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Diabetes & Primary Care Australia Vol 2 No 2 2017 The primary care diabetes journal for healthcare professionals in Australia Pre-gestational diabetes in pregnancy This issue includes guidance on how to optimise pregnancy outcomes through pre-conception care and the resources available for mothers with pre-gestational diabetes and healthcare professionals who care for them. E-learning on pre-conception care for women with pre-gestational diabetes is available at www.pcdsa.au.org/cpd. Page 54 IN THIS ISSUE Bone health The relationship between diabetes and bone health, and the impact of poor bone health on patients. Page 61 Preventing falls A clinical review of the screening, assessment and management of older people at risk of falls. Page 69 Diabetes and skin Considering the skin of people with diabetes and the importance of skin care before and after ulceration. Page 75 WEBSITE Journal content online at www.pcdsa.com.au/journal

Diabetes<br />

& Primary Care Australia<br />

Vol 2 No 2 2017<br />

The primary care diabetes journal for healthcare professionals in Australia<br />

Pre-gestational diabetes in pregnancy<br />

This <strong>issue</strong> includes guidance on how<br />

to optimise pregnancy outcomes<br />

through pre-conception care and the<br />

resources available for mothers with<br />

pre-gestational diabetes and healthcare<br />

professionals who care for them.<br />

E-learning on pre-conception care for<br />

women with pre-gestational diabetes is<br />

available at www.pcdsa.au.org/cpd.<br />

Page 54<br />

IN THIS ISSUE<br />

Bone health<br />

The relationship between<br />

diabetes and bone health,<br />

and the impact of poor bone<br />

health on patients. Page 61<br />

Preventing falls<br />

A clinical review of the<br />

screening, assessment and<br />

management of older people<br />

at risk of falls. Page 69<br />

Diabetes and skin<br />

Considering the skin of<br />

people with diabetes and the<br />

importance of skin care before<br />

and after ulceration. Page 75<br />

WEBSITE<br />

Journal content online at<br />

www.pcdsa.com.au/journal


The PCDSA is a multidisciplinary society with the aim<br />

of supporting primary health care professionals to deliver<br />

high quality, clinically effective care in order to improve<br />

the lives of people with diabetes.<br />

The PCDSA will<br />

Share best practice in delivering quality diabetes care.<br />

Provide high-quality education tailored to health professional needs.<br />

Promote and participate in high quality research in diabetes.<br />

Disseminate up-to-date, evidence-based information to health<br />

professionals.<br />

Form partnerships and collaborate with other diabetes related,<br />

high level professional organisations committed to the care of<br />

people with diabetes.<br />

Promote co-ordinated and timely interdisciplinary care.<br />

Membership of the PCDSA is free and members get access to a quarterly<br />

online journal and continuing professional development activities. Our first<br />

annual conference will feature internationally and nationally regarded experts<br />

in the field of diabetes.<br />

To register, visit our website:<br />

www.pcdsa.com.au


Contents<br />

Diabetes<br />

& Primary Care Australia<br />

Volume 2 No 2 2017<br />

Website: www.pcdsa.com.au/journal<br />

Editorial<br />

Diabetes and pregnancy 45<br />

Rajna Ogrin introduces this <strong>issue</strong>, which has a focus on pregnancy and pre-conception care for women with pre-gestational diabetes.<br />

From the other side of the desk<br />

Through diagnosis to pregnancy: My journey with diabetes 47<br />

Karen Barrett gives a first-hand perspective on her journey with diabetes and how it affected her pregnancies.<br />

CPD module<br />

Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care 54<br />

Glynis Ross provides guidance to support pre-conception care for women with pre-gestational diabetes.<br />

Articles<br />

Resources to support preconception care for women with diabetes 50<br />

Melinda Morrison, Ralph Audehm, Alison Barry and colleagues describe the resources available for health professionals and women with<br />

diabetes and provide up-to-date, evidence-based information on pregnancy and diabetes.<br />

Diabetes and bone health 61<br />

Vidhya Jahagirdar and Neil J Gittoes explore the current literature on diabetes and bone health, its impact on patients and the management<br />

strategies that may be considered in primary care to minimise risk of diabetes-related bone disease and to improve outcomes.<br />

Falls prevention in older adults with diabetes: A clinical review of screening, assessment and management recommendations 69<br />

Anna Chapman and Claudia Meyer review the screening, assessment and management recommendations for fall prevention in older people.<br />

The effect of diabetes on the skin before and after ulceration 75<br />

Roy Rasalam and Lesley Weaving look at the changes that occur in the skin of people with diabetes and the importance of skin care in<br />

relation to ulceration.<br />

Editor-in-Chief<br />

Rajna Ogrin<br />

Senior Research Fellow, RDNS<br />

Institute, St Kilda, Vic<br />

Associate Editor<br />

Gary Kilov<br />

Practice Principal, The Seaport<br />

Practice, and Senior Lecturer,<br />

University of Tasmania,<br />

Launceston, Tas<br />

Editorial Board<br />

Ralph Audehm<br />

GP Director, Dianella Community<br />

Health, and Associate Professor,<br />

University of Melbourne,<br />

Melbourne, Vic<br />

Werner Bischof<br />

Periodontist, and Associate<br />

Professor, LaTrobe University,<br />

Bendigo, Vic<br />

Jessica Browne<br />

Senior Research Fellow, The<br />

Australian Centre for Behavioural<br />

Research in Diabetes, Deakin<br />

University, Melbourne, Vic<br />

Anna Chapman<br />

Research Fellow, RDNS Institute,<br />

St Kilda, Vic<br />

Laura Dean<br />

Course Director of the Graduate<br />

Certificate in Pharmacy<br />

Practice, Monash University, Vic<br />

Nicholas Forgione<br />

Principal, Trigg Health Care<br />

Centre, Perth, WA<br />

John Furler<br />

Principal Research Fellow and<br />

Associate Professor,<br />

University of Melbourne, Vic<br />

Mark Kennedy<br />

Medical Director, Northern Bay<br />

Health, Geelong, and Honorary<br />

Clinical Associate Professor,<br />

University of Melbourne,<br />

Melbourne, Vic<br />

Peter Lazzarini<br />

Senior Research Fellow,<br />

Queensland University of<br />

Technology, Brisbane, Qld<br />

Roy Rasalam<br />

Head of Clinical Skills and<br />

Medical Director,<br />

James Cook University, and<br />

Clinical Researcher, Townsville<br />

Hospital, Townsville, Qld<br />

Suzane Ryan<br />

Practice Principal, Newcastle<br />

Family Practice, Newcastle, NSW<br />

Editor<br />

Olivia Tamburello<br />

Editorial Manager<br />

Richard Owen<br />

Publisher<br />

Simon Breed<br />

© OmniaMed SB and the Primary Care<br />

Diabetes Society of Australia<br />

Published by OmniaMed SB,<br />

1–2 Hatfields, London<br />

SE1 9PG, UK<br />

All rights reserved. No part of this<br />

journal may be reproduced or transmitted<br />

in any form, by any means, electronic<br />

or mechanic, including photocopying,<br />

recording or any information retrieval<br />

system, without the publisher’s<br />

permission.<br />

ISSN 2397-2254<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 43


Call for papers<br />

Would you like to write an article<br />

for Diabetes & Primary Care Australia?<br />

The new journal from the Primary Care Diabetes Society of Australia<br />

To submit an article or if you have any queries, please contact: gary.kilov@pcdsa.com.au.<br />

Title page<br />

Please include the article title, the full names of the authors<br />

and their institutional affiliations, as well as full details of<br />

each author’s current appointment. This page should also have<br />

the name, address and contact telephone number(s) of the<br />

corresponding author.<br />

Article points and key words<br />

Four or five sentences of 15–20 words that summarise the major<br />

themes of the article. Please also provide four or five key words<br />

that highlight the content of the article.<br />

Abstract<br />

Approximately 150 words briefly introducing your article,<br />

outlining the discussion points and main conclusions.<br />

Introduction<br />

In 60–120 words, this should aim to draw the reader into the<br />

article as well as broadly stating what the article is about.<br />

Main body<br />

Use sub-headings liberally and apply formatting to differentiate<br />

between heading levels (you may have up to three heading levels).<br />

The article must have a conclusion, which should be succinct and<br />

logically ordered, ideally identifying gaps in present knowledge and<br />

implications for practice, as well as suggesting future initiatives.<br />

Tables and illustrations<br />

Tables and figures – particularly photographs – are encouraged<br />

wherever appropriate. Figures and tables should be numbered<br />

consecutively in the order of their first citation in the text. Present<br />

tables at the end of the articles; supply figures as logically labelled<br />

separate files. If a figure or table has been published previously,<br />

acknowledge the original source and submit written permission<br />

from the copyright holder to reproduce the material.<br />

References<br />

In the text<br />

Use the name and year (Harvard) system for references in the<br />

text, as exemplified by the following:<br />

● As Smith and Jones (2013) have shown …<br />

● As already reported (Smith and Jones, 2013) …<br />

For three or more authors, give the first author’s surname<br />

followed by et al:<br />

● As Robson et al (2015) have shown …<br />

Simultaneous references should be ordered chronologically first,<br />

and then alphabetically:<br />

● (Smith and Jones, 2013; Young, 2013; Black, 2014).<br />

Statements based on a personal communication should be<br />

indicated as such, with the name of the person and the year.<br />

In the reference list<br />

The total number of references should not exceed 30 without prior<br />

discussion with the Editor. Arrange references alphabetically first,<br />

and then chronologically. Give the surnames and initials of all<br />

authors for references with four or fewer authors; for five or more,<br />

give the first three and add “et al”. Papers accepted but not yet<br />

published may be included in the reference list as being “[In press]”.<br />

Journal article example: Robson R, Seed J, Khan E et al (2015)<br />

Diabetes in childhood. Diabetes Journal 9: 119–23<br />

Whole book example: White F, Moore B (2014) Childhood<br />

Diabetes. Academic Press, Melbourne<br />

Book chapter example: Fisher M (2012) The role of age. In: Merson<br />

A, Kriek U (eds). Diabetes in Children. 2nd edn. Academic Press,<br />

Melbourne: 15–32<br />

Document on website example: Department of Health (2009)<br />

Australian type 2 diabetes risk assessment tool (AUSDRISK).<br />

Australian Government, Canberra. Available at: http://www.<br />

health.gov.au/preventionoftype2diabetes (accessed 22.07.15)<br />

Article types<br />

Articles may fall into the categories below. All articles should be<br />

1700–2300 words in length and written with consideration of<br />

the journal’s readership (general practitioners, practice nurses,<br />

prescribing advisers and other healthcare professionals with an<br />

interest in primary care diabetes).<br />

Clinical reviews should present a balanced consideration of a<br />

particular clinical area, covering the evidence that exists. The<br />

relevance to practice should be highlighted where appropriate.<br />

Original research articles should be presented with sections<br />

for the background, aims, methods, results, discussion and<br />

conclusion. The discussion should consider the implications<br />

for practice.<br />

Clinical guideline articles should appraise newly published<br />

clinical guidelines and assess how they will sit alongside<br />

existing guidelines and impact on the management of diabetes.<br />

Organisational articles could provide information on newly<br />

published organisational guidelines or explain how a particular<br />

local service has been organised to benefit people with diabetes.<br />

— Diabetes & Primary Care Australia —


Editorial<br />

Diabetes and pregnancy<br />

It is well known that diabetes is a systemic<br />

condition and, if not managed efficiently,<br />

can have a life-changing impact on the eyes,<br />

feet and kidneys. In this <strong>issue</strong>, we consider<br />

the impact of uncontrolled hyperglycaemia on<br />

other body systems and functions – from skin<br />

to bone, and from pregnancy to older age. On<br />

page 75, Roy Rasalam and Lesley Weaving<br />

discuss the practical aspects of maintaining<br />

healthy skin in people with diabetes, and<br />

Neil Gittoes and Vidhya Jahagirdar provide a<br />

clinical review of the potential complications<br />

to bone health as a result of diabetes (page 61).<br />

There is a special section on diabetes and<br />

pregnancy covering preconception care in<br />

primary care and the resources available<br />

for women with diabetes and health care<br />

professionals (starting from page 47). Finally,<br />

there is a paper by Anna Chapman and<br />

Claudia Meyer on the increased risk of falls<br />

in older people with diabetes and what can be<br />

done to lower the risk (page 69). This topic is<br />

especially pertinent with the growing ageing<br />

population seen in Australia and globally.<br />

Diabetes and pregnancy<br />

One relatively new area of research in<br />

diabetes and pregnancy that has caught my<br />

eye is epigenetics – the effect of environment<br />

on genetics. Questions are being raised<br />

as to whether the maternal environment<br />

(e.g. maternal obesity, poor nutrition and<br />

hyperglycaemia) may “program” type 2<br />

diabetes in offspring. There is some evidence<br />

that suggests that shared genetic and<br />

environmental risk, as well as developmental<br />

programming, may lead to children born to<br />

women with diabetes during pregnancy at<br />

greater risk of developing type 2 diabetes in<br />

later life (Berends and Ozanne, 2012). If the<br />

female offspring then have their own children,<br />

it is thought that an intergenerational<br />

cycle of diabetes risk could be established<br />

(Dabelea and Crume, 2011). The intricacies<br />

of this are important to understand, as many<br />

women with pre-existing type 2 diabetes<br />

are often overweight or obese. They often<br />

continue to gain weight with each additional<br />

pregnancy and are sometimes reluctant to<br />

engage with health services (Bandyopadhyay<br />

et al, 2011). Women of South East Asian<br />

origin are at particularly high risk of diabetes<br />

during pregnancy, so by developing effective<br />

strategies to specifically address these factors,<br />

the risk of future diabetes to offspring may be<br />

reduced (Greenhalgh et al, 2015).<br />

What other considerations need to be<br />

made to avoid the increased risk of adverse<br />

pregnancy outcomes as a result of diabetes?<br />

Pre-gestational diabetes (type 1 and<br />

type 2 diabetes) is present in approximately<br />

1% of pregnant women in Australia and the<br />

prevalence is increasing not only here, but<br />

around the world. Women with pre-existing<br />

diabetes are at high risk of complications<br />

during pregnancy, with up to four times<br />

the rate of congenital malformations, and<br />

up to a five-fold increased risk of stillbirth<br />

and perinatal mortality compared to women<br />

without diabetes. By safely optimising blood<br />

glucose management, women can significantly<br />

reduce their risk of complications, and<br />

preconception care has been shown to reduce<br />

these risks (Inkster et al, 2006).<br />

Women of child-bearing age with diabetes<br />

need to be informed of the availability and<br />

importance of preconception care, which<br />

can be provided by both primary and<br />

specialised diabetes services; many women<br />

with type 1 diabetes access diabetes specialist<br />

services, while the majority of women with<br />

type 2 diabetes are managed in primary care.<br />

Included in preconception care is appropriate<br />

contraception advice. Here, primary care<br />

providers can make a real difference in<br />

promoting and providing appropriate<br />

contraception to women with diabetes to<br />

prevent unplanned pregnancies.<br />

In this pregnancy special, there are three<br />

pieces related to pregnancy and diabetes. There<br />

is a CPD module outlining the requirements<br />

of preconception care for women with<br />

Rajna Ogrin<br />

Editor of Diabetes & Primary Care<br />

Australia, and Senior Research<br />

Fellow, RDNS Institute,<br />

St Kilda, Vic.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 45


Editorial<br />

“By considering the<br />

health and wellbeing of<br />

women with diabetes<br />

prior to pregnancy,<br />

we anticipate<br />

that meaningful<br />

improvements in<br />

pregnancy outcomes<br />

are possible.”<br />

diabetes, including practical information for<br />

health care providers, as well as case studies to<br />

highlight the application of this information<br />

in clinical practice (page 54). There is also<br />

a wealth of resources for the clinician and<br />

woman with diabetes to optimise healthy<br />

pregnancy outcomes. Melinda Morrison from<br />

the National Diabetes Services Scheme and<br />

colleagues outline the resources available,<br />

such as apps, booklets and online resources<br />

(page 50). We also have the first “From<br />

the other side of the desk” feature – a<br />

new series to inform clinical care from the<br />

perspectives of people with diabetes. In the<br />

first of the series, Karen Barrett discusses her<br />

journey with diabetes and how it affected her<br />

pregnancies (page 47).<br />

By considering the health and wellbeing<br />

of women with diabetes prior to pregnancy,<br />

and utilising the resources that have been<br />

developed specifically to support this group<br />

before, during and after pregnancy, we<br />

anticipate that meaningful improvements in<br />

pregnancy outcomes are possible. n<br />

2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

pcdsa.com.au<br />

Bandyopadhyay M, Small R, Davey MA et al (2011) Lived<br />

experience of gestational diabetes mellitus among immigrant<br />

South Asian women in Australia. Aust N Z J Obstet Gynaecol<br />

51: 360–4<br />

Berends LM, Ozanne SE (2012) Early determinants of type 2<br />

diabetes. Best Pract Res Clin Endocrinol Metab 26: 569–80<br />

Dabelea D, Crume T (2011) Maternal environment and the<br />

transgenerational cycle of obesity and diabetes. Diabetes 60:<br />

1849–55<br />

Greenhalgh T, Clinch M, Afsar N et al (2015) Socio-cultural<br />

influences on the behaviour of South Asian women with<br />

diabetes in pregnancy: qualitative study using a multi-level<br />

theoretical approach. BMC Med 13: 120<br />

Inkster ME, Fahey TP, Donnan PT et al (2006) Poor glycated<br />

haemoglobin control and adverse pregnancy outcomes in<br />

type 1 and type 2 diabetes mellitus: Systematic review of<br />

observational studies BMC Pregnancy Childbirth 6: 30<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017


From the other side of the desk<br />

From the other side of the desk:<br />

Patient perspective<br />

Through diagnosis to pregnancy:<br />

My journey with diabetes<br />

Karen Barrett<br />

I<br />

was diagnosed with type 1 diabetes on Valentine’s<br />

Day, 1983, a day meant for chocolates, roses<br />

and sweets. What an irony it turned out to be.<br />

Dressed in my school uniform and ready for school,<br />

my Mum, being a nurse, had known for some time<br />

that something wasn’t right. I had lost a substantial<br />

amount of weight and the bathroom seemed to<br />

be my best friend, as did my unquenchable thirst.<br />

“Oh what a bombshell!” my Mum’s colleague said<br />

that day after hearing my diagnosis. I never really<br />

comprehended the significance of the diagnosis at<br />

the time. I had felt fine.<br />

In the early days after my diagnosis, to see my<br />

diabetes specialist meant a day off school and a trip<br />

to Canberra – that was the good part. The not-sogood<br />

part became the endless questions from the<br />

doctor – what was I putting in my mouth and at<br />

exactly what time of the day – measurements on the<br />

scales, numbers in books, pathology results and eye<br />

tests. On and on it went. Would I pass or fail? Had<br />

I been good or bad? I hated it.<br />

There was never a time that I let my diabetes<br />

stand in the way. I was quite sporty growing up<br />

in a small country town, later trying triathlons<br />

and endurance sports. But in my school life, I was<br />

sometimes left out, missing the first school camp<br />

because everyone was so very nervous to have a<br />

person with diabetes at camp and friends’ parents<br />

being reluctant to have me over, afraid of what or<br />

what not to feed me.<br />

As an adolescent, I was studious and quite fit and<br />

healthy, with an obsessive personality. That was<br />

until my late teens, when I seemed to burn out with<br />

school, with life and with diabetes. Life became<br />

tricky. I found solace in food and subsequently paid<br />

the price, gaining weight.<br />

My family, of course, was concerned, but the<br />

constant questions about how many blood sugar<br />

tests I was doing and whether I was looking after<br />

myself was a continuous reminder of my diabetes,<br />

something I wanted to forget. I ate in secret and lied<br />

to keep them satisfied while continuing to silently<br />

struggle. I was tired of all the rules, tired of all the<br />

questions and tired of being different and feeling<br />

restricted. As I entered adulthood, I thought I kept<br />

my struggles well hidden from others for many<br />

years. I went on to study nursing at university and<br />

the big wide world gave me even more freedom<br />

to hide from the reality of diabetes. Somehow,<br />

I stayed on the tightrope of avoiding routine<br />

doctor’s appointments while also avoiding more<br />

serious hospital admissions. A visit to the doctor<br />

would mean tests, which I knew I would fail, and<br />

questions that I would be ashamed to answer – I<br />

wasn’t up for the interrogations and judgements.<br />

But, I didn’t feel like I was failing! I was eating what<br />

I wanted, when I wanted, and being like the rest of<br />

my friends and peers.<br />

Time to get real<br />

Then I found out I was pregnant…unplanned.<br />

For me, I realised it was not fair to have a child,<br />

with the high risk of complications to me and my<br />

baby as a result of me not looking after myself.<br />

A decision, that I feel to this day, even though I<br />

agreed, had already been made for me. Time to get<br />

real. If I was to ever create a family of my own, it<br />

meant facing the <strong>issue</strong>s I had so long avoided – the<br />

medical world testing me on passing or failing at<br />

diabetes.<br />

Unable, and not allowing myself, to be anything<br />

other than perfectly controlled, I became a<br />

Citation: Barrett K (2017) Through<br />

diagnosis to pregnancy: My journey<br />

with diabetes. Diabetes & Primary<br />

Care Australia 1: 47–8<br />

About this series<br />

The aim of the “From the other<br />

side of the desk” series is to<br />

provide a patient perspective on<br />

a topic within diabetes, to reflect<br />

on the doctor–patient relationship<br />

and to inform clinical care.<br />

Author<br />

Karen Barrett, Registered Nurse<br />

and Coordinator, Central Coast,<br />

NSW.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 47


From the other side of the desk<br />

“As a person with<br />

diabetes, my advice<br />

to the medical world<br />

would be to consider<br />

the person in front<br />

of you without their<br />

diabetes diagnosis.”<br />

champion of the tests. It was an intense time but<br />

my motivation to have healthy babies drove me<br />

to that perfection, and I went on to have three<br />

babies in 3 years. I told the medical team what they<br />

wanted to hear, but this time I wasn’t lying.<br />

It became my obsession to get the numbers<br />

right. Averaging about 12–14 blood sugars daily<br />

and the never-ending specialist appointments were<br />

vital to achieving the desired outcome. I was lucky<br />

that the care I received from my diabetes team<br />

during my pregnancies was excellent and well<br />

planned. I feel that it is vital to have a trusting<br />

relationship with an endocrinologist before, during<br />

and after pregnancies, and I was very fortunate<br />

to have that. But pregnancy with diabetes is not<br />

without its difficulties; the severe hypos during the<br />

first trimesters became frequent and increasingly<br />

exhausting, and with every pregnancy, I had<br />

another toddler to care for. My first-born was<br />

diagnosed with cerebral palsy (totally unrelated<br />

to my diabetes), and as if that was not sufficiently<br />

challenging, I became a single Mum when my<br />

youngest was 11 months old. Juggling three<br />

toddlers, a part-time job to survive financially and<br />

my diabetes became routine. The all-or-nothing<br />

personality has some advantages and in those<br />

3 years, I was switched to “all”, determined to be<br />

a good Mum.<br />

However, as the years went by, I let those<br />

numbers slip again. My three gorgeous children,<br />

my world, were growing up fast, and at aged 6, 7<br />

and 8 years, they kept me busy. I kept the medical<br />

team at length – I knew I wasn’t going to “pass the<br />

test”. My 7-year-old daughter, Presley, had spirit<br />

(sometimes too much!) and when she came down<br />

with a viral illness, as a mum with diabetes would,<br />

I checked her blood sugar. My Mum had suggested<br />

the “D” word as Presley kept sleeping through the<br />

day, which was very much unlike her. I still recall<br />

that moment, and I think I too knew something<br />

wasn’t right. Weeks later, Presley mentioned to me<br />

that she was waking through the night to go to the<br />

bathroom. I knew. I waited.<br />

My beautiful girl was dressed in her swimmers<br />

ready to go swimming. I did her blood sugar and<br />

there I was – the mother of a child with diabetes.<br />

Now it was me answering the questions not as a<br />

person with diabetes, but as a Mum. It was more<br />

than my own tests – I had to pass all of Presley’s<br />

tests as well.<br />

I felt my skills as a parent were put under the<br />

microscope. I believed it was all my fault if her<br />

numbers weren’t right. What was she eating when<br />

I wasn’t there? Was she exerting too much energy<br />

during lunchtime at school? Could she recognise<br />

a hypo? I felt like I had to live in her head, and<br />

I became the “helicopter” Mum. Presley too<br />

hated the medical world, clamming up at all the<br />

questions and hating the scales and numbers. At<br />

home, she dealt with the never-ending motherly<br />

concerns and requests to check her blood sugar,<br />

blaming every ailment or headache on diabetes,<br />

whether or not it was.<br />

Where I am now<br />

Despite some complications of my own, at 44 years<br />

of age, I now take care of myself and feel as well as<br />

I can feel, given my past “bad behaviour”. I have<br />

a good relationship with my team and appreciate<br />

the rapport I have with them, which has taken<br />

many years to establish and develop. I now take<br />

charge of my appointments and we talk about the<br />

concerns I have. The first questions asked are not<br />

“shall we look at the numbers?” or “how many<br />

highs/lows are you having?”; rather, “how are you,<br />

and what’s going on in your world?”<br />

I have had a lovely relationship with my<br />

psychologist who somehow allows me to be proud<br />

of who I am and what I have achieved. I am now<br />

free of the judgement calls that I thought were<br />

placed on me as a person with diabetes and then<br />

as the mother of a child with diabetes. Mistakes<br />

are human. Rough patches enable us all to make<br />

better choices, and experience allows us to call the<br />

shots. It’s OK not to be perfect. I truly hope that<br />

if anything, I can pass this on to my children and<br />

that they reach this point a whole lot sooner than<br />

I did.<br />

As a person with diabetes, my advice to the<br />

medical world would be to consider the person<br />

in front of you without their diabetes diagnosis.<br />

Diabetes management is far more than looking<br />

at the numbers. Consider their state of mind<br />

and the unsaid pressures they may have put on<br />

themselves. The bravest thing one can do is to ask<br />

for help and say that we’re not OK, and creating<br />

an environment where people with diabetes feel<br />

comfortable and safe to do so is vital. n<br />

48 Diabetes & Primary Care Australia Vol 2 No 2 2017


2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

<br />

<br />

<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

pcdsa.com.au


Article<br />

Resources to support preconception care<br />

for women with diabetes<br />

Citation: Morrison M, Audehm R,<br />

Barry A et al (2017) Resources to<br />

support preconception care for<br />

women with diabetes. Diabetes &<br />

Primary Care Australia 2: 50–3<br />

Article points<br />

1. Women with diabetes are<br />

at increased risk of adverse<br />

pregnancy outcomes. Early<br />

intervention and planning<br />

can reduce the risks.<br />

2. Primary health care<br />

professionals have a key role<br />

in providing appropriate<br />

contraception to women with<br />

diabetes to prevent unplanned<br />

pregnancies, as well as<br />

encouraging optimal pregnancy<br />

planning and preparation.<br />

3. To address the gap in<br />

information for women with<br />

diabetes who are seeking<br />

or already accessing prepregnancy<br />

advice and<br />

care, Diabetes Australia<br />

has developed a suite of<br />

resources with funding<br />

through the National<br />

Diabetes Services Scheme.<br />

Key words<br />

– Diabetes in pregnancy<br />

– Education<br />

– Preconception care<br />

– Pregnancy<br />

– Resources<br />

– Type 1 diabetes<br />

– Type 2 diabetes<br />

Authors<br />

See page 53 for details.<br />

Melinda Morrison, Ralph Audehm, Alison Barry, Christel Hendrieckx,<br />

Alison Nankervis, Cynthia Porter, Renza Scibilia, Glynis P Ross<br />

Preconception care has been shown to reduce the rates of adverse pregnancy outcomes<br />

in women with pre-existing type 1 or type 2 diabetes. With an increasing prevalence of<br />

diabetes among women of child-bearing age, health professionals working in primary<br />

care have an important role in encouraging women with diabetes to plan and prepare<br />

for pregnancy. New resources, described here, are available for health professionals and<br />

women with diabetes and provide up to date, evidence-based information on pregnancy<br />

and diabetes.<br />

Pre-existing diabetes (type 1 or<br />

type 2 diabetes) is estimated to affect<br />

approximately 1% of pregnant women<br />

in Australia (Australian Institute of Health and<br />

Welfare, 2016), and evidence suggests that the<br />

prevalence is increasing (Abouzeid et al, 2014).<br />

In particular, the prevalence of type 2 diabetes in<br />

pregnant women is expected to increase as a result<br />

of older maternal age, high rates of obesity and an<br />

ethnically diverse population (Cheung et al, 2005;<br />

Temple and Murphy, 2010).<br />

Diabetes in pregnancy has many welldocumented<br />

risks to both mother and baby<br />

(Macintosh et al, 2006; Dunne et al, 2009;<br />

Kitzmiller et al, 2010); however, these risks can<br />

be mitigated by effective preconception and<br />

pregnancy care, and most women with diabetes<br />

will go on to have a healthy pregnancy and a<br />

healthy baby (Ray et al, 2001; Wahabi et al, 2010;<br />

Holmes et al, 2017).<br />

While most women with type 1 diabetes access<br />

specialist services, the majority of women with<br />

type 2 diabetes are managed in primary care.<br />

Health professionals in primary care are often the<br />

first point of contact for women seeking pregnancy<br />

information, and have a key role in promoting and<br />

providing appropriate contraception to women<br />

with pre-existing diabetes to prevent unplanned<br />

pregnancies, and in specialist referral. They are<br />

also critically important in encouraging diabetesspecific<br />

preconception care in all women with<br />

pre-existing diabetes to optimise maternal and<br />

fetal outcomes (Temple and Murphy, 2010). In<br />

the National Diabetes Services Scheme (NDSS)*<br />

Contraception, Pregnancy & Women’s Health<br />

Survey (2015) women with type 1 or type 2<br />

diabetes (n=967) indicated that diabetes specialists<br />

(endocrinologists and diabetes educators) and<br />

general practitioners were the health professionals<br />

with whom pregnancy and diabetes was most<br />

frequently discussed. Interestingly, the majority<br />

of women reported that they, rather than health<br />

professionals, initiated the conversation about<br />

pregnancy and diabetes.<br />

Preconception care in the primary<br />

health setting<br />

Despite the documented benefits of preconception<br />

care for women with pre-existing diabetes (Ray<br />

et al, 2001; Wahabi et al, 2010), many women<br />

with diabetes do not plan their pregnancies. Zhu<br />

et al (2012) reported that 45% of pregnancies in<br />

women with diabetes attending a tertiary obstetric<br />

hospital in Western Australia during 2009–2010<br />

*The National Diabetes Services Scheme (NDSS) is an<br />

initiative of the Australian Government administered<br />

with the assistance of Diabetes Australia.<br />

50 Diabetes & Primary Care Australia Vol 2 No 2 2017


Resources to support preconception care for women with diabetes<br />

were unplanned. While in an earlier Australian<br />

multicentre study of pregnancies complicated<br />

by diabetes, pre-pregnancy counselling was<br />

documented in only 20% of women – 28% of<br />

those with type 1 diabetes and 12% of those with<br />

type 2 diabetes (McElduff et al, 2005).<br />

Planning for pregnancy<br />

The primary health care setting is where many<br />

women with diabetes seek advice on reproductive<br />

<strong>issue</strong>s and access contraception. However, in the<br />

NDSS Contraception, Pregnancy & Women’s<br />

Health Survey (2015) only 49% of Australian<br />

women with type 1 or type 2 diabetes could<br />

recall being advised by a health professional to<br />

use some form of contraception to prevent an<br />

unplanned pregnancy, and 55% could recall being<br />

advised by a health professional that they should<br />

access diabetes-specific pre-pregnancy care before<br />

becoming pregnant or planning a pregnancy.<br />

These results differed by type of diabetes, with<br />

those with type 2 diabetes being less likely to recall<br />

receiving advice. These findings are consistent<br />

with those reported in the TRIAD (Translating<br />

Research into Action for Diabetes) preconception<br />

study of US women aged 18–45 years enrolled<br />

in managed care (Kim et al, 2005). Of these<br />

women, 52% recalled discussions with a health<br />

professional regarding glucose control before<br />

conception, and 37% could recall receiving family<br />

planning advice.<br />

Due to the impact of an unplanned pregnancy<br />

on both the developing fetus and mother, adequate<br />

contraception should be maintained until<br />

glycaemia and all aspects of care are optimised.<br />

The longer-acting reversible contraceptives are an<br />

excellent choice (e.g. intrauterine contraceptive<br />

devices or implant) and are safe for women with<br />

diabetes to use. When reviewing contraception in<br />

women with diabetes, timing of pregnancy should<br />

be discussed. Preconception planning for women<br />

with diabetes should occur well before conception.<br />

If available, involvement of a specialist diabetes in<br />

pregnancy service is recommended.<br />

New NDSS resources to support<br />

preconception care<br />

To address the gap in information for<br />

women with diabetes who are seeking or<br />

already accessing pre-pregnancy advice<br />

and care, Diabetes Australia has developed<br />

a suite of resources with funding through<br />

the NDSS. These resources were developed<br />

following extensive consumer and stakeholder<br />

consultation, and provide up-to-date, evidencebased<br />

pregnancy information for women living<br />

with type 1 or type 2 diabetes. The NDSS<br />

resources available include the following:<br />

l www.pregnancyanddiabetes.com.au: A<br />

website dedicated to pregnancy and diabetes<br />

information.<br />

l Pregnancy planning checklist: A checklist<br />

to help women with diabetes prepare for a<br />

healthy pregnancy. The checklist can be<br />

completed as an online tool or downloaded<br />

as a printable checklist (Figure 1).<br />

l Having a Healthy Baby booklets: Booklets<br />

providing comprehensive information on<br />

planning and managing pregnancy. Separate<br />

booklets are available for women with<br />

type 1 or type 2 diabetes (Figure 2).<br />

l NDSS pregnancy and diabetes factsheet:<br />

Available for download in English, Arabic,<br />

Chinese, Vietnamese, Korean, Turkish,<br />

Urdu, Greek, Italian and Spanish.<br />

l Plan for the best start e-newsletter: A<br />

quarterly e-newsletter for women with<br />

diabetes and health professionals. It<br />

provides information on planning and<br />

preparing for pregnancy, and there is access<br />

to the latest NDSS resources and research<br />

updates.<br />

l Health professional continuing professional<br />

development learning: E-learning modules<br />

for primary health care providers on the<br />

topic of preconception care for women<br />

with type 1 or type 2 diabetes. The course<br />

includes three modules with two nonassessed<br />

case studies and can be accessed<br />

from the NDSS pregnancy and diabetes<br />

website. CPD points are available for<br />

eligible health professionals.<br />

These resources for patients and health<br />

care professionals can be accessed at<br />

www.pregnancyanddiabetes.com.au. Hard<br />

copies of the booklets can be ordered online or<br />

by phoning the NDSS Helpline (1300 136 588).<br />

Page points<br />

1. Due to the impact of an<br />

unplanned pregnancy on<br />

both the developing fetus and<br />

mother, adequate contraception<br />

should be maintained until<br />

glycaemia and all aspects of<br />

care are optimised.<br />

2. Preconception planning for<br />

women with diabetes should<br />

occur well before conception.<br />

3. Resources for patients and<br />

health care professionals<br />

can be accessed at www.<br />

pregnancyanddiabetes.com.au.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 51


Resources to support preconception care for women with diabetes<br />

Pregnancy Planning Checklist<br />

Plan and prepare at least 3-6 months before you start<br />

trying for a baby<br />

What you need to do BEFORE you fall pregnant<br />

Use contraception until you are ready to start trying for<br />

a baby (ask your doctor if this is the most reliable<br />

contraception suitable for you)<br />

Talk to your doctor for general pregnancy planning advice<br />

Make an appointment with health professionals who<br />

specialise in pregnancy and diabetes<br />

Aim for an HbA1c of less than 53mmol/mol (7%) if you<br />

have type 1 diabetes or 42mmol/mol (6%) or less if<br />

you have type 2 diabetes<br />

Review your diabetes management with your diabetes<br />

health professionals<br />

Have all your medications checked to see if they are<br />

safe to take during pregnancy<br />

Start taking a high-dose (2.5mg-5mg) folic acid<br />

supplement each day<br />

Have a full diabetes complications screening and<br />

your blood pressure checked<br />

Aim for a healthy weight before you fall pregnant<br />

For women<br />

with type 1<br />

or type 2<br />

diabetes<br />

Use this checklist as a guide to discuss with your health professionals<br />

www.pregnancyanddiabetes.com.au<br />

This checklist is intended as a guide only. It should not replace individual medical advice and if you have any<br />

concerns about your health or further questions, you should contact your health professional.<br />

The National Diabetes Services Scheme (NDSS) is an initiative of the Australian Government administered with the assistance of Diabetes Australia.<br />

Figure 1. Pregnancy planning checklist, to help women with diabetes<br />

prepare for a healthy pregnancy. Produced by the National Diabetes<br />

Service Scheme.<br />

Other resources<br />

The Australasian Diabetes in Pregnancy<br />

Society (ADIPS)-endorsed Pregnant<br />

with Diabetes app has been developed<br />

for pregnant women with diabetes, and<br />

women with diabetes who intend to<br />

become pregnant (Figure 3). It is written by<br />

Prof. Elisabeth R Mathiesen and Prof. Peter<br />

Damm and is based on the recommendations<br />

of the Centre for Pregnant Women with<br />

Diabetes at Rigshospitalet in Copenhagen,<br />

Denmark. The Australian version has been<br />

adapted by an Australian working party<br />

to reflect the ADIPS guidelines. The app<br />

can be downloaded from app stores free<br />

of charge. The information covered in the<br />

app is suitable for women with gestational,<br />

type 1 and type 2 diabetes and covers<br />

topics such as: how to plan for pregnancy,<br />

Figure 2. Booklets for women with type 1 and type 2<br />

diabetes. Produced by the National Diabetes Services<br />

Scheme.<br />

goal blood glucose levels, gestational weight<br />

gain, diet and carbohydrate intake, physical<br />

activity and insulin dosing.<br />

52 Diabetes & Primary Care Australia Vol 2 No 2 2017


Resources to support preconception care for women with diabetes<br />

National Development Program Expert<br />

Reference Group (2013–16). We acknowledge<br />

D. Charron-Prochownik for permission<br />

to reproduce questions from the RHAB<br />

questionnaire and V. Holmes for permission to<br />

use reproductive health knowledge questions<br />

in the NDSS Contraception, Pregnancy &<br />

Women’s Health Survey.<br />

Abouzeid M, Versace VL, Janus ED et al (2014) A population-based<br />

observational study of diabetes during pregnancy in Victoria,<br />

Australia, 1999–2008. BMJ Open 4: e005394<br />

Australian Institute of Health and Welfare (2016) Australia’s<br />

mothers and babies 2014-in brief. Perinatal statistics. AIHW,<br />

Canberra, ACT. Available at: http://www.aihw.gov.au/<br />

publication-detail/?id=60129557656 (accessed 14.03.17)<br />

“Primary care health<br />

professionals are<br />

also ideally placed to<br />

increase the awareness<br />

of women with<br />

diabetes about the<br />

available resources<br />

which are being<br />

actively reviewed and<br />

developed to meet<br />

their needs.”<br />

Cheung N, McElduff A, Ross G (2005) Type 2 diabetes in<br />

pregnancy: a wolf in sheep’s clothing. Aust N Z J Obstet<br />

Gynaecol 45: 479–83<br />

Figure 3. The Australasian Diabetes in Pregnancy<br />

Society (ADIPS)-endorsed Pregnant with Diabetes app.<br />

Conclusion<br />

Primary health care providers play an important<br />

role in promoting effective contraception use<br />

and encouraging women with pre-existing<br />

type 1 or type 2 diabetes to plan and prepare<br />

for pregnancy. They are also ideally placed to<br />

increase the awareness of women with diabetes<br />

about the available resources which are being<br />

actively reviewed and developed to meet their<br />

needs.<br />

n<br />

Acknowledgements<br />

The authors are grateful to the women who took<br />

part in the NDSS Contraception, Pregnancy<br />

& Women’s Health Survey, to the Australasian<br />

Diabetes in Pregnancy Society for approving the<br />

use of the image of the Pregnant with Diabetes<br />

app and to Effie Houvardas and Kaye Farrell,<br />

for their contribution to Diabetes in Pregnancy<br />

Dunne FP, Avalos G, Durkan M et al (2009) ATLANTIC DIP:<br />

pregnancy outcome for women with pregestational diabetes<br />

along the Irish Atlantic seaboard. Diabetes Care 32: 1205–6<br />

Holmes VA, Hamill, LL, Alderdice FA et al (2017) Effect of<br />

implementation of a preconception counselling resource for<br />

women with diabetes: A population based study. Primary Care<br />

Diabetes 11: 37–45<br />

Kim C, Ferrara A, McEwan LN et al (2005) Preconception care in<br />

managed care: the translating research into action for diabetes<br />

study. Am J Obstet Gynecol 192: 227–32<br />

Kitzmiller JL, Wallerstein R, Correa A, Kwan S (2010)<br />

Preconception care for women with diabetes and prevention of<br />

major congenital malformations. Birth Defects Res A Clin Mol<br />

Teratol 88: 791–803<br />

Macintosh MC, Fleming KM, Bailey JA et al (2006) Perinatal<br />

mortality and congenital anomalies in babies of women with<br />

type 1 or type 2 diabetes in England, Wales, and Northern<br />

Ireland: population based study. BMJ 333: 177<br />

McElduff A, Ross GP, Lagstrom JA et al (2005) Pregestational<br />

diabetes and pregnancy: an Australian experience. Diabetes<br />

Care 28: 1260–1<br />

National Diabetes Services Scheme (2015) NDSS Diabetes<br />

in Pregnancy National Development Program, Registrant<br />

Consultation and Needs Assessment Report. NDSS, Canberra,<br />

ACT<br />

Ray JG, O’Brien TE, Chan WS (2001) Preconception care and the<br />

risk of congenital anomalies in the offspring of women with<br />

diabetes mellitus: a meta-analysis. QJM 94: 435–44<br />

Temple RC, Murphy H (2010) Type 2 diabetes in pregnancy - an<br />

increasing problem. Best Pract Res Clin Endocrinol Metab 24:<br />

591–603<br />

Wahabi HA, Alzeidan RA, Bawazeer GA et al (2010)<br />

Preconception care for diabetic women for improving maternal<br />

and fetal outcomes: a systematic review and meta-analysis.<br />

BMC Pregnancy Childbirth 10: 63<br />

Zhu H, Graham D, Teh RW, Hornbuckle J (2012) Utilisation of<br />

preconception care in women with pregestational diabetes in<br />

Western Australia. Aust N Z J Obstet Gynaecol 52: 593–6<br />

Authors<br />

Melinda Morrison, NDSS<br />

Diabetes in Pregnancy Priority<br />

Area Leader*, Diabetes, NSW,<br />

Glebe, NSW; Ralph Audehm,<br />

General Practitioner, Carlton<br />

Family Medical and Department<br />

of General Practice, University<br />

of Melbourne, Vic; Alison Barry,<br />

Credentialled Diabetes Educator<br />

and Midwife, Mater Mothers’<br />

Hospital, South Brisbane, Qld;<br />

Christel Hendrieckx, Senior<br />

Research Fellow, The Australian<br />

Centre for Behavioural Research<br />

in Diabetes, Deakin University,<br />

Geelong, Vic; Alison Nankervis,<br />

Senior Physician to the Diabetes<br />

Service, The Royal Women’s<br />

Hospital and Clinical Head,<br />

Diabetes, Royal Melbourne<br />

Hospital, Parkville, Vic; Cynthia<br />

Porter, Advanced Accredited<br />

Practising Dietitian/Credentialled<br />

Diabetes Educator, Geraldton<br />

Diabetes Clinic, Geraldton, WA;<br />

Renza Scibilia, Manager Type 1<br />

Diabetes and Consumer Voice,<br />

Diabetes Australia, Melbourne,<br />

Vic; Glynis P Ross, Visiting<br />

Endocrinologist, Royal Prince<br />

Alfred Hospital, Camperdown,<br />

NSW, and Senior Endocrinologist,<br />

Bankstown-Lidcombe Hospital,<br />

Bankstown, NSW.<br />

*Melinda Morrison is representing<br />

Diabetes Australia/National<br />

Diabetes Service Scheme.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 53


CPD module<br />

Optimising pregnancy outcomes for<br />

women with pre-gestational diabetes in<br />

primary health care<br />

Glynis P Ross<br />

Citation: Ross GP (2017) Optimising<br />

pregnancy outcomes for women<br />

with pre-gestational diabetes in<br />

primary health care. Diabetes &<br />

Primary Care Australia 2: 54–9<br />

Learning objectives<br />

After reading this article, the<br />

participant should be able to:<br />

1. Identify the increased<br />

risks of adverse pregnancy<br />

outcomes to mother and<br />

baby that are associated with<br />

pre-gestational diabetes.<br />

2. Describe the ideal<br />

preconception care<br />

consultation and the key<br />

elements of care that a pregnant<br />

woman with pre-existing<br />

diabetes should receive.<br />

3. Implement a checklist for<br />

preconception care for<br />

women with diabetes.<br />

Key words<br />

– Preconception care<br />

– Pre-gestational diabetes<br />

– Pregnancy<br />

– Type 1 diabetes<br />

– Type 2 diabetes<br />

Author<br />

Glynis P Ross, Visiting<br />

Endocrinologist, Royal Prince<br />

Alfred Hospital, Camperdown<br />

NSW, and Senior Endocrinologist,<br />

Bankstown-Lidcombe Hospital,<br />

Bankstown, NSW.<br />

Preconception care for women with pre-existing diabetes (type 1 or type 2) is critical to<br />

optimise pregnancy outcomes and reduce the risk of adverse outcomes, including miscarriage,<br />

congenital anomalies, hypertension, caesarean deliveries and perinatal mortality. Pregestational<br />

diabetes is present in approximately 1% of pregnant women in Australia, and the<br />

prevalence is increasing. Women with pre-gestational diabetes need to be informed on the<br />

availability and importance of preconception care, which can be provided by both primary<br />

care and specialised diabetes services. The key elements of preconception care for women<br />

with diabetes are outlined in this article with two case examples to illustrate.<br />

Women with pre-gestational type 1<br />

or type 2 diabetes are at high risk<br />

of complications during pregnancy<br />

and of adverse outcomes including miscarriage,<br />

congenital anomalies and perinatal mortality.<br />

Despite advances in diabetes management, rates<br />

of congenital anomalies are 2–4 times higher<br />

than that of the background population and<br />

there is a 3–5 fold increased risk of stillbirth<br />

and perinatal mortality for births to women<br />

with diabetes (Macintosh et al, 2006; Dunne et<br />

al, 2009; Kitzmiller et al, 2010). Data from the<br />

Australian Institute of Health and Welfare (2010)<br />

show that in 2005–2007, more than half of all<br />

Australian women with pre-gestational diabetes<br />

underwent caesarean delivery (59%; 71% type 1<br />

and 56% type 2 diabetes), compared to a third of<br />

women without diabetes. Following birth, 58%<br />

of infants born to women with diabetes were<br />

admitted to a special care nursery or neonatal<br />

intensive care unit, compared to 14% of babies<br />

born to mothers without diabetes.<br />

Glycaemic control in early pregnancy is strongly<br />

associated with the risk of adverse pregnancy<br />

outcomes (Nielsen et al, 2004; Guerin et al, 2007,<br />

Jensen et al, 2009). Research shows that for every<br />

10.93 mmol/mol (1%) increase in HbA 1c<br />

above<br />

53 mmol/mol (7%), there is a 5.5% increase in<br />

risk of adverse outcomes (Nielsen et al, 2004). The<br />

American Diabetes Association (2017) states that<br />

the lowest rates of adverse pregnancy outcomes<br />

are seen in association with an early gestation<br />

HbA 1c<br />

of 42–48 mmol/mol (6.0–6.5%).<br />

Preconception care for women with existing<br />

diabetes provides an opportunity to optimise<br />

glycaemic control, as well as other aspects of<br />

maternal health such as folic acid supplementation,<br />

diabetes complications screening and<br />

discontinuation of teratogenic medications prior<br />

to conception (McElduff et al, 2005; Mahmud<br />

and Mazza, 2010; Egan et al, 2015). Attendance<br />

at diabetes-specific preconception care has<br />

been associated with a reduction in congenital<br />

anomalies (relative risk [RR], 0.25), perinatal<br />

mortality (RR, 0.35) and reduced first trimester<br />

HbA 1c<br />

by an average of 26 mmol/mol (2.4%;<br />

Wahabi et al, 2010).<br />

Advice<br />

Preconception planning and assessment is<br />

recommended for all women considering<br />

pregnancy, but it is particularly important for<br />

women with diabetes or other medical disorders.<br />

Primary health care providers are well placed to<br />

complete most of the preconception screening<br />

and risk assessment, and can facilitate many of<br />

54 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

the interventions and appropriate referrals that<br />

may be required. A checklist, such as below,<br />

may be useful when undertaking pre-pregnancy<br />

counselling.<br />

ADVICE AND CONSIDERATIONS<br />

FOR ALL WOMEN CONSIDERING<br />

PREGNANCY<br />

o Appropriate contraception until<br />

optimal situation for pregnancy.<br />

o Review ALL current medications<br />

and ensure they are safe and<br />

appropriate for pregnancy.<br />

o Check blood pressure.<br />

o (For women not known to<br />

have diabetes, assess risk,<br />

and test appropriately for<br />

abnormal glucose tolerance.)<br />

o Promote a healthy lifestyle<br />

with regard to diet, exercise<br />

and optimal weight – this is<br />

also advisable for partners!<br />

o Encourage smoking cessation.<br />

o Advise to cease alcohol intake.<br />

o Advise to stop any<br />

recreational drug use.<br />

o Reduce caffeine intake.<br />

o Dental check.<br />

o Complete breast check<br />

and pap smear.<br />

o Assess immunity to rubella<br />

and varicella zoster, and, if<br />

necessary, organise vaccinations<br />

with appropriate waiting<br />

periods before conception.<br />

o Consider vaccinations for<br />

influenza and whooping cough.<br />

o Commence folic acid 3 months<br />

prior to pregnancy at 0.5 mg daily<br />

(see below for dose adjustments<br />

for women with known diabetes).<br />

o Commence an iodine-containing<br />

supplement (unless active<br />

thyrotoxicosis is present).<br />

o Consider checking thyroid<br />

function, iron, B12 (especially if<br />

vegetarian or taking metformin)<br />

and vitamin D status (if at risk).<br />

ADDITIONAL ADVICE AND<br />

CONSIDERATIONS FOR WOMEN<br />

WITH PRE-GESTATIONAL DIABETES<br />

CONSIDERING PREGNANCY<br />

o Refer to a diabetes specialist<br />

or team if not already under<br />

their care for assessment.<br />

o Optimise glycaemic control<br />

o In type 1 diabetes, pre-pregnancy<br />

HbA 1c<br />

should ideally be<br />


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Page points<br />

1. Preconception care should be<br />

individualised.<br />

2. Women should be advised<br />

to continue to use effective<br />

contraception until the best<br />

possible conditions for a<br />

safe pregnancy and birth are<br />

achieved.<br />

3. Regular monitoring and<br />

recording of blood glucose<br />

levels during the preconception<br />

stage and pregnancy can be<br />

helpful in optimising pregnancy<br />

outcomes.<br />

Case studies<br />

Outlined on the following two pages are two case<br />

studies illustrating some of the considerations to<br />

address during the preconception period. Given<br />

the range of situations that may be encountered,<br />

all care needs to be individualised. Ideally, most<br />

women with diabetes should be assessed before<br />

conception by a diabetes specialist or team with<br />

expertise in diabetes and pregnancy. This is<br />

particularly important when there are diabetes<br />

complications or additional medical disorders.<br />

For women in rural and remote areas, review<br />

in a regional centre or via telehealth with a<br />

specialist centre may be an appropriate option.<br />

This is especially important for women with more<br />

complex situations such as type 1 diabetes, type 2<br />

diabetes requiring multiple medications, diabetes<br />

vascular complications and/or other vascular risk<br />

factors.<br />

Case 1<br />

Maria is a 41-year old woman and has come<br />

to see you for a pap smear. You last saw her<br />

4 months ago when she wanted a script for<br />

the oral contraceptive pill (OCP). On routine<br />

questioning when you are completing the<br />

pathology request for cervical cytology she says<br />

that she is considering having a break from the<br />

pill as she and her husband are thinking about<br />

having another baby.<br />

History<br />

Maria has two children aged 9 and 12 years.<br />

The first pregnancy was uncomplicated and she<br />

had spontaneous vaginal delivery at term. Her<br />

daughter weighed 3450 g and was breastfed<br />

for 12 months. Before her second pregnancy,<br />

Maria had gained 8 kg in weight and her BMI<br />

was 28 kg/m 2 . At 28 weeks during her second<br />

pregnancy, Maria was diagnosed with gestational<br />

diabetes. She was able to manage this with diet<br />

modification alone and had spontaneous vaginal<br />

delivery at 39 +3 weeks of a 3720 g son. He was<br />

also breastfed for 12 months.<br />

Three years ago (age 38 years), Maria’s<br />

weight had risen and her BMI was 31 kg/m 2<br />

(class 1 obesity range). Her fasting glucose was<br />

7.2 mmol/L and her HbA 1c<br />

was 49 mmol/mol<br />

(6.6%) and a diagnosis of type 2 diabetes was<br />

made. Initially she was treated with metformin<br />

XR 2 g daily. Despite the metformin and Maria<br />

trying to follow dietary guidelines, 4 months<br />

ago her HbA 1c<br />

was 62 mmol/mol (7.8%) and so<br />

empagliflozin was added to her regimen. She<br />

continued to struggle to find time to exercise.<br />

Maria has a strong family history of<br />

type 2 diabetes (both parents, her older brother<br />

and all grandparents) and hypertension (father<br />

and paternal grandmother). Her father had a<br />

myocardial infarct at the age of 39 years with<br />

subsequent stenting. For 7 years, Maria has also<br />

been treated for hypertension with telmisartan,<br />

and dyslipidaemia for which she is taking<br />

atorvastatin and fenofibrate. She and her husband<br />

smoke, but Maria has said she is trying to stop<br />

so is only smoking in the evenings after dinner.<br />

Discussion<br />

Maria has several factors that increase her<br />

risk of adverse pregnancy outcomes. She is of<br />

advanced maternal age, is obese, a smoker, and<br />

has type 2 diabetes, hypertension, dyslipidaemia<br />

and a family history of early-onset ischaemic<br />

heart disease.<br />

Her glycaemic control is not satisfactory for<br />

pregnancy, and although metformin can be<br />

continued during pregnancy, empagliflozin<br />

will need to be stopped and insulin therapy<br />

commenced and titrated. She will need to increase<br />

her blood glucose monitoring and recording of<br />

results, preferably including dietary information.<br />

Review with a dietitian, diabetes educator and<br />

preferably an exercise physiologist is advisable.<br />

She should be seen by a diabetes physician with<br />

expertise in diabetes and pregnancy.<br />

She has multiple vascular risk factors and is<br />

at a higher risk of developing pre-eclampsia in<br />

pregnancy. She should be appropriately counselled<br />

regarding smoking cessation. The medication she<br />

is on for hypertension needs to be changed and<br />

the lipid management will need to be stopped<br />

for pregnancy. As she has hypertension it would<br />

be preferable that she is also seen by a renal or<br />

obstetric medicine physician, especially if she<br />

fails to achieve blood pressure targets or if she<br />

has overt proteinuria. Given the multiple vascular<br />

risk factors, she should have a pre-pregnancy<br />

cardiac assessment.<br />

56 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Advice<br />

You advise Maria that she should stay on the<br />

OCP for the time being and that preconception<br />

planning is needed in view of her multiple medical<br />

conditions and medications. If she still wishes to<br />

become pregnant, she should commence highdose<br />

folic acid and have routine pre-pregnancy<br />

checks. If she conceives, her contraception choice<br />

should be reviewed following the pregnancy as it<br />

is not advisable for her to continue on the OCP<br />

given her age and vascular risk status.<br />

Case 2<br />

Jennifer has come to see you for a referral letter to<br />

her gynaecologist. She wants to have her intrauterine<br />

contraceptive device (IUCD) removed as she is<br />

keen to start a family. Jennifer is a 30-year-old<br />

woman who has had type 1 diabetes for 21 years.<br />

For the last 3 years, she has been using insulin<br />

pump therapy. Jennifer’s most recent HbA 1c<br />

of<br />

70 mmol/mol (8.6%) was higher than usual after a<br />

recent overseas holiday with her husband.<br />

History<br />

In her teens, Jennifer struggled with her diabetes<br />

control but in the past 5 years has been managing<br />

quite well. Her last episode of diabetic ketoacidosis<br />

was 18 months ago when there was a problem with<br />

insulin delivery through her pump. She has not<br />

had severe hypoglycaemia (requiring the assistance<br />

of another person) for 5 years and is using a<br />

continuous glucose monitoring system (CGMS)<br />

with predictive low-glucose suspend, as she knows<br />

that she does not reliably sense hypoglycaemia.<br />

Jennifer has diabetic retinopathy that has<br />

previously required laser photocoagulation.<br />

However, she has not had her eyes checked for<br />

about 2 years as she missed an appointment and<br />

did not find time to reschedule. She has overt<br />

proteinuria (0.5 g per day) and is on ramipril for<br />

nephroprotection. Her eGFR is 62 mL/min/1.73 m 2<br />

and she has previously been assessed for other<br />

causes of renal disease by a nephrologist. Her<br />

blood pressure and lipids are normal. She has<br />

a moderate degree of asymptomatic peripheral<br />

neuropathy with loss of distal sensation to light<br />

touch and vibration, as well as loss of ankle<br />

reflexes. She senses a monofilament and has had<br />

no diabetes-related foot complications.<br />

Discussion<br />

If conception is successful, this will be Jennifer’s<br />

first pregnancy. As she is on insulin pump therapy<br />

and uses a CGM device, she will already be under<br />

a specialist diabetes team. Her glycaemic control<br />

is sub-optimal and significantly increases her<br />

risk of adverse pregnancy outcomes, including<br />

miscarriage and congenital anomalies. Even<br />

though the recommended HbA 1c<br />

target for women<br />

with type 1 diabetes in the preconception stage is<br />

≤53 mmol/mol (7%), given her long duration<br />

of type 1 diabetes and poor hypoglycaemic<br />

awareness, it may not be safe to reduce her HbA 1c<br />

below 58 mmol/mol (7.5%) due to the increasing<br />

risk of severe hypoglycaemia at lower levels. She<br />

needs specific specialist assessment and advice<br />

regarding her HbA 1c<br />

as well as review of all<br />

aspects of her diabetes self-management (e.g. diet,<br />

exercise, BGL testing and recording, insulin pump<br />

settings review, pump management skills, driving<br />

considerations, and hypoglycaemia and diabetic<br />

ketoacidosis prevention and management).<br />

Jennifer also needs an urgent diabetes eye<br />

review. If there is active proliferative retinopathy or<br />

macular oedema she will need to delay pregnancy<br />

plans until the retinopathy has been treated and<br />

is stable. As she has overt proteinuria, she should<br />

be assessed pre-pregnancy by a renal or obstetric<br />

medicine physician who will be able to continue<br />

to manage her in pregnancy. Her risk of preeclampsia<br />

and poor fetal outcomes, including<br />

intrauterine growth restriction (IUGR), will be<br />

increased. Although she is not known to have<br />

autonomic neuropathy, she should be assessed for<br />

this by her diabetes specialist.<br />

Advice<br />

You advise Jennifer to not have the IUCD<br />

removed yet and that preconception planning is<br />

needed in view of her complex diabetes situation<br />

– especially her overall glycaemic control,<br />

nephropathy and retinopathy. You also ask her<br />

whether she has discussed pregnancy with her<br />

endocrinologist and check the date of her next<br />

scheduled appointment. Following diabetes<br />

complications assessment and optimising<br />

glycaemic management, Jennifer should<br />

commence high-dose folic acid and have routine<br />

pre-pregnancy checks.<br />

”If a woman has<br />

been diagnosed with<br />

retinopathy, it is<br />

important to ensure<br />

it has been treated<br />

and is stable prior to<br />

pregnancy.”<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 57


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

“Primary health<br />

care providers have<br />

critical roles to play<br />

in the assessment<br />

and management of<br />

contraception,<br />

pre-pregnancy<br />

assessment<br />

and care.”<br />

Conclusion<br />

Women of child-bearing age with pre-gestational<br />

type 1 or type 2 diabetes need to be counselled<br />

on the need for appropriate contraception at all<br />

times unless trying for pregnancy in the best<br />

possible circumstances to avoid adverse pregnancy<br />

outcomes. Most women with pre-gestational<br />

diabetes are able to have successful pregnancies.<br />

However, they are at much higher risk of having<br />

adverse pregnancy outcomes than women without<br />

diabetes (Macintosh et al, 2006; Dunne et al,<br />

2009). It has been shown that women who have<br />

had optimal pre-pregnancy care and best practice<br />

management of their diabetes, both before and<br />

throughout pregnancy, will have a substantially<br />

lower rate of adverse outcomes (Ray et al, 2001;<br />

Wahabi et al, 2010).<br />

Ideally, care should involve services that are<br />

specialised in diabetes in pregnancy. However,<br />

primary health care providers also have critical<br />

roles to play in the assessment and management of<br />

contraception, pre-pregnancy assessment and care,<br />

coordination of specialist services and ongoing<br />

support prior to, as well as throughout and<br />

following, the pregnancy. <br />

n<br />

Acknowledgement<br />

The author would like to acknowledge Melinda<br />

Morrison for assistance with article editing and<br />

referencing.<br />

American Diabetes Association (2017) Standards of Medical Care in<br />

Diabetes—2017. Diabetes Care 40(Suppl 1): S4–S5<br />

Australian Institute of Health and Welfare (2010) Diabetes in<br />

pregnancy: its impact on Australian women and their babies.<br />

AIHW, Canberra, ACT<br />

Dunne FP, Avalos G, Durkan M et al (2009) ATLANTIC DIP:<br />

pregnancy outcome for women with pregestational diabetes<br />

along the Irish Atlantic seaboard. Diabetes Care 32: 1205–6<br />

Egan, AM, Murphy HR, Dunne FP (2015) The management of type 1<br />

and type 2 diabetes in pregnancy. QJM: An International Journal<br />

of Medicine 108: 923–7<br />

Guerin A, Nisenbaum R, Ray JG (2007) Use of maternal GHb<br />

concentration to estimate the risk of congenital anomalies in the<br />

offspring of women with prepregnancy diabetes. Diabetes Care<br />

30: 1920–5<br />

Inkster ME, Fahey TP, Donnan PT et al (2006) Poor glycated<br />

haemoglobin control and adverse pregnancy outcomes in type 1<br />

and type 2 diabetes mellitus: Systematic review of observational<br />

studies. BMC Pregnancy Childbirth 6: 30<br />

Jensen DM, KorsholmL, Ovesen P et al (2009) Periconceptional A1C<br />

and risk of serious adverse pregnancy outcome in 933 women<br />

with type 1 diabetes. Diabetes Care 32: 1046–8<br />

Kitzmiller JL, Wallerstein R, Correa A, Kwan S (2010) Preconception<br />

care for women with diabetes and prevention of major congenital<br />

malformations. Birth Defects Res A Clin Mol Teratol 88: 791–803<br />

Macintosh MC, Fleming KM, Bailey JA et al (2006) Perinatal<br />

mortality and congenital anomalies in babies of women with<br />

type 1 or type 2 diabetes in England, Wales, and Northern<br />

Ireland: population based study. BMJ 333: 177<br />

Mahmud M, Mazza D (2010) Preconception care of women with<br />

diabetes: a review of current guideline recommendations. BMC<br />

Womens Health 10: 5<br />

McElduff A, Cheung NW, McIntyre HD et al (2005) The Australasian<br />

Diabetes in Pregnancy Society consensus guidelines for the<br />

management of type 1 and type 2 diabetes in relation to<br />

pregnancy. Med J Aust 183: 373–7<br />

Nielsen LR, Ekbom P, Damm P et al (2004) HbA1c levels are<br />

significantly lower in early and late pregnancy. Diabetes Care 27:<br />

1200–1<br />

Ray JG, O’Brien TE, Chan WS (2001) Preconception care and the risk<br />

of congenital anomalies in the offspring of women with diabetes<br />

mellitus: a meta-analysis. QJM 94: 435–44<br />

Wahabi HA, Alzeidan RA, Bawazeer GA et al (2010), Preconception<br />

care for diabetic women for improving maternal and fetal<br />

outcomes: a systematic review and meta-analysis. BMC<br />

Pregnancy Childbirth 10: 63<br />

58 Diabetes & Primary Care Australia Vol 2 No 2 2017


Optimising pregnancy outcomes for women with pre-gestational diabetes in primary health care<br />

Online CPD activity<br />

Visit www.pcdsa.com.au/cpd to record your answers and gain a certificate of participation<br />

Participants should read the preceding article before answering the multiple choice questions below. There is ONE correct answer to each question.<br />

After submitting your answers online, you will be immediately notified of your score. A pass mark of 70% is required to obtain a certificate of<br />

successful participation; however, it is possible to take the test a maximum of three times. A short explanation of the correct answer is provided.<br />

Before accessing your certificate, you will be given the opportunity to evaluate the activity and reflect on the module, stating how you will use what<br />

you have learnt in practice. The CPD centre keeps a record of your CPD activities and provides the option to add items to an action plan, which will<br />

help you to collate evidence for your annual appraisal.<br />

1. What percentage of pregnant women are<br />

affected by pre-gestational diabetes?<br />

Select ONE option only.<br />

A. 0.1%<br />

B. 1%<br />

C. 2.5%<br />

D. 5%<br />

E. 10%<br />

2. A woman with type 2 diabetes has an<br />

HbA 1c<br />

of 69 mmol/mol (8.5%) in early<br />

pregnancy. Which ONE of the following<br />

statements is NOT true?<br />

A. She is at increased risk of miscarriage.<br />

B. She is at increased risk of hypertension<br />

in late pregnancy.<br />

C. She is at increased risk of developing<br />

retinopathy in pregnancy.<br />

D. She will not have an increased risk of<br />

pregnancy complications unless she is<br />

obese.<br />

E. It is safe for her to continue taking<br />

metformin.<br />

3. A 31-year-old woman with type 2 diabetes<br />

has just found she is pregnant. She is<br />

currently being treated with gliclazide and<br />

metformin. Which of the following options<br />

is most appropriate? Choose ONE option<br />

only.<br />

A. Stop gliclazide immediately<br />

B. Continue gliclazide and metformin<br />

initially<br />

C. Check HbA 1c<br />

D. Start self-monitoring of blood glucose<br />

(finger-prick testing)<br />

E. B, C and D<br />

4. Attendance at diabetes-specific<br />

preconception care has been associated<br />

with which one of the following? Choose<br />

ONE option only.<br />

A. A reduction in congenital anomalies<br />

B. A reduction in perinatal mortality<br />

C. A reduction in first trimester HbA 1c<br />

D. A, B and C<br />

E. None of the above<br />

5. Rachel has long-standing type 1<br />

diabetes. Her most recent HbA 1c<br />

is<br />

70 mmol/mol (8.6%). She is keen to<br />

conceive soon. Which of the following<br />

statements is INCORRECT? Select ONE<br />

option only.<br />

A. She should avoid pregnancy until her<br />

HbA 1c<br />

is close to 53 mmol/mol (7%)<br />

while still minimising hypoglycaemia<br />

risk.<br />

B. She should start taking folic acid 5 mg<br />

daily at least 3 months before she starts<br />

trying to conceive.<br />

C. She should be referred to a specialist<br />

diabetes and pregnancy unit to<br />

optimise her diabetes management<br />

prior to conceiving.<br />

D. She should be advised to terminate the<br />

pregnancy if she falls pregnant before<br />

her HbA 1c<br />

has improved as risk to her<br />

and the fetus would be unacceptable.<br />

E. She should delay pregnancy plans if<br />

she has active retinopathy until it has<br />

been treated.<br />

6. A 43-year-old woman with type 2 diabetes<br />

is currently 6 weeks pregnant. She has<br />

a past medical history that includes<br />

pernicious anaemia, hypertension<br />

and hyperlipidaemia. Which of her<br />

medications, if any, should she now STOP?<br />

Choose ONE option only.<br />

A. Metformin<br />

B. Hydroxocobalamin 1 mg 3-monthly<br />

C. Labetalol 200 mg twice daily<br />

D. Simvastatin 20 mg daily<br />

E. None of the above<br />

7. Which of the following antidiabetes<br />

agents, if any, are SAFE to prescribe for<br />

a woman with type 2 diabetes planning<br />

pregnancy? Choose ONE option only.<br />

A. A sodium–glucose co-transporter 2<br />

(SGLT2) inhibitor<br />

B. A dipeptidyl peptidase-4 (DPP-4)<br />

inhibitor<br />

C. A glucagon-like peptide-1(GLP-1)<br />

receptor agonist<br />

D. Thiazolidinedione<br />

E. Insulin<br />

8. A 37-year-old woman with pre-gestational<br />

type 2 diabetes is advised to monitor<br />

her blood glucose levels as she has<br />

recently commenced insulin to control<br />

her diabetes. Which of the following<br />

is the most appropriate to monitor her<br />

glycaemia? Choose ONE option only.<br />

A. HbA 1c<br />

B. Self-monitoring of blood glucose<br />

(finger-prick testing)<br />

C. Fructosamine<br />

D. Continuous blood glucose monitoring<br />

E. A and B<br />

9. Which of the following insulins does not<br />

have regulatory approval for use during<br />

pregnancy? Select ONE option only.<br />

A. Insulin glulisine (Apidra ® )<br />

B. Protaphane/Humulin NPH<br />

C. Insulin detemir (Levemir ® )<br />

D. Insulin aspart (Novorapid ® )<br />

E. None of the above; they are all<br />

approved for use in pregnancy<br />

10. Ideally, what should the pre-pregnancy<br />

HbA 1c<br />

target for women with type 2<br />

diabetes be? Choose ONE option only.<br />

A.


2017 NATIONAL CONFERENCE<br />

Saturday 6th May 2017 – Melbourne Convention and Exhibition Centre, Victoria, Australia<br />

The conference has been specifically designed for all primary care health<br />

professionals working in diabetes care to:<br />

<br />

<br />

<br />

Advance their education and learning in the field of diabetes health care<br />

Promote best practice standards and clinically effective care in the management of diabetes<br />

Facilitate collaboration between health professionals to improve the quality of diabetes<br />

primary care across Australia<br />

6TH MAY 2017 CONFERENCE PROGRAM<br />

The 2017 PCDSA national conference program will combine cutting edge scientific content with<br />

practical clinical sessions, basing the education on much more than just knowing the guidelines.<br />

The distinguished panel of speakers will share their specialised experience in an environment<br />

conducive to optimal learning. The Speaking faculty include, amongst others:<br />

Associate Professor<br />

Neale Cohen<br />

Director Clinical Diabetes<br />

Baker Heart and<br />

Diabetes Institute<br />

“Diabetes management<br />

and research in primary<br />

care – key components<br />

to improving outcomes”<br />

Doctor Christel<br />

Hendrieckx<br />

Senior Research Fellow<br />

The Australian Centre<br />

for Behavioural Research<br />

in Diabetes<br />

“The emotional health of<br />

people living with diabetes”<br />

Ms Renza Scibilia<br />

Manager - Type 1 Diabetes<br />

and Consumer Voice<br />

Diabetes Australia<br />

“Engaging people with<br />

diabetes, the diabetes<br />

online community and<br />

apps for diabetes”<br />

Doctor Gautam<br />

Vaddadi<br />

Consultant Cardiologist<br />

Alfred Health, Northern Health,<br />

University of Melbourne<br />

“The emerging importance<br />

of cardiac failure diagnosis<br />

and management in people<br />

with type 2 diabetes”<br />

For further information including the full 2017 program<br />

and to register for the conference please visit:<br />

www.eventful.com.au/pcdsa2017<br />

If you have any questions regarding the conference,<br />

please contact the Conference Secretariat;<br />

Toll free telephone: 1800 898 499<br />

Email: pcdsa@eventful.com.au<br />

pcdsa.com.au


Article<br />

Diabetes and bone health<br />

Vidhya Jahagirdar, Neil J Gittoes<br />

Diabetes and osteoporosis represent two major public health challenges. Osteoporosis<br />

is characterised by decreased bone mineral density and micro-architectural changes of<br />

the bone leading to increased risk of low trauma (fragility) fractures. Both diabetes and<br />

osteoporosis are associated with significant morbidity, decreased quality of life and reduced<br />

life expectancy. This article will explore the current literature on the inter-relationships<br />

between diabetes and bone health, the impact on patients and the management strategies<br />

that may be considered in primary care to minimise risk of diabetes-related bone disease<br />

and improve outcomes.<br />

Preface<br />

Nick Forgione, General Practitioner, Trigg Health<br />

Care Centre, Perth, WA<br />

The connection between diabetes and<br />

osteoporosis is often overlooked in the<br />

busy management schedule of people<br />

with diabetes. However, there is an accumulation<br />

of evidence suggesting that type 2 diabetes may<br />

be an independent risk factor for osteoporosis.<br />

Despite the fact that bone mineral density<br />

(BMD) is often higher in people with<br />

type 2 diabetes compared to those without, it<br />

is paradoxical that people with type 2 diabetes<br />

have a higher risk of fracture. It is likely that the<br />

explanation for this paradox is multifactorial,<br />

including changes in trabecular bone,<br />

microarchitectural changes in bone leading<br />

to reduced bone strength and changes in the<br />

material property of bone due to accumulation<br />

of advanced glycation end products (AGEs).<br />

Medications used in the management of diabetes<br />

may also play a part.<br />

Diabetes and osteoporosis represent<br />

two major public health challenges.<br />

Osteoporosis is characterised by<br />

decreased bone mineral density (BMD) and<br />

micro-architectural changes of the bone leading<br />

to increased risk of low trauma or fragility<br />

fractures that are sustained as a result of a fall<br />

from standing height or less (Figure 1). Both<br />

There is much that remains unclear about<br />

people with diabetes-related osteoporosis.<br />

Assessment of fracture risk must be approached<br />

with caution as people with diabetes tend to<br />

have a higher fracture risk for a given BMD<br />

t-score compared to those without diabetes.<br />

Also it is unclear whether antiresorptive agents<br />

reduce fracture risk in type 2 diabetes to the<br />

same extent as those without diabetes (Rubin et<br />

al, 2013).<br />

As the number of people with type 2 diabetes<br />

increases and their life is extended through<br />

improvements in management, ensuring early<br />

detection and appropriate management of<br />

osteoporosis in this population becomes another<br />

priority for primary care management. Until<br />

there is further clarification of whether or not<br />

individuals with type 2 diabetes should be<br />

screened and managed differently to the rest<br />

of the population, it is important to at least<br />

ensure that the current RACGP guidelines for<br />

the detection and treatment of osteoporosis are<br />

followed.<br />

diabetes and osteoporosis are associated with<br />

significant morbidity, decreased quality of life<br />

and reduced life expectancy. In Australia, the<br />

total number of adults with diabetes is projected<br />

to rise to between 2 and 3 million by 2025<br />

(Magliano et al, 2009). Osteoporosis is also<br />

a condition that increases in prevalence with<br />

ageing (Figure 2). Age-related bone loss and<br />

Citation: Jahagirdar V, Gittoes NJ<br />

(2016) Diabetes and bone health.<br />

Diabetes & Primary Care Australia<br />

2: 61–8<br />

Article points<br />

1. Diabetes and osteoporosis are<br />

increasingly prevalent diseases.<br />

2. Diabetes and its complications<br />

influence important<br />

determinants of bone strength<br />

such as the material properties<br />

of bone, bone density and<br />

mineral content as well as<br />

bone micro-architecture<br />

and bone turnover.<br />

3. Diabetes is an important<br />

clinical risk factor for<br />

osteoporosis and fracture,<br />

and as clinicians it is<br />

important to remember this<br />

association when managing<br />

people with diabetes.<br />

Key words<br />

– Bone<br />

– Metabolic disorder<br />

– Osteoporosis<br />

Authors<br />

Vidhya Jahagirdar is Specialty<br />

Trainee Registrar in Diabetes,<br />

Endocrinology and General<br />

Internal Medicine; Neil Gittoes is<br />

Consultant & Honorary Professor<br />

of Endocrinology, Head, Centre<br />

for Endocrinology, Diabetes and<br />

Metabolism. Both are at the<br />

Department of Endocrinology,<br />

University Hospitals Birmingham<br />

NHS Foundation Trust,<br />

Birmingham, UK.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 61


Diabetes and bone health<br />

Page points<br />

1. The prevalence of osteoporosis<br />

based on bone mass density<br />

(BMD) is significantly lower in<br />

type 2 diabetes compared to<br />

age-matched controls.<br />

2. Age, female gender,<br />

glucocorticoid use and family<br />

history are well-recognised risk<br />

factors for osteoporosis and<br />

osteoporotic fractures, but the<br />

association between diabetes<br />

and osteoporosis is tantalising,<br />

but poorly understood.<br />

3. As type 1 diabetes is usually<br />

diagnosed in children, the early<br />

and chronic alterations in bone<br />

metabolism may result in lower<br />

peak bone mass.<br />

Figure 1. Osteoporosis is characterised by decreased<br />

bone mineral density and micro-architectural changes<br />

of the bone leading to increased risk of low trauma<br />

fractures (Blausen Medical Communications, 2016).<br />

post-menopausal physiological changes result in<br />

an increased prevalence of osteoporosis from 2%<br />

at 50 years to 25% at 80 years of age (NICE,<br />

2012). One in two women and one in five men<br />

sustain one or more osteoporotic fractures in their<br />

lifetime. In 2012, there were 140 822 fractures<br />

as a result of osteoporosis or osteopaenia in<br />

Australians over the age of 55 years, with a total<br />

cost of $2.75 billion. This is expected to increase to<br />

around $3.84 billion by 2022 (Watts et al, 2013).<br />

While age, female gender, glucocorticoid use<br />

and family history are well-recognised risk factors<br />

for osteoporosis and osteoporotic fractures, the<br />

association between diabetes and osteoporosis<br />

is tantalising, but poorly understood. Other<br />

disease conditions associated with diabetes, such<br />

as diabetic nephropathy, retinopathy, neuropathy<br />

and obesity, as well as medication used in<br />

the management of diabetes, may affect bone<br />

health, increase risk of falls and predispose<br />

patients to osteoporotic fractures. These factors<br />

are confounders in attempting to delineate causal<br />

links between diabetes and osteoporosis.<br />

The aim of this article is to explore the current<br />

literature on the inter-relationships between<br />

diabetes and bone health, the impact on patients<br />

and the management strategies that may be<br />

considered in primary care to minimise risk<br />

of diabetes-related bone disease and improve<br />

outcomes.<br />

Epidemiology of fractures in diabetes<br />

The interaction between diabetes and osteoporosis<br />

is poorly understood. Both type 1 and type 2<br />

diabetes are associated with increased risk of<br />

osteoporosis and fracture, and this risk is greater<br />

in type 1 than type 2 (Vestergaard, 2007).<br />

Various factors, such as type of diabetes, onset<br />

and duration, metabolic control, BMI, BMD,<br />

falls risk, diabetic complications and treatment,<br />

may influence bone health in diabetes. There are<br />

no well-designed randomised controlled trials<br />

(RCTs) or carefully evaluated epidemiological<br />

studies that have looked into all the above<br />

factors as potential attributors to fracture risk in<br />

diabetes.<br />

Figure 2. Peak bone mass is reached at 30 years of age. Bone mass then decreases with age, more<br />

so in women (Anatomy & Physiology, 2013).<br />

Type 1 diabetes<br />

BMD is lower in children and adolescents with<br />

type 1 diabetes than children without diabetes.<br />

As type 1 diabetes is usually diagnosed in<br />

children, the early and chronic alterations in<br />

bone metabolism may result in lower peak<br />

bone mass. This may contribute to osteoporosis<br />

and an increased risk of fracture in later life<br />

(Bonjour and Chevalley, 2014).<br />

According to a recent meta-analysis, type 1<br />

diabetes is associated with three times increased<br />

background risk of any fracture and the risk is<br />

elevated in both men and women. In individuals<br />

62 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

Secondary causes<br />

associated with diabetes<br />

l Coeliac disease<br />

l Graves thyrotoxicosis<br />

l Hypothyroidism<br />

l Hypogonadism<br />

l Vitamin D deficiency<br />

Anti-diabetes medication<br />

l TZDs<br />

l GLP-1 receptor agonists<br />

l DPP-4 inhibitors<br />

l SGLT2 inhibitors<br />

Falls risk<br />

l Diabetic retinopathy<br />

l Diabetic neuropathy<br />

l Obesity<br />

l Hypoglycaemia<br />

Decreased bone<br />

turnover<br />

CKD–MBD secondary to<br />

diabetic nephropathy<br />

Fracture risk<br />

Abnormal bone architecture<br />

Decreased bone mineral density<br />

via collagen cross links<br />

Decreased osteoblast differentiation<br />

Osteoblast dysfunction<br />

Increased osteoclast activity<br />

Increased adipogenesis<br />

Increased AGE<br />

Increased PPAR-gamma<br />

Decreased insulin/<br />

IGF-1 secretion<br />

Oxidative stress<br />

Figure 3. The factors influencing bone health and fracture risk in diabetes. AGE=advanced glycation end-products; CKD–MBD=chronic kidney<br />

disease–mineral and bone disorder; DPP-4=dipeptidyl peptidase-4; GLP-1=glucagon-like peptide-1; IGF-1=insulin-like growth factor-1; PPAR-gamma=<br />

peroxisome proliferator-activated receptor-gamma; SGLT2=sodium–glucose cotransporter 2; TZD=thiazolidinedione.<br />

with type 1 diabetes compared to people<br />

without the condition, the relative risk (RR) for<br />

hip fracture was 3.78 (95% confidence interval<br />

[CI], 2.05–6.98; P


Diabetes and bone health<br />

Page points<br />

1. Insulin deficiency and reduced<br />

insulin-like growth factor-1 have<br />

been linked to the inhibition of<br />

osteoblast differentiation and<br />

osteopaenia in type 1 diabetes.<br />

2. People with diabetes are at<br />

increased risk of falls and this is<br />

multifactorial due to advancing<br />

age, diabetes complications,<br />

hypoglycaemia and high BMI.<br />

3. Cortical bone mass is reduced<br />

in the feet and hands in severe<br />

diabetic peripheral neuropathy<br />

and may predispose to<br />

metatarsal fracture and diabetic<br />

Charcot’s osteoarthropathy.<br />

Fracture risk has also been reported to be<br />

independent of other usually reliable predictors<br />

of fracture risk in type 2 diabetes, including age,<br />

physical activity and BMI (RR 2.6 [95% CI],<br />

1.5–4.5; Janghorbani et al, 2007).<br />

How does diabetes affect bone?<br />

Diabetes and its complications influence<br />

important determinants of bone strength such<br />

as the material properties of bone, bone density<br />

and mineral content as well as bone microarchitecture<br />

and bone turnover (Figure 3).<br />

Oxidative stress<br />

Diabetes is reported to affect bone metabolism<br />

adversely through several mechanisms. Advanced<br />

glycation end-products (AGE) are produced as<br />

a result of oxidative stress in diabetes and are<br />

important mediators of diabetic complications<br />

such as diabetic retinopathy, nephropathy,<br />

neuropathy and atherosclerosis (Goh and<br />

Cooper, 2008). AGE accumulation in bones is<br />

also detrimental and leads to abnormal structure<br />

and alignment of collagen, contributing to bone<br />

fragility (Katayama et al, 1996).<br />

Insulin deficiency<br />

Insulin has an anabolic effect on bone. Insulin<br />

deficiency and reduced insulin-like growth<br />

factor-1 (IGF-1) have been linked to inhibition<br />

of osteoblast differentiation and osteopaenia<br />

in type 1 diabetes (Kanazawa et al, 2011).<br />

Treatment with insulin has been reported to<br />

stabilise BMD (Hofbauer et al, 2007). Hence,<br />

adequate optimisation of glycaemic control<br />

with insulin in type 1 diabetes may prevent<br />

osteopaenia and osteoporosis later in life.<br />

Diabetic nephropathy and chronic kidney<br />

disease (CKD)<br />

Diabetic nephropathy often leads to CKD and<br />

is the most common cause of end-stage renal<br />

disease in Australia (Kidney Health Australia,<br />

2015). The risk of developing moderate to severe<br />

CKD (stages 3b, 4 and 5) is eight times greater<br />

in women and twelve times greater in men with<br />

type 1 diabetes than in people without diabetes<br />

(Hippisley-Cox and Coupland, 2010). Similar to<br />

diabetes and osteoporosis, the risk of developing<br />

CKD increases with age.<br />

Clinical expression of mineral and bone disorders<br />

in CKD (CKD–MBD) is often asymptomatic<br />

until late in its course. Abnormalities in<br />

bone turnover and mineralisation can result<br />

in osteitis fibrosa cystica (brown tumours;<br />

Figure 4), adynamic bone disease, osteomalacia<br />

and secondary hyperparathyroidism caused by<br />

phosphate retention, decreased calcium and<br />

1,25-dihydroxy(OH) vitamin D (calcitriol)<br />

concentration, and uraemic osteodystrophy.<br />

These conditions increase the risk of fractures due<br />

to changes in bone quality. While abnormalities<br />

in calcium and phosphate levels are detected<br />

even at CKD stages 1 and 2, the clinical<br />

significance of these abnormalities is unclear.<br />

Hence, management is focussed on optimising<br />

calcium and phosphate levels in CKD stages 3,<br />

4 and 5.<br />

Factors affecting falls risk<br />

People with diabetes are at increased risk of falls<br />

and this is multifactorial due to advancing age,<br />

diabetes complications, hypoglycaemia and high<br />

BMI (Figure 3).<br />

Peripheral neuropathy<br />

The ABC health study showed that individuals<br />

with type 2 diabetes who develop fractures<br />

are more likely to have peripheral neuropathy,<br />

cerebrovascular disease and falls compared<br />

with people with diabetes without fractures<br />

(Strotmeyer et al, 2005). Cortical bone mass is<br />

reduced in the feet and hands in severe diabetic<br />

peripheral neuropathy and may predispose<br />

to metatarsal fracture and diabetic Charcot’s<br />

osteoarthropathy (Cundy et al, 1985), which can<br />

cause foot deformity and gait disturbance, further<br />

increasing fracture risk by increasing falls. People<br />

with diabetic peripheral neuropathy are more<br />

likely to fall when compared to age-matched<br />

controls. While the underlying causative factors<br />

are not entirely understood, reduced muscle<br />

strength and stability (Handsaker et al, 2014)<br />

and foot deformity are likely to be contributing<br />

factors.<br />

Retinopathy<br />

The Blue Mountain Eye study showed that, in<br />

64 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

Page points<br />

1. Individuals with diabetic<br />

retinopathy or cataracts, or<br />

both, with reduced visual acuity<br />

are prone to falls.<br />

2. Obesity is also associated with<br />

decreased bioavailability of<br />

vitamin D due to distribution in<br />

the subcutaneous t<strong>issue</strong> leading<br />

to vitamin D deficiency, another<br />

risk factor for osteoporosis.<br />

3. There is a high incidence of<br />

fragility fracture in people who<br />

experience hypoglycaemic<br />

events.<br />

Figure 4. Brown tumours of the hands in an individual with hyperparathyroidism (Gaillard, 2008).<br />

people with diabetes, there was a significantly<br />

increased risk of proximal humerus fracture<br />

associated with diabetic retinopathy, cortical<br />

cataract, longer diabetes duration (>10 years) and<br />

insulin treatment (Ivers et al, 2001). Individuals<br />

with diabetic retinopathy or cataracts, or both,<br />

with reduced visual acuity are prone to falls. Thus,<br />

the attendant increased risk of falls contributes to<br />

greater risk of fracture.<br />

Obesity<br />

In total, 90% of people with type 2 diabetes are<br />

overweight or obese. Obesity is commonly thought<br />

to have a protective effect on bone as BMD tends<br />

to increase with load bearing associated with<br />

being overweight. In post-menopausal women,<br />

obesity increased the risk of fractures at the<br />

humerus and ankle while decreased the risk at<br />

the hip, pelvis and wrist (Gonnelli et al, 2014).<br />

Fewer data are available for men. The reasons for<br />

site-specific fractures in obesity could be related<br />

to fat padding protecting the hip and pelvis and<br />

a tendency to fall backwards or sideways rather<br />

than fall forward on outstretched arm leading<br />

to wrist fracture. Obesity is also associated with<br />

decreased bioavailability of vitamin D due to<br />

distribution in the subcutaneous t<strong>issue</strong> leading<br />

to vitamin D deficiency, another risk factor<br />

for osteoporosis. Hence, in spite of increased<br />

BMD, obesity is associated with increased risk<br />

of fracture at particular sites, which is likely<br />

to be due to the pattern of fall and vitamin D<br />

deficiency.<br />

Hypoglycaemia<br />

There is a higher incidence of fragility fracture<br />

in people who experience hypoglycaemic events<br />

(Signorovitch et al, 2013). Intensive glycaemic<br />

control (HbA 1c<br />


Diabetes and bone health<br />

Page points<br />

1. Type 1 diabetes can be<br />

associated with other<br />

autoimmune conditions such as<br />

coeliac disease, hypothyroidism<br />

and Graves’ thyrotoxicosis,<br />

which also increase this risk of<br />

fracture and osteoporosis.<br />

2. Hyperthyroidism and overtreated<br />

hypothyroidism are<br />

associated with lower bone<br />

mineral density and increased<br />

risk of fracture.<br />

3. It is important to be aware<br />

of the effect different antidiabetes<br />

medication can have<br />

on bone mineral density and<br />

osteoporosis.<br />

relationship between hypoglycaemia and<br />

falls risk. It is intuitive, however, to speculate<br />

that with frequent hypoglycaemic episodes<br />

contributing to loss of consciousness, falls risk<br />

would increase. Thus, hypoglycaemia-induced<br />

falls with underlying low bone density in diabetes<br />

would increase risk of fragility fracture.<br />

Secondary causes for osteoporosis associated<br />

with diabetes<br />

Type 1 diabetes can be associated with other<br />

autoimmune conditions such as coeliac disease,<br />

hypothyroidism and Graves’ thyrotoxicosis.<br />

About one-third of people with coeliac disease<br />

have osteoporosis and may be at a higher risk of<br />

fractures. Both hyperthyroidism and over-treated<br />

hypothyroidism are associated with lower BMD<br />

and increased risk of fracture (Mirza and Canalis,<br />

2015). Hypogonadotrophic hypogonadism (low<br />

gonadotropins and low testosterone) is found<br />

in 25% of people with type 2 diabetes. Low<br />

testosterone levels in men are associated with<br />

low BMD and hypogonadism is a recognised<br />

cause of osteoporosis, but there are no reliable<br />

data available on fracture rates in people with<br />

type 2 diabetes and hypogonadism (Dandona<br />

and Dhindsa, 2011). Though epidemiological<br />

observational studies have shown associations<br />

between vitamin D deficiency and type 1 and<br />

type 2 diabetes, the evidence is inconclusive<br />

(Suzuki et al, 2006; Tahrani et al, 2010), as it<br />

is for many associations between suboptimal<br />

vitamin D and major health outcomes.<br />

Anti-diabetes medication<br />

Thiazolidinediones<br />

Expression of peroxisome proliferator-activated<br />

receptor-gamma (PPAR-gamma) is increased<br />

in diabetes. This induces adipogenesis and<br />

inhibits osteogenesis (Botolin and McCabe,<br />

2006; Montagnani and Gonnelli, 2013).<br />

Thiazolidinediones (pioglitazone and rosiglitazone)<br />

are PPAR-gamma agonists. They improve insulin<br />

sensitivity through their action on adipose t<strong>issue</strong><br />

and liver by increasing glucose utilisation and<br />

decreasing glucose production. Thiazolidinediones,<br />

through their action on PPAR-gamma, enhance<br />

the effect of inhibiting osteoblast formation and<br />

increase risk of fracture in type 2 diabetes.<br />

Both pioglitazone and rosiglitazone are<br />

associated with increased fractures in women<br />

but not in men. A meta-analysis by Zhu et al<br />

(2014) reported this risk as independent of age<br />

and with no clear association with duration of<br />

treatment. Thiazolidinedione use was associated<br />

with significant changes in BMD and increased<br />

fractures not only in the upper and lower limbs<br />

but also at the lumbar spine and femoral neck<br />

(Zhu et al, 2014). The benefit of improving<br />

glycaemic control versus the risk of fracture<br />

should be assessed carefully on an individual<br />

case basis, especially in post-menopausal women,<br />

before commencing treatment with pioglitazone<br />

in type 2 diabetes.<br />

Incretin-based medicines<br />

Glucagon-like peptide 1 (GLP-1) agonists are<br />

recommended in the management of obese people<br />

with type 2 diabetes and their effect on the risk<br />

of bone fractures is beginning to be established.<br />

In a meta-analysis of RCTs, liraglutide was<br />

associated with significantly reduced risk of<br />

fracture and exenatide was associated with an<br />

elevated risk of incident bone fractures (Su<br />

et al, 2015). Protective effects of dipeptidyl<br />

peptidase-4 (DPP-4) inhibitors on bone have<br />

also been reported in a recent meta-analysis.<br />

These data should be interpreted with caution as<br />

the trials included in the meta-analysis were not<br />

sufficiently long to assess fracture risk and the<br />

effect on bone was not assessed as a primary endpoint<br />

(Monami et al, 2011). The effects of DPP-4<br />

inhibitors and GLP-1 agonists on bone health<br />

need to be confirmed with well-designed RCTs.<br />

Sodium–glucose cotransporter 2 (SGLT2)<br />

inhibitors<br />

In October 2015, the US Food and Drug<br />

Administration (FDA; 2015) <strong>issue</strong>d a warning<br />

for the SGLT2 inhibitor canagliflozin relating to<br />

increased risk of hip fractures and fractures of the<br />

lower spine. More evidence is needed to ascertain<br />

if this is a drug class effect.<br />

Insulin<br />

One large longitudinal study, using a German<br />

database of over 100 000 people with type 2<br />

diabetes in general practice found non-significant<br />

66 Diabetes & Primary Care Australia Vol 2 No 2 2017


Diabetes and bone health<br />

increase in risk of fracture in people on basal<br />

insulin (glargine, insulin detemir and NPH<br />

insulin) compared to oral hypoglycaemia agents<br />

(Pscherer et al, 2016). This could possibly be<br />

due to increased insulin-induced hypoglycaemiarelated<br />

falls as discussed above, rather than direct<br />

effect of insulin on the bone. In the absence of<br />

RCT data at present, there is no clear evidence<br />

to suggest that insulin increases the risk of<br />

osteoporosis or fracture.<br />

Management<br />

There is no specific guideline for the management<br />

of bone disorders in diabetes. Investigations and<br />

treatment of osteoporosis should be based on<br />

patients’ absolute risk of fracture taking into<br />

consideration age, gender, menopausal status,<br />

personal and family history of fractures, body<br />

weight, falls risk, thiazolinediones use and<br />

associated secondary causes of osteoporosis.<br />

Fracture risk assessment based on FRAX,<br />

Garvan or QFracture assessment tools can help<br />

predict the risk of fracture. However, these may<br />

under-estimate fracture risk in type 2 diabetes,<br />

as paradoxically, BMD is often higher than in<br />

those without diabetes, despite the increased risk<br />

of fracture (Schwartz et al, 2011). Type 2 diabetes<br />

is not an explicitly recognised risk factor included<br />

in the risk assessment tool and BMD in type 2<br />

diabetes can be normal or elevated in spite of<br />

increased fracture risk. As BMD does not predict<br />

fracture risk in renal osteodystrophy, it need not<br />

be performed routinely in CKD stages 3–5 in<br />

the presence of CKD-MBD (Kidney Disease:<br />

Improving Global Outcomes [KDIGO] CKD-<br />

MBD Work Group, 2009).<br />

Bone mineral disorders in CKD can be identified<br />

early by detecting decreasing serum calcium,<br />

phosphate and vitamin D concentrations, and<br />

increasing serum parathyroid hormone (PTH)<br />

concentrations. The KDIGO clinical practice<br />

guideline suggests monitoring for serum calcium,<br />

phosphorus, 25-hydroxy vitamin D deficiency<br />

and PTH routinely for CKD stages 3–5 with the<br />

frequency of monitoring based on stage, rate of<br />

progression and whether specific therapies have<br />

been initiated (KDIGO CKD-MBD Work Group,<br />

2009). PTH and bone alkaline phosphatase can<br />

be used to evaluate CKD–MBD.<br />

Anti-resorptive agents such as bisphosphonates<br />

can be used as first-line agents to treat osteoporosis<br />

and high fracture risk in diabetes and in CKD<br />

stages 1, 2 and 3 (estimated glomerular filtration<br />

rate [GFR] >30 mL/min/1.73 m 2 ) in the absence<br />

of abnormal bone mineral markers. The effect of<br />

drug treatment should be reviewed after 5 years<br />

for alendronate and after 3 years for intravenous<br />

zolendronic acid with a view to making a decision<br />

regarding a drug holiday or continuing or switching<br />

treatment. No studies have specifically looked at<br />

optimal treatment for people with fractures where<br />

thiazolidinediones have been implicated.<br />

Screening for coeliac disease with t<strong>issue</strong><br />

transglutaminase antibodies (TTG) is<br />

recommended at the time of diagnosis of type 1<br />

diabetes and if a young adult with type 1 develops<br />

intestinal or extra-intestinal symptoms consistent<br />

with coeliac disease (NICE, 2009). Annual<br />

screening for thyroid status is also recommended.<br />

Screening for hypogonadism in people with type 2<br />

diabetes and replacing with testosterone if found<br />

deficient is also recommended (Dandona and<br />

Dhindsa, 2011).<br />

Good glycaemic control and blood pressure<br />

control delays the progression of microvascular<br />

complications, which are associated with increased<br />

risk of falls and fracture. HbA 1c<br />

targets should be<br />

individualised and less stringent control (HbA 1c<br />


Diabetes and bone health<br />

“It is important,<br />

where possible, to<br />

ensure that messages<br />

from different<br />

clinicians pertaining<br />

to lifestyle factors are<br />

aligned and overlap as<br />

much as possible.”<br />

Conclusion<br />

Diabetes and osteoporosis are increasingly<br />

prevalent diseases. Diabetes is an important<br />

clinical risk factor for osteoporosis and fracture,<br />

and as clinicians it is important to remember this<br />

association when managing people with diabetes.<br />

Diabetes-related complications, hypoglycaemia<br />

and obesity could increase the risk of falls<br />

and fragility fracture. HbA 1c<br />

targets should be<br />

individualised taking into consideration age,<br />

frailty, diabetes complications and falls risk.<br />

While there is much to learn regarding the<br />

associations between diabetes, osteoporosis<br />

and fractures, it is important to recognise the<br />

value of performing a multifactorial fracture<br />

risk assessment, including falls risk. Tools are<br />

available to conveniently assess this risk and<br />

measurement of BMD by performing a DXA<br />

scan may provide additional useful information<br />

to help target those patients who are most<br />

at risk of fracture with appropriate fracture<br />

prevention drug therapies. The value of lifestyle<br />

modification to address fracture and falls risk<br />

cannot be underestimated. It is also convenient<br />

that the lifestyle modifications required to<br />

optimise bone health very much overlap with<br />

the lifestyle guidance that is offered to optimise<br />

the management of the underlying diabetes and<br />

obesity. It is important, where possible, to ensure<br />

that our messages to patients pertaining to<br />

lifestyle factors are aligned and overlap as much<br />

as possible, rather than conveying different sets<br />

of instructions for different disease areas. This<br />

is where diabetes and osteoporosis management<br />

from a self-help perspective very much align. n<br />

Acknowledgement<br />

This article has been modified from one<br />

previously published in Diabetes & Primary Care<br />

(2016, 2: 68–74).<br />

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68 Diabetes & Primary Care Australia Vol 2 No 2 2017


Article<br />

Falls prevention in older adults<br />

with diabetes: A clinical review of<br />

screening, assessment and management<br />

recommendations<br />

Anna Chapman, Claudia Meyer<br />

Older adults with diabetes have an increased rate of falls, recurrent falls and rate of<br />

fracture following a fall. Falls can contribute to a heightened fear of further falling, social<br />

isolation, avoidance of daily activities, and can increase the likelihood of premature<br />

admission to residential aged-care facilities. The most common risk factors for falls within<br />

this population group include peripheral neuropathy, foot complications, impaired postural<br />

control, polypharmacy and insulin use, sub-optimal glycaemic control and hypoglycaemia,<br />

as well as vision and cognitive impairment. Falls risk screening should be undertaken every<br />

12 months for all older people with diabetes, followed by a more detailed falls assessment<br />

for those deemed high risk to identify the contributory risk factors and management<br />

strategies. Individualised strategies should be co-designed with individuals and where<br />

appropriate, their carer(s), may involve referral to other health professionals, and should<br />

be monitored and reviewed at regular intervals.<br />

Falls are a complication of diabetes and<br />

are being increasingly acknowledged<br />

as impacting the overall health and<br />

wellbeing of older adults (International Diabetes<br />

Federation [IDF], 2013). Within the general<br />

community-dwelling population of older adults,<br />

approximately one in three people fall per<br />

year (Moyer, 2012). The combination of age<br />

(≥65 years) and diabetes increases the risk of<br />

recurrent falls by 67% (Pijpers et al, 2012); and<br />

older adults with diabetes are twice as likely to<br />

have injurious falls (Roman de Mettelinge et al,<br />

2013). At the individual level, falls can contribute<br />

to a loss of confidence and reduced activity levels,<br />

loss of lower-limb muscle and bone strength<br />

(Karinkanta et al, 2010), and a heightened<br />

fear of further falling (Zijlstra et al, 2007). For<br />

the public health system, there are expanding<br />

costs associated with falls-related hospitalisations<br />

(Bradley, 2012).<br />

Key to the prevention of falls is the identification<br />

of at-risk individuals and the implementation of<br />

appropriate interventions. Given the increased<br />

prevalence and negative consequences associated<br />

with falls among older adults with diabetes, falls<br />

prevention should be considered an integral<br />

component of diabetes care, and primary care<br />

practitioners are well-placed to offer proactive,<br />

comprehensive and individualised falls prevention<br />

strategies. This article will assist primary care<br />

practitioners in this role, providing an overview<br />

of potential screening tools and outlining fallsrelated<br />

risk factors pertinent to an older person<br />

with diabetes. In addition, this paper will<br />

consider the evidence and recommend actions<br />

for older adults with diabetes, specifically for the<br />

community-dwelling population (rather than the<br />

hospital or residential aged-care setting).<br />

Falls risk screening<br />

Falls risk screening refers to the process of<br />

identifying individuals who are at-risk of a fall,<br />

to determine if a detailed falls assessment is<br />

appropriate. To be effective, screening tools need<br />

Citation: Chapman A, Meyer C<br />

(2017) Falls prevention in older<br />

adults with diabetes: A clinical<br />

review of screening, assessment and<br />

management recommendations.<br />

Diabetes & Primary Care Australia<br />

2: 69–74<br />

Article points<br />

1. Falls-related risk factors<br />

for older people with<br />

diabetes include peripheral<br />

neuropathy, impaired postural<br />

control, polypharmacy,<br />

visual impairment,<br />

cognitive impairment, foot<br />

complications, and suboptimal<br />

glycaemic control.<br />

3. Valid and reliable risk screens<br />

exist to identify individuals<br />

at-risk of falls. As with all<br />

older adults, individuals with<br />

diabetes should be screened for<br />

falls at least once every year.<br />

4. Individuals at increased risk<br />

of falls require a multifactorial<br />

assessment that examines<br />

the wide range of fallsrelated<br />

risk factors.<br />

5. Falls prevention interventions<br />

should systematically address<br />

the risk factors identified and<br />

should be developed with the<br />

older person with diabetes, and<br />

where applicable their carer(s).<br />

Key words<br />

– Falls<br />

– Older people<br />

Authors<br />

Author details are on page 74.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 69


Falls prevention in older adults with diabetes<br />

Page points<br />

1. Falls risk screening tools need<br />

to be validated, quick and easy<br />

to administer, cost-effective and<br />

clinically relevant.<br />

2. Falls risk screening should<br />

be incorporated into routine<br />

consultations, involving<br />

assessment of an individual’s<br />

falls history over the last<br />

12 months together with<br />

examination of balance and<br />

mobility.<br />

3. When classified as high risk,<br />

individuals should undergo a<br />

comprehensive falls assessment<br />

in a timely manner to guide<br />

appropriate and individualised<br />

falls prevention strategies.<br />

to be validated, quick and easy to administer,<br />

cost-effective and clinically relevant. The<br />

selection of a screening tool should complement<br />

the setting (community, hospital or residential<br />

aged-care) and the older adult being screened,<br />

particularly with regard to age, ethnicity, as<br />

well as cognitive and functional status.<br />

The Global Guideline for Managing Older<br />

People with Type 2 Diabetes recommends that<br />

falls risk screening be performed during an<br />

initial visit to a health care provider, reviewed<br />

annually at a minimum and additionally<br />

following a fall event (IDF, 2013). Falls<br />

risk screening should be incorporated into<br />

routine consultations, involving assessment<br />

of an individual’s falls history over the last<br />

12 months (frequency of falls, circumstances<br />

surrounding each fall, and number of injurious<br />

falls), together with examination of balance<br />

and mobility. Table 1 provides a summary<br />

of available tools and tests for use in the<br />

primary care setting. As with any screening<br />

procedure, all falls risk screening outcomes<br />

should be documented and discussed with the<br />

older person and their carer(s), and information<br />

provided to individuals.<br />

Falls risk assessment to identify fallsrisk<br />

factors<br />

Falls risk screening identifies individuals at<br />

high risk of falls. When classified as such,<br />

individuals should undergo a comprehensive<br />

falls assessment in a timely manner to guide<br />

appropriate and individualised falls prevention<br />

strategies.<br />

A recommended falls assessment tool can<br />

be used to assess the overall risk of falls (as<br />

summarised in Table 2). In addition, specific<br />

assessment of individual factors known to<br />

contribute to falls risk among older adults with<br />

diabetes can be undertaken. It is important to<br />

acknowledge, that although falls-related risk<br />

factors are often referred to independently,<br />

most falls occur as a result of the interaction<br />

between intrinsic and extrinsic risk factors<br />

(Tinetti et al, 1986). A description of the<br />

specific risk factors that are primarily targeted<br />

for further assessment with older adults with<br />

diabetes are discussed below with assessment<br />

and management recommendations provided<br />

(Australian Commission on Safety and Quality<br />

in Healthcare, 2009; American Geriatrics<br />

Society and British Geriatrics Society, 2010).<br />

Table 1. Summary of validated tools and tests recommended for screening of falls risk.<br />

Falls risk screen Description Time to implement Scoring interpretation*<br />

Balance and mobility tests<br />

Timed Up and Go (TUG) test<br />

(Podsiadlo and Richardson, 1991)<br />

A measure of dynamic balance that assesses the time taken for an individual<br />

to rise from a chair, walk 3 metres, turn around, walk back to the chair, and<br />

sit down. Requires a stop-watch and a 43 cm-high straight-backed chair<br />

with solid seat.<br />

1–2 minutes<br />

≥12 seconds is indicative of<br />

an increased risk of falling.<br />

Five Times Sit To Stand<br />

(FTSTS) test<br />

(Tiedemann et al, 2008)<br />

A measure of lower-limb strength that assesses the time taken for an<br />

individual to stand up and sit down as quickly as possible five times, with<br />

their arms folded across their chest. Requires a stop-watch and a 43 cm-high<br />

straight-backed chair with solid seat.<br />

1–2 minutes<br />

≥12 seconds is indicative of<br />

an increased risk of falling.<br />

Alternate Step Test (AST)<br />

(Tiedemann et al, 2008)<br />

A measure of lateral stability that involves weight shifting. An individual<br />

is required to alternately place the right and left feet (no shoes) as fast as<br />

possible on a step that is 18 cm high and 40 cm deep, for a total of eight<br />

steps. A stop-watch is required.<br />

1–2 minutes<br />

≥10 seconds is indicative of<br />

an increased risk of falling.<br />

Multi-item screening tool<br />

Falls Risk for Older People in the<br />

Community (FROP-Com) Screen<br />

(Russell et al, 2009)<br />

A 3-item screening tool that addresses 12-month falls history, self-perceived<br />

need for assistance to perform activities of daily living, and the objective<br />

assessment of steadiness through the observation of an individual standing,<br />

walking a few metres, turning and sitting.<br />

Available at: http://bit.ly/2m6PXZX<br />

1–2 minutes<br />

Responses for each item are<br />

scored from 0–3. A total<br />

score between 0–3 indicates<br />

low-risk. Scores between<br />

4–9 indicate high-risk.<br />

*Scoring criterion based on cut-off scores specified within best practice guidelines for falls prevention (Australian Commission on Safety and Quality in Healthcare, 2009).<br />

Note: Above mentioned tools not specifically validated for older adults with diabetes.<br />

70 Diabetes & Primary Care Australia Vol 2 No 2 2017


Falls prevention in older adults with diabetes<br />

Table 2. Summary of recommended falls assessment tools.<br />

Falls assessment tool Description Time to implement Scoring interpretation*<br />

FallScreen © : Physiological<br />

Profile Assessment<br />

(Lord et al, 2003)<br />

The short form is a validated five-item instrument that includes a single<br />

assessment of vision, peripheral sensation, lower-limb strength, reaction<br />

time and body sway. There is an associated cost for the purchase of the<br />

tool.<br />

Available at: http://bit.ly/2lYqPU7<br />

15–20 minutes<br />

≥1 is indicative of an<br />

increased risk of falling.<br />

FROP-Com<br />

(Russell et al, 2008)<br />

A detailed falls risk factor assessment tool that includes 26 items that<br />

address 13 falls-related risk factors. The tool includes guidelines for<br />

scoring, and evidence-based referrals and interventions. No equipment is<br />

required and the tool is available at no cost.<br />

Available at: http://bit.ly/2mFR8mD<br />

10–15 minutes<br />

Total score range is 0–60.<br />

Scores >18 is indicative of<br />

high risk.<br />

QuickScreen ©<br />

(Tiedemann et al, 2008)<br />

A multifactorial falls assessment tool comprised of the following items:<br />

previous falls, medication usage, vision, peripheral sensation, lower-limb<br />

strength, balance and co-ordination. Minimal equipment is required. There<br />

is an associated cost for the purchase of the tool.<br />

Available at: http://bit.ly/2mlM7P5<br />

10 minutes<br />

≥4 is indicative of an<br />

increased risk of falling.<br />

*Scoring criterion based on cut-off scores specified within best practice guidelines for falls prevention (Australian Commission on Safety and Quality in Healthcare, 2009).<br />

The above scores should be used for the purpose of assessment and re-assessment over time.<br />

Note: Above mentioned tools not specifically validated for older adults with diabetes.<br />

Peripheral neuropathy<br />

The most common falls-related risk factor related<br />

to diabetes is peripheral neuropathy, present<br />

in approximately 50–70% of older adults with<br />

diabetes (Kirkman et al, 2012). Peripheral<br />

neuropathy results in changes to the motor<br />

and/or sensory components of the foot and<br />

ankle, potentially leading to postural instability,<br />

foot complications, altered walking function<br />

and muscle atrophy (Boulton, 2004; Palma et al,<br />

2013; Brown et al, 2015). Clinical emphasis is<br />

placed on the prevention of peripheral neuropathy<br />

by means of optimal glycaemic control, as well as<br />

the early recognition of the condition (Royal<br />

Australian College of General Practitioners<br />

[RACGP], 2016). Peripheral neuropathy should<br />

be assessed annually using either the Diabetic<br />

Neuropathy Symptom (DNS) score (Meijer<br />

et al, 2002) and/or routine sensory tests (i.e.<br />

a 10-g monofilament and palpating foot).<br />

Postural instability<br />

An increase in postural instability is a risk factor<br />

for falls (Ganz et al, 2007; Drootin, 2011), which<br />

is particularly important for people with diabetes<br />

who experience a decrease in the functioning of<br />

the neuromuscular and sensorimotor systems<br />

(Crews et al, 2013). Control of balance to<br />

maintain postural stability involves a complex<br />

interplay of the sensory and motor systems and<br />

integration of, and reaction to, this information<br />

by the central nervous system.<br />

In the primary care setting, the assessment<br />

of postural stability can be easily performed<br />

by balance and mobility tests (e.g. Table 1).<br />

To address postural instability, falls prevention<br />

exercise programs are encouraged (Australian<br />

Commission on Safety and Quality in Healthcare,<br />

2009; Gillespie et al, 2012). Exercise interventions<br />

have recently been found to be effective for older<br />

adults with diabetes with regard to lower-limb<br />

strength, static balance and gait measures<br />

(outcomes vital in the maintenance of postural<br />

stability; Chapman et al, 2016). In particular,<br />

individuals are likely to benefit from exercise<br />

programs that incorporate a challenge to balance,<br />

when delivered with sufficient frequency (e.g. total<br />

of 50 hours, preferably at least 2 hours per week).<br />

It should also be noted that walking programs,<br />

although beneficial for metabolic control and<br />

improvement of cardiovascular disease risk, have<br />

been associated with an increased risk of falls<br />

(Sherrington et al, 2011). Exercise programs<br />

should be tailored to existing levels of fitness<br />

and should consider an individual’s lifestyle<br />

and any medical contraindications. Referral<br />

to an appropriate health professional (e.g. a<br />

physiotherapist or exercise physiologist) may be<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 71


Falls prevention in older adults with diabetes<br />

Page points<br />

1. Foot complications, including<br />

foot pain, foot ulceration and<br />

consequent amputations, are<br />

common among older adults<br />

with diabetes and are significant<br />

contributors to increased falls<br />

risk.<br />

2. Falls risk among adults with<br />

diabetes has been found to<br />

increase steadily at four or more<br />

prescription medications.<br />

3. It is important that primary care<br />

practitioners comprehend the<br />

overall medication burden as<br />

it has the potential to lead to<br />

medication-related problems<br />

including non-adherence,<br />

hypoglycaemia and increased<br />

risk of falls.<br />

warranted for a detailed assessment of balance,<br />

and the design of challenging, yet safe exercise<br />

programs (Australian Commission on Safety<br />

and Quality in Healthcare, 2009).<br />

Foot complications<br />

Foot complications, including foot pain, foot<br />

ulceration and consequent amputations, are<br />

common among older adults with diabetes and<br />

are significant contributors to increased falls<br />

risk (Al-Rubeaan et al, 2015). In brief, foot-care<br />

education should be provided to all people<br />

with diabetes to assist in the prevention of foot<br />

complications. Education should consist of basic<br />

foot-care recommendations and, of particular<br />

relevance to falls, advice regarding appropriate<br />

footwear. Screening and risk stratification for<br />

potential foot complications should also be<br />

performed for all adults with diabetes, with the<br />

intensity of monitoring and review dependent<br />

on the associated level of risk. For individuals<br />

classified as being at intermediate or high risk,<br />

a podiatry assessment is an integral component<br />

of a foot protection program (Menz et al, 2006;<br />

R ACGP, 2016).<br />

Diabetes-related foot ulcers deserve specific<br />

mention when considering falls risk. Offloading<br />

footwear is a common recommendation for<br />

foot ulcers, yet it has a negative effect on<br />

postural stability (van Deursen, 2008). In<br />

particular, total contact casts and removable<br />

or non-removable cast-walkers are problematic<br />

for falls. Given their rigid nature, they do not<br />

allow the foot to make its usual adjustments on<br />

uneven terrain.<br />

Sub-optimal glycaemic control<br />

and hypoglycaemia<br />

Hypoglycaemia, hypoglycaemic unawareness<br />

and severe hyperglycaemia are well-established<br />

risk factors for falls among older adults with<br />

diabetes (Jafari and Britton, 2015; Sinclair et<br />

al, 2015). Optimising an individual’s glycaemic<br />

control can reduce short- and long-term<br />

complications of diabetes, and can improve<br />

quality of life, and functional and cognitive<br />

ability. However, the potential harmful effects<br />

of hypoglycaemia should be considered when<br />

setting individual glycaemic targets. Targets<br />

need be personalised and balanced against<br />

factors such as an individual’s capabilities,<br />

life expectancy, medical comorbidities, and<br />

the potential risk of severe hypoglycaemia,<br />

especially among frail, older adults with an<br />

increased risk of falls (RACGP, 2016). For older<br />

adults with diabetes who have a life expectancy<br />

>10 years and are functionally independent and<br />

fit, an HbA 1c<br />

target of 53 mmol/mol (7.0%) is<br />

often appropriate. However, less stringent HbA 1c<br />

targets (i.e. 64 mmol/mol [8%]) are appropriate<br />

for those with long-standing diabetes, a<br />

history of severe hypoglycaemia, limited life<br />

expectancy, advanced complications, and/or<br />

extensive comorbid conditions (RACGP, 2016).<br />

Medication and polypharmacy<br />

Older adults with diabetes are often required<br />

to take multiple medications in an effort to<br />

control diabetes-related outcomes and other<br />

comorbidities, and a significant proportion of<br />

individuals take upwards of eight medications<br />

(RACGP, 2016). Falls risk among adults with<br />

diabetes has been found to increase steadily at<br />

four or more prescription medications (Huang<br />

et al, 2010). Falls risk can be heightened as a<br />

result of medication interaction, medication<br />

side effects (e.g. dizziness) and even the intended<br />

effects of medications (e.g. glucose-lowering<br />

leading to hypoglycaemia). Certain classes of<br />

medication are more likely to increase the risk<br />

of falls, and those commonly implicated in falls<br />

related to older people with diabetes include<br />

insulin, psychoactive medications (in particular<br />

benzodiazepines), diuretics, antiarrhythmics<br />

(class 1a), digoxin, and antidepressants (Berlie<br />

and Garwood, 2010; Huang et al, 2010).<br />

It is important that primary care practitioners<br />

comprehend the overall medication burden<br />

as it has the potential to lead to medicationrelated<br />

problems including non-adherence,<br />

hypoglycaemia and increased risk of falls.<br />

Medication use (both conventional and<br />

complementary), should be reviewed at least<br />

once per year as part of the annual cycle of<br />

care (RACGP, 2016). Referral for a Home<br />

Medicines Review has the potential to identify<br />

medications implicated in falls and consider the<br />

ongoing need for these medications.<br />

72 Diabetes & Primary Care Australia Vol 2 No 2 2017


Falls prevention in older adults with diabetes<br />

Vision impairment<br />

Vision impairment is an important risk factor<br />

for falls in community-dwelling older adults,<br />

with vision being a key sensory input for the<br />

maintenance of balance and the avoidance of<br />

obstacles. Diabetic retinopathy, occurring as<br />

a result of microvascular disease of the retina,<br />

causes visual impairment and blindness, and<br />

affects more than 30% of adults with diabetes<br />

(Dirani, 2013).<br />

All older adults with diabetes should have a<br />

visual acuity assessment at diagnosis, and at least<br />

every 2 years (more frequently if vision noted to<br />

have concerns). Primary care practitioners can<br />

monitor individuals for retinopathy via retinal<br />

photography or by examining the eyes through<br />

dilated pupils. If practitioners are not confident<br />

with fundoscopy and assessment of the retina,<br />

referral to an eye specialist is recommended.<br />

Older people may additionally benefit from an<br />

assessment by an eye specialist for the provision<br />

of appropriate spectacle correction (RACGP,<br />

2016). The use of bifocal or multifocal lenses<br />

by older people in the community is associated<br />

with a doubled risk of falls as a result of<br />

tripping. Individuals with an increased risk of<br />

falls or established falls history are, therefore,<br />

recommended to wear single-vision distance<br />

spectacles when walking and negotiating steps<br />

(Australian Commission on Safety and Quality<br />

in Healthcare, 2009; Haran et al, 2010). Other<br />

effective fall prevention strategies for vision<br />

include maximising vision through cataract<br />

surgery on the first eye (Lord et al, 2010).<br />

Cognition<br />

Cognitive impairment is a risk factor for falls,<br />

with 50–80% of people with dementia falling<br />

in a given year (Allan et al, 2009), and mild<br />

cognitive impairment linked to greater risk of<br />

injurious and multiple falls (Delbaere et al, 2012).<br />

There appears to be a crucial link between the<br />

decline of cognition and the use of executive<br />

functioning for the purposes of balance, with this<br />

decline evident in decreasing ability to control and<br />

integrate cognitive abilities related to attention<br />

and perception (Liu-Ambrose et al, 2008). People<br />

with cognitive impairment may have difficulty<br />

with planning and executing movements related<br />

to balance and mobility, and may have difficulty<br />

limiting sensory input which affects attention to a<br />

task (e.g. walking while talking; Liu-Ambrose et<br />

al, 2008). Medication use in people with cognitive<br />

impairment also impacts falls risk, particularly<br />

psychotropic medications that may magnify side<br />

effects of other medications (Hill and Wee, 2012).<br />

There is no specific literature relating falls,<br />

diabetes and cognitive impairment. There<br />

is, however, an emerging body of evidence for<br />

effective falls prevention strategies for people with<br />

dementia (Drootin, 2011), with studies showing<br />

“traditional” falls prevention programs to be<br />

unsuccessful with people with dementia (Shaw<br />

et al, 2003). However, a different approach to<br />

adoption of falls prevention strategies may be<br />

beneficial with elements of health professional<br />

involvement, inclusion of the caregiving dyad<br />

and accommodation of individual needs and<br />

preferences likely to be important (Meyer et al,<br />

2013).<br />

Built environment<br />

Environmental hazards are considered a risk for<br />

falls: clutter can be a tripping hazard; lighting<br />

should be sufficient in order to prevent shadows;<br />

flooring should be clear of rugs and provide a<br />

contrast to furniture; and bathroom setup needs<br />

to prevent slippage on wet surfaces, with grab<br />

rails provided as needed. Home safety assessment<br />

and modification interventions are effective in<br />

decreasing falls risk and rates, especially for<br />

people with severe visual impairment, which is of<br />

relevance to the person with diabetes (Gillespie et<br />

al, 2012).<br />

Adaptation and modification of the environment<br />

with an occupational therapist who is trained<br />

to identify and maximise the benefits of the<br />

person–environment fit is the crucial factor in<br />

reducing risk (Clemson et al, 2014). Shared<br />

decision-making processes with the person with<br />

diabetes, and with their carer(s) if appropriate, will<br />

most likely enhance the uptake of environmental<br />

modifications.<br />

Conclusion<br />

Reducing the number of falls among older adults<br />

with diabetes is dependent upon the identification<br />

of at-risk individuals and the coordination of<br />

Page points<br />

1. Vision impairment is an<br />

important risk factor for falls<br />

in community-dwelling older<br />

adults, with vision being a<br />

key sensory input for the<br />

maintenance of balance and the<br />

avoidance of obstacles.<br />

2. There appears to be a crucial<br />

link between the decline<br />

of cognition and the use of<br />

executive functioning for the<br />

purposes of balance.<br />

3. Environmental hazards are<br />

considered a risk for falls, and<br />

efforts should be made to avoid<br />

them where possible.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 73


Falls prevention in older adults with diabetes<br />

“All primary care<br />

practitioners should<br />

have access to<br />

education about<br />

falls prevention, and<br />

every attempt should<br />

be made to provide<br />

comprehensive<br />

and individualised<br />

education about falls<br />

to older adults with<br />

diabetes and where<br />

appropriate, their<br />

caregivers and family.”<br />

Authors<br />

Anna Chapman, Research Fellow,<br />

School of Primary Health Care,<br />

Monash University, Melbourne, Vic;<br />

Claudia Meyer, Research Fellow,<br />

Centre for Health Communication,<br />

School of Public Health and Human<br />

Biosciences, La Trobe University,<br />

Melbourne, Vic. Both are at the<br />

RDNS Institute, St Kilda, Vic.<br />

appropriate preventive strategies. A diagnosis<br />

of diabetes in an older adult should trigger to<br />

primary care practitioners the potential for<br />

increased falls risk. Systems need to be established<br />

in the diabetes care pathway to enable falls<br />

risk screening to be performed annually. All<br />

primary care practitioners should have access<br />

to education about falls prevention, and every<br />

attempt should be made to provide comprehensive<br />

and individualised education about falls to older<br />

adults with diabetes and where appropriate, their<br />

caregivers and family. <br />

n<br />

Al-Rubeaan K, Al Derwish M, Ouizi S et al (2015) Diabetic foot<br />

complications and their risk factors from a large retrospective<br />

cohort study. PLoS ONE 10: e0124446<br />

Allan L, Ballard C, Rowan E, Kenny R (2009) Incidence and prediction<br />

of falls in dementia: A prospective study in older people. PLoS ONE<br />

4: e5521<br />

American Geriatrics Society & British Geriatrics Society (2010)<br />

Prevention of Falls in Older Persons: AGS/BGS Clinical Practice<br />

Guideline. AGS/BGS<br />

Australian Commission On Safety And Quality In Healthcare (2009)<br />

Preventing falls and harm from falls in older people: Best practice<br />

guidelines for Australian community care. ACSQHC, Canberra,<br />

ACT<br />

Berlie HD, Garwood CL (2010) Diabetes medications related to an<br />

increased risk of falls and fall-related morbidity in the elderly. Ann<br />

Pharmacother 44: 712–7<br />

Boulton AJ (2004) The diabetic foot: from art to science. The 18th<br />

Camillo Golgi lecture. Diabetologia 47: 1343–53<br />

Bradley C (2012) Hospitalisations due to falls in older people, Australia<br />

2008-09. Australian Institute for Health and Welfare, Canberra,<br />

ACT. Available at: http://bit.ly/2mlESXq (accessed 08.03.17)<br />

Brown SJ, Handsaker JC, Bowling FL et al (2015) Diabetic peripheral<br />

neuropathy compromises balance during daily activities.<br />

Diabetes Care 38: 1116–22<br />

Chapman A, Meyer C, Renehan E et al (2016) Exercise interventions<br />

for the improvement of falls-related outcomes among older adults<br />

with diabetes mellitus: A systematic review and meta-analyses.<br />

J Diabetes Complications 31: 631–45<br />

Clemson L, Donaldson A, Hill K, Day L (2014) Implementing personenvironment<br />

approaches to prevent falls: a qualitative inquiry in<br />

applying the Westmead approach to occupational therapy home<br />

visits. Aust Occup Ther J 61: 325–34<br />

Crews R, Yalla S, Fleischer A, Wu S (2013) A growing troubling triad:<br />

diabetes, aging, and falls. J Aging Res 2013: 342650<br />

Delbaere K, Kochan NA, Close JC et al (2012) Mild cognitive<br />

impairment as a predictor of falls in community-dwelling older<br />

people. Am J Geriatr Psychiatry 20: 845–53<br />

Dirani M (2013) Out of sight: A report into diabetic eye disease in<br />

Australia. Baker IDI Heart and Diabetes Institute and Centre for Eye<br />

Research Australia, Australia<br />

Drootin M (2011) Summary of the updated American Geriatrics<br />

Society/British Geriatrics Society clinical practice guideline for<br />

prevention of falls in older persons. J Am Geriatr Soc 59: 148–57<br />

Ganz D, Bao Y, Shekelle P, Rubenstein L (2007) Will my patient fall?<br />

JAMA 297: 77–86<br />

Gillespie L, Robertson M, Gillespie W et al (2012) Interventions for<br />

preventing falls in older people living in the community. Cochrane<br />

Database Syst Rev 12: CD007146<br />

Haran MJ, Cameron ID, Ivers RQ et al (2010) Effect on falls of<br />

providing single lens distance vision glasses to multifocal glasses<br />

wearers: VISIBLE randomised controlled trial. BMJ 340: c2265<br />

Hill K, Wee R (2012) Psychotropic drug-induced falls in older people:<br />

A review of interventions aimed at reducing the problem. Drugs<br />

Aging 29: 15–30<br />

Huang ES, Karter AJ, Danielson KK et al (2010) the association<br />

between the number of prescription medications and incident falls<br />

in a multi-ethnic population of adult type-2 diabetes patients: The<br />

Diabetes and Aging Study. J Gen Intern Med 25: 141–6<br />

International Diabetes Federation (2013) IDF Global Guideline for<br />

Managing Older People with Type 2 Diabetes. International<br />

Diabetes Federation, Brussels, Belgium<br />

Jafari B, Britton ME (2015) Hypoglycaemia in elderly patients with<br />

type 2 diabetes mellitus: a review of risk factors, consequences and<br />

prevention. J Pharmacy Practice Research 45: 459–69<br />

Karinkanta S, Piirtola M, Sievanen H et al (2010) Physical therapy<br />

approaches to reduce fall and fracture risk among older adults.<br />

Nature Reviews Endocrinology 6: 396–407<br />

Kirkman MS, Briscoe VJ, Clark N et al (2012) Diabetes in older adults.<br />

Diabetes Care 35: 2650–64<br />

Liu-Ambrose T, Ahamed Y, Graf P et al (2008) Older fallers with poor<br />

working memory overestimate their postural limits. Arch Phys Med<br />

Rehabil 89: 1335–40<br />

Lord SR, Menz HB, Tiedemann A (2003) A physiological profile<br />

approach to falls risk assessment and prevention. Phys Ther 83:<br />

237–52<br />

Lord SR, Smith ST, Menant JC (2010) Vision and falls in older people:<br />

Risk factors and intervention strategies. Clinics Geriatr Med 26:<br />

569–81<br />

Meijer JW, Smit AJ, Sonderen EV et al (2002) Symptom scoring<br />

systems to diagnose distal polyneuropathy in diabetes: the Diabetic<br />

Neuropathy Symptom score. Diabet Med 19: 962–5<br />

Menz G, Morris M, Lord S (2006) Foot and ankle risk factors for falls<br />

in older people: a prospective study. J Gerontol A Biol Sci Med Sci<br />

61: 866–70<br />

Meyer C, Hill S, Dow B et al (2013) Translating falls prevention<br />

knowledge to community-dwelling older PLWD: A mixed-method<br />

systematic review. Gerontologist 55: 560–74<br />

Moyer VA (2012) Prevention of falls in community-dwelling older<br />

adults: U.S. Preventive Services Task Force recommendation<br />

statement. Ann Intern Med 157: 197–204<br />

Palma F, Antigual D, Martinez S et al (2013) Static balance in patients<br />

presenting diabetes mellitus type 2 with and without diabetic<br />

polyneuropathy. Arch Endocrinol Metab 57: 722–6<br />

Pijpers E, Ferreira I, De Jongh R et al (2012) Older individuals<br />

with diabetes have an increased risk of recurrent falls: analysis<br />

of potential mediating factors: the Longitudinal Ageing Study<br />

Amsterdam. Age Ageing 41: 358–65<br />

Podsiadlo D, Richardson S (1991) The Timed “Up & Go”: A test of<br />

basic functional mobility for frail elderly persons. J Amer Geriatr<br />

Soc 39: 142–8<br />

Roman De Mettelinge T, Cambier D, Calders P et al (2013)<br />

Understanding the relationship between type 2 diabetes mellitus<br />

and falls in older adults: A Prospective Cohort Study. PLoS ONE 8:<br />

e67055<br />

Royal Australian College Of General Practitioners (2016) General<br />

practice management of type 2 diabetes: 2016-18. RACGP, East<br />

Melbourne, Vic<br />

Russell MA, Hill KD, Blackberry I et al (2008) The reliability and<br />

predictive accuracy of the falls risk for older people in the<br />

community assessment (FROP-Com) tool. Age Ageing 37: 634–9<br />

Russell MA, Hill KD, Day L et al (2009) Development of the Falls Risk<br />

for Older People in the Community (FROP-Com) screening tool.<br />

Age Ageing 38: 40–6<br />

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after a fall in older people with cognitive impairment and<br />

dementia presenting to the accident and emergency department:<br />

Randomised controlled trial. BMJ 326:<br />

Sherrington C, Tiedemann A, Fairhall N et al (2011) Exercise to prevent<br />

falls in older adults: An updated meta-analysis and best practice<br />

recommendations. N S W Public Health Bull 22: 78–83<br />

Sinclair A, Dunning T, Rodriguez-Mañas L (2015) Diabetes in older<br />

people: new insights and remaining challenges. Lancet Diabetes<br />

Endocrinol 3: 275–85<br />

Tiedemann A, Shimada H, Sherrington C et al (2008) The comparative<br />

ability of eight functional mobility tests for predicting falls in<br />

community-dwelling older people. Age Ageing 37: 430–5<br />

Tinetti ME, Franklin Williams T, Mayewski R (1986) Fall risk index for<br />

elderly patients based on number of chronic disabilities. Am J Med<br />

80: 429–34<br />

van Deursen, R (2008) Footwear for the neuropathic patient:<br />

offloading and stability. Diabetes Metab Res Rev 24: S96–S100<br />

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Interventions to reduce fear of falling in community-living older<br />

people: A systematic review. J Am Geriatr Soc 55: 603–15<br />

74 Diabetes & Primary Care Australia Vol 2 No 2 2017


Article<br />

The effect of diabetes on the skin<br />

before and after ulceration<br />

Lesley Weaving, Roy Rasalam<br />

Diabetes affects the skin in many different ways at a microcirculatory level, making it<br />

more prone to injury and ulceration. These changes not only have an impact on healing<br />

but also on the resulting scar t<strong>issue</strong>, which is not as strong as the skin was prior to injury.<br />

Eight-five percent of amputations are preceded by ulceration, with re-ulceration rates<br />

reported to be as high as 70% after 5 years. This article looks at the changes that occur<br />

in the skin of people with diabetes and the importance of skin care before and after<br />

ulceration.<br />

A<br />

history of ulceration is considered<br />

to be a significant risk factor for<br />

re-ulceration, and as such, people<br />

with diabetes are classed as high risk if they<br />

have a history of foot ulceration (National<br />

Institute for Health and Care Excellence,<br />

2015). Australia’s amputation rate as a result<br />

of diabetes appears to have increased in the<br />

last decade and is a major contributor to the<br />

national burden of condition (Lazzarini et al,<br />

2012). Eighty-five per cent of amputations are<br />

preceded by ulcers (International Diabetes<br />

Federation, 2016); therefore, the prevention of<br />

re-ulceration is an important consideration in<br />

reducing amputation rates. Varying rates of reulceration<br />

have been reported in the literature,<br />

but the rate of re-ulceration is known to<br />

increase over time from initial ulceration;<br />

Miller et al (2014) reported 34% re-ulceration<br />

at 1 year, 61% at 3 years and 70% at 5 years.<br />

A critical triad of neuropathy, minor foot<br />

trauma and foot deformity is present in >63%<br />

of patients’ causal pathways to foot ulceration<br />

(Reiber et al, 1999). There are many reasons<br />

that determine whether people with diabetes<br />

develop ulcers, including their vascular<br />

status, nutritional status and compliance with<br />

preventative therapies, such as custom-made<br />

shoes or insoles (Miller et al, 2014). Despite<br />

these interventions, one study has reported a<br />

30% re-ulceration rate over a 2-year period,<br />

during which individuals received regular<br />

podiatric review (Westphal et al, 2011). With<br />

this in mind, do we need to consider other<br />

factors, such as the health of the skin? What is<br />

the effect of ulceration on the skin during and<br />

after healing, and does it play a role in the risk<br />

of re-ulceration?<br />

The skin<br />

The skin is the largest organ of the body.<br />

Its main functions are to act as a barrier<br />

to substances entering the body and in the<br />

prevention of moisture loss. It helps to regulate<br />

temperature and provides sensory information<br />

(e.g. pain, touch and temperature). It has<br />

three layers: the epidermis, the dermis and a<br />

fat (subcutaneous) layer (see Figure 1). The<br />

epidermis is the thin outer layer, made of five<br />

layers. The outermost layer is the stratum<br />

corneum, which consists of dead cells and is the<br />

major barrier to chemical and bacterial transfer<br />

through the skin. The epidermis is thicker on<br />

the plantar aspect of the foot and is relatively<br />

waterproof. The second layer of the skin is the<br />

dermis, which contains nerve endings, sweat<br />

glands, oil (sebaceous) glands, hair follicles<br />

and blood vessels. It consists of a thick layer<br />

of fibrous and elastic t<strong>issue</strong>, giving the skin its<br />

flexibility and strength. Below the dermis is a<br />

Citation: Weaving L,<br />

Rasalam R (2017) The effect<br />

of diabetes on the skin before<br />

and after ulceration. Diabetes &<br />

Primary Care Australia 2: 75–9<br />

Article points<br />

1. People with diabetes<br />

are more prone to skin<br />

injury and ulceration.<br />

2. Diabetes impairs the<br />

skin’s ability to heal.<br />

3. Scar t<strong>issue</strong> is not as strong as<br />

the t<strong>issue</strong> was before injury.<br />

4. Skin should be kept in the<br />

best condition possible to<br />

prevent re-ulceration.<br />

Key words<br />

– Healing<br />

– Re-ulceration<br />

– Scar t<strong>issue</strong><br />

– Skin<br />

Authors<br />

Lesley Weaving is diabetes<br />

specialist podiatrist, Leicestershire<br />

Partnership Trust, Coalville<br />

Community Hospital, Coalville,<br />

Leicestershire, UK; Roy Rasalam<br />

is Director of Clinical Studies,<br />

College of Medicine, James Cook<br />

University, Qld, Australia.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 75


The effect of diabetes on the skin before and after ulceration<br />

80% of the tensile strength of normal skin<br />

(Ousey, 2009). Many factors play a role in<br />

how closely the healed skin resembles the<br />

original uninjured t<strong>issue</strong>, including the size,<br />

depth and location of the wound, as well as<br />

the nutritional status and overall health of the<br />

individual (Teller and White, 2009).<br />

Figure 1. Cross-section through the skin.<br />

Page points<br />

1. Skin conditions, such as<br />

infection, xerosis and<br />

psoriasis, are common in<br />

people with diabetes.<br />

2. Regular moisturising of dry skin<br />

is recommended as part of a<br />

routine foot care regimen.<br />

3. Scar t<strong>issue</strong> is not as strong<br />

as the original uninjured<br />

t<strong>issue</strong> and so is at increased<br />

risk of damage.<br />

subcutaneous layer of fat that helps insulate the<br />

body from heat and cold, provides protective<br />

padding and serves as an energy store (Health<br />

and Safety Executive, 2016).<br />

The healing process<br />

When the skin is damaged, a complex healing<br />

process takes place that can be divided<br />

into four phases (Box 1). The final stage<br />

of healing, maturation, lasts from 21 days<br />

to 2 years. During this process, epithelial<br />

cells reduce the size of the wound. This is<br />

followed by re-organisation of the collagen<br />

by macrophages to form a scar (Brown, 2015).<br />

In healthy individuals, the resulting scar<br />

t<strong>issue</strong> formed after injury has approximately<br />

Box 1. The wound healing process.<br />

l Vascular response (haemostasis): injured<br />

vessels constrict, a clot forms consisting<br />

of a fibrin mesh that forms a scab, and<br />

vasodilation of the vessels commences.<br />

l Inflammation: occurs in acute wounds<br />

3–5 days after injury and is prolonged in<br />

chronic wounds.<br />

l Proliferation: collagen fibres form to<br />

replace lost t<strong>issue</strong>.<br />

l Maturation: in healthy individuals, this<br />

stage commences 21 days after injury.<br />

Scarring develops, and the new t<strong>issue</strong> is<br />

avascular and contains no hair, sebaceous<br />

or sweat glands.<br />

The effect of diabetes on skin healing<br />

Diabetes can affect the skin in different<br />

ways. Autonomic neuropathy is a common<br />

complication of diabetes leading to dry<br />

skin, loss of sweating and the subsequent<br />

development of fissures and cracks that break<br />

the skin barrier, allowing microorganisms to<br />

enter (Vinik et al, 2003).<br />

It is now understood that a complex<br />

relationship exists between sensory<br />

nerve function and vascular response in<br />

type 2 diabetes. Dermal neurovascular<br />

function is regulated by peripheral<br />

C fibre neurons, which are damaged in<br />

diabetic neuropathy. This results in an<br />

imbalance between vasodilators (nitric<br />

oxide, substance P, and calcitonin generelated<br />

peptide) and vasoconstrictors<br />

(angiotensin II and endothelin). This<br />

dysregulation leads to decreased pain and<br />

warm thermal perception, leaving skin<br />

vulnerable to heat and t<strong>issue</strong> injury (Vinik et<br />

al, 2001).<br />

It has also been demonstrated that there is<br />

a reduced oxygen supply within the t<strong>issue</strong> of<br />

people with diabetes, which is accentuated<br />

in the presence of neuropathy (Greenman<br />

et al, 2005). Other skin conditions are also<br />

commonly seen in people with diabetes,<br />

the prevalences of which are reported to be<br />

between 30% and 91.2% (Demirseren et al,<br />

2014). The most frequently reported skin<br />

condition in people with diabetes is cutaneous<br />

infection (mainly fungal), followed by xerosis<br />

(dry skin) and inflammatory skin diseases<br />

such as psoriasis (Figure 2). These conditions<br />

are more common in people with diabetes<br />

who have nephropathy than in those without<br />

nephropathy, and those who have an HbA 1c<br />

of >64 mmol/mol (8%) are at the greatest risk<br />

(Demirseren et al, 2014).<br />

76 Diabetes & Primary Care Australia Vol 2 No 2 2017


The effect of diabetes on the skin before and after ulceration<br />

Figure 2. Psoriasis is one of the most common skin<br />

conditions experienced by people with diabetes.<br />

Vascular endothelial cells line the entire<br />

circulatory system, from the heart to<br />

capillaries. These cells are important for<br />

vascular biology and become impaired not only<br />

with age but also as a result of hyperglycaemia,<br />

which results in the impairment of blood flow<br />

to the t<strong>issue</strong>s (Petrofsky, 2011). When pressure<br />

is applied to healthy skin, the affected t<strong>issue</strong><br />

can become hypoxic; once the pressure is<br />

released there is reactive hyperaemia (increase<br />

in blood flow) to oxygenate the t<strong>issue</strong>. Vascular<br />

endothelial dysfunction can diminish this<br />

response. It has also been demonstrated that<br />

in a standing position, the average person still<br />

has circulation in the skin but in people with<br />

diabetes (even those with normal weight) there<br />

is occlusion to the skin (McLellan et al, 2009).<br />

This occlusion, together with reduced or no<br />

post-occlusive hyperaemia, may be the reason<br />

that feet are so susceptible to wounds and<br />

skin injury, particularly in people with type 2<br />

diabetes (Petrofsky, 2011).<br />

Emollients<br />

Regular moisturising of dry skin is<br />

recommended as part of a routine foot care<br />

regimen to reduce the risk of cracking and<br />

ulceration. What is not always clear is which<br />

emollient to use. There is little evidence<br />

available as to the most effective emollient,<br />

not only for the general population, but also<br />

for people with diabetes. A moisturiser that<br />

the patient is willing or happy to use that<br />

is supported by the available evidence is<br />

preferable. The clinician should also check<br />

that the patient likes the smell, texture and<br />

absorption of the cream before recommending<br />

or prescribing one. There is some evidence<br />

that high-concentration, urea-based emollients<br />

are beneficial, and these have been shown to<br />

improve dryness on the feet of people with<br />

diabetes (Bristow, 2013).<br />

For twice-a-day application, it is<br />

recommended that an emollient is applied just<br />

before getting into bed. Covering the foot with<br />

a damp undersock and then a dry oversock may<br />

enhance the effect of the emollient (Bristow,<br />

2013). For once-a-day application, the cream<br />

should form part of a patient’s daily regimen<br />

of washing, drying and checking their feet<br />

thoroughly. It is recommended that emollients<br />

be used to lubricate the skin, but not between<br />

the toes (International Working Group on<br />

the Diabetic Foot, 2015). A pump dispenser<br />

is considered by some clinicians a more userfriendly<br />

way of delivering the right amount of<br />

emollient than a tub and also decreases the risk<br />

of contamination (Carr et al, 2008), although<br />

tubes are also commonly used.<br />

Silicones<br />

Once skin has healed, silicone gel has been<br />

proven to be effective in scar-t<strong>issue</strong> management<br />

on non-weight-bearing areas; however there<br />

is little evidence to support its use on weightbearing<br />

areas (Westphal et al, 2011). Figure 3<br />

and Figure 4 demonstrate that silicone gel may<br />

be useful in protecting newly healed skin<br />

during the maturation process. A person with<br />

type 2 diabetes who suffered from psoriasis<br />

had developed ulceration and subsequent<br />

osteomyelitis at the base of the fifth metatarsal<br />

Page points<br />

1. Regular moisturising of dry<br />

skin is recommended as<br />

part of a routine foot-care<br />

regimen to reduce the risk<br />

of cracking and ulceration.<br />

2. Once skin has healed,<br />

silicone gel has been proven<br />

to be effective in scar-t<strong>issue</strong><br />

management on non-weightbearing<br />

areas; however there<br />

is little evidence to support its<br />

use on weight-bearing areas.<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 77


The effect of diabetes on the skin before and after ulceration<br />

Page points<br />

1. There are many factors<br />

affecting a person’s skin<br />

when they have diabetes.<br />

2. From available evidence, the<br />

healing of a diabetic foot ulcer<br />

should not be considered<br />

the end result of a patient’s<br />

journey, but the beginning of<br />

a process to remain healed.<br />

3. Further research is required<br />

on the most-effective<br />

way to care for the skin of<br />

people with diabetes.<br />

head, which had healed well with the use of<br />

a removable cast device. However, once they<br />

returned to wearing their bespoke shoes with<br />

total contact insole, the skin re-ulcerated<br />

(Figure 3). Silicone sheeting was used to protect<br />

the area once epithelisation was achieved and for<br />

8 weeks afterwards, and no further ulceration<br />

occurred during this time (Figure 4). This<br />

suggests that the silicone sheeting provided<br />

some protection to the newly healed skin during<br />

the early stages of the maturation process<br />

(Weaving, 2014). However, a pilot study of<br />

30 people with diabetes found that silicone gel<br />

sheeting did not reduce the risk of ulceration<br />

(Westphal, 2011).<br />

Why it’s important to keep the<br />

skin healthy<br />

There are many factors affecting a person’s skin<br />

when they have diabetes. These factors can lead<br />

to ulceration and contribute to delayed healing.<br />

Poor glycaemic control of diabetes has been<br />

shown to affect the microcirculation, along<br />

with poor oxygen supply, occlusion in the skin<br />

during weight bearing, changes to the vascular<br />

endothelial cells, dry skin and reduction in<br />

elasticity all putting the skin at greater risk<br />

of injury. This is further complicated by the<br />

reduced strength of the scar t<strong>issue</strong> that forms<br />

after the ulcer has healed.<br />

Eighty per cent of ulcers are caused by some<br />

form of trauma and are, therefore, considered<br />

to be preventable (Healy et al, 2013). While<br />

custom-made footwear is used to prevent<br />

re-ulceration, it appears to be most effective for<br />

those with foot deformity (Reiber et al, 2002).<br />

Not every insole or shoe is a perfect fit to each<br />

patient’s foot (Miller et al, 2014). It is therefore<br />

important that the skin on the foot is kept in the<br />

best condition it can be to cope with the stresses<br />

placed upon it, whether it is from shoe wear or<br />

simple day-to-day weight-bearing activities.<br />

Conclusion<br />

There is little evidence on how best to look<br />

after the skin of people with diabetes. From<br />

the available evidence, the healing of a diabetic<br />

foot ulcer should not be considered the end<br />

result of a patient’s journey, but the beginning<br />

Figure 3. A patient with type 2 diabetes and psoriasis<br />

experienced re-ulceration after changing from a<br />

removable cast device back to their bespoke shoes.<br />

Figure 4. The patient continued to use silicone sheeting<br />

for 8 weeks after the ulcer had healed, which prevented<br />

re-ulceration.<br />

of a process to remain “healed”. We want<br />

patients to be active and keep mobile to<br />

help with their overall health and wellbeing;<br />

however, the impact of diabetes on their skin<br />

makes them vulnerable to skin breakdown,<br />

particularly where there is scar t<strong>issue</strong> from<br />

previous ulceration. Further research is<br />

required on the most-effective way to care<br />

for the skin of people with diabetes not just<br />

when dry, but also post-healing during the<br />

maturation process when the stresses and<br />

strains of simple weight bearing could lead<br />

to re-ulceration and, subsequently, potential<br />

78 Diabetes & Primary Care Australia Vol 2 No 2 2017


The effect of diabetes on the skin before and after ulceration<br />

loss of a limb. This is a worthwhile endeavour<br />

when we consider that every 30 seconds a<br />

lower limb is lost somewhere in the world as a<br />

consequence of diabetes (Boulton et al, 2005).<br />

<br />

n<br />

Acknowledgement<br />

This article has been modified from one<br />

previously published in The Diabetic Foot Journal<br />

(2016, 3: 142–8).<br />

Lazzarini PA, Gurr JM, Rogers JR et al (2012) Diabetes foot<br />

disease: the Cinderella of Australian diabetes management?<br />

J Foot Ankle Res 5: 24<br />

McLellan K, Petrofsky JS, Zimmerman G et al (2009) The<br />

influence of environmental temperature on the response<br />

of the skin to local pressure: the impact of aging and<br />

diabetes. Diabetes Technol Ther 11: 791–8<br />

Miller JD, Salloum M, Button A et al (2014) How can I<br />

maintain my patient with diabetes and history of foot ulcer<br />

in remission? Int J Low Extrem Wounds 13: 371–7<br />

“This is a worthwhile<br />

endeavour when we<br />

consider that every<br />

30 seconds a lower<br />

limb is lost somewhere<br />

in the world as a<br />

consequence of<br />

diabetes.”<br />

Boulton AJ, Vilikyte L, Ragnarson-Tennvall G et al (2005)<br />

The global burden of diabetic foot disease. Lancet 366:<br />

1719–24<br />

National Institute for Health and Care Excellence (2015)<br />

NICE guideline 19. Diabetic foot problems: prevention<br />

and management. NICE, London, UK. Available at: www.<br />

nice.org.uk/guidance/ng19 (accessed 02.09.2016)<br />

Bristow I (2013) Emollients in the care of the diabetic foot.<br />

The Diabetic Foot Journal 16: 61–6<br />

Ousey K (2009) Chronic wounds – an overview. J Commun<br />

Nursing 21: 4–9<br />

Brown A (2015) Wound management 1: Phases of the wound<br />

healing process. Nursing Times 111: 12–3<br />

Carr J, Akram M, Sultan A et al (2008) Contamination of<br />

emollient creams and ointments with Staphylococcus<br />

aureus in children with atopic dermatitis. Dermatitis 19:<br />

282<br />

Demirseren DD, Emre S, Akoglu G et al (2014) Relationship<br />

between skin diseases and extracutaneous complications<br />

of diabetes mellitus: clinical analysis of 750 patients.<br />

Am J Dermatol 15: 65–70<br />

Greenman RL, Panasyuk S, Wang X et al (2005) Early<br />

changes in the microcirculation and muscle metabolism<br />

of the diabetic foot. Lancet 366: 1711–5<br />

Healy A, Naemi R, Chockalingam N (2013) The effectiveness<br />

of footwear as an intervention to prevent or to reduce<br />

biomechanical risk factors associated with diabetic foot<br />

ulceration: a systematic review. J Diabetes Complications<br />

27: 391–400<br />

Petrofsky JS (2011) The effect of type-2-diabetes-related<br />

vascular endothelial dysfunction on skin physiology and<br />

activities of daily living. J Diabetes Sci Technol 5: 657–67<br />

Reiber GE, Vileikyte L, Boyko EJ et al (1999) Causal pathways<br />

for incident lower-extremity ulcers in patients with diabetes<br />

from two settings. Diabetes Care 22: 157–62<br />

Reiber GE, Smith DG, Wallace C et al (2002) Effect of<br />

therapeutic footwear on foot reulceration in patients<br />

with diabetes. A randomised controlled trial. JAMA 287:<br />

2552–8<br />

Teller P, White TK (2009) The physiology of wound healing:<br />

injury through maturation. Surg Clin North Am 89: 599–<br />

610<br />

Vinik AI, Erbas T, Park TS (2001) Dermal neurovascular<br />

dysfunction in type 2 diabetes. Diabetes Care 24: 1468–75<br />

Health and Safety Executive (2016) Structure and<br />

functions of the skin. HSE, London, UK. Available at:<br />

http://bit.ly/ZIW36y (accessed 02.09.16)<br />

Vinik AI, Maser RE, Mitchell BD, Freeman R (2003) Diabetic<br />

autonomic neuropathy. Diabetes Care 26: 1553–66<br />

International Diabetes Federation (2016) Diabetes<br />

and the Foot. IDF, Brussels, Belgium. Available at:<br />

http://bit.ly/2cUTPJB (accessed 13.09.16)<br />

Weaving L (2014) KerraPro pressure reducing pads<br />

in preventing pressure ulceration. Harrogate 2014<br />

Conference Posters. Harrogate, Wounds UK, UK. Available<br />

at: http://bit.ly/2m75Rab (accessed 02.09.16)<br />

International Working Group on the Diabetic Foot (2015)<br />

Prevention and management of foot problems in diabetes:<br />

a Summary Guidance for daily practice 2015. IWGDF<br />

Guidance documents. IDF, Brussels, Belgium. Available at:<br />

http://bit.ly/2kLpS69 (accessed 22.02.16)<br />

Westphal C, Neame IM, Harrison JC, et al (2011) A diabetic<br />

foot ulcer pilot study: does silicone gel shee ting reduce<br />

the incidence of reulceration? J Am Podiatr Med Assoc<br />

101: 116–23<br />

Diabetes & Primary Care Australia Vol 2 No 2 2017 79


The PCDSA is a multidisciplinary society with the aim<br />

of supporting primary health care professionals to deliver<br />

high quality, clinically effective care in order to improve<br />

the lives of people with diabetes.<br />

The PCDSA will<br />

Share best practice in delivering quality diabetes care.<br />

Provide high-quality education tailored to health professional needs.<br />

Promote and participate in high quality research in diabetes.<br />

Disseminate up-to-date, evidence-based information to health<br />

professionals.<br />

Form partnerships and collaborate with other diabetes related,<br />

high level professional organisations committed to the care of<br />

people with diabetes.<br />

Promote co-ordinated and timely interdisciplinary care.<br />

Membership of the PCDSA is free and members get access to a quarterly<br />

online journal and continuing professional development activities. Our first<br />

annual conference will feature internationally and nationally regarded experts<br />

in the field of diabetes.<br />

To register, visit our website:<br />

www.pcdsa.com.au

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