Recommendations for SMBG

Recommendations for SMBG Recommendations for SMBG

A Diabetes Update<br />

What’s new since the 2008 clinical<br />

practice guidelines


Objectives<br />

To gain knowledge related to:<br />

‣ History of diabetes<br />

‣ Current diabetes statistics<br />

‣ Current diabetes practice<br />

‣ New models in organization of diabetes<br />

care<br />

‣ Implications <strong>for</strong> future diabetes care and<br />

management


History<br />

‣ 1552 BCE- Egyptian physician makes the first known<br />

mention of diabetes as passing of too much urine<br />

‣ 1776- First diagnostic tests <strong>for</strong> diabetes- evaporating 2<br />

quarts of urine leaving saccharine compounds and<br />

tasting urine <strong>for</strong> sweetness<br />

‣ 1920, Oct.-Banting first conceives of insulin<br />

‣ 1921, Summer-Banting and Best discover insulin<br />

‣ 1922, Jan.-1 st patient treated with insulin<br />

‣ 1950’s-first oral medications <strong>for</strong> Type 2<br />

‣ 1966- first pancreas transplant<br />

‣ 1971- first portable blood glucose monitor<br />

‣ 1999- first islet cell transplant


Incidence and Prevalence<br />

KB IH BC<br />

Prevalence 6.1% 6.6% 6.9-7.4%<br />

Incidence 4,482 43,536 202,442- 338,000<br />

Sources: Primary Health Care registry (DAD); Discharge Abstract Database (DAD), Medical Services Plan (MSP),<br />

2008/09.<br />

http://www.diabetes.ca/documents/get-involved/CDA_BC_Cost_Model_Report_Backgrounder_FINAL.pdf<br />

http://www40.statcan.ca/l01/cst01/health54a-eng.htm


Type 1 Diabetes<br />

‣ Absolute insulin<br />

deficiency<br />

‣ Rapid onset<br />

‣ Always fatal prior to<br />

1922<br />

‣ 10% of all diabetes


Type 2 Diabetes<br />

‣ Predominantly insulin<br />

resistance with<br />

relative insulin<br />

deficiency<br />

‣ Slow onset and<br />

decline<br />

‣ 90% of all diabetes


Gestational Diabetes<br />

‣ glucose intolerance<br />

with onset or first<br />

recognition during<br />

pregnancy<br />

‣ Usually a transitory<br />

state<br />

‣ Approx. 50- 60 % go<br />

on to Type 2 diabetes<br />

later in life


Diagnosis Type 1 or 2<br />

Fasting PG >7.0 mmol/L<br />

or<br />

casual PG >11.1 mmol/L + symptoms<br />

polyuria, polydipsia and unexplained weight loss<br />

or<br />

2hPG in a 75-g OGTT<br />

11.1 mmol/L<br />

or<br />

Hemoglobin A1C > 6.5%


A1C: evolved recommendation<br />

‣ A1C >6.5% has been added as a<br />

diagnostic criterion <strong>for</strong> Type II DM<br />

• confirmatory test still required<br />

• A1C


Diagnosis Gestational<br />

IADPSG diagnostic criteria <strong>for</strong> gestational<br />

diabetes mellitus (75-g OGTT)<br />

Fasting plasma glucose 5.1<br />

1 hr plasma glucose 10.0<br />

2 hr plasma glucose 8.5<br />

One abnormal value constitutes GDM.<br />

http://www.perinatalservicesbc.ca/sites/bcrcp/files/Guidelines/Obstetrics/Updated_guideline10b.pdf


GDM -evolved recommendation.<br />

‣ Not without controversy<br />

‣ Consensus guideline<br />

‣ HAPO study-23,316 participants<br />

‣ Strong associations of increased birth<br />

weight and increased cord blood c-peptide<br />

below previous diagnostic levels <strong>for</strong> GDM


Blood Glucose Targets<br />

<strong>for</strong> Management


Targets Type 1 and Type 2-<br />

Adult<br />

A1C (%) ≤ 7.0<br />

FPG or pre-prandial PG (mmol/L) 4.0-7.0<br />

(5.0–8.0 if angina )<br />

2-hr postprandial PG (mmol/L) 7.0-10.0<br />

(5.0–8.0 if A1C targets not being met)<br />

Canadian Diabetes Association 2008 Clinical Practice Guidelines <strong>for</strong> the Prevention and Management of Diabetes<br />

in Canada


Target Implications<br />

‣ Was a trend to tighter targets HbA1c< 6.5% (IDF and<br />

ACE)<br />

‣ ACCORD Trial- intensive and routine managed groups<br />

‣ Halted early- increased mortality in intensive group<br />

http://www.accordtrial.org/public/index.cfm?CFID=55793&CFTOKEN=e8ea93ef16f5646d-560D983A-AF4E-7E83-27265E2B83ED8592


Targets Type 1 and Type 2<br />

Pregnant and Gestational<br />

‣ Fasting/preprandial PG: 3.8 to 5.2 mmol/L<br />

‣ • 1h postprandial PG: 5.5 to 7.7 mmol/L<br />

‣ • 2h postprandial PG l: 5.0 to 6.6 mmol/L<br />

Canadian Diabetes Association 2008 Clinical Practice Guidelines <strong>for</strong> the Prevention and Management of Diabetes in<br />

Canada


Other follow-up Laboratory Tests<br />

‣ A1C q3 months<br />

‣ Lab/glucose meter comparison at least annually<br />

‣ Annual random urine <strong>for</strong> ACR<br />

‣ Annual serum creatinine (every 6mos <strong>for</strong> people<br />

with nephropathy)<br />

‣ Type 1 should test <strong>for</strong> ketones with elevated BG<br />

during acute illness (>14.0mmol/L pre-prandial) or<br />

having symptoms of DKA


Beyond the <strong>Recommendations</strong>:<br />

Common Practice<br />

‣ electrolytes, BUN, Cr q 6 months with A1C<br />

‣ ACR<br />

‣ AST, ALT <strong>for</strong> people being treated with met<strong>for</strong>min or a<br />

statin<br />

‣ FBG yearly<br />

‣ TSH (thyroid disease & diabetes tend to co-occur)<br />

‣ Blood lipids @ diagnosis then q1-3 years as clinically<br />

indicated<br />

‣ Evolving use of hs-CRP to evaluate cardiovascular risk<br />

‣ Apo-B to monitor hyperlipidemia


Tools


Medication


Insulin<br />

Insulin categories referred to now as<br />

bolus, basal and premixed<br />

Inhaled insulin was not released<br />

BC- Insulin pumps covered <strong>for</strong><br />

pediatric Type 1


Other New Medications<br />

‣ Victoza- GLP1 receptor agonist<br />

‣ Byetta- incretin mimetic<br />

Use early to preserve insulin function<br />

‣ Otelixizumab- investigational<br />

immunotherapeutic<br />

http://clinicaltrials.gov/ct2/show/NCT01123083?term=defend-2&rank=1<br />

.


Tools SBGM


Canadian Optimal Medication Prescribing and Utilization<br />

Service (COMPUS)<br />

takes the position that:<br />

Routine self-monitoring of blood<br />

glucose by most adults with type 2<br />

diabetes using oral anti-diabetes<br />

drugs is<br />

not recommended.<br />

COMPUS Volume 3, Issue 6 July 2009<br />

http://www.bcguidelines.ca/guideline_diabetes.html#controversies_in_care_smbg<br />

http://www.cadth.ca/index.php/en/compus/blood-glucose<br />

http://www.cadth.ca/index.php/en/compus/blood-glucose/reports


The CDA maintains…<br />

‣ “[the COMPUS study] significantly undervalues<br />

safety and clinical considerations including<br />

hypoglycemia and diabetes complications”<br />

‣ The frequency of self-monitoring of blood glucose<br />

should be individualized depending on glycemic<br />

control and type of therapy and should include both<br />

pre- and postprandial measurements of blood<br />

glucose levels.<br />

‣ There is clear evidence <strong>for</strong> reduced episodes of<br />

hypoglycemia in patients with type 2 diabetes who<br />

practice frequent self-monitoring of blood glucose<br />

http://www.diabetes.ca/<strong>for</strong>-professionals/css-news-entry/position-statement-and-paper/


The Canadian Journal of Diabetes:<br />

‣ “<strong>SMBG</strong>… …valuable <strong>for</strong> both patients and healthcare<br />

professionals”<br />

‣ <strong>SMBG</strong> recommended, though:<br />

• no consensus within & between professional groups<br />

• highly individual<br />

Celeste Latter BSc MHI, Pam McLean-Veysey BSc(Pharm), Peggy Dunbar MED PDt, Dawn<br />

Frail BSc(Pharm) MSc, Ingrid Sketris PharmD MPA(HSA), Wayne Putnam MD FCFP<br />

CANADIAN JOURNAL OF DIABETES. 2011;35(1):31-38.<br />

‣ The new version of the clinical practice guidelines will be<br />

available in 2013. The evidence is mounting quickly that<br />

health professionals working with people with type 2<br />

diabetes who do not require insulin must use <strong>SMBG</strong> in<br />

more selective and limited circumstances (7).<br />

http://www.diabetes.ca/documents/<strong>for</strong>-professionals/CJD--March_2011--H.Dean_.pdf


BC MoH<br />

‣ Recently CADTH (Canadian Agency <strong>for</strong> Drugs<br />

and Technologies in Health) investigated the<br />

evidence relating to <strong>SMBG</strong>. Their findings<br />

identified that evidence supporting routine<br />

<strong>SMBG</strong> <strong>for</strong> individuals not on insulin therapy is<br />

poor and associated costs are escalating. As<br />

such the Ministry of Health is requesting Health<br />

Authorities review their practice and policy<br />

relating to … <strong>SMBG</strong> practice.


Organization of Care


Organization of Care<br />

‣ Self Management- Goal setting and action<br />

planning<br />

‣ Attachment to practice, Primary Care<br />

Home<br />

‣ Integrated Health Networks, Family Health<br />

Care teams


Attachment to Practice Evaluation<br />

• Clear inverse relationship between the level of<br />

attachment to a primary care practice, and costs, <strong>for</strong><br />

higher care needs patients<br />

• Most of the differential in costs is in hospital costs<br />

• There<strong>for</strong>e, activities which foster greater attachment of<br />

patients to a particular primary care practice have the<br />

potential to reduce health care costs<br />

Hollander, M.J., Kaldec, H., Hamdi, R., & Tessaro, T. (2009)<br />

Increasing value <strong>for</strong> money in the Canadian healthcare system:<br />

New findings on the contribution of primary care.<br />

Healthcare Quarterly, 12(4), 30-42.<br />

Adapted from BCMA


Implications<br />

‣ Need <strong>for</strong> improved self management options<br />

‣ Need <strong>for</strong> more primary care providers<br />

‣ Health professionals will need training in self<br />

management support<br />

‣ Better electronic communication tools<br />

‣ Patient registries<br />

‣ Reminders<br />

‣ Access- expanded hours and locations, Dr.’s offices,<br />

education (in person and on line), labs, pharmacies,<br />

point of care tools and supplies<br />

‣ Improved prevention ef<strong>for</strong>ts<br />

‣ Consider costs to the patient<br />

http://www.diabetes.ca/documents/<strong>for</strong>-professionals/CJD--June_2008--Cameron,_D.pdf


KB IHN outcomes<br />

‣decrease in ER visits 22-63%<br />

‣decrease in acute admissions 25-<br />

88%<br />

‣decrease in hospital LOS 23-85%


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