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Book of Medical Disorders in Pregnancy - Tintash

Book of Medical Disorders in Pregnancy - Tintash

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Risk factors:<br />

The risk <strong>of</strong> GDM <strong>in</strong>creases with<br />

<strong>in</strong>creas<strong>in</strong>g age, and high BMI before<br />

pregnancy, Smok<strong>in</strong>g doubles the risk <strong>of</strong><br />

gestational diabetes Increase <strong>in</strong> weight<br />

between pregnancies, Short <strong>in</strong>terval<br />

between pregnancies, previous<br />

unexpla<strong>in</strong>ed stillbirth, previous<br />

macrosomia and Family history <strong>of</strong><br />

GDM, also <strong>in</strong>creases risk <strong>of</strong> develop<strong>in</strong>g<br />

GDM.<br />

Screen<strong>in</strong>g:<br />

Because the condition may be<br />

asymptomatic but have serious<br />

consequences that can be reduced by<br />

treatment the patient should be screened.<br />

There is lack <strong>of</strong> consensus about who to<br />

screen and the criteria for diagnosis.<br />

Ur<strong>in</strong>e should be checked for glucose at<br />

every antenatal visit and if it is present at<br />

++, further <strong>in</strong>vestigation is required. The<br />

World Health Organi-zation advice that<br />

a 75 g oral glucose tolerance test<br />

(OGTT) should be conducted if the<br />

blood glucose exceeds 5.5 mmol/l at 2<br />

hours or more after food, or exceeds 7<br />

mmol/l with<strong>in</strong> 2 hours <strong>of</strong> food. The<br />

criteria recommended for diagnosis <strong>of</strong><br />

GDM are fast<strong>in</strong>g venous plasma glucose<br />

over 5.5 mmol/l or 2 hours after OGTT<br />

over 9mmol/l. Screen-<strong>in</strong>g will detect<br />

50% or more <strong>of</strong> all cases which means<br />

that up to half will not be screened or<br />

detected. Hence vigilance is required<br />

dur<strong>in</strong>g antenatal care, especially if there<br />

is glycosuria.<br />

Causes <strong>of</strong> diabetes: There is <strong>in</strong>creased<br />

level <strong>of</strong> hormones such as cortisol, and<br />

human growth hormone dur<strong>in</strong>g<br />

pregnancy. These hormones are <strong>in</strong>sul<strong>in</strong><br />

<strong>in</strong>hibitor. Hypertension coexists with<br />

type II <strong>in</strong> about 40% at age 45 ris<strong>in</strong>g to<br />

60% at age 75. 70% <strong>of</strong> type II patients<br />

19<br />

die from cardio-vascular disease and at<br />

least 60% <strong>of</strong> patients will require 2 or 3<br />

antihypertensive agents to achieve tight<br />

control.<br />

Critical balance which is ma<strong>in</strong>ta<strong>in</strong>ed<br />

between these hormones dur<strong>in</strong>g normal<br />

health is upset dur<strong>in</strong>g pregnancy.<br />

The student will realize that <strong>in</strong>sul<strong>in</strong> is<br />

released from pancreatic islet cells <strong>in</strong><br />

response to hyperglycemia and hyper<br />

am<strong>in</strong>oacidemia. The blood level <strong>of</strong> the<br />

<strong>in</strong>sul<strong>in</strong> is ma<strong>in</strong>ta<strong>in</strong>ed by both synthesis<br />

and transport <strong>of</strong> the hormone. In cases <strong>of</strong><br />

output failure, <strong>in</strong>sul<strong>in</strong> dependent<br />

diabetes results. The primary output<br />

failure may be due to <strong>in</strong>herent deficiency<br />

<strong>in</strong> pancreas. The secondary output<br />

failure may be due to destruction <strong>of</strong><br />

islets, pancreatitis, and pancreatic<br />

replacement with tomur,<br />

hemochromatosis and exhaustion <strong>of</strong><br />

pancreas associated with <strong>in</strong>creased<br />

requirements. The pancreatic release <strong>of</strong><br />

<strong>in</strong>sul<strong>in</strong> may be blocked by drugs such as<br />

Thiazide and Ep<strong>in</strong>ephr<strong>in</strong>e. The failure<br />

may also be idiopathic or secondary to<br />

known antagonist <strong>of</strong> <strong>in</strong>sul<strong>in</strong> like cortisol,<br />

ep<strong>in</strong>ephr<strong>in</strong>e and human growth hormone<br />

(HGH). The half life <strong>of</strong> <strong>in</strong>sul<strong>in</strong> is 10<br />

m<strong>in</strong>utes.<br />

Classification: There are number <strong>of</strong><br />

classi-fications reported <strong>in</strong> the literature.<br />

These are shown below. Some <strong>of</strong> these<br />

are based on history <strong>of</strong> the patient while<br />

the other on laboratory f<strong>in</strong>d<strong>in</strong>gs and<br />

cl<strong>in</strong>ical symptoms.<br />

From obstetrical po<strong>in</strong>t, classification<br />

presented by Pris-cilla Whites is<br />

considered to be most useful and<br />

practical.<br />

A. Glucose tolerance test abnormal;<br />

no symptoms, euglycemia

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