Book of Medical Disorders in Pregnancy - Tintash
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