Venous
thromboembolism is globally recognized a
leading cause of maternal
mortality. However in West
Incidence 1 in 1500
deliveries (West) 1 in 1000 (India). This may postpartum or post operative. Postpartum
DVT is 3 times more than antepartum (3-16 times)
More after cesarean
section than normal delivery :-The incidence is approximately in 1 in 1500 deliveries seen in
the west and according to an Indian study, antenatal DVT is 0.1%. The risk is
lower for Asian and Hispanic women, higher for white and highest for black
women. Postpartum DVT has been reported to occur 3 to 5 times more often than
antepartum DVT and 3 to 16 times more frequent after cesarean section compared
to vaginal delivery.
MMR & DVT:_Venous
thromboembolism is leading cause of maternal mortality in western world and
accounts for 17% of all maternal deaths.
Mortality is primarily due to massive pulmonary embolism which
commonly occurs from a thrombus embolising from deep veins of lower
extremities. Pulmonary embolism can occur in up to 24% of untreated patients of
deep vein thrombosis. Thrombosis of
ileo-femoral veins is more common than thrombosis of calf vein in pregnancy and
has a higher risk of pulmonary embolism. Early diagnosis and treatment in
patients with acute venous thromboembolism decreases the mortality rate to
<1%. Risk factors associated with increased risk for venous thromboembolism
have been identified. Primary prophylaxis decreases the rate of thromboembolic
events in high risk patients.
Hemostasis is a
physiological process of four major steps occurring in set order.
Step 1: Vasoconstriction
Step 2: Activation and
aggregation of platelets
Step 3: Formation of
fibrin clot
Step 4: Dissolution of
clot by plasmin
Hypercoagulability, venous
stasis and vascular damage are components of Virchow's triad, all of which
occur in pregnancy.
Various physiological
changes occur in pregnancy which predispose to a procoagulant state:
Increase in factors VII,
VIII, and IX, X and XII and fibrinogen.
Increase in plasminogen
activator inhibitors such as tissue plasminogen activator inhibitor and
decrease in the levels of tissue plasminogen activator

12) Hypovolemia – so in
obese women one can continue the drip for 36 hrs or more 13) , massive
blood loss 14)
Hyperemesis, 15) dehydration
16) Nonpreg or even pregàif Long distance travel 17) Prolonged immobilization.
18)
Prolonged labor 19) septic
abortion, peritonitis or severe
infection, e.g. pyelonephritis 20 ) Ovarian hyperstimulation syndrome21) Operations
for ca Cx /Ca ovary à Malignancy
especially pelvic and abdominal
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