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Book of Medical Disorders in Pregnancy - Tintash

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hours. The maximal effect takes 36 to 72<br />

hours to develop, after <strong>in</strong>itial<br />

adm<strong>in</strong>istration <strong>of</strong> the drug.<br />

The cl<strong>in</strong>ical target <strong>in</strong> achiev<strong>in</strong>g<br />

desired anticoagulant effect is to reduce<br />

the prothromb<strong>in</strong> time or activity to about<br />

20 per cent <strong>of</strong> normal control The effect<br />

<strong>of</strong> these drugs can be reversed by<br />

<strong>in</strong>travenous <strong>in</strong>jection <strong>of</strong> 50 to 150 mg <strong>of</strong><br />

Vitam<strong>in</strong> K" given very slowly and no<br />

more than 10 mg per m<strong>in</strong>ute. The<br />

activity <strong>of</strong> Vitam<strong>in</strong> K dependent clott<strong>in</strong>g<br />

factors reaches to safe level with<strong>in</strong> 4 to 8<br />

hours. Oral anticoagulants cross the<br />

placenta and may cause serious bleed<strong>in</strong>g.<br />

Warfar<strong>in</strong> is preferred over other<br />

agents s<strong>in</strong>ce it produce less side effects.<br />

The <strong>in</strong>itial dose is around 35 to 40 mg<br />

followed by 10 mg, depend<strong>in</strong>g upon the<br />

prothromb<strong>in</strong> time.<br />

Fig 10.4: Shows embolism <strong>in</strong> place <strong>in</strong><br />

one <strong>of</strong> the lungs<br />

Pulmonary embolism is the<br />

second most common cause <strong>of</strong> maternal<br />

death <strong>in</strong> pregnancy. This occurs when a<br />

thrombus breaks free from the ve<strong>in</strong>. It<br />

enters <strong>in</strong>to the pulmonary artery at the<br />

141<br />

time <strong>of</strong> right ventricular systole,<br />

becomes impacted <strong>in</strong> its branch whose<br />

lumen is narrow and the thrombus<br />

cannot pass through it. The effect <strong>of</strong> the<br />

embolism on the patient depends upon<br />

the size <strong>of</strong> the embolus. The cl<strong>in</strong>ical<br />

symptoms may be delayed until the<br />

fourth or fifth week after delivery, when<br />

the patient has returned home.<br />

Etiology: The causes <strong>of</strong> pulmonary<br />

embolism are the same as for deep<br />

venous phlebothrombosis. Pulmonary<br />

embolism is a recurrent disease. The<br />

woman who has c<strong>in</strong>e attack is liable to<br />

have another with<strong>in</strong> a few hours or day.<br />

Pathology: Embolism can occur before<br />

there is any sign <strong>of</strong> venous thrombosis.<br />

Pulmonary <strong>in</strong>farction occurs when a<br />

large clot is lodged <strong>in</strong> one <strong>of</strong> the ma<strong>in</strong><br />

branches <strong>of</strong> the pulmonary artery. This<br />

clot comes from the femoral or iliac ve<strong>in</strong><br />

<strong>in</strong> majority <strong>of</strong> cases, but <strong>in</strong> few cases it<br />

may come from the pelvic ve<strong>in</strong>s.<br />

The emulous can be lethal if half<br />

<strong>of</strong> the lung capacity is affected, An<br />

immense spasm <strong>of</strong> the unblocked<br />

pulmonary arteries play an important<br />

role <strong>in</strong> produc<strong>in</strong>g this fatal effect. Small<br />

emboli do not produce <strong>in</strong>farction <strong>of</strong><br />

healthy lungs, therefore they go<br />

unnoticed and the student may confuse<br />

the cl<strong>in</strong>ical features with pleurisy or<br />

pneumonia. However, multiple and<br />

recurrent small emboli can result <strong>in</strong><br />

pulmonary hypertension if left untreated.<br />

Pathophysiology <strong>of</strong> <strong>in</strong>fraction:<br />

The emboli can stop venous flow<br />

from the pulmonary segment supplied by<br />

these vessels. The alveoli cont<strong>in</strong>ue to be<br />

no rushed by the bronchial arteries<br />

which carry oxygenated blood.

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