Key result
Transplacental procainamide therapy successfully managed fetal tachycardia and hydrops in two cases after digoxin failed, with both infants developing Wolff-Parkinson-White syndrome postnatally.
Why the study?
Does transplacental procainamide therapy control rapid heart rate in fetuses with hydrops and tachycardia unresponsive to digoxin?
Case Report (n=2)
Does transplacental procainamide therapy control rapid heart rate in fetuses with hydrops and tachycardia unresponsive to digoxin?
Transplacental procainamide may be an effective second-line therapy for fetal tachycardia with hydrops when digoxin fails.
May support procainamide after digoxin failure in fetal hydrops; hypothesis-generating and requires prospective confirmation.
We describe two fetuses presenting with hydrops and tachycardia who were treated by prolonged dosage with procainamide. Initial therapy with digoxin in both had been unsuccessful in controlling the rapid heart rate. The first child was delivered after five weeks of transplacental therapy, and demonstrated Wolff-Parkinson-White syndrome on the second day which was controlled with flecainide. The second fetus required three and a half weeks of intrauterine treatment. Wolff-Parkinson-White syndrome became manifest four days after premature labor at 33 weeks gestation. No tachycardia occurred postnatally and the infant has been well during follow-up. The implications of treatment are discussed.
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Triedman et al. (1996) conducted a case report in Fetal tachycardia and hydrops (n=2). Transplacental procainamide therapy was evaluated on Control of rapid heart rate and postnatal outcome. Transplacental procainamide therapy successfully managed fetal tachycardia and hydrops in two cases after digoxin failed, with both infants developing Wolff-Parkinson-White syndrome postnatally.
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