2017
DOI: 10.1080/24734306.2017.1411322
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A case of neonatal single twin flecainide toxicity after therapeutic in utero exposure for fetal SVT

Abstract: A case of neonatal single twin flecainide toxicity after therapeutic in utero exposure for fetal SVT, Toxicology Communications, 1:1, 41-44, ABSTRACTA 9 hour old twin neonate, who was treated with flecainide in utero for fetal supraventricular tachycardia, presented with hypotension and a wide complex tachycardia concerning for flecainide toxicity. The patient was given a bolus of sodium bicarbonate with transient narrowing of her QRS complex. She was then intubated and started on a sodium bicarbonate drip wit… Show more

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(4 citation statements)
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“…Flecainide, a class IC antiarrhythmic drug, works by blocking fast-acting sodium channels to slow down depolarization in myocytes. 7 It is an effective second-line agent for the treatment of refractory SVT in infants, 8 but, in large doses, flecainide can lead to conduction disturbances such as widening of the QRS complex that can escalate into ventricular tachycardia and cardiovascular collapse. 7 Most reported causes of toxicity in infants have been due to dosing errors.…”
Section: Discussionmentioning
confidence: 99%
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“…Flecainide, a class IC antiarrhythmic drug, works by blocking fast-acting sodium channels to slow down depolarization in myocytes. 7 It is an effective second-line agent for the treatment of refractory SVT in infants, 8 but, in large doses, flecainide can lead to conduction disturbances such as widening of the QRS complex that can escalate into ventricular tachycardia and cardiovascular collapse. 7 Most reported causes of toxicity in infants have been due to dosing errors.…”
Section: Discussionmentioning
confidence: 99%
“…7 It is an effective second-line agent for the treatment of refractory SVT in infants, 8 but, in large doses, flecainide can lead to conduction disturbances such as widening of the QRS complex that can escalate into ventricular tachycardia and cardiovascular collapse. 7 Most reported causes of toxicity in infants have been due to dosing errors. In our patient, we believe that flecainide toxicity was contributed by reduced metabolism secondary to an unfavorable genetic polymorphism.…”
Section: Discussionmentioning
confidence: 99%
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