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胎儿心动过速的管理结果与随访

Management outcome and follow-up of fetal tachycardia.

作者信息

van Engelen A D, Weijtens O, Brenner J I, Kleinman C S, Copel J A, Stoutenbeek P, Meijboom E J

机构信息

Division of Pediatric Cardiology, University of Utrecht, The Netherlands.

出版信息

J Am Coll Cardiol. 1994 Nov 1;24(5):1371-5. doi: 10.1016/0735-1097(94)90122-8.

Abstract

OBJECTIVES

The aim of this study was to evaluate fetal tachycardia and the efficacy of maternally administered antiarrhythmic agents and the effect of this therapy on delivery and postpartum management.

BACKGROUND

Sustained fetal tachycardia is a potentially life-threatening condition in which pharmacologic therapy is reported to be effective. There is ongoing discussion about optimal management.

METHODS

A group of 51 patients with M-mode echocardiographically documented fetal tachycardia was studied retrospectively.

RESULTS

Thirty-three fetuses had supraventricular tachycardia; 15 had atrial flutter; 1 had two episodes of both; and 2 had ventricular tachycardia. Fetal hydrops was seen in 22 patients. Thirty-four fetuses received maternal therapy with either digoxin or flecainide as the first administered drug (additional drugs were given in 12). Drug treatment was successful in establishing acceptable rhythm control in 82% (84% without, 80% with hydrops). In the latter group the median number of drugs and number of days to conversion were higher. Three patients with fetal hydrops died. In 50% of cases, tachycardia reappeared at delivery: 9 neonates presented with atrial flutter, 14 with supraventricular tachycardia and 1 with ventricular tachycardia. Seventy-eight percent of the group had pharmacologic therapy by 1 month of age and 14% by 3 years.

CONCLUSIONS

Fetal tachycardia can be treated adequately in the majority of patients, even in the presence of hydrops, and therefore emergency delivery might not be indicated. Digoxin and flecainide were drugs of first choice and produced no serious adverse effects in this series of patients. The majority of patients do not require prolonged therapy.

摘要

目的

本研究旨在评估胎儿心动过速、母亲使用抗心律失常药物的疗效以及该治疗对分娩和产后管理的影响。

背景

持续性胎儿心动过速是一种潜在的危及生命的情况,据报道药物治疗有效。关于最佳管理方法的讨论仍在进行中。

方法

回顾性研究了一组51例经M型超声心动图记录有胎儿心动过速的患者。

结果

33例胎儿为室上性心动过速;15例为心房扑动;1例有两种情况的发作各两次;2例为室性心动过速。22例患者出现胎儿水肿。34例胎儿接受了母亲使用地高辛或氟卡尼作为首次给药药物的治疗(12例加用了其他药物)。药物治疗成功地使82%的患者建立了可接受的心律控制(无水肿患者为84%,有水肿患者为80%)。在后一组中,药物的中位数和转为正常心律的天数更高。3例有胎儿水肿的患者死亡。50%的病例在分娩时心动过速复发:9例新生儿为心房扑动,14例为室上性心动过速和1例为室性心动过速。该组78%的患者在1月龄时接受了药物治疗,14%的患者在3岁时接受了药物治疗。

结论

即使存在水肿,大多数胎儿心动过速患者也能得到充分治疗,因此可能无需紧急分娩。地高辛和氟卡尼是首选药物,在这组患者中未产生严重不良反应。大多数患者不需要长期治疗。

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