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产前诊断的法洛四联症结局:对保留瓣膜修复与跨瓣环补片的影响。

Outcomes of prenatally diagnosed tetralogy of Fallot: Implications for valve-sparing repair versus transannular patch.

机构信息

The Hospital for Sick Children, Labatt Family Heart Centre, Toronto, Canada.

出版信息

Can J Cardiol. 2010 Jan;26(1):e1-6. doi: 10.1016/s0828-282x(10)70330-5.

Abstract

OBJECTIVES

To assess outcomes of prenatally diagnosed tetralogy of Fallot and determine factors associated with the choice to undergo a valvesparing repair versus transannular patch, and the use of prostaglandins at birth.

METHODS

All cases at The Hospital for Sick Children (Toronto, Ontario) with a fetal diagnosis of tetralogy of Fallot from 1998 to 2006, were reviewed for demographic and fetal echocardiographic data to determine factors associated with the valve-sparing repair and need for perinatal support.

RESULTS

Sixty-four fetuses met inclusion criteria (median gestational age 22 weeks) with 47 live births. Twenty-six underwent valve-sparing repair (median age 5.7 months) and 14 underwent transannular patch repair (median age 4.5 months). There were seven deaths before surgery and one post-transannular patch repair. One patient required a transannular patch repair after the initial valve-sparing repair. Twelve of 29 (41%) patients received prostaglandins at birth. Type of surgical repair, use of prostaglandins and postnatal death were among the outcomes investigated. The mean pulmonary valve (PV) z-score was -3.0+/-2.0 and the mean PV/aortic valve (AoV) ratio was 0.65+/-0.10. Lower PV z-score (P=0.04), smaller PV/AoV ratio (P=0.04) and the presence of nonantegrade arterial duct flow (P=0.02) were associated with prostaglandin use. A higher PV/AoV ratio was associated with valvesparing repair (P=0.04). Fetal z-scores of the PV, AoV and right pulmonary artery at 29 to 32 weeks gestational age correlated with respective postnatal z-scores (P=0.01).

CONCLUSION

Fetal echocardiographic variables were associated with the use of prostaglandins and valve-sparing repair in fetuses with tetralogy of Fallot, and at 29 weeks, correlated with postnatal valve diameters.

摘要

目的

评估产前诊断出的法洛四联症的结局,并确定与选择行保留瓣膜修复术与跨瓣环补片修补术相关的因素,以及出生时使用前列腺素的相关因素。

方法

对 1998 年至 2006 年期间在多伦多 SickKids 医院(安大略省)接受胎儿法洛四联症诊断的所有病例进行了回顾性分析,以获取人口统计学和胎儿超声心动图数据,从而确定与保留瓣膜修复术和围产期支持相关的因素。

结果

64 例胎儿符合纳入标准(中位孕龄 22 周),其中 47 例存活分娩。26 例行保留瓣膜修复术(中位年龄 5.7 个月),14 例行跨瓣环补片修补术(中位年龄 4.5 个月)。手术前有 7 例死亡,1 例跨瓣环补片修补术后死亡。1 例患者在初始保留瓣膜修复术后需要行跨瓣环补片修补术。29 例患者中有 12 例(41%)出生时接受了前列腺素治疗。研究的结果包括手术修复类型、前列腺素的使用和新生儿死亡。平均肺动脉瓣(PV)Z 评分-3.0+/-2.0,平均 PV/主动脉瓣(AoV)比值 0.65+/-0.10。较低的 PV Z 评分(P=0.04)、较小的 PV/AoV 比值(P=0.04)和非前向动脉导管血流的存在(P=0.02)与前列腺素的使用相关。较高的 PV/AoV 比值与保留瓣膜修复术相关(P=0.04)。29 至 32 孕周胎儿的 PV、AoV 和右肺动脉 Z 评分与相应的新生儿 Z 评分相关(P=0.01)。

结论

法洛四联症胎儿的胎儿超声心动图变量与前列腺素的使用和保留瓣膜修复术相关,在 29 孕周时与出生后瓣膜直径相关。

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