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胎儿房室传导阻滞的围产期结局:来自单一机构的116例病例

Perinatal outcome of fetal atrioventricular block: one-hundred-sixteen cases from a single institution.

作者信息

Lopes Lilian M, Tavares Gláucia Maria Penha, Damiano Ana Paula, Lopes Marco Antônio Borges, Aiello Vera Demarchi, Schultz Regina, Zugaib Marcelo

机构信息

Department of Obstetrics and Gynecology, Fetal Medicine and Cardiology Unit, São Paulo University Medical School, São Paulo, SP, Brazil.

出版信息

Circulation. 2008 Sep 16;118(12):1268-75. doi: 10.1161/CIRCULATIONAHA.107.735118. Epub 2008 Sep 2.

Abstract

BACKGROUND

Fetal atrioventricular (AV) block is an uncommon lesion with significant mortality. Because of the rarity of this disorder, the natural course, extensive evaluation of untreated fetuses, and late follow-up remain unclear.

METHODS AND RESULTS

Of the 116 consecutive cases of fetal AV block studied from 1988 to 2006, only 1 was terminated, and 75% were live births. Fifty-nine cases of AV block were associated with major structural heart disease, mainly left atrial isomerism (n=40), with only 26% of neonatal survivors. Of the 57 fetuses with normal cardiac anatomy, 41 (72%) were positive for maternal antinuclear antibodies, and 32 of these seropositive mothers did not receive any treatment. This untreated group had live-birth and 1-year infant survival rates of 93% and 90% [corrected], respectively. Five fetuses from seronegative mothers showed regression to sinus rhythm during pregnancy. The presence of major structural heart disease, hydrops, an atrial rate <or=120 bpm, and a ventricular rate <or=55 bpm were identified as risk factors for mortality. Logistic regression analysis of the whole group showed that the presence of structural heart disease was the only independent predictor of death (P<0.001).

CONCLUSIONS

This long-term study confirms that fetal AV block has a poor outcome when associated with structural heart disease and that spontaneous regression of AV block is possible in seronegative forms. The survival rate of >90% of our untreated patients with isolated forms of AV block raises concerns about any decision to intervene with immunosuppressive agents.

摘要

背景

胎儿房室传导阻滞是一种罕见的病变,死亡率较高。由于这种疾病罕见,其自然病程、未经治疗胎儿的广泛评估以及长期随访情况仍不明确。

方法与结果

在1988年至2006年连续研究的116例胎儿房室传导阻滞病例中,仅1例终止妊娠,75%为活产。59例房室传导阻滞与主要结构性心脏病相关,主要是左心房异构(n = 40),新生儿幸存者仅占26%。在57例心脏解剖结构正常的胎儿中,41例(72%)母亲抗核抗体呈阳性,其中32例血清学阳性母亲未接受任何治疗。这个未治疗组的活产率和1岁婴儿生存率分别为93%和90%[校正后]。5例血清学阴性母亲的胎儿在孕期窦性心律恢复正常。主要结构性心脏病、水肿、心房率≤120次/分以及心室率≤55次/分被确定为死亡的危险因素。对整个队列进行逻辑回归分析显示,结构性心脏病的存在是唯一的独立死亡预测因素(P<0.001)。

结论

这项长期研究证实,胎儿房室传导阻滞合并结构性心脏病时预后不良,血清学阴性形式的房室传导阻滞可能会自发恢复正常。我们未治疗的孤立性房室传导阻滞患者90%以上的生存率引发了对于使用免疫抑制剂进行干预决策的担忧。

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