Rein A J J T, Mevorach D, Perles Z, Gavri S, Nadjari M, Nir A, Elchalal U
Department of Pediatric Cardiology, Hadassah-Hebrew University Medical Center, Kiryat Hadassah, Jerusalem, Israel.
Circulation. 2009 Apr 14;119(14):1867-72. doi: 10.1161/CIRCULATIONAHA.108.773143. Epub 2009 Mar 30.
A fetus exposed to maternal anti-SSA/Ro or anti-SSB/La antibodies (or both) may develop complete atrioventricular block (AVB), which results in high prenatal and postnatal morbidity and mortality. Until recently, only high-grade AVB could be diagnosed in utero. The tissue velocity-based fetal kinetocardiogram (FKCG) enables accurate measurement of AV conduction time and diagnosis of low-grade AVB. In the present multicenter observational study, we used FKCG to detect first-degree AVB in fetuses at risk.
FKCG was performed in 70 fetuses of 56 mothers who were positive for anti-SSA/Ro and/or anti-SSB/La. Fetuses were monitored with weekly FKCG from 13 to 24 weeks' gestation, followed by monthly assessments until delivery in unaffected fetuses and weekly assessments in affected fetuses. AV conduction in 70 at-risk and 109 normal fetuses was compared. FKCG was obtained readily in all fetuses; 6 showed first-degree AVB (AV conduction time >2 z scores above normal mean) at 21 to 34 gestational weeks. Immediate maternal treatment with dexamethasone resulted in normalization of AV conduction in all affected fetuses within 3 to 14 days. AV conduction time in the remaining 64 untreated fetuses remained normal throughout gestation. The ECG PR interval immediately after birth was normal in all affected newborns. No child developed AVB or cardiomyopathy in the subsequent 1- to 6-year (median 4-year) follow-up.
The present findings suggest that an FKCG can detect first-degree AVB in the fetus exposed to maternal anti-SSA/Ro or anti-SSB/La antibodies (or both). Dexamethasone given on detection was associated with normalized AV conduction in fetuses with first-degree AVB. No fetus in the present study developed complete prenatal or postnatal AVB.
暴露于母体抗SSA/Ro或抗SSB/La抗体(或两者)的胎儿可能会发生完全性房室传导阻滞(AVB),这会导致较高的产前和产后发病率及死亡率。直到最近,子宫内仅能诊断出高度AVB。基于组织速度的胎儿心动图(FKCG)能够准确测量房室传导时间并诊断低度AVB。在本多中心观察性研究中,我们使用FKCG来检测有风险胎儿的一度AVB。
对56名抗SSA/Ro和/或抗SSB/La阳性母亲的70名胎儿进行了FKCG检查。从妊娠13至24周开始,每周对胎儿进行FKCG监测,未受影响的胎儿随后每月评估一次直至分娩,受影响的胎儿则每周评估一次。比较了70名有风险胎儿和109名正常胎儿的房室传导情况。所有胎儿均能顺利获得FKCG;6例在妊娠21至34周时出现一度AVB(房室传导时间比正常平均值高出>2个标准差)。母亲立即接受地塞米松治疗后,所有受影响胎儿的房室传导在3至14天内恢复正常。其余64例未治疗胎儿的房室传导时间在整个妊娠期均保持正常。所有受影响新生儿出生后立即进行的心电图PR间期均正常。在随后1至6年(中位时间4年)的随访中,没有儿童发生AVB或心肌病。
目前的研究结果表明,FKCG能够检测出暴露于母体抗SSA/Ro或抗SSB/La抗体(或两者)的胎儿的一度AVB。检测到一度AVB的胎儿给予地塞米松后,房室传导恢复正常。本研究中没有胎儿发生完全性产前或产后AVB。