Cuneo Bettina F, Strasburger Janette F, Wakai Ronald T, Ovadia Marc
The Heart Institute for Children, Rush Medical College, Chicago, IL 60612, USA.
Fetal Diagn Ther. 2006;21(3):307-13. doi: 10.1159/000091362.
To determine the prevalence of 1st and 2nd degree AV block in fetuses with an irregular cardiac rhythm, and to summarize outcome of these pregnancies.
The diagnosis of irregular cardiac rhythm or 'skipped beats' includes isolated ectopy that resolves spontaneously. Recently, Doppler measurements of the 'mechanical' PR interval have been shown to identify AV conduction disease prenatally. Prenatal therapy of these conduction abnormalities may limit the progression to more advanced disease either in utero or after birth.
A retrospective review was performed of fetuses evaluated between 1996 and 2004 with the findings of irregular cardiac rhythm. 1st or 2nd degree AV block was diagnosed on Doppler and M-mode recordings, and confirmed using either fetal magnetocardiography (fMCG) or postnatal 12-lead ECG. Dexamethasone was administered to 4 mothers with abnormal fetal AV conduction in the setting of anti-Ro/anti-La antibodies.
Of 702 fetuses initially referred for arrhythmia, 306 had an irregular rhythm. Eight (2.6%) had intermittent 1st or 2nd degree AV block confirmed by fMCG and/or postnatal 12-lead ECG. AV block was presumed idiopathic in 2, associated with congenital long QT syndrome in 2 or with clinically unsuspected maternal anti-Ro or anti-La antibodies in 4. During the intrauterine period there was no progression to complete AV block and all were born alive at 34-40 weeks of gestation.
A small but clinically significant population of fetuses with irregular rhythm will have 1st or 2nd degree AV block. Transplacental therapy may limit the intrauterine progression to more advanced disease.
确定心律不齐胎儿中一度和二度房室传导阻滞的患病率,并总结这些妊娠的结局。
心律不齐或“漏跳”的诊断包括自发缓解的孤立性异位心律。最近,已证明对“机械性”PR间期进行多普勒测量可在产前识别房室传导疾病。对这些传导异常进行产前治疗可能会限制其在子宫内或出生后发展为更严重的疾病。
对1996年至2004年间评估的心律不齐胎儿进行回顾性研究。根据多普勒和M型记录诊断一度或二度房室传导阻滞,并使用胎儿心磁图(fMCG)或产后12导联心电图进行确认。4名胎儿房室传导异常且母亲存在抗Ro/抗La抗体的母亲接受了地塞米松治疗。
在最初因心律失常转诊的702例胎儿中,306例心律不齐。8例(2.6%)经fMCG和/或产后12导联心电图确认存在间歇性一度或二度房室传导阻滞。2例房室传导阻滞被认为是特发性的,2例与先天性长QT综合征相关,4例与临床未怀疑的母亲抗Ro或抗La抗体相关。在子宫内期间,均未进展为完全性房室传导阻滞,所有胎儿均在妊娠34 - 40周时存活出生。
一小部分但具有临床意义的心律不齐胎儿会出现一度或二度房室传导阻滞。经胎盘治疗可能会限制其在子宫内发展为更严重的疾病。