Fetal sinus bradycardia and the long QT syndrome

被引:44
作者
Beinder, E
Grancay, T
Menédez, T
Singer, H
Hofbeck, M
机构
[1] Univ Hosp Erlangen, Dept Pediat Cardiol, Erlangen, Germany
[2] Univ Hosp Erlangen, Dept Cardiovasc Dis & Internal Med 2, Erlangen, Germany
[3] Univ Hosp Erlangen, Dept Obstet & Gynecol, Erlangen, Germany
关键词
kong QT syndrome; sudden infant death syndrome; fetal bradycardia; prenatal diagnosis; cardiotocography;
D O I
10.1067/mob.2001.117973
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Recent evidence in literature shows that the long QT syndrome accounts for a fraction of the sudden infant death syndrome. Newborn infants with prolongation of the Q-T interval often show sinus bradycardia, which led us to test whether children who were diagnosed with long QT syndrome also show sinus bradycardia in the cardiotocogram before birth. STUDY DESIGN: We identified 18 children who were born from singleton pregnancies at or near term in whom long QT syndrome (corrected QT interval, >0.440 second) was diagnosed after birth or in childhood. Cardiograms during pregnancy and delivery were available from 17 of the 18 children. RESULTS: The cardiotocogram showed persistent fetal sinus bradycardia (baseline heart rate permanently below 120 beats/min) in 12 of 17 fetuses (71 %) with long QT syndrome. Two fetuses had additional intermittent tachyarrhythmias. CONCLUSION: Sinus bradycardia in the cardiotocogram during delivery or in pregnancy may indicate long QT syndrome in the fetus. Postnatal electrocardiography should be performed in these children to rule out or confirm a prolongation of the Q-T interval.
引用
收藏
页码:743 / 747
页数:5
相关论文
共 27 条
[1]  
Desmyttere S., 1994, Genetic Counseling, V5, P289
[2]   Fetal presentation of congenital long QT syndrome [J].
Donofrio, MT ;
Gullquist, SD ;
O'Connell, NG ;
Redwine, FO .
PEDIATRIC CARDIOLOGY, 1999, 20 (06) :441-444
[3]   SIDS EPIDEMIOLOGY AND INCIDENCE [J].
DWYER, T ;
PONSONBY, AL .
PEDIATRIC ANNALS, 1995, 24 (07) :350-&
[4]   THE LONG QT SYNDROME IN CHILDREN - AN INTERNATIONAL STUDY OF 287 PATIENTS [J].
GARSON, A ;
DICK, M ;
FOURNIER, A ;
GILLETTE, PC ;
HAMILTON, R ;
KUGLER, JD ;
VANHARE, GF ;
VETTER, V ;
VICK, GW .
CIRCULATION, 1993, 87 (06) :1866-1872
[5]  
Hamada H, 1999, PRENATAL DIAG, V19, P677, DOI 10.1002/(SICI)1097-0223(199907)19:7<677::AID-PD597>3.0.CO
[6]  
2-Z
[7]   Prenatal findings in patients with prolonged QT interval in the neonatal period [J].
Hofbeck, M ;
Ulmer, H ;
Beinder, E ;
Sieber, E ;
Singer, H .
HEART, 1997, 77 (03) :198-204
[8]   CONGENITAL DEAF-MUTISM, FUNCTIONAL HEART DISEASE WITH PROLONGATION OF THE Q-T INTERVAL, AND SUDDEN DEATH [J].
JERVELL, A ;
LANGENIELSEN, F .
AMERICAN HEART JOURNAL, 1957, 54 (01) :59-68
[9]   Prenatal diagnosis of QT prolongation by magnetocardiography [J].
Menéndez, T ;
Achenbach, S ;
Beinder, E ;
Hofbeck, M ;
Schmid, O ;
Singer, H ;
Moshage, W ;
Daniel, WG .
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2000, 23 (08) :1305-1307
[10]   Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management parts I and II [J].
Priori, SG ;
Barhanin, J ;
Hauer, RNW ;
Haverkamp, W ;
Jongsma, HJ ;
Kleber, AG ;
McKenna, WJ ;
Roden, DM ;
Rudy, Y ;
Schwartz, K ;
Schwartz, PJ ;
Towbin, JA ;
Wilde, AM .
CIRCULATION, 1999, 99 (04) :518-528