HIGH PREVALENCE OF MUSCULAR VENTRICULAR SEPTAL-DEFECT IN NEONATES

被引:151
作者
ROGUIN, N [1 ]
DU, ZD [1 ]
BARAK, M [1 ]
NASSER, N [1 ]
HERSHKOWITZ, S [1 ]
MILGRAM, E [1 ]
机构
[1] WESTERN GALILEE HOSP NAHARIYA, TECHNION FAC MED, DEPT NEONATOL, IL-22100 NAHARIYYA, ISRAEL
关键词
D O I
10.1016/0735-1097(95)00358-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study sought to use echocardiography to evaluate the prevalence of muscular ventricular septal defect in neonates. Background. Ventricular septal defect is usually asymptomatic and closes spontaneously. An increase in its prevalence has been noted recently. One reason is the improved detection of small defects, especially with the increased use of echocardiography. Therefore, one would expect a higher prevalence in neonates on the basis of echocardiographic screening. Methods. Color Doppler echocardiography was performed in 1,053 consecutive neonates 6 to 170 h old at Western Galilee Hospital, Israel. Data on the neonates, parents and family were obtained to analyze the influencing factors. The identified patients were followed up for 1 to 10 months or until ventricular septal defect closure. Results. Muscular ventricular septal defect was found in 56 (25 male, 31 female) of the 1,053 neonates, a prevalence of 53.2/1,000 live births. All neonates were asymptomatic. Six had a systolic murmur. Electrocardiographic findings were normal in 44 (97.8%) of 45 neonates followed up, and left ventricular hypertro-phy occurred in 1 (2.2%). By echocardiography, 50 ventricular septal defects (89.3%) were single and 6 (10.7%) were multiple. The defects (range 1 to 5 mm in diameter, mean [+/-SD] 2.3 +/- 0.8) occurred anywhere along the muscular septum; 43 (76.8%) were detectable only on color Doppler imaging. The left atrium and left ventricle were mildly dilated. Of 45 neonates who were followed up for 6 to 10 months or until closure of the defects, 40 (88.9%) had defects that closed spontaneously. The risk of ventricular septal defect was not significantly associated with gestational age, birth weight, birth order, maternal age, diabetes, smoking, exposure to drugs or infection, paternal age, familial congenital heart disease, religion or consanguinity. Conclusions. There is a prevalence of muscular ventricular septal defect in neonates of 53.2/1,000 live births. The patients were asymptomatic, and 88.9% had defects that closed spontaneously within 1 to 10 months. These defects may be caused by environmental factors. In many cases, muscular ventricular septal defect may also result from delayed physiologic development.
引用
收藏
页码:1545 / 1548
页数:4
相关论文
共 21 条
[1]  
ALPERT BS, 1979, PEDIATRICS, V63, P204
[2]  
[Anonymous], 1980, Pediatrics, V65, P375
[3]   CONGENITAL HEART-DISEASE - PREVALENCE AT LIVEBIRTH - THE BALTIMORE WASHINGTON INFANT STUDY [J].
FERENCZ, C ;
RUBIN, JD ;
MCCARTER, RJ ;
BRENNER, JI ;
NEILL, CA ;
PERRY, LW ;
HEPNER, SI ;
DOWNING, JW .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1985, 121 (01) :31-36
[4]   TRENDS IN CONGENITAL HEART-DISEASE IN DALLAS COUNTY BIRTHS 1971-1984 [J].
FIXLER, DE ;
PASTOR, P ;
CHAMBERLIN, M ;
SIGMAN, E ;
EIFLER, CW .
CIRCULATION, 1990, 81 (01) :137-142
[5]  
FREUNDLICH E, 1984, ISRAEL J MED SCI, V20, P1035
[6]   CONSANGUINITY AND CONGENITAL HEART-DISEASE IN THE RURAL ARAB POPULATION IN NORTHERN ISRAEL [J].
GEV, D ;
ROGUIN, N ;
FREUNDLICH, E .
HUMAN HEREDITY, 1986, 36 (04) :213-217
[7]   TWO-DIMENSIONAL AND COLOR DOPPLER ASSESSMENT OF VENTRICULAR SEPTAL-DEFECT OF CONGENITAL ORIGIN [J].
HELMCKE, F ;
DESOUZA, A ;
NANDA, NC ;
VILLACOSTA, I ;
GATEWOOD, R ;
COLVIN, E ;
SOTO, B .
AMERICAN JOURNAL OF CARDIOLOGY, 1989, 63 (15) :1112-1116
[9]   CONGENITAL HEART-DISEASE IN A COHORT OF 19,502 BIRTHS WITH LONG-TERM FOLLOW-UP [J].
HOFFMAN, JIE ;
CHRISTIANSON, R .
AMERICAN JOURNAL OF CARDIOLOGY, 1978, 42 (04) :641-647
[10]   ELUCIDATION OF THE NATURAL-HISTORY OF VENTRICULAR SEPTAL-DEFECTS BY SERIAL DOPPLER COLOR FLOW MAPPING STUDIES [J].
HORNBERGER, LK ;
SAHN, DJ ;
KRABILL, KA ;
SHERMAN, FS ;
SWENSSON, RE ;
PESONEN, E ;
HAGENANSERT, S ;
CHUNG, KJ .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1989, 13 (05) :1111-1118