IMPROVED SURVIVAL FOR CONGENITAL DIAPHRAGMATIC-HERNIA, BASED ON PRENATAL ULTRASOUND DIAGNOSIS AND REFERRAL TO A COMBINED OBSTETRIC-PEDIATRIC SURGICAL CENTER

Citation
Ks. Shaw et al., IMPROVED SURVIVAL FOR CONGENITAL DIAPHRAGMATIC-HERNIA, BASED ON PRENATAL ULTRASOUND DIAGNOSIS AND REFERRAL TO A COMBINED OBSTETRIC-PEDIATRIC SURGICAL CENTER, Journal of pediatric surgery, 29(9), 1994, pp. 1268-1269
Citations number
4
Categorie Soggetti
Pediatrics,Surgery
ISSN journal
00223468
Volume
29
Issue
9
Year of publication
1994
Pages
1268 - 1269
Database
ISI
SICI code
0022-3468(1994)29:9<1268:ISFCDB>2.0.ZU;2-E
Abstract
Between January 1990 and January 1993, 36 patients with antenatal ultr asound (US) diagnosis and/or postnatal diagnosis of congenital diaphra gmatic hernia (CDH) were referred to the authors' high-risk obstetric and pediatric hospital. Among the 36, there were four spontaneous abor tions (11%). five deaths after live births (14%), one false-positive U S examination, and 26 patients who underwent surgery, 23 of whom survi ved (66% overall, 74% of live births, and 89% postoperatively). Only o ne survivor had extracorporeal membrane oxygenation (ECMO). Thirty-fiv e ultrasound examinations were performed in 24 patients; there were 18 true-positives results (51%), one false-positive (3%), and 16 false-n egatives (46%). In this series, there were 25 left-sided CDHs, eight r ight-sided, one bilateral, and one central. Of the four right-sided he rnias having antenatal US, only one was diagnosed prenatally; 15 of th e 17 left-sided CDHs were diagnosed correctly (88%). All 19 babies wit h the prenatal diagnosis were born at the authors' institution. US dia gnosis before 25 weeks' gestation and polyhydramnios separately result ed in a mortality rate of only 50%. Patients born at this institution tend to be sicker than those transferred from elsewhere, as reflected by the lower 1- and 5-minute Apgar scores (3.7 v 6.9, P < .001, and 5. 4 v 6.9, P < .16, respectively), lower gestational ages (37.0 v 39.2 w eeks, P < .007), and lower birth weights (2,525 v 3,049 g, P < .02). N evertheless, transferred patients had a mortality rate (3 of 15 patien ts, 20%) similar to that of nontransferred patients (5 of 20 patients, 25%). The authors conclude that (1) systematic prenatal US can diagno se CDH and enable referral to a center that provides high risk obstetr ic and pediatric surgical care, thus providing optimal postnatal treat ment, and (2) contrary to other reports, antenatal diagnosis of CDH di d not presage a high mortality rate. Copyright (C) 1994 by W.B. Saunde rs Company