Sapin E, Kurzenne J Y, Bargy F, Wakim A, Esteve C, Egu J F, Helardot P G
Service de Chirurgie Pédiatrique, Hôpital Saint-Vincent-de-Paul, Paris.
Chir Pediatr. 1988;29(5):247-51.
In a consecutive series of 275 infants with esophageal atresia seen at Saint-Vincent-de-Paul's Hospital (Paris) between 1971 to 1987, the authors report the experience with 37 infants weighed under 2,000 g (13.45%). 19 had severe additional malformations (51.35%) and 10 (27%) had a respiratory distress syndrome. As Abrahamson in 1972 (3), Cozzi an Wilkinson in 1975 (4), Rickham in 1981 (5) reported, according to the criteria suggested in 1962 by Waterston (1), survival rate are related to additional congenital anomalies and initial respiratory distress (pulmonary dysmaturity or pneumonia) but seems more related to maturity (small-for-date babies) than to birth weight. The authors recommend to perform a primary division of the tracheo-esophageal fistula and end-to-end esophageal anastomosis whenever possible.
在1971年至1987年间于圣文森特 - 德保罗医院(巴黎)接诊的连续275例食管闭锁婴儿中,作者报告了37例体重低于2000克婴儿(占13.45%)的治疗经验。19例有严重的其他畸形(占51.35%),10例(占27%)有呼吸窘迫综合征。正如1972年亚伯拉罕森(3)、1975年科齐和威尔金森(4)、1981年里克姆(5)所报告的,根据1962年沃特斯顿(1)提出的标准,存活率与其他先天性异常和初始呼吸窘迫(肺发育不全或肺炎)有关,但似乎与成熟度(足月小样儿)的关系比与出生体重的关系更大。作者建议尽可能进行一期气管食管瘘分离和食管端端吻合术。