Mooney D, Lewis J E, Connors R H, Weber T R
Am J Surg. 1987 Apr;153(4):347-9. doi: 10.1016/0002-9610(87)90574-5.
From 1973 through 1983, 20 newborns with congenital duodenal atresia were treated. These patients are compared with our previous series and with other published series. There were no fatalities among the 19 patients who underwent operation, an improvement from the 72 percent survival rate in our previous series. Fifty-five percent of the patients had associated congenital anomalies, which frequently complicated their management. The use of a transanastomotic jejunal feeding tube resulted in delayed oral feeding and prolonged hospitalization, and cannot be recommended.
1973年至1983年期间，对20例先天性十二指肠闭锁的新生儿进行了治疗。将这些患者与我们之前的系列病例以及其他已发表的系列病例进行了比较。接受手术的19例患者中无死亡病例，较我们之前系列病例72%的生存率有所提高。55%的患者伴有先天性畸形，这常常使他们的治疗复杂化。使用经吻合口空肠喂养管导致经口喂养延迟和住院时间延长，因此不推荐使用。
