Crankson Stanley J, Al Jadaan Saud A, Namshan Mohammed A, Al-Rabeeah Abdullah A, Oda Omar
Division of Pediatric Surgery, Department of Surgery-MC1446, King Abdulaziz Medical City-Riyadh, King Fahad National Guard Hospital, P.O. Box 22490, 11426, Riyadh, Kingdom of Saudi Arabia.
Pediatr Surg Int. 2006 Apr;22(4):335-40. doi: 10.1007/s00383-006-1643-6. Epub 2006 Feb 3.
In spite of the innovations in the management of newborns with congenital diaphragmatic hernia (CDH) presenting with respiratory distress at birth, mortality and ongoing morbidity still remain high. This is a retrospective analysis of newborns with CDH to determine the immediate and long-term outcomes among survivors. Medical records of newborns with CDH and respiratory distress at birth between January 1993 and March 2002 were reviewed retrospectively. There were 45 newborns, 29 males and 16 females. Eleven newborns (24%) died during the period of preoperative stabilization, 9 from pulmonary hypoplasia and 2 with complex anomalies who were not resuscitated. Surgery was performed in 34 newborns (76%). Three died postoperatively from severe pulmonary hypoplasia and pulmonary hypertension. Eleven newborns (24%) had sepsis from coagulative-negative staphylococci. Thirty-one of 43 newborns (72%) with isolated CDH were discharged home. Twenty-seven of 31 survivors (87%) had adverse long-term outcome and 2 late deaths were from pulmonary complications. Twenty-nine of 43 newborns (67%) with isolated CDH survived. The principal determinant of survival was pulmonary hypoplasia. Eighty-seven percent of survivors have associated morbidity including ongoing pulmonary, nutritional and neuro-developmental problems. Nevertheless preoperative stabilization and delayed surgery have been a satisfactory mode of management.
尽管在出生时出现呼吸窘迫的先天性膈疝(CDH)新生儿的管理方面有创新,但死亡率和持续发病率仍然很高。这是一项对CDH新生儿的回顾性分析,以确定幸存者的近期和长期结局。回顾性分析了1993年1月至2002年3月期间出生时患有CDH和呼吸窘迫的新生儿的病历。共有45例新生儿,男29例,女16例。11例新生儿(24%)在术前稳定期死亡,9例死于肺发育不全,2例因复杂畸形未复苏。34例新生儿(76%)接受了手术。3例术后死于严重肺发育不全和肺动脉高压。11例新生儿(24%)发生凝固酶阴性葡萄球菌败血症。43例孤立性CDH新生儿中有31例(72%)出院回家。31例幸存者中有27例(87%)有不良长期结局,2例晚期死亡死于肺部并发症。43例孤立性CDH新生儿中有29例(67%)存活。生存的主要决定因素是肺发育不全。87%的幸存者有相关的发病率,包括持续的肺部、营养和神经发育问题。尽管如此,术前稳定和延迟手术一直是一种令人满意的管理方式。