腹壁缺损的远期疗效分析澳大利亚悉尼韦斯特米德儿童医院胃裂回顾性单中心研究

Nageia Younis, Danny Cass, Andrew Holland
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摘要

目的:探讨在韦斯特米德儿童医院确诊腹壁缺陷病例的自然病史和详细结果。方法:对1998年10月1日至2007年1月1日在韦斯特米德儿童医院收治的所有腹壁缺损病例进行回顾性单中心研究。本研究通过对所有诊断为脐膨出和腹裂的新生儿、儿科手术记录和后续随访资料进行回顾性分析。结果:收治前腹壁缺损90例。大多数病例出生在韦斯特米德医院。腹裂新生儿25例(女27例,男28例),外凸新生儿35例(女15例,男20例)。81例新生儿进行了产前超声诊断。一些新生儿有相关的先天性异常,导致5例死亡(4例外腹畸形,1例胃裂)。术后并发症常见,术后住院时间长。90例患者中有25例(15例腹裂,10例腹外裂)需要进一步手术,这与他们最初诊断的腹裂或腹外裂有关,主要是腹壁疝。结论:大多数腹壁缺损病例的长期预后良好,死亡率基本上发生在伴有相关异常的新生儿中。术后疝气患者需要再手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Long-Term Outcome of Abdominal Wall Defects Exomphalos & Gastroschisis Retrospective Single Centre Study Children Hospital at Westmead, Sydney, Australia
Objective: To examine the natural history and detailed outcome of diagnosed cases of abdominal wall defects that admitted to The Children`s Hospital at Westmead. Methods: This was A retrospective single centre study of all cases of abdominal wall defects admitted between the 1st of October 1998 and the 1st of January 2007 to The Children`s Hospital at Westmead. The study had been conducted through a retrospective review of the neonatal, pediatric surgery records and subsequent follow-up information of all cases of Omphalocele and Gastroschisis diagnosed. Results: Ninety cases with anterior abdominal wall defects were admitted. Majority of the cases were born at Westmead Hospital. There were 25 neonates with Gastroschisis (27 females, 28 males), and 35 neonates with Exomphalos (15 females, 20 males). Eighty-one neonates had prenatal ultrasound diagnosis. Some neonates had associated congenital anomalies which results in five deaths (4 Exomphalos, 1 Gastroschisis). Post operative complications were common and the postoperative hospital stay was often lengthy. Twenty-five patients out of the ninety (15 Gastroschisis, 10 exomphalos) required further operations which were related to their primary diagnosis of Gastroschisis or Exomphalos, mostly for abdominal wall hernias. Conclusions: Long-term outcome was favourable in majority of cases with abdominal wall defects and mortality substantially happened in neonates with associated anomalies. Reoperations were necessary in those patients who had postoperative hernias.
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