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单纯食管闭锁延迟一期吻合术的长期结果:27年随访

Long-term results of delayed primary anastomosis for pure oesophageal atresia: a 27-year follow up.

作者信息

Sri Paran Thambipillai, Decaluwe Diane, Corbally Martin, Puri Prem

机构信息

Children's Research Centre, Our Lady's Hospital for Children, University Hospital, Crumlin, Dublin 12, Ireland.

出版信息

Pediatr Surg Int. 2007 Jul;23(7):647-51. doi: 10.1007/s00383-007-1925-7. Epub 2007 May 22.

Abstract

The management of a newborn with pure oesophageal atresia continues to be challenging. We started treating babies with pure oesophageal atresia by delayed primary anastomosis in 1977. The purpose of this study was to review the long-term outcome in infants with pure oesophageal atresia (EA) treated by delayed primary anastomosis with special emphasis on gastroesophageal reflux (GOR) related morbidity. The medical charts of all patients treated by delayed primary anastomosis between 1977 and 2004 were retrospectively reviewed. All survivors were followed up with completion of a questionnaire and personal/phone interviews. There were 26 patients in total admitted during the 27-year study period with the diagnosis of pure oesophageal atresia. Three died prior to surgery due to associated anomalies; two had almost no distal oesophageal segment and underwent oesophageal replacement surgery. The remaining 21 children were treated with delayed primary anastomosis and made up our study group. There were four deaths (19%) in this group, and all were prior to 1980. The median gestational age was 35.5 weeks and the median birth weight was 2.6 kg; median initial gap was 3.7 cm and median preoperative gap was 1.5 cm; median age at operation was 80 days and the median hospital stay was 5.5 months. The median follow-up period was 13.5 years. Fourteen children (66%) developed symptomatic gastroesophageal reflux and nine of these needed fundoplication (43%). Sixteen children developed strictures at the anastomotic site; ten responded to repeated dilatations while six needed resection and reanastomosis. At the time of this study, 15 out of the 17 survivors (88%) were on normal diet with no respiratory problems and 2 (12%) were dependent on gastrostomy feeds. Our long-term follow-up data shows that the delayed primary anastomosis provides excellent functional results in patients born with pure oesophageal atresia. The high incidence of gastroesophageal reflux and associated morbidity requires early intervention to prevent ongoing feeding problems due to oesophagitis and stricture formation.

摘要

单纯食管闭锁新生儿的管理仍然具有挑战性。1977年,我们开始采用延迟一期吻合术治疗单纯食管闭锁的婴儿。本研究的目的是回顾采用延迟一期吻合术治疗的单纯食管闭锁(EA)婴儿的长期预后,特别关注与胃食管反流(GOR)相关的发病率。对1977年至2004年间采用延迟一期吻合术治疗的所有患者的病历进行了回顾性分析。所有幸存者均通过完成问卷调查和个人/电话访谈进行随访。在27年的研究期间,共有26例患者被诊断为单纯食管闭锁并入院。3例因合并畸形在手术前死亡;2例几乎没有远端食管段,接受了食管置换手术。其余21名儿童接受了延迟一期吻合术,构成了我们的研究组。该组中有4例死亡(19%),均在1980年之前。中位孕周为35.5周,中位出生体重为2.6kg;中位初始间隙为3.7cm,中位术前间隙为1.5cm;中位手术年龄为80天,中位住院时间为5.5个月。中位随访期为13.5年。14名儿童(66%)出现有症状的胃食管反流,其中9名需要进行胃底折叠术(43%)。16名儿童在吻合口处出现狭窄;10名对反复扩张有反应,而6名需要切除并重新吻合。在本研究时,17名幸存者中有15名(88%)饮食正常,无呼吸问题,2名(12%)依赖胃造口喂养。我们的长期随访数据表明,延迟一期吻合术为单纯食管闭锁患儿提供了良好的功能结果。胃食管反流的高发病率及相关发病率需要早期干预,以防止因食管炎和狭窄形成而导致持续的喂养问题。

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