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胆管闭锁修复的二次手术。

Second operation for repair of biliary atresia.

作者信息

Freitas L, Gauthier F, Valayer J

机构信息

Department of Pediatrics, Hôpital de Bicêtre, France.

出版信息

J Pediatr Surg. 1987 Sep;22(9):857-60. doi: 10.1016/s0022-3468(87)80655-3.

Abstract

In our experience with biliary atresia, there are few cases amenable to reoperation for recurrent jaundice. All authors would agree that specific conditions such as complete bile flow recovery from the first operation followed by early recurrence should be an unquestionable case for revision of the anastomosis, inasmuch as no biologic signs of ongoing cholangitis can be traced. The same decision would apply to the problem of bile leakage after hepatoportocholecystostomy. In other cases, however, one should be aware that these reoperations expose the child to ascitis, poor healing of the abdominal wound, liver failure, and also bring with the decision to reoperate undue hopes to the parents of the child. Moreover, if the child should be a future candidate for liver transplantation, it may be wiser to avoid useless laparotomies and abdominal dissections that are known to complicate the task of hepatectomy.

摘要

根据我们对胆道闭锁的治疗经验,因复发性黄疸而适合再次手术的病例很少。所有作者都认同,对于某些特定情况,比如首次手术后胆汁流完全恢复但随后又早期复发,只要没有持续胆管炎的生物学迹象,就无疑是吻合口修复的病例。这同样适用于肝门胆囊吻合术后胆汁漏的问题。然而,在其他情况下,应该意识到这些再次手术会使患儿面临腹水、腹部伤口愈合不良、肝衰竭的风险,同时也会给患儿父母带来再次手术的不当希望。此外,如果患儿将来可能成为肝移植的候选者,明智的做法可能是避免进行已知会使肝切除术复杂化的无用剖腹术和腹部解剖。

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