Rothenberg Steven S, Chin Anthony
Department of Pediatric Surgery, The Rocky Mountain Hospital for Children, Denver, Colorado 80218, USA.
J Laparoendosc Adv Surg Tech A. 2010 Nov;20(9):787-90. doi: 10.1089/lap.2010.0111. Epub 2010 Sep 1.
Patients following esophageal atresia repair may often have a congenitally short esophagus, leading to severe reflux and failed fundoplications. This report evaluates the efficacy of a laparoscopic Collis-Nissen fundoplication in this group of patients who have failed a previous fundoplication.
From January 2005 to February 2010, 6 patients born with esophageal atresia presented with recurrent gastroesophageal reflux disease (GERD) and hiatal hernia (H/H). Patient's ages ranged from 5 to 12 years and weights from 17 to 32 kg. All patients had undergone at least three previous fundoplications and hiatal hernia repair. Four of 5 patients had at least one open laparotomy for their previous repair. Patient 6 had had a previous open Collis gastroplasty. The procedure was performed through five ports and consisted of a takedown of the previous fundoplication, elongation of the esophagus using an endoscopic stapler, closure of the hiatus using Teflon pledgets to buttress the repair, and formation of the fundoplication.
All procedures were completed successfully laparoscopically. Procedure times ranged from 180 to 300 minutes. A nasogastric (NG) tube was left for an average of 3 days in 5 patients. Patient 6 had a delayed perforation on day 3 and required reexploration and an NG tube that was left for 10 days. Five of 6 patients were started on feeds on day 4 and were discharged on day 5. Patient 6 with the perforation was discharged on day 14. At an average follow-up of 42 months, all patients have intact wraps and no recurrence of their hiatal hernia.
A laparoscopic Collis-Nissen in a child with previous failed fundoplication is a complex, but efficacious, procedure. Elongating the esophagus in patients with esophageal atresia may decrease the high recurrence rate of hiatal hernia in these patients and should be considered if the patient fails their primary repair.
食管闭锁修复术后的患者常伴有先天性食管短缩,导致严重反流和胃底折叠术失败。本报告评估腹腔镜科利斯-尼森胃底折叠术在既往胃底折叠术失败的这类患者中的疗效。
2005年1月至2010年2月,6例先天性食管闭锁患儿出现复发性胃食管反流病(GERD)和食管裂孔疝(H/H)。患者年龄5至12岁,体重17至32千克。所有患者此前至少接受过三次胃底折叠术和食管裂孔疝修补术。5例患者中有4例此前至少接受过一次开腹手术进行修复。患者6曾接受过一次开放性科利斯胃成形术。手术通过五个端口进行,包括拆除先前的胃底折叠术、使用内镜吻合器延长食管、使用聚四氟乙烯垫片封闭裂孔以加强修复以及形成胃底折叠术。
所有手术均通过腹腔镜成功完成。手术时间为180至300分钟。5例患者平均留置鼻胃管3天。患者6在第3天出现延迟穿孔,需要再次探查,鼻胃管留置了1十天。6例患者中有5例在第4天开始进食,并于第5天出院。穿孔的患者6在第14天出院。平均随访42个月时,所有患者胃底折叠术均完好,食管裂孔疝无复发。
既往胃底折叠术失败的儿童患者行腹腔镜科利斯-尼森手术是一项复杂但有效的手术。延长食管闭锁患者的食管可能会降低这些患者食管裂孔疝的高复发率,如果患者初次修复失败,应考虑该手术。