儿童孤立性及相关先天性直肠外瘘的外科治疗

O.Р. Dzham, O. Sliepov
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引用次数: 0

摘要

先天性肛肠畸形(CARM)包括许多不同的选择,不同的解剖和功能特征。其中一种选择是直肠会阴瘘(RPF)。目的:评估儿童先天性RPF的手术治疗效果,采用鉴别诊断方法和孤立及相关形式的矫正方法。材料和方法。该研究包括28例RPF患者,占所有治疗CARM的18.2%:男孩18例(64.3%),女孩10例(35.7%)。主要疾病和相关发育缺陷的验证是在临床和仪器研究方法的基础上进行的。儿童15例(53.6%),男童8例(53.3%),女童7例(46.7%),男童13例(46.4%),男童10例(76.9%),女童3例(23.1%)。结果。2例(7.1%)伴有ARM的患者接受一期手术治疗。26例(92.9%)患儿进行了分阶段的手术治疗,包括结肠造口切除和肛肠成形术。行前矢状直肠成形术的患儿14/26(53.8%),男童10例(71.4%),女童4例(28.6%);最小后矢状面- 26.9%(7/26):男孩2例(28.6%),女孩5例(71.4%);后矢状面穿刺,适用于19.2%(5/26),且仅适用于男孩。第三阶段的治疗包括关闭局部通道的造口。25例(96.1%)患者切除结肠造口并形成端到端吻合,无并发症。结论。采用不同的诊断方法和肛门直肠成形术,以及对孤立和相关形式的ARM使用复杂的康复治疗,使81.5%的儿童获得良好的结果,18.5%的儿童获得满意的结果。手术矫正RPF的策略的选择应因人而异,考虑到缺陷的解剖和功能特征、性别和一定范围的相关畸形的存在。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案经所有参与机构的当地伦理委员会批准。获得患者的知情同意进行研究。作者未声明存在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical treatment of isolated and associated congenital rectoperinetic fistura in children
Congenital anorectal malformations (CARM) include a number of different options that differ in their anatomical and functional features. One of these options is rectoperineal fistula (RPF). Purpose - to evaluate the results of surgical treatment of congenital RPF in children, using a differentiated approach to diagnosis and methods of correction of its isolated and associated forms. Materials and methods. The study included 28 patients with RPF, which accounted for 18.2% of all treated CARM: boys - 18 (64.3%), girls - 10 (35.7%). Verification of the main disease and associated developmental defects was carried out on the basis of clinical and instrumental research methods. Isolated anorectal malformation (ARM) was diagnosed in 15 (53.6%) children, 8 (53.3%) boys, 7 (46.7%) girls, and associated - in 13 (46.4%) patients, 10 (76.9%) boys, 3 (23.1%) girls. Results. One-stage surgical treatment was performed in 2 (7.1%) patients with associated ARM. Staged surgical treatment, with colostomy removal and anorectoplasty, was performed in 26 (92.9%) children. Anterosagittal anorectoplasty was performed in 14/26 (53.8%) of children: 10 (71.4%) boys, 4 (28.6%) girls; minimal posterior sagittal - in 26.9% (7/26): 2 (28.6%) boys, 5 (71.4%) girls; posterior sagittal according to Pen, applied in 19, 2% (5/26), and only in boys. The third stage of treatment included closing the stoma from local access. Removal of the colostomy and formation of an end-to-end anastomosis was performed in 25 (96.1%) patients without complications. Conclusions. The use of a differentiated approach to diagnostics and methods of anorectoplasty, as well as the use of a complex of rehabilitation treatment for isolated and associated forms of ARM, allowed to obtain good results - in 81.5% and satisfactory results - in 18.5% of children. The choice of tactics for surgical correction of RPF should be individual for each patient, considering the anatomical and functional features of the defect, gender and the presence of a certain range of associated malformations. The research was carried out in accordance with the principles of the Helsinki Declaration. The study protocol was approved by the Local Ethics Committee of all participating institutions. The informed consent of the patient was obtained for conducting the studies. No conflict of interests was declared by the authors.
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