Suppr超能文献

畸形:加纳一家教学医院5年的病例报告及管理回顾

Malformations: A 5-year review of the presentation and management in a Teaching Hospital in Ghana.

作者信息

Yifieyeh Abiboye C, Duduyemi Babatunde M, Enimil Anthony, Amoah Michael, Nimako Boateng

机构信息

Department of Surgery, Komfo Anokye Teaching Hospital, Kumasi, Ghana.

Departments of Pathology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

Afr J Paediatr Surg. 2018 Apr-Jun;15(2):118-120. doi: 10.4103/ajps.AJPS_10_18.

Abstract

BACKGROUND

Anorectal malformations (ARMs) are congenital defects affecting the distal gastrointestinal tract and anus with frequent fistulous connections to the genitourinary system. The spectrum of the disease is considerably wide, and thus, an individualised approach to its management is required. There are few recent publications about the burden of this malformation in Africa and the outcome of surgical intervention. We present our experiences with the management of ARM, peculiar challenges and the outcome at a tertiary hospital catering for the Northern and Central parts of Ghana.

MATERIALS AND METHODS

This was a retrospective folder review of children with ARM at the Paediatric Surgical Unit of Komfo Anokye Teaching Hospital, Kumasi, Ghana, from 2011 to 2015. The data extracted included diagnosis, associated features, initial and definitive surgical treatment and post-operative complications.

RESULTS

Of the 53 records that were conclusively retrieved, the sex ratio was 1:1. The median age of presentation was 4.5 days (neonates), 4.5 months (infants) and 1.6 years (older children). There were 12 (44%) rectoperineal and 18 (69%) rectovestibular fistulas, representing the most common types of ARM in boys and girls, respectively. Posterior sagittal anorectoplasty and abdominoperineal pull-through were the corrective procedures performed. The overall complication rate was <10%.

CONCLUSION

Our patients generally presented later than their Western counterparts, making a single-stage correction rare. The types of ARM documented in our study suggest the existence of a geographical variation.

摘要

背景

肛门直肠畸形(ARMs)是影响远端胃肠道和肛门的先天性缺陷,常与泌尿生殖系统存在瘘管连接。该疾病谱相当广泛,因此需要采取个体化的治疗方法。关于非洲这种畸形的负担以及手术干预结果的近期出版物较少。我们介绍了在一家为加纳北部和中部地区服务的三级医院处理肛门直肠畸形的经验、特殊挑战及结果。

材料与方法

这是对2011年至2015年期间加纳库马西Komfo Anokye教学医院小儿外科病房收治的肛门直肠畸形患儿病历进行的回顾性研究。提取的数据包括诊断、相关特征、初始和确定性手术治疗以及术后并发症。

结果

在最终检索到的53份记录中,男女比例为1:1。就诊的中位年龄为4.5天(新生儿)、4.5个月(婴儿)和1.6岁(大龄儿童)。分别有12例(44%)直肠会阴瘘和18例(69%)直肠前庭瘘,分别是男孩和女孩中最常见的肛门直肠畸形类型。所施行的矫正手术为后矢状位肛门直肠成形术和腹会阴拖出术。总体并发症发生率<10%。

结论

我们的患者就诊时间通常比西方患者晚,单阶段矫正很少见。我们研究中记录的肛门直肠畸形类型表明存在地域差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00ac/6615007/7a6f96344ab6/AJPS-15-118-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验