Evidence map›Paper›PMID 38259012›Full record

ArticleAfrican journal of paediatric surgery : AJPS2024

Outcome of Transanal Endorectal Pull-Through in Patients with Hirschsprung's Disease.

Tunde Talib Sholadoye, Oluseyi Oyebode Ogunsua, Yakubu Alfa, Philip Mari Mshelbwala, Emmanuel Adoyi Ameh

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Article in African journal of paediatric surgery : AJPS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tunde Talib SholadoyeDepartment of Surgery, Division of Paediatric Surgery, Ahmadu Bello University and Ahmadu Bello University Teaching Hospital, Shika-Zaria, Nigeria.
Oluseyi Oyebode OgunsuaDepartment of Surgery, Division of Paediatric Surgery, Ahmadu Bello University and Ahmadu Bello University Teaching Hospital, Shika-Zaria, Nigeria.
Yakubu AlfaDepartment of Surgery, Division of Paediatric Surgery, Ahmadu Bello University Teaching Hospital, Shika-Zaria, Nigeria.
Philip Mari MshelbwalaDepartment of Surgery, University of Abuja and University of Abuja Teaching Hospital, Abuja, Nigeria.
Emmanuel Adoyi AmehDepartment of Surgery, Division of Paediatric Surgery, National Hospital, Abuja, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransanal endorectal pull-through (TERPT) has become one of the preferred treatments for Hirschsprung's disease (HD) in our setting. This report aims to evaluate the current outcome of TERPT in the setting. MATERIALS AND

methodsA retrospective review of 71 children who had TERPT for histologically-confirmed HD in 11 years (2006-2017) in Nigeria.

resultsThere were 48 boys and 23 girls; aged 3 days-12 years at initial presentation (median = 10 months). Three (4.2%) patients had associated anomalies (duodenal atresia; anorectal malformation and sensorineural deafness with hypopigmented skin patches each). Age at TERPT was 2 months to 15 years (median = 3 years), with surgery waiting time of 1 month-14.9 years (median = 18 months). Sixty-six (93.0%) patients had rectosigmoid, four (5.6%) patients had long segment and one (1.4%) had total colonic disease. Five (7.0%) patients with large megacolon and one (1.4%) with the total colonic disease had assisted abdominal resection of the colon at TERPT. Seventeen (23.9%) patients had post-operative complications, including post-operative enterocolitis 8 (11.3%); anastomotic dehiscence 3 (4.2%); retained aganglionic segment 2 (2.8%); anastomotic stenosis 2 (2.8%), resulting in prolonged hospital stay (P = 0.0001; range = 1-30 days; median = 5 days). The mortality rate was 4.2% (3) from malignant hyperthermia in one patient and in 2 patients, the cause of mortality was unclear. Patients were followed up for 3-6 years (median = 3.5 years). Bowel movement stabilised to 2-4 times daily by 6 weeks after surgery.

conclusionTERPT is a safe treatment for HD in this setting with good short-term outcomes. Longer follow-up is necessary to further evaluate the long-term bowel movement outcomes.!

Indexed as

Anorectal MalformationsColonic DiseasesHirschsprung DiseaseAnastomosis, SurgicalChildFemaleHumansMale

Identifiers

PMID38259012
PMCPMC10903729

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