Evidence map›Paper›PMID 41865325›Full record

SynthesisWorld journal of urology2026

Hirschsprung disease and associated urological morbidities: institutional experience and systemic review.

Quang Thanh Nguyen, Hien Duy Pham, Dung Boi Ly, Trang Thu Dang, Hanh Thi My Do, Nhung Thi Nguyen, Quynh Anh Tran

Abstract readSystematic Review
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In one paragraph

Synthesis in World journal of urology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Quang Thanh NguyenCollege of Health Sciences, VinUniversity, Da Ton, Gia Lam, Hanoi, Vietnam. quangmd85@gmail.com.ORCID http://orcid.org/0000-0001-8413-1910
Hien Duy PhamDepartment of Pediatric Surgery, Vietnam National Children's Hospital, La Thanh, Dong Da, Hanoi, Vietnam.
Dung Boi LyCollege of Health Sciences, VinUniversity, Da Ton, Gia Lam, Hanoi, Vietnam.
Trang Thu DangCollege of Health Sciences, VinUniversity, Da Ton, Gia Lam, Hanoi, Vietnam.
Hanh Thi My DoCollege of Health Sciences, VinUniversity, Da Ton, Gia Lam, Hanoi, Vietnam.
Nhung Thi NguyenCollege of Health Sciences, VinUniversity, Da Ton, Gia Lam, Hanoi, Vietnam.
Quynh Anh TranDepartment of Pediatric Surgery, Vietnam National Children's Hospital, La Thanh, Dong Da, Hanoi, Vietnam.

Funding

VinUniversity Seed Grant
6 · The paper itself

Abstract

purposeHirschsprung disease (HSCR) may be accompanied by urological comorbidities such as congenital anomalies of the kidney and urinary tract (CAKUT) and lower urinary tract symptoms (LUTS). However, their actual burden remains under-characterized. This study aimed to assess the prevalence and clinical impact of CAKUT and urinary dysfunction in HSCR patients using institutional data and a systematic literature review.

methodsWe retrospectively analyzed 310 pediatric HSCR patients who underwent definitive surgery between January 2020 and December 2021. All underwent renal ultrasonography; additional imaging (voiding cystourethrogram [VCUG], magnetic resonance imaging [MRI], scintigraphy) was performed as clinically indicated. Postoperative voiding function was evaluated in 160 children ≥ 4 years of age using the Dysfunctional Voiding Scoring System (DVSS). A systematic review was performed per PRISMA guidelines.

resultsCongenital anomalies of the kidney and urinary tract were found in 6.5% (20/310) of patients, predominantly unilateral hydronephrosis. The mean anteroposterior renal pelvic diameter was 13.7 ± 4.8 mm. Surgical intervention was required in 25% of these cases. Only 2 of 160 patients (1.3%) had abnormal DVSS scores. No link was observed between the extent of aganglionosis and urological outcomes. Literature review (24 studies) showed highly variable CAKUT (0–21.8%) and LUTS (0.5–27.9%) prevalence.

conclusionCongenital anomalies of the kidney and urinary tract and urinary dysfunction are underrecognized comorbidities in HSCR. Routine ultrasonographic screening and selective advanced imaging support early detection. Our low postoperative dysfunction rates suggest favorable outcomes with standardized multidisciplinary care.

Indexed as

Hirschsprung DiseaseLower Urinary Tract SymptomsUrinary TractUrogenital AbnormalitiesChild, PreschoolFemaleHumansMalePrevalenceRetrospective StudiesVesico-Ureteral RefluxCAKUTHirschsprung’s diseaseLower urinary tract symptomsPediatric urologyUrinary tract anomalies

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.