Long-term Outcomes of Pediatric Urethroplasty: A Systematic Review and Meta-analysis

Abstract Background Short-term outcomes of pediatric urethroplasty for hypospadias have been extensively reported, but the long-term morbidity — including complications emerging years after the index procedure — has been synthesised less systematically. Objective To systematically review and quantitatively synthesise the long-term (mean or median ≥ 2 years) outcomes of pediatric urethroplasty, restricted to hypospadias for the quantitative synthesis, and to explore the extent to which the pooled estimates are limited by clinical, methodological, and study-quality heterogeneity. Methods PubMed, MEDLINE, Embase, Scopus, and CENTRAL were searched from inception to 31 December 2024, following PRISMA 2020 (PROSPERO CRD420261470670). Random-effects meta-analysis with the DerSimonian–Laird estimator was used to pool proportions; heterogeneity was assessed with I²; sensitivity analyses were performed restricted to high-quality studies (Newcastle–Ottawa Scale ≥ 7) and to prospective cohorts. Certainty of evidence was rated using GRADE (post-hoc protocol amendment). Results Twenty-two studies (3,842 patients; mean follow-up 8.6 years, range 2–22) met inclusion criteria; 18 hypospadias cohorts (n = 3,842) contributed to the quantitative synthesis. The pooled long-term complication rate was 22.9% (95% CI 20.8–25.2; I² = 68.4%). Urethrocutaneous fistula (11.4%) was the commonest anatomical complication; the pooled reoperation rate was 22.1%. In a sensitivity analysis restricted to the 14 high-quality studies (NOS ≥ 7), the pooled complication rate was 21.8% (95% CI 19.4–24.5). Cumulative complications increased throughout follow-up but with a decelerating rate over time. Certainty of evidence was Moderate for objective anatomical outcomes and Low to Very Low for patient-reported outcomes. Conclusions In this synthesis of pediatric hypospadias urethroplasty cohorts, approximately one in five patients experienced at least one long-term complication and a similar proportion underwent reoperation. Estimates should be interpreted in the context of substantial between-study heterogeneity, inconsistent outcome definitions, and a shortage of cohorts with genuinely adolescent or adult follow-up. Long, structured follow-up and standardised outcome reporting are required before firm conclusions about the trajectory of late complications — including any pubertal effect — can be drawn. Registration Registered in PROSPERO on 05 August 2026 (CRD420261470670). The timing of registration relative to data extraction is disclosed and discussed under limitations.

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Publication Details

Journal
Research Square
Published
2026-11-01
DOI
https://doi.org/10.21203/rs.3.rs-10663190/v1
Primary Topic
Urological Disorders and Treatments
Type
preprint
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preprint

Long-term Outcomes of Pediatric Urethroplasty: A Systematic Review and Meta-analysis

Fayaz Ahmad Najar, Gowhar Nazir Mufti, Mohamad Altaf Ganayee, Ubayer Nabi
1 links
Research Square
Urological Disorders and Treatments
preprint

Long-term Outcomes of Pediatric Urethroplasty: A Systematic Review and Meta-analysis

Fayaz Ahmad Najar, Gowhar Nazir Mufti, Mohamad Altaf Ganayee, Ubayer Nabi
preprint en

Abstract

Abstract Background Short-term outcomes of pediatric urethroplasty for hypospadias have been extensively reported, but the long-term morbidity — including complications emerging years after the index procedure — has been synthesised less systematically. Objective To systematically review and quantitatively synthesise the long-term (mean or median ≥ 2 years) outcomes of pediatric urethroplasty, restricted to hypospadias for the quantitative synthesis, and to explore the extent to which the pooled estimates are limited by clinical, methodological, and study-quality heterogeneity. Methods PubMed, MEDLINE, Embase, Scopus, and CENTRAL were searched from inception to 31 December 2024, following PRISMA 2020 (PROSPERO CRD420261470670). Random-effects meta-analysis with the DerSimonian–Laird estimator was used to pool proportions; heterogeneity was assessed with I²; sensitivity analyses were performed restricted to high-quality studies (Newcastle–Ottawa Scale ≥ 7) and to prospective cohorts. Certainty of evidence was rated using GRADE (post-hoc protocol amendment). Results Twenty-two studies (3,842 patients; mean follow-up 8.6 years, range 2–22) met inclusion criteria; 18 hypospadias cohorts (n = 3,842) contributed to the quantitative synthesis. The pooled long-term complication rate was 22.9% (95% CI 20.8–25.2; I² = 68.4%). Urethrocutaneous fistula (11.4%) was the commonest anatomical complication; the pooled reoperation rate was 22.1%. In a sensitivity analysis restricted to the 14 high-quality studies (NOS ≥ 7), the pooled complication rate was 21.8% (95% CI 19.4–24.5). Cumulative complications increased throughout follow-up but with a decelerating rate over time. Certainty of evidence was Moderate for objective anatomical outcomes and Low to Very Low for patient-reported outcomes. Conclusions In this synthesis of pediatric hypospadias urethroplasty cohorts, approximately one in five patients experienced at least one long-term complication and a similar proportion underwent reoperation. Estimates should be interpreted in the context of substantial between-study heterogeneity, inconsistent outcome definitions, and a shortage of cohorts with genuinely adolescent or adult follow-up. Long, structured follow-up and standardised outcome reporting are required before firm conclusions about the trajectory of late complications — including any pubertal effect — can be drawn. Registration Registered in PROSPERO on 05 August 2026 (CRD420261470670). The timing of registration relative to data extraction is disclosed and discussed under limitations.

Research Square
Government Medical College (IN), Sher-i-Kashmir Institute of Medical Sciences (IN)
Good health and well-being
Urological Disorders and Treatments
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