Evidence map›Paper›PMID 42360745›Full record

ArticleJAMA network open2026

Kidney Morbidity in Pediatric Patients With Spina Bifida.

Hannah S Thomas, Rano Matta, Samantha Morais, Drew Wilton, Refik Saskin, Michael Chua, Amanda Hird, Robert K Nam, Sender Herschorn, Sarah Neu

Abstract read
In one paragraph

Article in JAMA network open, 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

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Hannah S ThomasDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Rano MattaDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Samantha MoraisICES, Toronto, Ontario, Canada.
Drew WiltonICES, Toronto, Ontario, Canada.
Refik SaskinICES, Toronto, Ontario, Canada.
Michael ChuaDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Amanda HirdDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Robert K NamDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Sender HerschornDivision of Urology, University of Toronto, Toronto, Ontario, Canada.
Sarah NeuDivision of Urology, University of Toronto, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: With improved medical care, patients with spina bifida are living longer, making kidney morbidity an increasingly important source of disease burden. Objective: To measure the incidence rate, age of onset, and clinical factors associated with kidney morbidity among a pediatric cohort of patients with spina bifida. Design, Setting, and Participants: This cohort study included all publicly insured individuals born in Ontario, Canada, between April 1, 1992, and March 31, 2023, stratified by those with and without spina bifida. Data was sourced from inpatient and outpatient administrative health record databases. Patients were followed up from birth until August 31, 2023, termination of health insurance, or death. Exposure: Patients with spina bifida were identified and compared with the general population born within the same time frame. Main Outcomes and Measures: Incidence rate and age of onset of chronic kidney disease (CKD) and end-stage renal disease (ESRD) (ie, long-term dialysis and/or kidney transplant), captured through administrative diagnosis codes. A multivariate Cox proportional hazards model identified clinical factors associated with the development of CKD among patients with spina bifida. Results: A total of 4 380 749 individuals were included: 12 868 with spina bifida (median [IQR] age at diagnosis, 1 [0-8] years) and 4 367 881 without spina bifida. The median (IQR) follow-up was 15 (7-23) years. Among patients with spina bifida, the incidence rate of CKD was 2.7 (95% CI, 2.5-2.9) per 1000 person-years compared with 0.3 (95% CI, 0.3-0.3) per 1000 person-years among the general population. The incidence rates of ESRD were 0.3 (95% CI, 0.2-0.4) and 0.01 (95% CI, 0.01-0.01) per 1000 person-years for patients with and without spina bifida, respectively. Patients with spina bifida were diagnosed with CKD earlier than controls (median [IQR], 5 [1-13] years vs 10 [2-18] years; P < .001; standardized difference = 0.411) and progressed to ESRD at a younger age as well (median [IQR], 8 [2-15] years vs 15 [7-22] years; P < .001; standardized difference = 0.614). Earlier birth year, male sex, higher comorbidity score, history of diabetes, upper tract calculi, recurrent complex urinary tract infections, and urologic surgery were significantly associated with CKD among patients with spina bifida. Conclusions and Relevance: In this cohort study, pediatric patients with spina bifida faced a higher risk of CKD and ESRD, with onset about 5 to 7 years earlier compared with the general population. Several identified clinical factors were associated with kidney decline, warranting close pediatric surveillance.

Indexed as

Kidney Failure, ChronicRenal Insufficiency, ChronicSpinal DysraphismAdolescentAge of OnsetChildChild, PreschoolCohort StudiesFemaleHumansIncidenceInfantMaleOntarioProportional Hazards ModelsRisk Factors

Identifiers

PMID42360745
PMCPMC13309867

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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.