Capacity assessment for EHR-based medical device post-market surveillance for synthetic mid-urethral slings among women with stress urinary incontinence: a NEST consortium study
Matheny M, Perkins A, Rieger-Christ K, Ross J, Mao J, Sedrakyan A, Shah N, Winter R, Reynolds W, Mourtzinos A, Schulz W, Bartlett V, Solotke M, Pandya S, Aryal S, Cho A, Frankenberger E, Park D, Bostrom D, Robbins S, Yustein A, Chughtai B, Trabuco E. Capacity assessment for EHR-based medical device post-market surveillance for synthetic mid-urethral slings among women with stress urinary incontinence: a NEST consortium study. BMJ Surgery Interventions & Health Technologies 2025, 7: e000193. PMID: 39949784, PMCID: PMC11822424, DOI: 10.1136/bmjsit-2023-000193.Peer-Reviewed Original ResearchElectronic health record dataElectronic health recordsHealth systemStress urinary incontinenceSynthetic mesh implantsTertiary care academic medical centerSurgical approachManual chart reviewChart reviewAcademic medical centerMedical device surveillanceHealth recordsAdverse event surveillanceMesh implantationUrinary incontinenceDuration of surveillanceAscertainment rateMid-urethral sling (MUSOutcome measuresSynthetic mid-urethral slingsTreat stress urinary incontinenceDetermination of surgical approachEvent surveillanceRetrospective observational studyMedical Center
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