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Participants were selected retrospectively from a list of patients who had undergone surgical intervention for POP using polypropylene mesh at Prisma Health Greenville Memorial Hospital, as detailed in Waugh et al [10]. The patients were randomly identified and recruited via phone call until 10 patients with mesh exposure and 10 without were enrolled for this study. Participants with POP recurrence or those taking medications that could affect inflammatory responses were excluded from the study.
JMIR Form Res 2025;9:e59631
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Challenges for Data Quality in the Clinical Data Life Cycle: Systematic Review
J Med Internet Res 2025;27:e60709
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