Breakthrough Improvement Collaborative for Ventral Mesh Rectopexy

N/AEnrolling By InvitationNCT05728554

KU Leuven320 enrolled

Overview

Different studies showed large variation between care processes in multiple diseases, this leads to large variation in outcomes. Better adherence to evidence-based guidelines for these diseases can reduce this variation and can improve the health outcomes. Ventral mesh rectopexy has gained popularity in Europe to treat different rectal prolapse syndromes. This procedure has been shown to achieve acceptable anatomic results with low recurrence rates, few complications, and improvements of both constipation and fecal incontinence. However, there is limited data on the care process and outcomes. Moreover, there is no insight in the variation between different centers for patients undergoing ventral mesh rectopexy. This study aims to map the variation in care for patients undergoing ventral mesh rectopexy in Flemish hospitals and to get an overview about the variation within and between these hospitals. Hereby, this will be a repeat of the studies for colorectal cancer, fragility hip fractures, stroke and breast cancer surgery.

Study Type

OBSERVATIONAL

Enrollment

320

Conditions

Rectal Prolapse

Interventions

Learning session 1OTHER

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Minimum age of 18 years; * Elective admission for ventral mesh rectopexy * Total rectal prolapse * Grade III Internal prolapse with incontinence or obstructed defaecation Exclusion Criteria: * Colpo posterior * Patients diagnosed with severe dementia (DSM IV) or severe concomitant disease that may affect very short-term outcome (life expectancy less than 3 months) and hence influence deviations from standard acute care.