Rectal Prolapse Surgery in Switzerland: Hospital Volume and Patient Outcomes
Prolapse · Switzerland · Outcome Assessment · Rectopexy · Mortality
De qué trata este estudio
El registro no identifica actualmente este estudio como reclutando. Consulta su estado antes de planificar una evaluación.
- Tipo de estudio
- Observacional
- Fase
- No aplica / no indicada
- Rango de edad
- 20 años - No especificado
- Sexo admitido
- Todos los sexos
- Voluntarios sanos
- No aceptados
- Participantes
- 4257 Real
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Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.
Acerca de la investigación
Rectal Prolapse Surgery in Switzerland: Hospital Volume and Postoperative Outcomes
¿Quién podría participar?
La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.
Inclusion Criteria:
- Age 20 years or older.
- Hospitalization in Switzerland between January 1, 2013, and December 31, 2022.
- Diagnosis of rectal prolapse (ICD-10-GM K62.3).
- Elective surgical treatment of rectal prolapse identified by Swiss CHOP codes 48.49, 48.74, 48.75, or 48.76.11.
Exclusion Criteria:
- Age below 20 years.
- Emergency surgery.
- Non-operative treatment of rectal prolapse.
- Incomplete documentation.
- Unspecified surgical procedures or CHOP codes not corresponding to the predefined eligible procedures (e.g., 48.76.00).
Población del estudio
This nationwide retrospective observational study included 4,257 adult patients aged 20 years or older who underwent elective surgery for rectal prolapse in Switzerland between January 1, 2013, and December 31, 2022. Patients were identified using ICD-10 and Swiss CHOP procedure codes from the anonymized national inpatient database of the Swiss Federal Statistical Office. The study included abdominal rectopexy, Delorme's procedure, perineal stapled prolapse resection, and Altemeier's procedure. Postoperative outcomes were evaluated according to annual hospital procedure volume.
Entiende la evaluación inicialTratamiento, grupos y participación
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- Asignación
- No informado
- Enmascaramiento
- No informado
Rectal Prolapse Surgery Cohort
Adult patients aged 20 years or older who underwent elective surgery for rectal prolapse in Switzerland between 2013 and 2022. The cohort includes patients treated by abdominal rectopexy, Delorme's procedure, perineal stapled prolapse resection, or Altemeier's procedure. Postoperative outcomes were evaluated according to annual hospital procedure volume. All surgical procedures were performed as part of routine clinical care without study-assigned interventions.
Procedure: Surgical Treatment of Rectal Prolapse
Surgical Treatment of Rectal Prolapse PROCEDURE
Patients underwent elective surgical treatment for rectal prolapse as part of routine clinical care. Procedures included abdominal rectopexy (open, laparoscopic, or robotic), Delorme's procedure, perineal stapled prolapse resection (PSP), and Altemeier's procedure. Surgical approaches were identified using Swiss CHOP procedure codes. No interventions were assigned by the investigators, as this was a retrospective observational study.
Qué evalúan los investigadores
Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.
Medidas principales
In-Hospital mortality following rectal prolapse surgery
Plazo: During the index hospitalization, from admission until hospital discharge or in-hospital death. As data from the Federal statistical office was completely anonymised no longer follow-up was possible. Mean length of stay was 7 days.
In-hospital mortality was defined as death from any cause during the index hospitalization following elective rectal prolapse surgery. Mortality was assessed using anonymized inpatient data from the Swiss Federal Statistical Office and analysed in relation to annual hospital procedure volume.
Medidas secundarias
Postoperative complication rate
Plazo: During the index hospitalization, from admission until hospital discharge or in-hospital death. As data from the Federal statistical office was completely anonymised no longer follow-up was possible. Mean length of stay was 7 days.
Occurrence of postoperative complications during the index hospitalization following elective rectal prolapse surgery. Complications were identified using predefined ICD-10 and CHOP codes from the Swiss national inpatient database.
Failure-to-rescue rate
Plazo: During the index hospitalization, from admission until hospital discharge or in-hospital death. As data from the Federal statistical office was completely anonymised no longer follow-up was possible. Mean length of stay was 7 days.
Failure-to-rescue was defined as in-hospital death following at least one major postoperative complication. The rate was calculated as the proportion of patients with major complications who died during the index hospitalization.
Length of hospital stay
Plazo: During the index hospitalization, from admission until hospital discharge or in-hospital death. As data from the Federal statistical office was completely anonymised no longer follow-up was possible. Mean length of stay was 7 days.
Duration of the index hospitalization, measured in days. Length of stay was assessed using administrative inpatient data.
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Abrir resultados oficiales ↗Centros de investigación (0)
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No hay centros indicados. Usa el contacto oficial del estudio.
Equipo y fechas
- Patrocinador principal
- Lukas Marti
- Inicio del estudio
- 1 ene 2013 Real
- Finalización primaria
- 31 dic 2022 Real
- Finalización del estudio
- 31 dic 2022 Real
- Primera publicación
- 10 nov 2026 Real
- Última actualización
- 10 nov 2026 Real
Contactos oficiales del estudio
No hay un contacto central indicado. Revisa los centros y el registro oficial.
Título oficial del estudio
Mortality After Rectal Prolapse Surgery in Switzerland: a Nationwide Population-based Analysis of Hospital Volume and Shorterm Outcomes (2013-2022)
Consulta a Wellness Clinical Research
Tu mensaje va a WCR, incluso si otra organización realiza este estudio. WCR puede orientarte, pero podría no realizar este estudio, tener acceso a su equipo ni poder inscribirte.
Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.
Consultado: 11 nov 2026 · Última actualización del registro: 10 nov 2026
