Impact of an Improved Rehabilitation Program After a Scheduled Hysterectomy. (RAACHYS)

Centre Hospitalier Régional Metz-Thionville

Status: Completed

Conditions: Post-Op Complication

Study type: Observational

Funder types: Other

Identifiers

NCT04268576

2018-08-CHRMT

Details and patient eligibility

About

It is an observational study, prospective in order to assess the impact of the implementation of an early rehabilitation program on post-operative recovery. this is measured by the qOR15 questionnaire in patients operated on for a programmed hysterectomy, it takes place in the gynecology department of the CHR Metz-Thionville hospital.

Full description

This program implemented will comply with HAS recommendations. The only change in management for patients participating in the study is the completion of the self-questionnaire QOR-15 on D-1 (the day before surgery), D0 (the day of the surgery) and D1 (the day after the surgery).

It is planned to include 74 patients before the implementation of the early rehabilitation protocol and 74 patients after the implementation of the early rehabilitation protocol. The total duration of inclusion is established at 18 months.

The measures applied should improve the patient's well-being and accelerate his return to normal life and therefore reduce the length of his stay.

Enrollment: 220 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Indication of a scheduled hysterectomy
• Presence of a utero-ovarian affection, deemed resectable and requiring a regulated hysterectomy (outside the context of the emergency) associated or not with pelvic or lumbar-aortic dissection.
• classified ASA 1 to 3
• informed about the principles of improved rehabilitation by the surgeon and the anesthesiologist + written document (accessible on the site www.grace-asso.fr).
• able to return home after discharge from the hospital, having a telephone and being able to contact their doctor or the service if necessary or transferred to a convalescent home at their request.

Exclusion criteria

• Patients included in another study
• Refusal to use data by the patient
• Inability to respond to self-questionnaires due to cognitive impairment, difficulties in reading or understanding the French language
• Patients included in another study
• Patients with severe or unbalanced associated conditions