Overview
Assessing the clinical and organisational impact of a home-based post-operative monitoring strategy incorporating the MultiSense® device involving 80 patients aged 65 years and over who have undergone major surgery.
Description
Evaluate the clinical and organisational impact of a post-operative home monitoring strategy incorporating the MultiSense® device in elderly patients.
The study will be conducted in a multicentre setting, involving 80 patients aged 65 years and over who have undergone major surgery.
Eligibility
Inclusion Criteria :
- Patient aged 65 or over
- Patient eligible for remote monitoring using the MultiSense® device
- No psychiatric illness that would prevent them from giving informed consent or receiving optimal treatment and follow-up care
- Subject affiliated with a health insurance scheme
- Subject able to read and understand English
- Subject who has signed an informed consent form
- Subjects indicated for scheduled surgery
- Patients indicated for scheduled surgery :
- Transverse colectomy, by laparotomy
- Hepatic laparoscopy
- Laparoscopic or laparoscopic liver surgery (code hlfc or hlfa for procedures)
- Hysterectomy
- Adnexectomy
- Parietal surgery (eventration)
- Rectal resection
- Right and left colectomy
- Stoma closure by direct approach
Exclusion Criteria :
- Patients already participating in an interventional clinical trial.
- Patients subject to legal protection measures, guardianship, curatorship, or deprived of their liberty by judicial or administrative decision.
- Patients hospitalised without consent.
- Patients unable to complete a questionnaire and without a close relative to assist them in using the solution.
- Patients admitted to or residing in a health or social care facility (other than for the surgery itself).
- Persons admitted to or residing in a health or social care institution (other than for the surgery itself);
- Persons unable to give their free and informed consent.
