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Characteristics and Evolution of Hospitalized Patients in Post-Resuscitation Rehabilitation Care Units (SRPR) (Cohorte-SRPR)

A

Assistance Publique - Hôpitaux de Paris

Status

Enrolling

Conditions

Hospitalization in a Post-Resuscitation Rehabilitation Care Units

Treatments

Other: Data gathering

Study type

Observational

Funder types

Other

Identifiers

NCT03768700
2018-A00743-52 (Other Identifier)
NI17008J

Details and patient eligibility

About

Non-interventional cohort study (on data), prospective national multicenter. Inclusion of patients as they enter in a post-intensive care rehabilitation unit (SRPR) .

Collection of data after inclusion, from patients' records during their stay (weekly follow-up) to the SRPR and at their discharge, to D28, D90 and at 1 year after their hospitalization from hospital reports or call of the attending physician.

Full description

For one year, all patients, adults and children hospitalized in a post-intensive care rehabilitation unit (SRPR) of Ile de France and Rouen will be offered to participate in the SRPR Cohort in order to have a completeness of data on a new practice.

The study of these data will make it possible to know the future of the patients and to establish criteria prior to the admission in the SRPR which could make it possible to predict this future and to select the patients as well as possible. It will also make it possible to know the impact of care on the outcome of patients at discharge, at 28 days, 90 days and 1 year of their admission to SRPR to improve practices.

This research will focus on the collection of data from patients' medical records. General information about their stay in the intensive care unit - including the patient's ventilatory status - will be collected upon arrival at the SRPR units, during their stay (weekly follow-up), at the exit of the SRPR, at D28, and in the longer term. (J90 and J365 of the entry into the SRPR unit) where will be listed more comprehensive data with, in addition to general information, data on nutritional, neurological, neuromuscular, respiratory and biological hemodynamic assessments will be collected.

In addition to the common data base, each type of SRPR (respiratory and pediatric neurology) will collect data that is specific to its specialty.

Enrollment

1,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalization in a Post-Resuscitation Rehabilitation Care Units (SRPR) of Ile de France and Rouen

Exclusion criteria

  • Refusal of access to the data by the patient or the designated trusted person or the holder (s) of parental authority (pediatric population)

Trial design

1,000 participants in 1 patient group

Cohort
Description:
Hospitalization in a Post-Resuscitation Rehabilitation Care Units (SRPR)
Treatment:
Other: Data gathering

Trial contacts and locations

10

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Central trial contact

Julie DELEMAZURE, Dr; Alexandre DEMOULE, Pr

Data sourced from clinicaltrials.gov

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