Intensive Care Unit Activity in France From the National Database Between 2013 and 2019 (ICU_ACTIVITY)

Intensive Care Unit Activity in France From the National Database Between 2013 and 2019: More Critically Ill Patients, Shorter Stay and Lower Mortality Rate

Using data from the French National Uniform Hospital Discharge Database (systematically collecting administrative and medical information related to all hospitalized patients in France for care reimbursement purposes), the present study retrospectively assesses the activity of the French Intensive Care Unit (ICU)(1,594,801 ICU admissions):

  • In-ICU and in-hospital mortality rates
  • Length of stay in ICU and hospital
  • Mortality-associated factors during the study period.
  • Number of organ failures
  • Bed occupancy,
  • Regional variations in previous indicators

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

1594801

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Nîmes, France, 30029
        • Intensive care Unit CHU Nîmes

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All adults patients admitted in French ICU between January 1st, 2013, to December 31st, 2019

Description

Inclusion Criteria:

All adults patients admitted in French ICU between January 1st, 2013, to December 31st, 2019

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
ICU ADMISSION
All patients admitted in a French intensive care unit over a 7-year period (2013 to 2019) using the French National Uniform Hospital Discharge Database (PMSI)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evolution in mortality rate
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the mortality rate of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019
Evolution in organ failure rate
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the organ failure rate of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019
Evolution in ICU stay
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the ICU stay of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019
Evolution in SAPS (Simplified Acute Physiology Score) II score at admission
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the SAPS II score at admission of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019
Evolution in age at admission
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the age at admission of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019
Evolution in sex ratio
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the sex ratio of ICU patients over the study period (2013-19)
from January 1st, 2013, to December 31st, 2019

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of patients admitted in ICU with at least 2 different organ failures
Time Frame: from January 1st, 2013, to December 31st, 2019
evolution of the proportion of patients admitted in ICU with at least 2 different organ failures corresponding to the definition of ICU in France.
from January 1st, 2013, to December 31st, 2019
- Proportion of patients admitted in ICU with a SAPS II score over 15 and with a specific ICU supportive therapy
Time Frame: from January 1st, 2013, to December 31st, 2019
Evolution of the proportion of patients admitted in ICU with a SAPS II score over 15 and with a specific ICU supportive therapy leading to a reimbursement by the French national health insurance.
from January 1st, 2013, to December 31st, 2019
Factors Associated with in-ICU mortality
Time Frame: from January 1st, 2013, to December 31st, 2019
Effect of year-time on in-ICU mortality
from January 1st, 2013, to December 31st, 2019
Regional variations
Time Frame: from January 1st, 2013, to December 31st, 2019
Evolution and potential differences between French regions in admission level
from January 1st, 2013, to December 31st, 2019

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jean Yves LEFRANT, Centre Hospitalier Universitaire de Nimes

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2013

Primary Completion (Actual)

December 31, 2019

Study Completion (Actual)

December 31, 2019

Study Registration Dates

First Submitted

April 25, 2022

First Submitted That Met QC Criteria

April 25, 2022

First Posted (Actual)

April 29, 2022

Study Record Updates

Last Update Posted (Actual)

April 29, 2022

Last Update Submitted That Met QC Criteria

April 25, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • LOCAL/2022/JYL-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Critical Illness

3
Subscribe