Factors Associated With Early Readmission in Critical Care

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSociété Française d'Anesthésie et de Réanimation

About this trial

The COVID-19 health crisis has highlighted pre-existing challenges in patient flow management within healthcare facilities, especially in critical care units. This has sparked debate regarding the sufficiency of critical care beds in France, while drawing attention to the lack of downstream structures. Inefficient patient flow, leading to bed occupancy bottlenecks, has been correlated with both critical care length of stay and morbidity. Unplanned early readmission to critical care further exacerbates these strains and prolongs hospital length of stay. Currently, no standardized criteria are available to guide safe discharge from critical care. A recent Delphi consensus study proposed a set of criteria, although largely subjective. The primary outcome of the present study is to identify factors associated with unplanned early readmission to critical care within 48 hours of discharge. Delayed discharge from critical care represents another major bottleneck contributing to system strain. The secondary outcome of this study is therefore to assess the proportion of critical care beds occupied by patients deemed ready for discharge by the medical team, as well as to analyze the reasons underlying such delayed transfers.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over 18 years of age

Hospitalized or admitted to the ICU

Disqualifiers

Objection to the use of their data (by patient or a relative when applicable)

Patients under legal protection

Trial population

All patients aged 18 years or older admitted to the ICU

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • No intervention

    Other intervention

    Only observation

Treatment groups

1,000 Participants
are divided into 1 treatment group
Group A: No intervention /Observation1 intervention

Trial outcomes

Primary outcomes

1

Early Readmission to the ICU

Patients readmitted to the ICU less than 48 hours after their first discharge

Time frame
From the first day of recruitment to 48 hours after the end of recruitment

Secondary outcomes

1

Readmission to the ICU

Patients readmitted to the ICU less than 30 days after their first discharge

Time frame
From the first day of admission to 30 days of follow up
2

30-days mortality

Patients dead by day 30 of the follow-up

Time frame
From the first day of admission to 30 days of follow up
3

Rate of bed occupancy by patients deemed fit for discharged

Patients still hospitalized in the ICU the day after they were deemed fit for discharge by the medical team

Time frame
From the first day of the study to the 7th day of the study

Other outcomes

Sponsors and contacts

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