Elsevier

Journal of Critical Care

Volume 27, Issue 4, August 2012, Pages 422.e1-422.e9
Journal of Critical Care

Prognosis and Outcomes
A model to predict short-term death or readmission after intensive care unit discharge,☆☆,

https://doi.org/10.1016/j.jcrc.2011.08.003Get rights and content

Abstract

Objective

Early unplanned readmission to the intensive care unit (ICU) carries a poor prognosis, and post-ICU mortality may be related, in part, to premature ICU discharge. Our objectives were to identify independent risk factors for early post-ICU readmission or death and to construct a prediction model.

Design

Retrospective analysis of a prospective database was done.

Setting

Four ICUs of the French Outcomerea network participated.

Patients

Patients were consecutive adults with ICU stay longer than 24 hours who were discharged alive to same-hospital wards without treatment-limitation decisions.

Main results

Of 5014 admitted patients, 3462 met our inclusion criteria. Age was 60.6 ± 17.6 years, and admission Simplified Acute Physiology Score II (SAPS II) was 35.1 ± 15.1. The rate of death or ICU readmission within 7 days after ICU discharge was 3.0%. Independent risk factors for this outcome were age, SAPS II at ICU admission, use of a central venous catheter in the ICU, Sepsis-related Organ Failure Assessment and Systemic Inflammatory Response Syndrome scores before ICU discharge, and discharge at night. The predictive model based on these variables showed good calibration. Compared with SAPS II at admission or Stability and Workload Index for Transfer at discharge, discrimination was better with our model (area under receiver operating characteristics curve, 0.74; 95% confidence interval, 0.68-0.79).

Conclusion

Among patients without treatment-limitation decisions and discharged alive from the ICU, 3.0% died or were readmitted within 7 days. Independent risk factors were indicators of patients' severity and discharge at night. Our prediction model should be evaluated in other ICU populations.

Introduction

Many critically ill patients experience clinical deterioration or death shortly after discharge from the intensive care unit (ICU). In earlier studies, 8% to 10% of patients discharged from the ICU died or required ICU readmission during the same hospital stay [1], [2], [3], [4], [5]. Studies have demonstrated that ICU discharge decisions depend on organizational factors such as workload and ICU bed availability [6], [7], [8]. Furthermore, premature ICU discharge was responsible for 22% to 42% of readmissions [9], [10] and has led to rank ICU readmission among the top indicators for ICU quality [11]. Intensive care unit readmission has been associated with worsening of the original disease process, higher hospital costs, and increase in hospital mortality [5], [7], [10], [12]. Therefore, knowledge of the risk factors for ICU readmission may help to identify high-risk patients before determining whether discharge is appropriate [7], [9], [12]. A rating scale based on the subjective prognosis by attending intensivists has been reported to predict hospital mortality after ICU discharge [13]. In several countries, critical care outreach teams are available for assessing patients being considered for ICU admission [14]. A tool based on objective data could help discriminating which patients should not be discharged without risk of bad outcome and/or should undergo a special surveillance after the ICU stay [15]. Our objective was to develop a tool for prediction of early ICU readmission or death during the same hospital stay of patients without treatment-limitation decisions. Using a population-based cohort ICU records, we hypothesized that objective factors could discriminate between patients who were and were not likely to die or be readmitted to the ICU within 7 days of ICU discharge.

Section snippets

Methods

We retrospectively studied a prospective cohort of patients from 4 ICUs (named A, B, C, and D) in tertiary care hospitals filling the Outcomerea database. A is a 10-bed medical surgical ICU; B, an 18-bed medical ICU; C, a 10-bed surgical ICU; and D, a 14-bed medical surgical ICU. A and C are located in the same 460-bed nonprofit private hospital, B is located in a 1500-bed public university-affiliated hospital, and D is located in a 600-bed public hospital. In each center, the study was active

Study population

The patient selection is shown on Fig. 1. The age of the 3462 patients included in the study was 60.6 ± 17.6 years, and their admission SAPS II was 35.1 ± 15.1 points. Before ICU admission, they were either in a ward (51.4%), at the emergency department (47.9%), or at home (0.6%). The most common reasons for ICU admission were acute respiratory failure (21.1%), shock (18.1%), coma (13.3%), and acute renal failure (5.2%).

Of the 3462 patients, 224 (6.5%) were either readmitted or died during the

Discussion

In our cohort of patients without treatment-limitation decisions, the incidence of death or ICU readmission after ICU discharge was 6.6%. The incidence was 3.0% within 7 days of ICU discharge, and independent risk factors for this outcome were the patients' age, indicators of severity during the ICU stay, sepsis, organ dysfunction at ICU discharge, and discharge at night. We developed a probability model that predicted death or ICU readmission within 7 days after ICU discharge with good

Conclusion

In a cohort of ICU patients without treatment-limitation decisions, the rate of death or ICU readmission within 7 days after ICU discharge was 3.0%. The independent risk factors for this outcome reflect disease severity during the ICU stay and discharge at night. They are easy to identify in current databases. Our MIR probability model is well calibrated and better in terms of discrimination than prior published models. Its validity should be evaluated in other ICU populations.

The following are

Contributions of the authors to the manuscript

Conception and design: IO, JFT, and BM.

Acquisition of data, analysis and interpretation of data: All.

Participation in writing the article: IO, CS, AF, MGO, JFT, and BM.

Critical revision for intellectual content: All.

Approval of version to be published: All.

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    Conflicts of interest: The authors have no personal or financial conflicts of interest to declare.

    ☆☆

    Financial support: Outcomerea is supported by nonexclusive educational grants from Pfizer, Aventis Pharma France, Wyeth France, and Ely Lilly and by public grants from the Centre National de la Recherche Scientifique and Institut National de la Santé et la Recherche Medicale. The Outcomerea data warehouse project was also supported by a grant from the Agence Nationale de Valorisation de la Recherche. These grants had no role in the design or conduct of the study; the collection, management, analysis, or interpretation of the data; or the preparation, review, or approval of the manuscript.

    The results reported in this manuscript were presented, in part, at the 2009 annual meetings of the French Society of Intensive Care Medicine, French Society of Anesthesia and Intensive Care, and European Society of Intensive Care Medicine.

    1

    The members of the Outcomerea Study Group are listed in the appendix.

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