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Efficacy of a home discharge care bundle after acute exacerbation of COPD

Authors Cousse S, Gillibert A, Salaün M, Thiberville L, Cuvelier A, Patout M

Received 25 June 2018

Accepted for publication 17 December 2018

Published 22 January 2019 Volume 2019:14 Pages 289—296

DOI https://doi.org/10.2147/COPD.S178147

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Cristina Weinberg

Peer reviewer comments 2

Editor who approved publication: Dr Richard Russell


Stéphanie Cousse,1 André Gillibert,2 Mathieu Salaün,1,3 Luc Thiberville,1,3 Antoine Cuvelier,1,4 Maxime Patout1,4

1Pulmonary, Thoracic Oncology and Respiratory Intensive Care Department, Rouen University Hospital, Rouen, France; 2Department of Biostatistics, Rouen University Hospital, Rouen, France; 3Normandy University, UNIROUEN, CIC INSERM 1404, Rouen, France; 4Normandy University, UNIROUEN, EA3830-GRHV, Institute for Research and Innovation in Biomedicine (IRIB), Rouen, France

Purpose: Acute exacerbations of COPD (AECOPD) are frequent and associated with a poor prognosis. A home discharge care bundle, the PRADO-BPCO program, has been set up by the French National Health System in order to reduce readmission rate after hospitalization for AECOPD. This program includes early consultations by the general practitioner, a nurse, and a physiotherapist after discharge. The aim of our study was to evaluate the effect of the PRADO-BPCO program on the 28-days readmission rate of COPD patients after hospitalization for AECOPD.
Patients and methods: This was a retrospective cohort study including all patients admitted for AECOPD in our center between November 2015 and January 2017. The readmission or death rate at 28 days after hospitalization for AECOPD was compared between patients included in the PRADO-BPCO program and patients with standard care after discharge. Inclusion in the program was decided by the physician in charge of the patient.
Results: A total of 62 patients were included in the PRADO-BPCO group and 202 in the control group. At baseline, patients in the PRADO group had a more severe COPD disease and more severe exacerbations than the control group and mean inpatient stay was shorter in the PRADO group: 8.6±4.3 vs 10.4±7.4 days (P=0.034). Readmission or death rate at 28 days was similar between groups: 10 (16.1%) in the PRADO group vs 30 (14.9%) in the control group (P=0.81). Ninety-days readmission or death rate and overall survival were similar in the two groups.
Conclusion: In our center, despite more severe COPD and a shorter hospitalization time, the PRADO-BPCO program failed to prove a benefit on the 28 days readmission or death rate when compared with standard care.

Keywords: COPD, exacerbation, patient readmission, patient care bundles, continuity of patient care


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