BMC Public Health (Oct 2010)

Effectiveness and cost-effectiveness of early assisted discharge for Chronic Obstructive Pulmonary Disease exacerbations: the design of a randomised controlled trial

  • van der Pouw Anouschka,
  • de Bruijn Peter J,
  • van de Pas Brigitte,
  • Demunck Dirk RAJ,
  • Seezink Wiel,
  • van Vliet Monique,
  • Janssen Annet,
  • van Litsenburg Walter,
  • van Schayck Onno CP,
  • Smeenk Frank WJM,
  • Goossens Lucas MA,
  • Utens Cecile MA,
  • Retera Jeroen MAM,
  • de Laat-Bierings Petra,
  • van Eijsden Loes,
  • Braken Maria,
  • Eijsermans Riet,
  • Rutten-van Mölken Maureen PMH

DOI
https://doi.org/10.1186/1471-2458-10-618
Journal volume & issue
Vol. 10, no. 1
p. 618

Abstract

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Abstract Background Exacerbations of Chronic Obstructive Pulmonary Disease (COPD) are the main cause for hospitalisation. These hospitalisations result in a high pressure on hospital beds and high health care costs. Because of the increasing prevalence of COPD this will only become worse. Hospital at home is one of the alternatives that has been proved to be a safe alternative for hospitalisation in COPD. Most schemes are early assisted discharge schemes with specialised respiratory nurses providing care at home. Whether this type of service is cost-effective depends on the setting in which it is delivered and the way in which it is organised. Methods/Design GO AHEAD (Assessment Of Going Home under Early Assisted Discharge) is a 3-months, randomised controlled, multi-centre clinical trial. Patients admitted to hospital for a COPD exacerbation are either discharged on the fourth day of admission and further treated at home, or receive usual inpatient hospital care. Home treatment is supervised by general nurses. Primary outcome is the effectiveness and cost effectiveness of an early assisted discharge intervention in comparison with usual inpatient hospital care for patients hospitalised with a COPD exacerbation. Secondary outcomes include effects on quality of life, primary informal caregiver burden and patient and primary caregiver satisfaction. Additionally, a discrete choice experiment is performed to provide insight in patient and informal caregiver preferences for different treatment characteristics. Measurements are performed on the first day of admission and 3 days, 7 days, 1 month and 3 months thereafter. Ethical approval has been obtained and the study has been registered. Discussion This article describes the study protocol of the GO AHEAD study. Early assisted discharge could be an effective and cost-effective method to reduce length of hospital stay in the Netherlands which is beneficial for patients and society. If effectiveness and cost-effectiveness can be proven, implementation in the Dutch health care system should be considered. Trial registration Netherlands Trial Register NTR1129.