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Effect of a postdischarge virtual ward on readmission or death for high-risk patients: a randomized clinical trial.
Dhalla, Irfan A; O'Brien, Tara; Morra, Dante; Thorpe, Kevin E; Wong, Brian M; Mehta, Rajin; Frost, David W; Abrams, Howard; Ko, Françoise; Van Rooyen, Patrick; Bell, Chaim M; Gruneir, Andrea; Lewis, Geraint H; Daub, Stacey; Anderson, Geoff M; Hawker, Gillian A; Rochon, Paula A; Laupacis, Andreas.
Afiliación
  • Dhalla IA; Department of Medicine, University of Toronto, Toronto, Ontario, Canada2Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto3Department of Medicine, St Michael's Hospital, Toronto4Li Ka Shing Knowledge Institute of St Mich.
  • O'Brien T; Department of Medicine, University of Toronto, Toronto, Ontario, Canada6Department of Medicine, Women's College Hospital, Toronto.
  • Morra D; Department of Medicine, University of Toronto, Toronto, Ontario, Canada7Trillium Health Partners, Mississauga, Ontario.
  • Thorpe KE; Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto8Dalla Lana School of Public Health, University of Toronto, Toronto.
  • Wong BM; Department of Medicine, University of Toronto, Toronto, Ontario, Canada9Department of Medicine, Sunnybrook Health Sciences Centre, Toronto10Centre for Quality Improvement and Patient Safety, University of Toronto, Toronto.
  • Mehta R; Department of Medicine, University of Toronto, Toronto, Ontario, Canada9Department of Medicine, Sunnybrook Health Sciences Centre, Toronto.
  • Frost DW; Department of Medicine, University of Toronto, Toronto, Ontario, Canada11Department of Medicine, University Health Network, Toronto.
  • Abrams H; Department of Medicine, University of Toronto, Toronto, Ontario, Canada11Department of Medicine, University Health Network, Toronto.
  • Ko F; Taddle Creek Family Health Team, Toronto.
  • Van Rooyen P; Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto.
  • Bell CM; Department of Medicine, University of Toronto, Toronto, Ontario, Canada5Institute for Clinical Evaluative Sciences, Toronto, 13Department of Medicine, Mount Sinai Hospital, Toronto.
  • Gruneir A; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto5Institute for Clinical Evaluative Sciences, Toronto, 14Women's College Research Institute, Women's College Hospital, Toronto.
  • Lewis GH; NHS England, London, England.
  • Daub S; Toronto Central Community Care Access Centre, Toronto.
  • Anderson GM; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto.
  • Hawker GA; Department of Medicine, University of Toronto, Toronto, Ontario, Canada5Institute for Clinical Evaluative Sciences, Toronto, 6Department of Medicine, Women's College Hospital, Toronto.
  • Rochon PA; Department of Medicine, University of Toronto, Toronto, Ontario, Canada2Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto5Institute for Clinical Evaluative Sciences, Toronto, 6Department of Medicine, Women's College Hos.
  • Laupacis A; Department of Medicine, University of Toronto, Toronto, Ontario, Canada2Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto4Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto5Institute for Clinical Evaluati.
JAMA ; 312(13): 1305-12, 2014 Oct 01.
Article en En | MEDLINE | ID: mdl-25268437
ABSTRACT
IMPORTANCE Hospital readmissions are common and costly, and no single intervention or bundle of interventions has reliably reduced readmissions. Virtual wards, which use elements of hospital care in the community, have the potential to reduce readmissions, but have not yet been rigorously evaluated.

OBJECTIVE:

To determine whether a virtual ward-a model of care that uses some of the systems of a hospital ward to provide interprofessional care for community-dwelling patients-can reduce the risk of readmission in patients at high risk of readmission or death when being discharged from hospital. DESIGN, SETTING, AND PATIENTS High-risk adult hospital discharge patients in Toronto were randomly assigned to either the virtual ward or usual care. A total of 1923 patients were randomized during the course of the study 960 to the usual care group and 963 to the virtual ward group. The first patient was enrolled on June 29, 2010, and follow-up was completed on June 2, 2014.

INTERVENTIONS:

Patients assigned to the virtual ward received care coordination plus direct care provision (via a combination of telephone, home visits, or clinic visits) from an interprofessional team for several weeks after hospital discharge. The interprofessional team met daily at a central site to design and implement individualized management plans. Patients assigned to usual care typically received a typed, structured discharge summary, prescription for new medications if indicated, counseling from the resident physician, arrangements for home care as needed, and recommendations, appointments, or both for follow-up care with physicians as indicated. MAIN OUTCOMES AND

MEASURES:

The primary outcome was a composite of hospital readmission or death within 30 days of discharge. Secondary outcomes included nursing home admission and emergency department visits, each of the components of the primary outcome at 30 days, as well as each of the outcomes (including the composite primary outcome) at 90 days, 6 months, and 1 year.

RESULTS:

There were no statistically significant between-group differences in the primary or secondary outcomes at 30 or 90 days, 6 months, or 1 year. The primary outcome occurred in 203 of 959 (21.2%) of the virtual ward patients and 235 of 956 (24.6%) of the usual care patients (absolute difference, 3.4%; 95% CI, -0.3% to 7.2%; P = .09). There were no statistically significant interactions to indicate that the virtual ward model of care was more or less effective in any of the prespecified subgroups. CONCLUSIONS AND RELEVANCE In a diverse group of high-risk patients being discharged from the hospital, we found no statistically significant effect of a virtual ward model of care on readmissions or death at either 30 days or 90 days, 6 months, or 1 year after hospital discharge. TRIAL REGISTRATION clinicaltrials.gov Identifier NCT01108172.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Readmisión del Paciente / Servicios de Salud Comunitaria / Continuidad de la Atención al Paciente / Atención Ambulatoria Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Readmisión del Paciente / Servicios de Salud Comunitaria / Continuidad de la Atención al Paciente / Atención Ambulatoria Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: JAMA Año: 2014 Tipo del documento: Article