BMJ 1998;316:1939-1944 ( 27 June )

Papers

Effectiveness of home care programmes for patients with incurable cancer on their quality of life and time spent in hospital: systematic review

Frank W J M Smeenk, pulmonologista Jolanda C M van Haastregt, health scientistb Luc P de Witte, executive directorc Harry F J M Crebolder, professor of general practiced

a Departments of Multidisciplinary Oncology and Pulmonology, Catharina Hospital, PO Box 1350, 5602 ZA Eindhoven, Netherlands, b Institute for Rehabilitation Research (IRV), PO Box 192, 6430 AD Hoensbroek, Netherlands, c Health Care Interventions and Services Department, Institute for Rehabilitation Research (IRV), PO Box 192, 6430 AD Hoensbroek, d Department of General Practice, Maastricht University, PO Box 616, 6200 MD Maastricht, Netherlands

Correspondence to: Dr Smeenk fsk{at}iaehv.nl

Objective: To investigate whether for patients with incurable cancer comprehensive home care programmes are more effective than standard care in maintaining the patients' quality of life and reducing their "readmission time" (percentage of days spent in hospital from start of care till death).
Design: Systematic review.
Methods: A computer aided search was conducted using the databases of Medline, Embase, CancerLit, and PsychLit. The search for studies and the assessment of the methodological quality of the relevant studies were performed by two investigators, blinded from each other. Prospective, controlled studies investigating the effects of a home care intervention programme on patients' quality of life or on readmission time were included in the analyses.
Results: Only 9 prospective controlled studies were found; eight were performed in the United States and 1 in the United Kingdom. Their methodological quality was judged to be moderate (median rating 62 on a 100 point scale). None of the studies showed a negative influence of home care interventions on quality of life. A significantly positive influence on the outcome measures was seen in 2 out of the 5 studies measuring patients' satisfaction with care, in 3/7 studies measuring physical dimensions of quality of life, in 1/6 studies measuring psychosocial dimensions, and in 2/5 studies measuring readmission time. The incorporation of team members' visits to patients at home or regular multidisciplinary team meetings into the intervention programme seemed to be related to positive results.
Conclusions: The effectiveness of comprehensive home care programmes remains unclear. Given the enormity of the problems faced by society in caring for patients with terminal cancer, further research is urgently needed.

Key messages

  • Only nine controlled prospective studies have compared the effects of home care intervention programmes for patients with terminal cancer with those of standard care, in relation to patients' quality of life and time spent in hospital between start of care and death

  • The methodological quality of these studies seemed to be moderate

  • Home care programmes did not have a negative influence on quality of life or time spent in hospital; some studies observed positive effects on these outcome measures

  • Enabling team members to visit patients at home and holding regular multidisciplinary team meetings seem important elements for obtaining favourable results

  • The general belief that home care programmes are effective for patients with terminal cancer is not supported scientifically




© BMJ 1998

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Relevant Article

Benefits of home care for incurable cancer are unclear
BMJ 1998 316: 0. [Full Text]

This article has been cited by other articles:

  • Simon, S, Higginson, I. (2009). Evaluation of hospital palliative care teams: strengths and weaknesses of the before-after study design and strategies to improve it. Palliat Med 23: 23-28 [Abstract]  
  • Zimmermann, C., Riechelmann, R., Krzyzanowska, M., Rodin, G., Tannock, I. (2008). Effectiveness of Specialized Palliative Care: A Systematic Review. JAMA 299: 1698-1709 [Abstract] [Full text]  
  • Lorenz, K. A., Lynn, J., Dy, S. M., Shugarman, L. R., Wilkinson, A., Mularski, R. A., Morton, S. C., Hughes, R. G., Hilton, L. K., Maglione, M., Rhodes, S. L., Rolon, C., Sun, V. C., Shekelle, P. G. (2008). Evidence for Improving Palliative Care at the End of Life: A Systematic Review. ANN INTERN MED 148: 147-159 [Abstract] [Full text]  
  • Shnoor, Y., Szlaifer, M., Aoberman, A. S., Bentur, N. (2007). The Cost of Home Hospice Care for Terminal Patients in Israel. AM J HOSP PALLIAT CARE 24: 284-290 [Abstract]  
  • Killaspy, H. (2007). From the asylum to community care: learning from experience. Br Med Bull 0: ldl017v1-14 [Abstract] [Full text]  
  • Winkler, M. F., Ross, V. M., Piamjariyakul, U., Gajewski, B., Smith, C. E. (2006). Technology Dependence in Home Care: Impact on Patients and Their Family Caregivers. Nutr Clin Pract 21: 544-556 [Abstract] [Full text]  
  • Currow, D. C, Abernethy, A. P, Shelby-James, T. M, Phillips, P. A (2006). The impact of conducting a regional palliative care clinical study. Palliat Med 20: 735-743 [Abstract]  
  • Taft, S. H., Pierce, C. A., Gallo, C. L. (2005). From Hospital to Home and Back Again: A Study in Hospital Admissions and Deaths for Home Care Patients. Home Health Care Management Practice 17: 467-480 [Abstract]  
  • Winkler, M. F. (2005). Quality of Life in Adult Home Parenteral Nutrition Patients. JPEN J Parenter Enteral Nutr 29: 162-170 [Abstract] [Full text]  
  • Cowan, J. D. (2004). Hospital charges for a community inpatient palliative care program. AM J HOSP PALLIAT CARE 21: 177-190 [Abstract]  
  • Cowan, J. D., Burns, D., Palmer, T. W., Scott, J., Feeback, E. (2003). A palliative medicine program in a community setting: 12 points from the first 12 months. AM J HOSP PALLIAT CARE 20: 415-433 [Abstract]  
  • Ingleton, C, Payne, S, Nolan, M, Carey, I (2003). Respite in palliative care: a review and discussion of the literature. Palliat Med 17: 567-575 [Abstract]  
  • Douglas, H-R, Normand, C E, Higginson, I J, Goodwin, D M, Myers, K (2003). Palliative day care: what does it cost to run a centre and does attendance affect use of other services?. Palliat Med 17: 628-637 [Abstract]  
  • Stevens, T., Wilde, D., Paz, S., Ahmedzai, S. H, Rawson, A., Wragg, D. (2003). Palliative care research protocols: a special case for ethical review?. Palliat Med 17: 482-490 [Abstract]  
  • Costantini, M., Higginson, I. J, Boni, L., Orengo, M. A., Garrone, E., Henriquet, F., Bruzzi, P. (2003). Effect of a palliative home care team on hospital admissions among patients with advanced cancer. Palliat Med 17: 315-321 [Abstract]  
  • Saunders, L. D., Soomro, G. M., Buckingham, J., Jamtvedt, G., Raina, P. (2003). Assessing the Methodological Quality of Nonrandomized Intervention Studies. West J Nurs Res 25: 223-237 [Abstract]  
  • Needham, D S, Wong, I C K, Campion, P D (2002). Evaluation of the effectiveness of UK community pharmacists' interventions in community palliative care. Palliat Med 16: 219-225 [Abstract]  
  • Jordhoy, M. S., Fayers, P., Loge, J. H., Ahlner-Elmqvist, M., Kaasa, S. (2001). Quality of Life in Palliative Cancer Care: Results From a Cluster Randomized Trial. JCO 19: 3884-3894 [Abstract] [Full text]  
  • Serra-Prat, M., Gallo, P., Picaza, J. M (2001). Home palliative care as a cost-saving alternative: evidence from Catalonia. Palliat Med 15: 271-278 [Abstract]  
  • Borras, J M, Sanchez-Hernandez, A, Navarro, M, Martinez, M, Mendez, E, Ponton, J L L, Espinas, J A, Germa, J R (2001). Compliance, satisfaction, and quality of life of patients with colorectal cancer receiving home chemotherapy or outpatient treatment: a randomised controlled trial. BMJ 322: 826-826 [Abstract] [Full text]  
  • Melville, A, Eastwood, A, Morris, E, Forman, D (2001). Management of upper gastrointestinal cancers. Qual Saf Health Care 10: 57-64 [Full text]  
  • Grande, G E, Todd, C J, Barclay, S I G, Farquhar, M C (2000). A randomized controlled trial of a hospital at home service for the terminally ill. Palliat Med 14: 375-385 [Abstract]  
  • Morrison, R. S., Siu, A. L., Leipzig, R. M., Cassel, C. K., Meier, D. E. (2000). The Hard Task of Improving the Quality of Care at the End of Life. Arch Intern Med 160: 743-747 [Full text]  
  • Grande, G E, Todd, C J (2000). Why are trials in palliative care so difficult?. Palliat Med 14: 69-74  
  • Keeley, D. (1999). Rigorous assessment of palliative care revisited. BMJ 319: 1447-1448 [Full text]  
  • Grande, G. E, Todd, C. J, Barclay, S. I G, Farquhar, M. C (1999). Does hospital at home for palliative care facilitate death at home? Randomised controlled trial. BMJ 319: 1472-1475 [Abstract] [Full text]  



Access jobs at BMJ Careers
Whats new online at Student 

BMJ