Background Each year more than 220,000 Medicare beneficiariesreceive care from hospice programs designed to enhance the qualityof the end of life. Enrollment requires certification by a physicianthat the patient has a life expectancy of less than six months.We examined how long before death patients enrolled in hospiceprograms.
Methods Using 1990 Medicare claims data, we analyzed the characteristicsand survival of 6451 hospice patients followed for a minimumof 27 months with respect to mortality.
Results The patients' mean age was 76.4 years; 92.4 percentwere white. Half the patients were women, and 80.2 percent hadcancer of some type. The most common diagnoses were lung cancer(21.4 percent), colorectal cancer (10.5 percent), and prostatecancer (7.4 percent). The median survival after enrollment wasonly 36 days, and 15.6 percent of the patients died within 7days. At the other extreme, 14.9 percent of the patients livedlonger than six months. Survival varied substantially accordingto diagnosis, even after adjustment for age and coexisting conditions.The unadjusted survival after enrollment was shortest for thosewith renal failure, those with leukemia or lymphoma, and thosewith liver or biliary cancer; it was longest for those withchronic lung disease, those with dementia, and those with breastcancer. Patients at for-profit, larger, outpatient, or newerhospices lived longer after enrollment than those in other typesof hospice programs.
Conclusions Most patients who enter hospice care do so latein the course of their terminal illnesses. The timing of enrollmentin hospice programs varies substantially with the characteristicsof the patients and the hospices.
Source Information
From the Section of General Internal Medicine, Department of Medicine, and the Department of Sociology, University of Chicago, Chicago (N.A.C.); and the Division of General Internal Medicine, Department of Medicine, and the Leonard Davis Institute of Health Economics, University of Pennsylvania, Philadelphia (J.J.E.).
Address reprint requests to Dr. Christakis at the Section of General Internal Medicine, University of Chicago Medical Center, 5841 S. Maryland Ave., MC 6098, Chicago, IL 60637.
Medicare Hospice Programs
Roda P. I., Gandhi H., Mor V., Castle N. G., Christakis N. A., Escarce J. J.
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N Engl J Med 1996;
335:1926-1927, Dec 19, 1996.
Correspondence
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(2007). A 93-Year-Old Man With Advanced Dementia and Eating Problems. JAMA
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(2007). Definition, epidemiology and natural history of COPD. Eur Respir J
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[Abstract][Full Text]
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(2007). Prostate Cancer Quality of Life: Beyond Initial Treatment and the Patient. JCO
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(2007). Palliative Care Consultation, Quality-of-Life Measurements, and Bereavement for End-of-Life Care in Patients With Lung Cancer: ACCP Evidence-Based Clinical Practice Guidelines (2nd Edition). Chest
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[Abstract][Full Text]
Temel, J. S., Jackson, V. A., Billings, J. A., Dahlin, C., Block, S. D., Buss, M. K., Ostler, P., Fidias, P., Muzikansky, A., Greer, J. A., Pirl, W. F., Lynch, T. J.
(2007). Phase II Study: Integrated Palliative Care in Newly Diagnosed Advanced Non-Small-Cell Lung Cancer Patients. JCO
25: 2377-2382
[Abstract][Full Text]
Stone, P., Lund, S
(2007). Predicting prognosis in patients with advanced cancer. Ann Oncol
18: 971-976
[Abstract][Full Text]
Aminoff, B. Z.
(2007). The New Israeli Law "The Dying Patient" and Relief of Suffering Units. AM J HOSP PALLIAT CARE
24: 54-58
[Abstract]
Yabroff, K. R., Davis, W. W., Lamont, E. B., Fahey, A., Topor, M., Brown, M. L., Warren, J. L.
(2007). Patient Time Costs Associated With Cancer Care. JNCI J Natl Cancer Inst
99: 14-23
[Abstract][Full Text]
Formiga, F., Olmedo, C., Lopez-Soto, A., Navarro, M., Culla, A., Pujol, R.
(2007). Dying in hospital of terminal heart failure or severe dementia: the circumstances associated with death and the opinions of caregivers. Palliat Med
21: 35-40
[Abstract]
Carrese, J.
(2006). Refusal of Care by Patients--Reply. JAMA
296: 2923-2923
[Full Text]
Aminoff, B. Z., Adunsky, A.
(2006). Their last 6 months: suffering and survival of end-stage dementia patients. Age Ageing
35: 597-601
[Abstract][Full Text]
Davison, S. N.
(2006). Facilitating Advance Care Planning for Patients with End-Stage Renal Disease: The Patient Perspective. CJASN
1: 1023-1028
[Abstract][Full Text]
Keating, N. L., Herrinton, L. J., Zaslavsky, A. M., Liu, L., Ayanian, J. Z.
(2006). Variations in hospice use among cancer patients.. JNCI J Natl Cancer Inst
98: 1053-1059
[Abstract][Full Text]
Zimmermann, C., Wennberg, R.
(2006). Integrating Palliative Care: A Postmodern Perspective. AM J HOSP PALLIAT CARE
23: 255-258
[Abstract]
Han, B., Remsburg, R. E., McAuley, W. J., Keay, T. J., Travis, S. S.
(2006). National trends in adult hospice use: 1991-1992 to 1999-2000.. Health Aff (Millwood)
25: 792-799
[Abstract][Full Text]
Earle, C. C., Ayanian, J. Z.
(2006). Looking Back From Death: The Value of Retrospective Studies of End-of-Life Care. JCO
24: 838-840
[Full Text]
Waldrop, D. P.
(2006). At the Eleventh Hour: Psychosocial Dynamics in Short Hospice Stays. Gerontologist
46: 106-114
[Abstract][Full Text]
Casey, M. M., Moscovice, I. S., Virnig, B. A., Durham, S. B.
(2005). Providing hospice care in rural areas: Challenges and strategies. AM J HOSP PALLIAT CARE
22: 363-368
[Abstract]
Morita, T., Akechi, T., Ikenaga, M., Kizawa, Y., Kohara, H., Mukaiyama, T., Nakaho, T., Nakashima, N., Shima, Y., Matsubara, T., Uchitomi, Y.
(2005). Late Referrals to Specialized Palliative Care Service in Japan. JCO
23: 2637-2644
[Abstract][Full Text]
Toscani, F., Brunelli, C., Miccinesi, G., Costantini, M., Gallucci, M., Tamburini, M., Paci, E., Di Giulio, P., Peruselli, C.
(2005). Predicting survival in terminal cancer patients: clinical observation or quality-of-life evaluation?. Palliat Med
19: 220-227
[Abstract]
Fine, P. G.
(2005). The Evolving and Important Role of Anesthesiology in Palliative Care. Anesth. Analg.
100: 183-188
[Abstract][Full Text]
Bradley, E. H., Prigerson, H., Carlson, M. D.A., Cherlin, E., Johnson-Hurzeler, R., Kasl, S. V.
(2004). Depression Among Surviving Caregivers: Does Length of Hospice Enrollment Matter?. Am. J. Psychiatry
161: 2257-2262
[Abstract][Full Text]
Formiga, F., Chivite, D., Ortega, C., Casas, S., Ramon, J.M., Pujol, R.
(2004). End-of-life preferences in elderly patients admitted for heart failure. QJM
97: 803-808
[Abstract][Full Text]
Aupperle, P. M., MacPhee, E. R., Strozeski, J. E., Finn, M., Heath, J. M.
(2004). Hospice use for the patient with advanced Alzheimer's disease: The role of the geriatric psychiatrist. AM J HOSP PALLIAT CARE
21: 427-437
[Abstract]
Mertens, W. C., Hoople, N. E., Rodrigues, C., Lindenauer, P. K., Benjamin, E. M.
(2004). Association of admission date with cancer patient survival at a regional hospice: Utility of a statistical process control analysis. AM J HOSP PALLIAT CARE
21: 275-284
[Abstract]
Morrison, R. S., Meier, D. E.
(2004). Palliative Care. NEJM
350: 2582-2590
[Full Text]
Mitchell, S. L., Kiely, D. K., Hamel, M. B., Park, P. S., Morris, J. N., Fries, B. E.
(2004). Estimating Prognosis for Nursing Home Residents With Advanced Dementia. JAMA
291: 2734-2740
[Abstract][Full Text]
Celli, B.R., MacNee, W., Agusti, A., Anzueto, A., Berg, B., Buist, A.S., Calverley, P.M.A., Chavannes, N., Dillard, T., Fahy, B., Fein, A., Heffner, J., Lareau, S., Meek, P., Martinez, F., McNicholas, W., Muris, J., Austegard, E., Pauwels, R., Rennard, S., Rossi, A., Siafakas, N., Tiep, B., Vestbo, J., Wouters, E., ZuWallack, R.
(2004). Standards for the diagnosis and treatment of patients with COPD: a summary of the ATS/ERS position paper. Eur Respir J
23: 932-946
[Full Text]
Pantilat, S. Z., Steimle, A. E.
(2004). Palliative Care for Patients With Heart Failure. JAMA
291: 2476-2482
[Abstract][Full Text]
Sanders, B. S., Burkett, T. L., Dickinson, G. E., Tournier, R. E.
(2004). Hospice referral decisions: The role of physicians. AM J HOSP PALLIAT CARE
21: 196-202
[Abstract]
Covinsky, K. E., Yaffe, K.
(2004). Dementia, Prognosis, and the Needs of Patients and Caregivers. ANN INTERN MED
140: 573-574
[Full Text]
Yabroff, K R., Mandelblatt, J. S, Ingham, J.
(2004). The quality of medical care at the end-of-life in the USA: existing barriers and examples of process and outcome measures. Palliat Med
18: 202-216
[Abstract]
Currow, D. C, Abernethy, A. P, Fazekas, B. S
(2004). Specialist palliative care needs of whole populations: a feasibility study using a novel approach. Palliat Med
18: 239-247
[Abstract]
Aupperle, P. M., MacPhee, E. R., Strozeski, J. E., Finn, M., Heath, J. M.
(2004). Hospice use for the patient with advanced Alzheimer's disease: The role of the geriatric psychiatrist. AM J ALZHEIMERS DIS OTHER DEMEN
19: 94-104
[Abstract]
Rabow, M. W., Dibble, S. L., Pantilat, S. Z., McPhee, S. J.
(2004). The Comprehensive Care Team: A Controlled Trial of Outpatient Palliative Medicine Consultation. Arch Intern Med
164: 83-91
[Abstract][Full Text]
Jerant, A. F., Azari, R. S., Nesbitt, T. S., Meyers, F. J.
(2004). The TLC Model of Palliative Care in the Elderly: Preliminary Application in the Assisted Living Setting. Ann Fam Med
2: 54-60
[Abstract][Full Text]
Miceli, P. J., Mylod, D. E.
(2003). Satisfaction of families using end-of-life care: Current successes and challenges in the hospice industry. AM J HOSP PALLIAT CARE
20: 360-370
[Abstract]
McCarthy, E. P., Burns, R. B., Ngo-Metzger, Q., Davis, R. B., Phillips, R. S.
(2003). Hospice Use Among Medicare Managed Care and Fee-for-Service Patients Dying With Cancer. JAMA
289: 2238-2245
[Abstract][Full Text]
Schonwetter, R. S., Han, B., Small, B. J., Martin, B., Tope, K., Haley, W. E.
(2003). Predictors of six-month survival among patients with dementia: An evaluation of hospice Medicare guidelines. AM J HOSP PALLIAT CARE
20: 105-113
[Abstract]
McCarthy, E. P., Burns, R. B., Davis, R. B., Phillips, R. S.
(2003). Barriers to Hospice Care Among Older Patients Dying With Lung and Colorectal Cancer. JCO
21: 728-735
[Abstract][Full Text]
George, L. K.
(2002). Research Design in End-of-Life Research: State of Science. Gerontologist
42: 86-98
[Abstract][Full Text]
Silvestri, G. A., Sherman, C., Williams, T., Leong, S.-S., Flume, P., Turrisi, A.
(2002). Caring for the Dying Patient With Lung Cancer*. Chest
122: 1028-1036
[Full Text]
Formiga, F, Espel, E, Chivite, D, Pujol, R
(2002). Dying from heart failure in hospital: palliative decision making analysis. Heart
88: 187-187
[Full Text]
Cowan, J. D., Walsh, D., Homsi, J.
(2002). Palliative medicine in a United States cancer center: A prospective study. AM J HOSP PALLIAT CARE
19: 240-250
[Abstract]
Green, J. S.A.
(2002). An investigation into the use of palliative care services by patients with prostate cancer. AM J HOSP PALLIAT CARE
19: 259-262
[Abstract]
Gogel, H. K., Liron, M., Laks, M. P., Rotblat, M., Redelmeier, D. A., Bell, C. M.
(2002). Mortality among Patients Admitted to Hospitals on Weekends as Compared with Weekdays. NEJM
346: 1500-1501
[Full Text]
Bruera, E., Russell, N., Sweeney, C., Fisch, M., Palmer, J. L.
(2002). Place of Death and Its Predictors for Local Patients Registered at a Comprehensive Cancer Center. JCO
20: 2127-2133
[Abstract][Full Text]
Huang, J., Boyd, C., Tyldesley, S., Zhang-Salomons, J., Groome, P. A., Mackillop, W. J.
(2002). Time Spent in Hospital in the Last Six Months of Life in Patients Who Died of Cancer in Ontario. JCO
20: 1584-1592
[Abstract][Full Text]
Terry, P. B.
(2002). Hospice and Pulmonary Medicine. Chest
121: 11-12
[Full Text]
Abrahm, J. L., Hansen-Flaschen, J.
(2002). Hospice Care for Patients With Advanced Lung Disease. Chest
121: 220-229
[Abstract][Full Text]
Hayley, D. C., Muir, J. C., Stocking, C., Hougham, G., Sachs, G. A.
(2001). Not ready for hospice: Characteristics of patients in a pre-hospice program. AM J HOSP PALLIAT CARE
18: 377-382
[Abstract]
Miller, S C, Mor, V
(2001). The emergence of Medicare hospice care in US nursing homes. Palliat Med
15: 471-480
[Abstract]
Snyder, L., Sulmasy, D. P., for the Ethics and Human Rights Committee, America,
(2001). Physician-Assisted Suicide. ANN INTERN MED
135: 209-216
[Abstract][Full Text]
Johnston, G. M., Boyd, C. J., Joseph, P., MacIntyre, M.
(2001). Variation in Delivery of Palliative Radiotherapy to Persons Dying of Cancer in Nova Scotia, 1994 to 1998. JCO
19: 3323-3332
[Abstract][Full Text]
Lamont, E. B., Christakis, N. A.
(2001). Prognostic Disclosure to Patients with Cancer near the End of Life. ANN INTERN MED
134: 1096-1105
[Abstract][Full Text]
Casarett, D., Abrahm, J. L.
(2001). Patients With Cancer Referred to Hospice Versus a Bridge Program: Patient Characteristics, Needs for Care, and Survival. JCO
19: 2057-2063
[Abstract][Full Text]
Owens, M. R., Simmons, B., Gibson, P. S., Weeks, D.
(2001). A longitudinal study of pain in hospice and pre-hospice patients. AM J HOSP PALLIAT CARE
18: 124-128
[Abstract]
Navari, R. M., Stocking, C. B., Siegler, M.
(2000). Preferences of Patients With Advanced Cancer for Hospice Care. JAMA
284: 2449-2449
[Full Text]
Zerzan, J., Stearns, S., Hanson, L.
(2000). Access to Palliative Care and Hospice in Nursing Homes. JAMA
284: 2489-2494
[Abstract][Full Text]
Emanuel, L. L., von Gunten, C. F., Ferris, F. D.
(2000). Gaps in End-of-Life Care. Arch Fam Med
9: 1176-1180
[Abstract][Full Text]
Larson, D. G., Tobin, D. R.
(2000). End-of-Life Conversations: Evolving Practice and Theory. JAMA
284: 1573-1578
[Abstract][Full Text]
Vigano, A., Dorgan, M., Buckingham, J., Bruera, E., Suarez-Almazor, M. E
(2000). Survival prediction in terminal cancer patients: a systematic review of the medical literature. Palliat Med
14: 363-374
[Abstract]
Christakis, N. A, Lamont, E. B, Smith, J. L, Parkes, C. M.
(2000). Extent and determinants of error in doctors' prognoses in terminally ill patients: prospective cohort study • Commentary: Why do doctors overestimate? • Commentary: Prognoses should be based on proved indices not intuition. BMJ
320: 469-473
[Abstract][Full Text]
Fox, E., Landrum-McNiff, K., Zhong, Z., Dawson, N. V., Wu, A. W., Lynn, J., for the SUPPORT Investigators,
(1999). Evaluation of Prognostic Criteria for Determining Hospice Eligibility in Patients With Advanced Lung, Heart, or Liver Disease. JAMA
282: 1638-1645
[Abstract][Full Text]
Christakis, N. A., Iwashyna, T. J.
(1998). Attitude and Self-reported Practice Regarding Prognostication in a National Sample of Internists. Arch Intern Med
158: 2389-2395
[Abstract][Full Text]
Berger, J. T.
(1998). Culture and Ethnicity in Clinical Care. Arch Intern Med
158: 2085-2090
[Full Text]
Byock, I. R, Merriman, M. P
(1998). Measuring quality of life for patients with terminal illness: the Missoula-VITAS(R) quality of life index. Palliat Med
12: 231-244
[Abstract]
Meyer, G. S., Gibbons, R. V.
(1997). House Calls to the Elderly -- A Vanishing Practice among Physicians. NEJM
337: 1815-1820
[Abstract][Full Text]
Burke, J., Steel, R. K.
(1997). Contempo 1997: End-of-Life Care. JAMA
278: 1150-1151
[Abstract]
(1997). Fair Allocation of Intensive Care Unit Resources. Am. J. Respir. Crit. Care Med.
156: 1282-1301
[Full Text]
Farnon, C., Hofmann, M.
(1997). Factors contributing to late hospice admission and proposals for change. AM J HOSP PALLIAT CARE
14: 212-218
[Abstract]
Bascom, P. B.
(1997). A hospital-based comfort care team: Consultation for seriously ill and dying patients. AM J HOSP PALLIAT CARE
14: 57-60
[Abstract]
Roda, P. I., Gandhi, H., Mor, V., Castle, N. G., Christakis, N. A., Escarce, J. J.
(1996). Medicare Hospice Programs. NEJM
335: 1926-1927
[Full Text]
Cassel, C. K., Vladeck, B. C.
(1996). ICD-9 Code for Palliative or Terminal Care. NEJM
335: 1232-1234
[Full Text]
Lynn, J.
(1996). Caring at the End of Our Lives. NEJM
335: 201-202
[Full Text]