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Perceptions by Family Members of the Dying Experience of Older and Seriously Ill Patients
Abstract
BACKGROUND: Alleviating the problems faced by dying persons and their families has drawn substantial public attention, but little is known about the experience of dying. OBJECTIVE: To characterize the experience of dying from the perspective of surrogate decision makers, usually close family members (89%). DESIGN: Prospective cohort study. SETTING: Five teaching hospitals. PATIENTS: Persons who had one of nine serious medical conditions or were 80 years of age or older who died and for whom a surrogate decision maker completed an interview about the death. MEASUREMENTS: Medical records were reviewed and surrogate decision makers were interviewed. RESULTS: 4124 of 9105 seriously ill patients died (46%); 408 of 1176 elderly patients died (35%). The patients' family members were interviewed after 3357 persons (73%) had died. Of 1541 patients who survived the enrollment hospitalization, 46% died during a later hospitalization. In the last 3 days of life, 55% of patients were conscious. Among these patients, pain, dyspnea, and fatigue were prevalent. Four in 10 patients had severe pain most of the time. Severe fatigue affected almost 8 in 10 patients. More than 1 in 4 patients had moderate dysphoria. Sixty-three percent of patients had difficulty tolerating physical or emotional symptoms. Overall, 11% of patients had a final resuscitation attempt. A ventilator was used in one fourth of patients, and a feeding tube was used in four tenths of patients. Most patients (59%) were reported to prefer a treatment plan that focused on comfort, but care was reported to be contrary to the preferred approach in 10% of cases. CONCLUSIONS: Most elderly and seriously ill patients died in acute care hospitals. Pain and other symptoms were commonplace and troubling to patients. Family members believed that patients preferred comfort, but life-sustaining treatments were often used. These findings indicate important opportunities to improve the care of dying patients.
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Citations
Cited by
Quality End-of-Life Care: Patients' Perspectives
Singer, P. A., Martin, D. K., & Kelner, M. (1999) · JAMA · doi:10.1001/jama.281.2.163 · Cited by 1,287
Solano, J. P., Gomes, B., & Higginson, I. J. (2006) · Journal of Pain and Symptom Management · doi:10.1016/j.jpainsymman.2005.06.007 · Cited by 1,191
Azoulay, E., Chevret, S., Leleu, G., Pochard, F., Barboteu, M., Adrie, C., Canoui, P., Le Gall, J. R., & Schlemmer, B. (2000) · Critical Care Medicine · doi:10.1097/00003246-200008000-00061 · Cited by 746
Impact of an Inpatient Palliative Care Team: A Randomized Controlled Trial
Gade, G., Venohr, I., Conner, D., McGrady, K., Beane, J., Richardson, R. H., Williams, M. P., Liberson, M., Blum, M., & Penna, R. D. (2008) · Journal of Palliative Medicine · doi:10.1089/jpm.2007.0055 · Cited by 564
Jaarsma, T., Beattie, J. M., Ryder, M., Rutten, F. H., McDonagh, T., Mohacsi, P., Murray, S. A., Grodzicki, T., Bergh, I., Metra, M., et al. (2009) · European Journal of Heart Failure · doi:10.1093/eurjhf/hfp041 · Cited by 542
Metadata
- Authors
- Lynn, J., Teno, J. M., Phillips, R. S., Wu, A. W., Desbiens, N., Harrold, J., Claessens, M. T., Wenger, N., Kreling, B., & Connors Jr., A. F.
- Venue
- Annals of Internal Medicine
- Publisher
- American College of Physicians
- Published
- 1997-01-15
- Volume
- 126
- Issue
- 2
- Pages
- 97-106
- ISSN
- 0003-4819 (ISSN-L)
- 1539-3704
- OpenAlex
- W2067517055
- Cited by
- 767
- References
- 0
- FWCI
- 46.09
- Type
- journal article
- Language
- en
- Open access
- closed
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- Lynn, J., Teno, J. M., Phillips, R. S., Wu, A. W., Desbiens, N., Harrold, J., Claessens, M. T., Wenger, N., Kreling, B., & Connors Jr., A. F. (1997). Perceptions by Family Members of the Dying Experience of Older and Seriously Ill Patients. Annals of Internal Medicine. https://doi.org/10.7326/0003-4819-126-2-199701150-00001
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