TY - JOUR
T1 - Perceptions by family members of the dying experience of older and seriously ill patients
AU - Lynn, Joanne
AU - Teno, Joan M.
AU - Phillips, Russell S.
AU - Wu, Albert W.
AU - Desbiens, Norman
AU - Harrold, Joan
AU - Claessens, Michael T.
AU - Wenger, Neu
AU - Kreling, Barbara
AU - Connors, Alfred F.
PY - 1997
Y1 - 1997
N2 - 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.
AB - 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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U2 - 10.7326/0003-4819-126-2-199701150-00001
DO - 10.7326/0003-4819-126-2-199701150-00001
M3 - Article
C2 - 9005760
AN - SCOPUS:0031018538
SN - 0003-4819
VL - 126
SP - 97
EP - 106
JO - Annals of internal medicine
JF - Annals of internal medicine
IS - 2
ER -