Elements of Palliative Care in the Last 6 Months of Life: Frequency, Predictors, and Timing

被引:30
作者
Ernecoff, Natalie C. [1 ]
Wessell, Kathryn L. [2 ]
Hanson, Laura C. [2 ,3 ]
Dusetzina, Stacie B. [4 ]
Shea, Christopher M. [5 ]
Weinberger, Morris [5 ]
Bennett, Antonia V. [5 ]
机构
[1] Univ Pittsburgh, Sch Med, Div Gen Internal Med, Pittsburgh, PA 15260 USA
[2] Univ N Carolina, Cecil G Sheps Ctr Hlth Serv Res, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, Div Geriatr Med, Chapel Hill, NC 27515 USA
[4] Vanderbilt Univ, Dept Hlth Policy, 221 Kirkland Hall, Nashville, TN 37235 USA
[5] Univ N Carolina, Dept Hlth Policy & Management, Chapel Hill, NC 27515 USA
关键词
PATIENT-REPORTED OUTCOMES; QUALITY-OF-LIFE; CANCER CARE; END; PREVALENCE; GOALS; HOSPICE; COHORT; SCALE;
D O I
10.1007/s11606-019-05349-0
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Importance Persons living with serious illness often need skilled symptom management, communication, and spiritual support. Palliative care addresses these needs and may be delivered by either specialists or clinicians trained in other fields. It is important to understand core elements of palliative care to best provide patient-centered care. Objective To describe frequency, predictors, and timing of core elements of palliative care during the last 6 months of life. Design Retrospective chart review. Setting Inpatient academic medical center. Participants Decedents with cancer, dementia, or chronic kidney disease (CKD) admitted during the 6 months preceding death. Exposures We identified receipt and timing of core elements of palliative care: pain and symptom management, goals of care, spiritual care; and specialty palliative care utilization; hospital encounters; demographics; and comorbid diagnoses. We ran Poisson regression models to assess whether diagnosis or hospital encounters were associated with core elements of palliative care. Results Among 402 decedents, the mean (SD) number of appropriately screened and treated symptoms was 2.9 (1.7)/10. Among 76.1% with documented goals of care, 58.0% had a primary goal of comfort; 55.0% had documented spiritual care. In multivariable models, compared with decedents with cancer, those with dementia or CKD were less likely to have pain and symptom management (respectively, 31% (incidence rate ratio [IRR], 0.69; 95% CI, 0.56-0.85) and 17% (IRR, 0.83; CI, 0.71-0.97)). There was a median of 3 days (IQR, 0-173) between transition to a goal of comfort and death, and a median of 12 days (IQR, 5-47) between hospice referral and death. Conclusions and Relevance Although a high proportion of patients received elements of palliative care, transitions to a goal of comfort or hospice happened very near death. Palliative care delivery can be improved by systematizing existing mechanisms, including prompts for earlier goals-of-care discussion, symptom screening, and spiritual care, and by building collaboration between primary and specialty palliative care services.
引用
收藏
页码:753 / 761
页数:9
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