Correspondence between patients' preferences and surrogates' understandings for dying and death

被引:47
作者
Engelberg, RA
Patrick, DL
Curtis, JR
机构
[1] Univ Washington, Div Pulm & Crit Care Med, Dept Med, Seattle, WA 98104 USA
[2] Univ Washington, Dept Hlth Serv, Seattle, WA 98104 USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98104 USA
[4] Univ Washington, Dept Sociol, Seattle, WA 98104 USA
关键词
dying; family; proxy; agreement; hospice; communication;
D O I
10.1016/j.jpainsymman.2005.06.006
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
We examined the agreement between hospice patients' perferences for desired experiences during the last week of life and their surrogates' understandings of those preferences (n = 92 pairs). Analyses included percent agreement, intraclass correlation coefficients, and Bland-Altman plots. Demographic characteristics and communication measures associated with better agreement were identified using t-tests and analysis of variance. The median number of items on which patients and family members agreed was 14 of 30 (interquartile range, IQR 10, 16). Preferences with good agreement included both observable and nonobservable experiences. Patients who reported having had conversations about treatment preferences and who reported that their surrogates knew their preferences reported higher agreement. Surrogates display a better understanding of what is important to patients at the end of life if they had discussions about patients preferences. These discussions may enable surrogates and clinicians to more accurately follow patient preferences.
引用
收藏
页码:498 / 509
页数:12
相关论文
共 54 条
[1]   THE SICKNESS IMPACT PROFILE - DEVELOPMENT AND FINAL REVISION OF A HEALTH-STATUS MEASURE [J].
BERGNER, M ;
BOBBITT, RA ;
CARTER, WB ;
GILSON, BS .
MEDICAL CARE, 1981, 19 (08) :787-805
[2]   COMPARING METHODS OF MEASUREMENT - WHY PLOTTING DIFFERENCE AGAINST STANDARD METHOD IS MISLEADING [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1995, 346 (8982) :1085-1087
[3]   Measuring quality of life for patients with terminal illness:: the Missoula-VITAS® quality of life index [J].
Byock, IR ;
Merriman, MP .
PALLIATIVE MEDICINE, 1998, 12 (04) :231-244
[4]  
Cohen SR, 1997, PALLIATIVE MED, V11, P3
[5]  
Cole R.E., 1993, FAMILIES COPE CHRONI
[6]   Communication and decision-making in seriously ill patients: Findings of the SUPPORT project [J].
Covinsky, KE ;
Fuller, JD ;
Yaffe, K ;
Johnston, CB ;
Hamel, MB ;
Lynn, J ;
Teno, JM ;
Phillips, RS .
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY, 2000, 48 (05) :S187-S193
[7]   Barriers to communication about end-of-life care in AIDS patients [J].
Curtis, JR ;
Patrick, DL .
JOURNAL OF GENERAL INTERNAL MEDICINE, 1997, 12 (12) :736-741
[8]   A measure of the quality of dying and death: Initial validation using after-death interviews with family members [J].
Curtis, JR ;
Patrick, DL ;
Engelberg, RA ;
Norris, K ;
Asp, C ;
Byock, I .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2002, 24 (01) :17-31
[9]   Patient-physician communication about end-of-life care for patients with severe COPD [J].
Curtis, JR ;
Engelberg, RA ;
Nielsen, EL ;
Au, DH ;
Patrick, DL .
EUROPEAN RESPIRATORY JOURNAL, 2004, 24 (02) :200-205
[10]   Patients' perspectives on physician skill in end-of-life care - Differences between patients with COPD, cancer, and AIDS [J].
Curtis, JR ;
Wenrich, MD ;
Carline, JD ;
Shannon, SE ;
Ambrozy, DM ;
Ramsey, PG .
CHEST, 2002, 122 (01) :356-362