Factors Associated With Quality-of-Dying-and-Death Classes Among Critically Ill Patients

被引:1
作者
Wen, Fur-Hsing [1 ]
Chou, Wen-Chi [2 ,3 ]
Huang, Chung-Chi [4 ,5 ]
Hu, Tsung-Hui [6 ]
Chuang, Li-Pang [4 ]
Tang, Siew Tzuh [2 ,7 ,8 ,9 ]
机构
[1] Soochow Univ, Dept Int Business, Taipei, Taiwan
[2] Chang Gung Mem Hosp Linkou, Div Hematol Oncol, Tao Yuan, Taiwan
[3] Chang Gung Univ, Coll Med, Tao Yuan, Taiwan
[4] Chang Gung Mem Hosp Linkou, Dept Internal Med, Div Pulm & Crit Care Med, Tao Yuan, Taiwan
[5] Chang Gung Univ, Dept Resp Therapy, Tao Yuan, Taiwan
[6] Chang Gung Mem Hosp Kaohsiung, Div Hepatogastroenterol, Dept Internal Med, Kaohsiung, Taiwan
[7] Chang Gung Mem Hosp Kaohsiung, Dept Nursing, Taoyuan, Taiwan
[8] Chang Gung Univ, Coll Med, Sch Nursing, 259 Wen Hwa 1st Rd, Tao Yuan 333, Taiwan
[9] Chang Gung Univ Sci & Technol, Dept Nursing, Tao Yuan, Taiwan
关键词
INTENSIVE-CARE-UNIT; LIFE-CARE; FAMILY SATISFACTION; SOCIAL SUPPORT; MEDICAL-RECORD; VALIDATION; ICU; ACCOUNTABILITY; OPPORTUNITIES; SYMPTOMS;
D O I
10.1001/jamanetworkopen.2024.20388
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ImportanceImproving end-of-life care in the intensive care unit (ICU) is a priority, but clinically modifiable factors of quality of dying and death (QODD) are seldom identified. ObjectivesTo comprehensively identify factors associated with QODD classes of dying ICU patients, emphasizing clinically modifiable factors based on the integrative framework of factors associated with for bereavement outcomes. Design, Setting, and ParticipantsThis observational cohort study was conducted at medical ICUs of 2 Taiwanese medical centers from January 2018 to March 2020 with follow-up through December 2022. Eligible participants included primary family surrogates responsible for decision making for critically ill ICU patients at high risk of death (Acute Physiology and Chronic Health Evaluation II score >20) but who survived more than 3 days after ICU admission. Data analysis was conducted from July to September 2023. Main Outcomes and MeasuresQODD was measured by the 23-item ICU-QODD questionnaire. Factors associated with patient membership in 4 previously determined QODD classes (high, moderate, poor to uncertain, and worst) were examined using a 3-step approach for latent class modeling with the high QODD class as the reference category. ResultsA total of 309 family surrogates (mean [SD] age, 49.83 [12.55] years; 184 women [59.5%] and 125 men [40.5%]) were included in the study. Of all surrogates, 91 (29.4%) were the patients' spouse and 66 (53.7%) were the patients' adult child. Patient demographics were not associated with QODD class. Two family demographics (age and gender), relationship with the patient (spousal or adult-child), and length of ICU stay were associated with QODD classes. Patients of surrogates perceiving greater social support were less likely to be in the poor to uncertain (adjusted odds ratio [aOR], 0.89; 95% CI, 0.83-0.94) and worst (aOR, 0.92; 95% CI, 0.87-0.96) QODD classes. Family meetings were associated with the poor to uncertain QODD class (aOR, 8.61; 95% CI, 2.49-29.74) and worst QODD class (aOR, 7.28; 95% CI, 1.37-38.71). Death with cardiopulmonary resuscitation was associated with the worst QODD class (aOR, 7.51; 95% CI, 1.12-50.25). Family presence at patient death was uniformly negatively associated with the moderate QODD class (aOR, 0.16; 95% CI, 0.05-0.54), poor to uncertain QODD class (aOR, 0.21; 95% CI, 0.05-0.82), and worst QODD class (aOR, 0.08; 95% CI, 0.02-0.38). Higher family satisfaction with ICU care was negatively associated with the poor to uncertain QODD class (aOR, 0.93; 95% CI, 0.87-0.98) and worst QODD class (aOR, 0.86; 95% CI, 0.81-0.92). Conclusions and RelevanceIn this cohort study of critically ill patients and their family surrogates, modifiable end-of-life ICU-care characteristics played a more significant role in associations with patient QODD class than did immutable family demographics, preexisting family health conditions, patient demographics, and patient clinical characteristics, thereby illuminating actionable opportunities to improve end-of-life ICU care.
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相关论文
共 48 条
[1]   WHAT MATTERS TO PATIENTS AND THEIR FAMILIES DURING AND AFTER CRITICAL ILLNESS: A QUALITATIVE STUDY [J].
Auriemma, Catherine L. ;
Harhay, Michael O. ;
Haines, Kimberley J. ;
Barg, Frances K. ;
Halpern, Scott D. ;
Lyon, Sarah M. .
AMERICAN JOURNAL OF CRITICAL CARE, 2021, 30 (01) :11-+
[2]   Identifying Core Domains to Assess the "Quality of Death": A Scoping Review [J].
Bhadelia, Afsan ;
Oldfield, Leslie E. ;
Cruz, Jennifer L. ;
Singh, Ratna ;
Finkelstein, Eric A. .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2022, 63 (04) :E365-E386
[3]   Quality of dying and death with cancer in Israel [J].
Braun, Michal ;
Hasson-Ohayon, Ilanit ;
Hales, Sarah ;
Zimmermann, Camilla ;
Rydall, Anne ;
Peretz, Tamar ;
Rodin, Gary .
SUPPORTIVE CARE IN CANCER, 2014, 22 (07) :1973-1980
[4]   Associations between Family Satisfaction with End-of-Life Care and Chart-Derived, Process-Based Quality Indicators in Intensive Care Units [J].
Chou, Wen-Chi ;
Huang, Chung-Chi ;
Hu, Tsung-Hui ;
Chuang, Li-Pang ;
Chiang, Ming Chu ;
Tang, Siew Tzuh .
JOURNAL OF PALLIATIVE MEDICINE, 2022, 25 (03) :368-375
[5]   Quality indicators for end-of-life care in the intensive care unit [J].
Clarke, EB ;
Curtis, JR ;
Luce, JM ;
Levy, M ;
Danis, M ;
Nelson, J ;
Solomon, MZ .
CRITICAL CARE MEDICINE, 2003, 31 (09) :2255-2262
[6]  
COHEN S, 1985, PSYCHOL BULL, V98, P310, DOI 10.1037//0033-2909.98.2.310
[7]   Using Electronic Health Records for Quality Measurement and Accountability in Care of the Seriously Ill: Opportunities and Challenges [J].
Curtis, J. Randall ;
Sathitratanacheewin, Seelwan ;
Starks, Helene ;
Lee, Robert Y. ;
Kross, Erin K. ;
Downey, Lois ;
Sibley, James ;
Lober, William ;
Loggers, Elizabeth T. ;
Fausto, James A. ;
Lindvall, Charlotta ;
Engelberg, Ruth A. .
JOURNAL OF PALLIATIVE MEDICINE, 2018, 21 :S52-S60
[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]   Guidelines for Family-Centered Care in the Neonatal, Pediatric, and Adult ICU [J].
Davidson, Judy E. ;
Aslakson, Rebecca A. ;
Long, Ann C. ;
Puntillo, Kathleen A. ;
Kross, Erin K. ;
Hart, Joanna ;
Cox, Christopher E. ;
Wunsch, Hannah ;
Wickline, Mary A. ;
Nunnally, Mark E. ;
Netzer, Giora ;
Kentish-Barnes, Nancy ;
Sprung, Charles L. ;
Hartog, Christiane ;
Coombs, Maureen ;
Gerritsen, Rik T. ;
Hopkins, Ramona O. ;
Franck, Linda S. ;
Skrobik, Yoanna ;
Kon, Alexander A. ;
Scruth, Elizabeth A. ;
Harvey, Maurene A. ;
Lewis-Newby, Mithya ;
White, Douglas B. ;
Swoboda, Sandra M. ;
Cooke, Colin R. ;
Levy, Mitchell M. ;
Azoulay, Elie ;
Curtis, J. Randall .
CRITICAL CARE MEDICINE, 2017, 45 (01) :103-128
[10]   Comparing Quality of Dying and Death Perceived by Family Members and Nurses for Patients Dying in US and Dutch ICUs [J].
Gerritsen, Rik T. ;
Koopmans, Matty ;
Hofhuis, Jose G. M. ;
Curtis, J. Randall ;
Jensen, Hanne Irene ;
Zijlstra, Jan G. ;
Engelberg, Ruth A. ;
Spronk, Peter E. .
CHEST, 2017, 151 (02) :298-307