Bereavement services for family caregivers: How often used, why, and why not

被引:68
作者
Cherlin, Emily J.
Barry, Colleen L.
Prigerson, Holly G.
Schulman-Green, Dena
Johnson-Hurzeler, Rosemary
Kasl, Stanislav V.
Bradley, Elizabeth H.
机构
[1] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06520 USA
[2] Dana Farber Canc Inst, Ctr Psychooncol & Palliat Care Res, Boston, MA 02115 USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Psychiat, Boston, MA 02115 USA
[4] Yale Univ, Sch Nursing, New Haven, CT 06536 USA
[5] Connecticut Hospice, Branford, CT USA
[6] John D Thompson Hospice Inst Educ Training & Res, Branford, CT USA
[7] Yale Univ, Sch Med, Dept Med, Robert Wood Johnson Clin Scholars Program, New Haven, CT 06510 USA
关键词
D O I
10.1089/jpm.2006.0108
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
Background: Bereavement services are central to high-quality end-of-life care, however, little is known about how frequently and why such bereavement services are used and not used. We examined family caregiver reports about how often they used bereavement services, predictors of their use, and reported reasons for not using bereavement services. Methods: Prospective cohort study of family caregivers (n = 161) of patients with cancer enrolled with hospice between October 1999 and September 2001. We conducted bivariate and multivariable analyses to determine predictors of bereavement service use, adjusted for a broad range of factors including caregiving experiences, major depressive disorder (MDD), relationship with the deceased, and demographic factors. We used content analysis to summarize responses to open-ended questions concerning why individuals did not use bereavement services. Results: We found that approximately 30% of family caregivers used bereavement services in the year postloss, and the majority of these caregivers used services in the first 6 months postloss. Even among bereaved caregivers with MDD, less than half (47.6%) used bereavement services. Factors associated with using bereavement services included being a spouse caregiver, younger age, having MDD at study enrollment, witnessing highly distressing events pertaining to the patient's death, having assisted the patient with more Instrumental Activities of Daily Living (IADLs) prior to the patient's death, having greater availability of instrumental support for oneself, and physician communication with the caregiver about the patient's prognosis before the patient's death. The most common given reason for nonuse was the perception that bereavement services were not needed or would not help. Conclusion: Addressing caregiver receptivity to bereavement services will be an important aspect of increasing appropriate use of such services. Future studies might examine specific interventions for reducing barriers and increasing receptivity to bereavement service use.
引用
收藏
页码:148 / 158
页数:11
相关论文
共 39 条
  • [1] Effectiveness of grief therapy: A meta-analysis
    Allumbaugh, DL
    Hoyt, WT
    [J]. JOURNAL OF COUNSELING PSYCHOLOGY, 1999, 46 (03) : 370 - 380
  • [2] AREEJ RE, IN PRESS J PALLIAT M
  • [3] Report on bereavement and grief research
    Ayers, T
    Balk, D
    Bolle, J
    Bonanno, GA
    Connor, SR
    Cook, AS
    Doka, K
    Goodkin, K
    Hall, M
    Hansson, RO
    Klass, D
    Moss, M
    Nadeau, JW
    Neimeyer, RA
    Oltjenbruns, KA
    Prigerson, H
    Rosenblatt, P
    Sandler, I
    Shapiro, ER
    Silver, RC
    Tancredy, C
    Weiss, RS
    Neimeyer, RA
    [J]. DEATH STUDIES, 2004, 28 (06) : 491 - 575
  • [4] The stigma receptivity scale and its association with mental health service use among bereaved older adults
    Bambauer, KZ
    Prigerson, HG
    [J]. JOURNAL OF NERVOUS AND MENTAL DISEASE, 2006, 194 (02) : 139 - 141
  • [5] Depression among surviving caregivers: Does length of hospice enrollment matter?
    Bradley, EH
    Prigerson, H
    Carlson, MDA
    Cherlin, E
    Johnson-Hurzeler, R
    Kasl, SV
    [J]. AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (12) : 2257 - 2262
  • [6] BEREAVED OLDER ADULTS WHO SEEK EARLY PROFESSIONAL HELP
    CASERTA, MS
    LUND, DA
    [J]. DEATH STUDIES, 1992, 16 (01) : 17 - 30
  • [7] Communication between physicians and family caregivers about care at the end of life: When do discussions occur and what is said?
    Cherlin, Emily
    Fried, Terri
    Prigerson, Holly G.
    Schulman-Green, Dena
    Johnson-Hurzeler, Rosemary
    Bradley, Elizabeth H.
    [J]. JOURNAL OF PALLIATIVE MEDICINE, 2005, 8 (06) : 1176 - 1185
  • [8] Crabtree BF, 1999, DOING QUALITATIVE RE
  • [9] Adaptation to bereavement
    Dutton, YC
    Zisook, S
    [J]. DEATH STUDIES, 2005, 29 (10) : 877 - 903
  • [10] First M, 2017, Structured Clinical Interview for DSM-5 Personality Disorders (SCID-5-PD)