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Bereave Care. 2013;32(3):117-123. doi: 10.1080/02682621.2013.854544. Epub 2013 Dec 16.
2
Toward a model of continuous care: A necessity for caregiving partners.迈向持续护理模式:护理伙伴的必要性。
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The experiences of suffering of palliative care informal caregivers in Malaysia: a thematic analysis.马来西亚姑息治疗非正式照护者的痛苦经历:一项主题分析。
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Trajectory and influencing factors of depressive symptoms in family caregivers before and after the death of terminally ill patients with cancer.癌症晚期患者死亡前后家庭照顾者抑郁症状的轨迹及影响因素
Oncol Nurs Forum. 2013 Jan;40(1):E32-40. doi: 10.1188/13.ONF.E32-E40.
5
Course and predictors of depressive symptoms among family caregivers of terminally ill cancer patients until their death.临终癌症患者家属的抑郁症状的过程和预测因素,直至患者死亡。
Psychooncology. 2013 Jun;22(6):1312-8. doi: 10.1002/pon.3141. Epub 2012 Jul 27.
6
The care strategy for families of terminally ill cancer patients who become unable to take nourishment orally: recommendations from a nationwide survey of bereaved family members' experiences.无法经口进食的终末期癌症患者家属的照护策略:一项全国性调查中对丧亲家庭成员经历的建议。
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丧亲第一年之后家庭照顾者的心理社会健康状况

Psychosocial Health Outcomes for Family Caregivers Following the First Year of Bereavement.

作者信息

Masterson Melissa P, Hurley Karen E, Zaider Talia, Corner Geoffrey, Schuler Tammy, Kissane David W

机构信息

a Department of Psychiatry & Behavioral Sciences , Memorial Sloan-Kettering Cancer Center , New York , New York , USA.

b Teachers College , Columbia University , New York , New York , USA.

出版信息

Death Stud. 2015;39(10):573-8. doi: 10.1080/07481187.2014.985406. Epub 2015 Feb 4.

DOI:10.1080/07481187.2014.985406
PMID:25651502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11623306/
Abstract

The authors examined psychosocial outcomes following the first year of bereavement, for 51 family caregivers, including both spouses and offspring. Researchers assessed caregivers during palliative care and again during the second year of bereavement, for social functioning, depression, and distress. For all family caregivers, only depression scores declined significantly between T1 and T2 (p < 0.05). Caregiver relationship and gender did not make a difference in recovery. Results demonstrate that poor psychosocial health outcomes exist beyond the first year of bereavement. Early identification of these caregivers is necessary to provide mental health professionals the opportunity to intervene proactively.

摘要

作者对51名家庭照顾者(包括配偶和子女)在丧亲第一年之后的心理社会结果进行了研究。研究人员在姑息治疗期间以及丧亲第二年再次对照顾者的社会功能、抑郁和痛苦程度进行了评估。对于所有家庭照顾者而言,仅抑郁得分在T1和T2之间显著下降(p<0.05)。照顾者关系和性别对恢复情况没有影响。结果表明,丧亲一年之后仍存在不良的心理社会健康结果。尽早识别这些照顾者,以便为心理健康专业人员提供积极干预的机会,这很有必要。