成年癌症患者照顾者的创伤性压力:范围界定综述

Elizaveta Klekovkina , Maya A. Stern , Carmine Malfitano , Esme Fuller-Thomson
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引用次数: 0

摘要

目的对成人癌症患者照护者创伤应激的相关研究文献进行综述。目的包括确定显著创伤应激症状的流行程度、文献中的主题以及与该人群中创伤应激相关的因素。方法检索APA PsycInfo、MEDLINE、Embase和CINAHL。两位作者筛选摘要和全文,并从纳入的文章中提取数据。共鉴定出1150篇独特的标题和摘要,其中2f篇文章在标题和摘要筛选后进行全文筛选。共有23项研究被纳入综述。结果大多数研究报告PTSD患病率为15%及以上。新确诊患者、癌症复发患者和接受积极治疗的患者的护理人员最痛苦。完成治疗的患者和长期幸存者的护理人员的痛苦程度较低。研究发现,照顾者创伤压力、照顾者与患者的心理共病、较低的社会支持、较高的照顾者负担和患者较大的身体症状之间存在显著关联。结论本综述揭示了相当比例的成年癌症患者的照顾者经历创伤性应激。然而,大多数已发表的研究都是横断面的,样本量小,缺乏种族和性别多样性。迫切需要进一步研究,包括在诊断或疾病复发时提供积极和有针对性的干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Traumatic stress in caregivers of adult patients with cancer: A scoping review

Objective

The goal of this review was to critically review the research literature on traumatic stress in caregivers of adult cancer patients. Objectives included identifying the prevalence of significant traumatic stress symptoms, themes within the literature, and factors that are associated with traumatic stress in this population.

Methods

A search was conducted of APA PsycInfo, MEDLINE, Embase, and CINAHL. Two authors screened abstracts and full-texts and extracted data from included articles. A total of 1,150 unique titles and abstracts were identified, with 2f articles selected for full-text screening after title and abstract screening. There were 23 studies which were included in the review.

Results

Most studies reported a prevalence of PTSD of 15 % and above. The caregivers of newly diagnosed patients, those with recurrent cancer, and those on active treatment were the most distressed. Caregivers of patients who had completed treatment and those of longer-term survivors were less distressed. Significant associations were identified between caregiver traumatic stress and caregiver and patient psychological comorbidity, lower social support, higher caregiver burden, and patient's greater physical symptoms.

Conclusion

This scoping review reveals that a substantial proportion of caregivers of adult patients with cancer experience traumatic stress. However, the majority of published studies are cross-sectional, with small sample sizes, and a lack of racial and gender diversity. There is an urgent need for further research, including on proactive and tailored interventions provided at the time of diagnosis or recurrence of the disease.
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