Krista A Brown, Katrina Poppert Cordts, Robin M Lally
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引用次数: 0
摘要
问题识别：本综述旨在确定和综合已发表的关于晚期（美国癌症联合委员会 [AJCC] III）和转移性（AJCC IV）CRC 幸存者生活质量（QoL）和未满足需求的文献：检索的数据库包括 PubMed、CINAHL 和 Embase（2010 年至 2023 年）。共检索到 512 篇文章，其中 5 篇符合纳入标准：数据评估/综述：共确定了五项研究，对 CRC 幸存者的 QoL 和未满足的需求进行了调查。其中三项研究仅评估了 III 期和 IV 期病例。可能影响 QoL 的核心因素包括年龄较小、来自社交圈的情感支持以及治疗后期间的心理支持。CRC 幸存者报告的未满足的需求包括帮助他们控制痛苦，以及对癌症进展恐惧的心理支持：对晚期和转移性 CRC 幸存者未满足需求的探索研究有限。需要进一步开展研究，了解影响生活质量和未满足需求的患者因素，以支持最佳护理实践。
Quality of life and unmet needs of late-stage and metastatic colorectal cancer survivors: An integrative review.
Problem identification: The purpose of this review was to identify and synthesize the published literature on Quality of Life (QoL) and unmet needs of late-stage (American Joint Committee on Cancer [AJCC] III) and metastatic (AJCC IV) CRC survivors.
Literature search: Databases searched included PubMed, CINAHL, and Embase from 2010 to 2023. Articles were included if they focused on self-reported CRC experiences of late-stage and metastatic survivors, identifying 512 articles, of which five met the inclusion criteria.
Data evaluation/synthesis: Five studies were identified that examined QoL and unmet needs of CRC survivors. Three studies assessed only stage III and IV cases. Core factors that may impact QoL included younger age, emotional support from social circles, and psychological support during post-therapy periods. Unmet needs reported by CRC survivors included help managing distress and psychological support for fear of cancer progression.
Conclusions: Limited research has explored unmet needs of late-stage and metastatic CRC survivors. Further research is needed to understand patient factors that impact QoL and unmet needs to support best care practices.
期刊介绍：
Here is your single source of integrated information on providing the best psychosocial care possible from the knowledge available from many disciplines.The Journal of Psychosocial Oncology is an essential source for up-to-date clinical and research material geared toward health professionals who provide psychosocial services to cancer patients, their families, and their caregivers. The journal—the first interdisciplinary resource of its kind—is in its third decade of examining exploratory and hypothesis testing and presenting program evaluation research on critical areas, including: the stigma of cancer; employment and personal problems facing cancer patients; patient education.
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