Quality of end-of-life care for women diagnosed with metastatic breast cancer.

IF 4.7 3区 医学 Q1 ONCOLOGY
Rachel Brazee, Margaret Q. Rosenzweig
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Abstract

238 Background: Metastatic breast cancer (MBC) is a progressive, non-curative disease, with multiple therapy options. The toxicities and side effects from these therapies, as well as the signs and symptoms of advancing cancer, can cause patient and family related distress. To address these end-of-life (EOL) care needs, standards of care were established and recommendations provided. However, it is not clear if these standards are comprehensive in describing current MBC populations and their EOL experiences. Methods: This study used a sequential quantitative-qualitative mixed methods design to examine the quality of EOL care. The deceased patient’s designated personal representative (DPR) completed the Quality of Death and Dying (QODD) survey, with a subsequent/optional telephone interview. Results: The DPRs were predominately male (n=18; 72%), white (n=23; 92%), had some college education or more (n=24; 96%), and was the spouse/partner (n=16; 64%). The range in age was 25-95 years (SD 14.51), with the length of relationship varying between 7-63 years (SD 14.38). In the QODD survey (N=25), 40% (n=10), rated the overall quality of their loved one’s dying experience as ‘poor’ (score 0-4), yet 60% (n=15) rated the care they received from their healthcare team as ‘excellent.’ During the interview (N=16), the DPR was then asked to explore what made or what would have made for high quality EOL care. Four major categories emerged: resilience in response to transitions of care and adaptations to lifestyle changes; communication between healthcare providers and the patient/DPR in both content quality and delivery style; perceived support from the healthcare team, family, or spiritual advisors, specifically during changes in treatment goals; and knowledge as it relates to past experiences, when it was perceived as missing, or lack the knowledge regarding how to gather new information. Conclusions: The care needs for both the patient and DPR dynamically evolve throughout an MBC diagnosis and treatment. While resilience, communication, support, and knowledge all play a key role in the perception of the DPR regarding the quality of death experienced by their loved one, it is important to note that these experiences took place well before the EOL occurred and should be considered at the start of MBC treatment.
诊断为转移性乳腺癌的妇女的临终关怀质量。
238背景:转移性乳腺癌(MBC)是一种进行性、不可治愈的疾病,有多种治疗选择。这些疗法的毒性和副作用,以及癌症进展的体征和症状,可能会给患者和家属带来痛苦。为了解决这些生命末期(EOL)护理需求,建立了护理标准并提供了建议。然而,尚不清楚这些标准是否全面地描述了目前的MBC人口及其EOL经历。方法:本研究采用序贯定量-定性混合方法设计来检验EOL护理的质量。死亡患者的指定个人代表(DPR)完成了死亡和临终质量(QODD)调查,并进行了随后的/可选的电话访谈。结果:DPRs以男性为主(n=18;72%),白色(n=23;92%),受过大学或以上教育(n=24;96%),配偶/伴侣(n=16;64%)。年龄范围为25 ~ 95岁(SD 14.51),关系长度为7 ~ 63岁(SD 14.38)。在QODD的调查中(N=25), 40% (N= 10)的人认为他们所爱的人临终体验的整体质量“差”(0-4分),但60% (N= 15)的人认为他们从医疗团队那里得到的护理“非常好”。在访谈期间(N=16), DPR被要求探讨是什么造就了高质量的EOL护理,或者是什么造就了高质量的EOL护理。出现了四个主要类别:应对护理转变和适应生活方式变化的复原力;医疗保健提供者与患者/DPR之间在内容质量和交付方式方面的沟通;感受到来自医疗团队、家庭或精神顾问的支持,特别是在治疗目标改变期间;和过去的经验有关的知识,当它被认为是缺失的,或者缺乏关于如何收集新信息的知识。结论:在整个MBC诊断和治疗过程中,患者和DPR的护理需求都是动态变化的。虽然复原力、沟通、支持和知识都在DPR对亲人所经历的死亡质量的感知中发挥关键作用,但重要的是要注意,这些经历发生在EOL发生之前很久,应在MBC治疗开始时予以考虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
7.50%
发文量
518
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