Belkora Jeffrey K, Miller Melissa F, Dougherty Kasey, Gayer Christopher, Golant Mitch, Buzaglo Joanne S
Institute for Health Policy Studies, University of California, San Francisco, California, USA.
Public Health Research Scientist, Fairfax, Virginia, USA.
J Community Support Oncol. 2015 Mar;13(3):104-12. doi: 10.12788/jcso.0116.
Qualitative studies have identified barriers to communication and informed decision making among breast cancer survivors making treatment decisions. The prevalence of these barriers is unknown.
To quantify the need for decision support among breast cancer survivors.
We surveyed 2,521 breast cancer survivors participating in an online registry hosted by the Cancer Support Community to find out what proportion of breast cancer patients: made decisions during their first visit with a specialist; received satisfactory information before that visit; asked questions and received responses; and endorsed expanded use of decision support.
We received 1,017 (41%) responses and analyzed 917 surveys from women who lived in the United States. Most of the respondents recalled making treatment decisions during their first visit (52%). A minority (14%) received information before the first specialist visit. At least 25% of respondents rated their satisfaction below 7 on a scale of 10 for decision-making, information, and questions asked and answered. Respondents endorsed the need for assistance with obtaining information, listing questions, taking notes, and making audio-recordings of visits.
The respondent sample skewed younger and had higher-stage cancer compared with all breast cancer survivors. Responses were subject to recall bias.
Cancer survivors expressed gaps in their care with respect to reviewing information, asking questions, obtaining answers, and making decisions. Implementing decision and communication aids immediately upon diagnosis, when treatment decisions are being made, would address these gaps.
定性研究已确定乳腺癌幸存者在做出治疗决策时存在沟通障碍和知情决策障碍。这些障碍的发生率尚不清楚。
量化乳腺癌幸存者对决策支持的需求。
我们对参与癌症支持社区主办的在线登记的2521名乳腺癌幸存者进行了调查,以了解乳腺癌患者的以下比例:在首次就诊专科医生时做出决策;在就诊前获得满意的信息;提出问题并得到答复;以及支持扩大决策支持的使用。
我们收到了1017份(41%)回复,并分析了来自美国女性的917份调查问卷。大多数受访者回忆说在首次就诊时做出了治疗决策(52%)。少数人(14%)在首次就诊专科医生之前获得了信息。至少25%的受访者在决策、信息以及提问和回答方面给自己的满意度打分为10分制中的7分以下。受访者支持在获取信息、列出问题、做笔记以及对就诊进行录音方面获得帮助。
与所有乳腺癌幸存者相比,受访者样本年龄偏轻且癌症分期较高。回复存在回忆偏差。
癌症幸存者在信息审查、提问、获取答案和决策方面表示护理存在差距。在做出治疗决策时,即诊断后立即实施决策和沟通辅助工具,将弥补这些差距。