同伴支持和患者指导在增强乳腺癌幸存者能力方面的作用:对社区癌症控制的影响

Marc Sleiman, M. R. Yockel, A. Fleischmann, E. Silber, Mingqian Liu, Olivia Young, Sahana Arumani, K. Tercyak
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引用次数: 0

摘要

社区组织(CBO)为乳腺癌高危妇女(例如,患有 BRCA 致病变异的妇女)和乳腺癌幸存者提供支持,包括患者指导(PN)。然而,CBO 的工作对提高幸存者能力(如控制力、自信心、知识/技能、应对能力)的影响在很大程度上是未知的。 作为一项质量改进计划(N = 2,247)的一部分,我们对 CBO 护理服务模式进行了二次分析,重点关注 PN、护理满意度、同伴支持和生活质量(QoL)。 在 CBO 领导下的癌症控制中,妇女的能力得到了很大的提高:大多数幸存者(71.2%)对自己的护理管理充满信心,(66.4%)对护理知识也有所了解。对护理质量的评价也很高(91%):可向他人推荐(93.9%)、有帮助(92.7%)、信息丰富(92.6%)、及时(92.2%)、可靠(91.5%)、支持(91.3%)和有效(88.7%)。在社区组织护理满意度方面,幸存者感到得到了丰富的资源(92.8%)和项目(91.2%)的支持、理解(92.0%)和帮助(91.6%)。同伴支持(提供给超过 25% 的幸存者)显示出较高的参与度(超过 85%)。在生活质量方面,25.3%的人健康状况一般/较差,25.6%的人经常感到精神痛苦(过去一个月内身体不健康天数为 7.2 天,精神不健康天数为 7.8 天,活动受限天数为 6.4 天)。根据幸存者 QoL 的函数,可以观察到赋权方面的差异:精神痛苦(t = -2.13,P < .05)、精神不健康天数(r = -0.083,P < .05)和活动受限天数(r = -0.058,P < .05)较多的幸存者赋权最低。)这些负担可能会影响幸存者的赋权感,尤其是那些没有同伴支持的幸存者(t = 3.77,P < .001),他们会降低 PN 的质量(t = 0.60,P < .01),并且对 CBO 癌症控制最不满意(t = 0.57,P < .01)。在调整精神痛苦的多变量模型中,感知到的 PN 质量(B = 0.16,SE = 0.01,P < .001)和同伴支持(B = 0.24,SE = 0.13,P = .05)与增强能力呈正相关:对其 PN 评价较高并提供同伴支持的幸存者感到更有能力。 社区组织的癌症控制可以提升大多数幸存者的能力:通过同伴支持等计划来解决社会决定的差异,可以提高其有效性,尤其是在那些心理健康状况不佳的幸存者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of peer support and patient navigation for empowerment in breast cancer survivors: implications for community cancer control
Community-based organizations (CBO) offer support, including patient navigation (PN), to women at-risk for (eg, those with BRCA pathogenic variants) and surviving with breast cancer. However, the impacts of CBO efforts on survivors' empowerment (eg, control, self-confidence, knowledge/skills, coping) are largely unknown. As part of a quality improvement initiative (N = 2,247) focused on PN, care satisfaction, peer support, and quality of life (QoL), we conducted a secondary analysis of a CBO care delivery model on women's empowerment. Under CBO led cancer control, empowerment was high: most survivors felt confident in (71.2%) and knowledgeable about (66.4%) managing their care. Perceived care quality was also high (91%): it was recommendable to others (93.9%), helpful (92.7%), informative (92.6%), timely (92.2%), reliable (91.5%), supportive (91.3%), and effective (88.7%). Regarding CBO care satisfaction, survivors felt supported by abundant resources (92.8%) and programs (91.2%), understood (92.0%), and helped (91.6%). Peer support (offered to >25%) demonstrated high engagement (>85%). Regarding QoL, 25.3% were in fair/poor health and 25.6% endorsed frequent mental distress (M = 7.2 physically unhealthy days, M = 7.8 mentally unhealthy days, and M = 6.4 activity-limited days within the past month). Disparities in empowerment were observed as a function of survivors' QoL: lowest among those with more frequent mental distress (t = −2.13, P < .05), mentally unhealthy days (r = −0.083, P < .05), and activity-limited days (r = −0.058, P < .05)). These burdens may have influenced survivors' feelings of empowerment, especially among those without peer support (t = 3.77, P < .001), who downgraded the quality of PN (t = 0.60, P < .01), and were least satisfied with CBO cancer control (t = 0.57, P < .01). In a multivariable model adjusting for mental distress, both perceived PN quality (B = 0.16, SE = 0.01, P < .001) and peer support (B = 0.24, SE = 0.13, P = .05) were positively associated with empowerment: survivors who rated their PN higher, and offered peer support, felt more empowered. CBO cancer control can uplift most survivors: addressing socially determined disparities, through programs such as peer support, may enhance their effectiveness and particularly among those with poor mental health.
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