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乳腺癌诊断后在一家保障医院的社会需求负担和轨迹。

Burden and trajectory of social needs after breast cancer diagnosis at a safety-net hospital.

机构信息

Boston University Chobanian and Avedisian School of Medicine, Boston, MA, 02118, USA.

Section of General Internal Medicine, Women's Health Unit, Department of Medicine, Boston University Chobanian and Avedisian School of Medicine, Boston, MA, 02118, USA.

出版信息

Breast Cancer Res Treat. 2024 Oct;207(3):579-585. doi: 10.1007/s10549-024-07389-5. Epub 2024 Jun 8.

Abstract

PURPOSE

Unmet social needs pose barriers to cancer care, contributing to adverse outcomes and health inequities. A better understanding of how social needs change after cancer diagnosis can inform more effective, equity-focused interventions.

METHODS

In this study, we examined self-reported social needs at 0, 3, and 6 months after a breast cancer diagnosis in a racially diverse, multilingual sample (n = 222) enrolled in patient navigation intervention at an urban safety-net hospital. At each timepoint, respondents completed surveys about social needs related to employment, disability benefits, housing and utilities, and personal and family stability.

RESULTS

Over three-quarters (78%, n = 175) reported ≥ 1 social need, and 46% (n = 102) reported ≥ 3 social needs. The most frequently reported need was housing and utilities (64%, n = 142), followed by employment (40%, n = 90). Individuals from minoritized groups more frequently reported an increased number of social needs over time, compared with their White counterparts (p = 0.02).

CONCLUSION

Our findings suggest that despite navigation, many cancer patients from historically underrepresented populations continue to experience social concerns over the first 6 months of treatment. Further research, conducted with historically underrepresented populations in research, is needed to better understand the social needs of breast cancer patients to inform effective and equitable interventions.

摘要

目的

未满足的社会需求是癌症护理的障碍,导致不良结局和健康不平等。更好地了解癌症诊断后社会需求的变化方式,可以为更有效、以公平为重点的干预措施提供信息。

方法

在这项研究中,我们在一家城市社区医院的患者导航干预中,对 222 名种族多样化、会多种语言的参与者在乳腺癌诊断后 0、3 和 6 个月时的自我报告社会需求进行了研究。在每个时间点,受访者都完成了与就业、残疾福利、住房和水电费以及个人和家庭稳定相关的社会需求调查。

结果

超过四分之三(78%,n=175)的人报告了≥1 项社会需求,46%(n=102)的人报告了≥3 项社会需求。最常报告的需求是住房和水电费(64%,n=142),其次是就业(40%,n=90)。与白人相比,少数族裔群体的个体随着时间的推移报告的社会需求数量增加更多(p=0.02)。

结论

我们的研究结果表明,尽管有导航,但许多来自历史上代表性不足的人群的癌症患者在治疗的头 6 个月中仍然面临社会问题。需要对历史上代表性不足的人群进行更多的研究,以更好地了解乳腺癌患者的社会需求,为有效的公平干预措施提供信息。

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