Impact of Social Determinants of Health on Cancer Treatment Referrals in Patients Living with HIV in the United States: A Narrative Review.

IF 2 Q3 HEALTH POLICY & SERVICES Journal of Cancer Policy Pub Date : 2024-12-31 DOI:10.1016/j.jcpo.2024.100555
Shebin George, Heena Mansuri, Michael Qureshi, Sebastian Lopez, Alejandra Viera, Jeremy Purow, Stephanie Ocejo, Jannelle Vicens, Marco Ruiz Andia
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Abstract

Introduction: This narrative review aims to identify and explore the social determinants that prevent people living with HIV (PWH) from accessing specialized cancer centers in the United States and compare to patient experiences in other countries.

Methods: The review includes randomized controlled trials, cohort studies, case-control studies, qualitative studies, case series, and non-peer reviewed articles. The risk of bias was assessed using standardized tools, and data were synthesized narratively due to the heterogeneity of study designs and outcomes.

Results: Our findings highlight that PWH in the U.S. typically depend on public insurance or programs such as the Ryan White HIV/AIDS Program (RWHP), which offer better cancer care outcomes but are limited by income restrictions. Integrated health systems, such as Veterans Affairs (VA) centers, have successful cancer screening programs but limited accessibility. Limited health literacy among PWH is associated with poor clinical knowledge, misinterpretation of treatment outcomes, and underreporting of medical conditions. Although higher health literacy improves screening rates, its impact on referrals to specialized cancer centers is unclear. Racial and ethnic disparities result in lower screening rates and fewer referrals to specialized care, with Hispanic, Asian, and Black patients facing barriers like distrust in healthcare, cultural factors, and insurance status. HIV stigma further leads to healthcare avoidance and delayed interventions.

Conclusion: The review addresses systemic barriers including healthcare access, health literacy, racial, and ethnic disparities, and cultural stigma and highlights solutions to improve cancer treatment referrals among PWH. Recommendations include improving access to integrated health centers and developing culturally competent interventions to enhance referrals to advanced cancer care for PWH.

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健康的社会决定因素对美国艾滋病毒感染者癌症治疗转诊的影响:叙述性回顾。
引言:这篇叙述性综述旨在确定阻止艾滋病毒感染者进入专门的癌症中心的社会决定因素,并探讨阻止这些患者转诊到美国专门的艾滋病毒/癌症护理中心的因素,并与其他国家的患者经历进行比较。方法:综述包括随机对照试验、队列研究、病例对照研究、定性研究、病例系列和非同行评议文章。使用标准化工具评估偏倚风险,由于研究设计和结果的异质性,对数据进行叙述性综合。结果:该综述强调,PWH通常依赖于公共保险或瑞安·怀特艾滋病毒/艾滋病计划(RWHP)等项目,这些项目提供了更好的结果,但受到收入限制的限制。综合卫生系统,如退伍军人事务(VA)中心,有成功的癌症筛查项目,但可及性有限。PWH的健康素养有限与临床知识贫乏、对治疗结果的误解以及对医疗状况的少报有关。虽然更高的健康素养提高了筛查率,但它对进入癌症中心的影响尚不清楚。种族和民族差异导致较低的筛查率和较少的专科护理转诊,西班牙裔、亚裔和黑人患者面临着诸如对医疗保健、文化因素和保险状况的不信任等障碍。艾滋病毒污名进一步导致逃避保健和延迟干预。结论:该综述呼吁解决系统性问题,如医疗保健可及性、健康素养、种族和民族差异以及文化耻辱感,以改善PWH之间的癌症治疗转诊。建议包括综合保健中心和文化上有能力的干预措施,以增加PWH获得晚期癌症护理的机会。
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来源期刊
Journal of Cancer Policy
Journal of Cancer Policy Medicine-Health Policy
CiteScore
2.40
自引率
7.70%
发文量
47
审稿时长
65 days
期刊最新文献
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