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社会决定因素对健康的影响:亚裔美国人群肝细胞癌患者数据采集有待改善。

Social determinants of health: a need for better data capture in Asian American patients with hepatocellular cancer.

机构信息

Department of Oncology, Mayo Clinic, 200 First Street SW, Rochester, MN, 55905, USA.

Division of Gastroenterology, Mayo Clinic, Phoenix, AZ, USA.

出版信息

Support Care Cancer. 2023 Aug 30;31(9):543. doi: 10.1007/s00520-023-08016-7.

Abstract

BACKGROUND

Social determinants of health lead to better cancer care. This multi-site, single-institution study sought to capture data on social determinants of health data in Asian Americans with hepatocellular carcinoma; this group constitutes 60% of patients with this malignancy and are often undertreated or not treated at all.

METHODS

This study took advantage of an institutional initiative designed to capture and integrate social determinants of health data into the electronic medical record for all patients. Medical records of Asian Americans with hepatocellular cancer were reviewed to acquire data on housing instability, lack of transportation, financial concerns, and social isolation; a score of 1 indicated poor social determinants of health.

RESULTS

Of 112 adult Asian American patients with hepatocellular cancer, 22 (20%) were Southeast Asian, and 74 (67%) described English proficiency/preference. Total noncompletion per domain (no question answered within that domain) was observed in 90 patients (80%) for housing instability; 90 (80%) for lack of transportation; 92 (82%) for financial hardship; and 90 (80%) for social isolation. A score of 1 (highest risk) was observed in 1 patient (0.9%) for housing instability; 1 (0.9%) lack of transportation; no patient for financial hardship; and 1 (0.9%) for social isolation. Of note, institution-wide benchmark total noncompletion rates were 0.3%, 0.3%, 47%, and 39% for these respective domains.

CONCLUSION

High total noncompletion rates make social determinants of health data challenging to interpret and underscore the need for evidence-based guidelines on how best to capture such data in underserved patients.

摘要

背景

健康的社会决定因素可改善癌症护理。这项多地点、单机构研究旨在收集亚裔美国人肝癌患者健康社会决定因素的数据;该人群构成了 60%的此类恶性肿瘤患者,他们往往治疗不足或根本不治疗。

方法

本研究利用了一项机构倡议,旨在将健康社会决定因素数据纳入所有患者的电子病历中。对亚裔美国人肝癌患者的病历进行了回顾,以获取住房不稳定、缺乏交通工具、经济困难和社会孤立的数据;1 分表示健康社会决定因素较差。

结果

在 112 名成年亚裔美国人肝癌患者中,22 名(20%)是东南亚人,74 名(67%)表示精通/偏好英语。在住房不稳定、缺乏交通工具、经济困难和社会孤立方面,有 90 名患者(80%)未完成任何一个领域的全部问题;90 名患者(80%)缺乏交通工具;92 名患者(82%)经济困难;90 名患者(80%)社会孤立。1 名患者(0.9%)住房不稳定、1 名患者(0.9%)缺乏交通工具、没有患者经济困难、1 名患者(0.9%)社会孤立的风险最高。值得注意的是,在这些领域,机构范围内的总不完整率分别为 0.3%、0.3%、47%和 39%。

结论

总不完整率高使得健康社会决定因素数据难以解释,并强调了需要制定基于证据的指南,以最佳方式在服务不足的患者中获取此类数据。

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