Provision of disaggregated race and ethnicity information in hospital visits.

IF 2.7
Health affairs scholar Pub Date : 2025-03-07 eCollection Date: 2025-04-01 DOI:10.1093/haschl/qxaf047
Charleen Hsuan, Donald Miller, Alexis M Zebrowski, Jeannette A Rogowski, Eric K Wei, Yasmin Mahmud, Amy Yeung, Ninez A Ponce
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引用次数: 0

Abstract

Although federal and state policies support collection of detailed race and ethnicity, little research has examined how organizations and patients respond to these requests. New York State encourages hospitals to collect detailed race and ethnic group information for Hispanic, Asian, and Native Hawaiian or Pacific Islander (NHPI) patients, with more than 70% of hospitals complying. Using New York hospital discharge data from 2016-2022, we found that visit-responses for Asian and NHPI patients were more than 40 percentage points more likely to have detailed race and ethnic group information than patients identified as other races. Hospitals collecting detailed ethnic group information for Asian and NHPI patients were more likely to be larger and more urban, located in counties with less deprivation. This descriptive study suggests that patients will report detailed race and ethnic group information when prompted, and policies encouraging hospitals to record detailed race and ethnic group information may be effective.

在医院就诊时提供分类的种族和族裔信息。
虽然联邦和州的政策支持收集详细的种族和民族,但很少有研究调查组织和患者如何回应这些要求。纽约州鼓励医院为西班牙裔、亚裔和夏威夷原住民或太平洋岛民(NHPI)患者收集详细的种族和族裔信息,超过70%的医院遵守了这一规定。使用纽约2016-2022年的出院数据,我们发现亚洲和NHPI患者的就诊反应比其他种族的患者更有可能拥有详细的种族和族裔群体信息,这一比例超过40个百分点。为亚洲患者和NHPI患者收集详细族裔群体信息的医院更有可能是规模更大、更城市化的医院,位于贫困程度较低的县。这项描述性研究表明,患者会在提示时报告详细的种族和民族信息,鼓励医院记录详细的种族和民族信息的政策可能是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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