Bertolli Jeanne, Lee Lisa M, Sullivan Patrick S
Office of Health Disparities, National Center for HIV, STD, and TB Prevention, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Public Health Rep. 2007 May-Jun;122(3):382-92. doi: 10.1177/003335490712200312.
We examined racial misidentification of American Indians/Alaska Natives (AI/AN) reported to the human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS) Reporting Systems (HARS) of five U.S. states and one county.
To identify AI/AN records with misidentified race, we linked HARS data from 1984 through 2002 to the Indian Health Service National Patient Information and Reporting System (NPIRS), excluding non-AI/AN dependents, using probabilistic matching with clerical review. We used chi-square tests to examine differences in proportions and logistic regression to examine the associations of racial misidentification with HARS site, degree of AI/AN ancestry, mode of exposure to HIV, and urban or rural location of residence at time of diagnosis.
A total of 1,523 AI/AN individuals was found in both NPIRS and HARS; race was misidentified in HARS for 459 (30%). The percentages of racially misidentified ranged from 3.7% (in Alaska) to 55% (in California). AI/AN people were misidentified as white (70%), Hispanic (16%), black (11%), and Asian/Pacific Islander (2%); for 0.9%, race was unspecified. Logistic regression results (data from all areas, all variables) indicated that urban residence at time of diagnosis, degree of AI/AN ancestry, and mode of exposure to HIV were significantly associated with racial misidentification of AI/AN people reported to HARS.
Our findings add to the evidence that racial misidentification of AI/AN in surveillance data can result in underestimation of AI/AN HIV/AIDS case counts. Racial misidentification must be addressed to ensure that HIV/ AIDS surveillance data can be used as the basis for equitable resource allocation decisions, and to inform and mobilize public health action.
我们调查了向美国五个州和一个县的人类免疫缺陷病毒(HIV)/获得性免疫缺陷综合征(AIDS)报告系统(HARS)报告的美洲印第安人/阿拉斯加原住民(AI/AN)的种族误认情况。
为了识别种族被误认的AI/AN记录,我们将1984年至2002年的HARS数据与印第安卫生服务局国家患者信息和报告系统(NPIRS)进行了关联,排除了非AI/AN家属,采用概率匹配并进行人工审核。我们使用卡方检验来检验比例差异,并使用逻辑回归来检验种族误认与HARS站点、AI/AN血统程度、接触HIV的方式以及诊断时居住的城市或农村地点之间的关联。
在NPIRS和HARS中总共发现了1523名AI/AN个体;HARS中459人(30%)的种族被误认。种族误认的百分比从3.7%(在阿拉斯加)到55%(在加利福尼亚)不等。AI/AN人群被误认的种族为白人(70%)、西班牙裔(16%)、黑人(11%)和亚太岛民(2%);0.9%的种族未明确指定。逻辑回归结果(来自所有地区、所有变量的数据)表明,诊断时居住在城市、AI/AN血统程度以及接触HIV的方式与向HARS报告的AI/AN人群的种族误认显著相关。
我们的研究结果进一步证明,监测数据中AI/AN的种族误认可能导致AI/AN HIV/AIDS病例数被低估。必须解决种族误认问题,以确保HIV/AIDS监测数据可作为公平资源分配决策的基础,并为公共卫生行动提供信息和推动行动。