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Historically Marginalized and Minority Populations With Pulmonary Arterial Hypertension: A Deeper Dive Into a Complex
Roberto J Bernardo1, Victor E Ortega2, Jason Glenn3
1Division of Pulmonary, Allergy and Critical Care Medicine, Stanford University, Stanford, CA; Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford University, Stanford, CA.
Topic Importance:
Pulmonary arterial hypertension (PAH) is a progressive cardiopulmonary disorder with disparities in epidemiologic features, clinical outcomes, and health care access that disproportionately affect historically neglected populations, including Black Americans, Hispanic Americans, and American Indians.
Review Findings:
This state-of-the-art review examined PAH disparities through cross-cutting themes and population-specific evidence. First, we examined the role of race and ethnicity as social constructs; the historical roots of medical mistrust arising from documented exploitation of Black, Hispanic, and American Indian communities; and the implications of genetic ancestry research within the framework of race as a social, rather than biological, variable. We then reviewed population-specific evidence on clinical phenotypes, survival, and access to care and reviewed the significance of socioeconomic deprivation in clinical outcomes across populations.
Summary:
This review highlights existing gaps in knowledge and proposes a framework for shared efforts toward the common goal of achieving health equity in pulmonary hypertension care.
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