Congenital heart disease | 2019

A model for geographic and sociodemographic access to care disparities for adults with congenital heart disease.

 
 
 
 
 

Abstract


BACKGROUND\nFollow-up at a regional adult congenital heart disease (ACHD) center is recommended for all ACHD patients at least once per the 2018 ACC/AHA guidelines. Other specialties have demonstrated poorer follow-up and outcomes correlating with increased distance from health care providers, but driving time to regional ACHD centers has not been examined in the US population.\n\n\nOBJECTIVE\nTo identify and characterize potential disparities in access to ACHD care in the US based on drive time to ACHD centers and compounding sociodemographic factors.\n\n\nMETHODS\nMid- to high-volume ACHD centers with ≥500 outpatient ACHD visits and ≥20 ACHD surgeries annually were included based on self-reported, public data. Geographic Information System mapping was used to delineate drive times to ACHD centers. Sociodemographic data from the 2012-2016 American Community Survey (US Census) and the Environmental Systems Research Institute were analyzed based on drive time to nearest ACHD center. Previously established CHD prevalence estimates were used to estimate the similarly located US ACHD population.\n\n\nRESULTS\nNearly half of the continental US population (45.1%) lives >1\xa0hour drive to an ACHD center. Overall, 39.7% live 1-4\xa0hours away, 3.4% live 4-6\xa0hours away, and 2.0% live >6\xa0hours away. Hispanics were disproportionately likely to live a >6\xa0hour drive to a center (p\xa0<\xa0.001). Compared to people with <1\xa0hour drive, those living >6\xa0hours away have higher proportions of uninsured adults (29% vs. 18%; p\xa0<\xa0.001), households below the federal poverty level (19% vs. 13%; p\xa0<\xa0.001), and adults with less than college education (18% vs. 12%; p\xa0<\xa0.001).\n\n\nCONCLUSIONS\nWe estimate that ~45% of the continental US population lives >1\xa0hour to an ACHD center, with 5.4% living >4\xa0hours away. Compounding barriers exist for Hispanic, uninsured, lower socioeconomic status, and less-educated patients. These results may help drive future policy changes to improve access to ACHD care.

Volume None
Pages None
DOI 10.1111/chd.12819
Language English
Journal Congenital heart disease

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