Barriers to Care Among Sexual and Gender Minority Individuals With Chronic Inflammatory Skin Diseases in the US
Clinical Summary
View sourceWhat was studied
A US cross-sectional analysis (May 31, 2017–July 1, 2022) of adults ≥18 years in the All of Us program with chronic inflammatory skin diseases compared sexual and gender minority (SGM) vs non‑SGM patients on cost and noncost barriers to care using multivariable logistic regression.
Key findings
Among 19,743 patients (SGM 1,877; non‑SGM 17,866), SGM patients had higher adjusted odds of delaying specialist care (AOR 1.23; 95% CI 1.03-1.47), mental health care (AOR 1.62; 95% CI 1.37-1.91), and filling a prescription (AOR 1.30; 95% CI 1.11-1.52) due to cost; and higher odds of delaying care due to transportation (AOR 1.49; 95% CI 1.22-1.80) and because providers were from different backgrounds (AOR 1.39; 95% CI 1.19-1.62). They were also more likely to report not always being treated with respect (AOR 1.47; 95% CI 1.30-1.65).
Study limitations
Cross-sectional survey data preclude causal inference; some associations attenuated after adjusting for socioeconomic factors (e.g., delaying general doctor visit lost significance); small cell sizes (1–20) were suppressed per policy, limiting detail.
Clinical implications
Expect more cost- and transport-related delays and perceived disrespect among SGM patients with chronic inflammatory skin diseases; proactively ask about affordability, prescription costs, transportation, and provider fit, and address these barriers within clinic workflows.
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