ArticleHealth affairs scholar2026
Healthcare access, utilization, and care experiences for American Indian and Alaska Native populations.
Article in Health affairs scholar, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Despite targeted health reforms, differences in healthcare access, utilization, and mortality have persisted between American Indian and Alaska Native (AI/AN) and non-AI/AN people and within the AI/AN population. Methods: Using the 2015-2019 Medical Expenditure Panel Survey Household Component (MEPS-HC), we examined healthcare access, utilization, and care experiences for AI/AN people relative to non-AI/AN people and disaggregate the AI/AN population by race (ie, single race and one or more races) and ethnicity (ie, Hispanic and non-Hispanic). Results: We found that AI/AN people had a lower probability of at least one dental and ambulatory visit annually than non-Hispanic White people. Conversely, non-Hispanic AI/AN people were more likely than non-Hispanic White people to have at least one emergency-department (ED) visit. Non-Hispanic AI/AN people who reported multiple races had higher rates of delayed or unmet needs due to cost than non-Hispanic White people. People solely identifying as AI/AN reported worse care experiences, and non-Hispanic AI/AN people rated their healthcare lower than non-Hispanic White people. Conclusion: Our findings highlight the importance of efforts to improve healthcare access and care experiences of AI/AN people and shed light on how decisions about disaggregating race and ethnicity may affect study results.
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Registered trials
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