ArticleJournal of the American Medical Informatics Association : JAMIA2021
Promoting health equity for deaf patients through the electronic health record.
Article in Journal of the American Medical Informatics Association : JAMIA, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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.
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Who cites it
8 citing papers in PubMed.
- Reframing EHR Policy in China: Towards Balanced Implementation and Ethical Foundations.Journal of evaluation in clinical practice · 2025Article
- Article
- Emergency department patient-centred care perspectives from deaf and hard-of-hearing patients.Health expectations : an international journal of public participation in health care and health policy · 2023Article
- Governance of Electronic Health Record Modification at U.S. Academic Medical Centers.Applied clinical informatics · 2023Article
- Spotlighting Disability in a Major Electronic Health Record: Michigan Medicine's Disability and Accommodations Tab.JMIR formative research · 2022Article
- Emergency department condition acuity, length of stay, and revisits among deaf and hard-of-hearing patients: A retrospective chart review.Academic emergency medicine : official journal of the Society for Academic Emergency Medicine · 2022Observational
- Equitable Research PRAXIS: A Framework for Health Informatics Methods.Yearbook of medical informatics · 2022Article
- Emergency department utilization among deaf and hard-of-hearing patients: A retrospective chart review.Disability and health journal · 2022Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Language status can be conceptualized as an equity-relevant variable, particularly for non-English-speaking populations. Deaf and hard-of-hearing (DHH) individuals who use American Sign Language (ASL) to communicate comprise one such group and are understudied in health services research. DHH individuals are at high-risk of receiving lower-quality care due to ineffective patient-provider communication. This perspective outlines barriers to health equity research serving DHH ASL-users due to systems developed by large-scale informatics networks (eg, the Patient-Centered Clinical Outcomes Research Network), and institutional policies on self-serve cohort discovery tools. We list potential to help adequate capture of language status of DHH ASL-users to promote health equity for this population.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.