| Literature DB >> 29854231 |
Hiral Soni1, Adela Grando1, Anita Murcko1, Mike Bayuk1, Pramod Chandrashekar1, Madhumita Mukundan1, Meredith Abrams1, Marcela P Aliste1, Megan Hiestand1, Julia Varkey1, Wentao Zhou1, Caroline Horrow2, Michael Saks3, Richard Sharp2, Mary Jo Whitfield4, Mark Callesen4, Christy Dye5, Darwyn Chern5.
Abstract
An integral element of value-based care is care team access to both physical and behavioral health data. Data release processes in both environments are governed by federal and state statutes. The requirements for obtaining consent are complex and often confusing. Little is known about the consent processes and practices in the behavioral health setting, specifically how patients and surrogates engage in the process and their interactions with electronic consent tools. This study analyzes the consent processes from the patient perspective at two community behavioral health clinics. Outcomes include description of the processes using electronic consent, workflows and consenter-provider interactions. Conclusions include need to streamline and standardize consent technologies and improve consenter engagement. This study supports the development of an electronic consent tool, My Data Choices (MDC), funded by the National Institute of Mental Health, that offers individuals with behavioral health conditions more control over their medical records.Entities:
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Year: 2018 PMID： 29854231 PMCID： PMC5977724
Source DB: PubMed Journal: AMIA Annu Symp Proc ISSN： 1559-4076