Today, the US Access Board announced that it is seeking final public comment on its newly proposed Americans with Disabilities Act (ADA) guidelines for the use of lower transfer heights for medical diagnostic equipment in medical diagnostics and treatment. The US Access Board is the federal organization that develops guidelines for the ADA. It works with professionals and advocacy groups to develop guidelines for various aspects of the ADA to provide greater access to goods and services. The Access Board is required to seek public comment before finalizing its proposed guidelines. After receiving public comment, the Access Board presents its proposed guidelines to the Department of Justice (DOJ) which then adopts all or part of the proposed guidelines into the ADA.
The Access board has been working for some time on the development of formal guidelines for lower transfer heights of medical diagnostic equipment. Once implemented, these guidelines will have an immediate impact on diagnostic equipment manufacturers, hospitals, clinics, and doctors’ offices throughout the country. The lower height requirements are intended to provide easier transfer for patients using wheelchairs, walkers, or other assistive devices. These diagnostic devices typically include, among other things, examination tables, scanning devices, and chairs for diagnosis.
Historically, medical diagnostic equipment (MDE) has been, and continues to be, inaccessible to many people in wheelchairs, which can lead to misdiagnosis or barriers to basic care and examinations. Continue ›