domingo, 22 de julio de 2012

When access is an issue: exploring barriers ... [Eur J Hum Genet. 2012] - PubMed - NCBI

When access is an issue: exploring barriers ... [Eur J Hum Genet. 2012] - PubMed - NCBI


2012 Jul 11. doi: 10.1038/ejhg.2012.147. [Epub ahead of print]

When access is an issue: exploring barriers to predictive testing for Huntington disease in British Columbia, Canada.

Source

Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.

Abstract

Predictive testing (PT) for Huntington disease (HD) requires several in-person appointments. This requirement may be a barrier to testing so that at risk individuals do not realize the potential benefits of PT. To understand the obstacles to PT in terms of the accessibility of services, as well as exploring mechanisms by which this issue may be addressed, we conducted an interview study of individuals at risk for HD throughout British Columbia, Canada. Results reveal that the accessibility of PT can be a barrier for two major reasons: distance and the inflexibility of the testing process. Distance is a structural barrier, and relates to the time and travel required to access PT, the financial and other opportunity costs associated with taking time away from work and family to attend appointments and the stress of navigating urban centers. The inflexibility of the testing process barrier relates to the emotional and psychological accessibility of PT. The results of the interview study reveal that there are access barriers to PT that deter individuals from receiving the support, information and counseling they require. What makes accessibility of PT services important is not just that it may result in differences in quality of life and care, but because these differences may be addressed with creative and adaptable solutions in the delivery of genetic services. The study findings underscore the need for us to rethink and personalize the way we deliver such services to improve access issues to prevent inequities in the health care system.European Journal of Human Genetics advance online publication, 11 July 2012; doi:10.1038/ejhg.2012.147.

PMID:
22781094
[PubMed - as supplied by publisher]

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