Introducing personalized health for the family: the experience of a single hospital system. - PubMed - NCBI

Introducing personalized health for the family: the experience of a single hospital system. - PubMed - NCBI

Pharmacogenomics. 2017 Oct 24. doi: 10.2217/pgs-2017-0112. [Epub ahead of print]

Introducing personalized health for the family: the experience of a single hospital system.

Huddleston KL1, Klein E1, Fuller A1, Jo G1, Lawrence G1, Haga SB2.

Author information

Abstract

Pharmacogenetic testing is leading the personalized health movement, gradually being implemented in a variety of healthcare settings. To inform the efforts of other hospital and clinical practices implementing personalized health or medicine applications, we describe the implementation of a newborn pharmacogenetic testing program at Inova Health System (VA, USA). In particular, we describe the efforts to gather patient feedback through focus groups, the training and program staff, the pilot program and our experiences to date. In our experience, a multidisciplinary team was essential to address the myriad facets of program development and implementation as well as an in-person approach to introduce testing and patient education.

KEYWORDS:

newborns; patient education; pharmacogenetic testing; pre-emptive testing

PMID:

 

29061078

 

DOI:

 

10.2217/pgs-2017-0112