TY - JOUR
T1 - Genomic medicine and the “loss of chance” medical malpractice doctrine
AU - Wagner, Jennifer K.
AU - Meyer, Michelle N.
N1 - Funding Information:
The content of this article is the authors’ responsibility and might not represent the views of the authors’ funding sources, employers, clients, or any other person or entity. This research was funded by the National Human Genome Research Institute (NHGRI) award no. 1R01HG009671-01A1 . The authors thank Adam Buchanan (PI) for imbedding this research into that project and Jessica Roberts for her helpful guidance during the development and conduct of this research. The authors also thank Gary Marchant for providing access to the table of cases (see Marchant and Lindor 1 at FN68, p.16) and Leah Lebeau for law library assistance obtaining copies of many of the items in that table of cases, both of which enabled the secondary analysis reported here.
Publisher Copyright:
© 2021 The Author(s)
PY - 2021/7/8
Y1 - 2021/7/8
N2 - As genomic medicine expands, interest in how medical malpractice law will apply to such questions as whether and when to return new or updated genomic results has grown. Given that access to some genomic results (such as those pertaining to minors or those for which scientific interpretations are unsettled) is delayed for years, the “loss of chance” (LOC) doctrine is of particular potential relevance. Yet it has received relatively little attention among scholars of law and genomics. We performed legal research to determine the status of this malpractice doctrine across the United States and consider its potential applicability to genomic medicine. We further examined known genomic medicine malpractices to assess whether this doctrine had yet been invoked in that context. We identified a trend toward adoption of the LOC doctrine, finding 29 states (58%) have adopted, 15 states (30%) have rejected, and six states (12%) have deferred or not yet addressed the doctrine. Attempts to invoke or apply the doctrine in the known genomic medical malpractice cases were also found. While our findings do not provide cause for substantial concern, the availability of the LOC medical malpractice doctrine is a potentially important factor to consider when making programmatic decisions for genomic medicine. Future research examining whether liability risks posed by this doctrine prompt defensive medicine practices would be useful.
AB - As genomic medicine expands, interest in how medical malpractice law will apply to such questions as whether and when to return new or updated genomic results has grown. Given that access to some genomic results (such as those pertaining to minors or those for which scientific interpretations are unsettled) is delayed for years, the “loss of chance” (LOC) doctrine is of particular potential relevance. Yet it has received relatively little attention among scholars of law and genomics. We performed legal research to determine the status of this malpractice doctrine across the United States and consider its potential applicability to genomic medicine. We further examined known genomic medicine malpractices to assess whether this doctrine had yet been invoked in that context. We identified a trend toward adoption of the LOC doctrine, finding 29 states (58%) have adopted, 15 states (30%) have rejected, and six states (12%) have deferred or not yet addressed the doctrine. Attempts to invoke or apply the doctrine in the known genomic medical malpractice cases were also found. While our findings do not provide cause for substantial concern, the availability of the LOC medical malpractice doctrine is a potentially important factor to consider when making programmatic decisions for genomic medicine. Future research examining whether liability risks posed by this doctrine prompt defensive medicine practices would be useful.
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U2 - 10.1016/j.xhgg.2021.100032
DO - 10.1016/j.xhgg.2021.100032
M3 - Article
C2 - 34250511
AN - SCOPUS:85120448998
SN - 2666-2477
VL - 2
JO - Human Genetics and Genomics Advances
JF - Human Genetics and Genomics Advances
IS - 3
M1 - 100032
ER -