Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research

被引:3
|
作者
Blumling, Amy A. [1 ]
Prows, Cynthia A. [1 ]
Harr, Margaret H. [2 ]
Chung, Wendy K. [3 ]
Clayton, Ellen Wright [4 ]
Holm, Ingrid A. [5 ,6 ]
Wiesner, Georgia L. [4 ]
Connolly, John J. [2 ]
Harley, John B. [7 ]
Hakonarson, Hakon [2 ,8 ]
McGowan, Michelle L. [9 ,10 ]
Miller, Erin M. [1 ,11 ]
Myers, Melanie F. [1 ,11 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
[2] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Columbia Univ, Dept Pediat, New York, NY 10032 USA
[4] Vanderbilt Univ, Dept Med, Div Genet Med, Med Ctr, Nashville, TN 37232 USA
[5] Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA
[6] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
[7] US Dept Vet Affairs Med Ctr, Cincinnati, OH 45220 USA
[8] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
[9] Mayo Clin, Dept Quantitat Hlth Sci, Biomed Eth Res Program, Rochester, MN 55905 USA
[10] Univ Cincinnati, Coll Arts & Sci, Dept Womens Gender & Sexual Studies, Cincinnati, OH 45221 USA
[11] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH 45267 USA
来源
JOURNAL OF PERSONALIZED MEDICINE | 2022年 / 12卷 / 11期
基金
美国国家卫生研究院;
关键词
genomic screening; pediatric genomics; return of genomic results; healthcare outcomes; CLINICAL EXOME; RECOMMENDATIONS;
D O I
10.3390/jpm12111910
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Purpose: The electronic Medical Records and Genomics (eMERGE) Phase III study was undertaken to assess clinical utility of returning medically actionable genomic screening results. We assessed pediatric clinical outcomes following return of pathogenic/likely pathogenic (P/LP) variants in autosomal dominant conditions with available effective interventions. Methods: The two eMERGE III pediatric sites collected outcome data and assessed changes in medical management at 6 and 12 months. Results: We returned P/LP results to 29 participants with outcome data. For 23 of the 29 participants, the P/LP results were previously unknown. Five of the 23 participants were already followed for conditions related to the P/LP variant. Of those receiving novel results and not being followed for the condition related to the P/LP result (n = 18), 14 (77.8%) had a change in healthcare after return of results (RoR). Following RoR, cascade testing of family members occurred for 10 of 23 (43.5%). Conclusions: The most common outcomes post-RoR included imaging/laboratory testing and health behavior recommendations. A change in healthcare was documented in 77.8% of those receiving results by 6 months. Our findings demonstrate how return of genomic screening results impacts healthcare in pediatric populations.
引用
收藏
页数:12
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