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Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.
Blumling, Amy A; Prows, Cynthia A; Harr, Margaret H; Chung, Wendy K; Clayton, Ellen Wright; Holm, Ingrid A; Wiesner, Georgia L; Connolly, John J; Harley, John B; Hakonarson, Hakon; McGowan, Michelle L; Miller, Erin M; Myers, Melanie F.
Afiliación
  • Blumling AA; Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
  • Prows CA; Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
  • Harr MH; Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Chung WK; Department of Pediatrics, Columbia University, New York, NY 10032, USA.
  • Clayton EW; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Holm IA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA.
  • Wiesner GL; Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.
  • Connolly JJ; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
  • Harley JB; Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Hakonarson H; US Department of Veterans Affairs Medical Center, Cincinnati, OH 45220, USA.
  • McGowan ML; Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
  • Miller EM; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Myers MF; Biomedical Ethics Research Program, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN 55905, USA.
J Pers Med ; 12(11)2022 Nov 16.
Article en En | MEDLINE | ID: mdl-36422086
ABSTRACT

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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Pers Med Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: J Pers Med Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos