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Using the Delphi method to identify clinicians' perceived importance of pediatric exome sequencing results.
Stevens Smith, Hadley; Russell, Heidi V; Lee, Brendan H; Morain, Stephanie R.
Afiliación
  • Stevens Smith H; Baylor College of Medicine, Department of Molecular and Human Genetics, Houston, TX, USA.
  • Russell HV; Baylor College of Medicine, Center for Medical Ethics and Health Policy, Houston, TX, USA.
  • Lee BH; Baylor College of Medicine, Center for Medical Ethics and Health Policy, Houston, TX, USA.
  • Morain SR; Baylor College of Medicine, Department of Pediatrics, Houston, TX, USA.
Genet Med ; 22(1): 69-76, 2020 01.
Article en En | MEDLINE | ID: mdl-31273346
ABSTRACT

PURPOSE:

Information obtained from clinical exome sequencing (ES) may impact clinical care or other aspects of a patient's life. Little is known about clinicians' perceptions regarding either the value of ES results or which among various outcomes are most relevant to determine value. This study aims to assess clinicians' opinions of the importance of ES results for medical decision making and identify a set of outcomes to be measured in future ES evaluations.

METHODS:

Expert opinion regarding the value of remarkable (diagnostic/positive) and unremarkable (nondiagnostic/negative) ES results was elicited via the Delphi method, consisting of two survey rounds and a teleconference. Participants had expertise in caring for clinically diverse infants and children with suspected underlying genetic etiologies. Descriptive statistics and (dis)agreement were calculated for each survey item.

RESULTS:

Remarkable ES results were considered important for 17 outcome domains. Unremarkable ES results were also perceived as important in terms of psychological impact and ability to inform follow-up diagnostic test decisions.

CONCLUSION:

Clinicians regard remarkable ES results as more important in many ways than findings from other diagnostic modalities. Unremarkable ES results were not considered unimportant for decision making, but rather uncertain in most outcome domains.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médicos / Técnica Delphi / Secuenciación del Exoma Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médicos / Técnica Delphi / Secuenciación del Exoma Tipo de estudio: Prognostic_studies / Qualitative_research Límite: Female / Humans / Male Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos