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Patient perspectives on variant reclassification after cancer susceptibility testing.
Halverson, Colin M E; Connors, Laurie M; Wessinger, Bronson C; Clayton, Ellen W; Wiesner, Georgia L.
Afiliação
  • Halverson CME; Center for Bioethics, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Connors LM; Regenstrief Institute, Indianapolis, IN, USA.
  • Wessinger BC; School of Nursing, Vanderbilt University, Nashville, TN, USA.
  • Clayton EW; Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Wiesner GL; Center for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, TN, USA.
Mol Genet Genomic Med ; 8(7): e1275, 2020 07.
Article em En | MEDLINE | ID: mdl-32329193
ABSTRACT

BACKGROUND:

Little is known about the impact of reclassification on patients' perception of medical uncertainty or trust in genetics-based clinical care.

METHODS:

Semistructured telephone interviews were conducted with 20 patients who had received a reclassified genetic test result related to hereditary cancer. All participants had undergone genetic counseling and testing for cancer susceptibility at Vanderbilt-Ingram Cancer Center Hereditary Cancer Clinic within the last six years.

RESULTS:

Most of the participants did not express distress related to the variant reclassification and only a minority expressed a decrease in trust in medical genetics. However, recall of the new interpretation was limited, even though all participants were recontacted by letter, phone, or clinic visit.

CONCLUSION:

Reclassification of genetic tests is an important issue in modern healthcare because changes in interpretation have the potential to alter previously recommended management. Participants in this study did not express strong feelings of mistrust or doubt about their genetic evaluation. However, there was a low level of comprehension and information retention related to the updated report. Future research can build on this study to improve communication with patients about their reclassified results.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes / Atitude / Predisposição Genética para Doença / Aconselhamento Genético / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pacientes / Atitude / Predisposição Genética para Doença / Aconselhamento Genético / Neoplasias Idioma: En Ano de publicação: 2020 Tipo de documento: Article