Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms. (December 2018)
- Record Type:
- Journal Article
- Title:
- Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms. (December 2018)
- Main Title:
- Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms
- Authors:
- Vears, Danya
Niemiec, Emilia
Howard, Heidi
Borry, Pascal - Abstract:
- Abstract There are several key unsolved issues relating to the clinical use of next generation sequencing, such as: should laboratories report variants of uncertain significance (VUS) to clinicians and/or patients? Should they reinterpret VUS in response to growing knowledge in the field? And should patients be recontacted regarding such results? We systematically analyzed 58 consent forms in English used in the diagnostic context to investigate their policies for (a) reporting VUS, (b) reinterpreting variants, including who should initiate this, and (c) recontacting patients and the mechanisms for undertaking any recontact. One-third (20/58) of the forms did not mention VUS in any way. Of the 38 forms that mentioned VUS, only half provided some description of what a VUS is. Approximately one-third of forms explicitly stated that reinterpretation of variants for clinical purposes may occur. Less than half mentioned recontact for clinical purposes, with variation as to whether laboratories, patients, or clinicians should initiate this. We suggest that the variability in variant reporting, reinterpretation, and recontact policies and practices revealed by our analysis may lead to diffused responsibility, which could result in missed opportunities for patients or family members to receive a diagnosis in response to updated variant classifications. Finally, we provide some suggestions for ethically appropriate inclusion of policies for reporting VUS, reinterpretation, andAbstract There are several key unsolved issues relating to the clinical use of next generation sequencing, such as: should laboratories report variants of uncertain significance (VUS) to clinicians and/or patients? Should they reinterpret VUS in response to growing knowledge in the field? And should patients be recontacted regarding such results? We systematically analyzed 58 consent forms in English used in the diagnostic context to investigate their policies for (a) reporting VUS, (b) reinterpreting variants, including who should initiate this, and (c) recontacting patients and the mechanisms for undertaking any recontact. One-third (20/58) of the forms did not mention VUS in any way. Of the 38 forms that mentioned VUS, only half provided some description of what a VUS is. Approximately one-third of forms explicitly stated that reinterpretation of variants for clinical purposes may occur. Less than half mentioned recontact for clinical purposes, with variation as to whether laboratories, patients, or clinicians should initiate this. We suggest that the variability in variant reporting, reinterpretation, and recontact policies and practices revealed by our analysis may lead to diffused responsibility, which could result in missed opportunities for patients or family members to receive a diagnosis in response to updated variant classifications. Finally, we provide some suggestions for ethically appropriate inclusion of policies for reporting VUS, reinterpretation, and recontact on consent forms. … (more)
- Is Part Of:
- European journal of human genetics. Volume 26:Number 12(2018)
- Journal:
- European journal of human genetics
- Issue:
- Volume 26:Number 12(2018)
- Issue Display:
- Volume 26, Issue 12 (2018)
- Year:
- 2018
- Volume:
- 26
- Issue:
- 12
- Issue Sort Value:
- 2018-0026-0012-0000
- Page Start:
- 1743
- Page End:
- 1751
- Publication Date:
- 2018-12
- Subjects:
- Human genetics -- Periodicals
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://www.nature.com/ejhg/index.html ↗
https://www.karger.com/Journal/Home/224162 ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41431-018-0239-7 ↗
- Languages:
- English
- ISSNs:
- 1018-4813
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.730020
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11054.xml