Should Health Systems Share Genetic Findings With At-Risk Relatives When the Proband Is Deceased? Interviews With Individuals Diagnosed With Lynch Syndrome
Purpose: Genetic information has health implications for patients and their biological relatives. Death of a patient before sharing a genetic diagnosis with at-risk relatives is a missed opportunity to provide important information that could guide interventions to minimize cancer-related morbidity...
Main Authors: | Jessica Ezzell Hunter, Jennifer L. Schneider, Alison J. Firemark, James V. Davis, Sara Gille, Pamala A. Pawloski, Su-Ying Liang, Victoria Schlieder, Alanna Kulchak Rahm |
---|---|
Format: | Article |
Language: | English |
Published: |
Advocate Aurora Health
2022-10-01
|
Series: | Journal of Patient-Centered Research and Reviews |
Subjects: | |
Online Access: | https://institutionalrepository.aah.org/cgi/viewcontent.cgi?article=1945&context=jpcrr |
Similar Items
-
“Go ahead and screen” - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients
by: Jennifer L. Schneider, et al.
Published: (2023-11-01) -
Economic Evaluation of Universal Lynch Syndrome Screening Protocols among Newly Diagnosed Patients with Colorectal Cancer
by: Jing Hao, et al.
Published: (2021-12-01) -
Comparison of suspected Lynch syndrome patients carrying BRCA and BRCA‐like variants with Lynch syndrome probands: Phenotypic characteristics and pedigree analyses
by: Yun Xu, et al.
Published: (2020-08-01) -
Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts
by: Alanna Kulchak Rahm, et al.
Published: (2018-10-01) -
To use or not to use? an ethical analysis of access to data and samples of a deceased patient for genetic diagnostic and research purposes
by: Mahshad Noroozi, et al.
Published: (2022-12-01)