0 92

Cited 0 times in

Awareness of genetic counseling and genetic testing for hereditary gynecologic cancers among Korean healthcare providers: A survey

Authors
 Miseon Kim  ;  Myong Cheol Lim  ;  Eun Ji Nam  ;  Dan Huang  ;  Sue Kim  ;  Heon Jong Yoo  ;  Yoo-Young Lee  ;  Yoon-Jung Chang 
Citation
 JOURNAL OF GENETIC COUNSELING, Vol.31(2) : 546-553, 2022-04 
Journal Title
JOURNAL OF GENETIC COUNSELING
ISSN
 1059-7700 
Issue Date
2022-04
MeSH
Female ; Genetic Counseling / methods ; Genetic Predisposition to Disease ; Genetic Testing / methods ; Genital Neoplasms, Female* / genetics ; Health Personnel ; Humans ; Ovarian Neoplasms* / diagnosis ; Ovarian Neoplasms* / genetics ; Republic of Korea ; Surveys and Questionnaires
Keywords
genetic counseling ; genetic testing ; healthcare providers ; hereditary breast and ovarian cancer syndrome ; lynch syndrome ; survey
Abstract
We conducted a survey to evaluate the awareness of genetic counseling and testing for hereditary gynecologic cancers among Korean healthcare providers. We performed an on-the-spot survey using 29 questions on respondents' basic information, awareness of pre/post-test genetic counseling, genetic information management, and related social issues. We surveyed healthcare providers who attended the 2019 Hereditary Gynecologic Cancer Symposium organized by the Korean Society of Gynecologic Oncology. Of the 108 attendees, 85 (78.7%) participated in the survey. Among them, 45% (37/83) and 40% (33/83) did not have a separate clinic and had a dedicated team for genetic counseling in their institutions, respectively. Most respondents (60/76, 79%) recommended genetic testing for all women diagnosed with epithelial ovarian cancer. Many respondents simultaneously (20/85, 24%) or sequentially (45/85, 53%) tested for both pathogenic somatic and germline variants, whereas a few respondents (2/85, 2%) checked for only pathogenic somatic variants using tissue samples. Only 20% (17/85) of the respondents recommended genetic testing for all women with endometrial cancer; meanwhile, 68% (58/86) offered the test based on the results of the screening test or family history. Risk-reducing salpingo-oophorectomy was recommended to unaffected women with pathogenic BRCA1/2 variants by 69.4% of the respondents (59/85). Most respondents (73/85, 85.9%) needed a manual on bioethics law; a few required a clinical update of hereditary cancer (73/85, 85.9%). The awareness of genetic counseling and testing and the pattern of clinical practice for hereditary gynecologic cancers differ among institutions and regions in Korea. A discussion on these issues and the development of an integrated manual for healthcare providers are required.
Full Text
https://onlinelibrary.wiley.com/doi/10.1002/jgc4.1524
DOI
10.1002/jgc4.1524
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Obstetrics and Gynecology (산부인과학교실) > 1. Journal Papers
3. College of Nursing (간호대학) > Dept. of Nursing (간호학과) > 1. Journal Papers
Yonsei Authors
Kim, Sue(김수) ORCID logo https://orcid.org/0000-0003-3785-2445
Nam, Eun Ji(남은지) ORCID logo https://orcid.org/0000-0003-0189-3560
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/188447
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links