Investigating genetic counselors' communication with Lynch syndrome patients about cascade testing: Barriers, facilitators, and strategies

被引:0
|
作者
Zhong, Lingzi [1 ,2 ,5 ]
Rodriguez, Yanete [3 ]
Espinel, Whitney [1 ]
Ozanne, Elissa M. [4 ]
Kaphingst, Kimberly A. [1 ,2 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[2] Univ Utah, Dept Commun, Salt Lake City, UT USA
[3] Univ Utah, Dept Human Genet, Grad Program Genet Counseling, Salt Lake City, UT USA
[4] Univ Utah, Dept Populat Hlth Sci, Salt Lake City, UT USA
[5] Univ Minnesota Duluth, Dept Commun, Duluth, MN USA
关键词
barriers; cascade testing; communication; counseling techniques; facilitators; family; Lynch syndrome; AT-RISK RELATIVES; COLORECTAL-CANCER; INDIVIDUALS; DUTY;
D O I
10.1002/jgc4.1937
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cascade testing is an imperative process to engage Lynch syndrome patients' at-risk relatives in early cancer risk reduction interventions. How genetic counselors communicate about cascade testing is crucial to patients' intentions of and actual involvement in family communication. Based on data from 20 interviews with genetic counselors, this qualitative study examined their perceptions of barriers and facilitators of offering cascade testing to at-risk relatives and the specific communication strategies they use to discuss cascade testing with patients. We identified patient-level, genetic counselor-level, and system-level barriers and facilitators of having discussions with Lynch syndrome patients about cascade testing. The qualitative data also revealed four prominent communication strategies that genetic counselors use for such discussions: build rapport, reframe the benefits of family communication, adapt communication, and provide various resources. These findings highlight genetic counselors' needs of practical and structural support to facilitate their communication about cascade testing, especially when patients are hesitant or lack resources or skills to notify at-risk relatives about cascade testing.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome
    Hadley, Donald W.
    Eliezer, Dina
    Addissie, Yonit
    Goergen, Andrea
    Ashida, Sato
    Koehly, Laura
    SCIENTIFIC REPORTS, 2020, 10 (01)
  • [22] Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome
    Donald W. Hadley
    Dina Eliezer
    Yonit Addissie
    Andrea Goergen
    Sato Ashida
    Laura Koehly
    Scientific Reports, 10
  • [23] The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
    Mvundura, Mercy
    Grosse, Scott D.
    Hampel, Heather
    Palomaki, Glenn E.
    GENETICS IN MEDICINE, 2010, 12 (02) : 93 - 104
  • [24] Cost-Effectiveness Analysis of Different Genetic Testing Strategies for Lynch Syndrome in Taiwan
    Chen, Ying-Erh
    Kao, Sung-Shuo
    Chung, Ren-Hua
    PLOS ONE, 2016, 11 (08):
  • [25] Interpretation of Genetic Testing for Lynch Syndrome in Patients With Putative Familial Colorectal Cancer
    Rybak, Christina
    Hall, Michael J.
    JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2011, 9 (11): : 1311 - 1320
  • [26] Swiss cost-effectiveness analysis of universal screening for Lynch syndrome of patients with colorectal cancer followed by cascade genetic testing of relatives
    Salikhanov, Islam
    Heinimann, Karl
    Chappuis, Pierre
    Buerki, Nicole
    Graffeo, Rossella
    Heinzelmann, Viola
    Rabaglio, Manuela
    Taborelli, Monica
    Wieser, Simon
    Katapodi, Maria C.
    JOURNAL OF MEDICAL GENETICS, 2021, : 924 - 930
  • [27] Barriers and Motivators for Referral of Patients with Suspected Lynch Syndrome to Cancer Genetic Services: A Qualitative Study
    Tan, Yen Y.
    Fitzgerald, Lisa J.
    JOURNAL OF PERSONALIZED MEDICINE, 2014, 4 (01) : 20 - 34
  • [28] Whole genome sequencing completes the molecular genetic testing workflow of patients with Lynch syndrome
    Horti-Oravecz, Klaudia
    Bozsik, Aniko
    Pocza, Timea
    Vereczkey, Ildiko
    Strausz, Tamas
    Toth, Erika
    Sedlackova, Tatiana
    Rusnakova, Diana
    Szemes, Tomas
    Liko, Istvan
    Olah, Edit
    Butz, Henriett
    Patocs, Attila
    Papp, Janos
    Grolmusz, Vince Kornel
    NPJ GENOMIC MEDICINE, 2025, 10 (01)
  • [29] Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline
    Kanga-Parabia, Anaita
    Gaff, Clara
    Flander, Louisa
    Jenkins, Mark
    Keogh, Louise A.
    FAMILIAL CANCER, 2018, 17 (04) : 547 - 555
  • [30] Discussions about predictive genetic testing for Lynch syndrome: the role of health professionals and families in decisions to decline
    Anaita Kanga-Parabia
    Clara Gaff
    Louisa Flander
    Mark Jenkins
    Louise A. Keogh
    Familial Cancer, 2018, 17 : 547 - 555