The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine

被引:159
作者
Stoll, Katie [1 ]
Kubendran, Shobana [2 ]
Cohen, Stephanie A. [3 ]
机构
[1] Genet Support Fdn, 1800 Cooper Point Rd SW 14, Olympia, WA 98502 USA
[2] Kansas Univ, Sch Med, Wichita, KS USA
[3] St Vincent Hosp, Indianapolis, IN USA
关键词
genetic counseling; precision medicine; service delivery models; workforce; CLINICAL DOCTORATE; PROGRAM DIRECTORS; INCIDENTAL FINDINGS; AMERICAN-COLLEGE; NATIONAL-SOCIETY; RISK-ASSESSMENT; TASK-FORCE; CANCER; MODEL; TIME;
D O I
10.1002/ajmg.c.31602
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Precision medicine aims to approach disease treatment and prevention with consideration of the variability in genes, environment, and lifestyle for each person. This focus on the individual is also key to the practice of genetic counseling, whereby foundational professional values prioritize informed and autonomous patient decisions regarding their genetic health. Genetic counselors are ideally suited to help realize the goals of the precision medicine. However, a limited genetic counseling workforce at a time in which there is a rapidly growing need for services is challenging the balance of supply and demand. This article provides historical context to better understand what has informed traditional models of genetic counseling and considers some of the current forces that require genetic counselors to adapt their practice. New service delivery models can improve access to genetic healthcare by overcoming geographical barriers, allowing genetic counselors to see a higher volume of patients and supporting other healthcare providers to better provide genetic services to meet the needs of their patients. Approaches to genetic counseling service delivery are considered with a forward focus to the challenges and opportunities that lie ahead for genetic counselors in this age of precision health.
引用
收藏
页码:24 / 37
页数:14
相关论文
共 84 条
[1]  
ACGC, 2018, ACCR PROGR
[2]   Follow-up effects of a tailored pre-counseling website with question prompt in breast cancer genetic counseling [J].
Albada, Akke ;
van Dulmen, Sandra ;
Spreeuwenberg, Peter ;
Ausems, Margreet G. E. M. .
PATIENT EDUCATION AND COUNSELING, 2015, 98 (01) :69-76
[3]   Communication challenges for nongeneticist physicians relaying clinical genomic results [J].
Arora, Nonie S. ;
Davis, J. Kelly ;
Kirby, Christine ;
McGuire, Amy L. ;
Green, Robert C. ;
Blumenthal-Barby, J. S. ;
Ubel, Peter A. .
PERSONALIZED MEDICINE, 2017, 14 (05) :423-431
[4]   The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results [J].
Baldridge, Dustin ;
Heeley, Jennifer ;
Vineyard, Marisa ;
Manwaring, Linda ;
Toler, Tomi L. ;
Fassi, Emily ;
Fiala, Elise ;
Brown, Sarah ;
Goss, Charles W. ;
Willing, Marcia ;
Grange, Dorothy K. ;
Kozel, Beth A. ;
Shinawi, Marwan .
GENETICS IN MEDICINE, 2017, 19 (09) :1040-1048
[5]  
Bergner A., 2017, 2017 NSGC ANN ED C C, V26, P1432, DOI [10. 1007/s10897-017-0156-x, DOI 10.1007/S10897-017-0156-X, 10.1007/s10897-017-0156-x]
[6]   A two-stage approach to genetic risk assessment in primary care [J].
Biswas, Swati ;
Atienza, Philamer ;
Chipman, Jonathan ;
Blackford, Amanda L. ;
Arun, Banu ;
Hughes, Kevin ;
Parmigiani, Giovanni .
BREAST CANCER RESEARCH AND TREATMENT, 2016, 155 (02) :375-383
[7]  
Blazer K. R., 2006, JAMA ONCOLOGY, V2, P723
[8]   Outcomes from intensive training in genetic cancer risk counseling for clinicians [J].
Blazer, KR ;
MacDonald, DJ ;
Ricker, C ;
Sand, S ;
Uman, GC ;
Weitzel, JN .
GENETICS IN MEDICINE, 2005, 7 (01) :40-47
[9]  
Boudreault P., 2017, J GENETIC COUNSELING, V10, P23
[10]   Recommendations for the integration of genomics into clinical practice [J].
Bowdin, Sarah ;
Gilbert, Adel ;
Bedoukian, Emma ;
Carew, Christopher ;
Adam, Margaret P. ;
Belmont, John ;
Bernhardt, Barbara ;
Biesecker, Leslie ;
Bjornsson, Hans T. ;
Blitzer, Miriam ;
D'Alessandro, Lisa C. A. ;
Deardorff, Matthew A. ;
Demmer, Laurie ;
Elliott, Alison ;
Feldman, Gerald L. ;
Glass, Ian A. ;
Herman, Gail ;
Hindorff, Lucia ;
Hisama, Fuki ;
Hudgins, Louanne ;
Innes, A. Micheil ;
Jackson, Laird ;
Jarvik, Gail ;
Kim, Raymond ;
Korf, Bruce ;
Ledbetter, David H. ;
Li, Mindy ;
Liston, Eriskay ;
Marshall, Christian ;
Medne, Livija ;
Meyn, M. Stephen ;
Monfared, Nasim ;
Morton, Cynthia ;
Mulvihill, John J. ;
Plon, Sharon E. ;
Rehm, Heidi ;
Roberts, Amy ;
Shuman, Cheryl ;
Spinner, Nancy B. ;
Stavropoulos, D. James ;
Valverde, Kathleen ;
Waggoner, Darrel J. ;
Wilkens, Alisha ;
Cohn, Ronald D. ;
Krantz, Ian D. .
GENETICS IN MEDICINE, 2016, 18 (11) :1075-1084