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Assessment of genetic testing and related counseling services: current research and future directions

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  • Wang, Catharine
  • Gonzalez, Richard
  • Merajver, Sofia D.

Abstract

With the recent completion of the sequencing of the Human Genome, genetic testing will increasingly become available for a greater number of medical conditions, many of which are those that manifest in adulthood (e.g., various cancers, cardiovascular disease, diabetes) or for which little or no treatments are available (e.g., Alzheimer disease). Genetic services, defined here as those relating to genetic testing and counseling, will be with helping more individuals deal with medical information that affects their health directly, as opposed to affecting primarily the health of their offspring. This paper reviews the existing research in the genetic testing and counseling literature and presents an evaluation framework outlining the intended outcomes of genetic services. The purpose of this framework is to provide an overview of the potential outcomes of these services and highlight constructs for future research in this area. In addition, other issues that will affect the assessment of genetic services are raised, using examples from the existing literature. Ultimately, the goal of this paper is to highlight and suggest directions researchers can take to produce the information needed to guide genetic testing and counseling practice. Moreover, as genetic knowledge is increasingly applied towards the prevention and treatment of various common, chronic disease conditions, genetic information will have implications for providers outside of the traditional medical genetics realm, such as primary care providers and public health practitioners. A better understanding of the outcomes of genetic testing and counseling will provide a basis from which to ensure an appropriate application of genetic information by all those who eventually provide care and "genetic" services.

Suggested Citation

  • Wang, Catharine & Gonzalez, Richard & Merajver, Sofia D., 2004. "Assessment of genetic testing and related counseling services: current research and future directions," Social Science & Medicine, Elsevier, vol. 58(7), pages 1427-1442, April.
  • Handle: RePEc:eee:socmed:v:58:y:2004:i:7:p:1427-1442
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    Citations

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    Cited by:

    1. Albada, Akke & Ausems, Margreet G.E.M. & van Dulmen, Sandra, 2014. "Counselee participation in follow-up breast cancer genetic counselling visits and associations with achievement of the preferred role, cognitive outcomes, risk perception alignment and perceived perso," Social Science & Medicine, Elsevier, vol. 116(C), pages 178-186.
    2. Miller, Fiona Alice & Ahern, Catherine & Ogilvie, Jacqueline & Giacomini, Mita & Schwartz, Lisa, 2005. "Ruling in and ruling out: Implications of molecular genetic diagnoses for disease classification," Social Science & Medicine, Elsevier, vol. 61(12), pages 2536-2545, December.
    3. Gooding, Holly C. & Organista, Kurt & Burack, Jeffrey & Biesecker, Barbara Bowles, 2006. "Genetic susceptibility testing from a stress and coping perspective," Social Science & Medicine, Elsevier, vol. 62(8), pages 1880-1890, April.
    4. Payne, Katherine & Nicholls, Stuart G. & McAllister, Marion & MacLeod, Rhona & Ellis, Ian & Donnai, Dian & Davies, Linda M., 2007. "Outcome measures for clinical genetics services: A comparison of genetics healthcare professionals and patients' views," Health Policy, Elsevier, vol. 84(1), pages 112-122, November.
    5. Mette Bergman & Caroline Graff & Maria Eriksdotter & Marja Schuster & Kerstin S. Fugl‐Meyer, 2017. "Overall and domain‐specific life satisfaction when living with familial Alzheimer's disease risk: A quantitative approach," Nursing & Health Sciences, John Wiley & Sons, vol. 19(4), pages 452-458, December.
    6. Peyron, Christine & Pélissier, Aurore & Béjean, Sophie, 2018. "Preference heterogeneity with respect to whole genome sequencing. A discrete choice experiment among parents of children with rare genetic diseases," Social Science & Medicine, Elsevier, vol. 214(C), pages 125-132.
    7. Azimatun Noor Aizuddin & Abdul Rahman Ramdzan & Sharifah Azween Syed Omar & Zuria Mahmud & Zarina A. Latiff & Salleh Amat & Keng Wee Teik & Ch’ng Gaik Siew & Haniza Rais & Syed Mohamed Aljunid, 2021. "Genetic Testing for Cancer Risk: Is the Community Willing to Pay for It?," IJERPH, MDPI, vol. 18(16), pages 1-11, August.
    8. Shim, Jae-Mahn & Kim, Jibum, 2020. "Contextualizing geneticization and medical pluralism: How variable institutionalization of traditional, complementary, and alternative medicine (TCAM) conditions effects of genetic beliefs on utilizat," Social Science & Medicine, Elsevier, vol. 267(C).

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