Table of Contents
Advances in Nursing
Volume 2014, Article ID 725968, 19 pages
http://dx.doi.org/10.1155/2014/725968
Review Article

Effectiveness of the Interventions Utilized in Genetic Counseling

1College of Nursing, University of Wisconsin-Milwaukee, 1921 E. Hartford Avenue, Cunningham Hall Room 685, Milwaukee, WI 53211-3060, USA
2Division of Biomedical Informatics, Department of Medicine, University of California, San Diego, 9500 Gilman Drive No. 0728, Building 2, La Jolla, CA 92093-0728, USA

Received 12 April 2014; Revised 11 June 2014; Accepted 12 June 2014; Published 3 July 2014

Academic Editor: Caroline Sanders

Copyright © 2014 Jeeyae Choi and Hyeoneui Kim. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. A. Trepanier, M. Ahrens, W. McKinnon et al., “Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors,” Journal of Genetic Counseling, vol. 13, no. 2, pp. 83–114, 2004. View at Publisher · View at Google Scholar · View at Scopus
  2. K. A. Calzone, A. Cashion, S. Feetham et al., “Nurses transforming health care using genetics and genomics,” Nursing Outlook, vol. 58, no. 1, pp. 26–35, 2010. View at Publisher · View at Google Scholar · View at Scopus
  3. L. Godino, D. Turchetti, and H. Skirton, “Genetic counseling: a survey to explore knowledge and attitudes of Italian nurses and midwives,” Nursing and Health Sciences, vol. 15, no. 1, pp. 15–21, 2013. View at Publisher · View at Google Scholar · View at Scopus
  4. A. J. Lloyd, “The extent of patients' understanding of the risk of treatments,” Quality in Health Care, vol. 10, no. 1, pp. 14–18, 2001. View at Google Scholar · View at Scopus
  5. D. W. Hutton, J. K. Belkora, R. D. Shachter, and D. H. Moore, “Are patients getting the gist in risk communication? Patient understanding of prognosis in breast cancer treatment,” Journal of Cancer Education, vol. 24, no. 3, pp. 194–199, 2009. View at Publisher · View at Google Scholar · View at Scopus
  6. P. C. Schroy III, J. T. Glick, S. Wilson, P. A. Robinson, and T. C. Heeren, “An effective educational strategy for improving knowledge, risk perception, and risk communication among colorectal adenoma patients,” Journal of Clinical Gastroenterology, vol. 42, no. 6, pp. 708–714, 2008. View at Publisher · View at Google Scholar · View at Scopus
  7. R. T. Croyle and C. Lerman, “Risk communication in genetic testing for cancer susceptibility,” Journal of the National Cancer Institute Monographs, no. 25, pp. 59–66, 1999. View at Google Scholar · View at Scopus
  8. C. L. Gaff, A. J. Clarke, P. Atkinson et al., “Process and outcome in communication of genetic information within families: a systematic review,” European Journal of Human Genetics, vol. 15, no. 10, pp. 999–1011, 2007. View at Publisher · View at Google Scholar · View at Scopus
  9. S. Feetham and E. Thomson, “Keeping the individual and family in focus,” in Individuals, Families and the New Era of Genetics, Biopsychosocial Aspect, S. H. McDaniel, S. M. Miller, and J. S. Rolland, Eds., pp. 3–28, W.W. Norton, 2006. View at Google Scholar
  10. K. G. Meilleur and M. T. Littleton-Kearney, “Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review,” American Journal of Medical Genetics A, vol. 149, no. 4, pp. 819–830, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. M. Paneque, J. Sequeiros, and H. Skirton, “Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles,” Genetic Testing and Molecular Biomarkers, vol. 16, no. 1, pp. 36–45, 2012. View at Publisher · View at Google Scholar · View at Scopus
  12. S. Sivell, G. Elwyn, C. L. Gaff et al., “How risk is perceived, constructed and interpreted by clients in clinical genetics, and the effects on decision making: Systematic review,” Journal of Genetic Counseling, vol. 17, no. 1, pp. 30–63, 2008. View at Publisher · View at Google Scholar · View at Scopus
  13. C. Julian-Reynier, M. Welkenhuysen, L. Hagoel et al., “Risk communication strategies: state of the art and effectiveness in the context of cancer genetic services,” European Journal of Human Genetics, vol. 11, no. 10, pp. 725–736, 2003. View at Publisher · View at Google Scholar · View at Scopus
  14. F. C. Fraser, “Genetic counseling,” The American Journal of Human Genetics, vol. 26, no. 5, pp. 636–661, 1974. View at Google Scholar · View at Scopus
  15. B. A. Bernhardt, B. B. Biesecker, and C. L. Mastromarino, “Goals, benefits, and outcomes of genetic counseling: client and genetic counselor assessment,” The American Journal of Medical Genetics, vol. 94, pp. 189–197, 2000. View at Google Scholar
  16. R. Resta, B. B. Biesecker, R. L. Bennett et al., “A new definition of genetic counseling: National Society of Genetic Counselors' Task Force report,” Journal of Genetic Counseling, vol. 15, no. 2, pp. 77–83, 2006. View at Publisher · View at Google Scholar · View at Scopus
  17. L. Ellington, A. Maxwel, B. J. Baty, D. Roter, W. N. Dudley, and A. Y. Kinney, “Genetic counseling communication with an African American BRCA1 kindred,” Social Science and Medicine, vol. 64, no. 3, pp. 724–734, 2007. View at Publisher · View at Google Scholar · View at Scopus
  18. L. F. Ross, “Good ethics requires good science: why transplant programs should not disclose misattributed parentage,” The American Journal of Transplantation, vol. 10, pp. 742–746, 2010. View at Google Scholar
  19. E. Rothwell, W. Kohlmann, K. Jasperson, A. Gammon, B. Wong, and A. Kinney, “Patient outcomes associated with group and individual genetic counseling formats,” Familial Cancer, vol. 11, no. 1, pp. 97–106, 2012. View at Publisher · View at Google Scholar · View at Scopus
  20. A. Albada, S. van Dulmen, M. G. E. M. Ausems, and J. M. Bensing, “A pre-visit website with question prompt sheet for counselees facilitates communication in the first consultation for breast cancer genetic counseling: findings from a randomized controlled trial,” Genetics in Medicine, vol. 14, no. 5, pp. 535–542, 2012. View at Publisher · View at Google Scholar · View at Scopus
  21. A. Albada, S. van Dulmen, D. Lindhout, J. M. Bensing, and M. G. E. M. Ausems, “A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling,” Familial Cancer, vol. 11, no. 1, pp. 85–95, 2012. View at Publisher · View at Google Scholar · View at Scopus
  22. K. D. Graves, L. Wenzel, M. D. Schwartz et al., “Randomized controlled trial of a psychosocial telephone counseling intervention in BRCA1 and BRCA2 mutation carriers,” Cancer Epidemiology Biomarkers and Prevention, vol. 19, no. 3, pp. 648–654, 2010. View at Publisher · View at Google Scholar · View at Scopus
  23. T. Pal, C. Stowe, A. Cole, J.-H. Lee, X. Zhaoa, and S. Vadaparampil, “Evaluation of phone-based genetic counselling in African American women using culturally tailored visual aids,” Clinical Genetics, vol. 78, no. 2, pp. 124–131, 2010. View at Publisher · View at Google Scholar · View at Scopus
  24. C. H. Halbert, L. Kessler, A. B. Troxel, J. E. Stopfer, and S. Domchek, “Effect of genetic counseling and testing for BRCA1 and BRCA2 mutations in African American women: a randomized trial,” Public Health Genomics, vol. 13, no. 7-8, pp. 440–448, 2010. View at Publisher · View at Google Scholar · View at Scopus
  25. P. Roussi, K. A. Sherman, S. Miller et al., “Enhanced counselling for women undergoing BRCA1/2 testing: impact on knowledge and psychological distress-results from a randomised clinical trial,” Psychology and Health, vol. 25, no. 4, pp. 401–415, 2010. View at Publisher · View at Google Scholar · View at Scopus
  26. C. Castellani, S. Perobelli, V. Bianchi et al., “An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests,” American Journal of Medical Genetics A, vol. 155, no. 4, pp. 778–785, 2011. View at Publisher · View at Google Scholar · View at Scopus
  27. A. H. Roshanai, R. Rosenquist, C. Lampic, and K. Nordin, “Does enhanced information at cancer genetic counseling improve counselees' knowledge, risk perception, satisfaction and negotiation of information to at-risk relatives? A randomized study,” Acta Oncologica, vol. 48, no. 7, pp. 999–1009, 2009. View at Publisher · View at Google Scholar · View at Scopus
  28. M. D. Schwartz, H. B. Valdimarsdottir, T. A. DeMarco et al., “Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction,” Health Psychology, vol. 28, no. 1, pp. 11–19, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. J. Bodurtha, J. M. Quillin, K. A. Tracy et al., “Mammography screening after risk-tailored messages: The Women Improving Screening through Education and Risk Assessment (WISER) randomized, controlled trial,” Journal of Women's Health, vol. 18, no. 1, pp. 41–47, 2009. View at Publisher · View at Google Scholar · View at Scopus
  30. C. E. Wakefield, B. Meiser, J. Homewood et al., “Randomized trial of a decision aid for individuals considering genetic testing for hereditary nonpolyposis colorectal cancer risk,” Cancer, vol. 113, no. 5, pp. 956–965, 2008. View at Publisher · View at Google Scholar · View at Scopus
  31. C. E. Wakefield, B. Meiser, J. Homewood et al., “A randomized trial of a breast/ovarian cancer genetic testing decision aid used as a communication aid during genetic counseling,” Psycho-Oncology, vol. 17, no. 8, pp. 844–854, 2008. View at Publisher · View at Google Scholar · View at Scopus
  32. K. M. Kelly, L. Senter, H. Leventhal, G. Ozakinci, and K. Porter, “Subjective and objective risk of ovarian cancer in Ashkenazi Jewish women testing for BRCA1/2 mutations,” Patient Education and Counseling, vol. 70, no. 1, pp. 135–142, 2008. View at Publisher · View at Google Scholar · View at Scopus
  33. K. Glanz, A. D. Steffen, and L. A. Taglialatela, “Effects of colon cancer risk counseling for first-degree relatives,” Cancer Epidemiology Biomarkers and Prevention, vol. 16, no. 7, pp. 1485–1491, 2007. View at Publisher · View at Google Scholar · View at Scopus
  34. E. M. Ozanne, C. Annis, K. Adduci, J. Showstack, and L. Esserman, “Pilot trial of a computerized decision aid for breast cancer prevention,” Breast Journal, vol. 13, no. 2, pp. 147–154, 2007. View at Publisher · View at Google Scholar · View at Scopus
  35. E. A. Lobb, P. N. Butow, A. Moore et al., “Development of a communication aid to facilitate risk communication in consultations with unaffected women from high risk breast cancer families: a pilot study,” Journal of Genetic Counseling, vol. 15, no. 5, pp. 393–405, 2006. View at Publisher · View at Google Scholar · View at Scopus
  36. D. J. Bowen, W. Burke, J. O. Culver, N. Press, and S. Crystal, “Effects of counseling Ashkenazi jewish women about breast cancer risk,” Cultural Diversity and Ethnic Minority Psychology, vol. 12, no. 1, pp. 45–56, 2006. View at Publisher · View at Google Scholar · View at Scopus
  37. S. Charles, L. Kessler, J. E. Stopfer, S. Domchek, and C. H. Halbert, “Satisfaction with genetic counseling for BRCA1 and BRCA2 mutations among African American women,” Patient Education and Counseling, vol. 63, no. 1-2, pp. 196–204, 2006. View at Publisher · View at Google Scholar · View at Scopus
  38. E. T. Matloff, A. Moyer, K. M. Shannon, K. B. Niendorf, and N. F. Col, “Healthy women with a family history of breast cancer: impact of a tailored genetic counseling intervention on risk perception, knowledge, and menopausal therapy decision making,” Journal of Women's Health, vol. 15, no. 7, pp. 843–856, 2006. View at Publisher · View at Google Scholar · View at Scopus
  39. N. Arimori, “Randomized controlled trial of decision aids for women considering prenatal testing: the effect of the Ottawa Personal Decision Guide on decisional conflict,” Japan Journal of Nursing Science, vol. 3, no. 2, pp. 119–130, 2006. View at Publisher · View at Google Scholar · View at Scopus
  40. S. M. Miller, L. Fleisher, P. Roussi et al., “Facilitating informed decision making about breast cancer risk and genetic counseling among women calling the NCI's Cancer Information Service,” Journal of Health Communication, vol. 10, no. 1, supplement, pp. 119–136, 2005. View at Publisher · View at Google Scholar · View at Scopus
  41. S. M. Miller, P. Roussi, M. B. Daly et al., “Enhanced counseling for women undergoing BRCA1/2 testing: impact on subsequent decision making about risk reduction behaviors,” Health Education and Behavior, vol. 32, no. 5, pp. 654–667, 2005. View at Publisher · View at Google Scholar · View at Scopus
  42. J. M. Griffith, J. R. Sorenson, J. M. Bowling, and T. Jennings-Grant, “Assessment of an interactive computer-based patient prenatal genetic screening and testing education tool,” Health Education and Behavior, vol. 32, no. 5, pp. 613–626, 2005. View at Publisher · View at Google Scholar · View at Scopus
  43. K. Brain, S. Sivell, K. Bennert et al., “An exploratory comparison of genetic counselling protocols for HNPCC predictive testing,” Clinical Genetics, vol. 68, no. 3, pp. 255–261, 2005. View at Publisher · View at Google Scholar · View at Scopus
  44. D. Braithwaite, S. Sutton, J. Mackay, J. Stein, and J. Emery, “Development of a risk assessment tool for women with a family history of breast cancer,” Cancer Detection and Prevention, vol. 29, no. 5, pp. 433–439, 2005. View at Publisher · View at Google Scholar · View at Scopus
  45. M. J. Green, S. K. Peterson, M. W. Baker et al., “Use of an educational computer program before genetic counseling for breast cancer susceptibility: Effects on duration and content of counseling sessions,” Genetics in Medicine, vol. 7, no. 4, pp. 221–229, 2005. View at Publisher · View at Google Scholar · View at Scopus
  46. C. Wang, R. Gonzalez, K. J. Milliron, V. J. Strecher, and S. D. Merajver, “Genetic counseling for BRCA1/2: a randomized controlled trial of two strategies to facilitate the education and counseling process,” American Journal of Medical Genetics, vol. 134, no. 1, pp. 66–73, 2005. View at Publisher · View at Google Scholar · View at Scopus
  47. A. McInerney-Leo, B. B. Biesecker, D. W. Hadley et al., “BRCA1/2 testing in hereditary breast and ovarian cancer families II: impact on relationships,” The American Journal of Medical Genetics, vol. 133, no. 2, pp. 165–169, 2005. View at Publisher · View at Google Scholar · View at Scopus
  48. M. J. Green, S. K. Peterson, M. W. Baker et al., “Effect of a computer-based decision aid on knowledge, perceptions, and intentions about genetic testing for breast cancer susceptibility: a randomized controlled trial,” Journal of the American Medical Association, vol. 292, no. 4, pp. 442–452, 2004. View at Publisher · View at Google Scholar · View at Scopus
  49. K. M. Emmons, M. Wong, E. Puleo, N. Weinstein, R. Fletcher, and G. Colditz, “Tailored computer-based cancer risk communication: correcting colorectal cancer risk perception,” Journal of Health Communication, vol. 9, no. 2, pp. 127–141, 2004. View at Publisher · View at Google Scholar · View at Scopus
  50. M. S. van Roosmalen, P. F. M. Stalmeier, L. C. G. Verhoef et al., “Randomised trial of a decision aid and its timing for women being tested for a BRCA1/2 mutation,” British Journal of Cancer, vol. 90, no. 2, pp. 333–342, 2004. View at Publisher · View at Google Scholar · View at Scopus
  51. K. Brain, P. Norman, J. Gray, C. Rogers, R. Mansel, and P. Harper, “A randomized trial of specialist genetic assessment: psychological impact on women at different levels of familial breast cancer risk,” British Journal of Cancer, vol. 86, no. 2, pp. 233–238, 2002. View at Publisher · View at Google Scholar · View at Scopus
  52. D. J. Bowen, W. Burke, Y. Yasui, A. McTiernan, and D. McLeran, “Effects of risk counseling on interest in breast cancer genetic testing for lower risk women,” Genetics in Medicine, vol. 4, no. 5, pp. 359–365, 2002. View at Publisher · View at Google Scholar · View at Scopus
  53. G. J. Hurt, R. P. McQuellon, R. Michielutte, D. M. Conrad, S. Carter, and H. Anderson, “Risk assessment of first-degree relatives of women with breast cancer: a feasibility study.,” Oncology Nursing Forum, vol. 28, no. 7, pp. 1097–1104, 2001. View at Google Scholar · View at Scopus
  54. M. D. Schwartz, J. Benkendorf, C. Lerman, C. Isaacs, A. Ryan-Robertson, and L. Johnson, “Impact of educational print materials on knowledge, attitudes, and interest in BRCA1/BRCA2,” The American Cancer Society, vol. 92, no. 4, pp. 932–940, 2001. View at Google Scholar
  55. M. J. Green, A. M. McInerney, B. B. Biesecker, and N. Fost, “Education about genetic testing for breast cancer susceptibility: patient preferences for a computer program or genetic counselor,” American Journal of Medical Genetics, vol. 103, no. 1, pp. 24–31, 2001. View at Publisher · View at Google Scholar
  56. M. J. Green, A. M. McInerney, B. B. Biesecker, and N. Fost, “An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility,” American Journal of Medical Genetics, vol. 103, no. 1, pp. 16–23, 2001. View at Publisher · View at Google Scholar · View at Scopus
  57. E. R. Drake, L. Engler-Todd, A. M. O'Connor, L. C. Surh, and A. Hunter, “Development and evaluation of a decision aid about prenatal testing for women of advanced maternal age,” Journal of Genetic Counseling, vol. 8, no. 4, pp. 217–233, 1999. View at Publisher · View at Google Scholar · View at Scopus
  58. A. Baum, A. L. Friedman, and S. G. Zakowski, “Stress and Genetic Testing for Disease Risk,” Health Psychology, vol. 16, no. 1, pp. 8–19, 1997. View at Google Scholar · View at Scopus
  59. G. Marks, J. L. Richardson, J. W. Graham, and A. Levine, “Role of health locus of control beliefs and expectations of treatment efficacy in adjustment to cancer,” Journal of Personality and Social Psychology, vol. 51, no. 2, pp. 443–450, 1986. View at Publisher · View at Google Scholar · View at Scopus
  60. S. E. Taylor, M. E. Kemeny, L. G. Aspinwall, S. G. Schneider, R. Rodriguez, and M. Herbert, “Optimism, coping, psychological distress, and high-risk sexual behavior among men at risk for acquired immunodeficiency syndrome (AIDS),” Journal of Personality and Social Psychology, vol. 63, no. 3, pp. 460–473, 1992. View at Publisher · View at Google Scholar · View at Scopus