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Erschienen in: Journal of Genetic Counseling 1/2016

01.02.2016 | Original Research

Comparison of Informed Consent Preferences for Multiplex Genetic Carrier Screening among a Diverse Population

verfasst von: Ashley Reeves, Angela Trepanier

Erschienen in: Journal of Genetic Counseling | Ausgabe 1/2016

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Abstract

Multiplex genetic carrier screening is increasingly being integrated into reproductive care. Obtaining informed consent becomes more challenging as the number of screened conditions increases. Implementing a model of generic informed consent may facilitate informed decision-making. Current Wayne State University students and staff were invited to complete a web-based survey by blast email solicitation. Participants were asked to determine which of two generic informed consent scenarios they preferred: a brief versus a detailed consent. They were asked to rank the importance of different informational components in making an informed decision and to provide demographic information. Comparisons between informational preferences, demographic variables and scenario preferences were made. Six hundred ninety three participants completed the survey. When evaluating these generic consents, the majority preferred the more detailed consent (74.5 %), and agreed that it provided enough information to make an informed decision (89.5 %). Those who thought it would be more important to know the severity of the conditions being screened (p = .002) and range of symptoms (p = .000) were more likely to prefer the more detailed consent. There were no significant associations between scenario preferences and demographic variables. A generic consent was perceived to provide sufficient information for informed decision making regarding multiplex carrier screening with most preferring a more detailed version of the consent. Individual attitudes rather than demographic variables influenced preferences regarding the amount of information that should be included in the generic consent. The findings have implications for how clinicians approach providing tailored informed consent.
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Literatur
Zurück zum Zitat American College of Obstetricians and Gynecologists Committee on Genetics. (2011). ACOG committee opinion no. 486. Update on carrier screening for cystic fibrosis. Obstetrics and Gynecology, 117(4), 1028–31. doi:10.1097/AOG.0b013e31821922c2.CrossRef American College of Obstetricians and Gynecologists Committee on Genetics. (2011). ACOG committee opinion no. 486. Update on carrier screening for cystic fibrosis. Obstetrics and Gynecology, 117(4), 1028–31. doi:10.​1097/​AOG.​0b013e31821922c2​.CrossRef
Zurück zum Zitat Bekker, H., Thornton, J. G., Airey, C. M., Connelly, J. B., Hewison, J., Robinson, M. B., & Pearman, A. D. (1999). Informed decision making: an annotated bibliography and systematic review. Health Technology and Assessments, 3(1), 1–156. Bekker, H., Thornton, J. G., Airey, C. M., Connelly, J. B., Hewison, J., Robinson, M. B., & Pearman, A. D. (1999). Informed decision making: an annotated bibliography and systematic review. Health Technology and Assessments, 3(1), 1–156.
Zurück zum Zitat Berger, K. (2003). Informed consent: information or knowledge? Medicine and Law, 22(4), 743–50.PubMed Berger, K. (2003). Informed consent: information or knowledge? Medicine and Law, 22(4), 743–50.PubMed
Zurück zum Zitat Bradbury, A. R., Patrick-Miller, L., & Domcheck, S. (2014). Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencing. Commentary. Genetics in Medicine. doi:10.1038/gim.2014.85.PubMedCentral Bradbury, A. R., Patrick-Miller, L., & Domcheck, S. (2014). Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencing. Commentary. Genetics in Medicine. doi:10.​1038/​gim.​2014.​85.PubMedCentral
Zurück zum Zitat Dormandy, E., Tsui, E.Y., & Marteau, T. M. (2007). Development of a measure of informed choice suitable for use in low literacy populations. Patient Education and Counseling, 66(3), 278–95. doi:10.1016/j.pec.2007.01.001. Dormandy, E., Tsui, E.Y., & Marteau, T. M. (2007). Development of a measure of informed choice suitable for use in low literacy populations. Patient Education and Counseling, 66(3), 278–95. doi:10.​1016/​j.​pec.​2007.​01.​001.
Zurück zum Zitat Edwards, J. G., Feldman, G., Goldberg, J., Gregg, A. R., Norton, M. E., Rose, N. C., Schneider, A., Stoll, K., Wapner, R., & Watson, M. S. (2015). Expanded carrier screening in reproductive medicine-points to consider. A joint statement of the American college of medical genetics, American college of obstetricians and gynecologists, national society of genetic counselors, perinatal quality foundation, and society for maternal fetal medicine. Obstetrics and Gynecology, 125(3), 653–662. doi:10.1097/AOG.0000000000000666.CrossRefPubMed Edwards, J. G., Feldman, G., Goldberg, J., Gregg, A. R., Norton, M. E., Rose, N. C., Schneider, A., Stoll, K., Wapner, R., & Watson, M. S. (2015). Expanded carrier screening in reproductive medicine-points to consider. A joint statement of the American college of medical genetics, American college of obstetricians and gynecologists, national society of genetic counselors, perinatal quality foundation, and society for maternal fetal medicine. Obstetrics and Gynecology, 125(3), 653–662. doi:10.​1097/​AOG.​0000000000000666​.CrossRefPubMed
Zurück zum Zitat Flesch, R. (1948). A new readability yardstick. Journal of Applied Psychology, 32(3), 221–233.CrossRefPubMed Flesch, R. (1948). A new readability yardstick. Journal of Applied Psychology, 32(3), 221–233.CrossRefPubMed
Zurück zum Zitat Geller, G., Strauss, M., Bernhardt, B. A., & Holtzman, N. A. (1997). Decoding” informed consent. Insights from women regarding breast cancer susceptibility testing. Hastings Center Report, 27(2), 28–33.CrossRefPubMed Geller, G., Strauss, M., Bernhardt, B. A., & Holtzman, N. A. (1997). Decoding” informed consent. Insights from women regarding breast cancer susceptibility testing. Hastings Center Report, 27(2), 28–33.CrossRefPubMed
Zurück zum Zitat Grody, W. W., Thompson, B. H., Gregg, A. R., Bean, L. H., Monaghan, K. G., Schneider, A., & Lebo, R. V. (2013). ACMG position statement on prental/preconception expanded carrier screening. Genetics in Medicine, 15(6), 482–483. doi:10.1038/gim.2013.47.CrossRefPubMed Grody, W. W., Thompson, B. H., Gregg, A. R., Bean, L. H., Monaghan, K. G., Schneider, A., & Lebo, R. V. (2013). ACMG position statement on prental/preconception expanded carrier screening. Genetics in Medicine, 15(6), 482–483. doi:10.​1038/​gim.​2013.​47.CrossRefPubMed
Zurück zum Zitat Kloza, E. M., Haddow, P. K., Halliday, J. V., O’Brien, B. M., Lambert-Messerlian, G. M., & Palomaki, G. E. (2015). Evaluation of patient education materials: the example of circulating cell free DNA testing for aneuploidy. Journal of Genet Counsel, 24, 259–266. doi:10.1007/s10897-014-9758-8.CrossRef Kloza, E. M., Haddow, P. K., Halliday, J. V., O’Brien, B. M., Lambert-Messerlian, G. M., & Palomaki, G. E. (2015). Evaluation of patient education materials: the example of circulating cell free DNA testing for aneuploidy. Journal of Genet Counsel, 24, 259–266. doi:10.​1007/​s10897-014-9758-8.CrossRef
Zurück zum Zitat National Human Genome Research Institute (2008). Population-based carrier screening for single gene disorders: Lessons learned and new opportunities. Meeting Summary. Rockville, MD. Last accessed on 11/12/14 at http://www.genome.gov/27026048. National Human Genome Research Institute (2008). Population-based carrier screening for single gene disorders: Lessons learned and new opportunities. Meeting Summary. Rockville, MD. Last accessed on 11/12/14 at http://​www.​genome.​gov/​27026048.
Zurück zum Zitat Ormond, K. E., Iris, M., Banuvar, S., Minogue, J., Annas, G. J., & Elias, S. (2007). What do patients prefer: informed consent models for genetic carrier testing. Journal of Genetic Counseling, 16(4), 539–50. doi:10.1007/s10897-007-9094-3.CrossRefPubMed Ormond, K. E., Iris, M., Banuvar, S., Minogue, J., Annas, G. J., & Elias, S. (2007). What do patients prefer: informed consent models for genetic carrier testing. Journal of Genetic Counseling, 16(4), 539–50. doi:10.​1007/​s10897-007-9094-3.CrossRefPubMed
Zurück zum Zitat Ormond, K. E., Banuvar, S., Daly, A., Iris, M., Minogue, J., & Elias, S. (2009). Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening. Patient Education and Counseling, 75(2), 244–50. doi:10.1016//j.pec.2008.09.020.CrossRefPubMed Ormond, K. E., Banuvar, S., Daly, A., Iris, M., Minogue, J., & Elias, S. (2009). Information preferences of high literacy pregnant women regarding informed consent models for genetic carrier screening. Patient Education and Counseling, 75(2), 244–50. doi:10.​1016/​/​j.​pec.​2008.​09.​020.CrossRefPubMed
Zurück zum Zitat Tanner, A. K., Valencia, C. A., Rhodenizer, D., Espirages, M., DaSilva, C., Borsuk, L., & Hegde, M. (2014). Development and performance of a comprehensive targeted sequencing assay for pan-ethnic screening of carrier status. Journal of Molecular Diagnostics, 16(3), 350–360. doi:10.1016/j.jmoldx.2013.12.003.CrossRefPubMed Tanner, A. K., Valencia, C. A., Rhodenizer, D., Espirages, M., DaSilva, C., Borsuk, L., & Hegde, M. (2014). Development and performance of a comprehensive targeted sequencing assay for pan-ethnic screening of carrier status. Journal of Molecular Diagnostics, 16(3), 350–360. doi:10.​1016/​j.​jmoldx.​2013.​12.​003.CrossRefPubMed
Metadaten
Titel
Comparison of Informed Consent Preferences for Multiplex Genetic Carrier Screening among a Diverse Population
verfasst von
Ashley Reeves
Angela Trepanier
Publikationsdatum
01.02.2016
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 1/2016
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-015-9854-4

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