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. 2014 Jun;164A(6):1496-502.
doi: 10.1002/ajmg.a.36525. Epub 2014 Apr 4.

Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice

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Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice

Setareh Ashtiani et al. Am J Med Genet A. 2014 Jun.

Abstract

Little is currently known about how parents experience the medical genetics appointment at which their child receives a genetic diagnosis. We conducted semi-structured in-person interviews with 13 parents of 10 index children to explore their experience in the medical genetics appointment in which they received their child's genetic diagnosis. Guided by grounded theory, we used a constant comparative approach to data analysis. Transcribed interviews were coded and sorted, and thematic categories identified. Sixty-one and a half percent of parents experienced the diagnosis session as negative, 23% felt the experience was positive, and 15.5% were ambivalent. Receiving emotional support, an outline of the follow-up plans, and messages of hope and perspective during the session seemed to positively influence parents' experience, while feeling that their role was as a passive receiver of information and the use of difficult medical terminology negatively influenced parents' overall experience. Parental preparedness for the information, and the parents' emotional reaction to the diagnosis were also factors that influenced the parental experience. Few participants understood the role of the genetic counselor. Our results provide in-depth insight into the parental experience of the pediatric medical genetics diagnosis session. We propose a mechanism through which parental experience shapes their perception of the medical genetics session.

Keywords: genetic counseling; genetic diagnosis; parental experience; pediatric genetics; receiving bad news.

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Figures

FIGURE 1
FIGURE 1
Model illustrating the factors shaping parents’ experience of receiving their child’s genetic diagnosis at the Medical Genetics clinic.

References

    1. Babul-Hirji R, Hewson S, Frescura M. A sociolinguistic exploration of genetic counseling discourse involving a child with a new genetic diagnosis. Patient Educ Couns. 2010;78(1):40–45. - PubMed
    1. Barr O, Millar R. Parents of Children with Intellectual Disabilities: Their Expectations and Experience of Genetic Counselling. J Appl Res Intellect Disabil. 2003;16:189–204.
    1. Barr O, McConkey R. A different type of appointment: the experiences of parents who have children with intellectual disabilities referred for genetic investigation. J Res Nurs. 2007;12(6):637–652.
    1. Boyd JR. A process for delivering bad news: supporting families when a child is diagnosed. J Neurosci Nurs. 2001;33(1):14–20. - PubMed
    1. Carmichael B, Pembrey M, Barnicoat GTA. Diagnosis of fragile-X syndrome: the experiences of parents. J Intellect Disabil Res. 1999;43(Pt1):47–53. - PubMed

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