TY - JOUR
T1 - Risk Communication in Families of Children with Familial Hypercholesterolemia
T2 - Identifying Motivators and Barriers to Cascade Screening to Improve Diagnosis at a Single Medical Center
AU - Wurtmann, Elisabeth
AU - Steinberger, Julia
AU - Veach, Pat Mc Carthy
AU - Khan, Mindi
AU - Zierhut, Heather
N1 - Publisher Copyright:
© 2018 National Society of Genetic Counselors
PY - 2019/2
Y1 - 2019/2
N2 - Familial hypercholesterolemia (FH) is severely underdiagnosed in the USA; yet, factors influencing family notification about risk for FH in the US pediatric setting have not been well elucidated. Most previous research on these factors has occurred in adult patient populations in European countries with organized cascade screening programs; therefore, we sought to characterize parent experiences with cascade screening in the US pediatric setting. A quantitative survey measuring family notification of FH risk information was administered to 38 parents of children with FH identified within a pediatric cardiology clinic. Participants were also asked if family notification was impacted by intrapersonal, interpersonal, institutional, community, and public policy factors identified previously in other populations. Notification of at least one of the proband's living grandparents or aunts/uncles was reported by 76% (n = 25/33) and 71% (n = 24/34) of participants, respectively. The most common reason for notification was to protect relatives from heart disease. Two of the most common reasons participants did not notify relatives were a lack of information about FH and concern that the relative would have difficulty understanding the information. Yet, only a minority of participants (39%) accessed institutional resources such as educational materials to share with relatives or assistance drafting a family letter that could address these barriers. Based on the identified barriers and motivators for family communication, we suggest facilitators to improve implementation of cascade screening.
AB - Familial hypercholesterolemia (FH) is severely underdiagnosed in the USA; yet, factors influencing family notification about risk for FH in the US pediatric setting have not been well elucidated. Most previous research on these factors has occurred in adult patient populations in European countries with organized cascade screening programs; therefore, we sought to characterize parent experiences with cascade screening in the US pediatric setting. A quantitative survey measuring family notification of FH risk information was administered to 38 parents of children with FH identified within a pediatric cardiology clinic. Participants were also asked if family notification was impacted by intrapersonal, interpersonal, institutional, community, and public policy factors identified previously in other populations. Notification of at least one of the proband's living grandparents or aunts/uncles was reported by 76% (n = 25/33) and 71% (n = 24/34) of participants, respectively. The most common reason for notification was to protect relatives from heart disease. Two of the most common reasons participants did not notify relatives were a lack of information about FH and concern that the relative would have difficulty understanding the information. Yet, only a minority of participants (39%) accessed institutional resources such as educational materials to share with relatives or assistance drafting a family letter that could address these barriers. Based on the identified barriers and motivators for family communication, we suggest facilitators to improve implementation of cascade screening.
KW - Cascade screening
KW - Disclosure
KW - Familial hypercholesterolemia
KW - Family communication
KW - Genetic predisposition to disease
KW - Prevention
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U2 - 10.1007/s10897-018-0290-0
DO - 10.1007/s10897-018-0290-0
M3 - Article
C2 - 30109451
AN - SCOPUS:85051721507
SN - 1059-7700
VL - 28
SP - 50
EP - 58
JO - Journal of Genetic Counseling
JF - Journal of Genetic Counseling
IS - 1
ER -