TY - JOUR
T1 - Parents' perceptions of genetics services for congenital heart disease
T2 - The role of demographic, clinical, and psychological factors in determining service attendance
AU - Kasparian, Nadine A.
AU - Fidock, Blake
AU - Sholler, Gary F.
AU - Camphausen, Christoph
AU - Murphy, David N.
AU - Cooper, Stephen G.
AU - Kaul, Ritik
AU - Jones, Owen
AU - Winlaw, David S.
AU - Kirk, Edwin P.E.
PY - 2014/6
Y1 - 2014/6
N2 - Purpose:We sought to identify the demographic, clinical, and psychological factors associated with parents' attendance at clinical genetics services for congenital heart disease.Methods:A survey assessing access to cardiac genetics services and a range of other variables was sent to the families of 213 children diagnosed with congenital heart disease between the years 2000 and 2009 at the Sydney Children's Hospital, Australia.Results:Of the 114 respondents, 22% had accessed cardiac genetics services. Variables strongly associated with service attendance included presence of a syndrome associated with congenital heart disease (odds ratio = 17.93; P < 0.001) and antenatal diagnosis of congenital heart disease (odds ratio = 4.13; P = 0.02). Most participants (87%) perceived genetic factors as "quite" or "extremely important" in the development of congenital heart disease, and many (73%) believed that receiving information about congenital heart disease and genetics was "quite" or "extremely important"; however, only 36% of participants could recall receiving information of this nature. Forty-two percent of parents reported current concerns about their child's health, and a substantial subset reported levels of depression (26%), anxiety (27%), and stress (32%) warranting clinical attention.Conclusion:There is a strong desire among parents of children with congenital heart disease for greater information about the role of genetic factors; however, most families do not access cardiac genetics services and report limited recall of information gathered from other sources.Genet Med 16 6, 460-468.
AB - Purpose:We sought to identify the demographic, clinical, and psychological factors associated with parents' attendance at clinical genetics services for congenital heart disease.Methods:A survey assessing access to cardiac genetics services and a range of other variables was sent to the families of 213 children diagnosed with congenital heart disease between the years 2000 and 2009 at the Sydney Children's Hospital, Australia.Results:Of the 114 respondents, 22% had accessed cardiac genetics services. Variables strongly associated with service attendance included presence of a syndrome associated with congenital heart disease (odds ratio = 17.93; P < 0.001) and antenatal diagnosis of congenital heart disease (odds ratio = 4.13; P = 0.02). Most participants (87%) perceived genetic factors as "quite" or "extremely important" in the development of congenital heart disease, and many (73%) believed that receiving information about congenital heart disease and genetics was "quite" or "extremely important"; however, only 36% of participants could recall receiving information of this nature. Forty-two percent of parents reported current concerns about their child's health, and a substantial subset reported levels of depression (26%), anxiety (27%), and stress (32%) warranting clinical attention.Conclusion:There is a strong desire among parents of children with congenital heart disease for greater information about the role of genetic factors; however, most families do not access cardiac genetics services and report limited recall of information gathered from other sources.Genet Med 16 6, 460-468.
KW - causal attributions
KW - congenital heart disease
KW - genetic counseling
KW - genetics services
KW - health services
KW - psychological stress
UR - http://www.scopus.com/inward/record.url?scp=84902077315&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84902077315&partnerID=8YFLogxK
U2 - 10.1038/gim.2013.169
DO - 10.1038/gim.2013.169
M3 - Article
C2 - 24202083
AN - SCOPUS:84902077315
SN - 1098-3600
VL - 16
SP - 460
EP - 468
JO - Genetics in Medicine
JF - Genetics in Medicine
IS - 6
ER -