Genetic counselling in parents of children with congenital heart disease significantly improves knowledge about causation and enhances psychosocial functioning

被引:25
|
作者
Blue, Gillian M. [1 ,2 ,3 ]
Kasparian, Nadine A. [2 ,4 ]
Sholler, Gary F. [1 ,2 ,3 ]
Kirk, Edwin P. [4 ,5 ]
Winlaw, David S. [1 ,2 ,3 ]
机构
[1] Childrens Hosp Westmead, Kids Heart Res, Sydney, NSW, Australia
[2] Childrens Hosp Westmead, Heart Ctr Children, Sydney, NSW, Australia
[3] Univ Sydney, Sch Med, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
[4] Univ New S Wales, UNSW Med, Sch Womens & Childrens Hlth, Discipline Paediat, Sydney, NSW, Australia
[5] Childrens Hosp, Dept Med Genet, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Congenital heart disease; Genetic counselling; Genetics education; Intervention; Guilt and shame; Psychological stress; PERCEIVED PERSONAL CONTROL; INHERITANCE;
D O I
10.1016/j.ijcard.2014.10.119
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: One of the key questions asked by parents of children with congenital heart disease (CHD) is 'why' and 'how did this happen?'. Receiving more information in response to these questions is therefore important to parents. This study sought to assess the efficacy of individualised genetic counselling sessions in improving knowledge of causation and psychosocial functioning in parents of children with CHD. Methods: Parents of children undergoing surgery for CHD were offered individualised genetic counselling during their child's hospital admission. Assessments occurred at three time-points (immediately pre-, immediately post-, and two months post- session) using questionnaires comprising a purpose-designed knowledge measure, as well as validated psychological measures. Results: Of the 94 participants approached, 57 attended the genetic counselling session (participation rate = 60.6%). Knowledge scores for the participants who completed all three questionnaires improved significantly from pre( (x) over bar = 7.38/16, SD = 3.53) to post- session ((x) over bar = 13.33/16, SD = 2.82) (p < 0.001). Participants retained this knowledge over time, with no changes in scores at two-month follow-up (p = 0.11). Perceived personal control also increased post-session, while reported guilt, shame, depression, anxiety and stress decreased. Overall satisfaction was high, with 96.4% of participants indicating they would recommend this service to other parents of children with CHD. Conclusion: Individualised genetic counselling sessions were highly beneficial to parents of children with CHD in regards to improving knowledge about the causes of CHD and enhancing psychosocial functioning, and should be considered as part of 'best care' practices. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:124 / 130
页数:7
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