Literature DB >> 16352205

Counselling strategies in the prenatal diagnosis of major heart abnormality.

Samuel Menahem1, James Grimwade.   

Abstract

BACKGROUND: Prenatal diagnosis of a major cardiac abnormality precipitates a crisis in the parents. To their grief and/or anger may be added the burden of whether to continue with the pregnancy if the fetus is previable. AIMS: We reviewed our counselling strategies to determine if the parents were satisfied with our approach and whether in their perception it provided the knowledge and understanding of the abnormality detected to help them in their decision.
METHODS: Questionnaires highlighting parental perception of their experiences, were developed and sent to a cohort of parents following the birth of their infant or at least 6 months after termination. The parents were seen over 3 years in a private obstetric ultrasound practice, diagnosed with or specifically referred because of the diagnosis of a major heart abnormality in the fetus, confirmed at a subsequent scan with the paediatric cardiologist in attendance. Both clinicians explained the abnormality, 'working off each other'. The obstetrician ensured the explanations were in lay terms. Anatomical detail, while important to the clinicians, was not emphasised, but rather function, quality of life issues and probable outcome and attendant risks of intervention. An appointment with the cardiologist was offered as was the need/option for further scans.
RESULTS: 39 patients were reviewed, 13 of whom elected to terminate their pregnancy. Of the 30 who responded, 70% reported that the explanations of the abnormality were clear to very clear, whilst 85% considered the detail given was 'just right'. Only 60% rated their understanding of the diagnosis as 'good to excellent', improving to 80% with subsequent scans. These results were especially meaningful when 70% of the respondents described themselves as being distressed or very distressed following the initial diagnosis.
CONCLUSIONS: These results suggest that parents seemed satisfied with our approach of two clinicians working together emphasising function and outcome, rather than anatomical detail. Their perceived understanding seemed to allow them to make their decision concerning continuation or termination of their pregnancy.

Entities:  

Year:  2004        PMID: 16352205     DOI: 10.1016/j.hlc.2004.06.009

Source DB:  PubMed          Journal:  Heart Lung Circ        ISSN: 1443-9506            Impact factor:   2.975


  9 in total

1.  Exploring the perceptions and the role of genetic counselors in the emerging field of perinatal palliative care.

Authors:  Charlotte Wool; Martha Dudek
Journal:  J Genet Couns       Date:  2013-04-18       Impact factor: 2.537

2.  Is counselling for CCAM that difficult? Learning from parental experience.

Authors:  Lucia Aite; Antonio Zaccara; Alessandro Trucchi; Antonella Nahom; Irma Capolupo; Luisa Mobili; Pietro Bagolan
Journal:  J Prenat Med       Date:  2011-07

3.  Ethical issues in fetal management: a cardiac perspective.

Authors:  Atul Malhotra; Samuel Menahem; Lynn Gillam
Journal:  Int J Pediatr       Date:  2010-03-24

4.  Content and quality of information websites about congenital heart defects following a prenatal diagnosis.

Authors:  Tommy Carlsson; Gunnar Bergman; Anna-Malin Karlsson; Elisabet Mattsson
Journal:  Interact J Med Res       Date:  2015-01-21

Review 5.  "Functionally" univentricular hearts: impact of pre-natal diagnosis.

Authors:  Antonio Francesco Corno
Journal:  Front Pediatr       Date:  2015-02-27       Impact factor: 3.418

6.  Information following a diagnosis of congenital heart defect: experiences among parents to prenatally diagnosed children.

Authors:  Tommy Carlsson; Gunnar Bergman; Ulla Melander Marttala; Barbro Wadensten; Elisabet Mattsson
Journal:  PLoS One       Date:  2015-02-18       Impact factor: 3.240

7.  Involvement of persons with lived experience of a prenatal diagnosis of congenital heart defect: an explorative study to gain insights into perspectives on future research.

Authors:  Tommy Carlsson; Ulla Melander Marttala; Barbro Wadensten; Gunnar Bergman; Elisabet Mattsson
Journal:  Res Involv Engagem       Date:  2016-12-15

8.  Experiences of informational needs and received information following a prenatal diagnosis of congenital heart defect.

Authors:  Tommy Carlsson; Gunnar Bergman; Barbro Wadensten; Elisabet Mattsson
Journal:  Prenat Diagn       Date:  2016-04-24       Impact factor: 3.050

9.  Quality of Patient Information Websites About Congenital Heart Defects: Mixed-Methods Study of Perspectives Among Individuals With Experience of a Prenatal Diagnosis.

Authors:  Tommy Carlsson; Ulla Melander Marttala; Barbro Wadensten; Gunnar Bergman; Ove Axelsson; Elisabet Mattsson
Journal:  Interact J Med Res       Date:  2017-09-12
  9 in total

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