European Journal of Pediatrics

, Volume 177, Issue 3, pp 319–336 | Cite as

Children’s experiences of congenital heart disease: a systematic review of qualitative studies

  • Lauren S. H. Chong
  • Dominic A. Fitzgerald
  • Jonathan C. Craig
  • Karine E. Manera
  • Camilla S. Hanson
  • David Celermajer
  • Julian Ayer
  • Nadine A. Kasparian
  • Allison Tong
Review

Abstract

We aimed to describe the experiences of children and adolescents with congenital heart disease (CHD). Electronic databases were searched until August 2016. Qualitative studies of children’s perspectives on CHD were included. Data was extracted using thematic synthesis. From 44 studies from 12 countries involving 995 children, we identified 6 themes: disrupting normality (denying the diagnosis, oscillating between sickness and health, destabilizing the family dynamic), powerlessness in deteriorating health (preoccupation with impending mortality, vulnerability to catastrophic complications, exhaustion from medical testing), enduring medical ordeals (traumatized by invasive procedures, disappointed by treatment failure, displaced by transition, valuing empathy and continuity in care, overcoming uncertainty with information), warring with the body (losing stamina, distressing inability to participate in sport, distorted body image, testing the limits), hampering potential and goals (feeling disabled, unfair judgment and exclusion, difficulties with academic achievement, limiting attainment and maintenance of life milestones), and establishing one’s own pace (demarcating disease from life, determination to survive, taking limitations in their stride, embracing the positives, finding personal enrichment, relying on social or spiritual support).

Conclusion: Children with CHD feel vulnerable and burdened by debilitating physical symptoms, unpredictable complications, and discrimination. Clinicians may support patients by sharing recognition of these profound psychosocial consequences.

What is Known:

CHD is associated with difficulties in learning and attention, school absenteeism, decreased endurance, poor body image, and peer socialization

What is lesser known is how young patients cope with the symptoms, prognostic uncertainty, and treatment burden

What is New:

We found that children are challenged by lifestyle restrictions, fear of invasive procedures, impaired body image, discrimination, and uncertainty about the future. Feelings of disempowerment are intensified by the unpredictability of disease progression

Thus, strategies to improve outcomes include improved patient education on disease and lifestyle management and partnership with school teachers and counselors for unique psychosocial support

Keywords

Qualitative research Pediatrics Cardiology Congenital heart disease Systematic review 

Abbreviations

CHD

Congenital heart disease

QOL

Quality of life

Notes

Authors’ Contributions

Lauren Chong: conceptualized the study, carried out the data collection and analysis, coding of data,drafted the initial manuscript, drafted the manuscript, and approved the final manuscript as submitted.

Dominic Fitzgerald: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Jonathan Craig: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Karine Manera: conceptualized the study, carried out the data collection and analysis, coding of data, drafted the initial manuscript, and approved the final manuscript as submitted.

Camilla Hanson: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

David Celermajer: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Julian Ayer: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Nadine Kasparian: conceptualized the study, reviewed and revised the manuscript, and approved the final manuscript as submitted.

Allison Tong: conceptualized the study, carried out the data collection and analysis, coding of data, drafted the initial manuscript, and approved the final manuscript as submitted.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflicts of interest.

Informed consent

No informed consent was required for this systematic review.

Supplementary material

431_2017_3081_MOESM1_ESM.docx (110 kb)
ESM 1 (DOCX 109kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Lauren S. H. Chong
    • 1
    • 2
  • Dominic A. Fitzgerald
    • 3
    • 4
  • Jonathan C. Craig
    • 1
    • 2
  • Karine E. Manera
    • 1
    • 2
  • Camilla S. Hanson
    • 1
    • 2
  • David Celermajer
    • 5
    • 6
  • Julian Ayer
    • 4
    • 6
  • Nadine A. Kasparian
    • 6
    • 7
  • Allison Tong
    • 1
    • 2
  1. 1.Sydney School of Public HealthThe University of SydneySydneyAustralia
  2. 2.Centre for Kidney ResearchKids Research Institute, The Children’s Hospital at WestmeadSydneyAustralia
  3. 3.Respiratory MedicineThe Children’s Hospital at WestmeadWestmeadAustralia
  4. 4.Paediatrics and Child HealthThe Children’s Hospital at WestmeadWestmeadAustralia
  5. 5.Central Clinical SchoolThe University of SydneySydneyAustralia
  6. 6.Heart Centre for ChildrenThe Sydney Children’s Hospitals Network (Westmead and Randwick)SydneyAustralia
  7. 7.Discipline of Paediatrics, School of Women’s and Children’s Health, UNSW MedicineThe University of New South WalesKensingtonAustralia

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