The quality of life of children with heart disease in Tanzania: a single center study
- PMID: 40448087
- PMCID: PMC12124094
- DOI: 10.1186/s12887-025-05761-y
The quality of life of children with heart disease in Tanzania: a single center study
Abstract
Background: The demand for surgical intervention for congenital heart disease (CHD) exceeds the available resources in low- and middle-income countries (LMICs). This has resulted in a growing population of children with CHD, with only few receiving surgery and many more waiting. Health-related quality of life (HRQoL) and its impact on the pediatric CHD population in these settings have been largely overlooked, and limited research has been conducted. Therefore, this study aimed to explore HRQoL in the pediatric CHD population in Tanzania by comparing unoperated and operated patients, thus bridging the knowledge gap.
Methods: This cross-sectional study included patients with CHD, 2 to 18 years old, without severe comorbidities, at the Jakaya Kikwete Cardiac Institute, either unoperated or operated, at least six months after cardiac surgery. Clinical and sociodemographic variables (scored 0 to 1, resp. poorest to highest) were collected. The Pediatric HRQoL Generic Core Scale (PedsQL™ 4.0 SF15, Swahili Version) provided HRQoL scores by parental report and self-report (5 years and above) for different domains (physical, social, emotional, and school). Questions were scored on a Likert linear analogue scale; higher scores indicated better HRQoL. The between-group scores were compared with Student's t test and the Mann‒Whitney U test. Generalized linear models were used to identify predictors of HRQoL.
Results: Mean age of the study group was 6.3 ± 3.7 years, with a slight female predominance (n = 110, 53.9%). Operated patients had a higher socioeconomic status score (0.71/1 vs. 0.66/1) and more frequent early diagnosis (< 1 year; 67.8% vs. 47.1%). The complexity of cardiac diagnosis (simple, moderate or complex) was significantly different between groups (p = 0.001). Parent-reported HRQoL scores were significantly higher for the post-operative group (90.8 ± 10.2 vs. 80.5 ± 16.7, p < 0.001), with the most noticeable difference in the physical domain (effect size d=-0.813, p < 0.001). Being post palliative or curative surgery and higher socioeconomic status were found to be significant predictors of better HRQoL. HRQoL significantly decreased with increasing severity of heart failure symptoms.
Conclusions: The HRQoL of operated Tanzanian children with CHD differed significantly from that of their unoperated counterparts. Reducing symptoms for those on the waiting list can improve their HQoL. In this setting, HQoL in children with CHD is strongly predicted and influenced by socioeconomic status, emphasizing the need for interventions to address socioeconomic disparities and improve patient outcomes.
Clinical trial number: Not applicable.
Keywords: Africa; Cardiac surgery; Congenital heart disease; Health-related quality of life; Lower-middle-income country.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was approved by the Ethics Committee of the Jakaya Kikwete Cardiac Institute (JKCI) (#AB.123/307/01H/40) and followed the ethical guidelines of the 1975 Declaration of Helsinki. All parents or legal guardians in the study signed a written informed consent before participation. As patients were minors, parental written consent and verbal assent of the child over four years of age were sufficient for participation after carefully explaining the study. The physical records are stored at the Jakaya Kikwete Cardiac Institute, Department of Pediatric Cardiology. Data was stored with encrypted personal information to secure patient confidentiality. Consent for publication: Not applicable. Competing interests: The authors declare no competing interests.
Figures
Similar articles
-
Health-related quality of life in surgical children and adolescents with congenital heart disease compared with their age-matched healthy sibling: a cross-sectional study from a lower middle-income country, Pakistan.Arch Dis Child. 2019 May;104(5):419-425. doi: 10.1136/archdischild-2018-315594. Epub 2018 Dec 15. Arch Dis Child. 2019. PMID: 30554150
-
Parental perceptions of disease-severity and health-related quality of life in school-age children with congenital heart disease.J Spec Pediatr Nurs. 2018 Jan;23(1). doi: 10.1111/jspn.12204. Epub 2017 Dec 20. J Spec Pediatr Nurs. 2018. PMID: 29266743
-
[Impact of the family socioeconomic status on health related quality of life in children operated on for congenital heart defects].Acta Med Croatica. 2010 Mar;64(1):9-16. Acta Med Croatica. 2010. PMID: 20653120 Croatian.
-
Health-related quality of life in congenital heart disease surgery in children and young adults: a systematic review and meta-analysis.Arch Dis Child. 2019 Apr;104(4):340-347. doi: 10.1136/archdischild-2017-313653. Epub 2018 Mar 23. Arch Dis Child. 2019. PMID: 29572215
-
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217. Cochrane Database Syst Rev. 2022. PMID: 36321557 Free PMC article.
References
-
- Van Der Linde D, et al. Birth prevalence of congenital heart disease worldwide: A systematic review and meta-analysis. J Am Coll Cardiol. 2011;58:2241–7. - PubMed
-
- Higashi H, Barendregt JJ, Kassebaum NJ, Weiser TG, Bickler SW, Vos T. The burden of selected congenital anomalies amenable to surgery in low and Middle-Income regions: cleft lip and palate, congenital heart anomalies and neural tube defects. Arch Dis Child. 2015;100(3):233–8. 10.1136/archdischild-2014-306175 - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous