Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 May 30;25(1):436.
doi: 10.1186/s12887-025-05761-y.

The quality of life of children with heart disease in Tanzania: a single center study

Affiliations

The quality of life of children with heart disease in Tanzania: a single center study

Joëlle R Koster et al. BMC Pediatr. .

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.

PubMed Disclaimer

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

Fig. 1
Fig. 1
Distribution of age groups for unoperated (green) and operated (blue) children

Similar articles

References

    1. 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
    1. Zimmerman MS, et al. Global, regional, and National burden of congenital heart disease, 1990–2017: a systematic analysis for the global burden of disease study 2017. Lancet Child Adolesc Heal. 2020;4:185–200. - PMC - PubMed
    1. Hoffman J. I. review Article the global burden of congenital heart disease. Cardiovasc J Afr. 2013;24:141–5. - PMC - PubMed
    1. Dominique Vervoort H, Jin F, Edwin RK, Kumar M, Malik N, Tapaua A, Verstappen BS. Hasan,Global access to comprehensive care for pediatricpediatric and congenital heart disease,cjc pediatric and congenital heart disease,2, Issue 6, Part B, 2023,Pages 453–463,ISSN 2772–8129. - PMC - PubMed
    1. 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

LinkOut - more resources