Perception of Quality of Life by Primary Caregivers of Children with Congenital Zika Syndrome: a Cross-Sectional Study
- PMID: 39841322
- DOI: 10.1007/s10995-025-04057-y
Perception of Quality of Life by Primary Caregivers of Children with Congenital Zika Syndrome: a Cross-Sectional Study
Abstract
Objective: The study aimed to evaluate the quality of life (QoL) of caregivers of children diagnosed with CZS and to assess the association of findings with socioeconomic and CZS-associated variables.
Methods: This was a cross-sectional, quantitative study, carried out over three days of multidisciplinary care for patients with CZS. Sixty-four participants underwent a quality of life assessment using the World Health Organization Quality of Life questionnaire (WHOQOL-BREF) in Portuguese.
Results: Both groups of caregivers attributed regular scores for Global QoL, and all WHOQOL-BREF domains. Among caregivers of children with CZS, QoL correlated with three of the four WHOQOL-BREF domains (psychological health: rho = 0.49, p < 0.001; social relationships: rho = 0.28, p < 0.023; and environment: rho = 0.11, p < 0.006), while general health perception correlated with three other domains (physical health: rho = 0.49, p < 0.001; psychological health: rho = 0.31, p < 0.012; and social relationships: rho = 0.30, p < 0.016). The environment domain was associated with the level of education in this population (p < 0.001). Macular scarring and focal pigmentary retinal mottling were significantly associated with the physical environment (p = 0.039), negative feelings (p = 0.035), support and social aid (p = 0.020).
Conclusion: The present study demonstrates that the WHOQOL-BREF is an effective method to evaluate the general perception of QoL among caregivers of children with CZS. Our results also suggest that caregivers of children with CZS do not experience a reduced quality of life compared to caregivers of typically developing children.
Keywords: Caregivers; Craniofacial abnormalities; Microcephaly; Quality of life; Zika virus.
© 2025. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
Conflict of interest statement
Declarations. Conflict of interest: The authors declare that there is no conflict of interest. Ethical Approval: This study was performed in line with the principles of the Declaration of Helsinki. Approval was granted by the Ethics Committees of Federal University of Ceará (3.588.279) and Albert Sabin Children’s Hospital (4.985.603). Consent to Participate: Informed consent was obtained from all individual participants included in the study.
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References
-
- Abbasi, S., Sajedi, F., Hemmati, S., Najafi Fard, T., Azadchehr, M. J., & Poursadoghi, A. (2016). Evaluation of quality of life in mothers of children with down syndrome. Practice in Clinical Psychology, 4(2), 81–88. https://doi.org/10.15412/J.JPCP.06040202 - DOI
-
- Aslan, B. I., Gülşen, A., Tirank, ŞB., Findikçioğlu, K., Uzuner, F. D., Tutar, H., & Üçüncü, N. (2018). Family functions and life quality of parents of children with cleft lip and palate. The Journal of Craniofacial Surgery, 29(6), 1614–1618. https://doi.org/10.1097/SCS.0000000000004611 - DOI - PubMed
-
- Baker, S. R., Owens, J., Stern, M., & Willmot, D. (2009). Coping strategies and social support in the family impact of cleft lip and palate and parents’ adjustment and psychological distress. The Cleft Palate-Craniofacial Journal: Official Publication of the American Cleft Palate-Craniofacial Association, 46(3), 229–236. https://doi.org/10.1597/08-075.1 - DOI - PubMed
-
- Barros, A. L. O., de Gutierrez, G. M., Barros, A. O., & Santos, M. T. B. R. (2019). Quality of life and burden of caregivers of children and adolescents with disabilities. Special Care in Dentistry: Official Publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry, 39(4), 380–388. https://doi.org/10.1111/scd.12400 - DOI - PubMed
-
- Beluci, M. L., da Silva Demoro Mondini, C. C., Trettene, A. D. S., & Dantas, R. A. S. (2019). Correlation between quality of life and burden of family caregivers of infants with cleft lip and palate. Revista Da Escola De Enfermagem Da USP, 53, e03432. https://doi.org/10.1590/S1980-220X2017047603432 - DOI
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