Pediatric Liver Transplantation: Caregivers’ Quality of Life
10.5223/pghn.2022.25.6.489
- Author:
Ana Paula BASTOS TAVARES
1
;
Lucas Belém Pessôa de MELO GUERRA SEIXAS
;
Caren Lopes Wanderlei JAYME
;
Gilda PORTA
;
Renata Belém Pessôa de MELO SEIXAS
;
Elisa de CARVALHO
Author Information
1. Department of Pediatric Gastroenterology, Brasília José de Alencar Children’s Hospital, Brasília, Brazil
- Publication Type:Original Article
- From:Pediatric Gastroenterology, Hepatology & Nutrition
2022;25(6):489-499
- CountryRepublic of Korea
- Language:English
-
Abstract:
Purpose:The survival rate of pediatric patients undergoing liver transplantation has increased considerably. Despite this, the period after transplantation is still complex and poses several challenges to the recipient’s family, which is responsible for care management. Recently, more attention has been paid to the impact of this complex procedure on the quality of life of caregivers. Hence, this study is aimed at assessing the quality of life of caregivers of patients who have undergone liver transplantation and the aspects that influence it.
Methods:This was an observational and cross-sectional study. From November 2020 to January 2021, short-form-36 questionnaires and additional questions were given to the main caregivers of children and adolescents who underwent pediatric liver transplantation.
Results:Thirty-eight questionnaires were completed and the results revealed a lower quality of life in comparison to Brazilian standards, primarily in the mental domains (41.8±14.1 vs. 51.1±2.8; p<0.001). It did not show a significant association with socioeconomic or transplant-related factors, but it did show a negative impact on parents’ perception of the child’s health. Parents who reported worse health status for their children had a lower mental quality of life (44.1±13.8 vs. 33.3±12.6; p<0.05).
Conclusion:The caregivers of transplanted children have a lower quality of life than those of the local population. Psychological assistance should be routinely provided to parents for long-term follow-up to mitigate potential negative effects on the transplanted child’s care.
