Affiliation:
1. Department of Pediatric Nephrology, Celal Bayar University School of
Medicine, Manisa, Turkey
2. Pediatric Nephrology, Aksaray Training and Research Hospital,
Department of Paediatric Nephrology, Aksaray, Turkey
3. Department of Child and Adolescent Psychiatry, Celal Bayar University
School of Medicine, Manisa, Turkey
Abstract
Abstract
Background Familial Mediterranean fever (FMF) is a chronic disease
characterized by recurrent episodes of fever and polyserositis. This study aimed
to assess children’s quality of life (QoL), as reported by children and their
parents, and to compare the results according to clinical variables.
Material and Methods The study examined 107 children with FMF, evaluating
their demographic and genetic data, utilizing the Pediatric Quality of Life
Inventory (PedsQL) to assess QoL, and comparing scores based on disease
severity.
Results The severity of FMF is inversely correlated with QoL scores, with
mild cases having the highest scores (97±4), followed by moderate (76±11) and
severe cases (52±10.3) (p<0,001). Disease severity, treatment adherence,
healthcare utilization, genetic mutations, family income, and maternal age at
birth all significantly impact perceived quality of life in FMF patients
(p<0,001). Additionally, parents reported lower QoL for children with FMF who
experienced various adverse factors such as low family income, household
smoking, frequent attacks, hospitalizations, irregular medication use, and low
maternal education levels (p<0,001).
Conclusion Children’s daily activities, academic performance, and family
functioning are all significantly impacted by FMF. Physicians caring for
patients with FMF should be aware of the QoL changes in the management of these
patients. As a result, medical therapy, patient education, and indicators of
psychological and social support can all be offered more effectively.