Iranian Journal of Pediatrics
Tehran University of Medical Sciences Press
Vol. 23, No. 2, 2013, pp. 149-153
Bioline Code: pe13027
Full paper language: English
Document type: Research Article
Document available free of charge
Iranian Journal of Pediatrics, Vol. 23, No. 2, 2013, pp. 149-153
© Copyright 2013 - Iran Journal of Pediatrics
Quality of Life in Cystic Fibrosis Children|
Kianifar, Hamid-Reza; Bakhshoodeh, Banafsheh; Hebrani, Paria & Behdani, Fatemeh
Objective: Cystic fibrosis (CF) is a chronic, multisystem genetic disease with a wide variability in clinical
severity. The measurement of quality of life in CF provides additional information about the impact of this
disease. This article tries to assess quality of life (QoL) in children and adolescents with CF and to compare it
with control group.
Methods: Patients 2-18 years old with admission diagnosis of cystic fibrosis entered the study. QoL was
observed in CF patients and compared with control group.
Findings: Based on children's reports, significant differences between the CF patients and control group were
noted for emotional, physical, social, school performance, and total scores (P<0.05). Based on parents' reports,
quality of life score in CF patients from the physical point of view as well as social and total scores were
Conclusion: QoL in CF patients seems to be low, and therapy programs should take into account the
suggestive perceived quality of life.
Cystic fibrosis; Quality of life; Child; Adolescence
Alternative site location: http://diglib.tums.ac.ir/pub/