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Economic Burden And Health-Related Quality Of Life Of Patients With Cystic Fibrosis In Bulgaria.
Iskrov, Georgi G; Stefanov, Rumen S; López-Bastida, Julio; Linertová, Renata; Oliva-Moreno, Juan; Serrano-Aguilar, Pedro.
Afiliação
  • Stefanov RS; Department of Social Medicine and Public Health, Faculty of Public Health, Medical University, Plovdiv, Bulgaria
  • López-Bastida J; Institute for Rare Diseases, Plovdiv, Bulgaria
  • Linertová R; University of Castilla-La Mancha, Talavera de la Reina, Toledo, Spain
  • Oliva-Moreno J; Red de Investigación en Servicios Sanitarios en Enfermedades Crónicas (REDISSEC), Spain
  • Serrano-Aguilar P; Red de Investigación en Servicios Sanitarios en Enfermedades Crónicas (REDISSEC), Spain
Folia Med (Plovdiv) ; 57(1): 56-64, 2015.
Article em En | MEDLINE | ID: mdl-26431096
OBJECTIVE: The aim of this study was to determine the economic burden from a societal perspective and health-related quality of life (HRQOL) of patients with cystic fibrosis (CF) in Bulgaria. MATERIALS AND METHODS: We conducted a cross-sectional study of 33 patients with CF and 17 caregivers from Bulgaria. Data on socio-demographic characteristics, health resource utilisation, informal care, labor productivity losses and HRQOL were collected from questionnaires completed by patients or their caregivers. HRQOL was evaluated with the EuroQol 5-domain (EQ-5D-3L) questionnaire. RESULTS: Median annual costs of CF in Bulgaria were € 24 152 per patient in 2012 as a reference year. Median annual costs for children were found to be significantly higher than those for adults - € 31 945 vs. € 15 714 (p = 0.012). This outcome came from statistically significant differences in costs for main informal carer (p < 0.001) and costs for other informal carers (p = 0.022). As a single cost item, drugs had the biggest monetary impact. Median annual drug costs were € 13 059. Bulgarian CF patients showed low HRQOL results - 50 median VAS score and 0.592 median health utilities. A quarter of patients even rated their health state as worse than death. CONCLUSION: CF patients from Eastern Europe remain a vulnerable population with risk factors for worse health outcomes. Our study provided a state-of-the art analysis that facilitates the elaboration, adoption and application of targeted public health policies to tackle CF-related problems at national and European level.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Fibrose Cística Tipo de estudo: Health_economic_evaluation / Observational_studies / Prevalence_studies / Qualitative_research / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Fibrose Cística Tipo de estudo: Health_economic_evaluation / Observational_studies / Prevalence_studies / Qualitative_research / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article