Literature DB >> 26584153

Mortality from cystic fibrosis in Europe: 1994-2010.

Esther Quintana-Gallego1,2, Miguel Ruiz-Ramos3, Isabel Delgado-Pecellin4, Carmen Calero1,2, Joan B Soriano5, Jose Luis Lopez-Campos2,6.   

Abstract

OBJECTIVE: To date, available mortality trends due to cystic fibrosis (CF) have been limited to the analysis of certain countries in different parts of the world showing that mortality trends have been constantly decreasing. However, no studies have examined Europe as a whole. The present study aims to analyze CF mortality trends by gender within the European Union (EU) and to quantify potential years of life lost (PYLL).
DESIGN: Deaths from the 27 EU countries were obtained from the statistical office of the EU from the years 1994-2010. Crude and age-standardized mortality rates (ASR) were estimated for women and men using the standard European population, expressed in deaths per 1,000,000 persons. The PYLL from ages 0 up to 30 years were estimated. Trends were studied by a joinpoint regression analysis.
RESULTS: During the study period, 5,130 deaths (2,443 in males and 2,687 in females) were identified. Females had a slightly higher mortality rate than males, with a downward trend observed for both genders. In males, the ASR changed from 1.34 in 1994 to 1.03 in 2010. In females, the ASR changed from 1.42 in 1994 to 0.92 in 2010. The mean age at death and PYLL increased for both genders. The joinpoint analysis did not identify any significant joinpoint for either gender for ASR or PYLL.
CONCLUSIONS: Our data suggest a continued downward trend of CF mortality throughout the EU, with differences by country and gender.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  cystic fibrosis; epidemiology; mortality

Mesh:

Year:  2015        PMID: 26584153     DOI: 10.1002/ppul.23337

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  6 in total

Review 1.  Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis.

Authors:  Meike Hohwieler; Lukas Perkhofer; Stefan Liebau; Thomas Seufferlein; Martin Müller; Anett Illing; Alexander Kleger
Journal:  United European Gastroenterol J       Date:  2016-09-21       Impact factor: 4.623

2.  How are the ancient cystic fibrosis patients? Cystic fibrosis diagnosed over 60 years-old.

Authors:  C Prados; M Lerín; J J Cabanillas; L Gómez-Carrera; R Álvarez-Sala
Journal:  Respir Med Case Rep       Date:  2017-03-24

3.  Mortality Due to Cystic Fibrosis over a 36-Year Period in Spain: Time Trends and Geographic Variations.

Authors:  Ana Villaverde-Hueso; Germán Sánchez-Díaz; Francisco J Molina-Cabrero; Elisa Gallego; Manuel Posada de la Paz; Verónica Alonso-Ferreira
Journal:  Int J Environ Res Public Health       Date:  2019-01-04       Impact factor: 3.390

4.  Cardiac involvement in cystic fibrosis evaluated using cardiopulmonary magnetic resonance.

Authors:  Jakub Lagan; Josephine H Naish; Joshua Bradley; Christien Fortune; Charlie Palmer; David Clark; Erik B Schelbert; Matthias Schmitt; Rowland Bright-Thomas; Christopher A Miller
Journal:  Int J Cardiovasc Imaging       Date:  2022-01-07       Impact factor: 2.357

Review 5.  A Practical Approach to Glucose Abnormalities in Cystic Fibrosis.

Authors:  Gregory C Jones; Christopher A R Sainsbury
Journal:  Diabetes Ther       Date:  2016-10-17       Impact factor: 2.945

6.  Managing Cystic Fibrosis in Polish Healthcare.

Authors:  Marta Rachel; Stanisław Topolewicz; Andrzej Śliwczyński; Sabina Galiniak
Journal:  Int J Environ Res Public Health       Date:  2020-10-20       Impact factor: 3.390

  6 in total

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