Risk factors for rate of decline in FEV(1) in adults with cystic fibrosis |
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Authors: | Konstan Michael W Wagener Jeffrey S Vandevanter Donald R Pasta David J Yegin Ashley Rasouliyan Lawrence Morgan Wayne J |
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Affiliation: | Case Western Reserve University School of Medicine and Rainbow Babies and Children's Hospital, 11100 Euclid Avenue, Cleveland, OH 44106. Electronic address: Michael.Konstan@UHhospitals.org. |
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Abstract: | BackgroundPreviously we assessed risk factors for FEV1 decline in children and adolescents using the Epidemiologic Study of Cystic Fibrosis (J Pediatr 2007;151:134–139); the current study assessed risk factors in adults.MethodsRisk factors for FEV1 decline over 3–5.5 years for ages 18–24 and ≥ 25 years were assessed using mixed-model regression.ResultsMean rates of FEV1 decline (% predicted/year) were − 1.92 for ages 18-24y (n = 2793) and − 1.45 for ages ≥ 25y (n = 1368). For the 18-24y group, B. cepacia, pancreatic enzyme use, multidrug-resistant P. aeruginosa, cough, mucoid P. aeruginosa, and female sex predicted greater decline; low baseline FEV1 and sinusitis predicted less decline. For the ≥ 25y group, only pancreatic enzyme use predicted greater decline; low baseline FEV1 and sinusitis predicted less decline.ConclusionsRisk factors for FEV1 decline in adults < 25 years are similar to those previously identified in children and adolescents; older adults had few statistically significant risk factors. |
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