268 Renal function impairment in cystic fibrosis
نویسندگان
چکیده
منابع مشابه
Renal impairment following aminoglycoside therapy in cystic fibrosis.
Cystic fibrosis (CF) is a chronic respiratory, life limiting illness in the Caucasian population. Chronic infection with Pseudomonas aeruginosa occurs in more than 80% of adults and this contributes to deterioration in lung function over time. A reported long term complication includes renal impairment from presumed cumulative aminoglycoside antibiotics. Aminoglycosides are highly effective aga...
متن کاملSexual Function in Cystic Fibrosis*
#{176}Fromthe Department of Psychiatry and the Cystic Fibrosis Center, Department of Pediatrics, Case Western Reserve University, and Rainbow Babies and Childrens Hospital, Cleveland. tAssociate Professor of Psychiatry. lAssociate Professor of Pediatrics. Supported in part by grant AM 08305 from the National Institutes of Health and by grants from the Rainbow Cystic Fibrosis Foundation and Unit...
متن کاملMaintaining Respiratory Health in Cystic Fibrosis Patients
Cystic fibrosis (CF) is an inherited disease that primarily affects the lungs and the digestive system, however, it also affects a number of other organs and systems. More than 90% of mortality of CF patients is due to lung complications. Healthy lungs are important for a long life for people with CF, We will discuss two important topics for maintaining respiratory health. Chronic use of drug...
متن کاملPrevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran
Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common mutations in CF patients and to assess its possible relationship with clinical presentations. Materials and Methods: This cross sectional study was conducted on 36 CF patients who were referred to a tertiary ped...
متن کاملLung function in infants with cystic fibrosis.
Lung function was measured in 28 infants with cystic fibrosis and repeated in 17 of the infants during the first year of life. Thoracic gas volume (TGV) and specific airway conductance (sGaw) were measured plethysmographically and maximum forced expiratory flow at functional residual capacity (VmaxFRC) was derived from the partial expiratory flow-volume curve. At the time of the initial evaluat...
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ژورنال
عنوان ژورنال: Journal of Cystic Fibrosis
سال: 2013
ISSN: 1569-1993
DOI: 10.1016/s1569-1993(13)60409-9