کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4209528 1280487 2008 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Efficacy and safety of intravenous meropenem and tobramycin versus ceftazidime and tobramycin in cystic fibrosis
موضوعات مرتبط
علوم پزشکی و سلامت پزشکی و دندانپزشکی پزشکی ریوی و تنفسی
پیش نمایش صفحه اول مقاله
Efficacy and safety of intravenous meropenem and tobramycin versus ceftazidime and tobramycin in cystic fibrosis
چکیده انگلیسی

BackgroundCystic fibrosis (CF) is characterized by chronic bacterial broncho-pulmonary infection. Although intravenous (IV) antibiotic therapy is regarded as standard treatment in CF, only few randomised trials comparing different antibiotic compounds exist.MethodsWe report on a prospective multicenter interventional trial of IV meropenem (120 mg/kg/day) or IV ceftazidime (200–400 mg/kg/day), each administered together with IV tobramycin (9–12 mg/kg/day). Outcome measures were changes in lung function, microbiological sputum burden and blood inflammatory marker. Liver and renal function values were measured to assess safety.ResultsOne hundred eighteen patients (59/59) were included into the study with the following indications: first infection of P. aeruginosa (n = 6), acute pulmonary exacerbation (n = 34) and suppression therapy of chronic P. aeruginosa colonization (n = 78). Both treatments improved lung function measures, bacterial sputum burden and CRP levels with no differences between treatment groups observed. A significant higher elevation for alkaline phosphatase (p < 0.0001) was observed for patients in the meropenem/tobramycin group.ConclusionsIV antibiotic therapy in CF patients with meropenem/tobramycin is as effective as with ceftazidime/tobramycin regarding lung function, microbiological sputum burden and systemic inflammatory status. Hepato-biliary function should be monitored carefully during IV treatment, possibly important in CF patients with pre-existing liver disease.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Cystic Fibrosis - Volume 7, Issue 2, March 2008, Pages 142–146
نویسندگان
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