دورية أكاديمية

Imipenem/cilastatin (1.5 g daily) versus meropenem (3.0 g daily) in patients with intra-abdominal infections: results of a prospective, randomized, multicentre trial.

التفاصيل البيبلوغرافية
العنوان: Imipenem/cilastatin (1.5 g daily) versus meropenem (3.0 g daily) in patients with intra-abdominal infections: results of a prospective, randomized, multicentre trial.
المؤلفون: Basoli A; Department of Surgery, Università degli Studi La Sapienza, Policlinico Umberto I., Rome, Italy., Meli EZ, Mazzocchi P, Speranza V
المصدر: Scandinavian journal of infectious diseases [Scand J Infect Dis] 1997; Vol. 29 (5), pp. 503-8.
نوع المنشور: Clinical Trial; Comparative Study; Journal Article; Multicenter Study; Randomized Controlled Trial
اللغة: English
بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 0215333 Publication Model: Print Cited Medium: Print ISSN: 0036-5548 (Print) Linking ISSN: 00365548 NLM ISO Abbreviation: Scand J Infect Dis Subsets: MEDLINE
أسماء مطبوعة: Publication: 2007-2014 : London : Informa Healthcare
Original Publication: Stockholm, Society for the Publication of Acta medica Scandinavica.
مواضيع طبية MeSH: Abdomen*, Anti-Bacterial Agents/*therapeutic use , Bacterial Infections/*drug therapy , Cilastatin/*therapeutic use , Imipenem/*therapeutic use , Protease Inhibitors/*therapeutic use , Thienamycins/*therapeutic use, APACHE ; Adult ; Aged ; Anti-Bacterial Agents/administration & dosage ; Cilastatin/administration & dosage ; Female ; Humans ; Imipenem/administration & dosage ; Infusions, Intravenous ; Male ; Meropenem ; Middle Aged ; Prospective Studies ; Protease Inhibitors/administration & dosage ; Thienamycins/administration & dosage ; Treatment Outcome
مستخلص: An open-label prospective, randomized, parallel multicentre study was undertaken to compare the efficacy and tolerability of 1.5 g/day intravenous imipenem/cilastatin with 3 g/day intravenous meropenem in the treatment of intra-abdominal infections. A total of 287 patients were enrolled: 201 patients, divided between the 2 treatment groups, were evaluable. Clinical outcome, bacteriological outcome, untoward microbiological effects, and clinical and laboratory adverse experiences were evaluated. 98% of patients receiving imipenem/cilastatin therapy were cured, with 96% showing eradication of infection. 95% of those on meropenem were cured, with 98% showing eradication. These differences in clinical and bacteriological outcome between the 2 treatments were not statistically significant. Two patients receiving imipenem/cilastatin and 5 receiving meropenem had untoward microbiological effects. There was a 0.7% frequency (1/139 patients) of possibly or probably drug-related clinical or laboratory adverse experiences with imipenem/cilastatin and a 2.7% frequency (4/148) with meropenem. The mean time to defervescence was significantly less for patients in the imipenem/cilastatin treatment group than for those receiving meropenem. This study shows that 1.5 g/day of imipenem/cilastatin is equivalent to 3.0 g/day meropenem in clinical and bacteriological outcome, as well as in incidence of side effects.
المشرفين على المادة: 0 (Anti-Bacterial Agents)
0 (Protease Inhibitors)
0 (Thienamycins)
141A6AMN38 (Cilastatin)
71OTZ9ZE0A (Imipenem)
FV9J3JU8B1 (Meropenem)
تواريخ الأحداث: Date Created: 19970101 Date Completed: 19980203 Latest Revision: 20181201
رمز التحديث: 20240627
DOI: 10.3109/00365549709011863
PMID: 9435041
قاعدة البيانات: MEDLINE
الوصف
تدمد:0036-5548
DOI:10.3109/00365549709011863