Double-blind, prospective, multicenter trial comparing ceftazidime with moxalactam in the treatment of serious gram-negative infections
- 1 July 1986
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 30 (1) , 90-95
- https://doi.org/10.1128/aac.30.1.90
Abstract
Ceftazidime is a new antimicrobial agent possessing excellent in vitro activity against most members of the family Enterobacteriaceae and against Pseudomonas aeruginosa. We conducted a double-blind, prospective, multicenter trial to compare ceftazidime with moxalactam in the treatment of serious gram-negative infections. The overall favorable response rates for the two regimens were similar (93 of 106 [88%] and 84 of 97 [86%], respectively). Among these, the response rates of the 56 gram-negative bacteremias and the 23 P. aeruginosa infections were comparable. Both groups had similar incidences of subsequent infections with P. aeruginosa, enterococci, and yeasts. A total of 13% of the patients in the moxalactam group developed a prolonged prothrombin time (P less than 0.01), and three patients demonstrated clinical bleeding. These results suggest that although the overall efficacy of both regimens was similar, treatment with moxalactam resulted in a higher incidence of prolongation of prothrombin time with an attendant risk of bleeding. In nonneutropenic patients, ceftazidime as a single agent is safe and effective in gram-negative bacillary infections.This publication has 18 references indexed in Scilit:
- Production of Menaquinones by Intestinal AnaerobesThe Journal of Infectious Diseases, 1984
- Hypoprothrombinemia in Febrile, Neutropenic Patients with Cancer: Association with Antimicrobial Suppression of Intestinal MicrofloraThe Journal of Infectious Diseases, 1984
- Clinical efficacy of ceftazidime. Treatment of serious infection due to multiresistant Pseudomonas and other gram-negative bacteriaArchives of internal medicine (1960), 1984
- Use of ceftazidime in the therapy of serious infections, including those due to multiresistant organismsAntimicrobial Agents and Chemotherapy, 1983
- Oral or Intravenous Trimethoprim-Sulfamethoxazole Therapy for ShigellosisClinical Infectious Diseases, 1982
- Comparative antipseudomonal activity of some newer beta-lactam agentsAntimicrobial Agents and Chemotherapy, 1982
- Moxalactam therapy of infections caused by cephalothin-resistant bacteria: influence of serum inhibitory activity on clinical response and acquisition of antibiotic resistance during therapyAntimicrobial Agents and Chemotherapy, 1981
- The combination of pivmecillinam and pivampicillin in the treatment of acute enteric feverJournal of Antimicrobial Chemotherapy, 1981
- Double-Blind Comparison of the Nephrotoxicity and Auditory Toxicity of Gentamicin and TobramycinNew England Journal of Medicine, 1980
- Comparative Activities of the Oxa-β-Lactam LY127935, Cefotaxime, Cefoperazone, Cefamandole, and Ticarcillin Against Multiply Resistant Gram-Negative BacilliAntimicrobial Agents and Chemotherapy, 1980