Cefpirome and cefepime are two fourth-generation cephalosporins recently introduced in Brazil. They have a very similar range of in vitro antimicrobial activity, but some differences have been noticed. The goal of this study was to compare the in vitro activity of cefpirome and cefepime against bacterial samples isolated in Brazilian hospitals. We studied 931 samples taken from hospitalized patients between April and June, 1998. The minimum inhibitory concentration (MIC) was determined by the Etest method. The potency of cefpirome was similar to that of cefepime, except against enterococci and coagulase-negative staphylococci, where cefpirome proved 2-fold more potent. The MIC(90) for cefepime were inferior to cefpirome in response to Klebsiella pneumoniae (MIC(90), 24 and 96µg/mL, respectively), Pseudomonas aeruginosa (MIC(90), 48 and 128µg/mL, respectively), and other Gram-negative organisms (MIC(90), 64 and 256µg/mL, respectively). Despite the fact that cefpirome presented a slightly broader range of action against Gram-positive bacteria (90% sensitive vs. 78% sensitive to cefepime), and that cefepime presented an equally broad range against Gram-negative bacteria (74% sensitive vs. 65% sensitive to cefpirome), these differences were not considered clinically significant because the sensitivity differed in MIC by less than 2 dilutions. Only 16 (1.7%) of the 931 samples tested showed a significant difference in sensitivity. This study suggests that, except for Acinetobacter sp. and P. aeruginosa, laboratories may routinely test only cefpirome and apply the same category result to cefepime. Since category discrepancies are very rare and cefpirome is slightly less active than cefepime against Enterobacteriaceae, isolates susceptible to cefepime will certanly also be susceptible to cefpirome. To optimize the treatment of severely infected patients, especially where species such as Acinetobacter sp and P. aeruginosa are involved, we recommend that both cephalosporins be tested by using the same susceptibility test method to determine the MIC.
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Ann Clin Microbiol Antimicrob
September 2023
Department of Microbiology and Immunology, Faculty of Pharmacy (Girls), El-Azhar University, Cairo, Egypt.
Background: Klebsiella pneumoniae is a significant healthcare-associated pathogen. We investigated the antimicrobial interaction pattern between zinc sulfate and antibiotics against K. pneumoniae biofilm on the phenotypic and genotypic levels.
View Article and Find Full Text PDFPharmaceuticals (Basel)
September 2020
Department of Chemical Engineering, Universitat Politecnica de Catalunya. ETSEIB. Av. Diagonal, 647, 08028 Barcelona, Spain.
Angiotensin converting enzyme 2 (ACE2) downregulation is a key negative factor for the severity of lung edema and acute lung failure observed in patients infected with SARS-CoV-2. ACE2 downregulation affects the levels of diverse peptide mediators of the renin-agiotensin-aldestosterone and kallikrein-kinin systems, compromising vascular hemostasis. Increasing evidence suggests that the inflammatory response observed in covid-19 patients is initiated by the action of kinins on the bradykinin receptors.
View Article and Find Full Text PDFAntimicrob Agents Chemother
May 2020
Division of Infectious Diseases, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan
Carbapenems are currently the preferred agents for the treatment of serious infections. However, whether cefepime-cefpirome can be used to treat an bloodstream infection (BSI) if it is active against the causative pathogen(s) is not clear. This study aimed to compare the efficacy of cefepime-cefpirome and carbapenem monotherapy in patients with BSI.
View Article and Find Full Text PDFJ Assoc Physicians India
April 2019
Director-Professor, Department of Microbiology, ESIC Medical College, Faridabad, Haryana; *Corresponding Author.
Background: Antibiotic resistance to multiple antibiotics among P aeruginosa are on rise due to acquisition of various beta-lactamase enzymes. P aeruginosa possessing such enzymes can cause major break down in therapy and are responsible for substantial clinical challenges.
Objectives: To know the antibiotic susceptibility pattern, common resistance mechanisms of P aeruginosa and document baseline antibiotic resistance data to implement effective infection control program.
Antimicrob Agents Chemother
June 2019
Department of Microbiology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
A novel VIM-type metallo-β-lactamase variant, VIM-60, was identified in multidrug-resistant clinical isolates in Japan. Compared with VIM-2, VIM-60 had two amino acid substitutions (Arg228Leu and His252Arg) and higher catalytic activities against fourth-generation cephalosporins. The genetic context for was - on the chromosome.
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