[Bronchial diffusion of new anti-pseudomonal beta-lactams. Clinical significance]. 1984

E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern

In treating severe respiratory infections due to Pseudomonas aeruginosa and in patients with cystic fibrosis, new anti-pseudomonal beta-lactams constitute a good alternative to the traditional aminoglycoside antibiotic therapy. Among several criteria for the choice of an antibiotic, estimation of intrabronchial levels is to be taken into account. The authors report the results of the study of a new semi-synthetic penicillin, apalcillin, and two cephalosporins (cefsulodin, ceftazidime), active in vitro against Pseudomonas; their penetration into respiratory secretions was evaluated in 48 patients, intubated, tracheostomized, or undergoing fiberoptic bronchoscopy. Antibiotic concentrations were measured by the microbiological procedure. Bronchial penetration of apalcillin was early and noticeable, reaching a bronchial peak representing 20% of the simultaneous seric concentration. The local levels of cefsulodin and of ceftazidime did not differ from those achieved with cephalosporins studied previously; the bronchial peak reached 5,6 micrograms/ml for both drugs 2 hours after administration; this bronchial level corresponded to 15 to 20% of the serum concentration. The clinical response could not be evaluated due to the severe underlying pathology which compromised the outcome of the disease in the patients of this study. However, at least for apalcillin, a significant correlation was noted between bronchial levels, susceptibility of bacteria isolated in patients, and eradication of susceptible organisms.

UI MeSH Term Description Entries
D007700 Kinetics The rate dynamics in chemical or physical systems.
D011552 Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. Infections, Pseudomonas,Pseudomonas aeruginosa Infection,Infection, Pseudomonas,Pseudomonas Infection,Pseudomonas aeruginosa Infections
D001980 Bronchi The larger air passages of the lungs arising from the terminal bifurcation of the TRACHEA. They include the largest two primary bronchi which branch out into secondary bronchi, and tertiary bronchi which extend into BRONCHIOLES and PULMONARY ALVEOLI. Primary Bronchi,Primary Bronchus,Secondary Bronchi,Secondary Bronchus,Tertiary Bronchi,Tertiary Bronchus,Bronchi, Primary,Bronchi, Secondary,Bronchi, Tertiary,Bronchus,Bronchus, Primary,Bronchus, Secondary,Bronchus, Tertiary
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000900 Anti-Bacterial Agents Substances that inhibit the growth or reproduction of BACTERIA. Anti-Bacterial Agent,Anti-Bacterial Compound,Anti-Mycobacterial Agent,Antibacterial Agent,Antibiotics,Antimycobacterial Agent,Bacteriocidal Agent,Bacteriocide,Anti-Bacterial Compounds,Anti-Mycobacterial Agents,Antibacterial Agents,Antibiotic,Antimycobacterial Agents,Bacteriocidal Agents,Bacteriocides,Agent, Anti-Bacterial,Agent, Anti-Mycobacterial,Agent, Antibacterial,Agent, Antimycobacterial,Agent, Bacteriocidal,Agents, Anti-Bacterial,Agents, Anti-Mycobacterial,Agents, Antibacterial,Agents, Antimycobacterial,Agents, Bacteriocidal,Anti Bacterial Agent,Anti Bacterial Agents,Anti Bacterial Compound,Anti Bacterial Compounds,Anti Mycobacterial Agent,Anti Mycobacterial Agents,Compound, Anti-Bacterial,Compounds, Anti-Bacterial
D047090 beta-Lactams Four-membered cyclic AMIDES, best known for the PENICILLINS based on a bicyclo-thiazolidine, as well as the CEPHALOSPORINS based on a bicyclo-thiazine, and including monocyclic MONOBACTAMS. The BETA-LACTAMASES hydrolyze the beta lactam ring, accounting for BETA-LACTAM RESISTANCE of infective bacteria. beta-Lactam,4-Thia-1-Azabicyclo(3.2.0)Heptanes,4-Thia-1-Azabicyclo(4.2.0)Octanes,beta Lactam,beta Lactams

Related Publications

E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
November 2010, The Cochrane database of systematic reviews,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
April 2023, Open forum infectious diseases,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
June 2023, Open forum infectious diseases,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
April 2006, Bioorganic & medicinal chemistry letters,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
January 1984, Antonie van Leeuwenhoek,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
October 2006, Current opinion in pharmacology,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
September 1991, The Journal of antimicrobial chemotherapy,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
January 2021, The Journal of antimicrobial chemotherapy,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
December 1975, Helvetica chimica acta,
E Bergogne-Berezin, and J Pierre, and G Berthelot, and H Kafe, and P Even, and C Gibert, and D Safran, and M Stern
April 1977, Journal of the American Chemical Society,
Copied contents to your clipboard!