Literature DB >> 10678785

Antimicrobial chemotherapy in the control of surgical infectious complications.

F de Lalla1.   

Abstract

In spite of the progress in surgical technique and antibiotic prophylaxis, postoperative infection still accounts for both the commonest surgical complication and one of the most frequent nosocomial infections, also causing an increase in duration and costs of hospital stay. The choice of treatment for post-surgical infections requires an understanding of the usual infecting flora, available antimicrobial agents, and susceptibility patterns. The most common organisms in simple wound infection are gram-positive cocci and mainly Staphylococcus aureus. Staphylococcus epidermidis and S. aureus (quite often methicillin-resistant strains) are the organisms which predominate in the infectious complications following clean surgical procedures with implantation of vascular grafts or prosthetic devices. Mixed aerobic and anaerobic flora are mainly responsible for cases of intra-abdominal and intra-pelvic postoperative infections: the most common aerobes are Enterobacteriaceae (Escherichia coli, Proteus spp., and others) and enterococci, and among anaerobes Bacteroides fragilis group prevails. Adequate drainage and surgical control of the source of infection, when needed, and adjunctive effective antimicrobial therapy are important factors in successful treatment of postoperative infections. Semisynthetic penicillinase-resistant penicillins and glycopeptides (vancomycin and teicoplanin) are the drugs of choice for the treatment of infections caused by penicillin-resistant methicillin-sensitive, and methicillin-resistant, respectively, S. aureus and S. epidermidis. For the treatment of intra-abdominal and intra-pelvic infections, animal and human studies support the recommendation that treatment should be directed against both gram-negative enteric and anaerobic bacteria. Combinations of aminoglycosides with clindamycin or metronidazole have been widely used with great success; however adverse reactions such as nephrotoxicity and ototoxicity have been a problem in some patients. In recent years monotherapy with either a carbapenem (imipenem/cilastatin or meropenem) or a penicillin/beta-lactamase inhibitor combination has been proposed. Among these combination antimicrobials, piperacillin combined with tazobactam is a very well designed formulation. Indeed, piperacillin is active against a broad range of gram-negative and gram-positive pathogens, and tazobactam is a potent beta-lactamase inhibitor which acts on a variety of clinically important plasmid and chromosomal beta-lactamases. This combination seems particularly attractive for the treatment of mixed polymicrobial anaerobic-aerobic infections such as intra-abdominal and intra-pelvic postoperative infections.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10678785     DOI: 10.1179/joc.1999.11.6.440

Source DB:  PubMed          Journal:  J Chemother        ISSN: 1120-009X            Impact factor:   1.714


  4 in total

1.  Antiangiogenic, antimicrobial, and cytotoxic potential of sponge-associated bacteria.

Authors:  Archana N Thakur; Narsinh L Thakur; Madhavi M Indap; Reena A Pandit; Vrushali V Datar; Werner E G Müller
Journal:  Mar Biotechnol (NY)       Date:  2005-03-24       Impact factor: 3.619

2.  TRPV1 regulators mediate gentamicin penetration of cultured kidney cells.

Authors:  Sigrid E Myrdal; Peter S Steyger
Journal:  Hear Res       Date:  2005-06       Impact factor: 3.208

3.  Cinnamon Oil and Chitosan Coating on Orthopaedic Implant Surface for Prevention of Staphylococcus Epidermidis Biofilm Formation.

Authors:  R Magetsari PhD; P Dewo PhD; B K Saputro Md; Z Lanodiyu Md
Journal:  Malays Orthop J       Date:  2014-11

4.  Antimicrobial Activity of Protein Fraction from Naja ashei Venom Against Staphylococcus epidermidis.

Authors:  Aleksandra Bocian; Ewa Ciszkowicz; Konrad K Hus; Justyna Buczkowicz; Katarzyna Lecka-Szlachta; Monika Pietrowska; Vladimír Petrilla; Monika Petrillova; Ľubomír Legáth; Jaroslav Legáth
Journal:  Molecules       Date:  2020-01-10       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.