Literature DB >> 16103664

Current guidelines for the treatment of severe pneumonia and sepsis.

K F Bodmann1.   

Abstract

UNLABELLED: Infections in intensive care unit (ICU) patients like severe pneumonia, e.g. nosocomial (NP) and community-acquired pneumonia (CAP), or septicemia must be treated promptly and effectively because of the ensuing high mortality. Treatment is thus empirical and starts before the results of microbiological cultures are known. The risk factors affecting mortality include severity of illness, virulence of etiologic pathogens and the use of inappropriate antibiotic therapy. Several studies have shown that modifying initially inadequate therapy, according to microbiological results, does not result in a better outcome. Due to this, antibiotic treatment requires agents which have an appropriate spectrum covering the likely pathogens causing these infections. In critically ill patients, the need for empirical first-line treatment covering a broad spectrum of Gram-negative and Gram-positive bacteria, as recommended in international guidelines (e.g. those of the American Thoracic Society or the Infectious Diseases Society of America), is justified in the presence of resistant organisms commonly documented in these patients. To choose an appropriate, initial antibiotic regimen, local and national resistance data have to be considered. With respect to new German resistance trends in Gram-negative and Gram-positive bacteria, the Paul Ehrlich Society of Chemotherapy has recently published guidelines for the treatment of infections in hospitalized patients. Especially in ICU patients with severe pneumonia (NP or CAP) or septicemia and risk factors like underlying diseases, antibiotic pretreatment or mechanical ventilation, agents with an appropriate spectrum encompassing Pseudomonas aeruginosa as well as other Gram-negative bacteria like Escherichia coli, Klebsiella spp., Enterobacter spp. and Gram-positive bacteria (e.g. Staphylococcus aureus, pneumococci and streptococci) are recommended as treatment of choice. Combination therapy with an anti-pseudomonal beta-lactam and a fluoroquinolone or an aminoglycoside are recommended for these patients to provide the necessary spectrum of activity and to prevent the emergence of resistant organisms. On the other hand, clinical trials and meta-analyses have shown the efficacy, tolerability and cost-effectiveness of monotherapy regimens even in critically ill and immunocompromised patients.
CONCLUSION: Appropriate beta-lactam antibiotics recommended in international and German guidelines for the treatment of severe CAP, NP and septicemia, either as monotherapy or as combination therapy, are the 4th generation cephalosporin cefepime, the carbapenems imipenem and meropenem, and the acylamino-beta-lactamase inhibitor combination piperacillin-tazobactam.

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Year:  2005        PMID: 16103664     DOI: 10.1159/000087452

Source DB:  PubMed          Journal:  Chemotherapy        ISSN: 0009-3157            Impact factor:   2.544


  18 in total

1.  In vivo pharmacodynamic activity of tomopenem (formerly CS-023) against Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus in a murine thigh infection model.

Authors:  Kiyoshi Sugihara; Chika Sugihara; Yoko Matsushita; Naotoshi Yamamura; Mitsutoshi Uemori; Akane Tokumitsu; Harumi Inoue; Masayo Kakuta; Eiko Namba; Hatsumi Nasu; Tetsufumi Koga
Journal:  Antimicrob Agents Chemother       Date:  2010-10-04       Impact factor: 5.191

2.  S-nitrosothiol tethered polymer hexagons: synthesis, characterisation and antibacterial effect.

Authors:  S Priya; R Nithya; Sheela Berchmans
Journal:  J Mater Sci Mater Med       Date:  2013-08-31       Impact factor: 3.896

3.  A Multicenter Evaluation of Off-Label Medication Use and Associated Adverse Drug Reactions in Adult Medical ICUs.

Authors:  Pamela L Smithburger; Mitchell S Buckley; Mark A Culver; Sarah Sokol; Ishaq Lat; Steven M Handler; Levent Kirisci; Sandra L Kane-Gill
Journal:  Crit Care Med       Date:  2015-08       Impact factor: 7.598

4.  MALDI-ToF short incubation identification from blood cultures is associated with reduced length of hospitalization and a decrease in bacteremia associated mortality.

Authors:  J A Delport; A Strikwerda; A Armstrong; D Schaus; M John
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2017-01-20       Impact factor: 3.267

5.  [Severe bacterial infection: increased mortality in elderly women with low body weight taking drugs prolonging the QTc interval].

Authors:  S Suefke; H Djonlagić; T Kibbel
Journal:  Med Klin Intensivmed Notfmed       Date:  2012-04-29       Impact factor: 0.840

6.  Eradication of Pathogenic Bacteria by Remote Delivery of Nitric Oxide via Light-Triggering of Nitrosyl-Containing Materials.

Authors:  Genevieve M Halpenny; Kavita R Gandhi; Pradip K Mascharak
Journal:  ACS Med Chem Lett       Date:  2010-01-01       Impact factor: 4.345

7.  Incidence and outcome of sepsis in Japanese intensive care units: The Japanese nosocomial infection surveillance system.

Authors:  Machi Suka; Katsumi Yoshida; Jun Takezawa
Journal:  Environ Health Prev Med       Date:  2006-11       Impact factor: 3.674

8.  Comparison of biophysical and biologic properties of alpha-helical enantiomeric antimicrobial peptides.

Authors:  Yuxin Chen; Adriana I Vasil; Linda Rehaume; Colin T Mant; Jane L Burns; Michael L Vasil; Robert E W Hancock; Robert S Hodges
Journal:  Chem Biol Drug Des       Date:  2006-02       Impact factor: 2.817

Review 9.  Carbapenems versus other beta-lactams in treating severe infections in intensive care: a systematic review of randomised controlled trials.

Authors:  S J Edwards; M J Clarke; S Wordsworth; C E Emmas
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2008-03-29       Impact factor: 3.267

10.  Use of in vitro critical inhibitory concentration, a novel approach to predict in vivo synergistic bactericidal effect of combined amikacin and piperacillin against Pseudomonas aeruginosa in a systemic rat infection model.

Authors:  Eli Chan; Shufeng Zhou; Sahasranaman Srikumar; Wei Duan
Journal:  Pharm Res       Date:  2006-03-29       Impact factor: 4.200

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