Literature DB >> 21923444

Monotherapy or combination therapy? The Pseudomonas aeruginosa conundrum.

Kristi A Traugott1, Kelly Echevarria, Pamela Maxwell, Kay Green, James S Lewis.   

Abstract

Abstract The use of combination antibiotic therapy for severe pseudomonal infections is a standard practice in many hospitals; however, the data supporting its use are somewhat unclear. Possible benefits of combination therapy for Pseudomonas aeruginosa infections include in vitro antibiotic synergy, prevention of the emergence of bacterial resistance while receiving therapy, and improved adequacy of empiric therapy. Unfortunately, the potential disadvantages are also considerable, the most worrisome of which are drug toxicity and creation of multidrug-resistant organisms in the environment. Many in vitro and animal studies have attempted to shed light on this clinically challenging issue; however, these studies have often yielded conflicting results and used different study methods, which limits the clinical utility of the results. Clinical studies have also attempted to clarify this issue, particularly in patients with serious pseudomonal infections such as bacteremia and ventilator-associated pneumonia, but again, often resulted in conflicting conclusions. Thus, we performed a MEDLINE search (1950-May 2010) of clinical and in vitro studies evaluating the use of antibiotic combination therapy and monotherapy for bacteremia and pneumonia due to P. aeruginosa. Although a clear answer still eludes this controversy, combination therapy for seriously ill patients suspected of having pseudomonal infection has been shown, with considerable evidence, to improve the likelihood of an active agent being included in the initial antibiotic regimen of these patients. The clinical status of the patient and true likelihood of encountering a multidrug-resistant organism should be evaluated before deciding on empiric combination therapy. Future research may be able to better identify which patient populations might receive the most benefit from combination therapy rather than using combination therapy for everyone at risk for these infections.

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Year:  2011        PMID: 21923444     DOI: 10.1592/phco.31.6.598

Source DB:  PubMed          Journal:  Pharmacotherapy        ISSN: 0277-0008            Impact factor:   4.705


  24 in total

1.  Community acquired Pseudomonas pneumonia in an immune competent host.

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2.  Ceftolozane/tazobactam for febrile UTI due to multidrug-resistant Pseudomonas aeruginosa in a patient with neurogenic bladder.

Authors:  Aurélien Dinh; Benjamin Davido; Ruxandra Calin; Julie Paquereau; Clara Duran; Frédérique Bouchand; Véronique Phé; Emmanuel Chartier-Kastler; Martin Rottman; Jérôme Salomon; Patrick Plésiat; Anaïs Potron
Journal:  Spinal Cord Ser Cases       Date:  2017-05-11

3.  Chitosan sponges for local synergistic infection therapy: a pilot study.

Authors:  J Keaton Smith; Abteen R Moshref; Jessica A Jennings; Harry S Courtney; Warren O Haggard
Journal:  Clin Orthop Relat Res       Date:  2013-04-20       Impact factor: 4.176

Review 4.  Antibiotic therapy in necrotising external otitis: case series of 32 patients and review of the literature.

Authors:  C Pulcini; P Mahdyoun; E Cua; I Gahide; L Castillo; N Guevara
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2012-07-19       Impact factor: 3.267

5.  Activities of antibiotic combinations against resistant strains of Pseudomonas aeruginosa in a model of infected THP-1 monocytes.

Authors:  Julien M Buyck; Paul M Tulkens; Françoise Van Bambeke
Journal:  Antimicrob Agents Chemother       Date:  2014-10-27       Impact factor: 5.191

6.  Outcome of bloodstream infections among spinal cord injury patients and impact of multidrug-resistant organisms.

Authors:  M Saliba; D Saadeh; F Bouchand; B Davido; C Duran; B Clair; C Lawrence; D Annane; P Denys; J Salomon; L Bernard; A Dinh
Journal:  Spinal Cord       Date:  2016-12-20       Impact factor: 2.772

7.  Antipseudomonal monotherapy or combination therapy for older adults with community-onset pneumonia and multidrug-resistant risk factors: a retrospective cohort study.

Authors:  Obiageri O Obodozie-Ofoegbu; Chengwen Teng; Eric M Mortensen; Christopher R Frei
Journal:  Am J Infect Control       Date:  2019-03-21       Impact factor: 2.918

8.  Potentiation of Aminoglycoside Activity in Pseudomonas aeruginosa by Targeting the AmgRS Envelope Stress-Responsive Two-Component System.

Authors:  Keith Poole; Christie Gilmour; Maya A Farha; Erin Mullen; Calvin Ho-Fung Lau; Eric D Brown
Journal:  Antimicrob Agents Chemother       Date:  2016-05-23       Impact factor: 5.191

9.  Novel phytochemical-antibiotic conjugates as multitarget inhibitors of Pseudomononas aeruginosa GyrB/ParE and DHFR.

Authors:  Premkumar Jayaraman; Kishore R Sakharkar; ChuSing Lim; Mohammad Imran Siddiqi; Sarinder K Dhillon; Meena K Sakharkar
Journal:  Drug Des Devel Ther       Date:  2013-06-17       Impact factor: 4.162

10.  Impact of adequate empirical combination therapy on mortality from bacteremic Pseudomonas aeruginosa pneumonia.

Authors:  So-Youn Park; Hyun Jung Park; Song Mi Moon; Ki-Ho Park; Yong Pil Chong; Mi-Na Kim; Sung-Han Kim; Sang-Oh Lee; Yang Soo Kim; Jun Hee Woo; Sang-Ho Choi
Journal:  BMC Infect Dis       Date:  2012-11-16       Impact factor: 3.090

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