Literature DB >> 12019085

Randomized controlled trial of sequential intravenous (i.v.) and oral moxifloxacin compared with sequential i.v. and oral co-amoxiclav with or without clarithromycin in patients with community-acquired pneumonia requiring initial parenteral treatment.

R Finch1, D Schürmann, O Collins, R Kubin, J McGivern, H Bobbaers, J L Izquierdo, P Nikolaides, F Ogundare, R Raz, P Zuck, G Hoeffken.   

Abstract

The objective of the present trial was to compare the efficacy, safety, and tolerability of moxifloxacin (400 mg) given intravenously (i.v.) once daily followed by oral moxifloxacin (400 mg) for 7 to 14 days with the efficacy, safety, and tolerability of co-amoxiclav (1.2 g) administered by i.v. infusion three times a day followed by oral co-amoxiclav (625 mg) three times a day, with or without clarithromycin (500 mg) twice daily (i.v. or orally), for 7 to 14 days in adult patients with community-acquired pneumonia requiring initial parenteral therapy. A total of 628 patients were enrolled and assessed by evaluation of their clinical and bacteriological responses 5 to 7 days and 21 to 28 days after administration of the last dose of study medication. Although the trial was designed, on the basis of predefined outcomes, to demonstrate the equivalence of the two regimens, the results showed statistically significant higher clinical success rates (for moxifloxacin, 93.4%, and for comparator regimen, 85.4%; difference [Delta], 8.05%; 95% confidence interval [CI], 2.91 to 13.19%; P = 0.004) and bacteriological success rates (for moxifloxacin, 93.7%, and for comparator regimen, 81.7%; Delta, 12.06%; 95% CI, 1.21 to 22.91%) for patients treated with moxifloxacin. This superiority was seen irrespective of the severity of the pneumonia and whether or not the combination therapy included a macrolide. The time to resolution of fever was also statistically significantly faster for patients who received moxifloxacin (median time, 2 versus 3 days), and the duration of hospital admission was approximately 1 day less for patients who received moxifloxacin. The treatment was converted to oral therapy immediately after the initial mandatory 3-day period of i.v. administration for a larger proportion of patients in the moxifloxacin group than patients in the comparator group (151 [50.2%] versus 57 [17.8%] patients). There were fewer deaths (9 [3.0%] versus 17 [5.3%]) and fewer serious adverse events (38 [12.6%] versus 53 [16.5%]) in the moxifloxacin group than in the comparator group. The rates of drug-related adverse events were comparable in both groups (38.9% in each treatment group). The overall incidence of laboratory abnormalities was similar in both groups. Thus, it is concluded that monotherapy with moxifloxacin is superior to that with a standard combination regimen of a beta-lactam and a beta-lactamase inhibitor, co-amoxiclav, with or without a macrolide, clarithromycin, in the treatment of patients with community-acquired pneumonia admitted to a hospital.

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Year:  2002        PMID: 12019085      PMCID: PMC127227          DOI: 10.1128/AAC.46.6.1746-1754.2002

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  16 in total

1.  General guidelines for the clinical evaluation of anti-infective drug products. Infectious Diseases Society of America and the Food and Drug Administration.

Authors:  T R Beam; D N Gilbert; C M Kunin
Journal:  Clin Infect Dis       Date:  1992-11       Impact factor: 9.079

Review 2.  The crisis in antibiotic resistance.

Authors:  H C Neu
Journal:  Science       Date:  1992-08-21       Impact factor: 47.728

3.  Community-acquired pneumonia: the annual cost to the National Health Service in the UK.

Authors:  J F Guest; A Morris
Journal:  Eur Respir J       Date:  1997-07       Impact factor: 16.671

4.  Incidence of community-acquired pneumonia requiring hospitalization. Results of a population-based active surveillance Study in Ohio. The Community-Based Pneumonia Incidence Study Group.

Authors:  B J Marston; J F Plouffe; T M File; B A Hackman; S J Salstrom; H B Lipman; M S Kolczak; R F Breiman
Journal:  Arch Intern Med       Date:  1997 Aug 11-25

5.  A prospective randomized study of inpatient iv. antibiotics for community-acquired pneumonia. The optimal duration of therapy.

Authors:  R E Siegel; N A Halpern; P L Almenoff; A Lee; R Cashin; J G Greene
Journal:  Chest       Date:  1996-10       Impact factor: 9.410

Review 6.  Community-acquired pneumonia.

Authors:  T J Marrie
Journal:  Clin Infect Dis       Date:  1994-04       Impact factor: 9.079

7.  Advances in antimicrobial therapy of community-acquired pneumonia.

Authors:  L A Mandell
Journal:  Curr Opin Infect Dis       Date:  1999-04       Impact factor: 4.915

8.  Cost-effectiveness of gatifloxacin vs ceftriaxone with a macrolide for the treatment of community-acquired pneumonia.

Authors:  L D Dresser; M S Niederman; J A Paladino
Journal:  Chest       Date:  2001-05       Impact factor: 9.410

Review 9.  Guidelines for the management of community-acquired pneumonia in adults admitted to hospital. The British Thoracic Society.

Authors: 
Journal:  Br J Hosp Med       Date:  1993 Mar 3-16

10.  Early switch from intravenous to oral cephalosporins in the treatment of hospitalized patients with community-acquired pneumonia.

Authors:  J A Ramirez; L Srinath; S Ahkee; A Huang; M J Raff
Journal:  Arch Intern Med       Date:  1995-06-26
View more
  41 in total

1.  Moxifloxacin for community-acquired pneumonia.

Authors:  Bart J A Rijnders
Journal:  Antimicrob Agents Chemother       Date:  2003-01       Impact factor: 5.191

2.  Efficacy and safety of sequential moxifloxacin for treatment of community-acquired pneumonia associated with atypical pathogens.

Authors:  G Hoeffken; D Talan; L S Larsen; S Peloquin; S H Choudhri; D Haverstock; P Jackson; D Church
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2004-10       Impact factor: 3.267

Review 3.  [Pneumonia - pathogen-based or constellation-based therapy?].

Authors:  A Kuhnke; T Welte; N Suttorp
Journal:  Internist (Berl)       Date:  2006-06       Impact factor: 0.743

Review 4.  Optimal therapy for severe pneumococcal community-acquired pneumonia.

Authors:  Manel Luján; Miguel Gallego; Jordi Rello
Journal:  Intensive Care Med       Date:  2006-05-10       Impact factor: 17.440

5.  Moxifloxacin pharmacokinetic profile and efficacy evaluation in empiric treatment of community-acquired pneumonia.

Authors:  Kristina Öbrink-Hansen; Tore Forsingdal Hardlei; Birgitte Brock; Søren Jensen-Fangel; Marianne Kragh Thomsen; Eskild Petersen; Mads Kreilgaard
Journal:  Antimicrob Agents Chemother       Date:  2015-02-09       Impact factor: 5.191

Review 6.  Treating acute exacerbations of chronic bronchitis and community-acquired pneumonia: how effective are respiratory fluoroquinolones?

Authors:  M Balter; K Weiss
Journal:  Can Fam Physician       Date:  2006-10       Impact factor: 3.275

Review 7.  Elderly patients with community-acquired pneumonia: optimal treatment strategies.

Authors:  Ulrich Thiem; Hans-Jürgen Heppner; Ludger Pientka
Journal:  Drugs Aging       Date:  2011-07-01       Impact factor: 3.923

Review 8.  Mycoplasma pneumoniae and its role as a human pathogen.

Authors:  Ken B Waites; Deborah F Talkington
Journal:  Clin Microbiol Rev       Date:  2004-10       Impact factor: 26.132

Review 9.  Community-acquired pneumonia.

Authors:  Mark Loeb
Journal:  BMJ Clin Evid       Date:  2008-07-17

10.  Respiratory fluoroquinolones for the treatment of community-acquired pneumonia: a meta-analysis of randomized controlled trials.

Authors:  Konstantinos Z Vardakas; Ilias I Siempos; Alexandros Grammatikos; Zoe Athanassa; Ioanna P Korbila; Matthew E Falagas
Journal:  CMAJ       Date:  2008-12-02       Impact factor: 8.262

View more

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