Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (3)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Darley, E. S. R.
Right arrow Articles by Macgowan, A. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Darley, E. S. R.
Right arrow Articles by Macgowan, A. P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (2000) 45, 247-250
© 2000 The British Society for Antimicrobial Chemotherapy


Brief reports

Use of meropenem 3 g once daily for outpatient treatment of infective exacerbations of bronchiectasis

Elizabeth S. R. Darleya,*, Karen E. Bowkera, Andrew M. Loveringa, John E. Harveyb and Alasdair P. Macgowana

a Bristol Centre for Antimicrobial Research and Evaluation, North Bristol NHS Trust and University of Bristol, Department of Medical Microbiology, and b Department of Respiratory Medicine, Southmead Hospital, Westbury-on-Trym, Bristol BS10 5NB, UK

Meropenem administered as a single iv 3 g dose once every 24 h was used to treat nine ambulatory patients with infective exacerbations of bronchiectasis. Serum meropenem concentrations were measured before dosing and at 30 min after each 30 min infusion. Mean pre-dose concentrations were <0.1 mg/L and mean post-dose concentrations 93.9 ± 29.5 mg/L (95% confidence interval (CI) 86.2–101.6, n = 59). A pathogen was cultured from sputum in six patients and eradicated (<100 cfu/g sputum) in all but one by day 6 of therapy. Previous work on animals has shown that a bacteriostatic effect is seen with meropenem when t > MIC is greater than 20–30% of the dose interval. In these nine patients, this could be achieved and was associated with successful outcome for pathogens for which MICs are <= 0.5 mg/L. Therefore, once-a-day meropenem therapy may be a useful option for outpatient treatment for isolates for which MICs are <= 0.5 mg/L.

* Corresponding author. Tel: +44-117-959-5651; Fax: +44-117-959-3154.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Eur Respir JHome page
M. P. Murray, K. Turnbull, S. MacQuarrie, and A. T. Hill
Assessing response to treatment of exacerbations of bronchiectasis in adults
Eur. Respir. J., February 1, 2009; 33(2): 312 - 318.
[Abstract] [Full Text] [PDF]


Home page
ChestHome page
P. Scheinberg, E. Shore, and on behalf of the PC-TNDS-008 Study Group
A Pilot Study of the Safety and Efficacy of Tobramycin Solution for Inhalation in Patients With Severe Bronchiectasis
Chest, April 1, 2005; 127(4): 1420 - 1426.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
A. P. MacGowan, A. R. Noel, C. A. Rogers, and K. E. Bowker
Antibacterial Effects of Amoxicillin-Clavulanate against Streptococcus pneumoniae and Haemophilus influenzae Strains for Which MICs Are High, in an In Vitro Pharmacokinetic Model
Antimicrob. Agents Chemother., July 1, 2004; 48(7): 2599 - 2603.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.