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 (12)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sirgel, F.
Right arrow Articles by Mitchison, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sirgel, F.
Right arrow Articles by Mitchison, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (2001) 47, 177-182
© 2001 The British Society for Antimicrobial Chemotherapy

Sources of variation in studies of the early bactericidal activity of antituberculosis drugs

Frik Sirgela, Amour Ventera and Denis Mitchisonb,*

a National Tuberculosis Research Programme, Medical Research Council, PO Box 19070, Tygerberg, 7505 South Africa; b Department of Medical Microbiology, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK

The early bactericidal activity (EBA) of antituberculosis drugs can be measured as the daily fall in cfu counts of Mycobacterium tuberculosis in sputum, usually during the first 2 days of treatment. In studies of low potency drugs, it is necessary to compare the treated group of patients with a group who receives no chemotherapy (Nil group). Over the past 10 years, five Nil groups of between five and 13 patients have been studied in Cape Town and two Nil groups in Hong Kong. There was a suggestion of an increase in variation within the Cape Town groups, as shown by a regression of variance size against study date (P = 0.06), which could not be attributed to technical causes. It might indicate increasing host resistance in the Western Cape epidemic of tuberculosis. Since the weighted mean of all Nil groups at Cape Town was 0.00036, very close to zero, it would seem safe to test means of treated groups against zero thus increasing precision and avoiding ethical problems in delaying treatment. In contrast to Nil groups, the variation found in five groups who received 300 mg isoniazid daily (INH 300) was uniform and homoscedastic, possibly because the additional variation was caused mainly by individual differences in plasma isoniazid concentrations and patient body weights. The mean EBA in the INH 300 series was 0.575 with 95% confidence limits of 0.515 and 0.636.

* Corresponding author. Tel: +44-20-8725-5704; Fax: +44-20-8672-0234; E-mail: dmitchis{at}sghms.ac.uk


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
Antimicrob. Agents Chemother.Home page
M. W. R. Pletz, A. De Roux, A. Roth, K.-H. Neumann, H. Mauch, and H. Lode
Early Bactericidal Activity of Moxifloxacin in Treatment of Pulmonary Tuberculosis: a Prospective, Randomized Study
Antimicrob. Agents Chemother., March 1, 2004; 48(3): 780 - 782.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
R. D. Gosling, L. Heifets, and S. H. Gillespie
A multicentre comparison of a novel surrogate marker for determining the specific potency of anti-tuberculosis drugs
J. Antimicrob. Chemother., September 1, 2003; 52(3): 473 - 476.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
A. Jindani, C. J. Dore, and D. A. Mitchison
Bactericidal and Sterilizing Activities of Antituberculosis Drugs during the First 14 Days
Am. J. Respir. Crit. Care Med., May 15, 2003; 167(10): 1348 - 1354.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
C. J. Dore, A. J. Nunn, S. H. Gillespie, R. D. Gosling, and B. M. Charalambous
Bactericidal activity of antituberculosis drugs
Am. J. Respir. Crit. Care Med., February 15, 2003; 167(4): 663 - 663.
[Full Text]


Home page
Am. J. Respir. Crit. Care Med.Home page
D. A. Mitchison, S. H. Gillespie, B. M. Charalambous, and R. D. Gosling
A reiterative method for calculating bactericidal activity
Am. J. Respir. Crit. Care Med., February 15, 2003; 167(4): 663 - 664.
[Full Text]


Home page
Am. J. Respir. Crit. Care Med.Home page
S. H. Gillespie, R. D. Gosling, and B. M. Charalambous
A Reiterative Method for Calculating the Early Bactericidal Activity of Antituberculosis Drugs
Am. J. Respir. Crit. Care Med., July 1, 2002; 166(1): 31 - 35.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
P. R. Donald, F. A. Sirgel, A. Venter, E. Smit, D. P. Parkin, B. W. Van de Wal, and D. A. Mitchison
The early bactericidal activity of a low-clearance liposomal amikacin in pulmonary tuberculosis
J. Antimicrob. Chemother., December 1, 2001; 48(6): 877 - 880.
[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.