Title
Randomised controlled comparison of single-dose ciprofloxacin and doxycycline for cholera caused by Vibrio cholerae 01 or 0139
Date Issued
03 August 1996
Access level
metadata only access
Resource Type
journal article
Author(s)
Publisher(s)
Elsevier B.V.
Abstract
Background. Effective antimicrobial therapy can reduce the duration and volume of cholera diarrhoea by half. However, such treatment is currently limited by Vibrio cholerae resistance to the drugs commonly prescribed for cholera, and by the difficulties involved in the administration of multi-drug doses under field conditions. Because of its favourable pharmacokinetics we thought it likely that single-dose ciprofloxacin would be effective in the treatment of cholera. Methods. In this double-blind study treatment was either a single 1 g oral dose of ciprofloxacin plus doxycycline placebo, or a single 300 mg oral dose of doxycycline plus ciprofloxacine placebo. 130 severely moderately or dehydrated men infected with V cholerae 01 and 130 infected with V cholerae 0139 were randomly assigned treatment. Patients stayed in hospital for 5 days. We measured fluid intake and stool volume every 6 h, and a sample of stool for culture was obtained daily. The primary outcome measures were clinical success - the cessation of watery stool within 48 h; and bacteriological success - absence of V cholerae from cultures of stool after study day 2. Findings. Among patients infected with V cholerae 01, treatment was clinically successful in 62 (94%) of 66 patients who received ciprofloxacin and in 47 (73%) of 64 who receive doxycycline (difference 21% [95% CI 8-33]); the corresponding proportions with bacteriological success were 63 (95%) and 44 (69%) (27% [14-39]). Among patients infected with V cholerae 0139, treatment successful in 54 (92%) of 59 patients ciprofloxacin and in 65 (92%) of 71 who received doxycycline (< 1% [-9 to 9]), and bacteriologically successful in 58 (98%) and 56 (79%), respectively (19% [9-30]). Total volume of watery stool did not differ significantly between ciprofloxacin-group and doxycycline-group patients infected with either V cholerae 01 or 0139. All but one of the V cholerae 01 and all of the 0139 isolates were susceptible in vitro to doxycycline, whereas 48 (37%) of the V cholerae 01 isolates and none of the 0139 isolates were resistant to tetracycline. Treatment clinically failed in 14 (52%) of 27 doxycycline-treated patients infected with a tetracycline-resistant V cholerae 01 strain, compared with three (8%) of 37 patients infected with a tetracycline-susceptible strain (44% [23-65]). Interpretation. Single-dose ciprofloxacin is effective in the treatment of cholera caused by V cholerae 01 or 0139 and is better than single-dose doxycycline in the eradication of V cholerae from stool. Single-dose ciprofloxacin may also be the preferred treatment in areas where tetracycline resistant V cholerae are common. In V cholerae, in-vitro doxycycline susceptibilities are not a useful indicator of the in vivo efficacy of the drug.
Start page
296
End page
300
Volume
348
Issue
9023
Language
English
OCDE Knowledge area
Pediatría
Farmacología, Farmacia
Scopus EID
2-s2.0-0030567832
PubMed ID
Source
Lancet
ISSN of the container
01406736
Sponsor(s)
This study was supported by grants from: Bayer AG, Wuppertal, Germany, and by the International Centre for Diarrhoeal Disease Research, Bangladesh (supported by the governments of Australia, Bangladesh, Belgium, Canada, Denmark, France, Japan, the Netherlands, Norway, Sweden, Switzerland, the United Kingdom, and the United States, the United Nations Development Program, the United Nations Children's Fund, and the World Health Organization, and the Ford and Sasakawa Foundations). CS was supported by a fellowship from the Swedish Agency for Research Cooperation with Developing Countries. Doxycycline tablets were supplied by Pfizer, Germany. We thank Monira Begum for laboratory support, Humayun Kabir for assistance with data entry, William Rand for advice on statistical methods, Marcia Barbiero for carrying out the doxycycline assay, and Stuart Levy for helpful suggestions and assistance with susceptibility determinations.
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