Comparison of single-dose azithromycin and 12-dose, 3-day erythromycin for childhood cholera: a randomised, double-blind trial
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Khan, Wasif A. | - |
dc.contributor.author | Saha, Debasish | - |
dc.contributor.author | Rahman, Anisur | - |
dc.contributor.author | Salam, Mohammad A. | - |
dc.contributor.author | Bogaerts, Joseph | - |
dc.contributor.author | Bennish, Michael L. | - |
dc.date.accessioned | 2015-04-27T03:54:46Z | - |
dc.date.available | 2015-04-27T03:54:46Z | - |
dc.date.issued | 2002 | - |
dc.identifier.citation | Lancet. 2002 Nov 30;360(9347):1722-7 | en |
dc.identifier.uri | http://hdl.handle.net/123456789/5714 | - |
dc.description.abstract | Abstract BACKGROUND: Cholera is a major public-health problem, with children most affected. However, effective single-dose antimicrobial regimens have been identified only for adults. Our aim was to compare the efficacy of azithromycin and erythromycin regimens in the treatment of children. METHODS: We did a double-blind, randomised study of 128 severely dehydrated children (age 1-15 years) with cholera, treated at one of two treatment centres in Bangladesh in 1999. Children were assigned single-dose azithromycin (20 mg/kg bodyweight, maximum individual dose 1 g; n=65) or 12.5 mg/kg erythromycin (maximum dose 500 mg; n=63) every 6 h for 3 days. Patients stayed in hospital for 5 days. We measured fluid balance every 6 h, and obtained a rectal swab or stool sample for culture daily. Our primary outcome measures were clinical success of treatment-ie, cessation of watery diarrhoea within 48 h-and bacteriological success-ie, absence of Vibrio cholerae O1 or O139 from cultures of stool or rectal swab samples after study day 2. Analysis was per protocol. FINDINGS: Two children in both groups withdrew from the study, and we excluded one child in the erythromycin group. Treatment was clinically successful in 48 (76%) patients who received azithromycin and 39 (65%) who received erythromycin (difference 11%, 95% CI -5 to 27, p=0.244); and bacteriologically successful in 45 (71%) and 49 (82%) patients, respectively (10%, -5 to 25, p=0.261). Patients treated with azithromycin had a shorter duration of diarrhoea (median 24 h vs 42 h; difference 12 h, 0-18 h, p=0.019) and fewer episodes of vomiting (1 vs 4; difference 1 episode, 0-3 episodes, p=0.023). INTERPRETATION: Single-dose azithromycin is as effective for treatment of cholera in children as standard erythromycin therapy, but is associated with less vomiting | en |
dc.format.extent | 92004 bytes | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | en | en |
dc.subject | Anti-bacterial agents | en |
dc.subject | Azithromycin | en |
dc.subject | Bangladesh | en |
dc.subject | Double-blind method | en |
dc.subject | Drug administration schedule | en |
dc.subject | Erythromycin | en |
dc.subject | Treatment outcome | en |
dc.subject | Vibrio cholerae O1/isolation & purification | en |
dc.title | Comparison of single-dose azithromycin and 12-dose, 3-day erythromycin for childhood cholera: a randomised, double-blind trial | en |
dc.type | Article | en |
Appears in Collections: | A. Original papers |
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