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   A multi-center randomized trial to assess the efficacy of gatifloxacin versus ciprofloxacin for the treatment of shigellosis in Vietnamese children  
   
نویسنده vinh h. ,anh v.t.c. ,anh n.d. ,campbell j.i. ,van minh hoang n. ,nga t.v.t. ,nhu n.t.k. ,van minh p. ,thuy c.t. ,duy p.t. ,phuong l.t. ,loan h.t. ,chinh m.t. ,thao n.t.t. ,tham n.t.h. ,mong b.l. ,van be bay p. ,day j.n. ,dolecek c. ,lan n.p.h. ,diep t.s. ,farrar j.j. ,van vinh chau n. ,wolbers m. ,baker s.
منبع plos neglected tropical diseases - 2011 - دوره : 5 - شماره : 8
چکیده    Background: the bacterial genus shigella is the leading cause of dysentery. there have been significant increases in the proportion of shigella isolated that demonstrate resistance to nalidixic acid. while nalidixic acid is no longer considered as a therapeutic agent for shigellosis,the fluoroquinolone ciprofloxacin is the current recommendation of the world health organization. resistance to nalidixic acid is a marker of reduced susceptibility to older generation fluoroquinolones,such as ciprofloxacin. we aimed to assess the efficacy of gatifloxacin versus ciprofloxacin in the treatment of uncomplicated shigellosis in children. methodology/principal findings: we conducted a randomized,open-label,controlled trial with two parallel arms at two hospitals in southern vietnam. the study was designed as a superiority trial and children with dysentery meeting the inclusion criteria were invited to participate. participants received either gatifloxacin (10 mg/kg/day) in a single daily dose for 3 days or ciprofloxacin (30 mg/kg/day) in two divided doses for 3 days. the primary outcome measure was treatment failure; secondary outcome measures were time to the cessation of individual symptoms. four hundred and ninety four patients were randomized to receive either gatifloxacin (n = 249) or ciprofloxacin (n = 245),of which 107 had a positive shigella stool culture. we could not demonstrate superiority of gatifloxacin and observed similar clinical failure rate in both groups (gatifloxacin; 12.0% and ciprofloxacin; 11.0%,p = 0.72). the median (inter-quartile range) time from illness onset to cessation of all symptoms was 95 (66-126) hours for gatifloxacin recipients and 93 (68-120) hours for the ciprofloxacin recipients (hazard ratio [95%ci] = 0.98 [0.82-1.17],p = 0.83). conclusions: we conclude that in vietnam,where nalidixic acid resistant shigellae are highly prevalent,ciprofloxacin and gatifloxacin are similarly effective for the treatment of acute shigellosis. trial registration: controlled trials number isrctn55945881. © 2011 vinh et al.
آدرس the hospital for tropical diseases,ho chi minh city,viet nam,the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, huu nghi hospital,cao lanh,dong thap province, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom, the hospital for tropical diseases,ho chi minh city,viet nam,the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,ho chi minh city,viet nam,the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,ho chi minh city,viet nam,the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city, Viet Nam, huu nghi hospital,cao lanh,dong thap province, Viet Nam, the hospital for tropical diseases,ho chi minh city, Viet Nam, the hospital for tropical diseases,ho chi minh city, Viet Nam, school of medicine and pharmacy,ho chi minh city, Viet Nam, huu nghi hospital,cao lanh,dong thap province, Viet Nam, huu nghi hospital,cao lanh,dong thap province, Viet Nam, huu nghi hospital,cao lanh,dong thap province, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom, the hospital for tropical diseases,ho chi minh city, Viet Nam, the hospital for tropical diseases,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom, the hospital for tropical diseases,ho chi minh city, Viet Nam, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom, the hospital for tropical diseases,wellcome trust major overseas programme,oxford university clinical research unit,ho chi minh city,viet nam,centre for tropical medicine,nuffield department of clinical medicine,oxford university,oxford, United Kingdom
 
     
   
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