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诺氟沙星与安慰剂预防旅行者腹泻的对比研究。

Norfloxacin versus placebo for prophylaxis against travellers' diarrhoea.

作者信息

Wiström J, Norrby S R, Burman L G, Lundholm R, Jellheden B, Englund G

机构信息

Department of Infectious Diseases, University of Umeå, Sweden.

出版信息

J Antimicrob Chemother. 1987 Oct;20(4):563-74. doi: 10.1093/jac/20.4.563.

Abstract

In a randomized, double blind study, 127 subjects travelling to countries outside Northern Europe were given norfloxacin 200 mg or placebo bid as prophylaxis against diarrhoea. Fifty-six subjects randomized to norfloxacin and 59 to placebo fulfilled criteria for evaluation of efficacy and of those, respectively six and 20 (P = 0.0006) developed diarrhoea. The mean duration of symptoms in the placebo group was 3.6 days, while all subjects on norfloxacin had symptoms for one day only. In travellers to Mediterranean Europe or the Canary Islands, no significant differences were seen between norfloxacin and placebo. Among subjects going to Africa, Asia or Latin America, 4/32 subjects on norfloxacin and 16/30 on placebo developed diarrhoea (P = 0.0004). Adverse effects were few and mild. Faeces for aerobic cultures was obtained before travelling and three weeks and then three months post-treatment. Treatment with norfloxacin resulted in a significant reduction of samples yielding aerobic Gram-negative rods but did not affect enterococci. In the placebo group, Gram-negative organisms other than Escherichia coli were increased on return to Sweden and the subjects frequently acquired Gram-negative organisms resistant to antibiotics. In none of the groups was there a tendency towards increased norfloxacin resistance. Biotyping of E. coli showed that in both groups the subjects changed their E. coli strains frequently during and after travelling. This trial showed that norfloxacin is a safe and effective prophylactic agent with no adverse effect on bacterial flora, but that its use should be restricted to travellers to non-European countries.

摘要

在一项随机双盲研究中,127名前往北欧以外国家的受试者被给予200毫克诺氟沙星或安慰剂,每日两次,以预防腹泻。随机分配到诺氟沙星组的56名受试者和分配到安慰剂组的59名受试者符合疗效评估标准,其中分别有6名和20名(P = 0.0006)出现腹泻。安慰剂组症状的平均持续时间为3.6天,而所有服用诺氟沙星的受试者仅出现症状一天。在地中海欧洲或加那利群岛的旅行者中,诺氟沙星和安慰剂之间未观察到显著差异。在前往非洲、亚洲或拉丁美洲的受试者中,服用诺氟沙星的32名受试者中有4名出现腹泻,服用安慰剂的30名受试者中有16名出现腹泻(P = 0.0004)。不良反应少且轻微。在旅行前、治疗后三周和三个月采集粪便进行需氧培养。诺氟沙星治疗导致产生需氧革兰氏阴性杆菌的样本显著减少,但对肠球菌没有影响。在安慰剂组中,返回瑞典后除大肠杆菌外的革兰氏阴性菌增加,并且受试者经常获得对抗生素耐药的革兰氏阴性菌。在所有组中均未出现诺氟沙星耐药性增加的趋势。大肠杆菌的生物分型显示,在两组中,受试者在旅行期间和旅行后经常更换其大肠杆菌菌株。该试验表明,诺氟沙星是一种安全有效的预防药物,对细菌菌群无不良影响,但其使用应仅限于前往非欧洲国家的旅行者。

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