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头孢呋辛酯在上呼吸道感染中的疗效及耐受性。与头孢羟氨苄的对比研究。

[Efficacy and tolerability of cefuroxime-axetil in infections of the upper respiratory tract. Comparative study with cefadroxil].

作者信息

Dupuis G, Ebbo D, Evennou A, Pappo M

出版信息

Rev Laryngol Otol Rhinol (Bord). 1989;110(1):123-6.

PMID:2491707
Abstract

Cefuroxime-axetil is the first oral broad spectrum cephalosporin to be naturally stable in the presence of bêta-lactamases. The aim of this randomized trial was to evaluate the efficacy and safety of cefuroxime-axetil (250 mg twice daily after meal) with cefadroxil (1 g twice daily during meal) for the treatment of upper respiratory tract infection. In this study 150 patients were enrolled. Before treatment, the two groups were comparable. Clinical success was achieved for 94.3% of the patients treated with cefuroxime-axetil versus 90.4% for cefadroxil. Statistical significance was reached (p less than 0.05) concerning the number of days with facial pain for sinusitis (3 days for the cefuroxime-axetil treated group versus 4 days), the rate of normal tympanum at the second examination (58.3% vs 20% respectively) for otitis, and the number of day with painful dysphagia for tonsillitis (2.6 vs 3.8 days respectively). Cefuroxime-axetil was safe (a few advers events occurred, almost all gastro-intestinal). Cefuroxime-axetil is a safe and effective treatment of upper respiratory tract infections.

摘要

头孢呋辛酯是首个在β-内酰胺酶存在下天然稳定的口服广谱头孢菌素。本随机试验的目的是评估头孢呋辛酯(餐后每日两次,每次250毫克)与头孢羟氨苄(进餐期间每日两次,每次1克)治疗上呼吸道感染的疗效和安全性。本研究纳入了150例患者。治疗前,两组具有可比性。接受头孢呋辛酯治疗的患者临床成功率为94.3%,而接受头孢羟氨苄治疗的患者为90.4%。在鼻窦炎面部疼痛天数方面(头孢呋辛酯治疗组为3天,头孢羟氨苄治疗组为4天)、中耳炎第二次检查时鼓膜正常率方面(分别为58.3%和20%)以及扁桃体炎吞咽痛天数方面(分别为2.6天和3.8天)达到了统计学显著性(p小于0.05)。头孢呋辛酯是安全的(发生了一些不良事件,几乎均为胃肠道事件)。头孢呋辛酯是治疗上呼吸道感染的一种安全有效的药物。

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