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β-内酰胺类药物治疗与肠道菌群

Betalactam therapy and intestinal flora.

作者信息

Novelli A, Mazzei T, Fallani S, Dei R, Cassetta M I, Conti S

机构信息

Dipartimento di Farmacologia, Università degli Studi di Firenze, Italy.

出版信息

J Chemother. 1995 May;7 Suppl 1:25-31.

PMID:8618110
Abstract

Betalactams, mainly when orally administered, may lead to intestinal flora modifications related to their spectrum of activity, rate of absorption and degradation. therefore it is important to investigate the possible influence of recently developed oral cephem derivatives on normal human microflora. We have investigated the impact on normal human intestinal flora in a 10-day course with cefetamet-pivoxil (CET, 500 mg BID) in comparison to cefixime (CFX, 400 mg qD) or cefuroxime axetil (CA, 250 mg BID) in 24 patients suffering from acute exacerbation of chronic bronchitis. Stool specimens were taken before (day 0), at the end (day 10) and 14 days after treatment (day 24) and quali-quantitative microflora composition was determined with a detection limit of 10 CFU/g dry weight. Treatment with CET caused slight and non-significant modifications of normal intestinal flora. On the contrary CFX and CA significantly affect Enterobacteriaceae and clostridia with a concomitant increase in enterococci for CFX. With both CFX and CA there was a new appearance of Salmonella spp. as well as Clostridium difficile in 4 and 2 cases, respectively. Therefore CET seems to affect normal bowel flora minimally in comparison to other oral cephalosporins. This aspect might contribute to the low incidence of GI related side effects in patients treated with CEt for longer than 1 week.

摘要

β-内酰胺类药物,主要是口服给药时,可能会因其活性谱、吸收和降解速率而导致肠道菌群发生改变。因此,研究最近开发的口服头孢菌素衍生物对正常人体微生物群的可能影响具有重要意义。我们研究了在24例慢性支气管炎急性加重患者中,头孢他美酯(CET,500mg,每日两次)与头孢克肟(CFX,400mg,每日一次)或头孢呋辛酯(CA,250mg,每日两次)进行为期10天的疗程对正常人体肠道菌群的影响。在治疗前(第0天)、结束时(第10天)和治疗后14天(第24天)采集粪便标本,采用检测限为10CFU/g干重的方法测定菌群的定性和定量组成。CET治疗对正常肠道菌群产生了轻微且无显著意义的改变。相反,CFX和CA显著影响肠杆菌科和梭菌,CFX还使肠球菌同时增加。CFX和CA治疗分别有4例和2例出现了沙门氏菌属以及艰难梭菌。因此,与其他口服头孢菌素相比,CET对正常肠道菌群的影响似乎最小。这一方面可能有助于解释接受CET治疗超过1周的患者胃肠道相关副作用发生率较低的原因。

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