Bryson H M, Brogden R N
Adis International Limited, Auckland, New Zealand.
Drugs. 1993 Apr;45(4):589-621. doi: 10.2165/00003495-199345040-00009.
Cefetamet pivoxil is an oral third-generation cephalosporin which is hydrolysed to form the active agent, cefetamet. Cefetamet has excellent in vitro activity against the major respiratory pathogens Streptococcus pneumoniae, Haemophilus influenzae, Moraxella (Branhamella) catarrhalis and group A beta-haemolytic streptococci; it is active against beta-lactamase-producing strains of H. influenzae and M. catarrhalis, but has poor activity against penicillin-resistant S. pneumoniae. Cefetamet has marked activity against Neisseria gonorrhoeae and possesses a broad spectrum of activity against Enterobacteriaceae. Both staphylococci and Pseudomonas spp. are resistant to cefetamet. Cefetamet pivoxil has been investigated in the treatment of both upper and lower community-acquired respiratory tract infections and has demonstrated equivalent efficacy to a number of more established agents, namely cefaclor, amoxicillin and cefixime. In patients with group A beta-haemolytic streptococcal pharyngotonsillitis, a 7-day course of cefetamet pivoxil was as effective as a 10-day course of the standard agent, phenoxymethylpenicillin, in this indication. In complicated urinary tract infections, cefetamet pivoxil showed similar efficacy to cefadroxil, cefaclor and cefuroxime axetil. Cefetamet pivoxil was effective in the treatment of otitis media, pneumonia, pharyngotonsillitis and urinary tract infections in children. Preliminary data indicate that single dose cefetamet pivoxil can effectively eradicate N. gonorrhoeae from both men and women. Cefetamet pivoxil has a tolerability profile similar to that of other oral cephalosporins, with gastrointestinal effects being the most commonly reported adverse events. To date, no symptoms of carnitine deficiency have been reported with cefetamet pivoxil. Cefetamet pivoxil offers effective alternative oral therapy for outpatient treatment of community-acquired respiratory tract infections, with the advantage of improved activity against H. influenzae and increased beta-lactamase stability. However, its use in areas with a high incidence of penicillin-resistant S. pneumoniae is likely to be limited. Cefetamet pivoxil is also effective in the treatment of urinary tract infections, although further trials are required to define any comparative advantages over other oral agents.
头孢他美酯是一种口服第三代头孢菌素,可水解形成活性剂头孢他美。头孢他美对主要呼吸道病原体肺炎链球菌、流感嗜血杆菌、卡他莫拉菌(布兰汉菌)和A组β溶血性链球菌具有优异的体外活性;它对产β-内酰胺酶的流感嗜血杆菌和卡他莫拉菌菌株有活性,但对青霉素耐药的肺炎链球菌活性较差。头孢他美对淋病奈瑟菌有显著活性,对肠杆菌科具有广谱活性。葡萄球菌和假单胞菌属均对头孢他美耐药。头孢他美酯已用于治疗上下呼吸道社区获得性感染,并已证明与一些更常用的药物(即头孢克洛、阿莫西林和头孢克肟)疗效相当。在A组β溶血性链球菌性咽扁桃体炎患者中,7天疗程的头孢他美酯在该适应症中与10天疗程的标准药物苯氧甲基青霉素效果相同。在复杂性尿路感染中,头孢他美酯与头孢羟氨苄、头孢克洛和头孢呋辛酯疗效相似。头孢他美酯对儿童中耳炎、肺炎、咽扁桃体炎和尿路感染有效。初步数据表明,单剂量头孢他美酯可有效根除男性和女性体内的淋病奈瑟菌。头孢他美酯的耐受性与其他口服头孢菌素相似,胃肠道反应是最常报告的不良事件。迄今为止,尚未有头孢他美酯引起肉碱缺乏症状的报道。头孢他美酯为社区获得性呼吸道感染的门诊治疗提供了有效的口服替代疗法,具有增强对流感嗜血杆菌的活性和提高β-内酰胺酶稳定性的优点。然而,在青霉素耐药肺炎链球菌高发地区,其使用可能会受到限制。头孢他美酯在治疗尿路感染方面也有效,尽管需要进一步试验来确定其相对于其他口服药物的比较优势。