Bryson H M, Brogden R N
Adis International Limited, Auckland, New Zealand.
Drugs. 1994 Mar;47(3):506-35. doi: 10.2165/00003495-199447030-00008.
Combining tazobactam, a beta-lactamase inhibitor, with the ureidopenicillin, piperacillin, successfully restores the activity of piperacillin against beta-lactamase-producing bacteria. Tazobactam has inhibitory activity, and therefore protects piperacillin against Richmond and Sykes types II, III, IV and V beta-lactamases, staphylococcal penicillinase and extended-spectrum beta-lactamases. However, tazobactam has only species-specific activity against class I chromosomally-mediated enzymes. Resistant organisms include some Citrobacter spp., Enterobacter spp., Serratia spp., Xanthomonas maltophilia and Enterococcus faecium. Consistent with its in vitro activity, preliminary clinical data indicate that the fixed combination of piperacillin/tazobactam (dose ratio 8:1) is effective in the treatment of moderate to severe polymicrobial infections, including intra-abdominal, skin and soft-tissue and lower respiratory tract infections. In limited comparative trials, piperacillin/tazobactam demonstrated equivalent or better efficacy than standard comparator regimens in these infections. Piperacillin/tazobactam in combination with an aminoglycoside was effective in the empirical treatment of fever in patients with neutropenia and compared favourably with ceftazidime in combination with an aminoglycoside, although second-line therapy with a glycopeptide antibiotic may be indicated in unresponsive episodes. Data from phase III trials indicate that piperacillin/tazobactam has a tolerability profile typical of a penicillin agent. Piperacillin/tazobactam provides a broad spectrum of antibacterial activity in a convenient single formulation suitable for use in the treatment of polymicrobial infections. Possible limitations concern its restricted activity against class I beta-lactamases, enzymes that are becoming increasingly important in the nosocomial environment. Combined therapy with an aminoglycoside may be necessary in more serious infections.
将β-内酰胺酶抑制剂他唑巴坦与脲基青霉素哌拉西林联合使用,可成功恢复哌拉西林对产β-内酰胺酶细菌的活性。他唑巴坦具有抑制活性,因此可保护哌拉西林免受里士满和赛克斯II、III、IV和V型β-内酰胺酶、葡萄球菌青霉素酶及超广谱β-内酰胺酶的破坏。然而,他唑巴坦仅对I类染色体介导的酶具有种属特异性活性。耐药菌包括一些柠檬酸杆菌属、肠杆菌属、沙雷菌属、嗜麦芽窄食单胞菌和粪肠球菌。与其体外活性一致,初步临床数据表明,哌拉西林/他唑巴坦固定复方制剂(剂量比8:1)可有效治疗中度至重度混合感染,包括腹腔内感染、皮肤及软组织感染和下呼吸道感染。在有限的对照试验中,哌拉西林/他唑巴坦在这些感染中的疗效与标准对照方案相当或更佳。哌拉西林/他唑巴坦与氨基糖苷类药物联合使用对中性粒细胞减少患者的发热进行经验性治疗有效,与头孢他啶联合氨基糖苷类药物相比具有优势,不过在无反应的情况下可能需要使用糖肽类抗生素进行二线治疗。III期试验数据表明,哌拉西林/他唑巴坦具有青霉素类药物典型的耐受性。哌拉西林/他唑巴坦以方便的单一制剂形式提供了广泛的抗菌活性,适用于治疗混合感染。可能的局限性在于其对I类β-内酰胺酶的活性有限,而这类酶在医院环境中变得越来越重要。在更严重的感染中可能需要联合使用氨基糖苷类药物。