Perry C M, Markham A
Adis International Limited, Mairangi Bay, Auckland, New Zealand.
Drugs. 1999 May;57(5):805-43. doi: 10.2165/00003495-199957050-00017.
Piperacillin/tazobactam is a beta-lactam/beta-lactamase inhibitor combination with a broad spectrum of antibacterial activity encompassing most Gram-positive and Gram-negative aerobic bacteria and anaerobic bacteria, including many pathogens producing beta-lactamases. Evidence from clinical trials in adults has shown that piperacillin/tazobactam, administered in an 8:1 ratio, is an effective treatment for patients with lower respiratory tract, intra-abdominal, urinary tract, gynaecological and skin/soft tissue infections, and for fever in patients with neutropenia. Combination regimens of piperacillin/tazobactam plus an aminoglycoside are used to treat patients with severe nosocomial (hospital-acquired) infections. In clinical trials, piperacillin/tazobactam was significantly more effective than ticarcillin/clavulanic acid in terms of clinical and microbiological outcome in patients with community-acquired pneumonia. In patients with intra-abdominal infections, clinical and bacteriological response rates were significantly higher with piperacillin/tazobactam than with imipenem/cilastatin (administered at a dosage lower than is recommended in countries outside Scandinavia). Piperacillin/tazobactam in combination with amikacin was at least as effective as ceftazidime plus amikacin in the treatment of ventilator-associated pneumonia and was significantly more effective than ceftazidime plus amikacin in the empirical treatment of febrile episodes in patients with neutropenia or granulocytopenia. In other trials, the efficacy of piperacillin/tazobactam was similar to that of standard aminoglycoside-containing and other treatment regimens in patients with intra-abdominal, skin/soft tissue or gynaecological infections. Piperacillin/tazobactam is generally well tolerated. The most frequent adverse events are gastrointestinal symptoms (most commonly diarrhoea) and skin reactions. The incidence of adverse events with piperacillin/tazobactam is higher when the combination is given in combination with an aminoglycoside than when given as monotherapy.
Because of the broad spectrum of antibacterial activity provided by piperacillin/tazobactam, it is useful for the treatment of patients with polymicrobial infections caused by aerobic or anaerobic beta-lactamase-producing bacteria. Piperacillin/tazobactam appears to have a particularly useful role in the treatment of patients with intra-abdominal infections and, in combination with amikacin, in the treatment of patients with febrile neutropenia, especially given the current prevalence of Gram-positive infections in this group.
哌拉西林/他唑巴坦是一种β-内酰胺/β-内酰胺酶抑制剂组合,具有广泛的抗菌活性,涵盖大多数革兰氏阳性和革兰氏阴性需氧菌以及厌氧菌,包括许多产生β-内酰胺酶的病原体。成人临床试验的证据表明,以8:1的比例给药的哌拉西林/他唑巴坦对下呼吸道、腹腔内、泌尿系统、妇科和皮肤/软组织感染患者以及中性粒细胞减少患者的发热是一种有效的治疗方法。哌拉西林/他唑巴坦加氨基糖苷类的联合治疗方案用于治疗严重的医院获得性感染患者。在临床试验中,就社区获得性肺炎患者的临床和微生物学结果而言,哌拉西林/他唑巴坦比替卡西林/克拉维酸显著更有效。在腹腔内感染患者中,哌拉西林/他唑巴坦的临床和细菌学反应率显著高于亚胺培南/西司他丁(以低于斯堪的纳维亚以外国家推荐剂量给药)。哌拉西林/他唑巴坦与阿米卡星联合使用在治疗呼吸机相关性肺炎方面至少与头孢他啶加阿米卡星一样有效,并且在中性粒细胞减少或粒细胞缺乏患者发热发作的经验性治疗中比头孢他啶加阿米卡星显著更有效。在其他试验中,哌拉西林/他唑巴坦在腹腔内、皮肤/软组织或妇科感染患者中的疗效与含标准氨基糖苷类的治疗方案及其他治疗方案相似。哌拉西林/他唑巴坦一般耐受性良好。最常见的不良事件是胃肠道症状(最常见的是腹泻)和皮肤反应。当哌拉西林/他唑巴坦与氨基糖苷类联合使用时,不良事件的发生率高于单一疗法给药时。
由于哌拉西林/他唑巴坦具有广泛的抗菌活性,它可用于治疗由需氧或厌氧产β-内酰胺酶细菌引起的混合感染患者。哌拉西林/他唑巴坦在腹腔内感染患者的治疗中似乎具有特别有用的作用,并且与阿米卡星联合使用时,在发热性中性粒细胞减少患者的治疗中也具有特别有用的作用,特别是考虑到该组中目前革兰氏阳性感染的流行情况。