Daniel K P, Krop L C
Department of Pharmacy, Bay Pines VA Medical Center, Florida 33504, USA.
Pharmacotherapy. 1996 Mar-Apr;16(2):149-62.
We reviewed the spectrum of activity, pharmacokinetics, clinical efficacy, adverse effects, and relative advantages of piperacillin-tazobactam, a new beta-lactam-beta-lactamase inhibitor. Piperacillin-tazobactam has a wide spectrum of activity that includes gram-positive organisms such as staphylococci and streptococci, as well as many gram-negative aerobic and anaerobic bacteria. The combination distributes rapidly after parenteral administration and penetrates well into skin, lung, and intestinal mucosa. Compared with other beta-lactam-beta-lactamase inhibitor combinations, piperacillin-tazobactam has comparable efficacy in the treatment of intraabdominal infections, skin and soft tissue infections, and upper and lower respiratory tract infections. It may have better in vitro activity than the currently available combinations against selective bacteria that produce class I beta-lactamases (Richmond-Sykes classification). The combination is well tolerated, with diarrhea being the most common reported adverse effect. Additional controlled trials and clinical experience are required to define its role in clinical practice.
我们回顾了新型β-内酰胺类-β-内酰胺酶抑制剂哌拉西林-他唑巴坦的抗菌谱、药代动力学、临床疗效、不良反应及相对优势。哌拉西林-他唑巴坦抗菌谱广,包括葡萄球菌和链球菌等革兰氏阳性菌,以及许多革兰氏阴性需氧菌和厌氧菌。该复方制剂经胃肠外给药后迅速分布,并能很好地渗透到皮肤、肺和肠黏膜中。与其他β-内酰胺类-β-内酰胺酶抑制剂复方制剂相比,哌拉西林-他唑巴坦在治疗腹腔内感染、皮肤及软组织感染以及上、下呼吸道感染方面疗效相当。对于产生I类β-内酰胺酶(里士满-赛克斯分类法)的某些细菌,它可能比目前可用的复方制剂具有更好的体外活性。该复方制剂耐受性良好,腹泻是最常报告的不良反应。需要更多的对照试验和临床经验来明确其在临床实践中的作用。