Department of Infectious Diseases and Clinical Microbiology, Zonguldak Karaelmas University School of Medicine, 67600 Zonguldak, Turkey.
Jpn J Clin Oncol. 2010 Aug;40(8):761-7. doi: 10.1093/jjco/hyq046. Epub 2010 Apr 28.
Empirical beta-lactam monotherapy has become the standard therapy in febrile neutropenia. The aim of this study was to compare the efficacy and safety of piperacillin-tazobactam versus carbapenem therapy with or without amikacin in adult patients with febrile neutropenia.
In this prospective, open, single-center study, 127 episodes were randomized to receive either piperacillin-tazobactam (4 x 4.5 g IV/day) or carbapenem [meropenem (3 x 1 g IV/day) or imipenem (4 x 500 mg IV/day)] with or without amikacin (1 g IV/day). Doses were adjusted according to renal function. Clinical response was determined during and at completion of therapy.
One hundred and twenty episodes were assessable for efficacy (59 piperacillin-tazobactam, 61 carbapenem). Mean duration of treatment was 14.8 +/- 9.6 days in the piperacillin-tazobactam group and 14.7 +/- 8.8 days in the carbapenem group (P > 0.05). Mean days of fever resolution were 5.97 and 4.48 days for piperacillin-tazobactam and carbapenem groups, respectively (P > 0.05). Similar rates of success without modification were found in the piperacillin-tazobactam (87.9%) and in the carbapenem groups (75.4%; P > 0.05). Fungal infection occurrence rates were 30.5 and 18% in piperacillin-tazobactam and carbapenem groups, respectively (P = 0.05). Antibiotic modification rates were 30.5 and 13.1% (P = 0.02) and the addition of glycopeptides to empirical antibiotic regimens rates were 15.3 and 44.3% for piperacillin-tazobactam and carbapenem groups, respectively (P = 0.001). The rude mortality rates were 14% (6/43) and 29.3% (12/41) in piperacillin-tazobactam and carbapenem groups, respectively (P = 0.08).
The effect of empirical regimen of piperacillin-tazobactam regimen is equivalent to carbapenem in adult febrile neutropenic patients.
经验性β-内酰胺单药治疗已成为发热性中性粒细胞减少症的标准治疗方法。本研究旨在比较哌拉西林-他唑巴坦与碳青霉烯类药物(无论是否联合应用阿米卡星)治疗成人发热性中性粒细胞减少症的疗效和安全性。
在这项前瞻性、开放、单中心研究中,127 例患者随机分为哌拉西林-他唑巴坦(4×4.5g IV/天)或碳青霉烯类药物[美罗培南(3×1g IV/天)或亚胺培南(4×500mg IV/天)]联合或不联合阿米卡星(1g IV/天)治疗。剂量根据肾功能进行调整。在治疗期间和治疗结束时评估临床反应。
120 例患者可评估疗效(哌拉西林-他唑巴坦 59 例,碳青霉烯类药物 61 例)。哌拉西林-他唑巴坦组的平均治疗时间为 14.8±9.6 天,碳青霉烯类药物组为 14.7±8.8 天(P>0.05)。哌拉西林-他唑巴坦组和碳青霉烯类药物组的发热缓解天数分别为 5.97 和 4.48 天(P>0.05)。哌拉西林-他唑巴坦组(87.9%)和碳青霉烯类药物组(75.4%;P>0.05)的无修正成功率相似。哌拉西林-他唑巴坦组和碳青霉烯类药物组的真菌感染发生率分别为 30.5%和 18%(P=0.05)。抗生素调整率分别为 30.5%和 13.1%(P=0.02),经验性抗生素治疗方案中添加糖肽类抗生素的比率分别为 15.3%和 44.3%,哌拉西林-他唑巴坦组和碳青霉烯类药物组(P=0.001)。哌拉西林-他唑巴坦组和碳青霉烯类药物组的粗死亡率分别为 14%(6/43)和 29.3%(12/41)(P=0.08)。
在成人发热性中性粒细胞减少症患者中,经验性哌拉西林-他唑巴坦方案的疗效与碳青霉烯类药物相当。