摘要
目的:评价比阿培南经验性治疗重度及以上(Ⅲ、Ⅳ级)慢性阻塞性肺疾病急性加重期的疗效和安全性。方法:80例慢性阻塞性肺疾病急性加重期(AECOPD)患者随机分为比阿培南治疗组和头孢他啶对照组,疗程均为7~10d。结果:治疗组临床疗效和细菌清除率(72.6%,88.2%)均优于对照组(60.0%,68.6%),肺功能改善优于对照组,两组药物不良反应发生率均较低。结论:比阿培南经验性治疗重度及以上AECOPD有效且安全。
OBJECTIVE To evaluate the clinical efficacy and safety of biapenem in the treatment of severe and very severe acute exacerbation of chronic obstructive pulmonary disease(AECOPD). METHODS 80 patients with AECOPD were randomly divided into two groups, the trial and the control groups. Biapenem or ceftazidime were administered by intravenous infusion for 7 - 10 days. RESULTS The effective rates for trial group were higher than the control group (72.6% ,60. 0%). The bacterial eradication rates for trial group were also higher than the control group(88. 2% ,68. 6%). The lung function of trial group was significantly improved compared to the control group. The incidence of drug adverse reaction were all low. CONCLUSION Biapenem is both effective and safe drug for severe and very severe AECOPD.
出处
《中国医院药学杂志》
CAS
CSCD
北大核心
2011年第24期2035-2038,共4页
Chinese Journal of Hospital Pharmacy
关键词
比阿培南
头孢他啶
慢性阻塞性肺疾病
临床疗效
细菌清除率
biapenem
ceftazidime
acute exacerbation of chronic obstructive pulmonary disease
clinical efficacy
bacterial eradication rate