头孢硫脒治疗急性细菌性鼻窦炎70例临床疗效观察  被引量:3

Treatment of Acute Bacterial Sinusitis with Cefathiamidine: Analysis of 70 Cases

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作  者:陈小梅[1] 高春生[1] 王欢[1] 

机构地区:[1]深圳市南山区人民医院耳鼻咽喉科,深圳市518052

出  处:《中国医院用药评价与分析》2010年第3期257-259,共3页Evaluation and Analysis of Drug-use in Hospitals of China

摘  要:目的:评价头孢硫脒治疗急性细菌性鼻窦炎(ABS)的临床疗效。方法:将135例住院确诊为ABS患者,随机分为治疗组70例,对照组65例,治疗组用头孢硫脒2.0g,1日2次肌内注射,对照组用头孢哌酮/舒巴坦,2.0g,q12h静脉滴注,疗程均为7~14d,按照卫生部颁发的《抗菌药物临床应用指导原则》进行临床观察对比研究。结果:临床疗效分别为85.71%和89.23%;细菌学疗效分别为82.26%和85.96%,头孢硫脒与头孢哌酮/舒巴坦疗效相当。不良反应发生率头孢硫脒组为10.0%(7/70),头孢哌酮/舒巴坦组为9.23%(6/65)。均未见光毒性和肝毒性不良反应。结论:头孢硫脒与头孢哌酮/舒巴坦对ABS治疗同样安全有效。OBJECITVE: To evaluate the clinical efficacy of Cefathiamidine for acute bacterial sinusitis (ABS). METHODS: 135 patients who were confirmed as having ABS were randomly assigned to receive either Cefathiamidine (2. 0 g qd) for 7 ~14 days (treatment group,n =70) or Cefoperazon/sulbactam (2. 0 g q12 h iv gtt) for 7 ~14 days (control group,n = 65). A clinical comparative study was done according to the"Guiding Principle for Clinical Research of Antibiotics"issued by the National Health Ministry. RESULTS: The clinical response rates in the two groups were 85. 71% and 89. 23% ,respectively,with equivalent bacteriological response rate of 82. 26% vs. 85. 96% . The incidence of adverse reactions was 10. 0% (7 /70) for Cefathiamidine group vs. 9. 23% (6 /65) for Cefoperazon /sulbactam group. Neither phototoxicity nor hepatotoxicity was noted. CONCLUSION: Both Cefathiamidine and Cefoperazon / sulbactam are proved to be safe and effective for ABS.

关 键 词:头孢硫脒 头孢哌酮/舒巴坦 急性细菌性鼻窦炎 临床对比研究 

分 类 号:R978.1[医药卫生—药品]

 

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