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头孢吡肟与头孢他啶治疗严重感染的安全性和有效性

Safety and efficacy of cefepime versus ceftazidime in the treatment of severe infections.

作者信息

Huang Chun-Kai, Chen Yao-Shen, Lee Susan Shin-jung, Lin Wei-Ru, Tsai Hung-Chin, Lin Hsi-Hsun, Wann Shue-Ren, Chen Joanna Yan-wan, Yen Muh-Yong, Liu Yung-Ching

机构信息

Department of Internal Medicine, Kaohsiung Veterans General Hospital, Taiwan, ROC.

出版信息

J Microbiol Immunol Infect. 2002 Sep;35(3):159-67.

Abstract

An open-label, randomized study was conducted to evaluate the safety and efficacy of cefepime versus ceftazidime in the treatment of severe bacterial infections, including septicemia, urinary tract infection, bacterial bronchitis, bacterial pneumonia, and intraabdominal infection. Fifty-two patients with severe infections were eligible and prospectively randomized to receive cefepime (26 patients) or ceftazidime (26 patients) during a 15-month period. Forty-two patients were evaluable (24 in the cefepime group and 18 in the ceftazidime group). Most (86%) of the patients had urinary tract infections and the most commonly isolated pathogen was Escherichia coli (79%). Satisfactory clinical response rates of 71% and 61%, and bacteriological eradication rates of 87.5% and 89% were achieved for the cefepime and ceftazidime groups, respectively. Two patients treated with cefepime died, one from superinfection and one from suspected paraneoplastic syndrome. Cultures of the blood obtained at entry into the study were positive in 19 (45%) of the 42 evaluable cases. In the cefepime group, a patient with Salmonella paratyphi A septicemia was cured, which has not been previously reported. Adverse effects attributable to therapy were minimal in both groups of patients, and none required discontinuation or dose reduction. In conclusion, these results suggest that cefepime is as efficacious and well tolerated as ceftazidime in the treatment of severe bacterial infections, such as septicemia, urinary tract infection, bacterial bronchitis, bacterial pneumonia, and intraabdominal infection.

摘要

开展了一项开放标签的随机研究,以评估头孢吡肟与头孢他啶治疗严重细菌感染(包括败血症、尿路感染、细菌性支气管炎、细菌性肺炎和腹腔内感染)的安全性和疗效。52例严重感染患者符合条件,并在15个月期间前瞻性随机分组接受头孢吡肟(26例患者)或头孢他啶(26例患者)治疗。42例患者可评估(头孢吡肟组24例,头孢他啶组18例)。大多数(86%)患者患有尿路感染,最常分离出的病原体是大肠杆菌(79%)。头孢吡肟组和头孢他啶组的临床有效率分别为71%和61%,细菌清除率分别为87.5%和89%。两名接受头孢吡肟治疗的患者死亡,一名死于二重感染,一名死于疑似副肿瘤综合征。在42例可评估病例中,19例(45%)在进入研究时采集的血培养呈阳性。在头孢吡肟组,一名甲型副伤寒沙门菌败血症患者治愈,此前未见报道。两组患者因治疗引起的不良反应均最小,无一例需要停药或减量。总之,这些结果表明,在治疗严重细菌感染(如败血症、尿路感染、细菌性支气管炎、细菌性肺炎和腹腔内感染)方面,头孢吡肟与头孢他啶疗效相当且耐受性良好。

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