Ige O M, Okesola A O
Department of Medicine, University College Hospital, Ibadan, Nigeria.
Dept. of Medical Micro. & Parasitology, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Ann Ib Postgrad Med. 2015 Dec;13(2):72-8.
Initial antibiotic therapy in upper and lower respiratory tract infections is usually empirical. However, the decreasing susceptibility of respiratory pathogens to antibacterials have raised concerns about the decreasing efficacy of currently available antibiotics.
This study was conducted to compare the efficacy and safety of cefixime and ciprofloxacin in the empirical treatment of community-acquired pneumonia among adult Nigerian patients in Ibadan.
This was an open-labelled, randomized, parallel-group study of seventy-three (73) radiologically and bacteriologically confirmed adult cases of community-acquired pneumonia, between July 1 and September 31, 2011 at two health care facilities in Ibadan, Nigeria. All of these patients had severity index (CURB 65) scores of either 1 or 2. They were treated with either Cefixime, 400mg twice daily or Ciprofloxacin 500mg twice daily for 14 days. They were evaluated four times during the course of their treatment for clinical responses, radiological and bacteriological clearances and safety of therapy.
There were 39 (53.4%) patients in the Cefixime group and 34(46.6%) in Ciprofloxacin group. On day 7, patients on cefixime had a statistically significant lower temperature than patients on ciprofloxacin (P<0.01). By day 14, only 10.3% of patients in cefixime group still had persistent residual radiological changes compared to 38.2% in the ciprofloxacin group (P < 0.01). Bacteria cure was obtained in 96% of the patients in the cefixime group and 83% in the ciprofloxacin group.
Cefixime was found to be superior to ciprofloxacin in terms of efficacy in the treatment of community-acquired pneumonia in adults in Nigeria. However, both antibiotics were well-tolerated by all the patients as there were no reports or documentation of adverse events.
上、下呼吸道感染的初始抗生素治疗通常是经验性的。然而,呼吸道病原体对抗菌药物的敏感性下降引发了人们对现有抗生素疗效降低的担忧。
本研究旨在比较头孢克肟和环丙沙星在伊巴丹成年尼日利亚患者社区获得性肺炎经验性治疗中的疗效和安全性。
这是一项开放标签、随机、平行组研究,于2011年7月1日至9月31日在尼日利亚伊巴丹的两家医疗机构对73例经放射学和细菌学确诊的社区获得性肺炎成年病例进行研究。所有这些患者的严重程度指数(CURB 65)评分均为1或2。他们分别接受每日两次400mg头孢克肟或每日两次500mg环丙沙星治疗,为期14天。在治疗过程中对他们进行了4次评估,以观察临床反应、放射学和细菌学清除情况以及治疗安全性。
头孢克肟组有39例(53.4%)患者,环丙沙星组有34例(46.6%)患者。在第7天,服用头孢克肟的患者体温在统计学上显著低于服用环丙沙星的患者(P<0.01)。到第14天,头孢克肟组只有10.3%的患者仍有持续的残留放射学改变,而环丙沙星组为38.2%(P < 0.01)。头孢克肟组96%的患者细菌清除,环丙沙星组为83%。
在尼日利亚成年人社区获得性肺炎的治疗中,头孢克肟在疗效方面优于环丙沙星。然而,所有患者对这两种抗生素耐受性良好,因为没有不良事件的报告或记录。