Piippo T, Stefansson S, Pitkäjärvi T, Lundberg C
Community Health Centre of the City of Tampere, Finland.
Scand J Infect Dis. 1991;23(4):459-65. doi: 10.3109/00365549109075094.
In a double-blind study cefixime, an oral cephalosporin of the third generation, was compared to cefaclor in the treatment of acute otitis media in 397 children aged 6 months to 12 years. Clinical evaluation was carried out at the beginning, at day 10-12 and day 28-35 after the start of the treatment. Specimens for bacterial culture and sensitivity testings were taken from the nasopharynx at the initial visit. Patients were randomized either to cefixime in a dose of 8 mg/kg/day or cefaclor in a dose 40 mg/kg/day in the proportion of 2 cefixime patients to 1 cefaclor patient. Two daily doses were administered for 7 days. At day 10-12, 93.5% in the cefixime group and 90.5% in the cefaclor group (p = 0.08) were clinically cured or improved. At day 28-35 the rate of cured or improved patients had decreased, mostly due to reinfections, to 90.1% in the cefixime group and to 86.6% in the cefaclor group (p = 0.12), respectively. 375 patients (69.9%) had positive bacterial culture in the nasopharynx of at least one strain of Haemophilus influenzae, Streptococcus pneumoniae, Branhamella (Moraxella) catarrhalis or combinations of these 3.73.6% of the B. catarrhalis strains were beta-lactamase producing and 11.4% of the H. influenzae strains, respectively. All isolated bacteria were sensitive to cefixime. Adverse events were reported in 17.9% in the cefixime and 10.6% in the cefaclor group. Most reactions were of moderate or mild nature and mostly affected skin or the gastrointestinal region. No serious adverse experiences occurred. In view of the good clinical results obtained cefixime seems to be at least as effective as cefaclor in the treatment of acute otitis media in children.
在一项双盲研究中,将第三代口服头孢菌素头孢克肟与头孢克洛用于治疗397名6个月至12岁儿童的急性中耳炎。在治疗开始时、第10 - 12天和第28 - 35天进行临床评估。初诊时从鼻咽部采集细菌培养和药敏试验标本。患者按2例头孢克肟患者比1例头孢克洛患者的比例随机分为接受8mg/kg/天剂量的头孢克肟或40mg/kg/天剂量的头孢克洛治疗组。每日给药2次,疗程7天。在第10 - 12天,头孢克肟组93.5%、头孢克洛组90.5%(p = 0.08)临床治愈或好转。在第28 - 35天,治愈或好转患者比例下降,主要是由于再次感染,头孢克肟组降至90.1%,头孢克洛组降至86.6%(p = 0.12)。375例患者(69.9%)鼻咽部至少有一种流感嗜血杆菌、肺炎链球菌、卡他莫拉菌(布兰汉菌属)(莫拉菌属)或这三种菌的组合的细菌培养呈阳性。卡他莫拉菌菌株中分别有73.6%产β-内酰胺酶,流感嗜血杆菌菌株中有11.4%产β-内酰胺酶。所有分离出的细菌对头孢克肟敏感。头孢克肟组有17.9%、头孢克洛组有10.6%报告了不良事件。大多数反应为中度或轻度,主要累及皮肤或胃肠道。未发生严重不良事件。鉴于取得的良好临床结果,头孢克肟在治疗儿童急性中耳炎方面似乎至少与头孢克洛一样有效。