Rodriguez W J, Ross S, Schwartz R, Goldenberg R, Khan W
Postgrad Med J. 1979;55 Suppl 4:35-8.
Cefaclor is a new oral cephalosporin with in vitro activity against a wide variety of organisms including S. aureus, S. pneumoniae, S. pyogenes and H. influenzae (including ampicillin-resistant strains). Seventy-nine patients ranging in age from 2 months to 14 years with soft tissue infections (17 cases), otitis media (17), and streptococcal pharyngitis (45) were studied. They received cefaclor orally at a dose of 40 mg/kg per day in three or four divided doses for a minimum of five days. Results were generally good with favourable clinical and bacteriological responses obtained in 90% of cases. Most patients became afebrile within 48 hours after starting cefaclor. Two patients with H. influenzae cellulitis and bacteraemia defervesced within 24 hours and their blood cultures became negative promptly. Hepatic, renal and haematopoietic studies showed no adverse reactions except for an occasional increase in the eosinophil count with no clinical counterpart of hypersensitivity. Pharmacokinetic studies revealed that following a 10 mg/kg oral dose, peak serum levels of 8 micrograms/ml were observed at one hour, followed by a rather rapid tapering off so that at the end of four hours, virtually no cefaclor was detectable in serum.
头孢克洛是一种新型口服头孢菌素,对包括金黄色葡萄球菌、肺炎链球菌、化脓性链球菌和流感嗜血杆菌(包括耐氨苄西林菌株)在内的多种微生物具有体外活性。研究了79例年龄在2个月至14岁之间的患者,他们患有软组织感染(17例)、中耳炎(17例)和链球菌性咽炎(45例)。他们口服头孢克洛,剂量为每日40mg/kg,分三或四次给药,至少服用五天。结果总体良好,90%的病例获得了良好的临床和细菌学反应。大多数患者在开始使用头孢克洛后48小时内退热。两名患有流感嗜血杆菌蜂窝织炎和菌血症的患者在24小时内退热,他们的血培养迅速转阴。肝脏、肾脏和血液学研究未显示不良反应,只是偶尔嗜酸性粒细胞计数增加,但无过敏反应的临床对应表现。药代动力学研究表明,口服10mg/kg剂量后,1小时时血清峰值水平为8μg/ml,随后迅速下降,以至于在4小时末,血清中几乎检测不到头孢克洛。