Akita H, Sato Y, Kusumoto Y, Iwata S, Takeuchi Y, Aoyama T, Yokota T, Sunakawa K
Department of Pediatrics, Yamato City Hospital.
Jpn J Antibiot. 1996 Oct;49(10):899-916.
Azithromycin (AZM), a new macrolide antibiotic, in fine granules and in capsules was studied for pharmacokinetic and clinical evaluation in the pediatric patients. Antibacterial activity of AZM against 43 clinical isolates: AZM exhibited slightly lower activity against Gram-positive bacteria and 2-8-fold higher activity against Gram-negative bacteria than erythromycin or clarithromycin. Plasma or urine samples were collected from eight patients receiving the drug in fine granular form, and two patients receiving it in capsules for the determination of drug levels. The elimination half-lives of AZM after administration at dose of 10 mg/kg/day for 3 days were 50.0 and 51.2 hours for fine granules, and 41.5 hours for capsules. AUC0-infinity was 11.7 and 24.3 micrograms.hr/ml for fine granules, and 8.3 micrograms.hr/ml for capsules. The cumulative excretion rates up to 120 hours after the start of treatment were 8.24 and 13.84% for fine granules, and 3.83% for capsules. AZM was administered to 123 patients once daily at 3.7-20.0 mg/kg body weight over 3 to 5 days with reference to the standard dose of 10 mg/kg. The drug was used to treat patients with pharyngitis, tonsillitis, scarlet fever, pneumonia, mycoplasmal pneumonia, chlamydial pneumonia, otitis media, pertussis, intestinal infection, and SSTI. The effectiveness of AZM was evaluated in 109 cases. The drug was rated "excellent" in 65.1% of the patients and "good" in 29.4%, resulting in an efficacy rate of 94.5%. Furthermore, AZM eradicated 43 of 46 (93.5%) bacteria that had been identified before the treatment. Three patients complained of side effects of urticaria (1 case) and diarrhea (2 cases). Abnormal laboratory changes were reported as follows: decreased leukocyte (3 cases), increased eosinophil (5), increased platelet (2), increased eosinophil and platelet, elevated GPT (1), and elevated GOT and GPT (1). The abnormalities, however, were mild enough to raise no clinically significant problems. In conclusion, AZM in once daily regimen was effective and safe in treatment of pediatric infections.
阿奇霉素(AZM)是一种新型大环内酯类抗生素,对其细颗粒剂和胶囊剂在儿科患者中进行了药代动力学和临床评价研究。AZM对43株临床分离菌的抗菌活性:与红霉素或克拉霉素相比,AZM对革兰氏阳性菌的活性略低,对革兰氏阴性菌的活性高2 - 8倍。从8例接受细颗粒剂型药物的患者和2例接受胶囊剂型药物的患者中采集血浆或尿液样本,用于测定药物水平。以10mg/kg/天的剂量给药3天后,AZM细颗粒剂的消除半衰期分别为50.0小时和51.2小时,胶囊剂为41.5小时。细颗粒剂的AUC0-∞为11.7和24.3μg·hr/ml,胶囊剂为8.3μg·hr/ml。治疗开始后120小时内的累积排泄率,细颗粒剂为8.24%和