Fujita K, Murono K, Saijyo M, Yoshioka H, Maruyama S, Sakata H, Inyaku F
Department of Pediatrics, Asahikawa Medical College.
Jpn J Antibiot. 1992 Jun;45(6):718-26.
Forty-five children were treated with meropenem (MEPM) and the clinical efficacy and side effects were evaluated. The ages of the patients ranged from 1 month to 9 years and their body weights from 5.2 to 25 kg. Doses given were 17.2-45.5 mg/kg every 6 to 8 hours for 2 to 24.5 days. Those patients who responded to the MEPM treatment included 15 children with pneumonia, 7 with pharyngitis, 3 with cervical lymphadenitis, 3 with cellulitis, 10 with urinary tract infections and 4 with other infections. Among 42 children, the results were excellent in 29, good in 12 and fair in 1. The drug was well tolerated, although slightly elevated serum concentrations of transaminases occurred in 5 patients, eosinophilia in 2 patients, and neutropenia in 1 patient among 45 patients examined. The pharmacokinetic studies on MEPM were done in 6 patients. Their ages ranged from 2 to 9 years and body weights from 14.5 to 23.2 kg. In 4 patients, plasma concentrations at the end of 30 minutes drip infusion of 20 mg/kg were 29.28 +/- 10.29 micrograms/ml and those 3 hours later were 0.49 +/- 0.26 micrograms/ml. Serum elimination half-lives of the drug were 0.66 +/- 0.12 hours in these patients. Excretion rates of this drug into urine in the first 6 hours after initiation of drug administration were 53 and 40% in 2 of these patients. In 2 patients with 35 and 44 mg/kg of drug administration, plasma concentrations were higher than those given 20 mg/kg of the drug.(ABSTRACT TRUNCATED AT 250 WORDS)
45名儿童接受了美罗培南(MEPM)治疗,并对其临床疗效和副作用进行了评估。患者年龄从1个月至9岁,体重从5.2千克至25千克。给药剂量为每6至8小时17.2 - 45.5毫克/千克,持续2至24.5天。对MEPM治疗有反应的患者包括15名肺炎患儿、7名咽炎患儿、3名颈淋巴结炎患儿、3名蜂窝织炎患儿、10名尿路感染患儿和4名其他感染患儿。在42名儿童中,结果为优的有29名,良的有12名,中平的有1名。该药物耐受性良好,尽管在45名接受检查的患者中,有5名患者血清转氨酶浓度略有升高,2名患者出现嗜酸性粒细胞增多,1名患者出现中性粒细胞减少。对6名患者进行了美罗培南的药代动力学研究。他们的年龄从2岁至9岁,体重从14.5千克至23.2千克。在4名患者中,静脉滴注20毫克/千克30分钟结束时的血浆浓度为29.28±10.29微克/毫升,3小时后的血浆浓度为0.49±0.26微克/毫升。这些患者中该药物的血清消除半衰期为0.66±0.12小时。在开始给药后的前6小时内,其中2名患者该药物的尿排泄率分别为53%和40%。在2名分别给予35毫克/千克和44毫克/千克药物的患者中,血浆浓度高于给予20毫克/千克药物的患者。(摘要截取自250字)