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头孢唑肟在新生儿和婴幼儿中的临床疗效及药代动力学评价

[Clinical efficacy and pharmacokinetic evaluation of ceftizoxime in neonates and young infants].

作者信息

Sakata H, Fujita K, Murono K, Kakehashi H, Kaeriyama M, Oka T, Yoshioka H, In-yaku F

机构信息

Department of Pediatrics, Asahikawa Medical College.

出版信息

Jpn J Antibiot. 1988 Aug;41(8):1046-52.

PMID:3050189
Abstract

Thirteen neonates and young infants, including 5 infants with very low birth weight, were treated with ceftizoxime (CZX) and its clinical efficacy and side effects were evaluated. The ages of the patients ranged from 0 to 96 days, and their body weights ranged from 580 to 5,050 g. Doses given were 20-54 mg/kg every 6 to 12 hours for 2.5 to 7.5 days. Two infants with sepsis, one with urinary tract infection, one with sepsis and urinary tract infection, and 1 with fetal infection were considered to have responded satisfactorily to the CZX treatment. The drug was well tolerated and side effects was not apparent. Pharmacokinetic studies were done on CZX in 8 patients including 4 infants with very low birth weight. Their ages ranged from 2 to 91 days, and body weights from 545 to 5,050 g. Serum concentrations at 2 hours after single 20 mg/kg intravenous bolus injections were 19.2 to 44.2 micrograms/ml and the levels were 2.11 to 26.3 micrograms/ml at 8 hours. Elimination half-lives of CZX ranged 1.90 to 9.57 hours in these patients. In 2 infants with very low birth weights with ages 7 and 91 days, half-lives were as long as 9.57 and 8.24 hours, respectively. Urinary recovery in 6 hours was 31.9-66.9% in 5 patients. Urine concentrations of the drug in 24 samples collected at various time from the 7 patients ranged from 130 to 3,219 micrograms/ml. Influence of CZX on the fecal flora was studied in 1 patient given 20 mg/kg X 4/day of the drug.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

13名新生儿和小婴儿,包括5名极低出生体重儿,接受了头孢唑肟(CZX)治疗,并对其临床疗效和副作用进行了评估。患者年龄为0至96天,体重为580至5050克。给药剂量为每6至12小时20 - 54毫克/千克,持续2.5至7.5天。2名败血症婴儿、1名尿路感染婴儿、1名败血症合并尿路感染婴儿和1名胎儿感染婴儿被认为对CZX治疗反应良好。该药物耐受性良好,未出现明显副作用。对8名患者(包括4名极低出生体重儿)进行了CZX的药代动力学研究。他们的年龄为2至91天,体重为545至5050克。单次静脉推注20毫克/千克后2小时的血清浓度为19.2至44.2微克/毫升,8小时时为2.11至26.3微克/毫升。这些患者中CZX的消除半衰期为1.90至9.57小时。在2名年龄分别为7天和91天的极低出生体重儿中,半衰期分别长达9.57小时和8.24小时。5名患者6小时的尿回收率为31.9 - 66.9%。从7名患者在不同时间采集的24份尿液样本中,药物尿液浓度为130至3219微克/毫升。对1名每天给予20毫克/千克×4次该药物的患者研究了CZX对粪便菌群的影响。(摘要截断于250字)

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