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本文引用的文献

1
Single-dose pharmacokinetics of the monobactam azthreonam (SQ 26,776) in healthy subjects.健康受试者中单环β-内酰胺类氨曲南(SQ 26,776)的单剂量药代动力学。
Antimicrob Agents Chemother. 1982 Jun;21(6):944-9. doi: 10.1128/AAC.21.6.944.
2
Azthreonam (SQ 26,776), a synthetic monobactam specifically active against aerobic gram-negative bacteria.氨曲南(SQ 26,776),一种对需氧革兰氏阴性菌有特效的合成单环β-内酰胺抗生素。
Antimicrob Agents Chemother. 1982 Jan;21(1):85-92. doi: 10.1128/AAC.21.1.85.
3
Comparative in vitro study of SQ26,776.SQ26,776的体外对比研究。
Antimicrob Agents Chemother. 1982 Feb;21(2):294-8. doi: 10.1128/AAC.21.2.294.
4
Pharmacokinetics of aztreonam in patients with various degrees of renal dysfunction.氨曲南在不同程度肾功能不全患者中的药代动力学。
Antimicrob Agents Chemother. 1983 Aug;24(2):252-61. doi: 10.1128/AAC.24.2.252.
5
Single-dose pharmacokinetics of aztreonam in pediatric patients.氨曲南在儿科患者中的单剂量药代动力学。
Antimicrob Agents Chemother. 1984 Aug;26(2):196-9. doi: 10.1128/AAC.26.2.196.
6
Evaluation of aztreonam in experimental bacterial meningitis and cerebritis.氨曲南在实验性细菌性脑膜炎和脑脓肿中的评估。
Antimicrob Agents Chemother. 1983 Nov;24(5):682-8. doi: 10.1128/AAC.24.5.682.
7
Serial dilution antibiotic sensitivity testing with the microtitrator system.使用微量滴定仪系统进行系列稀释抗生素敏感性测试。
Am J Clin Pathol. 1966 May;45(5):548-51. doi: 10.1093/ajcp/45.5.548.
8
Microbioassay of antimicrobial agents.抗菌剂的微生物测定法。
Appl Microbiol. 1970 Apr;19(4):573-9. doi: 10.1128/am.19.4.573-579.1970.
9
Aztreonam therapy in experimental meningitis due to Haemophilus influenzae type b and Escherichia coli K1.氨曲南治疗由b型流感嗜血杆菌和大肠杆菌K1引起的实验性脑膜炎。
Antimicrob Agents Chemother. 1985 Apr;27(4):655-6. doi: 10.1128/AAC.27.4.655.

氨曲南在低体重儿中的药代动力学及血浆杀菌活性

Pharmacokinetics and plasma bactericidal activity of aztreonam in low-birth-weight infants.

作者信息

Likitnukul S, McCracken G H, Threlkeld N, Darabi A, Olsen K

出版信息

Antimicrob Agents Chemother. 1987 Jan;31(1):81-3. doi: 10.1128/AAC.31.1.81.

DOI:10.1128/AAC.31.1.81
PMID:3105443
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC174656/
Abstract

Aztreonam (30 mg/kg) was administered intravenously every 12 h during week 1 and every 8 h during weeks 2 to 4 of life to 26 low-birth-weight (less than 2,000 g) infants, and plasma concentration-time curves were measured on two occasions. The pharmacokinetics were described equally well by one-compartment and noncompartment models, and the values on day 1 were similar to those measured during the steady state on days 3 to 6. The mean peak plasma concentrations at completion of the 10-min infusion were from 65 to 83 micrograms/ml, the higher concentrations being seen in the larger infants. The half-lives of aztreonam ranged from 5.4 to 8.6 h and did not change significantly with birth weight. The median peak and trough plasma bactericidal titer against a strain of Escherichia coli (MBC, 10 micrograms/ml) was 1:16. Against a strain of Pseudomonas aeruginosa (MBC, 16 micrograms/ml), the median peak and trough bactericidal titers were 1:8 to 1:16 and 1:4, respectively. The urinary concentrations of aztreonam on day 1 of therapy were from 24 to 460.7 micrograms/ml (mean +/- 1 standard deviation, 254 +/- 113 micrograms/ml).

摘要

对26名低体重(小于2000克)婴儿在出生后第1周每12小时静脉注射氨曲南(30毫克/千克),在第2至4周每8小时静脉注射一次,并在两个时间点测量血浆浓度-时间曲线。单室模型和非房室模型对药代动力学的描述效果相当,第1天的值与第3至6天稳态时测量的值相似。在10分钟输注结束时,平均血浆峰浓度为65至83微克/毫升,较大婴儿的浓度更高。氨曲南的半衰期为5.4至8.6小时,且不随出生体重显著变化。针对一株大肠杆菌(最低杀菌浓度,10微克/毫升),血浆峰和谷杀菌效价中位数为1:16。针对一株铜绿假单胞菌(最低杀菌浓度,16微克/毫升),血浆峰和谷杀菌效价中位数分别为1:8至1:16和1:4。治疗第1天氨曲南的尿浓度为24至460.7微克/毫升(平均值±1标准差,254±113微克/毫升)。