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口服β-内酰胺类药物治疗儿童流感嗜血杆菌感染时达到所需药效学暴露的概率。

Probability of achieving requisite pharmacodynamic exposure for oral beta-lactam regimens against Haemophilus influenzae in children.

作者信息

Pichichero Michael E, Doern Gary V, Kuti Joseph L, Nicolau David P

机构信息

Department of Microbiology and Immunology, University of Rochester, Rochester, New York 14642, USA.

出版信息

Paediatr Drugs. 2008;10(6):391-7. doi: 10.2165/0148581-200810060-00006.

Abstract

OBJECTIVE

To define contemporary levels of resistance of Haemophilus influenzae to antibacterials commonly used to treat children for bacterial respiratory infections, and to assess the probability of achieving the requisite pharmacodynamic exposures for regimens against recent respiratory H. influenzae isolates using Monte Carlo simulation.

METHODS

233 H. influenzae isolates obtained from pediatric outpatients with acute otitis media (n = 55), sinusitis (n = 58), or lower respiratory tract infections ( n = 120) from 1 November 2004 to 30 April 2005 were characterized for beta-lactamase production and susceptibility to a panel of 10 beta-lactam antimicrobials. 5000 concentration-time profiles were simulated for US FDA-approved doses of oral amoxicillin, amoxicillin/clavulanic acid, cefpodoxime, cefprozil, ceftibuten, and cefuroxime using pharmacokinetics and weights of 5-year old male children. The probability of attaining free drug concentrations above the minimum inhibitory concentration (MIC) for 50% of the dosing interval (50% fT > MIC) was assessed for each regimen against this population of H. influenzae.

RESULTS

beta-Lactamase production was demonstrated in 67 (28.8%) of the H. influenzae isolates and varied by isolation site (38% acute otitis media, 36% sinusitis, and 21% lower respiratory tract infections). Regarding susceptibility, the rank order of the tested antimicrobials was ceftriaxone = cefixime (100%) > cefpodoxime (99.6%) > ceftibuten = amoxicillin/clavulanic acid (99.1%) > cefdinir (98.7%) > cefuroxime (97.4%) > cefprozil (93.1%) > cefaclor (92.3%) > amoxicillin (63.1%). The most active agents based on pharmacodynamic assessment (50% fT > MIC) were cefpodoxime (98.9%), ceftibuten (95.3%), and high-dose amoxicillin/clavulanic acid (90.4%). Several amoxicillin regimens also achieved a high likelihood of pharmacodynamic target attainment (91.8- 98.6%) when beta-lactamase-positive strains were excluded from the analysis.

CONCLUSION

Against H. influenzae, the antibacterials most likely to achieve optimal in vivo exposures in children are cefpodoxime, ceftibuten, and amoxicillin/clavulanic acid.

摘要

目的

确定流感嗜血杆菌对常用于治疗儿童细菌性呼吸道感染的抗菌药物的当代耐药水平,并使用蒙特卡洛模拟评估针对近期呼吸道流感嗜血杆菌分离株的治疗方案达到所需药效学暴露水平的概率。

方法

从2004年11月1日至2005年4月30日期间患有急性中耳炎(n = 55)、鼻窦炎(n = 58)或下呼吸道感染(n = 120)的儿科门诊患者中获得233株流感嗜血杆菌分离株,对其β-内酰胺酶产生情况及对一组10种β-内酰胺类抗菌药物的敏感性进行了表征。使用5岁男性儿童的药代动力学和体重,模拟了美国食品药品监督管理局(FDA)批准剂量的口服阿莫西林、阿莫西林/克拉维酸、头孢泊肟、头孢丙烯、头孢布烯和头孢呋辛的5000个浓度-时间曲线。针对这组流感嗜血杆菌分离株,评估了每种治疗方案在给药间隔的50%时间内达到游离药物浓度高于最低抑菌浓度(MIC)(50% fT > MIC)的概率。

结果

67株(28.8%)流感嗜血杆菌分离株检测到β-内酰胺酶产生,且因分离部位而异(急性中耳炎为38%,鼻窦炎为36%,下呼吸道感染为21%)。关于敏感性,受试抗菌药物的排序为头孢曲松 = 头孢克肟(100%)> 头孢泊肟(99.6%)> 头孢布烯 = 阿莫西林/克拉维酸(99.1%)> 头孢地尼(98.7%)> 头孢呋辛(97.4%)> 头孢丙烯(93.1%)> 头孢克洛(92.3%)> 阿莫西林(63.1%)。基于药效学评估(50% fT > MIC),最有效的药物是头孢泊肟(98.9%)、头孢布烯(95.3%)和高剂量阿莫西林/克拉维酸(90.4%)。当分析中排除β-内酰胺酶阳性菌株时,几种阿莫西林治疗方案也有很高的概率达到药效学目标(91.8 - 98.6%)。

结论

针对流感嗜血杆菌,最有可能在儿童体内实现最佳暴露的抗菌药物是头孢泊肟、头孢布烯和阿莫西林/克拉维酸。

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