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九种口服制剂对社区获得性感染中革兰氏阳性菌和革兰氏阴性菌的活性:在β-内酰胺类和大环内酯类抗菌药物的比较评估中使用药代动力学/药效学断点

Activity of nine oral agents against gram-positive and gram-negative bacteria encountered in community-acquired infections: use of pharmacokinetic/pharmacodynamic breakpoints in the comparative assessment of beta-lactam and macrolide antimicrobial agents.

作者信息

Peric Mihaela, Browne Frederick A, Jacobs Michael R, Appelbaum Peter C

机构信息

Hershey Medical Center, Hershey, Pennsylvania 17033, USA.

出版信息

Clin Ther. 2003 Jan;25(1):169-77. doi: 10.1016/s0149-2918(03)90021-x.

Abstract

BACKGROUND

The application of pharmacokinetic (PK) and pharmacodynamic (PD) data in conjunction with minimum inhibitory concentrations (MICs) of antibacterial agents has been shown to allow for improved selection and appropriate dosing of antimicrobial agents for specific infections, increasing the likelihood of bacteriologic cure and, through this, reducing the risk for the development of resistant organisms.

OBJECTIVES

This study was undertaken to provide data on current levels of resistance among common community-acquired bacterial species to 7 betalactam antimicrobial agents (including the combination product amoxicillin/clavulanate), azithromycin, and clarithromycin, determined through application of the PK/PD breakpoints based on time-above-MIC for the beta-lactams and the nonazalide macrolide clarithromycin, and on 24-hour serum area under the curve divided by MIC for the azalide macrolide azithromycin.

METHODS

The antimicrobial products tested were amoxicillin/clavylanate, cefpodoxime, cefdinir, cefditoren, cefprozil, cefuroxime, cefixime, azithromycin, and clarithromycin. The bacterial species comprised 70 penicillin-susceptible, 68 penicillin-intermediate, and 69 penicillin-resistant strains of Streptococcus pneumoniae; 46 beta-lactamase-positive and 54 beta-lactamase-negative strains of Haemophilus influenzae; 49 strains of Moraxella catarrhalis; and 100 methicillin-sensitive strains of Staphylococcus aureus (MSSA). Strains were isolated from clinical specimens obtained from outpatient-acquired infections in 1 clinical center in the Northeast and 1 in the north-central area of the United States within the past 2 years. National Committee for Clinical Laboratory Standards microdilution MIC methodology was used. PK/PD breakpoints were obtained from previously published studies and were based on blood values.

RESULTS

Amoxicillin/clavulanate was the product to which the greatest percentage of susceptible, intermediate, and resistant strains of pneumococci were sensitive at the PK/PD breakpoint, followed by cefditoren, cefpodoxime, cefuroxime, cefdinir, and cefprozil. None of the cephalosporins were active against penicillin-resistant pneumococci. Cefditoren and cefpodozime were the agents to which the greatest percentage of beta-lactamase-positive and beta-lactamase-negative strains of H influenzae were sensitive, followed by amoxicillin/clavulanate, cefdinir, and cefuroxime. Cefprozil was inactive against H influenzae. All of the beta-lactam products were active against M catarrhalis. All but cefpodoxime, cefditoren, and cefixime were active against MSSA.

CONCLUSIONS

In this study, based on PK/PD breakpoints, amoxicillin/clavulanate had the best overall activity of the 9 antimicrobial products tested. Cefpodoxime and cefditoren were active against >or=90% of strains of penicillin-susceptible and penicillin-intermediate pneumococci, H influenzae, and M catarrhalis. The macrolides azithromycin and clarithromycin were active against penicillin-susceptible and penicillin-intermediate pneumococci and M catarrhalis; they were inactive against H influenzae and penicillin-resistant pneumococci.

摘要

背景

药代动力学(PK)和药效学(PD)数据与抗菌药物的最低抑菌浓度(MIC)相结合,已被证明有助于为特定感染更好地选择抗菌药物并确定合适的剂量,提高细菌学治愈的可能性,并由此降低耐药菌产生的风险。

目的

本研究旨在提供常见社区获得性细菌对7种β-内酰胺类抗菌药物(包括复方制剂阿莫西林/克拉维酸)、阿奇霉素和克拉霉素的当前耐药水平数据,这些数据通过应用基于β-内酰胺类和非氮杂内酯类大环内酯类克拉霉素的高于MIC时间的PK/PD折点,以及基于氮杂内酯类大环内酯类阿奇霉素的24小时血清曲线下面积除以MIC的PK/PD折点来确定。

方法

所测试的抗菌产品有阿莫西林/克拉维酸、头孢泊肟、头孢地尼、头孢托仑、头孢丙烯、头孢呋辛、头孢克肟、阿奇霉素和克拉霉素。细菌种类包括70株青霉素敏感、68株青霉素中介和69株青霉素耐药的肺炎链球菌;46株β-内酰胺酶阳性和54株β-内酰胺酶阴性的流感嗜血杆菌;49株卡他莫拉菌;以及100株甲氧西林敏感金黄色葡萄球菌(MSSA)。菌株从过去2年内在美国东北部1个临床中心和中北部1个临床中心获得的门诊获得性感染的临床标本中分离得到。采用美国国家临床实验室标准委员会微量稀释MIC方法。PK/PD折点取自先前发表的研究,基于血液值。

结果

在PK/PD折点下,阿莫西林/克拉维酸是对肺炎链球菌敏感、中介和耐药菌株敏感率最高的产品,其次是头孢托仑、头孢泊肟、头孢呋辛、头孢地尼和头孢丙烯。没有一种头孢菌素对青霉素耐药肺炎链球菌有活性。头孢托仑和头孢泊肟是对β-内酰胺酶阳性和β-内酰胺酶阴性流感嗜血杆菌敏感率最高的药物,其次是阿莫西林/克拉维酸、头孢地尼和头孢呋辛。头孢丙烯对流感嗜血杆菌无活性。所有β-内酰胺类产品对卡他莫拉菌均有活性。除头孢泊肟、头孢托仑和头孢克肟外,所有产品对MSSA均有活性。

结论

在本研究中,基于PK/PD折点,阿莫西林/克拉维酸在所测试的9种抗菌产品中总体活性最佳。头孢泊肟和头孢托仑对≥90%的青霉素敏感和青霉素中介肺炎链球菌、流感嗜血杆菌和卡他莫拉菌菌株有活性。大环内酯类阿奇霉素和克拉霉素对青霉素敏感和青霉素中介肺炎链球菌及卡他莫拉菌有活性;它们对流感嗜血杆菌和青霉素耐药肺炎链球菌无活性。

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