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反馈剂量调整对医院获得性肺炎中病原体清除的概率有显著影响。

Feedback dose alteration significantly affects probability of pathogen eradication in nosocomial pneumonia.

作者信息

Scaglione F, Esposito S, Leone S, Lucini V, Pannacci M, Ma L, Drusano G L

机构信息

Department of Pharmacology, Chemotherapy and Toxicology, Faculty of Medicine, University of Milan, Milan, Italy.

出版信息

Eur Respir J. 2009 Aug;34(2):394-400. doi: 10.1183/09031936.00149508. Epub 2009 Feb 12.

Abstract

Nosocomial pneumonia (NP) is associated with considerable morbidity and mortality. Data have shown that inadequate initial antibiotic therapy is a major risk for infection-attributed mortality. The aim of the present study was to measure antibiotic concentration and minimum inhibitory concentration (MIC) in infected hospitalised patients early in therapy, in order to determine whether dose alterations, in those with low drug concentrations, could affect outcomes. Only patients treated with aminoglycosides, fluoroquinolones, and beta-lactams were evaluated. MICs were determined using standard National Committee for Clinical Laboratory Standards procedures. Antibiotics were assayed using validated high-performance liquid chromatographic methods. Pharmacokinetic/pharmacodynamic markers adopted were: aminoglycoside peak/MIC ratio >or=8 mg L(-1); fluoroquinolone peak/MIC >or=10 mg L(-1); beta-lactam peak/MIC >or=4 mg L(-1) and time that plasma levels remain above the MIC >or=70%. 638 patients with NP were included in the study. In 205 patients, both drug concentration and isolate MIC were available, while in other patients, used as controls, one or both parameters were lacking. For clinical outcome, the Acute Physiology and Chronic Health Evaluation II score (p<0.0001), the presence of combination therapy (p = 0.0014) and whether both MIC and drug concentration(s) were measured (p = 0.0002) significantly affected the probability of a good outcome. For microbiological outcome, the MIC for the beta-lactams (<or=2 mg L(-1); p<0.0001) and whether the second drug was a fluoroquinolone or aminoglycoside (fluoroquinolones were better than aminoglycosides; p = 0.0177), as well as whether both MIC and drug concentration(s) were measured (p = 0.02), affected the probability of eradication. Measurement of drug concentrations and determination of pathogen MIC values with subsequent dose alteration significantly improves the probability of good clinical outcome and pathogen eradication in NP.

摘要

医院获得性肺炎(NP)与相当高的发病率和死亡率相关。数据表明,初始抗生素治疗不充分是感染归因死亡率的主要风险。本研究的目的是在治疗早期测量感染住院患者的抗生素浓度和最低抑菌浓度(MIC),以确定药物浓度低的患者调整剂量是否会影响治疗结果。仅对接受氨基糖苷类、氟喹诺酮类和β-内酰胺类治疗的患者进行评估。使用标准的美国国家临床实验室标准委员会程序测定MIC。采用经过验证的高效液相色谱法测定抗生素。采用的药代动力学/药效学指标为:氨基糖苷类峰浓度/MIC比值≥8 mg·L⁻¹;氟喹诺酮类峰浓度/MIC≥10 mg·L⁻¹;β-内酰胺类峰浓度/MIC≥4 mg·L⁻¹且血浆水平高于MIC的时间≥70%。638例NP患者纳入研究。205例患者可获得药物浓度和分离菌MIC,而其他用作对照的患者则缺少一个或两个参数。对于临床结局,急性生理与慢性健康状况评分II(p<0.0001)、联合治疗的使用情况(p = 0.0014)以及是否同时测量了MIC和药物浓度(p = 0.0002)显著影响良好结局的概率。对于微生物学结局,β-内酰胺类的MIC(≤2 mg·L⁻¹;p<0.0001)、第二种药物是氟喹诺酮类还是氨基糖苷类(氟喹诺酮类比氨基糖苷类更好;p = 0.0177)以及是否同时测量了MIC和药物浓度(p = 0.02)影响根除的概率。测量药物浓度并确定病原体MIC值,随后调整剂量可显著提高NP患者良好临床结局和病原体根除的概率。

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