Dosing strategies to optimize currently available anti-MRSA treatment options (Part 2: PO options)

被引:3
|
作者
Payne, Kenna D. [1 ]
Das, Amrita [2 ]
Ndiulor, Michelle [2 ]
Hall, Ronald G. [2 ,3 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Pharm Practice Dept, Amarillo, TX 79106 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Dallas, TX USA
[3] Dose Optimizat & Outcomes Res DOOR Program, Dallas, TX USA
关键词
Dose optimization; MRSA; antimicrobial; pharmacokinetics; pharmacodynamics; RESISTANT STAPHYLOCOCCUS-AUREUS; SKIN-STRUCTURE INFECTIONS; ACUTE BACTERIAL SKIN; RENAL REPLACEMENT THERAPY; TRIMETHOPRIM-SULFAMETHOXAZOLE; POPULATION PHARMACOKINETICS; THIGH INFECTION; LINEZOLID PHARMACOKINETICS; TEDIZOLID PHOSPHATE; MORBIDLY OBESE;
D O I
10.1080/17512433.2018.1411800
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Methicillin-resistant Staphylococcus aureus (MRSA) is a problematic pathogen in both outpatient and inpatient settings. Research to optimize the dosing of these agents is needed to slow the development of antimicrobial resistance and to decrease the likelihood of clinical failure. Areas covered: This review summarizes the available data for orally administered antimicrobials routinely used as monotherapy for MRSA infections. We make recommendations and highlight the current gaps in the literature. A PubMed (1966 - Present) search was performed to identify relevant literature for this review. Expert commentary: There is a vast divide in the amount of pharmacokinetic/pharmacodynamic data to guide dosing decisions for older MRSA agents compared with the oxazolidenones. Five-year view: Additional retrospective data will become available for the older MRSA agents in severe MRSA infections.
引用
收藏
页码:139 / 149
页数:11
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