Critical role of tedizolid in the treatment of acute bacterial skin and skin structure infections

被引:17
作者
Ferrandez, Olivia [1 ,2 ]
Urbina, Olatz [1 ]
Grau, Santiago [1 ,3 ]
机构
[1] Hosp Univ Mar, Hosp Pharm, Passeig Maritim 25-29, E-08003 Barcelona, Spain
[2] Univ Pompeu Fabra, Dept Nursing, Barcelona, Spain
[3] Univ Autonoma Barcelona, Med Dept, Barcelona, Spain
关键词
tedizolid; tedizolid phosphate; acute bacterial skin and skin structure infections; oxazolidinone; linezolid resistance; IN-VITRO ACTIVITY; RESISTANT STAPHYLOCOCCUS-AUREUS; TOREZOLID PHOSPHATE TR-701; GRAM-POSITIVE PATHOGENS; SOFT-TISSUE INFECTIONS; LINEZOLID RESISTANCE; ENTEROCOCCUS-FAECIUM; COMPLICATED SKIN; POPULATION PHARMACOKINETICS; OXAZOLIDINONE ANTIBIOTICS;
D O I
10.2147/DDDT.S84667
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Tedizolid phosphate has high activity against the Gram-positive microorganisms mainly involved in acute bacterial skin and skin structure infections, such as strains of Staphylococcus aureus (including methicillin-resistant S. aureus strains and methicillin-sensitive S. aureus strains), Streptococcus pyogenes, Streptococcus agalactiae, the Streptococcus anginosus group, and Enterococcus faecalis, including those with some mechanism of resistance limiting the use of linezolid. The area under the curve for time 0-24 hours/minimum inhibitory concentration (MIC) pharmacodynamic ratio has shown the best correlation with the efficacy of tedizolid, versus the time above MIC ratio and the maximum drug concentration/ minimum inhibitory concentration ratio. Administration of this antibiotic for 6 days has shown its noninferiority versus administration of linezolid for 10 days in patients with skin and skin structure infections enrolled in two Phase III studies (ESTABLISH-1 and ESTABLISH-2). Tedizolid's more favorable safety profile and dosage regimen, which allow once-daily administration, versus linezolid, position it as a good therapeutic alternative. However, whether or not the greater economic cost associated with this antibiotic is offset by its shorter treatment duration and possibility of oral administration in routine clinical practice has yet to be clarified.
引用
收藏
页码:65 / 82
页数:18
相关论文
共 99 条
[1]  
[Anonymous], 54 INT C ANT AG CHEM
[2]  
[Anonymous], 52 INT C ANT AG CHEM
[3]  
[Anonymous], 48 INT C ANT AG CHEM
[4]   Linezolid, a novel oxazolidinone antibiotic: Assessment of monoamine oxidase inhibition using presser response to oral tyramine [J].
Antal, EJ ;
Hendershot, PE ;
Batts, DH ;
Sheu, WP ;
Hopkins, NK ;
Donaldson, KM .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (05) :552-562
[5]  
Anti-infective drugs advisory committee, 2014, TED PHOSPH TREATM AC
[6]   Pharmacokinetics of DA-7218, a new oxazolidinone, and its active metabolite, DA-7157, after intravenous and oral administration of DA-7218 and DA-7157 to rats [J].
Bae, Soo K. ;
Yang, Si H. ;
Shin, Karen N. ;
Rhee, Jae K. ;
Yoo, Moohi ;
Lee, Myung G. .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2007, 59 (07) :955-963
[7]   Evaluation of tedizolid against Staphylococcus aureus and enterococci with reduced susceptibility to vancomycin, daptomycin or linezolid [J].
Barber, Katie E. ;
Smith, Jordan R. ;
Raut, Animesh ;
Rybak, Michael J. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2016, 71 (01) :152-155
[8]   European perspective and update on the management of complicated skin and soft tissue infections due to methicillin-resistant Staphylococcus aureus after more than 10years of experience with linezolid [J].
Bassetti, M. ;
Baguneid, M. ;
Bouza, E. ;
Dryden, M. ;
Nathwani, D. ;
Wilcox, M. .
CLINICAL MICROBIOLOGY AND INFECTION, 2014, 20 :3-18
[9]   Toxicity of extended courses of linezolid: results of an Infectious Diseases Society of America Emerging Infections Network survey [J].
Beekmann, Susan E. ;
Gilbert, David N. ;
Polgreen, Philip M. .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2008, 62 (04) :407-410
[10]   Linezolid resistance in Staphylococcus aureus:: Gene dosage effect, stability, fitness costs, and cross-resistances [J].
Besier, Silke ;
Ludwig, Albrecht ;
Zander, Johannes ;
Brade, Volker ;
Wichelhaus, Thomas A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (04) :1570-1572