Attainment of Target Antibiotic Levels by Oral Treatment of Left-sided Infective Endocarditis: A POET Substudy

被引:28
作者
Bock, Magnus [1 ]
Theut, Anna Marie [1 ]
van Hasselt, Johan G. C. [2 ]
Wang, Hengzhuang [1 ,3 ]
Fuursted, Kurt [4 ]
Hoiby, Niels [1 ,3 ]
Lerche, Christian Johann [1 ,5 ]
Ihlemann, Nikolaj [6 ]
Gill, Sabine [7 ]
Christiansen, Ulrik [8 ]
Nielsen, Hans Linde [9 ,10 ]
Lemming, Lars [11 ]
Elming, Hanne [12 ]
Povlsen, Jonas A. [13 ]
Bruun, Niels Eske [10 ,12 ,14 ]
Hofsten, Dan [15 ]
Fosbol, Emil L. [15 ]
Kober, Lars [14 ,15 ]
Schultz, Martin [16 ]
Pries-Heje, Mia M. [15 ]
Kristensen, Jonas Henrik [17 ,18 ]
Christensen, Jens Jorgen [14 ,19 ]
Rosenvinge, Flemming S. [20 ,21 ]
Pedersen, Christian Torp [22 ,23 ]
Helweg-Larsen, Jannik [24 ]
Tonder, Niels [22 ]
Iversen, Kasper [14 ,18 ]
Bundgaard, Henning [14 ,15 ]
Moser, Claus [1 ,3 ,25 ,26 ]
机构
[1] Copenhagen Univ Hosp, Dept Clin Microbiol, Rigshosp, Copenhagen, Denmark
[2] Leiden Univ, Leiden Acad Ctr Drug Res, Leiden, Netherlands
[3] Univ Copenhagen, Dept Immunol & Microbiol, Copenhagen, Denmark
[4] Statens Serum Inst, Dept Bacteria Parasites & Fungi, Copenhagen, Denmark
[5] Copenhagen Univ Hosp, Dept Clin Microbiol, Hvidovre, Denmark
[6] Bispebjerg Hosp, Dept Cardiol, Copenhagen, Denmark
[7] Odense Univ Hosp, Dept Cardiol, Odense, Denmark
[8] Aalborg Univ Hosp, Dept Cardiol, Aalborg, Denmark
[9] Aalborg Univ Hosp, Dept Clin Microbiol, Aalborg, Denmark
[10] Aalborg Univ, Dept Clin Med, Aalborg, Denmark
[11] Aarhus Univ Hosp, Dept Clin Microbiol, Aarhus, Denmark
[12] Zealand Univ Hosp, Dept Cardiol, Roskilde, Denmark
[13] Aarhus Univ Hosp, Dept Cardiol, Aarhus, Denmark
[14] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
[15] Copenhagen Univ Hosp, Dept Cardiol, Rigshosp, Copenhagen, Denmark
[16] Copenhagen Univ Hosp, Dept Internal Med, Copenhagen, Denmark
[17] Copenhagen Univ Hosp, Dept Cardiol, Copenhagen, Denmark
[18] Copenhagen Univ Hosp, Dept Emergency Med, Copenhagen, Denmark
[19] Reg Dept Clin Microbiol, Reg Zealand, Slagelse, Denmark
[20] Odense Univ Hosp, Dept Clin Microbiol, Odense, Denmark
[21] Univ Southern Denmark, Res Unit Clin Microbiol, Odense, Denmark
[22] Nordsjaellands Hosp, Dept Cardiol, Hillerod, Denmark
[23] Univ Copenhagen, Dept Publ Hlth, Copenhagen, Denmark
[24] Copenhagen Univ Hosp, Dept Infect Dis, Rigshosp, Copenhagen, Denmark
[25] Univ Copenhagen, Copenhagen Univ Hosp, Dept Clin Microbiol, Rigshosp, Henrik Harpestrengsvej 4A, DK-2100 Copenhagen, Denmark
[26] Univ Copenhagen, Copenhagen Univ Hosp, Dept Immunol & Microbiol, Henrik Harpestrengsvej 4A, DK-2100 Copenhagen, Denmark
关键词
infective endocarditis; pharmacokinetics; pharmacodynamics; oral antibiotics; target attainment; ANTIMICROBIAL THERAPY; PROTEIN-BINDING; PHARMACOKINETICS; PHARMACODYNAMICS; MICE;
D O I
10.1093/cid/ciad168
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. In the POET (Partial Oral Endocarditis Treatment) trial, oral step-down therapy was noninferior to full-length intravenous antibiotic administration. The aim of the present study was to perform pharmacokinetic/pharmacodynamic analyses for oral treatments of infective endocarditis to assess the probabilities of target attainment (PTAs). Methods. Plasma concentrations of oral antibiotics were measured at day 1 and 5. Minimal inhibitory concentrations (MICs) were determined for the bacteria causing infective endocarditis (streptococci, staphylococci, or enterococci). Pharmacokinetic/pharmacodynamic targets were predefined according to literature using time above MIC or the ratio of area under the curve to MIC. Population pharmacokinetic modeling and pharmacokinetic/pharmacodynamic analyses were done for amoxicillin, dicloxacillin, linezolid, moxifloxacin, and rifampicin, and PTAs were calculated. Results. A total of 236 patients participated in this POET substudy. For amoxicillin and linezolid, the PTAs were 88%-100%. For moxifloxacin and rifampicin, the PTAs were 71%-100%. Using a clinical breakpoint for staphylococci, the PTAs for dicloxacillin were 9%-17%. Seventy-four patients at day 1 and 65 patients at day 5 had available pharmacokinetic and MIC data for 2 oral antibiotics. Of those, 13 patients at day 1 and 14 patients at day 5 did only reach the target for 1 antibiotic. One patient did not reach target for any of the 2 antibiotics. Conclusions. For the individual orally administered antibiotic, the majority reached the target level. Patients with sub-target levels were compensated by the administration of 2 different antibiotics. The findings support the efficacy of oral step-down antibiotic treatment in patients with infective endocarditis.
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收藏
页码:242 / 251
页数:10
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