共 40 条
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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页码:242 / 251
页数:10
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