共 50 条
Pharmacokinetics of ertapenem in patients with multidrug-resistant tuberculosis
被引:26
|作者:
van Rijn, Sander P.
[1
]
van Altena, Richard
[2
]
Akkerman, Onno W.
[2
]
van Soolingen, Dick
[3
,4
,5
]
van der Laan, Tridia
[5
]
de Lange, Wiel C. M.
[2
]
Kosterink, Jos G. W.
[1
,6
]
van der Werf, Tjip S.
[7
,8
]
Alffenaar, Jan-Willem C.
[1
]
机构:
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, TB Ctr Beatrixoord, Haren, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Pulm Dis, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Med Ctr, Dept Med Microbiol, Nijmegen, Netherlands
[5] Natl Inst Publ Hlth & Environm RIVM, Natl TB Reference Lab, Bilthoven, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Pharm, Sect Pharmacotherapy & Pharmaceut Care, Groningen, Netherlands
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Internal Med, Groningen, Netherlands
[8] Univ Groningen, Univ Med Ctr Groningen, Dept Pulm Dis & TB, Groningen, Netherlands
关键词:
GROUP;
5;
DRUGS;
MYCOBACTERIUM-TUBERCULOSIS;
SUSCEPTIBILITY;
CARBAPENEMS;
CLAVULANATE;
MEROPENEM;
EFFICACY;
SAFETY;
MOXIFLOXACIN;
EXPERIENCE;
D O I:
10.1183/13993003.01654-2015
中图分类号:
R56 [呼吸系及胸部疾病];
学科分类号:
摘要:
Treatment of multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB) is becoming more challenging because of increased levels of drug resistance against second-line TB drugs. One promising group of antimicrobial drugs is carbapenems. Ertapenem is an attractive carbapenem for the treatment of MDR- and XDR-TB because its relatively long half-life enables once-daily dosing. A retrospective study was performed for all patients with suspected MDR-TB at the Tuberculosis Center Beatrixoord of the University Medical Center Groningen (Haren, the Netherlands) who received ertapenem as part of their treatment regimen between December 1, 2010 and March 1, 2013. Safety and pharmacokinetics were evaluated. 18 patients were treated with 1000 mg ertapenem for a mean (range) of 77 (5-210) days. Sputum smear and culture were converted in all patients. Drug exposure was evaluated in 12 patients. The mean (range) area under the concentration-time curve up to 24 h was 544.9 (309-1130) h.mg.L-1. The mean (range) maximum observed plasma concentration was 127.5 (73.9-277.9) mg.L-1. In general, ertapenem treatment was well tolerated during MDR-TB treatment and showed a favourable pharmacokinetic/pharmacodynamic profile in MDR-TB patients. We conclude that ertapenem is a highly promising drug for the treatment of MDR-TB that warrants further investigation.
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页码:1229 / 1234
页数:6
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