Telavancin pharmacokinetics in patients with chronic kidney disease receiving haemodialysis

被引:1
|
作者
Gharibian, Katherine N. [1 ]
Lewis, Susan J. [2 ,3 ]
Heung, Michael [4 ]
Segal, Jonathan H. [4 ]
Salama, Noha N. [5 ,6 ]
Mueller, Bruce A. [7 ]
机构
[1] Amgen Inc, Thousand Oaks, CA USA
[2] Univ Findlay, Coll Pharm, Dept Pharm Practice, Findlay, OH 45840 USA
[3] Mercy Hlth St Anne Hosp, Dept Pharm, Toledo, OH 43623 USA
[4] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USA
[5] Cairo Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo, Egypt
[6] Univ Hlth Sci & Pharm, St Louis Coll Pharm, Dept Pharmaceut & Adm Sci, St Louis, MO USA
[7] Univ Michigan, Coll Pharm, Dept Clin Pharm, 428 Church St, Ann Arbor, MI 48109 USA
关键词
IN-VITRO; INFECTIONS; BACTEREMIA;
D O I
10.1093/jac/dkab370
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Telavancin is a lipoglycopeptide antibiotic with limited pharmacokinetic data to guide drug dosing in patients receiving haemodialysis. Objectives: This study characterized telavancin pharmacokinetics in patients receiving haemodialysis. Patients and methods: This was a Phase IV, prospective, open-label, single-centre, crossover pharmacokinetic study (ClinicalTrials.gov: NCT02392208). Eight subjects with end-stage kidney disease requiring maintenance haemodialysis (mean +/- SD: 47 +/- 20 years, 69.5 +/- 17.1 kg) received 5 mg/kg telavancin IV 3 h before starting a 3.5 hour haemodialysis treatment with a high-permeability haemodialyser (haemodialysis period). After a 14 day washout period, a second 5 mg/kg dose was administered post-haemodialysis (control period). Telavancin plasma concentrations were measured over a 2 day period after each dose and non-compartmental pharmacokinetic analyses were performed. Results: The geometricmean (GM) of telavancin overall clearance was 11.2 mL/h/kg (intrinsic clearance and dialytic clearance) in the haemodialysis period and 5.9 mL/h/kg (off-haemodialysis clearance) in the control period [GM ratio (GMR) = 1.89; 90% CI: 1.70-2.10; P < 0.01]. The GM t(1/2) was 13.1 h when haemodialysis occurred 3 h post-dosing in the haemodialysis period but extended to 20.9 h with post-haemodialysis dosing in the control period (GMR = 0.63; 90% CI: 0.54-0.73; P < 0.01). The GM of telavancin plasma concentrations removed by haemodialysis was 27.7%. The GMR of peak plasma concentration and volume of distribution of the haemodialysis period and the control period were 0.88 (90% CI: 0.79-0.98; P = 0.08) and 1.17 (90% CI: 1.05-1.30; P = 0.048), respectively. Conclusions: Haemodialysis with high-permeability haemodialysers removes telavancin considerably (similar to 1/3 of body load). Telavancin 5 mg/kg every 48 h post-haemodialysis dosing is recommended, but dose adjustments may be warranted if haemodialysis starts within 3 h of telavancin administration.
引用
收藏
页码:174 / 180
页数:7
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