Telavancin pharmacokinetics in patients with chronic kidney disease receiving haemodialysis
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Gharibian, Katherine N.
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Amgen Inc, Thousand Oaks, CA USAAmgen Inc, Thousand Oaks, CA USA
Gharibian, Katherine N.
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Lewis, Susan J.
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Univ Findlay, Coll Pharm, Dept Pharm Practice, Findlay, OH 45840 USA
Mercy Hlth St Anne Hosp, Dept Pharm, Toledo, OH 43623 USAAmgen Inc, Thousand Oaks, CA USA
Lewis, Susan J.
[2
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Heung, Michael
[4
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Segal, Jonathan H.
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机构:
Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USAAmgen Inc, Thousand Oaks, CA USA
Segal, Jonathan H.
[4
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Salama, Noha N.
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机构:
Cairo Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo, Egypt
Univ Hlth Sci & Pharm, St Louis Coll Pharm, Dept Pharmaceut & Adm Sci, St Louis, MO USAAmgen Inc, Thousand Oaks, CA USA
Salama, Noha N.
[5
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Mueller, Bruce A.
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Univ Michigan, Coll Pharm, Dept Clin Pharm, 428 Church St, Ann Arbor, MI 48109 USAAmgen Inc, Thousand Oaks, CA USA
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.
机构:
UCL, Fac Med Sci, Div Med, London, EnglandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Slee, Adrian
Adamson, Gary
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Ulster Univ, Sch Psychol, Coleraine Campus, Coleraine, Londonderry, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Adamson, Gary
Davenport, Andrew
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UCL, Royal Free Hosp, UCL Ctr Nephrol, London, EnglandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Davenport, Andrew
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Farrington, Ken
Fouque, Denis
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Univ Lyon, Ctr Hosp Lyon Sud, Dept Nephrol, CARMEN, Pierre Benite, FranceQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Fouque, Denis
Kalantar-Zadeh, Kamyar
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Univ Calif Irvine, Div Nephrol & Hypertens, Orange, CA 92868 USAQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Kalantar-Zadeh, Kamyar
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Mallett, John
Maxwell, Alexander P.
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Queens Univ Belfast, Royal Victoria Hosp, Ctr Publ Hlth, Inst Clin Sci, Grosvenor Rd, Belfast BT12 6BA, Antrim, North Ireland
Belfast City Hosp, Reg Nephrol Unit, Belfast Hlth Social Care Trust, Belfast BT9 7AB, Antrim, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Maxwell, Alexander P.
Mullan, Robert
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Northern Hlth Social Care Trust, Antrim Area Hosp, Dept Nephrol, Antrim BT41 2RL, Antrim, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Mullan, Robert
Noble, Helen
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Queens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
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Bournemouth Univ, Dept Social Sci & Social Work, Bournemouth, Dorset, EnglandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Porter, Sam
Seres, David S.
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Columbia Univ, New York Presbyterian Hosp, Med Ctr, Dept Med, New York, NY USAQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Seres, David S.
Shields, Joanne
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Belfast City Hosp, Reg Nephrol Unit, Belfast Hlth Social Care Trust, Belfast BT9 7AB, Antrim, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Shields, Joanne
Witham, Miles
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Newcastle Univ, NIHR Newcastle Biomed Res Ctr, Newcastle Upon Tyne, Tyne & Wear, EnglandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland
Witham, Miles
Reid, Joanne
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Queens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North IrelandQueens Univ Belfast, Med Biol Ctr, Sch Nursing & Midwifery, Belfast, Antrim, North Ireland