The pharmacokinetics of meropenem and piperacillin-tazobactam during sustained low efficiency haemodiafiltration (SLED-HDF)
Objective We analysed the pharmacokinetics of meropenem and piperacillin-tazobactam in patients undergoing a standardised session of sustained low efficiency haemodiafiltration (SLED-HDF) to inform the dosing of these drugs in an acute setting. Participants Six stable patients with end-stage kidney...
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Veröffentlicht in: | European journal of clinical pharmacology 2020-02, Vol.76 (2), p.239-247 |
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Sprache: | eng |
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Zusammenfassung: | Objective
We analysed the pharmacokinetics of meropenem and piperacillin-tazobactam in patients undergoing a standardised session of sustained low efficiency haemodiafiltration (SLED-HDF) to inform the dosing of these drugs in an acute setting.
Participants
Six stable patients with end-stage kidney disease.
Methods
An open-label pilot pharmacokinetic study of meropenem and piperacillin-tazobactam. SLED-HDF was undertaken for 4 h. Plasma drug concentrations were measured pre- and post-filter and in the effluent at multiple time points. The pharmacokinetic data was analysed using non-compartmental methods. The fraction of time that individual plasma concentration profiles were predicted to remain above the MIC break-points for commonly isolated gram-negative pathogens during a prolonged SLED-HDF session was assessed using two targets;
fT >
MIC (fraction of time above the MIC) and the more aggressive
fT
>
4 × MIC (fraction of time above 4 × MIC).
Results
Meropenem total and SLED-HDF clearance ranged from 141 to 180 mL/min and 126–205 mL/min, respectively. Piperacillin total and SLED-HDF clearance values ranged from 131 to 252 mL/min and 135–162 mL/min, respectively. Our results suggest that prolonged SLED-HDF (12 h) will only maintain a sufficient meropenem and piperacillin-tazobactam plasma concentration to achieve a target of
fT >
MIC for gram-negative pathogens (MIC 2 mg/L-meropenem, 8 mg/L-piperacillin-tazobactam) for less than 40% of the time. Plasma concentrations would be inadequate to achieve the more aggressive target of 100 %
fT >
4xMIC target recommended for critically unwell patients.
Conclusions
The pharmacokinetic data obtained from this pilot study demonstrate significant quantities of meropenem and piperacillin are removed during a SLED-HDF session. This may lead to subtherapeutic concentrations of piperacillin and meropenem over the duration of HDF session.
Trial registration
Australasian Clinical Trials Registry Network (ACTRN12616000078459) |
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ISSN: | 0031-6970 1432-1041 |
DOI: | 10.1007/s00228-019-02792-0 |