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Removal of common antimicrobial agents by sustained low-efficiency dialysis
Joanna Q Hudson1,2, Madelyn N Hilgers1, Elvira O Gosmanova2
1Department of Clinical Pharmacy and Translational Science, The University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Abstract:
Adequate dosing of antimicrobials is paramount for treating infections in critically ill patients undergoing kidney replacement therapy; however, little is known about antimicrobial removal by sustained low-efficiency dialysis (SLED). The objective was to quantify the removal of cefepime, daptomycin, meropenem, piperacillin-tazobactam, and vancomycin in patients undergoing SLED. Adult patients ≥18 years with acute kidney injury (AKI) or end-stage kidney disease receiving one of the select antimicrobials and requiring SLED were included. Blood and dialysate flow rates were maintained at 250 and 100 mL/min, respectively. Simultaneous arterial and venous blood samples for the analysis of antibiotic concentrations were collected hourly for 8 hours during SLED (on-SLED). Arterial samples were collected every 2 hours for up to 6 hours while not receiving SLED (off-SLED) for the calculation of SLED clearance, half-life (t1/2) on-SLED and off-SLED, and the fraction of removal by SLED (fD). Twenty-one patients completed the study: 52% male, mean age (±SD) 53 ± 13 years, and mean weight of 98 ± 30 kg. Eighty-six percent had AKI, and 4 patients were receiving cefepime, 3 daptomycin, 10 meropenem, 6 piperacillin-tazobactam, and 13 vancomycin. The average SLED time was 7.3 ± 1.1 hours, and the mean ultrafiltration rate was 95 ± 52 mL/hour (range 10-211). The t1/2 on-SLED was substantially lower than the off-SLED t1/2 for all antimicrobials, and the SLED fD varied between 44% and 77%. An 8-hour SLED session led to significant elimination of most antimicrobials evaluated. If SLED is performed, modification of the dosing regimen is warranted to avoid subtherapeutic concentrations.
Insights
Sustained low-efficiency dialysis (SLED) significantly removes common antibiotics like cefepime, meropenem, and vancomycin in critically ill patients. Dosing adjustments are crucial during SLED to maintain effective antimicrobial levels and prevent treatment failure.
Area of Science:
- Pharmacokinetics
- Nephrology
- Critical Care Medicine
Background:
- Optimizing antimicrobial dosing is critical for critically ill patients with kidney dysfunction.
- Limited data exists on antimicrobial removal during sustained low-efficiency dialysis (SLED).
Purpose of the Study:
- To quantify the removal of key antimicrobials (cefepime, daptomycin, meropenem, piperacillin-tazobactam, vancomycin) during SLED.
- To evaluate the impact of SLED on antimicrobial pharmacokinetics, including clearance and half-life.
Main Methods:
- Conducted a study on adult patients with AKI or ESRD requiring SLED and receiving selected antimicrobials.
- Collected simultaneous arterial and venous blood samples hourly during SLED and arterial samples off-SLED for pharmacokinetic analysis.
- Calculated SLED clearance, half-life on- and off-SLED, and fraction of removal by SLED (fD).
Main Results:
- SLED significantly reduced the half-life of all evaluated antimicrobials compared to off-SLED conditions.
- The fraction of antimicrobial removal by SLED (fD) ranged from 44% to 77% across the studied drugs.
- An 8-hour SLED session resulted in substantial elimination of most tested antimicrobials.
Conclusions:
- SLED leads to significant antimicrobial removal in critically ill patients.
- Antimicrobial dosing regimens require modification during SLED to prevent subtherapeutic drug concentrations.
- Further research is needed to establish optimal dosing strategies for antimicrobials during SLED.
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