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Is Antimicrobial Treatment Effective During Therapeutic Plasma Exchange? Investigating the Role of Possible
Łukasz J Krzych1, Marcelina Czok2, Zbigniew Putowski2
1Department of Anesthesiology and Intensive Care, School of Medicine in Katowice, Medical University of Silesia, 14 Medyków Street, 40-752 Katowice, Poland.
Abstract:
Antimicrobial treatment during therapeutic plasma exchange (TPE) remains a complex issue. Recommendations based on a limited number of experimental studies should be implemented in clinical practice with caution. Effective management of infections due to plasma or albumin-related interactions, as well as impaired pharmacokinetics, in critical illness is difficult. Knowing the pharmacokinetics of the drugs concerned and the procedural aspects of plasmapheresis should be helpful in planning personalized treatment. In general, possessing a low distribution volume, a high protein-binding affinity, a low endogenous clearance rate, and long distribution and elimination half-lives make a drug more prone to elimination during TPE. A high frequency and longer duration of the procedure may also contribute to altering a drug's concentration. The safest choice would be to start and finish TPE before antimicrobial agent infusion. If this not feasible, a reasonable alternative is to avoid administering the drug just before TPE and to delay the procedure for the time of the administered drug's distributive phase. Ultimately, if plasma exchange must be performed urgently or the drug has a very narrow therapeutic index, monitoring its plasma concentration is advised.
Insights
Managing antimicrobial therapy during therapeutic plasma exchange (TPE) requires careful consideration of drug pharmacokinetics and TPE procedure details to ensure effective infection treatment.
Area of Science:
- Pharmacology
- Critical Care Medicine
- Nephrology
Background:
- Antimicrobial drug administration during therapeutic plasma exchange (TPE) presents complex clinical challenges.
- Limited experimental data necessitates cautious implementation of current recommendations in practice.
- Managing infections in critically ill patients undergoing TPE is complicated by drug-protein interactions and altered pharmacokinetics.
Purpose of the Study:
- To provide guidance on antimicrobial treatment strategies during TPE.
- To highlight the importance of understanding drug pharmacokinetics and TPE procedural aspects for personalized patient management.
- To inform clinical decision-making regarding antimicrobial dosing and timing in relation to TPE.
Main Methods:
- Review of existing literature on drug elimination during TPE.
- Analysis of pharmacokinetic properties influencing drug removal by TPE.
- Consideration of TPE procedural factors (frequency, duration) affecting drug concentrations.
Main Results:
- Drugs with low distribution volume, high protein binding, low endogenous clearance, and long half-lives are more susceptible to removal during TPE.
- TPE frequency and duration can significantly alter antimicrobial drug concentrations.
- Optimal timing involves completing TPE before or after antimicrobial administration, or delaying TPE to accommodate the drug's distributive phase.
Conclusions:
- Personalized antimicrobial treatment during TPE necessitates understanding drug pharmacokinetics and procedural variables.
- Strategic timing of antimicrobial administration and TPE is crucial for maintaining therapeutic drug levels.
- Drug concentration monitoring is advised for urgent TPE or when using agents with a narrow therapeutic index.
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