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Published on: August 30, 2018
[Plasmatic concentracion of piperacillin/tazobactam in pediatric patients on ECMO support. Preliminary analysis]
Brenda Zylbersztajn1, Giannina Izquierdo C1, Daniel Navea M1
1Clínica Las Condes, Chile.
Insights
Optimal dosing of piperacillin tazobactam (PT) is crucial for pediatric patients on extracorporeal membrane oxygenation (ECMO). This study found that current PT dosing often fails to achieve therapeutic piperacillin concentrations in these critically ill children.
Area of Science:
- Pediatric Critical Care Medicine
- Pharmacology
- Extracorporeal Life Support
Background:
- Optimal dosing of piperacillin tazobactam (PT) is not well-established in pediatric patients requiring extracorporeal membrane oxygenation (ECMO).
- Understanding drug pharmacokinetics in ECMO patients is essential for effective treatment.
Purpose of the Study:
- To determine piperacillin plasma concentrations in pediatric patients receiving PT during ECMO.
- To assess the achievement of pharmacokinetic/pharmacodynamic (PK/PD) targets with PT in this population.
Main Methods:
- A case series involving three pediatric patients on ECMO treated with PT.
- Piperacillin plasma levels were measured using high-performance liquid chromatography (HPLC) mid-dose interval.
Main Results:
- Piperacillin plasma concentrations varied significantly among patients (51.7, 14.1, and 6.5 μg/mL).
- Only one of the three patients achieved adequate therapeutic piperacillin concentrations.
Conclusions:
- Preliminary findings suggest that piperacillin dosing may need adjustment in pediatric ECMO patients.
- Monitoring plasma concentrations could help optimize PT therapy and improve PK/PD target attainment in this vulnerable group.
Background:
Pharmacokinetics and optimal dosing of piperacillin tazobactam (PT) have not been well studied in pediatric patients undergoing extracorporeal oxygenation membrane (ECMO).
Aim:
To describe piperacillin plasmatic concentration and evaluate achievement of pharmaccokinetic/pharmacodinamic objective in patients on ECMO support.
Method:
We report three pediatric patients admitted to the Pediatric Intensive Care Unit, treated with PT undergoing ECMO. Plasmatic concentrations of piperacillin were obtained in the middle of the dosing interval using high performance liquid chromatography.
Results:
Plasmatic concentrations were 51,7-14,1 and 6,5 μg/mL for patient A, B and C respectively. Only one patient reached adequate concentrations.
Conclusion:
These preliminary results suggest that availability of plasmatic concentrations of piperacillin could optimize the achievement of pharmacokinetic/pharmacodynamic objectives in pediatric patients on ECMO support.
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