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Pharmacokinetic Profile of Plasma Levobupivacaine

  • Writer: Scotia Biologics Ltd.
    Scotia Biologics Ltd.
  • Jun 15, 2020
  • 1 min read

Updated: Jun 3, 2021

Rebecca Parr, Hal Robinson, Gary Cameron, Gillian Broadbent, Keith Charlton, Heather Wallace, Thomas Engelhardt



Abstract


Introduction: Fascia iliaca compartment block (FICB) is commonly used in older patients to provide effective analgesia following hip fracture. However, only limited pharmacokinetic (PK) data about levobupivacaine are available to help clinical practice and establish safe volumes and amounts of local anesthetics.

Methods: Ten patients aged between 53 and 87 years, who underwent hemiarthroplasty following femoral neck fracture were recruited into this study. A fixed volume (40 mL) of 0.25% levobupivacaine was injected before the induction of anesthesia using ultrasound guidance. Venous blood samples were obtained at 0, 10, 20, 30, 45, 60, 75, 90, and 120 min time points and analyzed using mass spectrometry.

Results: The median (interquartile range) maximum observed plasma concentration (Cmax) of levobupivacaine was 0.48 (0.45-0.61) µg/mL, with the time to reach Cmax (tmax) of 38 minutes (30–105) after administration, a half-life of 2.8 h (1.65–5.8), and clearance rate of 0.72 L/min (0.36–1.26). The fixed volume (40 mL) of 0.25% levobupivacaine FICB did not exceed the recognized toxic threshold in adults (2.6 µg/mL).

Conclusion: The data described here indicate a similar levobupivacaine PK profile for older patients undergoing FICB for hip arthroplasty compared with the levobupivacaine PK profile for the general population.



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