Pharmacokinetics of anidulafungin during venovenous extracorporeal membrane oxygenation

Echinocandins are currently considered the first-line treatment for invasive candidiasis (IC) in the intensive care unit (ICU) [1, 2]. However, extracorporeal membrane oxygenation (ECMO), a rescue therapy used in patients with severe acute respiratory distress syndrome (ARDS) [3], could alter the pharmacokinetics of certain drugs [4]. We prescribed anidulafungin for suspected IC in a patient with severe ARDS on ECMO and measured the plasma concentrations of the drug using highperformance liquid chromatography (HPLC). A 69-year-old male patient was admitted to the ICU with septic shock secondary to peritonitis. The antiinfective treatment was based on surgical source control and broad spectrum antimicrobial therapy, including anidulafungin at usual doses. The patient developed severe ARDS. ECMO with Novalung iLA ActivveTM was initiated, maintaining ultraprotective ventilation. Femoral (23 F) and jugular (19 F) cannulas (NovalungTM, Germany) were inserted with 4.5 L/min blood flow and 4 L/min gas flow. Urine samples and pre-filter and postfilter blood samples were collected before starting the eight-dose anidulafungin infusion and 0.5, 1, 1.5, 2, 4, 6, 8, and 24 h after the infusion ended. Anidulafungin was well tolerated without relevant adverse effects. A non-compartmental pharmacokinetic analysis was performed using Abbottbase Pharmacokinetic SystemsTM (Abbott Laboratories, Illinois, USA). The maximum and trough plasma concentrations (Cmax and Cmin, respectively) were estimated directly from concentration-time data. The area under the plasma concentration-time curve over the 24-h dosing interval (AUC0–24) was estimated using the linear trapezoidal rule for both prefilter and post-filter data. Clearance (CL) was estimated as dose/AUC0–24. The apparent volume of distribution at steady state (Vss) was estimated as the product of CL and mean residence time (MRT). Cmax and Cmin were 13.5 and 2.19 mg/L, respectively (Fig. 1). Pre-filter and post-filter AUC0–24 were 107 and 111 mg/h/L, respectively; Vss was 18.9 L; CL was 0.933 L/h. Urine anidulafungin concentrations were negligible. All pharmacokinetic data were comparable to published data in critically ill patients with and without other types of extracorporeal support [5]. Regarding the use of anti-infective drugs in patients on ECMO, most pharmacokinetic data on this topic are from neonatal studies of antibiotics [4]. To the best of our knowledge, this report is the first on the pharmacokinetics of anidulafungin in a critically ill patient on ECMO. In our case, the therapy had little effect on the pharmacokinetics, suggesting that the dose of anidulafungin does not need adjustment. However, future studies are needed to confirm these findings.