The benefit of hydroxychloroquine (HCQ) in the treatment of coronavirus disease (COVID-19) is still under investigation, and randomized control trials worldwide are currently recruiting patients. Data on HCQ pharmacokinetics (PK) exist in lupus patients but are scarce in COVID-19 critically ill patients [1,2,3]. In our intensive care unit (ICU), patients were started on a 10-day oral course of HCQ 200 mg t.i.d, or 200 mg b.i.d if they had acute kidney injury (AKI) defined as creatinine clearance < 50 ml/min . Oral loading dose was 400 mg, or 200 mg if patients had AKI. We targeted trough blood concentrations between 1 and 2 mg/L [4, 5]. HCQ can induce critical side effects such as prolonged QT on electrocardiogram (EKG), severe arrhythmias, and hypoglycemia. This toxicity combined with lack of experience using HCQ led us to measure daily blood trough and peak concentrations over a 12-day period to evaluate PK parameters. Samples were also collected around first hemodialysis (HD) session and in dialysis bath.
We included eight patients with normal renal function, five patients with AKI of whom four required renal replacement therapy and one patient with veno-venous extracorporeal life support (ECLS) (eFig. 2). Median age was 58 (interquartile range 53–70) years, seven (50%) male, and Sequential Organ Failure Assessment (SOFA) score at admission was 5 (3–7). At day one of treatment, all patients were mechanically ventilated. Median albumin level was 27 (24–30) g/L, and total bilirubin serum level was 6 (4–8.5) µmol/l (eTable 1). We found median HCQ peak concentrations after loading dose of 400 mg and 200 mg were 0.5 (0.28–0.62) mg/L and 0.22 (0.2–0.24) mg/L, respectively (eTable 2). Median time to obtain concentration of 1 mg/L was 4 (3–7) days (Fig. 1), and median duration in therapeutic range was 3.3 days. Toxic levels were noted after day five of treatment (Fig. 1). We found unchanged HCQ concentrations before and after HD sessions and low HCQ concentration in dialysis bath: 0.01 mg/L and 0.032 mg/L at half-time and at disconnection of dialysis line, respectively. Finally, three out of 14 patients (21%) with blood concentration in therapeutic range had side effects: two with prolonged QT who needed a treatment cessation and one with severe hypoglycemia who required a decreased HCQ dosage.
Our results suggest that prescribing HCQ in COVID-19 patients is unsafe for several reasons. Because of drug accumulation and high volume of distribution, toxic threshold was reached by day 5 even in patients with normal renal function. We recorded side effects although patients’ blood concentrations were in therapeutic range, therefore making HCQ administration potentially harmful despite correct surveillance parameters. HD had little effect on HCQ concentrations, whereas the patient with ECLS expressed constant low HCQ blood concentration, possibly due to membrane adsorption. To avoid HCQ-related complications in COVID-19 critically ill patients, we suggest monitoring EKG and blood concentration daily. In summary, we believe that for safety reasons, HCQ should not be prescribed outside of randomized controlled trials anymore.
The local ethics committee approved the study (Institutional Review Board of the Rennes University Hospital, accord no 20.38). All patients signed written informed consent.
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Painvin, B., Guillot, P., Verdier, MC. et al. Hydroxychloroquine pharmacokinetic in COVID-19 critically ill patients: an observational cohort study. Intensive Care Med 46, 1772–1773 (2020). https://doi.org/10.1007/s00134-020-06142-y