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Hydroxychloroquine serum concentration in coronavirus disease 2019 (COVID-19) patients: a retrospective study
Saadi Fatima Zohra1,2,3, Lachgueur Nassima1,2
1Department of Toxicology, University Hospital, Oran, Algeria.
Insights
Algeria monitored hydroxychloroquine (HCQ) levels in COVID-19 patients, finding good tolerance and efficacy. This study confirms HCQ
Area of Science:
- Pharmacology
- Infectious Diseases
- Analytical Chemistry
Background:
- Algeria implemented hydroxychloroquine (HCQ) as a first-line COVID-19 treatment.
- Therapeutic drug monitoring is crucial for HCQ to prevent side effects.
- COVID-19 treatment protocols require careful patient management.
Purpose of the Study:
- To estimate hydroxychloroquine (HCQ) plasma concentrations in COVID-19 patients.
- To assess patient tolerance and safety during HCQ treatment.
- To validate an analytical method for HCQ quantification.
Main Methods:
- Retrospective descriptive study analyzing 267 blood samples from 240 COVID-19 patients.
- Quantification of HCQ using high-performance liquid chromatography with a diode array detector (HPLC-DAD).
- Patient monitoring followed French National Agency for Research on AIDS and Viral Hepatitis (ANRS) and STP-PT guidelines.
Main Results:
- A validated HPLC-DAD method demonstrated high accuracy (r²=0.9999) and sensitivity (LOQ=0.05 mg/L).
- The majority of patients (68%) had HCQ concentrations between 0.1-1 mg/L.
- Over 88% of patients exhibited HCQ levels within the therapeutic range (≥0.05 mg/L), with minimal toxicity.
Conclusions:
- Hydroxychloroquine (HCQ) demonstrated good tolerance and was safely administered to COVID-19 patients in Algeria.
- The validated HPLC-DAD method is reliable for therapeutic drug monitoring of HCQ.
- Adherence to monitoring guidelines ensures patient safety during HCQ treatment for COVID-19.
Abstract:
Algeria has adopted a therapeutic protocol using hydroxychloroquine (HCQ) as a first-line treatment for patients with coronavirus disease 2019 (COVID-19). The administration of HCQ must be accompanied by appropriate cardiac and therapeutic pharmacological monitoring to avoid side effects and toxicity. This work is a retrospective descriptive study aiming to estimate the HCQ levels of COVID-19 patients. HCQ concentrations in blood samples from COVID-19 patients were determined using high performance liquid chromatography with diode array detector (HPLC-DAD) after liquid-liquid extraction of plasma. The coefficient of determination (r 2) of this method was 0.9999. The limits of quantification and detection were 0.05 mg/L and 0.02 mg/L, respectively, with coefficients of variance less than 6%. Patient monitoring was performed following recommendations for the therapeutic pharmacological monitoring of HCQ in patients treated for SARS-CoV-2 (COVID-19) infection validated by the coordinated action (AC43) of the National Agency for Research on AIDS and Viral Hepatitis (ANRS) and Therapeutic Pharmacological Monitoring and Personalization of Treatments (STP-PT) group. A total of 267 blood samples from 240 patients were analyzed, 49% for males and 51% for females. More than a third of the patients were 60-80 years old. The majority (68%) of the HCQ concentrations were between 0.1 and 1 mg/L. Additionally, more than 20% were between 0.05 and 0.1 mg/L, while only 7.5% were less than 0.05mg/L and 1.5% were greater than 1 mg/L. In summary, patients with COVID-19 showed a good tolerance to HCQ in the majority of cases.Key PointsHCQ was proposed to be a promised treatment for COVID-19.A reverse phase HPLC-DAD method was validated for HCQ concentration determination in plasma.Patients hospitalized for COVID-19 were monitored according to the guideline established by the French National Team AC43 of the ANRS and the STP-PT group.Patients showed a very good tolerance to HCQ with no observed cases of toxicity.
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