Pharmacokinetics of Ribavirin in the Treatment of Lassa Fever: An Observational Clinical Study at the Irrua Specialist Teaching Hospital, Edo State, Nigeria

Author:

Groger Mirjam123,Akhideno Peter4,Kleist Christine J5,Babatunde Femi O4,Edeawe Osahogie4,Hinzmann Julia36,Akhigbe ThankGod4,Nwatuzor Joy4,Eifediyi Gloria4,Müller Jonas36,Hinrichs Mette36,Pahlmann Meike36,Sarpong Francisca Naana123,Wagner Christine123,Thielebein Anke36,Aihonwalan Louis4,Koch Till123,Riedner Maria7,Ogbaini-Emovon Ephraim4,Okogbenin Sylvanus4,Günther Stephan36,Wicha Sebastian G5,Ramharter Michael123ORCID,Oestereich Lisa36,Duraffour Sophie36,Erameh Cyril4

Affiliation:

1. Department of Tropical Medicine, Bernhard Nocht Institute for Tropical Medicine , Hamburg , Germany

2. Department of Medicine, University Medical Center Hamburg-Eppendorf , Hamburg , Germany

3. German Center for Infection Research (DZIF), Partner Site Hamburg–Lübeck–Borstel–Riems , Hamburg , Germany

4. Irrua Specialist Teaching Hospital , Irrua , Nigeria

5. Department of Clinical Pharmacy, Institute of Pharmacy, University of Hamburg , Hamburg , Germany

6. Department of Virology, Bernhard Nocht Institute for Tropical Medicine , Hamburg , Germany

7. Department of Chemistry, University of Hamburg , Hamburg , Germany

Abstract

Abstract Background Lassa fever is endemic in large parts of West Africa. The recommended antiviral treatment is ribavirin. Two treatment regimens are currently endorsed in Nigeria: the “McCormick regimen” based on a study published in 1986 and the “Irrua regimen” constituting a simplified schedule developed at the Irrua Specialist Teaching Hospital, Nigeria. Evidence for the safety and efficacy of ribavirin in Lassa fever patients is poor and pharmacokinetic data for both regimens are lacking Methods Polymerase chain reaction-confirmed Lassa fever patients with mild to moderate disease severity were invited to participate in this prospective, observational pharmacokinetic study. Pharmacokinetics of ribavirin, clinical, virologic, and clinical laboratory parameters were assessed. Results Using a population pharmacokinetic approach, plasma concentrations of ribavirin were best described by a 3-compartment model. Drug exposure was remarkably consistent between participants. Overall, drug clearance was 28.5% lower in female compared with male participants. Median (5th-95th percentile) time above half maximal inhibitory concentration (IC50) was 37.3% (16.9%–73.1%), 16.7% (8.2%–58.5%), and 9.6% (4.9%–38.4%) on days 1, 7, and 8, respectively. Clinical laboratory parameters indicated reduction of cell damage and development of hemolytic anemia in the course of the treatment period. Conclusions This observational study characterizes the pharmacokinetics of ribavirin in the treatment of Lassa fever indicating consistent exposure across patients. Whereas only a short time interval of concentrations above the IC50 implies rather low antiviral efficacy in vivo, the prominent reduction of cell damage markers might point to indirect—potentially anti-inflammatory—effects of ribavirin. The role of ribavirin in the treatment of Lassa fever requires further scrutiny.

Funder

Global Health Protection Programme of the German Federal Ministry of Health

German Research Foundation

Deutsche Forschungsgemeinschaft

Leibniz Association

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference26 articles.

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