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Pharmacokinetics of Hydroxychloroquine and Its Clinical Implications in Chemoprophylaxis against Malaria Caused by Plasmodium vivax

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TLDR
Hydroxychloroquine is an antimalarial drug used as chemoprophylaxis against malaria caused by Plasmodium vivax in the Republic of Korea Army (ROKA), and a significant cause of prophylactic failure among the individuals in ROKA was ascribed to plasma concentrations of HCQ lower than those predicted by the PK model.
Abstract
Hydroxychloroquine (HCQ) is an antimalarial drug used as chemoprophylaxis against malaria caused by Plasmodium vivax in the Republic of Korea Army (ROKA). In this study, we evaluated the pharmacokinetics (PK) of HCQ and its metabolites and the relationship between the PK of HCQ and the effect of treatment of HCQ on vivax malaria in South Koreans. Three PK studies of HCQ were conducted with 91 healthy subjects and patients with vivax malaria. Plasma concentrations were analyzed by noncompartmental and mixed-effect modeling approaches. A two-compartment model with first-order absorption best described the data. The clearance and the central and peripheral volumes of distribution were 15.5 liters/h, 733 liters, and 1,630 liters, respectively. We measured the plasma concentrations of HCQ in patients with prophylactic failure of HCQ and compared them with the prediction intervals of the simulated concentrations for HCQ from the final PK model built in this study. In 71% of the patients with prophylactic failure, the plasma concentrations of HCQ were below the lower bounds of the 95% prediction interval, while only 8% of them showed higher levels than the upper bounds of the 95% prediction interval. We report that a significant cause of prophylactic failure among the individuals in ROKA was ascribed to plasma concentrations of HCQ lower than those predicted by the PK model. However, prophylactic failure despite sufficient plasma concentrations of HCQ was confirmed in several individuals, warranting continued surveillance to monitor changes in the HCQ susceptibility of Plasmodium vivax in the Republic of Korea.

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Pharmacologic Treatments for Coronavirus Disease 2019 (COVID-19): A Review.

TL;DR: The COVID-19 pandemic represents the greatest global public health crisis of this generation and, potentially, since the pandemic influenza outbreak of 1918 and both the need and capability to produce high-quality evidence even in the middle of a pandemic.
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Therapy and pharmacological properties of hydroxychloroquine and chloroquine in treatment of systemic lupus erythematosus, rheumatoid arthritis and related diseases

TL;DR: This review examines the pharmacokinetics, modes of action and therapeutic properties of the anti-malarial drugs, HCQ and CQ, in the treatment of systemic lupus erythematosus (SLE), rheumatoid arthritis (RA) and related conditions, as well as osteoarthritis (OA).
References
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Journal Article

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TL;DR: An introduction to the R project for statistical computing (www.R-project.org) is presented to make the professional community aware of "R" as a potent and free software for graphical and statistical analysis of medical data.
Journal ArticleDOI

The economic and social burden of malaria

TL;DR: There are multiple channels by which malaria impedes development, including effects on fertility, population growth, saving and investment, worker productivity, absenteeism, premature mortality and medical costs.
Journal ArticleDOI

Inhibition by chloroquine of a novel haem polymerase enzyme activity in malaria trophozoites.

A. F. G. Slater, +1 more
- 09 Jan 1992 - 
TL;DR: The identification and characterization of a haem polymerase enzyme activity from extracts of Plasmodium fal-ciparum trophozoites are reported and show that this enzyme is inhibited by quinoline-containing drugs such as chloroquine and quinine, providing a possible explanation for the highly stage-specific anti-malarial properties of these drugs.
Journal ArticleDOI

Plasmodium vivax resistance to chloroquine

TL;DR: Two soldiers continued weekly prophylaxis with 300 mg chloroquine base on their return to Australia from Papua New Guinea but were not protected against Plasmodium vivax malaria, suggesting the emergence of strains of P v Vivax with a reduced susceptibility to chloroquines.
Journal ArticleDOI

Chloroquine Resistance in Plasmodium vivax

TL;DR: This minireview summarizes the present state of knowledge of CRPV as a scientific, clinical, and public health problem and examines the genesis of CQ therapy for P. vivax and the laboratory and clinical data underpinning the diagnosis.
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