Publications by authors named "Jindarat Kouhathong"

Article Synopsis
  • Antiviral drugs are crucial in preventing severe outcomes from COVID-19, and measuring the clearance of SARS-CoV-2 in patients helps assess their effectiveness.
  • A meta-analysis of data from the PLATCOV trial focused on how viral clearance rates change over time in patients to improve the design of future antiviral drug evaluations.
  • The study found that effective antiviral interventions speed up the initial phase of viral clearance, with the best results observed within the first five days after treatment begins.
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Article Synopsis
  • - The ongoing PLATCOV trial compares the antiviral effects of molnupiravir and ritonavir-boosted nirmatrelvir in treating early symptomatic COVID-19 patients across various countries including Thailand and Brazil, using viral clearance as the main measure of effectiveness.
  • - In this phase 2, open-label trial, low-risk adults aged 18-50 with COVID-19 symptoms were randomly assigned to one of seven treatment groups, including both antiviral drugs and a no-drug control group, ensuring at least 20% of participants received no medication.
  • - The study assesses the rate of viral clearance and treatment safety over one week using a Bayesian model to evaluate the effectiveness of the antiviral treatments, aiming to establish if either
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Background: There are no pharmacokinetic data of single low dose primaquine (SLDPQ) as transmission blocking in African children with acute Plasmodium falciparum and glucose-6-phosphate dehydrogenase deficiency (G6PDd).

Methods: Primaquine pharmacokinetics of age-dosed SLDPQ (shown previously to be gametocytocidal with similar tolerability as placebo) were characterised in falciparum-infected Ugandan and Congolese children aged 6 months to 11 years, treated on admission with standard 3-day dihydroartemisinin-piperaquine or artemether-lumefantrine plus SLDPQ: 6 m-<1 y: 1.25 mg, 1-5 y: 2.

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Background: The amplification of GTP cyclohydrolase 1 (pfgch1) in Plasmodium falciparum has been linked to the upregulation of the pfdhfr and pfdhps genes associated with resistance to the antimalarial drug sulfadoxine-pyrimethamine. During the 1990s and 2000s, sulfadoxine-pyrimethamine was withdrawn from use as first-line treatment in southeast Asia due to clinical drug resistance. This study assessed the temporal and geographic changes in the prevalence of pfdhfr and pfdhps gene mutations and pfgch1 amplification a decade after sulfadoxine-pyrimethamine had no longer been widely used.

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