Antimicrobial Agents and Chemotherapy · 2018 · 41 citations · 32 references
MedicinePharmacokineticsPharmacologyAntimicrobial PharmacologyPharmaceutical ToxicologyPharmacokinetic ModelingAnthelmintic PharmacologyAntiparasitic AgentsAntiparasitic PharmacologyAntiparasitic PharmacotherapyAntiparasitic TherapyPharmacokinetics Of AntimicrobialsAcaricidal TherapyAntiparasitic Drug PharmacokineticsPathogenesis Of ScabiesPesticide Pharmacokinetics In AnimalsPharmacokinetics Of Antiparasitic AgentsScabies TreatmentSingle-dose AdministrationUnmet Health Need
= 4). The response to treatment was assessed by the reduction of mite counts in skin scrapings as well as clinical and pruritus scores over time. Plasma and skin pharmacokinetics profiles for both AFX and IVM were evaluated. AFX efficacy was 100% at days 8 and 14 posttreatment and remained unchanged until the study end (day 45). IVM efficacy was 86% and 97% on days 8 and 14, respectively, with a few mites recovered at the study end. Clinical and pruritus scores decreased in both treated groups and remained constant in the control group. Plasma mean residence times (MRT) were 7.1 ± 2.4 and 1.1 ± 0.2 days for AFX and IVM, respectively. Skin MRT values were 16.2 ± 16.9 and 2.7 ± 0.5 days for AFX and IVM, respectively. Overall, a single oral dose of AFX was efficacious for the treatment of scabies in experimentally infested pigs and showed remarkably long MRTs in plasma and, notably, in the skin.
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Theo Vos, Abraham D Flaxman, Mohsen Naghavi et al. · The Lancet · 2012 · 8.4K citations · Full text
Global Skin Disease Morbidity and Mortality
Chanté Karimkhani, Robert P. Dellavalle, Luc E. Coffeng et al. · JAMA Dermatology · 2017 · 719 citations · Full text