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Objective: Prior studies have emphasized the importance of compliance with preoperative dual antiplatelet therapy (DAPT) in patients undergoing transcarotid artery revascularization (TCAR). This investigation examines differences in perioperative outcomes after TCAR in those receiving a loading dose of antiplatelet medications on the day of the procedure vs those already maintained on DAPT.
Methods: Consecutive TCAR procedures from the Vascular Quality Initiative (2016-2022) were identified. Patients were divided into (1) those on preoperative DAPT (aspirin and P2YI2 antagonist) taken at least within 36 hours of the procedure (61.9%); (2) those on at least one antiplatelet medication who received a supplemental dose of another antiplatelet within 4 hours before the procedure (AP + loading, 37.1%); and (3) patients receiving only a loading dose (of aspirin or P2Y12 antagonist) without prior use of antiplatelet therapy (1%). In-hospital and 30-day outcomes were compared between the three groups using univariable and multivariable analyses.
Results: A total of 22,310 patients were on DAPT; 13,392 were on at least one antiplatelet and received a supplemental dose (AP + loading) and 361 patients received a loading dose on the day of the intervention. On univariable analysis, there was no significant difference in in-hospital or 30-day outcomes between the three groups, except for an increased rate of in-hospital stent thrombosis/occlusion in patients loaded with antiplatelet medications on the day of TCAR (n = 2 [0.6%]), compared with those maintained on DAPT (n = 23 [0.1%]) and patients in the AP + loading group (n = 26 [0.2%]) (P = .01). After adjusting for baseline differences between the three groups, no significant association was observed between the groups and in-hospital stroke/death or bleeding complications. However, compared with patients maintained on DAPT, patients receiving antiplatelet loading had higher odds of stent thrombosis/occlusion (odds ratio, 1.92; 95% confidence interval, 1.08-3.4; P = .03). Among patients in the AP + loading group, those maintained on aspirin preoperatively and receiving another antiplatelet loading on the day of the intervention were more likely to have stent thrombosis.
Conclusions: This study demonstrates that administering loading or supplemental doses of antiplatelet medication(s) to rapidly achieve therapeutic levels on the day of TCAR is not associated with higher rates of in-hospital stroke or bleeding complications. However, an increase in stent thrombosis or occlusion was noted in patients receiving a loading dose or supplementation of antiplatelet medications and warrants further investigation. In elective cases, it might be safer to delay intervention until patients receive adequate DAPT regimen, especially if patients are not maintained on P2Y12 inhibitors preoperatively.
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http://dx.doi.org/10.1016/j.jvs.2024.12.038 | DOI Listing |
Int J Biol Macromol
September 2025
Faculty of Agronomy and Agricultural Sciences, University of Dschang, PO. Box 222, Dschang, Cameroon.
Dissolved organic matter (DOM) plays a key role in grassland carbon biogeochemistry and shows sensitivity to global climate change, particularly nitrogen (N) deposition. We investigated the soil DOM molecular composition by UV-Vis and fluorescence spectroscopy, and FT-ICR MS through a N addition experiment (CK, N5, N10, N20, and N40 [0, 5, 10, 20, and 40 g N m-2 year-1, respectively]) in a desert steppe of northwest China. Moderate N inputs (N5-N20) caused a dose-dependent increase in DOM content (9.
View Article and Find Full Text PDFLancet Infect Dis
September 2025
The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Background: Based on results from preclinical and clinical studies, a five-drug combination of isoniazid, rifapentine, pyrazinamide, ethambutol, and clofazimine was identified with treatment shortening potential for drug-susceptible tuberculosis; the Clo-Fast trial aimed to determine the efficacy and safety of this regimen. We compared 3 months of isoniazid, rifapentine, pyrazinamide, ethambutol, and clofazimine, administered with a clofazimine loading dose, to the standard 6 month regimen of isoniazid, rifampicin, pyrazinamide, and ethambutol in drug-susceptible tuberculosis.
Methods: Clo-Fast was a phase 2c open-label trial recruiting participants at six sites in five countries.
Acta Trop
September 2025
Guangdong Provincial Key Laboratory of Aquatic Economic Animals, State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-Sen University, Guangzhou 510275, China;. Electronic address:
Malaria is still one of the most important parasitic diseases with millions of cases reported globally every year. Combination therapies of artemisinin or its derivatives, with a partner drug, are the first-and second-line treatments for malaria. However, recently, artemisinin partial resistance or tolerance has emerged and emphasizes the need for new therapeutic approaches to malaria.
View Article and Find Full Text PDFDrug Deliv Transl Res
September 2025
Pharmaceutics and Drug Manufacturing Department, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Cairo, 11571, Egypt.
Oral lichen planus (OLP) is a chronic inflammatory disorder with limited topical treatment options and long-term corticosteroid dependency. This study investigates a novel atorvastatin-loaded hyalurosomal gel (ATV-Hyalugel) as a topical adjuvant to reduce systemic corticosteroid use in severe OLP. The objective of the study is to develop, optimize, characterize ATV-Hyalugel and evaluate its clinical efficacy in a randomized controlled clinical trial.
View Article and Find Full Text PDFInt J Antimicrob Agents
September 2025
Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai 200040, China; Key Laboratory of Clinical Pharmacology of Antibiotics, National Population and Family Planning Commission, Shanghai 200040, China; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan
Objectives: The pharmacokinetics of renally cleared vancomycin are significantly altered in critically ill patients undergoing renal replacement therapy (RRT), affecting the achievement of therapeutic targets. We evaluated the predictive performance of RRT patient-based PopPK models for model-informed precision dosing and subsequently simulated optimal dosing regimens for this population.
Methods: Six adult PopPK models were systematically identified and evaluated using a dataset of 226 concentrations from 23 adult patients on RRT from two study centers.