4 research outputs found
Abbreviated Antiplatelet Therapy After Coronary Stenting in Patients With Myocardial Infarction at High Bleeding Risk.
BACKGROUND
The optimal duration of antiplatelet therapy (APT) after coronary stenting in patients at high bleeding risk (HBR) presenting with an acute coronary syndrome remains unclear.
OBJECTIVES
The objective of this study was to investigate the safety and efficacy of an abbreviated APT regimen after coronary stenting in an HBR population presenting with acute or recent myocardial infarction.
METHODS
In the MASTER DAPT trial, 4,579 patients at HBR were randomized after 1 month of dual APT (DAPT) to abbreviated (DAPT stopped and 11 months single APT or 5 months in patients with oral anticoagulants) or nonabbreviated APT (DAPT for minimum 3 months) strategies. Randomization was stratified by acute or recent myocardial infarction at index procedure. Coprimary outcomes at 335 days after randomization were net adverse clinical outcomes events (NACE); major adverse cardiac and cerebral events (MACCE); and type 2, 3, or 5 Bleeding Academic Research Consortium bleeding.
RESULTS
NACE and MACCE did not differ with abbreviated vs nonabbreviated APT regimens in patients with an acute or recent myocardial infarction (n = 1,780; HR: 0.83; 95% CI: 0.61-1.12 and HR: 0.86; 95% CI: 0.62-1.19, respectively) or without an acute or recent myocardial infarction (n = 2,799; HR: 1.03; 95% CI: 0.77-1.38 and HR: 1.13; 95% CI: 0.80-1.59; Pinteraction = 0.31 and 0.25, respectively). Bleeding Academic Research Consortium 2, 3, or 5 bleeding was significantly reduced in patients with or without an acute or recent myocardial infarction (HR: 0.65; 95% CI: 0.46-0.91 and HR: 0.71; 95% CI: 0.54-0.92; Pinteraction = 0.72) with abbreviated APT.
CONCLUSIONS
A 1-month DAPT strategy in patients with HBR presenting with an acute or recent myocardial infarction results in similar NACE and MACCE rates and reduces bleedings compared with a nonabbreviated DAPT strategy. (Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen [MASTER DAPT]; NCT03023020)
Contactless Vital Sign Monitoring System for In-Vehicle Driver Monitoring Using a Near-Infrared Time-of-Flight Camera
We demonstrate a Contactless Vital Sign Monitoring (CVSM) system and road-test the system for in-cabin driver monitoring using a near-infrared indirect Time-of-Flight (ToF) camera. The CVSM measures both heart rate (HR) and respiration rate (RR) by leveraging the simultaneously measured grayscale and depth information from a ToF camera. For a camera-based driver monitoring system (DMS), key challenges from varying background illumination and motion-induced artifacts need to be addressed. In this study, active illumination and depth-based motion compensation are used to mitigate these two challenges. For HR measurements, active illumination allows the system to work under various lighting conditions, while our depth-based motion compensation has the advantage of directly measuring the motion of the driver without making prior assumptions about the motion artifacts. In addition, we can extract RR directly from the chest wall motion, circumventing the challenge of acquiring RR from the near-infrared photoplethysmography (PPG) signal of low signal quality. We investigate the system’s performance in various scenarios, including monitoring both drivers and passengers while driving on highways and local roads. Our results show that our CVSM system is ambient light agnostic, and the success rates of HR measurements on the highway are 82% and 71.9% for the passenger and driver, respectively. At the same time, we show that the system can measure RR on users driving on a highway with a mean deviation of −1.4 breaths per minute (BPM). With reliable HR and RR measurement in the vehicle, the CVSM system could one day be a key enabler to sudden sickness or drowsiness detection in DMS
The effect of reactive oxygen and nitrogen species on the structure of cytoglobin: a potential tumor suppressor
Impact of Medication Nonadherence in a Clinical Trial of Dual Antiplatelet Therapy.
BACKGROUND
Nonadherence to antiplatelet therapy after percutaneous coronary intervention (PCI) is common, even in clinical trials.
OBJECTIVES
The purpose of this study was to investigate the impact of nonadherence to study protocol regimens in the MASTER DAPT (Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen) trial.
METHODS
At 1-month after PCI, 4,579 high bleeding risk patients were randomized to single antiplatelet therapy (SAPT) for 11 months (or 5 months in patients on oral anticoagulation [OAC]) or dual antiplatelet therapy (DAPT) for ≥2 months followed by SAPT. Coprimary outcomes included net adverse clinical events (NACE), major adverse cardiac and cerebral events (MACE), and major or clinically relevant nonmajor bleeding (MCB) at 335 days. Inverse probability-of-censoring weights were used to correct for nonadherence Academic Research Consortium type 2 or 3.
RESULTS
In total, 464 (20.2%) patients in the abbreviated-treatment and 214 (9.4%) in the standard-treatment groups incurred nonadherence Academic Research Consortium type 2 or 3. At inverse probability-of-censoring weights analyses, NACE (HR: 1.01; 95% CI: 0.88-1.27) or MACE (HR: 1.07; 95% CI: 0.83-1.40) did not differ, and MCB was lower with abbreviated compared with standard treatment (HR: 0.51; 95% CI: 0.60-0.73) consistently across OAC subgroups; among OAC patients, SAPT discontinuation 6 months after PCI was associated with similar MACE and lower MCB (HR: 0.47; 95% CI: 0.22-0.99) compared with SAPT continuation.
CONCLUSIONS
In the MASTER DAPT adherent population, 1-month compared with ≥3-month DAPT was associated with similar NACE or MACE and lower MCB. Among OAC patients, SAPT discontinuation after 6 months was associated with similar MACE and lower MCB than SAPT continuation (Management of High Bleeding Risk Patients Post Bioresorbable Polymer Coated Stent Implantation With an Abbreviated Versus Prolonged DAPT Regimen [MASTER DAPT]; NCT03023020)