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BackgroundTranscatheter mitral valve repair is beneficial in patients with mitral regurgitation (MR), left ventricular dysfunction, and persistent symptoms despite maximally tolerated medical therapy.ObjectivesThe aim of this study was to evaluate the safety and feasibility of transcatheter mitral cerclage ventriculoplasty in patients with MR and either heart failure with reduced ejection fraction or preserved ejection fraction and in subjects with prior edge-to-edge repair but persistent or recurrent symptomatic MR.MethodsThe National Heart, Lung, and Blood Institute Division of Intramural Research Transcatheter Mitral Cerclage Ventriculoplasty Early Feasibility Study (NCT03929913) was an investigator-initiated prospective multicenter study. The primary endpoint was technical success measured at exit from the catheterization laboratory. Follow-up included heart failure quality-of-life assessments and serial imaging with echocardiography and cardiac computed tomography.ResultsNineteen subjects consented and underwent cerclage, 63% with heart failure with reduced ejection fraction and 37% with heart failure with preserved ejection fraction, with ischemic cardiomyopathy in 26% and nonischemic cardiomyopathy in 74%. There were no procedural deaths, strokes, or transient ischemic attacks or other major cardiovascular adverse events. The primary endpoint was met in 17 subjects. Cerclage induced sustained reductions in mitral regurgitant volume (-41%) and effective orifice area (-33%) after a median of 337 days. Cerclage resulted in improvements in 6-minute walking distance (+78 m) and Kansas City Cardiomyopathy Questionnaire Overall Summary Score (+22 points) at 30 days that were maintained after a median of 265 days. New complete heart block developed in 6 of 17 subjects. Three deaths occurred on postprocedural days 79, 159, and 756, unrelated to cerclage.ConclusionsTranscatheter mitral cerclage ventriculoplasty resulted in significant and sustained improvements in mitral regurgitation and in heart failure quality-of-life assessments.

Problem Based Learning (PBL) is widely used to educate tertiary health students, mainly because of the pedagogical benefits including promoting critical thinking, clinical reasoning and lifelong learning. However, delivering PBL can be challenging, particularly when students have demanding academic and clinical placement schedules. PBL online has the potential to allow students to participate remotely. In this study, a PBL case was designed and delivered using a synchronous online platform. A qualitative methodology was used to understand the participants' experiences and perspectives. Focus group and survey data revealed that PBL online is a flexible and accessible alternative to face-to-face PBL. Aspects of the functionality offered by the platform assisted the PBL process, however internet connectivity impacted the trial and students reported difficulties with rapport building and limited depth of discussion. These difficulties were not perceived as detrimental by the facilitator, however additional effort and preparation was required compared to face-to-face PBL.

Purpose: To introduce alternating current‐controlled, conductive ink‐printed marker that could be implemented with both custom and commercial interventional devices for device tracking under MRI using gradient echo, balanced SSFP, and turbo spin‐echo sequences. Methods: Tracking markers were designed as solenoid coils and printed on heat shrink tubes using conductive ink. These markers were then placed on three MR‐compatible test samples that are typically challenging to visualize during MRI scans. MRI visibility of markers was tested by applying alternating and direct current to the markers, and the effects of applied current parameters (amplitude, frequency) on marker artifacts were tested for three sequences (gradient echo, turbo spin echo, and balanced SSFP) in a gel phantom, using 0.55T and 1.5T MRI scanners. Furthermore, an MR‐compatible current supply circuit was designed, and the performance of the current‐controlled markers was tested in one postmortem animal experiment using the current supply circuit. Results: Direction and parameters of the applied current were determined to provide the highest conspicuity for all three sequences. Marker artifact size was controlled by adjusting the current amplitude, successfully. Visibility of a custom‐designed, 20‐gauge nitinol needle was increased in both in vitro and postmortem animal experiments using the current supply circuit. Conclusion: Current‐controlled conductive ink‐printed markers can be placed on custom or commercial MR‐compatible interventional tools and can provide an easy and effective solution to device tracking under MRI for three sequences by adjusting the applied current parameters with respect to pulse sequence parameters using the current supply circuit. [ABSTRACT FROM AUTHOR]

The performative context of higher education demands that practice-oriented academics shift their priorities from preparing practitioners for the profession, towards "productive" scholarship. We present narratives from occupational therapy academics at the end of a year-long journey through an action research project focussed on academic identity and scholarly growth. Our analysis captures subtle and striking shifts in being and becoming, doing and belonging. The findings, re-presented as an adapted "Hero's Journey", also reveal the powerful impacts on identity and practice that are enabled when academics have the opportunity to create spaces for scholarship that are experienced as caring, collaborative and collegial.

Purpose: We describe a clinical grade, "active", monopole antenna‐based metallic guidewire that has a continuous shaft‐to‐tip image profile, a pre‐shaped tip‐curve, standard 0.89 mm (0.035″) outer diameter, and a detachable connector for catheter exchange during cardiovascular catheterization at 0.55T. Methods: Electromagnetic simulations were performed to characterize the magnetic field around the antenna whip for continuous tip visibility. The active guidewire was manufactured using medical grade materials in an ISO Class 7 cleanroom. RF‐induced heating of the active guidewire prototype was tested in one gel phantom per ASTM 2182‐19a, alone and in tandem with clinical metal‐braided catheters. Real‐time MRI visibility was tested in one gel phantom and in‐vivo in two swine. Mechanical performance was compared with commercial equivalents. Results: The active guidewire provided continuous "profile" shaft and tip visibility in‐vitro and in‐vivo, analogous to guidewire shaft‐and‐tip profiles under X‐ray. The MRI signal signature matched simulation results. Maximum unscaled RF‐induced temperature rise was 5.2°C and 6.5°C (3.47 W/kg local background specific absorption rate), alone and in tandem with a steel‐braided catheter, respectively. Mechanical characteristics matched commercial comparator guidewires. Conclusion: The active guidewire was clearly visible via real‐time MRI at 0.55T and exhibits a favorable geometric sensitivity profile depicting the guidewire continuously from shaft‐to‐tip including a unique curved‐tip signature. RF‐induced heating is clinically acceptable. This design allows safe device navigation through luminal structures and heart chambers. The detachable connector allows delivery and exchange of cardiovascular catheters while maintaining guidewire position. This enhanced guidewire design affords the expected performance of X‐ray guidewires during human MRI catheterization. [ABSTRACT FROM AUTHOR]