800 results on '"Dhruva, Sanket S."'
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2. Deep Learning of Electrocardiograms in Sinus Rhythm From US Veterans to Predict Atrial Fibrillation
3. Informational Postcards Increase Engagement with Remote Monitoring Among Veterans with Pacemakers and Implantable Cardioverter-Defibrillators: a Stepped-Wedge Randomized Controlled Trial
4. Experts’ Views on FDA Regulatory Standards for Drug and High-Risk Medical Devices: Implications for Patient Care
5. Using real-world data from health systems to evaluate the safety and effectiveness of a catheter to treat ischemic ventricular tachycardia
6. Ventricular arrhythmia detection for contemporary Biotronik and Abbott implantable cardioverter defibrillators with markedly prolonged detection in Biotronik devices
7. Advancing the Real-World Evidence for Medical Devices through Coordinated Registry Networks
8. Gender Differences in Guideline-Directed Medical Therapy for Cardiovascular Disease Among Young Veterans
9. Evaluation of cardiovascular implantable electronic device leads post implant: ElectroPhysiology Predictable And SuStainable Implementation Of National Registries (EP PASSION)
10. A Policy Approach to Reducing Low-Value Device-Based Procedure Use
11. Utilization of Fixed-Dose Combination Treatment for Hypertension in Medicare and Medicaid From 2016 to 2020
12. Heart Watch Study: protocol for a pragmatic randomised controlled trial
13. Strategies to enhance remote monitoring adherence among patients with cardiovascular implantable electronic devices
14. Challenges and solutions to advancing health equity with medical devices
15. Physician responses to apple watch-detected irregular rhythm alerts
16. Payer-Negotiated Prices for Cardiac Electrophysiology Procedures at 2022-2023 Top 100 US News & World Report for Cardiology and Heart Surgery Hospitals
17. Identifying treatment heterogeneity in atrial fibrillation using a novel causal machine learning method
18. Cardiovascular implantable electronic device lead safety: Harnessing real-world remote monitoring data for medical device evaluation
19. Medicare Coverage and Patient Out-of-Pocket Costs for Cardiovascular-Kidney-Metabolic Medications
20. Funding of Evidence Included Within Public Comments Submitted to Inform Medicare National Coverage Determinations
21. Effectiveness, utilisation and cost associated with implantable loop recorders versus external monitors after ischaemic or cryptogenic stroke
22. Blood pressure control and maintenance in a prospective cohort of younger Veterans: Roles of sex, race, ethnicity, and social determinants of health
23. Intravascular Microaxial Left Ventricular Assist Device Manufacturer Payments to Cardiologists and Use of Devices
24. Informational letters or postcards to initiate remote monitoring among veterans with pacemakers and implantable cardioverter‐defibrillators: A randomized, controlled trial
25. Monitoring of Remotely Reprogrammable Implantable Loop Recorders With Algorithms to Reduce False‐Positive Alerts
26. Characterization of multi-domain postoperative recovery trajectories after cardiac surgery using a digital platform
27. Factors associated with remote monitoring adherence for cardiovascular implantable electronic devices
28. Medicare Coverage and Out-of-Pocket Costs of Quadruple Drug Therapy for Heart Failure
29. Ensuring Patient Safety and Benefit in Use of Medical Devices Granted Expedited Approval
30. Electrical abnormalities with St. Jude/Abbott pacing leads: A systematic review and meta-analysis
31. Use of Electronic Health Records to Characterize Patients with Uncontrolled Hypertension in Two Large Health System Networks
32. Hospital Prices for Physician-Administered Drugs for Patients with Private Insurance
33. Physicians’ Perspectives On FDA Regulation Of Drugs And Medical Devices: A National Survey
34. Systematic reprogramming of implantable cardioverter-defibrillators to match the 2019 consensus recommendations
35. Physical activity, patient-reported symptoms, and clinical events: Insights into postprocedural recovery from personal digital devices
36. Changing FDA Approval Standards: Ethical Implications for Patient Consent
37. Reporting of Demographics & Subgroup Analyses in Premarketing Studies of FDA Approved High-Risk Cardiovascular Devices, 2014–2022.
38. Cardiac coronary tomography angiography (CCTA) use across geographical regions in the USA and the UK: a cross-sectional study
39. Clinical Phenotyping with an Outcomes-driven Mixture of Experts for Patient Matching and Risk Estimation
40. The Need for Randomized Clinical Trials Demonstrating Reduction in All-Cause Mortality With Blood Tests for Cancer Screening
41. Financial Conflicts of Interest in Public Comments on Medicare National Coverage Determinations of Medical Devices
42. A Critical Examination of Independent Medical Review Decision-making for Cardiovascular Procedures Shows Low Rate of Evidence Citation in Reviews
43. Medical device risk (re)classification: lessons from the FDA’s 515 Program Initiative
44. Decreasing unnecessary use of continuous cardiac monitoring (telemetry) in hospitalised patients.
45. Aligning US Agency Policies for Cardiovascular Devices Through the Breakthrough Devices Program.
46. Assessing the use of observational methods and real-world data to emulate ongoing randomized controlled trials.
47. Unique Device Identifiers for Medical Devices at 10 Years
48. Use of Electronic Health Records to Characterize Patients with Uncontrolled Hypertension in Two Large Health System Networks
49. Barriers and Facilitators Associated With Remote Monitoring Adherence Among Veterans With Pacemakers and Implantable Cardioverter-Defibrillators: Qualitative Cross-Sectional Study (Preprint)
50. Availability of Unique Device Identifiers for Class I Medical Device Recalls From 2018 to 2022
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