All Stories

  1. Can machine learning complement traditional medical device surveillance? A case-study of dual-chamber implantable cardioverter–defibrillators
  2. Transcatheter Valve Therapy Registry Is A Model For Medical Device Innovation And Surveillance
  3. Editorial: Arthroplasty Devices: Registries and Beyond
  4. Tailoring study design to each stage of surgical innovation: the ideal recommendations
  5. The STS-ACC Transcatheter Valve Therapy National Registry
  6. The International Registry Infrastructure for Cardiovascular Device Evaluation and Surveillance
  7. Special Applications of Pharmacoepidemiology
  8. IDEAL framework for surgical innovation 3: randomised controlled trials in the assessment stage and evaluations in the long term study stage
  9. Association Between Endoscopic vs Open Vein-Graft Harvesting and Mortality, Wound Complications, and Cardiovascular Events in Patients Undergoing CABG Surgery
  10. Sex and Risk of Hip Implant Failure
  11. Risk of Revision for Fixed Versus Mobile-Bearing Primary Total Knee Replacements
  12. Long-Term Outcomes After Transmyocardial Revascularization
  13. Association Between Endoscopic vs Open Vein-Graft Harvesting and Mortality, Wound Complications, and Cardiovascular Events in Patients Undergoing CABG Surgery
  14. Evaluation of total hip arthroplasty devices using a total joint replacement registry
  15. Epidemiologic Studies of Medical Devices: Methodologic Considerations for Implantable Devices
  16. Evaluation of an automated safety surveillance system using risk adjusted sequential probability ratio testing
  17. The International Consortium of Orthopaedic Registries: Overview and Summary
  18. Stages and Tools for Multinational Collaboration: The Perspective from the Coordinating Center of the International Consortium of Orthopaedic Registries (ICOR)
  19. Comparative assessment of implantable hip devices with different bearing surfaces: systematic appraisal of evidence
  20. Disproportionality analysis for signal detection of implantable cardioverter-defibrillator-related adverse events in the Food and Drug Administration Medical Device Reporting System
  21. Elevated B-Type Natriuretic Peptide Is Associated With Increased In-Hospital Mortality or Cardiac Arrest in Patients Undergoing Implantable Cardioverter-Defibrillator Implantation
  22. Automated Surveillance to Detect Postprocedure Safety Signals of Approved Cardiovascular Devices
  23. Developing the Safety of Atrial Fibrillation Ablation Registry Initiative (SAFARI) as a collaborative pan-stakeholder critical path registry model: A Cardiac Safety Research Consortium “Incubator” Think Tank
  24. A Framework for Evidence Evaluation and Methodological Issues in Implantable Device Studies
  25. Rethinking Analytical Strategies for Surveillance of Medical Devices
  26. Planning the Safety of Atrial Fibrillation Ablation Registry Initiative (SAFARI) as a Collaborative Pan-Stakeholder Critical Path Registry Model: A Cardiac Safety Research Consortium “Incubator” Think Tank
  27. The FDA Advisory on Vacuum-Assisted Devices (1998)
  28. The Safety of Prenatal Ultrasound Exposure in Human Studies
  29. Comparison of women treated with Palmaz-Schatz stent and with balloon angioplasty
  30. Ethical Requirements and Guidelines for Epidemiological Studies of Medical Devices
  31. Clinical Epidemiology of Intrapartum Fetal Monitoring Devices
  32. Data Sources for Medical Device Epidemiology Studies and Data Mining