Dr. Joseph Drozda
Director of Outcomes Research
St. Louis, Missouri
After a career in the private practice of cardiology and as a senior health system and managed care executive, I retired and was hired by Mercy to start a health services research program for the four-state regional health system. The idea was to begin capturing and using data being generated by the system-wide Epic EHR to inform Mercy's care management strategies. Shortly after my arrival, an opportunity presented itself to develop systems, with FDA's support, for evaluating medical devices using device identifiers to join supply chain and clinical data. This soon burgeoned into formation of multi-system distributed data networks, adaptation of common data models to medical device work, and development of large data sets dealing with specific conditions, e.g., heart failure.
Current Research Interest:
National Evaluation System for health Technologies (NEST) projects:
Multi-system study using EHR data in support of an application to FDA for label expansion of cardiac ablation catheters
Development of a national system for medical device active surveillance using real world data
Drozda J, Zeringue A, Dummitt B, Yount B, Resnic F. How real-world evidence can really deliver: a case study of data source development and use. BMJ Surgery, Interventions, & Health Technologies 2020;2:e000024. doi: 10.1136/bmjsit-2019-000024
Drozda JP Jr, Roach J, Forsyth T, Helmering P, Dummitt B, Tcheng JE. Constructing the informatics and information technology foundations of a medical device evaluation system: a report from the FDA unique device identifier demonstration. J Am Med Inform Assoc 2018;25:111-120. Originally published on-line May 3, 2017. Available at https://doi.org/10.1093/jamia/ocx041.
Resnic FS, Majithia A, Marinac-Dabic D, Robbins S, Ssemaganda H, Hewitt K, Ponirakis A, Loyo-Berrios N, Moussa I, Drozda J, Normand S, Matheny ME. Registry-based prospective, active surveillance of medical-device safety. N Engl J Med 2017; 376:526-535. Originally published on-line January 25, 2017. http://www.nejm.org/doi/full/10.1056/NEJMoa1516333.
Tcheng JE., Drozda JP., Gabriel, D., Wilgus RW., Williams M., Windle TA., Windle JR. (2018). Improving Healthcare Interoperability Project Report. Pew Charitable Trusts and Duke Clinical Research Institute, 1-42. Retrieved from https://dcri.org/registry-data-standards/
Drozda JP Jr, Dudley C, Helmering P, Roach J, Hutchison L. The Mercy unique device identifier demonstration project; implementing point of use product identification in the cardiac catheterization laboratories of a regional health system. Healthcare 2016;4:116-119. doi:10.1016/j.hjdsi.2015.07.002. Originally published on-line July, 2015.
Tcheng JE, Crowley J, Tomes M, Reed TL, Dudas JM, Thompson KP, Garratt KN, Drozda Jr. JP. Unique device identifiers (udis) for coronary stent post-market surveillance and research: A report from the FDA's Medical Device Epidemiology Network (MDEpiNet) udi demonstration, American Heart Journal, 2014;168(4);405-13,e2., doi: 10.1016/j.ahj.2014.07.001.