Trial DesignThe design and implementation of a new surveillance system for venous thromboembolism using combined active and passive methods
Section snippets
Surveillance system objectives
The primary aims of our pilot surveillance system were to (1) develop and implement a population-based surveillance system for DVT and PE in Oklahoma County, OK, that includes both active and passive surveillance activities and which can accurately capture outpatient, inpatient, and death-related VTE events and distinguish first episode (incident) from recurrent VTE events; (2) estimate the annual incidence of first-episode VTE events and DVT and PE separately, (3) estimate the annual incidence
Results
All 13 inpatient facilities in Oklahoma County and the Oklahoma City VA Medical Center were included in this surveillance system. Fifty-six outpatient facilities were identified as being potentially eligible for surveillance; however, after contacting each facility, only 8 facilities met the criteria to be included in the surveillance, each of which contributed data to the surveillance system. As of February 1, 2015, we have screened 54,494 (99.5%) of 54,782 identified imaging records of
Discussion
We established a pilot population-based surveillance system for VTE using both active and passive methods in Oklahoma County, OK, to inform CDC regarding the development of future national VTE surveillance. We designed this system to (1) improve VTE-related estimates of the incidence of first-time and recurrent events and mortality rates, (2) differentiate between provoked and unprovoked events as well as describe these patients by demographic characteristics (including race/ethnicity), and (3)
Conclusions
In conclusion, we developed a pilot population-based surveillance system for VTE in Oklahoma County, OK. This novel system incorporates both active and passive elements. The most important factor in conducting our surveillance was the collaboration with CDC and the Oklahoma Commissioner of Health. This allowed us to work with all facilities in the county and collect the required information. We are in the process of better understanding the quality of individual ICD-9 CM codes in identifying
Disclosures
This project was funded by CDC funding: DD14-1407. Dr Bratzler would like to disclose a consultancy for CDC and Sanofi Pasteur. Dr Raskob would like to disclose a consultancy and honoraria for Bayer Healthcare, BMS, Boehringer Ingelheim, Daiichi Sankyo, Janssen Pharmaceuticals, Pfizer, and ISIS Pharmaceuticals. Dr Wendelboe would like to disclose an honoraria from Bristol-Myers Squibb. None of the other authors have any disclosures.
Acknowledgments
This surveillance system was funded by a cooperative agreement with the CDC DD14-1407. We are also deeply grateful for the work of the surveillance officer, Natalie Feland, Aubrey Balch, Jannate Ahmed, Evaren Page, and Ashley Sword-Buster, for their tireless dedication in collecting the data. We are also grateful for Pravina Kota for her information technology support, including the development of the database.
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CDC disclaimer: The findings and conclusions in this report are those of the author(s) and do not necessarily represent the official position of the CDC.
Funding provided by a cooperative agreement with CDCDD14-1407.