The objective of the study is to actively gather additional information on the use of CorMatrix ECM for pericardial reconstruction.
Up to 100 clinical sites will enroll subjects who have received CorMatrix ECM for pericardial reconstruction. The following clinical data will be collected at a single post-operative visit: * Demographic information * Pre-operative risk factors * Surgical procedure * Blood transfusion information, if applicable * Chest tube placement information * Surgical complications * Use of anticoagulation medication * Cardiac related procedures since surgical procedure * Device related adverse events
Study Type
OBSERVATIONAL
Enrollment
1,420
Proportion of Subjects With Device Related Adverse Events.
Data will be collected at the initial post-operative visit. This is a single visit study.
Time frame: Post-op visit, after an average of 30 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Cario-Thoracic Surgeons, P.C.
Birmingham, Alabama, United States
Cardiovascular Consultants, LTD
Glendale, Arizona, United States
Phoenix Cardiac Surgery
Phoenix, Arizona, United States
Southwest Heart & Lung
Phoenix, Arizona, United States
University of Arizona Medical Center
Tucson, Arizona, United States
Mercy Clinic Cardiac Thoracic & Vascular Surgery
Fort Smith, Arkansas, United States
Arkansas Heart Hospital
Little Rock, Arkansas, United States
Baptist Medical Center
Little Rock, Arkansas, United States
Arkansas Heart Hospital
Little Rock, Arkansas, United States
Heart & Lung Surgical Specialties
Rancho Mirage, California, United States
...and 33 more locations