Overview
Registry intended to provide a data repository and reporting infrastructure for the surveillance of CytoSorb device use in real-world critical care settings, and to serve as an objective, comprehensive, and scientifically-based resource to measure and improve the quality of patient care
Eligibility
Inclusion Criteria:
- Planned OR actual CytoSorb® 300 mL device utilization
- Informed consent for prospective registry participation
Exclusion Criteria:
- Use of the CytoSorb® 300 mL device for antithrombotic removal only
- Intraoperative use of CytoSorb® 300 mL device during cardiac surgery only
- The occurrence of a complication or other medically justified circumstance that arises after written informed consent has been obtained from the patient and before or during the planned therapy and as a result of which the use of CytoSorb® 300 mL Adsorber is contraindicated or no longer appropriate.