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Published on: September 15, 2023
Unexplained Obstruction of an Integrated Cardiotomy Filter During Cardiopulmonary Bypass
Insights
An integrated cardiotomy filter obstructed during cardiopulmonary bypass (CPB), necessitating circuit reconfiguration. This rare event highlights the need for preparedness and reporting during CPB procedures.
Area of Science:
- Cardiovascular Surgery
- Medical Device Safety
- Patient Safety
Background:
- Cardiopulmonary bypass (CPB) is a critical procedure in cardiac surgery.
- While generally safe, CPB carries potential complications.
- Integrated cardiotomy filters are designed to ensure circuit safety during CPB.
Observation:
- An integrated cardiotomy filter became obstructed approximately one hour after CPB initiation.
- The obstruction occurred gradually over several minutes.
- The patient required circuit reconfiguration using an external cardiotomy filter to maintain CPB functionality.
Findings:
- The cause of the integrated cardiotomy filter obstruction remained undetermined despite thorough analysis.
- Postoperative examination revealed no thrombus or mechanical damage to the filter.
- The patient experienced an otherwise routine hospital stay without complications related to the incident.
Implications:
- This case represents the first reported instance of an obstructed integrated cardiotomy filter.
- Highlights the importance of having a readiness plan for CPB circuit complications, including filter obstruction.
- Emphasizes the need for formal reporting systems for "near miss" and adverse events during CPB.
Abstract:
Cardiopulmonary bypass (CPB) is considered relatively safe in most cases, yet is not complication free. We present a case of an integrated cardiotomy filter obstruction during CPB, requiring circuit reconfiguration. Approximately an hour after uneventful initiation of CPB the integrated cardiotomy filter became obstructed over several minutes, requiring circuit reconfiguration using an external cardiotomy filter to maintain functionality. Following reconfiguration, CPB was maintained with a fully functional circuit allowing safe patient support throughout the remainder of CPB. Postoperatively, there was no sign of thrombus or mechanical obstruction of the filter, which was sent to the manufacturer for analysis. The cause of the obstruction was unclear even after chemical analysis, visual inspection, and a review of all techniques and products to which the patient was exposed. The patient had a generally routine hospital stay, with no signs or symptoms related to the incident. To our knowledge, this is the first report describing an obstructed integrated cardiotomy filter. An appropriate readiness plan for such an incident includes proper venting of the filter chamber, a method for detecting an obstruction, and a plan for circuit reconfiguration. This case illustrates the need for a formal reporting structure for incidents or "near miss" incidents during CPB.

