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Haemolysis after Amplatzer device closure of ventricular septal defect
Insights
Transcatheter closure of septal defects using Amplatzer devices can cause hemolysis. This case report details a patient experiencing self-limiting hemolysis after implantation of an Amplatzer perimembranous ventricular septal defect device.
Area of Science:
- Cardiology
- Medical Devices
- Hematology
Background:
- Transcatheter device closure is a common method for treating septal defects.
- Hemolysis has been observed following Amplatzer device implantation for various septal defects.
- Perimembranous ventricular septal defects (VSDs) are a subset of these defects.
Purpose of the Study:
- To report a case of hemolysis following Amplatzer perimembranous VSD device implantation.
- To highlight the occurrence of self-limiting hemolysis in this context.
- To contribute to the understanding of potential complications associated with transcatheter VSD closure.
Main Methods:
- Case report of a single patient.
- Review of clinical presentation and laboratory findings.
- Implantation of an Amplatzer perimembranous VSD device.
Main Results:
- The patient experienced hemolysis post-device implantation.
- The hemolysis was self-limiting and resolved without specific intervention.
- No long-term adverse effects were noted.
Conclusions:
- Amplatzer perimembranous VSD device closure can be associated with hemolysis.
- Hemolysis in this context may be self-limiting.
- Further monitoring and research are warranted for transcatheter VSD device complications.
Abstract:
Over the last few years, a vast variety of devices have been developed to close various septal defects through the transcatheter route. Haemolysis has been documented after Amplatzer device closure of patent ductus arteriousus, atrial septal defect, and ventricular septal defect. We report one patient with self-limiting haemolysis after implantation of an Amplatzer perimembranous VSD device.

