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Is antiarrhythmia device implantation safe under dual antiplatelet therapy?
Henryk Dreger1, Andrea Grohmann, Hansjürgen Bondke
1From the Medizinische Klinik für Kardiologie und Angiologie, Campus Mitte, Charité-Universitätsmedizin Berlin, Berlin, Germany. henryk.dreger@charite.de
Insights
Implanting devices in patients on dual antiplatelet therapy (DA-therapy) is safe. Using drainage systems prevents significant increases in clinically relevant hematoma, even with continued DA-therapy.
Area of Science:
- Cardiology
- Medical Devices
- Antiplatelet Therapy
Background:
- Dual antiplatelet therapy (DA-therapy) use is increasing in patients undergoing device implantation.
- Complications of antiarrhythmia device implantation in patients on DA-therapy require careful evaluation.
Purpose of the Study:
- To analyze complications associated with antiarrhythmia device implantation in patients on DA-therapy.
Main Methods:
- Prospective data collection for device implantations (Jan 2008-Feb 2009).
- Comparison between a DA-therapy group (n=109) and a control group (n=318) on single antiplatelet or no antiplatelet medication.
- Retrospective analysis of 71 DA-therapy patients (2002-2007).
Main Results:
- Longer procedure times observed for first-time pacemaker implants in DA-therapy patients.
- Increased fluid loss and drainage times in DA-therapy patients after pacemaker implantation, but not after ICD implantation.
- No significant difference in overall complication rates, including hematoma, between DA-therapy and control groups.
Conclusions:
- Antiarrhythmia device implantation can be safely performed in patients on continued DA-therapy.
- Utilizing drainage systems mitigates the risk of clinically relevant hematoma in this patient population.
Background:
Device implantations in patients on dual antiplatelet-therapy (DA-therapy) continue to rise. The aim of our study was to compile and analyze data on complications of antiarrhythmia device implantation under DA-therapy.
Methods:
We prospectively collected data on all device implantations in our department from January 2008 until February 2009. The control group was comprised of patients on acetylsalicylic acid alone or no antiplatelet medication at all (318 subjects). The DA-therapy group consisted of 109 patients of whom 71 were analyzed retrospectively (implantations from 2002 to 2007).
Results:
Procedure times were significantly longer in DA-therapy patients receiving a pacemaker for the first time. In contrast, procedure times did not differ significantly between the two study groups for implantable cardioverter defibrillator (ICD) implantations and for pacemaker replacements. Fluid losses via drainage systems and drainage times were significantly increased in the DA-therapy group as compared with the control group after pacemaker but not after ICD implantations. Importantly, there were no significant differences in complication rates, particularly the hematoma rate, between the DA-therapy and the control group.
Conclusions:
When drainage systems are used, antiarrhythmia device implantation is safe and can be performed without significantly increased risk of clinically relevant hematoma in patients on continued DA-therapy. (PACE 2010; 394-399).
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