Key result
Antiarrhythmia device implantation under continued dual antiplatelet therapy showed no significant differences in complication rates, particularly hematoma, compared to control.
Why the study?
Does continued dual antiplatelet therapy increase the risk of complications during antiarrhythmia device implantation in patients requiring such devices?
Cohort (n=427)
No
Does continued dual antiplatelet therapy increase the risk of complications during antiarrhythmia device implantation in patients requiring such devices?
Antiarrhythmia device implantation can be safely performed in patients on continued dual antiplatelet therapy without a significantly increased risk of hematoma when drainage systems are used.
Answers are grounded in this paper and cite their sources.
Supports continued DAPT feasibility in device implantation; hypothesis-generating and requires randomized confirmation before practice change.
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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Dreger et al. (2009) conducted a cohort in Antiarrhythmia device implantation (n=427). Dual antiplatelet therapy vs. Acetylsalicylic acid alone or no antiplatelet medication was evaluated on Complication rates, particularly hematoma rate. Antiarrhythmia device implantation under continued dual antiplatelet therapy showed no significant differences in complication rates, particularly hematoma, compared to control.
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