Abstract
Background
In the present study, we have focused upon rates and clinical determinants of inappropriate shock (IS) after implantable cardioverter-defibrillator (ICD).
Methods
Data were collected prospectively in the German Device II Registry.
Results
A total of 783 patients were included. Three sub-groups were identified: non-shock (NS) included 725 patients (92.6%), IS 24 (3.1%), and appropriate shock (AS) 34 (4.3%). IS patients were younger (AS 68 (58–77); IS 59 (51–68); NS 66 (56–75) years; p = 0.03), had been mainly referred for primary prophylaxis (AS 42.4%; IS 70.8%; NS 67.3%; p = 0.01), had a higher resting heart rate (AS 70 (63–80); IS 80 (71–98); NS 70 (60–81) BPM; p = 0.003), had more often atrial fibrillation (AF) (AS 14.7%; IS 45.8%; NS 18.8%; p = 0.006), and shorter QRS duration (AS 100 (90–120); IS 95 (90–100); NS 120 (98–150) msec.; p = 0.001). VVI-ICD was more common in IS (AS 64.7%; IS 83.3%; NS 49.8%; p = 0.002). At a follow-up of 18.2 months (75% IQR 13.6–22.4), no deaths were observed in the IS group, one (2.9%) in the AS, and 36 (4.9%) in the NS (p = 0.9). At logistic regression, VVI-ICD implantation was the strongest IS independent determinant (OR 5.0; 95% CI 1.6–15.9; p = 0.004) together with age < 70 years (OR 4.6; CI 1.4–14.7; p = 0.009), AF at time of ICD implantation (OR 3.5; CI 1.3–9.1; p = 0.01), and resting heart rate > 70/min (OR 2.8; CI 1.0–7.3; p = 0.03).
Conclusion
In a contemporary setting, some specific conditions such as VVI-ICD, younger age, and faster resting heart rates remain important IS determinants after ICD implantation.
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Data availability
This is a multicenter study and data are protected by local patients’ privacy regulations. In any case, data will be made available upon request.
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Funding
The registry has been supported by “Stiftung Institut für Herzinfarktforschung (IHF)” and by Biotronik, Medtronic, and St. Jude Medical.
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All authors have contributed to database designing and patients’ clinical management. GD, HI, JS, and MH have designed the study. GD has written the manuscript. MH has performed the analysis. LE and ES ha have given a first critical reading and correction to the original version of the manuscript. All other authors have read and approved the final version of the manuscript.
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A positive vote was obtained from the ethics committee of the Landesaerztekammer Rheinland-Pfalz in April 2011. All patients have given written informed consent to data collection and publication.
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Safak, E., Eckardt, L., Jung, W. et al. Determinants of inappropriate implantable cardioverter-defibrillator shocks: the German Device Registry perspective. J Interv Card Electrophysiol 56, 71–77 (2019). https://doi.org/10.1007/s10840-019-00600-4
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DOI: https://doi.org/10.1007/s10840-019-00600-4