defibrillator lead: observation of long-term performance of defibrillator leads
Study summary
All patients having an implantable cardiac defibrillator (ICD) implanted and having follow-up at the Cantonal Hospital Lucerne (LUKS), the investigator center, are included in this retrospective ICD lead registry from 2006 onwards. Data is collected prospectively from december 2016 onwards. After certain ICD-leads tended to fail early the investigators aimed for a registry monitoring our patient population with defibrillator leads and evaluating their long-term performance.
Eligibility
Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* all patients being implanted with a Defibrillator lead from 2006 onwards
Exclusion Criteria:
* documented refusal of data collection for scientific purposes
Primary outcome measure(s)
performance of lead impedance — regular clinical controls within 10 years electronic impedances in Ω
performance of lead threshold — during regular clinical controls within 10 years threshold values in V
performance of lead sensing — during regular clinical controls within 10 years sensing values in millivolt (mV)
lead parameters — during regular clinical controls within 10 years battery performance in %
performance of defibrillator — during regular clinical controls within 10 years inadequate/adequate shock release in numbers
control system of defibrillator — during regular clinical controls within 10 years software problems in numbers and descriptive
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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