Read more to learn how AVEIR™ VR LP has helped patients with a broad spectrum of health concerns live healthier, better lives.
AVEIR VR LP is an appropriate choice for patients indicated for permanent pacing but who may need temporary or interim pacing support following certain types of procedures like laser lead extractions (LLEs) and TAVR. For these patients, AVEIR offers:
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For patients with symptomatic AV block who have persistent atrial fibrillation (AF) or other atrial tachyarrhythmia (AT). AVEIR VR LP can provide:
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MAT-2209470 v1.0
AVEIR VR LP is an effective solution for this group of patients, e.g. patients in normal sinus rhythm with episodes of sinus arrest and in whom relatively infrequent ventricular pacing is expected, or who have significant existing comorbidities that are otherwise likely to impact or determine clinical outcomes. For these patients, AVEIR VR LP offers:
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Patients in this category may include those experiencing symptomatic intermittent AV block, those with AV block in whom infrequent pacing is expected, or who have significant existing comorbidities that are otherwise likely to impact or determine clinical outcomes. AVEIR VR LP is appropriate for these patients because:
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Patients in this category may experience symptomatic pauses secondary to persistent or chronic atrial fibrillation, slow ventricular response or malignant tachy-brady syndrome, severe comorbidities like end-stage kidney disease1 (ESKD) or access and mobility problems that would support leadless pacing as the preferred pacing option.
AVEIR VR LP is an appropriate option for these patients because:
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Young, vibrant, active – and living her best life with Abbott’s AVEIR VR Leadless Pacemaker.
Chelsey needed a pacemaker, and AVEIR VR’s leadless pacemaker design was the ideal solution for her active lifestyle. With no wires and no arm restrictions, Aveir VR LP got her back to the gym and back to life - it’s her safety net. “It catches me when I need it.”
Young Male Patient with Heart Block; Dr. James Ip (AVEIR™ VR Case Insights Series)
References
* The LP device electronics are designed to be enabled by future software, upon regulatory approval, to support dual chamber pacing in the future. Dual chamber pacing system is currently in clinical trial (ClinicalTrials.gov NCT #05252702) and limited to investigational use only
For additional information about specific MR Conditional, including warnings, precautions, adverse conditions to MRI scanning and potential adverse events, please refer to the MRI-Ready Leadless Systems Manual at medical.abbott/manuals or check our MRI Ready resources at cardiovascular.abbott/mriready
MAT-2302697 v2.0 | Item is approved for U.S. use only