Abstract 4354762: Safety and feasibility of magnetic resonance imaging within the first week following transvenous pacing system implantation

Introduction: Patients with transvenous cardiac implantable electrical devices (CIEDs) including pacemakers are typically excluded from magnetic resonance imaging (MRI) examinations for at least 6-weeks following implant. However, many MRI scans are required on urgent or emergency basis, potentially resulting in suboptimal management for patients following a recent CIED implant. The absolute risks of adverse lead/generator events with early MRI have not been quantified. Specific transvenous pacing systems from one manufacturer (Abbott) do not mandate a routine 6-week post-implant restriction for MRI conditionality, although real-world human data investigating lead parameter stability with MRI early (<7 days) post-implant are lacking. Research Question: Can MRI be performed early (<7 days) after pacemaker implantation without safety events or significant changes to lead parameters? Methods: Patients undergoing implantation of Abbott Assurity™ MRI pacemakers with active-fixation MRI conditional leads (Abbott Tendril™ 52cm/58cm or UltiPace™ 65cm) with no contraindication to MRI underwent cardiac MRI within 7 days of implant. Patients were scanned at 1.5 or 3T in an asynchronous pacing mode. Device interrogation was performed before and after MRI. All patients provided written consent. Pre- and post-MRI lead parameter measurements were compared using the two one-sided t-Tests (TOST) equivalence test. Equivalence margins were prespecified: lead impedance ±30Ω, lead sensing ±0.5mV, lead threshold ±0.25V. Results: 20 patients (median age 77 (IQR 72-80) years, 75% male) were recruited. 65% received right ventricular pacing and 35% conduction system pacing. Median time from implant to MRI was 3 [IQR 1-5] days. All lead parameters were statistically equivalent pre- and post-MRI: Atrial lead impedance mean difference 5 Ω (90% CI -3 to +12), TOST p<0.001 Ventricular lead impedance -1 Ω (90% CI -9.2 to +7.2), TOST p<0.001 Sensed P wave 0.04 mV (90% CI -0.13 to +0.22), TOST p<0.001 Sensed R wave -0.06 mV (90% CI -0.28 to +0.17), TOST p=0.001 Atrial capture threshold -0.01 mV (90% CI -0.04 to +0.01), TOST p<0.001 Ventricular capture threshold -0.01 mV (90% CI -0.05 to +0.03), TOST p<0.001 Conclusion: MRI within 7 days of pacemaker implantation was safe, with no adverse events and no significant change in lead parameters. These findings provide real-world data to complement manufacturer guidance and support access to early MRI when indicated for patients with conditional pacemaker systems.

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Journal
Circulation
Published
2025-11-03
DOI
https://doi.org/10.1161/circ.152.suppl_3.4354762
Primary Topic
Advanced MRI Techniques and Applications
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article
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article

Abstract 4354762: Safety and feasibility of magnetic resonance imaging within the first week following transvenous pacing system implantation

Dimitrios Panagopoulos, C Fielder Camm, Julian O.M. Ormerod, Oliver J. Rider et al.
Circulation
Advanced MRI Techniques and Applications
article

Abstract 4354762: Safety and feasibility of magnetic resonance imaging within the first week following transvenous pacing system implantation

Dimitrios Panagopoulos, C Fielder Camm, Julian O.M. Ormerod, Oliver J. Rider, Kim Rajappan, Timothy R. Betts, Pok‐Tin Tang, Matthew Ginks, Sheila Coelho Ramalho Vasconcelos Morais, Benjamin Mothibe Bussmann, Stefan Neubauer, James Gamble, Jonathan Raby, Andrew Lewis, Neil Herring, Michala Pedersen
article en

Abstract

Introduction: Patients with transvenous cardiac implantable electrical devices (CIEDs) including pacemakers are typically excluded from magnetic resonance imaging (MRI) examinations for at least 6-weeks following implant. However, many MRI scans are required on urgent or emergency basis, potentially resulting in suboptimal management for patients following a recent CIED implant. The absolute risks of adverse lead/generator events with early MRI have not been quantified. Specific transvenous pacing systems from one manufacturer (Abbott) do not mandate a routine 6-week post-implant restriction for MRI conditionality, although real-world human data investigating lead parameter stability with MRI early (<7 days) post-implant are lacking. Research Question: Can MRI be performed early (<7 days) after pacemaker implantation without safety events or significant changes to lead parameters? Methods: Patients undergoing implantation of Abbott Assurity™ MRI pacemakers with active-fixation MRI conditional leads (Abbott Tendril™ 52cm/58cm or UltiPace™ 65cm) with no contraindication to MRI underwent cardiac MRI within 7 days of implant. Patients were scanned at 1.5 or 3T in an asynchronous pacing mode. Device interrogation was performed before and after MRI. All patients provided written consent. Pre- and post-MRI lead parameter measurements were compared using the two one-sided t-Tests (TOST) equivalence test. Equivalence margins were prespecified: lead impedance ±30Ω, lead sensing ±0.5mV, lead threshold ±0.25V. Results: 20 patients (median age 77 (IQR 72-80) years, 75% male) were recruited. 65% received right ventricular pacing and 35% conduction system pacing. Median time from implant to MRI was 3 [IQR 1-5] days. All lead parameters were statistically equivalent pre- and post-MRI: Atrial lead impedance mean difference 5 Ω (90% CI -3 to +12), TOST p<0.001 Ventricular lead impedance -1 Ω (90% CI -9.2 to +7.2), TOST p<0.001 Sensed P wave 0.04 mV (90% CI -0.13 to +0.22), TOST p<0.001 Sensed R wave -0.06 mV (90% CI -0.28 to +0.17), TOST p=0.001 Atrial capture threshold -0.01 mV (90% CI -0.04 to +0.01), TOST p<0.001 Ventricular capture threshold -0.01 mV (90% CI -0.05 to +0.03), TOST p<0.001 Conclusion: MRI within 7 days of pacemaker implantation was safe, with no adverse events and no significant change in lead parameters. These findings provide real-world data to complement manufacturer guidance and support access to early MRI when indicated for patients with conditional pacemaker systems.

CirculationVol. 152(Suppl_3)
University of Oxford (GB), Oxford University Hospitals NHS Trust (GB)
Openalex Percentile: Top 53%
Advanced MRI Techniques and Applications
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