Authors
Michael A Quail, Oliver Tann, Romina Linton, Elena G Milano, Kristian Mortensen, Andrew M Taylor, Vivek Muthurangu
Published in
European heart journal. Imaging methods and practice. Volume 4. Issue 3. Pages qyag108. Epub Jun 15, 2026.
Abstract
Weight-based regadenoson dosing for paediatric stress perfusion cardiac magnetic resonance (CMR) achieves coronary vasodilation but may result in excessive drug exposure in some patients. We evaluated the feasibility, safety, and diagnostic performance of heart rate-targeted regadenoson titration as an individualized alternative to fixed-based dosing.
We performed a retrospective analysis of 31 consecutive regadenoson stress perfusion CMR studies (29 technically successful) in paediatric patients with known or suspected coronary artery disease (2015-2025). Regadenoson was administered incrementally, targeting ≥20% heart rate increase. Outcomes included achieved doses, haemodynamic responses, adverse events, image quality, and positivity rate. Results were compared with published weight-based dosing protocols.Mean age was 11.8 ± 4 years (range 3-18) and weight 50.4 ± 21 kg (range 14.9-91.8). Complete dosing data were available for 21/29 studies. Target heart rate response was achieved in all 29 studies (100% success) with a median dose 3.2 mcg/kg (range 1.6-8), representing 60% reduction compared with standard 8 mcg/kg protocols. Among patients >50 kg, 83% achieved adequate stress with ≤160 mcg (≤40% of the standard 400 mcg adult dose). Mean heart rate increased 42% (range 16-77%). Transient blood pressure reductions ≥10 mmHg occurred in nine patients. All studies yielded diagnostic-quality images. Stress-inducible perfusion defects were identified in 7/29 studies (24%). No major adverse events occurred.
Heart rate-targeted regadenoson titration for paediatric stress perfusion CMR is feasible, achieving diagnostic-quality images with substantially reduced drug exposure. Consistent haemodynamic responses and positivity rates comparable to published series suggest adequacy of pharmacological stress, though prospective validation with quantitative perfusion measurement is required.
PMID:
42405304
Bibliographic data and abstract were imported from PubMed on 06 Jul 2026.
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