Why the study?
The association between cardiac adrenergic innervation tools suggestive of arrhythmic risk and clinical risk scores predicting all-cause mortality in patients with heart failure needed further investigation.
Is there a correlation between mortality risk scores and cardiac sympathetic innervation assessed by 123 I-mIBG imaging in patients with heart failure?
Is there a correlation between mortality risk scores and cardiac sympathetic innervation assessed by 123 I-mIBG imaging in patients with heart failure?
Mortality risk scores have a weak association with cardiac sympathetic innervation, suggesting that both arrhythmic and general mortality risk tools should be integrated when evaluating heart failure patients for ICD implantation.
Answers are grounded in this paper and cite their sources.
Mortality risk scores poorly correlate with mIBG-assessed innervation; leaves open whether integrating both improves ICD selection in HF.
Introduction In the risk stratification and selection of patients with heart failure (HF) eligible for implantable cardioverter‐defibrillator (ICD) therapy, 123 I‐meta‐IodineBenzylGuanidine ( 123 I‐mIBG) scintigraphy has emerged as an effective non‐invasive method to assess cardiac adrenergic innervation. Similarly, clinical risk scores have been proposed to identify patients with HF at risk of all‐cause mortality, for whom the net clinical benefit of device implantation would presumably be lower. Nevertheless, the association between the two classes of tools, one suggestive of arrhythmic risk, the other of all‐cause mortality, needs further investigation. Objective To test the relationship between the risk scores for predicting mortality and cardiac sympathetic innervation, assessed through myocardial 123 I‐mIBG imaging, in a population of patients with HF. Methods In HF patients undergoing 123 I‐mIBG scintigraphy, eight risk stratification models were assessed: AAACC, FADES, MADIT, MADIT‐ICD non‐arrhythmic mortality score, PACE, Parkash, SHOCKED and Sjoblom. Cardiac adrenergic impairment was assessed by late heart‐to‐mediastinum ratio (H/M) <1.6. Results Among 269 patients suffering from HF, late H/M showed significant negative correlation with all the predicting models, although generally weak, ranging from −0.15 ( p = .013) for PACE to −0.32 ( p < .001) for FADES. The scores showed poor discrimination for cardiac innervation, with areas under the curve (AUC) ranging from 0.546 for Parkash to 0.621 for FADES. Conclusion A weak association emerged among mortality risk scores and cardiac innervation, suggesting to integrate in clinical practice tools indicative of both arrhythmic and general mortality risks, when evaluating patients affected by HF eligible for device implantation.
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Bencivenga et al. (2022) studied this question.
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