John LA, John II, Tedford RJ, Gregoski MJ, Gold MR, Field ME, Payne JE, Schoepf UJ, Suranyi P, Cochet H, Jaïs P, Santangeli P, and Winterfield JR
Background: The PAINESD (Pulmonary disease, Age, Ischemic cardiomyopathy, NYHA functional class, Ejection fraction, Storm, Diabetes mellitus) risk score has been validated as a predictor of periprocedural acute hemodynamic decompensation (AHD) in patients undergoing ventricular tachycardia (VT) ablation. Whether the addition of total scar volume (TSV) determined by preprocedure computed tomography imaging provides additional risk stratification has not been previously investigated., Objectives: The purpose of this study was to evaluate the impact of TSV on the risk of AHD and its adjunctive benefit to the PAINESD score newly modified as Pulmonary disease, Age, Ischemic cardiomyopathy, NYHA class, Ejection fraction, Storm, Scar volume, Diabetes mellitus (PAINES2D) based on the addition of scar volumes., Methods: This was a retrospective analysis of all index VT ablations at a quaternary care center from 2017 to 2022. Associations between TSV and AHD were evaluated among patients with structural heart disease., Results: Among 61 patients with TSV data, 13 (21%) had periprocedural AHD. TSV and PAINESD were independently associated with AHD risk. Both TSV and PAINESD were associated with AHD (P = 0.016 vs P = 0.053, respectively). The highest TSV tertile (≥37.30 mL) showed significant association with AHD (P = 0.018; OR: 4.80) compared to the other tertiles. The PAINESD and PAINES2D scores had significant impact on AHD (P = 0.046 and P = 0.010, respectively). The PAINES2D score had a greater impact on AHD compared to PAINESD (area under the curve: 0.73; P = 0.011; 95% CI: 0.56-0.91 and area under the curve: 0.67; P = 0.058; 95% CI: 0.49-0.85, respectively)., Conclusions: Addition of TSV to a modified PAINESD score, PAINES2D, enhances risk prediction of AHD. Further prospective study is needed to assess benefit in various cardiomyopathy populations undergoing VT ablation., Competing Interests: Funding Support and Author Disclosures Dr Tedford has consulting relationships with Medtronic, Abbott Medical, Aria CV Inc, Acceleron, Alleviant, CareDx, Cytokinetics, Itamar, Edwards LifeSciences, Eidos Therapeutics, Lexicon Pharmaceuticals, Gradient, and United Therapeutics; is the national principal investigator for the RIGHT-FLOW clinical trial (Edwards); serves on Steering Committee for Merck and Abbott and a Research Advisory Board for Abiomed; and also does hemodynamic core lab work for Merck. Dr Gold hasconsultation relationships with Medtronic, Boston Scientific, CVRX, EBR, and Abbott Medical. Dr Field has received research funding from Medtronic, Abbott Medical, and Biosense Webster. Dr Schoepf has received institutional research support and honoraria for speaking and consulting from Bayer, ElucidBio, Guerbet, HeartFlow, Inc, Keya Medical, and Siemens Healthineers. Dr Cochet is a cofounder of inHEART Medical. Dr Jaïs is a cofounder of inHEART Medical. Dr Santangeli has consultation relationships with Boston Scientific, Abbott Medical, and Biosense Webster. Dr Winterfield has received institutional research support from Abbott Medical and Biosense Webster; and has consultation relationships with Abbott Medical, Biosense Webster, Thermedical, and Biotronik. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose., (Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.)