{"title":"Disease-Specific Ventricular Unloading Responses to Impella Support Revealed by Three-Dimensional Pressure-Volume-Flow Landscape Analysis.","authors":"Hisato Takagi","doi":"10.1111/aor.70248","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Impella support alters left ventricular pressure-volume (PV) relations, but disease-specific unloading responses across the full support range remain incompletely characterized. We developed a three-dimensional pressure-volume-flow landscape (3D-PVL) framework to quantify and compare ventricular unloading in acute myocardial infarction (AMI), dilated cardiomyopathy (DCM), and DCM with mitral regurgitation (DCM + MR).</p><p><strong>Methods: </strong>PV loops were simulated using a closed-loop cardiovascular model at 51 Impella-flow levels from 0 to 5.0 L/min. Loop-centroid displacement and stroke work were normalized to their respective 0-L/min values, and their unscaled direction-sensitive derivatives were combined into a composite response. The response index (RI) quantified integrated response magnitude, while interior peak-response flow (Qpeak) identified the flow level of maximal incremental response among interior flow points. Pressure-volume area (PVA) provided energetic validation.</p><p><strong>Results: </strong>Unloading trajectories differed among disease states despite baseline normalization. Integrated response magnitudes were similar across the three disease models (RI: 1.33, 1.37, and 1.35 for AMI, DCM, and DCM + MR, respectively), whereas interior Qpeak differed at 3.40, 2.90, and 2.70 L/min. DCM + MR showed a renewed response increase at high flow, with its overall maximum occurring at the 5.0-L/min boundary. PVA-based analysis preserved the higher-flow response peak in AMI (3.60 vs. 3.10 and 2.90 L/min in DCM and DCM + MR).</p><p><strong>Conclusions: </strong>The underlying disease substrate influenced the distribution of ventricular unloading across the Impella-flow range despite similar integrated response magnitudes. The 3D-PVL framework provides quantitative descriptors of disease-specific unloading trajectories rather than clinically validated therapeutic targets.</p>","PeriodicalId":8450,"journal":{"name":"Artificial organs","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2026-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Artificial organs","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/aor.70248","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Impella support alters left ventricular pressure-volume (PV) relations, but disease-specific unloading responses across the full support range remain incompletely characterized. We developed a three-dimensional pressure-volume-flow landscape (3D-PVL) framework to quantify and compare ventricular unloading in acute myocardial infarction (AMI), dilated cardiomyopathy (DCM), and DCM with mitral regurgitation (DCM + MR).
Methods: PV loops were simulated using a closed-loop cardiovascular model at 51 Impella-flow levels from 0 to 5.0 L/min. Loop-centroid displacement and stroke work were normalized to their respective 0-L/min values, and their unscaled direction-sensitive derivatives were combined into a composite response. The response index (RI) quantified integrated response magnitude, while interior peak-response flow (Qpeak) identified the flow level of maximal incremental response among interior flow points. Pressure-volume area (PVA) provided energetic validation.
Results: Unloading trajectories differed among disease states despite baseline normalization. Integrated response magnitudes were similar across the three disease models (RI: 1.33, 1.37, and 1.35 for AMI, DCM, and DCM + MR, respectively), whereas interior Qpeak differed at 3.40, 2.90, and 2.70 L/min. DCM + MR showed a renewed response increase at high flow, with its overall maximum occurring at the 5.0-L/min boundary. PVA-based analysis preserved the higher-flow response peak in AMI (3.60 vs. 3.10 and 2.90 L/min in DCM and DCM + MR).
Conclusions: The underlying disease substrate influenced the distribution of ventricular unloading across the Impella-flow range despite similar integrated response magnitudes. The 3D-PVL framework provides quantitative descriptors of disease-specific unloading trajectories rather than clinically validated therapeutic targets.
期刊介绍:
Artificial Organs is the official peer reviewed journal of The International Federation for Artificial Organs (Members of the Federation are: The American Society for Artificial Internal Organs, The European Society for Artificial Organs, and The Japanese Society for Artificial Organs), The International Faculty for Artificial Organs, the International Society for Rotary Blood Pumps, The International Society for Pediatric Mechanical Cardiopulmonary Support, and the Vienna International Workshop on Functional Electrical Stimulation. Artificial Organs publishes original research articles dealing with developments in artificial organs applications and treatment modalities and their clinical applications worldwide. Membership in the Societies listed above is not a prerequisite for publication. Articles are published without charge to the author except for color figures and excess page charges as noted.