Leadless Ultrasound-Based Cardiac Resynchronization System in Heart Failure Results from the SOLVE-CRT Randomised Sub-study

Abstract Background Despite the well-established role of CRT in heart failure, major limitations of CRT are an occasional incidence of unsuccessful coronary sinus (CS) lead placement, one third non-responders in conventional CRT patients and higher complications risk in CRT upgrade procedures. The WiSE® Wireless Stimulation Endocardial) CRT System is designed to overcome these limitations. Prior non-randomised studies with the WiSE® CRT System have shown high implant success rates and improvement in LV remodeling and heart failure symptoms. Objectives Pivotal study to assess the safety and effectiveness of the WiSE® CRT System in an international, randomized, two-arm, double blinded, prospective study (randomized part only). Method 99 Patients with indication for CRT and previously failed CRT implant, considered as high-risk upgrade to conventional CRT, or non-responders to conventional CRT underwent device implantation and were then randomised into treatment (47 pts, System ON) and control (52 pts System OFF) groups for 6 months. Primary efficacy endpoints were change in LVESV, LVEDV, LVEF and QRS over 6 months in blinded Echo and ECG core lab analysis. Results Mean ΔLVESV (%) -14.6 (-19.6, -9.6); mean ΔLVEDV (%) -8.1 (-11.9, -4.3) and mean ΔQRS (ms) -41.9 (-50.1, -33.7) in the treatment group were significantly lower/shorter than mean ΔLVESV (%) -5.2 (-10.7, 0.2); mean ΔLVEDV (%) -3.0 (-7.0, 1.0) and mean ΔQRS (ms) -1.7 (-7.1,3.8) in the control group, p=0.005; p=0.027 and p=0.001, 95% CI. Mean ΔLVEF (%) 5.4 (3.2, 7.7) in the treatment group increased significantly compared to control group ΔLVEF (%) 2.4 (0.2, 4.5), p=0.048. 8 of 99 pts were attempted from WiSE CRT implant. Conclusion This randomized sub-study of the pivotal SOLVE-CRT trial demonstrates that leadless, ultrasound-based endocardial pacing for heart failure is feasible and efficacious showing evidence of left ventricular remodelling and electrical response after 6 months.Figure 1WISE® CRT System Figure 2Efficacy entire randomised population

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Journal
European Heart Journal Supplements
Published
2025-02-01
DOI
https://doi.org/10.1093/eurheartjsupp/suae124.002
Primary Topic
Cardiac pacing and defibrillation studies
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article
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article

Leadless Ultrasound-Based Cardiac Resynchronization System in Heart Failure Results from the SOLVE-CRT Randomised Sub-study

Michael R. Gold, Christopher A. Rinaldi, JoAnn M. Lindenfeld, Prashanthan Sanders et al.
European Heart Journal Supplements
Cardiac pacing and defibrillation studies
article

Leadless Ultrasound-Based Cardiac Resynchronization System in Heart Failure Results from the SOLVE-CRT Randomised Sub-study

Michael R. Gold, Christopher A. Rinaldi, JoAnn M. Lindenfeld, Prashanthan Sanders, Imran Khan Niazi, Christian Butter, Timothy R. Betts, Mary Norine Walsh, Emad F. Aziz, Simon James, Elisabetta Montemerlo, Angelo Auricchio, Mauro Biffi, Jagmeet Singh, Amir Zaidi, Jeffrey Alison, Giovanni Rovaris, Spencer H. Kubo
article en

Abstract

Abstract Background Despite the well-established role of CRT in heart failure, major limitations of CRT are an occasional incidence of unsuccessful coronary sinus (CS) lead placement, one third non-responders in conventional CRT patients and higher complications risk in CRT upgrade procedures. The WiSE® Wireless Stimulation Endocardial) CRT System is designed to overcome these limitations. Prior non-randomised studies with the WiSE® CRT System have shown high implant success rates and improvement in LV remodeling and heart failure symptoms. Objectives Pivotal study to assess the safety and effectiveness of the WiSE® CRT System in an international, randomized, two-arm, double blinded, prospective study (randomized part only). Method 99 Patients with indication for CRT and previously failed CRT implant, considered as high-risk upgrade to conventional CRT, or non-responders to conventional CRT underwent device implantation and were then randomised into treatment (47 pts, System ON) and control (52 pts System OFF) groups for 6 months. Primary efficacy endpoints were change in LVESV, LVEDV, LVEF and QRS over 6 months in blinded Echo and ECG core lab analysis. Results Mean ΔLVESV (%) -14.6 (-19.6, -9.6); mean ΔLVEDV (%) -8.1 (-11.9, -4.3) and mean ΔQRS (ms) -41.9 (-50.1, -33.7) in the treatment group were significantly lower/shorter than mean ΔLVESV (%) -5.2 (-10.7, 0.2); mean ΔLVEDV (%) -3.0 (-7.0, 1.0) and mean ΔQRS (ms) -1.7 (-7.1,3.8) in the control group, p=0.005; p=0.027 and p=0.001, 95% CI. Mean ΔLVEF (%) 5.4 (3.2, 7.7) in the treatment group increased significantly compared to control group ΔLVEF (%) 2.4 (0.2, 4.5), p=0.048. 8 of 99 pts were attempted from WiSE CRT implant. Conclusion This randomized sub-study of the pivotal SOLVE-CRT trial demonstrates that leadless, ultrasound-based endocardial pacing for heart failure is feasible and efficacious showing evidence of left ventricular remodelling and electrical response after 6 months.Figure 1WISE® CRT System Figure 2Efficacy entire randomised population

European Heart Journal SupplementsVol. 27(Supplement_1)
Rutgers, The State University of New Jersey (US), Royal Adelaide Hospital (AU), St Thomas' Hospital (GB), Harvard University (US), Medical University of South Carolina (US), King's College - North Carolina (US), King's College London (GB), Guy's and St Thomas' NHS Foundation Trust (GB), James Cook University Hospital (GB), Saint Vincent Health System (US), South Tees Hospitals NHS Foundation Trust (GB), Massachusetts General Hospital (US), Ente Ospedaliero Cantonale (CH), IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola (IT), Azienda Ospedaliera San Gerardo (IT), Aurora St. Luke's Medical Center (US), Monash Health (AU), St. Thomas Hospital (CA), EBR Systems (United States) (US), Oxford University Hospitals NHS Trust (GB), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Immanuel Klinikum Bernau (DE), Rutgers New Jersey Medical School (US), The University of Adelaide (AU)
Openalex Percentile: Top 95%
Cardiac pacing and defibrillation studies
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