Radial strain imaging-guided lead placement for improving response to cardiac resynchronization therapy in patients with ischaemic cardiomyopathy: the raise cardiac resynchronization therapy trial

Author:

Glikson Michael12ORCID,Beinart Roy2ORCID,Golovchiner Gregory3,Sheshet Alon Bar3,Swissa Moshe4,Bolous Munther5,Rosso Raphael6,Medina Aharon1,Haim Moti7,Friedman Paul8,Khalamaizer Vladimir9,Benzvi Shlomit10,Ito Saki8,Goldenberg Ilan1011ORCID,Klempfner Robert10,Vaturi Ori2,Oh Jae K8

Affiliation:

1. Integrated Heart Centre, Shaare Zedek Medical Centre, Hebrew University, Jerusalem, Israel

2. Arrhythmia center, Sheba Medical Centre, Tel Aviv University, Tel Hashomer, Israel

3. Department of cardiology, Rabin MC, Tel Aviv University, Petah Tikva, Israel

4. Department of cardiology, Kaplan MC, Hebrew University, Rehovot, Israel

5. Department of cardiology, Rambam MC, Technion Institute, Haifa, Israel

6. Department of cardiology, Tel Aviv Souraski MC, Tel Aviv University, Tel Aviv, Israel

7. Department of cardiology, Soroka MC, Ben Gurion University, Beer Sheba, Israel

8. Department of cardiovascular medicine, Mayo Clinic, Rochester, MN, USA

9. Department of cardiology, Barzilai MC, Ben Gurion University, Ashkelon, Israel

10. Israeli Centre for Cardiovascular Research, Tel Hashomer, Israel

11. University of Rochester, Rochester, NY, USA

Abstract

Abstract Aims To evaluate the benefit of speckle tracking radial strain imaging (STRSI)-guided left ventricular (LV) lead (LVL) positioning in cardiac resynchronization therapy (CRT) in patients (pts) with ischaemic cardiomyopathy with CRT indication. Methods and results We conducted a prospective randomized controlled trial. Patients were enrolled in nine centres with 2:1 randomization into two groups (guided vs. control). Patients underwent STRSI to identify the optimal LV position from six LV segments at midventricular level. Implantation via STRSI was attempted for recommended segment in the guided group only. Follow-up included echocardiography (6 months) and clinical evaluation (6 and 12 months). The primary endpoint was comparison % reduction in LV end-systolic volume at 6 months with baseline. Secondary endpoints included hospitalizations for heart failure and death, and improvement in additional echocardiographic measurements and quality of life score. A total of 172 patients (115 guided vs. 57 control) were enrolled. In the guided group, 60% of the implanted LV leads were adjudicated to be successfully located at the recommended segment, whereas in the control group 44% reached the best STRSI determined segment. There was no difference between the groups in any of the primary or secondary endpoints at 6 and 12 months. Conclusion Our findings suggest that echo-guided implantation of an LV lead using STRSI does not improve the clinical or echocardiographic response compared with conventional implantation.

Funder

Medtronic Inc.

Maurice Kahn Foundation via the Mayo Sheba Collaboration Fund

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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