Emergency and Compassionate Use of a Novel Ascending Endograft for Ascending and Arch Aortic Pathology

Author:

Patel Himanshu J.12ORCID,Preventza Ourania3,Roselli Eric E.4ORCID,Atkins Marvin D.5,Brinkman William6,Coselli Joseph3,Desai Nimesh7,Estrera Anthony8,Fleischman Fernando9ORCID,Taylor Bradley S.10,Reardon Michael J.5

Affiliation:

1. Frankel Cardiovascular Center, University of Michigan, Ann Arbor, MI, USA

2. Department of Cardiac Surgery, University of Michigan Hospitals, Cardiovascular Network of West Michigan, Ann Arbor, MI, USA

3. Baylor College of Medicine, Houston, TX, USA

4. Aortic Center, Department of Thoracic and Cardiovascular Surgery, Heart, Vascular & Thoracic Institute, Cleveland Clinic, Cleveland, OH, USA

5. Houston Methodist Hospital, Houston, TX, USA

6. Baylor Scott & White The Heart Hospital – Plano, Plano, TX, USA

7. University of Pennsylvania, Philadelphia, PA, USA

8. University of Texas, Houston, Houston, TX, USA

9. Keck Hospital of University of Southern California, Los Angeles, CA, USA

10. University of Maryland School of Medicine, Baltimore, MD, USA

Abstract

Purpose: Patients with complicated ascending aortic pathology, including patients with acute type A aortic dissection may be at extreme risk for open repair. Thoracic endovascular aortic repair (TEVAR), infrequently used for the ascending aorta, may be considered an alternative in this setting. We describe early results for emergency and compassionate (E&C) use of a novel endograft, specifically designed for use to treat pathology of the ascending aorta. Materials and Methods: This case series evaluated 19 patients (mean age, 68.84±13.12 years; 57.9% female) treated with ascending TEVAR for acute and chronic acute (4), subacute (1), or chronic (1) aortic dissection or pseudoaneurysm (13). Six of the 19 patients (31.5%) were treated under compassionate use and 13 patients (68.4%) were treated under the emergency use exemption. Ten patients (52.6%) received additional devices to extend treatment into the arch and descending aorta. Results: Device delivery was achieved in all patients (100%). Thirty-day mortality and stroke occurred in 3 patients (15.8%) and in 1 patient (5.3%), respectively. In 1 patient (5.3%), with an Unanticipated Adverse Device Event, the aorta ruptured when the endograft eroded into the adventitial portion of dissection site at the posterior aspect of the ascending wall. Devices were explanted in 2 patients (10.5%), 353 and 610 days after the index procedure, respectively. Six patients had endoleaks (31.6%), including type I (n=2, 10.5%), type II endoleaks (n=3, 15.8%), and indeterminate endoleak (n=1, 5.3%). Conclusions: Delivery and deployment of a novel ascending thoracic stent graft with or without an additional branched arch extension is feasible in patients with complex anatomy and pathology, including acute aortic dissection and pseudoaneurysm. Additional experience with this novel device will further refine the patient population most suitable for endovascular ascending aortic repair for these pathologies. Clinical Impact This study describes a novel stent graft specifically designed for treatment of ascending aortic pathology, including acute type A dissection. The patients described in this series constituted a group outside the formal US FDA sponsored clinical trial, and were those accepted as part of an emergency and compassionate use basis.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,Surgery

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