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One-Year Results of a Low-Profile Endograft in Acute, Complicated Type B Aortic Dissection

  • RelayPro-D Investigators
  • Medical College of Wisconsin
  • University of Pennsylvania
  • Northwestern University
  • Cleveland Clinic Foundation
  • Yale University
  • University of Colorado Anschutz Medical Campus
  • Temple University
  • St. Vincent Heart Center of Indiana
  • Georgetown University
  • Sentara Vascular Specialists
  • Case Western Reserve University
  • University of Iowa
  • University of Maryland Medical Center
  • Providence Heart Institute
  • Emory University
  • University of Southern California
  • Robert Wood Johnson University Hospital
  • Main Line Health
  • University of Washington
  • University of Michigan, Ann Arbor
  • Institute of Living

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Background: The safety and effectiveness of the RelayPro endograft (Terumo Aortic) was assessed for the treatment of acute, complicated type B aortic dissection (TBAD). Methods: A prospective pivotal trial analyzed a primary end point of all-cause mortality at 30 days. Secondary end points included technical success, major adverse events (disabling stroke, renal failure, and paraplegia/paralysis), endoleaks, patency, rupture, device integrity, false lumen perfusion, reinterventions, aortic expansion, and migration evaluated to 5 years. Results: The study involved 22 United States centers and enrolled 56 patients (mean age, 59.5 ± 11.4 years) from 2017 to 2021; of whom, 73.2% were men and 53.6% were African American. TBAD was complicated by malperfusion of the kidneys (51.8%), lower extremities (35.7%), and viscera (33.9%), and rupture (10.7%). Dissection extended proximally to zones 1/2 (14.3%) and zone 3 (78.6%) and distally to the iliac arteries (67.3%). Most procedures were percutaneous (85.5%). Technical success was 100%. Median hospitalization was 7 days (interquartile range, 5-12 days). All-cause mortality at 30 days was 1.8% (1 of 56; upper 95% CI, 8.2%; P < .0001). Seven major adverse events occurred in 6 patients (10.7%), consisting of paraplegia (n = 3), paraparesis (n = 2), disabling stroke (n = 1), and renal failure (n = 1). All paraplegia/paraparesis resolved with lumbar drainage. Kaplan-Meier analysis estimated a freedom from major adverse events of 89.1% at each interval from 30 days to 3 years. There was 1 endoleak (Type Ia), 2 retrograde dissections, and aortic diameter growth occurred in 2. There has been no rupture, fistula, component separation, patency loss, stenosis, kinking, twisting, bird beak, loss of device integrity, or fracture. Conclusions: RelayPro is safe and effective in acute, complicated TBAD. Follow-up is ongoing to evaluate longer-term outcomes and durability.

Original languageEnglish
Pages (from-to)336-343
Number of pages8
JournalAnnals of Thoracic Surgery
Volume117
Issue number2
DOIs
StatePublished - Feb 2024

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