THE DISCECTOMY DILEMMA
AT-RISK PATIENTS OFTEN HAVE DISCS WORTH SAVING
In a meta-analysis which includes 1,650+ patients2, it was found that large defects (>6mm) have:
- 2.5x risk of reherniation
- 2.3x risk of reoperation
>40% of disc herniations come from large defects3
73%
of all reoperations come from
high-risk patient population4
Patients who receive
a second surgery see
worse results.
53% receive fusions5
88% using opioids and at higher doses6
42% not working5
BARRICAID: A BIOMECHANICAL SOLUTION
Pressure in the lumbar disc has been measured as high as 334 PSI (10x average car tire pressure!)8. Unlike previous devices that have tried to solve this problem, Barricaid anchors to bone and is designed to close the annular defect from the inside, repressurizing the disc and preventing recurrence.
- Flexible polymer component designed to plug hole from inside annulus
- Titanium bone anchor prevents migration
- Maintains motion
- Does not impact future surgical options

MEASURE

TRIAL

IMPLANT
BARRICAID IS ONE OF THE MOST STUDIED DEVICES IN SPINE
Barricaid has been used to treat over 13,000 patients and is backed by 70+ peer reviewed publications.
- Prospective, single arm, 12 months
- 45 subjects
- 2.4% reherniation rate
- No device complications
- Prospective, single arm, 2 years
- 30 subjects
- 0% reherniation rate
- No device complications
- 2 year RCT
- 30 Barricaid/30 Control
- 5% vs 28.6% reherniation rate
- No device complications
BARRICAID IS ONE OF THE MOST STUDIED DEVICES IN SPINE
Sponsored and Non-sponsored RCTs, and multiple Level 1A Meta-Analyses
- 70+ peer reviewed publications
- Safety, efficacy, durability and health economics
- Proven superior vs. discectomy alone: significant reduction in reherniations, reoperations, and readmissions
81%
reduction in
reoperations for
reherniations*
PUBLISHED 5 YEAR RCT: THOME 2021
BARRICAID IS PROVEN TO BE DURABLE AND
NOT LIMIT FUTURE REOPERATION OPTIONS
Kursumovic 2017
- 6-year real-world evidence
- Single arm, 171 subjects
- 3.5% reherniation rate
Wang 2023
- Prospective, single arm, 2 years
- 30 subjects
- 0% reherniation rate
- No device complications
Klassen 2019
- 554 Patient RCT
- Reoperation choices, complications, and outcomes not impacted by Barricaid
Thome 2021
- 5 Year RCT
- Maintenance of benefits
HEAR FROM YOUR PEERS
- 1. Some studies outside US indications. Values at min 1 yr post-op. Minimum study size of 20 Barricaid subjects
- 2. Spine - Miller, 2018
- 3. FREEDOM Registry Data
- 4. J Bone Surg. Am. 2003- Carragee, et al
- 5. J.clineuor 2018 - Kerezoudis
- 6. Spine 2017 - O’Donnell J et al.
- 7. Clinicoecon Outcomes Res 2018 - Klassen
- 8. Wilke, 1999