The Supera™ Stent has been studied in over 2,000 patients worldwide in the SUPERB trial and 16 retrospective studies. Notably, in all of the 17 studies, the Supera™ Peripheral Stent showed durable results with zero fractures at 1 year.1,15-30
At 1 year the Supera™ Stent demonstrated primary patency of 91% when nominally* deployed. At 3 years, freedom from targeted lesion revascularization (TLR) was 94% when nominally* deployed.1
PATENCY (K-M) AT 1 YEAR
When nominally deployed*
FREEDOM FROM TLR AT 3 YEARS
When nominally deployed*
*Nominal deployment is defined as the stent length upon deployment being within +/- 10% of the labeled stent length. This data is from a non-powered post-hoc analysis. K-M=Kaplan Meier.
Supera Stent has demonstrated unmatched clinical outcomes in comparison to other US pivotal trial results which primarily included simple lesions.*,1-12
1-Year Patency (KM) | 3-Year Freedom from TLR | |||
---|---|---|---|---|
91% | Supera™ Stent Nominal1 | 94% | Supera™ Stent Nominal1 | |
87% | Eluvia‡12 | Not Reported | Eluvia‡ | |
84% | Zilver PTX‡2 | 84% | Zilver PTX‡2 | |
83% | Misago‡11 | Not Available | Misago‡ | |
81% | LifeStent‡3 | 76% | LifeStent‡4 | |
80% | S.M.A.R.T.‡5 | 79% | S.M.A.R.T.‡6 | |
77% | EverFlex‡7 | 70% | EverFlex‡8 | |
74% | Innova‡9 | Not Reported | Innova‡ | |
67% | Pulsar‡10 | Not Reported | Pulsar‡ |
* Study reported 93.8% with Trans-Atlantic Inter-Society Consensus Document (TASC) A & B lesions and/or Rutherford class 2 or 3 lesions
NOTE: Results from clinical trials are not directly comparable. Information provided for educational purposes only.
With some peripheral stents, increasing lesion lengths can lead to decreasing patency rates.31 The Supera™ Stent stands apart for its consistently high patency rates in lesions spanning lengths from 5.3 cm up to 28.0 cm.†
Whether treating simple (TASC A&B) or complex (TASC C&D) lesions, the Supera™ Stent is associated with impressive, consistent patency performance data at 1 year.13-15,32
Trial/Study | MUNICH REGISTRY13 | SUPERB32 | |
---|---|---|---|
Lesion Length | 5.3cm | 7.8cm | |
TASC A&B Lesions | 100% | 94% | |
1-Yr Patency | 86.7% | 90.5% | |
Sites | Single Center | Multicenter (46 sites) | |
# Patients | 70 | 264 |
Trial/Study | ST. LOUIS15 | SUPERSUB14 | |
---|---|---|---|
Lesion Length | 5.3cm | 7.8cm | |
TASC C&D Lesions | 78% | 100% | |
CTOs | Unknown | 100% | |
1-Yr Patency | 85.6% | 94.1% | |
Sites | Single Center | Single Center | |
# Patients | 48 | 34 |
TASC: Trans-Atlantic Inter-Society Consensus
MAT-2106532 v1.0
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