Focal stenting of complex femoropopliteal lesions with the multi-LOC multiple stent delivery system: 12-month results of the multicenter LOCOMOTIVE study
Introduction: The purpose of this observational study is to report the 12-month clinical outcomes with the novel Multiple Stent Delivery System (MSDS) to treat complex femoropopliteal lesions. Previously, we reported the 6-month clinical outcomes of the all-comers LOCOMOTIVE study, which demonstrate...
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| Main Author: | |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2019
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| In: |
CardioVascular and interventional radiology
Year: 2018, Volume: 42, Issue: 2, Pages: 169-175 |
| ISSN: | 1432-086X |
| DOI: | 10.1007/s00270-018-2095-9 |
| Online Access: | Verlag, Volltext: https://doi.org/10.1007/s00270-018-2095-9
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| Author Notes: | Martin Sigl, Ulrich Beschorner, Thomas Zeller, Matthias Waliszewski, Ralf Langhoff, Jörg Tautenhahn, Klaus Amendt |
MARC
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| 245 | 1 | 0 | |a Focal stenting of complex femoropopliteal lesions with the multi-LOC multiple stent delivery system |b 12-month results of the multicenter LOCOMOTIVE study |c Martin Sigl, Ulrich Beschorner, Thomas Zeller, Matthias Waliszewski, Ralf Langhoff, Jörg Tautenhahn, Klaus Amendt |
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| 500 | |a Published online: 25 October 2018 | ||
| 520 | |a Introduction: The purpose of this observational study is to report the 12-month clinical outcomes with the novel Multiple Stent Delivery System (MSDS) to treat complex femoropopliteal lesions. Previously, we reported the 6-month clinical outcomes of the all-comers LOCOMOTIVE study, which demonstrated the safety and efficacy of the MSDS with a favorable target lesion revascularization (TLR) rate of 5.3% and a 90.7% patency rate at 6 months in claudicants and critical limb ischemia patients. The 12-month outcomes of LOCOMOTIVE registry are presented in this report. ClinicalTrials.gov Identifier: NCT02531230. Methods: The LOCOMOTIVE study (Multi-LOC for flOw liMiting Outcomes after POBA and/or DCB Treatment in the infrainguinal position with the objecIVE to implant multiple stent segments) investigates the efficacy and safety of the MSDS approach in an all-comers population. Clinical follow-ups at 6 and 12 months are scheduled to assess TLR, ABI, and vessel patency based on sonographic imaging. Results: At 12 months, the primary unassisted patency was 85.7% and all-cause TLR rate was 9.3% in the overall cohort. Between baseline and 12 months, the target leg ABI increased from 0.62 ± 0.24 to 0.91 ± 0.38 (p < 0.001) and the mean Rutherford class improved from 3.5 to 1.9 (p < 0.001). Conclusions: Over a 12-month post-procedural period, MSDS for focal provisional stenting of complex femoropopliteal lesions demonstrated a promising primary patency and freedom from TLR after 12 months. In addition, significant improvements were observed in symptom classification and hemodynamics. | ||
| 534 | |c 2018 | ||
| 650 | 4 | |a Femoropopliteal lesions | |
| 650 | 4 | |a Multiple stent segments | |
| 650 | 4 | |a Patency | |
| 650 | 4 | |a Target lesion revascularization | |
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