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Autor(en) / Beteiligte
Titel
In-vivo Imaging of Femoral Artery Nitinol Stents for Deformation Analysis
Ist Teil von
  • Journal of vascular and interventional radiology, 2011-02, Vol.22 (2), p.244-249
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2011
Quelle
MEDLINE
Beschreibungen/Notizen
  • Abstract Purpose The authors have developed a direct method to study femoral artery stent deformations in vivo. A previously described imaging and analysis approach based on a calibrated phantom was used to examine stents in human volunteers treated for atherosclerotic disease. In this pilot study, forces on stents were evaluated under different in-vivo flexion conditions. Materials and Methods The optimized imaging protocol for imaging with a C-arm computed tomography system was first verified in an in-vivo porcine stent model. Human data were obtained by imaging 13 consenting volunteers with stents in femoral vessels. The affected leg was imaged in straight and bent positions to observe stent deformations. Semiautomatic software was used to calculate the changes in bending, extension, and torsion on the stents for the two positions. Results For the human studies, tension and bending calculation were successful. Bending was found to compress stent lengths by 4% ± 3% (−14.2 to 1.5 mm), increase their average eccentricity by 10% ± 9% (0.12 to −0.16), and change their mean curvature by 27% ± 22% (0 to −0.005 mm−1 ). Stents with the greatest change in eccentricity and curvature were located behind the knee or in the pelvis. Torsion calculations were difficult because the stents were untethered and are symmetric. In addition, multiple locations in each stent underwent torsional deformations. Conclusions The imaging and analysis approach developed based on calibrated in vitro measurements was extended to in-vivo data. Bending and tension forces were successfully evaluated in this pilot study.
Sprache
Englisch
Identifikatoren
ISSN: 1051-0443
eISSN: 1535-7732
DOI: 10.1016/j.jvir.2010.10.019
Titel-ID: cdi_pubmed_primary_21276917

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