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Application and Evaluation of Highly Automated Software for Comprehensive Stent Analysis in Intravascular Optical Coherence Tomography
H. Lu, J. Lee, M. Jakl, Z. Wang, P. Cervinka, HG. Bezerra, DL. Wilson,
Language English Country Great Britain
Document type Evaluation Study, Journal Article, Research Support, N.I.H., Extramural
Grant support
C06 RR012463
NCRR NIH HHS - United States
R01 HL114406
NHLBI NIH HHS - United States
R01 HL143484
NHLBI NIH HHS - United States
R21 HL108263
NHLBI NIH HHS - United States
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- MeSH
- Endovascular Procedures instrumentation methods MeSH
- Humans MeSH
- Tomography, Optical Coherence instrumentation methods MeSH
- Sensitivity and Specificity MeSH
- Software standards MeSH
- Stents adverse effects standards MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, N.I.H., Extramural MeSH
Intravascular optical coherence tomography (IVOCT) is used to assess stent tissue coverage and malapposition in stent evaluation trials. We developed the OCT Image Visualization and Analysis Toolkit for Stent (OCTivat-Stent), for highly automated analysis of IVOCT pullbacks. Algorithms automatically detected the guidewire, lumen boundary, and stent struts; determined the presence of tissue coverage for each strut; and estimated the stent contour for comparison of stent and lumen area. Strut-level tissue thickness, tissue coverage area, and malapposition area were automatically quantified. The software was used to analyze 292 stent pullbacks. The concordance-correlation-coefficients of automatically measured stent and lumen areas and independent manual measurements were 0.97 and 0.99, respectively. Eleven percent of struts were missed by the software and some artifacts were miscalled as struts giving 1% false-positive strut detection. Eighty-two percent of uncovered struts and 99% of covered struts were labeled correctly, as compared to manual analysis. Using the highly automated software, analysis was harmonized, leading to a reduction of inter-observer variability by 30%. With software assistance, analysis time for a full stent analysis was reduced to less than 30 minutes. Application of this software to stent evaluation trials should enable faster, more reliable analysis with improved statistical power for comparing designs.
Department of Biomedical Engineering Case Western Reserve University Cleveland OH 44106 USA
University of Defense Faculty of Military Health Sciences Hradec Kralove Czech Republic
References provided by Crossref.org
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