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- W1986044435 abstract "Methods: In BioFreedom-FIM and STEALTH-I, 43 lesions treated with standard-dose BioFreedom (NP-BES, n=13) or BioMatrix (BDP-BES, n=30) underwent volumetric IVUS at 4-6 months (nominal stent size: 2.5 or 3.0 mm). In addition to the standard IVUS parameters, a neointima-free frame ratio (number of frames without neointima / total frame number) was calculated to assess gross coverage of struts by IVUS-detectable neointima." @default.
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- W1986044435 date "2010-03-01" @default.
- W1986044435 modified "2023-09-26" @default.
- W1986044435 title "IS THERE A DIFFERENCE IN VASCULAR RESPONSE BETWEEN BIODEGRADABLE POLYMER-BASED VERSUS NONPOLYMER-BASED BIOLIMUS-ELUTING STENT? SHORT-TERM INTRAVASCULAR ULTRASOUND RESULTS FROM STEALTH AND BIOFREEDOM TRIAL" @default.
- W1986044435 doi "https://doi.org/10.1016/s0735-1097(10)61800-1" @default.
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