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GW24-e2200 In vivo virtual histology intravascular ultrasound comparison of neointimal hyperplasia within drug-eluting-versus bare metal stents

Jiao Zhang, Liu Huiliang

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Abstract

Objectives The process of in-stent neointimal hyperplasia (NIH) between durg-eluting stents (DES) and bare metal stents (BMS) might be different. We compared In vivo composition of in-stent NIH between DES and BMS using virtual histology-intravascular ultrasound (VH-IVUS). Methods Volumetric VH-IVUS was used to compare in-stent NIH between 61 DES and 25 BMS in 54 patients who underwent coronary angiography because of STEMI. The inner and outer VH-IVUS contours were drawn in a way to avoid the stent strut artefacts. Cross-sectional analysis was done at every VH-IVUS frame within the stent, thereby allowing volumetric measurement of stent, lumen, and NIH and its components. Results Baseline characteristics and IVUS measurements were similar between DES and BMS groups. The duration of follow-up was similar between DES (median 38 months [interquartile range,7–59]) vs. BMS(median 40 months [interquartile range, 7–99]), (p = 0.26).% necrotic core (NC) volume was significantly higher in DES than BMS: 19.5[16.3,25.6] vs.12.1[8.2,18.5] (p = 0.006).% NC volume significantly increased with time in BMS (p = 0.007), but not in DES (p = 0.24) so that at any given time point, %NC in DES was greater than in BMS. After adjustment for baseline differences, only DES (p = 0.003) and stent age (p = 0.043) were independent predictors of %NC volume. VH-IVUS in-stent thin-cap fibroatheromas were detected only in the DES group: 34.8% vs. 0%, p = 0.013. Conclusions In vivo composition of in-stent NIH between DES and BMS was different, suggesting that the process of in-stent NIH in DES and BMS is diverse in STEMI paient.

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Objectives The process of in-stent neointimal hyperplasia (NIH) between durg-eluting stents (DES) and bare metal stents (BMS) might be different. We compared In vivo composition of in-stent NIH between DES and BMS using virtual histology-intravascular ultrasound (VH-IVUS). Methods Volumetric VH-IVUS was used to compare in-stent NIH between 61 DES and 25 BMS in 54 patients who underwent coronary angiography because of STEMI. The inner and outer VH-IVUS contours were drawn in a way to avoid the stent strut artefacts. Cross-sectional analysis was done at every VH-IVUS frame within the stent, thereby allowing volumetric measurement of stent, lumen, and NIH and its components. Results Baseline characteristics and IVUS measurements were similar between DES and BMS groups. The duration of follow-up was similar between DES (median 38 months [interquartile range,7–59]) vs. BMS(median 40 months [interquartile range, 7–99]), (p = 0.26).% necrotic core (NC) volume was significantly higher in DES than BMS: 19.5[16.3,25.6] vs.12.1[8.2,18.5] (p = 0.006).% NC volume significantly increased with time in BMS (p = 0.007), but not in DES (p = 0.24) so that at any given time point, %NC in DES was greater than in BMS. After adjustment for baseline differences, only DES (p = 0.003) and stent age (p = 0.043) were independent predictors of %NC volume. VH-IVUS in-stent thin-cap fibroatheromas were detected only in the DES group: 34.8% vs. 0%, p = 0.013. Conclusions In vivo composition of in-stent NIH between DES and BMS was different, suggesting that the process of in-stent NIH in DES and BMS is diverse in STEMI paient.

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Available abstract

Objectives The process of in-stent neointimal hyperplasia (NIH) between durg-eluting stents (DES) and bare metal stents (BMS) might be different. We compared In vivo composition of in-stent NIH between DES and BMS using virtual histology-intravascular ultrasound (VH-IVUS). Methods Volumetric VH-IVUS was used to compare in-stent NIH between 61 DES and 25 BMS in 54 patients who underwent coronary angiography because of STEMI. The inner and outer VH-IVUS contours were drawn in a way to avoid the stent strut artefacts. Cross-sectional analysis was done at every VH-IVUS frame within the stent, thereby allowing volumetric measurement of stent, lumen, and NIH and its components. Results Baseline characteristics and IVUS measurements were similar between DES and BMS groups. The duration of follow-up was similar between DES (median 38 months [interquartile range,7–59]) vs. BMS(median 40 months [interquartile range, 7–99]), (p = 0.26).% necrotic core (NC) volume was significantly higher in DES than BMS: 19.5[16.3,25.6] vs.12.1[8.2,18.5] (p = 0.006).% NC volume significantly increased with time in BMS (p = 0.007), but not in DES (p = 0.24) so that at any given time point, %NC in DES was greater than in BMS. After adjustment for baseline differences, only DES (p = 0.003) and stent age (p = 0.043) were independent predictors of %NC volume. VH-IVUS in-stent thin-cap fibroatheromas were detected only in the DES group: 34.8% vs. 0%, p = 0.013. Conclusions In vivo composition of in-stent NIH between DES and BMS was different, suggesting that the process of in-stent NIH in DES and BMS is diverse in STEMI paient.

Key concepts: Medicine, Intravascular ultrasound, Interquartile range, Stent, Neointimal hyperplasia, Drug-eluting stent, Lumen (anatomy), Bare-metal stent

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