In vitro thrombogenicity of drug-eluting and bare metal stents. Issue 185 (January 2020)
- Record Type:
- Journal Article
- Title:
- In vitro thrombogenicity of drug-eluting and bare metal stents. Issue 185 (January 2020)
- Main Title:
- In vitro thrombogenicity of drug-eluting and bare metal stents
- Authors:
- Palmerini, Tullio
Barozzi, Chiara
Tomasi, Luciana
Riva, Diego Della
Marengo, Mario
Cicoria, Gianfranco
Bruno, Antonio G.
Bacchi-Reggiani, Maria-Letizia
Naldi, Marina
Bartolini, Manuela
Fanti, Stefano
Galiè, Nazzareno
Stone, Gregg W. - Abstract:
- Abstract: Aims: We sought to investigate the thrombogenicity of different DES and BMS in an in vitro system of stent perfusion. Material and methods: The experimental model consisted of a peristaltic pump connected to 4 parallel silicone tubes in which different stents were deployed. Blood was drawn from healthy volunteers and the amount of stent surfaced-induced thrombus deposition was determined using 125 I-fibrinogen. Results: Compared to Resolute, Biomatrix and Vision, Xience was associated with the lowest amount of stent surface-induced thrombus formation, with a significant difference compared to Vision ( 125 I-fibrinogen median value deposition [IQ range]: 50 ng [25–98] versus 560 ng [320–1520], respectively, p < 0.05), but not to other DES. In the second set of experiments Fluoropolymer-coated BMS not eluting drug was associated with a significant 3-fold reduction in 125 I-fibrinogen deposition (245 ng [80–300]) compared to Vision (625 ng [320–760], p < 0.05), but a 7-fold increase compared to Xience (35 ng [20–60], p < 0.05). Finally Xience was associated with a significantly greater absorption of albumin compared to BMS. Conclusions: In an in vitro system of stent perfusion, Xience was associated with the lowest amount of stent surface-induced thrombus formation compared with Resolute, Biomatrix and Vision, with a noted synergistic effect between the fluoropolymer and the drug. Highlights: The thrombogenicity of different stents was studied in an in vitro model.Abstract: Aims: We sought to investigate the thrombogenicity of different DES and BMS in an in vitro system of stent perfusion. Material and methods: The experimental model consisted of a peristaltic pump connected to 4 parallel silicone tubes in which different stents were deployed. Blood was drawn from healthy volunteers and the amount of stent surfaced-induced thrombus deposition was determined using 125 I-fibrinogen. Results: Compared to Resolute, Biomatrix and Vision, Xience was associated with the lowest amount of stent surface-induced thrombus formation, with a significant difference compared to Vision ( 125 I-fibrinogen median value deposition [IQ range]: 50 ng [25–98] versus 560 ng [320–1520], respectively, p < 0.05), but not to other DES. In the second set of experiments Fluoropolymer-coated BMS not eluting drug was associated with a significant 3-fold reduction in 125 I-fibrinogen deposition (245 ng [80–300]) compared to Vision (625 ng [320–760], p < 0.05), but a 7-fold increase compared to Xience (35 ng [20–60], p < 0.05). Finally Xience was associated with a significantly greater absorption of albumin compared to BMS. Conclusions: In an in vitro system of stent perfusion, Xience was associated with the lowest amount of stent surface-induced thrombus formation compared with Resolute, Biomatrix and Vision, with a noted synergistic effect between the fluoropolymer and the drug. Highlights: The thrombogenicity of different stents was studied in an in vitro model. Fluoropolymer coated drug-eluting stents are less thrombogenic than bare metal stents. Fluoropolymers have thromboresistant properties. Fluoropolymer-coated stents absorb albumin more avidly than bare metal stents. Fluoropolymers and everolimus have a synergistic antithrombotic action. … (more)
- Is Part Of:
- Thrombosis research. Issue 185(2020)
- Journal:
- Thrombosis research
- Issue:
- Issue 185(2020)
- Issue Display:
- Volume 185, Issue 185 (2020)
- Year:
- 2020
- Volume:
- 185
- Issue:
- 185
- Issue Sort Value:
- 2020-0185-0185-0000
- Page Start:
- 43
- Page End:
- 48
- Publication Date:
- 2020-01
- Subjects:
- Stent thrombosis -- Bare metal stent -- Drug-eluting stent
BMS bare metal stent -- DES drug-eluting stent -- HSA human serum albumin -- PBS phosphate buffered saline -- PCI percutaneous coronary intervention -- FP-BMS fluoropolymer coated bare metal stent
Thrombosis -- Periodicals
616.135 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00493848 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.thromres.2019.11.016 ↗
- Languages:
- English
- ISSNs:
- 0049-3848
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8820.365000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 12559.xml