Key result
Bioresorbable vascular scaffold thrombosis occurred early (<30 days) in 8 of 15 cases (53%) due to mechanical or antiplatelet factors, while late thrombosis featured peristrut low-intensity areas.
Why the study?
What are the angiographic and optical coherence tomography findings in patients experiencing bioresorbable vascular scaffold thrombosis?
Observational (n=14)
What are the angiographic and optical coherence tomography findings in patients experiencing bioresorbable vascular scaffold thrombosis?
Early bioresorbable scaffold thrombosis is primarily driven by mechanical factors and inadequate antiplatelet therapy, whereas late thrombosis is associated with peristrut low-intensity areas and intimal neovessels.
Answers are grounded in this paper and cite their sources.
Supports attention to procedural factors and platelet inhibition in early BVS use; leaves open neovessel roles in late thrombosis.
BACKGROUND: Everolimus-eluting bioresorbable vascular scaffolds have been developed to improve late outcomes after coronary interventions. However, recent registries raised concerns regarding an increased incidence of scaffold thrombosis (ScT). The mechanism of ScT remains unknown. METHODS AND RESULTS: The present study investigated angiographic and optical coherence tomography findings in patients experiencing ScT. Fifteen ScT (14 patients, 79% male, age 59±10 years) occurred at a median of 16 days (25%-75% interquartile range: 1-263 days) after implantation. Early ScT (<30 days) occurred in 8 cases (53%). Possible causal factors in these patients included insufficient platelet inhibition in 2 cases and procedural factors (scaffold underexpansion, undersizing, or geographical miss) in 4 cases. No obvious cause could be found in 2 early ScT. In late (>1 month) and very late (>1 year) ScT (respectively, 5 and 2 cases), 5 scaffolds showed intimal neovessels or marked peristrut low-intensity areas. Scaffold fractures were additionally found in 2 patients, and scaffold collapse was found in 1 patient with very late ScT. Extensive strut malapposition was the presumed cause for ScT in 1 case. One scaffold did not show any morphological abnormality. Thrombectomy specimens were analyzed in 3 patients and did not demonstrate increased numbers of inflammatory cells. CONCLUSIONS: The mechanisms of early ScT seem to be similar to metallic stents (mechanical and inadequate antiplatelet therapy). The predominant finding in late and very late ScT is peristrut low-intensity area.
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Cuculi et al. (2015) conducted an observational in Bioresorbable vascular scaffold thrombosis (n=14). Everolimus-eluting bioresorbable vascular scaffolds was evaluated on Angiographic and optical coherence tomography findings. Bioresorbable vascular scaffold thrombosis occurred early (<30 days) in 8 of 15 cases (53%) due to mechanical or antiplatelet factors, while late thrombosis featured peristrut low-intensity areas.
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