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. 2021 Nov 15;18(22):11970. doi: 10.3390/ijerph182211970

Table 2.

Selected differences and similarities between neoatherosclerosis within BMSs and DESs.

The analysis of 299 autopsies showed the incidence of neoatherosclerosis to be significantly greater in DESs (31%) than in BMSs (16%) (p < 0.001) [34].
Neoatherosclerosis occurs earlier in DESs (420 days (361–683)) in comparison to BMSs (2160 days (1800–2880)) (p < 0.001) [34].
Early neointima in DES consists of peristrut fibrin with a small amount of VSMCs within a proteoglycan-rich extracellular matrix with poor strut endothelialisation [35].
Neointima in BMS is relatively thick. It is mainly composed of VSMCs in a proteoglycan/collagenous matrix with endothelial coverage within 3 to 4 months [30].
In the case of stents implanted less than two years ago, in neoatherosclerosis within DES, there is a greater incidence of foamy macrophage clusters, as well as fibroatheromas [34].
It has been shown that neoatherosclerosis in BMSs occurs more frequently in the proximal than in the middle or distal segment. For DESs, no such difference was found [34].