Key result
14-day ex vivo perfusion of human saphenous veins increases intimal hyperplasia vs 7-day perfusion.
Why the study?
Does ex vivo perfusion for 14 days compared to 7 days increase intimal hyperplasia in human saphenous veins?
Does ex vivo perfusion for 14 days compared to 7 days increase intimal hyperplasia in human saphenous veins?
p-value: p=<0.05
An ex vivo perfusion model of human saphenous veins demonstrates progressive intimal hyperplasia and altered endothelial fibrinolytic function over 14 days while preserving muscular and endothelial integrity.
Ex vivo perfusion beyond 7 days should not yet guide clinical vein graft use; leaves open optimal duration for modeling intimal hyperplasia.
Intimal hyperplasia (IH) is a vessel wall remodeling process responsible of early failure after vascular surgery or endovascular interventions. An ex vivo perfusion was used to study human venous segments regarding functional, histomorphological, immunohistochemical and molecular alterations after 7 (group 1, n = 6) and 14 days (group 2, n = 6) of ex vivo perfusion. All vessel segments showed preserved smooth muscle function before and after perfusion. Histomorphometry revealed IH development which was more pronounced after 14 days rather than 7 days (p < 0.05). Expression of CD34, factor VIII, alpha-actin and MIB-1 was demonstrated in all segments from both groups indicating that muscular and endothelial integrity was preserved after ex vivo perfusion of up to 14 days. PAI-1 mRNA expression was significantly increased after perfusion (p < 0.05), suggesting that the endothelial fibrinolytic function may be modulated in this ex vivo perfusion model of human saphenous veins.
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Paroz et al. (2004) studied Intimal hyperplasia (n=12). Ex vivo perfusion for 14 days vs. Ex vivo perfusion for 7 days was evaluated on Intimal hyperplasia development (p=<0.05). Ex vivo perfusion of human saphenous veins for 14 days resulted in more pronounced intimal hyperplasia compared to 7 days (p < 0.05).
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