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Published on: May 14, 2013
Relevance of hemostasis on restenosis in clinically stable patients undergoing elective PTCA
F C Schoebel1, A J Peters, I Kreis
1Heinrich Heine Universität Düsseldorf, Medizinische Klinik und Poliklinik B, Klinik für Kardiologie, Pneumologie und Angiologie, Moorenstrasse 5, 40225 Düsseldorf, Germany.
Insights
A hypercoagulable state, indicated by thrombin generation, predicts restenosis after coronary angioplasty. This finding identifies high-risk patients for coronary renarrowing following percutaneous transluminal coronary angioplasty (PTCA).
Area of Science:
- Cardiovascular Medicine
- Hematology
- Interventional Cardiology
Background:
- Secondary coronary thrombus formation is a suspected factor in restenosis post-percutaneous transluminal coronary angioplasty (PTCA).
- Systemic hypercoagulable states may contribute to coronary renarrowing.
- While thrombin's role in injury-induced restenosis is suggested experimentally, clinical data are limited.
Purpose of the Study:
- To investigate the clinical relevance of hypercoagulable states and thrombin generation in restenosis after PTCA.
- To identify laboratory markers associated with restenosis in patients undergoing elective PTCA.
Main Methods:
- Sixty patients with stable coronary artery disease undergoing successful elective PTCA were assessed.
- Quantitative coronary angiography evaluated restenosis (luminal narrowing >50%) and late luminal loss.
- Laboratory variables including prothrombin fragment 1+2, red blood cell aggregation, and plasminogen-activator inhibitor were measured.
Main Results:
- Prothrombin fragment 1+2 levels were significantly higher in patients with restenosis (1.3+/-0.5 vs. 0.9+/-0.4 mmol/l, p<0.001).
- Red blood cell aggregation and plasminogen-activator inhibitor levels also differed between restenosis and non-restenosis groups (p<0.05).
- Late luminal loss correlated positively with prothrombin fragment 1+2 (r=0.41, p<0.001) and plasmin-alpha2-antiplasmin complex (r=0.39, p<0.01).
Conclusions:
- A hypercoagulable state, particularly involving thrombin generation, is associated with restenosis after PTCA.
- These findings identify a high-risk group prone to coronary renarrowing.
- Clinical data support the role of thrombin generation in restenosis pathogenesis.
Background:
Secondary coronary thrombus formation is considered to be co-factor in the pathogenesis of restenosis after percutaneous transluminal coronary angioplasty (PTCA). Therefore systemic factors indicating a hypercoagulable disease state may be relevant for the process of coronary renarrowing. Even though experimental data suggest that in particular thrombin may be of major relevance for restenosis induced by mechanical injury, only little clinical data has been presented so far.
Methods And Results:
In 60 consecutive patients, who had been clinical stable for at least 2 months, and who underwent elective and primarily successful PTCA, follow-up films were evaluated by means of quantitative coronary angiography in respect to a categorical and a continuous definition of restenosis, luminal narrowing >50% and late luminal loss respectively. Of the chosen laboratory variables prothrombin fragment 1+2 (1.3+/-0.5 vs. 0.9+/-0.4 mmol/l, p<0.001) red blood cell aggregation at low shear stress (13.5+/-2.9 vs. 11.6+/-2.8 units, p<0.05), and plasminogen-activator inhibitor (3.7+/-1.8 vs. 5.3+/-3.2 U/ml p<0.05) differentiated between patients with (n=18) and without restenosis (n=42). Late luminal loss correlated positively with prothrombin fragment 1+2 (r=0.41, p<0.001), plasminogen-activator inhibitor (r= -0.28, p<0.05) and plasmin-alpha2-antiplasmin complex (r=0.39, p<0.01).
Conclusions:
A hypercoagulable disease state and in particular thrombin generation characterize a high-risk group prone for restenosis in clinically stable coronary artery disease.
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