Fractal dimension: A novel clot microstructure biomarker use in ST elevation myocardial infarction patients

Autor: Lindsay D’Silva, Alexander Chase, Simon J. Davidson, Roger H. K. Morris, Phillip A. Evans, Phylip Rhodri Williams, Ahmed Sabra, Phillip Thomas, David Smith, Matthew Lawrence, Karl Hawkins, Daniel R. Obaid, Martin Rowan Brown
Jazyk: angličtina
Rok vydání: 2015
Předmět:
Male
medicine.medical_specialty
Time Factors
Platelet Aggregation
Point-of-care testing
medicine.medical_treatment
Myocardial Infarction
Coronary Angiography
Percutaneous Coronary Intervention
Fibrinolytic Agents
St elevation myocardial infarction
Predictive Value of Tests
Internal medicine
medicine
Coagulation testing
Humans
Myocardial infarction
Prospective Studies
Blood Coagulation
Aged
Aged
80 and over

business.industry
Viscosity
Coronary Thrombosis
Percutaneous coronary intervention
Anticoagulants
Reproducibility of Results
Venous blood
Middle Aged
medicine.disease
Thrombosis
Elasticity
Surgery
Fractals
Treatment Outcome
Point-of-Care Testing
Cardiology
Microscopy
Electron
Scanning

Biomarker (medicine)
Feasibility Studies
Female
Blood Coagulation Tests
Cardiology and Cardiovascular Medicine
business
Platelet Aggregation Inhibitors
Popis: Objectives Changes in clot microstructure are increasingly implicated in the pathology of atherosclerosis although most data are from techniques in the remote laboratory using altered blood. We validate the novel biomarker Gel Point in STEMI patients and assess therapeutic interventions. Gel Point marks the transition of blood from a visco-elastic liquid to visco-elastic solid and is rapidly measured using unadulterated blood. The Gel Point provides measurements of three parameters to reflect clot microstructure (fractal dimension ( d f )), real-time clot formation time ( T GP ) and blood clot strength (elasticity at the Gel Point ( G ′ GP )). Methods We prospectively recruited 38 consecutive patients with STEMI undergoing primary percutaneous coronary intervention (pPCI). Venous blood samples were collected on admission, after pPCI and 24 h after admission for assessment of the new biomarkers, standard coagulation tests and scanning electron microscopy (SEM). Results d f after pPCI was lower than d f on admission (mean 1.631 [SD 0.063] vs 1.751 [0.052], p d f at 24 h was similar to that on admission. G ′ GP also showed similar trend to d f (p T GP was prolonged at after-PCI measurement compared with admission (median 854 s [IQR 581–1801] vs 217 [179–305], p d f and G ′ GP were consistent with changes in the SEM images of the mature clot. Conclusions We characterise Gel Point derived markers of clot microstructure in patients admitted with emergency arterial thrombosis. This point of care test can potentially be used to assess the efficacy of therapeutic interventions by measuring changes in clot microstructure.
Databáze: OpenAIRE