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Prediction of Ischemic Events after Percutaneous Coronary Intervention: Thrombelastography Profiles and Factor XIIIa Activity.
Kreutz, Rolf P; Schmeisser, Glen; Schaffter, Andrea; Kanuri, Sri; Owens, Janelle; Maatman, Benjamin; Sinha, Anjan; von der Lohe, Elisabeth; Breall, Jeffrey A.
Afiliação
  • Kreutz RP; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Schmeisser G; Department of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Schaffter A; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Kanuri S; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Owens J; Department of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Maatman B; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Sinha A; Department of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • von der Lohe E; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
  • Breall JA; Krannert Institute of Cardiology, Indiana University School of Medicine, Indianapolis, Indiana, United States.
TH Open ; 2(2): e173-e181, 2018 Apr.
Article em En | MEDLINE | ID: mdl-30882064
ABSTRACT

BACKGROUND:

High plasma fibrin clot strength (MA) measured by thrombelastography (TEG) is associated with increased risk of cardiac events after percutaneous coronary interventions (PCIs). Factor XIIIa (FXIIIa) cross-links soluble fibrin, shortens clot formation time (TEG-K), and increases final clot strength (MA).

METHODS:

We analyzed platelet-poor plasma from patients with previous PCI. Kaolin-activated TEG (R, K, MA) in citrate platelet-poor plasma and FXIIIa were measured (n = 257). Combined primary endpoint was defined as recurrent myocardial infarction (MI) or cardiovascular death (CVD). Relationship of FXIIIa and TEG measurements on cardiac risk was explored.

RESULTS:

FXIIIa correlated with TEG-MA (p = 0.002) and inversely with TEG-K (p < 0.001). High MA (≥35.35 mm; p = 0.001), low K (<1.15 min; p = 0.038), and elevated FXIIIa (≥83.51%; p = 0.011) were associated with increased risk of CVD or MI. Inclusion of FXIIIa activity and low TEG-K in risk scores did not improve risk prediction as compared with high TEG-MA alone.

CONCLUSION:

FXIIIa is associated with higher plasma TEG-MA and low TEG-K. High FXIIIa activity is associated with a modest increase in cardiovascular risk after PCI, but is less sensitive and specific than TEG-MA. Addition of FXIIIa does not provide additional risk stratification beyond risk associated with high fibrin clot strength phenotype measured by TEG.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2018 Tipo de documento: Article