4.6 Article

Cardiac troponin-I on diagnosis predicts early death and refractoriness in acquired thrombotic thrombocytopenic purpura. Experience of the French Thrombotic Microangiopathies Reference Center

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 13, 期 2, 页码 293-302

出版社

WILEY
DOI: 10.1111/jth.12790

关键词

ADAMTS13 protein; human; prognosis; thrombotic microangiopathy; thrombotic thrombocytopenic purpura; troponin

资金

  1. Alexion
  2. Bayer Healthcare
  3. MSD
  4. Pfizer
  5. Gilead
  6. INSERM
  7. Societe de Reanimation de Langue Francaise
  8. LFB
  9. Astellas
  10. Novartis
  11. GlaxoSmithKline
  12. Roche
  13. Chugai
  14. Raison et Sante
  15. Janssen
  16. RESICARD
  17. AstraZeneca
  18. Bayer Pharma
  19. Boehringer Ingelheim
  20. Daiichi Sankyo
  21. Sanofi

向作者/读者索取更多资源

BackgroundCardiac involvement is a major cause of mortality in patients with thrombotic thrombocytopenic purpura (TTP). However, diagnosis remains underestimated and delayed, owing to subclinical injuries. Cardiac troponin-I measurement (cTnI) on admission could improve the early diagnosis of cardiac involvement and have prognostic value. ObjectivesTo assess the predictive value of cTnI in patients with TTP for death or refractoriness. Patients/MethodsThe study involved a prospective cohort of adult TTP patients with acquired severe ADAMTS-13 deficiency (<10%) and included in the registry of the French Reference Center for Thrombotic Microangiopathies. Centralized cTnI measurements were performed on frozen serum on admission. ResultsBetween January 2003 and December 2011, 133 patients with TTP (mean age, 4817years) had available cTnI measurements on admission. Thirty-two patients (24%) had clinical and/or electrocardiogram features. Nineteen (14.3%) had cardiac symptoms, mainly congestive heart failure and myocardial infarction. Electrocardiogram changes, mainly repolarization disorders, were present in 13 cases. An increased cTnI level (>0.1gL(-1)) was present in 78 patients (59%), of whom 46 (59%) had no clinical cardiac involvement. The main outcomes were death (25%) and refractoriness (17%). Age (P=0.02) and cTnI level (P=0.002) showed the greatest impact on survival. A cTnI level of >0.25gL(-1) was the only independent factor in predicting death (odds ratio [OR]2.87; 95% confidence interval [CI]1.13-7.22; P=0.024) and/or refractoriness (OR3.03; 95%CI1.27-7.3; P=0.01). ConclusionsA CTnI level of >0.25gL(-1) at presentation in patients with TTP appears to be an independent factor associated with a three-fold increase in the risk of death or refractoriness. Therefore, cTnI level should be considered as a prognostic indicator in patients diagnosed with TTP.

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