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A Systematic Review and Collaborative Meta-Analysis to Determine the Incremental Value of Copeptin for Rapid Rule-Out of Acute Myocardial Infarction

Journal

AMERICAN JOURNAL OF CARDIOLOGY
Volume 113, Issue 9, Pages 1581-1591

Publisher

EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.amjcard.2014.01.436

Keywords

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Funding

  1. Brahms Thermofisher
  2. Catalonian
  3. Spanish government
  4. Roche Diagnostics
  5. AstraZeneca
  6. Mitsubishi Chemicals
  7. Siemens Healthcare
  8. St. Jude Medical and Medtronic
  9. Clinical Research Hospital Program of the French Ministry of Health
  10. European Union
  11. Swiss National Science Foundation
  12. Swiss Heart Foundation
  13. Basel University
  14. University Hospital Basel
  15. Cardiovascular Research Foundation Basel
  16. Stanley Thomas Johnson Foundation
  17. Abbott
  18. ALERE
  19. Beckman Coulter
  20. Brahms
  21. Biihlmann
  22. Critical Diagnostics
  23. Nanosphere
  24. Pronota
  25. Roche
  26. Siemens
  27. 8sense

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Multiple studies have evaluated copeptin, a surrogate for arginine vasopressin, in the diagnosis of acute myocardial infarction (AMI) with mixed results. A systematic review and collaborative meta-analysis were performed for diagnosis of AMI and assessment of prognosis in patients presenting to the emergency department with chest pain. MEDLINE/PubMed, Cochrane CENTRAL, and EMBASE were searched for studies assessing copeptin in such patients. Study investigators were contacted, and many provided previously unpublished data. Random-effects methods were used to compare the data for copeptin, troponin, and their combination. There were a total of 9,244 patients from the 14 included studies. Mean age was 62 years; 64% were men; and 18.4% were ultimately diagnosed with AMI. Patients with AMI had a higher presentation copeptin level than those without AMI (22.8 vs 8.3 pmol/L, respectively, p <0.001). Although troponin had better diagnostic accuracy than copeptin for AMI, the combination of copeptin and troponin significantly improved the sensitivity (0.905 [0.888 to 0.921] vs 0.686 [0.661 to 0.710], respectively, p <0.001) and negative predictive value (0.97 [0.964 to 0.975] vs 0.93 [0.924 to 0.936], respectively, p <0.001) compared with troponin alone. Elevation in copeptin carried a similar risk of all-cause mortality to an elevation in troponin (odds ratio 5.84 vs 6.74, respectively, p = 0.67). In conclusion, copeptin not only identifies patients at risk of all-cause mortality, but its addition to troponin improved the sensitivity and negative likelihood ratio for diagnosis of AMI compared with troponin alone. Thus, copeptin may help identify patients who may be safely discharged early from the emergency department. (C) 2014 Elsevier Inc. All rights reserved.

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