Affiliations 

  • 1 Department of Cardiology, National Heart Centre Singapore, Singapore, Singapore
  • 2 Department of Cardiology, Universiti Teknologi MARA, Kuala Lumpur, Malaysia
  • 3 Department of Laboratory Medicine, Changi General Hospital, Singapore, Singapore
  • 4 Department of Cardiology, Philippine Heart Center, Manila, Philippines
  • 5 Department of Cardiology, Chi-Mei Hospital, Tainan, Taiwan
  • 6 Department of Cardiology, University Medical Center, Ho Chi Minh City, Vietnam
  • 7 Heart Institute, St Luke's Medical Centre, Quezon City, Philippines
  • 8 Department of Cardiology, Pondok Indah Hospital, Jakarta, Indonesia
  • 9 Department of Cardiology, Chiang Mai University, Chiang Mai, Thailand
  • 10 Department of Cardiology, National Cardiology Institute, Hanoi, Vietnam
  • 11 Department of Cardiology, Siriraj Hospital, Bangkok, Thailand
  • 12 Department of Medicine, Queen Mary Hospital, Hong Kong, Hong Kong
  • 13 Department of Emergency Medicine, Royal Brisbane and Women's Hospital, Brisbane, Australia
Heart Asia, 2017;9(1):81-87.
PMID: 28466882 DOI: 10.1136/heartasia-2016-010818

Abstract

OBJECTIVE: High-sensitivity troponin (hs-Tn) assays need to be applied appropriately to improve diagnosis and patient outcomes in acute coronary syndromes (ACS).

METHODS: Experts from Asia Pacific convened in 2015 to provide data-driven consensus-based, region-specific recommendations and develop an algorithm for the appropriate incorporation of this assay into the ACS assessment and treatment pathway.

RESULTS: Nine recommendations were developed by the expert panel: (1) troponin is the preferred cardiac biomarker for diagnostic assessment of ACS and is indicated for patients with symptoms of possible ACS; (2) hs-Tn assays are recommended; (3) serial testing is required for all patients; (4) testing should be performed at presentation and 3 hours later; (5) gender-specific cut-off values should be used for hs-Tn I assays; (6) hs-Tn I level >10 times the upper limit of normal should be considered to 'rule in' a diagnosis of ACS; (7) dynamic change >50% in hs-Tn I level from presentation to 3-hour retest identifies patients at high risk for ACS; (8) where only point-of-care testing is available, patients with elevated readings should be considered at high risk, while patients with low/undetectable readings should be retested after 6 hours or sent for laboratory testing and (9) regular education on the appropriate use of troponin tests is essential.

CONCLUSIONS: We propose an algorithm that will potentially reduce delays in discharge by the accurate 'rule out' of non-ACS patients within 3 hours. Appropriate research should be undertaken to ensure the efficacy and safety of the algorithm in clinical practice, with the long-term goal of improvement of care of patients with ACS in Asia Pacific.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.