Clinical and Economic Implications of High-Sensitivity Troponin-Informed Admission Strategies in Non-AMI Chest Pain

Wanyi Chen1, Allan S Jaffe2, Fred S Apple3,4

  • 1Medical Affairs, Siemens Healthcare Diagnostic Inc., Tarrytown, NY 10591, USA.

Insights

Using cardiac troponin I (cTnI) thresholds can safely reduce hospital admissions for chest pain patients without acute myocardial infarction (AMI). This approach improves diagnostic efficiency and lowers costs in emergency departments.

Area of Science:

  • Cardiology
  • Emergency Medicine
  • Health Economics

Background:

  • Most chest pain patients do not have acute myocardial infarction (AMI), yet disposition decisions after ruling out AMI are inconsistent.
  • Detectable but sub-99th percentile high-sensitivity cardiac troponin I (hs-cTnI) levels offer valuable prognostic insights.

Purpose of the Study:

  • To evaluate the economic value of using hs-cTnI-guided hospital admission strategies for patients presenting with chest pain but without AMI.

Main Methods:

  • Analysis of 1481 non-AMI chest pain visits with detectable baseline hs-cTnI from the prospective HIGH-US trial.
  • Comparison of standard-of-care admissions with modeled pathways using hs-cTnI thresholds and risk scores.
  • Assessment of admission rates, costs, and 30-day death/myocardial infarction (MI) diagnostic accuracy.

Main Results:

  • Standard-of-care admitted 59% of patients with 93% sensitivity and 41% specificity for 30-day death/MI.
  • A modeled pathway using hs-cTnI ≥ 5 ng/L plus non-low risk scores projected a 41% reduction in admissions, increased specificity to 60%, while maintaining 93% sensitivity.
  • Estimated per-patient diagnostic costs were lower in modeled scenarios compared to standard-of-care.

Conclusions:

  • Incorporating sub-99th percentile hs-cTnI thresholds with risk scores may enhance resource utilization and patient safety in chest pain evaluations.
  • This strategy could lead to more efficient hospital admissions without compromising diagnostic accuracy for adverse outcomes.
  • Further prospective validation is recommended to confirm these economic and clinical benefits.

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