All troponins are not created equal
S Jossi1, S L Gordon, M A Legge
1Department of Clinical Chemistry, North Shore Hospital, Takapuna, Auckland, New Zealand.
Different troponin assays show poor agreement in classifying results, leading to significant variations in diagnosing acute coronary syndromes. Clinicians must consider the clinical context over assay-specific normal ranges.
Area of Science:
- Cardiology
- Clinical Chemistry
- Biomarker Analysis
Background:
- Troponin assays are crucial for diagnosing acute coronary syndromes (ACS).
- Clinical decisions rely on categorizing troponin results as positive or negative.
- Variability between troponin assays may impact patient diagnosis and management.
Purpose of the Study:
- To evaluate the categorical agreement between four different troponin assays.
- To assess the impact of assay variability on the classification of troponin results.
Main Methods:
- Analysis of 60 blood samples using three troponin I assays (Centaur, Architect, i-STAT) and one troponin T assay (Roche Elecys).
- Determination of upper reference limits based on a 10% coefficient of variation.
- Assessment of continuous agreement using Pearson's correlation and categorical agreement using Cohen's kappa.
Main Results:
- Continuous agreement between assays was generally good (Pearson's r = 0.871-0.995).
- Categorical agreement varied from poor (kappa = 0.37-0.48) to good (kappa = 0.68).
- The percentage of positive results ranged from 37% to 72%, a nearly twofold variation.
Conclusions:
- Significant variations exist in the proportion of positive results among different troponin assays.
- This variability may lead to missed diagnoses or false positives, affecting ACS management.
- Clinical judgment and context are essential when interpreting troponin results, rather than relying solely on local assay normal ranges.
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