Switching From Cardiac Troponin I to T
NCT05748691 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 26000
Last updated 2024-05-28
Summary
Cardiac troponin is central to the diagnosis of myocardial infarction and high-sensitivity cardiac troponin (hs-cTn) assays are the preferred choice for the assessment of patients with suspected acute coronary syndrome.
Since the introduction of hs-cTn assays in Europe in 2010, most hospitals have switched from contemporary sensitive cardiac troponin assays to a hs-cTn assay. The implementation of hs-cTn assays has led to an increase in the number of patients identified with myocardial injury. Although both hs-cTnI and hs-cTnT assays are recommended in current guidelines, the impact of switching from a hs-cTnI assay to a hs-cTnT assay on clinical practice is unknown. At this point, no studies have evaluated the impact of implementing sex-specific hs-cTnT thresholds on the diagnosis of myocardial infarction and outcome in clinical practice.
The investigators propose to determine the proportion of patients with and without myocardial injury admitted to the hospital before and after implementation of a hs-cTnT assay and to evaluate the impact on investigations, care and clinical outcomes in consecutive patients with suspected acute coronary syndrome.
Conditions
- Acute Coronary Syndrome
- Acute Myocardial Infarction
- Acute Myocardial Ischemia
- Myocardial Injury
- Chest Pain
- Heart Failure
Interventions
- DIAGNOSTIC_TEST
-
Clinical implementation of hs-cTnT
To investigate the clinical impact on the transition from a hs-cTnI assay to a hs-cTnT assay in consecutive patients presenting to the Emergency Department or Acute Medical Unit with suspected acute coronary syndrome.
Sponsors & Collaborators
-
University of Edinburgh
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-10-25
- Primary Completion
- 2023-10-25
- Completion
- 2023-10-25
Countries
- United Kingdom
Study Locations
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