Usefulness of a 2-hour Delta Troponin-I During the ED Identification and Exclusion of Acute Myocardial Infarction

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02002546

Enrollment

240

Registered

2013-12-06

Start date

2014-01-31

Completion date

2015-09-04

Last updated

2018-01-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome

Keywords

Heart Attack, Myocardial Infarction, Angina, Chest Pain

Brief summary

1. In chest pain patients with suspected acute coronary syndrome, a 2-hr delta Troponin-I as measured by the i-STAT immunoassay reliably identifies and excludes an acute myocardial infarction. 2. In chest pain patients with suspected acute coronary syndrome whose baseline troponin is above the 99th percentile but less than 0.2ng/ml, a 2hr delta Troponin-I as measured by the i-STAT immunoassay accurately discriminates between acute myocardial infarction and non-acute myocardial infarction troponin elevations.

Detailed description

Primary Aims: 1) Demonstrate that a 2hr delta troponin as measured by the i-STAT platform can reliably identify and exclude MI on the initial ED evaluation. 2)Demonstrate that a 2hr delta troponin is useful in the discrimination AMI versus non-AMI conditions in patients with low abnormal baseline Troponin-I values. Secondary Aims: 1) Demonstrate that a positive 2-hr delta troponin-I identifies patients at highest risk for 30 day ACE. 2) Other Secondary aims TBD.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Adult patients 18 years of age or older 2. Chest pain suspicious for ACS 3. Absence of ST-segment elevation AMI (STEMI) or STEMI equivalent on the initial ECG 4. Baseline i-STAT troponin less or equal to 1.0 ng/ml 5. Enrollment initiated before 2 hour 'delt' troponin value available for review 6. Ability and willingness to participate and cooperate with telephone follow-up evaluations

Exclusion criteria

1. ST-elevation or other ECG criteria that results in the diagnosis of AMI and results in patient being sent for percutaneous coronary interventions (PCI) or being treated with thrombolytics 2. Patients with chest pain not deemed to warrant cardiac screening 3. Blunt chest trauma 4. Tachyarrhythmia (ventricular tachycardia, supraventricular tachycardia, or rapid atrial fibrillation) 5. Cardiac Arrest prior to arrival 6. Hemodynamically unstable patients 7. Pulmonary edema requiring CPAP, BIPAP, or mechanical ventilation 8. Baseline i-STAT troponin measurement greater than 1.0 ng/ml 9. Baseline and 2-hour i-STAT Troponin measurements not obtained 10. Patient (or Legal Representative) unable or unwilling to provide written informed consent 11. Subject unwilling or unlikely to comply with study procedures, including protocol-specific blood sampling 12. Subject unwilling, unable, or deemed unlikely to respond or participate in telephone follow-up 13. Vulnerable populations as deemed inappropriate for the study

Design outcomes

Primary

Measure	Time frame
Change in Troponin value over a two hour interval.	2 hours after baseline

Countries

United States

Outcome results