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About cTnI

With i-STAT cardiac troponin I (cTnI), healthcare professionals can obtain quantitative measurement of cardiac troponin I (cTnI) in ten minutes without leaving the patient's side. By incorporating i-STAT cTnI early in the patient experience, measurements of cardiac troponin I can improve diagnosis and treatment of myocardial infarction (MI) and aid in the risk stratification of patients with acute coronary syndromes (ACS) with respect to their relative risk of mortality.

Watch this short patient testimonial featuring George Hertner, MD, FACEM to see how process efficiencies achieved with i-STAT cTnI helped improve a particular patient’s care in his Emergency Department.

For an overview of i-STAT System test cartridges, browse the Test Cartridge Menu.

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Results in 10 Minutes

Providing lab-quality results fast when every
minute counts.

Related Items

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Ordering cTnI cartridges and other i-STAT System products is easy using our e-Abbott portal.

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Cartridge Details
 

cardiac_marker-icon.pngCardiac Markers
 
cTnI
Cardiac Troponin I (cTnI)

cTnI - INTENDED USE
The i-STAT cardiac troponin I (cTnI) test is an in vitro diagnostic test for the quantitative measurement of cardiac troponin I (cTnI) in whole blood or plasma. Measurements of cardiac troponin I are used in the diagnosis and treatment of myocardial infarction and as an aid in the risk stratification of patients with acute coronary syndromes with respect to their relative risk of mortality
The i-STAT cTnI cartridge meets the ACC/AHA guideline of 60-minute turnaround time 98% of the time, compared with 53% for the central lab1
Provides lab-quality results,2 which can improve adoption of serial cardiac marker testing
The 2012 Third Universal Definition of Myocardial Infarction recognizes troponin as the biomarker of choice3
Use of bedside testing in the ED has been shown to reduce:
  • time to anti-ischemic therapy by approximately 45 minutes4
  • time to discharge by 24 minutes1
  • ED length of stay by 1.9 hours5
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Description:

Rapid triage of chest pain patients, including those with ACS

Sample Size:

17μL

Sample type:

 

  • Heparinized whole blood or plasma samples collected in syringes or evacuated tubes containing lithium heparin, or
  • Non-heparinized whole blood samples tested within one minute of drawing from a patient into a plastic syringe or plastic evacuated tube containing no additives

 

Part Number:

06P23-25

Expected Values
 

cardiac_marker-icon.pngCardiac Markers
 
  Reportable Range Reference Range (Venous)
Cardiac Troponin I (cTnI) 0.00-50.00 ng/mL 0.00-0.08 ng/mL*
    * Represents the 0 to 99% range of results.

References: 1. ACEP Task Force Report on Boarding. Emergency Department Crowding: High-Impact Solutions. Irving, Tex: American College of Emergency Physicians; April 2008. 2. Ryan R, Lindsell C, Hollander J, et al. A multicenter randomized controlled trial comparing central laboratory and point-of-care marker testing strategies: The disposition impacted by serial point of care markers in acute coronary syndromes (DISPO-ACS) trial. Ann Emerg Med. 2009;53:321- 328. 3. Third Universal Definition of Myocardial Infarction (MI), Kristian Thygesen, Joseph S. Alpert, Allan S. Jaffe, Maarten L. Simoons, Bernard R. Chaitman and Harvey D. White, Circulation 2012;126:2020-2035 www.scpc.org/resources/PDFs/ThirdUniversalDefinitionofMyocardialInfarction_CIRC2012.pdf 4. Anderson JL, Adams CD, Antman EM, et al. ACC/AHA 2007 Guidelines for the Management of Patients With Unstable Angina/Non ST-Elevation Myocardial Infarction: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the 2002 Guidelines for the Management of Patients With Unstable Angina/Non ST-Elevation Myocardial Infarction). Circulation. 2007;116:e148-304. 5. Renaud B, Maison P, Ngako A, et al. Impact of point-of-care testing in the emergency department evaluation and treatment of patients with suspected acute coronary syndromes. Acad Emerg Med. 2008;15:216-224.

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