Epic Test Code LAB747 Troponin I High Sensitivity
Performing Location(s)
BMC,CRH,LFH,OCH,FTT,FOX
Specimen Type
Ordered alone or as STAT: Plasma
Any priority other than STAT: Serum
Preferred Container
Ordered alone or as STAT: Light Green top tube
Any priority other than STAT: Gold top tube
Blood Tube Draw Volume
Min 50% draw volume
Minumum Volume to Submit for Testing
0.5 mL Plasma or Serum
- Multiple test can be performed from this volume. For question please contact the lab at 547-3975.
Storage Requirements
Sample tubes should be centrifuged within 2 hours of collection followed by transfer of the plasma/serum to a labeled plastic, aliquot tube.
Place a “Plasma” sticker on the aliquot tube.
See Causes of Rejection for temperature requirements.
Transportation Needs
Deliver specimen to laboratory within 1 hour of collection if unspun. If not possible see "storage Requirements".
Causes for Rejection
Mislabeled or unlabeled specimen
Less than 50% draw for Vacutainer tubes
>48 hours refrigerated
>4 hour Room Temperature
>6 months Frozen
Hemolysis > 4000 mg/dL HgB
Lipemia > 3000 mg/dL Trig
Bilirubin > 40 mg/dL Bili
EDTA, NaF, Citrate, Oxalate
Limitations
Specimens should be free of particulate matter
Reference Values
Gender |
Reference Range |
Units |
Male |
≤ 20.0 |
pg/mL |
Female |
≤ 15.0 |
pg/mL |
Critical Value | >100 | pg/mL |
The normal range represents the 99th percentile of patients without cardiac injury. IFCC guidance states high sensitivity assays must have analytical imprecision ≤10% CV at the 99th percentile URL of healthy population. This assay has 10% CV limit at 6 pg/mL |
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A sequential sampling protocol is recommended. Serial samples from a patient with a myocardial injury taken at 6-8 hour intervals over the first 48 hours will result in the classic rise and fall in concentration. Sampling at 1-2 hrs after initial presentation may facilitate early identification of AMI. |
Available STAT
Yes
Days of Analysis
All
Additional Information
High sensitivity troponin provider >99% confidence in ruling out AMI in patients with values below the upper reference limit.
hs Troponin identifies ≥94% of true AMI patients within 1-3 hrs after presentation. Allows physicians to interpret small changes in borderline elevations for diagnosis and treatment.
Very low levels of hs Troponin on presentation or lack of any change and persistently normal hs Troponin values over 1-2 hr period after presentation can exclude acute myocardial injury and MI.
Methodology
Beckman AU/Dx/Access Series
CPT Code
84484
Last Updated
29-NOV-24 MS