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Information

Synonym/Acronym

Cardiac troponin, cardiac troponin I (cTnI), cardiac troponin T (cTnT).

Rationale

To assist in evaluating myocardial muscle damage related to disorders such as myocardial infarction (MI). Troponins are considered the gold standard for identification of MI and have largely replaced the use of myoglobin and lactate dehydrogenase with isoenzymes.

Patient Preparation

There are no food, fluid, activity, or medication restrictions unless by medical direction.

Normal Findings

Method: Electrochemiluminescent Immunoassay for Troponin I, Electrochemiluminescent Immunoassay, fifth generation (high sensitivity) for Troponin T.

Conventional UnitsSI Units (Conventional Units × 1)
Troponin I
AdultLess than 0.03 ng/mLLess than 0.03 mcg/L
Troponin T (high sensitivity)
Adult
MaleLess than or equal to 15 ng/LLess than or equal to 15 mcg/L
FemaleLess than or equal to 10 ng/LLess than or equal to 10 mcg/L

Normal values can vary significantly due to differences in test kit reagents and instrumentation. The testing laboratory should be consulted for comparison of results to the corresponding reference range.

Critical Findings and Potential Interventions

N/A

Overview

Study type: Blood. The laboratory should be contacted prior to specimen collection to determine the appropriate collection container. Collection requirements vary between different testing methods. Generally, green-top [heparin] tubes are required for (HScTnT), while some troponin I tests may be run on either plasma collected in a green-top [heparin] or lavender-top [EDTA] tube or run on serum collected in red/gray or red-top tube; related body system: Circulatory system. Care must be taken to use the same type of collection container if serial measurements are to be taken. It should also be noted that values obtained from different assays do not correlate, e.g., rapid point-of-care screen performed in the emergency department will not compare to the main laboratory’s automated assay.

Cardiovascular disease remains one of the leading causes of death in the United States. Troponin, considered the gold standard for diagnosing acute MI, is the preferred and sometimes sole cardiac marker used when a patient initially presents for evaluation of suspected MI. Troponin is a complex of three contractile proteins that regulate the interaction of actin and myosin. Troponin C is the calcium-binding subunit; it does not have a cardiac muscle–specific subunit. Troponin I and troponin T, however, do have cardiac muscle–specific subunits with separate and unique functions.

High-sensitivity cardiac troponin I (HScTnI) and high-sensitivity cardiac troponin T (HScTnT) assays have been approved by the U.S. Food and Drug Administration, and many laboratories have begun using the newer technology. While the high-sensitivity assays detect the presence of troponin sooner than the traditional methods, there is variability between the different test methods in cutoff values, sensitivity, and specificity of the protein segments or troponin epitopes being measured. These variations, as well as considerations regarding interpretation of results, require collaboration between assay manufacturers, laboratorians, and health-care providers during the process of evaluating and implementing high-sensitivity troponin assays.

Troponin I is only found in myocardial muscle tissue and is therefore thought to be a more specific marker of cardiac damage than troponin T. Cardiac troponin I begins to rise 3 to 6 hr after onset of chest pain accompanying MI, peaks between 12 and 16 hr, and resolves in 5 to 9 days.

Troponin T is present in the intracellular fluid of both striated cardiac and striated skeletal muscle cells and is therefore not considered as specific as cTnI for identifying MI. Levels of cTnT rise faster than cTnI and are detectable between 2 and 4 hr after MI, may peak somewhat later, and remain elevated longer (14 days or more).

Guidelines vary widely for concurrent serial testing of other cardiac markers including CK-MB. Multiple measurements of CK-MB may be used to identify cardiac injury subsequent to the initial infarct because unlike the release of CK-MB, once the troponin is increased to the point of being diagnostic for MI, further myocardial injury does not produce a new spike in troponin levels. Serial CK-MB measurements may also be used to rule out MI in the instance where the cTnT level is somewhat elevated related to a false positive caused by damage to striated skeletal muscle from other causes.

For additional information regarding screening guidelines for atherosclerotic cardiovascular disease (ASCVD), refer to the study titled “Cholesterol, Total and Fractions.”

Timing for Appearance and Resolution of Serum/Plasma Cardiac Markers in Acute MI
Cardiac MarkerAppearance (hr)Peak (hr)Resolution (d)
CK (total)4–6242–3
CK-MB4–615–202–3
Troponin I3–612–165–7
Troponin T2–416–2414

CK = creatine kinase; CK-MB = creatine kinase MB fraction.

Indications

Interfering Factors

cTnI and CK-MB assays can be used to rule out false-positive cTnT related to cTnT released from damaged skeletal muscle cells.

Potential Medical Diagnosis: Clinical Significance of Results

Increased In

Conditions that result in cardiac tissue damage; troponins are released from damaged skeletal and myocardial tissue into the circulation.

Decreased In

N/A

Nursing Implications, Nursing Process, Clinical Judgement

Potential Nursing Problems: Assessment & Nursing Diagnosis

ProblemsSigns and Symptoms
Cardiac output (decreased—prolonged myocardial ischemia, acute MI, reduced cardiac muscle contractility, rupture papillary muscle, mitral insufficiency)Weak peripheral pulses; slow capillary refill; decreased urinary output; cool, clammy skin; tachypnea; dyspnea; altered level of consciousness; abnormal heart sounds; fatigue; hypoxia; loud holosystolic murmur; electrocardiogram (ECG) changes; increased jugular venous distention
Pain (related to myocardial ischemia, MI)Reports of chest pain, new onset of angina, shortness of breath, pallor, weakness, diaphoresis, palpitations, nausea, vomiting, epigastric pain or discomfort, increased blood pressure, increased heart rate

Before the Study: Planning and Implementation

Teaching the Patient What to Expect

  • Discuss how this test can assist in evaluating heart damage.
  • Explain that a blood sample is needed for the test.
  • Serial markers including CK-MB may be requested to evaluate for subsequent cardiac damage.

Potential Nursing Actions

  • Follow the facility’s guidelines for cardiac biomarker testing.
  • Evaluate for the presence of other risk factors, such as family history of heart disease, smoking, obesity, diet, lack of physical activity, hypertension, diabetes, previous MI, and previous vascular disease, which should be investigated.
  • Explain that understanding genetics assists in identifying patients and family members who may benefit from additional education, risk assessment, and counseling.
  • Genetics is the study and identification of genes, genetic mutations, and inheritance. For example, genetics provides some insight into the likelihood of inheriting a medical condition such as CAD.
  • Genomic studies evaluate the interaction of groups of genes. The combined activity or combined expression of groups of genes allows assumptions or predictions to be made. As an example, genomic studies measure the levels of activity in multiple genes to predict how they, along with environmental and lifestyle decisions, influence the development of type 2 diabetes, CAD, MI, or ischemic stroke.

After the Study: Implementation & Evaluation Potential Nursing Actions

Treatment Considerations

Cardiac Output

  • Assess peripheral pulses and capillary refill, respiratory rate, breath sounds, orthopnea, skin color and temperature, and level of consciousness.
  • Monitor blood pressure and check for orthostatic changes and urinary output.
  • Use pulse oximetry to monitor oxygenation and monitor ECG.
  • Administer ordered inotropic and peripheral vasodilator medications, nitrates, and oxygen.

Pain

  • Assess pain characteristics: duration and onset (minimal exertion, sleep, or rest), squeezing pressure, and location in substernal back neck or jaw.
  • Discuss the importance of reporting chest pain as soon as it starts.
  • Identify pain relief modalities that have worked in the past.
  • Monitor and trend cardiac biomarkers (CK-MB, troponin). Collaborate with ancillary departments to complete ordered echocardiography, exercise stress testing, or pharmacological stress testing.
  • Administer ordered pain medication, anticoagulants, antiplatelets, beta blockers, calcium channel blockers, angiotensin-converting enzyme (ACE) inhibitors, angiotensin II receptor blockers (ARBs), and thrombolytic drugs.
  • Monitor and trend vital signs and administer prescribed oxygen.

Nutritional Considerations

  • Discuss ideal body weight and the purpose of and relationship between ideal weight and caloric intake to support cardiac health.
  • Review ways to decrease intake of saturated fats and increase intake of polyunsaturated fats.
  • Discuss limiting intake of refined processed sugar and sodium.
  • Discuss limiting cholesterol intake to less than 300 mg per day.
  • Encourage the intake of fresh fruits and vegetables, unprocessed carbohydrates, poultry, and grains.
  • Nutritional therapy is recommended for those with identified CAD risk, especially for those with elevated low-density lipoprotein cholesterol levels, other lipid disorders, diabetes, insulin resistance, or metabolic syndrome.
  • Always consider cultural influences with dietary choices to ensure better adherence to a change in lifestyle.
  • Variety of dietary patterns are beneficial for people with ASCVD. For additional information regarding nutritional guidelines, refer to the study titled “Cholesterol, Total and Fractions.”
  • Changeable risk factors warranting education include strategies to encourage regular participation in moderate aerobic physical activity three to four times per week, eliminating tobacco use, and adhering to a heart-healthy diet.
  • Those with elevated triglycerides should be advised to eliminate or reduce alcohol.

Clinical Judgement

  • Consider ways to discuss hospice and end-of-life care for those with a terminal diagnosis.

Follow-Up and Desired Outcomes

  • Acknowledges contact information provided for the American Heart Association (www.heart.org/HEARTORG), National Heart, Lung, and Blood Institute (www.nhlbi.nih.gov), and U.S. Department of Agriculture’s resource for nutrition (www.choosemyplate.gov).
  • Understands risk factors for CAD, necessary lifestyle changes (diet, smoking, alcohol use), the importance of weight management, and reportable signs and symptoms of heart attack.