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    Electrocardiogram: 12 Lead (Ambulatory) - CE

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    Jul.27.2023

    Electrocardiogram: 12 Lead (Ambulatory) - CE/NCPD

    ALERT

    Ensure the proper placement of electrodes to avoid incorrect interpretation of the 12-lead electrocardiogram (ECG), mistaken diagnosis, or patient mismanagement.undefined#ref2">2

    OVERVIEW

    The standard 12-lead ECG is the most widely used noninvasive diagnostic tool in the management of cardiac disease and is a source of information about the heart’s electrical system.2 The ECG has significant impact on medical decision-making, clinical management, and therapy. Common uses include diagnosing acute coronary syndromes, identifying arrhythmias and conduction disturbances, and determining the effects of medications or electrolytes on the heart’s electrical system (Box 1)Box 1.

    The ECG leads are the standard limb leads (I, II, III); augmented limb leads (augmented vector right [aVR], augmented vector foot [aVF], and augmented vector left [aVL]); and six chest leads (V1 to V6). The standard and augmented leads view the heart from the vertical or frontal plane (Figure 1)Figure 1, and the chest leads view the heart from the horizontal plane (Figure 2)Figure 2. The graphic display consists of the P, Q, R, S, and T waves, which represent electrical activity in the heart.2

    If myocardial ischemia or injury is suspected, serial ECGs are performed. Correct standardized electrode placement is crucial for accurate ECG interpretation.3 Advances in technology allow online or wireless transmission, networking capabilities, and computerized interpretation of the 12-lead ECG.

    SUPPLIES

    See Supplies tab at the top of the page.

    EDUCATION

    • Provide developmentally and culturally appropriate education based on the desire for knowledge, readiness to learn, and overall neurologic and psychosocial state.
    • Explain the equipment and the procedure.
    • Instruct the patient not to talk, to relax, to lie still, and to breathe normally.
    • Encourage questions and answer them as they arise.

    PROCEDURE

    1. Perform hand hygiene. Don appropriate personal protective equipment (PPE) based on the patient’s need for isolation precautions or the risk of exposure to bodily fluids.
    2. Introduce yourself to the patient.
    3. Verify the correct patient using two identifiers.
    4. Explain the procedure and ensure that the patient agrees to treatment.
    5. Ensure that evaluation findings are communicated to the clinical team leader per the organization’s practice.
    6. Ask if the patient is experiencing chest pain, shortness of breath, or palpitations.
    7. Ask about the patient’s history of cardiac arrhythmias or cardiac problems.
    8. Ask the patient about any current medications.
    9. Ask the patient to remove any jewelry (e.g., wristwatches, necklaces, body jewelry) that may interfere with the ECG.
    10. Check the cables and lead wires for fraying, broken wires, or discoloration.
      Rationale: Checking the cables and lead wires helps detect conditions that may give an inaccurate ECG tracing.
      If equipment is damaged, obtain alternative equipment and notify the appropriate health care team member for repair.
    11. Plug the ECG machine into a grounded alternating current (AC) wall outlet or ensure that the battery-operated machine is functioning.
    12. Turn the ECG machine on and input the required information.
      Rationale: Equipment may require a self-test and warm-up time. Multichannel machines (Figure 3)Figure 3 may require input of information (e.g., data about the patient) to store the ECG appropriately.
      Follow the manufacturer’s recommendations and requirements for inputting information and warm-up time.
    13. Assist the patient into a resting, supine position. Ensure that the patient is not touching any side rails or footboard, as applicable.
      Rationale: The supine position provides adequate support for the patient’s limbs so muscle activity is minimal. Touching side rails or a footboard may increase the chance of distorting the tracing. Body position changes can also cause alterations in the ECG tracing.
      The supine position is best, but Fowler or other positions may be used for comfort. Ensure that serial ECGs are recorded with the patient in the same position, so changes in body position do not cause changes in tracings. If another position is required clinically, document the position on the tracing or in the comment space of the machine input.
    14. Expose only the necessary parts of the patient’s legs, arms, and chest to provide privacy and warmth.
      Rationale: A lack of privacy may induce anxiety, which can alter the ECG reading. Shivering interferes with the recording.
    15. Identify the lead sites before placement.
      Rationale: Identifying and marking the lead sites ensures that the electrodes are accurately placed.
    16. Wash the patient’s skin with soap and water and dry it briskly with gauze pads or a washcloth.1 Ensure that the patient’s skin is dry before applying the electrodes.
      Rationale: Moist skin is not conducive to electrode adherence. Wiping the electrode area with a washcloth or gauze dries and roughens the skin to enhance conduction.1
      Do not use alcohol for skin preparation because it can dry the skin.1
      To ensure good skin contact with the electrodes, clip chest hair with surgical clippers as necessary.
    17. Prepare the electrodes.
      Rationale: Preparing the electrodes allows appropriate impulse conduction.
      1. For pregelled electrodes, remove the backing and test for moistness.
        Ensure that the gel is moist. Replace the electrodes if they are not moist.
      2. For adhesive electrodes, remove the backing and ensure that the adhesive pad is sticky or moist.
        Replace adhesive electrodes if they are not sticky.
    18. Place the limb electrodes (Figure 4)Figure 4 in fleshy areas, equidistant from the heart and in approximately the same place on each limb. Avoid bony prominences.
      Rationale: Accurate placement ensures correct electrical tracing of the heart from the vertical and frontal planes.2
    19. Place the chest electrodes (Figure 5)Figure 5, ensuring accurate placement.
      Rationale: Accurate placement ensures correct electrical tracing of the heart from the horizontal plane. Slight alterations in the position of a precordial lead may alter the ECG significantly and can have an impact on diagnosis and treatment.2
      1. Identify the sternal angle, also called the angle of Louis (Figure 5)Figure 5.
        Rationale: The sternal angle helps identify the second rib for placement of precordial leads in the appropriate intercostal spaces (ICSs).
        1. Palpate the upper sternum to identify where the clavicle joins the sternum (suprasternal notch).
        2. Slide the fingers down the center of the sternum to the obvious bony prominence; this is the sternal angle, which identifies the second rib and provides a landmark for locating the fourth ICS.
      2. When the fourth ICS is located, place the V electrodes in the appropriate locations.
        1. V1 at the fourth ICS, right sternal border
        2. V2 at the fourth ICS, left sternal border
        3. V4 at the fifth ICS, midclavicular line
        4. V3 equidistant between V2 and V4
        5. V5 horizontal to V4 at the anterior axillary line
        6. V6 horizontal to V4 at the midaxillary line
          Variations in precordial lead placement can result in important diagnostic errors, such as septal ischemia or infarction.2
          If leads cannot be accurately placed, clearly document the actual location of the electrode placement on the 12-lead ECG.
          Place precordial electrodes under the breasts of a patient with large breasts.
    20. Attach the lead wires to the electrodes.
    21. Turn the ECG machine on and program it according to the manufacturer’s instructions. Most machines have automatic settings for programming paper speed and calibration and to perform a self-test when turned on.
    22. Input patient information required for appropriate storage of the ECG into the machine according to the organization’s practice.
    23. Obtain a 12-lead ECG recording.
      1. Instruct the patient to remain still while the machine senses and translates the heart’s electrical activity to electrical waveforms on paper.
        Rationale: For correct interpretation, the ECG must be marked accurately and have a clear baseline without artifact.2
      2. Obtain a rhythm strip if needed.
        Rationale: A rhythm strip is a long recording of a specific lead; lead II is commonly used because P waves are best seen in lead II.
        Refer to the manufacturer’s instructions for use (IFU) on obtaining a rhythm strip.
    24. Examine the 12-lead ECG tracing to ensure that it is clear and without artifact; repeat the ECG if it is not clear. Compare the 12-lead ECG with previous 12-lead ECGs if possible.
      Rationale: A comparison helps determine normal and abnormal findings.
      Examine the ECG and determine whether the recording must be repeated while the patient is still connected to the machine.
    25. The clinical team leader interprets the recording, per the organization’s practice, and looks for:
      1. Rhythm
      2. Rate
      3. Presence and configuration of P waves
      4. Length of P–R intervals
      5. Length of QRS complexes
      6. Configuration and deviation of the ST segments
      7. Presence and configuration of T waves, length of Q-T intervals, presence of extra waves (e.g., U waves)
      8. Arrhythmias
      9. Signs of ischemia, injury, infarct, and other significant myocardial alterations
        Rationale: An evaluation identifies pathophysiologic processes that may require further evaluation or treatment.
    26. Disconnect the equipment, clean the gel off of the patient (if necessary), return removed clothing, and help the patient resume a comfortable position.
      Follow the manufacturer’s IFU and the organization’s practice for electrode use and removal.
    27. Clean the ECG leads and machine per the manufacturer’s instructions and the organization’s practice. Return the equipment to its assigned storage space.
    28. Discard supplies, remove PPE, and perform hand hygiene.
    29. Document the procedure in the patient’s record.

    EXPECTED OUTCOMES

    • A clear 12-lead ECG recording (Figure 6)Figure 6 is obtained.
    • Abnormalities are promptly identified.

    UNEXPECTED OUTCOMES

    • Altered skin integrity
    • Inaccurate lead placement or limb lead reversal (Figure 7)Figure 7
    • AC interference, also called 60-cycle interference (Figure 8)Figure 8
    • Wandering baseline (Figure 9)Figure 9
    • Motion artifact (Figure 10)Figure 10

    DOCUMENTATION

    • Education
    • Reason for the 12-lead ECG (documented by the clinical team leader)
    • Patient signs and symptoms of cardiac arrhythmias or cardiac problems (e.g., chest pain, syncope, dizziness, palpitations)
    • Any altered lead placement or patient position and reason for change
    • Follow-up to the 12-lead ECG, as indicated
    • Unexpected outcomes and related interventions
    • Evaluation findings communicated to the clinical team leader per the organization’s practice

    REFERENCES

    1. American Association of Critical-Care Nurses (AACN). (2018). AACN practice alert: Managing alarms in acute care across the life span: Electrocardiography and pulse oximetry. Critical Care Nurse, 38(2), e16-e20. doi:10.4037/ccn2018468 (Level VII)
    2. Brady, W.J., Harrigan, R.A., Chan, T.C. (2019). Chapter 14: Basic electrocardiographic techniques. In J.R. Roberts and others (Eds.), Roberts and Hedges’ clinical procedures in emergency medicine and acute care (7th ed., pp. 275-287). Philadelphia: Elsevier.
    3. Sandau, K.E. and others. (2017). Update to practice standards for electrocardiographic monitoring in hospital settings: A scientific statement from the American Heart Association. Circulation, 136(19), e273-e344. doi:10.1161/CIR.0000000000000527 (Level VII)

    Elsevier Skills Levels of Evidence

    • Level I - Systematic review of all relevant randomized controlled trials
    • Level II - At least one well-designed randomized controlled trial
    • Level III - Well-designed controlled trials without randomization
    • Level IV - Well-designed case-controlled or cohort studies
    • Level V - Descriptive or qualitative studies
    • Level VI - Single descriptive or qualitative study
    • Level VII - Authority opinion or expert committee reports
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