Procedure

Pacemaker

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Pacemaker, Twiddler's Syndrome, Pacemaker Interrogation, Pacemaker Associated Dysrhythmia, Pacemaker Generated Arrhythmia

  • Definition
  1. Thoracic-implanted, self-contained (with battery and circuitry)
  2. Cardiac sensing and pacing device indicated for Symptomatic Bradycardia or Syncope
  • Indications
  • Permanent Pacemaker - General
  1. Sinus Node Dysfunction with Symptomatic Bradycardia or Syncope
  2. Advanced second or third degree AV Block (see below)
  3. Chronic bifascicular block
  4. Acute Myocardial Infarction requiring ventricular pacing beyond acute phase
  5. Hypersensitive carotid sinus syndrome and Neurocardiogenic Syncope
  6. Cardiac Transplantation requiring post-operative pacing
  7. Symptomatic recurring SVT
  8. Congenital long QT Interval
  9. Cardiac Resynchronization Therapy with biventricular pacing
  10. Symptomatic Heart Block with Cardiomyopathy or Congenital Heart Disease
  • Indications
  • Permanent Pacemaker - AV Block
  1. Class I Indications (helpful)
    1. Sick Sinus Syndrome
      1. Symptomatic Bradycardia with frequent sinus pauses (>3 seconds) associated with symptoms
      2. Symptomatic chronotropic incompetence (inadequate Heart Rate response to Exercise or activity)
    2. Second Degree AV Block with Symptomatic Bradycardia
    3. Third Degree AV Block with one associated condition
      1. Symptomatic Bradycardia
      2. Documented Asystole (3 seconds or greater)
      3. Catheter ablation of the AV junction
      4. Neuromuscular disorder with AV Block
        1. Myotonic muscular disorder
        2. Kearns-Sayre Syndrome
        3. Erb's Dystrophy (limb-girdle)
        4. Peroneal muscular atrophy
  2. Class IIa Indications (probably helpful)
    1. Sick Sinus Syndrome
      1. Symptomatic Bradycardia with Heart Rate <40 bpm but symptom association with Bradycardia unclear
      2. Idiopathic Syncope and Sinoatrial Node dysfunction identified on electrophysiologic studies
    2. Asymptomatic third degree AV Block
    3. Asymptomatic Type II second degree AV Block
    4. Asymptomatic Type I AV Block at His level
    5. First degree AV Block and Pacemaker syndrome symptoms
  3. Class IIb Indications (Possibly helpful)
    1. Sick Sinus Syndrome
      1. Chronic awake rate <40 bpm in minimally symptomatic patients
    2. Marked First Degree AV Block (>0.3 seconds) with CHF
    3. Hypersensitive carotid sinus syndrome with recurrent Syncope
      1. ACC/AHA recommends if associated with ventricular Asystole for 3 or more seconds
      2. Cochrane review does not find sufficient evidence supporting Pacemakers for Carotid Sinus Syncope
      3. Romme (2011) Cochrane Database Syst Rev (10): CD004194 [PubMed]
  4. Class III Indications (Not helpful, possibly harmful)
    1. Asymptomatic Bradycardia due to medication
    2. Asymptomatic First Degree AV Block
    3. Asymptomatic Type I AV Block limited to supra-His
    4. Transient AV Block secondary to resolving condition
      1. Drug toxicity
      2. Lyme Disease
  • Components
  1. Pulse generator (Electronic device)
  2. Battery (e.g. 5-10 year Lithium ion)
  3. Pacing leads
  • Description
  • Pacemaker Codes
  1. Background
    1. Most Pacemakers in the U.S. are DDD (dual lead, dual sensed, dual response of trigger and inhibit)
    2. Some Pacemakers placed outside the U.S. are VVI (ventricle paced, ventricle sensed, ventricle inhibited)
  2. Position 1 (chamber paced)
    1. V - Ventricle
    2. A - Atrium
    3. D - Dual (A and V)
    4. O - None
  3. Position 2 (chamber sensed)
    1. V - Ventricle
    2. A - Atrium
    3. D - Dual (A and V)
    4. O - None
  4. Position 3 (response to sensing)
    1. V - Triggered
      1. Intrinsic P Wave with no QRS triggers the Pacemaker
    2. I - Inhibited
      1. Intrinsic P Wave with a QRS inhibits the Pacemaker
    3. D - Dual (T and I)
    4. O - None
  5. Position 4 (programmable functions and rate modulation)
    1. P - Programmable rate and output
    2. M - Muti-programmability of rate, output, sensitivity
    3. C - Communicating via telemetry
    4. R - Rate modulation
    5. O - None
  6. Position 5 (anti-tachyarrhythmia)
    1. P - Pacing (anti-tachyarrhythmia)
    2. S - Shock
    3. D - Dual (P and S)
    4. O - None
  • Types
  • Pacemaker modes
  1. Synchronous mode
    1. Synchronous with heart beat
  2. Asynchronous mode (fixed mode)
    1. Asynchronous in regards to heart beat (no response to sensing)
    2. Pacemakers revert to asynchronous mode when exposed to a magnet
  1. No signs or future risks for impaired AV conduction
    1. Rate response: Rate-responsive atrial pacer (AAIR)
    2. No rate response: Atrial Pacemaker (AAI)
  2. Impaired AV Conduction and no AV synchrony needed
    1. Rate response: Rate-responsive dual chamber (DDDR)
    2. No rate response: Ventricular Pacemaker (DDD)
  3. Impaired AV Conduction and AV synchrony needed
    1. Tachyarrhythmia (e.g. PSVT)
      1. Rate response: Rate-responsive dual chamber (DDDR)
      2. No rate response: Dual chamber Pacemaker (DDD)
    2. No Tachyarrhythmia
      1. Rate response: Rate-responsive dual and mode switch
      2. No rate response: Dual chamber with mode switching
  • Precautions
  1. Magnetic field exposure
    1. Pacemakers typically switch to asynchronous pacing at a set rate on exposure to magnetic field
    2. Cell phones should be held on the opposite side of body, away from Pacemaker
      1. Had been theoretical risk only in the past
      2. More powerful magnets are as of 2022 installed in phones for wireless charging (e.g. IPhone 12 MagSafe)
        1. Case reports of magnet triggered Syncope and other pacer adverse events are now more common
        2. Nadeem (2021) J Am Heart Assoc
          1. https://www.ahajournals.org/doi/10.1161/JAHA.121.020818
    3. Other wearable and personal use devices (e.g. Electronic Cigarettes) may interfere with Pacemaker function
      1. Shea (2020) HeartRhythm Case Rep 6(3): 121-3 [PubMed]
      2. Asher (2020) HeartRhythm Case Rep 7(3): 167-9 [PubMed]
    4. Magnets may be helpful in some emergency settings (e.g. applied to AICD that is delivering inappropriate shocks)
    5. MRI scans have been historically contraindicated
      1. Devices manufactured after 2000 are considered safe for non-thoracic MRI (after first 6 weeks)
      2. Avoid MRI with 6 weeks of placement due to device dislodgement
      3. Set Pacemaker to asynchronous mode (reset after scan), and turn AICD devices off
      4. Pacemaker may distort images
      5. Typically performed at tertiary centers with emergency backup and temporary Pacemaker reprogramming
      6. Russo (2017) N Engl J Med 376(8): 755-64 +PMID:28225684 [PubMed]
      7. Nazarian (2013) Circ Arrhythm Electrophysiol 6(2): 419-28 [PubMed]
  2. Battery life remaining in Pacemaker
    1. Pacers are interrogated to determine remaining battery life
    2. When battery life drops below ERI (Elective replacement indicator), Heart Rate will be be fixed at a manufacturer-set rate
    3. When battery life drops below EOL (End of life), Heart Rate will be fixed at a different fixed manufacturer-set rate
  3. External Defibrillation, cardioversion and external pacing
    1. Electrical shock may theoretically damage Pacemaker
    2. Emergency Defibrillation may be performed without regard to Pacemaker
    3. Avoid applying elective cardioversion pads directly over Pacemaker
      1. Try to apply pads at least 10-15 cm away from the device
  1. Indications
    1. May identify misplaced or damaged lead
    2. Identifies the Pacemaker type via a radiodense device stamp (requires a high penetration Chest XRay)
  2. Interpretation - Normal Pacemaker wire configuration
    1. Most newer Pacemakers are dual lead (but some may have only a single lead to either atrium or ventricle)
    2. Pacemaker tip positioning - PA View (or AP View)
      1. Pacemaker leads should coss the midline (from the left chest wall implantation site to the right heart)
      2. Atrial leads should be directed slightly upwards
      3. Ventricular leads should be directed slightly downwards
    3. Pacemaker tip positioning - Lateral View (or Lateral View)
      1. Pacemaker leads should be directed towards the Sternum (anteriorly)
      2. As with PA view, atrial leads are directed upward and ventricular leads downward
  1. Pacer spike
    1. Long, very narrow signal preceding a complex
  2. ST and T Waves
    1. Should always be discordant or opposite to the major QRS Complex (similar to a Left Bundle Branch Block)
      1. Discordance (or QRS Complex in the opposite direction as the ST Segment and T Wave) is normal
      2. Concordance (QRS and ST/T Wave in same direction) may suggest acute Myocardial Infarction
    2. Sgarbossa Criteria may distinguish Pacemaker altered ST-T morphology versus an acute Myocardial Infarction
      1. Applies to Left Bundle Branch Block induced with a right ventricular Pacemaker lead
      2. No guidelines directing Sgarbossa use in Pacemaker patients
        1. However original Sgarbossa study included a subset of Pacemaker patients
  3. QRS Complex
    1. Typically Left Bundle Branch Block (Pacemaker leads are typically placed in the right ventricle)
  • Diagnostics
  • Magnet placed over Pacemaker
  1. Indicated if Pacemaker malfunction is suspected
  2. Perform an Electrocardiogram before and after applying magnet
  3. Before magnet application (synchronous mode)
    1. Pacing is typically rate responsive via Pacemaker sensing functionality
  4. After magnet application (asynchronous mode, fixed mode)
    1. Turns off Pacemaker sensing functionality
    2. Pacemaker will now pace at an intrinsic rate (80-100 depending on manufacturer)
      1. QRS Complexes present after magnet application suggests a failure of Pacemaker sensing
      2. No QRS Complexes after magnet applications may suggest a failure of Pacemaker capture
  • Diagnostics
  • Pacemaker Interrogation
  1. All Pacemakers can perform Electrocardiograms (may be turned off to conserve battery life)
    1. Electrocardiogram functionality is enabled during interrogation
  2. Pacemaker programming head is placed directly over Pacemaker and push interrogate button
  3. Identify the patient's underlying rhythm
    1. Are the pacer spikes atrial or ventricular?
    2. Is the rhythm Pacemaker dependent?
      1. If uncertain, Pacemaker rate can be slowed to see if patient's rate also drops
  4. Can the Pacemaker sense the heart rhythm?
  5. Can the Pacemaker pace the heart?
  6. Are there other rhythm problems?
    1. Some Pacemakers can store abnormal rhythm events (e.g. VT runs) with a date-time stamp
  7. Is the Pacemaker programmed correctly?
  8. ERI (Elective replacement indicator)
    1. Battery life remaining before replacement is needed
  • Management
  • Troubleshooting a malfunctioning Pacemaker
  1. See Cardiac Pacemaker Infection
  2. Evaluation
    1. See Chest XRay (above) for Pacemaker lead positioning and device stamp
    2. See Magnet Application (above)
    3. See Electrocardiogram (above) for Pacemaker-related findings
    4. See Pacemaker Interrogation (above)
  3. Pacemaker device malfunction categories
    1. Failure to capture (despite pacer spike)
      1. Pacemaker spike present without ensuing QRS Complex
      2. May indicate lead Fracture or dislodgement, or malfunction central to the device
        1. Lead displacement is the most common cause and typically occurs in first month
      3. Other causes include cardiac ischemia or infarction, and Electrolyte abnormalities (esp. Hyperkalemia)
    2. Failure to output (without pacer spike, includes oversensing, exit block)
      1. Pacer spikes are absent
      2. May indicate lead Fracture or dislodgement, battery depletion
      3. May indicate device oversensing
        1. Pacemaker inhibited by a Hyperacute T Wave, muscle Fasciculation, cell phone within 10 cm
        2. Misinterpreted as an intrinsic beat
        3. Applying a magnet over the Pacemaker is diagnostic and therapeutic
      4. May indicate exit block
        1. Altered interface between Pacemaker lead and endocardium
        2. Causes include MI, fibrosis, Hyperkalemia, Antiarrhythmics
    3. Failure to sense (undersensing)
      1. Pacemaker fails to sense intrinsic cardiac activity and paces as if intrinsic activity is absent
      2. Pacer spike appear regardless of intrinsic rhythm
      3. May indicate lead dislodgement, altered position, acute right ventricular infarction
      4. Risk of R on T phenomenon
      5. Response depends on Pacemaker mode and programmed sensing parameters
      6. Placing a magnet over the Pacemaker will disable the aberrant functionality until it may be repaired
  4. Pacemaker Associated Dysrhythmia
    1. Pacemaker mediated Tachycardia (endless loop Tachycardia)
      1. Dual-Chamber Pacemaker mediated Tachycardia is a reentry Tachycardia
        1. Antegrade conduction via Pacemaker, retrograde conduction through AV Node
      2. Atrial sensing of retrograde impulses from the ventricle (e.g. PVC) trigger another atrial impulse
        1. Starts a cycle of Pacemaker impulses, followed by AV re-entry triggering another impulse
        2. Occurs if the Pacemaker postventricular atrial refractory period is too short
      3. EKG demonstrates a Wide Complex Tachycardia
        1. Retrograde P Waves may be present
        2. Ventricular pacer spikes are present, differentiating the ekg from Ventricular Tachycardia
      4. Treatment
        1. Apply magnet to Pacemaker to disable atrial sensing (and returning to a default pacer rate)
        2. Adenosine and AV Nodal blockers (e.g. Diltiazem, Beta Blockers) may also slow rate (as for AVRT)
    2. Runaway Pacemaker syndrome
      1. Rare, but life threatening
      2. A damaged Pacemaker theoretically could sporadically increase paced rates at well above 100
        1. Typically due to battery failure or Pacemaker damage (primarily older Pacemakers)
        2. Pacer spike bursts may trigger Ventricular Fibrillation
      3. Apply magnet to return Pacemaker to default rate
        1. Plan emergent replacement of the device
    3. Sensor-Induced Tachycardia
      1. Non-cardiac electrical stimulation triggers atrial-sensing and increases ventricular paced rate
      2. EKG demonstrates an inappropriate pacer rate
      3. Management
        1. Apply magnet to deactivate atrial sensing
        2. Eliminate non-cardiac stimuli
    4. References
      1. Berberian, Brady and Mattu (2024) Crit Dec Emerg Med 38(6): 14-5
  5. Other Specific Pacemaker problems
    1. Dislodged/displaced or Fractured Pacemaker lead
      1. Pacemaker lead displacement is most common
      2. Pacemaker leads are most prone to Fracture at the lead insertion site and under the clavicle or first rib
    2. Pacemaker syndrome (up to 20% of cases)
      1. Loss of atrial capture with only ventricle paced (atria contracts against a closed AV valve)
      2. Presents with retrograde pulsations into the neck
      3. Atrial distention results in diuresis and Hypotension
      4. Loss of Preload may result in secondary Heart Failure
      5. Symptoms include weakness, Fatigue, Dizziness, Orthostasis, Dyspnea and Chest Pain
    3. Inadequate pacer energy
    4. Twiddler's Syndrome
      1. Pacemaker patients may manipulate the Pacemaker site (subconsciously)
      2. Results in lead retraction and displacement
      3. Presentations
        1. Pacemaker failure (e.g. Syncope)
        2. Symptoms specific to new lead location (e.g. Hiccups, diaphragmatic spasm, arm twitching)
      4. Risk factors
        1. Elderly or obese (loose subcutaneous Pacemaker pocket)
        2. Dementia, Obsessive Compulsive Disorder or Developmental Delay
      5. Diagnosis
        1. Electrocardiogram (evaluate for appropriate sensing)
        2. See Chest XRay below regarding lead positioning (also observe for Fractured leads)
      6. References
        1. Jhun and Shoenberger in Herbert (2015) EM:Rap 15(7): 17
  6. Data to have available when communicating with Cardiology about a patient with possible Pacemaker-related problem
    1. Pacemaker information
      1. Most patients will have a card with Pacemaker information (device type, interrogation phone numbers)
      2. Pacemaker type can also be read from a high penetration Chest XRay
    2. Is the device a Pacemaker or Defibrillator?
    3. How many wires to heart are present?
    4. When and where was the device implanted?
  1. Most Pacemakers can not undergo MRI
    1. Risk of Arrhythmia or capture loss
    2. Certain tertiary centers perform MRI on non-MRI conditional devices with electrophysiologist present
      1. (2017) Am J Neuroradiol 38:2222 [PubMed]
  2. Abandoned leads can not typically undergo MRI
    1. Lead super-heating and local myocardial wall ablation
  3. MR Conditional Devices and leads may undergo MRI under certain conditions
    1. Most manufacturers as of 2018 produce MR conditional devices
    2. Obtain Chest XRay in advance of MRI
    3. Requires Pacemaker temporary reprogramming (off or asynchronous mode with higher rates and outputs)
    4. Expect scatter on imaging from the device (for targets near the device)
  4. References
    1. Abresch (2018) Cardiac Arrhythmia Conference, UMN, Minneapolis
  • Complications
  • Acute complications associated with placement
  1. Pneumothorax or Hemothorax (complicates 1-3% of Pacemaker placements)
  2. Myocardial perforation (with associated Cardiac Tamponade risk)
  3. Brachial nerve injury
  4. Pacemaker Infection (1-7% risk)
  5. Acute lead dislodgment (2-4% risk)
  • Complications
  • Chronic complications
  1. Atrial Fibrillation
    1. Increased risk with ventricular pacing (e.g. RV pacing)
  • References