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Anesthesia in patients with CIED*
in noncardiac surgery
*CIED: Cardiovascular Implantable Electronic Device (pace maker,ICD,CRT)
Dr. H. Moshtaghion Associated professor of Cardiac
anesthesia Yazd university
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Pacemakers
• A pacemaking system consists of an impulse generator
• and leads to carry the electrical impulse to the patient’s
• heart. Leads are connected to the heart’s chambers through
• the vena cava (transvenous leads), or they are directly
• sewn onto the surface of the heart (epicardial leads). Leads
• can be unipolar (one electrode per lead), bipolar (two electrodes
• per lead), or multipolar (multiple electrodes and
• wires contained within one lead with connections in multiple
• chambers)
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PACEMAKER CODE
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Pacemaker Indications
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Magnet
• Despite often repeated folklore, most PM manufacturers
• warn that magnets were never intended to treat PM
• emergencies or prevent the effects of EMI. Rather, magnet activated
• switches were incorporated to produce pacing
• behavior that demonstrates remaining battery life and,
• sometimes, pacing threshold safety factors.
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Predicting remaining battery life
• IFI(Intensified follow up)
• ERT(ERI)elective replacement time
• EOL (End of life)
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Threshold margin test(TMT)
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• Identify the generator manufacturer and model (pacemaker, transvenous
defibrillator, subcutaneous defibrillator) of the cardiovascular implantable
electronic device (CIED).
• Establish preoperative contact with the patient’s CIED physician or clinic to
obtain appropriate records and a perioperative prescription (Heart Rhythm
Society [HRS]).
Have the CIED interrogated (American Society of Anesthesiologists [ASA]) by a competent authority shortly before the anesthetic regimen.
Preoperatively
Anesthesia consideration
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• Obtain a copy of this interrogation. Obtain a perioperative prescription from the
CIED physician (HRS). Ensure that implantable cardioverter-defibrillator (ICD)
treatment settings are appropriate and that the CIED will pace the heart.
• Consider replacing any CIED near its elective replacement period in a patient
scheduled to undergo either a major surgical procedure or a surgical procedure
where monopolar electro surgery will be used within 25 cm of the generator.
• Determine the patient’s underlying rate and rhythm to determine the need for backup (external) pacing support.
Preoperatively
Anesthesia consideration
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• Ensure that all magnet behavior (pacing, suspension of shock
therapy) is appropriate if magnet use is planned.
• Program minute ventilation rate responsiveness “off,” if present.
• Consider increasing the lower rate limit to provide optimal oxygen
delivery for major procedures.
Preoperatively
Anesthesia consideration
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• If electromagnetic interference is likely,
(1) disable antitachycardia therapy if a defibrillator is present and
(2) consider asynchronous pacing for some pacing dependent
patients.
Magnet application may be acceptable for some ICDs (disable
antitachycardia therapy) or pacemakers (provide asynchronous
pacing).
Asynchronous pacing from an ICD always requires reprogramming.
Preoperatively
Anesthesia consideration
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Intraoperatively
Anesthesia consideration
• Monitor cardiac rhythm with the pulse oximeter (plethysmography) or arterial
waveform analysis.
• Consider disabling the “artifact filter” on the electrocardiogram monitor.
• Ask the surgeon to operate without the monopolar electrosurgical unit (ESU).
• Use a bipolar ESU if possible; if not possible, then pure “cut” electrosurgery is
better than “blend” or “coag,” and ESU should be applied in short bursts (<4 seconds) separated by at least 2 seconds.
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Intraoperatively
Anesthesia consideration
• Place the ESU dispersive electrode in such a way to prevent
electricity from crossing the generator-heart circuit, even if the
electrode must be placed on the distal forearm and the wire covered
with sterile drape.
• If the ESU causes ventricular oversensing with pacing quiescence
or atrial oversensing with inappropriate ventricular pacing, limit the
effect by using short ESU bursts, relocating the dispersive electrode, or placing a magnet over the pacemaker
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• Some patients require postoperative interrogation, especially if
preoperative reprogramming took place. For “low-risk cases,” HRS
(but not ASA) states that this interrogation can take place in an
ambulatory setting up to 1 month postoperatively.
Some rate enhancements can be reinitiated, and a determination of
optimum heart rate and pacing parameters should be made. Any
patient with disabled antitachycardia therapy must be monitored until the antitachycardia therapy is restored.
Postoperatively
Anesthesia consideration
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GLOSSARY Atrioventricular Delay
Lower Rate Limit
(LRL, also Automatic Rate or Programmed Rate)
Upper Tracking Rate
(UTR, also called Upper Rate Limit or URL)
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GLOSSARY…
Hysteresis
ICD (Implantable Cardioverter-Defibrillator) Mode
Mode Switch
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GLOSSARY…
Oversensing
Undersensing
Rate Modulation
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IMPLANTABLE CARDIOVERTER DEFIBRILATOR
• ICDs can work as defibrillator ;ATP and pacemaker
• It has been proven defibrillation is superior to drug therapy
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Icd code
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Indication
• Ventricular tachycardia
• Ventricular fibrillation
• Brugada syndrome (right bundle branch block, ST-segment
• elevation in electrocardiographic leads V1 to V3)
• Arrhythmogenic right ventricular dysplasia
• Long QT syndrome
• Hypertrophic cardiomyopathy
• Prophylactic use in the patient who has CM without electrophysiologic
• testing to justify placement: MADIT II (EF <30%,
• ischemic CM)98; MUSTT (EF <40%, ischemic CM with nonsustained
• ventricular tachycardia)97; SCD-HeFT (EF <35%, and
• CM of any cause)3
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Magnet behavior
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PREANESTHETIC EVALUATION AND REPROGRAMMING
• Management of comorbidity
• Interrogation or contact with CIED physician
• IF there is need for elective replacement
• Antithachycardia therapy should be disabled in the presence of ESU
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Intra and postoperative consideration
• Ability to deliver cardioversion and defibrillation
• Interrogation after surgery
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Diagnosis of VT from SVT include the following • 1. Onset criteria: In general, onset of VT is abrupt, whereasonset of SVT has
sequentially shortening R-R intervals.
• 2. Stability criteria: In general, the R-R interval of VT is relativelyconstant, whereas the R-R interval of atrial fibrillationwith rapid ventricular response is quite variable.
• 3. QRS width criteria: In general, the QRS complex widthin SVT is narrow (<110 msec), whereas the QRS widthin VT is wide (>120 msec).
• 4. “Intelligence” in dual-chamber devices attempts toassociate atrial activity with ventricular activity.
• 5. Morphology waveform analysis includes comparisonwith stored historical templates.
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