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Speaker -Dr Gowri shankar B
chair person – Dr Ashwini H R
 Basics of CIEDS functions “Cardiac Implanted
Electronic Devices”
 Indications for their use.
 Anaesthetic management
◦ Preoperative
◦ Intraoperative
◦ Postoperative
 Special situations
A Pacemaker is a device capable of generating artificial
pacing impulses and delivering them to the heart
Consists of a pulse generator, lead and appropriate
electrodes
 1958 : 1st battery operated pacemaker
 1969: AV sequential pacing
 1980: 1st AICD
 1985: AICD was approved by FDA
 1988: rate modulation
Pacemakers are evolving fast ..!
Pacemakers are evolving fast..!
2013
 Pulse Generator: It includes the
energy source (battery) and electric
circuits for pacing and sensory
function
 Leads: Insulated wires connecting
pulse generator and electrodes
 Electrode: An exposed metal end of
the lead in contact with the
endocardium or epicardium
Pacemaker leads as seen on fluroscopy
(Dual chamber system)
Atrial lead
Ventricular leads
 Unipolar Pacing: Current flows from the
cathode, stimulates the heart and
returns to anode on the casing of pulse
generator via the myocardium and
adjacent tissue to complete the circuit
 Bipolar Leads: Two separate electrodes,
anode (positive pole) and cathode
(negative pole), both located close to
each other within the chamber that is
being paced
 Pacing Threshold: minimum amount of energy
required to consistently cause depolarization and
contraction of the heart
 Sensitivity: The minimal voltage level of the patient’s
intrinsic R wave or P wave that must be exceeded for
the pacemaker to sense and activate the sensing
circuit of the pulse generator, resulting in inhibition
or triggering of the pacing circuit.
 Resistance: The impedance to the flow of current.
Abrupt changes in the impedance may indicate
problem with the lead system
 Pulse duration is the time in milliseconds between
the initiation and termination of the current flow
originating from the pacemaker
 Pulse amplitude is the height of the pacemaker
spike in millivolts
 Escape interval is the number of milliseconds
between the patient's own R wave and the next
paced beat
 Automatic interval is the number of milliseconds
between two pacing spikes
 Hysteresis is particularly useful in patients with sick
sinus syndrome. Hysteresis is the difference between
the escape and automatic intervals
Code Paced sensed Response Indication
example
AOO Atrium None None Sick sinus
syndrome
VOO Ventricle None None Complete HB
VVI Ventricle Ventricle Inhibited AF
DDD Both Both Inhibited AV + SA
disease
DDI Both Both Inhibited AV + SA
disease
 AICD system consists of a pulse generator and leads for
tachyarrhythmia detection and therapy
 Provides antitachycardia and antibradycardia pacing,
synchronized or nonsynchronized shocks, telemetry
and diagnostics including storing even electrograms
and history logs
 Modern ICD use transvenous lead systems for sensing,
pacing and shocks
 Cardiac arrest due to VT/VF which is not due to a
transient or reversible cause
 Spontaneous sustained VT
 Syncope with hemodynamically significant sustained
VT or VF
 NSVT with CAD, previous MI, LV dysfunction and
inducible VF or VT not suppressed by a class 1
antidysrhythmic
 Measures each R-R interval
 Categorize the rate (normal, too fast or too slow) If
sufficient number of short R-R interval within in a
period of time- will declare tachycardia episode
 Takes 5-20 seconds to sense VT/VF, another 5-15
seconds to charge. Delay 2.5-10 seconds before next
shock is administered. Total 5 shocks in a episode then
pauses
 Asynchronous pacing without rate responsiveness
 No apparent rhythm or rate change
 Continuous or transient loss of pacing
 Pacer enters diagnostic “Threshold Test Mode”
 Magnet mode disabled permanently by
programming or temporarily suspended
 Radio wave frequency between 0 -10 9 Hz and
microwaves frequency 109 – 10 11 Hz cause EMI
 Frequencies 5 -100 Hz overlap with intracardiac
signals
 Shielding of pulse generator, bipolar leads, and
filtering of incoming signals offers some protection
against EMI
 Asynchronous pacing
 Pacemaker inhibition or triggering
 Resetting or reprogramming pacemaker
 Damage to electronic circuits
 Burn injury to myocardium
 Inappropriate activation of rate adaptive feature
and anti tachycardia therapy
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
Intraoperative
Monitoring Conduct
Regional General
Postoperative
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
intraoperative
monitoring conduct
Regional General
postoperative
• Establish whether a patient has a CIED
o Conduct a focused history
o Conduct a focused physical examination
• Define the type of CIED
o Obtain manufacturer’s identification card from patient or
other source.
o Order chest x-ray studies if no other data are available.
o Refer to supplemental resources (e.g., manufacturer’s
databases).
• Determine dependency on pacing function of the
CIED
o History of symptomatic bradyarrhythmia resulting in CIED
implantation
o History of successful atrioventricular nodal ablation
• Determine CIED function
o Interrogate device
o Determine whether the device will capture when it paces
o Consider contacting the manufacturer for perioperative
recommendations
Pocket complications
Pocket hematoma
Infection
Erosion
Wound pain
Allergic reactions
Pacemaker complications
Lead dislodgement
Pneumothorax /air embolism
Cardiac perforation
Extracardiac stimulation
Venous thrombosis
Coronary sinus dissection
Twidller syndrome
Pacemaker malfunction
 Routine biochemical and hematological
investigation, coagulation screening
 Serum electrolyte measurement(specially k+ level)
 Well penetrated chest X-ray- model number of
pacemaker (radio opaque marker), integrity and
position of leads
 Baseline 12-lead ECG-
◦ No or intermittent pacing spike- own rhythm
◦ Pacing spike before every beat- pacemeker dependent
 Continue antiarrythmic drug and other cardiac drugs
as mandated
 Determine whether EMI is likely to occur during the
planned procedure
 Determine whether reprogramming pacing function
to asynchronous mode or disabling rate responsive
function is advantageous
 Temporary pacing and defibrillation equipment
should be immediately available
 Pacemaker dependent patients
 Major procedure in abdomen and chest
 Rate adaptive feature of pacemakers
 Suspension of antitachycardia function
 Surgical procedures with high chances
of EMI
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
Intraoperative
Monitoring Conduct
Regional General
Postoperative
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
Intraoperative
Monitoring Conduct
Regional General
Postoperative
 Monitoring
 Anesthetic technique
 Measures to prevent device malfunctioning
 Pacemaker failure trouble shooting
 Preparation for temporary pacemaker and
defibrillation
 ECG monitoring of a patient must include the
ability to detect pacing discharges. Artifact filtering
must be disabled so that the monitor will “paint”
pacing spikes onto the display
 Signs of peripheral perfusion-pulseoximetry or
arterial pressure waveform display
 Invasive monitoring –PAC, CVP- can dislodge when
less than 4 wks old
Regional-
 No guideline favoring or contradicting.
 Paced heart cannot compensate hypotension by
tachycardia- used cautiously
 case of pacemaker interference caused by activation of a
nerve stimulator has been reported
General anaesthesia
 Both narcotics and inhalational are safe
 Avoid using nitrous oxide, especially if CIED is reccently
inserted.
 Etomidate , ketamine should avoided
 Avoid shivering due to perioperative hypothermia
 Succinylcholine should avoided
 Non-depolarising muscle relaxant is safe
According to FDA 255 of 456 adverse events are due to
electro-cautery
The responses of pacemakers to electrocautery include:
 Inhibition of pacing
 Asynchronous pacing
 Reset to backup mode
 Myocardial burns (rare)
 VF (rare).
 Unipolar vs Bipolar vs Ultrasonic scalpel
 Distance to pulse generator
 Unipolar return pad
 Lowest energy possible in short bursts
 Generator failure: rare in a device that has previously been
evaluated and not near the end of useful battery life, unless
the generator (or leads) is struck directly by the ESU
 Lead failure :can result in undersensing , oversensing , or
failure to deliver sufficient energy to the myocardium to
produce depolarization
 Failure of capture: Myocardial changes that lengthen the
refractory period or increase the energy requirement for
depolarization can result from myocardial ischemia/infarction,
acid-base disturbance, electrolyte abnormalities, or abnormal
antiarrhythmic drug levels
 Myocardial ischaemia/infarct
 Electrolyte disturbance
 Acidosis or alkalosis
 Hypoxia or hypercapnia
 Abnormal antiarrythmic drug level especially Class
I and beta blockers
 Loss of pacing artifact in ECG in the absence of
spontaneous QRS wave
1. Absence of ‘P’or ‘QRS’ wave following atrial or
ventricular artifact in ECG
1. Pacing artifact in the middle of spontaneous ‘P’ or
‘QRS’ wave -no change in automatic interval
 Myocardial ischaemia/infarct
 Electrolyte disturbance
 Acidosis or alkalosis
 Hypoxia or hypercapnia
 Abnormal antiarrythmic drug level especially Class
I and beta blockers
 Temporary pacing can be initiated
 Disturbances in electrolyte balance, antiarrhythmic
drug levels, and acid-base equilibrium should be
investigated and corrected
 Sympathomimetic drugs can decrease depolarization
threshold or increase chronotropicity (or both)
 Causes of myocardial ischemia should be sought and
corrected
 Position defibrillation/cardioversion pads or paddles
as far as possible from the pulse generator
 Position defibrillation/cardioversion pads or paddles
perpendicular to the major axis of the CRMD to the
extent possible by placing them in an anterior
posterior location
 Use a clinically appropriate energy output
 Post shock interrogation/ reprogramming
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
Intraoperative
Monitoring Conduct
Regional General
Postoperative
Anaesthetic management
Preoperative
Assessment
History Examination Investigations
Preparation
Intraoperative
Monitoring Conduct
Regional General
Postoperative
 Device interrogation - For non-reprogrammed devices,
most manufacturers recommend interrogation to ensure
proper functioning and acceptable remaining battery life
if any electrosurgery was used
 Reprogramming- A Pacemaker that was reprogrammed
for the perioperative period should be reset
appropriately
 Monitoring- Continuously monitor cardiac rate and
rhythm and have backup pacing and defibrillation
equipment immediately available throughout the
immediatepostoperative period
 Shivering and fasciculation should be avoided
 Ventilation must be controlled and constant,otherwise
change pacemaker to asynchronous mode
 Function of pacemaker should be checked before and
after initiation of mechanical ventilation
 Coagulation current has no effect
 Cutting (high frequency) current can suppress bipolar
demand ventricular pacing
 Rx-convert preoperatively into asynchronous mode
 Therapeutic radiation can damage the complementary
metal oxide semiconductors (CMOS) that are the parts
of most modern pacemakers
 Doses in excess of 5000 rads are required to cause
pacemaker malfunction but as little as 1000 rads may
induce pacemaker failure or cause runaway pacemaker
 If pacemaker cannot be shielded from the field of
radiation, consideration should be given to
reimplanting the pacemaker generator at distant site
 Avoid focusing the lithotripsy beam near the pulse
generator
 Atrial pacing and rate adaptive function need to be
disabled
 Contraindicated in patients with piezoelectric circuit
implanted in abdominal wall
 Three types of powerful forces exist in the MRI suite
Static Magnetic Field: Torque effect on pulse generator
Radiofrequency Field (RF) :can cause interference with
pacemaker output circuits resulting in rapid pacing at
multiple of frequency between 60–300 bpm causing rapid
pacing rate
Gradient Magnetic Field: Magnetic field gradient closes
magnetic reed switch
 ECT is safe in patient with pacemaker, little current
pass through heart
 Seizures may cause inappropriate activation of
AICD and rate adaptive feature of pacemaker
 Pacemaker should be changed to asynchronous
mode, ECG monitoring is must
 In patients with inactivated AICD be prepared for
external defibrillation if VT/VF occurs
 TENS unit consists of several electrodes placed on the
skin and connected to a pulse generator that applies
20 μsec rectangular pulses of 1 to 200 V and 0 to 60
mA at a frequency of 20 to 110 Hz.
 Adverse interaction between these devices has been
frequently reported, so these patients should be
monitored during initial application of TENS
 Contact pacemaker or AICD clinic or manufacturer
 Reprogram the device function in selective group
of patients
 Monitoring and anesthesia technique with due
considerations to patients CVS status
 Avoid electrocautery use. If necessary consider use
of bipolar or harmonic scalpel
 Monitor ECG with interference. Frequently check
for pulse
 Diathermy should not be used within 15 cm from
pulse generator
 Frequency should be 1 second burst in every 10
seconds and Use minimum current
 Be sure about the availability of temporary pacing,
defibrillator and drugs for resuscitation
 Avoid drugs that cause myoclonic activity or
fasciculation
 Avoid hypothermia and shivering
 Central venous line or pulmonary artery catheter
should be used with caution
 Interrogate device following either elective or
emergency surgery at the earliest possible and
consider appropriate resetting if required
 Kaplan’s Cardiac Anesthesia:The Echo Era, 6thed.
 Millers anaesthesia, 8th ed.
 Clinical anaesthesia ,barash 5th ed.
 ATOTW 299 and 300 pacemakers and ICDs
 Yao and artusio Anesthesiology: Problem oriented
patient management 7th ed
 Short notes
Pacemakers may 2010 MD
CIED Anaesthetic Management

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CIED Anaesthetic Management

  • 1. Speaker -Dr Gowri shankar B chair person – Dr Ashwini H R
  • 2.  Basics of CIEDS functions “Cardiac Implanted Electronic Devices”  Indications for their use.  Anaesthetic management ◦ Preoperative ◦ Intraoperative ◦ Postoperative  Special situations
  • 3. A Pacemaker is a device capable of generating artificial pacing impulses and delivering them to the heart Consists of a pulse generator, lead and appropriate electrodes
  • 4.  1958 : 1st battery operated pacemaker  1969: AV sequential pacing  1980: 1st AICD  1985: AICD was approved by FDA  1988: rate modulation
  • 5.
  • 6.
  • 7.
  • 9. Pacemakers are evolving fast..! 2013
  • 10.  Pulse Generator: It includes the energy source (battery) and electric circuits for pacing and sensory function  Leads: Insulated wires connecting pulse generator and electrodes  Electrode: An exposed metal end of the lead in contact with the endocardium or epicardium
  • 11. Pacemaker leads as seen on fluroscopy (Dual chamber system) Atrial lead Ventricular leads
  • 12.  Unipolar Pacing: Current flows from the cathode, stimulates the heart and returns to anode on the casing of pulse generator via the myocardium and adjacent tissue to complete the circuit  Bipolar Leads: Two separate electrodes, anode (positive pole) and cathode (negative pole), both located close to each other within the chamber that is being paced
  • 13.  Pacing Threshold: minimum amount of energy required to consistently cause depolarization and contraction of the heart  Sensitivity: The minimal voltage level of the patient’s intrinsic R wave or P wave that must be exceeded for the pacemaker to sense and activate the sensing circuit of the pulse generator, resulting in inhibition or triggering of the pacing circuit.
  • 14.  Resistance: The impedance to the flow of current. Abrupt changes in the impedance may indicate problem with the lead system  Pulse duration is the time in milliseconds between the initiation and termination of the current flow originating from the pacemaker  Pulse amplitude is the height of the pacemaker spike in millivolts
  • 15.  Escape interval is the number of milliseconds between the patient's own R wave and the next paced beat  Automatic interval is the number of milliseconds between two pacing spikes  Hysteresis is particularly useful in patients with sick sinus syndrome. Hysteresis is the difference between the escape and automatic intervals
  • 16.
  • 17.
  • 18. Code Paced sensed Response Indication example AOO Atrium None None Sick sinus syndrome VOO Ventricle None None Complete HB VVI Ventricle Ventricle Inhibited AF DDD Both Both Inhibited AV + SA disease DDI Both Both Inhibited AV + SA disease
  • 19.
  • 20.
  • 21.  AICD system consists of a pulse generator and leads for tachyarrhythmia detection and therapy  Provides antitachycardia and antibradycardia pacing, synchronized or nonsynchronized shocks, telemetry and diagnostics including storing even electrograms and history logs  Modern ICD use transvenous lead systems for sensing, pacing and shocks
  • 22.
  • 23.  Cardiac arrest due to VT/VF which is not due to a transient or reversible cause  Spontaneous sustained VT  Syncope with hemodynamically significant sustained VT or VF  NSVT with CAD, previous MI, LV dysfunction and inducible VF or VT not suppressed by a class 1 antidysrhythmic
  • 24.
  • 25.  Measures each R-R interval  Categorize the rate (normal, too fast or too slow) If sufficient number of short R-R interval within in a period of time- will declare tachycardia episode  Takes 5-20 seconds to sense VT/VF, another 5-15 seconds to charge. Delay 2.5-10 seconds before next shock is administered. Total 5 shocks in a episode then pauses
  • 26.
  • 27.  Asynchronous pacing without rate responsiveness  No apparent rhythm or rate change  Continuous or transient loss of pacing  Pacer enters diagnostic “Threshold Test Mode”  Magnet mode disabled permanently by programming or temporarily suspended
  • 28.  Radio wave frequency between 0 -10 9 Hz and microwaves frequency 109 – 10 11 Hz cause EMI  Frequencies 5 -100 Hz overlap with intracardiac signals  Shielding of pulse generator, bipolar leads, and filtering of incoming signals offers some protection against EMI
  • 29.  Asynchronous pacing  Pacemaker inhibition or triggering  Resetting or reprogramming pacemaker  Damage to electronic circuits  Burn injury to myocardium  Inappropriate activation of rate adaptive feature and anti tachycardia therapy
  • 30.
  • 31. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation Intraoperative Monitoring Conduct Regional General Postoperative
  • 32. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation intraoperative monitoring conduct Regional General postoperative
  • 33. • Establish whether a patient has a CIED o Conduct a focused history o Conduct a focused physical examination • Define the type of CIED o Obtain manufacturer’s identification card from patient or other source. o Order chest x-ray studies if no other data are available. o Refer to supplemental resources (e.g., manufacturer’s databases).
  • 34. • Determine dependency on pacing function of the CIED o History of symptomatic bradyarrhythmia resulting in CIED implantation o History of successful atrioventricular nodal ablation • Determine CIED function o Interrogate device o Determine whether the device will capture when it paces o Consider contacting the manufacturer for perioperative recommendations
  • 35.
  • 36. Pocket complications Pocket hematoma Infection Erosion Wound pain Allergic reactions Pacemaker complications Lead dislodgement Pneumothorax /air embolism Cardiac perforation Extracardiac stimulation Venous thrombosis Coronary sinus dissection Twidller syndrome Pacemaker malfunction
  • 37.  Routine biochemical and hematological investigation, coagulation screening  Serum electrolyte measurement(specially k+ level)  Well penetrated chest X-ray- model number of pacemaker (radio opaque marker), integrity and position of leads  Baseline 12-lead ECG- ◦ No or intermittent pacing spike- own rhythm ◦ Pacing spike before every beat- pacemeker dependent
  • 38.  Continue antiarrythmic drug and other cardiac drugs as mandated  Determine whether EMI is likely to occur during the planned procedure  Determine whether reprogramming pacing function to asynchronous mode or disabling rate responsive function is advantageous  Temporary pacing and defibrillation equipment should be immediately available
  • 39.  Pacemaker dependent patients  Major procedure in abdomen and chest  Rate adaptive feature of pacemakers  Suspension of antitachycardia function  Surgical procedures with high chances of EMI
  • 40. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation Intraoperative Monitoring Conduct Regional General Postoperative
  • 41. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation Intraoperative Monitoring Conduct Regional General Postoperative
  • 42.  Monitoring  Anesthetic technique  Measures to prevent device malfunctioning  Pacemaker failure trouble shooting  Preparation for temporary pacemaker and defibrillation
  • 43.  ECG monitoring of a patient must include the ability to detect pacing discharges. Artifact filtering must be disabled so that the monitor will “paint” pacing spikes onto the display  Signs of peripheral perfusion-pulseoximetry or arterial pressure waveform display  Invasive monitoring –PAC, CVP- can dislodge when less than 4 wks old
  • 44. Regional-  No guideline favoring or contradicting.  Paced heart cannot compensate hypotension by tachycardia- used cautiously  case of pacemaker interference caused by activation of a nerve stimulator has been reported
  • 45. General anaesthesia  Both narcotics and inhalational are safe  Avoid using nitrous oxide, especially if CIED is reccently inserted.  Etomidate , ketamine should avoided  Avoid shivering due to perioperative hypothermia  Succinylcholine should avoided  Non-depolarising muscle relaxant is safe
  • 46. According to FDA 255 of 456 adverse events are due to electro-cautery The responses of pacemakers to electrocautery include:  Inhibition of pacing  Asynchronous pacing  Reset to backup mode  Myocardial burns (rare)  VF (rare).
  • 47.  Unipolar vs Bipolar vs Ultrasonic scalpel  Distance to pulse generator  Unipolar return pad  Lowest energy possible in short bursts
  • 48.  Generator failure: rare in a device that has previously been evaluated and not near the end of useful battery life, unless the generator (or leads) is struck directly by the ESU  Lead failure :can result in undersensing , oversensing , or failure to deliver sufficient energy to the myocardium to produce depolarization  Failure of capture: Myocardial changes that lengthen the refractory period or increase the energy requirement for depolarization can result from myocardial ischemia/infarction, acid-base disturbance, electrolyte abnormalities, or abnormal antiarrhythmic drug levels
  • 49.  Myocardial ischaemia/infarct  Electrolyte disturbance  Acidosis or alkalosis  Hypoxia or hypercapnia  Abnormal antiarrythmic drug level especially Class I and beta blockers
  • 50.  Loss of pacing artifact in ECG in the absence of spontaneous QRS wave
  • 51. 1. Absence of ‘P’or ‘QRS’ wave following atrial or ventricular artifact in ECG
  • 52. 1. Pacing artifact in the middle of spontaneous ‘P’ or ‘QRS’ wave -no change in automatic interval
  • 53.  Myocardial ischaemia/infarct  Electrolyte disturbance  Acidosis or alkalosis  Hypoxia or hypercapnia  Abnormal antiarrythmic drug level especially Class I and beta blockers
  • 54.  Temporary pacing can be initiated  Disturbances in electrolyte balance, antiarrhythmic drug levels, and acid-base equilibrium should be investigated and corrected  Sympathomimetic drugs can decrease depolarization threshold or increase chronotropicity (or both)  Causes of myocardial ischemia should be sought and corrected
  • 55.
  • 56.
  • 57.
  • 58.  Position defibrillation/cardioversion pads or paddles as far as possible from the pulse generator  Position defibrillation/cardioversion pads or paddles perpendicular to the major axis of the CRMD to the extent possible by placing them in an anterior posterior location  Use a clinically appropriate energy output  Post shock interrogation/ reprogramming
  • 59.
  • 60. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation Intraoperative Monitoring Conduct Regional General Postoperative
  • 61. Anaesthetic management Preoperative Assessment History Examination Investigations Preparation Intraoperative Monitoring Conduct Regional General Postoperative
  • 62.  Device interrogation - For non-reprogrammed devices, most manufacturers recommend interrogation to ensure proper functioning and acceptable remaining battery life if any electrosurgery was used  Reprogramming- A Pacemaker that was reprogrammed for the perioperative period should be reset appropriately  Monitoring- Continuously monitor cardiac rate and rhythm and have backup pacing and defibrillation equipment immediately available throughout the immediatepostoperative period
  • 63.  Shivering and fasciculation should be avoided  Ventilation must be controlled and constant,otherwise change pacemaker to asynchronous mode  Function of pacemaker should be checked before and after initiation of mechanical ventilation
  • 64.
  • 65.  Coagulation current has no effect  Cutting (high frequency) current can suppress bipolar demand ventricular pacing  Rx-convert preoperatively into asynchronous mode
  • 66.  Therapeutic radiation can damage the complementary metal oxide semiconductors (CMOS) that are the parts of most modern pacemakers  Doses in excess of 5000 rads are required to cause pacemaker malfunction but as little as 1000 rads may induce pacemaker failure or cause runaway pacemaker  If pacemaker cannot be shielded from the field of radiation, consideration should be given to reimplanting the pacemaker generator at distant site
  • 67.  Avoid focusing the lithotripsy beam near the pulse generator  Atrial pacing and rate adaptive function need to be disabled  Contraindicated in patients with piezoelectric circuit implanted in abdominal wall
  • 68.  Three types of powerful forces exist in the MRI suite Static Magnetic Field: Torque effect on pulse generator Radiofrequency Field (RF) :can cause interference with pacemaker output circuits resulting in rapid pacing at multiple of frequency between 60–300 bpm causing rapid pacing rate Gradient Magnetic Field: Magnetic field gradient closes magnetic reed switch
  • 69.  ECT is safe in patient with pacemaker, little current pass through heart  Seizures may cause inappropriate activation of AICD and rate adaptive feature of pacemaker  Pacemaker should be changed to asynchronous mode, ECG monitoring is must  In patients with inactivated AICD be prepared for external defibrillation if VT/VF occurs
  • 70.  TENS unit consists of several electrodes placed on the skin and connected to a pulse generator that applies 20 μsec rectangular pulses of 1 to 200 V and 0 to 60 mA at a frequency of 20 to 110 Hz.  Adverse interaction between these devices has been frequently reported, so these patients should be monitored during initial application of TENS
  • 71.  Contact pacemaker or AICD clinic or manufacturer  Reprogram the device function in selective group of patients  Monitoring and anesthesia technique with due considerations to patients CVS status  Avoid electrocautery use. If necessary consider use of bipolar or harmonic scalpel
  • 72.  Monitor ECG with interference. Frequently check for pulse  Diathermy should not be used within 15 cm from pulse generator  Frequency should be 1 second burst in every 10 seconds and Use minimum current  Be sure about the availability of temporary pacing, defibrillator and drugs for resuscitation
  • 73.  Avoid drugs that cause myoclonic activity or fasciculation  Avoid hypothermia and shivering  Central venous line or pulmonary artery catheter should be used with caution  Interrogate device following either elective or emergency surgery at the earliest possible and consider appropriate resetting if required
  • 74.  Kaplan’s Cardiac Anesthesia:The Echo Era, 6thed.  Millers anaesthesia, 8th ed.  Clinical anaesthesia ,barash 5th ed.  ATOTW 299 and 300 pacemakers and ICDs  Yao and artusio Anesthesiology: Problem oriented patient management 7th ed

Editor's Notes

  1. Very good afternoon every1 I welcome prf and hed of fdeptdr safiya mam, prof dr madhuri mam prof,dr umesh sir chirperson dr ashwinimam, all the staff members, senior pgs, co pgs and juniors Todays semiar topic is
  2. In the past few years electronic pacemaker systems have become extremely important in saving and sustaining the lives of cardiac patients whose normal pacing function of the heart have been impaired. Greater than 500,000 patients in the US population have pacemakers 115,000 implanted each year
  3. Dr. Rune Elmqvist designed the world's first implantable pacemaker in the yr 1958. It included a pulse generator delivering about two volts with an impulse period of two milliseconds. Av sequential pacing was inroduced in 1969 and in 1980 1st automated internal cardioverter defibrillator introduced and approved fy fda in1985
  4. In 1958, Arne Larsson (1915–2001) became the first to receive an implantable pacemaker. He had a total of 26 devices during his life and campaigned for other patients needing pacemakers
  5. Which was designed by Medtronic founder Earl Bakken in the late 1950s .
  6. This is another picture of pt with pacemaker PM-65 by Paul Zoll allowed the patient to ambulate (1955).
  7. Pacemakers are evolving fast continuously from the time of its invention, with higher technology becoming smaller n smaller, to the latest one being the capsule sized leadless paceamakers
  8. So as the no of pacemakers being implanted is incresing in huge numbers day by day we anaesthesiologist have to be ready deal with these pts.
  9. Pacemakers come with a variety of terms generally unfamiliar to us, to mention few- Mercury– Zinc batteries that were used in the early days had a short useful life (2–3 years). Currently Lithium-iodide batteries are being used which have longer life (5–10 years) and high energy density
  10. It’s a fluroscopic image showing two leads ,one in atria and other ventricle
  11. Unipolar Pacing: it has only one electrode, the cathode .Current flows from the cathode, stimulates the heart and returns to anode (positive pole) on the casing of pulse generator via the myocardium and adjacent tissue to complete the circuit. unipolar pacemaker is more likely to pick up extracardiac signals and myopotentials. Pacemaker spikes are large in this pacing Bipolar Leads: here both electrodes are located close to each other within the chamber that is being paced. As the electrodes are very close, the circuit is small and the possibility of extraneous noise disturbance is less Endocardial Pacing: Also called as transvenous pacing which implies that the leads/electrodes system has been passed through a vein to the right atrium or right ventricle. Epicardial Pacing: This type of pacing is accomplished by inserting the electrode through the epicardium into the myocardium and is generally done following cardiac surgery.
  12. Pacing Threshold: This is the minimum amount of energy required to consistently cause depolarization and contraction of the heart. it is measured in terms of both amplitude and duration for which it is applied to the myocardium. The amplitude is programmed in volts (V) or in milliamperes in some devices and the duration is measured in milliseconds. Sensitivity: The minimal voltage level of the patient’s intrinsic R wave or P wave that must be exceeded for the pacemaker to sense that R or a P wave and to activate the sensing circuit of the pulse generator, resulting in inhibition or triggering of the pacing circuit Sensing -Ability of device to detect intrinsic cardiac activity Undersensing: failure to sense Oversensing: too sensitive to activity
  13. Resistance: The impedance to the flow of current. In the pacemaker system it amounts to a combination of resistance in lead, resistance through the patient’s tissue and polarization that takes place when voltage and current are delivered into the tissues. Very high resistance can indicate a conductor fracture or poor connection to the pacemaker. A very low resistance indicates an insulation failure
  14. Hysteresis is particularly useful in patients with sick sinus syndrome. This feature allows a longer escape interval after a sensed event, giving the heart a greater opportunity to beat on its own. Here pacemaker is programmed to upper and lower rate and a programmable lower hysteresis rate.
  15. Runaway Pacemaker is pacemaker dysfunction characterized by fast and erratic spikes. This occurs with generator dysfunction due to battery failure or damage produced by leakage of the tissue fluids into the pulse generator. Treatment with antiarrhythmic drugs or cardioversion may be ineffective in such cases. It is necessary to change the pacemaker to an asynchronous mode, or reprogram it to lower outputs. If the patient is hemodynamically unstable temporary pacing should be done followed by changing of pulse generator Failure of capture because of a defect at the level of the myocardium (i.e., the generator continues to fire but no myocardial depolarization takes place) remains the most difficult problem to treat. Myocardial changes that result in noncapture include myocardial ischemia/infarction, acid-base disturbance, electrolyte abnormalities, or abnormal levels of antiarrhythmic drug
  16. Now moving on to Acc/asa recommended indications for permaanent pacemaker insertion..
  17. now to understand normal pacemaker behaviour we have to know the code. The currently used North American Pacing and Electrophysiology/British Pacing and Electrophysiology Group (NASPE/BPEG) pacemaker codes are used to describe pacemaker types and function.The original nomenclature involved a three-letter identification code, and later In 1 980, this code was extended to five letters; the last two letters can be deleted when not applicable. In 1 987, this five-letter coding system become known as the NBG pacemaker code after being adopted by both the NASPE (now known as the Heart Rhythm Society) and BPEG. The first letter describes the chamber(s) that the pacemaker can pace, the second letter describes the chamber(s) that it senses, and the third letter describes the responseof the pacemaker to sensed intrinsic activity. The last two letters describe additional features such as rate responsiveness that are commonly omitted when not used.
  18. For example, a VVI pacing mode paces in the ventricle, can sense intrinsic activity in the ventricle, and inhibits pacing when it senses intrinsic activity. A VOO pacing mode paces in the ventricle but does not sense intrinsic activity; nor does it inhibit pacing it simply paces ventricle regardless of the heart's electrical activity.
  19. Non sustained
  20. Measures each R-R interval Categorize the rate (normal, too fast or too slow) If sufficient number of short R-R interval within in a period of timeis present- will declare tachycardia episode based on the programmed algorithm and decides between antitachycardia pacing and shock Usually gives a shock of 25 joule ,Takes 5-20 seconds to sense VT/VF, another 5-15 seconds to charge. Delay 2.5-10 seconds before next shock is administered. Total 5 shocks in a episode then pauses . . Disadvantage is it may sense cautery as VF and deliver shock
  21. Application of magnet which was use earlier days is not recommedned nowadays because it can have varied effect on pace makers Like Asynchronous pacing without rate responsiveness -this is the most common behavior, no apparent rhythm or rate change Magnet mode disabled permanently by programming (possible with Biotronik, Boston Scientific, St. Jude Medical) or temporarily suspended (see Medtronic)
  22. EMI can also have varied effect on pacemakersuch as
  23. Device assessment Patient evaluation and preparation
  24. • Establish whether a patient has a CIED. o Conduct a focused history (patient interview, medical records review, review of available chest x-ray films, electrocardiogram, or any available monitor or rhythm strip information). o Conduct a focused physical examination (check for scars, palpate for device) • Define the type of CIED. o Obtain manufacturer’s identification card from patient or other source. o Order chest x-ray studies if no other data are available. o Refer to supplemental resources (e.g., manufacturer’s databases).
  25. Determine dependency on pacing function of the CIED o History of symptomatic bradyarrhythmia resulting in CIED implantation o History of successful atrioventricular nodal ablation o Inadequate escape rhythm at lowest programmable pacing rate • Determine CIED function. o Interrogate device by consultation with a cardiologist or pacemaker–ICD service clinic o Determine whether the device will capture when it paces (i.e., produce a mechanical systole with a pacemaker impulse). o also we should Consider contacting the manufacturer for perioperative recommendations.
  26. Due attention should be given to complications related pacemaker insertion perse specially wen it is implanted recently such as
  27. Determine whether EMI is likely to occur during the planned procedure Determine whether reprogramming pacing function to asynchronous mode or disabling rate responsive function is advantageous Suspend antitachyarrhythmia functions if present Advise individual performing the procedure to consider use of a bipolar electrocautery system or ultrasonic (harmonic) scalpel Temporary pacing and defibrillation equipment should be immediately available Evaluate the possible effects of anesthetic techniques and of the procedure on paccemaker function and patient pacemeaker interactions
  28. ECG monitoring of a patient must include the ability to detect pacing discharges. In their default settings, monitors often filter the pacing artifacts, and no pacing “spikes” will be shown. Artifact filtering must be disabled so that the monitor will “paint” pacing spikes onto the display Signs of peripheral perfusion-pulseoximetry or arterial pressure waveform display. Patient monitoring must include the ability to ensure that paced electrical activity is converted to mechanical systole Invasive monitoring Pulmonary artery catheter-caution (can dislodge <4wks old) Central venous line- caution. Manual palpation pulse. Capillary refilling. Trans esophageal or precordial stethoscope
  29. Based on the underlying disease case of pacemaker interference caused by activation of a nerve stimulator has been reported consider defasciculating dose of MR Fasciculations may inhibit firing due to the skeletal muscle contractions picked up by generator as intrinsic R waves
  30. Bipolar cautery should be used as much as possible ,If unipolar cautery is to be used during operation, the grounding plate should be placed close to the operative site (active cautery tip) and as far away as possible from the site of pacemaker Electrocautery should not be used within 15 cm of pacemaker Frequency of electrocautery should be limited to 1-second bursts in every 10 seconds to prevent repeated asystolic periods. Short bursts with long pauses of cautery are preferred.
  31. Recognise Assess haemodynamic status Identify the cause Manage Generator failure:rare in a device that has previously been evaluated and not near the end of useful battery life, unless the generator (or leads) is struck directly by the ESU Lead failure :unusual but reported during patient repositioning, can result in undersensing (intrinsic activity is not detected), oversensing (“detection” of events unrelated to intrinsic activity), or failure to deliver sufficient energy to the myocardium to produce depolarization (termed loss of capture). Failure of capture. Myocardial changes that lengthen the refractory period or increase the energy requirement for depolarization can result from myocardial ischemia/infarction, acid-base disturbance, electrolyte abnormalities, or abnormal antiarrhythmic drug levels
  32. Electrocardiographic tracing from a patient with a DDDR pacemaker. All ventricular pacing artifacts but one failed to result in ventricular depolarization— that is, failure to capture Causes Lead dislodgement or perforation Lead maturation(inflammation/fibrosis)(exit block) Battery depletion Circuit failure(coil fracture , insulation defect) Capture management algorithm failure Inappropriate programming Pseudo malfunction Functional non capture Metabolic , drugs , cardiomyopathies
  33. VVI pacemaker Pacing artifact present but no sensing(sensed beat doesn’t reset cycle) Causes are Defect in signal production – scar /fibrosis , BBB , ectopic , cardioversion , defibrillation , metabolic. Defect in signal transmission – lead fracture /dislodgement , insulation failure , partial open circuit. Defect in pacemaker – battery depletion , sensing circuit abnormalities , committed DVI.
  34. The response to PM failure depends on the clinical situation: a patient with a perfusing rhythm and stable vital signs can be observed while a plan is made to correct the problem. For a patient with inadequate perfusion, the following steps can be attempted (while cardiopulmonary resuscitation is in progress when appropriate
  35. Temporary pacing can be initiated, and it can be transthoracic (transcutaneous), transvenous, or transesophageal Sympathomimetic drugs can decrease depolarization threshold or increase chronotropicity (or both). Epinephrine (0.5 to 1 µg/min) or dopamine (5 to 20 µg/kg/min) should be considered. If none of the measures just presented succeed, consideration should be given to placement of epicardial leads by the surgical staff
  36. Several techniques are available to the anesthesiologist to establish reliable temporary pacing during the perioperative period or in the intensive care unit
  37. Discontinue any obvious source of EMI For external defibrillation: Position defibrillation/cardioversion pads or paddles as far as possible from the pulse generator. Position defibrillation/cardioversion pads or paddles perpendicular to the major axis of the CRMD to the extent possible by placing them in an anterior–posterior location. If it is technically impossible to place the pads or paddles in locations that help to protect the CRMD, defibrillate/cardiovert the patient in thequickest possible way and be prepared to provide pacing through other routes. Use a clinically appropriate energy output.
  38. Coagulation current used during TURP procedure has no effect, but the cutting current at high frequencies can suppress the output of a bipolar demand ventricular pacemaker. When electrosurgical unit (ESU) use is anticipated reprogramming of pacemaker preoperatively to the asynchronous (fixed rate) mode should be performed
  39. Generally Doses in excess of 5000 rads are required to cause pacemaker malfunction but as little as 1000 rads may induce pacemaker failure or cause runaway pacemaker
  40. High-energy vibrations produced by lithotripsy machine can cause closure of reed switch causing asynchronous pacing Activity’ rate responsive pacemaker can be affected due to the damage caused to the piezoelectric crystals by ESWL
  41. 1An intense static field is always present even if the scanner is not imaging. Most of the pacemakers contain ferromagnetic material, which gets attracted to the static magnetic field in the MRI and may exert a torque effect leading to discomfort at the pacemaker pocket The radiofrequency signals can cause interference with pacemaker output circuits resulting in rapid pacing at multiple of frequency between 60–300 bpm causing rapid pacing rate. It may cause pacemaker reprogramming and destruction of electronic components. It may also cause heating at the electrode-tissue boundary, which may cause thermal injury to endocardium and myocardium. MRI generally considered contraindicated in patients with pacemakers Latest models has less chance of torque effect
  42. TENS unit consists of several electrodes placed on the skin and connected to a pulse generator that applies 20 μsec rectangular pulses of 1 to 200 V and 0 to 60 mA at a frequency of 20 to 110 Hz. This repeated frequency is similar to the normal range of heart rates, so it can create a far field potential that may inhibit a cardiac pacemaker. Adverse interaction between these devices has been frequently reported, so these patients should be monitored during initial application of TENS
  43. patients undergoing elective surgery: Reprogram the device function in selective group of patients. Determine whether electromagnetic interference is likely to occur during the procedure. Determine whether reprogramming of pacemaker function needed or not
  44.  Monitor ECG with interference. Frequently check for pulse. If unipolar diathermy is to be used- Ground plate should close to operative site and away from pulse generator and close contact with skin. Diathermy should not be used within 15 cm from pulse generator. Frequency should be 1 second burst in every 10 seconds and Use minimum current Be sure about the availability of temporary pacing, defibrillator and drugs for resuscitation
  45. Pacemaker syndrome –av dysynchrony syndrome, hypotension, syncope, vertigo, light-headedness, fatigue, exercise intolerance, malaise, weakness, lethargy, dyspnoea, and induction of congestive heart failure. Cough, awareness of beat-to-beat variation of cardiac response from spontaneous to paced beats, neck pulsation or pressure sensation in the chest, neck, or head, headache, and chest pain are the other symptom