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
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
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
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
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
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
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
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
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
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
Which was designed by Medtronic founder Earl Bakken in the late 1950s .
This is another picture of pt with pacemaker PM-65 by Paul Zoll allowed the patient to ambulate (1955).
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
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.
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
It’s a fluroscopic image showing two leads ,one in atria and other ventricle
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.
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
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
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.
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
Now moving on to Acc/asa recommended indications for permaanent pacemaker insertion..
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.
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.
Non sustained
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
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)
EMI can also have varied effect on pacemakersuch as
Device assessment
Patient evaluation and preparation
• 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).
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.
Due attention should be given to complications related pacemaker insertion perse specially wen it is implanted recently such as
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
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
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
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.
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
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
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.
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
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
Several techniques are available to the anesthesiologist to establish reliable temporary pacing during the perioperative period or in the intensive care unit
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.
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
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
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
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
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
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
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
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