Discrimination Abbott

Abbott Device: ICD Field: Discrimination
  1. SINGLE CHAMBER DISCRIMINATION
  2. DUAL CHAMBER DISCRIMINATION
  3. LAST GENERATION DEFIBRILLATORS
This chapter first presents the discrimination parameters included in the older defibrillators manufactured by Saint Jude Medical and, in a second part, the modifications made in the most recent devices. 
The discriminators can be programmed in either or both VT zones but not in the VF zone.
The discrimination algorithms can be programmed to function in all, or only part of, the VT detection zones via a parameter called SVT Upper Limit.
The SVT Upper Limit defines the upper boundary of the SVT Overlap zone (i.e., the fastest rate that a patient’s SVT could achieve). Rates above this limit will not receive discrimination analysis.
The SVT Discrimination Timeout serves as a limit on the amount of time the device can consider a rhythm to be SVT before delivering VT therapy. It is a “fail-safe” feature that enables the system to override an SVT classification after the programmed timeout duration has expired and proceed to deliver VT therapy.
 

Single chamber discrimination 

The Saint Jude Medical single chamber defibrillators include 4 discrimination criteria:
  1. Sudden onset
  2. Rate stability
  3. Sinus Interval History (SIH)
  4. Ventricular complexes morphology
 
Sudden onset
 
The sudden onset criterion discriminates sinus tachycardia (gradual onset) from VT (sudden onset). This parameter, however, does not discriminate atrial fibrillation (AF) or flutter from VT.
Sudden onset criterion bases action on the past 8 intervals:
  • takes the interval average of every other detected ventricular event (4 out of 8)
  • compares the current interval average to each of the four previous interval averages
If the sudden onset difference is less than the programmed delta, the onset is classified as gradual, favoring sinus tachycardia. Otherwise, the onset is classified as sudden, favoring VT. The measurement can be programmed as an absolute value or a percentage. 
 
Rate stability 
 
The stability criterion discriminates AF (usually irregular) from VT (usually regular). It does not, however, discriminate sinus tachycardia, atrial tachycardia or atrial flutter from VT. 
The stability delta is the widest difference between the second longest and second shortest cycles, among 12 (programmable value) consecutive cycles of tachycardia detection (discards the fastest and the slowest intervals and subtracts the shortest interval from the longest interval). This measurement is always expressed as an absolute value. Rate stability is constantly re-evaluated throughout the episode. If the stability difference is less than the programmed delta, the rhythm is classified as stable, favoring VT. Otherwise, the parameter favors AF with AV conduction.
 
 
In this example: stability ignores longest (395 ms) and shortest (268 ms) intervals and subtracts second longest (378 ms) from second shortest (271 ms):  378 ms - 271 ms = 107 m (> 80 ms the programmed value); therefore interval stability indicates SVT (AF).
 
Sinus Interval History
 
The Sinus Interval History (SIH) operates in association with rate stability (programmed on: ON + SIH), in the single chamber models only. This function helps discriminate AF with long and regular ventricular cycles, operating only when the ventricular rate has been classified as stable (Interval Stability has classified a rhythm as a VT), i.e. after 12 cycles (nominal value) in the VT zone. 
The long cycles counter increases when:
  • the cycle is unclassified (either because the on-going RR interval is in the sinus rhythm zone, but not the average of 4 RR including the on-going cycle, or because the average interval is in the sinus rhythm zone but not the on-going interval);
  • the cycle is classified in the sinus rhythm zone (the on-going and the average cycle lengths are both in the sinus rhythm zone).
SIH counts the number of sinus average intervals during the detection phase and compares this count to a programmable SIH count (nominally set at 2). If more sinus intervals are counted in the detection phase than the programmable SIH count, the rhythm is classified an SVT.
 
discrimination_4.jpg
 
In this example, at detection, Interval Stability indicates VT, so SIH is checked; SIH count = 10 
2 the programmed value); SIH changes indication to SVT
Arrow indicates detection point (in this example, 12 intervals to detect)
 
Morphology
 
The analysis of the morphology has been consistently modified in the recent platforms. Until recently, the morphology was analyzed through the near-field channel. This has been modified in the contemporary devices that apply the morphology discriminator to a channel with more widely-spaced electrodes. We will present here the characteristics of morphology analysis on the old platforms (near-field signal). 
The morphology (sequence and number of positive and negative peaks and area ratios) of the ventricular complexes can be analyzed with each episode. The morphology of each tachycardia cycle is compared with a reference as soon as the episode is detected (12 cycles). Morphology compares a ventricular electrogram recorded during the tachycardia with a reference electrogram recorded in absence of tachycardia. This criterion relies on the principle that a ventricular complex produced during a SVT is likely to have the same morphology as a ventricular complex recorded during sinus rhythm. If the morphology of the tachycardia cycle is similar to the reference complex recorded during 
sinus rhythm, a percentage of similarity is assigned along with the “ν “ symbol. Otherwise, it is marked “x”. The “Morphology” criterion is constantly being re-evaluated. The onset of electrogram was used 
as the point of reference for alignment. 
If the number of similar complexes is greater than the programmed value (5 out of 8 or 7 out of 12 nominally according to the devices) the complexes are classified as conducted and the parameter favors SVT. Otherwise, it favors VT. 
 
 
Uses the four (4) largest contiguous peaks; aligns dominant peaks if polarities match; attempts alignment improvements if polarities do not match; marks the test complex a “Non-match” (e.g. assumed Ventricular in origin) if alignment fails. 
 
Example: SVT = Match (% match above 60% threshold)
The algorithm breaks the waveform apart into triangular chunks and compares the A pieces, the B pieces, etc. At each point, it determines how much discrepancy there is between template and test. In this case, there is none, which results in a 100% match. In such a scenario, the algorithm would determine the rhythm was an SVT (sinus in origin) rather than a VT.
 
Example: VT = Non-Match (35% match is less than 60% threshold)
 
Each part is compared (A to A, B to B) etc. This drawing shows how these particular pieces do not match exactly; the far right shows areas that one waveform has and the other does not (in other words, the blue areas is the one that does not match). The MD algorithm assesses this numerically; in this case, the waveforms are only a 35% match (in favor of VT).
 
MD starts its scoring process as soon as the first Tach interval is binned. Once a template is stored and MD is turned on, MD scores will be visible on real-time electrograms.
 
Combined criteria
 
Each criterion can be set on “ON”, “Stop” or “Passive”. The “Passive” mode assesses the performance of a criterion without its inclusion in the discrimination. If all criteria are set on “Passive” or “Stop”, discrimination is de-activated and therapy is delivered, regardless of the tachycardia origin. The greater the number of programmed criteria, the higher the specificity at the cost of sensitivity. Since these individual discriminators can produce conflicting results, the clinician can program the diagnosis criteria to adjudicate:
If “If All” is selected, then all three must indicate VT for VT to be declared. 
If “If 2 of 3” is selected, then two of the three discriminators being used must indicate VT for VT to be determined.

 

Dual chamber discrimination

Dual chamber devices are equipped with the same discriminators as those described previously, except for SIH, though they are applied differently, depending on the AV relationship used to classify the arrhythmia (V>A, V<A, V=A). The atrial lead enables a continuous comparison of the ventricular (i.e. the median of 12 ventricular cycles of the tachycardia episode) with the atrial rate (i.e. the median atrial rate in the same window) in order to identify the origin of the tachycardia. This comparison is the first discriminator. 
If “If Any” is selected, then the rhythm will be considered VT if any of the discriminators indicates VT.
  • V>A always diagnoses a VT/VF
  • V=A and V<A utilize SVT discriminators
  • V=A can be turned off, so that any rhythms with similar 1:1 AV response are classified as VT
The ventricular rate is faster than the atrial one in the majority (more than 80%) of the ventricular tachycardias or fibrillations, this proportion even increases with very fast rhythms. Therefore, the 2 other branches (V=A and V<A) apply for less than 20% of ventricular tachycardias.
 
VT arm (V>A)
 
When the ventricular rate is faster than the atrial rate, the tachycardia is classified as VT. No other discrimination criterion is analyzed.
 
Atrial fibrillation / flutter arm (V<A)
 
When the ventricular rate is slower than the atrial rate, one must distinguish AF, atrial tachycardia or flutter, and VT, using the following discriminators:
  • Rate stability and stability of AV association
  • QRS morphology
These discriminators may or may not be combined by programing “One of” or “All” criteria.
 
The rate stability and morphology criteria operate as described for single chamber devices. 
AV association operates on the same principle as rate stability, i.e. the AV association delta measures the difference between the second longest and second shortest AV intervals among the 12 tachycardia detection cycles.
When Interval Stability classifies a rhythm disorder as VT, AV association goes into effect.
 
 
The AV association option of the Interval Stability discriminator works by measuring the distance from a ventricular event to the atrial event that preceded it. The arrow shows the ventricular event and the atrial event that are “associated” for these purposes. The algorithm calculates these intervals for a 12-interval window, throws out the longest and shortest, then of the remaining intervals subtracts the shortest from the longest (measures time from ventricular event to the preceding atrial event and calculates the difference between the second-longest interval and the second-shortest interval). The result is compared to a programmable AV association delta value. If the AV association delta is the same or larger than the result, the rhythm disorder is classified a VT. If the difference is shorter than the programmed delta, the ventricular rhythm is associated, and the criterion favors SVT (atrial flutter or tachycardia conducted in n:1 ratio).
This criterion, intended to discriminate flutter with 2:1 or 3:1 conduction, intervenes only when the rhythm is stable, with a common programming: stability set to ON + AV delta.
 
Sinus tachycardia/atrial tachycardia arm (V=A)
 
The majority of tachycardias in the V=A with 1:1 relationship are SVT (predominance of sinus tachycardias). 
If the ventricular and the atrial rates are the same, sinus tachycardia, atrial tachycardia and VT must be discriminated, using the following criteria:
  • AV interval delta
  • Sudden onset
  • QRS morphology
When the AV Interval Delta is enabled and the rhythm is classified in the V=A Rate Branch, then AV Interval discrimination is evaluated first. The difference between the second longest and second shortest AV intervals in a recent history of tachycardia detection intervals must be less than the programmed AV Interval. 
Delta AV Interval Delta is programmable from 30 milliseconds (ms) to 150 ms (in 10 ms intervals). It was nominally ON at 60 ms in previous platforms and is now OFF in the most recent platforms.
  • If AV interval points to VT, then no other discrimination is applied, and VT therapy begins.
  • If AV interval points to SVT, then the rhythm is evaluated by 2 other discriminators in the V=A rate branch: the sudden onset and morphology criteria operating as described for single chamber devices.

These 2 criteria may or may not be associated: “One of” or “All” criteria.

In the last generation defibrillators, the chamber onset has been added in this arm (V=A)

 

Last generation defibrillators

The most recent St Jude Medical devices offer 3 new algorithms to lower the incidence of inappropriate shocks:
  • SecureSense™: discrimination of lead noise
  • Discrimination of far-field signal morphology
  • Discrimination of the chamber of onset of the tachycardia

With these new devices, the nominal discriminators have been changed:

  • single lead discrimination: onset and stability are passive (discrimination solely based on morphology)
  • dual lead discrimination: AV delta interval (A+V branch) is OFF
SecureSense™: discrimination of noise on the ventricular lead
 
The SecureSense™ algorithm compares the bipolar channel (RV distal to RV ring) with the unipolar channel (RV coil to can or RV distal to can). The Discrimination channel should have an R-wave amplitude greater than 1 mV with no noticeable myopotentials. If this is not the case with the RV coil to Can (nominal), the RV distal to can may be programmed. This algorithm operates in both the VT and VF therapy zones and has the capacity to detect short bursts of lead noise that are insufficient to reach VT/VF detection thresholds. When rapid signals are sensed on the bipolar but not on the unipolar channel, therapies are inhibited. When events are similarly classified on both channels, therapies are delivered. 
 
 
The supplemental SecureSense™ discrimination channel is activated after the sensing of 2 out of 3 cycles in the VT or VF zone. A counter is incremented with each short cycle sensed on that channel. If the discrimination channel senses short cycles (which are directly labeled VS² on the tracing), the counter is zeroed after each pair of cycles. At the time of diagnosis, if this counter is ≥10, therapy is inhibited. The counter is re-evaluated with each re-detection and before the delivery of a shock. It is de-activated after the first therapy.
 
Programming of the SecureSense algorithm
 
A warning can be programmed, which notifies the patient by vibration of the pulse generator and/or the caregiver by a remote alert (via the Merlin.net™ remote monitoring system). 
 
Far-field morphology discrimination: ShockGuard ™technology
 
The Far-field morphology discrimination (MD) algorithm uses the unipolar discrimination channel, which enables a finer analysis of the QRS morphology. The morphology of bipolar signals is often less effective than the far-field signals morphology. The bipolar signal strictly reflects local depolarization near the electrode. If the depolarization wavefront of a VT propagating near the detection dipole is similar to that of sinus rhythm, the morphology of a bipolar electrogram can be misleading. The far-field signal incorporates the depolarization of both ventricles and approaches that of a surface electrocardiogram. 
 
In this example, the bipolar morphology in sinus rhythm and during VT is close, whereas that of the far-field signal is totally dissimilar.
 
During the detection of a tachyarrhythmia, the far-field morphology discrimination algorithm examines cycle-by-cycle the unipolar discrimination channel (besides the bipolar channel) in order to compare the shape of each QRS complex on the unipolar channel with the far-field reference signal stored during sinus rhythm. From this comparison with the reference complex, a correlation score (or percentage of similarity) is calculated for each QRS recorded during the tachyarrhythmia, using 8 evenly spaced fiducial points on both electrograms. The bipolar channel is used to synchronize the measurements with the reference complex, while the unipolar channel is used to ascertain its similarity. 
 
A group of QRS complexes (eight or more) is ensemble averaged to generate a single QRS complex representative of sinus rhythm (template); offset alignment between the near field QRS complex and far field QRS complex is measured and marked on the far field QRS template; 7 additional evenly spaced correlation points along the template QRS complex are marked for future correlation use for a total of eight points.
 
 
The device automatically identifies PVCs and excludes them from the template ensemble average; ventricular extrasystoles are defined as:
  • 2 consecutive R waves without intervening P wave in DDD pacing mode;
  • RR interval <89% of the mean of 16 cycles
R waves following ventricular pacing are excluded.
The heart rate must be also lower than 120 bpm.
 
Periodic and automatic updates adjust the template ensemble average for changes in sinus morphology (more frequent and more progressive update of the reference morphology). Each new template update averages in the new representative QRS complex as 1/16th of the overall sinus QRS template.
To enable the update of the reference (automatic template updates) in the event that a template has not been acquired in more than a week due to high % pacing demands and to encourage intrinsic activity:
  • temporarily lengthens the AV Delay
  • temporarily turns off Negative Hysteresis
  • in VVI mode, temporarily decreases the Base Rate
The rate and AV delay hysteresis used to acquire the reference signal are programmable.
 
If the amplitude of the far-field signal is <1 mV, it should not be used in the update, a warning dialogue will appear suggesting to try the other configuration (RV tip - can). 
 
Identification of the source of onset of tachycardia
The sudden onset criterion is currently the same in single and dual chamber defibrillators, based on the ventricular rate and mean intervals only. In the A = V arm, sudden onset only discriminates sinus tachycardia, and is systematically confused by atrial tachycardias. 
This new algorithm applies simultaneously the atrial and ventricular intervals to identify the chamber responsible for the arrhythmia sharpening the discrimination between SVT and VT and, in particular, the discrimination of the following rhythms: 
  • Atrial tachycardia with 1:1 conduction;
  • Atrial fibrillation;
  • Atrial flutter
The discrimination by initial chamber is available in the last generations of dual and triple chamber St. Jude Medical™ defibrillators, in the V = A rate arm.
 
Algorithm operation 
 
In order to identify the source of arrhythmia and detect a significant increase in heart rate, the algorithm analyzes the atrial and ventricular channels simultaneously. The arrhythmia is classified as SVT or VT on the basis of 1) the chamber where it emerges first, and 2) the speed at which the heart rate increases. Gradual rate acceleration is classified as SVT. If the acceleration is sudden and starts in the atrium, it is classified as SVT. If the acceleration is sudden and starts in the ventricle, it is classified as VT.
Analysis of the atrial and ventricular rate to detect a sudden onset in both chambers:
  • Rate increase: > 40 ms decrease in the instantaneous cycle length;
  • 5 previous cycles with a > 20% difference in cycle length;
  • 5 next cycles with a > 10% difference in cycle length;
If the atrial sudden onset precedes the ventricular sudden onset by >8 ms → SVT
 
 

Theoritical features / Basic concepts

Discrimination in Single Chamber ICDs Discrimination in Dual Chamber ICDs   ICD Discrimination ALGORITHMS When programming an ICD, particular attention should be paid to the risk of inappropriate therapies. Modern ICDs offer several advanced criteria, which, alone or combined, can discriminate VT from SVT. The “heart rate” criterion cannot safely be used alone, as its specificity for the diagnosis of ventricular tachyarrhythmias is only 60%, while its sensitivity can be easily increased to 100%. Moreover, the lower the programmed VT zone, the lower its specificity. Without other discrimination criteria, the therapy will be delivered irrespective of the origin of the tachycardia. The VF zone is typically reserved for very high rate and left without other intervening criteria, which are...

Abbott paths associated with this specificity

Patient, recipient of a St Jude medical Current DR ICD was hospitalized for palpitations and an ICD shock.

This 64-year-old man, presenting with ischemic cardiomyopathy and episodes of sustained VT, received a St Jude medical Atlas single chamber ICD for secondary prevention and was seen for a routine follow-up.

Main programmed parameters

This 73-year old recipient of a St Jude medical Fortify single chamber ICD implanted for hypertrophic cardiomyopathy, a history of aborted sudden cardiac death and episodes of paroxysmal atrial fibrillation (AF) were discovered on a routine follow-up.

Main programmed parameters

This 71-year-old recipient of a St Jude medical Analyst Accel single chamber ICD implanted for primary prevention in the context of ischemic cardiomyopathy suffered from episodes of paroxysmal AF and was seen on routine follow-up.

Main programmed parameters

This 54-year-old man, recipient of a St Jude medical Atlas single chamber ICD implanted in the context of hypertrophic cardiomyopathy with a 32-mm thick septum, episodes of non-sustained VT and failure to adapt the blood pressure during exercise, was seen for a routine follow-up visit.

Main programmed parameters

This 66-year-old recipient of a St Jude medical Promote Accel CRT-D implanted for advanced dilated cardiomyopathy with a 30% LVEF and New York Heart Association functional class III, underwent His bundle ablation for chronic AF and was seen for a routine follow-up visit.

Main programmed parameters

This 44-year-old patient, recipient of a St Jude medical Atlas dual chamber ICD, implanted for primary prevention in the context of ischemic cardiomyopathy and a 27% LVEF, was seen for routine follow-up.

Main programmed parameters

This 77-year-old man, recipient of a St Jude medical CRT-D implanted for idiopathic dilated cardiomyopathy, a LVEF at 30%, a wide QRS and a prolonged PR, was seen for a routine follow-up. 

Main programmed parameters

A 38-year-old man presenting with hypertrophic cardiomyopathy underwent implantation of a St Jude medical Fortify dual chamber ICD after suffering an episode of aborted sudden death. He was seen in consultation, complaining of palpitations.

Main programmed parameters

A 41-year-old man suffering from advanced ischemic cardiomyopathy, recipient of a St Jude medical CRT-D implanted for secondary prevention of VT complicated by syncope, was seen for a routine follow-up.

Main programmed parameters

This 58-year-old lady received a St Jude medical Promote Accel CRT-D in the context of advanced idiopathic dilated cardiomyopathy with left bundle branch block and a history of AF ablation. She was seen in consultation, complaining of palpitations.

Main programmed parameters

This 51-year-old man presenting with a severely dilated cardiomyopathy, recipient of a St Jude medical dual chamber ICD, was seen in consultation for evaluation of palpitations.

A 33-year old recipient of a St Jude medical dual chamber ICD implanted for multiples episodes of VT refractory to treatment with beta-adrenergic blockers, in the context of arrhythmogenic right ventricular dysplasia, was seen in consultation after receiving multiples shocks during exercise.

Main programmed parameters

This 68-year old man, recipient of a St Jude medical CRT-D implanted in the background of dilated cardiomyopathy with conduction abnormalities and a history of paroxysmal AF, was seen for routine follow-up;

Main programmed parameters

This 69-year-old man suffering from ischemic cardiomyopathy received a St Jude medical Fortify dual chamber ICD for primary prevention and was seen for a routine follow-up.

Main programmed parameters

This 68-year-old woman, recipient of a St Jude medical Promote Accel CRT-D implanted in the context of dilated cardiomyopathy with left bundle branch block, had a history of paroxysmal AF and His bundle ablation and was seen for a routine follow-up.

Main programmed parameters