Circulation Journal
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Superior Rhythm Discrimination With the SmartShock Technology Algorithm ― Results of the Implantable Defibrillator With Enhanced Features and Settings for Reduction of Inaccurate Detection (DEFENSE) Trial ―
Yasushi OginosawaRitsuko KohnoToshihiro HondaKan KikuchiMasatsugu NozoeTakayuki UchidaHitoshi MinamiguchiKoichiro SonodaMasahiro OgawaTakeshi IdeguchiYoshihisa KizakiToshihiro NakamuraKageyuki ObaSatoshi HigaKeiki YoshidaSoichi TsunodaYoshihisa FujinoHaruhiko Abe
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論文ID: CJ-16-1330

この記事には本公開記事があります。
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Abstract

Background: Shocks delivered by implanted anti-tachyarrhythmia devices, even when appropriate, lower the quality of life and survival. The new SmartShock Technology® (SST) discrimination algorithm was developed to prevent the delivery of inappropriate shock. This prospective, multicenter, observational study compared the rate of inaccurate detection of ventricular tachyarrhythmia using the SST vs. a conventional discrimination algorithm.

Methods and Results: Recipients of implantable cardioverter defibrillators (ICD) or cardiac resynchronization therapy defibrillators (CRT-D) equipped with the SST algorithm were enrolled and followed up every 6 months. The tachycardia detection rate was set at ≥150 beats/min with the SST algorithm. The primary endpoint was the time to first inaccurate detection of ventricular tachycardia (VT) with conventional vs. the SST discrimination algorithm, up to 2 years of follow-up. Between March 2012 and September 2013, 185 patients (mean age, 64.0±14.9 years; men, 74%; secondary prevention indication, 49.5%) were enrolled at 14 Japanese medical centers. Inaccurate detection was observed in 32 patients (17.6%) with the conventional, vs. in 19 patients (10.4%) with the SST algorithm. SST significantly lowered the rate of inaccurate detection by dual chamber devices (HR, 0.50; 95% CI: 0.263–0.950; P=0.034).

Conclusions: Compared with previous algorithms, the SST discrimination algorithm significantly lowered the rate of inaccurate detection of VT in recipients of dual-chamber ICD or CRT-D.

The delivery of appropriate or inappropriate shocks by implantable devices lowers the quality of life and increases mortality.13 The delivery of unnecessary shocks may be prevented by 3 different methods.410 First, the device may be programmed with a high ventricular detection rate and a high number of intervals to detection (NID). Second, anti-tachycardia pacing (ATP) instead of shocks may be used to terminate ventricular tachycardia (VT). Third, special algorithms are available to eliminate the false detection of supraventricular tachycardia (SVT), lead noise, T-wave oversensing (TWOS) or to abort the shock delivery for a spontaneously terminated ventricular tachyarrhythmia. The programming of a high detection rate may not be appropriate, especially in secondary prevention, because of the need to protect against clinical VT.11 ATP may accelerate a tachyarrhythmia and cause the delivery of an unnecessary shock. Therefore, a highly discriminative algorithm is essential to lower the risk of shock delivery. SmartShock Technology® (SST) by Medtronic (Minneapolis, MN, USA) is a new discrimination algorithm, which operates in conjunction with conventional algorithms.12 A recent computer modeling study confirmed its efficacy in the prevention of inappropriate treatment at high detection rate settings.13 The question, however, of whether the SST algorithm, compared with conventional discriminating algorithms, further lowers the rate of delivery of unnecessary treatment remains unclear.

The aim of this clinical study was therefore to examine the added benefit of the SST algorithm in implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy defibrillator (CRT-D) recipients.

Methods

Study Design

This study was designed as a prospective, multicenter, non-randomized, observational trial (DEFENSE Trial; UMIN-CTR#R000008332 registered on 1 February 2012), which enrolled consecutive recipients of ICD or CRT-D equipped with the SST algorithm, followed remotely or in the regular outpatient clinic every 6 months, up to 2 years after device implantation. The devices were interrogated at all scheduled and unscheduled follow-up visits. The study protocol was approved by the institutional review board of each participating center and all patients provided written informed consent to participate in the study.

Patients

The patients included in this study had a primary or secondary prevention indication for de novo implantation, replacement or upgrade of a single (VR) or dual (DR) chamber ICD or CRT-D equipped with the SST algorithm (Protecta XT ICD [DR, VR], Protecta XT CRT-D [DR] and Evera XT ICD [DR, VR]; Medtronic, MN, USA). Patients (1) whose device programming did not match the study requirements (Table 1); (2) who were unable to complete 2 years of follow-up; or (3) who were unable to provide informed consent, were excluded from the study.

Table 1. Recommended Programing
  Status Criteria Therapy
Zone
 Ventricular fibrillation ON Cycle length; no. intervals to detection Physician discretion
 Ventricular tachycardia ON Cycle length <400 ms; Physician discretion
    No. intervals to:  
     Detection: 16  
     Re-detection: 12  
SVT limit zone   Physician discretion  
PR-Logic ON    
Wavelet ON or Monitor    
Discriminator
 T-wave oversensing ON    
 Lead noise ON or ON+Timeout    

SVT, supraventricular tachycardia.

Discrimination Algorithms

Conventional Algorithms The conventional tachyarrhythmia discrimination algorithms included in DR vs. VR devices are dissimilar. First, the PR logic algorithm, available only in DR ICD/CRT-D, analyzes the atrial and ventricular rates, pattern, regularity and the A and V timing relationship on a beat-by-beat basis, to distinguish ventricular from supraventricular tachyarrhythmia. Second, the Wavelet algorithm, available only in VR ICD/CRT-D, compares the ongoing QRS waveform with the QRS template previously sampled and stored during normal rhythm. VT/ventricular fibrillation (VF) detection is withheld when the ongoing waveform matches the template to a sufficient degree. Third, the sudden onset criterion is used to detect sinus tachycardia, in which the heart rate is typically changing gradually. And fourth, the stability criterion is used to detect atrial fibrillation (AF) with rapid ventricular response by the irregularity of the RR intervals. The sudden onset and stability criteria are available in both the DR and VR devices.

SST Algorithm The SST algorithm consists of 4 main components: (1) the PR logic and Wavelet algorithm, described earlier, are available together in DR devices; (2) the TWOS discriminator analyzes changes in signal amplitude, slew rate and patterns to distinguish R wave from T wave and lower the risk of inappropriate shock delivery due to TWOS; (3) Confirmation+ analyzes the rhythm to confirm the presence of VT/VF, after the detection of VT/VF, before a shock is delivered; if it is not confirmed, the shock is aborted and the device enters a phase of redetection; and (4) the Lead noise discriminator identifies oversensing due to noise artifacts and withholds the delivery of inappropriate shocks for detection of VT/VF by analyzing the far-field electrogram to validate near-field sensing and differentiate RV lead noise from VT/VF. The SST algorithm operates along with conventional algorithms to enhance their discriminative performance. Thus, the SST algorithm has additional functions, while also including the conventional algorithms.

Device Programming

The recommended device programming is shown in Table 1. The VT detection rate was ≥150 beats/min, and the SST and conventional discriminator algorithms were programmed “ON”. The NID and re-detection NID in the VT zone were 16 and 12 cycles, respectively. The detection, NID and redetection NID in the VF zone were left to physician discretion. Therapy in the VT or fast VT zone was optional and left to physician preference. The SVT limit zone was determined according to physician discretion. Most of the devices (74%), however, were programmed to the nominal setting of 260 ms (264±18 ms). The episodes detected by the device, including the electrograms and outcomes of the discrimination algorithms, were stored.

Rhythm Classification and Episodes Analysis

Figure 1 shows the decision tree used in the analysis of tachyarrhythmia episodes. We reviewed all episodes recorded by the devices, including the decisions of the discrimination algorithms. Episodes that the conventional discrimination algorithm classified as VT/fast VT/VF were analyzed. An independent adjudication committee (Appendix) reviewed the entire episode recorded by the device, to determine whether the discrimination as well as withholding was appropriate or inappropriate. When the Wavelet algorithm was programmed on “monitor”, the episodes were classified as withheld by the SST algorithm. Inaccurate detections with the SST algorithm (Figure 1A) were compared with inaccurate detections with the conventional algorithm, defined as inaccurate detections and appropriate withholding by the SST algorithm (Figure 1A+B).

Figure 1.

Episode analysis. Episodes judged as ventricular tachycardia (VT)/fast VT (FVT)/ventricular fibrillation (VF) by the conventional discrimination algorithm were analyzed. (A) Inaccurate detection with the SmartShock Technology (SST) algorithm is compared with (A+B) inaccurate detection with conventional algorithms, defined as inaccurate detection and appropriate withholding of false VT/VF by the SST algorithm. DR, dual chamber; F, false VT/VF; T, true VT/VF; TWOS, T-wave oversensing; VR, single chamber.

Endpoints

The primary endpoint was the time to first inaccurate detection by the conventional compared with the new SST discrimination algorithm during a 2-year follow-up. The secondary endpoints were the incidence and causes of accurate and inaccurate detection of ventricular tachyarrhythmia during the entire follow-up. The incidence of inappropriate withholding of treatment for ventricular tachyarrhythmia, and all-cause mortality were also recorded.

Statistical Analysis

Continuous variables are reported as mean±SD. Between-group comparisons were performed using Student’s t-test. Categorical variables are reported as counts and percentages. Event-free survival was measured using the Kaplan-Meier method. Hazard ratios (HR) were estimated using the Cox proportional hazards model with a baseline hazard unique to each individual. Incidence ratio was estimated with the multi-level Poisson regression model, and the logarithm of days of follow-up was included as an offset. P<0.05 was considered statistically significant. All analyses were performed using STATA version 14 (StataCorp LP, College Station, TX, USA).

Results

Patients

Between March 2012 and September 2013, 14 Japanese medical centers enrolled 185 consecutive patients in this study. After the exclusion of 3 patients whose follow-up data were missing, 182 patients were included in the final analysis (Figure 2; Table 2). DR devices were implanted in 152 patients (82%). Atrial tachyarrhythmia, including AF, atrial flutter (AFl) and atrial tachycardia (AT), were observed in 56 patients (30%).

Figure 2.

Patient selection.

Table 2. Subject Characteristics (n=182)
Characteristics Mean±SD or n (%)
Age (years) 63.8±14.8
Men 135 (74.2)
Implanted devices
 ICD
  DR 99 (54.4)
  VR 26 (14.3)
 CRT-D
  DR 53 (29.1)
  VR 4 (2.2)
Medical history
 Ischemic cardiomyopathy 54 (29.7)
 Hypertension 69 (37.9)
 Stroke 10 (5.5)
 Diabetes mellitus 44 (24.2)
Arrhythmia history
 Sick sinus syndrome 17 (9.3)
 Atrioventricular block 46 (25.3)
 Atrial fibrillation 45 (24.7)
 Atrial tachycardia/flutter 11 (6.0)
Secondary prevention 90 (49.5)
Cardiovascular function
 NYHA functional class (n=181)
  I 74 (40.9)
  II 53 (29.3)
  III 42 (23.2)
  IV 12 (6.6)
 LVEF (%) (n=180) 41.2±17.3
 QRS duration (ms) (n=178) 130.0±34.2

DR, dual chamber; CRT-D, cardiac resynchronization therapy defibrillator; ICD, implantable cardioverter defibrillator; LVEF, left ventricular ejection fraction; NYHA, New York Heart Association; VR, single chamber.

Device-Detected Ventricular Arrhythmia

During a follow-up of 620±228 days, 821 episodes of VT, fast VT or VF were identified by the conventional algorithms in 69 patients. Among these 821 episodes, 608 (74%) were adjudicated by the Event Committee as true ventricular tachyarrhythmia and 213 (26%) were adjudicated as other episodes, including 26 AF/AFl, 178 episodes of sinus tachycardia or AT, and 9 episodes of TWOS.

Primary Endpoint

Inaccurate detection of ventricular tachyarrhythmia was observed in 32 patients (18%) with the conventional discrimination algorithm, and in 19 patients (10%) with the SST algorithm. Kaplan-Meier survival free from first inaccurate detection of ventricular tachyarrhythmia during the 2-year follow-up for the entire group is shown in Figure 3A. While the rate of inaccurate detection tended to be lower with the SST than with the conventional algorithm (HR, 0.56; 95% CI: 0.31–1.00), the difference did not reach statistical significance (P=0.051). In the DR device group, however, a statistically significant decrease (P=0.034) was observed in the rate of inaccurate detection of ventricular tachyarrhythmia by the SST compared with the conventional algorithm (HR, 0.50; 95% CI: 0.263–0.950; Figure 3B). In the VR device group, the 2-year rate of inaccurate detection of ventricular tachyarrhythmia by the SST algorithm was similar to that with the conventional algorithm (data not shown).

Figure 3.

Time to first inaccurate detection of ventricular tachyarrhythmia with SmartShock Technology (SST) vs. conventional algorithm in (A) the whole group (dual chamber [DR]+single chamber) and (B) the DR device group.

Secondary Endpoints

Inaccurate Detection A total of 213 inaccurate detections of ventricular tachyarrhythmia occurred in the absence of SST algorithm during the entire follow-up period, representing a mean of 1.2±4.8events/patient and a maximum of 45 events/patient (Table 3). In contrast, 164 inaccurate detections of ventricular tachyarrhythmia occurred with the SST algorithm, representing a mean of 0.9±4.2 events/patient and a maximum of 36events/patient. The incidence rate ratio of SST to conventional algorithm was 0.77 (95% CI: 0.63–0.94; P=0.012). The incident rate ratio in the DR device group was 0.70 (95% CI: 0.55–0.89; P=0.004). It is noteworthy that inaccurate detection due to TWOS was totally eliminated by the SST algorithm, and that due to AT/AF and other SVT was decreased by 11.5% and 20.8%, respectively.

Table 3. Inaccurate Detection of Ventricular Tachyarrhythmia: 2-Year Follow-up
Cause of inaccurate detection Algorithm Reduction
Conventional SST
Atrial fibrillation/flutter 26 (12) 23 (14) 3 (13)
Other SV tachyarrhythmias 178 (84) 141 (86) 37 (21)
T-wave oversensing 9 (5) 0 9 (100)
Total 213 164 49 (23)

Data given as n (%). SST, SmartShock Technology; SV, supraventricular.

The mean cycle length of the tachycardias incorrectly detected by the conventional algorithm was 365±40 ms, compared with a mean cycle length of 337±48 ms for the accurately detected tachycardias (P<0.001). The mean cycle length of the incorrectly detected tachycardias with the conventional vs. the SST algorithm was identical (365±40 ms vs. 365±40 ms).

Inappropriate Withholding A total of 8 episodes of inappropriate withholding by the Wavelet algorithm was recorded in 3 patients, of which 7 episodes were observed in 2 DR CRT-D recipients. The template-matching score fulfilled the Wavelet criterion, causing withholding despite an episode of VT. One episode ended spontaneously within 11 s and the others ended with burst pacing because the Wavelet algorithm was programmed on “monitor”.

All-Cause Mortality Over a mean follow-up of 214±162 days 16 patients died: 7 of heart failure, 4 of septicemia, 1 of tuberculosis and 4 of undetermined causes. One of these patients had experienced an inaccurate detection by the conventional discrimination algorithm.

Discussion

The major finding of this study is that there was a significant decrease in the rate of inaccurate detection of ventricular tachyarrhythmia by SST compared with conventional discriminating algorithms in DR device recipients. This superiority of SST was mainly attributable to the TWOS discriminator and Wavelet algorithms. These beneficial effects were confirmed clinically in the setting of a ventricular tachyarrhythmia detection rate ≥150 beats/min.

Previous Studies

Volosin et al described a computer modeling simulation study estimating the shock reduction rate by combining a new discrimination algorithm, greater NID and ATP preceding the shock.13 The percentage of patient who received inappropriate shock during 5 years was decreased by 15%, and the decrease in the proportion of shocks delivered for non-VT/VF episodes was 82%. It is particularly noteworthy that the computer model was applied only to episodes faster than 188 beats/min, using the data of the SCD-HeFT study,1,14 which enrolled patients with a primary prevention indication and a single detection zone.

Auricchio et al conducted a prospective, multicenter clinical trial to measure the rate of inappropriate shocks delivered in a large sample population, including patients with secondary prevention indications, and to estimate the benefit conferred by ICD/CRT-D equipped with the SST algorithm.15 They programmed the VF detection rate at 188 beats/min and left the VT therapy zone to physician discretion (59% of patients had VT zone therapy enabled). During 2 years of follow-up, 3.7% of DR and 4.8% of VR recipients received inappropriate therapy, including shocks, ATP or both. They concluded that the SST algorithm combined with the routine implementation of modern programming strategies was associated with a very low rate of inappropriate treatment delivery. The inclusion of a VT zone had no effect on the rate of inappropriate shock delivery. Therefore, they hypothesized that the discrimination algorithms prevented an increase in the delivery of inappropriate therapies in the VT zone. The performance of the SST algorithm, however, was not clinically validated in that study because of the absence of a control group with conventional algorithms.

To the best of our knowledge, this is the first prospective clinical study comparing the pure effects of the SST algorithm with conventional algorithms and controlled programming of the ICD at a slow detection rate. The setting of the tachycardia detection rate (>150 beats/min) and NID (16 cycles) was determined based on a previous study, which recommended a relatively slow detection rate.16 The present results are concordant with previous studies in terms of the contribution to inaccurate detection of ventricular tachyarrhythmia.

Advantages of SST Over Conventional Algorithms

The decrease in incorrect detection of ventricular tachyarrhythmias was mainly due to the newly added Wavelet algorithm in DR devices in order to distinguish ventricular from supraventricular tachyarrhythmias. While the TWOS discriminator algorithm is diagnostically highly capable, its impact was modest because only 9 TWOS were observed in 4 DR patients. In addition, no episode of lead noise discrimination or Confirmation+ algorithm was observed in this study. Wavelet has already been included in VR devices as a conventional algorithm. Therefore, compared with conventional algorithms, in the present study the DR device had an added advantage as a result of the SST algorithm.

SST Algorithm: Inappropriate Withholding

A total of 8 instances of inappropriate withholding were observed in 3 patients. Seven instances occurred in CRT-D recipients, perhaps because the template morphology of the CRT-D Wavelet algorithm is not automatically renewed, in contrast to the ICD, with automatic renewal of the template with its own complexes. Careful attention should be paid to the programming of the Wavelet algorithm in CRT-D recipients, in particular. To avoid inappropriate withholding by Wavelet algorithm, the following are recommended: (1) “monitor” setting before the confirmation of discrimination; (2) strict setting of matching threshold to the template; and (3) early discovery of inappropriate withholding by remote monitoring.

Study Limitations

The present sample size, especially that of the VR device group, was relatively small, and insufficient to reliably compare SST with conventional algorithms in VR devices. Second, the primary endpoint was inaccurate detection of ventricular tachyarrhythmias. A decrease in inaccurate detection is not equivalent to a decrease in inappropriate shock delivery. Third, there is a possibility that the present results depend on device settings such as tachycardia detection rate and/or NID. Finally, we analyzed only the episodes with intracardiac electrograms recorded by the devices in the present study.

Conclusions

Compared with conventional discrimination algorithms, the new SST significantly decreased the rate of inaccurate detection of ventricular tachyarrhythmias in DR ICD or CRT-D recipients. This additional feature may lower the rate of inappropriate shock delivery in clinical practice.

Acknowledgments

We thank the staff of the core laboratory and the study coordinators of each medical center for their assistance in the data collection. This study was supported by a grant from Medtronic Japan.

Disclosures

The authors declare no conflict of interest.

Author Contributions

H.A., Y.O. and R.K. had full access to, and assume responsibility for the data and for the data analysis; they also conceived of and designed the study, drafted the manuscript, and supervised the study. H.A., Y.O., R.K., T.H., K.K., M.N., T.U., H.M., K.S., M.O., T.I., Y.K., T.N., K.O., S.H. and K.Y. carried out data collection. H.A., Y.O., R.K., S.T. and Y.F. analyzed and interpreted the data. H.A., Y.O. and Y.F. carried out the statistical analysis. All authors read and approved the final manuscript.

Appendix. Events Adjudication Committee

Toshiko Nakai, MD, PhD, Associate Professor, Department of Cardiology, Nihon University, Tokyo, Japan; Mitsuaki Takami, MD, Director, Takami Cardiology Clinic, Tokyo, Japan; Haruhiko Abe, MD, PhD, Professor of Medicine, Department of Heart Rhythm Management, University of Occupational and Environmental Health, Kitakyushu, Japan.

References
 
© 2017 THE JAPANESE CIRCULATION SOCIETY
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