Printer Friendly

Extended Use of the Wearable Cardioverter-Defibrillator: Which Patients Are Most Likely to Benefit?

1. Introduction

The implantable cardioverter-defibrillator has firmly established itself as a treatment option for patients at high risk for life-threatening ventricular tachyarrhythmias. In fact, several large randomized-controlled studies have supported its efficacy in preventing sudden cardiac death (SCD) and in reduction of mortality in patients with ischemic cardiomyopathy (ICM) and an ejection fraction (EF) [less than or equal to]35% at least 6 weeks after the ischemic event or nonischemic cardiomyopathy (NICM) and an EF [less than or equal to]35% after at least 3 months of optimal medical therapy (OMT) in primary prophylaxis [1-5]. The place for ICDs in secondary prophylaxis is clear, and it is indicated when a hemodynamically relevant tachycardia is diagnosed without a reversible cause or within 48 hours of an ischemic event [6-8]. Several controversies remain, however, regarding the optimal use of ICDs in primary prevention. In

particular, questions of risk stratification, including the optimal time point for implantation, are unresolved yet.

Moreover, there are clinical scenarios where the use of an implantable cardioverter-defibrillator (ICD) is not possible.

The wearable cardioverter-defibrillator is a noninvasive device used temporarily for the prevention of SCD in presumed high-risk patients, which do not meet ICD implantation criteria on the basis of current guidelines. So far, only one wearable cardioverter-defibrillator (WCD) is approved for clinical use (LifeVest, ZOLL, Pittsburgh, Pennsylvania, USA). The device is a wearable vest with built-in electrodes for rhythm sensing, and pads in case a shock must be delivered [9,10]. The WCD can detect ventricular tachycardia and ventricular fibrillation using an algorithm based on programmable heart rate cut-off values and ECG morphology analysis. Arrhythmia detection initiates a series of warnings before treatment ensues (Figure 1). Current recommendations, however, do not specify on the suggested WCD use duration except for ICM (40 days) [5]. On the contrary, WCD use is only a temporary protection against SCD. Prolonged use is defined as longer than the current recommended waiting period before implantation of an ICD, which is 3 months in the case of NICM and 40 days after the index event for ICM [11].

The aim of this study was to provide a systematic analysis of the published data on WCD-recorded appropriate shocks in different patient cohorts for extended time periods. The focus of our investigation was device wear length and time to the first appropriate shock. Our goal was to provide an overview of current data on prolonged WCD use in available literature and point out specific populations which seem to benefit most from it.

2. Methods

Studies were identified searching PubMed from the start of the database until the end of 2017 using the term "wearable cardioverter defibrillator" or "wearable cardioverter-defibrillator" and "wcd." Only English-written articles were considered. Abstracts of all search results were screened and only original clinical studies, excluding case reports and small case series with n < 10 patients, were analyzed. All original articles examining the clinical use of WCD were screened for baseline characteristics, number of appropriate shocks, available median and maximal WCD wear times, for the median time to the first appropriate shock, and maximal time to the first appropriate shock. Our objective was to describe the prevalence of prolonged WCD use and the possible benefit of prolonged use. Prolonged use was defined based on current guidelines as longer than the recommended waiting period to ICD implantation, if indicated: 3 months in case of NICM and 40 days in case of ICM. Since no randomized clinical trials are available on this subject, only studies reporting either maximal wear time or median and maximal time to the first appropriate shock were included in our study, thus providing a summary of prolonged use of WCD and its potential benefit for specific populations.

3. Results

The PubMed search resulted in a total of 127 publications. 101 were either not clinical studies or did not report on WCD use. The remaining 26 articles were screened, and 15 publications met the inclusion criteria. One study was excluded because of conflicting numbers reported in the dataset (the authors could not be reached for clarification) [12]. Study selection is shown in a flow chart in Figure 2.

The investigated 14 clinical studies were published between 2010 and 2017 (Table 1). 12 studies were retrospective based on registries, and data were collected by the manufacturer of the WCD device [13-24]. One study was a prospective observational investigation [25], and one study prescribed the WCD according to a prespecified algorithm and prospectively followed the study population [26]. Of the retrospective studies, one was labelled a review [24], but also reported on WCD experiences in Germany and fulfilled inclusion criteria. The main inclusion criterion in all studies was obviously WCD use, although the indications for use were variable. Seven studies included patients with any underlying heart disease as indication for WCD use, although one only included young patients, one only included patients of hemodialysis, and one examined patients with device infection only. The remaining five studies included patients with peripartum cardiomyopathy (PPCM), heart failure in general, and patients with ICM or NICM (Table 1).

The size of study populations ranged from 49 to 8453 patients in the investigated studies, and a total of 22908 patients were primarily reviewed for this analysis. All studies reported the median wear time (in 3 studies mean wear time [16,21,24]) ranging from 16 to 394 days and numbers of appropriate shocks (ranging from 0 to 309). Ten studies were reported on maximal wear time. 4 studies reported both median and maximal time to the first appropriate shock.

The prevalence of prolonged use was not specifically reported in either of the studies, except for the study of Lamichhane et al. which specifically only included long-term WCD users [18]. However, since three studies reported median wear times over 90 days and further six reported median wear times over 40 days, depending on the underlying condition prolonged use of WCD was highly prevalent. The shortest and longest median and maximal wear times and the shortest and longest maximal time to the first shock are summarized in Table 2.

The number of appropriate shocks per total study population varied greatly among the different indications. The highest rate observed was in patients on hemodialysis (136 appropriate shocks in 75 patients) [21]. A high rate was also observed in the study investigating patients with PPCM (5 appropriate shocks in 49 patients) [16]. No appropriate shocks were reported in one cohort with NICM, the only underage cohort ([less than or equal to]18 years), and in a mixed cohort of patients with heart failure [14,19,23]. Further study characteristics are illustrated in Table 1.

4. Discussion

We here provide the first systematic review of published data on prolonged WCD use in clinical practice and patients most likely to benefit from it.

4.1. Ischemic Cardiomyopathy. From the published data, it is evident that prolonged use of WCD was rarely reported in patients with ICM and ejection fraction [less than or equal to]35%. This is not surprising, considering current guidelines giving an IA indication for ICD implantation 3 months after an MI or PCI/ CABG with persistent symptomatic systolic heart failure based on the SCD-HeFT and MADIT-II trials [1,2,11]. Of the reviewed studies investigating WCD use in patients suffering from ICM, the majority report short median wear times and short times to the first appropriate shock. Epstein et al. reported a median time to the first appropriate shock of just 9 days after the start of the WCD use, which lies within the 40 days required by current guidelines before ICD implantation [22].

Singh et al. however report that only half of all shocks were in the first 40 days after an index MI suggesting that several cases of malignant arrhythmia occur after the initial waiting period. This difference to Epstein's results cannot clearly be explained, since EF and medication (including antiarrhythmic drugs) were not universally reported.

Furthermore, the event rates differed by a factor of 2 between the two studies. Similar to what Singh et al. reported, appropriate shocks reported after an ischemic event occurred within 40 days in a European cohort investigated by Kondo et al. (not fulfilling inclusion criteria for primary analysis of this study) [27].

Lamichhane et al., on the contrary, specifically investigated the use of WCD beyond three months. In their study population, 35% had ICM, and the main reason for prolonged use was ongoing evaluation for ICD implantation. Only 6 patients received appropriate shocks in this cohort, and the authors, however, did not report the time of the events/shocks [18]. In light of this data, patients suffering from ICM seldom benefited from prolonged use of WCD. On the contrary, WCD possibly has benefits in the first 40 days after MI where the risk of SCD is reported to be up to 5% [28]. The recently published VEST [29]was the first randomized clinical trial assessing this question. They found no benefit in the prevention of SCD with the use of WCD in addition to guideline-directed therapy in the early stages after myocardial infarction, although therapy adherence was low. This result underscores the problem of patient selection and ensuring compliance and adherence to therapy.

4.2. Nonischemic Cardiomyopathy. The reported wear time for NICM was generally longer compared to ICM in the reviewed studies [13,15,19,25,30]. A direct comparison of the ICM and NICM population was subject only in the study of Singh et al. They noted that, within their total population, the wear time was significantly longer for NICM patients compared to ICM patients. The authors, however, did not observe shocks in this cohort. Chung et al. also did not report any shocks in the NICM subpopulation [15]. Wafinig et al. found the longest wear times in the NICM subgroup but also low rates of appropriate shock. The WEARIT-II study reported 927 patients with NICM and WCD use. They report 1% arrhythmic events in this subpopulation, which was similar to Singh et al. and Wafinig et al.'s data, and significantly less than for the ICM patient subpopulation.

In light of the DANISH study [31], the question arises whether a prolonged waiting/risk stratification period and establishment of OMT is warranted in this subgroup, before ICD implantation is considered. The prolonged study specifically examined patients with HFrEF after 3 months of WCD use with the goal of preventing unnecessary ICD implantations. An extended therapy was used in patients who did not yet have OMT or showed an improvement of EF since previous visit but still had an EF [less than or equal to]35%. At the end of the follow-up (median 9 months), 33% of patients showed an improvement of EF to >35% [32]. They observed improvement more often in the NICM patients than ICM patients.

A further analysis from the WEARIT-II registry investigated patients using the WCD beyond 90 days and found a higher rate of extended use in NICM patients and furthermore discovered a further improvement in EF and thus obviating the need for an ICD in one-third of their patient cohort [33]. So far, the optimal timing of ICD implantation in NICM patients is still under debate. Whether prolonged WCD use in NICM patients is an option to prevent unnecessary ICD implantations, while minimizing the risk of sudden cardiac death remains an open question [34-36]. Hopefully, the currently recruiting HF-Opt trial (NCT03016754) examining EF improvement beyond 90 days of WCD use will hopefully provide some additional information on this subject.

Another possible indication for WCD use is PPCM, which however may have been reported in previous cohort investigating NICM as well. Duncker et al. provided the study examining only patients with PPCM [16]. They report a high prevalence of appropriate shocks. In contrast, in a study, Saltzberg et al. (not meeting inclusion criteria for primary analysis) compared patients with PPCM to NICM of other aetiology. The 107 patients included in their analysis wore the WCD 75 [+ or -] 81 days and had no events requiring intervention from the device [37]. It is noteworthy that this study was a retrospective analysis with patient inclusion based on the International Classification of Diseases coding and not according to current ESC criteria which may explain the much lower event rate compared to what Duncker et al. reported from their prospective study. Although the few other patient characteristics reported by all of the aforementioned three studies were similar (age, baseline EF, and parity), a more precise comparison is not feasible due to pronounced differences in methodology, reported variables, and outcome measures. Of note, another study reporting on cases of PPCM also reported on a high rate of appropriate shocks during prolonged wear time [38].

Current ESC guidelines recommend ICD implantation following standard guidelines for NICM, but also refer to WCD treatment (recommendation level class IIb). This is particularly noteworthy since EF recovery can be expected in a high rate of PPCM patients [11].

4.3. WCD in Patients with Device Infection. Data regarding WCD use and device removal were available in 6 studies, while Tanawuttiwat et al. only examined this cohort [13,15,20,21,24,25]. The largest number of patients examined was provided by Wassnig et al. [13]. Compared to the study of Ellenbogen et al. not meeting inclusion criteria for primary analysis, the median wear time was comparable but longer than what Tanawuttiwat et al. reported. Ellenbogen et al. demonstrated that 22% of their patients wore the WCD for over 3 months without reporting on the indication for this [39]. For obvious reasons, a prolonged wear time is only necessary in selected cases since the indication for ICD implantation has previously been made. Still an extended use is clearly indicated until the infection abates and surgery is again possible.

4.4. Heart Transplantation. Bridging the time to heart transplantation is another possible indication for WCD use [23, 24]. Although the reported number of appropriate shocks was low, since the perioperative risk of ICD implantation is especially high, these patients could especially benefit from extended WCD use. The ESC guidelines recommend an ICD implantation for all patients listed for transplant in a New York Heart Association class IV, whereas WCD use as a bridge to transplant is an alternative (recommendation level class IIa and IIb, respectively). In our opinion, extended wear for secondary prophylaxis of SCD is also an option in these patients.

4.5. Renal Failure. There are other, less frequent indications for WCD use. Wan et al. investigated patients on hemodialysis [21]. This patient group is not included in most pivotal ICD trials. They found that the main reason for WCD use was active infection and contraindication for ICD implant in this cohort, but they also pointed out that majority of patients used the device for an extended period of time until EF improvement or ICD implantation. Patients with end-stage renal disease represent a high-risk population for ICD implantation explaining the impressively high prevalence of arrhythmic events during the study period. Nevertheless, the same guidelines apply for ICD implantation in these patients as for the general population. Thus, prolonged WCD use was only considered in few cases in available literature.

4.6. Myocarditis. Myocarditis was infrequent in the reviewed studies. Only two studies were reported on wear time [13,25]. The current ESC guidelines give a weak recommendation for the use of WCD in these patients, similar to the PPCM population. Given the excellent long-term outcome of patients with myocarditis who recover from the impaired cardiac function, prolonged WCD use may be reasonable in this population.

4.7. Inherited Channelopathies. Few patients with channelopathies or congenital heart diseases were included in the assessed studies [15, 24, 25]. It seems prudent to thoroughly evaluate these patients before ICD implantation, while protecting them from SCD if necessary. To facilitate a safe risk stratification, WCD might be an option. Depending on the phenotype of underlying disease, this stratification period can be rather long depending on clinical judgment.

4.8. Children and Adolescent. Another population who may benefit from an extended use of WCD is children and younger adults. While they may have the highest lifetime benefit of an ICD implantation if indication is made correctly, they are also at higher risk of ICD complications such as multiple battery changes and thus increased risk of infection. Collins et al. examined a population [less than or equal to]21 years of age with a WCD use for any indication. The main causes of increased arrhythmogenic risk were cardiomyopathy, primary arrhythmia (without specification), and congenital heart disease especially in the [less than or equal to]18 years of age cohort. Since at the end of their study only 32% of patients had an ICD implanted, prolonged WCD use might be justified [14].

4.9. Summary of Reported Prolonged WCD Use. Several patient populations were reported to use the WCD for an extended period. Some subgroups were more prevalent probably due to the (assumed) reversibility of their elevated arrhythmogenic risk. In general, patients not yet receiving an OMT deserve a chance to improve their ejection fraction while being protected from SCD events. Patients possibly benefiting prolonged use after review available literature may be patients with PPCM and young patients in order to avoid unnecessary ICD implantation. These patients may be at higher risk of dying from SCD than dying of other cause, yet ICD implantation should be carefully evaluated after establishing OMT.

Clinicians also have to take into account patients' choice to refuse ICD while accepting a longer WCD use. The prolonged use of WCD in patients with NICM seems less clear particularly due to low treatment rates reported. There are several disadvantages of a prolonged WCD use. Wear comfort is an obvious problem especially over longer periods. The absence of pacing modalities (for bradycardia, antitachycardia pacing, or postshock pacing) can be an issue and fail to prevent SCD due to asystole. Lastly, a cost-benefit analysis is necessary to justify a longer WCD use.

4.10. Limitations. Our analysis has several limitations. The heterogeneity of clinical studies, which resulted in missing data on the time of appropriate shocks, is a limitation of this study. 11 of the 14 studies reported the database kept by ZOLL. It is therefore possible that patients fulfilling inclusion criteria for more than one of the listed studies in Table 1 were reported more than once.

5. Conclusions

Extended use of WCD is commonly reported in reviewed literature, although majority of it is of descriptive nature. Patients most likely to wear the device longer than 3 months seem to be patients with NICM, specifically PPCM likely due to the lack of other significant comorbidities and the high rate of disease improvement beyond the first 3 months often obviating the need for ICD implantation. On the contrary, patients listed for heart transplantation could also benefit from prolonged therapy to avoid risks of the more invasive ICD implantation. Question remains, however, what the rate of appropriate shock is during this prolonged use, if a true benefit is present compared to ICD implantation. To assess this true benefit, prospective and randomized data are needed.

https://doi.org/10.1155/2018/7373610

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

[1] G. H. Bardy, K. L. Lee, D. B. Mark et al., "Amiodarone or an implantable cardioverter-defibrillator for congestive heart failure," New England Journal of Medicine, vol. 352, no. 3, pp. 225-237, 2005.

[2] A. J. Moss, W. Zareba, W. J. Hall et al., "Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction," New England Journal of Medicine, vol. 346, no. 12, pp. 877-883, 2002.

[3] A. Kadish, A. Dyer, J. P. Daubert et al., "Prophylactic defibrillator implantation in patients with nonischemic dilated cardiomyopathy," New England Journal of Medicine, vol. 350, no. 21, pp. 2151-2158, 2004.

[4] A. S. Desai, J. C. Fang, W. H. Maisel, and K. L. Baughman, "Implantable defibrillators for the prevention of mortality in patients with nonischemic cardiomyopathy," JAMA, vol. 292, no. 23, p. 2874, 2004.

[5] S. G. Priori, C. Blomstrom-Lundqvist, A. Mazzanti et al., "2015 ESC guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: the task force for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death of the Europe," European Heart Journal, vol. 36, no. 41, pp. 2793-2867, 2015.

[6] S. J. Connolly, M. Gent, R. S. Roberts et al., "Canadian implantable defibrillator study (CIDS): a randomized trial of the implantable cardioverter defibrillator against amiodarone," Circulation, vol. 101, no. 11, pp. 1297-1302, 2000.

[7] K. H. Kuck, R. Cappato, J. Siebels, and R. Ruppel, "Randomized comparison of antiarrhythmic drug therapy with implantable defibrillators in patients resuscitated from cardiac arrest: the cardiac arrest study Hamburg (CASH)," Circulation, vol. 102, no. 7, pp. 748-754, 2000.

[8] D. G. Wyse, P. L. Friedman, and A. E. Epstein, "A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias," New England Journal of Medicine, vol. 337, no. 22, pp. 1576-1584, 1997.

[9] S. Reek, H. Burri, P. R. Roberts et al., "The wearable cardioverter-defibrillator: current technology and evolving indications," EP Europace, vol. 19, no. 3, pp. 335-345, 2017.

[10] H. U. Klein, I. Goldenberg, and A. J. Moss, "Risk stratification for implantable cardioverter defibrillator therapy: the role of the wearable cardioverter-defibrillator," European Heart Journal, vol. 34, no. 29, pp. 2230-2242, 2013.

[11] D. P. Zipes, A. J. Camm, M. Borggrefe et al., "ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association task force and the European society of cardiology com," Europace, vol. 8, no. 9, pp. 746-837, 2006.

[12] A. Bhaskaran, M. Bartlett, P. Kovoor, and L. M. Davis, "The wearable cardioverter defibrillator: an early single centre Australian experience. Some pitfalls and caveats for use," Heart, Lung and Circulation, vol. 25, no. 2, pp. 155-159, 2016.

[13] N. K. Wafinig, M. Gunther, S. Quick et al., "Experience with the wearable cardioverter-defibrillator in patients at high risk for sudden cardiac death," Circulation, vol. 134, no. 9, pp. 635-643, 2016.

[14] K. K. Collins, J. N. A. Silva, E. K. Rhee, and M. S. Schaffer, "Use of a wearable automated defibrillator in children compared to young adults," Pacing and Clinical Electrophysiology, vol. 33, no. 9, pp. 1119-1124, 2010.

[15] M. K. Chung, S. J. Szymkiewicz, M. Shao et al., "Aggregate national experience with the wearable cardioverter-defibrillator: event rates, compliance, and survival," Journal of the American College of Cardiology, vol. 56, no. 3, pp. 194-203, 2010.

[16] D. Duncker, R. Westenfeld, T. Konrad et al., "Risk for life-threatening arrhythmia in newly diagnosed peripartum cardiomyopathy with low ejection fraction: a German multicentre analysis," Clinical Research in Cardiology, vol. 106, no. 8, pp. 582-589, 2017.

[17] K. A. Dillon, S. J. Szymkiewicz, and T. E. Kaib, "Evaluation of the effectiveness of a wearable cardioverter defibrillator detection algorithm," Journal of Electrocardiology, vol. 43, no. 1, pp. 63-67, 2010.

[18] M. Lamichhane, J. C. Gardiner, N. R. Bianco, S. J. Szymkiewicz, and R. K. Thakur, "National experience with long-term use of the wearable cardioverter defibrillator in patients with cardiomyopathy," Journal of Interventional Cardiac Electrophysiology, vol. 48, no. 1, pp. 11-19, 2017.

[19] M. Singh, N. C. Wang, S. Jain, A. H. Voigt, S. Saba, and E. C. Adelstein, "Utility of the wearable cardioverter-defibrillator in patients with newly diagnosed cardiomyopathy: a decade-long single-center experience," Journal of the American College of Cardiology, vol. 66, no. 23, pp. 2607-2613, 2015.

[20] T. Tanawuttiwat, J. D. Garisto, A. Salow et al., "Protection from outpatient sudden cardiac death following ICD removal using a wearable cardioverter defibrillator," Pacing and Clinical Electrophysiology, vol. 37, no. 5, pp. 562-568, 2014.

[21] C. Wan, C. A. Herzog, W. Zareba, and S. J. Szymkiewicz, "Sudden cardiac arrest in hemodialysis patients with wearable cardioverter defibrillator," Annals of Noninvasive Electrocardiology, vol. 19, no. 3, pp. 247-257, 2014.

[22] A. E. Epstein, W. T. Abraham, N. R. Bianco et al., "Wearable cardioverter-defibrillator use in patients perceived to be at high risk early post-myocardial infarction," Journal of the American College of Cardiology, vol. 62, no. 21, pp. 2000-2007, 2013.

[23] A. C. Kao, S. W. Krause, R. Handa et al., "Wearable defibrillator use in heart failure (WIF): results of a prospective registry," BMC Cardiovascular Disorders, vol. 12, no. 1, p. 123, 2012.

[24] H. U. Klein, U. Meltendorf, S. Reek et al., "Bridging a temporary high risk of sudden arrhythmic death. Experience with the wearable cardioverter defibrillator (WCD)," Pacing and Clinical Electrophysiology, vol. 33, no. 3, pp. 353-367, 2010.

[25] J. W. Erath, M. Vamos, A. S. Sirat, and S. H. Hohnloser, "The wearable cardioverter-defibrillator in a real-world clinical setting: experience in 102 consecutive patients," Clinical Research in Cardiology, vol. 106, no. 4, pp. 300-306, 2017.

[26] S. Sasaki, Y. Shoji, Y. Ishida et al., "Potential roles of the wearable cardioverter-defibrillator in acute phase care of patients at high risk of sudden cardiac death: a single-center Japanese experience," Journal of Cardiology, vol. 69, no. 1, pp. 359-363, 2017.

[27] Y. Kondo, M. Linhart, R. P. Andrie, and J. O. Schwab, "Usefulness of the wearable cardioverter defibrillator in patients in the early post-myocardial infarction phase with high risk of sudden cardiac death: a single-center European experience," Journal of Arrhythmia, vol. 31, no. 5, pp. 293-295, 2015.

[28] M. A. Pfeffer, J. J. V. McMurray, E. J. Velazquez et al., "Valsartan, captopril, or both in myocardial infarction complicated by heart failure, left ventricular dysfunction, or both," New England Journal of Medicine, vol. 349, no. 20, pp. 1893-1906, 2003.

[29] J. E. Olgin, M. J. Pletcher, E. Vittinghoff et al., "Wearable cardioverter-defibrillator after myocardial infarction," New England Journal of Medicine, vol. 379, no. 13, pp. 1205-1215, 2018.

[30] A. J. Greenspon, J. D. Patel, E. Lauet al., "16-year-trends in the infection burden for pacemakers and implantable cardioverter-defibrillators in the United States 1993 to 2008," Journal of the American College of Cardiology, vol. 58, no. 10, pp. 1001-1006, 2011.

[31] L. K0ber, J. J. Thune, J. C. Nielsen et al., "Defibrillator implantation in patients with nonischemic systolic heart failure," New England Journal of Medicine, vol. 375, no. 13, pp. 1221-1230, 2016.

[32] D. Duncker, T. Konig, S. Hohmann, J. Bauersachs, and C. Veltmann, "Avoiding untimely implantable cardioverter/ defibrillator implantation by intensified heart failure therapy optimization supported by the wearable cardioverter/ defibrillator-the PROLONG study," Journal of the American Heart Association, vol. 6, no. 1, article e004512, 2017.

[33] V. Kutyifa, K. Vermilye, U. Daimee et al., "P6417-Extended wearable cardioverter defibrillator use in patients at-risk for sudden death," European Heart Journal, vol. 38, no. 1, article 4087435, 2017.

[34] E. Adelstein, "Long-term use of the wearable cardioverter-defibrillator: prolonging life or prolonging indecision?," Journal of Interventional Cardiac Electrophysiology, vol. 48, no. 1, pp. 9-10, 2017.

[35] E. Adelstein, A. Voigt, S. Saba, N. Wang, S. Jain, and M. Singh, "Reply: No utility of the wearable cardioverter-defibrillator in patients with nonischemic cardiomyopathy?," Journal of the American College of Cardiology, vol. 67, no. 23, p. 2808, 2016.

[36] A. E. Epstein, "The wearable cardioverter-defibrillator in newly diagnosed cardiomyopathy: treatment on the basis of perceived risk," Journal of the American College of Cardiology, vol. 66, no. 23, pp. 2614-2617, 2015.

[37] M. T. Saltzberg, S. Szymkiewicz, and N. R. Bianco, "Characteristics and outcomes ofperipartum versus nonperipartum cardiomyopathy in women using a wearable cardiac defibrillator," Journal of Cardiac Failure, vol. 18, no. 1, pp. 21-27, 2012.

[38] D. Duncker, A. Haghikia, T. Konig et al., "Risk for ventricular fibrillation in peripartum cardiomyopathy with severely reduced left ventricular function-value of the wearable cardioverter/defibrillator," European Journal of Heart Failure, vol. 16, no. 12, pp. 1331-1336, 2014.

[39] K. A. Ellenbogen, J. N. Koneru, P. S. Sharma, S. Deshpande, C. Wan, and S. J. Szymkiewicz, "Benefit of the wearable cardioverter-defibrillator in protecting patients after implantable-cardioverter defibrillator explant," JACC: Clinical Electrophysiology, vol. 3, no. 3, pp. 243-250, 2017.

Boldizsar Kovacs [ID], (1,2) Sven Reek, (3) Nazmi Krasniqi [ID], (2) Urs Eriksson [ID], (2) and Firat Duru (1)

(1) Arrhythmias and Electrophysiology Unit, Department of Cardiology, University Heart Center Zurich, University Hospital Zurich, Ramistrasse 100, 8091 Zurich, Switzerland

(2) Department of Cardiology, Regional Hospital Wetzikon, Spitalstrasse 66, 8620 Wetzikon, Switzerland

(3) Rain 34, 5000 Aarau, Switzerland

Correspondence should be addressed to Boldizsar Kovacs; boldizsar.kovacs@usz.ch

Received 24 May 2018; Revised 18 September 2018; Accepted 28 October 2018; Published 29 November 2018

Academic Editor: Terrence D. Ruddy

Caption: Figure 1: Ventricular flutter and fibrillation detected and appropriately terminated by a WCD in a patient.

Caption: Figure 2: Study selection flow chart. WCD = wearable cardioverter- defibrillator.
Table 1: Studies reviewed.

Year          Author              Indication         n     Median
                                                            wear
                                                            time

                              Any ([less than or     81       29
                              equal to] 18 years
                                    of age)
2010    Collins et al. [14]    Any (18-21 years
                                      of            103       35
                                     age)
2010     Chung et al. [15]            Any           3569      36
2010     Klein et al. [24]            Any           354    106 (a)
2010    Dillon et al. [17]            Any           2105      36
2012      Kao et al. [23]      Heart failure (b)     82       64
2013    Epstein et al. [22]           ICM           8453      57
2014      Wan et al. [21]        Hemodialysed        75    62.9 (a)
                                 patients [c]
        Tanawuttiwat et al.
2014           [20]            Device infection      97     21 (d)
                                      ICM           271       53
2015     Singh et al. [19]           NICM           254       71
         Lamichhane et al.
2016           [18]                HFrEF [e]        220      394
2016    Wafinig et al. [13]           Any           6043      59
2017     Erath et al. [25]            Any           1102      54
2017    Sasaki et al. [26]            Any            50       16
2017    Duncker et al. [16]          PPCM            49    120 (a)

Year          Author          Maximal    Number of     Median time
                               wear     appropriate    to the first
                               time       shocks      appropriate
                                                          shock

                                531          0           No shocks

2010    Collins et al. [14]
                                499          5               *

2010     Chung et al. [15]      1590         80              *
2010     Klein et al. [24]    >7 years       21              *
2010    Dillon et al. [17]      365          54              *
2012      Kao et al. [23]       277          0           No shocks
2013    Epstein et al. [22]      *          309              9
2014      Wan et al. [21]       308         136              *

        Tanawuttiwat et al.
2014           [20]              *           4              23
                                 *           6              34
2015     Singh et al. [19]       *           0           No shocks
         Lamichhane et al.
2016           [18]             2013         13              *
2016    Wafinig et al. [13]     163        * (f)             *
2017     Erath et al. [25]      166          8               *
2017    Sasaki et al. [26]      171          6              12
2017    Duncker et al. [16]      *           5              68

Year          Author          Maximal time
                              to the first
                              appropriate
                                  shock

                                No shocks

2010    Collins et al. [14]         *

2010     Chung et al. [15]          *
2010     Klein et al. [24]          *
2010    Dillon et al. [17]          *
2012      Kao et al. [23]       No shocks
2013    Epstein et al. [22]    > 9 months
2014      Wan et al. [21]           *

        Tanawuttiwat et al.
2014           [20]                38
                                   45
2015     Singh et al. [19]      No shocks
         Lamichhane et al.
2016           [18]                 *
2016    Wafinig et al. [13]         *
2017     Erath et al. [25]          *
2017    Sasaki et al. [26]         30
2017    Duncker et al. [16]      124 (g)

(a) Reported as a mean; (b) defined by own specific criteria; (c) only
patients with SCD events included; (d) median calculated for only 80
study patients; (e) wear time always >90 days; (f) 89% of treatments
occurred in the first 90 days; (g) calculated from the time of
diagnosis and not from the beginning of device therapy; * not
reported. Time is presented in days.

Table 2: Shortest and longest device parameters reported in the
included studies.

           Median wear    Maximal wear    Median time     Maximal time
               time           time        to the first    to the first
                                          appropriate     appropriate
                                              shock           shock

Shortest        16             163              9              30
Longest        394          >7 years           68           >9 months
COPYRIGHT 2018 COPYRIGHT 2010 SAGE-Hindawi Access to Research
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research Article
Author:Kovacs, Boldizsar; Reek, Sven; Krasniqi, Nazmi; Eriksson, Urs; Duru, Firat
Publication:Cardiology Research and Practice
Article Type:Clinical report
Date:Jan 1, 2018
Words:5272
Previous Article:The Reliability of the Use of Serum Neutrophil Gelatinase-Associated Lipocalin Levels in the Assessment of Renal Functions after Coronary Artery...
Next Article:Anxiety and Depression in Patients with Permanent Atrial Fibrillation: Prevalence and Associated Factors.
Topics:

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |