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Clinical Course After Cardioverter-Defibrillator Implantation: Chagasic Versus Ischemic Patients

Abstract

Background:

The outcome of Chagas disease patients after receiving implantable cardioverter defibrillator (ICD) is still controversial.

Objective:

To compare clinical outcomes after ICD implantation in patients with chronic Chagas cardiomyopathy (CCC) and ischemic heart disease (IHD).

Methods:

Prospective study of a population of 153 patients receiving ICD (65 with CCC and 88 with IHD). The devices were implanted between 2003 and 2011. Survival rates and event-free survival were compared.

Results:

The groups were similar regarding sex, functional class and ejection fraction. Ischemic patients were, on average, 10 years older than CCC patients (p < 0.05). Patients with CCC had lower schooling and monthly income than IHD patients (p < 0.05). The number of appropriate therapies was 2.07 higher in CCC patients, who had a greater incidence of appropriate shock (p < 0.05). Annual mortality rate and electrical storm incidence were similar in both groups. There was no sudden death in CCC patients, and only one in IHD patients. Neither survival time (p = 0.720) nor event-free survival (p = 0.143) significantly differed between the groups.

Conclusion:

CCC doubles the risk of receiving appropriate therapies as compared to IHD, showing the greater complexity of arrhythmias in Chagas patients.

Keywords:
Defibrillators Implantable; Chagas Disease; Myocardial Ischemia; Clinical Evolution

Resumo

Fundamento:

A evolução do paciente chagásico após implante de cardiodesfibrilador implantável (CDI) é tema ainda controverso.

Objetivo:

Comparar a evolução clínica pós-implante do CDI em pacientes com cardiopatia chagásica crônica (CCC) e cardiopatia isquêmica (CI).

Métodos:

Trata-se de um estudo prospectivo histórico de uma população de 153 pacientes portadores de CDI, sendo 65 com CCC e 88 com CI. Os dispositivos foram implantados entre janeiro de 2003 e novembro de 2011, tendo-se comparado a taxa de sobrevida e a sobrevida livre de eventos entre essas populações.

Resultados:

Os grupos foram similares na predominância do sexo masculino, classe funcional e fração de ejeção. Os pacientes isquêmicos são em média 10 anos mais velhos que os chagásicos (p < 0,05). Os pacientes chagásicos apresentavam escolaridade e renda mensal mais baixa do que os isquêmicos (p < 0,05). Foi demonstrado que o número de terapias apropriadas nos pacientes com CCC é 2,07 vezes maior do que naqueles com CI. A incidência de choque apropriado é maior na CCC (p < 0,05). As taxas de mortalidade anual nos dois grupos foram similares, assim como a incidência de tempestade elétrica. Não houve nenhuma morte súbita nos pacientes com CCC e apenas uma nos pacientes com CI. Não houve diferença estatisticamente significativa no tempo de sobrevida entre os dois grupos (p = 0,720) nem na sobrevida livre de eventos (p = 0,143).

Conclusão:

A CCC duplica o risco de receber terapias apropriadas em relação à CI, mostrando assim maior complexidade das arritmias nos pacientes chagásicos.

Palavras-chave:
Desfibriladores Implantáveis; Doença de Chagas; Isquemia Miocárdica; Evolução Clínica

Introduction

Sudden death is defined as of unexpected occurrence, usually less than one hour after symptom onset in an individual with no previous fatal condition.11 Myerburg RJ, Castellanos A. Cardiac arrest and sudden cardiac death. In: Braunwald E. Heart disease: a textbook of cardiovascular medicine. 4th ed. Philadelphia: WB Saunders; 1992. p. 756-89.

Cardiac sudden death (CSD) is a severe public health problem worldwide. In North America, 250,000 to 300,000 CSD per year are estimated to occur. Coronary artery disease (CAD) accounts for 80% of the CSD cases.22 Gillum RF. Sudden coronary death in the United States: 1980-1985. Circulation. 1989;79(4):756-65. The fatal event, ventricular tachycardia (VT) or ventricular fibrillation (VF), often occurs as the first manifestation of CAD, accounting for approximately 50% of the deaths due to that disease.33 Gillum RF. Geographic variations in sudden coronary death. Am Heart J. 1990;119(2Pt):380-9. Such estimates are only partially applicable to Brazil, which still has an expressive CSD rate due to chronic Chagas cardiomyopathy (CCC).44 Lopes, ER. Sudden death in patients with Chagas disease. Mem Inst Oswaldo Cruz. 1999;94 Suppl 1:321-4.,55 Martinelli M, Siqueira SF, Zimerman LI, Neto VA, Moraes AV Jr, Fenelon G. Sudden cardiac death in Brazil: study based on physicians´ perceptions of the public health care system. Pacing Clin Electrophysiol. 2012;35(11):1326-31.

Evidence on the efficacy of implantable cardioverter-defibrillator (ICD) to CSD prevention originates from large trials of secondary prevention (AVID,66 A comparison of antiarrhythmic drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias. The Antiarrhythmics versus Implantable Defibrillators (AVID) Investigators. N Engl J Med. 1997;337(22):1576-83. CASH77 Kuck KH, Cappato R, Siebels J, Ruppel R. Randomized comparison of antiarrhythmic drug therapy with implantable defibrillator in patients resuscitated from cardiac arrest: the Cardiac Arrest Study Hamburg (CASH). Circulation. 2000;102(7):748-54. and CIDS88 Bokhari F, Newman D, Greene M, Korley V, Mangat I, Dorian P. Long-term comparison of the implantable cardioverter versus amiodarone: eleven-year follow-up of a subset of patients in the Canadian Implantable Defibrillator Study (CIDS). Circulation. 2004;110(2):112-6.)) and primary prevention (MADIT I and II,99 Moss AJ, Zoreba Ç, Hall WJ, Klein H, Wilber DJ, Cannom DS, et al. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction (MADIT II). N Engl J Med. 2002;345(12):877-83. MUSTT1010 Moss AJ, Hall WJ, Cannom DS, Daubert JP, Higgins SL, Klein H, et al. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for ventricular arrhythmia. N Engl J Med. 1996;335(16):1933-40. and SCD-HEFT).1111 Kadish A, Mehra M. Heart failure devices: implantable cardioverter-defibrillators and biventricular pacing therapy. Circulation. 2005;111(24):3327-35. Those studies show the superiority of ICD over drugs, especially in ischemic and idiopathic cardiomyopathies. Data about the efficacy of ICD in patients with CCC are controversial. There is evidence from two registries1212 Muratore CA, Batista Sa LA, Chiale PA, Eloy R, Tentori MC, Escudero J, et al. Implantable cardioverter defibrillators and Chagas' disease: results of the ICD registry Latin America. Europace. 2009;11(2):164-8.,1313 Dubner S, Valero E, Pesce R, Zuelgaray JG, Mateos JC, Filho SG, et al. A Latin American registry of implantable cardioverter defibrillators: the ICD-LABOR study. Ann Noninvasive Electrocardiol. 2005;10(4):420-8. and two retrospective studies of secondary prevention.1414 Toro D, Muratore C, Aguinaga L, Batista L, Malan A, Greco O, et al. Predictors of all-cause 1-year mortality in implantable cardioverter defibrillator patients with chronic Chagas' cardiomyopathy. Pacing Clin Electrophysiol. 2011;34(9):1063-9.,1515 Cardinalli-Neto A, Bestetti RB, Cordeiro JA, Rodrigues VC. Predictors of all-cause mortality for patients with chronic Chagas' heart disease receiving implantable cardioverter defibrillator therapy. J Cardiovasc Electrophysiol. 2007;18(12):1236-40. The Brazilian Cardiac Implantable Electronic Devices Guideline makes no specific mention of the indication of ICD in patients with CCC.1616 Martinelli Filho M, Zimerman LI, Lorga AM, Vasconcelos JT, Rassi A Jr. Guidelines for implantable electronic cardiac devices of the Brazilian Society of Cardiology. Arq Bras Cardiol. 2007;89(6):e210-38.

Prospective and retrospective studies assessing the clinical course of patients with CCC and ICD are scarce.

The present study was aimed at comparing the clinical course after ICD implantation of patients with CCC and ischemic heart disease (IHD), and at assessing the survival and event-free survival curves (appropriate shocks, appropriate therapies and death).

Methods

The inclusion criterion was patients with CCC or IHD, ICD implanted for primary or secondary prevention of CSD, according to the Brazilian guidelines.88 Bokhari F, Newman D, Greene M, Korley V, Mangat I, Dorian P. Long-term comparison of the implantable cardioverter versus amiodarone: eleven-year follow-up of a subset of patients in the Canadian Implantable Defibrillator Study (CIDS). Circulation. 2004;110(2):112-6.,99 Moss AJ, Zoreba Ç, Hall WJ, Klein H, Wilber DJ, Cannom DS, et al. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction (MADIT II). N Engl J Med. 2002;345(12):877-83. Patients receiving ICD for primary prevention were those with indication for cardiac resynchronization and who never had syncope, sustained ventricular tachycardia or aborted sudden death by VT or VF.

This study patients had either CCC or IHD and received an ICD from January 2003 to November 2011, at the Walter Cantídio Hospital of the Federal University of Ceará (HUWC), Brazil. The exclusion criteria were: age below 18 years or concomitance of both diseases.

This historical prospective cohort study was approved by the Ethics Committee of the institution in January 2010 (protocol: 061.06.10). A databank system was designed to include the patients' clinical and epidemiological characteristics, indication for ICD and the functional results of ICD at the time of implantation and during follow-up. Those data were collected from medical records and during clinical visits. The ICD programming included antitachycardia pacing (ATP) followed by shock for VT and VF. Ventricular tachycardia was considered in the presence of sustained tachycardia with a cycle interval ranging from 300 to 400 ms, not identified as supraventricular tachycardia by specific algorithms. Ventricular fibrillation was considered when the interval cycle was shorter than 300 ms. The ICD therapy was classified as appropriate for VT / VF if the intracardiac electrogram recorded for the intervention was compatible. The ICD therapy was considered inappropriate when shock was applied to supraventricular tachycardia, noise, myopotential oversensing, or R-wave double counting. The follow-up protocol included regular clinical visits and device assessment three times a year or at shorter intervals, when deemed necessary. Death circumstances were classified as having a cardiac or non-cardiac cause, and the Hinkle and Thaler classification was used to assess the suspected mechanism of death.1717 Hinkle LE Jr, Thaler HT. Clinical classification of cardiac deaths. Circulation. 1982;65(3):457-64.

Statistical analysis

Data were entered into the EpiInfo software (3.5.1 version) and analyzed in the SPSS software, 17.0 version for Windows. Univariate analysis was performed to describe the study population.

Categorical variables were compared by using chi-square and Fisher exact tests, and tables with absolute values (n) and their proportions (%). Continuous variables of normal distribution were compared between groups using ANOVA, while the others were compared by using Kruskall-Wallis test, and tables with median or mean and standard deviations.

For bivariate analysis, log-ranks of the survival time differences for each variable concerning each outcome were calculated.

Kaplan-Meier curves were built for the variables with p-value < 0.05, compared by using two-tailed log-rank tests between strata.

Cox regression model was applied to the variables associated with survival on bivariate analysis (p < 0.20). Backward modeling with direct comparison of log likelihood, coefficients (β) and Wald test was used after each modeling step.

To assess proportional hazards associated with predictive factors, Schoenfeld test and graphic inspection of Cox-Snell residuals were performed.

The statistical significance level adopted was p < 0.05.

Results

This study included 153 patients submitted to ICD implantation from January 1st, 2003, to November 24th, 2011. Of the 153 patients, 65 (42.5%) had CCC and 88 (57.5%), IHD. Seven patients (4.6%) were lost to follow-up, five (5.7%) with IHD and two (3.1%) with CCC. Most of the study population consisted of men. Regarding the devices implanted, 101 patients (66.0%) received the dual-chamber device, 50 patients received the cardiac resynchronization therapy-defibrillator, and 2 patients received the single-chamber device. Secondary prevention of sudden death accounted for 65.4% of the implantations. During follow-up, 29 (18.3%) patients died (Table 1).

Table 1
Patients’ characteristics

The median follow-up time of the IHD group was 27 months, and of the CCC group, 35 months, with no statistically significant difference between them.

The mean age difference between the CCC and IHD groups was 10.2 years, a significant difference (p < 0.05). On average, ischemic patients were 10.2 years older than CCC patients.

Resuscitation from sudden death due to VF or VT was the indication for ICD implantation in 31 CCC patients and in 33 IHD patients. Syncope with induction of unstable VT on electrophysiological study was the reason for implantation in 20 CCC patients and in 16 IHD patients. Fourteen CCC patients and 39 IHD patients received ICD for primary prevention of sudden death (Table 1). Thus, secondary prevention was more prevalent in CCC than in IHD (p < 0.05), and primary prevention was more prevalent in IHD than in CCC (p < 0.05) (Table 3).

Table 2
Appropriate and inappropriate shocks according to indication (primary or secondary)
Table 3
Predisposing factors to appropriate therapies via ICD

The annual mortality rate (p = 0.721) and the incidence of sudden death (p = 0.253) and of arrhythmic storm (p = 0.240) were similar in CCC and IHD patients (Table 3). No surgical death occurred.

Left bundle-branch block was more frequently found in IHD than in CCC (p < 0.05), and right bundle-branch block associated with left anterior hemiblock was more frequently found in CCC (p < 0.05).

Patients with CCC more often used the association of beta-blockers and amiodarone than those with IHD (p < 0.05). The use of beta-blocker alone (p < 0.05) and of amiodarone alone (p < 0.05) was more frequent in IHD patients than in CCC patients. Regarding functional class, CCC and IHD differed only in functional class I, whose incidence was higher in CCC (p < 0.05). The incidence of normal ejection fraction was higher in CCC patients (p < 0.05) (Table 1).

The incidence of appropriate therapies (p < 0.05) and of appropriate shocks (p < 0.05) was higher in patients with CCC than with IHD (Table 1).

No statistically significant difference was found in the incidence of appropriate shocks when assessing functional class (p = 0.375) and ejection fraction (p = 0.837). However, patients receiving ICD for secondary prevention had more appropriate shocks than those receiving ICD for primary prevention (p < 0.05) (Table 2).

In the final Cox multivariate model, using all ICD patients, chagasic etiology, ejection fraction with mild dysfunction and no use of beta-blockers were significantly associated with predisposition to receive appropriate therapies (appropriate shock and ATP) (Table 3). Patients with ejection fraction with mild dysfunction had a 3.5-fold increased risk for the outcome 'appropriate therapy' when controlled by etiology and beta-blocker use. Patients with CCC had a twice-greater risk for appropriate therapy than those with IHD when controlled by ejection fraction with mild dysfunction and no beta-blocker use. No beta-blocker use is important in the model, although its significance is not at the 5% level (p < 0.05): no beta-blocker use increases 6.3 times the risk for receiving appropriate therapy.

No statistically significant difference in survival time and event-free survival time (appropriate shocks, appropriate therapies and death) was found between CCC and IHD (Figures 1 and 2). During follow-up, no sudden death occurred in the CCC group, and only one in the IHD group. In Kaplan-Meier univariate analysis, moderate to severe ejection fraction (p < 0.05) and functional class IV (p < 0.05) were associated with higher mortality. In the final Cox multivariate model, using all ICD patients, age (> 60 years) and functional class IV were significantly associated with higher mortality (Table 4). Patients in functional class IV had a 2.9-fold increased risk for the outcome 'death' when controlled by age.

Figure 1
Mean survival time [chronic Chagas cardiomyopathy (CCC) versus ischemic heart disease (IHD)]

Figure 2
Event-free survival time [chronic Chagas cardiomyopathy (CCC) versus ischemic heart disease (IHD)]

Table 4
Factors related to higher mortality

Discussion

Sudden death due to malignant ventricular arrhythmia (VT or VF) is a well-known complication of Chagas cardiomyopathy.1818 Rassi Jr A, Rassi SG, Rassi A. Sudden death in Chagas' disease. Arq Bras Cardiol. 2001;76(1):75-85. It occurs mainly between 30 years and 50 years of age, being rarer after the sixth decade of life, and predominates in the male sex. It usually occurs during routine activities, physical exertion or emotion, being instantaneous in half of the cases. In the other half, death is preceded by premonitory symptoms for seconds or, more rarely, minutes. Differently from IHD, whose sudden death frequency peaks in the morning, in CCC, deaths seem to predominate in the afternoon, between 12PM and 6PM.1919 Lopes ER, da Cunha LF, dos Santos TA, Resende AV, Jorge BH, Salomão LA, et al. [Daily and weekly circadian variations in sudden death in Chagas disease]. Arq Bras Cardiol. 1993;61(6):345-8. The therapeutic strategy to avoid sudden death in IHD is well established. In CCC, however, it is a great challenge.

One of the major findings of this study was the high number of CCC patients receiving appropriate ICD shock (36.5%) and appropriate therapy (42.9%), with a significant difference from that found in IHD patients (p < 0.05). Chronic Chagas cardiomyopathy increased 2.07 times the risk of receiving appropriate therapy [95% confidence interval (CI): 1.02 - 4.17]. That high percentage of appropriate shock and therapy triggered by ICD was similar to data of other studies, corroborating the concept relative to the severe arrhythmogenic nature of CCC, which is an inflammatory pancarditis with right injury to the electric system, and appearance of fibrosis, which feeds the reentry mechanism, the major responsible for the genesis of taquiarrhythmias.2020 Martinelli Filho M, De Siqueira SF, Moreira H, Fagundes A, Pedrosa A, Nishioka SD, et al. Probability of occurrence of life-threatening ventricular arrhythmias in Chagas´ disease versus non-Chagas´ disease. Pacing Clin Electrophysiol. 2000;23(11 Pt 2):1944-6.

21 Rabinovich R, Muratore C, Iglesias R, Gonzalez M, Darú V, Valentino M, et al. Time first shock in implantable cardioverter defibrillator (ICD) patients with Chagas cardiomyopathy. Pacing Clin Electrophysiol. 1999;22(1 Pt 2):202-5.

22 Barbosa MP, da Costa Rocha MO, Oliveira AB, Lombardi F, Ribeiro AL. Efficacy and safety of implantable cardioverter-defibrillators in patients with Chagas disease. Europace. 2013;15(7):957-62. Erratum in: Europace. 2013;15(11):1684.

23 da Fonseca SM, Belo LG, Carvalho H, Araujo N, Munhoz C, Siqueira L, et al. Clinical follow-up of patients with implantable cardioverter-defibrillator. Arq Bras Cardiol. 2007;88(1):8-16.

24 Muratore C, Rabinovich R, Iglesias R, González M, Darú V, Liprandi AS. Implantable cardioverter defibrillator in patients with Chagas disease: are they from patients with coronary disease? Pacing Clin Electrophysiol. 1997;29(6):194-7.

25 Martinelli M, de Siqueira SF, Sternick EB, Rassi A Jr, Costa R, Ramires JA, et al. Long-term follow-up of implantable cardioverter-defibrillator for secondary prevention in Chagas heart disease. Am J Cardiol. 2012;110(7):1040-5.

26 Cardinalli-Neto A, Bestetti RB, Cordeiro JA, Rodrigues VC. Predictors of all- cause mortality for patients with chronic Chagas' heart disease receiving implantable cardioverter defibrillator therapy. J Cardiovasc Eletrophysiol. 2007;18(12):1236-40.
-2727 Mateos JC, Lobo TJ, Mateos EI. Aspectos eletrofisiológicos da cardiopatia chagásica. Rev Soc Cardiol Estado de São Paulo. 2009;19(1):39-50. Barbosa et al2222 Barbosa MP, da Costa Rocha MO, Oliveira AB, Lombardi F, Ribeiro AL. Efficacy and safety of implantable cardioverter-defibrillators in patients with Chagas disease. Europace. 2013;15(7):957-62. Erratum in: Europace. 2013;15(11):1684. has shown an incidence of 62.7% of appropriate therapy in CCC patients and of 37.3% in non-chagasic patients during a median follow-up of 266 days, in addition to a 2.2-time increase in the risk of receiving appropriate therapy in CCC (95% CI: 1.2 - 4.3; p < 0.05). Martinelli et al.2020 Martinelli Filho M, De Siqueira SF, Moreira H, Fagundes A, Pedrosa A, Nishioka SD, et al. Probability of occurrence of life-threatening ventricular arrhythmias in Chagas´ disease versus non-Chagas´ disease. Pacing Clin Electrophysiol. 2000;23(11 Pt 2):1944-6., following up 11 CCC patients and 42 patients with either ischemic or idiopathic heart diseases, have shown a likelihood of fatal ventricular arrhythmia non-occurrence of 0% in chagasic patients and of 40% in non-chagasic patients, during a mean follow-up of 660 days.2020 Martinelli Filho M, De Siqueira SF, Moreira H, Fagundes A, Pedrosa A, Nishioka SD, et al. Probability of occurrence of life-threatening ventricular arrhythmias in Chagas´ disease versus non-Chagas´ disease. Pacing Clin Electrophysiol. 2000;23(11 Pt 2):1944-6. Other authors, assessing 20 CCC patients and 35 IHD patients submitted to ICD implantation, have reported 85% of chagasic patients receiving appropriate therapy as compared to 51% of the IHD group, during a mean follow-up of 180 days.2121 Rabinovich R, Muratore C, Iglesias R, Gonzalez M, Darú V, Valentino M, et al. Time first shock in implantable cardioverter defibrillator (ICD) patients with Chagas cardiomyopathy. Pacing Clin Electrophysiol. 1999;22(1 Pt 2):202-5. There are only two studies with opposite findings, showing no difference regarding appropriate shock or therapy between chagasic and non-chagasic patients.2323 da Fonseca SM, Belo LG, Carvalho H, Araujo N, Munhoz C, Siqueira L, et al. Clinical follow-up of patients with implantable cardioverter-defibrillator. Arq Bras Cardiol. 2007;88(1):8-16.,2424 Muratore C, Rabinovich R, Iglesias R, González M, Darú V, Liprandi AS. Implantable cardioverter defibrillator in patients with Chagas disease: are they from patients with coronary disease? Pacing Clin Electrophysiol. 1997;29(6):194-7. The difference in results might be attributed to the small number of chagasic patients included in those two studies (10 and 18, respectively).

Mild left ventricular dysfunction was shown to predict appropriate therapy. It is worth noting that the patients receiving ICD with mild left ventricular dysfunction were those undergoing ICD due to secondary prevention of sudden death; it is well known that patients receiving ICD due to secondary prevention are at higher risk of repeating the arrhythmic event.

In our study, ventricular dysfunction and functional class IV were predictors of mortality. This has been well demonstrated in other studies.2525 Martinelli M, de Siqueira SF, Sternick EB, Rassi A Jr, Costa R, Ramires JA, et al. Long-term follow-up of implantable cardioverter-defibrillator for secondary prevention in Chagas heart disease. Am J Cardiol. 2012;110(7):1040-5.,2828 Rassi A Jr, Rassi A, Little WC, Xavier SS, Rassi SG, Rassi AG, et al. Development and validation of a risk score for predicting death in Chagas' heart disease. N Engl J Med. 2006;355(8):799-808.,2929 di Toro D, Muratore C, Aguinaga L, Batista L, Malan A, Greco O, et al. Predictors of all-cause 1-year mortality in implantable cardioverter defibrillator patients with chronic Chagas´ cardiomyopathy. Pacing Clin Electrophysiol. 2011;34(9):1063-9.

In our study, the incidence of appropriate shock and therapy in CCC patients was higher than that in IHD patients; mortality, however, was similar. No sudden death occurred during the follow-up of CCC patients receiving ICD, as well as no death related to the device implantation procedure. This suggests the efficacy and safety of ICD implantation in CCC.

So far, no large randomized clinical trial, comparing the efficacy of ICD in CCC with that of active drug or placebo, has been published. Although Chagas disease was identified and described by the Brazilian researcher Carlos Justiniano Ribeiro Chagas more than 100 years ago, the best treatment for ventricular arrhythmias and sudden death prevention remain a challenge.

Study limitations

One limitation of this study was the lack of uniformity of the populations studied, such as the higher number of indication for secondary prevention in CCC.

This is an initial study suggesting the beneficial effect of using ICD in CCC, with efficacy similar to that in IHD. However, further more robust, controlled and uniform studies are required.

Conclusion

Chronic Chagas cardiomyopathy doubles the risk of receiving appropriate therapies as compared to IHD, thus showing the greater complexity of arrhythmias in chagasic patients, despite the similar mortality, suggesting the efficacy of using ICD in CCC.

  • Sources of Funding
    There were no external funding sources for this study.
  • Study Association
    This article is part of the thesis of master submitted by Francisca Tatiana Moreira Pereira, from Universidade Federal do Ceará.

References

  • 1
    Myerburg RJ, Castellanos A. Cardiac arrest and sudden cardiac death. In: Braunwald E. Heart disease: a textbook of cardiovascular medicine. 4th ed. Philadelphia: WB Saunders; 1992. p. 756-89.
  • 2
    Gillum RF. Sudden coronary death in the United States: 1980-1985. Circulation. 1989;79(4):756-65.
  • 3
    Gillum RF. Geographic variations in sudden coronary death. Am Heart J. 1990;119(2Pt):380-9.
  • 4
    Lopes, ER. Sudden death in patients with Chagas disease. Mem Inst Oswaldo Cruz. 1999;94 Suppl 1:321-4.
  • 5
    Martinelli M, Siqueira SF, Zimerman LI, Neto VA, Moraes AV Jr, Fenelon G. Sudden cardiac death in Brazil: study based on physicians´ perceptions of the public health care system. Pacing Clin Electrophysiol. 2012;35(11):1326-31.
  • 6
    A comparison of antiarrhythmic drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias. The Antiarrhythmics versus Implantable Defibrillators (AVID) Investigators. N Engl J Med. 1997;337(22):1576-83.
  • 7
    Kuck KH, Cappato R, Siebels J, Ruppel R. Randomized comparison of antiarrhythmic drug therapy with implantable defibrillator in patients resuscitated from cardiac arrest: the Cardiac Arrest Study Hamburg (CASH). Circulation. 2000;102(7):748-54.
  • 8
    Bokhari F, Newman D, Greene M, Korley V, Mangat I, Dorian P. Long-term comparison of the implantable cardioverter versus amiodarone: eleven-year follow-up of a subset of patients in the Canadian Implantable Defibrillator Study (CIDS). Circulation. 2004;110(2):112-6.
  • 9
    Moss AJ, Zoreba Ç, Hall WJ, Klein H, Wilber DJ, Cannom DS, et al. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction (MADIT II). N Engl J Med. 2002;345(12):877-83.
  • 10
    Moss AJ, Hall WJ, Cannom DS, Daubert JP, Higgins SL, Klein H, et al. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for ventricular arrhythmia. N Engl J Med. 1996;335(16):1933-40.
  • 11
    Kadish A, Mehra M. Heart failure devices: implantable cardioverter-defibrillators and biventricular pacing therapy. Circulation. 2005;111(24):3327-35.
  • 12
    Muratore CA, Batista Sa LA, Chiale PA, Eloy R, Tentori MC, Escudero J, et al. Implantable cardioverter defibrillators and Chagas' disease: results of the ICD registry Latin America. Europace. 2009;11(2):164-8.
  • 13
    Dubner S, Valero E, Pesce R, Zuelgaray JG, Mateos JC, Filho SG, et al. A Latin American registry of implantable cardioverter defibrillators: the ICD-LABOR study. Ann Noninvasive Electrocardiol. 2005;10(4):420-8.
  • 14
    Toro D, Muratore C, Aguinaga L, Batista L, Malan A, Greco O, et al. Predictors of all-cause 1-year mortality in implantable cardioverter defibrillator patients with chronic Chagas' cardiomyopathy. Pacing Clin Electrophysiol. 2011;34(9):1063-9.
  • 15
    Cardinalli-Neto A, Bestetti RB, Cordeiro JA, Rodrigues VC. Predictors of all-cause mortality for patients with chronic Chagas' heart disease receiving implantable cardioverter defibrillator therapy. J Cardiovasc Electrophysiol. 2007;18(12):1236-40.
  • 16
    Martinelli Filho M, Zimerman LI, Lorga AM, Vasconcelos JT, Rassi A Jr. Guidelines for implantable electronic cardiac devices of the Brazilian Society of Cardiology. Arq Bras Cardiol. 2007;89(6):e210-38.
  • 17
    Hinkle LE Jr, Thaler HT. Clinical classification of cardiac deaths. Circulation. 1982;65(3):457-64.
  • 18
    Rassi Jr A, Rassi SG, Rassi A. Sudden death in Chagas' disease. Arq Bras Cardiol. 2001;76(1):75-85.
  • 19
    Lopes ER, da Cunha LF, dos Santos TA, Resende AV, Jorge BH, Salomão LA, et al. [Daily and weekly circadian variations in sudden death in Chagas disease]. Arq Bras Cardiol. 1993;61(6):345-8.
  • 20
    Martinelli Filho M, De Siqueira SF, Moreira H, Fagundes A, Pedrosa A, Nishioka SD, et al. Probability of occurrence of life-threatening ventricular arrhythmias in Chagas´ disease versus non-Chagas´ disease. Pacing Clin Electrophysiol. 2000;23(11 Pt 2):1944-6.
  • 21
    Rabinovich R, Muratore C, Iglesias R, Gonzalez M, Darú V, Valentino M, et al. Time first shock in implantable cardioverter defibrillator (ICD) patients with Chagas cardiomyopathy. Pacing Clin Electrophysiol. 1999;22(1 Pt 2):202-5.
  • 22
    Barbosa MP, da Costa Rocha MO, Oliveira AB, Lombardi F, Ribeiro AL. Efficacy and safety of implantable cardioverter-defibrillators in patients with Chagas disease. Europace. 2013;15(7):957-62. Erratum in: Europace. 2013;15(11):1684.
  • 23
    da Fonseca SM, Belo LG, Carvalho H, Araujo N, Munhoz C, Siqueira L, et al. Clinical follow-up of patients with implantable cardioverter-defibrillator. Arq Bras Cardiol. 2007;88(1):8-16.
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Publication Dates

  • Publication in this collection
    11 July 2016
  • Date of issue
    Aug 2016

History

  • Received
    07 Sept 2015
  • Reviewed
    05 Mar 2016
  • Accepted
    07 Mar 2016
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