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Predictors of Arrhythmic Events Detected by Implantable Loop Recorders in Renal Transplant Candidates

Abstract

Background:

The recording of arrhythmic events (AE) in renal transplant candidates (RTCs) undergoing dialysis is limited by conventional electrocardiography. However, continuous cardiac rhythm monitoring seems to be more appropriate due to automatic detection of arrhythmia, but this method has not been used.

Objective:

We aimed to investigate the incidence and predictors of AE in RTCs using an implantable loop recorder (ILR).

Methods:

A prospective observational study conducted from June 2009 to January 2011 included 100 consecutive ambulatory RTCs who underwent ILR and were followed-up for at least 1 year. Multivariate logistic regression was applied to define predictors of AE.

Results:

During a mean follow-up of 424 ± 127 days, AE could be detected in 98% of patients, and 92% had more than one type of arrhythmia, with most considered potentially not serious. Sustained atrial tachycardia and atrial fibrillation occurred in 7% and 13% of patients, respectively, and bradyarrhythmia and non-sustained or sustained ventricular tachycardia (VT) occurred in 25% and 57%, respectively. There were 18 deaths, of which 7 were sudden cardiac events: 3 bradyarrhythmias, 1 ventricular fibrillation, 1 myocardial infarction, and 2 undetermined. The presence of a long QTc (odds ratio [OR] = 7.28; 95% confidence interval [CI], 2.01–26.35; p = 0.002), and the duration of the PR interval (OR = 1.05; 95% CI, 1.02–1.08; p < 0.001) were independently associated with bradyarrhythmias. Left ventricular dilatation (LVD) was independently associated with non-sustained VT (OR = 2.83; 95% CI, 1.01–7.96; p = 0.041).

Conclusions:

In medium-term follow-up of RTCs, ILR helped detect a high incidence of AE, most of which did not have clinical relevance. The PR interval and presence of long QTc were predictive of bradyarrhythmias, whereas LVD was predictive of non-sustained VT.

Keywords:
Arrhythmias, Cardiac; Myocardial Contraction; Kidney Transplantation; Difibrillators; Electric Countershock

Resumo

Fundamento:

A documentação de eventos arrítmicos (EA) em candidatos a transplante renal (CTR) submetidos à diálise é limitada pelo registro de eletrocardiograma convencional. Um monitoramento contínuo do ritmo cardíaco parece ser o procedimento mais adequado para a detecção automática de arritmia, contudo esse método não foi explorado anteriormente.

Objetivo:

O objetivo deste estudo foi investigar a incidência e os preditores de EA em CTR usando um gravador de eventos implantável, do inglês, “loop recorder implantável” (ILR).

Métodos:

Um estudo prospectivo observacional foi conduzido entre Junho/2009 a Janeiro/2011. Cem CTR ambulatoriais consecutivos foram submetidos ao ILR e acompanhados pelo menos por um ano. Uma regressão logística multivariada foi aplicada para definir os preditores de EA.

Resultados:

Durante o tempo médio de acompanhamento de 424 ± 127 dias, EA foram detectados em 98% dos pacientes, sendo que 92% deles tinham mais de um tipo de arritmia, a maioria não considerada potencialmente séria. Taquicardia atrial sustentada e fibrilação atrial ocorreram respectivamente em 7% e 13% dos pacientes; bradiarritmia em 25% e taquicardia ventricular (TV) não-sustentada ou sustentada em 57%. Ocorreram 18 óbitos, 7 por morte cardíaca súbita, 3 por bradiarritmias, 1 por fibrilação ventricular, 1 por infarto do miocárdio e 2 óbitos devido à causas desconhecidas. A presença de QTc longo (Razão de Probabilidade [RP] = 7,28; intervalo de confiança de 95% [IC] 2,01-26,35; p = 0,002) e duração do intervalo PR (RP = 1,05; IC 95%: 1,02-1,08; p < 0,001) foram associados independentemente a bradiarritmias. A dilatação ventricular esquerda (DVE) foi independentemente associada à TV não-sustentada (RP = 2,83; IC 95%: 1,01-7,96; p = 0,041).

Conclusões:

Em acompanhamento de médio prazo de CTR, o ILR detectou uma alta incidência de EA, a maioria sem relevância clínica. O intervalo PR e a presença de QTc longo foram preditivos de bradiarritmias e DVE de TV não‑sustentada.

Palavras-chave:
Arritmias Cardíacas; Contração Miocárdica; Transplante de Rim; Desfibriladores; Cardioversão Elétrica

Introduction

Patients with end-stage renal disease undergoing chronic hemodialysis have a high mortality rate1United States Renal Data System. 2010 Annual Data Report. [Internet]: atlas of chronic kidney disease and end-stage renal disease in the United States. Bethesda; 2010. [Cited in 2014 Jun 10]. Available from: http://www.usrds.org/2010/pdf/v1_00a_intros.PDF
http://www.usrds.org/2010/pdf/v1_00a_int...
. In 2010, the annual report of the United States Renal Data System (USRDS) showed a mortality rate of 210 deaths per 1000 patient-years, mainly attributable to cardiovascular disease. The single largest cause of death among dialysis patients is sudden cardiac death (SCD), accounting for 27% of all-cause mortality, and it is linked to arrhythmic mechanisms1United States Renal Data System. 2010 Annual Data Report. [Internet]: atlas of chronic kidney disease and end-stage renal disease in the United States. Bethesda; 2010. [Cited in 2014 Jun 10]. Available from: http://www.usrds.org/2010/pdf/v1_00a_intros.PDF
http://www.usrds.org/2010/pdf/v1_00a_int...

Herzog CA, Mangrum JM, Passman R. Sudden cardiac death and dialysis patients. Semin Dial. 2008;21(4):300-7.
-3Kanbay M, Afsar B, Goldsmith D, Covic A. Sudden death in hemodialysis: an update. Blood Purif. 2010;30(2):135-45..

The particular vulnerability of dialysis patients to SCD has been investigated earlier. Factors including obstructive coronary artery disease, left ventricular hypertrophy, electrolyte shift, and abnormal myocardial ultrastructure and function have been implicated in the increased risk of arrhythmia-mediated death. However, the relative contribution of individual factors to the overall hazard of SCD is still undertermined1United States Renal Data System. 2010 Annual Data Report. [Internet]: atlas of chronic kidney disease and end-stage renal disease in the United States. Bethesda; 2010. [Cited in 2014 Jun 10]. Available from: http://www.usrds.org/2010/pdf/v1_00a_intros.PDF
http://www.usrds.org/2010/pdf/v1_00a_int...
,2Herzog CA, Mangrum JM, Passman R. Sudden cardiac death and dialysis patients. Semin Dial. 2008;21(4):300-7.,4De Bie MK, van Dam B, Gassbeek A, van Buren M, van Erven L, Baxx JJ, et al. The current status of interventions aiming at reducing sudden cardiac death in dialysis patients. Eur Heart J. 2009;30(13):1559-64.

Myerburg RJ, Castellanos A. Emerging paradigms of the epidemiology and demographics of sudden cardiac arrest. Heart Rhythm. 2006;3(2):235-9.

Strippoli GF, Craig JC. Sunset for statins after AURORA? N Engl J Med. 2009;360(14):1455-7.
-7Wanner C, Krane V, Marz W, Olschewski M, Mann JF, Ruf G, et al; German Diabetes and Dialysis Study Investigators. Atorvastatin in patients with type 2 diabetes mellitus undergoing hemodialysis. N Engl J Med. 2005;353(3):238-48. Erratum in: N Engl J Med. 2005;353(15):1640..

In contrast, it has been previously reported that arrhythmic events (AE) are quite common in dialysis patients. To date, knowledge about the incidence of AE has been limited to detection by conventional resting electrocardiogram (ECG) and electrocardiographic ambulatory monitoring systems8Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9.

Blumberg A, Häusermann M, Strub B, Jenzer HR. Cardiac arrhythmias in patients on maintenance hemodialysis. Nephron. 1983;33(2):91-5.

10 Weber H, Schwarzer C, Stummvoll HK, Joskowics G, Wolf A, Steinbach K, et al. Chronic hemodialysis: high risk patients for arrhythmias? Nephron. 1984;37(3):180-5.

11 D'Elia JA, Weinrauch LA, Gleason RE, Hampton LA, Smith-Ossman S, Yoburn DC, et al. Application of the ambulatory 24-hour electrocardiogram in the prediction of cardiac death in dialysis patients. Arch Intern Med. 1988;148(11):2381-5.
-1212 Abe S, Yoshizawa M, Nakanishi N, Yazawa T, Yokota K, Honda M, et al. Electrocardiographic abnormalities in patients receiving hemodialysis. Am Heart J. 1996;131(6):1137-44.. However, documentation obtained by these traditional tools at randomly selected intervals may have resulted in huge gaps in temporal knowledge of the incidence of AE. Furthermore, the spontaneous and circadian variabilities of cardiac arrhythmias may have influenced their detection, and thus, its occurrence in dialysis patients may have been underdiagnosed. To date, studies using long-term cardiac monitoring to detect AE in dialysis patients have not been conducted.

The implantable loop recorder (ILR), with automatic detection of arrhythmias, allows for continuous detection, quantification, and documentation of AE during a long-term ECG monitoring period that extends to 36 months. Current clinical use and research with ILR have focused mostly on patients with syncope or ventricular dysfunction after myocardial infarction 1313 Brignole M, Vardas P, Hoffman E, Huikuri H, Moya A, Ricci R, et al; Task Force members of EHRA Scientific Documents Committee. Indications for the use of diagnostic implantable and external ECG loop recorders. Europace. 2009;11(5):671-87. Erratum in: Europace. 2009;11(6):836.,1414 Bloch Thomsen PE, Jons C, Raatikainen P, Moerch Joergensen R, Hartikainen J, Virtanen V, et al. Long-term recording of cardiac arrhythmias with an implantable cardiac monitor in patients with reduced ejection fraction after acute myocardial infarction. The Cardiac Arrhythmias and Risk Stratification After Acute Myocardial Infarction (CARISMA) Study. Circulation. 2010;122(13):1258-64.. The PRETRANSPLANT (Predictors of Arrhythmic Events Detected by ILRs in Hemodialysis Renal Transplant Candidates) study is a prospective observational study conducted to evaluate the incidence and predictors of AE occurrence by using long-term ILR monitoring in renal transplant candidates (RTCs) on hemodialysis.

Methods

Study Cohort Selection and Study setting

This study was conducted in a prospective ambulatory cohort of patients with end-stage renal disease (ESRD)referred to the Heart Institute (InCor) of the University of São Paulo Medical School, São Paulo, Brazil, for pretransplantation cardiovascular evaluation between March and December of 2009. A total of 383 consecutive outpatients awaiting a renal transplant were screened during routine clinical assessment. All of the patients who met the inclusion criteria of being on chronic hemodialysis therapy, having a high cardiologic risk profile for renal transplant surgery (defined by age > 50 years, diabetes, or clinically evident cardiovascular disease) and with < 2 years of baseline cardiovascular assessment were eligible for study participation (n = 176)1515 Gowdak LH, de Paula FJ, César LA, Bortolotto LA, de Lima JJ. A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates. Transplant Res. 2013;2(1):18.. From this cohort of included patients, 76 patients were further excluded because of refusal to participate (n = 63), planned cardiovascular intervention (n = 6), and previous renal transplantation (n = 3). Three patients died while waiting for ILR implantation and 1 patient was excluded because of inadequate R-wave amplitude measured in a preimplantation ILR test. Finally, 100 patients (mean age, 59 ± 8,8 years; men, 65%; white, 73%) underwent long-term ECG monitoring by ILR and were included in this analysis.

A comprehensive clinical and cardiovascular investigation was carried out for pretransplantation cardiovascular evaluation, including 12-lead resting ECG, signal-averaged electrocardiogram (SAECG), myocardial perfusion scintigraphy, and transthoracic echocardiogram conducted on interdialytic days.

Surface ECG parameters included the heart rate, PR interval, QRS duration, and QT interval. Values of corrected QT interval (QTc) were obtained by measuring the distance of QT interval on 12-lead ECG and then correcting using Bazett’s formula. QT dispersion was calculated by the difference from the longest to the shortest QT interval. A PR interval ≥ 200 ms, a QRS duration ≥120 ms, and a QTc interval > 450 ms (men) or > 470 ms (women) were considered abnormal1616 Pastore CA, Pinho C, Germiniani H, Samesima N, Mano R, Gruppi CJ, et al; Sociedade Brasileira de Cardiologia. Diretrizes da Sociedade Brasileira de Cardiologia sobre análise e emissão de laudos eletrocardiográficos. Arq Bras Cardiol. 2009;93(3 supl 2):1-19.. Four patients were excluded from QTc analyses due to left bundle branch block, atrial fibrillation (AF), or atrial flutter.

All patients provided written informed consent, and the local institutional ethics committee approved the study protocol (registration number: 1099/08). All phases of the study were free from interference by the ILR manufacturer, including study design, data collection, analysis, and description of the results. This company participated only in donating the devices used during the study.

ILR implantation and programming

This study used the Reveal® XT 9529 Implantable Cardiac Monitor (Medtronic Inc., Minneapolis, MN, USA), a 9 cm3, 15 g, subcutaneously implantable device for long-term ECG monitoring that is designed to continuously monitor cardiac rhythm for up to 3 years. The device is usually implanted, under local anesthesia, in the left parasternal region in the area indicated by a specific tool (Vector check).

The ECG data storage can be manually initiated or automatically triggered when AE fulfill the preprogrammed cut-off criteria: asystole (pause lasting >3 s); bradyarrhythmias (4 ventricular events <40 beats/min), ventricular tachycardia (5 ventricular events >120 beats/min), and accelerated ventricular tachycardia/ventricular fibrillation (9 ventricular events >200 beats/min from the past 12 events). AF and atrial tachycardia (AT) were automatically detected by the device using an internal algorithm programmed to detect AT/AF with default parameters. The dedicated AF detection algorithm uses irregularity and incoherence of RR intervals to identify and classify patterns in ventricular conduction. RR intervals were analyzed within each 2-min period, and the difference in duration between consecutive RR intervals (∆R-R) was calculated. Subsequently, the variability of these ∆R-R intervals is calculated, much as a Lorenz plot is constructed. When the RR intervals within the 2-min period show a certain pattern of irregularity, the heart rhythm in this period is classified as AF1717 Esperer HD, Esperer C, Cohen RJ. Cardiac arrhythmias imprint specific signatures on Lorenz plots. Ann Noninvasive Electrocardiol. 2008;13(1):44-60..

The device memory can automatically hold 28 AE with 30 s of preactivation and 27 s of postactivation ECG storage as well as 3 patient-activated events with 6.5 min of preactivation and 1 min of postactivation ECG storage. The sensitivity of AE detection was adjusted individually according to the number of false events observed at each visit. Patients were followed for at least 1 year after ILR implantation; the first evaluation occurred 2 weeks after hospital discharge and at 8-week intervals thereafter.

Outcomes

The outcomes were AE detected by ILR during the follow-up period. Each stored AE episode was analyzed and classified by a researcher as bradyarrhythmias and supraventricular or ventricular arrhythmias.

The bradyarrhythmias (heart rate < 40 beats/min) were classified as sinus pause, bradycardia, or atrioventricular (AV) block. Supraventricular arrhythmias were classified as premature atrial beats, non-sustained AT (an abrupt increase in heart rate [> 120 beats/min] lasting < 30 s), or sustained AT/AF (detected by the device according to irregularities in the RR intervals as noted on a Lorenz plot)1717 Esperer HD, Esperer C, Cohen RJ. Cardiac arrhythmias imprint specific signatures on Lorenz plots. Ann Noninvasive Electrocardiol. 2008;13(1):44-60.. Ventricular arrhythmias were categorized as premature ventricular beats, non-sustained ventricular tachycardia (VT), sustained VT (lasting > 30 s), or ventricular fibrillation.

Statistical analysis

The sample size was estimated as 92 patients based on the reported ventricular arrhythmia prevalence of 40% in a previous study published by Bozbas1818 Bozbas H, Atar I, Yildirir A, Ozqul A, Uyar M, Muderrisoqlu H, et al. Prevalence and predictors of arrhythmia in end stage renal disease patients on hemodialysis. Ren Fail. 2007;29(3):331-9., with a 10% variation in precision of the absolute estimate and a 95% reliability interval to analyze the proposed objectives and correlations1919 Lwanga SK, Lemeshow S. Sample size determination in health studies: a practical manual. Geneva: World Health Organization; 1991.. One patient was excluded due to localized infection 1 month after implantation. Statistical analysis of AE recorded by this ILR was conducted until device removal.

The incidence of AE was described in absolute and relative numbers, and continuous variables were expressed as mean ± standard deviation. Normality was assessed by means of the Kolmogorov-Smirnov test. Comparison of baseline characteristics of patients with and without AE was done with t tests for continuous variables and the chi-square test and Fisher’s exact test for categorical variables.

Multivariate logistic regression models using stepwise selection were applied to determine the independent association of baseline characteristics and AE incidence. A 2-sided p value of 0.05 was considered statistically significant and 95% confidence intervals (CIs) are presented for all odds ratios (ORs). All statistical analyses were conducted using a commercially available statistical software package (SPSS version 15.0 for Windows).

Results

One hundred patients were followed-up during a period of 424 ± 127 days after implantation of ILR, and no data were lost. All devices were inserted during a period of 8 months. Only 1 patient withdrew from the study due to a localized infection after 1 month of implantation, requiring removal of the ILR and antibiotic treatment. The mean duration of hemodialysis treatment was 53.8 ± 30 months. Hypertension was the most common comorbidity (97%), and 84% of patients were on beta-blockers. ECG findings demonstrated sinus rhythm in 99% of the patients, and 1 patient was in AF. The mean heart rate was 73 ± 15 beats/min, and 8% of patients had an intraventricular block. A prolonged QTc interval and an abnormal SAECG were documented in 33% and 3% of the patients, respectively. Echocardiographic characteristics showed mean left ventricular ejection fraction (LVEF) of 59 ± 10%, and 21% of patients had LVEF ≤50%. Abnormal myocardial scintigraphy was noted in 38% of the patients. Baseline clinical and demographic characteristics of patients are presented in Table 1.

Table 1
Clinicai, electrocardiographic, and functional characteristics of the study population

Incidence and factors associated to AE

During the ILR monitoring period, 98% of patients presented AE, with 92% of them presenting AE of more than one type. A total of 5075 AE were detected by ILR, resulting in a rate of 51.79 AE per patient. Supraventricular (94%) and ventricular arrhythmias (79%) were the most frequently diagnosed AE. Table 2 shows a descriptive panel of AE detected by ILR, and some examples of morphology are shown in Figure 1.

Table 2
Descriptive panel of arrhythmic events (AE) detected by implantable loop recorder in the study population
Figure 1
Examples of arrhythmic events recorded by implantable loop recorder during study follow-up. The tracing recorded in (A) shows isolated ventricular premature beats (*); the record in (B) shows polymorphic ventricular premature beats (**); episodes of non-sustained ventricular tachycardia are plotted in (C) and (D) (***), and an episode of atrial fibrillation is recorded in (E).

All clinical baseline, electrocardiographic, and functional characteristics were evaluated considering the occurrence of different types of AE, and predictors were identified exclusively for bradyarrhythmias and non-sustained VT. None of these variables was associated with the occurrence of AF or other supraventricular arrhythmias.

According to the AE detected by ILR, we observed that patients with bradyarrhythmias were significantly older (62.7 ± 6.9 years vs. 57.7 ± 9.1 years, p = 0.014), had lower mean HR (69.6 ± 8.7 beats/min vs. 75.5 ± 8.9 beats/min, p = 0.005), and had higher prevalence of coronary artery disease (CAD; 87% vs. 56%, p = 0.026) than those without bradyarrhythmias. Moreover, the PR interval was longer (190.2 ± 32.1 ms vs. 167.5 ± 17.6 ms, p < 0.001); there was a higher prevalence of first-degree AV block (36% vs. 3%, p < 0.001) and prolonged QTc interval (52% vs. 28%, p = 0.028) in patients with bradyarrhythmias. In contrast, there was no significant difference between patients with or without non-sustained VT, except that patients with non-sustained VT were less obese (9% vs. 27%, p = 0.01) and had higher prevalence of LV dilatation (31% vs. 14%, p = 0.04).

In a multivariate logistic regression model (Table 3), bradyarrhythmias were independently associated with PR interval duration (OR, 1.05 [95% CI, 1.02-1.08], p = 0.0008) and long QTc interval (OR, 7.28 [95% CI, 2.01-26.35], p = 0.002). When a cut-off of 200 ms for PR interval was used (first-degree AV block), the probability of bradyarrhythmias was 77% and 47% for patients with or without long QTc interval, respectively (Figure 2).

Table 3
Multivariate analysis demonstrating predictive factors for occurrence of arrhythmic events detected by the implantable loop recorder
Figure 2
Probability of bradyarrhythmia occurrence detected by implantable loop recorder in relation to PR interval duration stratified according to the type of QTc manifestation (with or without long QTc).

Furthermore, the presence of LV dilatation (OR, 2.83, [95% CI = 1.01-7.96], p = 0.04) was the only independent factor associated with non-sustained VT. Patients with LV dilatation were 2.8 times more likely to have non-sustained VT than those without it.

Clinical findings

Despite almost all patients (98%) presenting some type of AE, most had no significant clinical implication. All patients with AE reported at least 1 episode of palpitations, and no patient had syncope. Potentially serious bradyarrhythmias and ventricular tachyarrhythmias occurred in 4 and 1 patient, respectively. Three patients died suddenly due to bradyarrhythmia, and a patient with dilated cardiomyopathy developed advanced AV block (Figure 3), requiring pacemaker use and removal of the ILR. A 47-year-old man without structural heart disease died because of a malignant ventricular arrhythmia (Figure 4).

Figure 3
Recording of an advanced atrioventricular block episode by the implantable loop recorder. The marks (*) show three blocked P waves, indicating a pause of 3.1 s.
Figure 4
Fatal ventricular tachycardia/fibrillation episode recorded by the implantable loop recorder.

During the study follow-up period, 18 patients died, of whom 7 had SCD, 1 had heart failure (HF), and 10 died of non-cardiac causes. Among the cases of SCD, there were 3 bradyarrhythmias, 1 ventricular fibrillation, 1 acute myocardial infarction, and, in the remaining 2 cases, the ILR could not be analyzed and the causes of death have not been identified. Other nonfatal major cardiovascular events included acute pulmonary edema (9 patients), acute myocardial infarction (2 patients), acute peripheral vascular disease (2 patients), and ischemic stroke (1 patient). In addition, 14 patients underwent renal transplantation.

Discussion

In the PRETRANSPLANT study, continuous cardiac monitoring provided by ILR in RTCs on hemodialysis revealed a high incidence of arrhythmias. This new technology has recently been incorporated in this clinical setting, providing a prolonged period of cardiac monitoring that allows determination of relevant clinical and electrocardiographic correlations and solves the problem of spontaneous and circadian variabilities in AE. In addition, we identified several clinical factors independently associated with the most prevalent types of AE in the dialysis population. Importantly, supraventricular arrhythmias had no significant clinical implications; in contrast, bradyarrhythmias and ventricular arrhythmias were associated with serious and fatal clinical events.

Our findings showed the occurrence of at least some type of AE in 98% of patients. It is difficult to compare this study to others because none of the previous studies used an ILR for diagnosing cardiac arrhythmias. Normally, the ILR has been used to evaluate patients with recurrent syncope and a less severe cardiac risk profile1313 Brignole M, Vardas P, Hoffman E, Huikuri H, Moya A, Ricci R, et al; Task Force members of EHRA Scientific Documents Committee. Indications for the use of diagnostic implantable and external ECG loop recorders. Europace. 2009;11(5):671-87. Erratum in: Europace. 2009;11(6):836.. Moreover, previous studies using 24-h Holter monitoring for the detection of AE in the dialysis population reported a highly variable occurrence rate. Bozbas et al1818 Bozbas H, Atar I, Yildirir A, Ozqul A, Uyar M, Muderrisoqlu H, et al. Prevalence and predictors of arrhythmia in end stage renal disease patients on hemodialysis. Ren Fail. 2007;29(3):331-9. showed that 85.2% of 94 hemodialysis patients experienced an AE. Similar results were observed by Sforziniet al2020 Sforzini S, Latini R, Mingardi G, Vicentini A, Redaelli B. Ventricular arrhythmias and four-year mortality in haemodialysis patients. Gruppo Emodialisi e Patologie Cardiovascolari. Lancet. 1992;339(8787):212-3., who detected an AE in 76% of 127 hemodialysis patients. In contrast, D’Elia et al1111 D'Elia JA, Weinrauch LA, Gleason RE, Hampton LA, Smith-Ossman S, Yoburn DC, et al. Application of the ambulatory 24-hour electrocardiogram in the prediction of cardiac death in dialysis patients. Arch Intern Med. 1988;148(11):2381-5. reported AE in 26.2% of 122 patients, and 1 patient had an advanced AV block, and we observed the same rate in our study. This variability in the incidence of AE is most likely dependent on the specific characteristics of the population and on the different diagnostic criteria used for each study.

Many factors contributing to the increased incidence of AE in dialysis patients have been identified. Several studies have shown the influence of structural cardiac disease9Blumberg A, Häusermann M, Strub B, Jenzer HR. Cardiac arrhythmias in patients on maintenance hemodialysis. Nephron. 1983;33(2):91-5.,2121 Gross ML, Ritz E. Hypertrophy and fibrosis in the cardiomyopathy of uremia - beyond coronary heart disease. Semin Dial. 2008;21(4):308-18.,2222 de Lima JJ, Vieira ML, Lopes HF, Gruppi CJ, Medeiros CJ, Ianhez LE, et al. Blood pressure and the risk of complex arrhythmia in renal insufficiency, hemodialysis and renal transplant patients. Am J Hypertens. 1999;12(2 Pt 1):204-8., HF1111 D'Elia JA, Weinrauch LA, Gleason RE, Hampton LA, Smith-Ossman S, Yoburn DC, et al. Application of the ambulatory 24-hour electrocardiogram in the prediction of cardiac death in dialysis patients. Arch Intern Med. 1988;148(11):2381-5.,2323 Wizemann V, Kramer W, Funke T, Schutterle G. Dialysis-induced cardiac arrhythmias: fact or fiction? Importance of preexisting cardiac disease in the induction of arrhythmias during renal replacement therapy. Nephron. 1985;39(4):356-60.,2424 Burton JO, Korsheed S, Grundy BJ, McIntyre CW. Hemodialysis-induced left ventricular dysfunction is associated with an increase in ventricular arrhythmias. Ren Fail. 2008;30(7):701-9., electrolyte abnormalities8Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9.,1010 Weber H, Schwarzer C, Stummvoll HK, Joskowics G, Wolf A, Steinbach K, et al. Chronic hemodialysis: high risk patients for arrhythmias? Nephron. 1984;37(3):180-5., postdialysis hypokalemia1010 Weber H, Schwarzer C, Stummvoll HK, Joskowics G, Wolf A, Steinbach K, et al. Chronic hemodialysis: high risk patients for arrhythmias? Nephron. 1984;37(3):180-5., low potassium and calcium concentrations in the dialysate solution8Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9., silent ischemia related to dialysis2424 Burton JO, Korsheed S, Grundy BJ, McIntyre CW. Hemodialysis-induced left ventricular dysfunction is associated with an increase in ventricular arrhythmias. Ren Fail. 2008;30(7):701-9., the use of digoxin8Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9.,1010 Weber H, Schwarzer C, Stummvoll HK, Joskowics G, Wolf A, Steinbach K, et al. Chronic hemodialysis: high risk patients for arrhythmias? Nephron. 1984;37(3):180-5., the presence of left ventricular hypertrophy8Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9.,2121 Gross ML, Ritz E. Hypertrophy and fibrosis in the cardiomyopathy of uremia - beyond coronary heart disease. Semin Dial. 2008;21(4):308-18., hyperparathyroidism, and uncontrolled hypertension2222 de Lima JJ, Vieira ML, Lopes HF, Gruppi CJ, Medeiros CJ, Ianhez LE, et al. Blood pressure and the risk of complex arrhythmia in renal insufficiency, hemodialysis and renal transplant patients. Am J Hypertens. 1999;12(2 Pt 1):204-8.,2525 Ramirez G, Brueggemeyer CD, Newton JL. Cardiac arrhythmias on hemodialysis in chronic renal failure patients. Nephron. 1984;36(4):212-8.,2626 De Lima JJ, Lopes HF, Gruppi CJ, Abensur H, Giorgi MC, Krieger EM, et al. Blood pressure influences the occurrence of complex ventricular arrhythmia in hemodialysis patients. Hypertension. 1995;26(6 Pt 2):1200-3.; however, there are no studies that used continuous electrocardiographic monitoring methods. The present study showed that alterations in the conventional ECG and echocardiogram were independently associated with the AE detected by the ILR.

Previous studies reported that electrocardiographic alterations, such as prolonged PR and QT intervals, have been considered predictive factors for cardiovascular events and mortality in the end-stage renal disease and general populations2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6.,2828 Cheng S, Keyes MJ, Larson MG, McCabe EL, Newton-Cheh C, Levy D, et al. Long-term outcomes in individuals with prolonged PR interval or first-degree atrioventricular block. JAMA. 2009;301(24):2571-7.. In dialysis patients, all of these findings were more evident and have been associated with AE1212 Abe S, Yoshizawa M, Nakanishi N, Yazawa T, Yokota K, Honda M, et al. Electrocardiographic abnormalities in patients receiving hemodialysis. Am Heart J. 1996;131(6):1137-44.,2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6.,2929 Suzuki R, Tsumura K, Inoue R, Kishimoto H, Morii H. QT interval prolongation in the patients receiving maintenance hemodialysis. Clin Nephrol. 1998;49(4):240-4.. Abe et al1212 Abe S, Yoshizawa M, Nakanishi N, Yazawa T, Yokota K, Honda M, et al. Electrocardiographic abnormalities in patients receiving hemodialysis. Am Heart J. 1996;131(6):1137-44. showed that first-degree AV block is more prevalent in patients with chronic kidney disease undergoing hemodialysis (5.4%) than in those who were not receiving dialysis (1.4%) and in healthy controls. Hage et al2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6. identified prolonged PR interval on conventional ECG in 15% of patients, and this was not associated with worse survival. In our study, the prevalence of first-degree AV block was 11% and it was 12 times more prevalent in patients with bradyarrhythmias. For each 10-ms increase in the PR interval duration, the likelihood of a bradyarrhythmia increased by 5% during the follow-up.

Other studies have shown that the QT interval is significantly longer in dialysis patients than in healthy subjects. Furthermore, it has been demonstrated that the QT interval increases during dialysis and is associated with AE2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6.

28 Cheng S, Keyes MJ, Larson MG, McCabe EL, Newton-Cheh C, Levy D, et al. Long-term outcomes in individuals with prolonged PR interval or first-degree atrioventricular block. JAMA. 2009;301(24):2571-7.

29 Suzuki R, Tsumura K, Inoue R, Kishimoto H, Morii H. QT interval prolongation in the patients receiving maintenance hemodialysis. Clin Nephrol. 1998;49(4):240-4.

30 Green D, Roberts PR, New DI, Kalra PA. Sudden cardiac death in hemodialysis patients: an in-depth review. Am J Kidney Dis. 2011;57(6):921-9.

31 Selby NM, McIntyre CW. The acute cardiac effects of dialysis. Semin Dial. 2007;20(3):220-8.
-3232 Valentim B, Pereira A, Coelho P, Pereira T. Study of ventricular electrical systole in patients with end-stage kidney disease on hemodialysis. Arq Bras Cardiol. 2013;100(3):261-8.. In our study, the mean QTc interval (436.4 ± 27.6 ms) was similar to the results reported by Suzuki et al2929 Suzuki R, Tsumura K, Inoue R, Kishimoto H, Morii H. QT interval prolongation in the patients receiving maintenance hemodialysis. Clin Nephrol. 1998;49(4):240-4.(432.6 ± 24.9 ms) and slightly lower than those observed in the study by Hage et al2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6. (447 ± 35 ms). It is noteworthy that all of these measurements are within the normal range (≤450 ms in men and ≤470 ms in women)1616 Pastore CA, Pinho C, Germiniani H, Samesima N, Mano R, Gruppi CJ, et al; Sociedade Brasileira de Cardiologia. Diretrizes da Sociedade Brasileira de Cardiologia sobre análise e emissão de laudos eletrocardiográficos. Arq Bras Cardiol. 2009;93(3 supl 2):1-19.. Despite this, there was a high prevalence of long QTc in our study (33%), and this was similar to the results obtained by Hage et al.(39%)2727 Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6.. This is in agreement with the data in the literature, wherein the increase in the QT interval and the presence of a long QT have been associated with AE occurrence. Therefore, a careful evaluation using conventional ECG should be done routinely in this population, whereby these patients with higher risk of AE can be stratified.

Another interesting finding in our study was that LV dilatation occurred in 23% of patients and almost tripled the occurrence of non-sustained VT. Parfrey et al3333 Parfrey PS. Cardiac disease in dialysis patients: diagnosis, burden of disease, prognosis, risk factors and management. Nephrol Dial Transplant. 2000;15 Suppl 5:58-68. found that in a study of 432 patients, the prevalence of LV dilation (28%) was slightly higher than that in our study, and it was associated with CAD, hypertension, anemia, and hypoalbuminemia. Previous studies have shown that ventricular dilatation is a marker of poor prognosis in the dialysis population and is associated with LV volume overload3030 Green D, Roberts PR, New DI, Kalra PA. Sudden cardiac death in hemodialysis patients: an in-depth review. Am J Kidney Dis. 2011;57(6):921-9.,3333 Parfrey PS. Cardiac disease in dialysis patients: diagnosis, burden of disease, prognosis, risk factors and management. Nephrol Dial Transplant. 2000;15 Suppl 5:58-68.

34 Parfrey PS, Foley RN, Harnett JD, Kent GM, Murray DC, Barre PE. Outcome and risk factors for left ventricular disorders in chronic uraemia. Nephrol Dial Transplant. 1996;11(7):1277-85.
-3535 Shamseddin MK, Parfrey OS. Sudden cardiac death in chronic kidney disease: epidemiology and prevention. Nat Rev Nephrol. 2011;7(3):145-54.. The eccentric hypertrophy induced by this mechanism causes cardiomyocyte stretching, apoptosis, and cell death, which results in myocardial fibrosis. The combination of these factors with neurohormonal hyperactivity and HF may precipitate the occurrence of AE3636 Mall G, Huther W, Schneider J, Lundin P, Ritz E. Diffuse intermyocardiocytic fibrosis in uraemic patients. Nephrol Dial Transplant 1990;5(1):39-44.

37 Ritz E, Rambausek M, Mall G, Ruffmann K, Mandelbaum A. Cardiac changes in uraemia and their possible relationship to cardiovascular instability on dialysis. Nephrol Dial Transplant.1990;5 Suppl 1:93-7.

38 Remppis A, Ritz E. Cardiac problems in the dialysis patient: beyond coronary disease. Semin Dial. 2008;21(4):319-25.
-3939 Vonend O, Rump LC, Ritz E. Sympathetic overactivity - the Cinderella of cardiovascular risk factor in dialysis patients. Semin Dial. 2008;21(4):326-30.. Thus, an echocardiographic evaluation to diagnose structural changes may help identify patients at high risk of arrhythmias in the dialysis population.

Predictors of AE occurrence is a subject that is not well explored in the literature. Bozbas et al1818 Bozbas H, Atar I, Yildirir A, Ozqul A, Uyar M, Muderrisoqlu H, et al. Prevalence and predictors of arrhythmia in end stage renal disease patients on hemodialysis. Ren Fail. 2007;29(3):331-9. showed a predictive relationship between hypertension, CAD, and QT dispersion with complex ventricular arrhythmias. Moreover, they observed a causal relationship between the duration of dialysis therapy and premature atrial contraction. More specifically, Nishi et al4040 Nishi K, Fujimoto S, Hisanaga S, Ogawa O, Kitamura K. Electrocardiographic assessment of incident atrial fibrillation in hemodialysis patients. Ther Apher Dial. 2013;17(1):16-23. identified the age and presence of P-terminal force >0.04 mm/s as predictors of new-onset AF. Distinctly, our study could not establish any independent predictors of AF occurrences, but has identified predictors of bradyarrhythmia, which affected 3% of our patients, and non-sustained VT.

In summary, a conjunction of various risk factors may provide a very favorable scenario for the high occurrence of AE in the dialysis population. Moreover, taking into account the random characteristic of the occurrence of AE, and that its documentation requires absolute synchronism, it is important to emphasize that prolonged monitoring with an ILR may play a role in prospective investigations aiming to reduce cardiovascular events in this high-risk population.

Study Limitations

Some aspects of this analysis merit further consideration. First, the study population comprised consecutive hemodialysis patients derived from an academic institute rendering routine tertiary healthcare with interdisciplinary follow-up. Therefore, caution must be exercised when extrapolating these findings to other RTCs.

Second, the ILR may have some limitations related to detection properties; for example, the electrocardiographic analysis is taken from an isolated, single, subcutaneous ECG lead, and atrial depolarization is difficult to identify. The algorithm used by the device to identify AF expends 2 min in observation of RR-interval irregularity distribution in a Lorenz plot, which imposes a limit of inability to autoidentify AF episodes shorter than this duration. Another limitation of the ILR is a memory capacity limited to 30 AE recordings. When the memory was saturated, a new AE recording replaced the oldest, a feature known as loop memory recording. In patients with a high frequency of cardiac arrhythmias, this feature limits the AE recordings, and thus, results in underestimation of their real incidence. In the present study, it issue was minimized by reducing the intervals between the visits to 8 weeks. However, 40% of our patients had saturated ILR memory, which could have prevented analysis of certain types of AE.

Conclusions

The PRETRANSPLANT study is the first to report medium-term monitoring of AE recorded by an ILR in a high-risk population of RTCs. Most AE detected were not clinically relevant, but serious bradyarrhythmias and/or ventricular tachyarrhythmias occurred. Defining clinical characteristics that can stratify patients at higher risk of AE can help prevent complications or identify patients who require stricter monitoring. In our study, the factors independently associated with AE were the PR interval and the presence of long QTc for bradyarrhythmias and LV dilatation for non-sustained VT.

  • Sources of Funding
    There were no external funding sources for this study.
  • Study Association
    This article is part of the thesis of Doctoral submitted by Rodrigo Tavares Silva, from Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo.

References

  • 1
    United States Renal Data System. 2010 Annual Data Report. [Internet]: atlas of chronic kidney disease and end-stage renal disease in the United States. Bethesda; 2010. [Cited in 2014 Jun 10]. Available from: http://www.usrds.org/2010/pdf/v1_00a_intros.PDF
    » http://www.usrds.org/2010/pdf/v1_00a_intros.PDF
  • 2
    Herzog CA, Mangrum JM, Passman R. Sudden cardiac death and dialysis patients. Semin Dial. 2008;21(4):300-7.
  • 3
    Kanbay M, Afsar B, Goldsmith D, Covic A. Sudden death in hemodialysis: an update. Blood Purif. 2010;30(2):135-45.
  • 4
    De Bie MK, van Dam B, Gassbeek A, van Buren M, van Erven L, Baxx JJ, et al. The current status of interventions aiming at reducing sudden cardiac death in dialysis patients. Eur Heart J. 2009;30(13):1559-64.
  • 5
    Myerburg RJ, Castellanos A. Emerging paradigms of the epidemiology and demographics of sudden cardiac arrest. Heart Rhythm. 2006;3(2):235-9.
  • 6
    Strippoli GF, Craig JC. Sunset for statins after AURORA? N Engl J Med. 2009;360(14):1455-7.
  • 7
    Wanner C, Krane V, Marz W, Olschewski M, Mann JF, Ruf G, et al; German Diabetes and Dialysis Study Investigators. Atorvastatin in patients with type 2 diabetes mellitus undergoing hemodialysis. N Engl J Med. 2005;353(3):238-48. Erratum in: N Engl J Med. 2005;353(15):1640.
  • 8
    Morrison G, Michelson E, Brown S, Morganroth J. Mechanism and prevention of cardiac arrhythmias in chronic hemodialysis patients. Kidney Int. 1980;17(6):811-9.
  • 9
    Blumberg A, Häusermann M, Strub B, Jenzer HR. Cardiac arrhythmias in patients on maintenance hemodialysis. Nephron. 1983;33(2):91-5.
  • 10
    Weber H, Schwarzer C, Stummvoll HK, Joskowics G, Wolf A, Steinbach K, et al. Chronic hemodialysis: high risk patients for arrhythmias? Nephron. 1984;37(3):180-5.
  • 11
    D'Elia JA, Weinrauch LA, Gleason RE, Hampton LA, Smith-Ossman S, Yoburn DC, et al. Application of the ambulatory 24-hour electrocardiogram in the prediction of cardiac death in dialysis patients. Arch Intern Med. 1988;148(11):2381-5.
  • 12
    Abe S, Yoshizawa M, Nakanishi N, Yazawa T, Yokota K, Honda M, et al. Electrocardiographic abnormalities in patients receiving hemodialysis. Am Heart J. 1996;131(6):1137-44.
  • 13
    Brignole M, Vardas P, Hoffman E, Huikuri H, Moya A, Ricci R, et al; Task Force members of EHRA Scientific Documents Committee. Indications for the use of diagnostic implantable and external ECG loop recorders. Europace. 2009;11(5):671-87. Erratum in: Europace. 2009;11(6):836.
  • 14
    Bloch Thomsen PE, Jons C, Raatikainen P, Moerch Joergensen R, Hartikainen J, Virtanen V, et al. Long-term recording of cardiac arrhythmias with an implantable cardiac monitor in patients with reduced ejection fraction after acute myocardial infarction. The Cardiac Arrhythmias and Risk Stratification After Acute Myocardial Infarction (CARISMA) Study. Circulation. 2010;122(13):1258-64.
  • 15
    Gowdak LH, de Paula FJ, César LA, Bortolotto LA, de Lima JJ. A new risk score model to predict the presence of significant coronary artery disease in renal transplant candidates. Transplant Res. 2013;2(1):18.
  • 16
    Pastore CA, Pinho C, Germiniani H, Samesima N, Mano R, Gruppi CJ, et al; Sociedade Brasileira de Cardiologia. Diretrizes da Sociedade Brasileira de Cardiologia sobre análise e emissão de laudos eletrocardiográficos. Arq Bras Cardiol. 2009;93(3 supl 2):1-19.
  • 17
    Esperer HD, Esperer C, Cohen RJ. Cardiac arrhythmias imprint specific signatures on Lorenz plots. Ann Noninvasive Electrocardiol. 2008;13(1):44-60.
  • 18
    Bozbas H, Atar I, Yildirir A, Ozqul A, Uyar M, Muderrisoqlu H, et al. Prevalence and predictors of arrhythmia in end stage renal disease patients on hemodialysis. Ren Fail. 2007;29(3):331-9.
  • 19
    Lwanga SK, Lemeshow S. Sample size determination in health studies: a practical manual. Geneva: World Health Organization; 1991.
  • 20
    Sforzini S, Latini R, Mingardi G, Vicentini A, Redaelli B. Ventricular arrhythmias and four-year mortality in haemodialysis patients. Gruppo Emodialisi e Patologie Cardiovascolari. Lancet. 1992;339(8787):212-3.
  • 21
    Gross ML, Ritz E. Hypertrophy and fibrosis in the cardiomyopathy of uremia - beyond coronary heart disease. Semin Dial. 2008;21(4):308-18.
  • 22
    de Lima JJ, Vieira ML, Lopes HF, Gruppi CJ, Medeiros CJ, Ianhez LE, et al. Blood pressure and the risk of complex arrhythmia in renal insufficiency, hemodialysis and renal transplant patients. Am J Hypertens. 1999;12(2 Pt 1):204-8.
  • 23
    Wizemann V, Kramer W, Funke T, Schutterle G. Dialysis-induced cardiac arrhythmias: fact or fiction? Importance of preexisting cardiac disease in the induction of arrhythmias during renal replacement therapy. Nephron. 1985;39(4):356-60.
  • 24
    Burton JO, Korsheed S, Grundy BJ, McIntyre CW. Hemodialysis-induced left ventricular dysfunction is associated with an increase in ventricular arrhythmias. Ren Fail. 2008;30(7):701-9.
  • 25
    Ramirez G, Brueggemeyer CD, Newton JL. Cardiac arrhythmias on hemodialysis in chronic renal failure patients. Nephron. 1984;36(4):212-8.
  • 26
    De Lima JJ, Lopes HF, Gruppi CJ, Abensur H, Giorgi MC, Krieger EM, et al. Blood pressure influences the occurrence of complex ventricular arrhythmia in hemodialysis patients. Hypertension. 1995;26(6 Pt 2):1200-3.
  • 27
    Hage FG, de Mattos AM, Khamash H, Mehta S, Warnock D, Iskandrian AE. QT prolongation is an independent predictor of mortality in end-stage renal disease. Clin Cardiol. 2010;33(6):361-6.
  • 28
    Cheng S, Keyes MJ, Larson MG, McCabe EL, Newton-Cheh C, Levy D, et al. Long-term outcomes in individuals with prolonged PR interval or first-degree atrioventricular block. JAMA. 2009;301(24):2571-7.
  • 29
    Suzuki R, Tsumura K, Inoue R, Kishimoto H, Morii H. QT interval prolongation in the patients receiving maintenance hemodialysis. Clin Nephrol. 1998;49(4):240-4.
  • 30
    Green D, Roberts PR, New DI, Kalra PA. Sudden cardiac death in hemodialysis patients: an in-depth review. Am J Kidney Dis. 2011;57(6):921-9.
  • 31
    Selby NM, McIntyre CW. The acute cardiac effects of dialysis. Semin Dial. 2007;20(3):220-8.
  • 32
    Valentim B, Pereira A, Coelho P, Pereira T. Study of ventricular electrical systole in patients with end-stage kidney disease on hemodialysis. Arq Bras Cardiol. 2013;100(3):261-8.
  • 33
    Parfrey PS. Cardiac disease in dialysis patients: diagnosis, burden of disease, prognosis, risk factors and management. Nephrol Dial Transplant. 2000;15 Suppl 5:58-68.
  • 34
    Parfrey PS, Foley RN, Harnett JD, Kent GM, Murray DC, Barre PE. Outcome and risk factors for left ventricular disorders in chronic uraemia. Nephrol Dial Transplant. 1996;11(7):1277-85.
  • 35
    Shamseddin MK, Parfrey OS. Sudden cardiac death in chronic kidney disease: epidemiology and prevention. Nat Rev Nephrol. 2011;7(3):145-54.
  • 36
    Mall G, Huther W, Schneider J, Lundin P, Ritz E. Diffuse intermyocardiocytic fibrosis in uraemic patients. Nephrol Dial Transplant 1990;5(1):39-44.
  • 37
    Ritz E, Rambausek M, Mall G, Ruffmann K, Mandelbaum A. Cardiac changes in uraemia and their possible relationship to cardiovascular instability on dialysis. Nephrol Dial Transplant.1990;5 Suppl 1:93-7.
  • 38
    Remppis A, Ritz E. Cardiac problems in the dialysis patient: beyond coronary disease. Semin Dial. 2008;21(4):319-25.
  • 39
    Vonend O, Rump LC, Ritz E. Sympathetic overactivity - the Cinderella of cardiovascular risk factor in dialysis patients. Semin Dial. 2008;21(4):326-30.
  • 40
    Nishi K, Fujimoto S, Hisanaga S, Ogawa O, Kitamura K. Electrocardiographic assessment of incident atrial fibrillation in hemodialysis patients. Ther Apher Dial. 2013;17(1):16-23.

Publication Dates

  • Publication in this collection
    04 Sept 2015
  • Date of issue
    Nov 2015

History

  • Received
    14 Jan 2015
  • Reviewed
    21 May 2015
  • Accepted
    01 June 2015
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