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Arquivos Brasileiros de Cardiologia

Print version ISSN 0066-782XOn-line version ISSN 1678-4170

Arq. Bras. Cardiol. vol.105 no.5 São Paulo Nov. 2015  Epub Sep 04, 2015 

Original Articles

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

Rodrigo Tavares Silva1 

Martino Martinelli Filho1 

Giselle de Lima Peixoto1 

José Jayme Galvão de Lima1 

Sérgio Freitas de Siqueira1 

Roberto Costa1 

Luís Henrique Wolff Gowdak1 

Flávio Jota de Paula2 

Roberto Kalil Filho1 

José Antônio Franchini Ramires1 

1Instituto do Coração do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP - Brazil

2Unidade de Transplante Renal - Divisão de Urologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, SP - Brazil



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.


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


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.


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).


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


Patients with end-stage renal disease undergoing chronic hemodialysis have a high mortality rate1. 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 mechanisms1-3.

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 undertermined1,2,4-7.

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 systems8-12. 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 13,14. 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.


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)15. 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 abnormal16. 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 AF17.

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.


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)17. 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 Bozbas18, with a 10% variation in precision of the absolute estimate and a 95% reliability interval to analyze the proposed objectives and correlations19. 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).


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 

Characteristics n = 100
Age in years, mean ± SD (median) 59 ± 8.8 (59.1)
Male gender (%) 65
Ethnicity (%)  
White 73
Afro-Brazilian/Asian 21 / 6
Systemic arterial hypertension (%) 97
Diabetes mellitus (%) 70
Dyslipidemia (%) 54
Smoking/obesity (%) 9 / 17
Angina/previous myocardial infarction (%) 30 / 34
Heart failure (%) 27
Cerebrovascular disease/peripheral vascular insufficiency (%) 13/55
Duration of hemodialysis in months, mean ± SD (median) 53.8 ± 30 (48.3)
Medical therapy (%)  
Angiotensin-converting enzyme inhibitor or angiotensin receptor blockers 50
Beta-blockers/calcium channel antagonists 84 / 31
Acetylsalicylic acid/statins 84 / 62
Amiodarone 1
Conventional electrocardiogram (n = 100)  
Heart rate (beats/min) 73 ± 15.2
Sinus rhythm/atrial fibrillation 99% / 1%
PR interval (ms) 173.2 ± 24
QRS (ms) 91.4 ± 17.5
First-degree atrioventricular block 11%
Right bundle branch block/left bundle branch block 4% / 4%
Mean QTc interval (ms)/prolonged QTc (%) 436.4 ± 27.6 / 33%
QT dispersion (ms) 50.7 ± 24.7
Signal-averaged ECG positive (%), n = 100 3%
Echocardiogram (n = 99)  
Left atrium (mm), mean ± SD 40.6 ± 6.4
Interventricular septum/posterior wall (mm), mean ± SD 11.7 ± 2 / 11 ± 1.7
Left ventricular diastolic diameter/left ventricular systolic diameter (mm), mean ± SD 50.5 ± 6.1 / 34 ± 6.6
Left ventricular ejection fraction (%), mean ± SD 59.5 ± 10.8
Left ventricular ejection fraction ≤ 50% (%) 21
Cardiac mass index (g/m2), mean ± SD 125.2 ± 29.7
Diastolic dysfunction (%) 78
Segmental alterations (%) 26
Myocardial perfusion scintigraphy (n = 89)  
Normal/altered/ischemic (%) 62 / 27 / 11

SD: Standard deviation; ECG: Electrocardiogram.

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 

AE Incidence (n = 100) AE (number) AE Rate/pts
Follow-up: 424.7 ± 127.1 days
Bradyarrhythmias 25% 155 6.20
Asystole 4% 12 3.00
Bradycardia 24% 141 5.87
Advanced atrioventricular block 1% 2 2.00
Supraventricular arrhythmias 94% 3.702 39.38
Premature atrial beats 40% 276 6.90
Sinusal tachycardia 69% 1.972 28.58
Non-sustained atrial tachycardia 74% 1.362 18.41
Sustained atrial tachycardia 7% 50 7.14
Atrial fibrillation 13% 42 3.23
Ventricular Arrhythmias 79% 1.218 15.42
Premature ventricular beats 70% 947 13.53
Non-sustained ventricular tachycardia 56% 270 4.82
Sustained ventricular tachycardia/ventricular fibrillation 1% 1 1.00

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 

  Bradyarrhythmias Non-sustained ventricular tachycardia
  OR 95% CI p value OR 95% CI p value
Prolonged QTc 7.28 2.01-26.35 0.002 - - -
Duration of PR interval 1.05 1.02 to 1.08 0.0008 - - -
Left ventricular dilatation - - - 2.83 1.01-7.96 0.041

OR: Odds ratio; CI: Confidence interval.

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.


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 profile13. 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 al18 showed that 85.2% of 94 hemodialysis patients experienced an AE. Similar results were observed by Sforziniet al20, who detected an AE in 76% of 127 hemodialysis patients. In contrast, D’Elia et al11 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 disease9,21,22, HF11,23,24, electrolyte abnormalities8,10, postdialysis hypokalemia10, low potassium and calcium concentrations in the dialysate solution8, silent ischemia related to dialysis24, the use of digoxin8,10, the presence of left ventricular hypertrophy8,21, hyperparathyroidism, and uncontrolled hypertension22,25,26; 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 populations27,28. In dialysis patients, all of these findings were more evident and have been associated with AE12,27,29. Abe et al12 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 al27 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 AE27-32. In our study, the mean QTc interval (436.4 ± 27.6 ms) was similar to the results reported by Suzuki et al29(432.6 ± 24.9 ms) and slightly lower than those observed in the study by Hage et al27 (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)16. 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%)27. 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 al33 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 overload30,33-35. 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 AE36-39. 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 al18 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 al40 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.


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.


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: [ Links ]

Herzog CA, Mangrum JM, Passman R. Sudden cardiac death and dialysis patients. Semin Dial. 2008;21(4):300-7. [ Links ]

Kanbay M, Afsar B, Goldsmith D, Covic A. Sudden death in hemodialysis: an update. Blood Purif. 2010;30(2):135-45. [ Links ]

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. [ Links ]

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

Strippoli GF, Craig JC. Sunset for statins after AURORA? N Engl J Med. 2009;360(14):1455-7. [ Links ]

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. [ Links ]

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. [ Links ]

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

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

Esperer HD, Esperer C, Cohen RJ. Cardiac arrhythmias imprint specific signatures on Lorenz plots. Ann Noninvasive Electrocardiol. 2008;13(1):44-60. [ Links ]

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. [ Links ]

Lwanga SK, Lemeshow S. Sample size determination in health studies: a practical manual. Geneva: World Health Organization; 1991. [ Links ]

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. [ Links ]

Gross ML, Ritz E. Hypertrophy and fibrosis in the cardiomyopathy of uremia - beyond coronary heart disease. Semin Dial. 2008;21(4):308-18. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

Ramirez G, Brueggemeyer CD, Newton JL. Cardiac arrhythmias on hemodialysis in chronic renal failure patients. Nephron. 1984;36(4):212-8. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

Selby NM, McIntyre CW. The acute cardiac effects of dialysis. Semin Dial. 2007;20(3):220-8. [ Links ]

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. [ Links ]

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. [ Links ]

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. [ Links ]

Shamseddin MK, Parfrey OS. Sudden cardiac death in chronic kidney disease: epidemiology and prevention. Nat Rev Nephrol. 2011;7(3):145-54. [ Links ]

Mall G, Huther W, Schneider J, Lundin P, Ritz E. Diffuse intermyocardiocytic fibrosis in uraemic patients. Nephrol Dial Transplant 1990;5(1):39-44. [ Links ]

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. [ Links ]

Remppis A, Ritz E. Cardiac problems in the dialysis patient: beyond coronary disease. Semin Dial. 2008;21(4):319-25. [ Links ]

Vonend O, Rump LC, Ritz E. Sympathetic overactivity - the Cinderella of cardiovascular risk factor in dialysis patients. Semin Dial. 2008;21(4):326-30. [ Links ]

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. [ Links ]

Received: January 14, 2015; Revised: May 21, 2015; Accepted: June 01, 2015

Mailing Address: Martino Martinelli Filho, Instituto do Coração (InCor) – Hospital das Clínicas da Universidade de São Paulo. Rua Peixoto Gomide, 1628 AP 51, Cerqueira Cesar. Postal Code 01409-002, São Paulo, SP – Brazil. Email:,

Author contributions

Conception and design of the research: Silva RT, Martinelli M, Lima JJG, Siqueira SF, Costa R, Gowdak LHW, Paula FJ; Acquisition of data: Silva RT, Martinelli M, Peixoto GL, Siqueira SF, Costa R, Gowdak LHW, Paula FJ; Analysis and interpretation of the data: Silva RT, Martinelli M, Peixoto GL, Lima JJG, Siqueira SF, Gowdak LHW, Paula FJ; Statistical analysis: Silva RT, Martinelli M, Peixoto GL, Siqueira SF; Writing of the manuscript: Silva RT, Martinelli M, Peixoto GL, Lima JJG, Siqueira SF, Costa R; Critical revision of the manuscript for intellectual content: Silva RT, Martinelli M, Peixoto GL, Lima JJG, Siqueira SF, Costa R, Gowdak LHW, Paula FJ, Kalil Filho R, Ramires JAF.

Potential Conflict of Interest

No potential conflict of interest relevant to this article was reported.

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