Abstract
Background
Chagas disease is a neglected tropical disease that is still considered a global health emergency. In the Amazon region, most of the reports are of acute cases that are associated with oral transmission. This study aimed to evaluate myocardial injury in patients with acute Chagas disease before and after treatment.
Methods and Results
We evaluated 23 patients with acute Chagas disease in 3 different stages of progression. Group 1 had 12 patients evaluated during the acute phase, at the time of diagnosis, and 1 year after treatment, and Group 2 had 11 patients in the late postacute phase who were evaluated 5.2 years on average after diagnosis and treatment. ECGs with the Selvester score, 24‐hour Holter exam, and cardiovascular magnetic resonance imaging were performed. The mean age of the 23 patients was 44.3±18.9 years, and they were mostly men (15/65.24%) from Amazonas state (22/95.6%). In 69.6% (n=16) of the patients, some ECG alterations were found, the most frequent being left anterior fascicular block and ventricular repolarization. In Group 1, the 24‐hour Holter exam showed atrial tachycardia in 3 (25%) patients and ventricular extrasystoles in 2 (16.7%) patients. In Group 2, 1 patient had ventricular extrasystoles. Myocardial injury was observed in 7 patients (58.3%) at the acute phase and in 5 (50%) patients at the 1‐year follow‐up in Group 1 and in 2 (18.2%) patients in Group 2.
Conclusions
This article describes, for the first time, myocardial injury shown by cardiovascular magnetic resonance imaging in a group of patients with acute Chagas disease and reveals the importance of early detection and follow‐up of the cardiac impairment in these patients.
Keywords: acute Chagas disease, Brazilian Amazon, myocardial injury
Subject Categories: Magnetic Resonance Imaging (MRI), Electrocardiology (ECG)
Nonstandard Abbreviations and Acronyms
- ACD
acute Chagas disease
- CD
Chagas disease
- G1
group 1
- G1‐FU
group 1 with 1‐year follow‐up
- G2
group 2
- LGE
late gadolinium enhancement
- MF
myocardial fibrosis
- SS
Selvester score
Clinical Perspective
What Is New?
The prevalence of Chagas disease in western Amazonia has been growing significantly through the oral route transmission and attributed to the consumption of contaminated food.
Acute Chagas disease can cause myocardial injury that can be detected by cardiovascular magnetic resonance with potential prognostic and diagnostic value.
What Are the Clinical Implications?
A low‐cost and easily accessible tool such as the Selvester score could be an alternative in the detection of early myocardial injury in acute Chagas disease.
Chagas disease (CD) is a neglected tropical disease that is still considered a global health emergency. It is estimated that >7 million people are infected with Trypanosoma cruzi worldwide, and >70 million people live in areas with a constant risk of transmission. 1 , 2 In Latin America, the disease is endemic in 21 countries, including Brazil, where it is estimated that more than a million people are living with CD, and this results in ≈4000 deaths every year. 3
In the Amazon region, most reports are of acute cases associated with oral transmission that has occurred as the result of the ingestion of juices made from palm fruits (eg, açaí berry, palm tree wine, sugar cane, and guava juices). 4 Clinically, these acute cases may present nonspecific symptoms and for which treatment with benznidazole (Rochagan) is able to achieve 90% efficacy. 5
Chagas cardiomyopathy is the main cause of morbidity and mortality, and myocardial injury can be precisely detected by cardiovascular magnetic resonance (CMR) with late gadolinium enhancement (LGE) technique. 6 However, this condition is mostly described in the chronic phase of CD. 7 CMR is an imaging technique that is a significant technological development widely used in the diagnosis, monitoring, and treatment of cardiovascular diseases, especially in cardiomyopathies, with regard to diagnostic and prognostic differentiation. 8
Postinflammatory myocardial injury can be safely identified by CMR with delayed enhancement, which is as an important predictor of arrhythmia and sudden death in several nonischemic cardiomyopathies, such as hypertrophic cardiomyopathy and chronic chagasic cardiomyopathy, and may be useful in risk stratification in patients with CD. 9
To our knowledge, there are no studies that assessed the presence of myocardial injury by CMR involving a series of cases of acute CD (ACD) or with follow‐up evaluation after treatment. In addition, in the Amazon region, the aspects of the cardiac involvement of the disease, such as the evaluation of myocardial injury and cardiac arrhythmias, are not well known. Thus, the aim of this study was to investigate the presence and magnitude of myocardial injury in autochthonous patients with CD in the acute and posttreatment phases in the Brazilian Amazon using CMR.
Methods
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Study Design and Patient Population
This longitudinal study was carried out at the CD outpatient clinic of the Tropical Medicine Foundation Dr Heitor Vieira Dourado and followed up autochthonous patients from the western Amazon who were diagnosed with ACD.
Three groups at different stages of disease progression were included: group 1 (G1) with 12 patients with ACD evaluated before the start of treatment (G1) and with 1 year follow‐up (G1‐FU) after the end of treatment with benznidazole and group 2 (G2) with 11 late postacute patients evaluated 5.2 years on average after diagnosis and treatment. All patients were diagnosed by direct parasitological examination and a thick smear test and treated with benznidazole (Rochagan), 5 to 7 mg/kg for 60 days according to the II Brazilian Consensus on Chagas Disease, 2005 and 2015. 5 , 10
ECG Analysis and Dynamic Electrocardiography (24‐Hour Holter Exam)
All patients underwent a standard 12‐lead ECG (10 mm/mV and 25 mm/s). The ECG analysis was performed blindly by 2 experienced cardiologists, following the criteria established in the Brazilian Electrocardiogram Guidelines. 11 The evaluation of the Selvester score (SS) followed the recommendations established by Loring et al, 12 in which each point was designed to correspond to ≈3% of left ventricular injury. The patients underwent prolonged ECG monitoring (24‐hour Holter exam) to allow the detection and reproduction of arrhythmia tracings for a longer period.
Selvester QRS Score
The SS is a 12‐lead ECG analysis in which the QRS complex is adjusted for sex and age in the parameters of duration and amplitude (millivolt). Each column of the score table 12 represents an ECG alteration (right bundle branch block, left anterior fascicular block, left ventricular hypertrophy, left bundle branch block) or no alteration, and the score is recorded for each of these possibilities. The percentage of left ventricular scars estimated by ECG was calculated by multiplying the overall QRS score by 3 because each point in the score corresponds to 3% of total mass of the left ventricle (LV). Afterward, the differences in points and percentages obtained by the 2 observers were compared during a meeting, during which no disagreements were detected.
CMR Imaging and Analysis
CMR imaging with LGE was performed on all selected patients using a Philips Ingenia 1.5 T Scanner. The functional evaluation used conventional cine resonance using steady‐state free precession gradient echo. Tissue characterization assessed the presence of myocardial edema using T2‐weighted sequence with fat suppression and the presence of myocardial fibrosis (MF) by LGE with 2‐dimensional and 3‐dimensional acquisitions. The intravenous contrast material used was gadobutrol (0.1 mmol/kg), a gadolinium‐based contrast agent.
Data analysis was performed by a specialist in cardiac imaging with >5 years of experience in CMR analysis. A quantitative functional assessment was carried out to obtain the structural measurements of diastolic and systolic diameters of the LV, diastolic wall thickness, anterior systolic diameter of the left atrium, left atrial volume by biplane measurements, mean lateral diameter of the right ventricle, and the presence of pericardial effusion and the functional measurements of LV and right ventricle diastolic and systolic volumes and ejection fraction.
In LGE, image locations by the American Heart Association segmentation, degree of transmurality, pattern, and amount of LGE in grams and as a percentage of LV mass were measured. Quantitative measures of LGE used as specialized and dedicated software using a threshold method with a 5‐SD cutoff (pixel intensities 5 SDs above the normal myocardium were considered as LGE).
Statistical Analysis
Clinical and epidemiological data were organized using the Excel 2016 program and analyzed using the SPSS 28 IBM software. For categorical variables, the Fisher exact test was used, and the results are presented in tables with absolute and relative frequencies. The distribution of continuous variables was tested for normality using the Kolmogorov–Smirnov test. For those with normal distribution, the paired Student t test was used with the results presented as mean±SD.
To compare the percentage of LGE, the Fisher exact test was used. The correlation between the score of the SS and LGE (percentage in mass LV) was done using the Spearman correlation. A 95% CI was assumed for all statistical tests, and the results were considered statistically significant when P<0.05.
Ethical Considerations
This study is also part of a research funding call (No. 30/2013) issued by Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM/AM) and was approved by the Research Ethics Committee of Amazonas State University (Manaus, AM, Brazil) under the approval number 31812914.9.0000.5016/923.701, December 2014.
It was also supported by a previous call and approved by the Human Research Ethics Committee of the Fundação de Medicina Tropical Dr Heitor Vieira Dourado (FMTHVD) on March 7, 2007, under number 1836, Certification number 027.0.114.000‐06, and carried out in accordance with Resolution 466/12 of the Brazilian National Health Council and the ethical guidelines of the 1975 Declaration of Helsinki. All participants signed an informed consent form approved by the Research Ethics Committee of the Tropical Medicine Foundation Dr Heitor Vieira Dourado, Manaus, AM, Brazil, under the approval number 66077017.8.0000.0005/2.043.174 in May 2017.
Results
Baseline Characteristics
We included 23 patients whose average age was 44.3±18.9 years. The majority were men (15/65.24%) from the state of Amazonas (22/95.6%) and had an epidemiological history of acute oral disease (18/78.3%). In 16 (69.5%) patients, 2 T. cruzi strains (TcI and TcIV) were identified, with a predominance of 13 (81.2%) for the TcIV strain (Table 1). All patients were asymptomatic from the cardiovascular point of view.
Table 1.
Baseline Characteristics of Patients With Acute and Subacute Chagas Disease
| Variables | Total (N=23) | G1 (n=12) | G2 (n=11) | P value |
|---|---|---|---|---|
| Age, y | 44.3±18.9 | 47.6±23.2 | 40.6±12.9 | 0.392* |
| Sex | 0.027† | |||
| Female | 8 (34.8) | 7 (58.3) | 1 (9.1) | |
| Male | 15 (65.2) | 5 (41.7) | 10 (90.9) | |
| Origin, state | 1.000† | |||
| Amazonas | 22 (95.7) | 11 (91.7) | 11 (100) | |
| Roraima | 1 (4.3) | 1 (8.3) | 0 | |
| Transmission | 0.155 | |||
| Oral | 18 (78.3) | 11 (91.7) | 7 (63.7) | |
| Vectorial | 5 (21.7) | 1 (8.3) | 4 (36.3) | |
| T. cruzi DTU | 16 | 10 | 6 | 1.000† |
| TcI | 3 (18.8) | 2 (20) | 1 (16.7) | |
| TcIV | 13 (81.2) | 8 (80) | 5 (83.3) |
Data are provided as mean±SD, number, or number (percentage). DTU indicates discrete type unit; G1, group 1; G2, group 2; and T. cruzi, Trypanosoma cruzi.
Unpaired Student t test.
Fisher exact test.
ECG Analysis
The ECG was abnormal in 7/12 (58.3%) patients in G1, in 5/10 (50%) patients in G1‐FU, and in 4/11 (36.4%) patients in G2. The alterations found most frequently were left anterior fascicular block and ventricular repolarization alteration in 21.7% of patients. No alterations in ventricular repolarization were found in these patients after 1 year of follow‐up (Table 2).
Table 2.
Alterations in the ECG and 24‐Hour Holter Exam in Patients With Acute and Subacute Chagas Disease
| Variables | G1 (n=12) | G1‐FU (n=10) | P value |
|---|---|---|---|
| ECG | |||
| Ventricular repolarization alteration | 3 (25) | … | |
| Left anterior fascicular block | 2 (16.7) | 3 (25) | 0.070* |
| Atrial fibrillation | 1 (8.3) | 1 (8.3) | |
| Pre‐excitation | 1 (8.3) | 1 (8.3) | |
| 24‐h Holter exam | |||
| Ventricular extrasystoles | 3 (25) | … | |
| Paroxysmal supraventricular tachycardia | 3 (25) | … | |
| QRS Selvester score | 17.7±11.8 | 11.1±6.9 | 0.057† |
Data are provided as mean±SD or number (percentage). G1 indicates group 1; and G1‐FU, group 1 with 1‐year follow‐up.
Fisher exact test.
Paired Student t test.
Dynamic Electrocardiography (24‐Hour Holter Exam)
Dynamic electrocardiography (24‐hour Holter exam) in the G1 patients demonstrated the presence of isolated and monomorphic ventricular ectopic in 2 (16.7%) patients, supraventricular arrhythmias of the type unsupported supraventricular tachycardia (atrial tachycardia) in 3 (25%) patients, preventricular excitation in 1 (8.3%) patient, and atrial fibrillation as the base rhythm in 1 (8.3%) patient. In G2, 349 isolated and monomorphic ventricular ectopics were identified in 1 (9.1%) patient (Table 2).
Selvester QRS Score
In all patients, before the start of treatment (G1), an average score of 17% left ventricular mass injury was observed in the evaluation performed using the SS, with a variation between 3% and 39%. In the G1‐FU patients, after 1 year of treatment, an average score of 11% left ventricular mass injury was observed, with a variation between 0% and 21%. Regarding the percentage of injury in G2 patients, an average of 4% LV mass was observed and varied from 0% to 12% (Table 2).
Cardiovascular Magnetic Resonance
In CMR, the presence of LGE was observed in 7 patients (58.3%) in G1. In G1‐FU, there was loss of follow‐up in 2 patients and, of the 10 remaining patients evaluated, 7 (70%) showed delayed enhancement (Table 2). In G2, fibrosis was detected in 2 (18.2%) patients (Figure 1).
Figure 1. Delayed enhancement in cardiovascular magnetic resonance in (A) the medial inferolateral segment and (B) edema in the medial inferolateral.

Both arrows indicate delayed enhancement.
The assessment of left and right ventricular function were analyzed in all patients, and no alterations were observed in right ventricle function (Table 3). A total of 6 patients who presented fibrosis in the pretreatment phase underwent posttreatment evaluation, and 4 (66.75%) presented persistent MF.
Table 3.
Description of the Presence of Myocardial Fibrosis and Ejection Fraction in the Acute and Subacute Phases of Patients in 2 Groups Evaluated Using CMR
| Delayed enhancement | G1 (n=12) | G1‐FU (n=10) | P value |
|---|---|---|---|
| LGE present | 7 (58.3%) | 7 (70.0%) | 0.042* |
| LGE absent | 5 (41.7%) | 3 (30.0%) | |
| LV ejection fraction, % | 62.8±7.7 | 65.2±8.5 | 0.336† |
Data are described as mean±SD or number (percentage). CMR indicates cardiovascular magnetic resonance; GI, group 1; G1‐FU, group 1 with 1‐year follow‐up; LGE, late gadolinium enhancement; and LV, left ventricle.
Fisher exact test.
One‐way ANOVA post hoc Bonferroni.
In the G1‐FU patients, 1 developed MF that was previously undetected. The mean±SD percentage of LGE before treatment was 2.1±3.2. In the follow‐up, the mean±SD was 1.5±1.4. There was no statistical difference (P=0.607; Table 4). A very weak positive correlation was observed between the percentage of injured LV mass and the SS points (ρ=0.004; Figure 2).
Table 4.
Evolution of the Presence and Location of Injury on CMR Before and After CMR Treatment
| Identification No. | Age, y | Sex | DTU | Acute phase (n=12) | Follow‐up (n=10) | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Standard CMR | LGE segment | LGE (%) | Edema | Standard CMR | LGE segment | LGE (%) | Edema | ||||
| 01 | 28 | Male sex | TcIV | Subepicardium | Anteroseptal basal, anterolateral medial | 1.8 | Anterior lateral medial (3.9%, T2 ratio=1.8) | Lost to follow‐up | |||
| 02 | 43 | Male sex | TcIV | Absence of fibrosis | No | Lost to follow‐up | |||||
| 03 | 60 | Female sex | TcI | … | … | … | … | Junctional | Inferoseptal medial | 2.3 | No |
| 04 | 74 | Female sex | TcI | Focal | Inferolateral medial | 2.8 | No | Focal | Inferolateral medial | 1.3 | No |
| 05 | 51 | Female sex | TcIV | Absence of fibrosis | No | Absence of fibrosis | No | ||||
| 06 | 19 | Female sex | TcIV | Junctional | Inferoseptal medial | 0.7 | No | Junctional | Inferoseptal medial | 0.7 | No |
| 07 | 22 | Male sex | TcIV | Junctional, linear mesocardial | Inferoseptal medial and apical | 0.8 | No | Junctional, linear mesocardial | Inferoseptal medial and apical | 2.3 | No |
| 08 | 35 | Female sex | TcIV | … | … | … | … | Focal | Inferolateral basal | 1.1 | No |
| 09 | 65 | Female sex | TcIV | Absence of fibrosis | No | Absence of fibrosis | No | ||||
| 10 | 21 | Female sex | TcIV | Junctional, focal | Anteroseptal basal, inferior medial | 2.5 | No | Junctional, focal | Anteroseptal basal, inferior medial | 1.4 | No |
| 11 | 63 | Male sex | … | Multifocal | Inferolateral basal, inferior medial | 10.8 | Inferolateral medial (6.7%, T2 ratio=1.9) | Multifocal | Lateral, basal, medial, and apical | 4.7 | Lateral medial |
| 12 | 90 | Male sex | … | Focal | Inferolateral basal | 1.8 | No | Focal | Inferolateral basal | 1.6 | No |
CMR indicates cardiovascular magnetic resonance; DTU, discrete typing unit; and LGE, late gadolinium enhancement.
Figure 2. Spearman correlation between percentage of LV mass and the Selvester scoring points (P=0.991; ρ=0.004).

LGE indicates late gadolinium enhancement; and LV, left ventricle.
Table 4 describes the follow‐up of each patient in the G1/G1‐FU with regard to the presence or absence of delayed enhancement, edema, percentage of delayed enhancement, and location of alterations according to their pattern and myocardial segment.
Discussion
This study demonstrated for the first time that myocardial injury by CMR is present in patients with ACD. All patients were native to the western Brazilian Amazon, and most of the cases were the result of oral transmission attributed to a history of regional fruit juice consumption, such as açaí (Euterpe oleraceae), which is part of the local population’s diet. 13 This new epidemiological profile has been progressively registered in this region, and it is believed that food contamination by triatomines probably occurs when the juices are processed. As a result, this is now considered one of the most important routes of CD infection in Brazil. 14 , 15 , 16 , 17
As recommended by the Brazilian Ministry of Health, all ACD cases should be treated with benznidazole, and there should be a follow‐up of the patient during and after treatment. However, in the Amazon, this is not always the case because cases are rarely monitored, especially because most of them come from remote areas, which prevents patients from returning to the reference clinics. As a result, this compromises the recommendation for follow‐up and contributes to the evolution of the disease. 5
ECG Analysis
In our study, 56.63% of patients had an abnormal ECG in the acute period of the disease (G1), 25% being ventricular repolarization alteration, followed by left anterior fascicular block, atrial fibrillation, and pre‐excitation. The predominance of the ventricular repolarization alteration variable in G1 demonstrates a possible myocardial impairment in the pretreatment acute phase, which was not found in G1‐FU. This suggests that this alteration, which is related to the acute phase of the disease, may have disappeared as a result of early treatment. The ECG exam is considered the most appropriate, especially when it comes to mild impairment of the heart, 18 and the ventricular repolarization alterations found during the ECG exam are frequent and used in diagnostic screening and are thus considered the primary indicator of the disease. 19
Dynamic Electrocardiography (24‐Hour Holter Exam)
In a report presented by Marques et al, 20 after an outbreak attriuted to the consumption of guava juice at a school in Venezuela, the most common arrhythmias were supraventricular arrhythmias, which occurred in most cases. Ventricular arrhythmias were observed to be less common. During our study, the 24‐hour Holter exam showed that both ventricular extrasystoles and paroxysmal supraventricular tachycardia were found in G1, but subsequently not recorded in G1‐FU.
Selvester QRS Score
The SS has already been evaluated for testing chronic DC and presents good correlation with CMR; in addition, it may be important for risk stratification in this group of patients. 21 The SS in our study was positive for myocardial injury in G1 and G1‐FU (4.5 points [range, 3–7 points] and 4 points [range, 2–5 points], respectively); however, G2 did not present a score to confirm this alteration (1 point [range, 0–3 points]) because a positive result is given when the score is >3 points.
Cardiovascular Magnetic Resonance
Through CMR, the presence of late enhancement was detected in the patients in G1 and G1‐FU (58.3% and 50%, respectively); however, there was no significant difference in impairment when these patients were evaluated after 1 year of follow‐up. Nonetheless, fibrosis was detected in G2 in only 18.2% of the analyzed group. Fibrosis and myocardial inflammation have been demonstrated in all chronic phases of the disease, with or without heart disease, without ventricular dysfunction, and the amount of fibrosis correlates with the severity of the clinical form, functional class, LV ejection fraction, and LV dilation. 22
CMR has great accuracy in detecting regions of MF in patients with chronic CD. Because we know that these areas of fibrosis can be predictors of the development of malignant arrhythmias, this test becomes a fundamental tool and increases the possibility of detecting this risk early, even with preserved ventricular function. 9 Schmidt et al 22 also reported the potential of CMR in detecting the regions of MF in patients with chronic CD cardiomyopathy and confirmed that this is a potentially valuable tool in the noninvasive risk prediction of these patients suffering sudden death, even in those with LV ejection fraction still preserved.
The presence of MF in patients with CD with clinical cardiomyopathy is well established by the use of CMR. Its quantification is related to the Rassi score, 23 a prognostic score validated for CD. According to Uellendahl et al, 24 MF deserves to be investigated using CMR, as it is considered as an independent prognostic factor, which emphasizes its value as a prognostic tool for risk stratification of the disease. In the literature, there is only 1 case report study of ACD using CMR (de Sousa et al 25 ), in which fibrosis was not detected in three different periods after treatment initiation (Day 5, Day 26 and Day 56), only edema, which regressed after treatment. This is the first case series study that used this tool in the evolution, stratification, and follow‐up of cases.
Studies reinforce the hypothesis that MF in CD is related to arrhythmias and sudden death, which has already been suggested in electrophysiological evaluation. 22 However, the amount of myocardial injury detected in the evaluation of our patients was considered insufficient to generate arrhythmias of malignant character.
One of the limitations of the study is the fact that the patients in G2 were not the same as those evaluated in G1 and G1‐FU because they were recruited after diagnosis, although they were in fact all diagnosed and treated with benznidazole in the same way. The study presents a small number of patients because it is a rare disease and it occurs in sporadic outbreaks in remote regions that are difficult to access.
Conclusions
In this cohort of Amazon autochthonous patients with ACD, myocardial injury by CMR was detected in the pretreatment acute phase and also in the follow‐up 1 year after treatment. In another group of patients with 5.2 years of follow‐up after ACD, only a mildly persistent myocardial injury (18.2%) was detected. The occurrence of myocardial injury in autochthonous patients with ACD in the Amazon reveals the importance of follow‐up in the cardiology clinic.
The correlation between fibrosis detected by CMR and SS—a simple and easily accessible test—represents a good tool for the early detection and stratification of patients with myocardial involvement in the acute and subacute phases of CD. This is even more pertinent when one remembers that the Amazon is a region of vast territorial extension with many remote areas and access to CMR may prove difficult for many patients.
Sources of Funding
This study received financial support from Fundação de Amparo à Pesquisa do Estado do Amazonas under the Universal Program Notice N.30/2013.
Disclosures
None.
Acknowledgments
The authors would like to thank the Tropical Medicine Graduate Program (PPGMT/UEA) and the Amazonas State Research Support Foundation (FAPEAM) for supporting and funding the expenses regarding publication of this paper under Resolution N. 002/2008, 007/2018 and Notice N.005/2019–PRÓ‐ESTADO.
For Sources of Funding and Disclosures, see page 8.
References
- 1. World Health Organization . 2020. Available at: https://www.who.int/neglected_diseases/diseases/en/. Accessed February 3, 2021.
- 2. World Health Organization . Fourth WHO report on neglected tropical diseases: integrating neglected tropical diseases into global health and development. IV WHO Rep Neglected Trop Dis. 2017;4:1–271. [Google Scholar]
- 3. Sangenito LS, Branquinha MH, Santos ALS. Funding for Chagas disease: a 10‐year (2009–2018) survey. Trop Med Infect Dis. 2020;5:88. doi: 10.3390/tropicalmed5020088 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Dias JCP, Ramos AN Jr, Gontijo ED, Luquetti A, Shikanai‐Yasuda MA, Coura JR, Torres RM, Melo JRC, Almeida EA, Oliveira W Jr, et al. II Consenso Brasileiro em doença de Chagas. Epidemiol E Serviços Saúde. 2015;2016:7–86. [DOI] [PubMed] [Google Scholar]
- 5. Castro I, Andrade JPD, Paola AAVD, Vilas‐Boas F, Oliveira GMM, Marin Neto JA, Chagas ACP, Rocha EAV, Oliveira GMM, Zimerman LI, et al. I Diretriz Latino‐Americana para o diagnóstico e tratamento da cardiopatia chagásica. Arq Bras Cardiol. 2011;97:1–48. doi: 10.1590/S0066-782X2011001600001 [DOI] [PubMed] [Google Scholar]
- 6. Torreão JA, Ianni BM, Mady C, Naia E, Rassi CH, Nomura C, Parga JR, Avila LF, Ramires JAF, Kalil‐Filho R, et al. Myocardial tissue characterization in Chagas’ heart disease by cardiovascular magnetic resonance. J Cardiovasc Magn Reson. 2015;17:97. doi: 10.1186/s12968-015-0200-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Simões MV, Romano MMD, Schmidt A, Martins KSM, Marin‐Neto JA. Chagas disease cardiomyopathy. Int J Cardiovasc Sci. 2018;173–189. doi: 10.5935/2359-4802.20180011 [DOI] [Google Scholar]
- 8. Vitorino RR, Nacif MS. Ressonância magnética cardíaca na miocardiopatia dilatada: atualidades. Rev Bras Clin Med. São Paulo. 2011;225–233. [Google Scholar]
- 9. Pavão MLR, Leal EAMG, Marin‐Neto JA, Schmidt A. Morte súbita em Doença de Chagas – Conceitos atuais e perspectivas de novos avanços. JBAC. 2018;133–137. [Google Scholar]
- 10. da Saúde M. Consenso Brasileiro em Doença de Chagas. Rev Soc Bras Med Trop. 2005;1–29. [PubMed] [Google Scholar]
- 11. Pastore CA, Pinho JA, Pinho C, Samesima N, Pereira‐Filho HG, Kruse J, Paixão A, Pérez‐Riera AR, Ribeiro AL, Oliveira C, et al. III Diretrizes da Sociedade Brasileira de Cardiologia sobre análise e emissão de laudos eletrocardiográficos. Arq Bras Cardiol. 2016;106:1–23. doi: 10.5935/abc.20160054 [DOI] [PubMed] [Google Scholar]
- 12. Loring Z, Chelliah S, Selvester RH, Wagner G, Strauss DG. A detailed guide for quantification of myocardial scar with the Selvester QRS score in the presence of electrocardiogram confounders. J Electrocardiol. 2011;44:544–554. doi: 10.1016/j.jelectrocard.2011.06.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Santana RAG, Guerra MGVB, Sousa DR, Couceiro K, Ortiz JV, Oliveira M, Ferreira LS, Souza KR, Tavares IC, Morais RF, et al. Oral transmission of trypanosoma cruzi. Brazilian Amazon. Emer Infec Dis. 2019;132–135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Pinto AY, Valente VC, Coura JR, Valente SAS, Junqueira ACV, Santos LC, Ferreira AG Jr, Macedo RC. Clinical follow‐up of responses to treatment with benznidazol in amazon: a cohort study of acute chagas disease. PLoS One. 2013;8:e64450. doi: 10.1371/journal.pone.0064450 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Santos FACD, Braga APC, Ferreira IS, Arêde MDPSP, Baetas ALFD, Silva MVA, Lima LSA. Avaliação da prevalência e do perfil epidemiológico da doença de chagas aguda entre 2014 e 2017 no estado do Pará, Brasil. Braz J Hea Rev. 2014;2020:8974–8982. doi: 10.34119/bjhrv3n4-142 [DOI] [Google Scholar]
- 16. Valente SAS, da Costa Valente V, das Neves Pinto AY, de Jesus Barbosa César M, dos Santos MP, Miranda COS, Cuervo P, Fernandes O. Analysis of an acute Chagas disease outbreak in the Brazilian Amazon: human cases, triatomines, reservoir mammals and parasites. Trans R Soc Trop Med Hyg. 2009;103:291–297. doi: 10.1016/j.trstmh.2008.10.047 [DOI] [PubMed] [Google Scholar]
- 17. Souza‐Lima RC, Barbosa‐Guerra MGV, Coura JR, Arcanjo ARL, Nascimento AS, Barbosa‐Ferreira JMB, Magalhães LK, Albuquerque BC, Araujo GAN, Guerra JAO. Outbreak of acute Chagas disease associated with oral transmission in the Rio Negro region, Brazilian Amazon. Rev Soc Bras Med Trop. 2013;46:510–514. doi: 10.1590/0037-8682-1367-2013 [DOI] [PubMed] [Google Scholar]
- 18. Pinto AY, Ferreira AG Jr, Valente VC, Harada GS, Valente SAS. Urban outbreak of acute Chagas disease in Amazon region of Brazil: four‐year follow‐up after treatment with benznidazole. Rev Panam Salud Publica. 2009;25:77–83. doi: 10.1590/S1020-49892009000100012 [DOI] [PubMed] [Google Scholar]
- 19. Souza DSM, Povoa RMS. Aspectos epidemiológicos e clínicos da doença de Chagas aguda no Brasil e na América Latina. Rev Soc Cardiol Estado De São Paulo. 2016;222–229. [Google Scholar]
- 20. Marques J, Mendoza I, Noya B, Acquatella H, Palacios I, Marques‐Mejía M. As manifestações de ECG do maior surto da doença de Chagas devido a infecção oral na América Latina. Arq Bras Cardiol. 2013;249–254. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Rodríguez‐Zanella H, Meléndez‐Ramírez G, Velázquez L, Meave A, Alexanderson E. ECG score correlates with myocardial fibrosis assessed by magnetic resonance: a study in Chagas heart disease. Int J Cardiol. 2015;187:78–79. doi: 10.1016/j.ijcard.2015.03.337 [DOI] [PubMed] [Google Scholar]
- 22. Schmidt A, Romano MM, Maciel BC, Marin‐Neto JA. Cardiac magnetic resonance imaging for sudden cardiac death: much more than another method to measure LVEF. Curr Cardiovasc Imaging Rep. 2013;6:431–434. doi: 10.1007/s12410-013-9231-3 [DOI] [Google Scholar]
- 23. Rassi A, Rassi A, Little WC, Xavier SS, Rassi SG, Rassi AG, Rassi GG, Hasslocher‐Moreno A, Sousa AS, Scanavacca MI. Development and validation of a risk score for predicting death in Chagas’ heart disease. N Engl J Med. 2006;355:799–808. doi: 10.1056/NEJMoa053241 [DOI] [PubMed] [Google Scholar]
- 24. Uellendahl M, Uellendahl M, Siqueira ME, Calado EB, Kalil‐Filho R, Sobral D, Ribeiro C, Oliveira W, Martins S, Narula J, et al. Fibrose miocárdica definida por ressonância magnética cardíaca em doença de Chagas: correlações clínicas e estratificação de risco. Arq Bras Cardiol. 2016;460–466. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. de Sousa AS, Derenne ME, Hasslocher‐Moreno AM, Xavier SS, Gottlieb I. Myocardial edema without fibrosis by magnetic resonance T2 mapping in acute Chagas’ myocarditis. Arq Bras Cardiol. 2017;109:378–379. doi: 10.5935/abc.20170113 [DOI] [PMC free article] [PubMed] [Google Scholar]
