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Arq Bras Cardiol. 2017 February; 108(2): 122–128.
PMCID: PMC5344656

Dobutamine Stress Echocardiography Safety in Chagas Disease Patients

Abstract

Background

A few decades ago, patients with Chagas disease were predominantly rural workers, with a low risk profile for obstructive coronary artery disease (CAD). As urbanization has increased, they became exposed to the same risk factors for CAD of uninfected individuals. Dobutamine stress echocardiography (DSE) has proven to be an important tool in CAD diagnosis. Despite being a potentially arrhythmogenic method, it is safe for coronary patients without Chagas disease. For Chagas disease patients, however, the indication of DSE in clinical practice is uncertain, because of the arrhythmogenic potential of that heart disease.

Objectives

To assess DSE safety in Chagas disease patients with clinical suspicion of CAD, as well as the incidence of arrhythmias and adverse events during the exam.

Methods

Retrospective analysis of a database of patients referred for DSE from May/2012 to February/2015. This study assessed 205 consecutive patients with Chagas disease suspected of having CAD. All of them had their serology for Chagas disease confirmed.

Results

Their mean age was 64±10 years and most patients were females (65.4%). No patient had significant adverse events, such as acute myocardial infarction, ventricular fibrillation, asystole, stroke, cardiac rupture and death. Regarding arrhythmias, ventricular extrasystoles occurred in 48% of patients, and non-sustained ventricular tachycardia in 7.3%.

Conclusion

DSE proved to be safe in this population of Chagas disease patients, in which no potentially life-threatening outcome was found.

Keywords: Chagas Disease, Echocardiography, Stress, Atropine, Trypanosoma cruzi / drug effects

Introduction

Chagas disease continues to be a serious health problem, as well as an economic burden in most Latin-American countries. The World Health Organization has recently estimated that 18 million people are chronically infected with Trypanosoma cruzi, and approximately 200,000 new cases are diagnosed per year.1

A few decades ago, patients with Chagas disease were mainly rural workers, with low risk profile for coronary artery disease (CAD). As urbanization has increased since 1980, they became exposed to the same risk factors for CAD of uninfected individuals. Thus, the prevalence of CAD, as a cause of acute myocardial infarction, is expected to be similar in individuals with and without Chagas disease.2

The prevalence of CAD in patients with Chagas disease, however, is controversial.3-7 It is worth noting the inherent diagnostic difficulty concerning chest pain, which can be atypical or intense.8,9 Coronary angiography should only be indicated in special situations, such as typical angina and presence of classic CAD risk factors, or when large ischemic areas are seen on non-invasive tests.9

For 25 years, stress echocardiography has proven to be an important tool for the diagnosis of CAD. The dobutamine-atropine protocol [dobutamine stress echocardiography - DSE)] is safe and has accuracy similar to that of other non-invasive diagnostic methods, but higher specificity.10

Dobutamine is the most commonly used agent in most pharmacological stress tests.11,12 Severe ventricular arrhythmias can occur during the exam, but are rare, confirming, thus, the safety of using dobutamine for stress echocardiography.13,14

In clinical practice, however, the indication of DSE in chronic Chagas heart disease (CCHD) is controversial, because of the arrhythmogenic potential of the drug in an also arrhythmogenic heart disease. In the literature, there is no study aimed at specifically assessing the safety of DSE in a group of Chagas disease patients. Thus, this research, aimed at assessing the DSE safety for CAD diagnosis in that group of patients, is relevant.

Methods

Selection of patients and study site

This is a retrospective analysis of a database to raise a hypothesis. A population of consecutive patients with CCHD and suspected of having CAD was assessed. They were referred for DSE from May/2012 to February/2015 at two echocardiography centers, one of them outside a hospital.

Confirmation of serology for Chagas disease was required in all patients. Those who spontaneously presented with at least two positive serologies at the time of DSE were confirmed as having Chagas disease. Those who had no serology were invited, via telephone, to undergo the serological tests, and to provide written informed consent at the time of blood sample collection. They underwent at least two serological tests of different principles, which confirmed the existence of anti-T. cruzi antibodies. The following conventional serological tests were used: immunoenzymatic assay (ELISA); indirect immunofluorescence; and indirect hemagglutination assay. Patients refusing to undergo the tests were excluded from the analysis.

Echocardiographic assessment, analysis of safety and arrhythmias

Before DSE, the patients were asked about previous cardiovascular diseases, including Chagas disease, heart procedures they had already undergone, and regularly used medications.

Echocardiography was performed with a HD-11 echocardiographer (Philips Ultrasound Systems, Andover, MA, USA), by an echocardiography professional from a group of four, equally trained, and in a standardized and uniform way, according to the ASE recommendations.15 That group of professionals has a large experience with stress echocardiography, each performing, on average, 200 exams/month. The exams were performed systematically in all participants, regardless of the serological confirmation for Chagas disease.

Initially, the patients underwent a baseline echocardiographic study, with linear measurement of the heart structures and valvar flows. Ejection fraction was assessed by using the Teichholz or Simpson method, depending on the extent of the segmental contractility alteration. When using the latter, sometimes the end-systolic diameter was not measured. After acquiring baseline standard images in the parasternal, longitudinal, transverse, 4- and 2-chamber apical views, intravenous dobutamine infusion began, at an initial dose of 5 µg/kg/min, with increasing increments of 10, 20, 30 and 40 µg/kg/min every 3 minutes. If the patient had no echocardiographic sign of myocardial ischemia and did not reach the minimum heart rate of 100 bpm in the stage of 20 µg/kg/min, 0.25 mg/min of atropine was administered every 1 minute, up to the maximum cumulative dose of 2 mg. There was no standardization concerning monitoring time after the end of infusion, and the time necessary for heart rate to reach less than 100 beats per minute was respected.

The patients were kept under clinical, electrocardiographic and continuous blood pressure monitoring. The measures of blood pressure, heart rate and 12-lead electrocardiography were recorded at baseline, at the end of each stage and during recovery. The patients' symptoms were recorded either through direct questioning or direct patient's complaint at any time.

The DSE was effective when one of the following objectives was met: at least 85% of maximum heart rate predicted for age, calculated with the Karvonen equation (maximum heart rate = 220 - age);16 echocardiographic signs of ischemia (new changes in left ventricular contractility); or end of the infusion protocol.

The submaximal criteria for test interruption, considered non-diagnostic were: unbearable symptoms; limiting side effects, such as arterial hypertension (systolic blood pressure > 230 mm Hg or diastolic blood pressure > 120 mm Hg); relative or absolute hypotension (systolic blood pressure drop > 30 mm Hg at rest, or systolic blood pressure < 80 mm Hg); supraventricular arrhythmias (sustained supraventricular tachycardia and atrial fibrillation); and ventricular arrhythmias (non-sustained and sustained ventricular tachycardia).17

The safety criteria for exam interruption were established as life-threatening complications, defined in the meta-analysis by Geleijnse et al.18 as cardiac rupture, acute myocardial infarction, stroke, asystole, ventricular fibrillation, and sustained ventricular tachycardia.

The cardiac arrhythmias observed during the exam were defined as follows: supraventricular tachycardia, presence of well-defined, regular and similar narrow QRS complexes (<120 ms), in the absence of conduction disorder; atrial fibrillation, absence of P wave associated with irregular rhythm, narrow QRS complexes (<120 ms), in the absence of conduction disorder; frequent ventricular extrasystoles, presence of premature ventricular complexes with more than 6 complexes per minute; ventricular bigeminism, presence of ventricular extrasystoles alternating with normal QRS complexes; non-sustained ventricular tachycardia, presence of more than 3 premature complex ventricular beats, lasting less than 30 seconds and with heart rate greater than 100 beats per minute; and sustained ventricular tachycardia, presence of more than 3 premature complex ventricular beats, lasting more than 30 seconds and with heart rate greater than 100 beats per minute.19

The left ventricle was divided into 17 myocardial segments, according to the ASE recommendations.15 The qualitative analysis of segmental myocardial contractility was based on visual assessment of myocardial thickening and wall motility graded into a segmental contractility index, each segment being scored as follows: 1 - normal; 2 - hypokinesia; 3 - akinesia; and 4 - dyskinesia. The normal value of that index is 1 (17 points/17 segments). Any value greater than 1 was considered abnormal segmental contractility index. Segmental myocardial contractility was positive for ischemia in the presence of altered segmental myocardial contractility in at least one left ventricular segment during pharmacological stress.13,15

Statistical analysis

Non-probability convenience sampling was chosen and comprised patients with Chagas disease, suspected of having CAD, referred for DSE in the predetermined study period. The sample size was limited to the study's operational capacity.

Multivariate analysis was conducted using binary multiple logistic regression to identify covariables associated with the occurrence of binary outcome. When indicated, given the reduced number of binary outcome events, the use of penalized maximum likelihood ratio test was considered.

Multiple regression models were determined with the simultaneous introduction (full model) of the variables with p<0.05 in univariate regression analysis and that showed neither multicollinearity nor percentage loss greater than 10%.

Categorical variables were described as counts and percentages. Quantitative variables of normal and asymmetric distribution were described as mean ± standard deviation or median (interquartile range), respectively.

Normality was assessed via visual inspection of histograms. The R software (R Foundation, Vienna, Austria) was used for statistical analysis. All probabilities of significance presented are bilateral, and values smaller than 0.05 were considered statistically significant.

Results

The general population referred for DSE underwent 23,935 exams. Of that sample, 415 patients claiming to have Chagas disease were selected. Of those, 210 patients whose serology was not confirmed were excluded, resulting in a final group of 205 patients to be assessed.

The mean age of the 205 patients analyzed was 64±10 years, and most of them (65.4%) were of the female sex. Regarding pharmacological treatment, the most used drugs were angiotensin II receptor blockers (35,1%) and amiodarone (29.3%). Of the reported risk factors for CAD, dyslipidemia was the most frequent (33.2%). Regarding the presence of previous coronary event, 6.3% reported myocardial infarction, and 5.9% surgical or percutaneous myocardial revascularization. Table 1 shows the clinical characteristics of the group and pharmacological treatment, and Table 2, the risk factors for CAD.

Table 1
Clinical characteristics of the total sample
Table 2
Risk factors for atherosclerotic disease

Regarding the echocardiographic parameters and vital signs (Table 3), most patients had preserved ejection fraction, normal systolic and diastolic blood pressure, but heart rate tending to the lower limit of normality.

Table 3
Echocardiographic characteristics, blood pressure and heart rate

More than half of the group (105 patients - 51.2%) had some alteration in segmental contractility at rest: in the apical segments of the ventricle, 30 patients; in the basal segments of the inferior and/or inferolateral wall, 35; association of the two alterations described, 32; and diffuse hypokinesia, 8. Regarding electrocardiographic changes, 98 patients had the following tracing alterations at rest: isolated right bundle branch block, 60 patients; association of right bundle branch block with left anterior hemiblock, 27; left bundle branch block, 5; atrial fibrillation rhythm, 3; and pacemaker rhythm, 3. In addition, only segmental contractility alteration, electrocardiographic alteration, or association of both was present in 50, 43 and 55 patients, respectively.

Negative result for myocardial ischemia was the most frequent finding in 139 exams (67.9%). That result was positive in 29 exams (14.1%), and inconclusive (did not reach submaximal heart rate) in 37 (18%). Of the patients with inconclusive result, 22 (59.5%) used maximum dose of dobutamine and underwent all stages of the protocol, but some had their exams interrupted because of the following: severe chest pain, 1 (2.7%); important blood pressure elevation (> 230/120 mm Hg), 1 (2.7%); severe headache, 2 (5.4%); and cardiac arrhythmias, 11 (29.7%). Frequent and polymorphic ventricular extrasystoles and non-sustained ventricular tachycardia were the most common arrhythmias related to exam interruption. Most patients with frequent ventricular extrasystoles during the exam had isolated extrasystoles at rest. Likewise, most arrhythmias were dose-dependent, occurring at pharmacological stress peak. Of the patients receiving maximum dose of dobutamine, 16 (72.7%) were on negative chronotropic drugs, such as beta-blocker or amiodarone.

Table 4 shows the arrhythmias induced during DSE. Of the 205 patients, 18 (8.7%) had more than one type of arrhythmia during the exam.

Table 4
Arrhythmias induced during stress echocardiography

The protocol was interrupted because of the appearance of significant arrhythmias (atrial fibrillation, sustained supraventricular tachycardia, non-sustained ventricular tachycardia and sustained ventricular tachycardia). Those patients required neither specific drug nor electrical cardioversion. No patient had hemodynamic instability. All patients underwent routine observation.

Headache was the most frequent unwanted symptom (2.4%) during the exam, followed by chest pain (2.0%). No patient had hypotension during the exam, and only one (0.5%) had a hypertensive response.

No patient had significant adverse events, such as acute myocardial infarction, ventricular fibrillation, asystole, stroke, cardiac rupture or death.

Discussion

The use of DSE to diagnose CAD in patients who cannot undergo exercise test has increased. In addition, more aggressive protocols with high doses of dobutamine and atropine have been more often used.20

To our knowledge, this is the first study designed to assess the safety of DSE, as well as the occurrence of arrhythmias, in an exclusive population of patients with Chagas disease.

Despite the potential risk of complications, mainly arrhythmogenic ones, the method was safe when applied to 205 patients. None had significant complications, such as death, acute myocardial infarction, cardiac rupture, stroke, ventricular fibrillation or asystole. Most safety studies have reported a very low incidence of those events: the meta-analysis by Geleijnse et al.,18 with 55,071 patients, has found an incidence of death, cardiac rupture and stroke lower than 0.01%, of acute myocardial infarction of 0.02%, and a rate of major complications of 1:475 (adding sustained ventricular tachycardia, asystole and ventricular fibrillation). Those figures are in accordance with those reported in the International Stress Echo Complication Registry,21 with a rate of 1:595 in the assessment of 35,103 patients.

The population studied belongs to the same age group of those of the studies on DSE safety assessed in the meta-analysis cited.20 Recently, a study conducted by O'Driskll et al.22 with 550 octogenarian patients has demonstrated that DSE was safe in that population and capable of identifying individuals at high risk for cardiovascular event.

The patients with Chagas disease had a lower prevalence of risk factors for CAD as compared to those without Chagas disease, in previous studies.20,23,24 Of those risk factors, the most prevalent were hypertension and dyslipidemia, the only ones that got closer to those of the non-chagasic populations studied, such as the group assessed by San Roman et al.25, with the following prevalence: hypertension, 61%; diabetes mellitus, 29%; dyslipidemia, 46%; smoking, 23%; history of previous infarction, 23%; and revascularization, 31%.

Regarding pharmacological treatment, Chagas disease patients used less frequently antianginal therapy, such as beta-blockers, nitrates and calcium-channel blockers, as compared to those of previous studies.20,25 However, 30% of the patients used amiodarone, an antiarrhythmic and negatively chronotropic drug, which might have accounted for not reaching submaximal heart rate in most inconclusive results.

In our study, the positive result for ischemia was less frequent than in other studies, maybe because of the smaller number of risk factors for CAD in the group of patients with Chagas disease.20,23,24 A cohort of 4,033 patients conducted by Mathias et al.26 has shown a positive result in 37% of them, and inconclusive result in 10%. Sicari et al.,27 in a cohort of 7,333 patients, has reported a positive result for ischemia in 39% of the exams.

The only study published, assessing Chagas disease patients submitted to DSE, has been conducted by Aquatella et al.28 That study aimed at assessing whether the stimulation with dobutamine could trigger an abnormal contractility response, as seen in ischemic myocardium. In that small cohort (24 Chagas disease patients vs 10 controls), dobutamine has shown a chronotropic incompetence and a reduced contractile response, even in those without apparent cardiac manifestation. That study might explain part of the inconclusive results found in ours, because of that probable chronotropic deficit.

Most patients with Chagas disease studied had some degree of segmental impairment, frequent in that pathology.29 The segmental contractility index, which reflects the segmental myocardial impairment extent, was slightly altered (median value, 1.06), reflecting mild alterations and few impaired segments.

Regarding arrhythmias, ventricular extrasystoles were the most frequently found, similarly to that reported in the safety studies analyzed in the meta-analysis by Geleijnse et al.18 However, the incidence was higher than that reported in most studies, that by Takeuchi et al. 30 being the one that got closer. That study, with 1,090 patients, has assessed different dobutamine-atropine protocols, with a 43.6% incidence of ventricular extrasystoles.30 Non-sustained ventricular tachycardia had the second highest incidence, 15 patients (7.3%), which was also greater than those already published, with a mean of 2.19% (range, 0.2% to 7.3%).18 The study conducted by Bremer et al.,31 with 4,035 patients, assessing the safety of stress echocardiography performed by nurses, was the only to show an incidence similar to the one of that group. Sustained ventricular tachycardia occurred in 2 (1%) patients, and that incidence was also higher than the one reported in previous studies for patients without Chagas disease, whose mean was 0.15% (range, 0.0% to 0.78%). Regarding supraventricular arrhythmias, the incidence was similar to that of other studies, where atrial fibrillation had a mean incidence of 0.9%, and sustained supraventricular tachycardia, of 1.3%.18 Our patients had 0.5% and 1.0%, respectively.

Unwanted adverse effects, such as chest pain, had a lower incidence than in previous studies, such as that by Mathias et al.,32 San Roman et al.25 and Mertes et al.,20 where chest pain occurred in 12.6%, 8.5% and 12.7%, respectively. Headache had the same frequency of that in other studies, as demonstrated by Mathias et al.,32 Mertes et al.20 and San Roman et al.,25 with incidence of 1.9%, 4% and 1.9%, respectively.

In addition, the incidence of hypertensive response and hypotension was lower than that of the safety studies assessed in the meta-analysis by Geleijnse et al.,18 in which the mean incidence of hypertension as the cause of protocol interruption was 1.3%, and that of hypotension, 1.7%. A recent retrospective analysis by Abram et al.,33 with 2,968 patients with no cardiovascular disease and normal findings on stress echocardiography, has shown that blood pressure variation during the exam depends on age, sex and use of atropine. A greater increase in systolic blood pressure was seen in men and young individuals, with a more pronounced effect of atropine among the young.

Study limitations

This study is a retrospective analysis of a database, with the limitations inherent in that type of analysis. However, the exams were systematically performed by the same trained medical and nurse team, with large experience in that type of exam.

The database is small as compared to those of safety studies of stress echocardiography, but the identification of that type of patient is limited.

We had no coronary angiography of the patients who reported previous history of acute myocardial infarction. Thus, one might argue whether the segmental contractility alteration of such patients, when present, could be attributed to acute myocardial infarction or to Chagas heart disease. However, the number of those patients in our sample was reduced.

The interobserver variation analysis of the echocardiographic data could not be performed, because the digital images were not stored.

Conclusions

Stress echocardiography with dobutamine and atropine showed to be safe in the population of patients with Chagas disease, in which no life-threatening outcome was observed.

The incidence of arrhythmias during the exam was higher than that found in studies with populations without Chagas disease.

The incidence of adverse effects, such as chest pain, arterial hypertension and hypotension, was lower than that found in studies with populations without Chagas disease.

Footnotes

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 Daniela do Carmo Rassi, from Universidade Federal de Goiás.

References

1. World Health Organization World Health Tech Rep. Ser. 2002;905:1–109.
2. Marin-Neto JA, Simões MV, Ayres-Neto EM, Attab-Santos JL, Gallo L Jr, Amorim DS, et al. Studies of the coronary circulation in Chagas' heart disease. Sao Paulo Med J. 1995;113(2):826–834. [PubMed]
3. Melo EF, Melo RM, Aiello VD. Case 6 / 2011: decompensated heart failure in man of 65 years of age, suffering from cardiomyopathy of Chagas disease and coronary artery disease. Arq Bras Cardiol. 2011;97(6):e121–e127. [PubMed]
4. Garzon SA. Doença de Chagas associada a outras cardiopatias. In: Cançado JR, Chuster M, editors. Cardiopatia chagásica. Belo Horizonte, (MG): Fundação Carlos Chagas; 1985. pp. 255–265.
5. Rassi Jr A, Rassi A, Marin-Neto JA. Chagas heart disease: pathophysiologic mechanisms, prognostic factors and risk stratification. Mem Inst Oswaldo Cruz. 2009;104(Suppl 1):152–158. [PubMed]
6. Marin-Neto JA, Simões MV, Ayres-Neto EM, Attab-Santos JL, Gallo L Jr, Amorim DS, et al. Studies of the coronary circulation in Chagas' heart disease. Sao Paulo Med J. 1995;113(2):826–834. [PubMed]
7. Carvalho G, Rassi S, Bastos JM, Câmara SS. Asymptomatic coronary artery disease in chagasic patients with heart failure: prevalence and risk factors. Arq Bras Cardiol. 2011;97(5):408–412. [PubMed]
8. Marin-Neto JA, Cunha-Neto E, Maciel BC, Simões MV. Pathogenesis of chronic Chagas heart disease. Circulation. 2007;115(9):1109–1123. [PubMed]
9. Andrade JP, Marin-Neto JA, Paola AA, Vilas-Boas F, Oliveira GM, Bacal F, et al. Sociedade Brasileira de Cardiologia I Latin American guidelines for the diagnosis and treatment of Chagas cardiomyopathy. Arq Bras Cardiol. 2011;97(2) Suppl 3:1–48. [PubMed]
10. Sicari R, Nihoyannopoulos P, Evangelista A, Kasprzak J, Lancellotti P, Poldermans D, et al. European Association of Echocardiography Stress echocardiography expert consensus statement: European Association of Echocardiography (EAE) (a registered branch of the ESC) Eur J Echocardiogr. 2008;9(4):415–437. [PubMed]
11. Vieira C. Ecocardiografia sob estresse: algumas décadas depois. Rev Bras Ecocardiogr. 2008;21(1):36–44.
12. Bhattacharyya S, Chehab O, Khattar R, Lloyd G, Senior S, British Society of Echocardiography Stress echocardiography in clinical practice: a United Kingdom National Health Service Survey on behalf of the British Society of Echocardiography. Eur Heart J Cardiovasc Imaging. 2014;15(2):158–163. [PubMed]
13. Picano E. Stress echocardiography. 5th ed. 5th ed. Philadelphia: Springer; 2009. pp. 175–188.
14. Gottdiener JS. Overview of stress echocardiography: uses, advantages and limitations. Prog Cardiovasc Dis. 2001;43(4):315–334. [PubMed]
15. Pellikka PA, Nagueh SF, Elhendy AA, Kuehl CA, Sawada SG, American Society of Echocardiography American Society of Echocardiography recommendations for performance, interpretation, and application of stress echocardiography. J Am Soc Echocardiogr. 2007;41(9):1021–1034. [PubMed]
16. Karvonen NJ, Kentala E, Mustala O. The effects of training on heart rate: a "longitudinal" study. Ann Med Exp Biol Fenn. 1957;35(3):307–315. [PubMed]
17. Mathias Jr W, Tsutsui JM, editors. Ecocardiografia. Barueri(SP): Manole; 2012.
18. Geleijnse M, Krenning B, Nemes A, Van Dalen B, Soliman O, Cate F. Incidence, pathophysiology, and treatment of complications during dobutamine-atropine stress echocardiography. Circulation. 2010;121(15):1756–1767. [PubMed]
19. Pastore CA, Pinho C, Germiniani H, Samesima N, Mano R, 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. [PubMed]
20. Mertes H, Sawada SG, Ryan T, Segar DS, Kovacs R, Foltz J, et al. Symptoms, adverse effects, and complications associated with dobutamine stress echocardiography. Experience in 1118 patients. Circulation. 1993;8(1):15–19. [PubMed]
21. Varga A, Garcia MA, Picano E, International Stress Echo Complication Registry Safety of stress echocardiography (from the International Stress Echo Complication Registry) Am J Cardiol. 2006;98(4):541–543. [PubMed]
22. O'Driscoll JM, Marciniak A, Ray KK, Schmid K, Smith R, Sharma R. The safety and clinical usefulness of dobutamine stress echocardiography among octogenarians. Heart. 2014;100(13):1001–1007. [PubMed]
23. Kane GC, Hepinstall MJ, Kidd GM, Kuehl CA, Murphy AT, Nelson JM, et al. Safety of stress echocardiography supervised by registered nurses: results of a 2-year audit of 15,404 patients. J Am Soc Echocardiogr. 2008;21(4):337–341. [PubMed]
24. Fennich N, Ellouali F, Abdelali S, Chaara A, Berrada A, Elhajjaji I, et al. Stress echocardiography: safety and tolerability. Cardiovasc Ultrasound. 2013;11:30–30. [PMC free article] [PubMed]
25. San Roman JA, Sanz-Ruiz R, Ortega JR, Perez-Paredes M, Rollan MJ, Munoz AC, et al. Safety and predictors of complications with a new accelerated dobutamine stress echocardiography protocol. J Am Soc Echocardiogr. 2008;21(1):53–57. [PubMed]
26. Mathias W Jr, Arruda A, Santos FC, Arruda AL, Mattos E, Osorio A, et al. Safety of dobutamine atropine stress echocardiography: a prospective experience of 4,033 consecutive studies. J Am Soc Echocardiogr. 1999;12(10):785–791. [PubMed]
27. Sicari R, Pasanisi E, Venneri L, Landi P, Cortigiani L, Picano E, Echo Persantine International Cooperative (EPIC) Study Group. Echo Dobutamine International Cooperative (EDIC) Study Group Stress echo results predict mortality: a large-scale multicenter prospective international study. J Am Coll Cardiol. 2003;41(4):589–595. [PubMed]
28. Acquatella H, Perez JE, Condado JA, Sanchez I. Limited myocardial contractile reserve and chronotropic incompetence in patients with chronic Chagas' disease. J Am Coll Cardiol. 1999;33(2):522–529. [PubMed]
29. Acquatella H. Echocardiography in Chagas heart disease. Circulation. 2007;115(9):1124–1131. [PubMed]
30. Takeuchi M, Miura Y, Sonoda S, Kuroiwa A. Comparison of three different protocols for dobutamine stress echocardiography: does the addition of atropine increase complications, and does it improve diagnostic accuracy? Echocardiography. 1999;16(4):347–355. [PubMed]
31. Bremer ML, Monahan KH, Stussy VL, Miller FA Jr, Seward JB, Pellikka PA. Safety of dobutamine stress echocardiography supervised by registered nurse sonographers. J Am Soc Echocardiogr. 1998;11(6):601–605. [PubMed]
32. Mathias Junior W, Beneti LP, dos Santos FC, Duprat R, Beraldo A, Gil MA. Safety and feasibility of dobutamine-atropine stress echocardiography. Arq Bras Cardiol. 1997;69(1):31–34. [PubMed]
33. Abram S, Arruda-Olson AM, Scott CG, Pellikka PA, Nkomo VT, Oh JK, et al. Typical blood pressure response during dobutamine stress echocardiography of patients without known cardiovascular disease who have normal stress echocardiograms. Eur Heart J Cardiovasc Imaging. 2016;17(5):557–563. [PubMed]

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