Feasibility and safety of high-dose adenosine perfusion cardiovascular magnetic resonance
© Karamitsos et al; licensee BioMed Central Ltd. 2010
Received: 2 July 2010
Accepted: 16 November 2010
Published: 16 November 2010
Adenosine is the most widely used vasodilator stress agent for Cardiovascular Magnetic Resonance (CMR) perfusion studies. With the standard dose of 140 mcg/kg/min some patients fail to demonstrate characteristic haemodynamic changes: a significant increase in heart rate (HR) and mild decrease in systolic blood pressure (SBP). Whether an increase in the rate of adenosine infusion would improve peripheral and, likely, coronary vasodilatation in those patients is unknown. The aim of the present study was to assess the tolerance and safety of a high-dose adenosine protocol in patients with inadequate haemodynamic response to the standard adenosine protocol when undergoing CMR perfusion imaging.
98 consecutive patients with known or suspected coronary artery disease (CAD) underwent CMR perfusion imaging at 1.5 Tesla. Subjects were screened for contraindications to adenosine, and an electrocardiogram was performed prior to the scan. All patients initially received the standard adenosine protocol (140 mcg/kg/min for at least 3 minutes). If the haemodynamic response was inadequate (HR increase < 10 bpm or SBP decrease < 10 mmHg) then the infusion rate was increased up to a maximum of 210 mcg/kg/min (maximal infusion duration 7 minutes).
All patients successfully completed the CMR scan. Of a total of 98 patients, 18 (18%) did not demonstrate evidence of a significant increase in HR or decrease in SBP under the standard adenosine infusion rate. Following the increase in the rate of infusion, 16 out of those 18 patients showed an adequate haemodynamic response. One patient of the standard infusion group and two patients of the high-dose group developed transient advanced AV block. Significantly more patients complained of chest pain in the high-dose group (61% vs. 29%, p = 0.009). On multivariate analysis, age > 65 years and ejection fraction < 57% were the only independent predictors of blunted haemodynamic responsiveness to adenosine.
A substantial number of patients do not show adequate peripheral haemodynamic response to standard-dose adenosine stress during perfusion CMR imaging. Age and reduced ejection fraction are predictors of inadequate response to standard dose adenosine. A high-dose adenosine protocol (up to 210 mcg/kg/min) is well tolerated and results in adequate haemodynamic response in nearly all patients.
First pass perfusion cardiovascular magnetic resonance (CMR) is routinely performed under vasodilatory pharmacological stress with either adenosine or dipyridamole [1, 2]. Adenosine is the most widely used vasodilator agent because it is safe, well tolerated, and easily controlled . It generates systemic vasodilatation and reflex sympatho-excitation with consequent mild decrease in systolic blood pressure, slight increase in heart rate, and modest increase in double product . As a potent coronary vasodilator, adenosine causes up to a 4-fold increase in myocardial blood flow in areas supplied by normal coronary arteries. In contrast, in the presence of epicardial coronary stenoses, flow inhomogeneities give rise to regional perfusion defects during the first pass of a gadolinium based contrast .
With the standard adenosine dose of 140 mcg/kg/min most, but not all, patients develop maximal vasodilatation [4–6]. In patients with no or mild signs of peripheral vasodilatation however, the adequacy of coronary vasodilatation is questioned. Whether this inadequate cardiovascular response would respond to an increase in the rate of adenosine infusion is unknown. It is also unclear whether a high-dose adenosine infusion protocol is safe and would be tolerated by patients undergoing stress perfusion CMR. We hypothesized that an increase in the adenosine infusion rate up to 210 mcg/kg/min would result in an improved peripheral haemodynamic response in perfusion CMR subjects who failed to show characteristic changes in blood pressure and heart rate with the standard adenosine dose (140 mcg/kg/min).
The study population consisted of patients with known or suspected coronary artery disease (CAD) who underwent adenosine stress perfusion CMR imaging for clinical purposes. All patients gave informed consent before the CMR scan. All subjects were initially screened for the presence of contraindications to adenosine, which include asthma, unstable angina or acute myocardial infarction within two weeks of the study, 2nd or 3rd degree atrioventricular (AV) block and bifascicular block. A 12-lead ECG was performed before the CMR scan. All patients were asked to abstain from caffeine for at least 12 hours prior to the scan. However, patients who reported caffeine intake within the last 12 hours were still included in the study. Prior to the CMR scan, a physician carefully explained the procedure to subjects, with emphasis on potential adenosine-related symptoms. Subjects were continuously monitored with peripheral oxygen saturation, heart rate and 2-lead ECG throughout the CMR scan. Systemic blood pressure was periodically checked at every minute during adenosine stress and 15 min after the end of the infusion. The monitor tracing during the CMR scan does not allow for identification of 1st or Wenckebach 2nd degree AV block and therefore only advanced degrees of AV block (Mobitz II 2nd degree and 3rd degree) were noted. Each subject was questioned during and immediately after termination of adenosine infusion, specifically for the occurrence of the following symptoms: shortness of breath or dyspnea, chest pain and other minor symptoms (flushing, nausea, headache). At least two clinicians trained in cardiopulmonary resuscitation and CMR evacuation procedures were present during the adenosine infusion.
Adenosine infusion protocol
All patients initially had the standard adenosine (Adenoscan®, Sanofi-Synthelabo) infusion dose of 140 mcg/kg/min for at least 3 minutes through an antecubital vein using a syringe pump (Graseby® 3500). If after 3 minutes of continuous infusion at the standard rate, the haemodynamic response to adenosine was inadequate (heart rate increase < 10 beats per minute or systolic blood pressure decrease < 10 mmHg, and minimal or no reported side effects from the patient) then the infusion rate was increased to 170 mcg/kg/min for a further 2 minutes. The absence or minimal presence of classical adenosine side effects was not a criterion to increase the dose if an adequate haemodynamic response was evidenced. If still patients failed to show evidence of peripheral vasodilatation then the infusion was increased to a maximum of 210 mcg/kg/min for a further 2 minutes. The infusion was discontinued if patients developed persistent or symptomatic 3rd degree AV block, severe hypotension (systolic blood pressure < 90 mmHg) or bronchospasm. The attending physicians had aminophylline for adenosine receptor antagonism and nitroglycerine for persistent chest pain readily available, and a fully equipped resuscitation trolley with defibrillator was easily accessible.
All CMR examinations were performed with subjects in a supine position on a 1.5 MR Tesla (Siemens Avanto, Erlangen, Germany) with a 32-element phased-array coil. During the last minute of adenosine infusion a gadolinium-based contrast agent (Gadodiamide, Omniscan®, GE Healthcare or Gadoterate meglumine, Dotarem®, Guerbet S.A.) was administered intravenously at 0.075 mmol/kg body weight (injection rate 4 ml/s), followed by a 20 ml saline flush at the same rate. Perfusion imaging was performed every cardiac cycle during the first pass, using a T1-weighted fast (spoiled) gradient echo sequence (echo time 1.05 ms, repetition time 2 ms, saturation recovery time 100 ms, voxel size 2.3 × 2.8 × 10 mm; flip angle 12°). Three or four short-axis slices, positioned from the base to the apex of the left ventricle, were obtained. The same imaging sequence was repeated at least 10 minutes later without adenosine to obtain perfusion images at rest. For assessment of left ventricular function, steady-state free-precession cine images (TE/TR 1.1/2.6 ms, voxel size 2.0 × 2.0 × 7 mm, flip angle 55°) were acquired in three long-axis views, and a short-axis stack to obtain coverage of the entire left ventricle. Analysis of left ventricular function was performed with Argus Syngo MR software (version B15, Siemens Healthcare, Erlangen, Germany) using the short-axis SSFP images as previously described . The following left ventricular parameters were thereby determined: end-diastolic volume, end-systolic volume, ejection fraction and myocardial mass.
Based on clinical criteria, a proportion of patients underwent coronary angiography. The decision to proceed to coronary angiography on the basis of an abnormal perfusion CMR scan was left at the discretion of the referring consultant cardiologist. Significant CAD was defined visually as the presence of at least one stenosis of > 50% diameter in any of the main epicardial coronary arteries or their branches with a diameter of ≥ 2 mm.
Continuous variables are expressed as mean ± standard deviation. Categorical variables are expressed as counts and percentages. All continuous variables were found to be normally distributed by the Kolmogorov-Smirnov test. Differences in continuous variables between the standard- and high-dose groups were assessed by independent student's t-test. One-way analysis of variance (ANOVA) followed by post-hoc Bonferroni analysis was used to compare the haemodynamic response to stress in the high-dose group at several time points (baseline, standard dose and maximum infusion rate). Comparisons of categorical variables between groups were performed by χ2 test or Fisher's exact test as appropriate. We used binary logistic regression analysis to identify potential predictors of inadequate response to standard adenosine dose. Receiver operator characteristic analysis was used to identify cut-offs for continuous variables such as age and ejection fraction. Based on those cut-off values, ejection fraction and age were entered into the regression model as dichotomous variables. A probability value of p < 0.05 was considered significant and two-tailed p values were used for all statistics. Statistical analyses were performed using MedCalc for Windows, version 11.3 (MedCalc Software, Mariakerke, Belgium) and the SPSS Statistics software (version 17.0; SPSS Inc., Chicago, Ill., USA).
Characteristics of Study Population
Standard dose group (n = 80)
High dose group (n = 18)
56 ± 14
67 ± 10
172 ± 10
171 ± 11
84 ± 16
84 ± 19
1.99 ± 0.21
1.99 ± 0.28
Caffeine < 12 hours prior to scan
Family history of CAD
Single vessel CAD
End-diastolic volume (ml)
157 ± 46
183 ± 61
End-systolic volume (ml)
59 ± 38
99 ± 62
Ejection fraction (%)
65 ± 13
52 ± 19
Mass index (gr/m2)
71 ± 21
72 ± 18
Haemodynamic response to standard dose adenosine
Haemodynamic Parameters at Rest and During Adenosine Stress
Standard dose Adenosine
(n = 80)
High dose Adenosine
(n = 18)
70 ± 13
96 ± 16
66 ± 12
75 ± 11
81 ± 18*
137 ± 18
139 ± 19
139 ± 23
134 ± 24
132 ± 22
80 ± 12
81 ± 12
82 ± 12
79 ± 11
77 ± 14
9639 ± 2399
13304 ± 2781
8975 ± 1909
9945 ± 1694
10672 ± 2787
Haemodynamic response to high dose adenosine
Eighteen patients (18%) failed to show signs of adequate haemodynamic response during standard-dose adenosine infusion. Following an increase in the dose of adenosine (up to 170 mcg/kg/min in 6 patients; and up to 210 mcg/kg/min in 12 patients) 16 out of these 18 patients showed an improved haemodynamic response with greater rise in heart rate (p = 0.011) and a mild drop in systolic blood pressure (p = 0.57). There was a trend towards a significant increase to rate pressure product at maximum adenosine rate compared to baseline (p = 0.07). The mean duration of adenosine infusion was significantly longer for the high-dose group (387 ± 46 seconds; p < 0.001) compared to the standard dose group (246 ± 35 seconds). Table 2 shows the haemodynamic effects of adenosine in both groups. Of the 80 patients who received standard dose adenosine 50 patients (63%) had abnormal perfusion on CMR (defined as any defect at stress irrespective of the LGE findings). Similarly, of the 18 patients who received high dose adenosine 10 (56%) patients had abnormal perfusion on CMR (p = 0.6).
Adverse Effects of Adenosine
Standard dose Adenosine
(n = 80)
High dose Adenosine
(n = 18)
Shortness of breath
Flushing, headache or dizziness
Mobitz II 2nd or 3rd degree atrioventricular block
Angina requesting sublingual nitrates
Scan abandoned during adenosine on subject's request
Predictors of non-response to standard adenosine dose
The present study is the first to demonstrate the feasibility and safety of high-dose adenosine in patients with known or suspected CAD undergoing stress perfusion CMR. Our findings suggest that a substantial number of patients (18% in our cohort) do not show a sufficient haemodynamic response to adenosine stress. Independent predictors of an inadequate response to the standard adenosine dose of 140 mcg/kg/min were: age above 65 years and ejection fraction less than 57%. The attenuated response to adenosine can be surmounted by increasing adenosine dose up to 210 mcg/kg/min without significant adverse events. Our study has important clinical implications because a reduced peripheral haemodynamic response to standard dose intravenous administration of adenosine may reflect similarly inadequate effects on coronary vasodilatation, thereby affecting the diagnostic reliability of CMR perfusion imaging.
Adenosine is a powerful vasoactive substance. Activation of cardiac A2A and A2B adenosine receptors dilates the coronary and peripheral arterial beds (with the exception of renal glomerular afferent arteriole), increases myocardial blood flow, and causes sympatho-excitation . These effects cause mild decrease in blood pressure and baroreceptor-mediated reflex tachycardia [8, 9]. The majority of patients reach near maximal coronary vasodilatation and show signs of sufficient peripheral vasodilatory response after 2-3 minutes of adenosine infusion at the standard dose of 140 mcg/kg/min. However, as previous studies have demonstrated, some patients show reduced vasodilator response to the standard dose [4–6].
In our study 18% of patients showed inadequate peripheral haemodynamic response to the standard infusion dose. Similarly, Wilson et al. measured coronary blood flow invasively using Doppler and found that 16% of their subjects who received adenosine at 140 mcg/kg/min did not achieve maximal coronary hyperaemia as compared to that produced with papaverine . The mechanism of this phenomenon is not well understood, but it is interesting that similar differences in adenosine responsiveness have also been reported in dogs . Impairment of the baroreceptor reflex, resulting in decreased vascular reactivity in response to vasodilator stimuli is a possible cause of reduced heart rate response. As previously shown, diabetic or elderly patients have attenuated reflex tachycardia in response to vasodilator-induced decreased blood pressure, possibly attributable to autonomic dysfunction [5, 11]. Indeed, our study patients who showed reduced haemodynamic response were significantly older and were more likely to have history of diabetes mellitus than those with normal response to standard adenosine. Moreover, a left ventricular ejection fraction of less than 57% was also associated with inadequate peripheral haemodynamic response. This may be an effect of the already increased sympathetic nervous activity known to be present in heart failure. It is well known that patients with heart failure have high resting peripheral vasomotor tone which makes them less responsive to the vasodilator properties of adenosine [12, 13]. There is also an association between high catecholamine levels and endogenous adenosine formation which acts as a negative feedback system in patients with heart failure . Lastly, besides physiological considerations, genetic factors are likely to play an important role in determining response to adenosine. Potency of adenosine is strongly influenced by the number of adenosine receptors expressed in myocardial cells, the predominant type of receptor expressed, as well as the type of response that is measured from adenosine stimulation [14–17].
Our data suggest that there is a clear dose-response relation and when patients fail to show adequate vasomotor responsiveness, a further increase in adenosine dose can induce signs of improved peripheral hemodynamic effect. This dose-dependent vasodilator effect is also supported by previous studies using intravenous or intracoronary doses of adenosine [18–21]. Reyes and colleagues have used a high-dose adenosine protocol (210 mcg/kg/min) to overcome caffeine antagonism in patients undergoing myocardial perfusion scintigraphy . In total, 18 patients received the high dose after 200 mg of caffeine intake. The increased adenosine dose was well tolerated and was effective to surmount the inhibitory effect of caffeine. Our study is the first to use high dose adenosine in patients undergoing perfusion CMR imaging who fail to show an adequate cardiovascular response, irrespective of caffeine use. Although our patient cohort is small, all 18 patients who received high dose adenosine infusion tolerated it well without significant adverse clinical events. We did not measure caffeine levels in our patient population and, therefore, recent caffeine intake, despite the clear instructions to avoid it for 24 hours, cannot be excluded. However, as previously shown, even patients who consume coffee 1-2 hours before the scan and reach peak levels of caffeine during the infusion of adenosine may demonstrate similar hemodynamic response to stress with patients who had no caffeine [22–24]. Therefore, we believe that the insufficient response to adenosine stress which 18 of our patients showed is unlikely to be due to previous caffeine intake.
Previous studies looking into the relation between the peripheral hemodynamic actions of adenosine and its coronary vasodilator effect have shown that despite a lack of peripheral response to adenosine, coronary vasodilatation remains adequate for the purpose of myocardial perfusion imaging . This observation would suggest that a further increase to adenosine dose in order to induce better systemic and coronary vasodilatation to non-responders to standard dose is not needed. However, there are important differences between our study and the aforementioned study by Mishra and colleagues. First of all, we prospectively defined 'non-responders' to standard adenosine dose (HR rise < 10 bpm, SBPdrop < 10 mmHg) whereas Mishra and colleagues retrospectively looked into the lower tertile which had an average HR change of 13 bpm. Notwithstanding this, the patients in the lower tertile had lower hyperemic myocardial blood flow and higher coronary resistance compared to the patients in the intermediate (average HR increase 25 bpm) and upper tertiles (average HR change 37 bpm) . This observation supports our hypothesis that inadequate peripheral hemodynamic response to adenosine might indicate reduced coronary vasodilatation and slightly increased coronary resistance. Lastly, Mishra and colleagues did not test the peripheral and coronary haemodynamic effects of a high dose infusion protocol.
This study did not assess any potential advantage of high-dose adenosine perfusion CMR on the diagnostic performance of this technique in patients with reduced haemodynamic response to standard adenosine dose. To perform such a study the same cohort of patients with blunted vasodilatory response would need to undergo stress perfusion CMR twice using the standard- and the high-dose adenosine infusion with not only visual but also quantitative measurements of myocardial blood flow. Nevertheless, our aim was to show feasibility and initial safety data of the high-dose adenosine infusion protocol and not to assess the potential added clinical value of such an approach. Stress echocardiography using a high dose adenosine protocol has been shown to have incremental diagnostic value mainly by increasing sensitivity in patients with single-vessel disease . It is conceivable that this may also be true for stress perfusion CMR, but larger scale studies are needed to confirm our initial observations on safety of the proposed high-dose protocol and assess its diagnostic performance in everyday practice.
About one fifth of patients undergoing stress perfusion CMR show inadequate haemodynamic response to adenosine infusion at the standard dose of 140 mcg/kg/min, for which age > 65 years and ejection fraction < 57% were independent predictors. A high-dose protocol (up to 210 mcg/kg/min) improves the peripheral haemodynamic response to adenosine, suggesting better coronary vasodilatation. Our initial experience with a high dose adenosine infusion suggests it is well tolerated and safe, although further confirmation is needed in larger scale studies which will test also the clinical utility of this protocol.
This work was supported by the British Heart Foundation (PG/08/101/26126) and by the Oxford NIHR Biomedical Research Centre.
- Gerber BL, Raman SV, Nayak K, Epstein FH, Ferreira P, Axel L, Kraitchman DL: Myocardial first-pass perfusion cardiovascular magnetic resonance: history, theory, and current state of the art. J Cardiovasc Magn Reson. 2008, 10: 18-10.1186/1532-429X-10-18.PubMed CentralView ArticlePubMedGoogle Scholar
- Christiansen JP, Karamitsos TD, Myerson SG, Francis JM, Neubauer S: Stress Perfusion Imaging Using Cardiovascular Magnetic Resonance: A Review. Heart Lung Circ. 2010Google Scholar
- Karamitsos TD, Arnold JR, Pegg TJ, Cheng AS, van Gaal WJ, Francis JM, Banning AP, Neubauer S, Selvanayagam JB: Tolerance and safety of adenosine stress perfusion cardiovascular magnetic resonance imaging in patients with severe coronary artery disease. Int J Cardiovasc Imaging. 2009, 25: 277-283. 10.1007/s10554-008-9392-3.View ArticlePubMedGoogle Scholar
- Wilson RF, Wyche K, Christensen BV, Zimmer S, Laxson DD: Effects of adenosine on human coronary arterial circulation. Circulation. 1990, 82: 1595-1606.View ArticlePubMedGoogle Scholar
- Johnston DL, Hodge DO, Hopfenspirger MR, Gibbons RJ: Clinical determinants of hemodynamic and symptomatic responses in 2,000 patients during adenosine scintigraphy. Mayo Clin Proc. 1998, 73: 314-320. 10.4065/73.4.314.View ArticlePubMedGoogle Scholar
- Abidov A, Hachamovitch R, Hayes SW, Ng CK, Cohen I, Friedman JD, Germano G, Berman DS: Prognostic impact of hemodynamic response to adenosine in patients older than age 55 years undergoing vasodilator stress myocardial perfusion study. Circulation. 2003, 107: 2894-2899. 10.1161/01.CIR.0000072770.27332.75.View ArticlePubMedGoogle Scholar
- Karamitsos TD, Hudsmith LE, Selvanayagam JB, Neubauer S, Francis JM: Operator induced variability in left ventricular measurements with cardiovascular magnetic resonance is improved after training. J Cardiovasc Magn Reson. 2007, 9: 777-783. 10.1080/10976640701545073.View ArticlePubMedGoogle Scholar
- Cerqueira MD, Verani MS, Schwaiger M, Heo J, Iskandrian AS: Safety profile of adenosine stress perfusion imaging: results from the Adenoscan Multicenter Trial Registry. J Am Coll Cardiol. 1994, 23: 384-389. 10.1016/0735-1097(94)90424-3.View ArticlePubMedGoogle Scholar
- Biaggioni I, Olafsson B, Robertson RM, Hollister AS, Robertson D: Cardiovascular and respiratory effects of adenosine in conscious man. Evidence for chemoreceptor activation. Circ Res. 1987, 61: 779-786.View ArticlePubMedGoogle Scholar
- Olsson RA, Khouri EM, Bedynek JL, McLean J: Coronary vasoactivity of adenosine in the conscious dog. Circ Res. 1979, 45: 468-478.View ArticlePubMedGoogle Scholar
- Czernin J, Muller P, Chan S, Brunken RC, Porenta G, Krivokapich J, Chen K, Chan A, Phelps ME, Schelbert HR: Influence of age and hemodynamics on myocardial blood flow and flow reserve. Circulation. 1993, 88: 62-69.View ArticlePubMedGoogle Scholar
- Hasking GJ, Esler MD, Jennings GL, Burton D, Johns JA, Korner PI: Norepinephrine spillover to plasma in patients with congestive heart failure: evidence of increased overall and cardiorenal sympathetic nervous activity. Circulation. 1986, 73: 615-621.View ArticlePubMedGoogle Scholar
- Triposkiadis F, Karayannis G, Giamouzis G, Skoularigis J, Louridas G, Butler J: The sympathetic nervous system in heart failure physiology, pathophysiology, and clinical implications. J Am Coll Cardiol. 2009, 54: 1747-1762. 10.1016/j.jacc.2009.05.015.View ArticlePubMedGoogle Scholar
- Belardinelli L, Shryock JC, Snowdy S, Zhang Y, Monopoli A, Lozza G, Ongini E, Olsson RA, Dennis DM: The A2A adenosine receptor mediates coronary vasodilation. J Pharmacol Exp Ther. 1998, 284: 1066-1073.PubMedGoogle Scholar
- Mizuno M, Kimura Y, Tokizawa K, Ishii K, Oda K, Sasaki T, Nakamura Y, Muraoka I, Ishiwata K: Greater adenosine A(2A) receptor densities in cardiac and skeletal muscle in endurance-trained men: a [11C]TMSX PET study. Nucl Med Biol. 2005, 32: 831-836. 10.1016/j.nucmedbio.2005.07.003.View ArticlePubMedGoogle Scholar
- Mustafa SJ, Morrison RR, Teng B, Pelleg A: Adenosine receptors and the heart: role in regulation of coronary blood flow and cardiac electrophysiology. Handb Exp Pharmacol. 2009, 161-188. full_text.Google Scholar
- Talukder MA, Morrison RR, Jacobson MA, Jacobson KA, Ledent C, Mustafa SJ: Targeted deletion of adenosine A(3) receptors augments adenosine-induced coronary flow in isolated mouse heart. Am J Physiol Heart Circ Physiol. 2002, 282: H2183-2189.View ArticlePubMedGoogle Scholar
- Lopez-Palop R, Saura D, Pinar E, Lozano I, Perez-Lorente F, Pico F, Valdez M: Adequate intracoronary adenosine doses to achieve maximum hyperaemia in coronary functional studies by pressure derived fractional flow reserve: a dose response study. Heart. 2004, 90: 95-96. 10.1136/heart.90.1.95.PubMed CentralView ArticlePubMedGoogle Scholar
- Lindstaedt M, Bojara W, Holland-Letz T, Yazar A, Fadgyas T, Muller L, Mugge A, Germing A: Adenosine-induced maximal coronary hyperemia for myocardial fractional flow reserve measurements: comparison of administration by femoral venous versus antecubital venous access. Clin Res Cardiol. 2009, 98: 717-723. 10.1007/s00392-009-0056-7.View ArticlePubMedGoogle Scholar
- Kern MJ, Deligonul U, Tatineni S, Serota H, Aguirre F, Hilton TC: Intravenous adenosine: continuous infusion and low dose bolus administration for determination of coronary vasodilator reserve in patients with and without coronary artery disease. J Am Coll Cardiol. 1991, 18: 718-729. 10.1016/0735-1097(91)90795-B.View ArticlePubMedGoogle Scholar
- Djordjevic-Dikic AD, Ostojic MC, Beleslin BD, Stepanovic J, Petrasinovic Z, Babic R, Stojkovic SM, Stankovic G, Nedeljkovic M, Nedeljkovic I, Kanjuh V: High dose adenosine stress echocardiography for noninvasive detection of coronary artery disease. J Am Coll Cardiol. 1996, 28: 1689-1695. 10.1016/S0735-1097(96)00374-9.View ArticlePubMedGoogle Scholar
- Reyes E, Loong CY, Harbinson M, Donovan J, Anagnostopoulos C, Underwood SR: High-dose adenosine overcomes the attenuation of myocardial perfusion reserve caused by caffeine. J Am Coll Cardiol. 2008, 52: 2008-2016. 10.1016/j.jacc.2008.08.052.View ArticlePubMedGoogle Scholar
- Zoghbi GJ, Htay T, Aqel R, Blackmon L, Heo J, Iskandrian AE: Effect of caffeine on ischemia detection by adenosine single-photon emission computed tomography perfusion imaging. J Am Coll Cardiol. 2006, 47: 2296-2302. 10.1016/j.jacc.2005.11.088.View ArticlePubMedGoogle Scholar
- Aqel RA, Zoghbi GJ, Trimm JR, Baldwin SA, Iskandrian AE: Effect of caffeine administered intravenously on intracoronary-administered adenosine-induced coronary hemodynamics in patients with coronary artery disease. Am J Cardiol. 2004, 93: 343-346. 10.1016/j.amjcard.2003.10.017.View ArticlePubMedGoogle Scholar
- Mishra RK, Dorbala S, Logsetty G, Hassan A, Heinonen T, Schelbert HR, Di Carli MF: Quantitative relation between hemodynamic changes during intravenous adenosine infusion and the magnitude of coronary hyperemia: implications for myocardial perfusion imaging. J Am Coll Cardiol. 2005, 45: 553-558. 10.1016/j.jacc.2004.10.064.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.