Product Monograph
Pharmacologic Stress in Myocardial Perfusion Imaging: Adenoscan
Overview

Myocardial perfusion imaging has been shown to be of value in identifying areas affected by coronary artery disease.

Adequate coronary vasodilation is essential to myocardial perfusion imaging. Coronary vasodilation increases coronary blood flow. This increase creates differences in the distribution of the imaging agent great enough to identify regions supplied by stenosed coronary vessels and to distinguish ischemic from nonischemic areas.

Exercise stress testing often is employed for dilating coronary vessels, hence increasing coronary blood flow. However, maximal exercise levels are required for sufficient vasodilation, and exercise capacity varies greatly among patients. Therefore, exercise may not always be an option. Peripheral vascular disease, medications, poor patient motivation, and a variety of coexisting conditions all may preclude certain patients from exercising at maximal levels (Table 1).

Table 1. Potential Limitations to Maximal Exercise Testing
Peripheral vascular disease
Poor physical condition
Poor patient motivation
Lower limb amputation
Arthritis/rheumatism/orthopedic conditions
Other conditions that limit physical exertion


Intravenous Adenoscan is a pharmacologic stress agent indicated as an adjunct to thallium-201 myocardial perfusion scintigraphy in patients unable to exercise adequately. Adenoscan has shown consistency in producing maximal vasodilation of coronary arteries relative to intracoronary papaverine. The short half-life of Adenoscan is responsible for its short-acting pharmacologic effects, making it useful for diagnostic evaluation and risk stratification in coronary artery disease (Table 2).

Table 2. Clinical Uses for Myocardial Perfusion Imaging
Diagnosis of coronary artery disease1
Functional significance of coronary disease1
Surgical intervention assistance1
Assessment of therapeutic effects of interventions, including medical therapy and revascularization1
Assessment of myocardial viability1
Risk stratification of patients1
Evaluation of acute chest pain2


Chemical Description
Adenosine is an endogenous nucleoside found in small amounts throughout the body. Its chemical formula is C10H13N5O4, or 6-amino-9-beta-D-ribofuranosyl-9-H-purine, and its molecular weight is 267 (Figure 1). Adenosine is a white crystalline powder, soluble in water and practically insoluble in alcohol.

FIGURE 1. Chemical structure of adenosine.






IMPORTANT SAFETY INFORMATION

Intravenous Adenoscan® (adenosine injection) is indicated as an adjunct to thallium-201 myocardial perfusion scintigraphy in patients unable to exercise adequately.

Adenoscan is contraindicated in patients with 2nd- or 3rd-degree AV block, sinus node disease, and known or suspected bronchoconstrictive or bronchospastic lung disease.

Approximately 2.6% and 0.8% of patients developed second- and third-degree AV block, respectively. All episodes of AV block have been asymptomatic, transient, and did not require intervention; less than 1% required termination of adenosine infusion.

Fatal cardiac arrest, sustained ventricular tachycardia (requiring resuscitation), and nonfatal myocardial infarction have been reported coincident with Adenoscan infusion. Patients with unstable angina may be at greater risk.

Side effects that were seen most often included flushing (44%), chest discomfort (40%), and dyspnea (28%). Side effects usually resolve quickly when infusion is terminated and generally do not interfere with test results.

Despite adenosine’s short half-life, 10.6% of the side effects started several hours after the infusion terminated, and 8.4% of the side effects that began during the infusion persisted for up to 24 hours after infusion. In many cases, it is not possible to know whether these late adverse events are the result of Adenoscan infusion.

Please see full prescribing information.


Product Monograph
Overview
Pharmacology
Imaging Efficacy
Safety
Post-marketing Experience
Dosing and Administration
References