Sm. Mohiuddin et al., SAFETY OF DIFFERENT DOSAGES OF INTRAVENOUS ADENOSINE USED IN CONJUNCTION WITH DIAGNOSTIC MYOCARDIAL IMAGING TECHNIQUES, Pharmacotherapy, 13(5), 1993, pp. 476-480
Study Objective. To determine the safety of three different dosage reg
imens of intravenous adenosine. Design. Open-label, observational safe
ty evaluation. Setting. University hospital-based department of nuclea
r medicine. Patients. Cohort of 854 patients referred for myocardial p
erfusion imaging to evaluate their coronary artery disease and who wer
e judged unable to perform physical exercise Interventions. Subjects u
nderwent myocardial perfusion imaging in conjunction with one of three
intravenous dosage regimens: 1 = fixed dosage 140 mug/kg/minute for 6
minutes; 2 = dosage titration to a maximum of 140 mug/kg/minute; and
3 = dosage titration to a maximum of 200 mug/kg/minute. In regimens 2
and 3, maximum tolerated dosages were continued for a minimum of 3 min
utes prior to radioisotope injection. Measurements and Main Results. A
denosine-induced hemodynamic, electrocardiographic, and biochemical ch
anges were measured. Adverse effects of the different adenosine dosage
s were compared. Noncardiac side effects such as flushing, dyspnea, ne
ck tightness, and lightheadedness occurred at a significantly higher r
ate during regimens 2 and 3 than regimen 1. Chest pain and first- and
second-degree atrioventricular block were also more frequent during re
gimens 2 and 3. However, the frequency of other side effects such as c
omplete heart block, hypotension, and ST segment depression did not di
ffer among the regimens. High-dose adenosine was associated with a sig
nificant increase in serum uric acid, a significant decrease in blood
glucose, and a significant increase in serum triglyceride levels. Mean
changes in hemodynamics and electrocardiographic intervals were also
not different among the groups except for a greater increase in PR int
erval in regimens 2 and 3 than regimen 1. Discontinuation of adenosine
was infrequent (< 1 %) and did not differ among the regimens. Conclus
ions. Adenosine-assisted myocardial perfusion imaging procedures are r
elatively safe for evaluating coronary artery disease. Despite 82% of
patients reporting at least one side effect, only 10 (< 1%) had to dis
continue adenosine. No patient suffered any residual sequelae from the
adverse effects. The fixed-dose regimen is associated with fewer subj
ective side effects and is better tolerated than titration regimens. A
ppropriate safety precautions should nonetheless be taken during adeno
sine infusions.