A. Raviele et al., Comparison of diagnostic accuracy of sublingual nitroglycerin test and low-dose isoproterenol test in patients with unexplained syncope, AM J CARD, 85(10), 2000, pp. 1194-1198
Citations number
26
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Despite the widespread use of head-up tilt testing as a means for diagnosin
g vasovagal syncope, standardization of test methodology remains a controve
rsial issue. The aim of this study was to compare the diagnostic value of h
ead-up tilt testing potentiated with sublingual nitroglycerin with that of
head-vp tilt testing potentiated with law-dose isoproterenol. For this purp
ose, 71 patients with unexplained syncope (mean age 43 years) and 30 asympt
omatic controls were studied. All underwent the sublingual nitroglycerin an
d low-dose isoproterenol tests on separate days in a randomized fashion. Th
e protocol of the 2 tests was similar and consisted of 2 phases. Initially,
subjects were tilted at 60 degrees for 20 minutes without medication; then
, if syncope did not occur, patients and controls received sublingual nitro
glycerin (300 mu g) or low-dose intravenous isoproterenol (mean infusion ra
te 1.3 +/- 0.5 mu g/min) and continued to be tilted at 60 degrees for a fur
ther 20 minutes. During the sublingual nitroglycerin test, a positive respo
nse (syncope associated with sudden hypotension and bradycardia) occurred i
n 35 patients (49%), a negative response in 36 (51%), and drug intolerance
in none (0%). During the low-dose isoproterenol test, these percentages wer
e 41%, 59%, and 6%, respectively. A concordant response was observed in 53
cases (75%). Among controls, 3 subjects (10%) had a positive response to th
e sublingual nitroglycerin test and 4 (13%) to the low-dose isoproterenol t
est. It is concluded that sublingual nitroglycerin and low-dose isoproteren
ol are equivalent tests for evaluating patients with unexplained syncope. T
he sublingual nitroglycerin test, however, is simpler, better tolerated, an
d safer than the low-dose isoproterenol test and, thus, more suitable for r
outine clinical use. (C) 2000 by Excerpta Medica, Inc.