Background and Purpose-We sought to determine whether the introduction
of EEG monitoring during head-up tilt testing could significantly imp
rove the understanding of the cerebral events occurring during tilt-in
duced vasovagal syncope and the potential danger to the patient of thi
s diagnostic procedure. Method;-EEG monitoring was performed during he
ad-up tilt testing in a group of 63 consecutive patients (27 males and
36 females; mean age, 41.5 years) with a history of recurrent syncope
of unknown origin despite extensive clinical and laboratory assessmen
t. Results-Syncope occurred in 27 of 63 patients (42.8%) during head-u
p tilt testing and was found to be cardioinhibitory in 11 of 27 (40.7%
) and vasodepressor in 16 of 27 (59.3%). All patients with a negative
response to head-up tilt testing showed no significant EEG modificatio
ns. In patients with vasodepressor syncope, a generalized high-amplitu
de, 4- to 5-Hz (theta range) slowing of EEG activity appeared at the o
nset of syncope, followed by an increase of brain-wave amplitude with
the reduction of frequency at 1.5 to 3 Hz (delta range). The return to
the supine position was associated with brain-wave amplitude reductio
n and frequency increase to 4 to 5 Hz, followed by restoration of a no
rmal EEG pattern and arousal (mean total duration of syncope, 23.2 sec
onds.). In patients with cardioinhibitory syncope, a generalized high-
amplitude EEG slowing in the theta range was noted at the onset of syn
cope, followed by a brain-wave amplitude increase and slowing in the d
elta range. A sudden reduction of brain-wave amplitude then ensued, le
ading to the disappearance of electrocerebral activity (''flat'' EEG).
The return to the supine position did not allow either the immediate
resolution of EEG abnormalities or consciousness recovery, both of whi
ch occurred after a further time interval (mean total duration of sync
ope, 41.4 seconds.). Conclusions-EEG monitoring during head-up tilt te
sting allowed recording and systematic description of electrocerebral
abnormalities developing in the course of tilt-induced vasovagal synco
pe.