TRANSCRANIAL DOPPLER MONITORING DURING INDUCTION OF ANESTHESIA - EFFECTS OF PROPOFOL, THIOPENTAL, AND HYPERVENTILATION IN PATIENTS WITH LARGE MALIGNANT BRAIN-TUMORS
W. Schregel et al., TRANSCRANIAL DOPPLER MONITORING DURING INDUCTION OF ANESTHESIA - EFFECTS OF PROPOFOL, THIOPENTAL, AND HYPERVENTILATION IN PATIENTS WITH LARGE MALIGNANT BRAIN-TUMORS, Journal of neurosurgical anesthesiology, 5(2), 1993, pp. 86-93
Disturbed autoregulation and CO, reactivity have been reported in pati
ents with brain tumors. Therefore, we decided to monitor the cerebrova
scular effects of anesthetic drugs and hyperventilation. Transcranial
Doppler sonography (TCD) can measure noninvasively alterations of flow
velocities (v) and cross-sectional vessel area (VA) in large brain ar
teries. Twenty-eight patients with large malignant brain tumors in the
territory of the middle cerebral artery (MCA) randomly received propo
fol or thiopental for induction and maintenance of anesthesia. Mean ar
terial pressure (MAP), heart rate (HR), and TCD parameters (vMCA and V
A of the tumor or nontumor side) were determined at six data points (D
P). The first measurements (MAP, HR, and TCD of the nontumor side) wer
e performed before (DP I) and 60 s after (DP II) induction of anesthes
ia with either 2 mg/kg propofol or 4 mg/kg thiopental. After intubatio
n and normoventilation (50% O2 in air), 0.05-0.1 mg/kg midazolam and a
n alfentanil infusion (100 mug/kg x h) were initiated. Then MAP, HR, v
MCA, and VA of the tumor side were analyzed before (DP III) and 60 s a
fter (DP IV) either propofol (I mg/kg) or thiopental (2 mg/kg) were gi
ven. Finally, the effects of hyperventilation on HR, MAP, vMCA, and VA
(tumor side) were determined (DP V and VI). Mean +/- SD, thiopental o
r propofol reactivity (nontumor and tumor side) and CO2 reactivity (tu
mor side) were calculated; statistical comparison between DP I and II,
III and IV, and V and VI was performed by paired t tests (p < 0.05).
Unpaired t tests were used to evaluate differences between groups. By
injection of propofol or thiopental, MAP was reduced, whereas VA was n
ot markedly influenced. vMCA decreased by 24% after propofol and by 27
% after thiopental administration on the nontumor side. On the tumor s
ide, reduced or even paradoxical effects of propofol, thiopental, and
hyperventilation on vMCA occurred frequently. Nine patients developed
intraoperative brain swelling; five of these had the lowest drug react
ivity (tumor side) of their group. TCD can demonstrate disturbed vasor
eactivity caused by large brain tumors: Further studies are necessary
to define the role of TCD in neuroanesthesia.