関連する実験動画
Updated: Jan 15, 2026

In Vivo Real-Time Study of Drug Effects on Carotid Blood Flow in the Ovine Fetus
Published on: April 28, 2023
子癇前症患者における脊椎麻酔下帝王切開時のフェニレフリン初期予防注入速度と医師の介入:ランダム化二重盲検試験
M Mohta1, A Jain1, G T Chilkoti1
1Department of Anaesthesiology and Critical Care, University College of Medical Sciences and Guru Teg Bahadur Hospital, Delhi, India.
Background:
Patients with preeclampsia have greater sensitivity to vasopressors and require lower doses than patients without preeclampsia. The aim of the current study was to compare the number of required physician interventions using three initial prophylactic phenylephrine infusion rates titrated to maintain systolic blood pressure close to baseline values.
Methods:
In this randomised, controlled, double-blind trial, 102 patients with preeclampsia undergoing caesarean delivery under spinal anaesthesia were randomised to one of three prophylactic phenylephrine infusion rates: 15 µg/min, 25 µg/min, or 35 µg/min. The rate was titrated to maintain systolic blood pressure within 10% of baseline values. The primary outcome was the number of physician interventions; secondary outcome measures included the incidence of hypertension, hypotension and bradycardia, total phenylephrine dose, neonatal outcomes, and maternal complications.
Results:
The median [interquartile range] number of physician interventions was 6.5 [4-9], 6 [4-7.5] and 6.5 [4-9], respectively, for initial infusion rates of 15, 25, and 35 µg/min (P = 0.831). The total phenylephrine dose was greater with higher infusion doses (P < 0.001). No patient had bradycardia, and one patient had hypertension. Nineteen patients each in groups starting at 15 µg/min and 25 µg/min, and 22 patients starting at 35 µg/min developed hypotension (P = 0.695). Neonatal outcome and maternal complications were not different among groups.
Conclusions:
All three infusion regimens required a similar number of physician interventions to maintain systolic blood pressure close to the baseline. A starting dose of 15 µg/min may be considered in this patient population.
Clinical Trial Registration Number:
CTRI/2023/08/055926; registered on 1st August 2023.
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