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Background <p>Laryngoscopy and intubation provoke strong sympathetic activation and may cause hemodynamic instability in cardiovascular surgery patients. Maintaining adequate hypnotic depth and cerebral oxygenation during induction is essential. Although BIS and NIRS are widely used, their simultaneous behavior during induction in a homogeneous cardiovascular surgery population is not well established.</p> Objectives <p>To compare thiopental–low-dose fentanyl and midazolam–high-dose fentanyl induction protocols regarding their effects on BIS, regional cerebral oxygen saturation (rSO₂), and hemodynamic responses during the peri-intubation period.</p> Methods <p>This prospective, randomized study included 30 adults undergoing elective cardiovascular surgery. Patients received thiopental (5–7&#xa0;mg/kg) + fentanyl (1.5&#xa0;µg/kg) or midazolam (0.1&#xa0;mg/kg) + fentanyl (5&#xa0;µg/kg). BIS, bilateral rSO₂, arterial pressures, heart rate, and end-tidal CO₂ were recorded at four time points: before induction (T0), two minutes after induction (T1), immediately after intubation (T2), and two minutes post-intubation (T3). Statistical comparisons were performed within and between groups (<i>p</i> &lt; 0.05).</p> Results <p>Both protocols demonstrated similar BIS patterns: a marked decrease after induction, a rise at intubation, and a decline thereafter. rSO₂ increased significantly at T1–T2 and decreased at T3 in both groups. Hemodynamic responses showed parallel post-induction decreases and intubation-related increases. No significant intergroup differences were identified in BIS, rSO₂, or major hemodynamic variables.</p> Conclusions <p>Thiopental–low-dose fentanyl and midazolam–high-dose fentanyl induction yield comparable effects on hypnotic depth, cerebral oxygenation, and hemodynamic stability. Combined BIS–NIRS monitoring provides complementary information and may enhance peri-intubation safety in cardiovascular surgery.</p>

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Simultaneous bispectral index and near-infrared spectroscopy monitoring to evaluate two induction protocols in elective cardiovascular surgery

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月28日

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  • Hakan Eke,
  • Burak Toprak,
  • Elif Dilber Bozkurt

摘要

Background

Laryngoscopy and intubation provoke strong sympathetic activation and may cause hemodynamic instability in cardiovascular surgery patients. Maintaining adequate hypnotic depth and cerebral oxygenation during induction is essential. Although BIS and NIRS are widely used, their simultaneous behavior during induction in a homogeneous cardiovascular surgery population is not well established.

Objectives

To compare thiopental–low-dose fentanyl and midazolam–high-dose fentanyl induction protocols regarding their effects on BIS, regional cerebral oxygen saturation (rSO₂), and hemodynamic responses during the peri-intubation period.

Methods

This prospective, randomized study included 30 adults undergoing elective cardiovascular surgery. Patients received thiopental (5–7 mg/kg) + fentanyl (1.5 µg/kg) or midazolam (0.1 mg/kg) + fentanyl (5 µg/kg). BIS, bilateral rSO₂, arterial pressures, heart rate, and end-tidal CO₂ were recorded at four time points: before induction (T0), two minutes after induction (T1), immediately after intubation (T2), and two minutes post-intubation (T3). Statistical comparisons were performed within and between groups (p < 0.05).

Results

Both protocols demonstrated similar BIS patterns: a marked decrease after induction, a rise at intubation, and a decline thereafter. rSO₂ increased significantly at T1–T2 and decreased at T3 in both groups. Hemodynamic responses showed parallel post-induction decreases and intubation-related increases. No significant intergroup differences were identified in BIS, rSO₂, or major hemodynamic variables.

Conclusions

Thiopental–low-dose fentanyl and midazolam–high-dose fentanyl induction yield comparable effects on hypnotic depth, cerebral oxygenation, and hemodynamic stability. Combined BIS–NIRS monitoring provides complementary information and may enhance peri-intubation safety in cardiovascular surgery.