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Published on: December 17, 2014
Cerebrovascular carbon dioxide reactivity in children anaesthetized with sevoflurane
D A Rowney1, R Fairgrieve, B Bissonnette
1Department of Anaesthesia, The Hospital for Sick Children, University of Toronto, Ontario, Canada,.
Insights
Sevoflurane anesthesia preserves cerebrovascular carbon dioxide reactivity (CCO2R) in children. Middle cerebral artery blood flow velocity increased with CO2 levels, indicating maintained brain blood flow regulation.
Area of Science:
- Anesthesiology
- Pediatric Anesthesia
- Cerebrovascular Physiology
Background:
- Assessing the impact of sevoflurane on cerebrovascular carbon dioxide reactivity (CCO2R) is crucial for pediatric anesthesia.
- Cerebral blood flow velocity (CBFV) is a key indicator of cerebrovascular function.
Purpose of the Study:
- To evaluate the effect of sevoflurane on CCO2R in children undergoing surgery.
- To measure CBFV at varying end-tidal carbon dioxide (PE'CO2) levels.
Main Methods:
- Transcranial Doppler sonography was used to measure CBFV in 16 healthy children (18 months to 7 years).
- Anesthesia involved 1.0 MAC sevoflurane, air/oxygen, and caudal epidural block.
- PE'CO2 was adjusted to 25, 35, 45, and 55 mm Hg while maintaining ventilation.
Main Results:
- CBFV significantly increased as PE'CO2 rose from 25 to 45 mm Hg (P<0.001).
- No significant increase in CBFV was observed between 45 and 55 mm Hg PE'CO2.
- Mean heart rate and arterial pressure remained stable throughout the study.
Conclusions:
- Cerebrovascular carbon dioxide reactivity (CCO2R) is maintained in healthy children under sevoflurane anesthesia.
- Sevoflurane at 1.0 MAC appears safe for maintaining cerebrovascular regulation in this pediatric population.
Background:
To determine the effects of sevoflurane on cerebrovascular carbon dioxide reactivity (CCO2R), middle cerebral artery blood flow velocity (CBFV) was measured at different levels of PE'CO2 by transcranial Doppler sonography in 16 ASA I or II children, aged 18 months to 7 yr undergoing elective urological surgery.
Methods:
Anaesthesia comprised 1.0 MAC sevoflurane and air in 30% oxygen delivered through an Ayre's T piece by intermittent positive-pressure ventilation, and a caudal epidural block with 0.25% bupivacaine 1.0 ml kg(-1) without epinephrine. PE'CO2 was randomly adjusted to 25, 35, 45 and 55 mm Hg (3.3, 4.6, 5.9 and 7.2 kPa) with an exogenous source of CO2, while maintaining ventilation variables constant.
Results:
CBFV increased as PE'CO2 increased from 25 to 35, and to 45 mm Hg (P<0.001), but did not increase significantly with an increase in PE'CO2 from 45 to 55 mm Hg. Mean heart rate and arterial pressure remained constant.
Conclusion:
CCO2R is preserved in healthy children anaesthetized with 1.0 MAC sevoflurane.
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