Comparative Evaluation of Bolus Administration of Dexmedetomidine and Fentanyl for Stress Attenuation During Laryngoscopy and Endotracheal Intubation
Background: Laryngoscopy and endotracheal intubation can cause hypertension and tachycardia which can result in myocardial ischemia or stroke in vulnerable people. The objective of our study was to compare the efficacy of bolus dose of dexmedetomidine and fentanyl in attenuating haemodynamic st...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Private Limited
2015-09-01
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Series: | Journal of Clinical and Diagnostic Research |
Subjects: | |
Online Access: | https://jcdr.net/articles/PDF/6431/13827_CE[Ra1]_F(AK)_PF1(PAK)_PFA(AK)_PF2(PAG).pdf |
Summary: | Background: Laryngoscopy and endotracheal intubation
can cause hypertension and tachycardia which can result
in myocardial ischemia or stroke in vulnerable people. The
objective of our study was to compare the efficacy of bolus dose
of dexmedetomidine and fentanyl in attenuating haemodynamic
stress responses following laryngoscopy and intubation.
Materials and Methods: Sixty patients who were fixed to
undergo elective surgeries under general anaesthesia were
randomly divided into 2 groups. Group 1 received 1 mcg/kg of
dexmedetomidine over 10 minutes and group 2 received fentanyl
2mcg/kg before induction. Anaesthesia was standardized in
both the groups and vital parameters were recorded for up to
10 minutes after intubation.
Results: Dexmedetomidine in a dose of 1mcg/kg prevented an
increase in heart rate following laryngoscopy when compared to
fentanyl group. This effect lasted for 10 minutes after intubation
is performed. Though dexmedetomidine prevented an increase
in blood pressure, this effect was statistically significant only for
2 minutes after intubation when compared to fentanyl group.
Conclusion: Attenuation of rise in heart rate and blood pressure
following laryngoscopy and endotracheal intubation was
better with 1mcg/kg of dexmedetomidine when compared to
fentanyl. |
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ISSN: | 2249-782X 0973-709X |