Title of article :
Intravenous Dexmedetomidine or Propofol Adjuvant to Spinal Anesthesia in Total Knee Replacement Surgery
Author/Authors :
AlOweidi, Abdelkarim S. University of Jordan - Jordan University Hospital - Department of Anesthesia and Intensive Care, Jordan , Al-Mustafa, Mahmoud M. University of Jordan - Jordan University Hospital - Department of Anesthesia and Intensive Care, Jordan , Al Ajlouni, Jihad M. University of Jordan - Jordan University Hospital - Department of Special Surgery, Orthopedic Division, Jordan , Masad, Diana F. University of Jordan - Jordan University Hospital - Department of Family and Community Medicine, Jordan , Hamdan, Mohammad Q. University of Jordan - Jordan University Hospital - Department of Special Surgery, Orthopedic Division, Jordan , Alghanem, Subhi M. University of Jordan - Jordan University Hospital - Department of Special Surgery, Orthopedic Division, Jordan , Qudaisat, Ibraheem Y. University of Jordan - Jordan University Hospital - Department of Anesthesia and Intensive Care, Jordan , Abu Halaweh, Sami A. University of Jordan - Jordan University Hospital - Department of Anesthesia and Intensive Care, Jordan , Massad, Islam M. University of Jordan - Jordan University Hospital - Department of Anesthesia and Intensive Care, Jordan
From page :
174
To page :
183
Abstract :
Background: The purpose of this study was to compare the effect of intravenous dexmedetomidine with the intravenous propofol adjuvant to spinal intrathecal anesthesia on the duration of spinal anesthesia and hemodynamic parameters during total knee replacement surgery.Methods: Seventy five patients were enrolled into this randomized study from the 1st of April 2008 till the 30th of August 2009 for total knee replacement surgery under spinal anesthesia. They were randomly assigned into three groups, group D, group P and group C. Following intrathecal injection with bupivacaine 12.5 mg in all patients in the three groups, patients in group D received intravenous loading dose of 1^g/kg/hr dexmedetomidine over 10 minutes and a maintenance dose of 0.2 to 0.5 ^g/kg/hr. Patients in group P received intravenous propofol 4 mg/Kg/hr over 10 min and a maintenance dose of 0.5-2 mg/Kg/hr. Patients in group C (control group) received nothing extra to the regular IV fluid. The regression times to reach S1 sensory level and Bromage 0 motor scale, the hemodynamic parameters, the Bispectral Index level of Sedation (BIS), and arterial CO2 level were recorded.Results: The regression time to reach S1 dermatome was 149.4±14.6 min in group C, 152.8±16.6 min in group P and 209.6±25.9 min in group D. The regression to Bromage 0 was184.6±22.8 min in group C, 190.0±21.0 min in group P, and 255.8±36.7 min in group D. Statistical analysis of regression of sensory and motor block was significant among groups (C vs. D, P vs. D, P 0.05). The heart rate was significantly decreased in group D in comparison to groups C and P. Sedation levels were within accepted ranges in groups D and P and not affected in the control group. Minimal respiratory depression occurred in group P and D, clinically it was not significant.Conclusion: Supplementation of spinal anesthesia with intravenous dexmedetomidine or propofol produces good sedation levels without significant clinical hemodynamic changes. Adding dexmedetomidine produces significantly longer sensory and motor block than propofol.
Keywords :
Dexmedetomidine , Propofol , Spinal Anesthesia , Total Knee Replacement.
Journal title :
Jordan Medical Journal
Journal title :
Jordan Medical Journal
Record number :
2644836
Link To Document :
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