What is it about?
Study of Two Different Doses of Intrathecal Clonidine with Bupivacaine for Postoperative Analgesia
Featured Image
Photo by Leohoho on Unsplash
Why is it important?
Background: a2-agonist prolongs the duration of intrathecally administered local anaesthetics. This study was planned to investigate the effects of 45 µg and 90µg clonidine added to 0.5% intrathecal hyperbaric bupivacaine for postoperative analgesia. Materials and Methods: This prospective study was conducted in 90 patients of ASA grade I and II, both sex and aged between 20-60years. Patients were randomly allocated to Group A receiving normal saline+bupivacaine, Group B receiving a combination of 45µg clonidine+bupivacaine and Group C receiving combination of 90µg clonidine+bupivacaine. Sensory block, Motor block, sedation score and hemodynamic parameters were recorded. Results: Time for onset of sensory block (2.9±0.78 min) and motor block (6.27±0.98 min) was significantly lowest in group C (2.9±0.78 min). (p<0.01) The duration of analgesia was significantly higher in group C (495.33±34.2 min) (p<0.05). The motor block was most prolonged and intense in group C (2.0±0.0 score at 1.5 hr). Maximum sedation was seen at the end of 3 hrs with mean score of 2.1±0.37 in group C as compared to 2.1±0.3 in group B and 1.06±0.2 in Group A. There was no significance difference between the groups for fall of blood pressure. Hypotension and bradycardia were significantly higher in group B and group C as compared to group A, but was within acceptable limits. Conclusion: Intrathecal 90 µg clonidine seems to be the optimum safe dose because it significantly prolongs postoperative analgesia and markedly decreases supplementary analgesic demand with minimum hemodynamic changes.
Perspectives
Background: a2-agonist prolongs the duration of intrathecally administered local anaesthetics. This study was planned to investigate the effects of 45 µg and 90µg clonidine added to 0.5% intrathecal hyperbaric bupivacaine for postoperative analgesia. Materials and Methods: This prospective study was conducted in 90 patients of ASA grade I and II, both sex and aged between 20-60years. Patients were randomly allocated to Group A receiving normal saline+bupivacaine, Group B receiving a combination of 45µg clonidine+bupivacaine and Group C receiving combination of 90µg clonidine+bupivacaine. Sensory block, Motor block, sedation score and hemodynamic parameters were recorded. Results: Time for onset of sensory block (2.9±0.78 min) and motor block (6.27±0.98 min) was significantly lowest in group C (2.9±0.78 min). (p<0.01) The duration of analgesia was significantly higher in group C (495.33±34.2 min) (p<0.05). The motor block was most prolonged and intense in group C (2.0±0.0 score at 1.5 hr). Maximum sedation was seen at the end of 3 hrs with mean score of 2.1±0.37 in group C as compared to 2.1±0.3 in group B and 1.06±0.2 in Group A. There was no significance difference between the groups for fall of blood pressure. Hypotension and bradycardia were significantly higher in group B and group C as compared to group A, but was within acceptable limits. Conclusion: Intrathecal 90 µg clonidine seems to be the optimum safe dose because it significantly prolongs postoperative analgesia and markedly decreases supplementary analgesic demand with minimum hemodynamic changes.
Red Flower Publication Publications
Red Flower Publication Pvt Ltd
Read the Original
This page is a summary of: Comparative Study of Two Different doses of Intrathecal Clonidine with Bupivacaine for Postoperative Analgesia, Indian Journal of Anaesthesia and Analgesia, January 2018, Red Flower Publication Private, Ltd.,
DOI: 10.21088/ijaa.2349.8471.5518.8.
You can read the full text:
Contributors
The following have contributed to this page