Evaluation of Spinal Anaesthesia Using Low Dose Hyperbaric Bupivacaine for Day-Care Surgery

Journal Title: Journal of Medical Science And clinical Research - Year 2017, Vol 5, Issue 7

Abstract

Aim: To compare recovery time and evaluate home readiness time after different dosage of hyperbaric bupivacaine. Material and Methods: This study was performed in 3 different groups: group-I, group-II & group-III, each containing 50 patients. In study group-I, 6mg of hyperbaric bupivacaine, 8 mg in hyperbaric bupivacaine in group-II and in study group-III 10 mg hyperbaric bupivacaine was injected. The level of injection in all cases was at L2/3 vertebral interspace. Results: In study group-I (6mg bupivacaine) failure rate was 6%. Peri-operative complain of discomfort and pain was also high (12.76%). Study group-Ill (10mg bupivacaine) did not show any advantage over group-II (8 mg bupivacaine). The 10mg dose prolonged the stay in PACU and delayed home-readiness by 44 min when compared with the 8mg dose of spinal bupivacaine. Conclusion: Standardized spinal anaesthesia technique with 8mg dose of hyperbaric bupivacaine produced a good quality highly predictable spinal block with average duration of 57 minutes stay in PACU and average home readiness time was 4.15 hours. Furthermore, a small change in dose on upper and lower side (6mg or 10 mg) altered the reliability, spread and recovery of the spinal anaesthesia.

Authors and Affiliations

Dr Ravi Anand

Keywords

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  • EP ID EP526775
  • DOI -
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How To Cite

Dr Ravi Anand (2017). Evaluation of Spinal Anaesthesia Using Low Dose Hyperbaric Bupivacaine for Day-Care Surgery. Journal of Medical Science And clinical Research, 5(7), 25031-25036. https://europub.co.uk/articles/-A-526775