Published August 27, 2024 | Version https://impactfactor.org/PDF/IJPCR/16/IJPCR,Vol16,Issue8,Article18.pdf
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A Comparative Evaluation of Hyperbaric Ropivacaine 0.5% (18mg) versus Hyperbaric Bupivacaine 0.5% (18mg) for Elective Lower Abdominal Surgery under Spinal Anaesthesia

  • 1. Postgraduate, Department of Anaesthesiology and Critical Care, Sri Siddhartha Medical College and Research Institute, Tumkur, Karnataka, India
  • 2. Associate Professor, Department of Anaesthesiology and Critical Care, Sri Siddhartha Medical College and Research Institute, Tumkur, Karnataka, India
  • 3. Professor and Head, Department of Anaesthesiology and Critical Care, Sri Siddhartha Medical College and Research Institute, Tumkur, Karnataka, India

Description

Background: Ropivacaine is a novel long-acting amide local anaesthetic that is comparable to bupivacaine in terms of its structure and pharmacodynamics. ln comparison to bupivacaine, ropivacaine has a reduced propensity to affect the central nervous system and a lower cardio-toxicity. Aims and Objectives: The aim of our study was to compare and assess the effectiveness and compare the block characteristics of hyperbaric ropivacaine 0.5% (18mg) versus hyperbaric bupivacaine 0.5% (18mg) for elective lower abdominal surgeries under spinal Anaesthesia. Materials & Methods: After approval of Institutional Ethical Committee, this prospective comparative study was conducted on 60 patients aged 18-60 years posted for elective lower abdominal surgeries under spinal anaesthesia after taking informed consent. Patients were randomly divided into two groups; Group B: received 18 mg (3.6 ml) of 0.5% Hyperbaric Bupivacaine intrathecally, while Group R received 18 mg (3.6 ml) of 0.5% Hyperbaric Ropivacaine, prepared aseptically by adding 1.2 ml (300 mg) of autoclaved 25% dextrose from a 10 ml ampoule to 2.4 ml of commercially available sterile preservative-free isobaric 0.75% Ropivacaine solution immediately prior to injection. The onset time for sensory, motor blockade, duration of anaesthesia and duration of analgesia, VAS score were observed in both the groups. The haemodynamic variables and any untoward side effects were noted in both groups. Result: The onset of sensory and motor blockade was similar in both groups. Hemodynamic variables were found to be more stable in the Ropivacaine group. Conclusion: Hyperbaric Ropivacaine demonstrated comparable block quality to commonly used hyperbaric 0.5% bupivacaine when administered intrathecally for elective lower abdominal surgeries under spinal anesthesia.

 

 

 

Abstract (English)

Background: Ropivacaine is a novel long-acting amide local anaesthetic that is comparable to bupivacaine in terms of its structure and pharmacodynamics. ln comparison to bupivacaine, ropivacaine has a reduced propensity to affect the central nervous system and a lower cardio-toxicity. Aims and Objectives: The aim of our study was to compare and assess the effectiveness and compare the block characteristics of hyperbaric ropivacaine 0.5% (18mg) versus hyperbaric bupivacaine 0.5% (18mg) for elective lower abdominal surgeries under spinal Anaesthesia. Materials & Methods: After approval of Institutional Ethical Committee, this prospective comparative study was conducted on 60 patients aged 18-60 years posted for elective lower abdominal surgeries under spinal anaesthesia after taking informed consent. Patients were randomly divided into two groups; Group B: received 18 mg (3.6 ml) of 0.5% Hyperbaric Bupivacaine intrathecally, while Group R received 18 mg (3.6 ml) of 0.5% Hyperbaric Ropivacaine, prepared aseptically by adding 1.2 ml (300 mg) of autoclaved 25% dextrose from a 10 ml ampoule to 2.4 ml of commercially available sterile preservative-free isobaric 0.75% Ropivacaine solution immediately prior to injection. The onset time for sensory, motor blockade, duration of anaesthesia and duration of analgesia, VAS score were observed in both the groups. The haemodynamic variables and any untoward side effects were noted in both groups. Result: The onset of sensory and motor blockade was similar in both groups. Hemodynamic variables were found to be more stable in the Ropivacaine group. Conclusion: Hyperbaric Ropivacaine demonstrated comparable block quality to commonly used hyperbaric 0.5% bupivacaine when administered intrathecally for elective lower abdominal surgeries under spinal anesthesia.

 

 

 

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Dates

Accepted
2024-07-26

References

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