Miral G. Joshi 3rd Year Resident, Department of Anesthesia, M K Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India
Bipin M Patel HOD, Department of Anesthesia, MK Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India
Parth M. Shah Associate Professor, Department of Anesthesia, MK Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India
Dipal Kharsadiya Assistant Professor, Department of Anesthesia, MK Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India
Brijesh Bhayani 3rd Year Resident, Department of Anesthesia, M K Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India
Address for correspondence: Miral G. Joshi, 3rd Year Resident, Department of Anesthesia, M K Shah Medical College and Research Centre and S.M.S. Hospital, Ahmedabad, Ahmedabad 382424, Gujarat, India E-mail: parthshah1291@gmail.com
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Joshi MG, Shah PM, Patel BM, et al. Clinical utility of epidural volume extension following reduced intrathecal doses: a randomized controlled trial. Ind J Anesth Analg. 2024;11(4):198-203.
Timeline
Received : March 29, 2024
Accepted : May 31, 2024
Published : December 20, 2024
Abstract
Overview The study aimed to investigate the impact of Epidural Volume Extension (EVE) on sensory block height following intrathecal injections with reduced doses of bupivacaine. It was designed as a randomized, controlled, double-blind trial involving 80 adult male patients with ASA status I or II scheduled for orthopedic lower limb surgery under combined spinal epidural anaesthesia. Patients were randomly assigned to receive either a reduced intrathecal dose of bupivacaine (5 or 8 mg) with or without EVE, based on group allocation. The study aimed to compare the maximum sensory level (Smax) achieved with and without EVE application across the two different intrathecal doses. Further research is warranted to better understand the relationship between intrathecal dose and EVE efficacy, considering various factors such as instillation technique, timing, and patient characteristics.
Results: The study revealed that applying Epidural Volume Extension (EVE) alongside a 5 mg intrathecal bupivacaine dose significantly decreased the maximum sensory block height (Smax) compared to not using EVE However, there was no significant difference in Smax when EVE was applied alongside an 8 mg intrathecal bupivacaine dose compared to without it.
Conclusion: Avoiding the application of Epidural Volume Extension (EVE) to 5 mg plain bupivacaine during a combined spinal epidural block in patients undergoing lower limb orthopedic surgery is advisable. This caution stems from the observation that implementing EVE alongside this particular dosage of bupivacaine could lead to a reduction in the maximum sensory level.
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Author Contributions
All authors contributed significantly to the work and approve its publication.
Ethics Declaration
This article does not involve any human or animal subjects, and therefore does not require ethics approval.
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Conflicts of Interest
The authors report no conflicts of interest in this work.
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Joshi MG, Shah PM, Patel BM, et al. Clinical utility of epidural volume extension following reduced intrathecal doses: a randomized controlled trial. Ind J Anesth Analg. 2024;11(4):198-203.
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
This license enables reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.