Evidence map›Paper›PMID 40917380›Full record

ArticleGhana medical journal2021

Clonidine as an adjuvant to bupivacaine in spinal anaesthesia for infra-umbilical surgeries in children: a prospective randomized, double-blind trial.

Geeta Kamal, Raman Piplani, Anju Gupta, Nidhi Sehgal

Abstract read
In one paragraph

Article in Ghana medical journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Geeta KamalDepartment of Anaesthesia, Chacha Nehru Bal Chikitsalya, Geeta colony, Delhi - 110031, India.
Raman PiplaniDepartment of Anaesthesia, Chacha Nehru Bal Chikitsalya, Geeta colony, Delhi - 110031, India.
Anju GuptaDepartment of Anesthesiology, Pain Medicine and Critical Care, AIIMS, Delhi, India.
Nidhi SehgalDepartment of Anaesthesia, Chacha Nehru Bal Chikitsalya, Geeta colony, Delhi - 110031, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Spinal anaesthesia (SA) is a well-established technique for infra-umbilical surgeries but is underutilized in children. One important reason is the limited duration of action. Clonidine is a useful adjuvant in this regard but has not been studied in a dose of 1.5 µg/kg. Design: a prospective randomized study. Setting: A single centre study conducted at a Super speciality paediatric tertiary care centre. Participants: Sixty children (5-12yrs) scheduled for lower abdominal surgery with duration <90min were included. Interventions: The participants were randomized into two groups to receive 0.4mg/kg of 0.5% hyperbaric bupivacaine with clonidine 1.5µg/kg (Group-I, n=30) or 0.4mg/kg of 0.5% hyperbaric bupivacaine with saline (Group-II, n=30) in the subarachnoid block. Main outcome measures: The sensory and motor block duration, time to two-segment regression, time to first rescue analgesic, and the number of rescue doses required were recorded. Results: Mean duration of sensory blockade (147.5±7.28 vs 310.33±10.17min; P<0.001) and motor blockade (132.5±10.06 vs 283.33±11.77min; P < 0.001) and duration of analgesia (172±9.61 vs 364.50±28.75min; P < 0.001) were significantly prolonged in the clonidine group. In the control group, most patients needed three analgesic doses over 24hr while in the clonidine group, the majority needed two doses. Adverse effects were infrequent in both groups. Conclusions: Clonidine as an adjuvant to 0.5% hyperbaric bupivacaine significantly prolonged the duration of analgesia with improved quality of anaesthesia while maintaining safety. We recommend the routine use of clonidine 1.5 µg/kg dose as an adjuvant to 0.5% bupivacaine in paediatric SA. Funding: None.

Indexed as

adjuvantanaesthesiabupivacainechildclonidinespinal

Identifiers

PMID40917380
PMCPMC12410017

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