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Randomized Controlled Trial
. 2021 Jun 30;11(6):e044168.
doi: 10.1136/bmjopen-2020-044168.

Analgesic effects of intravenous ketamine after spinal anaesthesia for non-elective caesarean delivery: a randomised controlled trial

Affiliations
Randomized Controlled Trial

Analgesic effects of intravenous ketamine after spinal anaesthesia for non-elective caesarean delivery: a randomised controlled trial

Prahlad Adhikari et al. BMJ Open. .

Abstract

Objectives: This study aimed to determine if low dose intravenous ketamine is effective in reducing opioid use and pain after non-elective caesarean delivery.

Design: Prospective, randomised, double-blind.

Setting: Tertiary hospital, Bisheshwar Prasad Koirala Institute of Health Sciences, Dharan, Nepal PARTICIPANTS: 80 patients undergoing non-elective caesarean section with spinal anaesthesia.

Interventions: Patients were allocated in 1:1 ratio to receive either intravenous ketamine 0.25 mg/kg or normal saline before the skin incision.

Primary and secondary outcome measures: The primary outcome was the total amount of morphine equivalents needed up to postoperative 24 hours. Secondary outcome measures were postoperative pain scores, time to the first perception of pain, maternal adverse effects (nausea, vomiting, hypotension, shivering, diplopia, nystagmus, hallucination) and neonatal Apgar score at 1 and 5 min, neonatal respiratory depression and neonatal intensive-care referral.

Results: The median (range) cumulative morphine consumption during the first 24 hours of surgery was 0 (0-4.67) mg in ketamine group and 1 (0-6) mg in saline group (p=0.003). The median (range) time to the first perception of pain was 6 (1-12) hours and 2 (0.5-6) hours in ketamine and saline group, respectively (p<0.001). A significant reduction in postoperative pain scores was observed only at 2 hours and 6 hours in the ketamine group compared with placebo group (p<0.05). Maternal adverse effects and neonatal outcomes were comparable between the two groups.

Conclusions: Intravenous administration of low dose ketamine before surgical incision significantly reduced the opioid requirement in the first 24 hours in patients undergoing non-elective caesarean delivery.

Trial registration number: NCT03450499.

Keywords: anaesthesia in obstetrics; pain management.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Consort flow diagram of the study.
Figure 2
Figure 2
Total morphine equivalent for 24 hours postoperatively in patients receiving ketamine (KET group) and saline (NS group).
Figure 3
Figure 3
Postoperative Numerical Rating Scale (NRS) scores at various time points at rest. After adjustment for multiplicity significant difference between the groups was detected at 2 hours (p<0.05), PACU, postanaesthesia care unit. KET group received ketamine and NS group received normal saline.
Figure 4
Figure 4
Postoperative Numerical Rating Scale (NRS) scores at various time points during movement. After adjustment for multiplicity significant difference between the groups was detected at 2 hours and 6 hours (p<0.05), PACU, postanaesthesia care unit. KET group received ketamine and NS group received normal saline.

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