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Efficacy of adding ketamine to levobupivacaine in paravertebral block on acute and chronic pain in thoracotomy: a randomized controlled double-blinded trial.

Saad Ahmed Moharam, Amgad Elshikh, Mohamed Abdelbadie, Ahmed Mohamed Ibrahim, Mostafa Mohamed Khedr Shaheen, Mohammed Said Elsharkawy

Pain reports December 1, 2024 DOI: 10.1097/PR9.0000000000001206 via PubMed

Summary

AI-generated from the abstract

Adding ketamine to a thoracic paravertebral block (TPVB) improves immediate pain control after thoracotomy. In a randomized controlled trial of 60 patients, those receiving ketamine plus levobupivacaine requested pain relief significantly later, required less morphine in the first 24 and 48 hours, and reported lower pain scores at rest and during deep breathing compared to those receiving levobupivacaine alone. However, the addition of ketamine did not reduce the incidence of chronic post-thoracotomy pain syndrome or complications at 2 and 3 months.

Study at a glance

Characteristics Randomized controlled trial Double-blind Peer reviewed
Sample size 60
Population Patients scheduled for open thoracotomy
Interventions Ketamine Levobupivacaine
Dose 50 mg
Duration 48 hours for acute outcomes, with follow-up at 2 and 3 months for chronic pain
Topics Ketamine
Keywords Levobupivacaine Paravertebral block Pain management pain Pain control Acute pain
Citations 3
Key finding Adding ketamine to TPVB improved acute analgesia (delayed time to first rescue analgesia, lower opioid consumption, and lower pain scores) but did not affect chronic pain or complication rates at 2 and 3 months.

Abstract

The inappropriate management of pain after thoracotomy results in serious complications. Several adjuvants have been added to the thoracic paravertebral block (TPVB) to enhance its effects. This work aimed to evaluate the effect of adding ketamine to TPVB on thoracotomy-related acute and chronic pain. This randomized controlled double-blinded trial included 60 patients scheduled for open thoracotomy. Patients were equally randomized into 2 groups: group K: received TPVB + 1 mL ketamine (50 mg). Group C (n = 30): received TPVB (19 mL of 0.5% levobupivacaine + 1 mL normal saline) as a control arm. Group K exhibited a significant delay in requesting analgesia, required less morphine in the first 24 and 48 hours, and reported lower numerical rating scale at rest and at deep breathing at various time points compared with the control group. However, both groups were comparable in post-thoracotomy pain syndrome and the incidence of complications at 2 months and 3 months. Adding ketamine to TPVB resulted in better analgesia as demonstrated by significantly delayed time to first rescue analgesia, lower total amount of consumed opioid, and pain score without considerable effect on chronic pain and complications in patients undergoing thoracotomy.

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