Key result
Intermittent ropivacaine interpleural blockades did not significantly reduce the risk of severe postoperative pain (VAS-A≥70) compared to placebo (RR 1.3; 95% CI 0.4-3.8).
Why the study?
Does intermittent ropivacaine interpleural blockade reduce postoperative pain in patients undergoing posterolateral thoracic surgery receiving morphine epidurals?
RCT (n=90)
triple blind
randomised
Does intermittent ropivacaine interpleural blockade reduce postoperative pain in patients undergoing posterolateral thoracic surgery receiving morphine epidurals?
Relative Risk: 1.3 (95% CI 0.4–3.8)
The addition of interpleural ropivacaine to morphine epidurals is safe but does not improve postoperative pain following major thoracic surgery.
Background: Thoracic surgery is associated with high levels of postoperative pain. Interpleural blockades (IPB) can be effective in reducing this pain, but results after thoracotomy are controversial. The current study investigates the effects of the association of ropivacaine-based IPB and morphine epidurals after posterolateral thoracic surgery. Research Article British Journal of Medicine & Medical Research, 3(4): 841-854., 2013 842 Method: In this prospective, randomised, triple blind, placebo-controlled trial, patients received either intermittent ropivacaine IPB (R-group), (30 mg every 6 hours over 48 hours) or a placebo containing saline serum (P-group). The two groups had a morphine lumbar epidural. Pain was evaluated via patients’ reports and total morphine requirements. Results: 90 patients participated. There were no significant differences between levels of pain reported on mobilisation or morphine consumption between the two groups. For the principal criterion of VAS-A≥70 over the first 48 hours, this corresponds to a RR of 1.3(95%= 0.4-3.8). Patients in the R-group reported higher levels of pain at rest on day 2. The mean peak plasma concentrations of ropivacaine remained inferior to toxic plasma concentration levels. Conclusion: Postoperative interpleural infusions of 30 mg of ropivacaine every 6 hours in association with morphine epidurals are safe and feasible but do not improve postoperative experience of pain.
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Jean-Pierre Gékière (2013) conducted an RCT in postoperative pain following major thoracic surgery (n=90). ropivacaine interpleural blockades vs. placebo (saline serum) was evaluated on VAS-A≥70 over the first 48 hours (RR 1.3, 95% CI 0.4-3.8). Intermittent ropivacaine interpleural blockades did not significantly reduce the risk of severe postoperative pain (VAS-A≥70) compared to placebo (RR 1.3; 95% CI 0.4-3.8).
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