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• W4387392203 abstract "Abstract Background Optimizing pain management following cesarean section is crucial for the well‐being of both mother and infant. Various types of quadratus lumborum blocks have exhibited reduced opioid consumption and pain scores after cesarean section. However, duration of block effect is relatively short. The aim of this study was to investigate the analgesic efficacy of the anterior quadratus lumborum catheters for cesarean section. Methods All 32 enrolled participants were allocated to postoperative bilateral ultrasound‐guided anterior quadratus lumborum catheter placement with injection of 60 mL ropivacaine 0.375% after cesarean section. Randomization at 2 h resulted in either 60 mL ropivacaine 0.2% or 60 mL isotonic saline injected through the catheters, with subsequent 22‐h infusion of either ropivacaine 0.2% or isotonic saline with an infusion rate of 4 mL h −1 per catheter. Participants in the active group received a total of 697 mg ropivacaine during the first 24 h. All participants received the standard postoperative multimodal pain regimen, and a final bilateral injection at 24‐h post‐catheter placement of 60 mL ropivacaine 0.375% in total. The primary outcome was time to first opioid administration. Secondary outcomes were pain scores, time to first ambulation, nausea and vomiting, accumulated opioid consumption, and catheter displacement rates. Results No significant intergroup differences were observed following the randomized intervention. Median time to first opioid (IQR) was (active vs. placebo) 414 (283, 597) vs. 428 (245, 552) minutes, with a median difference (CI) of −14 (−184 to 262) min, p = .32. Conclusion Bilateral anterior quadratus lumborum catheters with continuous infusion did not prolong time to first opioid after elective cesarean section." @default.
• W4387392203 created "2023-10-07" @default.
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• W4387392203 date "2023-10-06" @default.
• W4387392203 modified "2023-10-07" @default.
• W4387392203 title "Anterior quadratus lumborum catheters for elective cesarean section: A double‐blind, randomized, placebo‐controlled trial" @default.
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• W4387392203 doi "https://doi.org/10.1111/aas.14335" @default.
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