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Reg Anesth Pain Med · Oct 2019
Anterior quadratus lumborum block analgesia for total hip arthroplasty: a randomized, controlled study.
- Promil Kukreja, Lisa MacBeth, Adam Sturdivant, Charity J Morgan, Elie Ghanem, Hari Kalagara, and ChanVincent W SVWSDepartment of Anesthesia, University of Toronto, Toronto, Ontario, Canada..
- Department of Anesthesiology and Perioperative Medicine, UAB, Birmingham, Alabama, USA pkukreja@uabmc.edu.
- Reg Anesth Pain Med. 2019 Oct 25.
Background And ObjectivesQuadratus lumborum (QL) block is a new regional analgesic technique for upper and lower abdominal surgeries as part of a multimodal analgesic regime. It has also been reported to relieve pain after total hip arthroplasty (THA). In this prospective, randomized, double-blind study, we compared QL block with control (no block) in patients undergoing primary THA.MethodsEighty patients undergoing primary THA surgery under spinal anesthesia were randomized into two groups, one with and one without QL block. The patients in both groups were randomized after sedation, positioning and ultrasound scanning. Both the patient and the researcher collecting data were blinded to the patient's group assignment. Opioid consumption and visual analog scores (VAS) pain scores were measured at 12, 24, and 48 hours after surgery. Also, the ambulation distance, patient satisfaction, and length of stay were recorded.ResultsThe study analysis included 36 patients in the QL group and 35 patients in the control group. Both VAS pain score at 24 hours (difference -1.76, 95% CI -2.87 to -0.64) and cumulative opioid consumption were significantly lower in the QL group at 12, 12-24, 24, 24-48, and 48 hours after surgery as compared with the control group (difference at 48 hours -36.13, 95% CI -62.89 to -9.37) (p<0.05). However, there was no difference in pain score at 12 and 48 hours, nor in the ambulation distance and duration of hospital stay between the two groups. The patient satisfaction score was significantly higher in the QL group.ConclusionsOur preliminary data show that the QL block provided effective analgesia and decreased opioid requirements up to 48 hours after primary THA.Trial Registration NumberNCT03408483.© American Society of Regional Anesthesia & Pain Medicine 2019. No commercial re-use. See rights and permissions. Published by BMJ.
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