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Intraoperative landmark-based genicular nerve block versus periarticular infiltration for postoperative analgesia in total knee arthroplasty: a randomized non-inferiority trial
  1. Wannida Kertkiatkachorn1,
  2. Srihatach Ngarmukos2,
  3. Aree Tanavalee2,
  4. Chottawan Tanavalee3 and
  5. Wirinaree Kampitak1
  1. 1 Department of Anesthesiology, King Chulalongkorn Memorial Hospital, Bangkok, Thailand
  2. 2 Department of Orthopaedics, Chulalongkorn University, Bangkok, Thailand
  3. 3 Department of Orthopaedics, King Chulalongkorn Memorial Hospital, Bangkok, Thailand
  1. Correspondence to Dr Wirinaree Kampitak, Anesthesiology, King Chulalongkorn Memorial Hospital, Bangkok, Thailand, 10400; nutong127{at}yahoo.com

Abstract

Introduction Genicular nerve blocks (GNBs) are an emerging technique that have been used as a part of multimodal analgesia for total knee arthroplasty. The efficacy of intraoperative landmark-based GNBs, a recently introduced technique, has been established. We hypothesized that it would provide non-inferior postoperative analgesia compared with periarticular infiltration (PAI) when combined with continuous adductor canal block.

Methods This study randomized 140 patients undergoing total knee arthroplasty to receive either intraoperative landmark-based GNB (GNB group) or PAI (PAI group), with 139 completing the study. The primary outcomes were the pain scores at rest and during movement at 12 hours postoperatively on an 11-point Numerical Rating Scale; the non-inferiority margin was 1. Pain scores at additional time points, intravenous morphine consumption, time to first rescue analgesia, functional performance and muscle strength tests, and sleep disturbance were also assessed.

Results At 12 hours postoperatively, the PAI and GNB groups had median resting pain scores of 0 (0–2) and 0 (0–2), respectively. The median difference was 0 (95% CI −0.4 to 0.4, p=1), with the 95% CI upper limit below the prespecified non-inferiority margin. The median pain score during movement was 1.5 (0–2.3) and 2 (1–3.1) in the PAI and GNB groups, respectively. The median difference was 0.9 (95% CI 0.3 to 1.6, p=0.004), failing to demonstrate non-inferiority. The GNB group had higher intravenous morphine consumption at 12 hours postoperatively and a shorter time to first rescue analgesia.

Conclusions GNB compared with PAI provides non-inferior resting pain relief. Non-inferiority was not established for pain during movement.

Trial registration number TCTR20220406001 (www.thaiclinicaltrials.org).

  • analgesia
  • Nerve Block
  • Pain, Postoperative
  • Lower Extremity
  • Ultrasonography

Data availability statement

Data are available on reasonable request.

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Data availability statement

Data are available on reasonable request.

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Footnotes

  • Contributors WIK was involved in the planning, conception and design of study, data acquisition, review of the literature, data analysis, data interpretation, and is the author responsible for the overall content as guarantor. WK was involved in the planning, design of the study, review of the literature, data interpretation, and preparation of the manuscript. SN was involved in reviewing the literature, data acquisition, and editing the manuscript. AT was involved in reviewing the literature, data acquisition, and editing the manuscript. CT was involved in reviewing the literature, reviewing the data, and editing the manuscript.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Supplemental material This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.