Primary ArthroplastyA Randomized Non-Inferiority Trial of Adductor Canal Block for Analgesia After Total Knee Arthroplasty: Single Injection Versus Catheter Technique
Section snippets
Materials and Methods
This study is a prospective randomized controlled trial conducted at an University affiliated academic hospital. Study approval was obtained from the University Research Ethics board in June 2016 (H16-01058) and the trial registered at ClinicalTrials.gov (NCT02798835). Adults over 18 years of age and with American Society of Anesthesiologists physical status I to III, scheduled to undergo primary unilateral TKA with spinal anesthesia, were eligible for enrolment. Exclusion criteria were
Results
Over a 5-month period (July-November 2016), 226 patients were approached and 180 were randomized into one of the 3 study groups (Fig. 1). Of the remainder, 6 patients were converted to general anesthesia for unsuccessful spinal, 1 refused participation, and 39 did not otherwise meet inclusion criteria. There was 1 protocol violation where a patient randomized into the catheter group was misidentified and received the single injection block instead. This patient remains in the catheter group per
Discussion
This study represents one of the largest prospective studies of ACB on TKA to date, with 177 patients. In accordance to the original hypothesis, single injection ACB with systemic Dex was shown to be non-inferior to a continuous catheter at 12 and 24 hour. Contrary to the hypothesis, the same was also found true for single injection ACB. Remarkably, the catheter group seemed to be the least beneficial modality of the 3 by having the most opioid consumption across all time points. There is a
Acknowledgments
The study authors thank Rebecca Grey, study coordinator, for patient recruitment; Boris Kuzeljevic, statistician, for statistical analysis and interpretation; Nicola Serreqi, anesthetic assistant, for assisting with blocks; and the study surgeons: Drs Bassam Masri, Donald Garbuz, and Nelson Greidanus from the Department of Orthopedics, University of British Columbia.
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Cited by (48)
Management of perioperative pain after TKA
2023, Orthopaedics and Traumatology: Surgery and ResearchCitation Excerpt :On the other hand, a nosocomial infection risk due to 48 hours’ catheterization has not been demonstrated [15,24,47]. There were no significant differences between the two [48,51–53,62]. According to some reports, postoperative pain is less with continuous blocks, but functional recovery is not better [48,50,52,63].
Continuous vs. single-shot adductor canal block for pain management following primary total knee arthroplasty: A systematic review and meta-analysis of randomized controlled trials
2022, Orthopaedics and Traumatology: Surgery and ResearchCitation Excerpt :For continuous ACB, seven studies [16,18,20–26] used basal rate infusion and four studies [16–18,24–26] used repeated bolus injections. Five studies [16–18,20–26] used intra or periarticular injections as part of their multimodal analgesia regimen for all patients and one study [25] used a block in the interspace between the popliteal artery and the posterior capsule of the knee (IPACK) in addition to single-shot ACB. All studies but one [26] reported opioid consumption.
Continuous vs. single-shot adductor canal block for pain management following primary total knee arthroplasty: A systematic review and meta-analysis of randomized controlled trials
2022, Revue de Chirurgie Orthopedique et Traumatologique
Steven Lee helped in study design, conduct of study, data analysis, manuscript preparation, and final approval; Nirooshan Rooban helped in study design, conduct of study, and manuscript preparation; Himat Vaghadia helped in study design, manuscript preparation, and final approval; Andrew N. Sawka helped in study design, manuscript preparation, and final approval; and Raymond Tang helped in study design, conduct of study, data analysis, manuscript preparation, and final approval.
Funding: Internal departmental funding from the Department of Anesthesia and Perioperative Care, Vancouver General Hospital, Vancouver, BC, Canada.
Institutional Review Board Approval: This study is a prospective randomized controlled trial conducted at the University of British Columbia Hospital. Study approval was obtained from the University of British Columbia Research Ethics Board in June 2016 (H16-01058).
Clinical Trial Number: NCT02798835 (https://clinicaltrials.gov/show/NCT02798835)
One or more of the authors of this paper have disclosed potential or pertinent conflicts of interest, which may include receipt of payment, either direct or indirect, institutional support, or association with an entity in the biomedical field which may be perceived to have potential conflict of interest with this work. For full disclosure statements refer to https://doi.org/10.1016/j.arth.2017.11.018.