Primary Arthroplasty
A Randomized Non-Inferiority Trial of Adductor Canal Block for Analgesia After Total Knee Arthroplasty: Single Injection Versus Catheter Technique

https://doi.org/10.1016/j.arth.2017.11.018Get rights and content

Abstract

Background

Adductor canal blocks (ACBs) provide effective analgesia following total knee arthroplasty. We hypothesized that ACB single injection plus intravenous (IV) dexamethasone (Dex) shows non-inferiority to catheter, while ACB single injection does not.

Methods

One hundred eighty patients were randomized and 177 analyzed from among 1 of 3 ACB interventions: (1) 0.5% ropivacaine 20 mL; (2) 0.5% ropivacaine 20 mL plus IV Dex 8 mg; (3) 0.5% ropivacaine 20 mL followed by continuous infusion of 0.2% ropivacaine at 5 mL/h for 48 hours. The primary endpoint was cumulative opioid consumption at 24 hours in oral morphine equivalents, with a non-inferiority limit of 30 mg. Secondary endpoints included opioid consumption at 12 and 48 hours, rest pain scores, quality of recovery survey, length of stay, and anti-emetic usage.

Results

For 24-hour opioid consumption, single injection ACB with and without IV Dex had a mean difference of −24.2 mg (confidence interval [CI] 0.5 to −48.9, P < .001) and −21 mg (CI 3.2 to −45.1, P < .001) relative to catheter, demonstrating non-inferiority. Non-inferiority was also shown at 12 hours by Dex and single injection over catheter with mean difference of −20.4 mg (CI −6.8 to −33.9, P < .001) and −15.1 mg (CI −2.1 to −28.2, P < .001), respectively. No intergroup difference was found for 48-hour opioid consumption. No differences in other secondary outcomes were observed across the 3 groups.

Conclusion

Single injection ACB, with and without IV Dex, is non-inferior to ACB catheters in 24-hour opioid consumption, and may be attractive options for early-discharge, fast-track total knee arthroplasty.

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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    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.

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