Continuous Adductor Canal Blockade In Perioperative Pain Management For Total Knee Replacement
- Authors: Torpudzhiyan M.A.1,2, Negovskiy A.A.1, Borzova N.Y.1, Novikov A.S.1, Gutnikov A.I.1, Sviridov S.V.1,3
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Affiliations:
- National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia
- Russian National Research Medical University named after N.I. Pirogov, Moscow, Russia
- The Russian National Research Medical University named after N.I. Pirogov, Moscow, Russia
- Section: Original study articles
- Submitted: 18.06.2025
- Accepted: 29.09.2025
- Published: 02.10.2025
- URL: https://rjraap.com/1993-6508/article/view/681932
- DOI: https://doi.org/10.17816/RA681932
- ID: 681932
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Abstract
BACKGROUND: Total knee replacement (TKR) is one of the commonly performed orthopedic procedures and remains the only definitive method for relieving pain and improving quality of life in patients with knee osteoarthritis. Despite significant progress in pain management, there is still no consensus on the optimal approach to postoperative analgesia in this patient population.
AIM: To compare the efficacy and safety of three prolonged postoperative analgesia techniques following TKR: continuous epidural analgesia (CEA — control group), continuous adductor canal block (CACB), and a combination of CACB with infiltration between the popliteal artery and the capsule of the knee (IPACK) — CACB+IPACK.
METHODS: Patients were enrolled between December 2023 and June 2024. A total of 184 patients aged 60 years and older were randomized into three groups: CEA (n=62), CACB (n=60), and CACB+IPACK (n=62). The primary endpoint was the proportion of patients achieving effective analgesia at 24 hours postoperatively. Secondary endpoints included muscle strength assessed using the Medical Research Council (MRC) Scale for Muscle Strength, presence of posterior knee pain at 24 hours, length of hospital stay, opioid analgesic requirements, and patient satisfaction with anesthesia measured by the QoR-40 questionnaire.
RESULTS: Effective analgesia was achieved in 70% of patients in the CACB group, compared to 91.9% in the CEA group (OR 0.21; 95% CI 0.07–0.6; p=0.0036). In the CACB+IPACK group, 90.3% of patients achieved effective analgesia, not significantly different from the CEA group (OR 0.81; 95% CI 0.24–2.84; p=0.752). Posterior knee pain was significantly more common in the CACB group (63.3%) compared to the CEA (14.5%) and CACB+IPACK (17.1%) groups (p <0.001). Muscle weakness rated as 4 on the MRC scale persisted at 28 hours in the CEA group. Tramadol use was required in 80% of cases in the CACB group, significantly more often than in the other groups. The duration of hospital stay was significantly longer in the CEA group. According to the QoR-40 questionnaire, patient satisfaction with anesthesia was higher in both peripheral nerve blockade groups.
CONCLUSIONS: CACB alone provided significantly less effective analgesia compared to CEA. However, the combination of CACB with IPACK demonstrated comparable efficacy to CEA.
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About the authors
Margarita A. Torpudzhiyan
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia; Russian National Research Medical University named after N.I. Pirogov, Moscow, Russia
Author for correspondence.
Email: margo-08.01@yandex.ru
ORCID iD: 0000-0002-7642-2918
SPIN-code: 9865-7998
Anesthesiologist-Intensivist of Federal State Autonomous Institution "National Medical Research Center for Rehabilitation Center" of the Ministry of Health of the Russian Federation, PhD Student at the Department of Anesthesiology and ICU, Pirogov RNRMU
Russian Federation, Moscow, Russia; Moscow, RussiaAndrey A. Negovskiy
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia
Email: negovskiy@mail.ru
ORCID iD: 0000-0001-6582-6565
SPIN-code: 4488-5040
Head of the Department of Anesthesiology and Resuscitation No. 1, Federal State Autonomous Institution "National Medical Research Center for Rehabilitation Center" of the Ministry of Health of the Russian Federation
Russian Federation, Moscow, RussiaNatalia Yu. Borzova
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia
Email: borzovan@mail.ru
ORCID iD: 0000-0002-8068-9674
SPIN-code: 3881-3119
Anesthesiologist-Intensivist of Federal State Autonomous Institution "National Medical Research Center for Rehabilitation Center" of the Ministry of Health of the Russian Federation
Russian Federation, Moscow, RussiaArtem S. Novikov
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia
Email: asnovikov82pochta@mail.ru
ORCID iD: 0009-0008-9550-7379
Anesthesiologist-Intensivist of Federal State Autonomous Institution "National Medical Research Center for Rehabilitation Center" of the Ministry of Health of the Russian Federation
Russian Federation, Moscow, RussiaAleksey I. Gutnikov
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia
Email: agutnik@mail.ru
SPIN-code: 7944-1160
Cand. Med. Sc., Anesthesiologist-Intensivist, Head of the Anesthesiology and Intensive Care Unit No. 2, National Medical Research Center for Rehabilitation Center (NMIRC RC), Ministry of Health of Russia
Russian Federation, Moscow, RussiaSergey V. Sviridov
National Medical Research Centre “Treatment and Rehabilitation Centre”, Moscow, Russia; The Russian National Research Medical University named after N.I. Pirogov, Moscow, Russia
Email: sergey.sviridov.59@mail.ru
ORCID iD: 0000-0002-9976-8903
SPIN-code: 4974-9195
MD, Dr. Sci. (Med.), Professor, Head of the department Anesthesiology and Resuscitation Pirogov RNRMU
Russian Federation, Moscow, Russia; Moscow, RussiaReferences
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