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The impact of central sensitization on perioperative pain in TKA: a retrospective cohort study

T. Sonobe, Takuya Nikaido, M. Sekiguchi, Yoichi Kaneuchi, Tadashi Kikuchi, Y. Matsumoto

Knee Surgery and Related Research, 2025

66 participants · 11 citations

Abstract

Total knee arthroplasty (TKA) is an established surgical procedure for severe knee osteoarthritis (KOA) that has provided excellent outcomes. While several studies have reported that patients with preoperative central sensitization (CS) experienced worse pre- and post-operative pain and outcomes, the evidence is limited. We conducted this study to determine the impact of CS on perioperative knee pain in TKA for severe KOA. A retrospective cohort study of 66 patients who underwent bilateral TKA for bilateral severe KOA was conducted. Multiple linear regression models that included covariates and scaled estimated regression coefficients were used to examine the impact of CS on the patients’ pre- and post-operative pain subscale values on the Knee Injury and Osteoarthritis Outcome Score (KOOS) and the improvement of KOOS pain. Postoperative KOOS pain was assessed at 3 months postoperatively, while other evaluation items including preoperative KOOS pain, CS, and pain self-efficacy were assessed on admission. CS had a negative impact on pre- and post-operative KOOS pain (preoperative, β: −0.28, 95% confidence interval [CI] −18.53, −0.92; postoperative, β: −0.26, 95%CI −14.09, −0.44; p < 0.05). High pain self-efficacy had a positive impact on preoperative KOOS pain (β: 0.25, 95%CI 0.32, 18.08; p < 0.05). However, CS did not influence the improvement of KOOS pain. These results demonstrate that CS had a negative impact on pre- and post-TKA knee pain in patients but did not affect…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 66 participants or records.

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