Dexiang Zhang, Yang Shen, Shaobing Zhang, Xiaolong Xiong
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引用次数: 0
Abstract
Objective: We aim to clarify the inhibitory effect of antibiotic-loaded bone cement (ALBC) on inflammatory factors, and its preventive effect on postoperative infections in unicompartmental knee arthroplasty (UKA).
Methods: This prospective randomized controlled trial enrolled 104 osteoarthritis patients undergoing UKA, randomly assigned to the non-ALBC group (n = 52, bone cement without antibiotics) and ALBC group (ALBC with 1.0 g vancomycin hydrochloride, n = 52). Primary outcomes were postoperative inflammatory markers (CRP, ESR, TNF-α, IL-6); secondary outcomes included infection rate and HSS score. Independent-samples t-tests were used for continuous variables, χ2 test for categorical variables (infection rate, efficacy), and repeated measures analysis of variance for intra-group longitudinal comparisons.
Results: The ALBC group demonstrated lower inflammatory markers at postoperative day 7 and at 3 months [CRP (3.52 ± 0.81 vs 6.92 ± 1.17, Cohen's d = 3.379), ESR (16.29 ± 2.31 vs 20.19 ± 4.05, Cohen's d = 1.183), TNF-α (29.71 ± 4.03 vs 36.25 ± 5.17, Cohen's d = 1.411), and IL-6 (17.05 ± 3.72 vs 22.05 ± 4.38, Cohen's d = 1.230)] (all p < 0.001), and also showed superior clinical outcomes, with lower postoperative infection rate (p = 0.016), higher HSS score (p < 0.001), and better overall clinical efficacy (p = 0.010) than the non-ALBC group.
Conclusion: The application of ALBC in UKA was associated with reduced postoperative inflammatory markers such as IL-6 and a lower incidence of postoperative infection. These findings suggest that ALBC may play a beneficial role in postoperative recovery and joint function rehabilitation.
期刊介绍:
The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal.
The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome.
With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more.
Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).