Lu Lu, Xie Yu, Gan Ke, Huang Xiao-Wen
Department of Rheumatology, Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Province Hospital of Chinese Medicine), Nanjing 210029, Jiangsu Province, China.
Department of Orthopedics, First Affiliated Hospital of Nanjing Medical University (Jiangsu Province Hospital), Nanjing 210029, Jiangsu Province, China.
World J Clin Cases. 2019 Dec 6;7(23):3971-3979. doi: 10.12998/wjcc.v7.i23.3971.
Non-steroid anti-inflammatory drugs (NSAIDs) have played a crucial role in the treatment of osteoarthritis, especially in the early stages. However, the cardiovascular risk and adverse gastrointestinal reactions of oral NSAIDs in elderly people cannot be underestimated. Intra-articular injection of NSAIDs may be a new attempt for early knee osteoarthritis treatment. Parecoxib may be a suitable drug for intra-articular injection.
To observe the clinical efficacy of the intra-articular injection of parecoxib for early knee osteoarthritis.
Early knee osteoarthritis patients ( = 110) were retrospectively analyzed. These patients were divided into three groups: Basic treatment + oral glucosamine (group A, = 37), oral celecoxib + basic treatment + oral glucosamine (group B, = 37), and intra-articular injection of parecoxib + basic treatment + oral glucosamine (group C, = 36). Intra-articular injection of parecoxib was performed once every 2 wk at a dose of 40 mg each time, for three times total. The three groups were compared in terms of visual analogue scale (VAS) scores, Hospital for Special Surgery (HSS) scores and patient satisfaction before and after treatment. The levels of inflammatory cytokines in the synovial fluid were detected in the three groups before and after treatment.
All patients were followed up for an average of 15.5 ± 2.7 mo. The clinical efficacy was estimated by VAS and HSS scores at 12 mo after treatment. Inflammatory cytokine levels in the synovial fluid were evaluated at 3 mo after treatment. VAS and HSS scores were significantly improved in each group compared with before ( < 0.001). There were significant differences among the three groups in VAS and HSS scores ( < 0.001). The clinical efficacy of group C was superior to that of groups A and B ( < 0.001), while group B outperformed group A in this respect ( < 0.001). The patient satisfaction was the highest in group C ( < 0.001). After treatment, the levels of tumor necrosis factor α (TNF-α) and interleukin (IL)-6 in the synovial fluid decreased in each group compared with before ( < 0.001), while the levels of IL-10 increased ( < 0.001). The three groups differed significantly in the levels of TNF-a, IL-6 and IL-10 in the synovial fluid after treatment ( < 0.001).
For patients with early knee osteoarthritis, intra-articular injection of parecoxib could effectively improve clinical symptoms. This method may be a reliable alternative for early knee osteoarthritis.
非甾体抗炎药(NSAIDs)在骨关节炎治疗中发挥了关键作用,尤其是在早期阶段。然而,老年人口服NSAIDs的心血管风险和胃肠道不良反应不容小觑。关节腔内注射NSAIDs可能是早期膝关节骨关节炎治疗的一种新尝试。帕瑞昔布可能是一种适合关节腔内注射的药物。
观察关节腔内注射帕瑞昔布治疗早期膝关节骨关节炎的临床疗效。
回顾性分析110例早期膝关节骨关节炎患者。这些患者分为三组:基础治疗+口服氨基葡萄糖(A组,n = 37)、口服塞来昔布+基础治疗+口服氨基葡萄糖(B组,n = 37)、关节腔内注射帕瑞昔布+基础治疗+口服氨基葡萄糖(C组,n = 36)。关节腔内注射帕瑞昔布每2周进行1次,每次剂量为40mg,共3次。比较三组治疗前后的视觉模拟评分(VAS)、美国特种外科医院(HSS)评分及患者满意度。检测三组治疗前后滑液中炎症细胞因子水平。
所有患者平均随访15.5±2.7个月。治疗12个月后用VAS和HSS评分评估临床疗效。治疗3个月后评估滑液中炎症细胞因子水平。与治疗前相比,每组VAS和HSS评分均显著改善(P < 0.001)。三组VAS和HSS评分差异有统计学意义(P < 0.001)。C组临床疗效优于A组和B组(P < 0.001),B组在这方面优于A组(P < 0.001)。C组患者满意度最高(P < 0.001)。治疗后,每组滑液中肿瘤坏死因子α(TNF-α)和白细胞介素(IL)-6水平较治疗前降低(P < 0.001),而IL-10水平升高(P < 0.001)。三组治疗后滑液中TNF-α、IL-6和IL-10水平差异有统计学意义(P < 0.001)。
对于早期膝关节骨关节炎患者,关节腔内注射帕瑞昔布可有效改善临床症状。该方法可能是早期膝关节骨关节炎一种可靠的替代治疗方法。