中国临床解剖学杂志 ›› 2023, Vol. 41 ›› Issue (1): 97-104.doi: 10.13418/j.issn.1001-165x.2023.1.18

• 临床研究 • 上一篇    下一篇

依那西普和传统合成改变病情抗风湿药序贯治疗轻中度强直性脊柱炎的中期疗效随访研究

江伟州1,    胡勇2,    宋旻恺1,    刘欢3,    黄文华4,    肖军1*   

  1. 1.南方医科大学附属南方医院关节与骨病外科,  广州   510515;    2.南方医科大学第五附属医院关节外科,  广州   510999;    3.西南医科大学附属中医医院骨伤科,  四川   泸州    646000;    4.南方医科大学基础医学院人体解剖学教研室,  广州   510515
  • 收稿日期:2021-07-19 出版日期:2023-01-25 发布日期:2023-02-08
  • 通讯作者: 肖军,副主任医师,副教授,硕士研究生导师,E-mail:orthopaedxj@163.com
  • 作者简介:江伟州(1993-),男,广东普宁人,住院医师,博士研究生,E-mail:orthopaedjoe@163.com
  • 基金资助:
    广东省教育厅高水平大学建设经费南方医科大学临床研究启动项目(LC2019ZD022);南方医科大学南方医院临床研究专项(2018CR001,2020CR028)

Sequential application of etanercept and csDMARDs in treating ankylosing spondylitis: A prospectively mid-term follow-up study

Jiang Weizhou1, Hu Yong2, Song Minkai1, Liu Huan3, Huang Wenhua4, Xiao Jun1*   

  1. 1. Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; 2.Department of Joint Surgery, The Fifth Affiliated Hospital of Southern Medical University, Guangzhou 510999, China; 3.Department of Orthopaedics, Affiliated Traditional Chinese Medicine Hospital, Southwest Medical University, Luzhou 646000, China; 4. Department of Human Anatomy, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China
  • Received:2021-07-19 Online:2023-01-25 Published:2023-02-08

摘要: 目的   随访评估依那西普和传统合成改变病情抗风湿药(conventional synthetic disease modifying anti-rheumatic drugs,csDMARDs)序贯治疗强直性脊柱炎(ankylosing spondylitis,AS)的药物组合方案治疗轻中度AS的中期疗效。  方法     纳入南方医院2017~2018年确诊的轻中度AS患者64例,疾病活动期短期选用依那西普,疾病缓解期改用csDMARDs药物组合口服维持。分别于治疗前,治疗后3、6、12个月评估临床缓解率,并应用BASFI、BASDAI、SQOL-AS量表评价治疗效果。  结果    随访3、6、12个月,Patient Global、BASFI、BASDAI及ASDAS-CRP评分,CRP及ESR值均下降(P<0.05),SQOL-AS评分提高(P<0.05)。随访终点分别有85.9%、79.7%的患者达到ASAS 20、ASAS 40缓解标准。随访期间无结核、机会感染、肿瘤发生。  结论    对于轻中度AS,依那西普和csDMARDs序贯组合方案展示了良好的中期疗效,有望成为低收入AS患者的替代治疗方案。

关键词:  强直性脊柱炎; ,  , 传统合成改变病情抗风湿药; ,  , 临床方案

Abstract: Objective    To evaluate etanercept and conventional synthetic disease modifying anti-rheumatic drugs (csDMARDs) in treating ankylosing spondylitis (AS) and its mid-term therapeutic effect among mild-to-moderate AS patients.   Methods   Sixty-four patients diagnosed with mild-to-moderate AS treating in our department from 2017 to 2018 were enrolled. Etanercept was used in the short term during the active stage of the disease, and csDMARDs combination was used for oral administration during the remission stage. Clinical remission rate was assessed before treatment, 3, 6 and 12 months after treatment. Tthe therapeutic effect was evaluated by BASFI, BASDAI and SQOL-AS scales.    Results   Patients Global, BASFI, BASDAI and ASDAS-CRP scores, CRP and ESR values decreased (P<0.05), while SQOL-AS scores increased (P<0.05) at 3, 6 and 12 months of follow-up. At the end of the follow-up, 85.9% and 79.7% of all enrolled patients achieved ASAS 20, ASAS 40 remission criteria, respectively. No tuberculosis, opportunistic infection or tumor occurred during the treatment.   Conclusions   For mild to moderate AS, the sequential combination of etanercept and csDMARDs shows satisfied mid-term therapeutic efficacy and expects to  be an alternative treatment for those low-income AS patients.

Key words:  Ankylosing spondylitis (AS); ,  Conventional synthetic disease modifying anti-rheumatic drugs (csDMARDs); ,  , Therapy

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