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根据当前建议,非甾体抗炎药治疗影像学和非影像学轴向脊柱关节炎患者的疗效

Efficiency of treatment with non-steroidal anti-inflammatory drugs according to current recommendations in patients with radiographic and non-radiographic axial spondyloarthritis.

作者信息

Baraliakos Xenofon, Kiltz Uta, Peters Soeren, Appel Heiner, Dybowski Friedrich, Igelmann Manfred, Kalthoff Ludwig, Krause Dietmar, Menne Hans-Juergen, Saracbasi-Zender Ertan, Schmitz-Bortz Elmar, Vigneswaran Mathura, Braun Juergen

机构信息

Rheumazentrum Ruhrgebiet Herne.

Department of Radiology, Bergmannsheil University Hospital, Ruhr-University Bochum.

出版信息

Rheumatology (Oxford). 2017 Jan;56(1):95-102. doi: 10.1093/rheumatology/kew367. Epub 2016 Oct 25.

Abstract

OBJECTIVE

NSAIDs are first-line therapy in axial SpA (axSpA). The proportion of patients responding to NSAIDs and differences between AS and non-radiographic axSpA (nr-axSpA) in this regard have not been studied in detail to date. The aim of this study was to examine the proportion of patients with AS and nr-axSpA responding to NSAIDs according to current treatment recommendations.

METHODS

Consecutive anti-TNF-naïve patients with nr-axSpA and AS (n = 50 each) were included if their BASDAI score was ⩾4 without having received maximal NSAID doses. In case of a BASDAI score ⩾4 1 week later, another NSAID was prescribed. For the next 3 weeks, continuous intake of maximal doses was recommended but patients could reduce doses in case of intolerance or improvement. MRI of the SI joints was performed at baseline and week 4.

RESULTS

All outcomes except for CRP and MRI scores improved significantly after 4 weeks of NSAIDs, with no difference between axSpA subgroups. An Assessment of SpondyloArthritis international Society 40% (ASAS40) response and partial remission rates were 35 and 16% at week 4, respectively. At the same time point, a BASDAI score ⩾4 was still present in 44% of patients, 30% of which had reduced NSAID doses, partly due to intolerance (38%). Only 13% of all patients had continuously taken NSAIDs at the maximal dosage, but there was no difference in the efficacy outcome compared with those who had taken reduced doses.

CONCLUSION

AS and nr-axSpA patients had similar response rates to NSAIDs while objective signs of inflammation did not change over 4 weeks. Only a minority of patients was willing to take maximal doses of NSAIDs, and ⩾40% patients remained candidates for TNF blockers. These results may influence future trial designs.

摘要

目的

非甾体抗炎药(NSAIDs)是中轴型脊柱关节炎(axSpA)的一线治疗药物。迄今为止,尚未对NSAIDs治疗有反应的患者比例以及强直性脊柱炎(AS)和非放射学中轴型脊柱关节炎(nr-axSpA)在这方面的差异进行详细研究。本研究的目的是根据当前治疗建议,检查AS和nr-axSpA患者对NSAIDs有反应的比例。

方法

纳入连续的未使用过肿瘤坏死因子(TNF)抑制剂、BASDAI评分≥4且未接受过最大剂量NSAIDs治疗的nr-axSpA和AS患者(各50例)。如果1周后BASDAI评分≥4,则换用另一种NSAIDs。在接下来的3周内,建议持续服用最大剂量,但患者如出现不耐受或病情改善可减少剂量。在基线和第4周时对骶髂关节进行磁共振成像(MRI)检查。

结果

使用NSAIDs 4周后,除CRP和MRI评分外,所有结局均有显著改善,axSpA各亚组之间无差异。第4周时,国际脊柱关节炎评估协会40%反应率(ASAS40)和部分缓解率分别为35%和16%。在同一时间点,44%的患者BASDAI评分仍≥4,其中30%的患者减少了NSAIDs剂量,部分原因是不耐受(38%)。所有患者中只有13%持续服用最大剂量的NSAIDs,但与服用减少剂量的患者相比,疗效结局无差异。

结论

AS和nr-axSpA患者对NSAIDs的反应率相似,而炎症的客观体征在4周内未发生变化。只有少数患者愿意服用最大剂量的NSAIDs,≥40%的患者仍是TNF阻滞剂的适用对象。这些结果可能会影响未来的试验设计。

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