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重度白塞氏葡萄膜炎的传统免疫抑制治疗:转换为生物制剂的比例

Conventional immunosuppressive therapy in severe Behcet's Uveitis: the switch rate to the biological agents.

作者信息

Celiker Hande, Kazokoglu Haluk, Direskeneli Haner

机构信息

Department of Ophthalmology, Marmara University School of Medicine, Fevzi Çakmak Mah. Muhsin Yazıcıoğlu Cad. No:10 Pendik, Istanbul, Turkey.

Division of Rheumatology, Marmara University School of Medicine Fevzi Çakmak Mah, Muhsin Yazıcıoğlu Cad. No:10 Pendik, Istanbul, Turkey.

出版信息

BMC Ophthalmol. 2018 Oct 5;18(1):261. doi: 10.1186/s12886-018-0929-5.

Abstract

BACKGROUND

To report the switch rate of conventional immunosuppressive (CIS) therapies to the biological agents (BA) in patients with refractory Behcet's uveitis (BU).

METHODS

In this retrospective study, clinical records were reviewed of 76 patients' 116 eyes presenting with BU who had been treated with immunosuppressive drug therapy. Mann Whitney U test was used for the intergroup comparisons of parameters without normal distribution as well as calculation of descriptive statistical methods (mean, standard deviation, median, frequency and rate). Wilcoxon Signed Ranks test was used for the intragroup comparisons of parameters without normal distribution. Pearson's Chi-Square test and Fisher-Freeman-Halton test were used for the comparisons of qualitative data.

RESULTS

Except for one, all patients were first treated with CIS regimens for BU. Thirty-one patients (41.3%) who were unresponsive to CIS regimens were switched to IFNα2a therapy. After that, eight of these cases were switched to the anti-TNF-α treatments. The presence of initial ocular complications were found to be statistically higher in BA treated patients than the CIS treated cases (p < 0.001). Both in CIS treated and in BA treated cases, an increase in visual acuity (VA) was observed during the last examination compared to the initial examination and was significant (p < 0.001 and p = 0.018, respectively).

CONCLUSIONS

CIS treatment was found to be effective and safe, as suggested in the management guidelines for severe BU. Biological therapy was also found effective for the improvement of the VA. We observed that 58.7% of cases could be treated with strong immunosuppressive therapies, however, nearly half of the patients could have lost their VA if BAs were not existent. During the treatment course of severe cases with BU, classical therapy stage must still be protected as the first-line therapy due to the their reasonable activity and safety.

摘要

背景

报告难治性白塞氏葡萄膜炎(BU)患者从传统免疫抑制(CIS)疗法转换为生物制剂(BA)的转换率。

方法

在这项回顾性研究中,对76例116眼接受免疫抑制药物治疗的BU患者的临床记录进行了回顾。Mann Whitney U检验用于非正态分布参数的组间比较以及描述性统计方法(均值、标准差、中位数、频率和率)的计算。Wilcoxon符号秩检验用于非正态分布参数的组内比较。Pearson卡方检验和Fisher-Freeman-Halton检验用于定性数据的比较。

结果

除1例患者外,所有患者均首先接受了用于治疗BU的CIS方案。31例(41.3%)对CIS方案无反应的患者转而接受IFNα2a治疗。此后,其中8例转而接受抗TNF-α治疗。发现接受BA治疗的患者初始眼部并发症的发生率在统计学上高于接受CIS治疗的患者(p < 0.001)。在接受CIS治疗和BA治疗的患者中,与初始检查相比,末次检查时视力(VA)均有提高,且差异有统计学意义(分别为p < 0.001和p = 0.018)。

结论

如重度BU管理指南中所建议的,发现CIS治疗有效且安全。生物治疗也被发现对改善VA有效。我们观察到58.7%的病例可以用强效免疫抑制疗法治疗,然而,如果没有生物制剂,近一半的患者可能已经丧失了视力。在重度BU病例的治疗过程中,由于经典治疗阶段具有合理的有效性和安全性,仍必须将其作为一线治疗加以保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4db/6173844/2670285431b0/12886_2018_929_Fig1_HTML.jpg

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