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根据专家的建议治疗系统性硬化症的方法。

Treatment Algorithms for Systemic Sclerosis According to Experts.

机构信息

University of Western Ontario, London, Ontario, Canada, and Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.

The Ottawa Hospital, University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Arthritis Rheumatol. 2018 Nov;70(11):1820-1828. doi: 10.1002/art.40560. Epub 2018 Sep 17.

Abstract

OBJECTIVE

There is a lack of agreement regarding treatment for many aspects of systemic sclerosis (SSc). We undertook this study to generate SSc treatment algorithms endorsed by a high percentage of SSc experts.

METHODS

Experts from the Scleroderma Clinical Trials Consortium and the Canadian Scleroderma Research group (n = 170) were asked whether they agreed with SSc algorithms from 2012. Two consensus rounds refined agreement; 62, 54, and 48 experts (36%, 32%, and 28%, respectively) completed the first, second, and third surveys, respectively.

RESULTS

For treatment of scleroderma renal crisis, 81% of experts agreed (first-, second-, and third-line treatments were angiotensin-converting enzyme inhibitors, then adding calcium-channel blockers [CCBs], then adding angiotensin receptor blockers [ARBs], respectively). For pulmonary arterial hypertension (PAH), 81% of experts agreed (for mild PAH, treatments were phosphodiesterase 5 [PDE5] inhibitors, then endothelin receptor antagonists plus PDE5 inhibitors, then prostanoids, respectively; for severe PAH, prostanoids were first-line treatment). For mild Raynaud's phenomenon (RP), 79% of experts agreed (treatments were CCBs, then adding PDE5 inhibitors, then ARBs or switching to another CCB, respectively; after the third line of treatment, mild RP was deemed severe). For severe RP, the first- through fourth-line treatments were CCBs, then adding PDE5 inhibitors or prostanoids, then adding PDE5 inhibitors (if not added as second-line treatment) or prostanoids (if not added as second-line treatment), then switching to another CCB, respectively. For active treatment of digital ulcers, 66% of experts agreed (first- and second-line treatments were CCBs and PDE5 inhibitors, respectively). For interstitial lung disease, 69% of experts agreed (for induction therapy, treatments were mycophenolate mofetil [MMF], intravenous cyclophosphamide [IV CYC], and rituximab, respectively; for maintenance, first-line treatment was MMF). For skin involvement, 71% of experts agreed (for a modified Rodnan skin thickness score [MRSS] of 24, first- and second-line treatments were methotrexate [MTX] and MMF, respectively; for an MRSS of 32, first- through fourth-line treatments were MMF, MTX, IV CYC, and hematopoietic stem cell transplantation, respectively). For inflammatory arthritis, 79% of experts agreed (first- through fourth-line treatments were MTX, low-dose glucocorticoids, hydroxychloroquine, and rituximab or tocilizumab, respectively). Algorithms for cardiac and gastrointestinal involvement had ≥75% agreement.

CONCLUSION

Total agreement for SSc algorithms was considerable. These algorithms may guide treatment.

摘要

目的

对于硬皮病(SSc)的许多方面的治疗,目前仍缺乏共识。我们开展了这项研究,旨在制定出能得到大量 SSc 专家认可的 SSc 治疗算法。

方法

来自硬皮病临床试验联盟和加拿大硬皮病研究组的 170 名专家被要求对 2012 年的 SSc 算法是否表示认可。两轮共识会议对意见进行了细化;分别有 62、54 和 48 名专家(分别占 36%、32%和 28%)完成了首轮、次轮和第三轮调查。

结果

对于硬皮病肾危象的治疗,81%的专家表示认可(一线、二线和三线治疗分别为血管紧张素转换酶抑制剂,然后加用钙通道阻滞剂[CCB],再添加血管紧张素受体阻滞剂[ARB])。对于肺动脉高压(PAH),81%的专家表示认可(对于轻度 PAH,治疗药物为磷酸二酯酶 5[PDE5]抑制剂,然后加用内皮素受体拮抗剂和 PDE5 抑制剂,再添加前列环素;对于重度 PAH,前列环素是一线治疗药物)。对于轻度雷诺现象(RP),79%的专家表示认可(治疗药物为 CCB,然后加用 PDE5 抑制剂,再添加 ARB 或换用另一种 CCB;三线治疗后,轻度 RP 被视为重度)。对于重度 RP,一线至四线治疗药物均为 CCB,然后加用 PDE5 抑制剂或前列环素,然后加用 PDE5 抑制剂(如果未作为二线治疗药物添加)或前列环素(如果未作为二线治疗药物添加),然后换用另一种 CCB。对于活动性指溃疡的治疗,66%的专家表示认可(一线和二线治疗药物分别为 CCB 和 PDE5 抑制剂)。对于间质性肺病,69%的专家表示认可(诱导治疗的药物分别为霉酚酸酯[MMF]、静脉环磷酰胺[IV CYC]和利妥昔单抗);对于维持治疗,一线治疗药物为 MMF。对于皮肤受累,71%的专家表示认可(对于改良 Rodnan 皮肤厚度评分[MRSS]为 24 的患者,一线和二线治疗药物分别为甲氨蝶呤[MTX]和 MMF;对于 MRSS 为 32 的患者,一线至四线治疗药物分别为 MMF、MTX、IV CYC 和造血干细胞移植)。对于炎症性关节炎,79%的专家表示认可(一线至四线治疗药物分别为 MTX、低剂量糖皮质激素、羟氯喹和利妥昔单抗或托珠单抗)。对于心脏和胃肠道受累的治疗算法,专家的认可比例均≥75%。

结论

SSc 治疗算法的总体一致程度较高。这些算法可以为治疗提供指导。

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