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德尔菲法和聚类分析辅助系统性硬化症专家和数据库制定潜在分类标准。

A Delphi exercise and cluster analysis to aid in the development of potential classification criteria for systemic sclerosis using SSc experts and databases.

机构信息

School of Medicine and Dentistry, Western University, London, ON, Canada.

出版信息

Clin Exp Rheumatol. 2013 Mar-Apr;31(2 Suppl 76):24-30. Epub 2013 Apr 2.

Abstract

OBJECTIVES

Since the 1980 ACR classification criteria for systemic sclerosis (SSc) do not identify 20% with SSc, revised criteria are necessary.

METHODS

Suggested new criteria from the literature were sent in random order to 96 SSc experts. A 3-round Delphi Consensus eliminated criteria. Then cluster analysis reduced items. The Canadian Scleroderma Research Group (CSRG) database was used to determine the prevalence of each item.

RESULTS

Seventy-one of 96 (71%) completed all 3 rounds; 47 items were expanded to 76 in round 2. Thirty items had at least 50% consensus and 18 had >75% agreement to include (a priori cut point). Clustering occurred for 4 categories: proximal to MCP skin involvement, vascular abnormalities, autoantibodies and tissue damage. Proximal to MCPs skin involvement identified 80% of patients. Adding one item from each of the other 3 categories or 1 or more items from 2 of 3 remaining categories increased the proportion of patients classified to 94% in CSRG patients. Categories included (1) Vascular (dilated capillaries, telangiectasia, Raynaud's phenomenon [RP]), (2) Autoantibodies (anticentromere [ACA] or antitopoisomeraseI [Topo1]) and (3) Fibrosis/damage (esophogeal dysmotility dysphagia, sclerodactyly, digital ulcers). In the CSRG, 98% were identified if using proximal skin involvement; or sclerodactyly plus one of: RP, ACA or Topo1.

CONCLUSIONS

This is a first step toward developing new SSc classification criteria. A Delphi exercise alone cannot suffice for item reduction. Also, validation prospectively in SSc patients and diseases that mimic SSc is needed in order to calculate sensitivity and specificity of future criteria.

摘要

目的

自 20 世纪 80 年代 ACR 系统性硬化症(SSc)分类标准以来,未能识别出 20%的 SSc 患者,因此需要修订标准。

方法

将文献中的新建议标准随机发送给 96 名 SSc 专家。经过三轮 Delphi 共识,淘汰了部分标准。然后通过聚类分析减少项目。使用加拿大硬皮病研究组(CSRG)数据库确定每个项目的患病率。

结果

96 名专家中有 71 名(71%)完成了全部 3 轮;第二轮将 47 项扩展到 76 项。30 项标准的共识率至少为 50%,18 项标准的同意率>75%(预设切点)。聚类发生在 4 个类别:近端掌指关节皮肤受累、血管异常、自身抗体和组织损伤。近端掌指关节皮肤受累可识别 80%的患者。从其他 3 个类别中的每一个类别中增加一个项目,或从 3 个剩余类别中的 2 个类别中增加 1 个或多个项目,可使 CSRG 患者中分类的患者比例增加到 94%。这些类别包括(1)血管(扩张毛细血管、毛细血管扩张、雷诺现象[RP])、(2)自身抗体(抗着丝点[ACA]或抗拓扑异构酶 I [Topo1])和(3)纤维化/损伤(食管运动障碍、吞咽困难、硬皮病、指溃疡)。在 CSRG 中,如果使用近端皮肤受累;或硬皮病加 RP、ACA 或 Topo1 之一,则可识别出 98%的患者。

结论

这是制定新 SSc 分类标准的第一步。仅进行 Delphi 练习不足以减少项目。还需要前瞻性验证 SSc 患者和模仿 SSc 的疾病,以计算未来标准的敏感性和特异性。

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