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早期免疫调节治疗的决策和影响:奥地利临床孤立综合征研究(ACISS)。

Decision-making for and impact of early immunomodulatory treatment: the Austrian Clinically Isolated Syndrome Study (ACISS).

机构信息

Department of Neurology, Medical University of Graz, Graz, Austria.

出版信息

Eur J Neurol. 2010 Jun 1;17(6):852-60. doi: 10.1111/j.1468-1331.2009.02943.x. Epub 2010 Jan 20.

DOI:10.1111/j.1468-1331.2009.02943.x
PMID:20100231
Abstract

BACKGROUND AND PURPOSE

When to start disease-modifying treatment (DMT) in patients with a clinically isolated syndrome (CIS) requires individual weighing of benefits versus possible burden of side effects and costs. How this occurs in a routine setting is barely known. The aim of the study was to investigate the decision-making process regarding immediate or later DMT and the ensuing impact on CIS patients in Austria.

METHODS

Demographic and (para) clinical characteristics of 296 CIS patients were recorded in 29 multiple sclerosis (MS) centres, and the patients' overall condition was rated on a visual analogue scale (VAS). Clinical follow-up and VAS ratings were repeated at 6-month intervals over 2 years. The decision for initiation of DMT was at the physician's and patient's discretion.

RESULTS

In 29% of patients, DMT was started within 3 months and this decision was independently associated with a T2-lesion number >or=9 on MRI and a worse VAS rating by the physician. DMT initiation in the subsequent 6 months was additionally associated with the presence of oligoclonal bands and rarely occurred thereafter. Adapted to the clinical course, later treatment was associated with the highest rate of conversion to clinically definite MS and greatest disability after 2 years whilst never treated patients fared best. Patient VAS ratings significantly improved during follow-up independently of treatment decisions.

CONCLUSION

The management of Austrian CIS patients relies strongly on MRI findings and the physicians' interpretation of the patients' overall situation which, after 2 years, depends primarily on the course of the disease.

摘要

背景与目的

对于临床孤立综合征(CIS)患者,何时开始疾病修正治疗(DMT)需要权衡利弊,既要考虑潜在的治疗效果,又要考虑不良反应和治疗费用等方面的负担。但在实际操作中,我们对这一过程知之甚少。本研究旨在调查奥地利 CIS 患者在决定即刻或延迟 DMT 治疗时的决策过程及其对患者的后续影响。

方法

在 29 家多发性硬化症(MS)中心,记录了 296 名 CIS 患者的人口统计学和(辅助)临床特征,并使用视觉模拟评分(VAS)对患者的整体状况进行评分。在接下来的 2 年内,每隔 6 个月对患者进行临床随访和 VAS 评分。DMT 的启动由医生和患者共同决定。

结果

29%的患者在 3 个月内开始 DMT,这一决策与 MRI 上 T2 病灶数量≥9 和医生评估的 VAS 评分更差独立相关。在接下来的 6 个月内开始 DMT 还与寡克隆带的存在相关,此后很少发生。根据临床病程,后期治疗与向临床确诊 MS 的转化率最高和 2 年后残疾程度最大相关,而从未接受治疗的患者情况最好。在整个随访过程中,患者的 VAS 评分显著改善,与治疗决策无关。

结论

奥地利 CIS 患者的管理主要依赖 MRI 结果和医生对患者整体状况的解读,而在 2 年后,这主要取决于疾病的发展情况。

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Eur J Neurol. 2010 Jun 1;17(6):852-60. doi: 10.1111/j.1468-1331.2009.02943.x. Epub 2010 Jan 20.
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