Suppr超能文献

口服 cladribine 片剂治疗复发性多发性硬化症——临床实践问题的专家意见。

Oral pulsed therapy of relapsing multiple sclerosis with cladribine tablets - expert opinion on issues in clinical practice.

机构信息

Klinik für Neurologie, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

Neurologische Praxis Eppendorf, Kümmellstr. 1, D-20249 Hamburg, Germany.

出版信息

Mult Scler Relat Disord. 2021 Sep;54:103075. doi: 10.1016/j.msard.2021.103075. Epub 2021 Jun 7.

Abstract

BACKGROUND

Oral cladribine is the first oral pulsed therapy licensed for relapsing multiple sclerosis (RMS). Three years after the introduction into the European market, we evaluated practical aspects in the use of cladribine tablets, incorporating the experience gained in routine clinical practice and real-world studies.

METHODS

Based on a structured review process, a panel of nine neurologists experienced in MS therapy discussed salient statements regarding the use of cladribine tables. For each statement the level of evidence was determined according to the levels of evidence recommended by the Centre for Evidence-Based Medicine, Oxford. The strength of each expert statement was then evaluated by means of a linear scale from 1 (very strong rejection) to 9 (very strong approval). Votes were collected by a formalized blinded process. Consent was considered to be reached if at least 75% of the experts agreed on a particular statement (i.e. voted for 7-9 points on the linear scale).

RESULTS

. Statements include efficacy in early RMS, risk of side effects and infections, vaccination, pregnancy, and monitoring requirements.

CONCLUSION

The consented recommendations summarize the practical experience inthe use of cladribine tablets in a real-world setting. These may provide guidance for unanswered questions arising with the introduction of new treatments such as cladribine tablets.

摘要

背景

口服克拉屈滨是首个获批用于治疗复发型多发性硬化症(RMS)的口服脉冲疗法。在克拉屈滨进入欧洲市场 3 年后,我们结合常规临床实践和真实世界研究中获得的经验,评估了克拉屈滨片剂的实际应用情况。

方法

根据结构化审查流程,一组 9 名具有 MS 治疗经验的神经病学家讨论了与克拉屈滨片剂使用相关的重要声明。根据牛津循证医学中心推荐的证据级别,对每个声明的证据级别进行了确定。然后,通过线性量表从 1(强烈反对)到 9(强烈赞成)对每个专家声明的强度进行评估。通过正式的盲法过程收集投票。如果至少 75%的专家对某个特定声明达成一致(即在线性量表上投票 7-9 分),则认为达成了共识。

结果

声明包括克拉屈滨在早期 RMS 中的疗效、副作用和感染风险、疫苗接种、妊娠和监测要求。

结论

达成共识的建议总结了在真实环境中使用克拉屈滨片剂的实际经验。这些建议可能为新治疗方法(如克拉屈滨片剂)引入后出现的未解决问题提供指导。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验