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Developing an international consensus guidance for myasthenia gravis using RAND/UCLA appropriateness method
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作者 Wei-Bin Liu Hao Ran +7 位作者 Chuang-Yi Ou Li Qiu Zhi-Dong Huang Zhong-Qiang Lin Yin-Kai Li Xiao-Xi Liu Hao Huang Wei Fang 《Neuroimmunology and Neuroinflammation》 2017年第3期54-60,共7页
Aim: Myasthenia gravis (MG) is a rare and heterogeneous disease for which there is no generally accepted standard of care. Thus, it is critical that MG experts develop consensus guidelines based on their practice and ... Aim: Myasthenia gravis (MG) is a rare and heterogeneous disease for which there is no generally accepted standard of care. Thus, it is critical that MG experts develop consensus guidelines based on their practice and disease management to assist clinicians and provide advice for insurance companies, health organizations and institutional review boards. Methods: An international treatment guidance was developed based on national guidelines established in the US, Denmark, Norway, Germany, Japan, Netherlands, United Kingdom and Europe. The RAND/UCLA appropriateness method (RAM) was applied to reach consensus among 15 worldly renowned experts and experienced clinicians. Results: This paper introduced the RAM procedure with its principles and applications and conducted a brief review of the resulting 2016 international consensus guidance for MG in comparison to clinical experience and management of Chinese MG patients. Conclusion: The 2016 international consensus guidance is a major contribution to the treatment and management of MG, providing an up-to-date expert consensus to assist clinicians around the world, especially those with limited experience and/or practice in countries/regions that have limited resources to develop local treatment guidelines. It is also an important contribution showing how RAM can help to develop consensus guidance for treatment of rare diseases based on scientific findings and expert experience. 展开更多
关键词 INTERNATIONAL treatment GUIDANCE myasthenia gravis rand/ucla APPROPRIATENESS method DEVELOPING CONSENSUS
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基于药典算法的无公害中药材农残限量通用标准的RAM研究 被引量:8
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作者 骆璐 董林林 +5 位作者 李孟芝 梁乙川 尉广飞 张蕴仪 钱忠直 陈士林 《中国中药杂志》 CAS CSCD 北大核心 2019年第11期2197-2207,共11页
中药材农残及重金属超标严重危害人类健康及中医药产业的可持续发展,为提升中药材质量,建立无公害中药材及饮片农药最大残留限量(MRL)通用标准,从根源上保障临床用药安全。采用《中国药典》的农药最大残留计算公式(MRL=A×W/100M)... 中药材农残及重金属超标严重危害人类健康及中医药产业的可持续发展,为提升中药材质量,建立无公害中药材及饮片农药最大残留限量(MRL)通用标准,从根源上保障临床用药安全。采用《中国药典》的农药最大残留计算公式(MRL=A×W/100M)计算出本标准MRL,与国内外现行标准及文献比较,通过RAND/UCLA合适度检测法(RAND/UCLA appropriateness method,RAM)形成专家咨询问卷并采用9分制的李克特量表(Likert scale)进行合适度分析,确定无公害中药材及饮片农药最大残留限量通用标准。结果表明:共计9位来自不同领域的专家分别就标准制定的必要性及206种农残限量进行了评分。206种农药进行RAND/UCLA合适度评分后分值均大于7,合适度为100%,专家意见达成了一致。采用RAND/UCLA(RAM)合适度检测法建立的无公害中药材质量标准达成了专家共识,形成的206种农药最大残留限量标准与CAC、欧盟、美国、韩国、日本、澳大利亚、新西兰及加拿大颁布相关标准进行了对比分析,结果表明,88.8%农药类型的MRL与国际标准规定的MRL范围一致,4.4%农药类型的MRL高于国际标准范围,6.8%农药类型的MRL低于国际标准范围。该标准的制定为规范无公害中药材的农药使用提供了依据。 展开更多
关键词 rand/ucla合适度检测法 农药最大残留限量 无公害 质量标准
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