本文旨在介紹如何進行知證衛生決策的組織方法。促進研究與實踐結合的一系列活動包括：與決策者高度相關的研究證據的生產和恰當的合成，促進研究與實踐結合的諸多努力，以及對其的評估。幾乎沒人知道如何更好地開展此類系列活動，直到最近才有很少幾個機構專門負責研究利用證據制定衛生政策。為此本文通過提出5 個問題來指導開展機構措施以支持研究證據在知證衛生決策中的使用：① 您所在機構進行知證決策的能力是什么? ② 應采用什么策略確保決策者、研究者和利益相關者之間的合作? ③ 應采用什么策略確保研究的獨立性和有效管理利益沖突? ④ 應采用什么策略確保使用系統和透明的方法獲取、評價和利用研究證據？⑤ 應采用什么策略以確保有足夠能力運用這些方法？
The development of evidence-based clinical practice guidelines is a sophisticated and systematic process, often requiring multidisciplinary efforts. The traditional approach to developing and updating clinical practice guidelines is usually time-consuming. These limitations obstacle the effective use of guideline recommendations and efficient transformation of most recent research evidence into practice. The MAGIC system is a novel method system for rapid creation and dissemination of high-quality clinical recommendations, including rapid creation of trustworthy recommendations, thus ensuring the scientific and efficient production of clinical practice guidelines; facilitating rapid dissemination and dynamic updating of clinical practice guidelines through recommendation release system (i.e., MAGICapp); and helping promote the production of relevant high-quality original research evidence by identifying the insufficiency of evidence in the process of creation of guideline recommendations. Ultimately, a complete closed-loop digital and trustworthy evidence ecosystem is developed. In order to further promote the effective transformation of research evidence into guideline recommendations, MAGIC China Center was established. We anticipate that the Center will assist the further development and effective use of clinical practice guideline in China.