tailieunhanh - Báo cáo y học: "The 32nd Annual Congress of the Society of Critical Care Medicine, 28 January – 2 February 2003, San Antonio, USA"

Tuyển tập các báo cáo nghiên cứu về y học được đăng trên tạp chí y học Critical Care giúp cho các bạn có thêm kiến thức về y học đề tài: The 32nd Annual Congress of the Society of Critical Care Medicine, 28 January – 2 February 2003, San Antonio, USA. | Available online http content 7 2 193 Meeting report The 32nd Annual Congress of the Society of Critical Care Medicine 28 January - 2 February 2003 San Antonio USA Daniel De Backer and Jacques Creteur Assistant Professor Department of Intensive Care Erasme University Hospital Free University of Brussels Brussels Belgium Correspondence Daniel De Backer ddebacker@ Published online 6 March 2003 Critical Care 2003 7 193-195 DOI cc2173 This article is online at http content 7 2 193 2003 BioMed Central Ltd Print ISSN 1364-8535 Online ISSN 1466-609X Keywords ARDS evaluation hemodynamics multiple organ failure proteomics The 32nd Annual Meeting of the Society of Critical Care Medicine was once again a well attended and very interesting meeting. The distinguished faculty of well recognized clinical and basic scientists from all parts of the world presented multiple sessions highlighting the tremendous advances being made in our understanding and treatment of a wide variety of problems encountered in critically ill patients. In addition more than 600 free communications were presented. These were too wide to be covered in the present report. Rather we focus on the seven outstanding plenary sessions in which distinguished speakers shared their views on the present and future of critical care practice and research. Proteomics system biology and the future of drug design Michael B Yaffe Cambridge MA USA In his lecture Michael Yaffe alluded to how fundamental science may help in the development of new therapeutic agents. In the past the search for new drugs was based on random selection of drugs of natural sources which were secondary tested in all possible models. When the drug was proven to have efficacy its chemical structure was isolated and the drug was then synthesized. Using this method unfortunately the rate of drug discovery has decreased. A more rational approach would be to take into account our understanding of the mechanism .

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