• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

每个患者口袋里的药物基因组学?基于快速响应码的原型。

Pharmacogenomics in the pocket of every patient? A prototype based on quick response codes.

机构信息

Section for Medical Expert and Knowledge-Based Systems, Center for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.

出版信息

J Am Med Inform Assoc. 2013 May 1;20(3):409-12. doi: 10.1136/amiajnl-2012-001275. Epub 2013 Jan 23.

DOI:10.1136/amiajnl-2012-001275
PMID:23345409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3628061/
Abstract

A sizable fraction of patients experiences adverse drug events or lack of drug efficacy. A part of this variability in drug response can be explained by genetic differences between patients. However, pharmacogenomic data as well as computational clinical decision support systems for interpreting such data are still unavailable in most healthcare settings. We address this problem by introducing the medicine safety code (MSC), which captures compressed pharmacogenomic data in a two-dimensional barcode that can be carried in a patient's wallet. We successfully encoded data about 385 genetic polymorphisms in MSC and were able to decode and interpret MSC quickly with common mobile devices. The MSC could make individual pharmacogenomic data and decision support available in a wide variety of healthcare settings without the set up of large-scale infrastructures or centralized databases.

摘要

相当一部分患者会经历药物不良反应或药物疗效不佳。药物反应的这种可变性部分可以通过患者之间的遗传差异来解释。然而,在大多数医疗保健环境中,仍然缺乏药物基因组学数据以及用于解释此类数据的计算临床决策支持系统。我们通过引入药物安全码(MSC)来解决这个问题,它将压缩的药物基因组学数据编码在二维条码中,可以放在患者的钱包里。我们成功地在 MSC 中编码了大约 385 种遗传多态性的数据,并能够使用常见的移动设备快速解码和解释 MSC。MSC 可以在各种医疗保健环境中提供个体药物基因组学数据和决策支持,而无需建立大规模基础设施或集中式数据库。

相似文献

1
Pharmacogenomics in the pocket of every patient? A prototype based on quick response codes.每个患者口袋里的药物基因组学?基于快速响应码的原型。
J Am Med Inform Assoc. 2013 May 1;20(3):409-12. doi: 10.1136/amiajnl-2012-001275. Epub 2013 Jan 23.
2
An ontology-based, mobile-optimized system for pharmacogenomic decision support at the point-of-care.一种基于本体论、针对移动设备优化的即时医疗点药物基因组学决策支持系统。
PLoS One. 2014 May 2;9(5):e93769. doi: 10.1371/journal.pone.0093769. eCollection 2014.
3
Towards a global IT system for personalized medicine: the Medicine Safety Code initiative.迈向个性化医疗的全球信息技术系统:药品安全代码倡议。
Stud Health Technol Inform. 2014;198:25-31.
4
Towards a global IT system for personalized medicine: the Medicine Safety Code initiative.迈向个性化医疗的全球信息技术系统:药品安全规范倡议。
Stud Health Technol Inform. 2014;205:261-5.
5
Examining perceptions of the usefulness and usability of a mobile-based system for pharmacogenomics clinical decision support: a mixed methods study.考察对基于移动设备的药物基因组学临床决策支持系统的有用性和易用性的认知:一项混合方法研究。
PeerJ. 2016 Feb 8;4:e1671. doi: 10.7717/peerj.1671. eCollection 2016.
6
Pharmacogenomic knowledge representation, reasoning and genome-based clinical decision support based on OWL 2 DL ontologies.基于OWL 2 DL本体的药物基因组学知识表示、推理及基于基因组的临床决策支持
BMC Med Inform Decis Mak. 2015 Feb 22;15:12. doi: 10.1186/s12911-015-0130-1.
7
Pharmacogenomic Primer for the Pediatrician-What Is Really Important?儿科医生的药物基因组学入门知识——真正重要的是什么?
Pediatr Ann. 2018 May 1;47(5):e217-e219. doi: 10.3928/19382359-20180429-01.
8
Integrating pharmacogenomics into electronic health records with clinical decision support.将药物基因组学与临床决策支持系统整合到电子健康记录中。
Am J Health Syst Pharm. 2016 Dec 1;73(23):1967-1976. doi: 10.2146/ajhp160030.
9
Physician perspectives of CYP2C19 and clopidogrel drug-gene interaction active clinical decision support alerts.医生对CYP2C19与氯吡格雷药物-基因相互作用的积极临床决策支持警报的看法。
Int J Med Inform. 2016 Feb;86:117-25. doi: 10.1016/j.ijmedinf.2015.11.004. Epub 2015 Nov 11.
10
Pharmacogenomics and Personalized Medicine.药物基因组学与个性化医学。
Genes (Basel). 2020 Jun 22;11(6):679. doi: 10.3390/genes11060679.

引用本文的文献

1
Pharmacogenomic testing in paediatrics: Clinical implementation strategies.儿科药物基因组学检测:临床实施策略
Br J Clin Pharmacol. 2022 Oct;88(10):4297-4310. doi: 10.1111/bcp.15181. Epub 2022 Feb 7.
2
Qualitative user evaluation of a revised pharmacogenetic educational toolkit.修订后的药物遗传学教育工具包的定性用户评估
Pharmgenomics Pers Med. 2018 Sep 4;11:139-146. doi: 10.2147/PGPM.S169648. eCollection 2018.
3
Incidence of Exposure of Patients in the United States to Multiple Drugs for Which Pharmacogenomic Guidelines Are Available.美国患者接触有药物基因组学指南的多种药物的发生率。
PLoS One. 2016 Oct 20;11(10):e0164972. doi: 10.1371/journal.pone.0164972. eCollection 2016.
4
Examining perceptions of the usefulness and usability of a mobile-based system for pharmacogenomics clinical decision support: a mixed methods study.考察对基于移动设备的药物基因组学临床决策支持系统的有用性和易用性的认知:一项混合方法研究。
PeerJ. 2016 Feb 8;4:e1671. doi: 10.7717/peerj.1671. eCollection 2016.
5
Pharmacogenomic knowledge representation, reasoning and genome-based clinical decision support based on OWL 2 DL ontologies.基于OWL 2 DL本体的药物基因组学知识表示、推理及基于基因组的临床决策支持
BMC Med Inform Decis Mak. 2015 Feb 22;15:12. doi: 10.1186/s12911-015-0130-1.
6
An ontology-based, mobile-optimized system for pharmacogenomic decision support at the point-of-care.一种基于本体论、针对移动设备优化的即时医疗点药物基因组学决策支持系统。
PLoS One. 2014 May 2;9(5):e93769. doi: 10.1371/journal.pone.0093769. eCollection 2014.
7
Making data on essential pharmacogenes available for every patient everywhere: the Medicine Safety Code initiative.让世界各地的每一位患者都能获取基本药物基因数据:药物安全编码倡议。
Pharmacogenomics. 2013 Oct;14(13):1529-31. doi: 10.2217/pgs.13.121.
8
Implementation of a clinical research pharmacogenomics program at an academic medical center: role of the genetics healthcare professional.在一家学术医疗中心实施临床研究药物基因组学项目:遗传学医疗专业人员的作用。
Pharmacogenomics. 2013 May;14(7):703-6. doi: 10.2217/pgs.13.46.

本文引用的文献

1
Implementing personalized medicine: development of a cost-effective customized pharmacogenetics genotyping array.实施个性化医学:开发一种具有成本效益的定制型药物基因组学分型基因芯片。
Clin Pharmacol Ther. 2012 Oct;92(4):437-9. doi: 10.1038/clpt.2012.125. Epub 2012 Aug 22.
2
The feasibility of QR-code prescription in Taiwan.台湾地区 QR 码处方的可行性。
J Clin Pharm Ther. 2012 Dec;37(6):643-6. doi: 10.1111/j.1365-2710.2012.01358.x. Epub 2012 May 21.
3
Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT project.前瞻性个体化医疗基因分型的实施:范德堡 PREDICT 项目的设计。
Clin Pharmacol Ther. 2012 Jul;92(1):87-95. doi: 10.1038/clpt.2011.371. Epub 2012 May 16.
4
DNA barcode goes two-dimensions: DNA QR code web server.DNA 条码进入二维时代:DNA QR 码网络服务器。
PLoS One. 2012;7(5):e35146. doi: 10.1371/journal.pone.0035146. Epub 2012 May 4.
5
Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial.即时检测指导抗血小板治疗个体化的研究(RAPID GENE):一项前瞻性、随机、概念验证试验。
Lancet. 2012 May 5;379(9827):1705-11. doi: 10.1016/S0140-6736(12)60161-5. Epub 2012 Mar 29.
6
Semantically enabling pharmacogenomic data for the realization of personalized medicine.使药物基因组学数据具有语义功能,以实现个性化医疗。
Pharmacogenomics. 2012 Jan;13(2):201-12. doi: 10.2217/pgs.11.179.
7
From pharmacogenomic knowledge acquisition to clinical applications: the PharmGKB as a clinical pharmacogenomic biomarker resource.从药物基因组学知识获取到临床应用:PharmGKB 作为临床药物基因组学生物标志物资源。
Biomark Med. 2011 Dec;5(6):795-806. doi: 10.2217/bmm.11.94.
8
Towards an interoperable information infrastructure providing decision support for genomic medicine.迈向为基因组医学提供决策支持的可互操作信息基础设施。
Stud Health Technol Inform. 2011;169:165-9.
9
Linked open drug data for pharmaceutical research and development.链接开放药物数据在药物研发中的应用。
J Cheminform. 2011 May 16;3(1):19. doi: 10.1186/1758-2946-3-19.
10
Pharmacogenetics: from bench to byte--an update of guidelines.药物遗传学:从实验室到字节——指南更新。
Clin Pharmacol Ther. 2011 May;89(5):662-73. doi: 10.1038/clpt.2011.34. Epub 2011 Mar 16.