IEEE J Biomed Health Inform. 2014 Mar;18(2):537-47. doi: 10.1109/JBHI.2013.2281505.
Drugs are frequently prescribed to patients with the aim of improving each patient's medical state, but an unfortunate consequence of most prescription drugs is the occurrence of undesirable side effects. Side effects that occur in more than one in a thousand patients are likely to be signaled efficiently by current drug surveillance methods, however, these same methods may take decades before generating signals for rarer side effects, risking medical morbidity or mortality in patients prescribed the drug while the rare side effect is undiscovered. In this paper, we propose a novel computational metaanalysis framework for signaling rare side effects that integrates existing methods, knowledge from the web,metric learning, and semisupervised clustering. The novel framework was able to signal many known rare and serious side effects for the selection of drugs investigated, such as tendon rupture when prescribed Ciprofloxacin or Levofloxacin, renal failure with Naproxen and depression associated with Rimonabant. Furthermore, for the majority of the drugs investigated it generated signals for rare side effects at a more stringent signaling threshold than existing methods and shows the potential to become a fundamental part of post marketing surveillance to detect rare side effects.
药物经常被开给患者,目的是改善每位患者的医疗状况,但大多数处方药的一个不幸后果是会出现不良副作用。当前的药物监测方法很可能能有效地发出每千名患者中就会出现一例以上的副作用信号,然而,这些方法可能需要数十年的时间才能为罕见副作用发出信号,从而使服用该药物的患者面临医疗发病率或死亡率的风险,而这种罕见的副作用尚未被发现。在本文中,我们提出了一种新颖的计算性元分析框架,用于发出罕见副作用信号,该框架集成了现有方法、来自网络的知识、度量学习和半监督聚类。该新颖的框架能够为所研究药物的选择发出许多已知的罕见和严重的副作用信号,例如环丙沙星或左氧氟沙星引起的肌腱断裂、萘普生引起的肾衰竭和利莫那班引起的抑郁。此外,对于大多数被研究的药物,它在比现有方法更严格的信号阈值下为罕见副作用生成信号,并显示出成为检测罕见副作用的上市后监测的基本组成部分的潜力。