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Precision Medicine-Personalized, Problematic, and Promising

机译:精准医学-个性化,有问题和有前途的

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Precision medicine is a term used to describe individualized treatment that encompasses the use of new diagnostics and therapeutics, targeted to the needs of a patient based on his/her own genetic, biomarker, phenotypic, or psychosocial characteristics. In particular, advances such as cell sorting, epigenetics, proteomics, metabolomics, and more are converging with informatics and other technologies in a manner that is rapidly expanding the scope of this field. This article highlights the variety of breakthroughs in the field and addresses challenges that precision medicine may face. Many current technologies are rapidly enhancing the field of precision medicine. Recombinant biologic agents can now be used as replacement therapies, such as in the treatment of hemophilia, and electronic health records have created a rich and accessible database of clinical information that can be used for research and for clinical care guideline creation. Gene therapy, genetics, and next-generation DNA sequencing methods are perhaps having the greatest effect; this will continue to advance with decreases in costs. Testing for specific abnormalities has aided in the treatment of certain types of cancers. In lung cancer, molecular testing of EGFR, MET, RAS, ALK, and other genetic markers can help identify patients who need treatment and protect patients who do not from costly and toxic therapies. Molecular testing can also screen patients for multiple endocrine neoplasia type 2, which allows for early prophylactic treatment and attention, sparing unaffected family members from unnecessary screening. Such advances decrease harm and create care specific to the individual. However, there are also challenges. One challenge is the misalignment of patient, physician, health system, payer, and industry interests. In greater detail, patients and physicians are primarily concerned with understanding and treating disease, but physicians must also consider utilization of heath care, which affects the health care system, payer, and industry interests and in turn also relates to costs of new diagnostics or finding more profitable therapies. Managing these interests in an efficacious and cost-effective manner may prove difficult. A second challenge is organizing the wealth of growing information. As disease classification trends toward more precise definitions and discrete disease entities, expanded decision algorithms and treatment options will be needed to properly address each type of treatment. Some conditions are caused by multiple different mutations in different genes, whereas in other cases different mutations in a single gene may lead to a range of diseases. As the complexity of disease becomes more apparent to us, physicians, especially primary care providers, will need to utilize informatics all within clinical guidelines in order to navigate these complex and specialized referral pathways. Future trends in precision medicine are most likely in targeting genetic pathways in cancer with medications, cancer immunotherapies, DNA sequencing, and use of technology in acute interventions (eg, automated defibrillator). Should stakeholders adapt to these changes, health providers streamline pathways that facilitate specialist access and proper care, and agencies and payers support a cost-effective field, then the advances in precision medicine may be limitless.
机译:精密医学是一个术语,用于描述个性化治疗,其中包括根据患者自身的遗传,生物标记,表型或社会心理特征,针对患者的需要使用新的诊断方法和治疗方法。特别是,诸如细胞分选,表观遗传学,蛋白质组学,代谢组学等方面的进展正以迅速扩展该领域范围的方式与信息学和其他技术融合。本文重点介绍了该领域的各种突破并解决了精密医学可能面临的挑战。当前的许多技术正在迅速扩大精密医学领域。重组生物制剂现在可以用作替代疗法,例如在血友病的治疗中,电子健康记录已经创建了丰富且可访问的临床信息数据库,可用于研究和临床护理指南的创建。基因治疗,遗传学和下一代DNA测序方法可能发挥最大的作用。随着成本的降低,这种情况将继续发展。对特定异常的测试有助于治疗某些类型的癌症。在肺癌中,对EGFR,MET,RAS,ALK和其他遗传标记进行分子检测可以帮助识别需要治疗的患者,并保护不需要昂贵和有毒疗法的患者。分子检测还可以筛查患者的2型多发性内分泌肿瘤,从而可以进行早期预防和治疗,使未受影响的家庭成员免受不必要的筛查。这种进步减少了伤害并创造了针对个人的护理。但是,也存在挑战。挑战之一是患者,医生,卫生系统,付款人和行业利益的错位。更详细地讲,患者和医师主要关注疾病的理解和治疗,但是医师还必须考虑使用保健服务,这会影响医疗保健系统,付款人和行业利益,进而也涉及新诊断或发现费用更有利可图的疗法。事实证明,以有效和具有成本效益的方式管理这些利益很困难。第二个挑战是组织越来越多的信息。随着疾病分类趋向于更精确的定义和离散的疾病实体,将需要扩展的决策算法和治疗选择以正确地解决每种治疗类型。某些情况是由不同基因中的多个不同突变引起的,而在其他情况下,单个基因中的不同突变可能导致一系列疾病。随着疾病的复杂性对我们变得越来越明显,医生(尤其是初级保健提供者)将需要在临床指南中充分利用信息学,以浏览这些复杂且专门的转诊途径。精准医学的未来趋势最有可能通过药物,癌症免疫疗法,DNA测序以及在急性干预措施(例如自动除颤器)中使用技术来靶向癌症的遗传途径。如果利益相关者适应这些变化,卫生服务提供者简化了促进专科医生就诊和适当护理的途径,并且机构和付款人支持了具有成本效益的领域,那么精密医学的进步将是无限的。

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