首页 > 最新文献

Expert opinion on medical diagnostics最新文献

英文 中文
Advances in personalized therapy for lung cancer. 肺癌个性化治疗的进展。
Pub Date : 2013-09-01 Epub Date: 2013-08-12 DOI: 10.1517/17530059.2013.826645
Eric S Kim, Kishan J Pandya

Introduction: Personalized medicine based on tumor characteristics is transforming the management of lung cancer. This review provides an overview of clinically approved strategies to personalize treatment for lung cancer as well as evolving strategies in various stages of clinical development.

Areas covered: Selecting therapy based on various tumor characteristics such as histology and presence of specific molecular alterations will be covered. This review will not only discuss the role of targeted agents in personalizing care for lung cancer but also the strategies to personalize traditional chemotherapeutic agents.

Expert opinion: Advances in genomic medicine to identify key genetic alterations with subsequent development of matching targeted agents are rapidly changing the management of lung cancer. Being able to target key driver molecular aberrations is certainly exciting and clinically meaningful, but only for a limited period of time. Intra- and intertumoral heterogeneity is a major contributor to therapy resistance, a substantial roadblock to durable response. Better understanding of resistance mechanism is at least as important as identifying new targetable genetic changes to effectively advance personalized therapy for lung cancer. Finally, optimization of biopsy specimens and rigorous validation steps to ensure reliability of diagnostic methods would be critical in moving forward.

基于肿瘤特征的个性化医疗正在改变肺癌的治疗方式。本文综述了临床批准的肺癌个体化治疗策略,以及在临床发展的各个阶段不断发展的策略。涵盖领域:根据不同的肿瘤特征,如组织学和特定分子改变的存在,选择治疗将被涵盖。本文将讨论靶向药物在肺癌个体化治疗中的作用,以及传统化疗药物的个体化治疗策略。专家意见:基因组医学在识别关键基因改变方面的进展以及随后匹配靶向药物的发展正在迅速改变肺癌的管理。能够靶向关键驱动分子畸变当然是令人兴奋的和有临床意义的,但只是在有限的时间内。肿瘤内部和肿瘤间的异质性是治疗耐药的主要因素,是持久疗效的重大障碍。更好地了解耐药机制至少与发现新的靶向基因变化对于有效推进肺癌的个性化治疗同样重要。最后,优化活检标本和严格的验证步骤以确保诊断方法的可靠性将是向前发展的关键。
{"title":"Advances in personalized therapy for lung cancer.","authors":"Eric S Kim,&nbsp;Kishan J Pandya","doi":"10.1517/17530059.2013.826645","DOIUrl":"https://doi.org/10.1517/17530059.2013.826645","url":null,"abstract":"<p><strong>Introduction: </strong>Personalized medicine based on tumor characteristics is transforming the management of lung cancer. This review provides an overview of clinically approved strategies to personalize treatment for lung cancer as well as evolving strategies in various stages of clinical development.</p><p><strong>Areas covered: </strong>Selecting therapy based on various tumor characteristics such as histology and presence of specific molecular alterations will be covered. This review will not only discuss the role of targeted agents in personalizing care for lung cancer but also the strategies to personalize traditional chemotherapeutic agents.</p><p><strong>Expert opinion: </strong>Advances in genomic medicine to identify key genetic alterations with subsequent development of matching targeted agents are rapidly changing the management of lung cancer. Being able to target key driver molecular aberrations is certainly exciting and clinically meaningful, but only for a limited period of time. Intra- and intertumoral heterogeneity is a major contributor to therapy resistance, a substantial roadblock to durable response. Better understanding of resistance mechanism is at least as important as identifying new targetable genetic changes to effectively advance personalized therapy for lung cancer. Finally, optimization of biopsy specimens and rigorous validation steps to ensure reliability of diagnostic methods would be critical in moving forward.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 5","pages":"475-85"},"PeriodicalIF":0.0,"publicationDate":"2013-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.826645","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31645102","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Diagnosis of thyroid cancer: state of art. 甲状腺癌的诊断:最新进展。
Pub Date : 2013-07-01 Epub Date: 2013-05-23 DOI: 10.1517/17530059.2013.800481
Myriem Boufraqech, Dhaval Patel, Yin Xiong, Electron Kebebew

Introduction: Thyroid cancer is the most common endocrine cancer in the USA and its incidence is increasing worldwide. Thyroid fine-needle aspiration biopsy (FNA) and cytologic analysis is the most cost-effective approach to distinguish between malignant and benign thyroid nodules. However, up to 30% of thyroid FNA biopsy results are inconclusive.

Areas covered: In this article, the authors provide an update on the current status and emerging approaches for improving thyroid cancer diagnosis. This review covers imaging, genetic and genomic approaches being used or in development to help distinguish between malignant and benign thyroid nodules.

Expert opinion: There has been considerable progress in improving thyroid cancer diagnosis. The molecular markers analysis to avoid diagnostic surgeries seems to be promising. However, the clinical utility and accuracy of some markers reported in this review are not conclusive and need to be validated as clinical diagnostic tool.

简介:甲状腺癌是美国最常见的内分泌癌,其发病率在世界范围内呈上升趋势。甲状腺细针穿刺活检(FNA)和细胞学分析是最经济有效的方法来区分恶性和良性甲状腺结节。然而,高达30%的甲状腺FNA活检结果是不确定的。涵盖领域:在这篇文章中,作者提供了一个最新的现状和新兴的方法,以提高甲状腺癌的诊断。本文综述了影像学、遗传学和基因组学方法正在使用或正在开发,以帮助区分恶性和良性甲状腺结节。专家意见:在改善甲状腺癌诊断方面已经取得了相当大的进展。分子标记分析避免诊断性手术似乎是有希望的。然而,本综述中报道的一些标志物的临床实用性和准确性尚不确定,需要作为临床诊断工具进行验证。
{"title":"Diagnosis of thyroid cancer: state of art.","authors":"Myriem Boufraqech,&nbsp;Dhaval Patel,&nbsp;Yin Xiong,&nbsp;Electron Kebebew","doi":"10.1517/17530059.2013.800481","DOIUrl":"https://doi.org/10.1517/17530059.2013.800481","url":null,"abstract":"<p><strong>Introduction: </strong>Thyroid cancer is the most common endocrine cancer in the USA and its incidence is increasing worldwide. Thyroid fine-needle aspiration biopsy (FNA) and cytologic analysis is the most cost-effective approach to distinguish between malignant and benign thyroid nodules. However, up to 30% of thyroid FNA biopsy results are inconclusive.</p><p><strong>Areas covered: </strong>In this article, the authors provide an update on the current status and emerging approaches for improving thyroid cancer diagnosis. This review covers imaging, genetic and genomic approaches being used or in development to help distinguish between malignant and benign thyroid nodules.</p><p><strong>Expert opinion: </strong>There has been considerable progress in improving thyroid cancer diagnosis. The molecular markers analysis to avoid diagnostic surgeries seems to be promising. However, the clinical utility and accuracy of some markers reported in this review are not conclusive and need to be validated as clinical diagnostic tool.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"331-42"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.800481","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31452257","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
MRI biomarkers for evaluation of treatment efficacy in preclinical diabetic retinopathy. 评价临床前糖尿病视网膜病变治疗效果的MRI生物标志物。
Pub Date : 2013-07-01 Epub Date: 2013-06-21 DOI: 10.1517/17530059.2013.814639
Bruce A Berkowitz, David Bissig, Oliver Dutczak, Shannon Corbett, Rob North, Robin Roberts

Introduction: One sober consequence of the current epidemic of diabetes mellitus is that an increasing number of people world-wide will partially or completely lose their sight to diabetic retinopathy. Clinically, the sight-threatening complications of diabetes are diagnosed and treated based on visible retinal lesions (e.g., dot-blot hemorrhages or retinal neovascularization). However, such anatomical microvascular lesions are slow to respond with treatment. Thus, there remains an urgent need for imaging biomarkers that are abnormal before retinal lesions are visibly apparent and are responsive to treatment.

Areas covered: Here, the development of new MRI methods, such as manganese-enhanced MRI, for evaluating early diabetes-evoked retinal pathophysiology, and its usefulness in guiding new treatments for diabetic retinopathy are reviewed.

Expert opinion: In diabetic retinopathy, not all important diagnostic and prognostic needs are well served by optical methods. In the absence of gross anatomy changes, critical times when drug intervention is most likely to be successful at reducing vision loss are missed by most light-based methods and thus provide little help in guiding diagnosis and treatment. For example, before clinical symptoms, is there an optimal time to intervene with drug therapy? Is a drug reaching its target? How does one assess optimal drug dose, schedule, and routes? How well do current experimental models mimic the clinical condition? As discussed herein, MRI is as an analytical tool for addressing these unmet needs. Future clinical applications of MRI can be envisioned such as in clinical trials to assess drug treatment efficacy, or as an adjunct approach to refine or clarify a difficult clinical case. New MRI-generated hypotheses about the pathogenesis of diabetic retinopathy and its treatment are discussed. In the coming years, a substantial growth in the development and application of MRI is expected to address relevant question in both the basic sciences and in the clinic.

导读:当前糖尿病流行的一个严重后果是,全世界越来越多的人将因糖尿病视网膜病变而部分或完全失明。临床上,糖尿病危及视力的并发症是根据可见的视网膜病变(如斑点出血或视网膜新生血管)进行诊断和治疗的。然而,这种解剖性微血管病变对治疗反应缓慢。因此,迫切需要在视网膜病变明显且对治疗有反应之前发现异常的成像生物标志物。本文综述了新的MRI方法的发展,如锰增强MRI,用于评估早期糖尿病引起的视网膜病理生理,及其在指导糖尿病视网膜病变新治疗中的作用。专家意见:在糖尿病视网膜病变中,并不是所有重要的诊断和预后需要都能通过光学方法得到很好的满足。在没有大体解剖变化的情况下,大多数基于光的方法都错过了药物干预最有可能成功减少视力丧失的关键时刻,因此对指导诊断和治疗帮助不大。例如,在出现临床症状之前,是否存在药物治疗干预的最佳时间?药物是否达到了目标?如何评估最佳药物剂量、方案和途径?目前的实验模型如何很好地模拟临床情况?正如本文所讨论的,MRI是解决这些未满足需求的分析工具。MRI的未来临床应用可以设想,如在临床试验中评估药物治疗效果,或作为一种辅助方法来完善或澄清一个困难的临床病例。本文讨论了关于糖尿病视网膜病变发病机制及其治疗的mri新假设。在未来的几年里,核磁共振成像的发展和应用有望在基础科学和临床中解决相关问题。
{"title":"MRI biomarkers for evaluation of treatment efficacy in preclinical diabetic retinopathy.","authors":"Bruce A Berkowitz,&nbsp;David Bissig,&nbsp;Oliver Dutczak,&nbsp;Shannon Corbett,&nbsp;Rob North,&nbsp;Robin Roberts","doi":"10.1517/17530059.2013.814639","DOIUrl":"https://doi.org/10.1517/17530059.2013.814639","url":null,"abstract":"<p><strong>Introduction: </strong>One sober consequence of the current epidemic of diabetes mellitus is that an increasing number of people world-wide will partially or completely lose their sight to diabetic retinopathy. Clinically, the sight-threatening complications of diabetes are diagnosed and treated based on visible retinal lesions (e.g., dot-blot hemorrhages or retinal neovascularization). However, such anatomical microvascular lesions are slow to respond with treatment. Thus, there remains an urgent need for imaging biomarkers that are abnormal before retinal lesions are visibly apparent and are responsive to treatment.</p><p><strong>Areas covered: </strong>Here, the development of new MRI methods, such as manganese-enhanced MRI, for evaluating early diabetes-evoked retinal pathophysiology, and its usefulness in guiding new treatments for diabetic retinopathy are reviewed.</p><p><strong>Expert opinion: </strong>In diabetic retinopathy, not all important diagnostic and prognostic needs are well served by optical methods. In the absence of gross anatomy changes, critical times when drug intervention is most likely to be successful at reducing vision loss are missed by most light-based methods and thus provide little help in guiding diagnosis and treatment. For example, before clinical symptoms, is there an optimal time to intervene with drug therapy? Is a drug reaching its target? How does one assess optimal drug dose, schedule, and routes? How well do current experimental models mimic the clinical condition? As discussed herein, MRI is as an analytical tool for addressing these unmet needs. Future clinical applications of MRI can be envisioned such as in clinical trials to assess drug treatment efficacy, or as an adjunct approach to refine or clarify a difficult clinical case. New MRI-generated hypotheses about the pathogenesis of diabetic retinopathy and its treatment are discussed. In the coming years, a substantial growth in the development and application of MRI is expected to address relevant question in both the basic sciences and in the clinic.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"393-403"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.814639","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31613614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Comment and reply on: ME is a distinct diagnostic entity, not part of a chronic fatigue spectrum. 评论和回复:ME是一种独特的诊断实体,而不是慢性疲劳谱的一部分。
Pub Date : 2013-07-01 Epub Date: 2013-05-02 DOI: 10.1517/17530059.2013.795147
Frank Nm Twisk, Rob Jw Arnoldus
{"title":"Comment and reply on: ME is a distinct diagnostic entity, not part of a chronic fatigue spectrum.","authors":"Frank Nm Twisk,&nbsp;Rob Jw Arnoldus","doi":"10.1517/17530059.2013.795147","DOIUrl":"https://doi.org/10.1517/17530059.2013.795147","url":null,"abstract":"","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"413-5"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.795147","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31490640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Molecular biomarkers in cervical cancer diagnosis: a critical appraisal. 分子生物标志物在宫颈癌诊断中的重要作用。
Pub Date : 2013-07-01 Epub Date: 2013-06-19 DOI: 10.1517/17530059.2013.808621
Rogier J N T M Litjens, Anton H N Hopman, Koen K van de Vijver, Frans C S Ramaekers, Roy F P M Kruitwagen, Arnold-Jan Kruse
INTRODUCTIONIt is expected that in the near future high-risk human papillomavirus (hr-HPV) testing will be implemented as the primary cervical cancer screening method in some countries. However, only a fraction of hr-HPV positive women will have a clinically relevant lesion. As a result, there is an urgent need for additional biomarkers that can detect these lesions and that can at the same time be applied to cytological specimens. This overview evaluates the most promising cytological biomarkers.AREAS COVEREDCytological biomarkers that can be used are being discussed in view of their molecular background. The most promising biomarkers are p16(INK4a)/Ki-67 dual immunostaining; methylation of the promoter region of the cell adhesion molecule 1 (CADM1) gene and the T-lymphocyte maturation associated protein (MAL) gene and viral integration. Their sensitivity, specificity and limitations are discussed in detail and their diagnostic accuracy is evaluated.EXPERT OPINIONThe most promising cytological biomarkers for cervical cancer screening are p16(INK4a)/Ki-67 dual immunostaining, methylation of CADM1 and MAL and viral integration. Although some of the biomarkers are very promising for this purpose, no studies have evaluated how accurately these biomarkers classify or predict the outcome. Additional clinical trials are needed to determine the true clinical value of these promising cytological biomarkers.
预计在不久的将来,一些国家将实施高危人乳头瘤病毒(hr-HPV)检测作为宫颈癌筛查的主要方法。然而,只有一小部分hr-HPV阳性的妇女会有临床相关的病变。因此,迫切需要额外的生物标志物来检测这些病变,同时可以应用于细胞学标本。本文综述了最有前途的细胞学生物标志物。涵盖领域:考虑到它们的分子背景,正在讨论可以使用的细胞学生物标志物。最有希望的生物标志物是p16(INK4a)/Ki-67双免疫染色;细胞粘附分子1 (CADM1)基因和t淋巴细胞成熟相关蛋白(MAL)基因启动子区甲基化与病毒整合详细讨论了它们的敏感性、特异性和局限性,并评估了它们的诊断准确性。专家意见:最有希望用于宫颈癌筛查的细胞学生物标志物是p16(INK4a)/Ki-67双免疫染色、CADM1和MAL的甲基化以及病毒整合。尽管一些生物标记物在这方面很有希望,但没有研究评估这些生物标记物分类或预测结果的准确性。需要更多的临床试验来确定这些有前途的细胞学生物标志物的真正临床价值。
{"title":"Molecular biomarkers in cervical cancer diagnosis: a critical appraisal.","authors":"Rogier J N T M Litjens,&nbsp;Anton H N Hopman,&nbsp;Koen K van de Vijver,&nbsp;Frans C S Ramaekers,&nbsp;Roy F P M Kruitwagen,&nbsp;Arnold-Jan Kruse","doi":"10.1517/17530059.2013.808621","DOIUrl":"https://doi.org/10.1517/17530059.2013.808621","url":null,"abstract":"INTRODUCTION\u0000It is expected that in the near future high-risk human papillomavirus (hr-HPV) testing will be implemented as the primary cervical cancer screening method in some countries. However, only a fraction of hr-HPV positive women will have a clinically relevant lesion. As a result, there is an urgent need for additional biomarkers that can detect these lesions and that can at the same time be applied to cytological specimens. This overview evaluates the most promising cytological biomarkers.\u0000\u0000\u0000AREAS COVERED\u0000Cytological biomarkers that can be used are being discussed in view of their molecular background. The most promising biomarkers are p16(INK4a)/Ki-67 dual immunostaining; methylation of the promoter region of the cell adhesion molecule 1 (CADM1) gene and the T-lymphocyte maturation associated protein (MAL) gene and viral integration. Their sensitivity, specificity and limitations are discussed in detail and their diagnostic accuracy is evaluated.\u0000\u0000\u0000EXPERT OPINION\u0000The most promising cytological biomarkers for cervical cancer screening are p16(INK4a)/Ki-67 dual immunostaining, methylation of CADM1 and MAL and viral integration. Although some of the biomarkers are very promising for this purpose, no studies have evaluated how accurately these biomarkers classify or predict the outcome. Additional clinical trials are needed to determine the true clinical value of these promising cytological biomarkers.","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"365-77"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.808621","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31514914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 35
The clinical and laboratory diagnosis of acute meningitis and acute encephalitis. 急性脑膜炎和急性脑炎的临床和实验室诊断。
Pub Date : 2013-07-01 Epub Date: 2013-05-30 DOI: 10.1517/17530059.2013.804508
Burke A Cunha

Introduction: Acute bacterial meningitis (ABM) is a life-threatening infectious disease requiring prompt antimicrobial therapy. ABM must be differentiated from systemic disorders with CNS manifestations that may mimic ABM. ABM should also be differentiated from acute meningoencephalitis (AME) and acute viral encephalitis (AVE). Nonviral causes of AME are treatable. Among the causes of AVE, Herpes simplex encephalitis (HSE) is treatable. This article reviews the clinical diagnostic approach to ABM, AME and AVE.

Areas covered: The differential diagnostic (DDx) approach to ABM, AME and AVE is based on clinical and laboratory findings. A specific pathogen diagnosis is based on serum/cerebrospinal fluid (CSF) tests. This overview presents the diagnostic approach to ABM, AME and AVE in normal hosts (excluding brain abscesses and chronic CNS infections).

Expert opinion: It is time critical to diagnose ABM and begin empiric antimicrobial therapy based on the known/most likely pathogen. The diagnosis of ABM depends on clinical features and the CSF profile. The CSF Gram stain and CSF lactic acid (LA) levels provide the most rapid, reliable and cost-effective tests to diagnose ABM. CSF LA levels are also the best way to diagnose partially treated acute bacterial meningitis (PTABM). In those cases of AME/AVE due to viruses with a CSF profile mimicking ABM, for example, HSE, unelevated CSF LA levels rapidly/reliably rule out ABM as a diagnostic possibility.

简介:急性细菌性脑膜炎(ABM)是一种危及生命的传染病,需要及时的抗菌治疗。ABM必须与可能模仿ABM的中枢神经系统表现的全身性疾病区分开来。ABM还应与急性脑膜脑炎(AME)和急性病毒性脑炎(AVE)相鉴别。AME的非病毒性病因是可以治疗的。在AVE的病因中,单纯疱疹脑炎(HSE)是可以治疗的。本文综述了ABM、AME和AVE的临床诊断方法,涵盖的领域:ABM、AME和AVE的鉴别诊断(DDx)方法是基于临床和实验室结果。具体的病原体诊断是基于血清/脑脊液(CSF)测试。本文概述了正常宿主(不包括脑脓肿和慢性中枢神经系统感染)ABM、AME和AVE的诊断方法。专家意见:诊断ABM并根据已知/最可能的病原体开始经验性抗菌治疗是非常关键的。ABM的诊断取决于临床特征和脑脊液剖面。脑脊液革兰氏染色和脑脊液乳酸(LA)水平为诊断ABM提供了最快速、可靠和经济的检测方法。CSF LA水平也是诊断部分治疗急性细菌性脑膜炎(PTABM)的最佳方法。在那些由脑脊液特征与ABM相似的病毒引起的AME/AVE病例中,例如HSE,未升高的脑脊液LA水平迅速/可靠地排除了ABM的诊断可能性。
{"title":"The clinical and laboratory diagnosis of acute meningitis and acute encephalitis.","authors":"Burke A Cunha","doi":"10.1517/17530059.2013.804508","DOIUrl":"https://doi.org/10.1517/17530059.2013.804508","url":null,"abstract":"<p><strong>Introduction: </strong>Acute bacterial meningitis (ABM) is a life-threatening infectious disease requiring prompt antimicrobial therapy. ABM must be differentiated from systemic disorders with CNS manifestations that may mimic ABM. ABM should also be differentiated from acute meningoencephalitis (AME) and acute viral encephalitis (AVE). Nonviral causes of AME are treatable. Among the causes of AVE, Herpes simplex encephalitis (HSE) is treatable. This article reviews the clinical diagnostic approach to ABM, AME and AVE.</p><p><strong>Areas covered: </strong>The differential diagnostic (DDx) approach to ABM, AME and AVE is based on clinical and laboratory findings. A specific pathogen diagnosis is based on serum/cerebrospinal fluid (CSF) tests. This overview presents the diagnostic approach to ABM, AME and AVE in normal hosts (excluding brain abscesses and chronic CNS infections).</p><p><strong>Expert opinion: </strong>It is time critical to diagnose ABM and begin empiric antimicrobial therapy based on the known/most likely pathogen. The diagnosis of ABM depends on clinical features and the CSF profile. The CSF Gram stain and CSF lactic acid (LA) levels provide the most rapid, reliable and cost-effective tests to diagnose ABM. CSF LA levels are also the best way to diagnose partially treated acute bacterial meningitis (PTABM). In those cases of AME/AVE due to viruses with a CSF profile mimicking ABM, for example, HSE, unelevated CSF LA levels rapidly/reliably rule out ABM as a diagnostic possibility.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"343-64"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.804508","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31467562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
The diagnostic evaluation of MelaFind multi-spectral objective computer vision system. MelaFind多光谱物镜计算机视觉系统的诊断评价。
Pub Date : 2013-07-01 Epub Date: 2013-03-31 DOI: 10.1517/17530059.2013.785520
Erine A Kupetsky, Laura K Ferris

Introduction: Over 75,000 people in the United States were diagnosed with melanoma in 2012. The incidence of melanoma continues to increase over time and early detection is currently the most promising strategy to decrease melanoma-related morbidity and mortality. Currently, most physicians perform skin cancer screenings with the unaided eye. However, the FDA recently approved, MelaFind, a multispectral objective computer vision system to assist dermatologists in making more accurate biopsy decisions to facilitate early melanoma diagnosis.

Areas covered: This review covers the sensitivity and specificity, limitations and clinical role of MelaFind and other devices available or under development to aid in the detection of melanoma.

Expert opinion: Physician screening with the aid of MelaFind device may improve detection of early melanoma and potentially reduce melanoma morbidity and mortality, if used widely. The strength of MelaFind is its high sensitivity, acceptable specificity, ease of use and objective output. Thus it has potential to improve biopsy decisions made by both dermatologists and less experienced clinicians. Currently, the use of MelaFind is not reimbursed by insurance and the cost, which is paid directly by the patient, will likely limit its use.

2012年,美国有超过75000人被诊断患有黑色素瘤。随着时间的推移,黑色素瘤的发病率持续增加,早期发现是目前最有希望降低黑色素瘤相关发病率和死亡率的策略。目前,大多数医生使用裸眼进行皮肤癌筛查。然而,FDA最近批准了MelaFind,这是一种多光谱物镜计算机视觉系统,可以帮助皮肤科医生做出更准确的活检决定,以促进黑色素瘤的早期诊断。涵盖领域:本综述涵盖了MelaFind和其他可用或正在开发的用于帮助检测黑色素瘤的设备的敏感性和特异性、局限性和临床作用。专家意见:如果广泛使用MelaFind设备,医生筛查可以提高早期黑色素瘤的发现,并有可能降低黑色素瘤的发病率和死亡率。MelaFind的优势在于其高灵敏度、可接受的特异性、易于使用和客观的输出。因此,它有可能改善皮肤科医生和经验不足的临床医生做出的活检决定。目前,使用MelaFind是不报销的,费用是由患者直接支付的,这可能会限制其使用。
{"title":"The diagnostic evaluation of MelaFind multi-spectral objective computer vision system.","authors":"Erine A Kupetsky,&nbsp;Laura K Ferris","doi":"10.1517/17530059.2013.785520","DOIUrl":"https://doi.org/10.1517/17530059.2013.785520","url":null,"abstract":"<p><strong>Introduction: </strong>Over 75,000 people in the United States were diagnosed with melanoma in 2012. The incidence of melanoma continues to increase over time and early detection is currently the most promising strategy to decrease melanoma-related morbidity and mortality. Currently, most physicians perform skin cancer screenings with the unaided eye. However, the FDA recently approved, MelaFind, a multispectral objective computer vision system to assist dermatologists in making more accurate biopsy decisions to facilitate early melanoma diagnosis.</p><p><strong>Areas covered: </strong>This review covers the sensitivity and specificity, limitations and clinical role of MelaFind and other devices available or under development to aid in the detection of melanoma.</p><p><strong>Expert opinion: </strong>Physician screening with the aid of MelaFind device may improve detection of early melanoma and potentially reduce melanoma morbidity and mortality, if used widely. The strength of MelaFind is its high sensitivity, acceptable specificity, ease of use and objective output. Thus it has potential to improve biopsy decisions made by both dermatologists and less experienced clinicians. Currently, the use of MelaFind is not reimbursed by insurance and the cost, which is paid directly by the patient, will likely limit its use.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":" ","pages":"405-11"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.785520","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40236256","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Prognostic markers for acute heart failure. 急性心力衰竭的预后指标。
Pub Date : 2013-07-01 DOI: 10.1517/17530059.2013.814638
Domingo A Pascual-Figal, Luis Caballero, Jesús Sanchez-Mas, Antonio Lax

Introduction: Acute heart failure (AHF) is the leading cause of hospitalization in patients over 65 years, representing a heterogenic syndrome and a major burden, as it is associated with elevated health expenditures and high rates of mortality and readmission.

Areas covered: This article provides a review of individual markers for risk stratification, including clinical, cardiorenal, hemodynamic, neurohormonal and cardiac biomarkers. In addition, aspects as complementary value, monitoring, risk models and events prediction are analyzed.

Expert opinion: In clinical practice, risk stratification of AHF is complex and relies on the integration of bedside evaluation and laboratory biomarkers. Measures of congestion and perfusion, renal function, natriuretic peptides and cardiac troponins have become standard risk markers of death and/or readmission. However, there are numerous research findings that do not translate into an improved clinical management of individuals and a reduction of health costs. Research on this field needs to be redirected in a prospective manner in order to evaluate risk models in the emergency department. This would allow safe identification of patients at lower risk - who could be transferred and managed in out-patient facilities - as well as those biomarkers that, by reflecting pathophysiological routes, could be used as a guide to related therapeutics for improving outcomes. In addition, the identification of specific markers and models closely related with the risk of recurrent AHF is mandatory. Consequently, it is the time for clinicians working in networks to assume a leading role in translating risk assessment in AHF into clinical practice.

急性心力衰竭(AHF)是65岁以上患者住院的主要原因,是一种异质综合征和主要负担,因为它与卫生支出增加、死亡率和再入院率高有关。涉及领域:本文综述了风险分层的个体标志物,包括临床、心肾、血流动力学、神经激素和心脏生物标志物。并从互补价值、监测、风险模型、事件预测等方面进行了分析。专家意见:在临床实践中,AHF的风险分层是复杂的,依赖于床边评估和实验室生物标志物的整合。充血和灌注、肾功能、利钠肽和心肌肌钙蛋白的测量已成为死亡和/或再入院的标准危险标志。然而,有许多研究结果并没有转化为改善个人的临床管理和降低医疗费用。这一领域的研究需要以前瞻性的方式重新定位,以评估急诊科的风险模型。这将允许安全识别风险较低的患者-可以在门诊设施转移和管理-以及那些通过反映病理生理途径可作为相关治疗方法指导以改善结果的生物标志物。此外,必须确定与AHF复发风险密切相关的特定标志物和模型。因此,是时候让在网络中工作的临床医生承担主导作用,将AHF的风险评估转化为临床实践。
{"title":"Prognostic markers for acute heart failure.","authors":"Domingo A Pascual-Figal,&nbsp;Luis Caballero,&nbsp;Jesús Sanchez-Mas,&nbsp;Antonio Lax","doi":"10.1517/17530059.2013.814638","DOIUrl":"https://doi.org/10.1517/17530059.2013.814638","url":null,"abstract":"<p><strong>Introduction: </strong>Acute heart failure (AHF) is the leading cause of hospitalization in patients over 65 years, representing a heterogenic syndrome and a major burden, as it is associated with elevated health expenditures and high rates of mortality and readmission.</p><p><strong>Areas covered: </strong>This article provides a review of individual markers for risk stratification, including clinical, cardiorenal, hemodynamic, neurohormonal and cardiac biomarkers. In addition, aspects as complementary value, monitoring, risk models and events prediction are analyzed.</p><p><strong>Expert opinion: </strong>In clinical practice, risk stratification of AHF is complex and relies on the integration of bedside evaluation and laboratory biomarkers. Measures of congestion and perfusion, renal function, natriuretic peptides and cardiac troponins have become standard risk markers of death and/or readmission. However, there are numerous research findings that do not translate into an improved clinical management of individuals and a reduction of health costs. Research on this field needs to be redirected in a prospective manner in order to evaluate risk models in the emergency department. This would allow safe identification of patients at lower risk - who could be transferred and managed in out-patient facilities - as well as those biomarkers that, by reflecting pathophysiological routes, could be used as a guide to related therapeutics for improving outcomes. In addition, the identification of specific markers and models closely related with the risk of recurrent AHF is mandatory. Consequently, it is the time for clinicians working in networks to assume a leading role in translating risk assessment in AHF into clinical practice.</p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"379-92"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.814638","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31528108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Circulating markers for prognosis of hepatocellular carcinoma. 肝细胞癌预后的循环标志物。
Pub Date : 2013-07-01 Epub Date: 2013-05-06 DOI: 10.1517/17530059.2013.795146
Kwong-Fai Wong, Zhi Xu, Jinfei Chen, Nikki P Lee, John M Luk
INTRODUCTION Hepatocellular carcinoma (HCC) is a lethal liver malignancy with an exceptionally high incidence in Asia and Africa. The number of new cases in America and Europe is rapidly increasing, making HCC a worldwide health problem. Patients with early HCC can be treated by potentially curative interventions such as tumor resection, liver transplantation, and radiofrequency ablation, but unfortunately a considerable portion of them would develop tumor recurrence, which in many cases cannot be detected early. As such, it remains imperative to develop accurate, noninvasive blood tests, which can be applied in most clinical laboratories, for the measurement of treatment responses and the surveillance for tumor recurrence. AREAS COVERED This review article focuses on the recent discoveries of circulating proteins, DNA, microRNAs, cancer cells, and regulatory T cells as serological prognostic biomarkers for patients with HCC. These biomarkers not only have prognostic implications, but also hold promises to help physicians stratify patients for different interventions. EXPERT OPINIONS: Biomarkers will certainly serve as accurate tools in disease prognostication, changing the ways physicians stratify patients for specific therapy and monitor patients' responses toward treatment.
简介:肝细胞癌(HCC)是一种致命的肝脏恶性肿瘤,在亚洲和非洲发病率异常高。美国和欧洲的新病例数量正在迅速增加,使HCC成为一个全球性的健康问题。早期HCC患者可以通过肿瘤切除、肝移植和射频消融等具有治愈潜力的干预措施进行治疗,但不幸的是,其中相当一部分患者会出现肿瘤复发,而且在许多情况下无法早期发现。因此,开发准确的、无创的血液测试仍然是当务之急,这种测试可以应用于大多数临床实验室,用于测量治疗反应和监测肿瘤复发。涵盖领域:这篇综述文章主要关注循环蛋白、DNA、microrna、癌细胞和调节性T细胞作为HCC患者血清学预后生物标志物的最新发现。这些生物标志物不仅具有预后意义,而且还有望帮助医生对不同干预措施的患者进行分层。专家意见:生物标志物肯定会作为疾病预测的准确工具,改变医生对患者进行特定治疗的分层方式,并监测患者对治疗的反应。
{"title":"Circulating markers for prognosis of hepatocellular carcinoma.","authors":"Kwong-Fai Wong,&nbsp;Zhi Xu,&nbsp;Jinfei Chen,&nbsp;Nikki P Lee,&nbsp;John M Luk","doi":"10.1517/17530059.2013.795146","DOIUrl":"https://doi.org/10.1517/17530059.2013.795146","url":null,"abstract":"INTRODUCTION Hepatocellular carcinoma (HCC) is a lethal liver malignancy with an exceptionally high incidence in Asia and Africa. The number of new cases in America and Europe is rapidly increasing, making HCC a worldwide health problem. Patients with early HCC can be treated by potentially curative interventions such as tumor resection, liver transplantation, and radiofrequency ablation, but unfortunately a considerable portion of them would develop tumor recurrence, which in many cases cannot be detected early. As such, it remains imperative to develop accurate, noninvasive blood tests, which can be applied in most clinical laboratories, for the measurement of treatment responses and the surveillance for tumor recurrence. AREAS COVERED This review article focuses on the recent discoveries of circulating proteins, DNA, microRNAs, cancer cells, and regulatory T cells as serological prognostic biomarkers for patients with HCC. These biomarkers not only have prognostic implications, but also hold promises to help physicians stratify patients for different interventions. EXPERT OPINIONS: Biomarkers will certainly serve as accurate tools in disease prognostication, changing the ways physicians stratify patients for specific therapy and monitor patients' responses toward treatment.","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"319-29"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.795146","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31404798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 23
Use of ultrasound-assisted arthroscopy in rheumatology: an experience in 11 patients with different rheumatic diseases. 超声辅助关节镜在风湿病中的应用:11例不同风湿病患者的经验
Pub Date : 2013-07-01 Epub Date: 2013-04-24 DOI: 10.1517/17530059.2013.794136
Erberto Paresce, Orazio De Lucia, Eleonora Bruschi, Luca Giacomelli, Oscar Massimiliano Epis

The 'real time' capability of ultrasound (US) allows dynamic assessment of joint and tendon movements, which can often aid in the detection of structural abnormalities. The simultaneous use of arthroscopy (AS) and US is therefore a logical progression. Here the results of a series of 11 patients with different rheumatic diseases in whom a combined use of US and AS was adopted are reported.

超声(US)的“实时”能力允许对关节和肌腱运动进行动态评估,这通常有助于检测结构异常。因此,同时使用关节镜(AS)和US是一个合乎逻辑的进展。本文报告了11例不同风湿病患者联合使用US和AS的结果。
{"title":"Use of ultrasound-assisted arthroscopy in rheumatology: an experience in 11 patients with different rheumatic diseases.","authors":"Erberto Paresce,&nbsp;Orazio De Lucia,&nbsp;Eleonora Bruschi,&nbsp;Luca Giacomelli,&nbsp;Oscar Massimiliano Epis","doi":"10.1517/17530059.2013.794136","DOIUrl":"https://doi.org/10.1517/17530059.2013.794136","url":null,"abstract":"<p><p>The 'real time' capability of ultrasound (US) allows dynamic assessment of joint and tendon movements, which can often aid in the detection of structural abnormalities. The simultaneous use of arthroscopy (AS) and US is therefore a logical progression. Here the results of a series of 11 patients with different rheumatic diseases in whom a combined use of US and AS was adopted are reported. </p>","PeriodicalId":72996,"journal":{"name":"Expert opinion on medical diagnostics","volume":"7 4","pages":"309-12"},"PeriodicalIF":0.0,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1517/17530059.2013.794136","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31383076","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Expert opinion on medical diagnostics
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1