Cerebrovascular disease

脑血管疾病
  • 文章类型: Journal Article
    背景:由于伴随挛缩的存在,先前存在神经系统疾病的患者对肩关节成形术(SA)外科医生提出了一系列独特的挑战,肌肉无力,痉挛,这可能会影响肩关节置换术后的预后和并发症发生率。本系统评价的目的是评估先有神经系统疾病的患者在SA后的临床和功能结果。关注并发症和再手术率。
    方法:本系统评价是根据CochraneCollaboration概述的系统评价和荟萃分析(PRISMA)首选报告项目进行的。搜索PubMed,Medline图书馆,和EMBASE从开始至2023年9月进行研究,以获得神经系统疾病患者SA后结局的报告.收集研究人口统计学和结果信息,包括患者报告的结果和并发症发生率。纳入的主要研究的方法学质量采用MINORS评分系统进行评价。
    结果:1997年至2023年发表的20篇文章符合纳入标准。总的来说,13,126名患有7种不同神经系统疾病的神经系统疾病患者(帕金森病(PD),癫痫和癫痫,脑瘫(CP),脊髓灰质炎,Charcot神经病(CN),包括脑血管疾病(CVD)和多发性硬化(MS)。患者平均年龄为64.3岁(范围,33.0-75.8年),51.4%的患者为男性,术后平均随访时间为5.1年(范围,1.4-9.9年)。PD是报告最多的神经系统疾病(9项研究,8033名患者),其次是癫痫(4项研究,3,783名患者),和MS(1项研究,1077名患者)。虽然这些患者在SA后的结果确实有所改善,观察到高并发症和翻修率.
    结论:与没有神经系统疾病的患者相比,患有神经系统疾病的患者在SA后疼痛和功能得到改善,但报告的并发症和翻修率更高。这项系统评价为外科医生和患者提供了有关神经系统疾病患者SA的预期临床结果和可能的并发症的宝贵数据,这些数据可能有助于在考虑SA时做出共同的决策。
    BACKGROUND: Patients with pre-existing neurologic disorders present a unique set of challenges for shoulder arthroplasty (SA) surgeons due to the presence of concomitant contractures, muscle weakness, and spasticity, which may affect outcomes and complication rates after shoulder arthroplasty. The goal of this systematic review was to evaluate the clinical and functional outcomes after SA in patients pre-existing with neurologic disorders, focusing on complication and reoperation rates.
    METHODS: This systematic review was performed in adherence to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines outlined by Cochrane Collaboration. A search of PubMed, the Medline Library, and EMBASE from inception until September 2023 was conducted to obtain studies reporting on outcomes after SA in patients with neurological disorders. Study demographics and information on outcomes including patient-reported outcomes and complication rates were collected. The methodological quality of included primary studies was appraised using the MINORS scoring system.
    RESULTS: Twenty articles published between 1997 and 2023 met inclusion criteria. In total, 13,126 patients with neurological conditions with 7 different neurological disorders (Parkinson\'s disease (PD), epilepsy and seizures, cerebral palsy (CP), poliomyelitis, Charcot neuropathy (CN), cerebrovascular disease (CVD) and multiple sclerosis (MS)) were included. The mean patient age was 64.3 years (range, 33.0 - 75.8 years), 51.4% of patients were male, and the mean postoperative follow-up time was 5.1 years (range, 1.4 - 9.9 years). PD was the most reported neurological disorder (9 studies, 8,033 patients), followed by epilepsy (4 studies, 3,783 patients), and MS (1 study, 1,077 patients). While these patients did experience improvements in outcomes following SA, high complication and revision rates were noted.
    CONCLUSIONS: Patients with neurologic disorders demonstrate improvements in pain and function after SA but have higher reported complication and revision rates when compared with patients without neurologic conditions. This systematic review offers valuable data for both the surgeon and patient regarding anticipated clinical results and possible complications from SA in patients with neurologic disorders that may aid in shared decision-making when considering SA.
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  • 文章类型: Journal Article
    血压变异性(BPV)通过影响大脑结构和脑血管疾病来影响大脑健康,虽然机制知之甚少。脑血管系统的变化可能导致迟发性抑郁症,认知障碍,和痴呆症,然而,BPV与抑郁和焦虑之间的关系尚不清楚,由于过去研究的方法差异和不一致。这篇综述旨在阐明成人BPV与抑郁和焦虑之间的关系,以了解BPV在认知健康中的作用机制。从开始到2024年1月的系统搜索在Embase上进行,PubMed,PsycINFO,和WebofScience。通过逐次跳动来评估BPV的研究,24小时,如果抑郁和/或焦虑的标准化评估报告为线性关联,或访视符合资格,或平均控制组和影响组之间的差异。共有14篇文章报告13个样本,N=5055人符合纳入标准(女性比例中位数=61%,范围0%-76%)。由于研究中BPV测量和指标的方法异质性,无法进行荟萃分析。在抑郁症研究中观察到混合结果,方向不一致和变化,联合的力量,和BPV指标。只有三项研究的证据表明收缩压变异系数与焦虑之间存在线性关系。总的来说,这些发现有助于理解BPV与大脑健康之间的关系,这表明BPV和对认知功能至关重要的大脑结构之间的任何关系都独立于抑郁,并且仅适度地涉及焦虑。
    Blood pressure variability (BPV) impacts brain health by influencing brain structure and cerebrovascular pathologies, though the mechanisms are poorly understood. Changes in the cerebrovasculature may lead to late-onset depression, cognitive impairment, and dementia, however the relationship between BPV with depression and anxiety remains unclear, due to methodological differences and inconsistencies in past research. This review aims to clarify the association between BPV with depression and anxiety in adults to inform understandings of the mechanisms implicating BPV in cognitive health. A systematic search from inception through to January 2024 was performed on Embase, PubMed, PsycINFO, and Web of Science. Studies that assessed BPV quantified by beat-to-beat, 24-hour, or visit-to-visit were eligible if the standardised assessment of depression and/or anxiety were reported as a linear association, or mean differences across control and affect groups. A total of 14 articles reporting on 13 samples and N = 5055 persons met the inclusion criteria (median female proportion = 61 %, range 0 % - 76 %). A meta-analysis was not possible due to methodological heterogeneity in BPV measurements and metrics across studies. Mixed results were observed across depression studies with inconsistencies and variation in the direction, strength of association, and BPV metric. There was weak evidence from only three studies to support a linear association between systolic coefficient of variation and anxiety. Collectively, the findings contribute to understanding the association between BPV and brain health, suggesting that any relationship between BPV and brain structures critical for cognitive function are independent of depression and only modestly implicate anxiety.
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  • 文章类型: Journal Article
    视网膜静脉阻塞(RVO)和脑血管疾病(CVD)具有共同的危险因素,并且可能是独立相关的;然而,这种联系的强度和性质尚不清楚.我们进行了系统评价和荟萃分析,根据PubMed的研究,Scopus,EMBASE,WebofScience,和谷歌学者直到2024年1月6日,旨在澄清这种关系。符合条件的研究包括观察RVO患者卒中发生率超过一年的队列。集合效应估计是使用随机效应模型计算的,通过亚组分析评估RVO类型(中央和分支)和卒中亚型(缺血性和出血性)之间的关联。共纳入了10项队列研究,共428,650名参与者(86,299名RVO患者)。与对照组相比,RVO患者出现卒中风险显著增加(合并风险比[RR]=1.38,95%置信区间(95CI)=1.34-1.41)。亚组分析表明,RVO患者发生缺血性卒中(RR=1.37,95CI=1.32-1.42)和出血性卒中(RR=1.55,95CI=1.08-2.22)的风险均升高。此外,中央(RR=1.50,95CI=1.27-1.78)和分支(RR=1.41,95CI=1.32-1.50)RVO均与卒中风险相关.敏感性分析证实了不同标准的一致结果,漏斗图显示无发表偏倚。RVO显着增加缺血性和出血性中风的风险,无论RVO类型,表明这些条件之间存在很强的独立联系。
    Retinal vein occlusion (RVO) and cerebrovascular disease share common risk factors and may be independently associated; however, the strength and nature of this association remain unclear. We conducted a systematic review and meta-analysis, informed by studies from PubMed, Scopus, EMBASE, Web of Science, and Google Scholar until January 6, 2024, aimed to clarify this relationship. Eligible studies included cohorts observing stroke incidence in RVO patients for over a year. Pooled effect estimates were calculated using random-effects models, with subgroup analyses evaluating associations between RVO types (central and branch) and stroke subtypes (ischemic and hemorrhagic). Ten cohort studies with a total of 428,650 participants (86,299 RVO patients) were included. Compared to controls, RVO patients exhibited a significantly increased risk of stroke (pooled risk ratio [RR]=1.38, 95 % confidence interval (95 %CI)=1.34-1.41). Subgroup analyses indicated elevated risk for both ischemic (RR=1.37, 95 %CI=1.32-1.42) and hemorrhagic (RR=1.55, 95 %CI=1.08-2.22) strokes in RVO patients. Additionally, both central (RR=1.50, 95 %CI=1.27-1.78) and branch (RR=1.41, 95 %CI=1.32-1.50) RVO were associated with stroke risk. Sensitivity analyses confirmed consistent results across various criteria, and funnel plots indicated no publication bias. RVO significantly increases the risk of both ischemic and hemorrhagic stroke, regardless of RVO type, suggesting a strong independent association between these conditions.
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  • 文章类型: Case Reports
    Millard-Gubler综合征是由下脑桥区域的病变引起的脑桥综合征。它的特征是同侧面瘫和VI轻瘫和对侧腕臂麻痹。我们介绍一个女病人的病例,G4P2A1,妊娠21周时,患有先兆子痫,视力模糊的投诉,复视,和右侧偏瘫,Millard-Gubler综合征的临床诊断。神经影像学检查显示,向球旁桥交界处中央部分的实质内出血。进行了广泛的病因研究,以确定妊娠期高血压疾病综合征的原因。早期死产分娩后,患者的神经功能缺损得到了令人满意的改善。
    Millard-Gubler syndrome is a pontine syndrome caused by a lesion in the lower pons region. It is characterised by ipsilateral facial paralysis and VI paresis and contralateral brachiocrural palsy. We present the case of a female patient, G4P2A1, at 21 weeks of gestation, with preeclampsia, complaints of blurred vision, diplopia, and right hemiparesis, in whom a clinical diagnosis of Millard-Gubler syndrome was made. Neuroimaging showed an intraparenchymal haemorrhage towards the central portion of the bulbopontine junction. An extensive aetiological study was carried out to determine the cause of the hypertensive disorder syndrome during pregnancy. The patient improved satisfactorily from the neurological deficit after delivery of an early stillbirth.
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  • 文章类型: Journal Article
    磁共振成像(MRI)的研究-可见血管周围空间(PVS)最近有所增加,因为对不同疾病和人群的研究结果正在巩固它们与睡眠的联系,疾病表型,和整体健康指标。随着世界范围内联盟的建立和大型数据库的可用性,允许自动处理所有这些丰富信息的计算方法正变得越来越重要。已经提出了几种计算方法来评估MRI的PVS,并努力总结和评估应用最广泛的方法。我们系统地审查和荟萃分析了截至2023年9月的所有出版物,描述了这一发展,改进,或应用MRI计算PVS定量方法。我们分析了67种方法和60种实施方法的应用,112种出版物两个应用最广泛的是使用形态滤波器来增强PVS样结构,Frangi是大多数人的首选,以及使用具有或不具有剩余连接的U-Net配置。从18岁开始的老年人或由成年人组成的人口研究是,总的来说,比使用临床样本的研究更频繁。PVS主要通过1.5T和/或3T扫描仪获得的T2加权MRI进行评估,尽管使用它与T1加权和FLAIR图像的组合也很丰富。研究的常见关联包括年龄,性别,高血压,糖尿病,白质高强度,睡眠和认知,与职业有关,种族,和遗传/可遗传特征也在探索中。尽管有希望的改进可以克服诸如噪音和与其他困惑的区别等障碍,现在最重要的是,需要共同努力进行更广泛的测试,并增加最有前途的方法的可用性。
    Research into magnetic resonance imaging (MRI)-visible perivascular spaces (PVS) has recently increased, as results from studies in different diseases and populations are cementing their association with sleep, disease phenotypes, and overall health indicators. With the establishment of worldwide consortia and the availability of large databases, computational methods that allow to automatically process all this wealth of information are becoming increasingly relevant. Several computational approaches have been proposed to assess PVS from MRI, and efforts have been made to summarise and appraise the most widely applied ones. We systematically reviewed and meta-analysed all publications available up to September 2023 describing the development, improvement, or application of computational PVS quantification methods from MRI. We analysed 67 approaches and 60 applications of their implementation, from 112 publications. The two most widely applied were the use of a morphological filter to enhance PVS-like structures, with Frangi being the choice preferred by most, and the use of a U-Net configuration with or without residual connections. Older adults or population studies comprising adults from 18 years old onwards were, overall, more frequent than studies using clinical samples. PVS were mainly assessed from T2-weighted MRI acquired in 1.5T and/or 3T scanners, although combinations using it with T1-weighted and FLAIR images were also abundant. Common associations researched included age, sex, hypertension, diabetes, white matter hyperintensities, sleep and cognition, with occupation-related, ethnicity, and genetic/hereditable traits being also explored. Despite promising improvements to overcome barriers such as noise and differentiation from other confounds, a need for joined efforts for a wider testing and increasing availability of the most promising methods is now paramount.
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  • 文章类型: Journal Article
    微RNA(miRNA)是通过与靶信使RNA(mRNA)结合来调节基因表达的非编码小RNA分子。miRNA与多种心血管和神经系统疾病有关,比如心肌梗塞,各种基因的心肌病,节律性疾病,神经退行性疾病和中风。许多研究都集中在miRNA模式的表达与心房颤动(AF)或急性缺血性卒中(AIS)相关。只有少数研究探讨了房颤和AIS患者中miRNAs的表达模式,以便不仅提供预防性信息,而且确定治疗潜力.因此,这篇综述的目的是总结18篇关于房颤和相关AIS这一综合主题的现有手稿,并阐明最常被提及的miRNAs-1,-19,-21,-145和-146的分子机制以及心脏和大脑的靶标.由此,可以得出未来可能的诊断和治疗后果。
    MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression by binding to target messenger RNAs (mRNAs). miRNAs have been implicated in a variety of cardiovascular and neurological diseases, such as myocardial infarction, cardiomyopathies of various geneses, rhythmological diseases, neurodegenerative illnesses and strokes. Numerous studies have focused on the expression of miRNA patterns with respect to atrial fibrillation (AF) or acute ischemic stroke (AIS) However, only a few studies have addressed the expression pattern of miRNAs in patients with AF and AIS in order to provide not only preventive information but also to identify therapeutic potentials. Therefore, the aim of this review is to summarize 18 existing manuscripts that have dealt with this combined topic of AF and associated AIS in detail and to shed light on the most frequently mentioned miRNAs-1, -19, -21, -145 and -146 with regard to their molecular mechanisms and targets on both the heart and the brain. From this, possible diagnostic and therapeutic consequences for the future could be derived.
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  • 文章类型: Journal Article
    有一个共同的共识,即阿尔茨海默病(AD)本质上是复杂的;否则,在其病因学基础上仍然存在普遍分歧,已经提出了许多替代假设。
    对描述过去几十年发表的AD假设和理论的原始手稿进行范围审查。
    我们审查了从开放数据库中提取的13,807篇参考文献中的131篇原始手稿,这些手稿符合我们的纳入标准。每个条目的特征是具有单因素或多因素焦点,并分配给15个理论分组之一。使用开放引文工具跟踪影响。
    从假设生成的角度可以看出三个阶段,四分之三的研究提出了一个以单焦点为特征的假设。最重要的理论分组是淀粉样蛋白组,其次是代谢和线粒体功能障碍,然后是感染和脑血管.最近,遗传学,尤其是肠道/大脑相互作用的证据脱颖而出。
    当一起查看时,这些多方面的报道强化了AD影响多个亚细胞的概念,细胞,解剖学,和生理系统同时存在,但个体之间的程度不同。提供所有系统及其相互作用的全面视图的挑战仍然存在,以及管理这种固有复杂性的方法。
    UNASSIGNED: There is a common agreement that Alzheimers disease (AD) is inherently complex; otherwise, a general disagreement remains on its etiological underpinning, with numerous alternative hypotheses having been proposed.
    UNASSIGNED: To perform a scoping review of original manuscripts describing hypotheses and theories of AD published in the past decades.
    UNASSIGNED: We reviewed 131 original manuscripts that fulfilled our inclusion criteria out of more than 13,807 references extracted from open databases. Each entry was characterized as having a single or multifactorial focus and assigned to one of 15 theoretical groupings. Impact was tracked using open citation tools.
    UNASSIGNED: Three stages can be discerned in terms of hypotheses generation, with three quarter of studies proposing a hypothesis characterized as being single-focus. The most important theoretical groupings were the Amyloid group, followed by Metabolism and Mitochondrial dysfunction, then Infections and Cerebrovascular. Lately, evidence towards Genetics and especially Gut/Brain interactions came to the fore.
    UNASSIGNED: When viewed together, these multi-faceted reports reinforce the notion that AD affects multiple sub-cellular, cellular, anatomical, and physiological systems at the same time but at varying degree between individuals. The challenge of providing a comprehensive view of all systems and their interactions remains, alongside ways to manage this inherent complexity.
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  • 文章类型: Journal Article
    目的:多血管疾病具有显著的全球负担,并且与每增加一个血管区域的主要不良心脏事件的风险增加相关。这篇综述的目的是强调风险因素,相关结果,新兴的遗传标记,和多血管疾病筛查和治疗的证据。
    结果:多血管疾病是在两个或多个血管床中存在动脉粥样硬化。它有一个巨大的全球负担,已知动脉粥样硬化患者的患病率为30-70%。多血管疾病患者心血管死亡率升高,心肌梗塞和中风,尤其是在2型糖尿病患者等高危亚组中,每增加一个血管区域,不良结局的风险就会逐步增加.遗传分析表明,一些个体可能具有遗传倾向,而其他人则表现出更高水平的动脉粥样硬化脂蛋白和炎症标志物。除非患者是高风险患者,否则目前主要的心血管社会不建议对无症状疾病进行常规筛查。虽然没有既定的升级治疗方案,现有指南提倡降脂治疗.此外,最近的研究已经证明了抗血栓药物的益处,如P2Y12抑制剂和低剂量抗凝,但是这些药物的最佳时机和剂量尚未确定,在多血管人群中,缺血获益必须与出血风险增加相平衡.由于与多血管疾病相关的高患病率和风险,早期识别和强化治疗对减少疾病进展至关重要.需要未来的研究来制定筛查方案,并确定预防缺血事件的最佳治疗时机和剂量。
    OBJECTIVE: Polyvascular disease has a significant global burden and is associated with increased risk of major adverse cardiac events with each additional vascular territory involved. The purpose of this review is to highlight the risk factors, associated outcomes, emerging genetic markers, and evidence for screening and treatment of polyvascular disease.
    RESULTS: Polyvascular disease is the presence of atherosclerosis in two or more vascular beds. It has a significant global burden, with a prevalence of 30-70% in patients with known atherosclerosis. Patients with polyvascular disease experience elevated rates of cardiovascular death, myocardial infarction and stroke, especially among high-risk subgroups like those with type 2 diabetes mellitus and there is a step-wise increased risk of adverse outcomes with each additional vascular territory involved. Genetic analyses demonstrate that some individuals may carry a genetic predisposition, while others exhibit higher levels of atherogenic lipoproteins and inflammatory markers. Routine screening for asymptomatic disease is not currently recommended by major cardiovascular societies unless patients are high-risk. While there are no established protocols for escalating treatment, existing guidelines advocate for lipid-lowering therapy. Additionally, recent studies have demonstrated benefit from antithrombotic agents, such as P2Y12 inhibitors and low-dose anticoagulation, but the optimal timing and dosage of these agents has not been established, and the ischemic benefit must be balanced against the increased risk of bleeding in the polyvascular population. Due to the high prevalence and risks associated with polyvascular disease, early identification and treatment intensification are crucial to reduce disease progression. Future research is needed to develop screening protocols and determine the optimal timing and dosing of therapy to prevent ischemic events.
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  • 文章类型: Journal Article
    目的:约束诱导运动疗法(CIMT),一种通过强化功能任务鼓励使用受影响的上肢的疗法,能有效促进慢性脑卒中患者的上肢功能。这项研究确定了使用远程康复的CIMT与传统CIMT在改善成年慢性中风患者轻中度上肢运动功能方面的有效性。
    方法:通过搜索电子数据库和扫描文章的参考列表来确定符合条件的研究。ReviewManager5.4用于确定组比较的标准化平均差异和95%置信区间的合并平均效应大小。视觉异质性,I2统计数据,采用卡方检验衡量纳入研究之间的异质性。我们使用GDT评估证据质量,用于创建证据摘要和医疗保健建议的软件。
    结果:本综述包括两项随机对照试验。共有109名参与者(70名男性,39名女性)进行了评估。一项研究中卒中时间≥6个月,另一项研究中卒中时间≥1年。使用Wolf运动功能测试测量进行功能性运动时上肢运动功能的改善。与传统CIMT相比,使用远程康复治疗的CIMT在改善慢性中风患者上肢功能方面的有效性具有中等质量。这表明两组之间没有显著差异(平均差[95%CI]:-0.04[-0.42,0.33])。
    结论:在改善慢性卒中患者上肢运动功能方面,使用远程康复的CIMT并不优于传统CIMT。使用远程康复的CIMT可能会改善获得治疗的机会,尽量减少SARS-CoV-2的风险,减少慢性中风患者的旅行。
    OBJECTIVE: Constraint-induced movement therapy (CIMT), a therapy that encourages the use of the affected upper limb through intensive functional tasks, effectively promotes upper limb function in patients with chronic stroke. This study determined the effectiveness of CIMT using telerehabilitation compared with traditional CIMT in improving mild to moderate upper limb motor function in adult patients with chronic stroke.
    METHODS: Eligible studies were identified by searching electronic databases and scanning the reference lists of articles. Review Manager 5.4 was used to determine the pooled mean effect size of the standardized mean difference and 95% confidence interval for the group comparison. Visual heterogeneity, I2 statistic, and chi-square test were used to measure the heterogeneity between the included studies. We evaluated the quality of evidence using GRADEpro GDT, software for creating evidence summaries and healthcare recommendations.
    RESULTS: Two randomized controlled trials were included in this review. A total of 109 participants (70 male, 39 female) were evaluated. The time since the stroke was ≥6 months in one study and ≥1 year in another study. Improvements in upper limb motor function while performing functional movements were measured using the Wolf Motor Function Test. The evidence for the effectiveness of CIMT using telerehabilitation compared with traditional CIMT in improving the upper extremity function in patients with chronic stroke is of moderate quality. This suggests no significant difference between the groups (mean difference [95% CI]: -0.04 [-0.42, 0.33]).
    CONCLUSIONS: CIMT using telerehabilitation is not superior to traditional CIMT in improving patients\' upper extremity motor function with chronic stroke. CIMT using telerehabilitation may improve access to treatment, minimize SARS-CoV-2 risk, and reduce travel in patients with chronic stroke.
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  • 文章类型: Journal Article
    颅内脑动脉狭窄(ICAS)的早期和准确分层对于指导治疗管理和提高脑血管疾病(CVD)患者的预后至关重要。数字减影血管造影(DSA)是一种侵入性且昂贵的手术,但却是诊断ICAS的金标准。近年来,经颅彩色编码多普勒超声(TCCD)已被认为是准确诊断ICAS的有用成像方法。然而,TCCD对CVD患者ICAS的分层诊断准确性尚不清楚.因此,本系统综述和荟萃分析旨在评估TCCD在CVD患者颅内狭窄闭塞分层中的诊断准确性.总共六个数据库-Embase,CINAHL,Medline,PubMed,谷歌学者,和WebofScience(核心集合)-搜索了评估TCCD在对ICAS进行分层时的诊断准确性的研究。使用Meta-DiSc1.4进行荟萃分析。诊断准确性研究的质量评估工具版本2(QUADAS-2)评估了偏倚的风险。18项研究符合所有资格标准。与DSA作为参考标准相比,TCCD在对患有CVD的患者的颅内狭窄闭塞进行分层方面表现出很高的合并诊断准确性(灵敏度=90%;特异性=87%;AUC=97%)。此外,超声参数收缩期峰值速度(PSV)和平均血流速度(MFV)的诊断准确率相当,为“AUC=0.96”。总之,TCCD可能是一个贵族,安全,和准确的DSA替代成像技术,可以为CVD患者的颅内狭窄闭塞分层提供有用的诊断信息。在获得DSA受限的临床病例中,应考虑TCCD。
    The early and accurate stratification of intracranial cerebral artery stenosis (ICAS) is critical to inform treatment management and enhance the prognostic outcomes in patients with cerebrovascular disease (CVD). Digital subtraction angiography (DSA) is an invasive and expensive procedure but is the gold standard for the diagnosis of ICAS. Over recent years, transcranial color-coded Doppler ultrasound (TCCD) has been suggested to be a useful imaging method for accurately diagnosing ICAS. However, the diagnostic accuracy of TCCD in stratifying ICASs among patients with CVD remains unclear. Therefore, this systematic review and meta-analysis aimed at evaluating the diagnostic accuracy of TCCD in the stratification of intracranial steno-occlusions among CVD patients. A total of six databases-Embase, CINAHL, Medline, PubMed, Google Scholar, and Web of Science (core collection)-were searched for studies that assessed the diagnostic accuracy of TCCD in stratifying ICASs. The meta-analysis was performed using Meta-DiSc 1.4. The Quality Assessment of Diagnostic Accuracy Studies tool version 2 (QUADAS-2) assessed the risk of bias. Eighteen studies met all of the eligibility criteria. TCCD exhibited a high pooled diagnostic accuracy in stratifying intracranial steno-occlusions in patients presenting with CVD when compared to DSA as a reference standard (sensitivity = 90%; specificity = 87%; AUC = 97%). Additionally, the ultrasound parameters peak systolic velocity (PSV) and mean flow velocity (MFV) yielded a comparable diagnostic accuracy of \"AUC = 0.96\". In conclusion, TCCD could be a noble, safe, and accurate alternative imaging technique to DSA that can provide useful diagnostic information in stratifying intracranial steno-occlusions in patients presenting with CVD. TCCD should be considered in clinical cases where access to DSA is limited.
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