high risk

高风险
  • 文章类型: Journal Article
    急性呼吸道感染(ARIs)是美国重大的公共卫生问题这项研究旨在描述ARIs的疾病负担,并确定患有并发症的高风险美国人群。
    此范围审查搜索了PubMed和EBSCO数据库,以分析2013年至2022年的美国研究,重点是疾病负担,并发症,以及与ARIs相关的高危人群。
    该研究包括60项研究,表明ARI与显着的疾病负担和医疗保健资源利用(HRU)有关。2019年,呼吸道感染和结核病每10万人中造成339703例,大多数病例是上呼吸道感染,大多数死亡是下呼吸道感染。ARI负责数百万的门诊就诊,尤其是流感和肺炎球菌肺炎,和数十亿美元的间接成本。ARI是由多种病原体引起的,并且对住院和门诊就诊造成显著负担。与ARI相关的HRU的危险因素包括年龄,慢性疾病,和社会经济因素。
    该综述强调了ARIs的巨大疾病负担和年龄的影响,慢性疾病,和社会经济地位对发展并发症的影响。它强调了针对高危人群的针对性策略和有效的病原体检测以预防严重并发症并减少HRU的必要性。
    UNASSIGNED: Acute respiratory infections (ARIs) represent a significant public health concern in the U.S. This study aimed to describe the disease burden of ARIs and identify U.S. populations at high risk of developing complications.
    UNASSIGNED: This scoping review searched PubMed and EBSCO databases to analyze U.S. studies from 2013 to 2022, focusing on disease burden, complications, and high-risk populations associated with ARIs.
    UNASSIGNED: The study included 60 studies and showed that ARI is associated with a significant disease burden and healthcare resource utilization (HRU). In 2019, respiratory infection and tuberculosis caused 339,703 cases per 100,000 people, with most cases being upper respiratory infections and most deaths being lower respiratory infections. ARI is responsible for millions of outpatient visits, especially for influenza and pneumococcal pneumonia, and indirect costs of billions of dollars. ARI is caused by multiple pathogens and poses a significant burden on hospitalizations and outpatient visits. Risk factors for HRU associated with ARI include age, chronic conditions, and socioeconomic factors.
    UNASSIGNED: The review underscores the substantial disease burden of ARIs and the influence of age, chronic conditions, and socioeconomic status on developing complications. It highlights the necessity for targeted strategies for high-risk populations and effective pathogen detection to prevent severe complications and reduce HRU.
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  • 文章类型: Journal Article
    背景:虽然强烈建议将约束诱导运动疗法作为单侧脑瘫婴儿的干预措施,最佳剂量仍未定义。这项系统评价旨在确定约束诱导运动疗法强度的最有效水平,以增强不对称脑部病变或单侧脑瘫诊断高危婴儿的手动功能。
    方法:这项具有荟萃分析的系统评价包括对四个电子数据库的全面搜索,以确定符合以下标准的文章:随机对照试验,0-6岁高危儿童或单侧脑瘫儿童,以及涉及上肢功能的约束诱导运动疗法的治疗。结果相似的研究通过计算每个亚组的标准化平均差异得分进行汇总。和亚组每30小时分层总干预剂量(30-60,61-90,>90小时)。使用CochraneCollaboration的工具评估偏倚风险。
    结果:共纳入17项研究。Meta分析显示亚组之间存在显著差异。30-60h亚组在双手表现期间对自发使用受影响的上肢的影响较弱,抓取功能,以及父母对儿童使用上肢的频率的看法。此外,该亚组对父母对儿童如何有效使用受影响的上肢的看法表现出中等影响。
    结论:在应用约束诱导运动治疗方案时,使用30至60小时的剂量有望成为改善上肢功能结局和父母感知的最适合年龄和成本效益的方法。
    BACKGROUND: While constraint-induced movement therapy is strongly recommended as an intervention for infants with unilateral cerebral palsy, the optimal dosage remains undefined. This systematic review aims to identify the most effective level of intensity of constraint-induced movement therapy to enhance manual function in infants at high risk of asymmetric brain lesions or unilateral cerebral palsy diagnosis.
    METHODS: This systematic review with meta-analysis encompassed a comprehensive search across four electronic databases to identify articles that met the following criteria: randomised controlled trials, children aged 0-6 with at high risk or with unilateral cerebral palsy, and treatment involving constraint-induced movement therapy for upper limb function. Studies with similar outcomes were pooled by calculating the standardised mean difference score for each subgroup, and subgroups were stratified every 30 h of total intervention dosage (30-60, 61-90, >90 h). Risk of bias was assessed with Cochrane Collaboration\'s tool.
    RESULTS: Seventeen studies were included. Meta-analyses revealed significant differences among subgroups. The 30-60 h subgroup showed a weak effect for spontaneous use of the affected upper limb during bimanual performance, grasp function, and parents\' perception of how often children use their affected upper limb. Additionally, this subgroup demonstrated a moderate effect for the parents\' perception of how effectively children use their affected upper limb.
    CONCLUSIONS: Using a dosage ranging from 30 to 60 h when applying a constraint-induced movement therapy protocol holds promise as the most age-appropriate and cost-effectiveness approach for improving upper limb functional outcomes and parent\'s perception.
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  • 文章类型: Journal Article
    早产是指在妊娠第37周之前分娩活胎儿。早产可能源于各种因素,包括胎膜早破,自发性早产,或医学诱导的情况。早产可能导致严重和持久的困难,即使是存活的婴儿,因为它是五岁以下婴儿死亡的主要原因。许多国家已经实施了检测和跟踪可能在预产期之前分娩的孕妇的举措。有许多疗法可用于保护这些高危人群免受早产的破坏性影响,考虑到早产危险因素的复杂性。在预防措施中,预防性孕酮似乎有很大的希望,而宫颈环扎术在宫颈机能不全的情况下证明是有效的。相反,子宫托在降低早产风险方面没有明显的有益作用。定期产前检查对于频繁的患者评估和筛查潜在的危险因素至关重要。采用健康的生活方式会影响先兆子痫的风险,有规律的身体活动,富含纤维的饮食,和戒烟有助于降低早产的风险。由于证据不足,卧床休息预防早产的疗效尚无定论。本研究旨在探讨高危妇女避免早产的各种预防策略。
    Preterm birth is the delivery of a live fetus before the 37th week of gestation. Preterm birth may stem from various factors, including premature rupture of membranes, spontaneous preterm labor, or medically induced circumstances. Premature delivery can result in serious and long-lasting difficulties even for infants who survive, as it is the leading cause of death for infants under five years old. Numerous nations have implemented initiatives to detect and track pregnant women who may give birth before their due date. Numerous therapies are available to protect these at-risk groups from the devastating effects of premature delivery, given the complex nature of preterm birth risk factors. Among the preventive measures, prophylactic progesterone appears to hold significant promise, while cervical cerclage proves effective in cases of cervical insufficiency. Conversely, pessaries show no discernible beneficial effects in reducing the risk of preterm birth. Regular antenatal visits are imperative for frequent patient evaluation and screening for potential risk factors. Adopting a healthy lifestyle can influence the risk of developing preeclampsia, with regular physical activity, a fiber-rich diet, and smoking cessation serving to mitigate the risk of preterm birth. The efficacy of bed rest in preventing preterm birth remains inconclusive due to insufficient evidence. This study aims to explore various preventive strategies for averting premature birth in high-risk women.
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  • 文章类型: Journal Article
    背景:非典型表现越来越被认为是导致内科诊断错误的重要因素。然而,由于缺乏被认为是非典型表现的广泛适用的定义和标准,因此尚未评估解决非典型表现与诊断错误之间关联的研究。
    目的:本研究的目的是描述如何在内科诊断错误的研究中定义和测量非典型表现,并利用这些新信息开发新的标准来识别高风险的非典型表现。
    方法:本研究将遵循已建立的范围审查框架。纳入标准是根据参与者制定的,概念,和上下文框架。这篇综述将考虑满足以下所有标准的研究:包括成年患者(参与者);使用任何定义探索非典型表现和诊断错误之间的关联,标准,或测量以识别非典型的表现和诊断错误(概念);并专注于内科(上下文)。关于来源的类型,这项范围审查将考虑定量,定性,和混合方法研究设计;系统评价;和意见文件纳入。病例报告,案例系列,会议摘要将被排除在外。数据将通过MEDLINE提取,WebofScience,CINAHL,Embase,科克伦图书馆,和谷歌学者搜索。语言没有限制,并将包括从数据库开始到2023年12月31日索引的论文。两名独立审稿人(YH和RK)将进行研究选择和数据提取。提取的数据将包括有关患者特征的具体细节(例如,年龄,性别,和疾病),非典型表现和诊断错误的定义和测量方法,临床设置(例如,科室和门诊或住院),证据来源类型,以及与复习问题相关的非典型演示和诊断错误之间的关联。提取的数据将以表格形式呈现,并带有描述性统计,使我们能够识别非典型表现的关键组成部分或类型,并开发新的标准来识别非典型表现,以便将来进行诊断错误的研究。制定新标准将遵循采用归纳法进行基本定性内容分析的指导。
    结果:截至2024年1月,正在通过多个数据库进行文献检索。我们将在2024年12月完成这项研究。
    结论:本范围审查旨在提供严格的证据,以开发新的标准,以识别内科诊断错误高风险的非典型表现。这样的标准可以促进全面概念模型的开发,以了解非典型表现与内科诊断错误之间的关联。
    背景:开放科学框架;www.osf.io/27d5m。
    DERR1-10.2196/56933。
    BACKGROUND: Atypical presentations have been increasingly recognized as a significant contributing factor to diagnostic errors in internal medicine. However, research to address associations between atypical presentations and diagnostic errors has not been evaluated due to the lack of widely applicable definitions and criteria for what is considered an atypical presentation.
    OBJECTIVE: The aim of the study is to describe how atypical presentations are defined and measured in studies of diagnostic errors in internal medicine and use this new information to develop new criteria to identify atypical presentations at high risk for diagnostic errors.
    METHODS: This study will follow an established framework for conducting scoping reviews. Inclusion criteria are developed according to the participants, concept, and context framework. This review will consider studies that fulfill all of the following criteria: include adult patients (participants); explore the association between atypical presentations and diagnostic errors using any definition, criteria, or measurement to identify atypical presentations and diagnostic errors (concept); and focus on internal medicine (context). Regarding the type of sources, this scoping review will consider quantitative, qualitative, and mixed methods study designs; systematic reviews; and opinion papers for inclusion. Case reports, case series, and conference abstracts will be excluded. The data will be extracted through MEDLINE, Web of Science, CINAHL, Embase, Cochrane Library, and Google Scholar searches. No limits will be applied to language, and papers indexed from database inception to December 31, 2023, will be included. Two independent reviewers (YH and RK) will conduct study selection and data extraction. The data extracted will include specific details about the patient characteristics (eg, age, sex, and disease), the definitions and measuring methods for atypical presentations and diagnostic errors, clinical settings (eg, department and outpatient or inpatient), type of evidence source, and the association between atypical presentations and diagnostic errors relevant to the review question. The extracted data will be presented in tabular format with descriptive statistics, allowing us to identify the key components or types of atypical presentations and develop new criteria to identify atypical presentations for future studies of diagnostic errors. Developing the new criteria will follow guidance for a basic qualitative content analysis with an inductive approach.
    RESULTS: As of January 2024, a literature search through multiple databases is ongoing. We will complete this study by December 2024.
    CONCLUSIONS: This scoping review aims to provide rigorous evidence to develop new criteria to identify atypical presentations at high risk for diagnostic errors in internal medicine. Such criteria could facilitate the development of a comprehensive conceptual model to understand the associations between atypical presentations and diagnostic errors in internal medicine.
    BACKGROUND: Open Science Framework; www.osf.io/27d5m.
    UNASSIGNED: DERR1-10.2196/56933.
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  • 文章类型: Meta-Analysis
    高危多发性骨髓瘤(HRMM)与低生存率相关,尽管在抗白血病策略方面取得了许多进展。与HRMM患者的串联自体干细胞移植(auto-allo-SCT)相比,自体干细胞移植(auto-allo-SCT)产生了有争议的结果。我们进行了这项荟萃分析,以比较自allo-SCT和串联自SCT在HRMM患者中的疗效和安全性。
    Embase,科克伦图书馆,和PubMed数据库一直搜索到2023年3月。纳入了比较自动allo-SCT和串联自动SCT效果的前瞻性或回顾性研究。事件发生时间结果的危险比(HR)和95%置信区间(CI),使用随机效应模型汇总二分结局的比值比(ORs)和95CI。
    纳入了三项涉及491名患者的研究。尽管自动全SCT似乎与无进展生存期(PFS)的改善有关(HR[95CI],0.71[0.51-1.00])和完全反应(CR)(OR[95CI],3.16[1.67-5.99]),并降低复发/进展率(47%vs.55%)与串联自动SCT相比,总生存期(OS)无明显改善。与串联自动SCT相比,接受自动allo-SCT的患者表现出更高的移植相关死亡率(TRM)风险(11.9%vs.4.1%)和非复发死亡率(NRM)(12.3%vs.3.1%)。
    在HRMM患者中,与串联自动SCT相比,自动allo-SCT似乎与PFS和CR的改善有关,但它并没有导致操作系统的显着改善。此外,auto-allo-SCT组患者发生TRM和NRM的风险较高.自体同种异体SCT移植不应常规纳入HRMM治疗,而应视为研究性移植。
    UNASSIGNED: High-risk multiple myeloma (HRMM) is associated with poor survival, despite many advances in antimyeloma strategies. Autologous followed by allogeneic stem cell transplantation (auto-allo-SCT) has yielded controversial results compared to tandem autologous stem cell transplantation (auto-SCT) in patients with HRMM. We conducted this meta-analysis to compare the efficacy and safety of auto-allo-SCT and tandem-auto-SCT in patients with HRMM.
    UNASSIGNED: Embase, Cochrane Library, and PubMed databases were searched until March 2023. Prospective or retrospective studies comparing the effects of auto-allo-SCT and tandem-auto-SCT were included. Hazard ratios (HRs) and 95% confidence intervals (CIs) for time-to-event outcomes, and odds ratios (ORs) and 95%CIs for dichotomous outcomes were pooled using random-effects models.
    UNASSIGNED: Three studies involving 491 patients were included. Despite auto-allo-SCT seemed to be associated with improvements in progression-free survival (PFS) (HR [95%CI], 0.71 [0.51-1.00]) and complete response (CR) (OR [95%CI], 3.16 [1.67-5.99]), and reduced relapse/progression rates (47% vs. 55%) in comparison with tandem-auto-SCT, no marked improvement in overall survival (OS). In comparison to tandem-auto-SCT, patients assigned to auto-allo-SCT exhibited a higher risk of transplant-related mortality (TRM) (11.9% vs. 4.1%) and non-relapse mortality (NRM) (12.3% vs. 3.1%).
    UNASSIGNED: Auto-allo-SCT seemed to be associated with improvements in PFS and CR when compared to tandem-auto-SCT in patients with HRMM, but it did not lead to a significant improvement in OS. Furthermore, patients in the auto-allo-SCT group were at a higher risk of developing TRM and NRM. Auto-allo-SCT transplantation should not be routinely incorporated into HRMM therapy but rather should be considered investigational.
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  • 文章类型: Meta-Analysis
    系统评价和荟萃分析的目的是确定进入印度新生儿重症监护病房(NICU)的高危新生儿的父母所经历的压力和压力源。我们包括定量和定性研究。JoannaBriggs研究所关键评估清单和关键评估技能计划清单用于评估纳入研究的质量。在PubMed进行了系统的搜索,EMBASE,Scopus,EBSCOhost,WebofScience,ProQuest,MicrosoftAcademic,DOAJ,印度引文索引,和J-Gate确定相关研究。此外,在印度相关机构的网站上进行了在线手工搜索,妇女和儿童卫生部门,存储库,登记册,和儿科期刊。21项定量研究中有12项发现,由于与婴儿的分离和新生儿的医疗状况,母亲的压力高于父亲。一项定性研究报告称,财政负担,育儿角色的改变,对家庭问题的关注是父亲压力的重要原因。纳入研究的荟萃分析评估了孕产妇的患病率,父系,和父母的压力,并报告说,在所有子量表中,母亲的压力水平都高于父亲。父母最典型的压力源是新生儿容貌的变化,行为,改变了父母的角色。除了立即的NICU护理和互动,在当地(印度)背景下设计多组分干预措施时,必须考虑父母之间压力的其他触发因素.此外,父母的心理支持和定期咨询可以纳入标准新生儿重症监护政策。
    The aim of the systematic review and meta-analysis is to determine the stress and stressors experienced by the parents of high-risk neonates admitted to the neonatal intensive care unit (NICU) in India. We included both quantitative and qualitative studies. The Joanna Briggs Institute Critical Appraisal Checklist and Critical Appraisal Skill Programme checklist were used to assess the quality of included studies. A systematic search was conducted in PubMed, EMBASE, SCOPUS, EBSCOhost, Web of Science, ProQuest, Microsoft Academic, DOAJ, Indian Citation Index, and J-Gate to identify relevant studies. Additionally, online hand searching was performed on Indian websites of relevant institutions, women and child health departments, repositories, registries, and paediatric journals. Twelve of the 21 quantitative studies found that maternal stress was higher than fathers due to the separation from their babies and the medical condition of the neonate. One qualitative study reported that financial burden, alterations in the parenting role, and concern over domestic issues are significant causes of fathers\' stress. A meta-analysis of the included studies assessed the prevalence of maternal, paternal, and parental stress and reported that mothers experienced higher stress levels than fathers across all subscales. The most typical stressors for parents were changes in neonatal looks, behaviour, and altered parental roles. Beyond the immediate NICU care and interactions, other triggering factors of stress among parents must be considered to design multicomponent interventions in a local (Indian) context. Moreover, parental psychological support and regular counselling can be incorporated into the standard neonatal intensive care policy.
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  • 文章类型: Journal Article
    精神分裂症(SCZ)和双相情感障碍(BD)是严重的精神疾病,具有共同的临床特征和几种风险基因。有关其遗传基础的重要信息来自中间表型(IP),与普通人群相比,在未受影响的患者亲属(REL)中更为普遍,并且与疾病共同隔离。在IP中,神经心理学功能和神经影像学检查有可能为SCZ和BD的病理生理学提供有用的见解。在这种情况下,本叙述性综述全面概述了SCZ(SCZ-RELs)和BD(BD-RELs)未受影响亲属的神经心理功能缺陷和神经影像学改变的现有证据.总的来说,包括智力在内的认知功能缺陷,记忆,注意,执行功能,社会认知可以被认为是SCZ的IP。虽然BD-REL中认知改变的情况不太明确,与执行功能的控制相比,BD-RELs似乎表现更差,包括适应性思维,规划,自我监控,自我控制,和工作记忆。在神经成像标记中,SCZ-RELs的特征似乎在于皮质-纹状体-丘脑网络的结构和功能改变,虽然BD风险似乎与前额叶异常有关,temporal,丘脑,和边缘区域。总之,SCZ-RELs和BD-RELs呈现了患者和健康个体之间的认知和神经影像学改变的模式。SCZ-RELs和BD-RELs的类似异常可能是两种疾病共同遗传机制的表型表达,而神经心理学和神经影像学的特异性可能与两种疾病的差异症状表达有关。
    Schizophrenia (SCZ) and bipolar disorder (BD) are severe psychiatric disorders that share clinical features and several risk genes. Important information about their genetic underpinnings arises from intermediate phenotypes (IPs), quantifiable biological traits that are more prevalent in unaffected relatives (RELs) of patients compared to the general population and co-segregate with the disorders. Within IPs, neuropsychological functions and neuroimaging measures have the potential to provide useful insight into the pathophysiology of SCZ and BD. In this context, the present narrative review provides a comprehensive overview of the available evidence on deficits in neuropsychological functions and neuroimaging alterations in unaffected relatives of SCZ (SCZ-RELs) and BD (BD-RELs). Overall, deficits in cognitive functions including intelligence, memory, attention, executive functions, and social cognition could be considered IPs for SCZ. Although the picture for cognitive alterations in BD-RELs is less defined, BD-RELs seem to present worse performances compared to controls in executive functioning, including adaptable thinking, planning, self-monitoring, self-control, and working memory. Among neuroimaging markers, SCZ-RELs appear to be characterized by structural and functional alterations in the cortico-striatal-thalamic network, while BD risk seems to be associated with abnormalities in the prefrontal, temporal, thalamic, and limbic regions. In conclusion, SCZ-RELs and BD-RELs present a pattern of cognitive and neuroimaging alterations that lie between patients and healthy individuals. Similar abnormalities in SCZ-RELs and BD-RELs may be the phenotypic expression of the shared genetic mechanisms underlying both disorders, while the specificities in neuropsychological and neuroimaging profiles may be associated with the differential symptom expression in the two disorders.
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  • 文章类型: Journal Article
    背景:保留生育力手术(FSS)对于患有早期宫颈癌(ECC)的年轻女性是可行的选择;然而,某些危险因素可能需要额外的治疗并影响生育能力.这篇综述研究了这些危险因素的患病率和可用的治疗方案。
    方法:对包括ECC患者(IA1伴LVSI,接受FSS的IA2,IB1(FIGO2009)。
    结果:64篇文章,由计划参加FSS的4118名妇女组成,包括在内。在638名(15.5%)女性中发现了高危或中危组织学特征:5.1%的患者淋巴结阳性,4.1%的切缘阳性,0.3%有宫旁受累,1.0%有未指定的高风险特征,5.1%的患者有中危组织学(主要基于Sedlis标准).辅助治疗损害了所有使用辅助子宫切除术和/或(化学)放疗的妇女的生育能力(58.7%)。1351例(32.8%)患者接受辅助化疗,这可能会降低生育率。
    结论:在大多数女性中可以实现生育力保护;但是高危或中危因素需要更广泛的手术或放疗导致不孕。考虑到其有效性,辅助化疗可能是一种替代治疗选择,安全性和生育力保存的更高变化。宫旁受累的低发生率证明在<2cm的肿瘤中放弃宫旁切除术是合理的。
    BACKGROUND: Fertility-sparing surgery (FSS) is a viable option for young women with early-stage cervical cancer (ECC); however, certain risk factors may necessitate additional treatments and impact fertility. This review examines the prevalence of these risk factors and available treatment options.
    METHODS: A systematic search was conducted of studies including patients with ECC (IA1 with LVSI, IA2, IB1 (FIGO 2009)) who underwent FSS.
    RESULTS: Sixty-four articles, comprising a total of 4118 women planned for FSS, were included. High- or intermediate-risk histologic features were found in 638 (15.5%) women: 5.1% had positive lymph node(s), 4.1% had positive resection margins, 0.3% had parametrial involvement, 1.0% had unspecified high-risk features, and 5.1% had intermediate-risk histology (primarily based on the Sedlis criteria). Adjuvant treatment impaired fertility in all women with adjuvant hysterectomy and/or (chemo)radiation (58.7%). Adjuvant chemotherapy was given to 1351 (32.8%) patients, which may reduce fertility.
    CONCLUSIONS: Fertility preservation could be achieved in most women; but high- or intermediate-risk factors necessitate more extensive surgery or radiotherapy leading to infertility. Adjuvant chemotherapy could be an alternative treatment option considering its effectiveness, safety and higher change in fertility preservation. The low incidence of parametrial involvement justifies waiving parametrectomy in tumors < 2 cm.
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  • 文章类型: Journal Article
    精神病患者的一级亲属患精神分裂症的风险增加,但在符合既定临床高风险(CHR)标准的人群中,风险甚至更高,一种临床结构,最常包括减弱的精神病经历。据报道,三年内CHR青年的精神病转化率约为15-35%。准确识别精神病症状会恶化的个体将有助于早期干预,但这很难单独使用行为措施。基于大脑的风险标志物有可能提高CHR青年预测结果的准确性。这篇叙述性综述概述了用于调查精神病风险的神经影像学研究,包括涉及结构的研究,功能,和扩散成像,功能连接,正电子发射断层扫描,动脉自旋标记,磁共振波谱,和多模态方法。我们分别介绍了在CHR状态下观察到的发现以及与精神病进展或韧性相关的发现。最后,我们讨论了未来的研究方向,这些研究方向可以改善精神病高危人群的临床护理。
    The risk for developing schizophrenia is increased among first-degree relatives of those with psychotic disorders, but the risk is even higher in those meeting established criteria for clinical high risk (CHR), a clinical construct most often comprising of attenuated psychotic experiences. Conversion to psychosis among CHR youth has been reported to be about 15-35% over three years. Accurately identifying individuals whose psychotic symptoms will worsen would facilitate earlier intervention, but this has been difficult to do using behavior measures alone. Brain-based risk markers have the potential to improve the accuracy of predicting outcomes in CHR youth. This narrative review provides an overview of neuroimaging studies used to investigate psychosis risk, including studies involving structural, functional, and diffusion imaging, functional connectivity, positron emission tomography, arterial spin labeling, magnetic resonance spectroscopy, and multi-modality approaches. We present findings separately in those observed in the CHR state and those associated with psychosis progression or resilience. Finally, we discuss future research directions that could improve clinical care for those at high risk for developing psychotic disorders.
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  • 文章类型: Journal Article
    未经证实:先兆子痫是一种以轻度至重度高血压为特征的非常复杂的多系统疾病。
    UNASSIGNED:PubMed和Cochrane图书馆于2002年1月1日至2022年3月31日进行了检索,检索词为“先兆子痫”和“妊娠期高血压疾病”。我们还寻求国际学会和临床专业学院的指南,我们专注于2015年以后的出版物。
    UNASSIGNED:与这种病理生理学相关的主要问题是子宫胎盘灌注和缺血的减少。先兆子痫具有多因素成因,其预防重点包括识别高危和中危临床因素.先兆子痫的临床表现从无症状到胎儿和母亲的致命并发症不等。在严重的情况下,母亲可能会出现肾脏,神经学,肝,或血管疾病。主要的预防策略是使用低剂量的阿司匹林,从妊娠中期的开始到结束,并一直持续到妊娠结束。
    UNASSIGNED:先兆子痫是一种多系统疾病;我们不知道如何准确预测它。乙酰水杨酸在低剂量,以防止低百分比,尤其是远未足月子痫前期的患者。有证据表明,每周运动至少140分钟可减少妊娠期高血压和先兆子痫。目前,最安全的方法是终止妊娠。有必要提高子痫前期的预测和预防,此外,在长期的产后随访中需要更好的研究。
    UNASSIGNED: Preeclampsia is a very complex multisystem disorder characterized by mild to severe hypertension.
    UNASSIGNED: PubMed and the Cochrane Library were searched from January 1, 2002 to March 31, 2022, with the search terms \"pre-eclampsia\" and \"hypertensive disorders in pregnancy\". We also look for guidelines from international societies and clinical specialty colleges and we focused on publications made after 2015.
    UNASSIGNED: The primary issue associated with this physiopathology is a reduction in utero-placental perfusion and ischemia. Preeclampsia has a multifactorial genesis, its focus in prevention consists of the identification of high and moderate-risk clinical factors. The clinical manifestations of preeclampsia vary from asymptomatic to fatal complications for both the fetus and the mother. In severe cases, the mother may present renal, neurological, hepatic, or vascular disease. The main prevention strategy is the use of aspirin at low doses, started from the beginning to the end of the second trimester and maintained until the end of pregnancy.
    UNASSIGNED: Preeclampsia is a multisystem disorder; we do not know how to predict it accurately. Acetylsalicylic acid at low doses to prevent a low percentage, especially in patients with far from term preeclampsia. There is evidence that exercising for at least 140 min per week reduces gestational hypertension and preeclampsia. Currently, the safest approach is the termination of pregnancy. It is necessary to improve the prediction and prevention of preeclampsia, in addition, better research is needed in the long-term postpartum follow-up.
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