Neurobehavioral manifestations

神经行为表现
  • 文章类型: Journal Article
    背景:神经行为合并症对癫痫患者的生活质量有不利影响,然而追踪它们的影响是具有挑战性的,因为行为可能会随着癫痫发作和抗癫痫药物(ASM)副作用而变化.智能手机有可能客观地监测日常神经行为模式。我们介绍了一个二十多岁的男性患有抗药性局灶性癫痫的病例,其中我们确定了ASM戒断和惊厥性癫痫发作对其触摸屏互动的影响。
    方法:使用专用应用程序,我们记录了超过185天的718,357次互动的时间戳。我们通过使用联合间隔分布(JID)根据交互的下一个间隔动态来划分各种智能手机行为。在两个ASM负载转换期间,即在逐渐减少和逐渐减少与重新开始药物治疗之前,我们使用基于集群的置换测试来比较JID。我们还将癫痫发作日的JID与前3天的平均值进行了比较。
    结果:基于聚类的排列检验显示出显著差异,随着逐渐减少和药物重新开始时的逆转,下一个间隔的动态加速。与前3天相比,惊厥当天的下一个间隔动态显着减慢。
    结论:我们的研究结果表明,智能手机触摸屏交互的时间动态可能有助于监测神经系统护理中的神经行为合并症。
    BACKGROUND: Neurobehavioural comorbidities have a detrimental effect on the quality of life of people with epilepsy, yet tracking their impact is challenging as behaviour may vary with seizures and anti-seizure medication (ASM) side effects. Smartphones have the potential to monitor day-to-day neurobehavioural patterns objectively. We present the case of a man in his late twenties with drug-resistant focal epilepsy in whom we ascertained the effects of ASM withdrawal and a convulsive seizure on his touchscreen interactions.
    METHODS: Using a dedicated app, we recorded over 185 days the timestamps of 718,357 interactions. We divided the various smartphone behaviours according to the next-interval dynamics of the interactions by using a joint interval distribution (JID). During two ASM load transitions, namely before versus during tapering and tapering versus restarting medication, we used cluster-based permutation tests to compare the JIDs. We also compared the JID of the seizure day to the average of the previous 3 days.
    RESULTS: The cluster-based permutation tests revealed significant differences, with accelerated next-interval dynamics during tapering and a reversal upon medication restart. The day of the convulsion exhibited a marked slowing of next-interval dynamics compared to the preceding 3 days.
    CONCLUSIONS: Our findings suggest that the temporal dynamics of smartphone touchscreen interactions may help monitor neurobehavioural comorbidities in neurological care.
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  • 文章类型: Journal Article
    在日本,高级脑功能障碍(HBD)的诊断标准于2005年提出,以满足社会对患者及其家属的支持需求.脑外伤后的认知功能障碍问题并非日本独有。本研究旨在从HBD患者家属的角度揭示其现状,重点关注日本诊断标准建立前后的变化。我们对支持HBD患者的家庭成员进行了问卷调查。问卷包括病因情况,卫生专业人员对HBD的解释,和他们遇到的问题/困难。这项研究涉及278例HBD患者的家庭成员(男性=211,年龄49岁)。主要原因是头部损伤(n=139)。与2005年前诊断的患者相比,2005年后获得急性期(一个月内)病情信息的家庭成员比例明显更高(p<0.001),包括医生(p<0.001)。近一半的家庭认为专业人员对HBD缺乏认识是一个问题。在日本,社会对HBD的认识逐渐提高,特别是在现行诊断标准实施后,随着时间的推移,早期诊断也在稳步增加。然而,仍然存在那些没有得到适当诊断的人。为了挽救那些病人和留下的家属,我们提出了一些建议,以进一步加强日本的临床实践和医疗保健系统.
    In Japan, the diagnostic criteria for the higher brain dysfunction (HBD) emerged in 2005 in response to social needs for support for the patients and their families. The issue of cognitive dysfunction after brain trauma is not unique to Japan. The purpose of this study was to reveal the current status of family members of HBD patients from their perspective, focusing on the changes before and after the establishment of diagnostic criteria in Japan. We conducted a questionnaire survey for family members supporting the HBD patients. The questionnaire included the causative condition, explanation on HBD by health professionals, and problems/difficulties they encountered. This research involved family members of 278 HBD cases (males = 211, age 49 years). The major underlying cause was head injury (n = 139). Compared to patients diagnosed pre-2005, a significantly larger proportion of family members after 2005 received information on the condition during the acute phase (within one month) (p < 0.001), including that from physicians (p < 0.001). Nearly half of the families cited a lack of awareness of HBD among the professionals as a problem. In Japan, awareness of HBD in the society is gradually increasing especially after the current diagnostic criteria were implemented, and there has been a steady increase over time in early diagnosis. Yet, there still remain those not appropriately diagnosed. To salvage those patients and the families left behind, we are suggesting several recommendations to further augment clinical practice and the healthcare systems in Japan.
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  • 文章类型: Preprint
    我们找到了LLM,传统的机器学习,深度学习在认知衰退识别方面有不同的错误特征,和LLM的合奏,机器学习,和深度学习实现了最先进的表现。
    早期发现老年人认知能力下降有助于临床试验登记和及时的医疗干预。本研究旨在应用,评估,并比较先进的自然语言处理技术,以识别临床笔记中认知能力下降的迹象。
    这项研究,在弥撒将军布莱根(MGB)进行,波士顿,MA,包括2019年诊断为轻度认知障碍(MCI)前4年≥50岁患者的临床记录。关于认知衰退的注释部分是手动标记的。使用与认知功能相关的关键字过滤的4,949个注释部分的随机样本用于传统AI模型开发,和200个随机子集用于LLM和提示开发;另一个1996年没有关键字过滤的笔记部分的随机样本用于测试。大型语言模型(LLM)的提示模板,亚马逊网络服务上的Llama2和微软Azure上的GPT-4,采用多种提示方法开发,以选择最佳的基于LLM的方法。使用XGBoost和基于分层注意力的深度神经网络模型进行基线比较。然后使用多数票构建了三个模型的集合。
    GPT-4表现出优于Llama2的准确性和效率。集成模型优于单个模型,达到90.3%的精度,召回94.2%,F1评分为92.2%。值得注意的是,与表现最好的单一模型相比,集成模型的精度显着提高(从70%-79%到90%以上)。误差分析显示,至少有一个模型错误地预测了63个样本;然而,只有2例(3.2%)是所有模型的相互错误,表明它们之间存在不同的误差曲线。
    我们的研究结果表明,LLM和传统模型表现出不同的误差曲线。在EHR数据上的LLM和本地训练的机器学习模型的集合被发现是互补的,提高性能和提高诊断的准确性。
    UNASSIGNED: Large language models (LLMs) have shown promising performance in various healthcare domains, but their effectiveness in identifying specific clinical conditions in real medical records is less explored. This study evaluates LLMs for detecting signs of cognitive decline in real electronic health record (EHR) clinical notes, comparing their error profiles with traditional models. The insights gained will inform strategies for performance enhancement.
    UNASSIGNED: This study, conducted at Mass General Brigham in Boston, MA, analyzed clinical notes from the four years prior to a 2019 diagnosis of mild cognitive impairment in patients aged 50 and older. We used a randomly annotated sample of 4,949 note sections, filtered with keywords related to cognitive functions, for model development. For testing, a random annotated sample of 1,996 note sections without keyword filtering was utilized. We developed prompts for two LLMs, Llama 2 and GPT-4, on HIPAA-compliant cloud-computing platforms using multiple approaches (e.g., both hard and soft prompting and error analysis-based instructions) to select the optimal LLM-based method. Baseline models included a hierarchical attention-based neural network and XGBoost. Subsequently, we constructed an ensemble of the three models using a majority vote approach.
    UNASSIGNED: GPT-4 demonstrated superior accuracy and efficiency compared to Llama 2, but did not outperform traditional models. The ensemble model outperformed the individual models, achieving a precision of 90.3%, a recall of 94.2%, and an F1-score of 92.2%. Notably, the ensemble model showed a significant improvement in precision, increasing from a range of 70%-79% to above 90%, compared to the best-performing single model. Error analysis revealed that 63 samples were incorrectly predicted by at least one model; however, only 2 cases (3.2%) were mutual errors across all models, indicating diverse error profiles among them.
    UNASSIGNED: LLMs and traditional machine learning models trained using local EHR data exhibited diverse error profiles. The ensemble of these models was found to be complementary, enhancing diagnostic performance. Future research should investigate integrating LLMs with smaller, localized models and incorporating medical data and domain knowledge to enhance performance on specific tasks.
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  • 文章类型: Systematic Review
    研究表明,妊娠期咖啡因暴露与不良结局之间存在关联,然而,证据仍然有限。因此,我们进行了系统评价,以调查产前咖啡因暴露与神经行为障碍之间的关系.MEDLINE(PubMed),EMBASE,Scopus,WebofScience,和LILACS数据库进行了搜索。涉及怀孕期间记录咖啡因摄入量的女性的观察性研究有资格纳入。评估的结果是行为和智力发展,注意力缺陷多动障碍,和相关行为。通过定性综合分析数据。ROBINS-I工具被用来评估偏差的风险,并使用GRADE(PROSPERO:CRD42023421164)评估证据的确定性。搜索产生了14项符合纳入/排除标准的研究。孕妇的样本量为173至64,189,儿童的样本量为88至49,190。孕妇在怀孕期间的咖啡因摄入量为0至1000毫克/天,在怀孕中期观察到的最高水平。七项研究表明,产前咖啡因暴露与神经行为/神经发育缺陷之间存在潜在关联,一项研究表明,产前咖啡因暴露改善了同伴问题,6项研究未显示产前咖啡因摄入对神经行为障碍有显著影响.纳入的研究被归类为中度偏倚风险,证据确定性非常低。因此,证据不足以确定产前咖啡因暴露会导致神经行为障碍。研究异质性,以及它们的可变质量和几个混杂因素的存在,产生不确定性。
    Studies have suggested associations between gestational exposure to caffeine and adverse outcomes, however the evidence is still limited. Therefore, a systematic review was conducted to investigate the association between prenatal caffeine exposure and neurobehavioral disorders. The MEDLINE (PubMed), EMBASE, Scopus, Web of Science, and LILACS databases were searched. Observational studies involving women with documented caffeine consumption during pregnancy were eligible for inclusion. The outcomes evaluated were behavioral and intellectual development, Attention Deficit Hyperactivity Disorder, and related behaviors. The data were analyzed by qualitative synthesis. The ROBINS-I tool was employed to assess the risk of bias, and the certainty of evidence was evaluated using GRADE (PROSPERO: CRD42023421164). The search yielded fourteen studies that met the inclusion/exclusion criteria. The sample size among pregnant women ranged from 173 to 64,189, and among children ranged from 88 to 49,190. Maternal caffeine consumption during pregnancy ranged from 0 to 1000 mg/day, with the highest levels observed during mid-pregnancy. Seven studies indicated a potential association between prenatal caffeine exposure and neurobehavioral/neurodevelopment deficits, one study showed that prenatal caffeine exposure improved peer problems, and six studies did not show a significant effect of prenatal caffeine consumption on neurobehavioral disorders. The included studies were classified as moderate for the risk of bias and with very low certainty of evidence. Thus, the evidence is insufficient to confirm with certainty that the prenatal caffeine exposure leads to neurobehavioral disorders. Studies heterogenicity, as well as their variable quality and the presence of several confounding factors, generate uncertainty.
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  • 文章类型: Systematic Review
    目的:运动神经元病(MND)是一种神经退行性疾病,逐步影响功能和自我感知的生活质量(QoL)。高达50%的MND患者会出现认知和行为障碍,与相关的增加照顾者的负担或紧张。然而,对于MND中QoL与认知或行为障碍之间的关系尚未有系统的研究.目的是确定在MND中QoL与认知/行为障碍之间是否存在关系,同时补充寻找确定这些研究中使用的认知/行为和QoL测量的类型。
    方法:在多个数据库中进行了系统搜索(PsychINFO,Embase,Medline,AMED)为截至2023年2月22日发表的研究。利用定量方法测量QoL的研究,包括认知/行为功能/损害.提取并综合了检查QoL-认知/行为损害之间关系的结果。
    结果:共确定了488项研究,14项研究纳入系统评价。所有14项研究均为观察性研究(11项横断面研究,3纵向)。13项研究使用了MND非特异性措施,特别是与QoL和认知障碍有关。在8项测量行为障碍的研究中,62.5%(N=5)发现QoL差异或相关性较低。在测量认知障碍的12项研究中,只有33.3%(N=4)发现较低的QoL差异或相关性。
    结论:本系统评价显示行为损害可能对MND患者的生活质量有影响。用于测量QoL和认知/行为损害的评估类型存在差异,其中大多数是非特异性疾病。未来研究的建议是使用全面的疾病特异性,多领域措施,以进一步阐明QoL-认知/行为损害关系。
    OBJECTIVE: Motor neuron disease (MND) is a neurodegenerative disease, progressively impacting function and self-perceived quality of life (QoL). Up to 50% of people with MND can present with cognitive and behavioural impairment, with an associated increase in caregiver burden or strain. However, there has been no systematic exploration of the relationship between QoL and cognitive or behavioural impairment in MND. The aim was to determine if there is a relationship between QoL and cognitive/behavioural impairment in MND, while also supplementarily looking to determine the types of cognitive/behavioural and QoL measures utilised in these studies.
    METHODS: A systematic search was performed across multiple databases (PsychINFO, Embase, Medline, AMED) for research published up to the date of February 22, 2023. Studies utilising quantitative methods of measuring QoL, cognitive/behavioural functioning/impairment were included. Findings examining relationships between QoL-cognitive/behavioural impairment were extracted and synthesised.
    RESULTS: A total of 488 studies were identified, with 14 studies included in the systematic review. All 14 studies were observational (11 cross-sectional, 3 longitudinal). 13 studies utilised MND non-specific measures, particularly in relation to QoL and cognitive impairment. Of 8 studies measuring behavioural impairment 62.5% (N = 5) found either a lower QoL difference or association. Only 33.3% (N = 4) of 12 studies measuring cognitive impairment found a lower QoL difference or association.
    CONCLUSIONS: This systematic review shows that behavioural impairment may have an impact on QoL in MND. There is variability in types of assessments used to measure QoL and also cognitive/behavioural impairment, most of which are disease-non-specific. Recommendations for future research are to use comprehensive disease-specific, multidomain measures to further elucidate the QoL-cognitive/behavioural impairment relationship.
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  • 文章类型: Journal Article
    临床指南建议将轻度行为障碍(MBI)和睡眠障碍(SD)等非认知标志物纳入痴呆筛查中以提高检测。
    我们调查了MBI,SD,和痴呆症事件。
    参与者的数据来自美国国家阿尔茨海默氏症协调中心。MBI是使用已发布的算法从神经精神清单问卷(NPI-Q)得出的。SD是使用NPI-Q夜间行为项目确定的。MBI与时间相关变量的Cox比例风险回归,SD,和认知诊断用于建立基线1)MBI和事件SD(n=11,277)之间的关联模型;2)SD和事件MBI(n=10,535);3)MBI并发SD和事件性痴呆(n=13,544);和4)MBI无并发SD和事件性痴呆(n=11,921)。模型根据首次就诊年龄进行了调整,性别,教育,认知诊断,种族,并使用Benjamini-Hochberg方法进行多重比较。
    与没有MBI的人相比,基线时患有MBI的老年人的SD发生率高3.1倍(95%CI:2.8-3.3)。具有基线SD的老年人的MBI发展速率比没有SD的老年人高1.5倍(95%CI:1.3-1.8)。患有MBI和SD的老年人患痴呆症的比率是2.2倍。与单独的SD相反(95%CI:1.9-2.6)。
    MBI和SD之间存在双向关系。与MBI同时发生时,患有SD的老年人患痴呆症的比率更高。未来的研究应该探索这些关系背后的机制,通过评估MBI和SD可以改善痴呆筛查。
    UNASSIGNED: Clinical guidelines recommend incorporating non-cognitive markers like mild behavioral impairment (MBI) and sleep disturbance (SD) into dementia screening to improve detection.
    UNASSIGNED: We investigated the longitudinal associations between MBI, SD, and incident dementia.
    UNASSIGNED: Participant data were from the National Alzheimer\'s Coordinating Center in the United States. MBI was derived from the Neuropsychiatric Inventory Questionnaire (NPI-Q) using a published algorithm. SD was determined using the NPI-Q nighttime behaviors item. Cox proportional hazard regressions with time-dependant variables for MBI, SD, and cognitive diagnosis were used to model associations between baseline 1) MBI and incident SD (n = 11,277); 2) SD and incident MBI (n = 10,535); 3) MBI with concurrent SD and incident dementia (n = 13,544); and 4) MBI without concurrent SD and incident dementia (n = 11,921). Models were adjusted for first-visit age, sex, education, cognitive diagnosis, race, and for multiple comparisons using the Benjamini-Hochberg method.
    UNASSIGNED: The rate of developing SD was 3.1-fold higher in older adults with MBI at baseline compared to those without MBI (95% CI: 2.8-3.3). The rate of developing MBI was 1.5-fold higher in older adults with baseline SD than those without SD (95% CI: 1.3-1.8). The rate of developing dementia was 2.2-fold greater in older adults with both MBI and SD, as opposed to SD alone (95% CI:1.9-2.6).
    UNASSIGNED: There is a bidirectional relationship between MBI and SD. Older adults with SD develop dementia at higher rates when co-occurring with MBI. Future studies should explore the mechanisms underlying these relationships, and dementia screening may be improved by assessing for both MBI and SD.
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  • 文章类型: Journal Article
    由于临床表现相似,区分功能性癫痫发作(FS)和癫痫发作(ES)构成了挑战。创建有助于准确诊断FS患者的临床评分系统将是对医疗实践的宝贵贡献。该评分有可能增强临床决策并促进FS患者的及时诊断。
    符合入选标准的参与者被随机分为三个不同的组:训练,验证,和测试队列。通过单变量分析在训练队列中分析了人口统计学和符号学变量。然后在两个多变量逻辑回归模型中进一步检查显示FS和ES之间存在显着差异的变量。CFSS是根据判别变量的比值比开发的。使用验证组,最佳临界值是根据AUC确定的,然后在测试队列中评估CFSS以评估其性能。
    在验证队列中,开发的评分得出的AUC为0.78,并且建立了6的截止点,重点是在不显著损害特异性的情况下最大化灵敏度.然后将分数应用于测试队列中,其灵敏度为86.96%,特异性为73.81%。
    我们开发了一种新工具,该工具在识别可疑FS的患者方面显示出可喜的结果。通过前瞻性研究的进一步分析,这种创新,简单的工具可以集成到FS的诊断过程中。
    UNASSIGNED: Distinguishing functional seizures (FS) from epileptic seizures (ES) poses a challenge due to similar clinical manifestations. The creation of a clinical scoring system that assists in accurately diagnosing patients with FS would be a valuable contribution to medical practice. This score has the potential to enhance clinical decision-making and facilitate prompt diagnosis of patients with FS.
    UNASSIGNED: Participants who met the inclusion criteria were randomly divided into three distinct groups: training, validation, and test cohorts. Demographic and semiological variables were analyzed in the training cohort by univariate analyses. Variables that showed a significant difference between FS and ES were then further scrutinized in two multivariate logistic regression models. The CFSS was developed based on the odds ratio of the discriminating variables. Using the validation group, the optimal cutoff value was determined based on the AUC, and then the CFSS was evaluated in the test cohort to assess its performance.
    UNASSIGNED: The developed score yielded an AUC of 0.78 in the validation cohort, and a cutoff point of 6 was established with a focus on maximizing sensitivity without significantly compromising specificity. The score was then applied in the test cohort, where it achieved a sensitivity of 86.96% and a specificity of 73.81%.
    UNASSIGNED: We have developed a new tool that shows promising results in identifying patients suspicious of FS. With further analysis through prospective studies, this innovative, simple tool can be integrated into the diagnostic process of FS.
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  • 文章类型: Systematic Review
    目的:主要目的是评估与西班牙裔/拉丁美洲人认知障碍相关的冷漠评估措施。
    方法:根据系统评价和荟萃分析(PRISMA)指南的首选报告项目,并使用APAPsycInfo,对西班牙裔/拉丁美洲人在正常衰老和神经认知障碍中的冷漠与认知障碍之间的关系进行了系统评价。Embase,和PubMed数据库。纳入标准要求(1)18岁及以上的英语或西班牙语成人样本,(2)采取冷漠的措施,(3)认知功能评估或神经认知障碍的诊断,(4)样本中至少有18.5%的西班牙裔/拉丁美洲人代表。
    结果:只有14篇论文符合纳入本综述的标准。在12项横断面研究中,9显示了冷漠增加和认知障碍之间的显著关联,1显示了冷漠和认知状态之间的描述性差异(即,未进行假设检验),而2表现出无效效果。这些横断面研究包括北美和南美参与者的社区和临床样本。在北美进行的两项纵向研究表明,冷漠与认知状态之间没有显着关联。
    结论:神经精神量表(NPI)和神经精神量表(NPI-Q)冷漠分量表是本综述中最常用的冷漠指标(纳入研究的85.7%)。然而,对冷漠措施进行审查后得出的有效性证据表明,在冷漠筛查的背景下,应谨慎使用NPI.西班牙裔/拉丁美洲人冷漠研究的这种潜在测量偏差限制了从本评论得出的结论。
    OBJECTIVE: The primary aim was to evaluate apathy assessment measures in relation to cognitive impairment among Hispanic/Latin Americans.
    METHODS: A systematic review on the relationship between apathy and cognitive impairment among Hispanic/Latin Americans across normal aging and neurocognitive disorders was conducted according to preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines and using APA PsycInfo, Embase, and PubMed databases. Inclusion criteria required (1) a sample of English or Spanish-speaking adults ages 18 years and older, (2) with measures of apathy, (3) assessment of cognitive functioning or diagnosis of neurocognitive disorder, (4) with at least 18.5% Hispanic/Latin American represented in the sample.
    RESULTS: Only 14 papers met criteria to be included in this review. Of the 12 cross-sectional studies, 9 demonstrated significant associations between increased apathy and cognitive impairment, 1 demonstrated a descriptive difference between apathy and cognitive status (ie, no hypothesis test conducted), while 2 demonstrated null effects. These cross-sectional studies consisted of community and clinic samples of participants across North and South America. Two longitudinal studies conducted in North America demonstrated non-significant associations of apathy with cognitive status.
    CONCLUSIONS: The Neuropsychiatric Inventory (NPI) and Neuropsychiatric Inventory Questionnaire (NPI-Q) apathy subscales were the most used measures for apathy in this review (85.7% of included studies). However, validity evidence from a review of apathy measures has warranted caution against the use of the NPI outside the context of screening for apathy. This potential measurement bias with Hispanic/Latin Americans apathy research limits conclusions drawn from the present review.
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  • 文章类型: Case Reports
    描述严重急性呼吸综合征冠状病毒-2(SARS-CoV-2)病毒感染以高度的症状多样性而著称。新出现的证据表明病毒侵入中枢神经系统。因此,严重的神经和精神表现预计。我们介绍了一名67岁的男性医生,他有稳定的双相情感障碍病史数十年,最近因持续的COVID-19症状住院,血清学记录为阳性。他在病毒感染附近出现了新的和急性发作的神经精神症状。我们假设神经侵袭是患者精神不稳定的推定起源。此外,需要进行一项调查,以扩大我们对与SARS-CoV-2相关的神经精神病发病率的潜在认识,以便及时诊断和适当管理.目前也没有研究解决患有持续性慢性精神疾病的SARS-CoV-2感染患者的神经和精神症状的风险。
    Description Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) viral infection is notable for a high degree of symptom diversity. Emerging evidence suggests viral invasion of the central nervous system. Therefore, serious neurological and psychiatric manifestations are anticipated. We present the case of a 67-year-old male physician who has a history of stable bipolar disorder for decades and was recently hospitalized for persistent COVID-19 symptoms with documented positive serology. He presented with new and acute onset neuropsychiatric symptoms of disinhibition proximate to the viral infection. We postulate neuroinvasion as the putative origin of the patient\'s psychiatric instability. Furthermore, an investigation is needed to expand upon our understanding of the potential for neuropsychiatric morbidity related to SARS-CoV-2 for prompt diagnosis and appropriate management. There are also no current studies addressing the risks for neurological and psychiatric symptomatology in SARS-CoV-2 infected patients with persistent chronic mental illness.
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  • 文章类型: Journal Article
    研究表明,妊娠接触铅(Pb)与自然流产有关,早产,较低的婴儿出生体重和身长,和神经功能障碍。然而,关于其在怀孕期间暴露对胎儿和儿童发育的影响的证据仍然很少。因此,本系统评价的目的是验证产前铅暴露与神经行为缺陷发生之间的关系,流产,和儿童死亡率。包括在怀孕期间暴露于铅的孕妇的观察性研究,没有性别或种族限制。MEDLINE,科克伦图书馆,EMBASE,Scopus,WebofScience,和LILACS数据库进行了搜索。进行了标题和摘要的阅读,然后以全格式阅读和数据提取,由两名审稿人独立进行。纳入的研究通过Downs和Black工具进行评估并进行定性合成。通过建议评估的分级来评估证据的确定性,发展,和评价(等级)。研究方案已在前瞻性系统评价注册中心(PROSPERO;CRD42022296750)注册。在21项研究中,16人被归类为前瞻性队列,两个病例控制,一个嵌套的案例控件,一个队列,和一项纵向研究。没有发现评估与妊娠铅暴露相关的儿童死亡率的研究。在妊娠铅暴露与神经行为缺陷或流产之间的关联中,证据的确定性非常低。本系统综述反映了人类毒理学研究的不良证据和挑战,因为不可能将妊娠铅暴露与神经行为缺陷联系起来,流产,和儿童死亡率。
    Studies suggest that gestational exposure to lead (Pb) is related to spontaneous abortions, preterm birth, lower infant birth weight and length, and neurological dysfunctions. However, the evidence about its effects during pregnancy exposure on fetal and child development is still poor. Thus, the aim of this systematic review was to verify the association between prenatal exposure to Pb and the occurrence of neurobehavioral deficits, miscarriages, and child mortality. Observational studies with pregnant women exposed to Pb during pregnancy were included, without gender or ethnicity restrictions. The MEDLINE, Cochrane Library, EMBASE, Scopus, Web of Science, and LILACS databases were searched. The reading of titles and abstracts was conducted, followed by reading in full format and data extraction, that were performed independently by two reviewers. The included studies were evaluated by Downs and Black tool and qualitatively synthesized. Certainty of evidence was assessed by Grading of Recommendations Assessment, Development, and Evaluations (GRADE). The study protocol was registered with the Prospective Registry of Systematic Reviews (PROSPERO; CRD42022296750). Among twenty-one studies included, sixteen were classified as prospective cohort, two case-control, one nested case-control, one cohort, and one longitudinal study. No study that evaluated child mortality associated with gestational Pb exposure was found. There is a very low certainty of evidence in the association of gestational Pb exposure and neurobehavioral deficits or miscarriages. This systematic review reflects the poor evidence and the challenges of human toxicology studies, since it was not possible to associate gestational Pb exposure to neurobehavioral deficits, miscarriages, and child mortality.
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