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A Conceptual Framework for the Development of Chatbots Addressing COVID-19 Vaccine Hesitancy 解决COVID-19疫苗犹豫问题的聊天机器人开发概念框架
Pub Date : 2022-12-28 DOI: 10.17816/pavlovj91196
D. R. Neog, Rhythm Grover, R. Ransing, R. Ramalho
Aim of this letter is to review Chatbots that answer questions of vaccine-hesitant people, their utility, and their limitations in addressing psycho-social determinants of COVID-19 vaccine hesitancy. The authors propose a conceptual framework that could guide the development of artificial intelligence-based Chatbots and summarise the salient features of the four Chatbots discussed in the literature today, developed to address COVID-19 vaccine hesitancy.
这封信的目的是回顾聊天机器人,它们回答了疫苗犹豫者的问题,它们的效用,以及它们在解决COVID-19疫苗犹豫的心理社会决定因素方面的局限性。作者提出了一个概念框架,可以指导基于人工智能的聊天机器人的发展,并总结了今天文献中讨论的四种聊天机器人的显著特征,这些聊天机器人是为了解决COVID-19疫苗犹豫而开发的。
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引用次数: 0
Comparative Characteristics of Quality Parameters of Waters of the Oka River in Places of Water Intake of Utility and Drinking Water System in Ryazan 梁赞市公用取水点与饮用水系统取水点奥卡河水质参数比较特征
Pub Date : 2022-12-28 DOI: 10.17816/pavlovj89568
A. A. Litvinova, Aleksey A. Dement’yev, Alexsandr A. Lyapkalo, E. P. Korshunova
INTRODUCTION: Surface water sources play an important role in supply of large cities with water. Their waters are subject to anthropogenic pollution with different chemical compounds which may be significant risk factors for the health of the population. The article presents the results of comparative sanitary-hygienic characteristics of the water quality of the Oka river in places of water intake of utility and drinking water supply system of Ryazan. Being the only surface source of water supply, the Oka river provides 53% of the total water consumption of the Ryazan population, therefore a rational choice of the place of water intake can have a considerable impact on the effectiveness of water conditioning and purification and on the final quality of drinking water. AIM: To give a comparative sanitary-hygienic characteristic of the water quality of the Oka river in places of the water intake of the utility and drinking water supply system of Ryazan. MATERIALS AND METHODS: A comparative evaluation of the water quality of the Oka river, as a surface source of water supply, was carried out based on the average long-term values of control parameters (organoleptic, microbiological, chemical) and the proportion of samples that do not meet hygienic standards in the sections of three water intakes in Ryazan in 20122019. The average parameters were compared by the method of variance analysis; for paired comparisons, Scheffe and Tamhein criteria were used, taking into account the results of Levene test. The statistical parameters were calculated in SPSS Statistics 19 program. RESULTS: The chemical composition of the Oka river water was characterized by the greatest pollution with iron (2+) and aluminum. The water of Oksky and Borkovskoy water intakes was characterized by higher average concentrations of iron (2+) and ammonia, as well as greater contamination with generalized and thermotolerant coliform bacteria, compared with the water of Sokolovsky water intake. CONCLUSION: A lower initial quality of the water in Oksky and Borkovskoy water intakes may be due to their location in the 'blind' river course characterized by the processes of eutrophication and slowed down water exchange. High concentrations of iron (2+) may be associated with supply of stream water from the underground sources or with anthropogenic pollution.
地表水在大城市的供水中起着重要的作用。它们的水受到各种化合物的人为污染,这些化合物可能是影响人口健康的重大危险因素。本文介绍了梁赞市公用取水点和饮水系统取水点奥卡河水质卫生特征的比较结果。奥卡河是梁赞地区唯一的地表水源,其供水量占梁赞人口总用水量的53%,因此合理选择取水地点对水的调理和净化效果以及最终的饮用水质量有相当大的影响。目的:对梁赞市公用事业取水点和饮用水供水系统取水点的奥卡河水质进行比较卫生特征分析。材料与方法:以梁赞市3个取水口2012 - 2019年水质控制参数(感官、微生物、化学)的长期平均值和不符合卫生标准的样品比例为基础,对作为地表水源的奥卡河水质进行对比评价。采用方差分析法比较平均参数;配对比较采用Scheffe和Tamhein标准,并考虑Levene检验的结果。统计参数用SPSS Statistics 19软件计算。结果:奥卡河水体化学成分以铁(2+)和铝污染最大。与Sokolovsky取水口相比,Oksky取水口和borkovsky取水口的水具有更高的平均铁(2+)和氨浓度,以及更大的广义和耐热大肠菌群污染。结论:Oksky和borkovskay取水口的初始水质较低可能是由于它们位于富营养化过程和水交换缓慢的“盲”河道中。高浓度的铁(2+)可能与地下水源的水流供应或人为污染有关。
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引用次数: 0
Analysis of Causes of Sudden Death Among Russian Railway Workers 俄罗斯铁路工人猝死原因分析
Pub Date : 2022-12-28 DOI: 10.17816/pavlovj110985
E. Zhidkova, E. Gutor, K. Gurevich, Nikita V. Makogon, Z. Shugushev, D. O. Orlov, O.N. Dzhioyeva, O. Drapkina
INTRODUCTION: Health protection of railway workers of various professional groups increases the safety of railway transport, the prestige of the profession and reduces morbidity and mortality from the most common causes in this group of patients. AIM: To analyze the risk factors of sudden death among Russian Railways workers. MATERIALS AND METHODS: The design of the study is made according to the case-control type. Analysis was carried out of all cases of sudden death (SD) of employees of JSCo Russian Railways (RR) in the period from 2009 to 2021 (n = 412). The comparison group consisted of 411 employees of RR who were undergoing periodical medical examination. The groups were formed on the basis of age, employment period, gender, profession. To assess the diagnostic significance of the quantitative signs in predicting a certain outcome, the method of analysis of ROC curves was used. RESULTS: The chances of death for workers of RR increased in case of past myocardial infarction, and also depended on the type of intervention (p 0.001). The threshold value of the BMI index in the cut-off point, which corresponded to the highest value of Youden index, was 27.1 kg/m2. In the group of sudden deaths, there were 1.8 times more smokers and 2 times less individuals with total cholesterol level exceeding 5 mmol/l than in the comparison group (p 0.001). A prognostic model was developed by ROC-analysis to determine the probability of mortality. The sensitivity and specificity of the model were 79.5% and 91.9%, respectively. CONCLUSION: A prognostic model was developed to determine the probability of sudden death in Russian railway workers, with the sensitivity and specificity 79.5% and 91.9%, respectively. However, the present study did not permit to reveal predictors of sudden death specific of the workers of RR.
导读:对各专业群体的铁路工人进行健康保护,可以提高铁路运输的安全性,提高该行业的声誉,并减少这类患者中最常见原因的发病率和死亡率。目的:分析俄罗斯铁路职工猝死的危险因素。材料与方法:本研究按病例-对照法设计。对2009 - 2021年JSCo俄罗斯铁路公司(RR)员工猝死(SD)的所有病例(n = 412)进行分析。对照组为定期体检的RR员工411人。这些群体是根据年龄、就业期、性别、职业组成的。为了评估定量指标对预测某一结局的诊断意义,采用ROC曲线分析的方法。结果:有心肌梗死病史的RR工人死亡几率增加,且与干预方式有关(p < 0.001)。分界点BMI指数阈值为27.1 kg/m2,与约登指数最高值相对应。在猝死组中,吸烟者比对照组多1.8倍,总胆固醇水平超过5 mmol/l的人少2倍(p < 0.001)。通过roc分析建立预后模型以确定死亡概率。该模型的敏感性为79.5%,特异性为91.9%。结论:建立了预测俄罗斯铁路职工猝死概率的预后模型,敏感性79.5%,特异性91.9%。然而,目前的研究并没有允许揭示突发死亡的预测特异性的工人RR。
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引用次数: 0
The Role and Significance of Polymorphisms of Certain Genes in Patients with Abdominal Aortic Aneurysm 某些基因多态性在腹主动脉瘤患者中的作用和意义
Pub Date : 2022-12-28 DOI: 10.17816/pavlovj108311
E. Kalmykov, I. Suchkov, R. Kalinin, Okildyhon Ne’matzoda, J. Dodkhoev
INTRODUCTION: To date, many factors that influence the risk and course of abdominal aortic aneurysm (AAA) are not studied. Increasing significance in the etiology and development of AAA is assigned to the existence of some genetic polymorphisms, the role of many of them is not studied either. AIM: To analyze the existence of association of the abdominal aortic aneurysm with some gene polymorphisms (GPs). MATERIALS AND METHODS: Gene polymorphisms were analyzed in 20 patients with AAA (study group, SG); 18 men (90%) and 2 women (10%), the mean age 68.1 7.3 years), and in 5 patients without AAA (control group, CG; 4 men (80%) and 1 woman (20%), the mean age 64.2 7.2 years). The frequency of concomitant diseases and risk factors for AAA were determined. The following GPs were studied: : Lys198Asn in the EDN1 gene; C-786T in the NOS3 gene; Leu28Pro in the APOE gene; Val174Ala in the SLC01B1 gene; Thr715Pro in the SELP gene; C807T in the ITGA2 gene; Ser447Ter in the LpL gene; Thr174Met in the AGT gene; Met235Thr in the AGT gene. Statistical analysis was performed using IBM SPSS Statistics 21, correlation analysis ― according to Pearson. The results were considered statistically significant at p 0.05. RESULTS: In the SG, correlation relationships were identified in Ser447Ter polymorphism in the LpL gene: direct relationships with Lys198Asn polymorphism (r = 0.63; р 0.001) in the EDN1 gene, Leu28Pro (r = 0.70; р 0.001) in the APOE gene and Thr715Pro (r = 0.63; р 0.001) in the SELP gene; a reverse relationship with С786Т polymorphism (r = -0.35; р = 0.006) in the NOS3 gene. The same amount of relationships were found in Leu28Pro polymorphism in the APOE gene: besides with Ser447Ter in the LpL gene, there is also a direct relationship with Lys198Asn (r = 0.70; р 0.001) in the EDN1 gene and Thr715Pro (r = 0.63; р 0.001) in the SELP gene; a reverse relationship with С786Т (r = -0.35; р = 0.006) in the NOS3 gene. Thr715Pro polymorphism in the SELP gene, along with relationships with Ser447Ter (r = 0.63; р 0.001) in the LpL gene and Leu28Pro in the APOE gene, has an additional direct relationship with Lys198Asn (r = 0.55; р 0.001) in the EDN1 gene. Thr174Met polymorphism in the AGT gene has a reverse relationship with Leu28Pro (r = -0.35; р = 0.006) in the APOE gene and direct relationship with Val174Ala (r = 0.40; р = 0.002) in the SLC01B1 gene. With this, Met235Thr polymorphism in the AGT gene has a direct relationship with Val174Ala (r = 0.33; p = 0.011) in the SLC01B1 gene and reverse relationship with C807T in the ITGA2 gene. CONCLUSION: The existence of direct correlations of some gene polymorphisms in patients with abdominal aortic aneurysm has been established, which indicates their probable role in the development of this pathology and may be used as a screening test for determination of the likelihood for its development.
迄今为止,许多影响腹主动脉瘤(AAA)风险和病程的因素尚未得到研究。一些遗传多态性的存在在AAA的病因和发展中具有越来越重要的意义,其中许多遗传多态性的作用也未得到研究。目的:分析腹主动脉瘤与某些基因多态性(gp)的相关性。材料与方法:分析20例AAA患者的基因多态性(研究组,SG);男性18例(90%),女性2例(10%),平均年龄68.1 ~ 7.3岁,无AAA患者5例(对照组,CG;男性4例(80%),女性1例(20%),平均年龄64.2 ~ 7.2岁。测定AAA伴发疾病的频率及危险因素。研究了以下gp:: EDN1基因中的Lys198Asn;NOS3基因中的C-786T;APOE基因中的Leu28Pro;SLC01B1基因中的Val174Ala;SELP基因中的Thr715Pro;ITGA2基因中的C807T;LpL基因Ser447Ter;AGT基因中的Thr174Met;AGT基因中的Met235Thr。统计学分析采用IBM SPSS Statistics 21,相关性分析-根据Pearson。p < 0.05认为结果有统计学意义。结果:在SG中,LpL基因的Ser447Ter多态性存在相关关系:与Lys198Asn多态性直接相关(r = 0.63;EDN1基因,Leu28Pro基因(r = 0.70;APOE基因和Thr715Pro (r = 0.63;SELP基因为0.001);与С786Т多态性呈负相关(r = -0.35;NOS3基因的差异为0.006)。在APOE基因的Leu28Pro多态性中也发现了同样数量的关系:除了与LpL基因的Ser447Ter有直接关系外,还与Lys198Asn有直接关系(r = 0.70;EDN1基因和Thr715Pro基因的差异(r = 0.63;SELP基因为0.001);与С786Т呈负相关(r = -0.35;NOS3基因的差异为0.006)。SELP基因的Thr715Pro多态性,以及与Ser447Ter的关系(r = 0.63;LpL基因中的Leu28Pro和APOE基因中的Leu28Pro与Lys198Asn有直接关系(r = 0.55;EDN1基因的差异为0.001)。AGT基因Thr174Met多态性与Leu28Pro呈负相关(r = -0.35;与Val174Ala有直接关系(r = 0.40;在SLC01B1基因中,r = 0.002)。由此可见,AGT基因Met235Thr多态性与Val174Ala有直接关系(r = 0.33;p = 0.011),与ITGA2基因中C807T呈负相关。结论:腹主动脉瘤患者中某些基因多态性存在直接相关性,提示其可能在该病理的发生发展中发挥作用,可作为确定其发生可能性的筛选试验。
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引用次数: 0
Potentials of Minimally Invasive Technologies in Treatment for Early Gastric Cancer 微创技术在早期胃癌治疗中的潜力
Pub Date : 2022-12-28 DOI: 10.17816/pavlovj108923
A. Dylenok, V. Rybachkov, V. N. Malashenko, S. Kashin, Leonid B. Shybin
INTRODUCTION: Gastric cancer remains one of the leading causes of oncological morbidity and mortality. AIM: To determine the effectiveness and safety of wedge resections of stomach in patients with early gastric cancer (EGC) in comparison with endoscopic intraluminal treatment methods. MATERIALS AND METHODS: Assessment of the immediate and long-term (5 years) prognosis of 164 patients with EGC who underwent wedge resection of stomach and endoscopic intraluminal interventions was performed. One hundred twenty eight patients were operated on in the volume of endoscopic intraluminal mucosal resection or submucosal dissection (the mean age 68.5 9.2 years; men 53.7%). In 36 patients (the mean age 65.3 7.8 years; men 66.7%), according to gastroscopy in combination with chromogastroscopy, narrow-band magnification endoscopy, the tumor dimensions exceeded those recommended for endoscopic methods. Due to contraindications for classic resection interventions in such patients, wedge resections of the stomach were performed. RESULTS: In the comparison groups there was no postoperative mortality, however, in the group with use of endoscopic methods, complications were noted (perforations of the stomach and bleeding). All the complications were eliminated endoscopically. In the group of wedge resections, there were no postoperative complications, but in the long-term result, the five-year survival rate was lower than in the group of endoscopic treatment (75.0% versus 92.2%; 2 = 8.10, p = 0.004) due to a more severe comorbid pathology in the patients of wedge resection group. CONCLUSION: Safety and equal effectiveness of wedge gastric resections was established in the long-term oncological result in patients with EGC in comparison with intraluminal endoscopic methods.
导读:胃癌仍然是肿瘤发病率和死亡率的主要原因之一。目的:探讨胃楔形切除术治疗早期胃癌(EGC)的有效性和安全性,并与内镜腔内治疗方法进行比较。材料和方法:对164例接受胃楔形切除术和内镜腔内介入治疗的EGC患者的近期和长期(5年)预后进行评估。128例患者行内镜下腔内粘膜切除或粘膜下剥离术,平均年龄68.5 - 9.2岁;男人53.7%)。36例患者(平均年龄65.3 - 7.8岁;男性66.7%),经胃镜检查联合胃镜染色、窄带放大内镜检查,肿瘤尺寸超出内镜方法推荐值。由于这类患者的经典切除干预的禁忌症,我们进行了胃楔形切除术。结果:在对照组中,无术后死亡,但在使用内镜方法的组中,注意到并发症(胃穿孔和出血)。所有并发症均经内镜检查消除。楔形切除组无术后并发症,但长期观察,5年生存率低于内镜治疗组(75.0% vs 92.2%;2 = 8.10, p = 0.004),因为楔形切除组患者的合并症病理更为严重。结论:与腔内内镜方法相比,楔形胃切除术在EGC患者的长期肿瘤学结果中具有安全性和同等有效性。
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引用次数: 0
Intracellular Location and Function of Nuclear Factor of Erythroid Origin 2 (Nrf2) in Modeling Oxidative Stress in vitro 红细胞起源核因子2 (Nrf2)在体外模拟氧化应激中的细胞内定位和功能
Pub Date : 2022-10-07 DOI: 10.17816/pavlovj105574
Y. Abalenikhina, P. Erokhina, A. A. Seidkuliyeva, Ol’ga A. Zav’yalova, A. V. Shchul’kin, E. Yakusheva
INTRODUCTION: Nuclear factor E2-related factor 2 (Nrf2) is a member of capncollar (CNC) family of subfamily of leucine zipper transcription factors that regulates cell protection against toxic substances and oxidants. AIM: To determine location, mechanism of activation and role of Nrf2 in conditions of oxidative stress in vitro. MATERIALS AND METHODS: The study was performed on human colon adenocarcinoma cell line (Caco-2). Oxidative stress (OS) was modeled by adding hydrogen peroxide (Н2О2) at concentrations of 0.1 М100 М to the nutritive medium and incubation for 24 and 72 hours. In assessment of Nrf2 function, its inhibitor ― AEM1 ― was added to cells at a concentration of 5 М. The extent of OS development was determined using photometric methods by the concentration of protein SH-groups and carbonyl derivatives of protein, and the activity of superoxide dismutase (SOD). Viability of cells was assessed by the results of cytotoxic test (MTT assay), the amount of Nrf2 in the cytoplasm and nucleus was determined by heterogenous ELISA method. RESULTS: Incubation of Caco-2 cells with Н2О2 resulted in decrease in the level of protein SH-groups and increase in the concentration of carbonyl derivatives of protein. In incubation with H2O2 at concentrations of 0.1 М10 М for 24 hours and 10 М for 72 hours, the activity of SOD increased. At concentrations of Н2О2 of 50 М and 100 М (24 hour and 72 hour), SOD activity and viability of cells decreased. Exposure to Н2О2 led to translocation of Nrf2 from the cytoplasm into nucleus. Direct correlation dependence was revealed between concentration of protein SH-groups and the amount of Nrf2 in the cytoplasm in incubation with H2O2 for 24 hour (r = 0.44, р = 0.03), 72 hour (r = 0.34, р = 0.05). The amount of Nrf2 in the nucleus positively correlated with SOD activity in the cytoplasm on exposure to H2O2 for 24 hour (r = 0.77, р = 0.0001) and 72 hour (r = 0.36, р = 0.06). In inhibition of Nrf2 in conditions of exposure to H2O2, the viability of cells decreased to a larger extent. CONCLUSION: Hydrogen peroxide induces the nuclear translocation of Nrf2, which promotes activation of antioxidant enzyme SOD and preserves viability of cells of OS conditions in vitro.
简介:核因子e2相关因子2 (Nrf2)是亮氨酸拉链转录因子亚家族capncollar (CNC)家族的成员,调节细胞对有毒物质和氧化剂的保护。目的:探讨Nrf2在体外氧化应激条件下的定位、激活机制及其作用。材料与方法:本研究在人结肠腺癌细胞系(Caco-2)上进行。通过在营养培养基中加入浓度为0.1 М100 М的过氧化氢(Н2О2)并孵育24和72小时来模拟氧化应激(OS)。为了评估Nrf2的功能,将其抑制剂AEM1以5 М的浓度添加到细胞中。通过光度法测定蛋白质sh基团和蛋白质羰基衍生物的浓度以及超氧化物歧化酶(SOD)的活性来确定OS的发育程度。采用细胞毒性试验(MTT法)评价细胞活力,采用异种ELISA法测定细胞质和细胞核中Nrf2的含量。结果:Н2О2与Caco-2细胞孵育后,Caco-2细胞中蛋白sh组水平降低,蛋白羰基衍生物浓度升高。与浓度为0.1 М10 М的H2O2孵育24 h和浓度为10 М的H2O2孵育72 h, SOD活性均有所提高。当Н2О2浓度为50 М和100 М(24小时和72小时)时,细胞SOD活性和活力下降。暴露于Н2О2导致Nrf2从细胞质转位到细胞核。H2O2孵育24 h (r = 0.44, r = 0.03)、72 h (r = 0.34, r = 0.05)细胞质中Nrf2含量与sh蛋白组浓度呈直接相关关系。H2O2处理24小时(r = 0.77, r = 0.0001)和72小时(r = 0.36, r = 0.06),细胞核中Nrf2的数量与细胞质中SOD活性呈正相关。在H2O2暴露条件下,Nrf2受到抑制,细胞活力下降幅度更大。结论:过氧化氢诱导Nrf2核易位,促进体外OS条件下抗氧化酶SOD的活化,保持细胞活力。
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引用次数: 0
Morphometric Characteristics of Axial Length of Eye in Population of the Southern Urals (according to “Ural Very Old Study” and “Ural Eye and Medical Study” Research) 乌拉尔南部人群眼轴长度形态计量学特征(根据“乌拉尔太古研究”和“乌拉尔眼与医学研究”研究)
Pub Date : 2022-10-07 DOI: 10.17816/pavlovj105239
M. Bikbov, T. R. Gil’manshin, G. Israfilova, E. M. Yakupova
INTRODUCTION: Currently, ametropias are the most important medical and social problem, which occupies one of the leading places in modern ophthalmology. Determination of the length of the anteroposterior eyeball axis (APEA) in myopia ― a type of ametropia directly associated with increase in the axial length of the eyeball ― is an objective method of its diagnosis and identification of progression. Due to the fact that myopia is a multifactorial disease, the study of correlation relationships of the length of the eyeball seems to be extremely relevant. AIM: To give a statistical assessment of the peculiarities of the axial length of the eyeball in the population of the Southern Urals, depending on age, gender and the respondents' settlement sites, and to determine the correlation relationships of this parameter. MATERIALS AND METHODS: The analysis was conducted on the base of Ufa Research Institute of Ophthalmology within large clinical and population studies Ural Eye and Medical Study (UEMS) and Ural Very Old Study (UVOS). Inclusion criteria: signing of voluntary consent to participation in the project, permanent residence in the territory of study; for inclusion in UEMS ― age from 40 to 85 years, in UVOS ― age above 85. UEMS study involved 5899 respondents, UVOS ― 1526. The study protocol suggested evaluation of 683 criteria, 293 of which were answers of respondents to questions of the questionnaire and the results of the general somatic examination, 355 criteria concerned the results of the ophthalmologic examination, 35 ― of laboratory tests. Axial length of the eyeball was measured by the method of ultrasound echo-biometry (A-scanning) (Ultra-compact A/B/P ultrasound system, Quantel Medical, France). RESULTS: The mean length of the APEA in the UEMS population was 23.31 1.08 mm, in the UVOS population ― 23.11 1.08 mm (p 0.001). The length of the eyeball axis was 23.31 1.08 mm in the age group 40-84 years and 23.11 1.08 mm in patients in the age category 85 years and older. The multivariate linear regression analysis in UEMS study showed the highest statistically significant association of APEA length with such factors as age (p 0.001), height (p 0.001), presence of arterial hypertension (p = 0.02), education level (p 0.001 ), intraocular pressure (IOP) (p 0.001), spherical refractive error (p0.001), depth of anterior chamber (p 0.001) and angle of anterior chamber (p 0.001), mosaicism of the eye fundus in the macular region (p 0.001), presence of myopic maculopathy (p 0.001), refractive power of the cornea (p 0.001), corneal volume (p 0.001), macular pigment density (p 0.001), thickness of peripapillary layer of nerve fibers (p 0.001), presence of the epiretinal membrane (p = 0.01). The multivariate linear regression analysis in UVOS study showed statistically significant association of the APEA length with such factors as height (p 0.001), education level (p = 0.002), corneal refractive power (p 0.001), spherical refraction error (p 0.001
简介:屈光不正是目前最重要的医学和社会问题,在现代眼科学中占主导地位。近视是一种与眼球轴长增加直接相关的屈光不正,测定眼球前后轴的长度是诊断和识别近视进展的一种客观方法。由于近视是一种多因素疾病,因此研究眼球长度的相关关系似乎非常重要。目的:对乌拉尔南部人口眼球轴长随年龄、性别和居住地的特殊性进行统计评估,并确定该参数的相关关系。材料和方法:分析基于乌法眼科研究所的大型临床和人口研究乌拉尔眼科和医学研究(UEMS)和乌拉尔高龄研究(UVOS)。入选标准:签署自愿参与项目的同意书,在研究地区永久居住;年龄介乎40至85岁,年龄介乎85岁以上。UEMS研究涉及5899名受访者,UVOS - 1526名。研究方案建议评估683项标准,其中293项是应答者对问卷问题的回答和一般身体检查的结果,355项标准涉及眼科检查的结果,35项涉及实验室检查。眼球轴向长度采用超声回声生物测定法(A扫描)测量(Ultra-compact A/B/P超声系统,Quantel Medical, France)。结果:UEMS人群APEA平均长度为23.31 1.08 mm, UVOS人群APEA平均长度为23.11 1.08 mm (p < 0.001)。40 ~ 84岁患者眼球轴长23.31 1.08 mm, 85岁及以上患者眼球轴长23.11 1.08 mm。UEMS研究的多变量线性回归分析显示,APEA长度与年龄(p0.001)、身高(p0.001)、动脉高血压(p = 0.02)、文化程度(p0.001)、眼压(p0.001)、球面屈光不正(p0.001)、前房深度(p0.001)、前房角度(p0.001)、眼底黄斑区嵌合程度(p0.001)、是否存在近视黄斑病变(p = 0.001)、角膜屈光度(p = 0.001)、角膜体积(p = 0.001)、黄斑色素密度(p = 0.001)、乳头周围神经纤维层厚度(p = 0.001)、视网膜前膜的存在(p = 0.01)。UVOS研究的多元线性回归分析显示,APEA长度与身高(p 0.001)、文化程度(p = 0.002)、角膜屈光度(p 0.001)、球面屈光误差(p 0.001)等因素有统计学意义。结论:在乌拉尔南部人群中,眼球轴长度与身高、文化程度、角膜屈光度和球面屈光不正等因素有统计学意义。此外,在UEMC研究人群中,还注意到与年龄、动脉高血压的存在、眼压、前房深度和前房角度、眼底黄斑区的镶嵌性、近视黄斑病的存在、角膜体积、黄斑色素密度、乳头周围神经纤维层的厚度、视网膜前膜的存在有关。
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引用次数: 0
Coronary-Vertebral Collaterals in Takayasu Arteritis: Case Report 高须动脉炎的冠状椎侧支1例
Pub Date : 2022-10-07 DOI: 10.17816/pavlovj104656
Andey V. Chupin, A. Zotikov, A. S. Kutovaya, A. L. Golovyuk, Aleksandr F. Kharazov, V. A. Kul’bak, A. Kozhanova, A. Varava, Irina E. Tiimina
INTRODUCTION: PNonspecific aortoarteritis is a rare autoimmune disease with the involvement and narrowing of the aorta and its branches leading to ischemia of the respective arterial region. In the territory of the Russian Federation, the most common manifestation of Takayasu nonspecific aortoarteritis is lesion of the branches of the aortic arch, which in rare cases leads to development of the so called bald arch syndrome. In response to hypoxia, intersystemic collaterals are formed through the neoangiogenesis or redirection of the blood flow from the occluded vessels to small-diameter vessels. In patients with bald arch syndrome, the key role in blood supply to the brain is played by the vertebral arteries. Here, collateral blood supply is realized through the intersystemic anastomoses, most often through the anastomotic leaks between the intercostal and internal thoracic arteries. In the literature, single cases of formation of collaterals between coronary and bronchial arteries are reported. The article presents a clinical case of coronary-vertebral anastomoses in a patient with extremely severe course of Takayasu arteritis with occlusion of the brachiocephalic trunk, right common carotid artery (CA), left common CA, right internal CA, left internal CA (bald arch syndrome). The probable cause of such course of the disease was late referral for medical help by the patient and lack of adequate basic therapy. CONCLUSION: The demonstrated case is the fourth case in the world literature describing the existence of collaterals between the coronary arteries and cerebral arteries, and the first case in the world describing the existence of collaterals from the right and left coronary arteries to the vertebral artery. Such unusual pathway of collateral blood supply in the patient is explained by the absence of the possibility for collateral compensation from the systems of subclavian and intercostal arteries, severe chronic cerebral ischemia. Usually, the causes of angina pectoris in patients with nonspecific aortoarteritis are spread of arteritis to the coronary arteries, insufficiency of the aortic valve, hypertrophy of the left ventricle. In the described case, none of these conditions was present, and angina can only be attributed to the existence of unusual collaterals and the development of a transient steal syndrome.
简介:非特异性大动脉炎是一种罕见的自身免疫性疾病,主要表现为主动脉及其分支受累和变窄,导致相应动脉区域缺血。在俄罗斯联邦境内,Takayasu非特异性大动脉炎最常见的表现是主动脉弓分支的病变,在极少数情况下导致所谓的秃弓综合征的发展。在缺氧的情况下,通过新生血管生成或血流从闭塞血管转向小直径血管形成系统间侧枝。在秃顶弓综合征患者中,椎动脉在脑供血中起着关键作用。在这里,侧枝血供是通过系统间吻合实现的,最常见的是通过肋间动脉和胸内动脉之间的吻合口。在文献中,有冠状动脉和支气管动脉之间形成侧支的单一病例报道。本文报道一例重症高松动脉炎伴头臂干、右颈总动脉、左颈总动脉、右内颈总动脉、左内颈总动脉(秃弓综合征)闭塞的临床病例。这种病程的可能原因是病人转诊较晚和缺乏适当的基本治疗。结论:本病例是世界文献中第4例冠状动脉与脑动脉之间存在络的病例,也是世界文献中第1例左右冠状动脉至椎动脉之间存在络的病例。这种不寻常的侧支血供途径可以解释为锁骨下和肋间动脉系统缺乏侧支代偿的可能性,严重的慢性脑缺血。通常,非特异性大动脉炎患者心绞痛的原因是动脉炎向冠状动脉扩散、主动脉瓣功能不全、左心室肥厚。在上述病例中,这些条件都不存在,心绞痛只能归因于不寻常的络的存在和短暂性窃血综合征的发展。
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引用次数: 0
Parameters of Functional Lateral Organization of Students of Medical University with Different Levels of Physical Fitness 不同体质水平医科大学学生的功能横向组织参数
Pub Date : 2022-10-07 DOI: 10.17816/pavlovj96768
I. Mazikin, M. Lapkin, Mariya V. Akulina, P. A. Kulagin
INTRODUCTION: One of the parameters of the functional reserves of the human body is the level of physical fitness, which depends not only on the improvement of various methods used in the education of students in physical culture, but also on the individual characteristics of students, including parameters of their functional lateralization. AIM: To establish the character of the interrelations between the parameters of functional lateralization and the parameters of physical fitness in medical university students. MATERIALS AND METHODS: Functional lateralization was determined by both the conventional test methods and by the method of neuro-energo mapping in 120 practically healthy medical university students of male gender aged 18 to 23 years. Physical fitness was assessed in conventional tests for determination of strength fitness, speed-strength fitness, speed endurance. All the data were processed using non-parametric statistical methods and correlation and cluster analysis. RESULTS: Based on the criterion of physical fitness, young men were divided to two groups: a group with a relatively high level of speed and strength endurance and flexibility (cluster 1, n = 71), and a group with a relatively high level of strength fitness (cluster 1, n = 49). Both the integral (coefficient of lateral organization profile CLOP) and partial parameters (manual and sensory asymmetry) of the functional lateralization were higher in the representatives of cluster 2, with this, the analysis of changes of the permanent potential level (method of neuro-energo mapping) in functional tests showed only an emerging tendency in the differences between the clusters. Also, in cluster 1, weak (r 0.3, р 0.05) negative relationships between the parameters of functional lateralization were found in behavioral tests, and between changes in the permanent potential level of the left and right cerebral hemispheres (TdTs lead) in load tests. In the representatives of the second cluster, no correlations were found. CONCLUSION: The results of the performed comprehensive analysis evidence, in the authors opinion, the differences in the central-peripheral relationships in the systemic organization of physiological functions that determine non-uniform physical fitness in young men with a relatively high level of speed-strength endurance and flexibility (cluster 1) and those with a relatively high level of strength fitness (cluster 2).
人体功能储备的参数之一是体质水平,这不仅取决于对学生进行体育教育的各种方法的改进,还取决于学生的个体特征,包括其功能偏侧参数。目的:探讨医科大学生功能偏侧参数与体质参数之间的相互关系特征。材料与方法:对120名年龄在18 ~ 23岁的实际健康男医科大学生,采用常规测试方法和神经能量定位法测定功能偏侧。身体素质是通过常规测试来评估的,以确定力量适能、速度-力量适能和速度耐力。所有数据均采用非参数统计方法、相关分析和聚类分析进行处理。结果:以体能标准为依据,将青年男性分为速度、力量耐力、柔韧性水平较高的组(第1组,n = 71)和力量体能水平较高的组(第1组,n = 49)。功能侧化的积分(侧组织剖面CLOP系数)和部分参数(手动和感觉不对称)在集群2的代表中都较高,因此,功能测试中永久电位水平(神经能量映射法)的变化分析显示集群之间的差异只是一个新兴的趋势。此外,在第1类中,行为测试中功能侧化参数之间以及负载测试中左右脑半球永久电位水平变化之间存在弱负相关(r 0.3, r 0.05)。在第二组的代表中,没有发现相关性。结论:综合分析结果表明,在速度-力量耐力和柔韧性水平较高的青年男性(第1类)和力量素质较高的青年男性(第2类)中,生理功能系统组织中中枢-外周关系的差异决定了身体素质的不均匀性。
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引用次数: 0
Complex Neuropsychiatric and Laboratory-Instrumental Diagnostics in Determination of Tactics of Therapeutic Management of Patients with Spinal Muscular Atrophy: Regional Experience 复杂神经精神病学和实验室仪器诊断在确定脊髓性肌萎缩症患者治疗管理策略中的作用:区域经验
Pub Date : 2022-10-07 DOI: 10.17816/pavlovj100672
A. Gayduk, P. Cumming, Viktoriya V. Chernikova, Y. V. Vlasov, D. Smirnova
INTRODUCTION: Spinal muscular atrophy (SMA) is a rare hereditary disabling disease and the most common hereditary cause of infant deaths. The timely comprehensive diagnosis of SMA permits to plan therapeutic tactics and preserve the quality of patients life. One of the objectives of the given work is a review of the actual literature data on etiopathogenesis, clinical presentation, valid diagnosis and modern effective tactics of SMA management. AIM: To evaluate the management tactics of patients with SMA taking into account neuropsychiatric symptoms, to analyze problems of proposal and organization of measures aimed at improvement of the quality of medical care, on the basis of the practical experience of the Samara region and with consideration of the current state of the problem. MATERIALS AND METHODS: In the work, the data of the archive of Seredavin Samara Regional Clinical Hospital were analyzed, 132 medical histories of 77 patients were processed with discharge dates from January 2008 to February 2022 with the following diagnoses (according to the code of the International Classification of Diseases and Health Related Problem, 10th revision (ICD-10)): G12.0 (spinal muscular atrophy, type I [WerdnigHoffmann disease], G12.1 (other hereditary SMA), G12.8 (other SMA and related syndromes) and G12.9 (unspecified SMA). The analysis of the results of clinical, laboratory, instrumental and neuropsychiatric diagnostic methods was performed in comparison with the tactics of therapeutic management of these patients. For statistical processing of the data, methods of descriptive statistics were used. RESULTS: Socio-demographic data. As of February 2022, 58 patients were registered (mean age 38.4 (41.3) years, of them 32 (55.2%) were individuals of female gender including 21 children (mean age 12.3 (7.4) years, 14 (24.1%) girls), with the following diagnoses according to ICD-10: G12.0 (n = 7; 12.0%; only children), G12.1 (children: n = 14; 24.1%; adults: n = 29; 50.0%), G12.8 (n = 6; 10.3%; only adults), G12.9 (n = 2; 3.4%; only adults). Clinical data. Motor disorders from a mild proximal lower paraparesis (n = 13; 22.4%) to pronounced tetraparesis (n = 7; 12.0%). The study of mental status was limited to evaluation of the state of consciousness and effectiveness of contact. Data on therapy. Until 2021, symptomatic therapy of SMA was conducted in the region, since March 2021, 8 children (13.8% of the total sample) aged 7.3 (8.8) years received nusinersen, another 8 children (13.8%) aged 9.5 (6.9) years received risdiplam; parents of 3 more children (5.2%) refused taking drugs. Of adult patients (n = 37; 63.8%; 35.3 (23.6) years) with confirmed SMA 5q (n = 10; 17.2%, 35.3 (19.0) years), 1 patient received nusinersen, the rest 9 patients (15.5%) did not receive therapy, 3 (5.2%) were achieving the right to receive drugs (at the moment of the analysis). CONCLUSION: The data analysis revealed deficit of early SMA diagnosis (at the moment of the diagnosi
简介:脊髓性肌萎缩症(SMA)是一种罕见的遗传性致残疾病,也是婴儿死亡最常见的遗传性原因。及时全面的诊断SMA允许计划治疗策略和保持患者的生活质量。本文的目的之一是对SMA的发病机制、临床表现、有效诊断和现代有效治疗策略的文献资料进行综述。目的:根据萨马拉地区的实践经验,结合问题现状,评价考虑神经精神症状的SMA患者的管理策略,分析提出和组织旨在提高医疗质量的措施的问题。材料与方法:对塞雷达文萨马拉地区临床医院档案资料进行分析,处理了2008年1月至2022年2月出院的77例患者的132例病史,诊断如下(根据国际疾病与健康相关问题分类代码,第十次修订(ICD-10)):G12.0(脊髓性肌萎缩,I型[WerdnigHoffmann病]),G12.1(其他遗传性SMA), G12.8(其他SMA及相关综合征)和G12.9(未指明的SMA)。分析临床、实验室、仪器和神经精神诊断方法的结果,并与这些患者的治疗管理策略进行比较。对数据进行统计处理,采用描述性统计方法。结果:社会人口统计学数据。截至2022年2月,共有58例患者登记,平均年龄38.4(41.3)岁,其中32例(55.2%)为女性,其中21例为儿童(平均年龄12.3(7.4)岁,14例为女孩(24.1%)),根据ICD-10诊断如下:G12.0 (n = 7);12.0%;独生子女),G12.1(儿童:n = 14;24.1%;成人:29人;50.0%), G12.8 (n = 6;10.3%;仅成人),G12.9 (n = 2;3.4%;只有成年人)。临床数据轻度近端下肢截瘫引起的运动障碍(n = 13;22.4%)到明显的四肢麻痹(n = 7;12.0%)。对心理状态的研究仅限于对意识状态和接触效果的评价。治疗数据。直到2021年,该地区对SMA进行了对症治疗,自2021年3月以来,8名7.3(8.8)岁的儿童(占总样本的13.8%)接受了nusinersen,另外8名9.5(6.9)岁的儿童(13.8%)接受了risdiplam;另有3名家长(5.2%)拒绝服药。成人患者(n = 37;63.8%;35.3(23.6)岁),确认SMA 5q (n = 10;17.2%, 35.3(19.0)年),1例患者接受了nusinersen治疗,其余9例(15.5%)患者未接受治疗,3例(5.2%)患者获得了药物接受权(截至分析时)。结论:数据分析揭示了早期SMA诊断的缺陷(在诊断时,所有患者都已经有明显的症状),情感和认知障碍的评估,治疗效果的监测(缺乏有效的运动技能评估量表),也显示了成人患者治疗的可获得性较低,这需要根据所揭示的因素重新调整该地区SMA患者的护理。
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I.P. Pavlov Russian Medical Biological Herald
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