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Open educational resources for medical community 面向医学界的开放式教育资源
Pub Date : 2024-05-19 DOI: 10.34215/1609-1175-2024-1-92-99
L. L. Sadovskaya
The study reveals the great importance of open educational resources (OER) in the field of medical education and scientific activity. Objective. To develop an “OER navigator for medical community”, containing metadata of information resources with open free access. These resources are intended for use in curricula at all stages of medical education, in scientific activities and self-education. At the present stage, the social significance of education in terms of the world concept of “sustainable development” is defined as the most important component and means of survival for civilization (UNESCO). In medicine, with its special mission to preserve the health of the population, the urgent task consists in the training of highly qualified personnel. Close connection of the future of mankind with the processes of digitalization determines the availability of information resources and the use of modern technologies as key aspects of the organization of educational processes. The analysis of the scientific literature and the study of the experience of OER application revealed that OER represent an important tool in the information support of the scientific and educational sphere. OER contribute to forming a personal educational environment, learning continuously and improving skills worldwide, in perpetuity and regardless of financial capabilities. The amount of data presented on the Internet is huge, therefore, the search for necessary information takes a significant amount of time. The developed Navigator (http://lib-os.ru/obrazovatelnye-resursy/navigator-oor-medicinskogo-soobshhestva/) provides meta-data of information resources with open free access, thereby allowing representatives of the medical community at all levels of education and research to quickly and effectively find reliable scientific data and peer-reviewed sources of information.
这项研究揭示了开放式教育资源(OER)在医学教育和科学活动领域的重要意义。目标开发一个 "医学界开放教育资源导航器",其中包含免费开放的信息资源元数据。这些资源将用于医学教育各个阶段的课程、科学活动和自我教育。现阶段,从世界 "可持续发展 "的概念来看,教育的社会意义被定义为文明最重要的 组成部分和生存手段(联合国教科文组织)。医学肩负着维护人类健康的特殊使命,当务之急是培养高素质的人才。人类的未来与数字化进程密切相关,这就决定了信息资源的可用性和现代技术的使用是组织教育过程的关键方面。对科学文献的分析和对开放式教育资源应用经验的研究表明,开放式教育资源是科学和教育领域信息支持的重要工具。开放式教育资源有助于形成个人的教育环境,在全球范围内持续学习和提高技能,而且是永久性的,与经济能力无关。互联网上的数据量巨大,因此,搜索必要信息需要花费大量时间。已开发的导航器 (http://lib-os.ru/obrazovatelnye-resursy/navigator-oor-medicinskogo-soobshhestva/) 提供信息资源的元数据,并开放免费访问,从而使各级教育和研究机构的医学界代表能够快速有效地找到可靠的科学数据和经同行评审的信息来源。
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引用次数: 0
Difficulties in the diagnosis of spinal tuberculosis (clinical observation) 脊柱结核的诊断困难(临床观察)
Pub Date : 2024-05-19 DOI: 10.34215/1609-1175-2024-1-75-78
G. A. Torohtij, S. A. Belov
Neurological disorders are widely recognized as the most frequent and dangerous complication of neglected forms of spinal tuberculosis, typically leading to disability. Since tuberculous spondylitis remains free from pathognomonic clinical symptoms, the disease should be suspected in case of ineffective treatment of a non-tuberculous disease with a particular form of spinal tuberculosis to be behind. The diagnostic algorithm, being implemented from the initial stage of tuberculous osteitis formation, involves timely anti-tuberculosis treatment and correct management of patients, thereby making the basis for preventing the neurological disorders and disability of patients. The presented clinical cases indicate the advantage of an integrated approach in the diagnosis of this pathology in terms of establishing the tuberculous etiology of spondylitis.
神经系统疾病被公认为是被忽视的脊柱结核最常见、最危险的并发症,通常会导致残疾。由于结核性脊柱炎没有明显的临床症状,因此在非结核性疾病治疗无效的情况下,应怀疑脊柱结核。诊断算法从结核性骨炎形成的初期阶段开始实施,包括及时的抗结核治疗和对患者的正确管理,从而为预防患者的神经功能紊乱和残疾奠定基础。所介绍的临床病例表明,在确定脊柱炎的结核病因方面,采用综合方法诊断该病症具有优势。
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引用次数: 0
Using flow-vacuum-washing isolation device for comprehensive treatment of maxillofacial purulent-inflammatory wounds 使用流动真空清洗隔离装置综合治疗颌面部化脓性炎症伤口
Pub Date : 2024-05-19 DOI: 10.34215/1609-1175-2024-1-88-91
M. K. Kubanychbekov, D. B. Shayakhmetov, D. A. Adambekov, A. R. Tsoi, I. S. Aldzhambayeva
Purulent-inflammatory diseases of the maxillofacial region (MFR) refer to frequent complications of odontogenic inflammatory processes. The successful treatment of this pathology is based on adequate drainage of the pustule, complete evacuation of wound exudates and effective local therapy of the wound. The paper presents the flow-vacuum-washing isolation device as an effective method of comprehensive treatment for MFR abscesses and phlegmons caused by antibiotic-resistant strains of microorganisms and in patients with poor immunologic resistance.
颌面部化脓性炎症(MFR)是指牙源性炎症过程中经常出现的并发症。这种病症的成功治疗基于脓疱的充分引流、伤口渗出物的完全排空和有效的伤口局部治疗。本文介绍了流动-真空清洗隔离装置,它是综合治疗由抗生素耐药微生物菌株引起的 MFR 脓肿和痰的有效方法,也适用于免疫抵抗力差的患者。
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引用次数: 0
Case of successful treatment of spinal infection in a patient with high comorbidity and septic manifestations 成功治疗一名高度合并症和脓毒症患者脊柱感染的病例
Pub Date : 2024-05-19 DOI: 10.34215/1609-1175-2024-1-82-87
A. Yarikov, A. Vishnevsky, A. S. Filyaeva, E. A. Pavlova, O. Perlmutter, A. Fraerman, V. N. Voloshin
The study presents a clinical case of complex treatment of a patient with high comorbidity (Charlson comorbidity index = 6 points) who had severe sepsis (SOFA score = 8 points) with multiple foci of pyogenic infection (spinal epiduritis, paravertebral and subdural abscesses, purulent meningitis, bilateral lower lobe pneumonia). The syndrome-based approach with the use of minimally invasive approaches in the early stages (no later than 12 hours from the onset of clinical manifestations of the disease) ensured a favorable outcome. Based on the results of surgical treatment, a conclusion was made about the tactics of surgical treatment in patients with spinal infection against the background of sepsis.
本研究介绍了一例复杂治疗的临床病例,患者合并症较高(夏尔森合并症指数=6分),患有严重脓毒症(SOFA评分=8分),并伴有多个化脓性感染病灶(脊髓外尿道炎、椎旁和硬膜下脓肿、化脓性脑膜炎、双侧下叶肺炎)。以综合征为基础,在早期阶段(不迟于疾病出现临床表现的 12 小时)使用微创方法,确保了良好的治疗效果。根据手术治疗的结果,对脓毒症背景下脊柱感染患者的手术治疗策略做出了结论。
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引用次数: 0
Clinical case of median arcuate ligament syndrome in the practice of a pediatric surgeon 一名小儿外科医生的正中弓形韧带综合征临床病例
Pub Date : 2024-05-19 DOI: 10.34215/1609-1175-2024-1-79-81
N. A. Surkov, O. M. Dondup, F. S. Piloyan, D. M. Redkina, A. A. Zaripova
Recurrent abdominal pain in childhood and adolescence may be indicative of chronic mesenteric ischemia with median arcuate ligament syndrome as a result of compression of the celiac artery by the median arcuate ligament of the diaphragm and its internal crura, neurofibrous tissue of the celiac plexus. The presence of symptoms characteristic of various diseases of gastrointestinal tract organs, absence of pathognomonic signs and complex approach in diagnostics of abdominal cavity vascular system, insufficient awareness of specialists of children’s outpatient clinics determine the urgency of timely diagnostics and treatment of patients with this pathology. Median arcuate ligament syndrome, or Dunbar syndrome, is more often a congenital malformation. This syndrome can be considered as an acquired pathology in the case of compression of the celiac artery by enlarged lymph nodes and neurofibrous tissue of the celiac plexus. In addition to hemodynamically significant disorders of blood supply to the gastrointestinal tract, Dunbar syndrome in children and adolescents is also accompanied by psycho-emotional disorders due to the presence of unstable stools, recurrent abdominal pain, and often repeated ineffective requests for medical care. Clinical observation, methods of diagnosis and surgical treatment of median arcuate ligament syndrome in a 14-year-old patient are presented in the study.
儿童和青少年时期反复发作的腹痛可能是慢性肠系膜缺血并伴有正中弓状韧带综合征,这是腹腔动脉受到膈肌正中弓状韧带及其内部嵴、腹腔神经丛的神经纤维组织压迫的结果。胃肠道器官各种疾病的特征性症状的出现、病理征兆的缺失、腹腔血管系统诊断方法的复杂性、儿童门诊专家的认识不足,都决定了及时诊断和治疗该病症患者的紧迫性。弓状韧带中段综合征或邓巴综合征通常是一种先天性畸形。如果腹腔动脉被肿大的淋巴结和腹腔神经丛的神经纤维组织压迫,这种综合征可被视为后天性病变。儿童和青少年的邓巴综合征除了在血液动力学上造成胃肠道供血障碍外,还伴有心理情绪障碍,表现为大便不稳定、反复腹痛、经常反复求医无效。本研究介绍了一名 14 岁患者正中弓状韧带综合征的临床观察、诊断方法和手术治疗。
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引用次数: 0
Fatal case of haemorrhagic fever with renal syndrome 肾综合征出血热死亡病例
Pub Date : 2024-05-18 DOI: 10.34215/1609-1175-2024-1-72-74
A. F. Popov, V. Ivanis, V. I. Verkhoturova, E. V. Safronova, T. A. Kabantsevа, S. I. Yehlakov, V. А. Pavlov
The Far Eastern Federal District comprises an epidemic focus of hemorrhagic fever with renal syndrome (HFRS), where the incidence is determined by two orthohantaviruses: Hantaan (including its variant Amur) and Seoul. In Primorsky Krai, the average long-term incidence rate for 13 years (2011–2023) accounted for 2.7% (in some years up to 4.4% per 100 thousand population), and the mortality rate comprised 3.2% (9.1% in 2018). The distribution of clinical forms of the disease over the past 13 years revealed the prevalence of its moderate forms (66%), severe forms accounted for about 30% of all cases. The study presents a clinical case of severe course of HFRS with lethal outcome in a young male with no concomitant pathology.
远东联邦区是出血热并发肾综合征(HFRS)的流行区,其发病率由两种正交汉坦病毒决定:汉坦病毒(包括其变种阿穆尔病毒)和首尔病毒。在滨海边疆区,13年(2011-2023年)的长期平均发病率为2.7%(某些年份高达每10万人口4.4%),死亡率为3.2%(2018年为9.1%)。在过去 13 年中,该疾病临床形式的分布显示,中度形式的发病率为 66%,重度形式的发病率约占所有病例的 30%。本研究介绍了一例无并发症的年轻男性重度 HFRS 临床病例。
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引用次数: 0
Comparative characterization of interleukin genotypes and risks of bronchial asthma phenotypes in children 白细胞介素基因型与儿童支气管哮喘表型风险的比较表征
Pub Date : 2024-05-18 DOI: 10.34215/1609-1175-2024-1-5-10
V. B. Shumatov, E. V. Prosekova, M. S. Dolgopolov, A. I. Turyanskaya, V. K. Kovalchuk, V. A. Sabynych
The present paper analyses genetic predictors of various endotypes and phenotypes of bronchial asthma in children. The review of data on the structure and prevalence of single-nucleotide polymorphisms of interleukin genes demonstrates their correlation with the risk of virus-induced and allergen-induced phenotypes of bronchial asthma. Significant differences in genotypes correlate with aberrant production of interleukin and the risks for developing various phenotypes of the disease. The studies into genetic factors indicate the significance of functional polymorphisms of interleukin genes as predictors associated with phenotypes and risk of the disease.
本文分析了儿童支气管哮喘各种内型和表型的遗传预测因素。对白细胞介素基因单核苷酸多态性的结构和流行情况的数据回顾表明,它们与病毒诱发和过敏原诱发支气管哮喘表型的风险相关。基因型的显著差异与白细胞介素的异常产生和该病各种表型的发病风险相关。对遗传因素的研究表明,白细胞介素基因的功能多态性是与疾病表型和风险相关的重要预测因素。
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引用次数: 0
Variant anatomy of structures in Calot’s triangle 卡洛三角区结构的变异解剖学
Pub Date : 2024-05-18 DOI: 10.34215/1609-1175-2024-1-24-28
A. N. Shilova, T. Zharikova, K. R. Koychuev, Yury O Zharikov, V. Nikolenko
The variant anatomy of the biliary tract and its sources of blood supply causes technical difficulties and increases the risk of damage to these main structures in the area of the porta hepatis and hepatoduodenal ligament during hepatobiliary operations, especially laparoscopic cholecystectomy. The main structures form a single topographic formation – the Calot’s triangle, with possible multiple anatomical variations, considered in the literature review.
胆道及其供血来源的解剖结构多变,给肝胆手术,尤其是腹腔镜胆囊切除术带来了技术上的困难,并增加了肝门和肝十二指肠韧带区域这些主要结构受损的风险。这些主要结构形成了一个单一的地形--卡洛氏三角,文献综述中考虑了可能存在的多种解剖变异。
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引用次数: 0
Decreased antioxidant capacity in children with diabetic ketoacidosis 糖尿病酮症酸中毒患儿抗氧化能力下降
Pub Date : 2024-05-18 DOI: 10.34215/1609-1175-2024-1-39-42
Yu. V. Bykov, V. Baturin, A. P. Vorobyova, A. A. Vartanyan
Objective. To analyze the levels of antioxidant enzyme superoxide dismutase (SOD) and glutathione peroxidase (GP) against the background of diabetic ketoacidosis (DKA) in type 1 diabetes mellitus (DM) children and adolescents. Materials and methods. The study involved examination of 74 children: 50 DKA children (study group) and 24 relatively healthy children (control group). The study group children were divided into two subgroups: subgroup 1 included children with DKA against the background of type 1 DM onset (n=27), subgroup 2 consisted of children with DKA against the background of chronic type 1 DM (n=23). SOD and GP concentrations in blood plasma were determined in all children by enzyme immunoassay. The reliability between the data was estimated using the Mann-Whitney test, Kruskal-Wallis test and Spearman coefficient. Results. A significant decrease in SOD and GP in children with DKA was revealed as follows: 13130 [13005–18255] Pg/ml and 50.085 [42.02–70.325] Ng/ml, compared to controls: 16415 [13370–19935] Pg/ml and 84.695 [52.49–144.5] Ng/ml, respectively. Minimal SOD and GP were noted in patients with DKA at the background of chronic type 1 DM, compared to DM onset children. The study indicates a reliable correlation between age, duration of the disease, number of DKA in the history and low values of SOD and GP. Conclusion. Decreased antioxidant capacity was found in children with DKA in type 1 DM. SOD and GP can be considered in pediatric practice as markers of oxidative stress in DKA. In addition, an early detection of SOD and GP contributes to the efficient therapy of DKA in children and adolescents.
目的分析 1 型糖尿病(DM)儿童和青少年在糖尿病酮症酸中毒(DKA)背景下的抗氧化酶超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GP)的水平。材料和方法。该研究对 74 名儿童进行了检查:50 名 DKA 儿童(研究组)和 24 名相对健康的儿童(对照组)。研究组儿童分为两个亚组:亚组 1 包括在 1 型 DM 发病背景下患有 DKA 的儿童(人数=27),亚组 2 包括在慢性 1 型 DM 背景下患有 DKA 的儿童(人数=23)。所有患儿血浆中的 SOD 和 GP 浓度均通过酶免疫测定法测定。使用曼-惠特尼检验(Mann-Whitney test)、克鲁斯卡尔-瓦利斯检验(Kruskal-Wallis test)和斯皮尔曼系数(Spearman coefficient)估算数据之间的可靠性。结果显示结果显示,患 DKA 儿童的 SOD 和 GP 明显下降,具体情况如下:与对照组相比,分别为 13130 [13005-18255] Pg/ml 和 50.085 [42.02-70.325] Ng/ml:对照组分别为 16415 [13370-19935] Pg/ml 和 84.695 [52.49-144.5] Ng/ml。与 DM 发病儿童相比,慢性 1 型糖尿病背景下的 DKA 患者的 SOD 和 GP 最低。研究表明,年龄、病程、DKA 病史次数与 SOD 和 GP 值偏低之间存在可靠的相关性。结论研究发现,1 型糖尿病患儿的抗氧化能力降低。在儿科实践中,SOD 和 GP 可被视为 DKA 中氧化应激的标志物。此外,早期检测 SOD 和 GP 有助于有效治疗儿童和青少年的 DKA。
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引用次数: 0
Concentration of fatty acid binding protein as a new indicator of ejaculate fertility 脂肪酸结合蛋白浓度作为射精生育能力的新指标
Pub Date : 2024-05-18 DOI: 10.34215/1609-1175-2024-1-60-63
D. Sosnin, K. R. Galkovich
Objective. To determine the marker function of fatty acid binding protein (FABP) concentration in seminal plasma (SP) in order to assess ejaculate fertility used in in vitro fertilization (IVF) treatment of infertility in couples. Materials and methods. The study involved semen samples of 96 men of reproductive age: the study group (n=63) – patients with a decrease in concentration and/or total content of spermatozoa in ejaculate, the comparison group (n=33) – men with normal concentration and number of spermatozoa in ejaculate. The content of FABP in SP was determined by enzyme-linked immunosorbent assay using the test system “FABP – ELISA – BEST” (A-9102, Vector-Best, Russia). In order to determine the informative value of using the concentration of FABP in SP as a criterion of ejaculate fertility of men of the study group, the predictive value of positive and negative IVF results was determined by calculating the diagnostic sensitivity, specificity and efficiency. Results. The content of FABP in SP accounted for 1.29 ± 0.24 ng/mL, the median and interquartile range comprised 1.23 [1.13–1.35] ng/mL, ranging from 1.08 to 2.79 ng/mL. The study revealed statistically significant intergroup differences (Mann-Whitney test U=79.00; p=0.000016), a weak correlation between the level of FABP and the concentration of spermatozoa (R=0.578008) and their number in ejaculate (R=0.583599). The diagnostic sensitivity of the test for FABP in SP of the men of the study group accounted for 81.82%, specificity – 78.95%, efficiency – 80.95%. Conclusion. Seminal plasma FABP can act as a marker of spermatogenesis disorders. The study of this protein in ejaculate provides the accuracy of predicting the outcome of in vitro fertilization.
研究目的确定精浆(SP)中脂肪酸结合蛋白(FABP)浓度的标记功能,以评估用于体外受精(IVF)治疗不孕症夫妇的射精生育能力。材料与方法研究涉及96名育龄男性的精液样本:研究组(63人)--射精中精子浓度和/或总含量下降的患者;对比组(33人)--射精中精子浓度和数量正常的男性。精液中 FABP 的含量是通过酶联免疫吸附试验测定的,使用的试验系统是 "FABP - ELISA - BEST"(A-9102,Vector-Best,俄罗斯)。为了确定将 SP 中 FABP 的浓度作为研究组男性射精生育能力标准的信息价值,通过计算诊断灵敏度、特异性和效率,确定了试管婴儿阳性和阴性结果的预测价值。结果SP中的FABP含量为1.29 ± 0.24纳克/毫升,中位数和四分位数范围为1.23 [1.13-1.35]纳克/毫升,范围在1.08至2.79纳克/毫升之间。研究显示,组间差异具有统计学意义(Mann-Whitney 检验 U=79.00;P=0.000016),FABP 水平与精子浓度(R=0.578008)和精子在射精中的数量(R=0.583599)之间存在弱相关性。研究组男性 SP 中 FABP 检测的诊断灵敏度为 81.82%,特异性为 78.95%,有效率为 80.95%。结论精浆FABP可作为精子发生障碍的标志物。通过研究射精中的这种蛋白质,可以准确预测体外受精的结果。
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引用次数: 0
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Pacific Medical Journal
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