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The role of miRNAs in the development of cholangiopathies. Part 2 mirna在胆管疾病发展中的作用。第2部分
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1619
A.E. Abaturov, V.L. Babуch
The role of miRNA in the development of cho­langiopathies is considered in the scientific review. This article discusses the role of miRNA in biliary atresia, polycystic liver disease, and cholangiocarcinoma. To write the article, information was searched using Scopus, Web of Science, MedLine, PubMed, Google Scholar, EMBASE, Global Health, The Cochrane Library databases. The results of experimental studies indicate that the influence of miRNA causes the development of biliary atresia. It is found that, according to the results of ­miRNA expression profiling of extrahepatic bile ducts and gallbladder, miR-133a/b, ­miR-30b/c, miR-200a, miR-195, miR-365 and miR-320 are involved in the pathogenesis of biliary atresia. The article states that the scientists demonstrated a high level of ADD3 mRNA expression in the liver tissue of patients with biliary atresia. ADD3 overexpression promotes the adhesion and accumulation of epithelial cells in the bile ducts, which can lead to obstruction of the bile ducts and cholestasis. In turn, an excess of bile acids stimulates the proliferation of cholangiocytes and causes the development of liver fibrosis. Given that hyperproli­feration of epithelial cells of the bile ducts due to an impaired cell cycle is a key feature of cystogenesis in polycystic liver disease, researchers hypothesized that miRNAs, changing the cell cycle, may contribute to hepatic cystogenesis. The authors showed that polycystic liver disease is accompanied by a decrease in the expression of miR-15a, whose target is the mRNA of the cell division cycle 25A regulator. Numerous miRNAs are involved in the development of cholangiocarcinoma, changes in the expression and content of which in blood serum were noted in patients with this form of neoplasms. Thus, after a comprehensive review using the latest information search databases, it was found that in the modern scientific literature, the authors determine the association of micro-RNA generation activity and the development of cholangiopathies, namely: biliary atresia, polycystic liver disease, cholangiocarcinoma.
在科学综述中考虑了miRNA在cho - langopathy的发展中的作用。本文讨论了miRNA在胆道闭锁、多囊性肝病和胆管癌中的作用。为了撰写这篇文章,我们使用Scopus、Web of Science、MedLine、PubMed、Google Scholar、EMBASE、Global Health、Cochrane Library等数据库进行了信息搜索。实验研究结果表明,miRNA的影响导致了胆道闭锁的发生。我们发现,根据肝外胆管和胆囊的-miRNA表达谱结果,miR-133a/b、-miR-30b /c、miR-200a、miR-195、miR-365和miR-320参与了胆道闭锁的发病机制。这篇文章指出,科学家们在胆道闭锁患者的肝组织中发现了高水平的ADD3 mRNA表达。ADD3过表达可促进胆管上皮细胞的粘附和积聚,从而导致胆管阻塞和胆汁淤积。反过来,过量的胆汁酸刺激胆管细胞的增殖,导致肝纤维化的发展。鉴于由于细胞周期受损导致的胆管上皮细胞的过度增殖是多囊性肝病膀胱形成的一个关键特征,研究人员假设,改变细胞周期的mirna可能有助于肝脏膀胱形成。作者发现多囊性肝病伴随着miR-15a的表达降低,其靶点是细胞分裂周期25A调控因子的mRNA。许多mirna参与胆管癌的发展,在这种形式的肿瘤患者中,其在血清中的表达和含量发生了变化。因此,在使用最新的信息检索数据库进行综合审查后发现,在现代科学文献中,作者确定了微rna生成活性与胆管疾病的发展之间的关联,即:胆道闭锁、多囊性肝病、胆管癌。
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引用次数: 0
Personalized genotype-associated diagnosis of the progression of atopic march in children 儿童特应性进行曲进展的个性化基因型相关诊断
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1614
V.O. Dytiatkovskyi
Background. Atopic march (AM) is the progression of atopic lesions (AL) from monoorganic phenotypes (MOPh), usually atopic dermatitis (AD), to a combination with allergic rhinitis/rhinoconjunctivitis (AR/ARC) and bronchial asthma (BA) in the full-scope polyorganic phenotype (POPh) AD + AR/ARC + BA. At the same time, AD is the initial and basic AM MOPh. The basis of AL and AM is the human genotype, in particular, single nucleotide variants (SNV) of genes that predispose to the development of AL phenotypes. Namely, these are SNV of thymic stromal lymphopoietin (TSLP) and orоsomucoid-1-like protein 3 (ORMDL3): SNV rs_11466749 TSLP and rs_7216389 ORMDL3. The purpose of this study was to detect the associations and risks of developing AM POPh AD + AR/ARC and AD + AR/ARC + BA related to baseline MOPh AD and to each other in children with different SNV rs_11466749 TSLP and rs_7216389 ORMDL3 genotypes. Materials and methods. Two hundred and thirty-two children aged 3 to 18 years took part in the study. The main group consisted of 127 patients with 3 studied AM phenotypes: one MOPh AD (n = 58) and two POPh: AD + AR/ARC (n = 43) and AD + AR/ARC + BA (n = 26). The control group included 105 children without AL, suffering from gastrointestinal diseases. All children in the study groups underwent a buccal swab of the DNA material, which then was studied using the real-time polymerase chain reaction with restriction fragment length polymorphism to determine the genotypes of SNV candidates: A/A, A/G, G/G rs_11466749 TSLP and C/C, C/T, T/T rs_7216389 ORMDL3. Pearson’s χ2 criterion and Fisher’s exact test, Bravais-Pearson contingency coefficient (r), logistic regression analysis with determination of odds ratio (OR) with 95% confidence interval (95% CI), receiver operating characteristic (ROC) analysis with calculation of the area under the ROC curve with a 95% CI and operating characteristics — sensitivity and specificity were used for statistical processing. The critical level of statistical significance of the results during testing of all hypotheses was p < 0.05, the tendency to probability was determined at p = 0.05–0.1. Results. The following statistically significant differences were detected in the occurrence of genotypes related to the control group: for POPh AD + AR/ARC: SNV rs_7216389 ORMDL3: C/C — 14.0 %, T/T — 39.5 to 27.6 and 15.2 %, respectively (p = 0.08 and p < 0.05); for POPh AD + AR/ARC + BA: SNV rs_11466749 TSLP: A/A — 77.0 %, A/G — 11.5 to 50.5 and 45.7 %, respectively (p < 0.05 and p < 0.01). Among the phenotypes of the main group, the following statistically significant differences in the genotypes incidence had been detected: AD + AR/ARC related to AD: G/G rs_11466749 TSLP — 9.3 to 1.7 % (p = 0.08), T/T rs_7216389 ORMDL3 — 39.5 to 19.0 % (p < 0.05); AD + AR/ARC + BA related to AD: SNV rs_11466749 TSLP: A/A — 77.0 to 55.2 % (p = 0.06), A/G — 11.5 to 43.1 % (p < 0.01), G/G — 11.5 to 1.7 % (p = 0.09). The following associations were found bet
背景。特应性进行(AM)是特应性病变(AL)从单有机表型(MOPh),通常是特应性皮炎(AD),到与过敏性鼻炎/鼻结膜炎(AR/ARC)和支气管哮喘(BA)在全范围多有机表型(POPh) AD + AR/ARC + BA的结合的进展。同时,AD是初始和基本的AM MOPh。AL和AM的基础是人类基因型,特别是易导致AL表型发展的基因的单核苷酸变异(SNV)。即,这些SNV分别是胸腺基质淋巴生成素(TSLP)和orovsomucoid -1样蛋白3 (ORMDL3): SNV rs_11466749 TSLP和rs_7216389 ORMDL3。本研究的目的是检测不同SNV rs_11466749 TSLP和rs_7216389 ORMDL3基因型儿童发生AM - POPh AD + AR/ARC和AD + AR/ARC + BA与基线MOPh AD以及彼此之间的关联和风险。材料和方法。232名3至18岁的儿童参加了这项研究。主组127例患者,共有3种AM表型:1例MOPh AD (n = 58)和2例POPh: AD + AR/ARC (n = 43)和AD + AR/ARC + BA (n = 26)。对照组为105例无胃肠疾病的AL患儿。所有研究组的儿童均采用口腔拭子拭取DNA材料,然后使用限制性片段长度多态性实时聚合酶链反应进行研究,以确定SNV候选基因型:a / a, a /G, G/G rs_11466749 TSLP和C/C, C/T, T/T rs_7216389 ORMDL3。采用Pearson χ2标准和Fisher精确检验、Bravais-Pearson偶然性系数(r)、确定95%置信区间(95% CI)的优势比(OR)的logistic回归分析、计算95% CI的ROC曲线下面积的受试者工作特征(ROC)分析和工作特征-敏感性和特异性进行统计处理。所有假设检验结果的统计显著性临界水平为p <0.05,在p = 0.05 - 0.1时确定概率趋势。结果。与对照组相关基因型的发生差异有统计学意义:POPh AD + AR/ARC: SNV rs_7216389 ORMDL3: C/C - 14.0%, T/T - 39.5 ~ 27.6%, 15.2% (p = 0.08, p <0.05);对于POPh AD + AR/ARC + BA: SNV rs_11466749 TSLP分别为A/A - 77.0%、A/G - 11.5 ~ 50.5%和45.7% (p <0.05和p <0.01)。在主组表型中,AD + AR/ARC与AD相关:G/G rs_11466749 TSLP - 9.3 ~ 1.7% (p = 0.08), T/T rs_7216389 ORMDL3 - 39.5 ~ 19.0% (p <0.05);AD + AR/ARC + BA与AD相关:SNV rs_11466749 TSLP: A/A - 77.0 ~ 55.2% (p = 0.06), A/G - 11.5 ~ 43.1% (p <G/G - 11.5% ~ 1.7% (p = 0.09)。POPh AM与MOPh AD的相关性如下:AD + AR/ARC与AD相关:G/G rs_11466749 TSLP, r = 0.173 (p = 0.08), T/T rs_7216389 ORMDL3, r = 0.227 (p <0.05);AD + AR/ARC + BA与AD相关:SNV rs_11466749 TSLP: A/A, r = 0.207 (p = 0.06), A/G, r = -0.310 (p <0.01), G/G, r = 0.213 (p = 0.09)。与MOPh AD相关的有统计学意义的发生POPh AM的风险如下:AD + AR/ARC: G/G rs_11466749 TSLP, OR = 5.85 (95% CI 0.63-54.31, p = 0.08), T/T rs_7216389 ORMDL3, OR = 2.79 (95% CI 1.14-6.85, p <0.05);AD + AR/ARC + BA与AD相关:SNV rs_11466749 TSLP: A/A, OR = 2.71 (95% CI 0.95 ~ 7.73, p = 0.06), A/G, OR = 0.17 (95% CI 0.05 ~ 0.64, p <0.01)、G / G或= 7.43 (95% CI 0.73 - -75.23, p = 0.09)。结论。G/G rs_11466749 TSLP基因型携带者发生POPh AD + AR/ARC的风险是MOPh AD的5.85倍。T/T rs_7216389 ORMDL3基因型携带者与发生与MOPh AD相关的POPh AD + AR/ARC的风险(高达2.79倍)有显著的直接关联。不同类型的SNV rs_11466749 TSLP决定了AD + AR/ARC + BA发生与基本MOPh AD相关的完全性POPh的风险:A/A和G/G具有趋势显著性的直接低相关性,分别使该风险增加了2.71和7.43倍,A/G具有显著性的直接低相关性,使该风险降低了0.17倍。
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引用次数: 1
Impact of stress on adolescents during puberty (part 1) 青春期压力对青少年的影响(第一部分)
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1616
L.A. Strashok, L.I. Rak, H.M. Danylenko, A.V. Yeshchenko, V.L. Kashina-Yarmak, E.M. Zavelya, M.Yu. Isakova
The first part of the presented article deals with the actual problem of stress impact of on the body in adolescence. Puberty is characterized by significant anatomical and physiological, neuroendocrine and psychological changes. During the war in Ukraine, there are many significant factors that provoke stresses, which are superimposed on the stress of puberty. Stressors can lead to significant psychological pressure, physical problems and, as a result, an impact on the physical health and well-being of children and adolescents. A significant stress factor is a change of residence and lifestyle. The article presents the data of own research on the study of the impact of military operations in Ukraine on the psycho-emotional state and health of internally displaced school-aged children and adolescents. An increase in the tense psycho-emotional state with an increase in negative emotions among migrant adolescents compared to the pre-war period is shown. The adolescents’ optimistic view of the future indicated a certain potential for resilience. Increased sensitivity to stressful events in adolescents is due to the maturation of stress-sensitive parts of the brain and rela­ted changes in hormonal reactivity. The course of a stress reaction is coordinated by an interaction of the stress-realizing and stress-li­miting systems. The first part of the article details the neuroendocrine changes in the hypothalamus of an adolescent provoked by a combination of stress and puberty. The effects of corticotropin-releasing hormone, gonadotropin-releasing hormone and gonadotropin-inhibitory hormone, dopamine, serotonin, gamma-aminobutyric acid, and others have been described. In adolescence, the adaptive stress reactions are superimposed on the process of adaptation to sexual maturation, physical growth and psychosocial development. The relationship of hormones and neurotransmitters of the hypothalamus with other neuroendocrine factors is presented in the second part of the article.
本文的第一部分讨论了压力对青少年身体影响的实际问题。青春期以显著的解剖生理、神经内分泌和心理变化为特征。在乌克兰战争期间,有许多重要的因素引发了压力,这些因素叠加在青春期的压力上。压力源可导致严重的心理压力和身体问题,从而对儿童和青少年的身体健康和福祉产生影响。一个重要的压力因素是居住地和生活方式的改变。本文介绍了自己对乌克兰军事行动对国内流离失所学龄儿童和青少年心理情绪状态和健康影响的研究数据。与战前相比,流动青少年的紧张心理情绪状态有所增加,负面情绪也有所增加。青少年对未来的乐观态度显示出一定的弹性潜力。青少年对压力事件的敏感性增加是由于大脑对压力敏感部分的成熟以及激素反应的相关变化。应力反应的过程是由应力实现系统和应力限制系统的相互作用协调的。文章的第一部分详细介绍了由压力和青春期共同引起的青少年下丘脑神经内分泌的变化。促肾上腺皮质激素释放激素、促性腺激素释放激素和促性腺激素抑制激素、多巴胺、血清素、γ -氨基丁酸等的作用已被描述。在青春期,适应性应激反应叠加在性成熟、身体生长和心理社会发展的适应过程中。下丘脑的激素和神经递质与其他神经内分泌因子的关系在文章的第二部分。
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引用次数: 0
The effect of vitamin D supplementation on the frequency and course of recurrent respiratory diseases in children 补充维生素D对儿童复发性呼吸道疾病发生频率和病程的影响
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1612
Yu.V. Marushko, S.I. Yesipova, T.V. Hyshchak
Background. Recurrent and prolonged course of respiratory infections leads to the formation of chronic foci of inflammation, the persistence of viruses, impaired physical and psychomotor development, and a decrease in the child’s immunity. Given the participation of vitamin D (VD) in the regulation of the body’s immune response, the study of its role in the development and course of recurrent respiratory diseases in children remains re­levant. The purpose is to study the effect of vitamin D supplementation on the frequency and course of recurrent respiratory diseases in children. Materials and methods. We examined 52 children with recurrent respiratory infections aged 4 to 10 years. Children were examined before and after VD supplementation according to the study criteria: the average frequency of acute respiratory infection (ARI) episodes per year, the severity of the clinical manifestations of ARI episode, its average duration, the frequency of antibiotic prescriptions and outpatient visits to the doctor. Results. It was found that at the beginning of the exa­mination, the level of 25(OH)D in the blood serum ranged from 11.1 to 29.9 ng/ml, 22 (42.3 %) children had VD deficiency. An analysis of the frequency of ARI episodes per year showed that children with VD deficiency were ill more often than children with a sufficient level of VD (p < 0.001). According to the results of the study, it was found that VD supplementation contributes to a decrease in the frequency of ARI episodes from 8.7 ± 1.7 to 6.8 ± 1.2 times a year (p < 0.001), a decrease in the average number of symptoms of an episode of acute respiratory infections per year from 5.5 ± 0.5 to 4.5 ± 0.5 and their manifestations from 9.2 to 7.41 points (p < 0.001), a decrease in the duration of ARI episode from 6.0 ± 1.7 to 5.7 ± 1.5 days (p = 0.003), as well as a decrease in the number of outpatient visits from 5 to 4 (p = 0.004) and antibiotic prescriptions from 61 to 38 (p < 0.001). Conclusions. VD supplementation improves the course of respiratory diseases in children. The study was carried out in accordance with the Declaration of Helsinki principles. The study protocol was adopted by the ethics committee of the institution indicated in the work. The informed consent of the children’s parents was obtained.
背景。呼吸道感染的反复发作和病程延长导致慢性炎症灶的形成、病毒的持续存在、身体和精神运动发育受损以及儿童免疫力下降。鉴于维生素D (VD)参与机体免疫反应的调节,研究其在儿童复发性呼吸道疾病的发展和进程中的作用仍然具有重要意义。目的是研究补充维生素D对儿童复发性呼吸道疾病的频率和病程的影响。材料和方法。我们检查了52名4至10岁的复发性呼吸道感染儿童。根据研究标准:每年急性呼吸道感染(ARI)发作的平均频率、ARI发作的临床表现的严重程度、平均持续时间、抗生素处方的频率和门诊就诊的次数,对儿童进行VD补充前后的检查。结果。结果发现,在检查开始时,血清25(OH)D水平在11.1 ~ 29.9 ng/ml之间,22例(42.3%)患儿为VD缺乏。一项对每年ARI发作频率的分析表明,VD缺乏的儿童比VD充足的儿童更常患病(p <0.001)。根据研究结果,发现补充VD有助于将ARI发作的频率从每年8.7±1.7次降低到每年6.8±1.2次(p <0.001),每年急性呼吸道感染发作的平均症状次数从5.5±0.5减少到4.5±0.5,其表现从9.2减少到7.41分(p <急性呼吸道感染发作的持续时间从6.0±1.7天减少到5.7±1.5天(p = 0.003),门诊次数从5次减少到4次(p = 0.004),抗生素处方从61次减少到38次(p <0.001)。结论。补充VD可改善儿童呼吸道疾病的病程。这项研究是按照《赫尔辛基宣言》的原则进行的。研究方案由工作中所述机构的伦理委员会通过。得到了孩子父母的知情同意。
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引用次数: 0
Food intolerance in premature babies: possibilities of additional diagnostics 早产儿食物不耐受:其他诊断的可能性
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1617
T.K. Mavropulo, A.A. Khorosh
Due to the immaturity of the digestive system and gastrointestinal motility the preterm infants have a critical challenge in establishing adequate enteral nutrition, which is a frequent cause of gastrointestinal complications such as food intolerance and necrotizing enterocolitis. Modern clinical methods of assessing the maturity of the intestines and the child's readiness for enteral nutrition are subjective, this slows down the expansion of enteral nutrition, increases the duration of parenteral nutrition, and accordingly , period of a child`s hospitalizing. Objective methods of diagnosis are needed, which would contribute to the effective diagnosis and monitoring of food intolerance in preterm infants. Therefore, the purpose of our review was to search and summarize literature data on objective methods of diagnosing impaired food tolerance in premature baby, which could to provide daily monitoring, would be safe, cost-effective and easily accessible. Results and their discussion. Accordingly, three leading and most promising methods of examining the newborns gastrointestinal tract were analyzed. The were ultrasound examination (absence or reverse diastolic blood flow in the umbilical artery, high pulsation index in the fetal venous duct, indicators of blood flow in the upper mesenteric artery of the newborn), near-infrared spectroscopy (estimation of oxygen saturation of splanchnic tissue), and auscultation of intestinal sounds (phonoenterogram). Each of these methods has advantages and disadvantages, but to solve these existing problems, there has been recently an increasing amount of research on the bowel sounds using (namely their computerized assessment) as a new diagnostic tool. New research and further study of intestinal murmurs in premature newborns of different gestational ages with the development of clear criteria for data interpretation are needed to assess the maturity of the gastrointestinal tract, to create a diagnosis plan of food intolerance, and to develop an algorithm for early intervention.
由于消化系统和胃肠运动的不成熟,早产儿在建立足够的肠内营养方面面临重大挑战,这是食物不耐受和坏死性小肠结肠炎等胃肠道并发症的常见原因。评估肠道成熟度和儿童肠内营养准备的现代临床方法是主观的,这减缓了肠内营养的扩展,增加了肠外营养的持续时间,相应地,儿童住院的时间。需要客观的诊断方法,这将有助于有效地诊断和监测早产儿的食物不耐受。因此,我们的目的是检索和总结诊断早产儿食物耐受障碍的客观方法的文献资料,这些方法可以提供日常监测,安全、经济、容易获取。结果和讨论。据此,本文分析了三种主要的、最有前途的新生儿胃肠道检查方法。超声检查(脐动脉舒张期无血或逆血、胎儿静脉导管脉动指数高、新生儿肠系膜上动脉血流指标)、近红外光谱检查(内脏组织氧饱和度估计)、肠音听诊(肠音图)。这些方法各有优缺点,但为了解决这些存在的问题,最近越来越多的研究将肠道声音(即其计算机化评估)作为一种新的诊断工具。需要对不同胎龄早产儿肠道杂音进行新的研究和进一步研究,并制定明确的数据解释标准,以评估胃肠道的成熟度,制定食物不耐受的诊断计划,并制定早期干预的算法。
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引用次数: 0
The program of multidisciplinary online support of children with spina bifida in Ukraine during the war 战争期间乌克兰脊柱裂儿童多学科在线支持项目
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1615
O.R. Boyarchuk, M.V. Koshmaniuk
Background. The Russian aggression against Ukraine has exacerbated the challenges faced by children with spina bifida (SB). Access to healthcare is severely impacted due to security concerns, restricted mobility, and mass displacement. To address these issues and improve access to medical care, we launched a project titled “The program of multidisciplinary online support of children with spina bifida in Ukraine”. The aim: to present the program of multidisciplinary online support of patients with SB and their families during the war for improving healthcare for this vulnerable group of patients at a time of limited opportunities. Methods. The project ran from June to December 2022 and involved collaboration of the NGO “Lights of Spirit”, doctors, and specialists including a lawyer, a psychologist, a social worker, a teacher. This multidisciplinary team worked together to provide comprehensive assistance to families with children having SB. Results. Overall, 149 families with children with SB and hydrocephalus from nearly all regions of Ukraine participated in the project. Initially, 82 online consultations were conducted. Nineteen online meetings were organized for parents with the involvement of a physical therapist, an occupational therapist, and a psychologist and 87 families took part in these meetings. Parents and children with SB received online consultations from doctors of the multidisciplinary team, as well as examination, treatment, necessary care products, and medicine tailored to their individual needs. The project also provided educational, informational, and psychological support. Conclusions. The program of multidisciplinary online support of children with SB in Ukraine during the Russian invasion confirmed its significance, necessity, and effectiveness. It facilitated the formation of partnerships between patients, parents, and clinicians. The project showed the problems of prevention and care of children with SB and also prospects for future development in this field.
背景。俄罗斯对乌克兰的侵略加剧了脊柱裂儿童面临的挑战。由于安全问题、行动受限和大规模流离失所,获得医疗保健的机会受到严重影响。为了解决这些问题并改善获得医疗服务的机会,我们启动了一个名为“乌克兰脊柱裂儿童多学科在线支持方案”的项目。目的:在战争期间为SB患者及其家属提供多学科在线支持方案,以便在机会有限的情况下改善对这一弱势患者群体的医疗保健。方法。该项目从2022年6月持续到12月,涉及非政府组织“精神之光”、医生和专家的合作,包括律师、心理学家、社会工作者和教师。这个多学科团队共同努力,为有SB孩子的家庭提供全面的帮助。总体而言,来自乌克兰几乎所有地区的149个患有SB和脑积水儿童的家庭参加了该项目。最初,进行了82次在线咨询。在一名物理治疗师、一名职业治疗师和一名心理学家的参与下,为父母组织了19次在线会议,87个家庭参加了这些会议。患有SB的家长和儿童接受了多学科团队医生的在线咨询,以及为他们量身定制的检查、治疗、必要的护理产品和药物。该项目还提供教育、信息和心理支持。结论。在俄罗斯入侵乌克兰期间,对患有SB的儿童进行多学科在线支持的项目证实了其重要性、必要性和有效性。它促进了患者、家长和临床医生之间伙伴关系的形成。该项目显示了SB儿童的预防和护理存在的问题,并对该领域的未来发展进行了展望。
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引用次数: 0
Cardiovascular disorders in children with COVID-19 COVID-19患儿的心血管疾病
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1613
V.V. Yevtushenko, I.Yu. Seriakova, S.O. Kramarov, N.S. Kyrytsia, V.O. Shadrin, O.O. Voronov
Background. The purpose of the work is to study the prevalence of cardiac disorders in hospitalized children with coronavirus disease (COVID-19). Materials and methods. A retrospective, cohort, monocenter study of the medical records of children who underwent inpatient treatment between September and December 2021 at the Kyiv City Children’s Clinical Infectious Disease Hospital was conducted. For our study, we selected the medical records of patients with polymerase chain reaction-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the presence of at least one result of cardiac activity examination by electrocardiography (ECG) and/or echocardiography. The first study of cardiac activity by ECG and/or echocardiography was carried out in the first three days of inpatient treatment. Standard methods of descriptive statistics were used for data processing. Non-parametric statistical methods (Mann-Whitney test, chi-square, Pearson’s exact test) were used for mathematical analysis. The research was carried out in accordance with the Declaration of Helsinki principles. The study was approved by the bioethics committee of the hospital. Results. Among 305 children hospitalized with a diagnosis of U07.1 (2019-nCoV acute respiratory disease), there were selected 195 medical histories of patients aged 15 days to 18 years (median of 5.37 years), who were examined for cardiac activity by ECG and/or echocardiography. The most common changes were rhythm disturbances in the form of sinus tachycardia (20.8 %), bradycardia (11.9 %) and sinus arrhythmia (7.9 %), ventricular conduction disorders (25.7 %), deviation of the electrical axis of the heart (10.9 %) and repolarization disorders (31.7 %). During echocardiographic examination, structural abnormalities in the form of myocardial hypertrophy were detected in 3.1 % of patients, dilated heart chambers in 2 %, and pericardial effusion in 9.2 %. Among the functional changes, we observed: a decrease in left ventricular contractility in 4.1 % of cases, in cardiac output in 28.6 %, and an increase in total peripheral resistance in 41.8 %. Heart rhythm disturbances in the form of sinus tachycardia, deviation of the electrical axis of the heart, a decrease in the amplitude of the ECG waves, repolarization disorders, and pericardial effusion were associated with an increased risk of death in children with COVID-19. Clinical cases of cardiovascular complications in the form of jugular vein thrombosis and infectious endocarditis illustrate the role of the cardiovascular system in the pathogenesis of coronavirus disease. Conclusions. SARS-CoV-2 infection is often associated with damage to the cardiovascular system. In most pediatric patients, this occurs in the form of subclinical changes registered during laboratory or instrumental studies, but the development of manifest forms such as myocarditis, endocarditis, pericarditis, heart attack, coronary disease, thrombotic complications, and hear
背景。研究新型冠状病毒病(COVID-19)住院患儿心脏疾病的患病率。材料和方法。对2021年9月至12月期间在基辅市儿童临床传染病医院接受住院治疗的儿童的医疗记录进行了一项回顾性、队列、单中心研究。在我们的研究中,我们选择了聚合酶链反应确诊的严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染患者的医疗记录,并通过心电图(ECG)和/或超声心动图检查至少存在一项心脏活动结果。通过心电图和/或超声心动图对心脏活动的首次研究是在住院治疗的前三天进行的。数据处理采用标准的描述性统计方法。采用非参数统计方法(Mann-Whitney检验、卡方检验、Pearson精确检验)进行数学分析。这项研究是按照《赫尔辛基宣言》的原则进行的。该研究得到了医院生命伦理委员会的批准。结果。在305例诊断为U07.1 (2019-nCoV急性呼吸系统疾病)的住院儿童中,选择195例15天至18岁(中位5.37岁)的病史患者,通过心电图和/或超声心动图检查心脏活动。最常见的变化是心律失常,表现为窦性心动过速(20.8%)、心动过缓(11.9%)和窦性心律失常(7.9%)、心室传导障碍(25.7%)、心电轴偏离(10.9%)和复极障碍(31.7%)。在超声心动图检查中,3.1%的患者发现心肌肥大的结构异常,2%的患者发现心腔扩张,9.2%的患者发现心包积液。在功能变化中,我们观察到:4.1%的病例左心室收缩力下降,28.6%的病例心输出量下降,41.8%的病例总外周阻力增加。窦性心动过速、心电轴偏离、心电图波幅下降、复极障碍和心包积液等形式的心律紊乱与COVID-19患儿死亡风险增加相关。颈静脉血栓形成和感染性心内膜炎等心血管并发症的临床病例说明心血管系统在冠状病毒病发病机制中的作用。结论。SARS-CoV-2感染通常与心血管系统损伤有关。在大多数儿科患者中,这以在实验室或仪器研究中记录的亚临床变化的形式发生,但也可能发展为明显的形式,如心肌炎、心内膜炎、心包炎、心脏病发作、冠心病、血栓性并发症和心力衰竭。在筛查过程中使用简单的无创方法(心电图和超声心动图),可以诊断心血管系统的损害,并检测心血管系统的变化,这些变化是亚临床的,但对于因SARS-CoV-2感染住院的儿童的不良病程具有重要的预后价值。
{"title":"Cardiovascular disorders in children with COVID-19","authors":"V.V. Yevtushenko, I.Yu. Seriakova, S.O. Kramarov, N.S. Kyrytsia, V.O. Shadrin, O.O. Voronov","doi":"10.22141/2224-0551.18.5.2023.1613","DOIUrl":"https://doi.org/10.22141/2224-0551.18.5.2023.1613","url":null,"abstract":"Background. The purpose of the work is to study the prevalence of cardiac disorders in hospitalized children with coronavirus disease (COVID-19). Materials and methods. A retrospective, cohort, monocenter study of the medical records of children who underwent inpatient treatment between September and December 2021 at the Kyiv City Children’s Clinical Infectious Disease Hospital was conducted. For our study, we selected the medical records of patients with polymerase chain reaction-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the presence of at least one result of cardiac activity examination by electrocardiography (ECG) and/or echocardiography. The first study of cardiac activity by ECG and/or echocardiography was carried out in the first three days of inpatient treatment. Standard methods of descriptive statistics were used for data processing. Non-parametric statistical methods (Mann-Whitney test, chi-square, Pearson’s exact test) were used for mathematical analysis. The research was carried out in accordance with the Declaration of Helsinki principles. The study was approved by the bioethics committee of the hospital. Results. Among 305 children hospitalized with a diagnosis of U07.1 (2019-nCoV acute respiratory disease), there were selected 195 medical histories of patients aged 15 days to 18 years (median of 5.37 years), who were examined for cardiac activity by ECG and/or echocardiography. The most common changes were rhythm disturbances in the form of sinus tachycardia (20.8 %), bradycardia (11.9 %) and sinus arrhythmia (7.9 %), ventricular conduction disorders (25.7 %), deviation of the electrical axis of the heart (10.9 %) and repolarization disorders (31.7 %). During echocardiographic examination, structural abnormalities in the form of myocardial hypertrophy were detected in 3.1 % of patients, dilated heart chambers in 2 %, and pericardial effusion in 9.2 %. Among the functional changes, we observed: a decrease in left ventricular contractility in 4.1 % of cases, in cardiac output in 28.6 %, and an increase in total peripheral resistance in 41.8 %. Heart rhythm disturbances in the form of sinus tachycardia, deviation of the electrical axis of the heart, a decrease in the amplitude of the ECG waves, repolarization disorders, and pericardial effusion were associated with an increased risk of death in children with COVID-19. Clinical cases of cardiovascular complications in the form of jugular vein thrombosis and infectious endocarditis illustrate the role of the cardiovascular system in the pathogenesis of coronavirus disease. Conclusions. SARS-CoV-2 infection is often associated with damage to the cardiovascular system. In most pediatric patients, this occurs in the form of subclinical changes registered during laboratory or instrumental studies, but the development of manifest forms such as myocarditis, endocarditis, pericarditis, heart attack, coronary disease, thrombotic complications, and hear","PeriodicalId":338009,"journal":{"name":"CHILD`S HEALTH","volume":"31 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135258781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A case of tetanus in a previously immunized person 曾经接种过疫苗的人的破伤风病例
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1618
V.O. Rybak, V.H. Sudakevych, T.V. Nasalskyi, I.I. Dobryanska, V.V. Yevtushenko, S.O. Kramarov, N.S. Kyrytsia, O.O. Voronov, I.V. Skrytskyi
Tetanus is an acute infectious disease of humans and animals caused by anaerobic wound bacteria. The nervous system structural damage caused by toxin of the pathogen leads to tonic tension of the skeletal muscles and periodic generalized convulsions. If proper medical care is not provided in time, tetanus ends fatally. The incidence of tetanus is relatively low due to the widespread vaccination, but this infection can also occur in previously immunized individuals. The infection is widespread mainly in countries with a low economic level and weak health system. The tetanus poses a risk for all population segments, but the newborns and pregnant women are most vulnerable. Accor­ding to the Center for Public Health, 14 cases of tetanus were registered in Ukraine in 2022. The clinical picture of tetanus, as defined by the World Health Organization, includes painful muscle contractions, risus sardonicus (persistent spasm of facial muscles) and trismus (inability to open the mouth). Such patients have a history of trauma or damage to soft tissues, skin or mucous membranes. However, tetanus is a disease with multiple lesions, because in addition to the nervous system, the cardiovascular, respiratory and other systems are involved in the process. In the treatment, it is important to promptly introduce specific human tetanus immunoglobulin, perform debridement, antibiotic therapy and situational therapy. However, it should be borne in mind that the most effective and important direction is tetanus vaccination. The article presents a clinical case of tetanus in an 18-year-old pre-immunized patient who was admitted to a district hospital as a result of an injury. The purpose of publishing this case is to remind physicians to be alert for tetanus. In addition, the authors wanted to emphasize the risk of developing the disease even in previously vaccinated patients. The presence of prior vaccination and a high level of antitoxic antibodies cannot rule out a diagnosis of tetanus.
破伤风是一种由厌氧菌引起的人畜急性传染病。病原菌毒素引起的神经系统结构损伤导致骨骼肌强直性紧张和周期性全身性抽搐。如果不及时提供适当的医疗护理,破伤风就会致命。由于广泛接种疫苗,破伤风的发病率相对较低,但这种感染也可能发生在以前接种过疫苗的个体中。这种感染主要在经济水平较低和卫生系统薄弱的国家广泛存在。破伤风对所有人群都构成威胁,但新生儿和孕妇是最脆弱的。根据公共卫生中心的数据,乌克兰在2022年登记了14例破伤风病例。根据世界卫生组织的定义,破伤风的临床表现包括肌肉收缩疼痛、面部肌肉持续痉挛和牙关紧闭(无法张嘴)。此类患者有外伤或软组织、皮肤或粘膜损伤史。然而,破伤风是一种多病变的疾病,因为除了神经系统外,心血管、呼吸等系统都参与了这一过程。在治疗中,应及时引入破伤风特异性免疫球蛋白,进行清创、抗生素治疗和情境治疗。但是,应该记住,最有效和最重要的方向是破伤风疫苗接种。这篇文章介绍了一个18岁的破伤风临床病例,病人事先接种了疫苗,因受伤而住进了一家地区医院。发表这个病例的目的是提醒医生警惕破伤风。此外,作者想强调即使在以前接种过疫苗的患者中也有患病的风险。事先接种疫苗和高水平的抗毒抗体不能排除破伤风的诊断。
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引用次数: 0
Hormonal profiles and adjustment disorders in adolescent girls with menstrual abnormalities and comorbid pathology 有月经异常和共病病理的青春期女孩的激素谱和调节障碍
Pub Date : 2023-09-17 DOI: 10.22141/2224-0551.18.5.2023.1611
V.O. Dynnik, О.О. Dynnik, H.О. Havenko, Yu.V. Volkova, O.G. Verchoshanova
Background. The reproductive health of girls has acquired great social significance in connection with the problem of quantitative and qualitative reproduction of the population. The purpose of the study was to determine the hormonal status of adolescent females with menstrual disorders and various somatic pathologies and to investigate the state of adaptive-compensatory capacities in these patients. Materials and methods. The hormonal background was studied in 391 girls aged 12–17 years: 175 with abnormal uterine bleeding (AUB) and 216 with oligomenorrhea (OM). All patients were examined by a multidisciplinary team. Results. A comorbid pathology was found in the absolute majority of girls with menstrual abnormalities. Endocrine disorders were noted more often (pϕ < 0.001–0.00001). Indicators of hormone concentration in patients with menstrual disorders had no significant differences depending on the type of comorbidity. Probable changes in the content of some hormones were observed depending on the type of menstrual disorders. A significant increase in the level of luteinizing hormone (pu < 0.02) and a decrease in estradiol (pu < 0.02) were observed in patients with OM compared to those with AUB. The assessment of the adjustment state revealed that in girls with menstrual disorders, the average cortisol content did not differ from that of controls, and insulin was higher than in the comparison group (pu < 0.001). Ho­wever, high cortisol values (above 90 percentile) were noted in 8–13 % of patients with AUB and OM. The stress index (C/In) as a marker of a nonspecific stress response was lower than in the comparison group (pu < 0.0001), and it was probably higher in girls with OM than in adolescents with AUB (pu < 0.004). Conclusions. An interdisciplinary approach is a mo­dern strategy in the treatment of menstrual disorders in adolescence. A decrease in the stress index was found in girls with menstrual disorders, which may indicate a decrease in adaptive capacity. Moreover, adolescents with OM are more adjusted to menstrual disorders than girls with AUB.
背景。女孩的生殖健康在人口数量和质量上的再生产问题方面具有重要的社会意义。本研究的目的是确定患有月经紊乱和各种躯体疾病的青春期女性的激素状态,并调查这些患者的适应代偿能力状态。材料和方法。本文对391例12 ~ 17岁少女的激素背景进行了研究,其中175例为子宫异常出血(AUB), 216例为少月经(OM)。所有患者均由一个多学科小组进行检查。结果。在绝大多数月经异常的女孩中发现了共病病理。内分泌失调更常被注意到(pϕ <0.001 - -0.00001)。月经紊乱患者的激素浓度指标根据合并症的类型无显著差异。根据月经紊乱的类型,观察到一些激素含量的可能变化。黄体生成素(pu <0.02),雌二醇降低(p <与AUB患者相比,OM患者观察到0.02)。调节状态评估显示,月经紊乱的女孩平均皮质醇含量与对照组无显著差异,而胰岛素含量高于对照组(p <0.001)。然而,8 - 13%的AUB和OM患者存在高皮质醇值(高于90百分位数)。应激指数(C/In)作为非特异性应激反应的标志低于对照组(pu <0.0001),并且OM女孩的患病率可能高于AUB青少年(p <0.004)。结论。跨学科的方法是治疗青春期月经紊乱的现代策略。在月经紊乱的女孩中发现压力指数下降,这可能表明适应能力下降。此外,OM的青少年比AUB的女孩更能适应月经紊乱。
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引用次数: 0
Acute hepatitis of unknown origin in children: analysis of probable etiologies 儿童不明原因急性肝炎:可能病因分析
Pub Date : 2023-07-14 DOI: 10.22141/2224-0551.18.4.2023.1605
O. Boyarchuk, V.V. Pavlyshak
Background. An outbreak of hepatitis of unknown origin in children aged 1 month — 16 years was first reported by the WHO in April 2022. It was accompanied by a high frequency of acute liver failure, and up to 5 % of children required liver transplantation. The purpose of the review was to determine probable etiological factors and mechanisms of acute hepatitis of unknown origin based on a systematic analysis of literary sources. Materials and methods. We conducted a search for studies on cases or case series of acute hepatitis of unknown origin in the PubMed between January 2022 and February 2023. A combination of the following terms was used for the search: “unknown hepatitis”, “hepatitis of unknown origin”, “non-A-E hepatitis”, “hepatitis of unknown etiology” and “children”. Results. According to the search results, 312 publications were found. After the selection, 14 publications were included in the review. A systematic analysis of 1,188 cases of acute hepatitis of unknown origin, which corresponded to the identified case, showed a high variability of causative agents. However, most children were tested positive for adenovirus (almost 57 %), and 14 % of children had a positive PCR for SARS-CoV-2. Among other viruses detected in children, viruses of the herpes family should be noted, especially human herpesvirus 7 (34.2 %), human herpesvirus 6 (20 %), Epstein-Barr virus (18.2 %), cytomegalovirus (9.2 %). Rhinovirus (40.7 %), enterovirus/rhinovirus (28.7 %), parainfluenza virus (15.4 %), streptococcal infection, and other pathogens were also found. Conclusions. Viruses, genetic predisposition and other factors that change the body’s immune response play an important role in the development of an outbreak of severe hepatitis. Systematic analysis has shown that human adenovirus most often acts as a helper for adeno-associated virus 2, which plays a major role in initiating an immune response in genetically predisposed individuals, causing acute hepatitis and acute liver failure. SARS-CoV-2 infection probably also plays a certain role in immune activation and in the development of hyperinflammation, as do other viruses that act as helpers for adeno-associated virus 2. Continued collection of detailed clinical, microbiological, and epidemiological data on probable cases, as well as well-planned and coordinated follow-up studies are necessary to identify risk factors and other etiological factors associated with this disease.
背景。世卫组织于2022年4月首次报告了1个月至16岁儿童中爆发的不明原因肝炎。它伴随着急性肝功能衰竭的频率很高,高达5%的儿童需要肝移植。本综述的目的是在系统分析文献资料的基础上,确定不明原因急性肝炎的可能病因和发病机制。材料和方法。我们在PubMed检索了2022年1月至2023年2月期间不明原因急性肝炎病例或病例系列的研究。搜寻时所使用的关键词包括:“不明原因肝炎”、“不明原因肝炎”、“非戊型肝炎”、“不明原因肝炎”及“儿童”。结果。根据检索结果,共发现312篇论文。经筛选,14篇文献被纳入综述。一项对1188例来历不明的急性肝炎的系统分析显示,病因具有很高的可变性。然而,大多数儿童的腺病毒检测呈阳性(近57%),14%的儿童的SARS-CoV-2 PCR阳性。在儿童中检出的其他病毒中,应注意疱疹家族病毒,特别是人疱疹病毒7(34.2%)、人疱疹病毒6(20%)、eb病毒(18.2%)、巨细胞病毒(9.2%)。鼻病毒(40.7%)、肠病毒/鼻病毒(28.7%)、副流感病毒(15.4%)、链球菌感染和其他病原体。结论。病毒、遗传易感性和其他改变人体免疫反应的因素在严重肝炎爆发的发展中起着重要作用。系统分析表明,人类腺病毒通常是腺相关病毒2的辅助者,而腺相关病毒2在启动遗传易感个体的免疫反应中起主要作用,导致急性肝炎和急性肝功能衰竭。SARS-CoV-2感染也可能在免疫激活和过度炎症的发展中发挥一定作用,其他病毒也可以作为腺相关病毒2的助手。有必要继续收集有关可能病例的详细临床、微生物学和流行病学数据,以及精心规划和协调的后续研究,以确定与该病相关的危险因素和其他病因。
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