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Rehabilitation of children with Lyme arthritis 莱姆病儿童的康复治疗
Pub Date : 2023-07-14 DOI: 10.22141/2224-0551.18.4.2023.1601
S. Nykytyuk, S. Levenets, S. Klymnyuk, L. Martynyuk, D.S. Pyvovarchuk, O.B. Dyakiv, G. Gabor
Background. Lyme disease is a common tick-borne infection. Untimely diagnosis and treatment lead to the chronicity of the process with the development of late lesions of various systems and organs and possible disability. The purpose of the study was to develop a program of rehabilitation measures for children with Lyme disease. Material and methods. The research was conducted on the basis of the Ternopil Regional Children’s Hospital. Twenty children, residents of the Ternopil region, who applied to the Ternopil Regio­nal Children’s Hospital for tick bites and, as a result, diagnosed Lyme arthritis, took part in the study. To assess the severity of pain, we used scales and questionnaires for the diagnosis of DN4 neuropathic pain. Laboratory and instrumental studies were performed such as evaluation of the level of malondialdehyde, diene conjugates, superoxide dismutase. Results. Clinical examination of tick-affected children with Lyme disease showed that the most common primary clinical manifestation is a typical skin lesion — erythema migrans. In case of arthritis, all children notice inflammatory changes and pain in the joints. As a result of the conducted studies, the activation of peroxidation in children with Lyme disease was detected (an increase in the level of malondialdehyde and a decrease in superoxide dismutase, diene conjugates). It was shown that combined therapy with the use of magnetic laser therapy leads to the normalization of lipid peroxidation. Conclusions. All children with Lyme arthritis have a pain syndrome of varying severity. In patients with Lyme disease, there is an increase in the activity of lipid peroxidation and a decrease in the functional capacity of the antioxidant defense system. Children who underwent traditional treatment for Lyme arthritis reported a partial normalization of lipid peroxidation as evidenced by a significantly decreased level of diene conjugates compared to controls. In the group of patients who underwent combined treatment for Lyme arthritis (antibacterial therapy + magnetic laser therapy), the activity of antioxidant defense was normalized. Combination of magnetic laser therapy with antibacterial therapy demonstrates an improvement of pain status and faster rehabilitation of children.
背景。莱姆病是一种常见的蜱传传染病。不及时的诊断和治疗会导致这个过程的长期性,发展到各个系统和器官的晚期病变,并可能导致残疾。这项研究的目的是为患有莱姆病的儿童制定一个康复措施计划。材料和方法。这项研究是在捷尔诺波尔地区儿童医院的基础上进行的。20名来自捷尔诺皮尔地区的儿童参加了这项研究,他们向捷尔诺皮尔地区儿童医院申请蜱虫叮咬,结果被诊断为莱姆病关节炎。为了评估疼痛的严重程度,我们使用量表和问卷来诊断DN4神经性疼痛。进行了实验室和仪器研究,如丙二醛,二烯偶联物,超氧化物歧化酶水平的评估。结果。莱姆病蜱病患儿的临床检查显示,最常见的主要临床表现是典型的皮肤病变-迁移性红斑。在关节炎的情况下,所有的孩子都注意到关节的炎症变化和疼痛。在进行的研究中,检测到莱姆病儿童过氧化活性(丙二醛水平升高,超氧化物歧化酶、二烯偶联物水平降低)。结果表明,联合使用磁激光治疗可导致脂质过氧化正常化。结论。所有患有莱姆病的儿童都有不同程度的疼痛综合征。在莱姆病患者中,脂质过氧化活性增加,抗氧化防御系统的功能能力下降。接受莱姆病传统治疗的儿童报告脂质过氧化部分正常化,与对照组相比,二烯偶联物水平显著降低。在莱姆病联合治疗组(抗菌治疗+磁激光治疗),抗氧化防御活性恢复正常。磁激光联合抗菌治疗可改善患儿的疼痛状况,加快患儿的康复。
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引用次数: 0
Association of single-nucleotide variants of the orsomucoid-1-like protein 3 gene with phenotypes of atopic march in children orsomucoid-1样蛋白3基因的单核苷酸变异与儿童特应性行军表型的关系
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1586
V. Dytiatkovskyi
Background. The problem of atopic march (AM), namely its progression from monoorganic phenotypes of atopic dermatitis (AD), allergic rhinitis/rhinoconjunctivitis (AR/ARC), bronchial asthma (BA) to their multiorgan combinations, is one of the biggest in the modern pediatrics. One of the most important causes for the development of these pathologies are single nucleotide variants (SNV) of the causative genes, orsomucoid-1-like protein 3 (ORMDL3), in particular rs_7216389 ORMDL3. The roles of T- and C-alleles in relation to monoorganic and polyorganic AM phenotypes have not been sufficiently studied. The objective was to study associations of the SNVs rs_7216389 ORMDL3 in the development of different AM phenotypes in children. Materials and methods. There were 293 children recruited into the main group and 105 controls aged 3 to 18 years. Children of the main group had monoorganic and polyorganic phenotypes of AM: AD, AR/ARC, BA, AD+AR/ARC, BA+AR/ARC, AD+AR/ARC+BA. Children of the control group suffered from organic and functional digestive pathology without clinical or paraclinical signs of AM. All children were genotyped for C/C, T/T, C/T variants of SNV rs_7216389 ORMDL3 by allelic discrimination method based on real time polymerase chain reaction with restriction fragment length polymorphism of the buccal swab obtained from each patient. Spearman’s correlation coefficient (rs) was used to determine associations; risks and protective effects were determined using logistic regression analysis by calculating odds ratios (OR) and 95% confidence intervals (CI). The results obtained were significant at p < 0.05 according to the Student’s test. Results. Risks and associations for the monoorganic AR/ARC phenotype: C/C SNV rs_7216389 ­ORMDL3: rs = 0.197, OR = 0.33 (95% CI 0.14–0.78, p < 0.05); T/T SNV rs_7216389 ORMDL3: rs = 0.246, OR = 3.21 (95% CI 1.57–6.59, p < 0.05). For the monoorganic BA phenotype: T/T SNV rs_7216389 ORMDL3: rs = 0.192, CI = 2.97 (95% CI 1.08–8.14, p < 0.05). For the polyorganic AD+AR/ARC phenotype: C/C SNV rs_7216389 ORMDL3: rs = 0.146, OR = 0.42 (95% CI 0.16–1.11, p = 0.05–0.1); T/T SNV rs_7216389 ­ORMDL3: rs = 0.265, OR = 3.64 (95% CI 1.62–8.18, p < 0.05). For the polyorganic BA+AR/ARC phenotype: C/C SNV rs_7216389 ORMDL3: rs = 0.163, OR = 0.42 (95% CI 0.19–0.93, p < 0.05); T/T SNV rs_7216389 ORMDL3: rs = 0.255, OR = 3.34 (95% CI 1.63–6.82, p < 0.01). The C/T SNV rs7216389 ORMDL3 genotype did not reveal significant associations or impact on the development of any AM phenotypes in children. Conclusions. The T-allele SNV rs7216389 ORMDL3 has an inductive impact on the development of AM in children — the homozygous T/T genotype of SNV rs7216389 ORMDL3 is significantly associated with and increases the risk of developing the monoorganic AR/ARC and BA phenotypes, as well as polyorganic AD+AR/ARC and BA+AR/ARC phenotypes. The C-allele SNV rs7216389 ORMDL3 has a protective impact on the development of AM in children — the homozygous ge
背景。特应性进行(AM)的问题,即从特应性皮炎(AD)、过敏性鼻炎/鼻结膜炎(AR/ARC)、支气管哮喘(BA)的单器官表型发展到它们的多器官组合,是现代儿科最大的问题之一。这些疾病发生的最重要原因之一是致病基因orsomucoid-1-like protein 3 (ORMDL3)的单核苷酸变异(SNV),特别是rs_7216389 ORMDL3。T和c等位基因在单有机和多有机AM表型中的作用尚未得到充分研究。目的是研究snv rs_7216389 ORMDL3在儿童不同AM表型发展中的关联。材料和方法。293名儿童被纳入主要组,105名儿童被纳入对照组,年龄在3至18岁之间。主组患儿存在AM单有机和多有机表型:AD、AR/ARC、BA、AD+AR/ARC、BA+AR/ARC、AD+AR/ARC+BA。对照组的儿童患有有机和功能性消化病理,没有AM的临床或临床体征。采用基于实时聚合酶链反应的等位基因鉴别方法,对每位患者口腔拭子的限制性片段长度多态性进行SNV rs_7216389 ORMDL3的C/C、T/T、C/T变异基因分型。Spearman相关系数(rs)用于确定相关性;通过计算优势比(OR)和95%置信区间(CI),采用逻辑回归分析确定风险和保护作用。根据学生检验,所得结果p < 0.05显著。结果。单有机AR/ARC表型的风险和相关性:C/C SNV rs_7216389 -ORMDL3: rs = 0.197, OR = 0.33 (95% CI 0.14-0.78, p < 0.05);T/T SNV rs_7216389 ORMDL3: rs = 0.246, OR = 3.21 (95% CI 1.57 ~ 6.59, p < 0.05)。单有机BA表型:T/T SNV rs_7216389 ORMDL3: rs = 0.192, CI = 2.97 (95% CI 1.08 ~ 8.14, p < 0.05)。对于多有机AD+AR/ARC表型:C/C SNV rs_7216389 ORMDL3: rs = 0.146, OR = 0.42 (95% CI 0.16-1.11, p = 0.05-0.1);T/T SNV rs_7216389 -ORMDL3: rs = 0.265, OR = 3.64 (95% CI 1.62 ~ 8.18, p < 0.05)。对于多有机BA+AR/ARC表型:C/C SNV rs_7216389 ORMDL3: rs = 0.163, OR = 0.42 (95% CI 0.19-0.93, p < 0.05);T/T SNV rs_7216389 ORMDL3: rs = 0.255, OR = 3.34 (95% CI 1.63 ~ 6.82, p < 0.01)。C/T SNV rs7216389 ORMDL3基因型未显示出与儿童AM表型发展的显著关联或影响。结论。T等位基因SNV rs7216389 ORMDL3对儿童AM的发展具有诱导作用,SNV rs7216389 ORMDL3的纯合T/T基因型与单有机AR/ARC和BA表型以及多有机AD+AR/ARC和BA+AR/ARC表型的发生显著相关并增加了发病风险。C等位基因SNV rs7216389 ORMDL3对儿童AM的发展具有保护作用- SNV rs7216389 ORMDL3的纯合基因型C/C与单有机AR/AR表型以及多有机AD+AR/AR和BA+AR/ARC表型的发展显著相关并降低了风险。
{"title":"Association of single-nucleotide variants of the orsomucoid-1-like protein 3 gene with phenotypes of atopic march in children","authors":"V. Dytiatkovskyi","doi":"10.22141/2224-0551.18.3.2023.1586","DOIUrl":"https://doi.org/10.22141/2224-0551.18.3.2023.1586","url":null,"abstract":"Background. The problem of atopic march (AM), namely its progression from monoorganic phenotypes of atopic dermatitis (AD), allergic rhinitis/rhinoconjunctivitis (AR/ARC), bronchial asthma (BA) to their multiorgan combinations, is one of the biggest in the modern pediatrics. One of the most important causes for the development of these pathologies are single nucleotide variants (SNV) of the causative genes, orsomucoid-1-like protein 3 (ORMDL3), in particular rs_7216389 ORMDL3. The roles of T- and C-alleles in relation to monoorganic and polyorganic AM phenotypes have not been sufficiently studied. The objective was to study associations of the SNVs rs_7216389 ORMDL3 in the development of different AM phenotypes in children. Materials and methods. There were 293 children recruited into the main group and 105 controls aged 3 to 18 years. Children of the main group had monoorganic and polyorganic phenotypes of AM: AD, AR/ARC, BA, AD+AR/ARC, BA+AR/ARC, AD+AR/ARC+BA. Children of the control group suffered from organic and functional digestive pathology without clinical or paraclinical signs of AM. All children were genotyped for C/C, T/T, C/T variants of SNV rs_7216389 ORMDL3 by allelic discrimination method based on real time polymerase chain reaction with restriction fragment length polymorphism of the buccal swab obtained from each patient. Spearman’s correlation coefficient (rs) was used to determine associations; risks and protective effects were determined using logistic regression analysis by calculating odds ratios (OR) and 95% confidence intervals (CI). The results obtained were significant at p < 0.05 according to the Student’s test. Results. Risks and associations for the monoorganic AR/ARC phenotype: C/C SNV rs_7216389 ­ORMDL3: rs = 0.197, OR = 0.33 (95% CI 0.14–0.78, p < 0.05); T/T SNV rs_7216389 ORMDL3: rs = 0.246, OR = 3.21 (95% CI 1.57–6.59, p < 0.05). For the monoorganic BA phenotype: T/T SNV rs_7216389 ORMDL3: rs = 0.192, CI = 2.97 (95% CI 1.08–8.14, p < 0.05). For the polyorganic AD+AR/ARC phenotype: C/C SNV rs_7216389 ORMDL3: rs = 0.146, OR = 0.42 (95% CI 0.16–1.11, p = 0.05–0.1); T/T SNV rs_7216389 ­ORMDL3: rs = 0.265, OR = 3.64 (95% CI 1.62–8.18, p < 0.05). For the polyorganic BA+AR/ARC phenotype: C/C SNV rs_7216389 ORMDL3: rs = 0.163, OR = 0.42 (95% CI 0.19–0.93, p < 0.05); T/T SNV rs_7216389 ORMDL3: rs = 0.255, OR = 3.34 (95% CI 1.63–6.82, p < 0.01). The C/T SNV rs7216389 ORMDL3 genotype did not reveal significant associations or impact on the development of any AM phenotypes in children. Conclusions. The T-allele SNV rs7216389 ORMDL3 has an inductive impact on the development of AM in children — the homozygous T/T genotype of SNV rs7216389 ORMDL3 is significantly associated with and increases the risk of developing the monoorganic AR/ARC and BA phenotypes, as well as polyorganic AD+AR/ARC and BA+AR/ARC phenotypes. The C-allele SNV rs7216389 ORMDL3 has a protective impact on the development of AM in children — the homozygous ge","PeriodicalId":338009,"journal":{"name":"CHILD`S HEALTH","volume":"20 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121684976","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
Prevalence of dental caries in pediatric patients with atopic dermatitis 儿童特应性皮炎患者龋齿的患病率
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1583
T. Volosovets, I. Dikova, O. Mozyrska, N. Slyusar
Background. Children with atopic dermatitis may be at increased risk of developing dental caries. This problem is poorly understood and needs attention. The aim of this study was to investigate the oral health status of children and adolescents with atopic dermatitis. Materials and methods. One hundred children with atopic dermatitis aged 2 to 17 years, median of 6 [3.5; 10], and 103 children without atopic dermatitis, median age 7 [5; 12.5] years, were included in the study. Clinical parameters included age, sex, age of onset and severity of atopic dermatitis according to the SCORing AD index (SCORAD). Patients with at least one type of caries at any stage of progression (from white spots to carious lesions with pulpal damage) were included in the caries group. The risk of caries in the atopic dermatitis group and in healthy children, and the significance of the presence of asthma and allergic rhinitis for the development of caries were evaluated using the odds ratio (OR) with a 95% confidence interval (CI). Results were considered statistically significant at the p < 0.05 level. Results. Caries was detected in 46 % of children with atopic dermatitis and 22 % controls (OR = 2.9630, CI 1.6131–5.4424, p = 0.0005). In the group of allergic rhinitis, 24 patients were found to have caries, and among those without allergic rhinitis, 22 children had caries. It was found that patients with concomitant allergic rhinitis were significantly more likely to develop caries (OR = 3.4406, CI 1.4693–8.0563, p = 0.0044). No such significance was found depending on the presence of asthma (OR = 1.3986, CI 0.4913–3.9814, p = 0.5). Conclusions. Children with atopic dermatitis have a significantly higher risk of dental caries than healthy children. Based on the results of our study, clinicians should be aware of dental manifestations in patients with atopic dermatitis and recommend regular dental examinations for early caries detection.
背景。患有特应性皮炎的儿童患龋齿的风险可能会增加。人们对这个问题知之甚少,需要引起注意。摘要本研究旨在探讨儿童及青少年特应性皮炎患者的口腔健康状况。材料和方法。2 ~ 17岁特应性皮炎患儿100例,中位数6例[3.5;[10],无特应性皮炎患儿103例,中位年龄7岁[5;12.5岁的女性被纳入研究。临床参数包括年龄、性别、发病年龄和特应性皮炎的严重程度,依据的是score AD指数(SCORAD)。在任何进展阶段至少有一种类型的龋齿(从白斑到牙髓损伤的龋齿病变)的患者被纳入龋齿组。使用比值比(OR)评估特应性皮炎组和健康儿童的龋齿风险,以及哮喘和变应性鼻炎的存在对龋齿发展的意义,其置信区间为95%。结果在p < 0.05水平上认为有统计学意义。结果。特应性皮炎患儿中有46%检出龋,对照组中有22%检出龋(OR = 2.9630, CI 1.6133 ~ 5.4424, p = 0.0005)。在变应性鼻炎组中,有24例患儿有龋齿,在非变应性鼻炎组中,有22例患儿有龋齿。结果发现,合并变应性鼻炎的患者发生龋齿的可能性显著增加(OR = 3.4406, CI 1.4693 ~ 8.0563, p = 0.0044)。没有发现哮喘存在的相关性(OR = 1.3986, CI 0.4913-3.9814, p = 0.5)。结论。患有特应性皮炎的儿童患龋齿的风险明显高于健康儿童。根据我们的研究结果,临床医生应该了解特应性皮炎患者的牙齿表现,并建议定期进行牙科检查,以早期发现龋病。
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引用次数: 0
The role of rhinomanometry in evaluating the effectiveness of laser surgical treatment in children with chronic hypertrophic rhinitis 鼻压测量在评估儿童慢性肥厚性鼻炎激光手术治疗效果中的作用
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1580
D.F. Fuculița
Background. Rhinomanometry is an objective way of assessing nasal patency. Due to advances in technology and the use of microcomputers connected to measuring instruments, the use of this approach has increased. Rhinomanometry evaluates nasal resistance by measuring airflow and transnasal pressure gradient. With the help of this examination, the presence of a nasal respiratory obstruction is detected, and it is evaluated which nosological structure continuously causes it, in this case the hypertrophy of the inferior nasal turbinates. The purpose of the research is to evaluate the effectiveness of the functional examination such as the anterior rhinomanometry in monitoring the results of laser surgical treatment in children with chronic hypertrophic rhinitis. Materials and methods. The given study was carried out in the pediatric otorhinolaryngology clinic of the Emilian Coţaga Republican Children’s Clinical Hospital. The research involved a group of 120 children with hypertrophic chronic rhinitis, aged between 8–17 years, divided into three groups of 40 children each, treated surgically by 3 techniques: group 1 — cauterization of the inferior nasal turbinates with bipolar forceps, group 2 — shaver mucotomy and group 3 — diode laser surgery. In all patients, rhinomanometry was performed as an objective preoperative and postoperative examination on the 7th day, after one month, one year and in 12 months. Results. The analysis of the functional examination results demonstrates that the surgical interventions had a beneficial effect in terms of the recovery of the space parameters of the nasal cavities. A more pronounced improvement of the endonasal architectural indices is determined in group 3 where the diode laser surgical technique was used compared to group 2 — only shaver mucotomy and group 1 where the standard surgical technique of cauterization with bipolar forceps was practiced. Conclusions. The functional rhinomanometric results were statistically different after the surgical treatment in all study groups that indicates an important diagnostic value of this examination in the monitoring of postoperative dynamics.
背景。鼻压测量法是评价鼻通畅程度的一种客观方法。由于技术的进步和与测量仪器相连的微型计算机的使用,这种方法的使用有所增加。鼻压测量法通过测量气流和经鼻压力梯度来评估鼻阻力。在这种检查的帮助下,检测到鼻呼吸阻塞的存在,并评估是哪种疾病结构连续引起的,在这种情况下是下鼻甲肥大。本研究的目的是评估前鼻测压等功能检查在监测慢性肥厚性鼻炎儿童激光手术治疗结果中的有效性。材料和方法。本研究是在艾米利亚Coţaga共和国儿童临床医院的小儿耳鼻喉科诊所进行的。研究对象为120例肥厚性慢性鼻炎患儿,年龄在8-17岁之间,分为三组,每组40例,采用三种手术方法治疗:组1 -双极钳烧化下鼻甲,组2 -刮胡刀粘膜切开术,组3 -二极管激光手术。所有患者均于术前第7天、术后1个月、1年和12个月进行鼻压测量作为客观的术前和术后检查。结果。功能检查结果分析表明,手术干预在鼻腔空间参数恢复方面有良好的效果。与仅使用剃须刀粘膜切开术的第2组和使用双极钳烧灼的标准手术技术的第1组相比,使用二极管激光手术技术的第3组鼻内结构指标得到了更明显的改善。结论。在所有研究组中,手术治疗后的功能性鼻压力测量结果有统计学差异,这表明该检查在监测术后动态方面具有重要的诊断价值。
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引用次数: 0
Prediction of the chronicity of inflammatory diseases of the urinary system in children 儿童泌尿系统炎症性疾病的慢性预测
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1582
H. O. Lezhenko, N. A. Zakharchenko
Background. The purpose was stratification of factors that lead to the chronicity of inflammatory diseases of the urinary system in children, as well as creation of a mathematical model for predicting their course. Materials and methods. The research group consisted of 97 children (average age — 10.0 ± 1.3 years). The main group was divided into subgroups: the first one — 43 children with acute urinary tract infections (UTIs), the second one — 34 patients with chronic UTIs. The control group consisted of 20 conditionally healthy children. The content of 1,25(OH)2D3, vitamin D-binding protein, inducible nitric oxide synthase (NOS2), cystatin C, cathelicidin, hepcidin, lactoferrin, interleukins 6, 15 was investigated by immunoenzymatic analysis. The impact of factor characteristics on the process of UTI chronicity was evaluated using factor and cluster analyses. A logistic regression equation was used to predict the probability of developing chronic UTIs. The quality of the constructed model was assessed by its sensitivity and specificity, and receiver operator characteristic (ROC) analysis was also used. Results. It was found that 6 factors had the greatest significance: the factor of functional disorders of the urinary tract, the factor of comorbid conditions, the protective factor, the immune factor, chronic foci of the disease, and the NOS2 factor. According to the results of logistic regression, the model for predicting the probability of developing chronic UTI in children had the form of an equation that included 6 variables (early manifestation of the disease, vitamin D level, vesicoureteral reflux, dysmetabolic nephropathy, neurogenic bladder, UTI in the mother in childhood). The classification ability of the model was determined based on the data of the training sample and was 75.0 %. The sensitivity of the model was 78.3 %, and the specificity was 76.5 %. The area under the ROC curve that corresponded to our mathematical model was equal to 0.776. The Gini index was 55.2 %, which corresponds to the good quality of the model. Conclusions. The process of chronicity of the inflammatory process in the urinary system in children occurs under the conditions of the interaction of some pathological factors. The leading risk factors for the chronicity of the inflammatory process are the presence of functional disorders of the urinary tract, early manifestation of the disease, the level of vitamin D, intestinal dysfunction, and the presence of UTI in the mother in childhood.
背景。目的是对导致儿童泌尿系统炎症性疾病的慢性因素进行分层,并建立一个预测其病程的数学模型。材料和方法。研究组共97例儿童,平均年龄- 10.0±1.3岁。主要分组分为急性尿路感染患儿43例,慢性尿路感染患儿34例。对照组为条件健康儿童20例。采用免疫酶分析方法研究了1,25(OH)2D3、维生素d结合蛋白、诱导型一氧化氮合酶(NOS2)、胱抑素C、抗菌肽、肝磷脂、乳铁蛋白、白细胞介素6,15的含量。采用因子分析和聚类分析评价因子特征对UTI慢性化过程的影响。采用logistic回归方程预测发生慢性尿路感染的概率。通过模型的敏感性和特异性评估模型的质量,并采用受试者操作特征(ROC)分析。结果。结果发现,尿路功能障碍因素、合并症因素、保护因素、免疫因素、疾病的慢性病灶、NOS2因素6个因素的意义最大。根据logistic回归结果,预测儿童慢性UTI发生概率的模型为包含6个变量(疾病早期表现、维生素D水平、膀胱输尿管反流、代谢异常肾病、神经源性膀胱、母亲儿童期UTI)的方程形式。根据训练样本的数据确定模型的分类能力为75.0%。该模型的敏感性为78.3%,特异性为76.5%。与我们的数学模型相对应的ROC曲线下的面积等于0.776。基尼系数为55.2%,说明模型质量较好。结论。儿童泌尿系统炎症过程的慢性过程是在一些病理因素相互作用的条件下发生的。慢性炎症过程的主要危险因素是尿路功能障碍的存在、疾病的早期表现、维生素D水平、肠道功能障碍以及母亲在儿童期存在尿路感染。
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引用次数: 0
Congenital heart defect — aortopulmonary window: diagnostic features in infants 先天性心脏缺损-主动脉肺窗:婴儿的诊断特征
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1591
A. Malska, O. Kuryliak, T. Yalynska, O. V. Stogova
Aortopulmonary window (APW) is a congenital heart defect characterized by the presence of an abnormal connection between the pulmonary artery and the proximal part of the aortic arch directly above the level of the semilunar valves. It is one of the rarest cardiac defects (frequency of 0.2–0.6 %). APW occurs as an isolated cardiac lesion or in association with other anomalies such as coarctation of the aorta, interrupted aortic arch, tetra­logy of Fallot, and atrial septal defect or patent ductus arteriosus. Treatment of APW comprises surgical correction of the defect, which should be performed immediately after diagnosis in order to prevent the development of pulmonary hypertension. Postoperative complications after surgical correction of APW occur rarely and depend on the association of this defect with other congenital heart defects, especially with an interrupted aortic arch. In this article, we present a retrospective analysis of patients with APW for 2003–2022, who were examined at the Lviv Regional Children’s Hospital OHMATDYT, and 2 clinical cases of APW in 2- and 10-month-old boys.
主动脉肺窗(APW)是一种先天性心脏缺陷,其特征是肺动脉与主动脉弓近端直接高于半月瓣水平的异常连接。它是最罕见的心脏缺陷之一(发生率为0.2 - 0.6%)。APW是一种孤立的心脏病变,或与其他异常有关,如主动脉缩窄、主动脉弓中断、法洛四联症、房间隔缺损或动脉导管未闭。APW的治疗包括手术矫正缺陷,应在诊断后立即进行手术,以防止肺动脉高压的发展。APW手术矫正后的术后并发症很少发生,并且依赖于该缺陷与其他先天性心脏缺陷的关联,特别是主动脉弓中断。在这篇文章中,我们回顾性分析了2003-2022年在利沃夫地区儿童医院OHMATDYT检查的APW患者,以及2例2月龄和10月龄男孩的APW临床病例。
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引用次数: 0
The role of vitamin D in the course of SARS-CoV-2 infection and long COVID in children (literature review) 维生素D在儿童SARS-CoV-2感染和长冠状病毒过程中的作用(文献复习)
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1590
L. Volianska, E. Burbela, T. Kosovska, V.O. Perestyuk, O. Boyarchuk
Long-term observation of the SARS-CoV-2 pandemic in the pediatric population revealed the presence of persistent symptoms in 1 : 4 to 1 : 10 children four or more weeks after the onset of this infection. The question about the role of vitamin D in the course of COVID-19 and the development of long-term health conditions is still debatable. The purpose of this review is to generalize and clarify the effect of vitamin D on the course of ­COVID-19 and the post-COVID period in children. Electronic search for scientific publications was done in the PubMed, Scopus, ResearchGate, Wiley Online Library and Google Scholar databases from 2019 to February 2023. Analysis of studies on COVID-19, the post-COVID period, and the impact of hypovitaminosis D on their course attests to the ambiguity of published results in the pediatric cohort. A number of resear­chers have linked vitamin D deficiency to higher mortality, higher hospitalization rates, and longer hospital stays. Hypovitaminosis D impairs the functioning of the immune system in an organism infected with the pandemic coronavirus, which increases the risk of severe course and mortality. But this hypothesis still needs in-depth study to understand the essence of the effect of vitamin D supplementation on the course of the coronavirus infection and long COVID. The hypothesis about the relationship between hypovitaminosis D and immunosuppression during infection with a pandemic coronavirus and its potential role in the formation of long-term health conditions after acute COVID-19 is still under permanent study.
对儿科人群中SARS-CoV-2大流行的长期观察显示,在感染发病后4周或更长时间内,1:4至1:10的儿童存在持续症状。关于维生素D在COVID-19过程中的作用和长期健康状况的发展仍然存在争议。本综述的目的是总结和阐明维生素D对儿童covid -19病程和covid -19后期的影响。从2019年到2023年2月,在PubMed、Scopus、ResearchGate、Wiley Online Library和Google Scholar数据库中进行了科学出版物的电子搜索。对COVID-19、covid后时期以及维生素D缺乏症对病程影响的研究分析证实了已发表的儿科队列研究结果的模糊性。许多研究人员将维生素D缺乏与更高的死亡率、更高的住院率和更长的住院时间联系起来。维生素D缺乏症会损害感染大流行冠状病毒的生物体的免疫系统功能,从而增加严重病程和死亡的风险。但这一假设仍需要深入研究,以了解补充维生素D对冠状病毒感染过程和长期COVID影响的本质。关于大流行冠状病毒感染期间维生素D缺乏症与免疫抑制之间的关系及其在急性COVID-19后长期健康状况形成中的潜在作用的假设仍在长期研究中。
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引用次数: 0
Chronic tonsillitis in adolescents: clinical features and the role of ultrasound diagnosis in the northern region of Ukraine 慢性扁桃体炎在青少年:临床特点和超声诊断在乌克兰北部地区的作用
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1579
Yuliia A Manko, O. I. Smiian, A. Loboda, S. V. Popov, P. I. Sichnenko, O. Vasylieva, K. Smiian, I. Vysotsky, T. Aleksakhina
Background. Chronic tonsillitis is the most common disease among children and adolescents in the structure of pathology of the ENT organs. Untimely diagnosis and irrational treatment lead to decompensation of chronic tonsillitis and the development of lesions of many organs and systems of the child’s body of tonsillogenic origin. The aim of the work was to study the clinical features and ultrasound changes of the palatine tonsils in adolescents with chronic tonsillitis. Materials and methods. We have examined 47 children aged 13 to 17 years suffering from chronic tonsillitis: group I — 27 patients with compensated chronic tonsillitis, group II — 20 patients suffering from decompensated chronic tonsillitis. The control group consisted of 16 practically healthy children, representative in terms of age and gender. We used clinical methods, ultrasonography of the palatine tonsils, and statistical methods. The study was approved by the Institutional Bioethics Committee and it conforms to the principles outlined in the Declaration of Helsinki. Results. According to the results of an ultrasound examination of the palatine tonsils in children with chronic tonsillitis, the main changes were an increase in their transverse dimensions by more than 15 mm, deepening of lacunae, thickening of the capsule, fibrous changes. In addition, in patients with tonsillogenic lesions of the cardiovascular system and a decompensated form of chronic tonsillitis, the pathological signs of the disease according to ultrasound were more significant and were manifested by unclear contours, increased echogenicity, heterogeneous hyperechoic structure, diffuse fibrous and cystic changes of the palatine tonsils. Conclusions. Ultrasonography of the palatine tonsils is a non-invasive, painless, accessible and informative method for studying the structure of the tonsils in normal and pathological conditions. It allows for a more thorough assessment of their changes in compensated and decompensated forms of chronic tonsillitis.
背景。慢性扁桃体炎是儿童和青少年耳鼻喉器官病理结构中最常见的疾病。不及时的诊断和不合理的治疗导致慢性扁桃体炎失代偿和扁桃体起源的儿童身体的许多器官和系统的病变的发展。研究慢性扁桃体炎青少年腭扁桃体的临床特征及超声改变。材料和方法。我们检查了47名13至17岁患有慢性扁桃体炎的儿童:I组- 27例代偿性慢性扁桃体炎,II组- 20例患有失代偿性慢性扁桃体炎。对照组由16名实际健康的儿童组成,在年龄和性别方面具有代表性。我们采用临床方法、腭扁桃体超声检查和统计学方法。该研究得到了机构生物伦理委员会的批准,并符合《赫尔辛基宣言》中概述的原则。结果。根据慢性扁桃体炎儿童的腭扁桃体超声检查结果,主要变化是其横向尺寸增加超过15毫米,腔隙加深,被膜增厚,纤维改变。此外,在心血管系统扁桃体源性病变和慢性扁桃体失代偿型的患者中,超声检查的病理征象更为明显,表现为轮廓不清、回声增强、异质高回声结构、腭扁桃体弥漫性纤维性和囊性改变。结论。腭扁桃体超声检查是一种无创、无痛、方便、信息丰富的研究扁桃体在正常和病理状态下结构的方法。它允许更彻底的评估他们在代偿和失代偿形式的慢性扁桃体炎的变化。
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引用次数: 0
Parental presence in the pediatric intensive care unit 父母在儿科重症监护病房的存在
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1589
V. Snisar, S. Egorov
Background. Currently, parental presence at the bedside of critically ill children in the pediatric intensive care unit (PICU) is a necessary family-oriented condition. In the published sources, there is enough evidence that shows the special emotional state of parents, their complex interactions with the medical staff of the PICU, as well as the attitude of doctors and nurses to parental presence in the department, especially during the manipulation on patients. In Ukraine, only in some pediatric medical centers parents were allowed to visit their children in the PICU, but permanent stay at the patient’s bedside was not allowed. In 2016, the order of the Ministry of Health of Ukraine No. 592 “On the approval of the Procedure for the admission of visitors to patients undergoing inpatient treatment in the intensive care unit” determined the procedure and rules for the admission of visitors to a patient who was in the intensive care unit. However, this Order established only rules for the admission of visitors to adult patients undergoing inpatient treatment in the intensive care units. The purpose of the work is to consider various strategic directions for ensuring access of parents to their sick children in the PICU and try to adapt some issues to the current state of our pediatric intensive care. Results. The article discusses issues such as the ethical and practical situation regarding the visiting and presence of parents at the bedside of a critically ill child in the PICU. The concepts of “visiting” or “presence” are considered, and the conditions are defined when parents can only visit, and when they can stay at the bedside of a sick child for a long time; the possibility of their presence during manipulations and procedures; the role of doctors and nurses in communicating with parents in the intensive care unit and the impact on their emotional state. Conclusions. Given the real need for parents to be present and visit their children in the intensive care unit, we must be careful and prudent in making this decision. You can face a lot of problems and inconveniences, but you must strive to change the established principles, because the presence of fa­mily members, their participation in providing assistance to children will improve the psychological environment in the intensive care unit and increase the humaneness of the work of its medical staff.
背景。目前,在儿童重症监护病房(PICU),父母陪伴在病重儿童的床边是一个必要的面向家庭的条件。在已发表的资料中,有足够的证据表明父母的特殊情绪状态,他们与PICU医务人员的复杂互动,以及医生和护士对父母在科室出现的态度,特别是在对患者进行操作时。在乌克兰,只有在一些儿科医疗中心,父母才被允许到重症监护病房探望他们的孩子,但不允许在病人床边永久停留。2016年,乌克兰卫生部第592号命令“关于批准探访在重症监护室接受住院治疗的病人的程序”,确定了探访在重症监护室的病人的程序和规则。但是,这项命令只规定了探视在重症监护病房接受住院治疗的成年病人的规则。这项工作的目的是考虑各种战略方向,以确保父母能够接触到PICU中的患病儿童,并试图使一些问题适应我国儿科重症监护的现状。结果。本文讨论的问题,如伦理和实际情况有关访问和父母在重症监护病房的床边存在的孩子。考虑了“探视”或“在场”的概念,并规定了父母只能探视和长时间陪伴患儿的条件;它们在操作和程序中存在的可能性;重症监护病房医护人员与家长沟通的作用及其对家长情绪状态的影响。结论。考虑到真正需要父母在重症监护病房探望他们的孩子,我们在做出这个决定时必须小心谨慎。你可能会面临很多问题和不便,但你必须努力改变既定的原则,因为家庭成员的存在,他们参与为儿童提供援助,将改善重症监护室的心理环境,增加医务人员工作的人性化。
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引用次数: 0
Healthcare-associated infections in children in Ukraine during 2009–2021 2009-2021年乌克兰儿童保健相关感染情况
Pub Date : 2023-07-06 DOI: 10.22141/2224-0551.18.3.2023.1588
O. Korniychuk, I. Tymchuk, S.Y. Pavliy, Y. Konechnyi
Background. Healthcare-associated infections (HCAIs) now include the development of infectious processes in various organ systems of patients and at hospitals of different work directions. It is believed that HCAIs are infections that first occur 48 hours or later after hospitalization or 30 days after receiving medical care. The aim of our research was a retrospective analysis of the incidence of HCAIs among children in Ukraine during 2009–2021. Materials and methods. Statistical analysis of the prevalence of registered cases of HCAIs in Ukraine for 2009–2021, according to the Center for Public Health of the Ministry of Health of Ukraine. Results. On average, 966 ± 489 cases of HCAIs were registered annually in Ukraine among children of various ages. According to the age distribution, the number of annual cases of HCAIs among newborns of up to 1 month of age averaged 65.8 %, for those aged 1 month to 1 year — 5.9 %, from 1 to 17 years — 28.3 %. According to the nosological structure of HCAIs, infections of certain conditions occurring in the perinatal period prevailed among children. On average, the number of such diseases for 2010–2021 was 49.5 ± 7.5 % (among children 0–17 years old) and 13.8 % of the total cases of HCAIs in Ukraine. Conclusions. In recent years, there has been an underestimation of HCAI cases in Ukraine among adult patients and children. Nevertheless, indicators provided by institutions of some regions (Odesa and Kyiv regions) make it possible, with a certain degree of probability, to get an idea of the structure of HCAI incidence in the country. According to the age structure, HCAIs in children (0–17 years) for 2009–2021 accounted for 22.06 % of the total number of HCAIs. Most cases during the specified period were recorded among newborns, 65.8 % of all children with HCAIs. Therefore, the primary efforts should be aimed at reducing HCAIs among newborns.
背景。医疗保健相关感染(HCAIs)现在包括在不同工作方向的患者和医院的各种器官系统的感染过程的发展。一般认为,hcai是在住院后48小时或更晚或接受医疗护理后30天首次发生的感染。本研究的目的是回顾性分析2009-2021年乌克兰儿童hcai发病率。材料和方法。根据乌克兰卫生部公共卫生中心的数据,2009-2021年乌克兰hcai登记病例流行率的统计分析。结果。乌克兰各年龄段儿童平均每年登记hcai 966±489例。根据年龄分布,1月龄以下新生儿hcai年平均病例数为65.8%,1月龄至1岁为5.9%,1岁至17岁为28.3%。根据hcai的分科结构,围产儿中出现的某些情况的感染在儿童中普遍存在。在乌克兰,2010-2021年这类疾病的数量平均为49.5%±7.5%(0-17岁儿童),占hcai总病例的13.8%。结论。近年来,乌克兰成人患者和儿童的HCAI病例被低估了。尽管如此,一些地区(敖德萨和基辅地区)的机构提供的指标在一定程度上可能使我们了解该国HCAI发病率的结构。从年龄结构看,2009-2021年0-17岁儿童hcai占hcai总数的22.06%。在指定期间记录的大多数病例为新生儿,占所有hcai儿童的65.8%。因此,主要的努力应以减少新生儿hcai为目标。
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引用次数: 0
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CHILD`S HEALTH
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