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Forensic Perspectives on Child Sexual Abuse Disclosure in Greece: A Retrospective Study. 希腊儿童性虐待披露的法医视角:一项回顾性研究。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-16 DOI: 10.3390/pediatric18010012
Konstantinos Dimitriou, Vasiliki Efthymiou, Kallirroi Fragkou, Pierre-Antoine Peyron, Laurent Martrille, Eric Baccino, Flora Bacopoulou, Stavroula Papadodima

Purpose: Child sexual abuse (CSA) is a major public health and forensic concern, often involving delayed disclosure that limits evidence collection and affects judicial outcomes. This study analyzed disclosure patterns, victim-perpetrator characteristics, and forensic findings in CSA cases evaluated in Greece, contributing to the limited Southern European evidence base. Material and Methods: A retrospective review of 89 CSA cases (2014-2024) examined by a certified forensic physician at the Department of Forensic Medicine and Toxicology, National and Kapodistrian University of Athens, was conducted. Data from official medico-legal reports included demographics, abuse context, forensic findings, and disclosure interval. Statistical analyses explored factors associated with delayed disclosure (>7 days). Results: Victims were predominantly female (69.7%) with a mean age of 9.8 years. Most perpetrators were adult males, and over half of cases (53.9%) involved intrafamilial abuse. The mean delay in disclosure was 79 days; only 29.2% reported within one week. Recurrent abuse correlated with delayed disclosure (p = 0.006), while early disclosure was associated with biological evidence collection (p < 0.001). Physical injuries were observed in 23.6% of victims, genital findings in 17%, and anal findings in 3.4%. Conclusions: Delayed disclosure was common and significantly reduced the likelihood of identifying forensic evidence. The early application of trauma-informed examinations, which adopt a child-centered approach emphasizing safety, emotional regulation, and the prevention of re-traumatization, is essential for the medical and forensic evaluation of abused children. Adopting hospital-based multidisciplinary units could improve forensic documentation, interagency coordination, and psychosocial care in Greece.

目的:儿童性虐待是一个重大的公共卫生和法医问题,往往涉及延迟披露,限制了证据收集并影响司法结果。本研究分析了在希腊评估的CSA案件的披露模式、受害者-犯罪者特征和法医调查结果,为有限的南欧证据基础做出了贡献。材料和方法:回顾性分析了89例CSA病例(2014-2024年),由雅典国立和卡波迪斯特兰大学法医学和毒理学系的一名认证法医检查。来自官方法医报告的数据包括人口统计、虐待背景、法医调查结果和披露时间间隔。统计分析探讨了延迟披露(7天)的相关因素。结果:患者以女性为主(69.7%),平均年龄9.8岁。大多数施暴者为成年男性,超过一半的案件(53.9%)涉及家庭内部虐待。平均延迟披露时间为79天;只有29.2%的人在一周内报告。反复虐待与延迟披露相关(p = 0.006),而早期披露与生物学证据收集相关(p < 0.001)。23.6%的受害者有身体损伤,17%的受害者有生殖器损伤,3.4%的受害者有肛门损伤。结论:延迟披露是常见的,并显著降低了鉴定法医证据的可能性。早期采用创伤知情检查,采用以儿童为中心的方法,强调安全、情绪调节和防止再次遭受创伤,这对受虐待儿童的医疗和法医评估至关重要。采用以医院为基础的多学科单位可以改善希腊的法医记录、机构间协调和社会心理护理。
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引用次数: 0
Parental Knowledge and Attitudes Toward Emergency Management of Dental Trauma in Children: A Cross-Sectional Croatian Study. 父母对儿童牙外伤急诊处理的知识和态度:一项克罗地亚横断面研究。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-15 DOI: 10.3390/pediatric18010011
Klaudia Aleric, Lidia Gavic, Mirna Draganja, Kristina Gorseta, Vesna Ambarkova, Antonija Tadin

Aim: Traumatic dental injuries (TDI) in children are a common but often underestimated emergency. Parental knowledge and timely response are crucial for successful treatment. This study aimed to evaluate parental knowledge, experiences, and awareness regarding dental trauma management and the use of protective mouthguards. Methods: A cross-sectional study was conducted using a self-administered questionnaire among 333 parents in dental clinics in Split and Zagreb, Croatia. The questionnaire assessed sociodemographic data, parental knowledge of TDIs, and prior experience with dental trauma. Statistical analysis included chi-square test (p < 0.05). Results: The overall level of parental knowledge regarding traumatic dental injuries was generally low (7.6 out of 15 points). Almost all parents correctly identified the age when children have primary or permanent teeth. However, less than half knew that an avulsed primary tooth should not be replanted, while about three-quarters recognized that professional help should be sought within 30 min after trauma. Overall, 43.5% of parents reported that their child had experienced dental trauma, most often affecting primary teeth (60.7%), particularly the maxillary central incisor (76.6%). Mothers demonstrated significantly higher knowledge than fathers (p = 0.025), and prior experience or information about dental trauma significantly improved awareness (p < 0.001). Although 54.3% of respondents were unaware of the purpose of dental shields, 82.3% considered them necessary during contact sports, yet only 12.9% reported that their child actually uses them. Conclusions: Within the limitations of this clinic-based study, the findings indicate gaps in parental knowledge regarding the appropriate management of dental trauma. Strengthening parents' understanding of emergency response and preventive measures may support timelier and appropriate care and contribute to improved outcomes for children experiencing traumatic dental injuries.

目的:儿童创伤性牙损伤(TDI)是一种常见但往往被低估的紧急情况。家长的知识和及时反应对成功治疗至关重要。本研究的目的是评估父母的知识,经验和意识,对牙外伤管理和使用保护齿套。方法:在克罗地亚斯普利特和萨格勒布牙科诊所的333名家长中进行了一项横断面研究,使用自我管理的问卷。问卷评估了社会人口统计数据、父母对tdi的了解程度以及先前的牙齿创伤经历。统计学分析采用卡方检验(p < 0.05)。结果:家长对创伤性牙损伤知识的总体水平普遍较低(7.6分/ 15分)。几乎所有的父母都能正确地判断出孩子长乳牙或恒牙的年龄。然而,不到一半的人知道撕脱的乳牙不应该再植,而大约四分之三的人认识到应该在创伤后30分钟内寻求专业帮助。总体而言,43.5%的父母报告他们的孩子经历过牙齿创伤,最常见的是影响乳牙(60.7%),特别是上颌中切牙(76.6%)。母亲对牙外伤的认知明显高于父亲(p = 0.025),既往经验或信息显著提高了对牙外伤的认知(p < 0.001)。虽然54.3%的受访者不知道牙护盾的用途,但82.3%的人认为在身体接触运动中使用牙护盾是必要的,但只有12.9%的人报告说他们的孩子实际上使用了牙护盾。结论:在本临床研究的局限性内,研究结果表明父母对牙外伤的适当管理知识存在差距。加强父母对应急反应和预防措施的了解,可能有助于更及时和适当的护理,并有助于改善遭受创伤性牙齿损伤的儿童的结局。
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引用次数: 0
Severe Abdominal Pain Mimicking Appendicitis Caused by Imperforate Hymen: Case Report and Narrative Review. 处女膜闭锁致严重腹痛模拟阑尾炎1例报告及叙述回顾。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-13 DOI: 10.3390/pediatric18010010
Julia Kleina, Marcin Wieczorek, Karolina Markowska, Katarzyna Nierzwicka, Julia Leszkowicz, Agnieszka Szlagatys-Sidorkiewicz

An imperforate hymen is a rare congenital genital anomaly causing menstrual blood retention during puberty. Treatment consists of a simple surgical incision of the hymenal membrane. We present a case of a 14-year-old girl who was admitted to the Emergency Department with severe lower abdominal pain mimicking appendicitis. Medical history revealed a lack of menses and several months of cyclic abdominal pain. Imaging diagnostics confirmed an imperforate hymen with hematometrocolpos. Hymenotomy was performed with full recovery without complications. An imperforate hymen should be considered in the differential diagnosis of abdominal pain in adolescent girls, especially without expected menstruation. Early recognition allows for prompt treatment and prevents complications.

处女膜闭锁是一种罕见的先天性生殖器异常,在青春期引起经血潴留。治疗包括一个简单的手术切口的处女膜。我们提出了一个14岁的女孩谁是入院急诊科严重的下腹疼痛模拟阑尾炎。病史显示没有月经和几个月的周期性腹痛。影像学诊断证实一处女膜闭锁合并血栓病。处女膜切开术完全恢复,无并发症。处女膜闭锁应考虑在鉴别诊断腹部疼痛的青春期女孩,特别是没有预期的月经。早期识别可以及时治疗并防止并发症。
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引用次数: 0
Testing the Reliability and Validity of the Turkish Adaptation of Sharenting Evaluation Scale. 土耳其语sharening量表的信度和效度检验。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-12 DOI: 10.3390/pediatric18010009
Fatih Bayraktar, Hale Ögel-Balaban

Objectives: The aim of the present study was to adapt the Sharenting Evaluation Scale to Turkish and to test its reliability and validity. Methods: Through an online data collection platform, we recruited 391 parents (Mage = 42.2, SDage = 5.6, 76% female). They have at least one child under 18 years of age and actively engage with social media. Sharenting Evaluation Scale consists of 17 items rated on a 6-point Likert scale. Its Turkish adaptation underwent a two-phase process: exploratory and confirmatory factor analyses, along with testing for construct validity. Results: The exploratory factor analysis revealed that the 17 items in the questionnaire were loaded onto two factors (Social Behavior and Implications). The confirmatory factor analysis indicated that the two-factor model fitted the current sample well. To evaluate the construct validity of the Sharenting Evaluation Scale, we compared groups at the extreme ends of the scoring spectrum. A t-test was conducted to compare the scores of both groups across subscales, revealing a significant difference. We observed positive correlations between sharenting and parental self-regulation, authoritative parenting, permissive parenting, and digital media literacy which indicate the criterion validity. Conclusions: In conclusion, the current study demonstrates that the Turkish version of the Sharenting Evaluation Scale is a reliable and valid tool.

目的:本研究的目的是将sharening量表适用于土耳其语,并检验其信度和效度。方法:通过在线数据收集平台,共招募391名家长(Mage = 42.2, SDage = 5.6, 76%为女性)。他们至少有一个18岁以下的孩子,并积极参与社交媒体。共享评估量表由17个项目组成,按6分李克特量表评分。其土耳其适应性经历了两个阶段的过程:探索性和验证性因素分析,以及结构效度测试。结果:探索性因子分析显示,问卷中的17个条目被加载到两个因子上(社会行为和影响)。验证性因子分析表明,双因子模型与当前样品拟合良好。为了评估Sharenting评价量表的结构效度,我们比较了得分谱的极端两端的组。进行t检验比较两组在各子量表上的得分,结果显示有显著差异。我们观察到育儿与父母自我调节、权威型父母、宽容型父母和数字媒体素养之间存在正相关,这表明了标准的效度。结论:总之,本研究表明,土耳其版Sharenting评估量表是一个可靠和有效的工具。
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引用次数: 0
Nationwide Study of Pediatric Drug-Resistant Epilepsy in Estonia: Lower Incidence and Insights into Etiology. 爱沙尼亚儿童耐药癫痫的全国研究:低发病率和病因学见解。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-06 DOI: 10.3390/pediatric18010008
Stella Lilles, Klari Heidmets, Kaisa Teele Oja, Karit Reinson, Laura Roht, Sander Pajusalu, Monica H Wojcik, Katrin Õunap, Inga Talvik

Background/objectives: Drug-resistant epilepsy (DRE) is a significant health problem leading to cognitive impairment and reduced quality of life. This study aimed to investigate the incidence and etiology of DRE in children in Estonia.

Methods: A retrospective, population-based study of childhood DRE was conducted in Estonia from 1 January 2013, to 31 December 2017. All cases were identified through the only two pediatric neurology departments in the country, both located at tertiary care hospitals (Tartu University Hospital and Tallinn Children's Hospital), ensuring complete nationwide coverage. Epidemiological, magnetic resonance imaging (MRI), and genetic data (chromosomal microarray, single-gene tests, gene panels, and exome/genome sequencing) were collected.

Results: The incidence rate of childhood epilepsy was 84.1 per 100,000. DRE developed in 10% of children with new-onset epilepsy, corresponding to an incidence rate of 8.5 per 100,000. Etiologically relevant MRI abnormalities were identified in 43% of patients with DRE, most commonly congenital brain malformations (19%). Pathogenic single-gene sequence variants were detected in 25 of 110 patients (23%), copy number variants in four patients (4%), and chromosomal aberrations in one patient (1%). Novel candidate disease genes of uncertain pathogenicity were identified in four patients (4%). The most frequent etiology of DRE was structural (29%), followed by genetic (19%), with combined etiologies (13%) also contributing significantly.

Conclusions: Our study is the first epidemiological study of DRE in children in Estonia and the Baltic region. The relatively low incidence observed may reflect the comprehensive national ascertainment and centralized management of pediatric epilepsy in tertiary care centers.

背景/目的:耐药癫痫(Drug-resistant epilepsy, DRE)是一种严重的健康问题,可导致认知障碍和生活质量下降。本研究旨在调查爱沙尼亚儿童DRE的发病率和病因。方法:2013年1月1日至2017年12月31日,在爱沙尼亚进行了一项基于人群的儿童DRE回顾性研究。所有病例都是通过全国仅有的两家儿科神经内科确诊的,这两家医院均位于三级保健医院(塔尔图大学医院和塔林儿童医院),确保了全国范围的全面覆盖。收集流行病学、磁共振成像(MRI)和遗传数据(染色体微阵列、单基因检测、基因面板和外显子组/基因组测序)。结果:儿童癫痫发病率为84.1 / 10万。10%的新发癫痫患儿出现DRE,相当于每10万人中有8.5例的发病率。在43%的DRE患者中发现了病因相关的MRI异常,最常见的是先天性脑畸形(19%)。110例患者中有25例(23%)检测到致病性单基因序列变异,4例(4%)检测到拷贝数变异,1例(1%)检测到染色体畸变。在4例(4%)患者中发现了致病性不确定的新的候选疾病基因。DRE最常见的病因是结构(29%),其次是遗传(19%),综合病因(13%)也有显著贡献。结论:我们的研究是爱沙尼亚和波罗的海地区儿童DRE的首次流行病学研究。相对较低的发病率可能反映了国家对儿童癫痫的全面确定和三级医疗中心的集中管理。
{"title":"Nationwide Study of Pediatric Drug-Resistant Epilepsy in Estonia: Lower Incidence and Insights into Etiology.","authors":"Stella Lilles, Klari Heidmets, Kaisa Teele Oja, Karit Reinson, Laura Roht, Sander Pajusalu, Monica H Wojcik, Katrin Õunap, Inga Talvik","doi":"10.3390/pediatric18010008","DOIUrl":"10.3390/pediatric18010008","url":null,"abstract":"<p><strong>Background/objectives: </strong>Drug-resistant epilepsy (DRE) is a significant health problem leading to cognitive impairment and reduced quality of life. This study aimed to investigate the incidence and etiology of DRE in children in Estonia.</p><p><strong>Methods: </strong>A retrospective, population-based study of childhood DRE was conducted in Estonia from 1 January 2013, to 31 December 2017. All cases were identified through the only two pediatric neurology departments in the country, both located at tertiary care hospitals (Tartu University Hospital and Tallinn Children's Hospital), ensuring complete nationwide coverage. Epidemiological, magnetic resonance imaging (MRI), and genetic data (chromosomal microarray, single-gene tests, gene panels, and exome/genome sequencing) were collected.</p><p><strong>Results: </strong>The incidence rate of childhood epilepsy was 84.1 per 100,000. DRE developed in 10% of children with new-onset epilepsy, corresponding to an incidence rate of 8.5 per 100,000. Etiologically relevant MRI abnormalities were identified in 43% of patients with DRE, most commonly congenital brain malformations (19%). Pathogenic single-gene sequence variants were detected in 25 of 110 patients (23%), copy number variants in four patients (4%), and chromosomal aberrations in one patient (1%). Novel candidate disease genes of uncertain pathogenicity were identified in four patients (4%). The most frequent etiology of DRE was structural (29%), followed by genetic (19%), with combined etiologies (13%) also contributing significantly.</p><p><strong>Conclusions: </strong>Our study is the first epidemiological study of DRE in children in Estonia and the Baltic region. The relatively low incidence observed may reflect the comprehensive national ascertainment and centralized management of pediatric epilepsy in tertiary care centers.</p>","PeriodicalId":45251,"journal":{"name":"Pediatric Reports","volume":"18 1","pages":""},"PeriodicalIF":1.4,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12821569/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146012695","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Inflammatory Biomarkers and Neurotrophic Factors in Preterm Newborns as Predictors of Motor Development: A Systematic Review. 炎症生物标志物和神经营养因子在早产新生儿中作为运动发育的预测因子:一项系统综述。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-05 DOI: 10.3390/pediatric18010007
Letícia Silva Gabriel, Vicente Donisete Ferreira Júnior, Marina Ornelas Anastácia Pereira, Dayanne Gabriela de Melo Marques, Virgínia Mendes Russo Vallejos, Melina Barros-Pinheiro

Background/Objectives: Preterm newborns (NBs) are at increased risk of motor developmental impairments. Evidence on inflammatory and neurotrophic biomarkers measured in the neonatal period as predictors of motor outcomes is scarce and heterogeneous. This systematic review synthesised data on inflammatory biomarkers and neurotrophic factors in Preterm NB as predictors of motor development (MD) up to 24 months of corrected age. Methods: MEDLINE, SciELO, Web of Science and Embase were searched for longitudinal observational studies of Preterm NB (World Health Organization definition) that measured one or more inflammatory biomarkers and/or neurotrophic factors in blood, urine or saliva and applied validated neurodevelopmental scales up to 24 months. Non-original reports, populations outside scope and studies with incomplete data were excluded. Methodological quality of primary studies was assessed with the Newcastle-Ottawa Scale (NOS). The protocol was registered in PROSPERO (CRD42022365839). Results: Of 1475 records, eight studies met the eligibility criteria. Higher neonatal concentrations of interleukin-6 (IL-6), interleukin-8 (IL-8), tumour necrosis factor-alpha (TNF-α) and C-reactive protein (CRP) were generally associated with poorer motor performance, although null findings occurred in some cohorts. One study assessing neurotrophic factors reported elevated urinary brain-derived neurotrophic factor (BDNF) and glial cell-derived neurotrophic factor (GDNF) among infants with below-expected MD. Conclusions: Inflammatory biomarkers show promise as early indicators of adverse MD in Preterm NB, but heterogeneity in populations, biospecimens, sampling windows, assays and outcome scales limits comparability and precludes definition of risk thresholds. Larger, standardised cohorts are needed to clarify the prognostic value of inflammatory and neurotrophic biomarkers and to inform early risk stratification.

背景/目的:早产儿(NBs)运动发育障碍的风险增加。在新生儿期测量炎症和神经营养生物标志物作为运动预后预测因子的证据很少且不一致。本系统综述综合了早产儿NB中炎症生物标志物和神经营养因子作为运动发育(MD)的预测因子的数据,直至矫正年龄24个月。方法:检索MEDLINE、SciELO、Web of Science和Embase对早产儿NB(世界卫生组织定义)的纵向观察研究,这些研究测量了血液、尿液或唾液中的一种或多种炎症生物标志物和/或神经营养因子,并应用了长达24个月的经过验证的神经发育量表。非原始报告、范围外人群和数据不完整的研究被排除在外。初步研究的方法学质量采用纽卡斯尔-渥太华量表(NOS)进行评估。该协议已在PROSPERO (CRD42022365839)中注册。结果:1475条记录中,8项研究符合入选标准。新生儿白细胞介素-6 (IL-6)、白细胞介素-8 (IL-8)、肿瘤坏死因子-α (TNF-α)和c反应蛋白(CRP)浓度较高通常与较差的运动表现相关,尽管在一些队列中没有发现任何结果。一项评估神经营养因子的研究报告了尿脑源性神经营养因子(BDNF)和神经胶质细胞源性神经营养因子(GDNF)在低于预期的MD婴儿中升高。结论:炎症生物标志物有望作为早产儿NB不良MD的早期指标,但人群、生物标本、采样窗口、分析和结果尺度的异质性限制了可比性,并排除了风险阈值的定义。需要更大的、标准化的队列来澄清炎症和神经营养生物标志物的预后价值,并为早期风险分层提供信息。
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引用次数: 0
Mandibular Distraction Osteogenesis Guided by 3D Model and Monitored with Ultrasonography: A Case Report. 三维模型引导下超声监测下颌骨牵张成骨1例。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-03 DOI: 10.3390/pediatric18010006
Barbora Hocková, Julien Issa, Miroslav Malček, Krzysztof Dowgierd, Rastislav Slávik, Yu-Chi Cheng, Karol Králinský, Adam Stebel

This case report describes mandibular distraction osteogenesis (DO) in a six-year-old patient with first and second branchial arch syndrome and obstructive sleep apnea, in whom 3D surgical planning was combined with ultrasonography (US) for postoperative monitoring. The aim was to illustrate how patient-specific 3D modeling and a structured ultrasonography protocol can support safe mandibular advancement while limiting radiation exposure in a pediatric patient with complex craniofacial deformity. Preoperatively, a 3D-printed model of the mandible, generated from a cone beam computed tomography (CBCT) scan, was used to guide precise osteotomy planning and vector orientation. The surgical procedure was conducted using a Risdon approach and piezoelectric tools to ensure minimal trauma. Postoperative monitoring incorporated serial panoramic radiography and US at predefined time points to assess gap size, callus formation, and vascularity during distraction and consolidation. US identified early callus formation, progressive cortical bridging, and preserved callus vascularity, and, together with radiographic findings, guided the timing of distraction termination and distractor removal at 16 weeks. This case adds to the limited literature on pediatric mandibular DO by demonstrating the feasibility of integrating patient-specific 3D virtual planning with US-based follow-up to improve the safety, precision, and radiation-conscious management of DO in pediatric patients with complex craniofacial deformities.

本病例报告描述了一名患有第一和第二鳃弓综合征并阻塞性睡眠呼吸暂停的六岁患者的下颌牵张成骨(DO),其中3D手术计划结合超声(US)进行术后监测。目的是说明患者特异性3D建模和结构化超声检查方案如何支持下颌安全推进,同时限制复杂颅面畸形儿科患者的辐射暴露。术前,由锥形束计算机断层扫描(CBCT)生成的下颌骨3d打印模型用于指导精确的截骨计划和矢量方向。手术过程采用Risdon入路和压电工具,以确保最小的创伤。术后监测包括在预定时间点的连续全景x线摄影和超声,以评估牵张和巩固期间的间隙大小、骨痂形成和血管状况。超声识别早期骨痂形成,皮质桥接进展,保留骨痂血管,并结合影像学结果,指导16周时牵张终止和牵张器移除的时机。本病例增加了关于儿童下颌DO的有限文献,证明了将患者特异性3D虚拟规划与基于美国的随访相结合的可行性,以提高复杂颅面畸形儿童DO的安全性、准确性和辐射意识管理。
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引用次数: 0
Procedural Pain and Situational Anxiety in Pediatric Patients: A Narrative Review of Assessment Tools. 儿科患者的程序性疼痛和情境性焦虑:评估工具的叙述性回顾。
IF 1.4 Q3 PEDIATRICS Pub Date : 2026-01-02 DOI: 10.3390/pediatric18010005
Anna Wojciechowska-Urbanek, Jowita Rosada-Kurasińska, Alicja Bartkowska-Śniatkowska

Background: Procedural pain and anxiety are common phenomena among children hospitalized in pediatric wards; however, they are often under-recognized. These experiences frequently accompany patients during various diagnostic and therapeutic procedures. Assessing pain is particularly challenging in pediatric care, as children may have difficulty clearly expressing their pain experiences, which can result in the underestimation of their symptoms. Accurate assessment using an appropriately selected scale should be regarded as an essential component of high-quality healthcare. Methods: This narrative review summarizes standardized tools for assessing procedural pain and anxiety in pediatric patients, focusing on instruments adapted to different ages and cognitive abilities and on their applicability in everyday clinical practice. Results: Numerous standardized scales are available, ranging from behavioral to numerical instruments tailored to specific developmental stages. Despite this, the implementation of these tools in routine care remains inconsistent, largely due to organizational, educational, and communication barriers among healthcare professionals. Conclusions: Medical staff must not only receive adequate training but also exhibit the motivation and readiness to utilize available pain assessment methods. Education and increased awareness among staff regarding pain and procedural anxiety are crucial for improving patient comfort and safety.

背景:程序性疼痛和焦虑是儿科病房住院儿童的常见现象;然而,他们经常被低估。在各种诊断和治疗过程中,这些经历经常伴随着患者。在儿科护理中,评估疼痛尤其具有挑战性,因为儿童可能难以清楚地表达他们的疼痛经历,这可能导致对其症状的低估。使用适当选择的量表进行准确评估应被视为高质量医疗保健的重要组成部分。方法:本文综述了评估儿科患者程序性疼痛和焦虑的标准化工具,重点介绍了适合不同年龄和认知能力的工具及其在日常临床实践中的适用性。结果:许多标准化的量表是可用的,从行为到量身定制的特定发展阶段的数字工具。尽管如此,这些工具在常规护理中的实施仍然不一致,主要是由于医疗保健专业人员之间的组织、教育和沟通障碍。结论:医务人员不仅要接受充分的培训,而且要表现出利用现有疼痛评估方法的积极性和准备性。教育和提高工作人员对疼痛和程序焦虑的认识对于改善患者的舒适度和安全性至关重要。
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引用次数: 0
Effects of a Media Prevention Program on Media-Related Knowledge and Awareness in Children and Their Parents: A Non-Randomized Controlled Cluster Study. 媒体预防计划对儿童及其家长媒体相关知识和意识的影响:一项非随机对照聚类研究。
IF 1.4 Q3 PEDIATRICS Pub Date : 2025-12-25 DOI: 10.3390/pediatric18010004
Tanja Poulain, Wieland Kiess, Team Drahtseil, Christof Meigen

Background/objectives: This study evaluates a media prevention program conducted in elementary schools.

Methods: A one-week media program, carried out with fourth graders in Leipzig, Germany, was evaluated using a non-randomized controlled cluster design. Program participants (experimental group (EG), n = 84 children, 41 parents) and non-participants (control group (CG), n = 19 children, 14 parents) completed questionnaires before the media program (t1), directly after the program (t2, EG only), and 3 months later (t3). The child questionnaire assessed media use frequency, rules at home, perceived and objective media-knowledge, and awareness of dangers on the Internet. The parent questionnaire assessed media-related topics discussed with their children and parents' confidence regarding media education.

Results: In the EG, children's perceived and objective knowledge and their awareness of dangers on the Internet increased significantly between t1 and t2 and remained stable until t3, while no changes were observed in the CG. The number of children reporting that there exist rules on social media use also increased significantly in the EG but not in the CG. The amount of media-related topics discussed within the family and parents' confidence regarding media education increased significantly from t1 to t3 in both EG and CG. Children's media use frequency did not change across time, neither in the EG nor in the CG.

Conclusions: Media prevention programs at school can have positive effects on children's knowledge and awareness of dangers on the Internet and might improve parents' confidence in and the realization of media education at home.

背景/目的:本研究评估在小学实施的媒体预防计划。方法:采用非随机对照聚类设计,对德国莱比锡市四年级学生进行为期一周的媒体计划进行评估。计划参与者(实验组(EG), n = 84名儿童,41名家长)和非参与者(对照组(CG), n = 19名儿童,14名家长)分别在媒体计划前(t1)、计划后(t2,仅EG)和3个月后(t3)完成问卷调查。儿童问卷评估了媒体使用频率、家庭规则、感知和客观的媒体知识以及对互联网危险的认识。家长问卷评估与子女讨论的媒体相关话题及家长对媒体教育的信心。结果:在EG中,儿童的感知知识和客观知识以及对网络危险的认知在t1和t2之间显著增加,并保持稳定至t3,而CG没有变化。报告存在社交媒体使用规则的儿童数量在EG中也显著增加,但在CG中没有。在EG和CG中,家庭内部讨论媒体相关话题的数量和父母对媒体教育的信心从t1显著增加到t3。儿童媒体使用频率没有随时间变化,EG和CG都没有。结论:学校媒体预防项目可以提高儿童对网络危险的认识和意识,并可能提高家长对家庭媒体教育的信心和实现。
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引用次数: 0
When Genes Reveal the Truth: Alport Syndrome Mimicking Steroid-Resistant Nephrotic Syndrome. 当基因揭示真相:阿尔波特综合征模仿类固醇抵抗性肾病综合征。
IF 1.4 Q3 PEDIATRICS Pub Date : 2025-12-19 DOI: 10.3390/pediatric18010003
John Dotis, Antonia Kondou, George Liapis, Athina Ververi, Konstantinos Kollios, Nikoleta Printza

Τargeted genetic sequencing in a 6-year-old with steroid-resistant nephrotic syndrome and biopsy findings of focal segmental glomerulosclerosis (FSGS) revealed a novel COL4A3 pathogenic variant (p.Arg341His). Combined with electron microscopy findings of glomerular basement membrane abnormality, this led to a diagnosis of type IV collagen-related nephropathy. This case underscores the benefit of early genetic testing in presumed FSGS for prognosis and avoiding unnecessary immunosuppression in pediatric nephrotic syndrome.

Τargeted一名6岁类固醇抵抗性肾病综合征患者的基因测序和局灶节段性肾小球硬化(FSGS)的活检结果显示,一种新的COL4A3致病变异(p.a g341his)。结合电镜检查肾小球基底膜异常,诊断为IV型胶原相关性肾病。该病例强调了在假定的FSGS中进行早期基因检测对预后的好处,并避免了儿童肾病综合征不必要的免疫抑制。
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引用次数: 0
期刊
Pediatric Reports
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