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Iodine Status in Cyprus and Neighboring Countries: A Review Article. 塞浦路斯及其邻国的碘状况:评论文章。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963275007231227051736
Nese Akcan, Ismet Zaimagaoglu

Despite the implementation of global iodine supplementation initiatives in the past decade, the problem of iodine deficiency persists as a significant public health concern in numerous countries. Although cretinism is now rare in developed countries, iodine deficiency can still lead to less severe cognitive deficits, which can negatively impact academic achievement, intellectual capacity, and work productivity. There is a scarcity of studies regarding the status of Cyprus, and the global database does not have any information pertaining to the prevalence of iodine deficiency in Cyprus. The geographical setting of the research is of importance as it pertains to the separation of Cyprus into two distinct areas. One region is predominantly inhabited by Greek Cypriots, where the practice of salt iodization is not mandatory. Conversely, the other region is primarily inhabited by Turkish Cypriots, who may potentially experience higher amounts of iodine contact due to their reliance on food imports from Turkey, where salt-iodisation is compulsory. The main objective of this study is to provide an overview of recent research conducted on the prevalence of iodine deficiency in Cyprus and neighboring Mediterranean nations. In this study, we assess the current method and subsequently offer public health recommendations for future research endeavors.

尽管过去十年间全球实施了多项补碘措施,但在许多国家,碘缺乏问题仍然是一个重大的公共卫生问题。虽然克汀病目前在发达国家已很少见,但碘缺乏仍会导致不太严重的认知障碍,从而对学习成绩、智力和工作效率产生负面影响。有关塞浦路斯现状的研究很少,全球数据库中也没有任何有关塞浦路斯碘缺乏症患病率的信息。研究的地理环境非常重要,因为塞浦路斯被分为两个不同的地区。一个地区主要由希族塞浦路斯人居住,他们不强制要求食盐加碘。相反,另一个地区主要由土族塞人居住,由于他们依赖从土耳其进口食品,而土耳其强制要求食盐加碘,因此土族塞人可能会接触到更多的碘。本研究的主要目的是概述近期对塞浦路斯及邻近地中海国家碘缺乏症患病率所做的研究。在这项研究中,我们评估了当前的方法,并随后为未来的研究工作提出了公共卫生建议。
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引用次数: 0
Late Relapse in Neuroblastoma: Case Report and Review of the Literature. 神经母细胞瘤的晚期复发:病例报告和文献复习。
IF 1.6 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963255648231024081333
Rejin Kebudi, Begum Koc, Banu Oflaz Sozmen

Background: Neuroblastoma is the most com mon extra-cranial solid tu mor in children. The survival rate of relapsed/refractory neuroblastoma is dismal. Late recurrence may occur rarely.

Case presentation: We have, herein, presented a case with stage IV neuroblastoma who relapsed after 11 years and had a subsequent relapse after 15 years from the initial diagnosis, and reviewed cases with late relapsed (after >5 years) neuroblastoma in the literature. The case presented with recurrent disease at the T7 vertebra after 11 years from the initial diagnosis. The patient received surgery, che motherapy, MIBG treatment, and antiGD2 combined with che motherapy, and had a further local recurrence in the paravertebral area of the re moved T7 vertebra after three years. The patient was operated, received anti-GD2 combined with che motherapy, and is still alive with no symptoms for 19 months after the last relapse.

Conclusion: There is not a well-established treatment regimen for the majority of these patients. MIBG treatment and antiGD2 combined with che motherapy may be promising options for relapsed/ refractory neuroblastoma.

背景:神经母细胞瘤是儿童最常见的颅外实体瘤。复发/难治性神经母细胞瘤的生存率令人沮丧。晚期复发可能很少发生。病例介绍:我们在本文中介绍了一例IV期神经母细胞瘤,从最初诊断起11年后复发,15年后再次复发,并回顾了文献中晚期复发(5年以上)的神经母细胞癌病例。该病例自最初诊断起11年后出现T7椎骨的复发性疾病。患者接受了手术、化疗、MIBG治疗和抗GD2联合化疗,三年后切除的T7椎骨的椎旁区域再次局部复发。该患者接受了手术,接受了抗GD2联合化疗,在最后一次复发后的19个月内仍然存活,没有任何症状。结论:对于这些患者中的大多数,没有一个完善的治疗方案。MIBG治疗和抗GD2联合化疗可能是治疗复发/难治性神经母细胞瘤的有希望的选择。
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引用次数: 0
Insights from Overviewing Selective International Guidelines for Pediatric Asthma. 选择性国际儿科哮喘指南概览》的启示。
IF 1.6 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963270829231221062201
Kam L E Hon, Daniel K K Ng, Wa K Chiu, Alexander K C Leung

Background: Asthma is a chronic atopic and inflammatory bronchial disease characterized by recurring symptoms, episodic reversible bronchial obstruction and easily triggered bronchospasms. Asthma often begins in childhood. International guidelines are widely accepted and implemented; however, there are similarities and differences in the management approaches. There is no national guideline in many cities in Asia. This review aims to provide a practical perspective on current recommendations in the management of childhood asthma, specifically in the following aspects: diagnosis, classification of severity, treatment options, and asthma control, and to provide physicians with up-to-date information for the management of asthma.

Methods: We used the PubMed function of Clinical Queries and searched keywords of "Asthma", "Pediatric" AND "Guidelines" as the search engine. "Clinical Prediction Guides", "Etiology", "Diagnosis", "Therapy," "Prognosis," and "Narrow" scope were used as filters. The search was conducted in November 2022. The information retrieved from this search was used in compiling the present article.

Results: Diagnosis is clinically based on symptom pattern, response to therapy with bronchodilators and inhaled corticosteroids, and spirometric pulmonary function testing (PFT). Asthma is classified in accordance with symptom frequency, peak expiratory flow rate (PEFR), forced expiratory volume in one second (FEV1), and atopic versus nonatopic etiology, where atopy means a predisposition toward a type 1 hypersensitivity reaction. Asthma is also classified as intermittent or persistent (mild to severe). Unfortunately, there is no disease cure for asthma. However, symptoms can be prevented by trigger avoidance and suppressed with inhaled corticosteroids. Antileukotriene agents or long-acting beta-agonists (LABA) may be used together with inhaled corticosteroids if symptoms of asthma are not controlled. Rapidly worsening symptoms are usually treated with an inhaled short-acting beta-2 agonist (SABA, e.g., salbutamol) and oral corticosteroids. Intravenous corticosteroids and hospitalization are required in severe cases of asthma attacks. Some guidelines also provide recommendations on the use of biologics and immunotherapy.

Conclusion: Asthma is diagnosed clinically, with supporting laboratory testing. Treatment is based on severity classification, from intermittent to persistent. Inhaled bronchodilator and anti-inflammatory corticosteroid form the main stay of management.

背景:哮喘是一种慢性特应性和炎症性支气管疾病,其特点是症状反复出现、发作性可逆支气管阻塞和易诱发支气管痉挛。哮喘通常始于儿童时期。国际指南已被广泛接受和实施,但在管理方法上却有异曲同工之妙。亚洲的许多城市都没有全国性的指南。本综述旨在从实用的角度介绍当前儿童哮喘管理的建议,特别是以下几个方面:诊断、严重程度分类、治疗方案和哮喘控制,并为医生提供哮喘管理的最新信息:我们使用 PubMed 的临床查询功能,以 "哮喘"、"儿科 "和 "指南 "为关键词进行搜索。筛选条件包括 "临床预测指南"、"病因学"、"诊断"、"治疗"、"预后 "和 "狭窄 "范围。搜索于 2022 年 11 月进行。从该搜索中检索到的信息被用于撰写本文:临床诊断基于症状模式、对支气管扩张剂和吸入皮质类固醇治疗的反应以及肺功能测试(PFT)。哮喘根据症状频率、呼气峰流速(PEFR)、一秒钟用力呼气容积(FEV1)、特应性病因与非特应性病因进行分类,其中特应性病因是指易发生 1 型超敏反应。哮喘还分为间歇性和持续性(轻度到重度)。遗憾的是,哮喘目前还没有根治的方法。不过,可以通过避免诱发因素来预防症状,并通过吸入皮质类固醇来抑制症状。如果哮喘症状未得到控制,抗白三烯药物或长效β-激动剂(LABA)可与吸入皮质类固醇一起使用。症状迅速恶化时,通常使用吸入式短效β2受体激动剂(SABA,如沙丁胺醇)和口服皮质类固醇。哮喘发作严重时需要静脉注射皮质类固醇和住院治疗。一些指南还对生物制剂和免疫疗法的使用提出了建议:结论:哮喘由临床诊断,并辅以实验室检测。治疗以严重程度分类为基础,从间歇性到持续性。吸入支气管扩张剂和类固醇抗炎药物是主要的治疗方法。
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引用次数: 0
Strategies for Pain Management after Extraction of Primary Teeth: A Systematic Review of Randomized Clinical Trials. 拔除基牙后的疼痛控制策略:随机临床试验的系统回顾。
IF 1.6 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963292710240725051920
Janina Rodrigues, Luiz Felipe Palma, Gabriela Seabra da Silva, Lucas Santiago Franca, Livia Araújo Alves, Daniela Prócida Raggio, Tamara Kerber Tedesco

Background: In dental extractions, particularly when local anesthesia is used, it usually offers analgesic relief for a few hours. However, pain can become a notable concern in the immediate postoperative period due to the trauma experienced by both soft and hard oral tissues.

Objectives: This systematic review aimed to evaluate the most effective strategies for managing postoperative pain in primary tooth extractions.

Methods: Two examiners conducted a search across electronic databases: MEDLINE (via PubMed), Embase, Scopus, Web of Science, CENTRAL, and OpenGray. Studies were included if they met the following criteria after reviewing their titles and abstracts: they involved children and evaluated pain management following primary tooth extraction. Subsequently, articles that described extractions performed under any form of sedation, were not conducted under local anesthesia, in an outpatient setting, and in children aged 0 to 12 years, or were not randomized controlled trials, were excluded.

Results: The search yielded 374 relevant articles, of which 9 were included. Among these, 5 utilized preoperative medications as a pain management strategy, one evaluated low-level laser therapy (LLLT) postoperatively, one assessed calendula drops postoperatively, and another explored virtual reality during the procedure and arnica in solution both pre and postoperatively.

Conclusion: Among all the strategies evaluated, the strategy involving analgesics administered 30 minutes before tooth extractions was supported by better-designed studies. However, there is a high risk of bias.

背景:在牙科拔牙手术中,尤其是使用局部麻醉时,通常可在数小时内缓解疼痛。然而,由于口腔软组织和硬组织受到的创伤,疼痛可能会在术后立即成为一个值得关注的问题:本系统综述旨在评估处理基牙拔除术后疼痛的最有效策略:方法: 两名审查员对五个电子数据库进行了检索:方法: 两名审查员在五个电子数据库中进行了检索:MEDLINE(通过 PubMed)、Embase、Scopus、Web of Science、CENTRAL 和 OpenGray。在审阅了研究的标题和摘要后,符合以下标准的研究均被纳入:涉及儿童并评估了拔除原牙后的疼痛管理。随后,排除了描述在任何形式的镇静剂下进行拔牙、未在局部麻醉下进行拔牙、在门诊环境下进行拔牙、拔牙对象为 0 至 12 岁儿童或非随机对照试验的文章:结果:搜索结果显示有 374 篇相关文章,其中 9 篇被纳入。其中,5 篇文章采用术前用药作为疼痛管理策略,1 篇文章评估了术后低强度激光疗法(LLLT),1 篇文章评估了术后金盏花滴剂,另一篇文章探讨了手术过程中的虚拟现实技术以及术前和术后的山金车溶液:结论:在所有评估策略中,拔牙前 30 分钟使用镇痛剂的策略得到了设计较好的研究的支持。然而,存在偏倚的风险很高。
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引用次数: 0
Prevalence of Bruxism in Children and Adolescents with Cerebral Palsy: Systematic Review and Meta-analysis. 脑瘫儿童和青少年的磨牙症患病率:系统回顾与元分析》。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963252499231120092148
Nathalia Kanhouche, Gabriela Godoy Pizzi, Nathalia Araujo Bim, Rafael Celestino de Souza, Ana Flávia Bissoto Calvo, Isabela Floriano, Thais Gimenez, José Carlos Pettorossi Imparato, Tamara Kerber Tedesco

Aims: To perform a systematic review and meta-analysis compiling data on the prevalence of bruxism in children and adolescents with cerebral palsy.

Methods and results: Searches were carried out in PubMed/Medline, Web of Science, and Scopus databases to identify the articles published by February 2023. Two independent reviewers, and in duplicate, employed a two-stage process to select publications. The same two reviewers performed the data extraction. Studies were included when the following eligibility criteria were met: performed in children and/or adolescents with cerebral palsy and reporting bruxism. Potentially eligible studies were read in full and excluded that: not presented numerical data on the prevalence of bruxism; not reported how the bruxism was assessed; not reported data about the cerebral palsy; and not an observational study. The risk assessment of bias was assessed by the Newcastle- Ottawa Scale. After reading the titles and abstracts of the 358 identified articles, eight articles from 1966 to 2020 were included. The main reason for not including the studies was not to report data about bruxism (59.3%), and 44.5% were excluded for not reporting data from patients with cerebral palsy. The studies were carried out in schools, university hospitals, or centers for patients with special needs (Brazil, the United States, and Egypt). The pooled prevalence of bruxism in children and adolescents with cerebral palsy was 46% (95%CI: 0.38-0.55) after removing one study.

Conclusion: The pooled prevalence of bruxism in children with cerebral palsy can be considered high since almost half of the studied population is affected by this condition. PROSPERO #CRD42021225781.

目的:对脑瘫儿童和青少年磨牙症的患病率进行系统回顾和荟萃分析:在PubMed/Medline、Web of Science和Scopus数据库中进行检索,以确定2023年2月之前发表的文章。两名独立的审稿人采用两阶段的方法对出版物进行筛选。由同两位审稿人进行数据提取。符合以下资格标准的研究均被纳入:研究对象为患有脑瘫的儿童和/或青少年,并报告了磨牙症。对可能符合条件的研究进行了全文阅读,并排除了以下情况的研究:未提供有关磨牙症发生率的数字数据;未报告如何评估磨牙症;未报告有关脑瘫的数据;非观察性研究。偏倚风险评估采用纽卡斯尔-渥太华量表。在阅读了 358 篇已确定文章的标题和摘要后,8 篇 1966 年至 2020 年的文章被纳入其中。未纳入研究的主要原因是未报告有关磨牙症的数据(59.3%),44.5%的研究因未报告脑瘫患者的数据而被排除。这些研究都是在学校、大学医院或特殊需要患者中心(巴西、美国和埃及)进行的。剔除一项研究后,汇总的脑瘫儿童和青少年磨牙症患病率为 46%(95%CI:0.38-0.55):结论:脑瘫儿童磨牙症的总患病率可以说很高,因为几乎一半的研究对象都患有这种疾病。PERROPO #CRD42021225781。
{"title":"Prevalence of Bruxism in Children and Adolescents with Cerebral Palsy: Systematic Review and Meta-analysis.","authors":"Nathalia Kanhouche, Gabriela Godoy Pizzi, Nathalia Araujo Bim, Rafael Celestino de Souza, Ana Flávia Bissoto Calvo, Isabela Floriano, Thais Gimenez, José Carlos Pettorossi Imparato, Tamara Kerber Tedesco","doi":"10.2174/0115733963252499231120092148","DOIUrl":"10.2174/0115733963252499231120092148","url":null,"abstract":"<p><strong>Aims: </strong>To perform a systematic review and meta-analysis compiling data on the prevalence of bruxism in children and adolescents with cerebral palsy.</p><p><strong>Methods and results: </strong>Searches were carried out in PubMed/Medline, Web of Science, and Scopus databases to identify the articles published by February 2023. Two independent reviewers, and in duplicate, employed a two-stage process to select publications. The same two reviewers performed the data extraction. Studies were included when the following eligibility criteria were met: performed in children and/or adolescents with cerebral palsy and reporting bruxism. Potentially eligible studies were read in full and excluded that: not presented numerical data on the prevalence of bruxism; not reported how the bruxism was assessed; not reported data about the cerebral palsy; and not an observational study. The risk assessment of bias was assessed by the Newcastle- Ottawa Scale. After reading the titles and abstracts of the 358 identified articles, eight articles from 1966 to 2020 were included. The main reason for not including the studies was not to report data about bruxism (59.3%), and 44.5% were excluded for not reporting data from patients with cerebral palsy. The studies were carried out in schools, university hospitals, or centers for patients with special needs (Brazil, the United States, and Egypt). The pooled prevalence of bruxism in children and adolescents with cerebral palsy was 46% (95%CI: 0.38-0.55) after removing one study.</p><p><strong>Conclusion: </strong>The pooled prevalence of bruxism in children with cerebral palsy can be considered high since almost half of the studied population is affected by this condition. PROSPERO #CRD42021225781.</p>","PeriodicalId":11175,"journal":{"name":"Current Pediatric Reviews","volume":" ","pages":"166-173"},"PeriodicalIF":1.3,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139511948","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
Lichen Striatus: An Updated Review. 地衣:最新综述。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963273945240101042423
Alexander K C Leung, Joseph M Lam, Benjamin Barankin, Kin Fon Leong

Background: Lichen striatus is a benign dermatosis that affects mainly children. This condition mimics many other dermatoses.

Objectives: The purpose of this article is to familiarize pediatricians with the clinical manifestations of lichen striatus to avoid misdiagnosis, unnecessary investigations, unnecessary referrals, and mismanagement of lichen striatus.

Methods: A search was conducted in June 2023 in PubMed Clinical Queries using the key term "Lichen striatus". The search strategy included all observational studies, clinical trials, and reviews published within the past ten years. Only papers published in the English literature were included in this review. The information retrieved from the above search was used in the compilation of this article.

Results: Lichen striatus is a benign self-limited T-cell mediated dermatosis characterized by a linear inflammatory papular eruption seen primarily in children. The onset is usually sudden with minimal or absent symptomatology. The eruption in typical lichen striatus consists of discrete, skin- colored, pink, erythematous, or violaceous, flat-topped, slightly elevated, smooth or scaly papules that coalesce to form a dull red, potentially scaly, interrupted or continuous band over days to weeks. Although any part of the body may be involved, the extremities are the sites of predilection. Typically, the rash is solitary, unilateral, and follows Blaschko lines. In dark-skinned individuals, the skin lesions may be hypopigmented at onset. Nails may be affected alone or, more commonly, along with the skin lesions of lichen striatus. The differential diagnoses of lichen striatus are many and the salient features of other conditions are highlighted in the text.

Conclusion: Lichen striatus is a self-limited condition that often resolves within one year without residual scarring but may have transient post-inflammatory hypopigmentation or hyperpigmentation. As such, treatment may not be necessary. For patients who desire treatment for cosmesis or for the symptomatic treatment of pruritus, a low- to mid-potency topical corticosteroid or a topical immunomodulator can be used. A fading cream can be used for post-inflammatory hyperpigmentation.

背景:条纹状苔藓是一种良性皮肤病,主要影响儿童。这种疾病与许多其他皮肤病相似:本文旨在让儿科医生熟悉苔藓样变的临床表现,以避免误诊、不必要的检查、不必要的转诊以及对苔藓样变的错误处理:方法:2023 年 6 月,使用关键词 "苔藓样变 "在 PubMed Clinical Queries 中进行了检索。搜索策略包括过去十年内发表的所有观察性研究、临床试验和综述。本综述仅包括英文文献中发表的论文。从上述检索中获取的信息用于本文的撰写:条纹状苔藓是一种由 T 细胞介导的良性自限性皮肤病,以线状炎性丘疹糜烂为特征,主要见于儿童。通常突然发病,症状轻微或无症状。典型的条纹状苔藓的疹子由离散的、皮肤色的、粉红色、红斑的或腥臭的、平顶的、稍隆起的、光滑的或有鳞屑的丘疹组成,这些丘疹在数天至数周内凝聚成暗红色、可能有鳞屑、间断的或连续的带状。虽然身体的任何部位都可能受累,但四肢是好发部位。典型的皮疹为单发、单侧、沿布拉什科线分布。皮肤黝黑的人在发病时皮损可能色素减退。指甲可能单独受累,或更常见的是与纹状苔藓的皮损同时受累。苔癣的鉴别诊断很多,文中强调了其他疾病的显著特征:苔癣是一种自限性疾病,通常在一年内消退,不会留下疤痕,但可能出现一过性的炎症后色素减退或色素沉着。因此,可能不需要治疗。如果患者希望通过治疗来改善外观或对症治疗瘙痒,可以使用中低效的外用皮质类固醇激素或外用免疫调节剂。炎症后色素沉着可使用褪色霜。
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引用次数: 0
Pinworm (Enterobius Vermicularis) Infestation: An Updated Review. 蛲虫(Enterobius Vermicularis)感染:最新综述。
IF 1.6 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963283507240115112552
Alexander K C Leung, Joseph M Lam, Benjamin Barankin, Alex H C Wong, Kin F Leong, Kam L Hon
<p><strong>Background: </strong>Pinworm infestation is an important public health problem worldwide, especially among children 5 to 10 years of age in developing countries with temperate climates. The problem is often overlooked because of its mild or asymptomatic clinical manifestations.</p><p><strong>Objectives: </strong>The purpose of this article was to familiarize pediatricians with the diagnosis and management of pinworm infestation.</p><p><strong>Methods: </strong>A search was conducted in August 2023 in PubMed Clinical Queries using the key terms "Enterobius vermicularis," OR "enterobiasis," OR "pinworm." The search strategy included all clinical trials, observational studies, and reviews published within the past 10 years. Only papers published in the English literature were included in this review. The information retrieved from the above search was used in the compilation of the present article.</p><p><strong>Results: </strong>Enterobiasis is a cosmopolitan parasitosis caused by Enterobius vermicularis. It affects approximately 30% of children worldwide and up to 60% of children in some developing countries. Predisposing factors include poor socioeconomic conditions, inadequate sanitation, poor personal hygiene, and overcrowding. Children aged 5 to 14 years have shown the highest prevalence of enterobiasis.. Egg transmission is mainly by the fecal-oral route. Approximately 30 to 40% of infested patients do not show any clinical symptoms of the disease. For symptomatic patients, the most common presenting symptom is nocturnal pruritus ani. The diagnosis of E. vermicularis infection is best established by the cellophane tape test. The sensitivity of one single test is around 50%; however, the sensitivity increases to approximately 90% with tests performed on three different mornings. If a worm is visualized in the perianal area or the stool, a pathological examination of the worm will yield a definitive diagnosis. As pinworms and eggs are not usually passed in the stool, examination of the stool is not recommended. The drugs of choice for the treatment of pinworm infestation are mebendazole (100 mg), pyrantel pamoate (11 mg/kg, maximum 1 g), and albendazole (400 mg), all of the above-mentioned drugs are given in a single dose and repeated in two weeks. Mebendazole and albendazole are both adulticidal and ovicidal, whereas pyrantel pamoate is only adulticidal. Given their safety and effectiveness, mebendazole and albendazole are currently the best available drugs for the treatment of pinworm infestation. For pregnant women, pyrantel is preferred to mebendazole and albendazole. Treatment of all household members should be considered, especially if there are multiple or repeated symptomatic infections because reinfection is common even when effective medication is given.</p><p><strong>Conclusion: </strong>In spite of effective treatment of pinworm infestation, recurrences are common. Recurrences are likely due to repeated cycles of reinfect
背景:蛲虫病是世界范围内一个重要的公共卫生问题,尤其是在温带气候的发展中国家的5至10岁儿童中。由于其临床表现轻微或无症状,该问题常常被忽视:本文旨在让儿科医生熟悉蛲虫病的诊断和处理方法:2023年8月,在PubMed临床查询中使用关键词 "Enterobius vermicularis "或 "enterobiasis "或 "蛲虫病 "进行了检索。搜索策略包括过去 10 年内发表的所有临床试验、观察性研究和综述。本综述仅包括英文文献中发表的论文。从上述检索中获取的信息用于本文的撰写:肠吸虫病是一种由蚯蚓肠吸虫引起的世界性寄生虫病。全世界约有 30% 的儿童患有肠吸虫病,在一些发展中国家,患病率高达 60%。致病因素包括社会经济条件差、卫生设施不足、个人卫生差和过度拥挤。5 至 14 岁的儿童是肠虫病的高发人群。虫卵主要通过粪-口途径传播。大约 30% 到 40% 的感染者不会出现任何临床症状。对于有症状的患者,最常见的症状是夜间肛门瘙痒。玻璃纸胶带试验是确诊蠕形虫感染的最佳方法。单次检测的灵敏度约为 50%;但在三个不同的早晨进行检测,灵敏度会提高到约 90%。如果在肛周或粪便中发现虫体,对虫体进行病理检查就能明确诊断。由于蛲虫和虫卵通常不会随粪便排出,因此不建议对粪便进行检查。治疗蛲虫病的首选药物是甲苯咪唑(100 毫克)、帕莫酸噻嘧啶(11 毫克/千克,最多 1 克)和阿苯达唑(400 毫克),上述药物均为单剂,两周后重复使用。甲苯咪唑和阿苯达唑都具有杀成虫和杀卵的作用,而戊唑醇只具有杀成虫的作用。鉴于其安全性和有效性,甲苯咪唑和阿苯达唑是目前治疗蛲虫病的最佳药物。对于孕妇来说,吡噻菌胺比甲苯咪唑和阿苯达唑更可取。应考虑对所有家庭成员进行治疗,尤其是在多次或反复出现无症状感染的情况下,因为即使使用了有效的药物,再次感染也很常见:结论:尽管对蛲虫病进行了有效治疗,但复发仍很常见。由于蛲虫成虫的寿命很短,复发很可能是由于反复循环的再感染(尤其是自身感染)造成的。良好的个人卫生,如勤洗手(尤其是便后和饭前)、剪指甲、避免吮吸手指、咬指甲和抓挠肛门生殖器部位,都是重要的预防措施。应考虑对所有家庭成员进行治疗,尤其是在有多个或重复症状的感染情况下。
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引用次数: 0
The Role of Newborn Pulse Oximetry Screening for Detecting Critical Congenital Heart Defects: A Narrative Review. 新生儿脉搏氧饱和度筛查在检测严重先天性心脏缺陷中的作用:叙述性综述。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963315664241024043935
Giuseppe De Bernardo, Maria Rosaria Arienzo, Flavia Barbieri, Fabio Centanni, Francesconina Moccia, Maurizio Giordano, Giuseppe Buonocore, Serafina Perrone

Critical congenital heart diseases are life-threatening, with a high morbidity rate and mortality among newborns; in fact, a newborn discharged from the hospital with undiagnosed heart disease may experience severe complications during the initial days or weeks of their life, necessitating emergency care and even death. Among all kinds of critical congenital heart disease, coarctation of the aorta is one of the most difficult to diagnose because it only becomes noticeable a few days after birth, when patients have already been discharged from the hospital. This underlines the importance of having a reliable diagnostic tool to discover these diseases. The identification of some of these patients can be achieved through newborn screening with pulse oximetry, but only a small number are diagnosed. Hence, the objective of this review was to determine the value of pulse oximetry screening for the early detection of congenital heart defects in newborns, with a focus on coarctation of the aorta. A literature search was conducted between December 2023 and February 2024 using four electronic databases: Pubmed, Google Scholar, Embase, and Scopus to identify studies that evaluated the efficacy of pre- and post-discharge neonatal ductal saturation monitoring for the diagnosis of critical congenital heart defects before discharge. Twenty research studies with a large number of patients, demonstrating moderate sensitivity and high specificity of pulse oximetry test in detecting critical heart defects, especially coarctation of the aorta, were selected and analyzed. Many confirmations have been found of how good the specificity of screening is, reaching an average value of 99.9% in each study analyzed. The problem still lies in the sensitivity of the screening, which is not as good as the specificity, never reaching 90% in any of the studies analysed. So, it is crucial to keep up with efforts to improve the efficacy of the pulse oximetry screening method.

危重先天性心脏病危及生命,在新生儿中发病率和死亡率都很高;事实上,未确诊心脏病的新生儿在出院后的最初几天或几周内可能会出现严重的并发症,需要急救,甚至死亡。在各种危重的先天性心脏病中,主动脉闭塞症是最难诊断的疾病之一,因为它只有在出生后几天,患者已经出院时才会被发现。这就强调了拥有可靠的诊断工具来发现这些疾病的重要性。通过脉搏血氧仪进行新生儿筛查,可以发现其中一些患者,但只有少数患者被确诊。因此,本综述的目的是确定脉搏血氧仪筛查对早期发现新生儿先天性心脏缺陷的价值,重点是主动脉闭塞。我们在 2023 年 12 月至 2024 年 2 月期间使用四个电子数据库进行了文献检索:Pubmed、Google Scholar、Embase 和 Scopus,以确定评估出院前后新生儿导管饱和度监测对出院前诊断危重先天性心脏缺陷疗效的研究。研究选取并分析了 20 项研究,这些研究涉及大量患者,证明脉搏血氧饱和度检测在发现危重心脏缺陷(尤其是主动脉共动脉瘤)方面具有中等灵敏度和较高特异性。许多研究证实了筛查的特异性有多高,每项分析研究的平均值都达到了 99.9%。问题仍然在于筛查的灵敏度,它没有特异性那么好,在所分析的研究中从未达到 90%。因此,继续努力提高脉搏血氧仪筛查方法的有效性至关重要。
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引用次数: 0
A Survey of the Course: 'How to Successfully Write a Scientific Article in Pediatric Settings'. “如何成功地写一篇科学论文”课程综述。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963277385230920054052
Tamara Sljivancanin Jakovljevic, Nadja Nikolic, Jelena Martic

Background: The aim of the present survey was to analyze the knowledge and skills in medical paper writing of physicians who attended the course "how to write successfully a scientific paper."

Methods: A blind survey was used to analyze participants' knowledge on the topic of the course "how to write successfully a scientific paper." Before starting the workshop, participants anonymously filled out the input questionnaire containing 12 preliminary data questions. The three-hour course included a lecture on the steps of creating and writing a scientific article with examples. At the end, all participants anonymously completed the exit questionnaire consisting of 18 questions. Differences and associations between the collected data were analyzed using appropriate statistical tests.

Results: The survey included 22 participants, most of whom were women (16, 72.7%). The participants' educational level was proportional to their age. 12 of the participants had an intermediate level, while the others reported higher English proficiency. Half of the participants had never published an article. A significant difference was observed between English level and being the first author of an article published in a scientific journal (p = 0.044). Before class, only 13.6% of participants knew that guidelines are mandatory for making clinical decisions according to evidence- based medicine. There was a significant positive correlation between sex and current affiliation (p = 0.038). A negative correlation was observed between sex and article publication (p = 0.037). A positive correlation was observed between English level and current affiliation (p = 0.020). There was a negative correlation observed between previous sources of learning scientific article writing and having already published an article (p = 0.025). A positive correlation was found between reading an article and publishing it (p = 0.046). Statistical analysis showed a significant difference between reading frequency, number of published articles, being the first author, and knowing the title of a scientific article (p = 0.036, p = 0.027, and p = 0.030, respectively).

Conclusion: The results of the questionnaires revealed discrepancies in prior research engagement and understanding of scientific concepts and rules. This survey highlights the importance of the course "how to successfully write a scientific article" in improving participants' knowledge of scientific work and the process of creating an article for submission to medical journals.

背景:本调查的目的是分析参加“如何成功撰写科学论文”课程的医生在医学论文撰写方面的知识和技能。方法:采用盲法调查分析参与者对“如何成功编写科学论文”主题的知识,参与者匿名填写了包含12个初步数据问题的输入问卷。这门三小时的课程包括一堂关于创建和撰写科学文章的步骤的讲座,并附有示例。最后,所有参与者匿名完成了由18个问题组成的退出问卷。使用适当的统计检验来分析所收集数据之间的差异和关联。结果:该调查包括22名参与者,其中大多数是女性(16,72.7%)。参与者的教育水平与年龄成正比。其中12名参与者的英语水平中等,其他人的英语水平较高。一半的参与者从未发表过文章。英语水平与在科学期刊上发表文章的第一作者之间存在显著差异(p=0.044)。在上课前,只有13.6%的参与者知道根据循证医学做出临床决策的指南是强制性的。性别和当前的隶属关系之间存在显著的正相关(p=0.038)。性别和文章发表之间存在负相关(p=0.037)。英语水平和当前的从属关系之间存在正相关(p=0.020)。以前学习科学文章写作的来源和已经学习科学文章的来源之间存在负相关性发表文章(p=0.025)。阅读文章和发表文章之间呈正相关(p=0.046)。统计分析显示,阅读频率、发表文章数量、第一作者、,以及知道科学文章的标题(分别为p=0.036、p=0.027和p=0.030)。结论:问卷调查结果显示,在先前的研究参与和对科学概念和规则的理解方面存在差异。这项调查强调了“如何成功撰写科学文章”课程在提高参与者对科学工作的认识以及撰写提交给医学期刊的文章的过程中的重要性。
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引用次数: 0
Acute Respiratory Tract Infections in Pediatric Populations of Slum Areas: Navigating Challenges and Dynamics of Immune Responses. 贫民区儿童急性呼吸道感染:应对免疫反应的挑战和动态变化。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-01-01 DOI: 10.2174/0115733963309043240703115735
Gayathri Gunasekaran, Dinesh Kumar Thirugnanam, Ashwath Balasubramaniam, N Nalini Jayanthi, K V Leela

The study presents a thorough examination of immune responses in pediatric populations within slum areas, specifically addressing respiratory infections. It explores the impact of slum conditions on respiratory health, detailing the epidemiology of infections, including common pathogens and environmental factors. The review delves into the etiology, clinical manifestations, and challenges associated with viral respiratory infections, co-infections, and complications in slum environments. The discussion extends to immune responses in pediatric respiratory infections, emphasizing unique challenges in diagnosis and treatment within slum areas. Prevention and intervention strategies are highlighted, encompassing vaccination programs, health education, and improving living conditions. It underscores the importance of targeted interventions, accounting for socio-economic factors, community-based strategies, and culturally sensitive approaches. It proposes the exploration of novel approaches and the development of vaccines tailored to prevalent respiratory pathogens in slum settings. Furthermore, the feasibility and impact of routine immunization programs, emphasizing accessibility, acceptance, and long-term sustainability are explored. It advocates strengthening primary healthcare systems, investing in healthcare workforce training, and improving diagnostic facilities. The potential of digital health technologies in enhancing surveillance, early detection, and the development of mobile applications or telemedicine platforms is discussed. In conclusion, the study emphasizes the multifaceted challenges faced by children in slum areas regarding respiratory infections, necessitating informed, interdisciplinary interventions. Addressing healthcare disparities, improving living conditions, and enhancing vaccination coverage are deemed crucial for mitigating the burden of respiratory infections. This review calls for collaborative efforts among researchers, healthcare professionals, policymakers, and community stakeholders to develop sustainable solutions for enhanced respiratory health in slum-dwelling pediatric populations.

该研究全面考察了贫民窟地区儿科人群的免疫反应,特别是呼吸道感染。研究探讨了贫民窟条件对呼吸系统健康的影响,详细介绍了感染的流行病学,包括常见病原体和环境因素。综述深入探讨了病因、临床表现以及贫民窟环境中与病毒性呼吸道感染、合并感染和并发症相关的挑战。讨论延伸到小儿呼吸道感染的免疫反应,强调贫民窟地区诊断和治疗的独特挑战。重点介绍了预防和干预策略,包括疫苗接种计划、健康教育和改善生活条件。报告强调了有针对性的干预措施的重要性,考虑到了社会经济因素、基于社区的战略和文化敏感性方法。报告建议探索新方法,并针对贫民窟环境中流行的呼吸道病原体开发疫苗。此外,还探讨了常规免疫计划的可行性和影响,强调了可及性、可接受性和长期可持续性。报告提倡加强初级医疗保健系统,投资于医疗保健人员培训,改善诊断设施。研究还讨论了数字医疗技术在加强监测、早期检测以及开发移动应用或远程医疗平台方面的潜力。总之,本研究强调了贫民窟地区儿童在呼吸道感染方面面临的多方面挑战,因此有必要采取知情的跨学科干预措施。解决医疗保健差异、改善生活条件和提高疫苗接种覆盖率被认为是减轻呼吸道感染负担的关键。本综述呼吁研究人员、医疗保健专业人员、政策制定者和社区利益相关者通力合作,制定可持续的解决方案,以提高贫民窟居住的儿科人群的呼吸系统健康水平。
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引用次数: 0
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Current Pediatric Reviews
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