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Impact of the 2022 American Academy of Pediatrics Hyperbilirubinemia Guideline on Hospitalization Rates and Short-Term Outcomes: A Single-Center Study. 2022年美国儿科学会高胆红素血症指南对住院率和短期结局的影响:一项单中心研究
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.25164
Ferhan Demirtaş, Büşra Kütükçü, Yasemin Ezgi Köstekçi, Emel Okulu, Ömer Erdeve, Begüm Atasay, Saadet Arsan

Objective: This study aimed to evaluate the impact of the revised 2022 American Academy of Pediatrics (AAP) guideline for hyperbilirubinemia on hospitalization rates and short-term outcomes. Materials and Methods: This retrospective observational study compared 2 periods, before (period 1: January 1-August 31, 2022) and after (period 2: September 1-December 31, 2022) implementation of the AAP 2022 guideline in a tertiary neonatal unit. Neonates born at ≥35 weeks' gestational age who met phototherapy criteria were included. In period 2, infants who would have been hospitalized under the previous 2004 guideline but not under the new one were followed to assess the need for hospitalization and the occurrence of neurotoxicity. Results: The rate of hospitalization due to hyperbilirubinemia decreased from 23% (n = 95/409) in period 1 to 14% (n = 25/173) in period 2 (P = .017). When the new guideline was retrospectively applied, it was found that 58% (n = 55) of previously hospitalized patients in period 1 would not have required admission under the new criteria. In period 2, 37 neonates met the previous criteria, but only 25 were hospitalized under the new guideline; 2 of the 25 required rehospitalization. The remaining 12 newborns were followed as outpatients without developing neurotoxicity. Overall, 51% (n = 67) of newborns who met previous criteria did not meet the new hospitalization thresholds. Conclusion: The implementation of the AAP 2022 guideline was associated with a reduced risk of hospitalization without an increased risk of bilirubin-related neurotoxicity. Structured followup and individualized risk assessment remain essential for safe outpatient management.

目的:本研究旨在评估修订后的2022年美国儿科学会(AAP)高胆红素血症指南对住院率和短期预后的影响。材料和方法:本回顾性观察性研究比较了在第三新生儿病房实施AAP 2022指南之前(第一期:2022年1月1日至8月31日)和之后(第二期:2022年9月1日至12月31日)两个阶段。符合光疗标准的≥35周孕龄新生儿纳入研究。在第二阶段,根据2004年以前的指南而不是根据新的指南将住院的婴儿被跟踪,以评估住院的必要性和神经毒性的发生。结果:高胆红素血症住院率由第1期的23% (n = 95/409)下降至第2期的14% (n = 25/173) (P = 0.017)。当回顾性应用新指南时,发现58% (n = 55)的第1期住院患者在新标准下不需要住院。在第2期,37名新生儿符合先前的标准,但只有25名根据新指南住院;25人中有2人需要再次住院。其余12名新生儿作为门诊患者随访,未出现神经毒性。总体而言,51% (n = 67)符合先前标准的新生儿未达到新的住院阈值。结论:AAP 2022指南的实施与住院风险降低相关,而胆红素相关神经毒性风险未增加。结构化的随访和个性化的风险评估仍然是安全门诊管理的必要条件。
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引用次数: 0
Evaluation of Pediatric Cardiomyopathy Patients in Pediatric Intensive Care Unit. 儿科重症监护病房小儿心肌病患者的评价。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.25111
Şeyda Kesen, Merve Havan, Mehmet Ramoğlu, Tayfun Uçar, Ercan Tutar, Tanıl Kendirli

Objective: Cardiomyopathies (CMP) are an important cause of end-stage heart failure in childhood. The study aims to evaluate the clinical features, treatments, and outcomes of the patients diagnosed with CMP followed in the pediatric intensive care unit (PICU). Materials and Methods: This retrospective study was conducted using the data of the patients followed in the PICU between January 1, 2008, and December 31, 2019. Demographic information of the patients, CMP types, informations of echocardiography and angiography, findings upon admission to the PICU, medical treatments applied, respiratory and circulatory support, cardiac transplantation status, and results were examined. Results: A total of 76 patients hospitalized with the diagnosis of CMP were included in the study. Among them, 39 (51%) patients were female. The majority (68.4%) were diagnosed with dilated CMP. The remaining patients were diagnosed with noncompaction left ventricular (LV) dilated CMP (14.5%), restrictive CMP (10.5%), hypertrophic CMP (5.3%), and noncompaction LV restrictive CMP (1.3%). Diuretics, inotropes, and invasive mechanical ventilation were used in 90.8%, 93.4%, and 75% of patients, respectively. While 43.4% (n = 33) of the patients needed extracorporeal membrane oxygenation (ECMO) support during their PICU hospitalization, 15.8% (n = 12) received LV assist device (LVAD) and 2.6% (n = 2) biventricular assist device (BiVAD) support. Heart transplantation was performed in 10 patients (13.2%). Finally, 40 (52.6%) of the patients died. Conclusion: Pediatric patients with CMP with severe heart failure require inotropes, mechanical ventilation, ECMO, LVAD, BiVAD, and heart transplantation, which are crucial for lifesaving measures, along with intensive care follow-up.

目的:心肌病(CMP)是儿童期终末期心力衰竭的重要原因。本研究旨在评估儿科重症监护病房(PICU)诊断为CMP的患者的临床特征、治疗方法和预后。材料与方法:本回顾性研究使用2008年1月1日至2019年12月31日在PICU随访的患者数据。检查患者的人口统计信息、CMP类型、超声心动图和血管造影信息、入PICU时的发现、所使用的药物、呼吸和循环支持、心脏移植情况和结果。结果:共纳入76例诊断为CMP的住院患者。其中女性39例(51%)。大多数(68.4%)被诊断为CMP扩张性。其余患者被诊断为非压实性左室(LV)扩张性CMP(14.5%)、限制性CMP(10.5%)、肥厚性CMP(5.3%)和非压实性左室限制性CMP(1.3%)。利尿剂、肌力剂和有创机械通气分别用于90.8%、93.4%和75%的患者。43.4% (n = 33)的患者在PICU住院期间需要体外膜氧合(ECMO)支持,15.8% (n = 12)的患者接受左室辅助装置(LVAD)支持,2.6% (n = 2)的患者接受双室辅助装置(BiVAD)支持。心脏移植10例(13.2%)。最终死亡40例(52.6%)。结论:小儿CMP合并严重心力衰竭患者需要肌力药物、机械通气、ECMO、LVAD、BiVAD、心脏移植等重要的救命措施,并配合重症监护随访。
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引用次数: 0
Cross-Sectional Analysis of Echocardiography Reports in Light of Guideline Recommendations. 根据指南建议的超声心动图报告的横断面分析。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.25123
Akif Kavgacı, Betül Erdoğdu, Serdar Kula, İpek Bozkurt

Objective: The aim of this study is to identify discrepancies in pediatric echocardiography reports across centers and emphasize the significance of establishing a standardized reporting approach. Materials and Methods: In this study, pediatric echocardiography reports from various institutions (university hospitals [UHs], training and research hospitals [TRHs], and private healthcare facilities) (33 reports from 29 centers) were evaluated for adherence to key criteria outlined in consensus guidelines by the European Association of Cardiovascular Imaging of the European Society of Cardiology and the Association for European Paediatric and Congenital Cardiology. Each echocardiography report was systematically categorized into distinct sections, including patient information, medical records, echocardiographic findings, and conclusions. Results: Systemic and pulmonary venous return was reported in 58.3% of cases from UHs, 77.7% from TRHs, and 66.7% from private healthcare institutions (PHIs). Pulmonary artery and aortic arch were documented in 83.3% of reports from PHIs, 88.8% from TRHs, and 25% from UHs. Coronary artery dimensions and course were reported in 58.3% of reports from UHs, 77.7% from TRHs, and 16.7% from PHIs. Physician interpretations and diagnoses were present in all reports. However, information regarding environmental factors, such as whether the patient was awake or agitated during the examination, was reported in 66.6% of cases from TRHs but was entirely absent in reports from other institutions. Conclusion: This study demonstrates important variability in pediatric echocardiography reports. Adopting international guidelines may facilitate standardized reporting, ensure consideration of underassessed parameters, and promote a unified terminology across institutions.

目的:本研究的目的是确定不同中心儿童超声心动图报告的差异,并强调建立标准化报告方法的重要性。材料和方法:在本研究中,来自不同机构(大学医院、培训和研究医院和私人医疗机构)的儿童超声心动图报告(来自29个中心的33份报告)被评估是否符合欧洲心血管成像协会、欧洲心脏病学会和欧洲儿科和先天性心脏病学会共识指南中概述的关键标准。每个超声心动图报告被系统地分为不同的部分,包括患者信息、医疗记录、超声心动图结果和结论。结果:综合医院58.3%的患者出现全身和肺静脉回流,综合医院77.7%,私立医疗机构66.7%。肺动脉和主动脉弓在公共卫生报告中占83.3%,在TRHs报告中占88.8%,在UHs报告中占25%。58.3%的UHs、77.7%的TRHs和16.7%的PHIs报告报告了冠状动脉尺寸和病程。所有报告均有医生的解释和诊断。然而,66.6%的TRHs病例报告了有关环境因素的信息,例如患者在检查过程中是否清醒或激动,但在其他机构的报告中完全没有。结论:本研究显示了儿科超声心动图报告的重要变异性。采用国际准则可以促进标准化报告,确保考虑被低估的参数,并促进各机构之间的统一术语。
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引用次数: 0
The Fifth Vital Sign in the First 1000 Days: Early Relational Health. 前1000天的第五个生命体征:早期关系健康。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.24317
İclal Ayrancı Sucaklı, Sıddika Songül Yalçın

Early childhood development forms the cornerstone for a healthy, fulfilling, and productive life. Research in health psychology and longevity highlights that social relationships are the most significant determinant of lifelong health and development. Among these, early attachment between children and caregivers, bolstered by positive experiences and nurturing environments, is pivotal for optimal growth, development, and well-being. This highlights the need for holistic approaches in healthcare, particularly during the critical first 1000 days of life. To address these needs, comprehensive evaluations must include assessments of childcaregiver interactions alongside biological, psychological, social, and environmental factors. Recognizing this, the American Academy of Pediatrics has embraced the Early Relational Health (ERH) framework, focusing on fostering healthy relationships during this crucial period. The framework encompasses all caregivers, including parents, extended family, and peers. The ERH framework emphasizes a broad assessment of factors affecting health-biological, psychological, interactional, economic, and environmental-within the child and caregivers' living contexts. The primary objective is not to teach parenting skills but to cultivate safe, stable, nurturing relationships supporting lifelong well-being. The ERH underscores the critical importance of assessing relational health as a "fifth vital sign," alongside traditional measures such as respiratory rate, heart rate, temperature, and blood pressure, in the first 1000 days. Integrating this framework into health systems can enhance the well-being of children and caregivers, ensuring a robust foundation for lifelong development.

儿童早期发展是健康、充实和富有成效的生活的基石。健康心理学和长寿研究强调,社会关系是终身健康和发展的最重要决定因素。其中,儿童与照顾者之间的早期依恋,在积极的经历和养育环境的支持下,对最佳的成长、发展和幸福至关重要。这突出表明,在医疗保健方面,特别是在生命关键的头1000天,需要采取综合办法。为了满足这些需求,综合评估必须包括对照顾儿童者的互动以及生物、心理、社会和环境因素的评估。认识到这一点,美国儿科学会采用了早期关系健康(ERH)框架,重点是在这个关键时期培养健康的关系。该框架涵盖所有照顾者,包括父母、大家庭和同伴。ERH框架强调在儿童和照料者的生活环境中对影响健康的因素——生物的、心理的、相互作用的、经济的和环境的——进行广泛的评估。主要目标不是传授育儿技巧,而是培养安全、稳定、养育的关系,支持终身幸福。ERH强调了在头1000天内评估关系健康作为“第五个生命体征”的重要性,以及传统的测量方法,如呼吸频率、心率、体温和血压。将这一框架纳入卫生系统可以增进儿童和照料者的福祉,确保为终身发展奠定坚实的基础。
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引用次数: 0
Erratum. 勘误表。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.251112
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引用次数: 0
RE: Comment On: Pediatric Urinary Stone Disease: A 10-Year SingleCenter Experience from Türkiye. 评论:儿童尿路结石疾病:来自<s:1> rkiye的10年单中心经验。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.250302
Utku Dönger
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引用次数: 0
Osteomyelitis with a Pathologic Fracture, Mortal Liver Abscess, and Cholelithiasis: Distinct Features in two Families with the Same p47-phox Mutation. 骨髓炎伴病理性骨折、致命肝脓肿和胆石症:两个相同p47-phox突变家族的不同特征
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.24231
Gulay Aksak Yigit, Gamze Sonmez, Kubra Deveci, Ilke Kılıc Topcu, Hacer Neslihan Bildik, Mehmet Ayvaz, Diclehan Orhan, Deniz Cagdas
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引用次数: 0
Kohlschütter-Tönz Syndrome: A Rare Clinical Entity with Amelogenesis Imperfecta in Two Siblings, Dental Management and Scoping Review. Kohlschütter-Tönz综合征:一个罕见的临床实体与两个兄弟姐妹的淀粉性发育不全,牙科管理和范围审查。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.25085
Ecem Akbeyaz Şivet, İsmail Hakkı Akbeyaz, Gülcan Berkel, Ahmet Yeşilyurt, Berkant Sezer, Ali Menteş

Kohlschütter-Tönz syndrome (KTS) (OMIM#226750) is a rare autosomal recessive disorder characterized by epileptic encephalopathy, developmental delay, and amelogenesis imperfecta. Early diagnosis and management are crucial, but the complexity of symptoms, particularly dental and neurological impairments, poses significant challenges. The aim of this report is to describe the clinical findings of 2 siblings and their dental management, whose dental examination led to genetic referral and subsequent diagnosis of KTS. Dental examinations revealed enamel defects consistent with amelogenesis imperfecta, including yellow-brown discoloration, soft enamel, and diastemas in both siblings. The younger sibling, a 9-year-old boy, exhibited early-onset seizures, intellectual disability, spasticity, and a history of kidney stones. The older sibling, a 13-year-old boy, presented with more severe neurodevelopmental delay, early-onset seizures, and drug-resistant epilepsy. Genetic testing confirmed homozygous deletions in the ROGDI gene, leading to the diagnosis of KTS in both siblings. The younger sibling received successful restorative treatment under general anesthesia, while the older sibling's oral care was managed conservatively due to contraindications for general anesthesia. These cases underscore the importance of pediatric dentists in the early identification of rare genetic disorders such as KTS, especially when dental anomalies like amelogenesis imperfecta are present. Timely referral for genetic evaluation can facilitate accurate diagnosis and appropriate care planning. Moreover, sharing clinical experiences and treatment outcomes contributes to a better understanding of this rare syndrome and helps guide future diagnostic and therapeutic strategies.

Kohlschütter-Tönz综合征(KTS) (OMIM#226750)是一种罕见的常染色体隐性遗传病,其特征为癫痫性脑病、发育迟缓和淀粉样变性不全。早期诊断和治疗至关重要,但症状的复杂性,特别是牙齿和神经损伤,构成了重大挑战。本报告的目的是描述2个兄弟姐妹的临床表现和他们的牙科管理,他们的牙科检查导致遗传转诊和随后诊断为KTS。牙科检查显示,两名兄弟姐妹的牙釉质缺陷与淀粉原性不完全性一致,包括黄棕色变色,软牙釉质和裂口。弟妹,一名9岁男孩,表现为早发性癫痫、智力残疾、痉挛和肾结石病史。哥哥是一名13岁的男孩,表现出更严重的神经发育迟缓、早发性癫痫和耐药性癫痫。基因检测证实了ROGDI基因的纯合缺失,从而在两个兄弟姐妹中诊断为KTS。弟弟妹妹在全身麻醉下接受了成功的恢复性治疗,而哥哥姐姐的口腔护理由于全身麻醉的禁忌症而被保守管理。这些病例强调了儿科牙医在早期识别罕见遗传疾病(如KTS)中的重要性,特别是当存在牙齿畸形(如无晶面发育不全)时。及时转诊进行遗传评估可以促进准确的诊断和适当的护理计划。此外,分享临床经验和治疗结果有助于更好地了解这种罕见综合征,并有助于指导未来的诊断和治疗策略。
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引用次数: 0
Unwitnessed Out-of-Hospital Cardiac Arrests in Children. Can Mesenchymal Stem Cells Work at Post-Resuscitation Care? 儿童院外无目击心脏骤停。间充质干细胞能在复苏后护理中发挥作用吗?
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.24275
Fevzi Kahveci
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引用次数: 0
High Frequency of Viral Etiology and Antibiotic Utilization Patterns in Pediatric Acute Diarrhea: A Cross-Sectional Study at a Tertiary Hospital in Vietnam. 儿童急性腹泻的高频率病毒病因学和抗生素使用模式:越南一家三级医院的横断面研究。
IF 1.7 Q3 PEDIATRICS Pub Date : 2025-09-01 DOI: 10.5152/TurkArchPediatr.2025.25146
Khai Quang Tran, Phuong Minh Nguyen, Uyen Thi Phuong Nguyen, Hung Hoang Tuan Nguyen, Nghia Quang Bui

Objective: The purpose of this research is to (1) determine the frequency of viral acute diarrheal disease in 2 months to 5 years of aged children admitted to the hospital; (2) describe the clinical and laboratory characteristics among children diagnosed with viral acute diarrheal disease; and (3) evaluate patterns of antibiotic utilization in treating pediatric acute diarrheal disease. Materials and Methods: A cross-sectional study involved 232 pediatric inpatients at the Department of Gastroenterology, Can Tho Children's Hospital from March 2023 to February 2024. This study utilized real-time polymerase chain reaction (PCR) to identify etiological pathogens responsible for infection. Results: Real-time PCR detected viruses in 140/232 (60.3%) of acute diarrhea cases, with 85/232 (36.6%) being only virus infections. Age, sex, and nutritional status showed no significant differences between the viral infection only and other case groups (P > .05). Vomiting predominated in viral infections only (P < .05), while mucoid-bloody stools and elevated C-reactive protein marked other cases (P < .05). Antibiotics were used in 52.9% of viral and 60.3% of total cases. The study found no differences in hospitalization time, fever length, or duration of diarrhea between the antibiotic use and non-antibiotic use groups (P > .05). Conclusion: Viruses were the predominant cause of acute diarrhea in children, yet antibiotics were frequently used without clinical benefit. Among children with confirmed viral infections, antibiotic use showed no advantage in reducing hospitalization duration, fever length, or diarrhea resolution. These findings support the need to limit unnecessary antibiotic use in pediatric diarrhea management.

目的:本研究的目的是:(1)确定2个月至5岁儿童入院时病毒性急性腹泻的发病频率;(2)描述诊断为病毒性急性腹泻病儿童的临床和实验室特征;(3)评价小儿急性腹泻病的抗生素使用模式。材料与方法:横断面研究纳入了2023年3月至2024年2月在Can Tho儿童医院消化内科住院的232名儿科患者。本研究利用实时聚合酶链反应(PCR)来鉴定引起感染的病原。结果:140/232例(60.3%)急性腹泻病例中检测到病毒,85/232例(36.6%)只为病毒感染。年龄、性别和营养状况在病毒感染组和其他病例组之间无显著差异(P < 0.05)。病毒感染以呕吐为主(P < 0.05),其他病例以粘液样血便和c反应蛋白升高为主(P < 0.05)。52.9%的病毒病例和60.3%的总病例使用抗生素。研究发现,抗生素使用组和非抗生素使用组在住院时间、发烧时间或腹泻持续时间方面没有差异(P < 0.05)。结论:病毒是引起儿童急性腹泻的主要原因,但抗生素的使用频繁且无临床效果。在确诊病毒感染的儿童中,使用抗生素在减少住院时间、发烧时间或腹泻缓解方面没有优势。这些发现支持在儿童腹泻管理中限制不必要的抗生素使用的必要性。
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引用次数: 0
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Turkish archives of pediatrics
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