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Association Between Frequency of Sugar and Protein Intake and Severity of Plaque-Induced Gingivitis in Children. 糖和蛋白质摄入频率与儿童菌斑性牙龈炎严重程度的关系
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24166
Ayshe Salim, Sirma Angelova, Bogdan Roussev, Todorka Sokrateva, Bistra Galunska, Pawel Olczyk, Katarzyna Komosinska-Vassev, Stefan Peev, Yoana Kiselova-Kaneva, Diana Ivanova

Objective: The aim of this study is to evaluate how the frequent sugar and protein intake is associated with the severity of plaque-induced gingivitis in children. Materials and Methods: A cross-sectional study was conducted, involving 38 subjects (4-14 years) at a mean age of 8.5 ± 2.32 years with diagnosed plaque-induced gingivitis based on the Löe-Silness Gingival Index (GI) (0 < GI ≤ 3). The gingival status was assessed by the Silness-Lőe Plaque Index (PLI), GI, and Papillary Bleeding Index by Saxer and Muhlemann. The nutritional status was established through an in-depth questionnaire on protein and sugar intake. Results: The increased frequency of sugar consumption in children with plaque-induced gingivitis is related to enhanced gingival inflammation. Higher values of PLI among the rep- resentatives were established with frequent sugar intake (P = .04). Frequent dairy protein con- sumption was associated with lower levels of PLI (P = .04). This index is indicative of the amount of accumulated dental plaque, which is the main etiological factor involved in plaque-induced gingivitis. Conclusion: It can be concluded that uncontrolled sugar consumption in children was asso- ciated with enhancement of the severity of plaque-induced gingivitis. Frequent dairy protein intake has the potential to serve as an essential prevention strategy regarding the onset and aggravation of plaque-induced gingival inflammation in childhood. A well-balanced diet, rich in proteins and with restricted sugar intake, is considered a possible tool in the prevention and control of plaque-induced gingivitis in childhood.

目的:本研究的目的是评估频繁的糖和蛋白质摄入与儿童菌斑性牙龈炎严重程度的关系。材料与方法:采用横断面研究方法,采用Löe-Silness牙龈指数(GI) (0 < GI≤3)诊断为菌斑性牙龈炎的38例受试者(4-14岁),平均年龄8.5±2.32岁。通过Saxer和Muhlemann的Silness-Lőe斑块指数(PLI)、GI和乳头状出血指数评估牙龈状况。通过深入的蛋白质和糖摄入量问卷来确定营养状况。结果:牙菌斑性牙龈炎患儿糖摄入频率的增加与牙龈炎症的增强有关。频繁摄入糖的人的PLI值较高(P = 0.04)。频繁食用乳制品蛋白与较低的PLI水平相关(P = 0.04)。该指标反映了牙菌斑的累积量,而牙菌斑是引起牙菌斑性牙龈炎的主要病因。结论:儿童不加控制的糖摄入与菌斑性牙龈炎的严重程度增加有关。经常摄入乳制品蛋白有可能作为一种重要的预防策略,预防儿童期菌斑引起的牙龈炎症的发生和恶化。均衡的饮食,富含蛋白质和限制糖的摄入,被认为是预防和控制儿童牙菌斑引起的牙龈炎的可能工具。
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引用次数: 0
Mother-to-Child Transmission of Human Immunodeficiency Virus and Its Determinants: Lessons Learnt from the Test and Treat Strategy at a Regional Hospital in Cameroon. 人类免疫缺陷病毒的母婴传播及其决定因素:从喀麦隆一家地区医院的检测和治疗战略中吸取的教训。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24144
Andreas Chiabi, Adel Vershiyi Bongakeh, Yolande Djike Puepi Fokam, Esther Neba Ngum, Samuel Angwafor, Denis Nsame Nforniwe

Objective: With the World Health Organization's (WHO) implementation of the "test and treat all" policy in 2016, there should have been a great change in mother-to-child transmission (MTCT) of human immunodeficiency virus (HIV), and its determinants. This study aimed to assess MTCT of HIV after the adoption of the universal "test and treat" policy. Materials and Methods: A retrospective cohort study of HIV-exposed infants (HEIs) between the ages of 6 weeks to 18 months enrolled from 1 January 1, 2017 to December 31, 2021. The study was carried out at the "Prevention of Mother to Child Transmission" center (PMTCT) of the HIV unit, Regional Hospital Bamenda (RHB) of the Northwest region of Cameroon. Data was col- lected from files with the aid of predesigned data collection forms. Results: During the study, out of the 294 HEIs included, 13 were positive, giving a frequency of 4.4%. Not taking antiretrovirals by the mother, or taking them 4 weeks prior to delivery, or after delivery, mixed feeding, and breastfeeding duration greater than 12 months were determinants of MTCT of HIV. Also, 4 out of the 294 exposed infants died, giving a death rate of 1.4%. No fac- tor analyzed was found to be significantly associated with the death rate of HEIs at 18 months. Conclusion: This study showed a reduction in the frequency of MTCT of HIV due to the imple- mentation and adoption of the universal "test and treat" policy. Also, starting maternal anti- retroviral treatment after delivery and a breastfeeding duration greater than 12 months were associated with MTCT of HIV.

目的:随着世界卫生组织(WHO)在2016年实施“检测和治疗所有人”政策,人类免疫缺陷病毒(HIV)的母婴传播(MTCT)及其决定因素应该会发生巨大变化。本研究旨在评估在普遍采用“检测和治疗”政策后的艾滋病毒母婴传播情况。材料和方法:对2017年1月1日至2021年12月31日期间6周至18个月的hiv暴露婴儿(HEIs)进行回顾性队列研究。这项研究是在喀麦隆西北地区巴门达地区医院艾滋病毒科的“预防母婴传播”中心进行的。通过预先设计的数据收集表格从文件中收集数据。结果:研究期间,294所高等教育机构中有13所呈阳性,阳性率为4.4%。母亲未服用抗逆转录病毒药物,或在分娩前4周或分娩后服用抗逆转录病毒药物,混合喂养和母乳喂养时间超过12个月是艾滋病毒母婴传播的决定因素。此外,294名受感染婴儿中有4人死亡,死亡率为1.4%。未发现任何因素与新生儿18个月时的死亡率有显著相关性。结论:本研究表明,由于实施和采用了普遍的“检测和治疗”政策,艾滋病毒母婴传播的频率有所下降。此外,分娩后开始抗逆转录病毒治疗和母乳喂养时间超过12个月与艾滋病毒母婴传播有关。
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引用次数: 0
Reliability and Validity of the Turkish Version of a Self-Reported Sizing Me Up and a Parent-Proxy Sizing Them Up: Obesity Specific Health- Related Quality of Life Measures. 土耳其版自我报告的信度和效度评估和父母代理评估:肥胖特定健康相关的生活质量措施。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24196
Deniz Özalp Kızılay, Derya Tepe, Betül Ersoy, Şermin Yalın Sapmaz

Objective: Investigating the validity and reliability of the Turkish versions of the obesity-specific health-related quality of life perception scales for children and parents , Sizing Me Up/Sizing Them Up (SMU/STU), was the aim of this study. Materials and Methods: Sizing me up/sizing them up were translated into Turkish following a standardized translation procedure. Test-retest reliability, internal consistency, discriminant and convergent validity, as well as confirmatory factor analysis (CFA) were all assessed. Results: Sizing me up /sizing them up had a total scale Cronbach's alpha of 0.873, 0.872. In the test-retest evaluations, significant correlation was found in the SMU (except the Teasing/ Marginalization subscale), while no correlation was found in the Physical Functioning, Teasing/ Marginalization, School and Mealtime Difficulties subscales in the STU. The Pediatric Quality of Life Generic Core Scales (PedsQL) total mean score and the SMU/STU total mean scores exhibited a significant correlation (r=0.671, P < .0001/r=0.663, P < .001). Regarding the SMU total scale score and other subscale scores, excluding the Social Avoidance subscale, and the STU total scale score and other subscale scores, excluding Mealtime and School Functioning, a significant difference was found between the OB and non-OB samples. In CFA, the com- parative fit index (CFI) and root mean square error of approximation (RMSEA) values were not compatible with the expected values. Conclusion: The results demonstrated that both scales are suitable for use in the Turkish context and showed the validity and reliability of the Turkish versions of the SMU/STU; however, some inconsistencies were found in the items related to social avoidance in the SMU scale and posi- tive social attributes, mealtime challenges, and school functioning in the STU, so it is recom- mended that these items should be interpreted separately and carefully when evaluating scale scores by researchers or clinicians.

目的:调查土耳其版儿童和家长肥胖相关健康生活质量感知量表的效度和可靠性,SMU/STU (Sizing Me Up/Sizing Them Up)是本研究的目的。材料和方法:根据标准化的翻译程序将其翻译成土耳其语。测试-重测信度、内部一致性、判别效度和收敛效度以及验证性因子分析(CFA)均进行了评估。结果:评定我/评定他们的总量表Cronbach's alpha为0.873,0.872。在重测评估中,SMU(戏弄/边缘化量表除外)与躯体功能量表、戏弄/边缘化量表、学校和用餐困难量表均无显著相关。儿童生活质量通用核心量表(PedsQL)总均分与SMU/STU总均分呈显著相关(r=0.671, P < 0.0001 /r=0.663, P < 0.001)。在SMU总量表得分和其他子量表得分(不包括社交回避子量表),以及STU总量表得分和其他子量表得分(不包括进餐时间和学校功能)方面,OB和非OB样本之间存在显著差异。在CFA中,比较拟合指数(CFI)和近似均方根误差(RMSEA)值与期望值不相容。结论:结果表明,两种量表都适合在土耳其语语境中使用,并显示了土耳其语版本的SMU/STU的有效性和可靠性;然而,在SMU量表中与社会回避相关的项目与STU中积极社会属性、用餐时间挑战和学校功能相关的项目中发现了一些不一致,因此建议研究人员或临床医生在评估量表得分时应单独仔细地解释这些项目。
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引用次数: 0
Subclinical Enthesitis in Children with Chronic Nonbacterial Osteomyelitis. 慢性非细菌性骨髓炎患儿的亚临床脓肿。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24300
Seher Sener, Adalet Elcin Yildiz, Ezgi Deniz Batu, Erdal Atalay, Ozge Basaran, Yelda Bilginer, Seza Ozen

Objective: Enthesitis is rare in chronic nonbacterial osteomyelitis (CNO) compared to enthesi- tis-related arthritis. It may be asymptomatic in CNO patients. This study aimed to evaluate the presence of subclinical enthesitis in patients with CNO using ultrasonography (US). Materials and Methods: Patients with CNO were included in this study and evaluated with US by an expert pediatric radiologist. The entheses of 7 tendons were assessed bilaterally, includ- ing the common extensor and flexor tendons, the quadriceps tendon, the proximal and distal patellar tendons, the Achilles tendon, and the plantar fascia. Results: Fifty CNO patients were included. The median age of the patients was 12.4 years, and 58% were female. Subclinical enthesitis was identified in 3 patients (6%). These 3 patients were male, older than 6 years at diagnosis, had bilateral sacroiliitis, and were positive for human leukocyte antigen-B27. The enthesitis was located in the right quadriceps, right plantar fascia, and bilateral Achilles. One of these patients also had a clinical history of enthesitis at diagnosis. Treatment modification was not done when subclinical enthesitis was detected since they were in clinical remission and acute phase reactants were within normal limits. However, the patient with bilateral subclinical Achilles enthesitis had a disease flare afterward, and methotrexate was switched to etanercept. Conclusion: Subclinical enthesitis can be observed especially in CNO patients with overlappin- genthesitis-related arthritis features. The use of US may prove beneficial in detecting subclini- cal enthesitis and predicting disease flare.

目的:慢性非细菌性骨髓炎(CNO)中阑尾炎较阑尾炎相关关节炎少见。CNO患者可能无症状。本研究旨在通过超声(US)评估CNO患者是否存在亚临床麻醉。材料和方法:本研究纳入CNO患者,并由儿科放射专家进行US评估。双侧评估7条肌腱的肌腱束,包括普通伸屈肌腱、股四头肌肌腱、髌骨近端和远端肌腱、跟腱和足底筋膜。结果:纳入50例CNO患者。患者的中位年龄为12.4岁,女性占58%。3例(6%)患者出现亚临床荨麻疹。这3例患者为男性,诊断时年龄大于6岁,患有双侧骶髂炎,人白细胞抗原b27阳性。炎位于右股四头肌、右足底筋膜和双侧跟腱。其中一名患者在诊断时也有鼻炎的临床病史。当检测到亚临床炎症时,不进行治疗修改,因为他们处于临床缓解期,急性期反应物在正常范围内。然而,患有双侧亚临床跟腱炎的患者随后出现疾病发作,甲氨蝶呤改为依那西普。结论:亚临床性全身炎在有重叠合成炎相关关节炎特征的CNO患者中尤为明显。超声在检测亚临床炎症和预测疾病爆发方面可能是有益的。
{"title":"Subclinical Enthesitis in Children with Chronic Nonbacterial Osteomyelitis.","authors":"Seher Sener, Adalet Elcin Yildiz, Ezgi Deniz Batu, Erdal Atalay, Ozge Basaran, Yelda Bilginer, Seza Ozen","doi":"10.5152/TurkArchPediatr.2025.24300","DOIUrl":"10.5152/TurkArchPediatr.2025.24300","url":null,"abstract":"<p><p>Objective: Enthesitis is rare in chronic nonbacterial osteomyelitis (CNO) compared to enthesi- tis-related arthritis. It may be asymptomatic in CNO patients. This study aimed to evaluate the presence of subclinical enthesitis in patients with CNO using ultrasonography (US). Materials and Methods: Patients with CNO were included in this study and evaluated with US by an expert pediatric radiologist. The entheses of 7 tendons were assessed bilaterally, includ- ing the common extensor and flexor tendons, the quadriceps tendon, the proximal and distal patellar tendons, the Achilles tendon, and the plantar fascia. Results: Fifty CNO patients were included. The median age of the patients was 12.4 years, and 58% were female. Subclinical enthesitis was identified in 3 patients (6%). These 3 patients were male, older than 6 years at diagnosis, had bilateral sacroiliitis, and were positive for human leukocyte antigen-B27. The enthesitis was located in the right quadriceps, right plantar fascia, and bilateral Achilles. One of these patients also had a clinical history of enthesitis at diagnosis. Treatment modification was not done when subclinical enthesitis was detected since they were in clinical remission and acute phase reactants were within normal limits. However, the patient with bilateral subclinical Achilles enthesitis had a disease flare afterward, and methotrexate was switched to etanercept. Conclusion: Subclinical enthesitis can be observed especially in CNO patients with overlappin- genthesitis-related arthritis features. The use of US may prove beneficial in detecting subclini- cal enthesitis and predicting disease flare.</p>","PeriodicalId":75267,"journal":{"name":"Turkish archives of pediatrics","volume":"60 2","pages":"289-293"},"PeriodicalIF":1.3,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12093391/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144045597","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
Evaluation of the Etiology of Granulomatous Lymphadenopathy in Children Admitted to a Tertiary Pediatric Infectious Clinic. 三级儿科感染诊所收治的儿童肉芽肿性淋巴结病的病因评估。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24316
Fatma Tugba Cetin, Ümmühan Çay, Özlem Özgür Gündeslioğlu, Derya Alabaz, Nazlı Totik, Aysun Hatice Uğuz

Objective: Pediatric patients with histopathologically confirmed granulomatous lymphade- nopathy were evaluated etiologically. Materials and Methods: In this study, patients who presented to the tertiary pediatric infec- tious disease clinic with histopathologically confirmed granulomatous lymphadenopathy were retrospectively reviewed, and the etiological evaluation of granulomatous inflammation based on patient history, clinical findings, and additional tests were presented. Results: The study included 91 patients. In the study, 48 (52.7%) patients underwent biopsy from the cervical region, 21 (23.1%) patients underwent biopsy from the axillary region, 13 (14.3%) patients underwent biopsy from the submandibular and 9 (9.9%) patients underwent biopsy from lymph node sites other than these regions. Cervical lymphadenopathy was more common in patients over the age of 10, while axillary lymphadenopathy was more common in patients under the age of 5. A statistically significant difference was found between the age groups in the biopsy sites (P=.007). When the etiology of the patients was examined, it was found that 78 (85.7%) patients had infectious and 3 (3.3%) patients had non-infectious causes. The cause could not be determined for 10 (11%). There was a difference in etiology frequency according to the lymphadenopathy locations (P=.001). Conclusion: In this study, the most common etiology of granulomatous lymphadenopathy was shown to be infections, especially mycobacteria. Less common were toxoplasmosis, aspergil- lus, and cat scratches. Among non-infectious causes, chronic granulomatous disease should be kept in mind.

目的:对经组织病理学证实的小儿肉芽肿性淋巴病变进行病因分析。材料和方法:在本研究中,回顾性分析了在第三期儿科传染病诊所就诊的组织病理学证实的肉芽肿性淋巴结病患者,并根据患者病史、临床表现和其他检查结果对肉芽肿性炎症的病因进行了评估。结果:共纳入91例患者。在本研究中,48例(52.7%)患者接受了颈部活检,21例(23.1%)患者接受了腋窝活检,13例(14.3%)患者接受了下颌下活检,9例(9.9%)患者接受了这些区域以外的淋巴结活检。宫颈淋巴结病多见于10岁以上的患者,而腋窝淋巴结病多见于5岁以下的患者。不同年龄组活检部位的差异有统计学意义(P=.007)。对患者进行病因检查,感染性78例(85.7%),非感染性3例(3.3%)。其中10例(11%)无法确定病因。不同淋巴结病变部位的发病频率有差异(P= 0.001)。结论:在本研究中,肉芽肿性淋巴结病最常见的病因是感染,尤其是分枝杆菌。较不常见的是弓形虫病、曲霉病和猫抓伤。在非感染性原因中,应注意慢性肉芽肿性疾病。
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引用次数: 0
Possible Factors Affecting Breast Milk Feeding Status Of Preterm Infants Monitored in the Neonatal Intensive Care Unit. 影响新生儿重症监护病房监测早产儿母乳喂养状况的可能因素
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24265
Funda Emren Yakar, Elif Ünver Korğalı

Objective: The aim was to investigate the rates, duration, and possible influencing factors of breast milk feeding (BMF) in preterm infants in the neonatal intensive care unit (NICU) at discharge and in the first year of life. Materials and Methods: In a retrospective cohort study, 173 preterm infants <37 weeks who were hospitalized in the NICU were evaluated. Information was obtained from hospital records and mothers via telephone. Results: The BMF rate was 90.7% with 62.4% exclusively breastfeeding (EBF) and 28.3% partially breastfeeding at discharge. The exclusive, partial, and formula feeding rates were 53.7%, 27.7%, 18.5% and 43.9%, 37%, 19.1% at 4 and 6 months, respectively. The median EBF and total BMF durations were 4 (1-6) and 12 (4.5-24) months, respectively. Very preterms were weaned at a higher rate in the first 6 months compared to moderate and late preterms (50%, 26.3%, 33.3%, P=.046, respectively). EBF at discharge was significantly associated with EBF at 4 and 6 months by chronological and corrected age. The BMF rate for >12 months was higher for multiparous mothers (56.40%, 36.10%, P=.02). Total BMF duration was shorter in preterms with sepsis compared to those without sepsis (median 5 (1-12) and 12.5 (5-24) months, P=.02). It was positively correlated with gestational age (P=.046, r = 0.13), birthweight (P=.012, r=0.17), APGAR (Appearance, Pulse, Grimace, Activity, Respiration) scores 1-minute (P=.002, r = 0.22) and 5-minutes (P=.016, r = 0.16), and maternal age (P < .001, r = 0.25) and negatively correlated with the length of stay in the NICU (P=.031, r=-0.14) and the intubation time (P=.006,r= -0.41). Conclusion: To improve breastfeeding, EBF should be aimed at discharge in all preterms. After discharge, breastfeeding support and close follow-up should be continued for all preterms, especially very preterms.

目的:探讨新生儿重症监护病房(NICU)早产儿出院时和1岁时母乳喂养(BMF)的发生率、持续时间及可能的影响因素。材料与方法:回顾性队列研究,173例12月龄早产儿在多胎母亲中较高(56.40%,36.10%,P= 0.02)。脓毒症早产儿的总BMF持续时间比无脓毒症早产儿短(中位5(1-12)个月和12.5(5-24)个月,P= 0.02)。与胎龄呈正相关(P=。046, r = 0.13),出生体重(P=。012, r=0.17), APGAR(外貌、脉搏、鬼脸、活动、呼吸)评分1分钟(P= 0.17)。002, r = 0.22)和5分钟(P=。016, r = 0.16),与产妇年龄(P < 0.001, r = 0.25)呈负相关,且与NICU住院时间呈负相关(P= 0.16, r = 0.16)。031, r=-0.14)和插管时间(P=。006年,r = -0.41)。结论:为改善母乳喂养,EBF应以所有早产儿出院为目标。出院后,应继续对所有早产儿,特别是非常早产儿进行母乳喂养支持和密切随访。
{"title":"Possible Factors Affecting Breast Milk Feeding Status Of Preterm Infants Monitored in the Neonatal Intensive Care Unit.","authors":"Funda Emren Yakar, Elif Ünver Korğalı","doi":"10.5152/TurkArchPediatr.2025.24265","DOIUrl":"10.5152/TurkArchPediatr.2025.24265","url":null,"abstract":"<p><p>Objective: The aim was to investigate the rates, duration, and possible influencing factors of breast milk feeding (BMF) in preterm infants in the neonatal intensive care unit (NICU) at discharge and in the first year of life. Materials and Methods: In a retrospective cohort study, 173 preterm infants <37 weeks who were hospitalized in the NICU were evaluated. Information was obtained from hospital records and mothers via telephone. Results: The BMF rate was 90.7% with 62.4% exclusively breastfeeding (EBF) and 28.3% partially breastfeeding at discharge. The exclusive, partial, and formula feeding rates were 53.7%, 27.7%, 18.5% and 43.9%, 37%, 19.1% at 4 and 6 months, respectively. The median EBF and total BMF durations were 4 (1-6) and 12 (4.5-24) months, respectively. Very preterms were weaned at a higher rate in the first 6 months compared to moderate and late preterms (50%, 26.3%, 33.3%, P=.046, respectively). EBF at discharge was significantly associated with EBF at 4 and 6 months by chronological and corrected age. The BMF rate for >12 months was higher for multiparous mothers (56.40%, 36.10%, P=.02). Total BMF duration was shorter in preterms with sepsis compared to those without sepsis (median 5 (1-12) and 12.5 (5-24) months, P=.02). It was positively correlated with gestational age (P=.046, r = 0.13), birthweight (P=.012, r=0.17), APGAR (Appearance, Pulse, Grimace, Activity, Respiration) scores 1-minute (P=.002, r = 0.22) and 5-minutes (P=.016, r = 0.16), and maternal age (P < .001, r = 0.25) and negatively correlated with the length of stay in the NICU (P=.031, r=-0.14) and the intubation time (P=.006,r= -0.41). Conclusion: To improve breastfeeding, EBF should be aimed at discharge in all preterms. After discharge, breastfeeding support and close follow-up should be continued for all preterms, especially very preterms.</p>","PeriodicalId":75267,"journal":{"name":"Turkish archives of pediatrics","volume":"60 2","pages":"280-288"},"PeriodicalIF":1.3,"publicationDate":"2025-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12093387/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144059460","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
Insights Into Pediatric Non-congenital Adrenal Hyperplasia: A Review Based on 5 Different Rare Cases with Primary Adrenal Insufficiency. 小儿非先天性肾上腺增生:基于5例罕见原发性肾上腺功能不全的回顾。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24339
Sirmen Kizilcan Cetin, Zeynep Siklar, Elif Ozsu, Zehra Aycan, Merih Berberoglu

Adrenal insufficiency presents a significant clinical challenge due to its diverse etiologies and potentially life-threatening consequences. This review highlights the spectrum of adrenal insuf- ficiency, focusing on primary adrenal insufficiency (PAI). Childhood PAI, predominantly con- genital, presents unique diagnostic and management considerations. An aspect of this review is the discussion of PAI related to non-congenital adrenal hyperpla- sia, particularly adrenocorticotropic hormone (ACTH) resistance syndromes and autoimmune adrenal insufficiency. The clinical presentation, diagnosis, and treatment management of these rare childhood PAI types are assessed through 5 case studies. Despite advancements in genetic understanding, some cases are unsolved and remain diag- nostic mysteries. There is a need for further research and elucidation of molecular etiopatho- genesis in adrenal insufficiency. Clinicians are pivotal in identifying these rare diseases and providing lifesaving outcomes.

由于其多种病因和潜在的危及生命的后果,肾上腺功能不全提出了一个重大的临床挑战。这篇综述强调了肾上腺功能不全的频谱,重点是原发性肾上腺功能不全(PAI)。儿童PAI,主要是外阴,提出了独特的诊断和管理考虑。本综述的一个方面是讨论PAI与非先天性肾上腺素亢进,特别是促肾上腺皮质激素(ACTH)抵抗综合征和自身免疫性肾上腺功能不全有关。通过5例病例研究,对这些罕见的儿童PAI类型的临床表现、诊断和治疗管理进行了评估。尽管对基因的理解有了进步,但有些病例仍未得到解决,仍然是诊断上的谜团。肾上腺功能不全的分子发病机制有待进一步研究和阐明。临床医生在识别这些罕见疾病和提供挽救生命的结果方面至关重要。
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引用次数: 0
Growth Hormone Therapy in Neurosecretory Dysfunction. 神经分泌功能障碍的生长激素治疗。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24319
Ebru Barsal Çetiner, Zeynep Donbaloğlu, Berna Singin, Kürşat Çetin, Yasemin Funda Bahar, Hale Tuhan, Mesut Parlak

Objective: Growth hormone neurosecretory dysfunction (GH-NSD) is a rare cause of short stat- ure. Diagnosis is established by evaluating nocturnal growth hormone secretion in patients with normal growth hormone stimulation tests. The aim of this study was to evaluate the first- and second-year treatment responses and final height in patients diagnosed with GH-NSD and treated with recombinant human growth hormone (rhGH). Materials and Methods: This retrospective study examined 500 patients treated with rhGH for short stature at a pediatric endocrinology clinic at Akdeniz University. Among them, 18 patients diagnosed with GH-NSD were included in the study. At the time of treatment initiation, param- eters such as insulin-like growth factor 1 (IGF-1), growth hormone (GH) stimulation test results, mean GH level during sleep, height standard deviation score (SDS), mid-parental height (MPH), and predicted adult height (PAH) were assessed. Treatment responses during the first and second years, as well as final height data, were analyzed. Results: GH therapy improved height velocity (HV) and overall height. The mean baseline height SDS of the patients was -3.13 ± 0.36. In the first year, Δheight SDS was 0.72 ± 0.44, and in the second year, Δheight SDS was 1.00 ± 0.70. Patients who reached their final height had a mean height SDS of -1.72 ± 0.83 and Δheight SDS of 1.46 ± 0.62. A correlation was found between the baseline height SDS, PAH SDS, MPH SDS, and first-year HV. Conclusion: Patients with GH-NSD treated with rhGH respond well to treatment, achieving genetic height potential.

目的:生长激素神经分泌功能障碍(GH-NSD)是一种罕见的矮个子原因。通过对生长激素刺激试验正常的患者夜间生长激素分泌情况的评价来确定诊断。本研究的目的是评估被诊断为GH-NSD并接受重组人生长激素(rhGH)治疗的患者的第一年和第二年的治疗反应和最终身高。材料和方法:本回顾性研究调查了在Akdeniz大学儿科内分泌学诊所接受rhGH治疗的500例矮小患者。其中18例诊断为GH-NSD的患者纳入研究。在治疗开始时,评估胰岛素样生长因子1 (IGF-1)、生长激素(GH)刺激试验结果、睡眠期间平均GH水平、身高标准偏差评分(SDS)、亲代中等身高(MPH)和预测成人身高(PAH)等参数。对第一年和第二年的治疗反应以及最终的身高数据进行分析。结果:生长激素治疗提高了身高速度(HV)和总身高。患者的平均基线身高SDS为-3.13±0.36。第一年Δheight SDS为0.72±0.44,第二年Δheight SDS为1.00±0.70。达到最终身高的患者平均身高SDS为-1.72±0.83,Δheight SDS为1.46±0.62。基线身高SDS、PAH SDS、MPH SDS与第一年HV之间存在相关性。结论:GH-NSD患者经rhGH治疗后疗效良好,达到遗传身高潜力。
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引用次数: 0
Hemodynamic Changes in the Transition Period in the Preterm and Term Infant: Basic Concepts. 早产儿和足月儿过渡期的血流动力学变化:基本概念。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24256
Fahri Fahri

The transition of the cardiovascular system from fetal life to extrauterine life occurs through different physiological mechanisms. The development of the lungs are parallel to the devel- opment of the cardiovascular system. Cardiac and vascular tone are affected by genetic and environmental factors, including hormonal influences and autonomic reflexes. During the tran- sition period, significant changes occur in preload, myocardial contractility, and afterload. The timing of cord clamping has a profound effect on these changes. Cerebral autoregulation is severely impaired in preterm infants, and cerebral blood flow is almost completely pressure- passive, especially in extremely preterm infants. Disrupted autoregulation is also more frequent in sick infants. Knowledge of transitional factors in different periods is essential for proper man- agement of newborn infants.

心血管系统从胎儿生命到子宫外生命的转变是通过不同的生理机制发生的。肺的发育与心血管系统的发育是平行的。心脏和血管张力受到遗传和环境因素的影响,包括激素影响和自主神经反射。在过渡期内,负荷前、心肌收缩力和负荷后发生显著变化。脐带夹紧的时间对这些变化有深远的影响。早产儿的大脑自我调节功能严重受损,脑血流几乎完全是压力被动的,尤其是在极早产儿中。自身调节紊乱在生病婴儿中也更为常见。了解不同时期的过渡性因素对新生儿的正确护理至关重要。
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引用次数: 0
Cardiovascular Response to Active Standing Test in Children with Overweight and Obesity. 超重和肥胖儿童对主动站立试验的心血管反应。
IF 1.3 Q3 PEDIATRICS Pub Date : 2025-05-02 DOI: 10.5152/TurkArchPediatr.2025.24243
Yasemin Nuran Donmez, Kutay Sel

Objective: The aim of this study was to assess active standing test responses in ovewrweight or obese children and to determine the factors that contribute to orthostatic abnormalities. Materials and Methods: Orthostatic responses were investigated in bothobese and overweight children. To provide an overview of the autonomic nervous system (ANS), blood pressure and heart rate measurements, laboratory parameters, and anthropometric measures were analyzed. Results: A total of 123 overweight or obese children, with a median age of 15.03 (range from 6.9 to 17.9), were included in this study. Seventy-seven patients (63%) were obese, whereas 46 (37%) were overweight. Orthostatic disturbances were observed in 78 patients (63%). In the standing test, 73 patients (59%) exhibited an abnormal response. Orthostatic hypotension (33%), ortho- static hypertension (30%), and postural orthostatic tachycardia syndrome (18%), were detected in the patients. The group that had orthostatic hypotension had a lower systolic pressure in the standing test after 10 min. The group with orthostatic hypertension had higher body mass index. Furthermore, the orthostatic group displayed significantly higher levels of Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), insulin, and HbA1c. Conclusion: The results of this study signifies a connection between obesity or being overweight and ANS, . highlighting the need for evaluation of the ANS in obese or overweight children to predict the adverse consequences and to prevent occuring during childhood.

目的:本研究的目的是评估超重或肥胖儿童的主动站立测试反应,并确定导致站立异常的因素。材料和方法:研究这些儿童和超重儿童的直立反应。为了提供自主神经系统(ANS)的概述,血压和心率测量,实验室参数和人体测量进行了分析。结果:本研究共纳入123例超重或肥胖儿童,年龄中位数为15.03岁(6.9 ~ 17.9岁)。77名患者(63%)肥胖,46名(37%)超重。78例(63%)患者出现直立性障碍。站立试验中,73例(59%)患者出现异常反应。体位性低血压(33%),体位性高血压(30%),体位性心动过速综合征(18%)。站立试验10 min后,体位性低血压组收缩压较低,体位性高血压组体重指数较高。此外,直立组胰岛素抵抗稳态模型评估(HOMA-IR)、胰岛素和HbA1c水平显著升高。结论:本研究结果表明肥胖或超重与ANS之间存在联系。强调需要对肥胖或超重儿童的ANS进行评估,以预测不良后果并防止在儿童时期发生。
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Turkish archives of pediatrics
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