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Psychobiotic properties of probiotic lactic acid bacteria and bifidobacteria in paediatric neurological disorders 益生菌乳酸菌和双歧杆菌在小儿神经系统疾病中的精神生物学特性
Pub Date : 2025-07-05 DOI: 10.1016/j.gpeds.2025.100266
Maria Teresa Rocchetti , Mariagiovanna Di Chiano , Iman Elouardi , Daniela Fiocco
Recent studies have highlighted a close relationship between intestinal dysbiosis and paediatric neurological disorders, such as autism spectrum disorders (ASD), attention deficit hyperactivity disorder (ADHD), epilepsy, cerebral palsy (CP). In the last decades, the relevance of a strong connection between the intestinal microbiota and the brain, i.e., the gut-brain axis, has been broadly ascertained. Through this association, gut microbes contribute to shape development, physiology, and cognitive functions of the brain. The bidirectional communication between gut microbiota and brain involves a complex set of molecular signals that influence synaptic plasticity, learning, memory, mood, and the brain's excitatory-inhibitory balance. Microbial metabolites play a fundamental role in modulating brain activity. Emerging scientific evidence suggests that neurological and psychiatric conditions, including ASD, ADHD, anxiety, and depression, may not simply stem from brain malfunctions, but rather from imbalances in the gut microbiota, which contribute to disrupt brain function and development. In this context, psychobiotics, i.e., a specific group of probiotic microorganisms, have garnered interest for their potential to modulate brain functions. Several pre-clinical studies on psychobiotics have shown promising results in managing paediatric neurological disorders, including ASD and ADHD. However, there is only a limited number of clinical studies to support the use of psychobiotics as therapeutics. This review summarizes and discusses the link between gut microbiota and neurological disorders in children, and the current status of studies investigating the potential application of psychobiotic lactic acid bacteria (LAB) and bifidobacteria for treating these paediatric disorders.
最近的研究强调了肠道生态失调与儿童神经系统疾病(如自闭症谱系障碍(ASD)、注意缺陷多动障碍(ADHD)、癫痫、脑瘫(CP))之间的密切关系。在过去的几十年里,肠道微生物群与大脑(即肠-脑轴)之间的紧密联系的相关性已被广泛确定。通过这种联系,肠道微生物有助于大脑的形状发育、生理和认知功能。肠道微生物群和大脑之间的双向交流涉及一组复杂的分子信号,这些信号影响突触可塑性、学习、记忆、情绪和大脑的兴奋-抑制平衡。微生物代谢物在调节大脑活动中起着重要作用。新出现的科学证据表明,包括ASD、ADHD、焦虑和抑郁在内的神经系统和精神疾病可能不仅仅源于大脑功能障碍,而是源于肠道微生物群的失衡,而肠道微生物群的失衡会破坏大脑功能和发育。在这种背景下,精神生物,即一组特定的益生菌微生物,因其调节大脑功能的潜力而引起了人们的兴趣。一些关于精神生物制剂的临床前研究在治疗儿童神经系统疾病,包括ASD和ADHD方面显示了有希望的结果。然而,只有有限数量的临床研究支持使用精神生物制剂作为治疗手段。本文综述并讨论了肠道微生物群与儿童神经系统疾病之间的联系,以及研究精神生物乳酸菌(LAB)和双歧杆菌在治疗这些儿科疾病中的潜在应用的研究现状。
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引用次数: 0
Measles vaccination dropout and its associated factors among children aged 15-23 months in Qardho district, Northeastern Somalia: A community-based cross-sectional study 索马里东北部Qardho地区15-23个月儿童麻疹疫苗接种失学率及其相关因素:一项基于社区的横断面研究
Pub Date : 2025-07-05 DOI: 10.1016/j.gpeds.2025.100267
Mohamed Yusuf , Agumasie Semahegn , Gezahegn Tesfaye , Maleda Tefera

Background

Although childhood vaccination is highly effective in preventing measles infection, dropout from the vaccination schedule remains a significant public health challenge in Low- and Middle-Income countries, including Somalia. There is a paucity of research evidence on the magnitude and the factors contributing to it in the study setting. Therefore, this study aimed to assess the magnitude of measles vaccination dropout and its associated factors among children aged 15–23 months in Qardho district, Northeastern, Somalia.

Method

A community-based cross-sectional study was conducted among 372 randomly selected participants who live in Qardho district, Northeastern Somalia. Data were collected using a structured tool developed in an Open Data Kit and exported to Stata version 17.0 for cleaning and analysis. Descriptive statistics were used to summarize the data. Bivariable and multivariable logistic regression analyses were performed to identify factors associated with children’s dropout from measles vaccination. Adjusted odds ratio at a 95 % confidence interval was used to declare statistically significant associations.

Results

The overall magnitude of measles vaccination dropout was 42.5 % (95 % CI: 37.3, 47.6 %). Children with a birth order of 2–4 (AOR = 3.09, 95 % CI: 1.38, 6.94), and ≥ 5 (AOR = 4.25, 95 % CI: 1.90, 9.48), born to a merchant mother (AOR = 3.63, 95 % CI: 1.64, 8.04), and whose mothers/caregivers had a negative attitude towards vaccination (AOR = 3.82, 95 % CI: 2.18, 6.69) were more likely to dropout from measles vaccination. Children whose mothers attended at least primary level of education (AOR = 0.28, 95 % CI: 0.12, 0.68), whose fathers attended primary education and above (AOR = 0.25, 95 % CI: 0.08, 0.81), and children from middle-income families (AOR = 0.32, 95 % CI: 0.13, 0.79) were less likely to experience measles vaccination dropout.

Conclusion

The findings of this study highlight that two in five children dropped out of the measles vaccine program. Parental educational status, attitude towards vaccination, mother’s occupation, family income and child’s birth order were significantly associated with measles vaccination dropout. Future intervention strategies could focus on promoting a positive attitude towards the vaccine.
尽管儿童疫苗接种在预防麻疹感染方面非常有效,但在包括索马里在内的低收入和中等收入国家,退出疫苗接种计划仍然是一个重大的公共卫生挑战。在研究环境中,对其大小和影响因素的研究证据不足。因此,本研究旨在评估索马里东北部Qardho地区15-23个月儿童麻疹疫苗接种失学率及其相关因素。方法对居住在索马里东北部Qardho区的372名随机选择的参与者进行了一项以社区为基础的横断面研究。使用Open Data Kit中开发的结构化工具收集数据,并导出到Stata 17.0版本进行清理和分析。采用描述性统计对数据进行汇总。进行了双变量和多变量logistic回归分析,以确定与儿童退出麻疹疫苗接种相关的因素。采用95%置信区间的校正优势比来宣布统计学上显著的关联。结果麻疹疫苗接种总体失接率为42.5% (95% CI: 37.3, 47.6%)。出生顺序为2-4 (AOR = 3.09, 95% CI: 1.38, 6.94)和≥5 (AOR = 4.25, 95% CI: 1.90, 9.48)、母亲为商人(AOR = 3.63, 95% CI: 1.64, 8.04)以及母亲/照顾者对疫苗接种持否定态度(AOR = 3.82, 95% CI: 2.18, 6.69)的儿童更容易退出麻疹疫苗接种。母亲至少接受过初等教育(AOR = 0.28, 95% CI: 0.12, 0.68)、父亲接受过初等教育及以上(AOR = 0.25, 95% CI: 0.08, 0.81)以及来自中等收入家庭(AOR = 0.32, 95% CI: 0.13, 0.79)的儿童发生麻疹疫苗接种辍学的可能性较小。结论:本研究结果强调,五分之二的儿童退出了麻疹疫苗接种计划。父母的教育程度、对疫苗接种的态度、母亲的职业、家庭收入和儿童的出生顺序与麻疹疫苗接种辍学率显著相关。今后的干预战略可侧重于促进对疫苗的积极态度。
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引用次数: 0
Rising incidence of feticide, neonaticide, and infanticide in Pakistan: An emerging crisis 巴基斯坦杀婴、杀新生儿和杀婴事件的上升:一个正在出现的危机
Pub Date : 2025-06-24 DOI: 10.1016/j.gpeds.2025.100265
Muneeb Saifullah , Fatima Yasin , Mishal Ihsan , Qasim Mehmood , Syed Ali Ahsan , Abbas M Mehdi , Javed Iqbal
Feticide, neonaticide, and infanticide are serious crimes under the law; however, they remain prevalent in South Asian countries, including Pakistan. Female feticide is much more common due to a preference for males based on social, economic, and cultural needs. Other contributing factors include poverty, Low literacy, honor killings, and unwanted or illegal pregnancies. Police rarely pursue these cases. This lack of accountability emboldens perpetrators and silences survivors. By improving education, health services, economic conditions, and legal accountability, Pakistan can begin to reduce the tragic incidence of feticide, neonaticide, and infanticide.
杀婴、杀婴、杀婴是严重犯罪;然而,它们在包括巴基斯坦在内的南亚国家仍然普遍存在。由于基于社会、经济和文化需求的对男性的偏好,女性堕胎更为常见。其他影响因素包括贫困、低文化水平、荣誉谋杀、意外怀孕或非法怀孕。警方很少追查这些案件。缺乏问责使肇事者更加大胆,使幸存者保持沉默。通过改善教育、卫生服务、经济条件和法律问责制,巴基斯坦可以开始减少杀婴、杀新生儿和杀婴的悲惨发生率。
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引用次数: 0
Patterns of multi-morbidity cluster for under five children in Tanzania 坦桑尼亚五岁以下儿童多发病群的模式
Pub Date : 2025-06-19 DOI: 10.1016/j.gpeds.2025.100264
Marystella Vicent, Maurice C.Y. Mbago, Amina S. Msengwa

Background

Despite progress in child health interventions, anemia, malaria, and fever remain prominent public health concerns for children under five in Tanzania. Geographic variability may influence disease patterns, necessitating the identification of high-risk clusters to inform targeted interventions. This study aimed to assess the spatial clustering of these three conditions among Tanzanian under-five children using three nationally representative surveys.

Methods

A cross-sectional, survey-based design was employed using data from the 2007–08 and 2011–12 Tanzania HIV/AIDS and Malaria Indicator Surveys (THMIS) and the 2015–16 Tanzania Demographic and Health Survey and Malaria Indicator Survey (TDHS-MIS). In total, 19,832 under-five children were included across the three surveys. Prevalences of anemia, malaria, and fever were determined, and spatial analyses were performed using STATA version 16, ArcGIS version 10.3, and SaTScan software. Moran’s I was calculated to test spatial autocorrelation, and the SaTScan Bernoulli model identified clusters with elevated risks.

Results

Overall, 5551 children from the 2007–08 THMIS, 6458 from the 2011–12 THMIS, and 7823 from the 2015–16 TDHS-MIS were analyzed. Anemia was the most prevalent condition, with rates ranging from 57.4 % to 69.7 %, followed by fever (18.6 % to 22.4 %), and malaria (9.3 % to 12.5 %). Spatial autocorrelation tests indicated non-random clustering for these conditions, with Moran’s I values ranging from 0.538 to 0.975 (p < 0.001). SaTScan analyses revealed recurrent high-risk clusters in Kigoma, Ruvuma, Lindi, and Mtwara across the three surveys. These clusters were statistically significant (p < 0.001) and highlighted persistent hotspots of childhood morbidity.

Conclusion

The study demonstrates pronounced spatial clustering of anemia, malaria, and fever among under-five children in Tanzania. Key regions including Kigoma, Ruvuma, Lindi, and Mtwara consistently emerged as hotspots. Targeted health interventions in these high-risk areas, including integrated approaches addressing multiple coexisting conditions, are critical for reducing disease burden and improving child health outcomes.
背景尽管在儿童保健干预措施方面取得了进展,但贫血、疟疾和发烧仍然是坦桑尼亚五岁以下儿童的主要公共卫生问题。地理差异可能影响疾病模式,因此有必要确定高风险群集,以便为有针对性的干预措施提供信息。本研究旨在通过三个具有全国代表性的调查来评估坦桑尼亚五岁以下儿童中这三种情况的空间聚类。方法采用横断面调查设计,使用2007-08年和2011-12年坦桑尼亚艾滋病毒/艾滋病和疟疾指标调查(THMIS)和2015-16年坦桑尼亚人口与健康调查和疟疾指标调查(TDHS-MIS)的数据。三次调查共包括19,832名五岁以下儿童。测定贫血、疟疾和发热的患病率,并使用STATA version 16、ArcGIS version 10.3和SaTScan软件进行空间分析。计算Moran 's I来测试空间自相关性,SaTScan伯努利模型识别出风险升高的集群。结果共纳入2007-08年度thhs - mis的儿童5551名,2011-12年度thhs - mis的儿童6458名,2015-16年度thhs - mis的儿童7823名。贫血是最普遍的疾病,发病率在57.4%至69.7%之间,其次是发烧(18.6%至22.4%)和疟疾(9.3%至12.5%)。空间自相关检验表明,这些条件存在非随机聚类,Moran 's I值范围为0.538 ~ 0.975 (p <;0.001)。SaTScan分析显示,在三次调查中,基戈马、鲁武马、林迪和姆特瓦拉都有复发性高风险聚集。这些聚类具有统计学意义(p <;0.001),并强调了儿童发病率的持续热点。结论该研究表明坦桑尼亚五岁以下儿童中存在明显的贫血、疟疾和发烧的空间聚集性。包括基戈马、鲁武马、林迪和姆特瓦拉在内的关键地区不断成为热点地区。在这些高风险地区采取有针对性的卫生干预措施,包括采取综合办法处理多种共存状况,对于减轻疾病负担和改善儿童健康结果至关重要。
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引用次数: 0
A 6.2 Kg macrosomia in a non-diabetic mother managed with no adverse outcomes in a resource limited setting: A case report 在资源有限的情况下,一位非糖尿病母亲的6.2公斤巨大儿没有出现不良后果
Pub Date : 2025-06-06 DOI: 10.1016/j.gpeds.2025.100262
Farhan Yusuf Sharif , Abdiwali mohamed Ahmed , Abdikafi Ibrahim Khayre , Mohamed Hassan Osman , Joshua Muhumuza

Introduction and importance

When a baby's birth weight surpasses the 90th percentile for a certain gestational week, it is referred to as macrosomia. The growing prevalence of fetal macrosomia presents an impending concern in the field of obstetrics. Numerous complications for both the mother and the fetus are linked to macrosomia. We present a case of macrosomia that weighed 6.2 kg, delivered in a low resource setting in which no early neonatal or maternal complication occurred.

Case presentation

We present a 41-year-old woman gravida 8 para 7 + 0 that presented at 42 weeks of amenorrhea. On examination at admission, the body mass index was 42.5kg/m2, Ultrasonography was suggestive of severe oligohydramnios with an estimated fetal weight of 5.5 kg. The decision to deliver the baby by an elective cesarean section was made. The baby weighed 6.2 kg and did not have any physical abnormalities. At discharge, both the mother and baby were healthy.

Clinical discussion

A positive outcome requires tailored therapy for each patient because macrosomia is linked to numerous maternal and fetal complications.

Conclusion

Making a timely decision to have a cesarean delivery when indicated, as was done in this instance, can lower the rate of maternal and neonatal morbidity.
当一个婴儿的出生体重在怀孕的某一周超过90个百分位数时,就被称为巨大儿。胎儿巨大症的日益流行提出了一个迫在眉睫的关注在产科领域。母亲和胎儿的许多并发症都与巨大儿有关。我们提出了一个体重6.2公斤的巨大儿病例,在低资源环境中分娩,没有发生早期新生儿或产妇并发症。病例介绍:我们报告一名41岁孕妇,妊娠第8段第7 + 0段,在闭经42周时出现。入院检查,体重指数42.5kg/m2,超声提示严重羊水过少,估计胎儿体重5.5 kg。决定择期剖宫产。婴儿体重6.2公斤,没有任何身体异常。出院时,母亲和婴儿都很健康。临床讨论一个积极的结果需要为每个患者量身定制的治疗,因为巨大儿与许多母体和胎儿并发症有关。结论及时决定剖宫产可降低产妇和新生儿的发病率,如本例所示。
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引用次数: 0
Outcome and its predictors of children with nosocomial infection in ayder pediatric ICU, Tigray, Ethiopia 埃塞俄比亚提格雷ayder儿科ICU院内感染患儿结局及其预测因素
Pub Date : 2025-05-31 DOI: 10.1016/j.gpeds.2025.100263
Hansa Haftu Lemma , Abdikarin Ahmed Mohamed , Amanuel Hadgu , Teklu Gebrehiwot Gebremichael

Objective

The main objectives of this study were to assess the outcomes and predictors of nosocomial infections in pediatric patients.

Method

A hospital-based retrospective observational study and a consecutive sampling technique were used to collect data. Categorical data were compared using Pearson’s Chi-square test/Fisher’s exact test. Additionally, Kaplan-Meier analysis was also used to assess survival. P-values < 0.05 were considered statistically significant.

Results

A total of 45 patients who developed nosocomial infections were analyzed. The incidence density of nosocomial infection was 41.1 per 1000 patient-days. Most patients were male (53.3 %) and under 14 (75.6 %), with a median age of 1 year. Statistically significant variables associated with increased mortality included female gender, transfer from the ward, prolonged maintenance fluid duration (>3 days), the need for mechanical ventilation, and the presence of comorbid illnesses, as indicated by chi-square analysis. Patients with nosocomial infections had a longer hospital stay (20 days vs. 10 days) and a higher mortality rate (26.7 % vs. 19.1 %) compared to those without nosocomial infections. Nosocomial infections resulted in an excess crude mortality rate of 7.5 %.

Conclusion

Preventive measures should be prioritized given the identified risk factors for nosocomial infections. Patients with nosocomial infections are at an increased risk of mortality.
目的本研究的主要目的是评估儿科患者院内感染的结局和预测因素。方法采用以医院为基础的回顾性观察研究和连续抽样技术收集资料。分类数据比较采用Pearson卡方检验/Fisher精确检验。此外,Kaplan-Meier分析也用于评估生存率。假定值& lt;0.05认为有统计学意义。结果共分析院内感染患者45例。医院感染的发生率密度为41.1 / 1000患者-日。大多数患者为男性(53.3%),14岁以下(75.6%),中位年龄为1岁。卡方分析显示,与死亡率增加相关的统计显著变量包括女性性别、从病房转出、维持液体持续时间延长(3天)、机械通气的需要以及合并症的存在。与没有医院感染的患者相比,医院感染患者的住院时间更长(20天对10天),死亡率更高(26.7%对19.1%)。医院感染导致的超额粗死亡率为7.5%。结论针对医院感染的危险因素,应优先采取预防措施。院内感染患者的死亡风险增加。
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引用次数: 0
Radiofrequency echographic multi-spectrometry for early bone health: The REMS-bone study protocol (Trial acronym: REMS-bone) 早期骨健康的射频超声多光谱:rem -bone研究方案(试验缩写:rem -bone)
Pub Date : 2025-05-23 DOI: 10.1016/j.gpeds.2025.100261
Serafina Perrone , Malgorzata Wasniewska , Maria-Elisabeth Street , Virginia Beretta , Elena Scarpa , Chiara Petrolini , Andrea Dall’Asta , Domenico Corica , Tommaso Aversa , Giorgia Pepe , Letteria Morabito , Federica Grassi , Anna-Mariia Shulhai , Valentina Bianco , Anna Maria Papini , Maria Cristina Albertini , Silvia Carloni , Giuseppe Maglietta , Matteo Puntoni , Caterina Caminiti , Tullio Ghi

Background

Bone health begins with maternal health and nutrition, which influences skeletal mass and bone mineral density (BMD) already in utero. Maximization of bone mass during skeletal growth has become the goal of primary prevention of osteopenia and osteoporosis. The amount of bone gained during growth and its subsequent rate of loss are closely linked to the final skeletal mass in adulthood. Radiofrequency Echographic Multi Spectrometry (REMS) technology has proven to be useful in the assessment of BMD in pregnant women. However, the feasibility of REMS for the assessment of bone status in newborns remains unknown. This multicenter longitudinal study aims at using REMS to evaluate skeletal status in fetuses, newborns and children until 12 months of age.

Methods

Two hundred mother-newborn dyads, with infants born at term of gestation, will be consecutively recruited during the prenatal period and followed up until 12 months of life. BMD will be assessed with REMS technology in mothers, fetuses, newborns and infants at 1, 3 6 and 12 months of life. In all enrolled patients, blood will be collected at specific time points and oxidative stress biomarkers, specific microRNAs, and several bone metabolites will be measured in blood, whereas endocrine disruptors will be measured in urine.

Discussion

This study is designed to provide robust data on the best method to identify and evaluate bone status starting from intrauterine life. The associations among BMD, maternal nutrition, early exposure to endocrine disruptors, and other investigated molecules will also be investigated in relationship with subsequent body composition and bone health.

Trial registration

The protocol was retrospectively registered on ClinicalTrials.gov on December 3rd, 2024, with the ID number NCT06750523.
骨骼健康始于孕产妇的健康和营养,它影响着已经在子宫内的骨量和骨矿物质密度(BMD)。在骨骼生长过程中使骨量最大化已成为预防骨质减少和骨质疏松的主要目标。生长期间获得的骨骼量及其随后的损失率与成年后的最终骨骼质量密切相关。射频超声多光谱(REMS)技术已被证明是有用的评估BMD在孕妇。然而,REMS评估新生儿骨骼状况的可行性尚不清楚。本多中心纵向研究旨在利用REMS评估胎儿、新生儿和12个月前儿童的骨骼状况。方法在产前连续招募200例足月出生的母新生儿,随访至出生后12个月。BMD将在母亲、胎儿、新生儿和婴儿1、6和12个月时用REMS技术进行评估。在所有入选的患者中,将在特定的时间点采集血液,并测量血液中的氧化应激生物标志物、特定的microrna和几种骨代谢物,而在尿液中测量内分泌干扰物。本研究旨在为从宫内生活开始识别和评估骨骼状态的最佳方法提供可靠的数据。骨密度、母体营养、早期暴露于内分泌干扰物和其他被研究分子之间的关联,也将被研究与随后的身体组成和骨骼健康的关系。试验注册该方案于2024年12月3日在ClinicalTrials.gov上回顾性注册,ID号NCT06750523。
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引用次数: 0
Fraser syndrome with extremely rare features of unilateral anophthalmia and penile torsion in an Afghan neonate: A case report 弗雷泽综合征与极其罕见的特征单侧眼失和阴茎扭转在阿富汗新生儿:一个案例报告
Pub Date : 2025-05-03 DOI: 10.1016/j.gpeds.2025.100258
Turyalai Hakimi , Mansoor Aslamzai

Background

Fraser syndrome is a very rare genetic disorder with multiple organ-system abnormalities. The diagnosis is usually made on the basis of clinical examination, and management requires a multidisciplinary approach.

Case Presentation

We present a case of Fraser syndrome with very rare manifestations of unilateral anophthalmia and moderate penile torsion in an Afghan neonate who was born to a 16-year-old mother. Physical findings and a CT scan of the brain and eyes were used to diagnose the aforementioned syndrome. The surgical repairs of cryptophthalmos and penile torsion were planned to be performed after infancy, and the baby was discharged in good health.

Conclusion

Anophthalmia and penile torsion are very rare components of Fraser syndrome. Very young maternal age may play a predisposing role in the pathogenesis of Fraser syndrome. The multiple organ defects in Fraser syndrome make this entity more challenging to deal with, particularly in low-resourced settings.
弗雷泽综合征是一种非常罕见的遗传性疾病,伴有多器官系统异常。诊断通常是在临床检查的基础上做出的,治疗需要多学科的方法。病例介绍我们提出一个病例弗雷泽综合征非常罕见的表现单侧无眼和中度阴茎扭转在阿富汗新生儿谁是由一个16岁的母亲所生。物理检查和CT扫描的大脑和眼睛被用来诊断上述综合征。隐眼和阴茎扭转的手术修复计划在婴儿期后进行,婴儿健康出院。结论无眼和阴茎扭转是弗雷泽综合征的罕见症状。非常年轻的母亲年龄可能在弗雷泽综合征的发病机制中起易感作用。弗雷泽综合征的多器官缺陷使该实体更具挑战性,特别是在资源匮乏的环境中。
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引用次数: 0
The impact of timing for initiating formula feeding on the short-term prognosis of very low birth weight infants 开始配方奶喂养时间对极低出生体重儿短期预后的影响
Pub Date : 2025-05-02 DOI: 10.1016/j.gpeds.2025.100259
Katsumi Mizuno

Background

For very low birth weight (VLBW) infants, breast milk, particularly mothers' own milk (MOM), is the optimal nutrition. Donor human milk (DHM) is recommended when MOM is insufficient. However, the optimal timing for transitioning from DHM to formula remains unclear. This study examines the impact of formula initiation timing on complications in VLBW infants.

Methods

We analyzed data from 744 VLBW infants (<1500 g) who initiated enteral feeding with DHM within 24 hours of birth using a human milk bank database (2018–2024). Postmenstrual age (PMA) at formula initiation was assessed for associations with bronchopulmonary dysplasia (BPD), home oxygen therapy (HOT), retinopathy of prematurity (ROP), and necrotizing enterocolitis (NEC).

Results

The median PMA at formula initiation was 34.6 weeks. Delayed formula initiation reduced the risk of BPD, HOT, and NEC. Compared to formula initiation before 32 weeks, odds ratios for BPD ranged from 0.186 (34–36 weeks) to 0.239 (no formula). Formula initiation at 32–34 weeks significantly lowered ROP requiring treatment (OR 0.305). Logistic regression analysis indicated a trend toward reduced NEC risk when formula initiation occurred after 34 weeks (p = 0.0504).

Conclusion

Delaying formula initiation until after 34 weeks PMA reduces complications in VLBW infants. Early enteral nutrition with MOM or DHM within 24 hours of birth is crucial, and later formula introduction may provide better outcomes. Further studies are needed to refine feeding guidelines
背景对于极低出生体重(VLBW)婴儿来说,母乳,特别是母亲的母乳(MOM)是最佳的营养来源。当母乳不足时,建议使用捐赠母乳(DHM)。然而,从DHM过渡到配方的最佳时机仍不清楚。本研究探讨配方奶粉起始时间对VLBW婴儿并发症的影响。方法使用母乳库数据库(2018-2024年)分析744名出生后24小时内开始肠内喂养DHM的VLBW婴儿(<1500 g)的数据。评估配方起始时经后年龄(PMA)与支气管肺发育不良(BPD)、家庭氧疗(HOT)、早产儿视网膜病变(ROP)和坏死性小肠结肠炎(NEC)的关系。结果开始配方时的中位PMA为34.6周。延迟配方起始降低了BPD、HOT和NEC的风险。与32周前开始使用配方奶粉相比,BPD的优势比从0.186(34-36周)到0.239(未使用配方奶粉)不等。32-34周时开始使用配方显著降低ROP (OR 0.305)。Logistic回归分析显示,34周后开始使用配方奶粉有降低NEC风险的趋势(p = 0.0504)。结论延迟至34周PMA后才开始使用配方奶粉可减少VLBW婴儿的并发症。出生24小时内早期肠内营养与MOM或DHM是至关重要的,以后引入配方可能会提供更好的结果。需要进一步的研究来完善喂养指南
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引用次数: 0
Determinants of survival of human immune deficiency virus infected children after commencing anti-retroviral therapy in Kembata-Tembaro zone: A facility-based retrospective cohort study 在Kembata-Tembaro地区开始抗逆转录病毒治疗后感染人类免疫缺陷病毒的儿童存活的决定因素:一项基于设施的回顾性队列研究
Pub Date : 2025-04-17 DOI: 10.1016/j.gpeds.2025.100257
Tarekegn Tessema , Mitiku Desalegn , Lonsako Abute , Tadele Yohannes

Background

HIV infection is one of the most significant challenges to global health faced by care providers. On the other hand, malnutrition is prevalent in developing countries; it remains a serious problem among HIV-positive children even with the provision of Anti-Retroviral Therapy (ART).

Objective

To explore determinants of survival of human immune deficiency virus-infected children after commencing Anti-Retroviral Therapy in Kembata-Tembaro Zone, Southern Ethiopia, 2022.

Methods

A facility-based retrospective cohort study was employed among 305 HIV-infected children on ART from May 5-June 4/2022 at public hospitals in Kembata-tembaro zone. The data were collected by using a checklist. Data were entered and cleaned using Epi info 3.5.3 and analysed using SPSS version 25.0 software. The cumulative survival time after initiation of ART was calculated using the Kaplan-Meier survival curve. A Multivariable Cox proportional model was fitted to identify factors affecting survival after initiation of ART and variables having P value≤ 0.05 were considered statistically significant predictors of mortality.

Results

Overall, 43(14.1 %) died with an overall survival rate of 3.3 per 1000 child-months of observation. Undernourished children had a lower survival time than well-nourished children with mean survival time of 92.7 and 62.3 months respectively. Children with advanced WHO clinical stage III or IV (AHR: 6.1; 95 %CI: 1.4, 26.7), severe wasting at the baseline (AHR: 8.7; 95 %CI: 3.2, 23.6), high viral load level (AHR: 3.5; 95 %CI: 0.15, 0.61) and fair/poor adherence to ART (AHR: 3.7; 95 %CI: 2.3, 13.5) were significantly associated with survival of HIV-positive children in this study.

Conclusion

a significant difference in survival time was observed between undernourished and well-nourished children with a high rate of mortality. Severe wasting, WHO clinical stage III or IV, high viral load level and fair/poor adherence were identified as the determinants of survival.
艾滋病毒感染是医护人员面临的全球卫生最重大挑战之一。另一方面,营养不良在发展中国家很普遍;即使提供抗逆转录病毒治疗,在艾滋病毒阳性儿童中,这仍然是一个严重的问题。目的探讨2022年埃塞俄比亚南部肯巴塔-坦巴罗地区人类免疫缺陷病毒感染儿童开始抗逆转录病毒治疗后存活的决定因素。方法对2022年5月5日至6月4日在肯巴塔-坦巴罗地区公立医院接受抗逆转录病毒治疗的305名艾滋病毒感染儿童进行回顾性队列研究。使用清单收集数据。使用Epi info 3.5.3进行数据录入和清理,使用SPSS 25.0软件进行数据分析。采用Kaplan-Meier生存曲线计算抗逆转录病毒治疗开始后的累积生存时间。拟合多变量Cox比例模型以确定影响ART开始后生存的因素,P值≤0.05的变量被认为是死亡率的有统计学意义的预测因子。结果死亡43例(14.1%),总生存率为3.3 / 1000儿童月。营养不良儿童的生存时间低于营养良好儿童,平均生存时间分别为92.7个月和62.3个月。世卫组织临床III期或IV期晚期儿童(AHR: 6.1;95% CI: 1.4, 26.7),基线时严重消瘦(AHR: 8.7;95% CI: 3.2, 23.6),高病毒载量水平(AHR: 3.5;95% CI: 0.15, 0.61)和ART依从性一般/较差(AHR: 3.7;95% CI: 2.3, 13.5)与本研究中hiv阳性儿童的生存率显著相关。结论营养不良儿童与营养良好儿童生存时间差异显著,死亡率高。严重消瘦、WHO临床III期或IV期、高病毒载量水平和一般/较差的依从性被确定为生存的决定因素。
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Global pediatrics
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