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Assessing the causal association between age at menarche and genetic susceptibility to future gastroesophageal reflux disease risks: A two-sample Mendelian randomization study 评估初潮年龄与未来胃食管反流疾病风险的遗传易感性之间的因果关系:一项双样本孟德尔随机化研究
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.10.012
Chung-Chih Liao , Chun-I Lee , Chia-Sheng Chu , Shih-An Wu , Jung-Miao Li

Objective

Evidence indicates that menarche onset is associated with various health outcomes. Gastroesophageal reflux disease (GERD) is a prevalent condition, which may be influenced by the age at menarche (AAM). The study aims to investigate the potential causal relationship between the AAM and GERD.

Methods

We conducted a two-sample Mendelian randomization (MR) analysis utilizing single nucleotide polymorphisms (SNPs) derived from genome-wide association studies summary statistics for AAM and GERD as instrumental variables. Various MR methods were applied to estimate causal effects, supplemented by sensitivity analyses to assess the robustness of our findings.

Results

Overall, 69 SNPs associated with the AAM were used after rigorous selection to ensure absence of linkage disequilibrium or association with confounding factors. The inverse variance-weighted (IVW) method indicated a significant inverse association between genetically predicted AAM and GERD (odds ratio, 0.89; 95 % confidence interval, 0.85–0.94). These findings were consistent across weighted median and weighted mode analyses. The MR-Egger regression analysis suggested no significant directional pleiotropy. Heterogeneity was detected among instrumental variables; however, the leave-one-out sensitivity analysis confirmed the association stability.

Conclusion

We provided robust evidence supporting an inverse causal relationship between the AAM and GERD risk.
目的:有证据表明初潮的发生与多种健康结果有关。胃食管反流病(GERD)是一种常见病,其发病可能与月经初潮年龄有关。本研究旨在探讨AAM与胃食管反流之间的潜在因果关系。方法:我们利用来自全基因组关联研究的单核苷酸多态性(snp)作为工具变量,对AAM和GERD进行了两样本孟德尔随机化(MR)分析。我们应用了各种核磁共振方法来估计因果效应,并辅以敏感性分析来评估我们研究结果的稳健性。结果:总的来说,经过严格的选择,使用了69个与AAM相关的snp,以确保没有连锁不平衡或与混杂因素相关。逆方差加权(IVW)方法显示遗传预测的AAM与GERD呈显著负相关(优势比0.89;95%置信区间,0.85-0.94)。这些发现在加权中位数和加权模式分析中是一致的。MR-Egger回归分析显示无显著的方向性多效性。工具变量间存在异质性;然而,留一敏感性分析证实了该关联的稳定性。结论:我们提供了强有力的证据支持AAM和GERD风险之间的反向因果关系。
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引用次数: 0
Effect of nocturnal enuresis on school-age children and their families in Thailand: A cross-sectional study 夜间遗尿对泰国学龄儿童及其家庭的影响:一项横断面研究。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.12.004
Ornatcha Sirimongkolchaiyakul , Chanon Sutheparank , Yupaporn Amornchaicharoensuk

Background

Nocturnal enuresis (NE) is a chronic problem that causes distress in children and their families. NE affects daily living activities, relationships, behavior, emotions, and social interactions. However, data on the effects of NE on Thai children are limited. This study aimed to evaluate the effects of NE and the associated factors on children with NE and their parents or guardians.

Methods

A cross-sectional study included 349 children with primary NE and 246 with secondary NE, all from Bangkok, Thailand. Their parents or guardians completed a validated questionnaire and rated the severity of the effects of NE on a Likert scale.

Results

Of the children with primary NE, 30.9 % rated it as not affecting them at all, 28.7 % as affecting them slightly, and 18.9 % as affecting them moderately. Of those with secondary NE, 36.2 % rated it as affecting them slightly, 28.9 % as not affecting them at all, and 18.3 % as affecting them moderately. Primary (32.1 %) and secondary NE (39.8 %) had the most effect on children's confidence. Primary and secondary NE affected 61.6 % and 60.2 % of parents or guardians, respectively, through the increased burden of housework from washing bedsheets.

Conclusion

NE demonstrated slight effects on children with NE and their parents or guardians. In the children, NE most affected their self-confidence, and in the parents and guardians, NE increased the burden of housework. In managing NE, physicians should evaluate its adverse effects on children and their parents or guardians.
背景:夜间遗尿症(NE)是一种给儿童及其家庭带来痛苦的慢性疾病。NE影响日常生活活动、人际关系、行为、情绪和社会互动。然而,关于NE对泰国儿童影响的数据是有限的。本研究旨在评估新脑障碍及其相关因素对新脑障碍患儿及其父母或监护人的影响。方法:一项横断面研究包括349名原发性NE和246名继发性NE,均来自泰国曼谷。他们的父母或监护人完成了一份有效的问卷,并在李克特量表上评估了NE影响的严重程度。结果:原发性NE患儿中,30.9%认为完全没有影响,28.7%认为轻微影响,18.9%认为中度影响。在继发性NE患者中,36.2%的人认为轻度影响,28.9%的人认为完全没有影响,18.3%的人认为中度影响。小学(32.1%)和中学(39.8%)对儿童自信心的影响最大。初级和次级NE通过增加洗床单的家务负担分别影响了61.6%和60.2%的父母或监护人。结论:NE对NE患儿及其父母或监护人的影响较小。在儿童中,NE对自信心的影响最大,在父母和监护人中,NE增加了家务劳动的负担。在处理NE时,医生应评估其对儿童及其父母或监护人的不良影响。
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引用次数: 0
Predictive risk factors for meconium-related ileus requiring surgical intervention in very low birth weight infants 极低出生体重儿需要手术干预的粪相关肠梗阻的预测危险因素。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.11.007
Yoshinobu Tsuno , Takeshi Kumagai , Mitsuhiko Riko , Taro Goda , Yasuyuki Mitani , Takuya Sugimoto , Mina Ueda , Manabu Kawai , Daisuke Tokuhara

Background

Meconium-related ileus (MRI) is a serious morbidity in very low birth weight infants (VLBWI). MRI can lead to intestinal perforation, which has a poor prognosis. Treatment may involve medical or surgical approaches. Our aim was to identify the risk factors predicting surgery in VLBWI with MRI, which are not well studied. We also compared clinical factors between VLBWI treated medically versus surgically.

Methods

We identified VLBWI with MRI who were admitted to our institution between January 2014 and December 2022. Infants were divided into those who underwent surgery and those who received conservative medical therapy. We compared various clinical factors between the groups. In each group, we calculated the ratio of maximum dilatational diameter of the intestinal tract to the maximum abdominal transverse diameter on abdominal X-rays at different time points; we called this ratio the “MRI index”. Using receiver operating characteristic curve analysis, we determined the MRI index cutoff value to predict surgery.

Results

We evaluated 34 VLBWI with MRI; 9 underwent surgery and 25 responded to conservative medical therapy. The MRI index on day 0 and the maximum MRI index in the surgical group were significantly higher than those in the medical group (p = 0.036 and p < 0.001, respectively). The MRI index cutoff value to predict surgery was 0.205 (area under the curve: 0.900, sensitivity: 0.92, specificity: 0.78). Compared with the medical group, the surgical group required significantly longer to achieve enteral feeding at 100 ml/kg/day, had a longer duration of hospital stay (p = 0.003 and p = 0.038, respectively) and a significantly higher incidence of sepsis (p = 0.042).

Conclusion

VLBWI with an MRI index ≥0.205 have a significantly high risk of requiring surgery.
背景:粪相关肠梗阻(MRI)是极低出生体重儿(VLBWI)的一种严重发病率。MRI可导致肠穿孔,预后较差。治疗可能包括药物或手术方法。我们的目的是通过MRI确定预测VLBWI手术的危险因素,这些因素尚未得到很好的研究。我们还比较了药物治疗和手术治疗VLBWI的临床因素。方法:对2014年1月至2022年12月在我院就诊的VLBWI患者进行MRI确诊。婴儿被分为接受手术的和接受保守药物治疗的两组。我们比较了两组间的各种临床因素。在每组中,我们计算不同时间点腹部x线上肠道最大扩张直径与腹部最大横径的比值;我们称这个比率为“MRI指数”。通过受试者工作特征曲线分析,我们确定了MRI指标临界值来预测手术。结果:我们对34例VLBWI进行MRI评估;9人接受手术治疗,25人接受保守药物治疗。手术组第0天MRI指数和最大MRI指数均显著高于内科组(p = 0.036和p)。结论:MRI指数≥0.205的VLBWI需要手术的风险显著增高。
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引用次数: 0
Giant Omental Lipoma in a Child 儿童巨大网膜脂肪瘤。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2025.08.003
Hyun Beak Shin , Yeon Jun Jeong
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引用次数: 0
lncRNA HCP5 regulates inflammation and oxidative stress of neonatal sepsis via modulating miR-93–5p lncRNA HCP5通过调节miR-93-5p调节新生儿脓毒症的炎症和氧化应激。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.10.013
Yueying Qi , Xin Li , Yuting Cai , Jiaxi Xie , Jinkai Yang

Background

Due to the high sensitivity to pathogenic microorganisms, newborns showed a high incidence and mortality of sepsis. The dysregulation of non-coding RNAs may play a key role in the immune regulation of neonatal sepsis. This study aimed to evaluate the potential function of lncRNA human histocompatibility leukocyte antigen complex P5 (HCP5) in the inflammation and oxidative stress of neonatal and to disclose its potential molecular mechanism.

Methods

The neonatal sepsis animal models were established with newborn rat pups by cecal ligation and perforation (CLP). The macrophage cells were induced by lipopolysaccharide (LPS) to mimic the sepsis injury. The expression of HCP5 was detected by polymerase chain reaction (PCR) and regulated by corresponding transfections. The inflammatory response was estimated by the levels of interleukin-6 (IL-6), interleukin-8 (IL-8), and tumor necrosis factor-α (TNF-α) using enzyme-linked immunosorbent assay (ELISA); and the oxidative stress was assessed by the levels of malondialdehyde (MDA) and superoxide dismutase (SOD). The proliferation of macrophage cells was evaluated by the CCK8 assay.

Results

HCP5 was significantly upregulated in neonatal sepsis rat models, of which the knockdown suppressed the inflammation and oxidative stress induced by CLP. In vitro, HCP5 was found to negatively regulate miR-93–5p in LPS-induced macrophage cells, which co-regulated the proliferation, inflammatory response, and oxidative stress in macrophage cells.

Conclusion

Upregulated HCP5 in neonatal sepsis rats regulated inflammation and oxidative stress, and it also modulated macrophage cell via regulating miR-93–5p.
背景:新生儿由于对病原微生物的高度敏感,脓毒症的发病率和死亡率较高。非编码rna的失调可能在新生儿败血症的免疫调节中起关键作用。本研究旨在评估lncRNA人组织相容性白细胞抗原复合物P5 (human histocompatibility leukocyte antigen complex P5, HCP5)在新生儿炎症和氧化应激中的潜在功能,并揭示其潜在的分子机制。方法:采用盲肠结扎穿孔法(CLP)建立新生儿脓毒症动物模型。采用脂多糖(LPS)诱导巨噬细胞模拟脓毒症损伤。采用聚合酶链反应(PCR)检测HCP5的表达,并通过相应的转染调节HCP5的表达。采用酶联免疫吸附试验(ELISA),通过白细胞介素-6 (IL-6)、白细胞介素-8 (IL-8)和肿瘤坏死因子-α (TNF-α)的水平来评估炎症反应;通过丙二醛(MDA)和超氧化物歧化酶(SOD)水平评估氧化应激。CCK8法检测巨噬细胞的增殖情况。结果:HCP5在新生儿脓毒症大鼠模型中显著上调,下调后可抑制CLP诱导的炎症和氧化应激。在体外实验中,我们发现HCP5在lps诱导的巨噬细胞中负调控miR-93-5p,共同调控巨噬细胞的增殖、炎症反应和氧化应激。结论:新生儿脓毒症大鼠HCP5上调可调节炎症和氧化应激,并通过调节miR-93-5p调节巨噬细胞。
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引用次数: 0
The outcome of kidney transplantation in lupus patients 狼疮患者肾移植的结果。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.09.008
Ting-Chih Lin , Meng-Kun Tsai , Jyh-Hong Lee , Yao-Hsu Yang , Yu-Tsan Lin , Hsin-Hui Yu , Bor-Luen Chiang , Li-Chieh Wang

Background

Kidney transplantation represents a therapeutic option for individuals with end-stage renal disease due to lupus. However, the influence of lupus activity and immunosuppressive medications on graft survival remains a matter of concern and it has not been thoroughly elucidated.

Methods

In this study, we conducted a retrospective review of 45 lupus patients who underwent kidney transplantation, with the aim of analyzing graft survival and identifying factors influencing the outcome of kidney transplantation in lupus patients.

Results

Graft survival rates at 1, 5, 10, 15, and 20 years were 98%, 98%, 88%, 85%, and 78%, respectively. Univariate logistic regression revealed hypertension, positive panel reactive antibodies against HLA class II antigens, retransplant, young age at lupus nephritis onset, low postoperative C4 levels, and HBsAg and/or anti-HBe antibody presence were significantly correlated with decreased graft survival (p < 0.05). Multiple regression confirmed the significant association of HBsAg and/or anti-HBe antibody with graft failure (p = 0.0161), with all patients testing negative for anti-HBc antibody. Preoperative markers (C3, C4, anti-dsDNA antibody) and recurrent lupus nephritis did not impact graft failure.

Conclusion

In lupus patients undergoing kidney transplantation, hepatitis B serology emerges as a potential singular predictor for graft failure, while preoperative lupus activity markers and recurrent lupus nephritis do not affect outcomes.
背景:对于狼疮引起的终末期肾病患者,肾移植是一种治疗选择。然而,狼疮活动和免疫抑制药物对移植物存活的影响仍然是一个值得关注的问题,并没有完全阐明。方法:本研究对45例接受肾移植的狼疮患者进行回顾性分析,目的是分析狼疮患者的移植物存活情况,并找出影响狼疮患者肾移植预后的因素。结果:移植1、5、10、15、20年生存率分别为98%、98%、88%、85%、78%。单因素logistic回归显示,高血压、HLAⅱ类抗体阳性、再移植、狼疮性肾炎发病年龄小、术后C4水平低、HBsAg和/或抗hbe抗体存在与移植物存活率降低显著相关(p)。在接受肾移植的狼疮患者中,乙型肝炎血清学成为移植失败的潜在单一预测因子,而术前狼疮活动标志物和复发性狼疮肾炎不影响结果。
{"title":"The outcome of kidney transplantation in lupus patients","authors":"Ting-Chih Lin ,&nbsp;Meng-Kun Tsai ,&nbsp;Jyh-Hong Lee ,&nbsp;Yao-Hsu Yang ,&nbsp;Yu-Tsan Lin ,&nbsp;Hsin-Hui Yu ,&nbsp;Bor-Luen Chiang ,&nbsp;Li-Chieh Wang","doi":"10.1016/j.pedneo.2024.09.008","DOIUrl":"10.1016/j.pedneo.2024.09.008","url":null,"abstract":"<div><h3>Background</h3><div>Kidney transplantation represents a therapeutic option for individuals with end-stage renal disease due to lupus. However, the influence of lupus activity and immunosuppressive medications on graft survival remains a matter of concern and it has not been thoroughly elucidated.</div></div><div><h3>Methods</h3><div>In this study, we conducted a retrospective review of 45 lupus patients who underwent kidney transplantation, with the aim of analyzing graft survival and identifying factors influencing the outcome of kidney transplantation in lupus patients.</div></div><div><h3>Results</h3><div>Graft survival rates at 1, 5, 10, 15, and 20 years were 98%, 98%, 88%, 85%, and 78%, respectively. Univariate logistic regression revealed hypertension, positive panel reactive antibodies against HLA class II antigens, retransplant, young age at lupus nephritis onset, low postoperative C4 levels, and HBsAg and/or anti-HBe antibody presence were significantly correlated with decreased graft survival (p &lt; 0.05). Multiple regression confirmed the significant association of HBsAg and/or anti-HBe antibody with graft failure (p = 0.0161), with all patients testing negative for anti-HBc antibody. Preoperative markers (C3, C4, anti-dsDNA antibody) and recurrent lupus nephritis did not impact graft failure.</div></div><div><h3>Conclusion</h3><div>In lupus patients undergoing kidney transplantation, hepatitis B serology emerges as a potential singular predictor for graft failure, while preoperative lupus activity markers and recurrent lupus nephritis do not affect outcomes.</div></div>","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":"66 6","pages":"Pages 534-541"},"PeriodicalIF":2.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143675011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Vitamin D status and the adequacy of its supplementation during the first year of life in preterm infants in northern Japan 日本北部早产儿第一年的维生素D状况及其补充是否充足。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2025.03.003
Fumikatsu Nohara , Toshio Okamoto , Kenta Takahashi , Tatsutoshi Sugiyama , Aiko Hashimoto , Mitsumaro Nii , Yukari Yamaki , Etsushi Tsuchida , Takashi Satou , Masaru Shirai , Ken Nagaya , Satoru Takahashi

Background

Vitamin D (VD) deficiency (VDD) is a major concern in preterm infants. The prevalence of VDD in mothers and infants varies between countries and is affected by a range of factors, such as geography and lifestyle. Thus, strategies aimed at preventing VDD must consider the status of each region. However, few reports have explored VDD in preterm infants in Japan and the safety and efficacy of VD supplementation in addressing VDD remain unclear.

Methods

This study was conducted between September 2019 and October 2022. The participants were 108 preterm infants who were divided into three groups based on their gestational age: <28 weeks (Group 1), 28–33 weeks (Group 2), and 34–36 weeks (Group 3). VD status at birth was assessed, and 25-hydroxyvitamin D (25OHD) levels and biochemical markers were monitored during supplementation with 400 IU/day of VD over the first year of life.

Results

Levels of 25OHD at birth were 10.0 (10.0–16.1), 10.5 (10.0–18.0), and 13.0 (10.0–19.0) nmol/L in Groups 1, 2, and 3, respectively. Infants in all three groups exhibited marked VDD. Their 25OHD levels gradually increased with VD supplementation before plateauing at 6 months. Nevertheless, VDD persisted in the majority of infants at 1 month of age. Serum intact parathyroid hormone levels peaked at 1 month of age and declined thereafter, negatively correlating with 25OHD levels. None of the infants exhibited symptoms of VD toxicity.

Conclusion

Preterm infants in northern Japan exhibited substantial VDD, regardless of gestational age. In our cohort, VD supplementation at 400 IU/day safely increased 25OHD levels. However, VD levels improved gradually over the months, and several of these infants developed secondary hyperparathyroidism. Further studies are warranted to determine the optimal VD supplementation dose for preterm infants in this region.
背景:维生素D (VD)缺乏症(VDD)是早产儿的一个主要问题。母亲和婴儿的VDD患病率因国家而异,并受到地理和生活方式等一系列因素的影响。因此,旨在预防VDD的战略必须考虑到每个区域的状况。然而,关于日本早产儿VDD的报道很少,补充VD治疗VDD的安全性和有效性仍不清楚。方法:本研究于2019年9月至2022年10月进行。参与者是108名早产儿,根据胎龄分为三组:结果:1、2和3组出生时25OHD水平分别为10.0(10.0-16.1)、10.5(10.0-18.0)和13.0 (10.0-19.0)nmol/L。三组婴儿均表现出明显的VDD。他们的25OHD水平随着VD的补充逐渐升高,在6个月时达到稳定。然而,大多数婴儿在1月龄时仍存在VDD。血清完整甲状旁腺激素水平在1月龄时达到峰值,随后下降,与25OHD水平呈负相关。没有婴儿表现出VD毒性症状。结论:无论胎龄大小,日本北部的早产儿都表现出大量的VDD。在我们的队列中,补充400 IU/天的VD可以安全地增加25OHD水平。然而,VD水平在几个月内逐渐改善,其中一些婴儿发展为继发性甲状旁腺功能亢进。需要进一步的研究来确定该地区早产儿的最佳VD补充剂量。
{"title":"Vitamin D status and the adequacy of its supplementation during the first year of life in preterm infants in northern Japan","authors":"Fumikatsu Nohara ,&nbsp;Toshio Okamoto ,&nbsp;Kenta Takahashi ,&nbsp;Tatsutoshi Sugiyama ,&nbsp;Aiko Hashimoto ,&nbsp;Mitsumaro Nii ,&nbsp;Yukari Yamaki ,&nbsp;Etsushi Tsuchida ,&nbsp;Takashi Satou ,&nbsp;Masaru Shirai ,&nbsp;Ken Nagaya ,&nbsp;Satoru Takahashi","doi":"10.1016/j.pedneo.2025.03.003","DOIUrl":"10.1016/j.pedneo.2025.03.003","url":null,"abstract":"<div><h3>Background</h3><div>Vitamin D (VD) deficiency (VDD) is a major concern in preterm infants. The prevalence of VDD in mothers and infants varies between countries and is affected by a range of factors, such as geography and lifestyle. Thus, strategies aimed at preventing VDD must consider the status of each region. However, few reports have explored VDD in preterm infants in Japan and the safety and efficacy of VD supplementation in addressing VDD remain unclear.</div></div><div><h3>Methods</h3><div>This study was conducted between September 2019 and October 2022. The participants were 108 preterm infants who were divided into three groups based on their gestational age: &lt;28 weeks (Group 1), 28–33 weeks (Group 2), and 34–36 weeks (Group 3). VD status at birth was assessed, and 25-hydroxyvitamin D (25OHD) levels and biochemical markers were monitored during supplementation with 400 IU/day of VD over the first year of life.</div></div><div><h3>Results</h3><div>Levels of 25OHD at birth were 10.0 (10.0–16.1), 10.5 (10.0–18.0), and 13.0 (10.0–19.0) nmol/L in Groups 1, 2, and 3, respectively. Infants in all three groups exhibited marked VDD. Their 25OHD levels gradually increased with VD supplementation before plateauing at 6 months. Nevertheless, VDD persisted in the majority of infants at 1 month of age. Serum intact parathyroid hormone levels peaked at 1 month of age and declined thereafter, negatively correlating with 25OHD levels. None of the infants exhibited symptoms of VD toxicity.</div></div><div><h3>Conclusion</h3><div>Preterm infants in northern Japan exhibited substantial VDD, regardless of gestational age. In our cohort, VD supplementation at 400 IU/day safely increased 25OHD levels. However, VD levels improved gradually over the months, and several of these infants developed secondary hyperparathyroidism. Further studies are warranted to determine the optimal VD supplementation dose for preterm infants in this region.</div></div>","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":"66 6","pages":"Pages 594-600"},"PeriodicalIF":2.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144112846","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Systemic air embolism 系统性空气栓塞。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2025.09.001
Shau-Ru Ho , Hsin-Chung Huang , Po-Nien Tsao
{"title":"Systemic air embolism","authors":"Shau-Ru Ho ,&nbsp;Hsin-Chung Huang ,&nbsp;Po-Nien Tsao","doi":"10.1016/j.pedneo.2025.09.001","DOIUrl":"10.1016/j.pedneo.2025.09.001","url":null,"abstract":"","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":"66 6","pages":"Pages 626-627"},"PeriodicalIF":2.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145309985","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gastric lavage for neonates with coffee-ground hematemesis in early postnatal period: Randomized controlled trial. 产后早期咖啡渣呕血新生儿洗胃:随机对照试验。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2025.05.014
M D Takashi Maeda, Yoshiaki Sato, Akihiro Hirakawa, Masahiro Nakatochi, Fumie Kinoshita, Takeshi Suzuki, Shintaro Ichimura, Hiroyuki Kidokoro, Jun-Ichi Kawada, Yoshiyuki Takahashi

Background: To evaluate the efficacy and safety of gastric lavage (GL) in neonates with coffee-ground hematemesis due to swallowing maternal blood by postnatal day 1.

Methods: This multicenter, randomized controlled trial included term neonates presenting coffee-ground hematemesis by postnatal day 1. Patients were randomly assigned to GL or non-GL groups. The primary outcome was the rate of feeding intolerance (FI) within 24 h. Secondary outcomes included onset of FI, residual gastric volume, vomiting episodes, weight changes, and bilirubin levels. Adverse events were monitored.

Results: Eighty neonates were analyzed (40 per group). FI occurred in 15.0 % of the GL group and 27.5 % of the non-GL group (p = 0.17). However, in the subgroup of neonates exclusively fed with formula, FI was significantly lower in the GL group than in the non-GL group (16.0 % vs. 47.4 %, p = 0.02). GL significantly reduced residual gastric volume but showed no significant differences in other secondary outcomes. No adverse events related to GL were observed. Post hoc analysis indicated that a larger sample size would be needed to detect statistical significance; and subgroup findings suggested potential benefit in selected populations.

Conclusions: GL did not significantly reduce the incidence of FI in neonates with coffee-ground hematemesis and thus it cannot be considered superior based on current results. However, it was well tolerated, and the study may have been underpowered. Exploratory analyses suggested potential benefits, particularly among formula-fed neonates, warranting further investigation.

背景:评价洗胃治疗产后第1天因吞母血而出现咖啡渣呕血的新生儿的疗效和安全性。方法:这项多中心随机对照试验纳入了出生后第1天出现咖啡渣呕血的足月新生儿。患者被随机分为GL组和非GL组。主要终点是24小时内进食不耐受(FI)的发生率。次要终点包括进食不耐受的发生、胃残量、呕吐次数、体重变化和胆红素水平。监测不良事件。结果:共分析80例新生儿,每组40例。GL组的FI发生率为15.0%,非GL组为27.5% (p = 0.17)。然而,在纯配方奶粉喂养的新生儿亚组中,GL组的FI显著低于非GL组(16.0%比47.4%,p = 0.02)。GL显著减少残胃量,但其他次要结局无显著差异。未观察到与GL相关的不良事件。事后分析表明,需要更大的样本量来检测统计显著性;亚组研究结果表明,在特定人群中可能有益处。结论:GL并没有显著降低咖啡渣呕血新生儿FI的发生率,因此根据目前的结果不能认为它是优越的。然而,它的耐受性很好,这项研究可能不够有力。探索性分析显示了潜在的益处,特别是对配方奶喂养的新生儿,值得进一步研究。
{"title":"Gastric lavage for neonates with coffee-ground hematemesis in early postnatal period: Randomized controlled trial.","authors":"M D Takashi Maeda, Yoshiaki Sato, Akihiro Hirakawa, Masahiro Nakatochi, Fumie Kinoshita, Takeshi Suzuki, Shintaro Ichimura, Hiroyuki Kidokoro, Jun-Ichi Kawada, Yoshiyuki Takahashi","doi":"10.1016/j.pedneo.2025.05.014","DOIUrl":"https://doi.org/10.1016/j.pedneo.2025.05.014","url":null,"abstract":"<p><strong>Background: </strong>To evaluate the efficacy and safety of gastric lavage (GL) in neonates with coffee-ground hematemesis due to swallowing maternal blood by postnatal day 1.</p><p><strong>Methods: </strong>This multicenter, randomized controlled trial included term neonates presenting coffee-ground hematemesis by postnatal day 1. Patients were randomly assigned to GL or non-GL groups. The primary outcome was the rate of feeding intolerance (FI) within 24 h. Secondary outcomes included onset of FI, residual gastric volume, vomiting episodes, weight changes, and bilirubin levels. Adverse events were monitored.</p><p><strong>Results: </strong>Eighty neonates were analyzed (40 per group). FI occurred in 15.0 % of the GL group and 27.5 % of the non-GL group (p = 0.17). However, in the subgroup of neonates exclusively fed with formula, FI was significantly lower in the GL group than in the non-GL group (16.0 % vs. 47.4 %, p = 0.02). GL significantly reduced residual gastric volume but showed no significant differences in other secondary outcomes. No adverse events related to GL were observed. Post hoc analysis indicated that a larger sample size would be needed to detect statistical significance; and subgroup findings suggested potential benefit in selected populations.</p><p><strong>Conclusions: </strong>GL did not significantly reduce the incidence of FI in neonates with coffee-ground hematemesis and thus it cannot be considered superior based on current results. However, it was well tolerated, and the study may have been underpowered. Exploratory analyses suggested potential benefits, particularly among formula-fed neonates, warranting further investigation.</p>","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":" ","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145483959","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hepatic tumors in Iranian children: Characteristics and survival predictors 伊朗儿童肝脏肿瘤:特征和生存预测因素。
IF 2.1 4区 医学 Q2 PEDIATRICS Pub Date : 2025-11-01 DOI: 10.1016/j.pedneo.2024.10.014
Fateme Ziyaee , Seyed Mohsen Dehghani , Mehdi Forooghi , Ali Bahador , Hamidreza Foroutan , Hamed Nikoupour , Bita Geramizadeh , Mahmood Haghighat , Mohammad Hadi Imanieh , Naser Honar , Iraj Shahramian , Maryam Ataollahi , Narges Ansary , Mehdi Ghasemian , Mahsa Rouhafshari , Zahra Radaei , Maryam Moradian Shahrebabaki , Mohammad Salehi Khatouni

Background

Hepatic tumors are rare in children. This study was conducted to determine the characteristics of liver masses in children and identify the independent predictors of their survival.

Methods

Medical records of children aged <18 years with a confirmed diagnosis of hepatic tumor diagnosed between January 2008 and December 2023 at two referral centers affiliated to Shiraz University of Medical Sciences, southern Iran, were reviewed.

Results

There were 153 children with hepatic tumors. The median age of the patients was 2 (IQR, 1–5) years. Abdominal pain and distension, and presence of a palpable mass and fever were the most common signs and symptoms at presentation. The most common tumor was hepatoblastoma (64.5 %) followed by hepatocellular carcinoma (HCC, 9.9 %). Right hepatectomy and hepatic segmentectomy were the most common surgical approach used. Children with hepatoblastoma were significantly (p < 0.001) younger than those with HCC. The risk of hepatoblastoma in males was twice that in females. Jaundice was not common in those with hepatoblastoma but it was in HCC. About a quarter of patients died. After adjusting for covariates, abdominal pain (adj OR = 4.90) and distension (adj OR = 3.17), and a diagnosis of HCC (adj OR = 13.63) were independent predictors of a poor prognosis.

Conclusions

The characteristics of pediatric hepatic tumors in our study were similar to those reported in most studies. Abdominal pain and distension and presence of HCC or jaundice were independent predictors of a poor prognosis.
背景:肝脏肿瘤在儿童中很少见。本研究旨在确定儿童肝脏肿块的特征,并确定其生存的独立预测因素。方法:查阅老年儿童病历。结果:153例肝肿瘤患儿。患者中位年龄为2岁(IQR, 1-5岁)。腹痛和腹胀,可触及肿块和发热是最常见的症状和体征。最常见的肿瘤是肝母细胞瘤(64.5%),其次是肝细胞癌(HCC, 9.9%)。右肝切除术和肝节段切除术是最常用的手术入路。结论:本研究中儿童肝脏肿瘤的特征与大多数研究报道的特征相似。腹痛和腹胀以及存在HCC或黄疸是预后不良的独立预测因素。
{"title":"Hepatic tumors in Iranian children: Characteristics and survival predictors","authors":"Fateme Ziyaee ,&nbsp;Seyed Mohsen Dehghani ,&nbsp;Mehdi Forooghi ,&nbsp;Ali Bahador ,&nbsp;Hamidreza Foroutan ,&nbsp;Hamed Nikoupour ,&nbsp;Bita Geramizadeh ,&nbsp;Mahmood Haghighat ,&nbsp;Mohammad Hadi Imanieh ,&nbsp;Naser Honar ,&nbsp;Iraj Shahramian ,&nbsp;Maryam Ataollahi ,&nbsp;Narges Ansary ,&nbsp;Mehdi Ghasemian ,&nbsp;Mahsa Rouhafshari ,&nbsp;Zahra Radaei ,&nbsp;Maryam Moradian Shahrebabaki ,&nbsp;Mohammad Salehi Khatouni","doi":"10.1016/j.pedneo.2024.10.014","DOIUrl":"10.1016/j.pedneo.2024.10.014","url":null,"abstract":"<div><h3>Background</h3><div>Hepatic tumors are rare in children. This study was conducted to determine the characteristics of liver masses in children and identify the independent predictors of their survival.</div></div><div><h3>Methods</h3><div>Medical records of children aged &lt;18 years with a confirmed diagnosis of hepatic tumor diagnosed between January 2008 and December 2023 at two referral centers affiliated to Shiraz University of Medical Sciences, southern Iran, were reviewed.</div></div><div><h3>Results</h3><div>There were 153 children with hepatic tumors. The median age of the patients was 2 (IQR, 1–5) years. Abdominal pain and distension, and presence of a palpable mass and fever were the most common signs and symptoms at presentation. The most common tumor was hepatoblastoma (64.5 %) followed by hepatocellular carcinoma (HCC, 9.9 %). Right hepatectomy and hepatic segmentectomy were the most common surgical approach used. Children with hepatoblastoma were significantly (p &lt; 0.001) younger than those with HCC. The risk of hepatoblastoma in males was twice that in females. Jaundice was not common in those with hepatoblastoma but it was in HCC. About a quarter of patients died. After adjusting for covariates, abdominal pain (adj OR = 4.90) and distension (adj OR = 3.17), and a diagnosis of HCC (adj OR = 13.63) were independent predictors of a poor prognosis.</div></div><div><h3>Conclusions</h3><div>The characteristics of pediatric hepatic tumors in our study were similar to those reported in most studies. Abdominal pain and distension and presence of HCC or jaundice were independent predictors of a poor prognosis.</div></div>","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":"66 6","pages":"Pages 573-578"},"PeriodicalIF":2.1,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144046347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Pediatrics and Neonatology
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