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Preventing Excess Fat Mass Gain in Severe Pediatric Obesity. 预防儿童严重肥胖中脂肪的增加。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-29 DOI: 10.1001/jamapediatrics.2025.5145
Martin Wabitsch,Stephanie Brandt-Heunemann,Kim Ulrich,Stefanie Zorn
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引用次数: 0
Hospital Formula Supplementation Postbreastfeeding Initiation, Neighborhood Economy, and Race. 母乳喂养开始后医院配方奶粉补充,社区经济和种族。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-29 DOI: 10.1001/jamapediatrics.2025.5379
Alison Mildon,Gillian D Alton,Jo-Anna B Baxter,Bronwyn Underhill,Daniel W Sellen,Deborah L O'Connor
ImportanceBreastfeeding supports lifelong health, but socioeconomic and racial disparities persist. Biases in hospital formula supplementation practices may be an underlying contributor.ObjectiveTo examine whether nonmedically indicated hospital formula supplementation of term-born breastfed newborns is associated with neighborhood socioeconomic status and/or maternal race.Design, Setting, and ParticipantsProvincial registry data were used to build a cohort of all live births of term-born singleton infants who initiated breastfeeding in Ontario, Canada, hospitals from April 1, 2015 through March 31, 2021, and for whom prenatal screening data were available. Of 570 936 eligible births, 148 888 were excluded, primarily due to missing outcome data, preterm birth, or not initiating breastfeeding. These data were analyzed from December 2023 through October 2025.ExposuresThe 2 exposures were socioeconomic status, derived by linking maternal postal codes with 2021 Ontario Marginalization Index neighborhood-level quintiles for material resources, and maternal race (Asian, Black, White, or other [Indigenous, multiracial, or unknown race]), determined from prenatal screening data.Main Outcome and MeasureThe primary outcome was nonmedically indicated formula supplementation, determined from hospital feeding records.ResultsThis cohort included 422 048 maternal-infant dyads, 28% of whom were in the Asian racial group, 7% in the Black racial group, 59% in the White racial group, and 5% in the other racial group. Overall, 27% of infants received nonmedically indicated formula supplementation, with an increase from 23% to 32% over the study period. Participants in the Asian, Black, and other racial groups were more likely than those in the White group to be in the most marginalized socioeconomic quintile (20%, 43%, and 23% vs 16%). Risk of nonmedically indicated formula supplementation increased in a gradient across quintiles of increasing socioeconomic marginalization (quintile 5 vs quintile 1: adjusted relative risk [aRR], 1.68; 95% CI, 1.64-1.72) and was significantly elevated for the Asian (aRR, 2.69; 95% CI, 2.64-2.74), Black (aRR, 2.07; 95% CI, 2.01-2.13), and other (aRR, 1.43; 95% CI, 1.39-1.48) racial groups compared with the White group.Conclusions and RelevanceIn this population-level analysis, nonmedically indicated formula supplementation prevalence was high and increased over time, with elevated risk associated with socioeconomic marginalization and maternal racialization. Increased hospital adherence to breastfeeding support guidelines is needed to improve health equity.
母乳喂养有助于终身健康,但社会经济和种族差异仍然存在。医院配方补充剂实践中的偏见可能是一个潜在的因素。目的探讨足月母乳喂养新生儿的非医学指证医院配方奶粉补充是否与社区社会经济地位和/或母亲种族有关。设计、环境和参与者使用省级登记数据建立了一个队列,该队列包括2015年4月1日至2021年3月31日在加拿大安大略省医院开始母乳喂养的所有足月单胎婴儿的活产,并提供了产前筛查数据。在570 936例符合条件的新生儿中,148 888例被排除在外,主要原因是缺少结局数据、早产或未开始母乳喂养。这些数据是从2023年12月到2025年10月进行分析的。这两项暴露是社会经济地位,通过将母亲的邮政编码与2021年安大略省边缘化指数(Ontario Marginalization Index)的物质资源邻里水平五分位数联系起来得出,以及母亲的种族(亚洲人、黑人、白人或其他[土著、多种族或未知种族]),这是根据产前筛查数据确定的。主要结局和测量主要结局是非医学指征的配方奶粉补充,由医院喂养记录确定。结果纳入422 048对母婴,其中亚洲种族占28%,黑人种族占7%,白人种族占59%,其他种族占5%。总体而言,27%的婴儿接受了非医学指示的配方补充剂,在研究期间从23%增加到32%。亚洲人、黑人和其他种族的参与者比白人更有可能处于最边缘化的社会经济五分之一(20%、43%和23%对16%)。非医学适应症配方补充剂的风险在社会经济边缘化增加的五分位数中呈梯度增加(五分位数5 vs五分位数1:调整相对风险[aRR], 1.68; 95% CI, 1.64-1.72),与白人组相比,亚洲人(aRR, 2.69; 95% CI, 2.64-2.74)、黑人(aRR, 2.07; 95% CI, 2.01-2.13)和其他种族(aRR, 1.43; 95% CI, 1.39-1.48)的风险显著升高。结论和相关性在这一人群水平的分析中,非医学指示的配方奶粉补充的患病率很高,并且随着时间的推移而增加,与社会经济边缘化和母亲种族化相关的风险增加。需要加强医院对母乳喂养支持指南的遵守,以改善卫生公平。
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引用次数: 0
Nirsevimab Against Hospitalizations and Emergency Department Visits for Lower Respiratory Tract Infection in Infants: A Meta-Analysis. 尼瑟维单抗对婴儿下呼吸道感染住院和急诊的影响:一项荟萃分析
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5280
Dewan Md Sumsuzzman,Congjie Shi,Joanne M Langley,Seyed M Moghadas
ImportanceNirsevimab, a long-acting monoclonal antibody available since 2023, has demonstrated effectiveness in preventing lower respiratory tract infection (LRTI) caused by respiratory syncytial virus (RSV) in clinical trials and postlicensure settings. However, its broader real-world associations with respiratory-related outcomes in infants remain unclear, and characterizing these associations is essential to inform pediatric immunization policy.ObjectiveTo evaluate the real-world association of nirsevimab with LRTI-related hospitalizations and emergency department (ED) visits in infants.Data SourcesMEDLINE, Embase, Web of Science, Scopus, Global Health, and medRxiv databases were systematically searched for observational studies published between January 1, 2023, and June 20, 2025. Data analysis was performed between January 1, 2025, and June 20, 2025.Study SelectionPostlicensure observational studies reporting original data on the effectiveness of nirsevimab immunization programs in infants and children aged 24 months or younger in routine clinical settings were eligible for inclusion.Data Extraction and SynthesisTwo reviewers independently extracted data and assessed study quality using the Critical Appraisal Checklist of the Joanna Briggs Institute. Random-effects meta-analysis was conducted to estimate pooled odds ratios (ORs) and 95% confidence intervals.Main Outcomes and MeasuresPrimary outcomes were all-cause LRTI-related hospitalization, all-cause hospitalization, all-cause LRTI-related ED visit, and RSV-LRTI-related ED visit.ResultsOf 1752 records screened, 15 studies met inclusion criteria; 11 studies were from 5 countries included in the meta-analysis, comprising 236 764 infants and children in the nirsevimab group and 27 522 in the control group. Compared with controls, nirsevimab was associated with lower odds of all-cause LRTI-related hospitalization (OR, 0.38; 95% CI, 0.28-0.53), all-cause LRTI-related ED visits (OR, 0.52; 95% CI, 0.37-0.73), and RSV-LRTI-related ED visits (OR, 0.24; 95% CI, 0.13-0.47). No significant difference was observed in all-cause hospitalizations (OR, 0.56; 95% CI, 0.14-2.20) between the nirsevimab and control groups.Conclusions and RelevanceIn this meta-analysis, nirsevimab was associated with reduced LRTI-related hospitalizations and ED visits in infants and young children. These findings support nirsevimab's potential to reduce respiratory-related morbidity in young children and health care utilization.
enirsevimab是一种长效单克隆抗体,于2023年上市,在临床试验和许可后环境中证明了预防呼吸道合胞病毒(RSV)引起的下呼吸道感染(LRTI)的有效性。然而,其与婴儿呼吸相关结局的更广泛的现实关联尚不清楚,表征这些关联对于告知儿科免疫政策至关重要。目的评估尼西维单抗与婴儿下呼吸道感染相关住院和急诊(ED)就诊的现实关系。数据来源medline、Embase、Web of Science、Scopus、Global Health和medRxiv数据库系统检索了2023年1月1日至2025年6月20日之间发表的观察性研究。数据分析时间为2025年1月1日至2025年6月20日。研究选择许可后的观察性研究报告了在常规临床环境中对24个月或更小的婴儿和儿童实施nirseimab免疫规划的有效性的原始数据,符合纳入条件。数据提取和综合两名审稿人独立提取数据并使用乔安娜布里格斯研究所的关键评估清单评估研究质量。随机效应荟萃分析用于估计合并优势比(or)和95%置信区间。主要结局和测量方法主要结局为全因lrti相关住院、全因住院、全因lrti相关ED就诊和rsv - lrti相关ED就诊。结果在筛选的1752份文献中,有15项研究符合纳入标准;荟萃分析纳入了来自5个国家的11项研究,包括236 764名婴儿和儿童在nirsevimab组和27 522名对照组。与对照组相比,尼西莫单抗与全因lrti相关住院(OR, 0.38; 95% CI, 0.28-0.53)、全因lrti相关ED就诊(OR, 0.52; 95% CI, 0.37-0.73)和rsv - lrti相关ED就诊(OR, 0.24; 95% CI, 0.13-0.47)相关。尼塞维单抗组和对照组的全因住院率无显著差异(OR, 0.56; 95% CI, 0.14-2.20)。结论和相关性:在这项荟萃分析中,尼塞维单抗与婴幼儿lrti相关住院和ED就诊减少相关。这些发现支持nirseimab在降低幼儿呼吸相关发病率和医疗保健利用率方面的潜力。
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引用次数: 0
Vaccine Policy and Eliminating Nonmedical Exemptions-Read the Room. 疫苗政策和消除非医疗豁免-阅读房间。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5290
Mark Christopher Navin,Douglas S Diekema
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引用次数: 0
Effectiveness and Impact of Maternal RSV Immunization and Nirsevimab on Medically Attended RSV in US Children. 母亲RSV免疫接种和尼瑟维单抗治疗美国儿童RSV的有效性和影响
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5778
Heidi L Moline,Ayzsa Tannis,Leah Goldstein,Janet A Englund,Mary A Staat,Julie A Boom,Rangaraj Selvarangan,Marian G Michaels,Geoffrey A Weinberg,Natasha B Halasa,Ariana P Toepfer,Rachel E Rutkowski,Abigail Salthouse,Leila C Sahni,Jennifer E Schuster,Laura S Stewart,John V Williams,Daniel C Payne,Eileen J Klein,Peter G Szilagyi,Fatimah S Dawood,
ImportanceDuring the 2024-2025 respiratory syncytial virus (RSV) season in the US, nirsevimab and maternal RSV vaccination became widely available to prevent severe RSV disease in infants. Assessments of the real-world effectiveness and impact of both products are needed to inform RSV prevention policy.ObjectivesTo estimate nirsevimab and maternal RSV vaccine effectiveness against medically attended RSV-associated acute respiratory illness (ARI) and to estimate the impact of these products on RSV-associated hospitalizations during 2024-2025.Design, Setting, and ParticipantsPopulation-based surveillance for medically attended ARI was conducted among children younger than 2 years with systematic molecular testing for RSV. Children were enrolled at 7 US pediatric medical centers from October 1, 2024, through April 30, 2025. A test-negative case-control design was used to estimate maternal RSV vaccine and nirsevimab effectiveness.ExposuresTo estimate maternal RSV vaccine effectiveness, the exposure was maternal RSV vaccination among newborns and infants younger than 6 months at medical encounters; to estimate nirsevimab effectiveness, the exposure was nirsevimab receipt among newborns and infants younger than 8 months as of October 1, 2024, or born after that date.Main Outcomes and MeasuresThe primary outcome was medically attended RSV-associated ARI and RSV-associated hospitalization. Immunization effectiveness was calculated as (1 - adjusted odds ratio) × 100%. To estimate population-level impact of RSV prevention products, relative rate reductions were estimated by comparing observed RSV-associated hospitalization rates during 2024-2025 to (1) observed rates in 2017-2020 or (2) counterfactual 2024-2025 rates estimated by a difference-in-differences approach; estimates from both approaches are presented as ranges.ResultsOverall, 5029 children younger than 2 years with medically attended ARI were enrolled during October 2024 to April 2025. Median (IQR) age was 10 months (5-16 months), and 2176 children (43.3%) were female. Among newborns and infants younger than 6 months, maternal RSV vaccine effectiveness was 64% (95% CI, 37%-79%) against any medically attended RSV-associated ARI and 70% (95% CI, 37%-86%) against RSV-associated hospitalization. Nirsevimab effectiveness was 81% (95% CI, 71%-87%) against RSV-associated hospitalization, and nirsevimab remained 77% (95% CI, 42%-92%) effective against RSV-associated hospitalization at 130 to 210 days after receipt. RSV-associated hospitalizations were reduced by 41% to 51% among newborns and infants aged 0 to 11 months, with the highest reduction of 56% to 63% in those aged 0 to 2 months.Conclusions and RelevanceAccording to the results of this population-based surveillance study, during 2024-2025, both maternal RSV vaccine and nirsevimab were estimated to be effective at protecting infants from RSV-associated hospitalizations in their first RSV season, and RSV-associated hospitalization rates in newbor
在2024-2025年美国呼吸道合胞病毒(RSV)流行季节,尼塞维单抗和母亲RSV疫苗接种广泛用于预防婴儿严重RSV疾病。需要对这两种产品的实际有效性和影响进行评估,以便为RSV预防政策提供信息。目的评估尼塞维单抗和母亲RSV疫苗对医疗护理的RSV相关急性呼吸道疾病(ARI)的有效性,并评估2024-2025年这些产品对RSV相关住院的影响。设计、环境和参与者对2岁以下的儿童进行了基于人群的ARI监测,并对RSV进行了系统的分子检测。从2024年10月1日到2025年4月30日,儿童在7个美国儿科医疗中心登记。采用检测阴性病例对照设计来评估母体RSV疫苗和nirseimab的有效性。暴露量为估计母亲RSV疫苗的有效性,暴露量为新生儿和小于6个月的婴儿在医疗接触中接种母亲RSV疫苗;为了估计尼瑟维单抗的有效性,在2024年10月1日或该日期之后出生的新生儿和小于8个月的婴儿中接受尼瑟维单抗暴露。主要结局和措施主要结局是接受医学治疗的与rsv相关的ARI和与rsv相关的住院。免疫效果计算为(1校正优势比)× 100%。为了估计RSV预防产品对人群水平的影响,通过将2024-2025年观察到的RSV相关住院率与(1)2017-2020年观察到的住院率或(2)通过差异中差法估计的2024-2025年反事实住院率进行比较,估计相对降低率;两种方法的估计值以范围表示。结果在2024年10月至2025年4月期间,共有5029名2岁以下的ARI儿童入组。中位(IQR)年龄为10个月(5-16个月),2176名儿童(43.3%)为女性。在新生儿和6个月以下的婴儿中,母亲RSV疫苗预防任何与RSV相关的医学治疗的有效性为64% (95% CI, 37%-79%),预防与RSV相关的住院治疗的有效性为70% (95% CI, 37%-86%)。对于与rsv相关的住院治疗,Nirsevimab的有效性为81% (95% CI, 71%-87%),并且在服用后130至210天,Nirsevimab对与rsv相关的住院治疗的有效性仍为77% (95% CI, 42%-92%)。在新生儿和0至11个月的婴儿中,与rsv相关的住院率降低了41%至51%,在0至2个月的婴儿中,降幅最大,为56%至63%。结论和相关性根据这项基于人群的监测研究的结果,在2024-2025年期间,估计母亲RSV疫苗和nirseimab都能有效地保护婴儿在第一个RSV季节免于RSV相关住院,与引入这些产品之前的季节相比,新生儿和0至11个月婴儿的RSV相关住院率降低了一半。
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引用次数: 0
Clarifying the Burden of Obesity in Youth: Measurement Choices-Reply. 澄清青少年肥胖负担:测量选择-回复。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5331
Ashwin K Chetty,Alissa S Chen,James T Nugent
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引用次数: 0
Change in US Pesticide Policy Still Needed to Protect Children. 美国农药政策仍需改变以保护儿童。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5109
Valerie J Watnick
{"title":"Change in US Pesticide Policy Still Needed to Protect Children.","authors":"Valerie J Watnick","doi":"10.1001/jamapediatrics.2025.5109","DOIUrl":"https://doi.org/10.1001/jamapediatrics.2025.5109","url":null,"abstract":"","PeriodicalId":14683,"journal":{"name":"JAMA Pediatrics","volume":"49 1","pages":""},"PeriodicalIF":26.1,"publicationDate":"2025-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145801000","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"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
What Parents Need to Know About Sleep in Children. 关于孩子的睡眠,父母需要知道什么。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5376
Cynthia-Mae M Hunt,Lindsay A Thompson
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引用次数: 0
Suicidality and Nonsuicidal Self-Injury in Transgender and Gender Diverse Youth: A Systematic Review and Meta-Analysis. 跨性别与性别多元青少年的自杀倾向与非自杀自伤:系统回顾与元分析。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5274
Brae Anne McArthur,Kristine Lyn Pesigan,Lindsay Berg,Glorianna Sin,Samarpreet Singh,Caitlin McClurg
ImportanceTransgender and gender diverse (TGD) youth face adversities that increase risks for suicidality and nonsuicidal self-injury (NSSI). However, substantial variability in prevalence rates have been reported across the literature.ObjectiveTo provide meta-analytic syntheses of research investigating the prevalence of suicidal ideation, suicide attempts, and NSSI in TGD youth and to examine the moderating effects of sample characteristics and study methods on estimates.Design, Setting, and ParticipantsMEDLINE, Embase, CINAHL, Web of Science, Social Work Abstracts, Scopus, PsycINFO, Cochrane Central Register of Controlled Trials, and ProQuest Dissertations & Theses Global databases were searched in January 2025. This meta-analysis included studies of TGD youth aged 25 years and younger measuring suicidal ideation, suicide attempts, and/or NSSI published in English. These data were analyzed from June 2025 to September 2025.Data Extraction and SynthesisData extraction followed the PRISMA guidelines. Random-effects meta-analyses were used to derive the pooled prevalence estimates.Main Outcomes and MeasuresOutcomes included prevalence rates of suicidal ideation, suicide attempts, and NSSI. Sample characteristics (ie, race and ethnicity and gender identity group) and study methods (ie, assessment modality, timeframe, geographical region, and study quality) acted as moderator variables.ResultsFrom 137 studies, 262 nonoverlapping samples with a total of 131 429 TGD youth (mean age, 17.0 [range, 7.5-23.4] years) were included. Pooled prevalence estimates of suicidal ideation, suicide attempts, and NSSI were 48.8% (95% CI, 45.6%-52.0%), 26.2% (95% CI, 23.9%-28.6%), and 46.6% (95% CI, 40.5%-52.7%), respectively. Survey studies yielded higher prevalence rates across all outcomes compared with interview and medical record reviews. Significant moderating effects for ethnicity, gender identity group, timeframe, geographical region, and study quality varied across outcomes.Conclusions and RelevanceIn this meta-analyis, pooled estimates suggested that 1 in 2 TGD youth globally are experiencing suicidal ideation and/or NSSI, and 1 in 4 have experienced a suicide attempt. These pooled estimates are 2 to 3.5 times greater in TGD youth compared with those established for cisgender peers. There is a critical need for improved prevention and intervention efforts to address TGD mental health concerns.
跨性别和性别多元化(TGD)青年面临的逆境增加了自杀和非自杀性自伤(NSSI)的风险。然而,文献中报道的患病率存在很大差异。目的对TGD青少年自杀意念、自杀企图和自伤的患病率进行meta分析,并检验样本特征和研究方法对估计的调节作用。设计、设置和参与者medline、Embase、CINAHL、Web of Science、Social Work Abstracts、Scopus、PsycINFO、Cochrane Central Register of Controlled Trials和ProQuest disserthesis & Theses全球数据库于2025年1月检索。本荟萃分析包括25岁及以下TGD青年的研究,测量自杀意念、自杀企图和/或自伤。这些数据的分析时间为2025年6月至2025年9月。数据提取和合成数据提取遵循PRISMA指南。随机效应荟萃分析用于得出汇总的患病率估计。主要结局和测量结果包括自杀意念、自杀企图和自伤的患病率。样本特征(即种族、民族和性别认同群体)和研究方法(即评估方式、时间框架、地理区域和研究质量)作为调节变量。结果137项研究共纳入262个非重叠样本,共131 429名TGD青年(平均年龄17.0[范围,7.5-23.4]岁)。自杀意念、自杀企图和自伤的合并患病率估计分别为48.8% (95% CI, 45.6%-52.0%)、26.2% (95% CI, 23.9%-28.6%)和46.6% (95% CI, 40.5%-52.7%)。与访谈和病历回顾相比,调查研究得出的所有结果的患病率都更高。种族、性别认同群体、时间框架、地理区域和研究质量的显著调节作用因结果而异。结论和相关性在这项荟萃分析中,综合估计表明,全球每2名TGD青年中就有1名有自杀意念和/或自伤,每4名中就有1名有自杀企图。这些综合估计在TGD青年中比在顺性别同龄人中高2至3.5倍。迫切需要改进预防和干预工作,以解决TGD心理健康问题。
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引用次数: 0
Clarifying the Burden of Obesity in Youth: Measurement Choices. 澄清青少年肥胖负担:测量选择。
IF 26.1 1区 医学 Q1 PEDIATRICS Pub Date : 2025-12-22 DOI: 10.1001/jamapediatrics.2025.5328
Josna Jojo
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引用次数: 0
期刊
JAMA Pediatrics
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