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Effectiveness of 2024-2025 COVID-19 Vaccines in Children in the United States - VISION, August 29, 2024-September 2, 2025. 2024-2025年新冠肺炎疫苗在美国儿童中的有效性——《视觉》杂志,2024年8月29日-2025年9月2日。
Pub Date : 2025-12-11 DOI: 10.15585/mmwr.mm7440a1
Stephanie A Irving,Elizabeth A K Rowley,Sean Chickery,Karthik Natarajan,Nicola P Klein,Shaun J Grannis,Toan C Ong,Sarah W Ball,Malini B DeSilva,Kristin Dascomb,Allison L Naleway,Melissa S Stockwell,Ashley B Stephens,Ousseny Zerbo,John Hansen,Lawrence Block,Karen B Jacobson,Brian E Dixon,Colin Rogerson,Tom Duszynski,Michelle A Barron,David Mayer,Catia Chavez,Zachary A Weber,Sarah E Reese,Inih Essien,Tamara Sheffield,Daniel Bride,Julie Arndorfer,Josh Van Otterloo,Padma Koppolu,Josephine Mak,Amber Kautz,Jennifer DeCuir,Ryan E Wiegand,Amanda B Payne,Ruth Link-Gelles
During September 2023-August 2024, approximately 38,000 COVID-19-associated hospitalizations occurred among children and adolescents aged <18 years in the United States, a rate of approximately 53 per 100,000 children, ranging from 600 per 100,000 children aged <6 months to 21 per 100,000 children and adolescents aged 5-17 years. On June 27, 2024, the Advisory Committee on Immunization Practices recommended that all persons aged ≥6 months receive a 2024-2025 COVID-19 vaccine, which targeted Omicron JN.1 and JN.1-derived sublineages. Investigators used a test-negative case-control design to estimate vaccine effectiveness (VE) of 2024-2025 COVID-19 vaccines against COVID-19-associated emergency department or urgent care (ED/UC) visits during August 29, 2024-September 2, 2025, among immunocompetent children aged 9 months-4 years and children and adolescents aged 5-17 years in the CDC-funded Virtual SARS-CoV-2, Influenza, and Other respiratory viruses Network (VISION), a multisite electronic health record-based network in nine states. Among children aged 9 months-4 years, VE against COVID-19-associated ED/UC visits was estimated at 76% (95% CI = 58%-87%) during the first 7-179 days after vaccination. Among children and adolescents aged 5-17 years, VE against COVID-19-associated ED/UC visits was an estimated 56% (95% CI = 35%-70%) during the first 7-179 days after vaccination. These findings suggest that vaccination with a 2024-2025 COVID-19 vaccine dose provided children with additional protection against COVID-19-associated ED/UC encounters compared with no 2024-2025 dose.
在2023年9月至2024年8月期间,美国18岁以下儿童和青少年中约有38,000例与covid -19相关的住院治疗,比率约为每10万名儿童53例,从每10万名6个月以下儿童600例到每10万名5-17岁儿童和青少年21例不等。2024年6月27日,免疫实践咨询委员会建议所有年龄≥6个月的人接种2024-2025年COVID-19疫苗,该疫苗针对欧米克隆JN.1和JN.1衍生亚谱系。在cdc资助的SARS-CoV-2、流感和其他呼吸道病毒虚拟网络(VISION)中,研究人员采用检测阴性病例对照设计,评估2024-2025年COVID-19疫苗在2024年8月29日至2025年9月2日期间对COVID-19相关急诊科或急诊(ED/UC)访问的疫苗有效性(VE),研究对象为9个月至4岁的免疫功能正常儿童和5-17岁的儿童和青少年。一个覆盖九个州的多站点电子健康记录网络。在9个月至4岁的儿童中,在接种疫苗后的头7-179天内,与covid -19相关的ED/UC就诊的VE估计为76% (95% CI = 58%-87%)。在5-17岁的儿童和青少年中,在接种疫苗后的头7-179天内,与covid -19相关的ED/UC就诊的VE估计为56% (95% CI = 35%-70%)。这些研究结果表明,与未接种2024-2025剂量相比,接种2024-2025剂量的COVID-19疫苗可为儿童提供额外的保护,以防止与COVID-19相关的ED/UC遭遇。
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引用次数: 0
Detection of Paraburkholderia in Clinical Specimens Associated with Use of Nonsterile Ultrasound Gel for Percutaneous Procedures - United States, Canada, and Israel, May 2023⎯April 2025. 与使用非无菌超声凝胶进行经皮手术相关的临床标本中副aburkholderia的检测-美国,加拿大和以色列,2023年5月- 2025年4月。
Pub Date : 2025-12-11 DOI: 10.15585/mmwr.mm7440a2
Sarah Lim,Paula Snippes Vagnone,Natalie C Marshall,Christine Lees,Jennifer L Dale,Becky Smith,Elizabeth Palavecino,Ruth Lynfield,Annastasia Gross,Krista Knowles,Ayelet Michael-Gayego,Violeta Temper,Jacob Strahilevitz,Yonatan Oster,Daniel Grupel,Dan Reshef,Yair Motro,Petrus J van der Walt,Matthew A Croxen,Stephanie W Smith,Bonita Lee,Graham A Tipples,Bobby Warren,Jacob Moran-Gilad
Contaminated nonsterile ultrasound gels have been implicated in outbreaks of Burkholderia infections associated with improper infection control practices before or during percutaneous procedures. In August 2024, the Minnesota Department of Health Public Health Laboratory noticed an increase in Paraburkholderia fungorum or Paraburkholderia species identified from referred clinical isolates. All isolates were recovered from blood cultures, and whole genome sequencing (WGS) confirmed that the isolates were genetically related. Because P. fungorum is not an established human pathogen and has rarely been reported in clinical specimens, an investigation was initiated, which was later joined by collaborators in Canada and Israel after similar observations in those countries. Forty-two patients from the United States, Canada, and Israel with genetically linked P. fungorum isolated from clinical specimens collected during May 2023-April 2025 were identified. Positive cultures were associated with the use of nonsterile ultrasound gel. Based on medical record review, treating clinicians deemed the isolate a culture contaminant in most cases; one patient had a confirmed invasive P. fungorum infection. WGS confirmed the relatedness of isolates from all three countries, including isolates cultured from clinical specimens as well as from nonsterile ultrasound gel products. Review of local practices revealed use of nonsterile ultrasound gel during point-of-care percutaneous procedures, including drawing blood, placing intravenous catheters, and paracentesis. This investigation underscores the continued importance of sterile gel use during percutaneous procedures and highlights the value of collaboration and shared WGS data for the investigation of international outbreaks.
受污染的非无菌超声凝胶与伯克氏菌感染暴发有关,这些感染暴发与经皮手术前或手术期间感染控制不当有关。2024年8月,明尼苏达州卫生部公共卫生实验室注意到,从转诊的临床分离株中发现的蕈样拟aburkholderia或拟aburkholderia种类增加。所有分离株均从血培养中恢复,全基因组测序(WGS)证实分离株具有遗传相关性。由于真菌假单胞菌不是一种确定的人类病原体,很少在临床标本中报告,因此开始了一项调查,后来加拿大和以色列的合作者在这些国家进行了类似的观察后加入了这项调查。从2023年5月至2025年4月期间收集的临床标本中鉴定出42例从美国、加拿大和以色列分离到遗传相关的真菌假单胞菌的患者。阳性培养与使用非无菌超声凝胶有关。根据医疗记录审查,在大多数情况下,治疗临床医生认为分离物是培养污染物;1例患者确诊为侵袭性真菌假体感染。WGS证实了来自所有三个国家的分离株的相关性,包括从临床标本中培养的分离株以及从非无菌超声凝胶产品中培养的分离株。对当地实践的回顾显示,在护理点经皮手术中使用非无菌超声凝胶,包括抽血、放置静脉导管和穿刺。这项调查强调了在经皮手术中使用无菌凝胶的持续重要性,并强调了合作和共享WGS数据对调查国际疫情的价值。
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引用次数: 0
Rabies Cluster Among Steers on a Dairy Farm - Minnesota, 2024. 2024年,明尼苏达州一家奶牛场的牛群中出现狂犬病。
Pub Date : 2025-12-11 DOI: 10.15585/mmwr.mm7440a3
Carrie Klumb,Malia Ireland,Bonnie Miller,Erik Jopp,Betsy Lempelius,Albert Rovira,Hemant Naikare,Carly Bauer,Katie Harry,Scott A Cunningham,Gongping Liu,Thomas F Czeck,Ryan Wallace,Brian Hoefs,Stacy Holzbauer
Rabies clusters in domestic livestock are rare but can result in human exposure and economic loss for farmers. During a 4-week period in May 2024, five of 35 steers on a Minnesota dairy farm developed neurologic signs consistent with rabies. Three clinically ill steers were euthanized, and brain specimens were submitted for rabies testing. Direct fluorescent antibody testing and whole genome sequencing confirmed rabies virus (North Central Skunk variant) in all three steers. After identification of the first two rabid steers, the remaining animals were quarantined for 120 days and vaccinated against rabies; three additional steers became ill during quarantine and were euthanized. The Minnesota Department of Health and Minnesota Board of Animal Health investigated human and animal exposures through interviews and site visits. Five persons were recommended to receive rabies postexposure prophylaxis because of known or potential exposures. The outbreak likely resulted from a single rabid skunk biting multiple cattle housed in a small pen, although steer-to-steer transmission cannot be ruled out. In addition to the loss of livestock, direct medical and veterinary costs associated with this outbreak totaled approximately $35,000. Preventive vaccination of cattle should be considered in areas with high activity of terrestrial rabies (i.e., rabies in land-based animals), presence of high-value livestock, and potential for human exposure.
家畜感染狂犬病群集的情况很少见,但可导致人类接触并给农民造成经济损失。在2024年5月的4周时间里,明尼苏达州一家奶牛场的35头牛中有5头出现了与狂犬病相符的神经症状。对临床上患病的3头牛实施安乐死,并采集脑标本进行狂犬病检测。直接荧光抗体检测和全基因组测序证实了所有3头牛的狂犬病毒(中北部臭鼬变种)。在鉴定出头两只患狂犬病的牛后,对其余的牛进行了120天的隔离,并接种了狂犬病疫苗;另外三头牛在隔离期间生病并被安乐死。明尼苏达州卫生部和明尼苏达州动物卫生委员会通过面谈和实地考察调查了人类和动物的接触情况。由于已知或潜在暴露,建议5人接受狂犬病暴露后预防。这次暴发可能是由于一只患狂犬病的臭鼬咬了饲养在一个小围栏里的多头牛,尽管不能排除牛与牛之间传播的可能性。除了牲畜损失外,与这次疫情有关的直接医疗和兽医费用总计约为35 000美元。在陆生狂犬病高发地区(即陆生动物狂犬病)、存在高价值牲畜以及人类可能接触狂犬病的地区,应考虑对牛进行预防性接种。
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引用次数: 0
Human-to-Human Rabies Transmission via Solid Organ Transplantation from a Donor with Undiagnosed Rabies - United States, October 2024-February 2025. 美国,2024年10月- 2025年2月,未确诊狂犬病的捐赠者通过实体器官移植传播狂犬病。
Pub Date : 2025-12-04 DOI: 10.15585/mmwr.mm7439a1
Rebecca Earnest,Kris K Carter,Sara F Margrey,Vaughn V Wicker,Rebecca Betz,Rebecca Reik,Eli Shiltz,Basmah Khalil,Brandon Palinski,Barbara Jordan,Daniel Dodson,Erin Epson,Curtis L Fritz,Juliet Stoltey,Alison Sikola,Ricardo Garcia,Monika Roy,Pallavi Annambhotla,Sridhar V Basavaraju,Sarah C Bonaparte,Shama Cash-Goldwasser,Ian Kracalik,David W McCormick,Faisal S Minhaj,Lillian A Orciari,Panayampalli S Satheshkumar,Pamela Yager,David A Crum,Nathan Koffarnus,Monica Beddo,Molly Baker,Erin C Phipps,Hanna Oltean,Hannah Schnitzler,Crystal M Gigante,Ryan M Wallace,Mary Grace Stobierski,Christine Hahn
Although rabies virus is typically transmitted through mammalian animal bites or scratches, human-to-human transmission has occurred through organ and tissue transplantation. From 1978 to 2013, three transplant-transmitted rabies events in the United States affected nine tissue or organ recipients. Rabies is almost always fatal without timely receipt of postexposure prophylaxis (PEP). In January 2025, clinicians in Ohio notified the Ohio Department of Health and CDC of a suspected case of rabies in a kidney transplant recipient who died 51 days after receiving the transplant. CDC confirmed the recipient's rabies diagnosis. Investigation revealed that the deceased donor had been scratched by a skunk approximately 6 weeks before death. No other organs from that donor were transplanted; however, three persons received cornea tissue grafts. While investigation of the donor's rabies status was ongoing, the cornea recipients underwent precautionary graft removal and received PEP. None developed signs or symptoms compatible with rabies. CDC detected rabies virus RNA in an archived sample of the donor's kidney, confirming organ-derived transmission. Investigation identified 370 persons with possible exposures to the donor or kidney recipient; 357 (96%) completed risk assessments. Among those who completed risk assessments, 46 (13%) were recommended to receive PEP. Early consultation with public health officials might prevent rabies-infected organ and tissue donation or lead to prompt PEP for transplant recipients. The risk for rabies should be considered among donors who have received rabies-susceptible animal bites or scratches within the previous year, particularly those donors with acute encephalopathy.
虽然狂犬病毒通常通过哺乳动物咬伤或抓伤传播,但也有通过器官和组织移植进行人际传播的情况。从1978年到2013年,美国发生了三起移植传播狂犬病事件,影响了9名组织或器官接受者。如果不及时接受暴露后预防,狂犬病几乎总是致命的。2025年1月,俄亥俄州的临床医生通知俄亥俄州卫生部和疾病预防控制中心,一名肾移植受者在接受移植后51天死亡,疑似患有狂犬病。疾控中心确认了接受者的狂犬病诊断。调查显示,死者在死前大约6周曾被一只臭鼬抓伤。没有移植该捐赠者的其他器官;然而,有3人接受了角膜组织移植。在对供体狂犬病状况进行调查的同时,角膜受者接受了预防性移植物切除和PEP治疗。没有人出现与狂犬病相符的体征或症状。疾病预防控制中心在供者肾脏的存档样本中检测到狂犬病毒RNA,证实了器官来源的传播。调查确定了370名可能与供体或肾受体有接触的人;357例(96%)完成风险评估。在完成风险评估的患者中,46例(13%)被推荐接受PEP治疗。与公共卫生官员的早期咨询可能会预防被狂犬病感染的器官和组织捐赠,或促使移植接受者及时采取PEP。在过去一年内受到狂犬病易感动物咬伤或抓伤的献血者,特别是患有急性脑病的献血者,应考虑患狂犬病的风险。
{"title":"Human-to-Human Rabies Transmission via Solid Organ Transplantation from a Donor with Undiagnosed Rabies - United States, October 2024-February 2025.","authors":"Rebecca Earnest,Kris K Carter,Sara F Margrey,Vaughn V Wicker,Rebecca Betz,Rebecca Reik,Eli Shiltz,Basmah Khalil,Brandon Palinski,Barbara Jordan,Daniel Dodson,Erin Epson,Curtis L Fritz,Juliet Stoltey,Alison Sikola,Ricardo Garcia,Monika Roy,Pallavi Annambhotla,Sridhar V Basavaraju,Sarah C Bonaparte,Shama Cash-Goldwasser,Ian Kracalik,David W McCormick,Faisal S Minhaj,Lillian A Orciari,Panayampalli S Satheshkumar,Pamela Yager,David A Crum,Nathan Koffarnus,Monica Beddo,Molly Baker,Erin C Phipps,Hanna Oltean,Hannah Schnitzler,Crystal M Gigante,Ryan M Wallace,Mary Grace Stobierski,Christine Hahn","doi":"10.15585/mmwr.mm7439a1","DOIUrl":"https://doi.org/10.15585/mmwr.mm7439a1","url":null,"abstract":"Although rabies virus is typically transmitted through mammalian animal bites or scratches, human-to-human transmission has occurred through organ and tissue transplantation. From 1978 to 2013, three transplant-transmitted rabies events in the United States affected nine tissue or organ recipients. Rabies is almost always fatal without timely receipt of postexposure prophylaxis (PEP). In January 2025, clinicians in Ohio notified the Ohio Department of Health and CDC of a suspected case of rabies in a kidney transplant recipient who died 51 days after receiving the transplant. CDC confirmed the recipient's rabies diagnosis. Investigation revealed that the deceased donor had been scratched by a skunk approximately 6 weeks before death. No other organs from that donor were transplanted; however, three persons received cornea tissue grafts. While investigation of the donor's rabies status was ongoing, the cornea recipients underwent precautionary graft removal and received PEP. None developed signs or symptoms compatible with rabies. CDC detected rabies virus RNA in an archived sample of the donor's kidney, confirming organ-derived transmission. Investigation identified 370 persons with possible exposures to the donor or kidney recipient; 357 (96%) completed risk assessments. Among those who completed risk assessments, 46 (13%) were recommended to receive PEP. Early consultation with public health officials might prevent rabies-infected organ and tissue donation or lead to prompt PEP for transplant recipients. The risk for rabies should be considered among donors who have received rabies-susceptible animal bites or scratches within the previous year, particularly those donors with acute encephalopathy.","PeriodicalId":18931,"journal":{"name":"Morbidity and Mortality Weekly Report","volume":"155 1","pages":"600-605"},"PeriodicalIF":0.0,"publicationDate":"2025-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145674144","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Notes from the Field: Outbreak of Escherichia coli O157:H7 Infections Linked to Organic Walnuts - Washington and California, 2024. 现场记录:与有机核桃有关的大肠杆菌O157:H7感染爆发-华盛顿和加利福尼亚,2024。
Pub Date : 2025-11-27 DOI: 10.15585/mmwr.mm7438a2
Angelica L Barrall,Laurie Stewart,Jeffrey Higa,Erin Jenkins,Brooke Whitney,Brandon Adcock,Anna Pickett,Bethan Swift,Peiman Aminabadi,Kenneth Zamora,Susan Shelton,Karen P Neil,Laura Gieraltowski
Outbreaks of Shiga toxin-producing Escherichia coli (STEC) O157 infections are associated primarily with beef and fresh vegetables, particularly leafy greens* (1). Only one reported STEC O157 outbreak in the United States has been linked to tree nuts, specifically a 2011 outbreak in Michigan, Minnesota, and Wisconsin associated with in-shell hazelnuts† (2). On March 25, 2024, the Washington State Department of Health alerted CDC to seven STEC O157 infections in Washington and California after determining that the isolates were highly genetically related by whole genome sequencing (WGS) (3).
产志贺毒素大肠杆菌(STEC) O157感染暴发主要与牛肉和新鲜蔬菜有关,尤其是绿叶蔬菜*(1)。在美国,只有一次报道的产大肠杆菌O157爆发与树坚果有关,特别是2011年在密歇根州、明尼苏达州和威斯康星州爆发的一次与带壳榛子有关的爆发(2)。2024年3月25日,华盛顿州卫生部在通过全基因组测序(WGS)确定分离株具有高度遗传相关性后,向疾病预防控制中心通报了华盛顿州和加利福尼亚州的7例产志毒素大肠杆菌O157感染(3)。
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引用次数: 0
Notes From the Field: Severe Illnesses After Self-Injection of Botulinum Toxin Purchased Online - New York, Texas, and Wisconsin, 2025. 现场记录:网上购买的自注射肉毒杆菌毒素后的严重疾病-纽约,德克萨斯州和威斯康星州,2025年。
Pub Date : 2025-11-27 DOI: 10.15585/mmwr.mm7438a1
Liz Lamere,Jennifer Cope,Robert Breazu,Sandra Peña,Michelle Chang,Joel Ackelsberg,Divya Pillendla,Olivia A Smith,Quoc Phung Than,Pilar Zaibaq,Suzanne Gibbons-Burgener,Ryan J Wozniak,Ethel Taylor
Cosmetic botulinum neurotoxin (BoNT) can be used to temporarily diminish facial wrinkles (1); however, injection for this purpose occasionally results in localized paralytic effects, even when BoNT that is approved by the Food and Drug Administration (FDA) and purchased from authorized sources is administered by licensed and trained medical professionals. Rarely, improperly procured or administered BoNT can lead to severe illness. During May-June 2025, hospital clinicians and health departments in New York, Texas, and Wisconsin each alerted CDC about a person in their jurisdiction who experienced severe illness after self-injecting cosmetic BoNT that was purchased online.* None of the three patients met their state's requirements for purchasing or administering BoNT; no link was reported among the patients. This report describes the patients' characteristics, treatment, and outcomes. This activity was reviewed by CDC, deemed not research, and conducted consistent with applicable federal law and CDC policy.†.
化妆品肉毒杆菌神经毒素(BoNT)可以用来暂时减少面部皱纹(1);然而,用于此目的的注射偶尔会导致局部麻痹效果,即使是经食品和药物管理局(FDA)批准并从授权来源购买的BoNT,也是由有执照和受过培训的医疗专业人员施用的。很少,不适当的获取或施用BoNT可导致严重的疾病。在2025年5月至6月期间,纽约、德克萨斯州和威斯康星州的医院临床医生和卫生部门都向疾病预防控制中心通报了他们管辖范围内的一名患者,该患者在自注射网上购买的BoNT化妆品后患上了严重疾病。*三个病人都没有达到他们所在州购买或使用BoNT的要求;患者之间没有联系的报道。本报告描述了患者的特点、治疗和结果。该活动经CDC审查,被视为非研究,并符合适用的联邦法律和CDC政策。
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引用次数: 0
Notes from the Field: Expanding Birthing Hospital Enrollment in the Vaccines for Children Program to Increase Infant Immunization Against Respiratory Syncytial Virus - United States, October 2023-March 2025. 现场记录:扩大分娩医院在儿童疫苗计划中的登记人数,以增加婴儿对呼吸道合胞病毒的免疫——美国,2023年10月至2025年3月。
Pub Date : 2025-11-20 DOI: 10.15585/mmwr.mm7437a2
Kerry E Olmsted,Terrin Ramsey-Omonua,Ebony S Thomas,James T Lee,Llandess Owens,Sam Graitcer,Jamie Mells
Respiratory syncytial virus (RSV), the leading cause of hospitalization among U.S. infants, results in 50,000-80,000 associated hospitalizations and 100-300 deaths among children aged <5 years each year (1). In 2023, the Advisory Committee on Immunization Practices (ACIP) recommended two options for preventing severe RSV in infants: maternal RSV vaccination during pregnancy (2) or administration of nirsevimab, a long-acting monoclonal antibody to infants (1). Nirsevimab is recommended for infants aged <8 months during their first RSV season (October-March in most of the United States); ideally, it should be administered during the birth hospitalization or within the first week of life. In September 2023, ACIP passed a resolution to add nirsevimab to the Vaccines for Children (VFC) Program, a public-private partnership that provides CDC-purchased vaccines to VFC-eligible children (those who are uninsured or underinsured, insured through Medicaid, or who are American Indian or Alaska Native) at no cost. Approximately one half (52.2%) of U.S. children aged 19-35 months are VFC-eligible, and among those, 93.4% are insured by Medicaid (3). Medicaid-insured infants have a higher incidence of severe RSV infection than do privately insured infants (4). Providers enrolled in the VFC program are able to administer nirsevimab at no cost to eligible children. Enrollment of birthing hospitals in VFC thus has the potential to expand infant immunization against RSV. This report describes enrollment of U.S. birthing hospitals (those with more than one birth during the previous year or at least one registered maternity bed) in the VFC program since the introduction of nirsevimab.
呼吸道合胞病毒(RSV)是美国婴儿住院的主要原因,每年在5岁以下儿童中导致50,000-80,000例相关住院和100-300例死亡(1)。2023年,免疫实践咨询委员会(ACIP)推荐了预防婴儿严重呼吸道合胞病毒的两种选择:怀孕期间母亲接种呼吸道合胞病毒疫苗(2)或使用尼瑟维单抗(nirsevimab),一种针对婴儿的长效单克隆抗体(1)。在第一个呼吸道合胞病毒季节(美国大部分地区为10月至3月),建议8个月以下的婴儿使用Nirsevimab;理想情况下,它应该在出生住院期间或生命的第一周内进行。2023年9月,ACIP通过了一项决议,将nirsevimab添加到儿童疫苗(VFC)计划中,该计划是一个公私合作伙伴关系,向符合VFC条件的儿童(那些没有保险或保险不足的儿童,通过医疗补助计划投保的儿童,或美国印第安人或阿拉斯加原住民)免费提供cdc购买的疫苗。大约一半(52.2%)的19-35个月的美国儿童符合vfc条件,其中93.4%的儿童参加了医疗补助(3)。医疗保险婴儿比私人保险婴儿有更高的严重呼吸道合胞病毒感染发生率(4)。参加VFC计划的提供者能够免费为符合条件的儿童管理nirsevimab。因此,在VFC登记分娩医院有可能扩大婴儿对呼吸道合胞病毒的免疫接种。本报告描述了自引进nirsevimab以来,美国分娩医院(上一年有一个以上分娩或至少有一个注册产科床位的医院)在VFC计划中的登记情况。
{"title":"Notes from the Field: Expanding Birthing Hospital Enrollment in the Vaccines for Children Program to Increase Infant Immunization Against Respiratory Syncytial Virus - United States, October 2023-March 2025.","authors":"Kerry E Olmsted,Terrin Ramsey-Omonua,Ebony S Thomas,James T Lee,Llandess Owens,Sam Graitcer,Jamie Mells","doi":"10.15585/mmwr.mm7437a2","DOIUrl":"https://doi.org/10.15585/mmwr.mm7437a2","url":null,"abstract":"Respiratory syncytial virus (RSV), the leading cause of hospitalization among U.S. infants, results in 50,000-80,000 associated hospitalizations and 100-300 deaths among children aged <5 years each year (1). In 2023, the Advisory Committee on Immunization Practices (ACIP) recommended two options for preventing severe RSV in infants: maternal RSV vaccination during pregnancy (2) or administration of nirsevimab, a long-acting monoclonal antibody to infants (1). Nirsevimab is recommended for infants aged <8 months during their first RSV season (October-March in most of the United States); ideally, it should be administered during the birth hospitalization or within the first week of life. In September 2023, ACIP passed a resolution to add nirsevimab to the Vaccines for Children (VFC) Program, a public-private partnership that provides CDC-purchased vaccines to VFC-eligible children (those who are uninsured or underinsured, insured through Medicaid, or who are American Indian or Alaska Native) at no cost. Approximately one half (52.2%) of U.S. children aged 19-35 months are VFC-eligible, and among those, 93.4% are insured by Medicaid (3). Medicaid-insured infants have a higher incidence of severe RSV infection than do privately insured infants (4). Providers enrolled in the VFC program are able to administer nirsevimab at no cost to eligible children. Enrollment of birthing hospitals in VFC thus has the potential to expand infant immunization against RSV. This report describes enrollment of U.S. birthing hospitals (those with more than one birth during the previous year or at least one registered maternity bed) in the VFC program since the introduction of nirsevimab.","PeriodicalId":18931,"journal":{"name":"Morbidity and Mortality Weekly Report","volume":"4 1","pages":"589-591"},"PeriodicalIF":0.0,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145559052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Influenza-Associated Pediatric Deaths - United States, 2024-25 Influenza Season. 流感相关的儿童死亡-美国,2024-25流感季节。
Pub Date : 2025-09-25 DOI: 10.15585/mmwr.mm7436a2
Katie Reinhart,Stacy Huang,Krista Kniss,Carrie Reed,Alicia Budd
Influenza-associated deaths among children aged <18 years have been nationally notifiable since 2004. The highest number of pediatric deaths reported during a single season since reporting of influenza-associated pediatric deaths began (excluding the 2009-10 influenza A[H1N1]pmd09 pandemic) occurred during the 2024-25 season. Through September 13, 2025, a total of 280 influenza-associated pediatric deaths were reported, representing a national rate of 3.8 deaths per 1 million children. The median age at death was 7 years, and 56% of children who died had at least one underlying medical condition. Influenza A viruses were associated with 240 (86%) of the deaths. Forty percent of children who died were treated with influenza antiviral medications. Among the 208 pediatric decedents with available data who were eligible for influenza vaccine, 89% were not fully vaccinated. CDC recommends that all persons aged ≥6 months who do not have contraindications receive the influenza vaccine each year, ideally by the end of October.
自2004年以来,18岁以下儿童中与流感相关的死亡已在全国范围内进行通报。自开始报告流感相关儿科死亡(不包括2009-10年甲型H1N1流感pmd09大流行)以来,单一季节报告的儿科死亡人数最多的是在2024-25年季节。截至2025年9月13日,共报告了280例与流感相关的儿科死亡病例,相当于全国每100万儿童中有3.8例死亡。死亡时的中位年龄为7岁,56%的死亡儿童至少有一种潜在的疾病。甲型流感病毒与240例(86%)死亡有关。40%的死亡儿童接受了流感抗病毒药物治疗。在208名有流感疫苗接种资格的儿童死亡病例中,89%没有完全接种流感疫苗。CDC建议所有年龄≥6个月且无禁忌症的人每年接种流感疫苗,最好在10月底前接种。
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引用次数: 0
Interim Effectiveness Estimates of 2025 Southern Hemisphere Influenza Vaccines in Preventing Influenza-Associated Outpatient and Hospitalized Illness - Eight Southern Hemisphere Countries, March-September 2025. 2025年南半球流感疫苗预防流感相关门诊和住院疾病的中期有效性评估——8个南半球国家,2025年3月至9月。
Pub Date : 2025-09-25 DOI: 10.15585/mmwr.mm7436a3
Savanah Russ,Francisco Nogareda,Annette K Regan,Estefanía Benedetti,Marina Pasinovich,Carla Voto,Monique Chilver,Nigel Stocks,Sheena G Sullivan,Allen C Cheng,Christopher C Blyth,Jenna Hassall,Walquiria Aparecida Ferreira de Almeida,Francisco José de Paula Júnior,Ana Catarina de Melo Araújo,Natalia Vergara,Paula Camila Rodríguez Ferrari,Rodrigo A Fasce,Christian Saavedra,Elena Penayo,Silvia Gómez,Chavely Domínguez,Andrew Anglemyer,Tim Wood,Q Sue Huang,Sibongile Walaza,Phindi Zwane,Nicole Wolter,Natalia Goñi,Jeremy Tairovich,Eduardo Silvera,Paula Couto,Jorge Jara,Rebecca J Kondor,Eduardo Azziz-Baumgartner,Anna N Chard
Seasonal influenza vaccination provides important protection from influenza illness and associated potential complications. Monitoring seasonal influenza vaccine effectiveness (VE) in Southern Hemisphere countries can apprise health authorities in Northern Hemisphere countries about the potential protection provided from vaccination. Using data from influenza-like illness (ILI) and severe acute respiratory infection (SARI) sentinel surveillance networks in eight Southern Hemisphere countries, investigators estimated interim VE against influenza-associated outpatient visits and hospitalization using a test-negative case-control study design. During March-September 2025, Australia and South Africa identified 2,122 patients with ILI; Argentina, Australia, Brazil, Chile, New Zealand, Paraguay, and Uruguay identified 42,752 patients with SARI. Overall, 21.3% of patients with ILI and 15.9% of patients with SARI were vaccinated against influenza. Adjusted VE against influenza-associated outpatient visits and hospitalization was 50.4% and 49.7%, respectively, for any influenza virus, and 45.4% and 46.1%, respectively, for influenza A viruses. Adjusted VE against hospitalization with the predominant influenza subtype, A(H1N1)pdm09, was 41.6%. These interim estimates suggest that vaccination reduced medically attended influenza-associated illness by approximately one half in eight Southern Hemisphere countries. Health authorities should prioritize vaccination of all eligible persons ≥6 months to reduce incidence of influenza disease.
季节性流感疫苗接种可提供预防流感疾病和相关潜在并发症的重要保护。在南半球国家监测季节性流感疫苗的有效性,可使北半球国家的卫生当局了解疫苗接种可能提供的保护。利用来自8个南半球国家流感样疾病(ILI)和严重急性呼吸道感染(SARI)哨点监测网络的数据,研究人员使用检测阴性病例对照研究设计估计了流感相关门诊就诊和住院的中期VE。在2025年3月至9月期间,澳大利亚和南非确定了2122例ILI患者;阿根廷、澳大利亚、巴西、智利、新西兰、巴拉圭和乌拉圭确定了42752例急性呼吸道感染患者。总体而言,21.3%的ILI患者和15.9%的严重急性呼吸道感染患者接种了流感疫苗。针对流感相关门诊就诊和住院的调整后VE,对于任何流感病毒分别为50.4%和49.7%,对于甲型流感病毒分别为45.4%和46.1%。与主要流感亚型A(H1N1)pdm09住院相比,调整后的VE为41.6%。这些中期估计表明,在南半球8个国家,疫苗接种使接受医疗护理的流感相关疾病减少了大约一半。卫生当局应优先为所有≥6个月的符合条件者接种疫苗,以减少流感发病率。
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引用次数: 0
Pediatric Influenza-Associated Encephalopathy and Acute Necrotizing Encephalopathy - United States, 2024-25 Influenza Season. 儿童流感相关脑病和急性坏死性脑病-美国,2024-25流感季节
Pub Date : 2025-09-25 DOI: 10.15585/mmwr.mm7436a1
Amara Fazal,Elizabeth J Harker,Varsha Neelam,Samantha M Olson,Melissa A Rolfes,Katie Reinhart,Krista Kniss,Aaron Frutos,Jerome Leonard,Carrie Reed,Vivien G Dugan,Haytham Safi,Theresa M Dulski,Adrianna Stanley-Downs,Aaliya Bhatti,Isaac Armistead,Suchitra Rao,Carola Torres-Diaz,Ashlin Thomas,Andy Weigel,Michael Patten,Mallory Sinner,Dawn Nims,Crystal Mattingly,Valerie Gosack,Amy Voris,Jaime Redkey,Felicia A Scaggs Huang,Danielle DeCesaris,Carrie Tuggle,Kristina A Betters,Julie Hand,Anna Krueger,Dina Z Potter,Curi Kim,Rachel Park,Sue Hong,Hannah E Edelman,Sue Kim,Justin Henderson,Melissa McMahon,Jeffrey Sanders,David A Hunstad,Emma L Doran,Khalil Harbi,Derek Julian,Hannah Ball,John Dreisig,Deepam Thomas,Justin Faybusovich,Yomei P Shaw,Nancy Eisenberg,Richa Chaturvedi,Ashleigh Faulstich,Rachel E Wester,Donna L Gowie,Nicholas Fisher,Melissa Sutton,Sameh W Boktor,Jonah M Long,Patricia Marshall,Abby L Berns,Lindsey McAda,Sarah Winders,Pamela Gomez Pinedo,Jade Murray,Ta'Kindra Westbrook,Anna Unutzer,Scott Lindquist,Thomas E Haupt,Kaylyn Baum,Molly Wilson-Murphy,Carol Glaser,Kathleen Harriman,James W Antoon,Keith P Van Haren,Adrienne G Randolph,Andrew Silverman,Annabelle de St Maurice,Sascha Ellington,Timothy M Uyeki,Shikha Garg,
In January 2025, CDC received several reports of deaths among children aged <18 years with a severe form of influenza-associated encephalopathy (IAE) termed acute necrotizing encephalopathy (ANE). Because no national surveillance for IAE currently exists, CDC requested notification of U.S. pediatric IAE cases from clinicians and health departments during the 2024-25 influenza season, a high-severity season with a record number of pediatric influenza-associated deaths. Among 192 reports of suspected IAE submitted to CDC, 109 (57%) were categorized as IAE, 37 (34%) of which were subcategorized as ANE, and 72 (66%) as other IAE; 82 reports did not meet IAE criteria and were categorized as other influenza-associated neurologic disease. The median age of children with IAE was 5 years and 55% were previously healthy, 74% were admitted to an intensive care unit, and 19% died; 41% of children with ANE died. Only 16% of children with IAE who were vaccination-eligible had received the 2024-25 influenza vaccine. Health care providers should consider IAE in children with encephalopathy or altered level of consciousness and a recent or current febrile illness when influenza viruses are circulating. Annual influenza vaccination is recommended for all children aged ≥6 months to prevent influenza and associated complications, potentially including severe neurologic disease such as IAE and ANE.
2025年1月,美国疾病控制与预防中心收到了几起未满18岁儿童死于严重形式的流感相关脑病(IAE)的报告,称为急性坏死性脑病(ANE)。由于目前没有针对IAE的全国性监测,CDC要求临床医生和卫生部门在2024-25年流感季节通报美国儿科IAE病例,这是一个高度严重的季节,儿童流感相关死亡人数创历史新高。在向CDC提交的192例疑似IAE报告中,IAE 109例(57%),ANE 37例(34%),其他IAE 72例(66%);82例报告不符合IAE标准,被归类为其他流感相关神经系统疾病。IAE患儿的中位年龄为5岁,55%以前健康,74%入住重症监护病房,19%死亡;41%的ANE患儿死亡。只有16%符合疫苗接种条件的IAE儿童接种了2024-25年流感疫苗。当流感病毒流行时,卫生保健提供者应考虑有脑病或意识水平改变以及近期或当前发热性疾病的儿童发生IAE。建议所有≥6个月的儿童每年接种流感疫苗,以预防流感及其相关并发症,可能包括严重的神经系统疾病,如IAE和ANE。
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Morbidity and Mortality Weekly Report
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