Prematurity

早产
  • 文章类型: Journal Article
    本文的目的是深入研究父亲在NICU和前所未有的卫生背景下应对早产婴儿的复杂性时面临的情感和心理挑战。
    我们使用了三种数据收集方法,例如访谈(叙事和高危婴儿父母的临床访谈-CLIP)和爱丁堡产后抑郁量表(EPDS),以全面了解病例。
    以下分析通过仔细研究两个上级主题,探讨了两个人在COVID-19大流行的第一波中成为第一次父亲的个人经历:“通过经历过的COVID-19限制的一系列分离”和“连接点”。“向父亲的过渡本质上是与他们的新生儿和感知的父亲身份的医学形式联系。就时间性而言,这些父亲经历了对婴儿长期发育和COVID-19健康问题的担忧。此外,他们使用精神分析框架显示出恐惧症或软骨病倾向的迹象,伴随着产后抑郁症的风险增加。
    UNASSIGNED: The aim of this paper is to delve into the emotional and psychological challenges that fathers face as they navigate the complexities of having a preterm infant in the NICU and in an unprecedented sanitary context.
    UNASSIGNED: We used three data collection methods such as interviews (narrative and the Clinical Interview for Parents of High-risk Infants- CLIP) and the Edinburgh Postnatal Depression Scale (EPDS) to gain a comprehensive understanding of the cases.
    UNASSIGNED: The following analysis explores two individuals\' personal experiences of becoming a first-time father during the first wave of the COVID-19 pandemic through a close examination of two superordinate themes: \"A series of separations through the experienced COVID- 19 restrictions\" and \"Moments of connection.\" The transition to fatherhood is essentially with a medicalized form of connection with their newborn and the perceived paternal identity. In terms of temporality, these fathers experienced a combination of concerns about their infants\' long-term development and COVID-19 health concerns. Furthermore, they showed indications of phobic or hypochondriac tendencies using a psychoanalytic framework, along with an increased risk of postpartum depression.
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  • 文章类型: Journal Article
    动脉导管未闭(PDA)是极早产(≤26周妊娠)的婴儿经常遇到的缺陷。历史上,使用环氧合酶抑制剂药物或通过手术结扎来封堵PDA.然而,使用这些疗法关闭PDA的益处从未得到证实,尽管以前的研究并不集中在极早产儿。因此,全球范围内的趋势是对PDA进行保守管理。随着极早产儿生存率的提高,与PDA相关的合并症增加了,从而为该人群找到替代治疗方法,例如经导管动脉导管未闭封堵术(TCPC)。目前,在这一高风险的小婴儿队列中,人们对PDA的选择性治疗产生了新的兴趣.这篇综合评论文章考察了早产儿PDA管理的全球变化趋势,特别关注TCPC的日益普及。此外,本文汇编了来自全球多个新生儿网络的数据,以帮助理解当前的问题。如果儿科心脏病专家要为该人群提供TCPC作为可行的治疗选择,了解早产儿的当前管理及其结局至关重要。本文旨在通过汇编有关PDA管理的具有里程碑意义的临床试验的结果以及这些试验引起的争议,为儿科心脏病专家提供有关该主题的指导。介绍了几个国家的比较结果,包括全球专家对数据的解释和意见。这是迈向早产儿PDA管理全球共识的一步。
    Patent ductus arteriosus (PDA) is a frequently encountered defect in infants born extremely premature (≤26 weeks\' gestation). Historically, closure of the PDA was performed using cyclooxygenase inhibitor medications or by surgical ligations. However, the benefits of PDA closure using these therapies have never been demonstrated, albeit studies have previously not focused on the extremely premature infants. Therefore, there was a worldwide trend toward conservative management of the PDA. With improved survival of extremely premature infants, comorbidities associated with the PDA has increased, resulting in finding alternate treatments such as transcatheter patent ductus arteriosus closure (TCPC) for this population. Currently, there is a renewed interest toward selective treatment of the PDA in this high-risk cohort of small infants. This Comprehensive Review article inspects the globally changing trends in the management of the PDA in premature infants, with a special focus on the rising adoption of TCPC. Moreover, this article compiles data from several neonatal networks worldwide to help understand the problem at hand. Understanding the current management of premature infants and their outcomes is fundamentally essential if pediatric cardiologists are to offer TCPC as a viable therapeutic option for this population. This article aims to serve as a guide for pediatric cardiologists on this topic by compiling the results on landmark clinical trials on PDA management and the controversies that arise from these trials. Comparative outcomes from several countries are presented, including interpretations and opinions of the data from experts globally. This is a step toward coming to a global consensus in PDA management in premature infants.
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  • 文章类型: Journal Article
    在明确干预之前,通常需要在CHD出生的婴儿中限制PBF以避免肺过度循环。目前的标准是手术放置肺动脉带,但这些都有局限性,并与并发症有关。
    这项研究的目的是通过一种相对新颖的技术来对先天性心脏病(CHD)的部分婴儿进行经皮限制肺血流(PBF)的单中心体验。
    由于出生体重不足或早产,选择患者进行此手术。他们都患有CHD,在没有PBF控制的情况下会导致过度循环。通过经皮方法,将改良的血管塞装置放置在双侧分支肺动脉中。
    7例CHD导致左侧梗阻的新生儿接受了该手术。所有患者均表现出限制性PBF的证据,平均氧饱和度从95%降低至84%。一名患者在手术后5天由于过度循环而需要放置肺动脉带。所有患者都进行了全面的手术干预,没有设备栓塞或需要进行肺动脉成形术。血流动力学表明,在5例接受术前心导管插入术的患者中,PBF的局限性足够大,平均肺血管阻力为1.52WU×m2,平均经肺梯度为5.9mmHg。
    经皮PBF限制似乎是安全的,并且是一种侵入性较小的选择,可以延迟选定人群的手术干预以允许体细胞生长和妊娠成熟。它导致胸骨的总数减少。
    UNASSIGNED: Restriction of PBF in infants born with CHD is often required to avoid pulmonary over-circulation prior to definitive intervention. The current standard is to surgically place pulmonary artery bands, but these have limitations and are associated with complications.
    UNASSIGNED: The purpose of this study was to a single-center experience with a relatively novel technique to percutaneously restrict pulmonary blood flow (PBF) in select infants with congenital heart disease (CHD).
    UNASSIGNED: Patients were selected to undergo this procedure either due to low birth weight or prematurity. All of them had CHD that would result in over-circulation without control of PBF. By a percutaneous method, modified vascular plug devices were placed in the bilateral branch pulmonary arteries.
    UNASSIGNED: Seven neonates with CHD resulting in left-sided obstruction underwent this procedure. All patients demonstrated evidence of restricted PBF with a decrease in mean oxygen saturation from 95% to 84%. One patient required pulmonary artery band placement due to over-circulation 5 days after the procedure. All patients proceeded to full surgical intervention without device embolization or need for pulmonary arterioplasty. Hemodynamics demonstrated adequate limitation of PBF in 5 patients who underwent presurgical cardiac catheterization with a mean pulmonary vascular resistance of 1.52 WU × m2 and a mean transpulmonary gradient of 5.9 mm Hg.
    UNASSIGNED: Percutaneous PBF restriction appears to be safe and a less invasive option to delay surgical intervention in a select population to allow for somatic growth and gestational maturation. It results in a decrease in the total number of sternotomies.
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  • 文章类型: Journal Article
    还原-氧化(氧化还原)化学在人体稳态中起着至关重要的作用。这些反应在能量产生中起着关键作用,作为先天免疫的一部分,以及产生具有各种功能的第二信使,例如细胞周期进程或神经递质的释放。尽管有这样的基石作用,如果不检查,身体可以过度产生活性氧(ROS)或活性氮(RNS)。当这些使内源性抗氧化系统不堪重负时,氧化应激(OS)发生。在新生儿中,OS与早产儿视网膜病变(ROP)有关,白质软化症,支气管肺发育不良(BPD)。鉴于其广泛的影响,研究已经开始检查OS是否在坏死性小肠结肠炎(NEC)中起作用。在本文中,我们将讨论氧化还原化学的基础知识以及人体如何控制这些。然后我们将讨论当这些出错时会发生什么,主要集中在新生儿的NEC。
    Reduction-oxidation (redox) chemistry plays a vital role in human homeostasis. These reactions play critical roles in energy generation, as part of innate immunity, and in the generation of secondary messengers with various functions such as cell cycle progression or the release of neurotransmitters. Despite this cornerstone role, if left unchecked, the body can overproduce reactive oxygen species (ROS) or reactive nitrogen species (RNS). When these overwhelm endogenous antioxidant systems, oxidative stress (OS) occurs. In neonates, OS has been associated with retinopathy of prematurity (ROP), leukomalacia, and bronchopulmonary dysplasia (BPD). Given its broad spectrum of effects, research has started to examine whether OS plays a role in necrotizing enterocolitis (NEC). In this paper, we will discuss the basics of redox chemistry and how the human body keeps these in check. We will then discuss what happens when these go awry, focusing mostly on NEC in neonates.
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  • 文章类型: Journal Article
    背景/目标:早产率仍然很高,对任何国家的公共卫生系统都是挑战,对新生儿死亡率有很大影响。本研究旨在评估一组产妇早产的频率和环境及母婴危险因素。他们的新生儿在一家私人参考医院的新生儿重症监护室接受监测。方法:在2013年至2018年期间,对居住在巴西东北部首都城市的产妇进行了队列研究,这些产妇的新生儿被送往新生儿重症监护病房。本研究得到福塔莱萨大学研究伦理委员会的批准。收集的信息包括来自医疗记录的数据和来自孕产妇家庭的水文卫生数据。结果:2013年至2018年,该医院活产(n=9778)的早产患病率为23%。符合条件的人(n=480)的早产频率为76.9%,在此期间,符合条件的早产儿(n=369)占分娩总数的频率为3.8%。在多变量分析中,早产的重要危险因素是初产妇(RR=1.104,95CI:1.004-1.213)和妊娠期高血压综合征(RR=1.262,95CI:1.161-1.371),且显著的保护因素是产前咨询次数最高(RR=0.924,95CI:0.901-0.947)。结论:这项研究有助于提高产前护理的知名度,以及对怀孕和分娩护理期间并发症的了解。这些结果表明,需要实施公共政策,促进改善人口的生活条件和照顾孕妇,以减少早产,因此,新生儿和婴儿死亡率。
    Background/Objectives: Prematurity rates remain high and represent a challenge for the public health systems of any country, with a high impact on neonatal mortality. This study aimed to evaluate the frequency and environmental and maternal-fetal risk factors for premature birth in a cohort of parturient women, with their newborns monitored in a neonatal intensive care unit at a private reference hospital. Methods: A cohort was carried out between 2013 and 2018 among parturient women living in a capital city in the Northeast of Brazil whose newborns were admitted to the neonatal intensive care unit. This study was approved by the Research Ethics Committee of the University of Fortaleza. The information collected comprised data from both medical records and hydrosanitary data from maternal homes. Results: The prevalence of prematurity among live births (n = 9778) between 2013 and 2018 at this hospital was 23%. The frequency of prematurity among those eligible (n = 480) was 76.9%, and the frequency of eligible premature babies (n = 369) in relation to the total number of births in this period was 3.8%. In the multivariate analysis, the significant risk factors for prematurity were primigravida (RR = 1.104, 95%CI: 1.004-1.213) and hypertensive syndromes during pregnancy (RR = 1.262, 95%CI: 1.161-1.371), and the significant protective factor was the highest number of prenatal consultations (RR = 0.924, 95%CI: 0.901-0.947). Conclusions: This study contributes to providing greater visibility to prenatal care and the understanding of complications during pregnancy and childbirth care. These results indicate the need to implement public policies that promote improvements in the population\'s living conditions and care for pregnant women to reduce premature births and, consequently, neonatal and infant mortality.
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  • 文章类型: Journal Article
    UNASSIGNED: Preeclampsia is a potentially life-threatening hypertensive pregnancy disorder that carries an acute risk of an unfavorable outcome of the pregnancy but also has consequences for the long-term health of the mother. Women who develop the early form of pre-eclampsia before the 32nd week of pregnancy have the highest risk and are also the most difficult to treat. The severity of pre-eclampsia is not characterized uniformly in Germany, so that the indication for delivery is rather individualized. The aim of this study was to reach a consensus on parameters that could serve as criteria for describing the severity of pre-eclampsia based on the urgency of delivery. To this end, a Delphi procedure was used to present a scenario in which a woman was admitted for preeclampsia before 32 gestational weeks and after completion of antenatal steroid therapy.
    UNASSIGNED: Clinicians specialized in maternal-fetal medicine from German-speaking countries completed five rounds of a modified Delphi questionnaire. Presented parameters were selected by the section \"Hypertensive Pregnancy Diseases and Fetal Growth Restriction\" of the German Society of Gynecology and Obstetrics after reviewing the literature. These included objectifiable laboratory or clinical parameters as well as subjective symptoms of the patient. In addition, nine fetal parameters were taken into account. The clinicians were asked to rate presented parameters as an indication for delivery on a Likert scale from 0 to 4 (no indication to absolute indication without delay). For each item, the predefined cut-off for group consensus was ≥ 70% agreement.
    UNASSIGNED: A total of 126 experts were approached. Sixty-nine experts (54.8%) took part in the first round; of those 50 completed the entire Delphi procedure. A consensus was reached on 14 parameters to be considered rapid preparation for delivery without delay (4 points on the Likert scale). These were among others hepatic hematoma or liver capsule rupture, acute liver failure with fulminant coagulation disorder or disseminated intravascular coagulation, eclampsia, pathologic findings in imaging (e.g. cMRI) or electrocardiogram arranged for new onset of headache or retrosternal pain, respectively. Twenty-six parameters were rated as factors that should be considered in the decision without being absolute (1 to 3 points), and 13 parameters should have no influence on the decision to deliver (0 points). No consensus on severe hypertension as an indication for delivery could be reached for blood pressure values below 220/140 mmHg.
    UNASSIGNED: A consensus was reached on whether to deliver in preeclampsia typic clinical findings and symptoms. The results can serve as guidance for current clinical practice and for the definition of clinical endpoints in intervention studies. Nevertheless, the isolated criteria are a theoretical construction since the combined deterioration or summation of several factors rather than a single factor most likely influences the decision to deliver and reflect the severity of preeclampsia. Moreover, the degree of hypertension as an indication for delivery remains controversial, unless the patient suffers additionally from complaints. Future research should be enforced to incorporate long-term risks for the mother into a decision aid.
    UNASSIGNED: Präeklampsie stellt eine potenziell lebensbedrohende hypertensive Schwangerschaftserkrankung dar, die mit einem akuten Risiko für ein ungünstiges Schwangerschaftsoutcome und mit Konsequenzen für die langfristige Gesundheit der Mutter verbunden ist. Das höchste Risiko haben Frauen, welche die Frühform von Präeklampsie vor der 32. Schwangerschaftswoche entwickeln, und die Behandlung dieser Frauen ist auch am schwierigsten. Der Schweregrad der Präeklampsie wird in Deutschland nicht einheitlich eingestuft. Das bedeutet, dass die Indikation zur Entbindung eher individuell erfolgt. Ziel dieser Studie war es, einen Konsens hinsichtlich der Parameter zu erreichen, die, basierend auf der Dringlichkeit der Entbindung, als Kriterien zur Beschreibung des Schweregrads der Präeklampsie dienen könnten. Es wurde dazu eine Delphi-Studie durchgeführt, die ein Szenario beschreiben sollte, bei der eine Frau wegen Präeklampsie vor der 32. Schwangerschaftswoche und nach Abschluss einer antenatalen Steroidtherapie stationär aufgenommen wird.
    UNASSIGNED: Fachärzte und -ärztinnen für mütterliche-fetale Medizin aus deutschsprachigen Ländern nahmen an 5 Runden einer modifizierten Delphi-Befragung teil. Die vorgestellten Parameter wurden von der Sektion Hypertensive Schwangerschaftserkrankungen und fetale Wachstumsrestriktion der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe nach Durchsicht der Literatur ausgewählt. Die Liste der Parameter umfasste objektivierbare Laborparameter und klinische Parameter sowie subjektive Symptome von Patientinnen. Es wurden auch 9 fetale Parameter berücksichtigt. Die Fachärzte und -ärztinnen wurden gebeten, die vorgestellten Parameter als Indikation für eine Entbindung auf einer Likert-Skala von 0 bis 4 (keine Indikation bis absolute Indikation ohne Verzug) zu bewerten. Für jeden Punkt war der vorgegebene kritische Wert für ein Gruppenkonsens eine Zustimmung ≥ 70%.
    UNASSIGNED: Insgesamt wurden 126 Fachärzte und -ärztinnen angeschrieben. Es nahmen 69 Fachärzte und -ärztinnen (54,8%) an der 1. Runde teil; davon haben 50 den gesamten Delphi-Prozess abgeschlossen. Ein Konsens wurde für 14 Parameter erreicht, die als Hinweise für eine schnelle Entbindung eingestuft wurden (4 Punkte auf der Likert-Skala). Dazu zählten u. a. Leberhämatom bzw. Leberkapselruptur, akutes Leberversagen mit fulminanter Gerinnungsstörung oder disseminierter intravasaler Gerinnung, Eklampsie, pathologische Befunde in der Bildgebung (z. B. cMRI) oder beim Elektrokardiogramm, das wegen erneutem Auftreten von Kopfschmerzen bzw. Brustbeinschmerzen durchgeführt wurde. 26 Parameter wurden als Faktoren eingestuft, die bei einer Entscheidung zur Entbindung berücksichtigt werden sollten, ohne dass sie absolut eine Entbindung erfordern (1 bis 3 Punkte); bei 13 Parametern war der Konsens, dass diese keinen Einfluss auf die Entscheidung zur Entbindung haben sollten (0 Punkte). Hinsichtlich des Punktes „schwerer Bluthochdruck als Indikation für eine Entbindung“ konnte kein Konsens erreicht werden, wenn die Blutdruckwerte unter 220/140 mmHg lagen.
    UNASSIGNED: Es wurde ein Konsens hinsichtlich der typischen klinischen Befunde und Symptome für eine dringliche Entbindung erreicht. Die Ergebnisse können als Anleitung für die aktuelle klinische Praxis und bei der Definition von klinischen Endpunkten in Interventionsstudien dienen. Dennoch stellen diese isolierten Kriterien ein theoretisches Konstrukt dar, da in der Praxis die Entscheidung zur Entbindung auf einer kombinierten Verschlechterung bzw. auf der Summierung mehrerer Faktoren anstelle eines einzigen Faktors beruht, da diese Konstellation eher den Schweregrad der Präeklampsie reflektiert. Hinzu kommt noch, dass die Schwere der Hypertonie als Indikation für eine Entbindung immer noch kontrovers diskutiert wird, es sei denn, dass die Patientin auch unter anderen Beschwerden leidet. Die zukünftige Forschung sollte auch mütterliche Langzeitrisiken in die Entscheidungshilfe integrieren.
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  • 文章类型: Journal Article
    背景:人乳库是向有健康并发症的早产和足月婴儿提供捐赠人乳(DHM)的重要设施。关于牛奶银行捐赠者以及他们的特征如何影响捐赠过程的特殊性知之甚少。本研究旨在评估捐献者及其新生儿的特征,以确定与DHM的数量以及开始和捐赠时间的关联。在科尔多瓦牛奶银行运营的第一年和第二年,西班牙。
    方法:这项横断面研究分三个阶段进行:牛奶库(PRE)的开业前,包括所有在2017年1月至5月期间分娩的新生儿和医院使用者的妇女;开业后第一年的捐赠者(第1期(P1):2019年4月至2020年3月);第二年(P2:2020年4月至2021年3月)。对于P1和P2,记录DHM数据。使用单变量和回归模型检查了供体和新生儿特征与捐赠过程之间的关系。
    结果:来自前一时期接受采访的391名女性,55人(14%)表示有意捐赠。在P1和P2中,有51和25人乳(HM)供体,分别。年龄,不同时期的胎龄(GA)和胎次相似.在P2中,受过高等教育的捐赠者比例更高(P1:46%;P2:70.8%,p=0.045)。在这两个时期,约有40%的捐助者休产假。在P1中,低出生体重婴儿(<2500g)的供体比体重≥2500g的供体捐赠了更多的HM(p=0.020)。在P2中,GA<37周的女性捐赠的量比≥37周的患者(p=0.002)。在这两个时期,产假与较短的捐赠开始时间有关(P1:p=0.002;P2:p<0.001)。
    结论:从西班牙人乳库获得的数据表明,早产和低出生体重似乎会影响DHM的含量。就业状况可能是启动HM捐赠的决定性因素。需要额外的努力来确定影响捐赠开始和数量的共同捐赠者特征。
    BACKGROUND: Human milk banks are essential facilities to provide donated human milk (DHM) to preterm and term infants with health complications. Little is known regarding milk bank donors and how their characteristics may influence the particularities of the donation process. The present study aims to assess characteristics of donors and their newborns to identify associations with the amount of DHM and initiation and donation time, during the first and second year of the milk bank operation in Córdoba, Spain.
    METHODS: This cross-sectional study was conducted in three periods: pre-opening of the milk bank (PRE) including all women who gave birth to a newborn between January - May 2017 and were hospital users; donors in the first year after the opening (Period 1 (P1): April 2019 - March 2020); and in the second year (P2: April 2020 - March 2021). For P1 and P2, DHM data were recorded. The relationships between donor and newborn characteristics and the donation process were examined using univariable and regression models.
    RESULTS: From 391 women interviewed in the PRE period, 55 (14%) showed intention to donate. In P1 and P2, there were 51 and 25 human milk (HM) donors, respectively. Age, gestational age (GA) and parity were similar between periods. In P2, a higher proportion of donors had higher education (P1: 46%; P2: 70.8%, p = 0.045). Around 40% of donors in both periods were on maternity leave. In P1, donors who had low birth weight infants (< 2500 g) donated more HM than those with infants weighing ≥ 2500 g (p = 0.020). In P2, women whose GA was < 37 weeks donated a higher volume vs. those with ≥ 37 weeks (p = 0.002). Maternity leave was linked to a shorter initiation time for donations in both periods (P1: p = 0.002; P2: p < 0.001).
    CONCLUSIONS: Data obtained from a Spanish human milk bank indicate that prematurity and low birth weight appear to influence the amounts of DHM. Employment status might be a decisive factor in initiating HM donation. Additional efforts are required to identify shared donor characteristics that influence the initiation and volume of donation.
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  • 文章类型: Journal Article
    调节性T细胞(Treg)在子宫内耐受非遗传母体抗原和调节出生时针对病原体的免疫应答中起着重要作用。这项研究调查了西非新生儿的Treg免疫,败血症仍然是一个主要的公共卫生问题。新生儿早发性败血症(EOS)亚组的Treg表型,假定脓毒症,并对有无产前危险因素的健康新生儿进行评估。Treg表型根据产前条件而变化,与无产前危险因素的健康新生儿相比,Treg频率和Foxp3表达增加。与有产前危险因素的健康新生儿相比,EOS新生儿Treg和Foxp3表达频率显著降低。在Treg池里,在EOS新生儿中观察到更高的活化Treg频率,提示败血症发作上游的子宫内激活。它们向感染部位的迁移可以解释循环整合素α4β1+Treg的频率降低,提示归巢至内皮组织。新生儿EOS显示Treg上CTLA-4,PD-1和CD39的表达增加,其负调节效应T细胞(Teff)的激活,这由EOS新生儿中Teff的较低频率证实。EOS非存活者中CD39+Treg的频率较高,整合素α4β1+Treg的频率较低,提示Treg耗尽和内皮归巢与结果严重程度相关。发展EOS的新生儿天生具有改变的Treg表型特征。CTLA-4、PD-1、CD39和整合素α4β1细胞标志物的Treg表达可被认为是EOS的早期预警或诊断标志物。
    Regulatory T cells (Treg) play a prominent role in utero tolerating non-inherited maternal antigens and in regulating immune responses against pathogens at birth. This study investigates Treg immunity in newborns in West Africa, where sepsis remains a major public health problem. Treg phenotypes on neonates subgroups with early-onset sepsis (EOS), presumed sepsis, and healthy newborn with and without prenatal risk factors were evaluated. Treg phenotypes varied according to prenatal conditions, with increase in Treg frequency and Foxp3 expression in healthy newborns with prenatal risk factors compared to those with none risk. Compared to healthy newborns with prenatal risk factors, EOS neonates had a significantly reduced frequency of Treg and Foxp3 expression. In the Treg pool, higher frequency of activated Treg was observed in EOS neonates, suggesting an in-utero activation upstream of the sepsis onset. Their migration to the infection site may explain the reduced frequency of circulating Integrin α4β1+ Treg suggestive of homing to the endothelial tissue. EOS neonates show increases expression of CTLA-4, PD-1 and CD39 on Treg, which negatively regulate the activation of effector T cells (Teff) corroborating by the lower frequency of Teff in EOS neonates. The higher frequency of CD39+ Treg and the lower frequency of integrinα4β1+ Treg in EOS non-survivor suggests that Treg exhaustement and endothelial homing are associated with outcome severity. Neonates developing EOS are born with an altered Treg phenotypic profile. Treg expression of CTLA-4, PD-1, CD39, and integrinα4β1 cell markers can be considered as early warning or diagnostic markers of EOS.
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  • 文章类型: Journal Article
    背景:脐带夹闭延迟(DCC)发生在大多数早产中。目的:评估DCC与急性肾损伤(AKI)和2年肾脏预后的关系。方法:对妊娠240/7至276/7周新生儿的早产促红细胞生成素神经保护试验进行二次分析。比较了患有DCC(分娩后≥30秒)的新生儿与患有早期脐带钳夹(ECC)(分娩后<30秒)的新生儿的AKI和两年肾脏结局。结果:AKI的发生率和严重程度在DCC组和ECC组之间没有差异(aOR1.17[95CI0.76-1.80])。在矫正两岁的时候,DCC与eGFR<90mL/min/1.73m2的校正几率增加4.5倍相关。DCC与白蛋白尿或血压升高之间没有显著关联。结论:DCC与新生儿AKI降低无关,但与2年时eGFR<90mL/min/1.73m2的校正几率较高相关。
    UNASSIGNED: Delayed cord clamping (DCC) occurs in most preterm births.
    UNASSIGNED: Evaluate the association of DCC with acute kidney injury (AKI) and two-year kidney outcomes.
    UNASSIGNED: Secondary analysis of the Preterm Erythropoietin Neuroprotection Trial of neonates born 240/7 to 276/7 weeks\' gestation. AKI and two year kidney outcomes were compared in neonates with DCC (≥30 seconds after delivery) to those with early cord clamping (ECC) (<30 seconds after delivery).
    UNASSIGNED: The incidence and severity of AKI did not differ between the DCC and ECC groups (aOR 1.17 [95%CI 0.76-1.80]). At two years corrected age, DCC was associated with a 4.5-fold times increased adjusted odds of eGFR <90 mL/min/1.73m2. No significant associations were noted between DCC and albuminuria or elevated BP.
    UNASSIGNED: DCC was not associated with decreased neonatal AKI, but was associated with higher adjusted odds of eGFR <90 mL/min/1.73m2 at two years.
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  • 文章类型: Journal Article
    种族不平等是健康结果的关键决定因素。我们量化了巴西出生不良结局和早期新生儿死亡率的种族不平等。
    我们在2012年至2019年期间使用行政关联数据在巴西进行了一项队列研究。估计整个群体(PAF)和特定群体(AF)的归因分数,如果所有女性的基线条件与白人女性相同,则可以避免的每种不良结局的比例,未调整和调整社会经济学和孕产妇风险因素。AF还通过比较不同母亲学校教育中每个母亲种族/肤色组的妇女来计算。以受过8年或8年以上教育的白人妇女为参照组,按年份划分。
    研究了21,261,936名新生儿。如果所有女性都经历了与白人女性相同的比率,1.7%的早产,7.2%的低出生体重(LBW),10.8%的小于胎龄(SGA)和11.8%的早期新生儿死亡本来可以预防。土著居民的可预防百分比更高(22.2%的早产,LBW的17.9%,SGA的20.5%和新生儿早期死亡的19.6%)和黑人妇女(早产的6%,LBW的21.4%,22.8%的SGA出生和20.1%的早期新生儿死亡)。土著受教育年限较少的群体AF较高,布莱克和帕达的所有结果。AF随时间增加,尤其是土著居民。
    如果巴西不存在种族不平等,则可以避免相当一部分不良出生结局和新生儿死亡。针对这些不平等的原因采取行动必须是妇幼保健政策的核心。
    比尔和梅琳达·盖茨基金会和惠康信托基金。
    UNASSIGNED: Ethno-racial inequalities are critical determinants of health outcomes. We quantified ethnic-racial inequalities on adverse birth outcomes and early neonatal mortality in Brazil.
    UNASSIGNED: We conducted a cohort study in Brazil using administrative linked data between 2012 and 2019. Estimated the attributable fractions for the entire population (PAF) and specific groups (AF), as the proportion of each adverse outcome that would have been avoided if all women had the same baseline conditions as White women, both unadjusted and adjusted for socioeconomics and maternal risk factors. AF was also calculated by comparing women from each maternal race/skin colour group in different groups of mothers\' schooling, with White women with 8 or more years of education as the reference group and by year.
    UNASSIGNED: 21,261,936 newborns were studied. If all women experienced the same rate as White women, 1.7% of preterm births, 7.2% of low birth weight (LBW), 10.8% of small for gestational age (SGA) and 11.8% of early neonatal deaths would have been prevented. Percentages preventable were higher among Indigenous (22.2% of preterm births, 17.9% of LBW, 20.5% of SGA and 19.6% of early neonatal deaths) and Black women (6% of preterm births, 21.4% of LBW, 22.8% of SGA births and 20.1% of early neonatal deaths). AF was higher in groups with fewer years of education among Indigenous, Black and Parda for all outcomes. AF increased over time, especially among Indigenous populations.
    UNASSIGNED: A considerable portion of adverse birth outcomes and neonatal deaths could be avoided if ethnic-racial inequalities were non-existent in Brazil. Acting on the causes of these inequalities must be central in maternal and child health policies.
    UNASSIGNED: Bill & Melinda Gates Foundation and Wellcome Trust.
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