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Ethics, obligations, and imperatives in neonatology 新生儿学的伦理、义务和必要性。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-07-12 DOI: 10.1016/j.semperi.2025.152113
Christy L. Cummings
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引用次数: 0
Parental mental health & well-being in the NICU: Addressing the surgeon general’s advisory 新生儿重症监护室的父母心理健康与福祉:解决外科医生的建议。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-07-01 DOI: 10.1016/j.semperi.2025.152111
Kara Hansen , Tiffany Gladdis , Stephanie Kukora
The 2023 U.S. Surgeon General’s Advisory on the Mental Health and Well-Being of Parents highlights the critical role parents play in family and societal health and underscores the urgent need to address the growing mental health challenges faced by parents. For parents with an infant in the Neonatal Intensive Care Unit, the key stressors identified in the advisory - such as financial strain, lack of childcare, lack of paid or universal leave from employment, social isolation, and mental health stigma– are often compounded by the trauma, uncertainty, and emotional toll of hospitalization. The advisory calls for coordinated, systemic efforts to support parental mental health, which is critical in the Neonatal Intensive Care Unit where parental well-being directly impacts child outcomes.
2023年美国卫生局局长关于父母心理健康和福祉的咨询强调了父母在家庭和社会健康中发挥的关键作用,并强调迫切需要解决父母面临的日益严重的心理健康挑战。对于在新生儿重症监护室有婴儿的父母来说,咨询中确定的主要压力源——如经济压力、缺乏托儿服务、缺乏带薪或普遍休假、社会孤立和精神健康耻辱——往往因住院的创伤、不确定性和情感损失而加剧。该咨询呼吁协调一致,系统地努力支持父母的心理健康,这在新生儿重症监护病房至关重要,因为父母的福祉直接影响到儿童的结局。
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引用次数: 0
Looking beyond diagnoses to functioning: using the F words and personalizing care in neonatology 从诊断到功能:在新生儿学中使用F词和个性化护理。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-19 DOI: 10.1016/j.semperi.2025.152102
Emilie Thivierge , Thuy Mai Luu , Peter Rosenbaum , Paige Terrien Church , Rebecca Pearce , Annie Janvier
Extreme prematurity is associated with significant risk of mortality and morbidities. Neonatal follow-up assesses health outcomes of babies as they grow older to improve care and contribute to research and quality improvement initiatives. Recent investigations demonstrate that parents and clinicians/researchers disagree about what is defined as a “severe outcome”. Families report they need balanced information about functioning rather than medical diagnoses. Many functional domains other than the presence/absence of impairment are not evaluated during neonatal follow-up. This article recommends how to shift communication with parents of preterm infants throughout the NICU hospitalization – from discussions that are medicalized and deficit-based to those that reflect the processes of growth and development. This includes understanding family-important outcomes and how to communicate with parents using the ‘F-words’ for child development based on the World Health Organization’s integrated biopsychosocial framework for health: Functioning, Family, Fitness, Fun, Friends, and Future.
极端早产与死亡率和发病率的显著风险相关。新生儿随访评估婴儿长大后的健康结果,以改善护理,促进研究和质量改进举措。最近的调查表明,家长和临床医生/研究人员对“严重后果”的定义存在分歧。家庭报告说,他们需要的是有关功能的平衡信息,而不是医学诊断。在新生儿随访期间,除了存在/不存在损伤外,许多功能域未进行评估。本文建议如何在新生儿重症监护室住院期间转变与早产儿父母的沟通-从医疗化和基于缺陷的讨论到反映生长和发育过程的讨论。这包括了解家庭的重要结果,以及如何根据世界卫生组织的综合生物心理社会健康框架(功能、家庭、健身、乐趣、朋友和未来),使用儿童发展的“f字”与父母沟通。
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引用次数: 0
Ethical challenges and justice concerns for infants and children with life-limiting conditions and significant disability, including trisomy 13 and 18 有生命限制条件和严重残疾的婴儿和儿童的伦理挑战和正义问题,包括13和18三体。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-14 DOI: 10.1016/j.semperi.2025.152101
Alaina K. Pyle , Mark R. Mercurio
Some life-limiting conditions associated with significant neurodevelopmental impairment, such as trisomy 13/18, have historically been considered lethal, thus medical or surgical treatments would be inappropriate. Evolving literature has shown that early death is not universal, and though all who survive with trisomy 13/18 will have significant impairments, some experience a positive quality of life. The presence of bias impacts counseling as well as what interventions are offered and/or provided to families of a child with anticipated significant disability. Shared decision-making processes should include parents receiving all relevant information about comfort care as well as available, indicated, and ethically permissible medical/surgical interventions. Ethical frameworks can help clarify which options would be permissible to offer or withhold on an individualized basis. Clinicians are encouraged to be open to revisiting past and sometimes long-established practices regarding patients with disability. A willingness to change should not be perceived as an indictment of past practice.
一些与严重神经发育障碍相关的限制生命的疾病,如13/18三体,历来被认为是致命的,因此药物或手术治疗是不合适的。不断发展的文献表明,早死并不普遍,尽管所有患有13/18三体的人都会有严重的损伤,但有些人的生活质量很好。偏见的存在会影响咨询以及提供和/或提供给预期严重残疾儿童家庭的干预措施。共同的决策过程应包括父母接受有关舒适护理的所有相关信息,以及可用的、指示的和道德上允许的医疗/手术干预措施。道德框架可以帮助明确哪些选择是允许提供或保留在个人的基础上。鼓励临床医生重新审视过去的,有时是长期建立的关于残疾患者的做法。改变的意愿不应被视为对过去做法的控诉。
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引用次数: 0
An end to genetic exceptionalism: reframing the ethics of genomic sequencing for rapid neonatal diagnosis 结束遗传例外论:重构用于新生儿快速诊断的基因组测序伦理。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-14 DOI: 10.1016/j.semperi.2025.152110
Kaiulani S Shulman , Kristen Fishler Malone , Hadley Stevens Smith , Bimal P. Chaudhari , Monica H Wojcik
Exome or genome sequencing (ES/GS) is increasingly used as the first-line test for postnatal diagnosis of rare genetic conditions, especially in intensive care units (ICUs). Early concerns regarding the use of broad genetic testing centered on the potential for psychosocial harm, particularly related to unexpected or uncertain findings. As the usage of ES/GS has grown and evolved, the ethical concerns initially raised have not borne out in empirical measurement of patient and family experience. We therefore review the use of diagnostic genomic sequencing in the neonatal intensive care unit with comparison to other standard diagnostic tests that have not elicited similar ethical questioning. We frame this landscape within the concept of genetic contextualism rather than exceptionalism and suggest that this approach may lead to a more productive future for applied genomic medicine, especially for sick neonates and infants in the NICU.
外显子组或基因组测序(ES/GS)越来越多地被用作产后罕见遗传疾病诊断的一线检测,特别是在重症监护病房(icu)。早期对广泛使用基因检测的关注集中在潜在的社会心理伤害上,特别是与意外或不确定的结果有关。随着ES/GS的使用不断发展和演变,最初提出的伦理问题并没有在患者和家庭经验的实证测量中得到证实。因此,我们回顾了诊断基因组测序在新生儿重症监护病房的使用,并与其他标准诊断测试进行了比较,这些测试没有引起类似的伦理质疑。我们在遗传情境主义而非例外论的概念中构建了这一景观,并建议这种方法可能会导致应用基因组医学的更富有成效的未来,特别是对新生儿和新生儿重症监护病房的婴儿。
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引用次数: 0
Climate change and environmental degradation: bioethical considerations and impact for neonatal care 气候变化和环境退化:对新生儿护理的生物伦理考虑和影响。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-12 DOI: 10.1016/j.semperi.2025.152099
McKenna F Parnes , Luke Mosley , Heather H Burris , Elliott Mark Weiss
Climate change has severe consequences for neonatal health. Neonates are uniquely vulnerable to the impacts of climate change due to their developing bodies and immature immune and thermoregulatory systems. Climate change increases the risk of severe weather events, including extreme heat and natural disasters, as well as pollution and chemical exposures. The physiologic fragility of neonates and dependence on a stable environment require healthcare systems and policymakers to ensure protections are in place to mitigate health risks and potential impacts that will have long-lasting effects on individual development and well-being. The current article details the impacts of climate change on neonatal health across the lifecycle as well as the disproportionate consequences for communities most vulnerable to climate change. We provide evidence as to why this is a bioethical issue and offer recommendations for policies to protect neonatal health and promote environmental and climate justice.
气候变化对新生儿健康造成严重后果。新生儿由于其发育中的身体和不成熟的免疫和体温调节系统,特别容易受到气候变化的影响。气候变化增加了极端天气事件的风险,包括极端高温和自然灾害,以及污染和化学品暴露。新生儿的生理脆弱性和对稳定环境的依赖性要求卫生保健系统和政策制定者确保采取保护措施,以减轻健康风险和可能对个人发展和福祉产生长期影响的潜在影响。本文详细介绍了气候变化对整个生命周期的新生儿健康的影响,以及对最易受气候变化影响的社区造成的不成比例的后果。我们提供证据说明为什么这是一个生物伦理问题,并为保护新生儿健康和促进环境和气候正义的政策提供建议。
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引用次数: 0
Disability, ableism, and decision-making at extreme prematurity 残疾,残障,以及过早的决策。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-11 DOI: 10.1016/j.semperi.2025.152098
Anne Sullivan , Jennifer Arnold , Sheria Wilson , Kaiulani Shulman , Fabiana Bacchini , Paige Church
Ableism plays a pervasive yet often unexamined role in decision-making at extreme prematurity. This review examines how ableist assumptions about quality of life, normalcy, and parental burden can shape clinical counseling and influence decisions regarding resuscitation and intensive care for extremely preterm infants. Drawing on literature from neonatology, disability studies, and bioethics, the article explores the historical and sociocultural roots of ableist thinking in medicine and its manifestations in prognostic framing, risk communication, and institutional norms. Strategies for recognizing and addressing ableism in clinical practice are reviewed, including approaches to anti-ableist communication, family-centered care, and medical education reform. The article argues that adopting an explicitly anti-ableist stance is essential for promoting ethical, inclusive, and genuinely shared decision-making in the neonatal intensive care unit (NICU) and calls for greater interdisciplinary collaboration to support systemic change.
残疾歧视在极度早产儿的决策中发挥着普遍但往往未经审查的作用。本综述探讨了关于生活质量、正常状态和父母负担的健康主义假设如何影响临床咨询,并影响极早产儿复苏和重症监护的决定。本文借鉴了新生儿学、残疾研究和生物伦理学的文献,探讨了医学中残疾主义思想的历史和社会文化根源,以及它在预后框架、风险沟通和制度规范方面的表现。本文回顾了在临床实践中识别和解决残疾歧视的策略,包括反残疾歧视沟通、以家庭为中心的护理和医学教育改革的方法。本文认为,采取明确的反残疾主义立场对于促进新生儿重症监护病房(NICU)的道德、包容和真正共享决策至关重要,并呼吁加强跨学科合作以支持系统性变革。
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引用次数: 0
Injustice and inequality in the provision of perinatal palliative care 提供围产期姑息治疗方面的不公正和不平等。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-04 DOI: 10.1016/j.semperi.2025.152097
Matthew Lin , Sophie Bertaud , Dominic Wilkinson
Perinatal palliative care (PnPC) is a relatively new branch of pediatric palliative care (PPC), which focuses on providing holistic care in the antenatal, delivery, and neonatal settings. In this paper, we address previously unexplored justice-based ethical questions related to the provision of PnPC. We examine why some families who receive the diagnosis of a potentially life-limiting condition in their baby before or after birth receive PnPC support whilst others do not. We describe current inequities in the access to, and delivery of, PnPC. Drawing on philosophical theory (the Capabilities Approach) we argue that palliative care represents a valuable capability for babies with life limiting illness and their families. Health professionals should advocate for and promote access to this option for all families, regardless of whether it is ultimately taken up.
围产期姑息治疗(PnPC)是儿科姑息治疗(PPC)的一个相对较新的分支,其重点是在产前、分娩和新生儿环境中提供整体护理。在本文中,我们解决了先前未探索的与PnPC提供相关的基于正义的伦理问题。我们研究了为什么一些在婴儿出生前或出生后被诊断出可能限制生命的家庭得到了PnPC支持,而另一些却没有。我们描述了目前在获取和提供PnPC方面的不公平现象。根据哲学理论(能力方法),我们认为姑息治疗对患有生命限制疾病的婴儿及其家庭来说是一种有价值的能力。卫生专业人员应倡导和促进所有家庭获得这种选择,无论最终是否采用这种选择。
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引用次数: 0
Preserving medical ethics in the era of artificial intelligence: Challenges and opportunities in neonatology 维护人工智能时代的医学伦理:新生儿科的挑战与机遇。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-04 DOI: 10.1016/j.semperi.2025.152100
Tanima Arora , Habeebah Muhammad-Kamal , Kristyn Beam
The integration of artificial intelligence (AI) into neonatology offers improved patient care while raising ethical challenges across four principles: beneficence, non-maleficence, justice, and autonomy. AI enhances prediction and early detection capabilities, but introduces concerns including the “black box” nature of many algorithms, which compromises transparency and may propagate existing biases. Justice considerations arise from potential inequities in AI development and deployment. Autonomy is challenged when clinicians cannot fully explain algorithmic decision-making, affecting shared decision-making with families. These ethical tensions are particularly acute in neonatology, where decisions impact vulnerable patients who cannot advocate for themselves. Mitigating these challenges requires developing transparent AI systems, ensuring diverse training data, maintaining human oversight of clinical decisions, and conducting rigorous validation across diverse healthcare settings. Responsible implementation requires balancing technological benefits with ethical principles.
将人工智能(AI)整合到新生儿医学中,在改善患者护理的同时,也提出了四个原则的伦理挑战:慈善、无害、正义和自主。人工智能增强了预测和早期检测能力,但也带来了一些担忧,包括许多算法的“黑箱”性质,这会损害透明度,并可能传播现有的偏见。在人工智能的开发和部署中,潜在的不公平现象引起了司法方面的考虑。当临床医生不能完全解释算法决策时,自主性受到挑战,影响与家庭的共同决策。这些伦理上的紧张关系在新生儿学中尤其严重,在新生儿学中,决定会影响那些无法为自己辩护的弱势患者。缓解这些挑战需要开发透明的人工智能系统,确保多样化的训练数据,维护人类对临床决策的监督,并在不同的医疗保健环境中进行严格的验证。负责任的实施需要平衡技术利益和道德原则。
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引用次数: 0
Infections during pregnancy: An ongoing threat 妊娠期感染:持续威胁。
IF 3.2 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Pub Date : 2025-06-01 DOI: 10.1016/j.semperi.2025.152075
Claudia Fernandes Lorea , Katherine Pressman , Lavinia Schuler-Faccini
Congenital infections are an ongoing relevant cause of congenital and perinatal abnormalities since effective vaccination is not available for many diseases. Moreover, climate change, mutational evolution of pathogens, or their vectors associated with intense human traveling predispose to outbreaks and modification of the geographic distribution of traditionally limited infectious diseases. Here, we review the so-called TORCH infections (toxoplasmosis, others, rubella, cytomegalovirus, herpes) with a special emphasis on the arboviral infections (zika, dengue, chikungunya, oropouche). Although respiratory viruses are rarely transmitted through the placenta, the maternal condition itself can cause adverse effects on the developing embryo/fetus (COVID-19, influenza). Some perinatal-acquired infections will also be briefly discussed due to their relevance in the child's development. The majority of teratogenic congenital and some perinatal-acquired infections have effects on the central nervous system or sensory organs with long-lasting disabilities. Vaccines are unavailable for several teratogenic or perinatal infections, and treatment options are still limited, particularly for arboviral and other emergent diseases. Social inequalities are associated with the prevalence, fetal outcomes and long-term disabilities of these diseases. The One Health approach could be an essential way to reduce the burden of these diseases in the population.
先天性感染是先天性和围产期异常的持续相关原因,因为许多疾病没有有效的疫苗接种。此外,气候变化、病原体的突变演变或与人类密集旅行有关的病媒容易导致传统上有限的传染病的暴发和地理分布的改变。在这里,我们回顾了所谓的TORCH感染(弓形虫病,其他,风疹,巨细胞病毒,疱疹),特别强调虫媒病毒感染(寨卡,登革热,基孔肯雅,oropouche)。虽然呼吸道病毒很少通过胎盘传播,但母体状况本身会对发育中的胚胎/胎儿造成不利影响(COVID-19、流感)。一些围产期获得性感染也将简要讨论,因为它们与儿童的发展有关。大多数先天性致畸和一些围产期获得性感染对中枢神经系统或感觉器官有影响,具有长期残疾。几种致畸或围产期感染无法获得疫苗,治疗选择仍然有限,特别是对虫媒病毒和其他紧急疾病。社会不平等与这些疾病的流行、胎儿结局和长期残疾有关。“同一个健康”方针可能是减轻这些疾病在人口中的负担的重要途径。
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引用次数: 0
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Seminars in perinatology
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