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Nursing Continuing Professional Development Activities: May/June 2025. 护理持续专业发展活动:2025年5月/ 6月。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/0730-0832.44.3.220
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引用次数: 0
The Ins and Outs of the Complete Blood Count With Differential: Back to Basics. 全血细胞计数的来龙去脉与差异:回到基础。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0072
Colleen Reilly Moss, Michele Savin, Curry Bordelon, Leann Baker

A complete blood count (CBC) with differential is an essential laboratory test used to evaluate overall physiologic health and detect potential disorders in neonates. This test provides valuable insights into various blood cell types and structures and offers information on infections, immune status, anemia, and other hematologic conditions. Given the unique physiology and susceptibility of neonates to infections and other complications, interpreting the CBC with differential results in this population requires a specialized approach. The purpose of this article is to describe the components of the CBC and provide the reader with a neonatal case study to analyze and calculate values from within the CBC. The article also highlights common disorders causing abnormal neonatal CBC values and potential outcomes.

全血细胞计数(CBC)与差异是一个必要的实验室测试,用于评估整体生理健康和发现潜在的疾病在新生儿。该测试提供了对各种血细胞类型和结构的有价值的见解,并提供了感染、免疫状态、贫血和其他血液学状况的信息。鉴于新生儿独特的生理和对感染和其他并发症的易感性,在这一人群中解释不同结果的CBC需要一个专门的方法。本文的目的是描述CBC的组成部分,并为读者提供新生儿案例研究,以分析和计算CBC内的值。文章还强调了引起新生儿异常CBC值和潜在结果的常见疾病。
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引用次数: 0
Parental Knowledge and Understanding of Respiratory Syncytial Virus and How to Decrease the Risk of Infection: The Canadian Premature Babies Foundation Survey 2023. 父母对呼吸道合胞病毒的知识和了解以及如何降低感染风险:加拿大早产儿基金会调查2023。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0064
Marianne Bracht, Fabiana Bacchini, Barry Rodgers-Gray, James O Edwards, Bosco A Paes

The purpose of this survey is to evaluate parental knowledge of respiratory syncytial virus (RSV) and its prevention. The study design used is an online survey. A total of 331 Canadian parents of preterm infants completed the survey. The main outcome variables used in the survey are knowledge of RSV, sources of information, and understanding strategies to decrease the risk of RSV infection. Of the participants, 99.4% understood the seriousness of RSV, but 19.6% were not confident in their knowledge. Respiratory syncytial virus education was provided to 75.6% in the hospital. 98.7% of uninformed parents wished they had been enlightened. Postdischarge, 60.5% felt unconfident in protecting their infant, and 70.8% searched for information. Health care professionals were the recommended source for RSV information (82.4-85.0%). Despite 98.6% understanding the importance of childhood immunizations, 24.1% remained anxious. Moreover, 65.4% received information about palivizumab, and 97.0% were confident about its use. Although 79.4% were unaware of nirsevimab, 75.4% would accept it. For maternal RSV vaccination, acceptability was 72.6%. Parents require accurate, reliable, and consistent information on RSV and its prevention, delivered to them in the NICU, following discharge, and via reputable online resources. Health care professionals, both in the NICU and community, should be well-informed and receive regular education throughout the year on RSV and the latest thinking on prevention.

本调查的目的是评估父母对呼吸道合胞病毒(RSV)及其预防的知识。使用的研究设计是在线调查。共有331名加拿大早产儿父母完成了这项调查。调查中使用的主要结果变量是对呼吸道合胞病毒的认识、信息来源以及对降低呼吸道合胞病毒感染风险的策略的了解。在参与者中,99.4%的人了解RSV的严重性,但19.6%的人对自己的知识没有信心。75.6%的患者接受了呼吸道合胞病毒教育。98.7%不知情的父母希望他们受到了启发。出院后,60.5%的人对保护婴儿没有信心,70.8%的人搜索过信息。卫生保健专业人员是RSV信息的推荐来源(82.4-85.0%)。尽管98.6%的人了解儿童免疫接种的重要性,但仍有24.1%的人感到焦虑。此外,65.4%的人获得了关于帕利珠单抗的信息,97.0%的人对其使用有信心。虽然79.4%的人不知道nirsevimab,但75.4%的人会接受它。对于母亲RSV疫苗接种,可接受度为72.6%。父母需要准确、可靠和一致的关于呼吸道合胞病毒及其预防的信息,在新生儿重症监护室,出院后,通过信誉良好的在线资源提供给他们。新生儿重症监护室和社区的卫生保健专业人员应充分了解情况,并全年定期接受关于呼吸道合胞病毒和最新预防思想的教育。
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引用次数: 0
Does Prehabilitative Oromotor Stimulation Have Any Impact on Feeding Performance of Preterm Infants During Hospital Stay and in Early Infancy: Findings From a Randomized Controlled Trial. 康复性运动刺激是否对早产儿住院期间和婴儿期早期的喂养表现有任何影响:一项随机对照试验的结果
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0071
Suvashri Sasmal, Asha P Shetty, Bijan Saha, Brenda Knoll, Suchandra Mukherjee, Sangita Mazumder

This study investigates the impact of a prehabilitative oromotor stimulation, namely, premature infant oral motor intervention (PIOMI), on feeding performance in preterm infants during hospitalization and early infancy. In this randomized, blinded clinical trial, 130 preterm infants (26-32 weeks PMA) were randomly assigned to either the intervention group, which received PIOMI, or the control group. PIOMI was administered twice daily for 5 minutes, approximately 15-20 minutes before feeding, starting at 30 weeks' gestation. Follow-up assessments were conducted until 6 months of corrected age. The results demonstrated that infants in the intervention group showed significantly improved feeding performance scores (p < .001), achieved independent oral feeding at lower body weights (p < .001), and had a shorter hospitalization period (p < .05). Additionally, a greater proportion of infants in the intervention group were on mothers' milk at discharge and sustained breastfeeding until 6 months of corrected age (p < 0.005). The findings highlight the effectiveness of PIOMI as a prehabilitative strategy to enhance feeding performance, reduce hospital stays, and promote sustained breastfeeding in preterm neonates.

本研究探讨了康复性口腔运动刺激,即早产儿口腔运动干预(PIOMI)对早产儿住院期间和婴儿期喂养表现的影响。在这项随机、盲法临床试验中,130名早产儿(PMA为26-32周)被随机分配到接受PIOMI治疗的干预组和对照组。从妊娠30周开始,每天两次,每次5分钟,大约在喂养前15-20分钟给药。随访评估一直进行到矫正年龄6个月。结果显示,干预组婴儿喂养表现评分显著提高(p < 0.001),实现了较低体重的独立口服喂养(p < 0.001),住院时间较短(p < 0.05)。此外,干预组婴儿出院时使用母乳并持续母乳喂养至矫正年龄6个月的比例更高(p < 0.005)。研究结果强调了PIOMI作为一种提高喂养性能、减少住院时间和促进早产儿持续母乳喂养的康复策略的有效性。
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引用次数: 0
Prevalence and Risk Factors of Congenital Hearing Loss in Turkey: A Systematic Review. 先天性听力损失的患病率和危险因素在土耳其:一个系统的回顾。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0054
Yasemin Sökmen, Resmiye Kaya Odabaş, Ayten Taşpinar

Congenital hearing loss hinders the child's social, emotional, and intellectual development. This systematic review was planned because the determination of congenital hearing loss and risk factors will guide health service planning. This systematic review was conducted based on previous studies in Turkey to determine the prevalence and the risk factors of newborn congenital hearing loss. This systematic review was conducted between November 2020 and February 2021; Google Scholar, PubMed, ScienceDirect, EBSCOhost, and Springer electronic databases were screened with the keywords "newborn hearing screening" and "congenital hearing loss." According to the results of the systematic review of 13 studies, 1 prospective and 12 retrospective, the prevalence of congenital hearing loss is 0.5% and 1.1% in those with risk factors; newborns are screened within 1 month, diagnosed within 2 months on average, and intervened with between the 3rd and 14th months; and the most common risk factors for hearing loss are admission in intensive care/mechanical ventilation for more than 5 days/history of ototoxic drug use, hyperbilirubinemia requiring an exchange transfusion/phototherapy, prematurity, consanguineous marriage, and family history of hearing loss, respectively.

先天性听力损失会阻碍儿童的社交、情感和智力发展。本系统综述计划是因为先天性听力损失和危险因素的确定将指导卫生服务计划。本系统综述是在土耳其以往研究的基础上进行的,以确定新生儿先天性听力损失的患病率和危险因素。该系统评价于2020年11月至2021年2月期间进行;谷歌Scholar、PubMed、ScienceDirect、EBSCOhost和施普林格电子数据库以“新生儿听力筛查”和“先天性听力损失”为关键词进行筛选。根据系统评价13项研究,1项前瞻性研究和12项回顾性研究的结果,先天性听力损失在有危险因素人群中的患病率分别为0.5%和1.1%;新生儿在1个月内进行筛查,平均在2个月内进行诊断,并在第3至14个月之间进行干预;最常见的听力损失危险因素分别为重症监护/机械通气超过5天/耳毒性药物使用史、需要换血/光疗的高胆红素血症、早产、近亲结婚和听力损失家族史。
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引用次数: 0
Genetics Review: Joubert Syndrome. 遗传学评论:Joubert综合征。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0052
Audrey M Tran, Amy J Jnah, Mauricio J De Castro Pretelt

Joubert syndrome (JS) is a rare neurodevelopmental and multisystem ciliopathy that affects 1 in 80,000-10,0000 infants globally per year. Classic defects include hypoplasia of the cerebellar vermis, thickened cerebellar peduncles, and deepened interpeduncular fossa, which is regarded as a "molar tooth" sign. More than 30 genes have been associated with JS. Gene mutations disrupt normal ciliary development and function during early embryogenesis and cause a vast array of symptoms and pathologies. The purpose of this article is to investigate this rare and complex medical condition. We present up-to-date information on the genetics, pathophysiology, clinical manifestations, diagnostics, and management of JS. We also include a valuable perspective from a pediatric geneticist who specializes in JS to enhance our understanding of challenges associated with making a molecular diagnosis and emphasize the importance of early recognition and diagnostics as a means to optimize the quality of care.

Joubert综合征(JS)是一种罕见的神经发育和多系统纤毛病,每年全球每8万至10万名婴儿中就有1人患病。典型的缺陷包括小脑蚓部发育不全,小脑梗增厚,小脑梗间窝加深,被认为是“磨牙”的征象。超过30个基因与JS相关。基因突变在胚胎发生早期破坏正常的纤毛发育和功能,并引起大量的症状和病理。本文的目的是研究这种罕见而复杂的医疗状况。我们介绍了JS的遗传学、病理生理学、临床表现、诊断和治疗方面的最新信息。我们还包括一位专门研究JS的儿科遗传学家的宝贵观点,以增强我们对与分子诊断相关的挑战的理解,并强调早期识别和诊断作为优化护理质量的手段的重要性。
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引用次数: 0
Bridging Knowledge and Practice: Insights Into Hirschsprung's Disease and Home Management. 衔接知识与实践:巨结肠疾病与家庭管理的见解。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0067
Stephanie Culnan, Alyssa Carlson, Meredith L Farmer

Hirschsprung's disease (HD) is a congenital intestinal motility disorder characterized by the absence of ganglionic cells in the distal intestine, leading to functional bowel obstruction and affecting 1 in every 5,000 neonates. A serious complication of HD is Hirschsprung-associated enterocolitis (HAEC), a life-threatening systemic illness responsible for a significant proportion of HD-related mortality. Proper management of HD, especially preventing HAEC, includes the use of rectal irrigations, which caregivers must master before their neonate's discharge. However, barriers such as short NICU stays and lack of standardized parental education hinder successful home care. This article provides an overview of HD pathophysiology, clinical manifestations, diagnostics, and management, alongside a practical parent education tool for rectal irrigation techniques to enhance at-home care and reduce morbidity.

先天性巨结肠病(HD)是一种先天性肠道运动障碍,其特征是远端肠缺乏神经节细胞,导致功能性肠梗阻,每5000名新生儿中就有1名患者。HD的一个严重并发症是先天性巨结肠相关小肠结肠炎(HAEC),这是一种危及生命的全身性疾病,占HD相关死亡率的很大比例。HD的正确管理,特别是预防HAEC,包括使用直肠冲洗,护理人员必须在新生儿出院前掌握。然而,诸如新生儿重症监护室停留时间短和缺乏标准化父母教育等障碍阻碍了成功的家庭护理。本文概述了HD的病理生理学、临床表现、诊断和管理,以及直肠冲洗技术的实用家长教育工具,以加强家庭护理和降低发病率。
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引用次数: 0
Academy News. 学院新闻。
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN.44.3.news
Debbie Fraser, Rachel Joseph, Sheron Wagner, Sandra Hubbard, Stephanie Abbu, Kathryn Rudd, Meredith L Farmer
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引用次数: 0
Transition to Practice: Are You Ready? 向实践过渡:你准备好了吗?
IF 0.6 Q4 NURSING Pub Date : 2025-06-01 DOI: 10.1891/NN-2024-0063
Curry Bordelon
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引用次数: 0
A Quality Improvement Initiative to Increase Skin-to-Skin Care and Positive Parent Touch. 一项质量改进倡议,以增加皮肤对皮肤的护理和积极的父母接触。
IF 0.6 Q4 NURSING Pub Date : 2025-04-01 DOI: 10.1891/NN-2024-0047
Rachelle Sey, Katherine Coughlin

Positive parent touch (PPT), including skin-to-skin care (STSC) and containment, is an evidence-based practice that provides short- and long-term benefits to preterm infants, while also improving parent-infant attachment and reducing parental stress. This quality improvement (QI) initiative aimed to decrease average days from birth to first STSC in infants born less than 29 weeks' gestation from 14.2 days to 7 days. A secondary aim was to decrease the average number of hours from birth to first PPT in the same population from 41.3 hours to ≤24 hours. Data were stratified by ethnicity to identify disparities. Using the Model for Improvement, a multidisciplinary team collaborated to identify barriers to early STSC implementing strategic interventions to improve STSC and PPT. Data were monitored and analyzed using statistical process control and run charts. An improvement was noted in mean days for STSC from a baseline of 14.2-3.3 days. Similarly, an improvement was noted in mean hours for PPT from a baseline of 41.3 hours to 28 hours. This NICU improved and sustained time to first STSC and PPT in preterm infants by combining QI methods with a family-centered care approach that emphasized neuroprotection and parent involvement.

积极的父母接触(PPT),包括皮肤对皮肤护理(STSC)和遏制,是一种基于证据的做法,可为早产儿提供短期和长期益处,同时还能改善亲子依恋并减轻父母的压力。这项质量改进(QI)计划旨在将妊娠不足29周的婴儿从出生到首次STSC的平均天数从14.2天减少到7天。第二个目标是将同一人群从出生到首次PPT的平均小时数从41.3小时减少到≤24小时。数据按种族分层,以确定差异。利用改进模型,一个多学科团队合作确定了早期STSC实施战略干预以改善STSC和PPT的障碍。采用统计过程控制和运行图对数据进行监测和分析。STSC的平均天数从14.2-3.3天的基线有所改善。同样,PPT的平均小时数也从41.3小时基线提高到28小时。该NICU通过将QI方法与强调神经保护和父母参与的以家庭为中心的护理方法相结合,改善并维持了早产儿首次STSC和PPT的时间。
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引用次数: 0
期刊
Neonatal Network
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