Neonatal death

新生儿死亡
  • 文章类型: Journal Article
    尽管努力减少死产和新生儿死亡,不一致的定义和报告做法继续阻碍全球进展。现有数据在质量和各国之间的可比性方面经常受到限制。本文通过概述新的国际疾病分类(ICD-11)建议来解决这一关键问题,以标准化记录和报告围产期死亡,以提高数据准确性和国际比较。ICD-11的主要进步包括使用胎龄作为报告的主要阈值,对测量和记录胎龄有更清晰的指导,并按胎龄亚组报告死亡率,以使国家比较能够包括相似的人群(例如,所有出生时间为154天[22+0周]或196天[28+0周])。此外,修订后的ICD-11指南进一步澄清了将终止妊娠(人工流产)从围产期死亡率统计中排除的问题.实施ICD-11中规定的标准化记录和报告方法对于有关死产和围产期死亡的准确全球数据至关重要。这种高质量的数据既可以进行适当的区域和国际比较,也可以作为改善临床实践以及流行病学和健康监测的资源,使有限的计划和研究资金能够集中于结束可预防的死亡,并改善每个妇女和每个婴儿的成果,无处不在。
    Despite efforts to reduce stillbirths and neonatal deaths, inconsistent definitions and reporting practices continue to hamper global progress. Existing data frequently being limited in terms of quality and comparability across countries. This paper addresses this critical issue by outlining the new International Classification of Disease (ICD-11) recommendations for standardized recording and reporting of perinatal deaths to improve data accuracy and international comparison. Key advancements in ICD-11 include using gestational age as the primary threshold to for reporting, clearer guidance on measurement and recording of gestational age, and reporting mortality rates by gestational age subgroups to enable country comparisons to include similar populations (e.g., all births from 154 days [22+0 weeks] or from 196 days [28+0 weeks]). Furthermore, the revised ICD-11 guidance provides further clarification around the exclusion of terminations of pregnancy (induced abortions) from perinatal mortality statistics. Implementing standardized recording and reporting methods laid out in ICD-11 will be crucial for accurate global data on stillbirths and perinatal deaths. Such high-quality data would both allow appropriate regional and international comparisons to be made and serve as a resource to improve clinical practice and epidemiological and health surveillance, enabling focusing of limited programmatic and research funds towards ending preventable deaths and improving outcomes for every woman and every baby, everywhere.
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  • 文章类型: Journal Article
    犬甲疱疹病毒-1(CaHV-1)可能导致新生儿幼崽高度致命的出血性疾病,并与生殖有关,老年犬的呼吸道和眼部疾病。虽然假设有一个世界范围的分布,在澳大利亚很少有CaHV-1的报道。这项研究的目的是调查汤斯维尔一个居住郊区的家犬中CaHV-1的血清阳性率,以及参加该地区两次狗展的狗。研究参与者是通过挨家挨户的非概率抽样招募的(道格拉斯狗,n=185)或被邀请参加(展示狗;n=76)。狗主人完成了一份调查问卷,调查了最近接触CaHV-1的可能危险因素。使用可商购的ELISA测定来自每只狗的血清样品的抗CaHV-1抗体。使用单变量分析和多变量逻辑回归模型分析了血清阳性犬与所有者报告的危险因素之间的关联。Douglas和Show犬的CaHV-1血清阳性率为11.4%(95%CI6.8-15.9%)和17.1%(95%CI5.5-28.8),分别,合并血清阳性率为13%(95%CI8.3-17.7%)。在过去3个月内患有结膜炎或参与繁殖的狗更有可能对CaHV-1呈血清阳性。没有发现其他显著的危险因素。总之,CaHV-1在北昆士兰州的狗中循环,可能导致该地区胎儿和新生儿的损失。
    Canid alphaherpesvirus-1 (CaHV-1) may cause a highly fatal haemorrhagic disease in neonatal pups and is associated with reproductive, respiratory and ocular disease in older dogs. Although assumed to have a world-wide distribution, there have been few reports of CaHV-1 in Australia. The aim of this study was to investigate the seroprevalence of CaHV-1 in household dogs in a residential suburb in Townsville, as well as in dogs attending two dog shows in the region. Study participants were recruited through door-to-door non-probability sampling (Douglas dogs, n = 185) or invited to participate (Show dogs; n = 76). Dog owners completed a questionnaire that investigated possible risk factors for recent exposure to CaHV-1. A serum sample from each dog was assayed for anti-CaHV-1 antibodies using a commercially available ELISA. Associations between seropositive dogs and owner-reported risk factors were analysed using univariable analysis and multivariable logistic regression models. The seroprevalence of CaHV-1 was 11.4 % (95 % CI 6.8-15.9 %) and 17.1 % (95 % CI 5.5-28.8) for the Douglas and Show dogs, respectively, with a pooled seroprevalence of 13 % (95 % CI 8.3-17.7 %). Dogs that had suffered from conjunctivitis within the previous 3 months or were involved in breeding were more likely to be seropositive to CaHV-1. No other significant risk factors were identified. In conclusion, CaHV-1 is circulating in dogs in North Queensland and may be contributing to foetal and neonatal losses in this region.
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  • 文章类型: Case Reports
    病人,一个34岁的primigravida没有既往病史,在23+0周出现妊娠期高血压和胎儿生长受限(FGR)。超声检查显示胎盘肿块,随后的重复超声扫描显示质量的回声变化,怀疑巨大的绒毛膜下血栓血肿(MST)。虽然血压轻度升高,但没有蛋白尿和器官功能障碍,血清可溶性fms样酪氨酸激酶-1/胎盘生长因子(sFlt-1/PlGF)的比值显着升高。由于胎儿状况不可靠,在29+2周时进行了剖宫产。女婴,在1/5分钟时Apgar评分为1/1,脐动脉pH值为7.16,在分娩后7小时仍无反应并死亡。病理检查显示绒毛膜下间隙有大量血肿,22毫米厚,脐带附件正下方。该病例强调了重复胎盘超声在MST诊断中的重要性,并表明sFlt-1/PlGF比值在预测不良结局中的潜在效用。
    The patient, a 34-year-old primigravida with no prior medical history, presented at 23 + 0 weeks with gestational hypertension and fetal growth restriction (FGR). Ultrasound examination showed a placental mass, and subsequent repeated ultrasound scans revealed changes in the mass\' echogenicity, raising suspicion of a massive subchorionic thrombohematoma (MST). While the blood pressure was mildly elevated without proteinuria and organ dysfunctions, serum soluble fms-like tyrosine kinase-1/placental growth factor (sFlt-1/PlGF) ratios showed significantly elevated values. A cesarean section was performed at 29 + 2 weeks due to the nonreassuring fetal status. The female infant, with Apgar scores of 1/1 at one/five minutes and an umbilical artery pH of 7.16, remained unresponsive and died seven hours postdelivery. Pathology examination revealed a massive hematoma in the subchorionic space, measuring 22 mm thick, directly beneath the umbilical cord attachment. This case underscores the importance of repetitive placental ultrasound in MST diagnosis and suggests the potential utility of sFlt-1/PlGF ratios in predicting adverse outcomes.
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  • 文章类型: Journal Article
    背景:双胎妊娠与围产期发病风险增加相关。此外,如果一个双胞胎发生宫内死亡,它增加了围生期和出生后存活的双胎的发病率。
    目的:本研究的目的是确定双胎妊娠中单胎宫内死亡(SIUFD)的发生率,以及根据存活的双胎并发症的维度定义的胎儿结局。
    方法:从医学研究生学院中央记录部(CRD)的劳动室记录中回顾性地收集了五年(从2015年到2019年)的双胎妊娠数据。教育和研究,昌迪加尔,印度。对SIUFD病例进行了单独研究,分娩后对新生儿进行了长达3至8年的随访。纳入标准是妊娠14周后双胎妊娠的SIUFD,妊娠早期超声检查预先定义的绒毛膜性。排除标准为高阶妊娠和单羊膜双胎。
    结果:在研究期间共进行了1246例(4.273%)双胎分娩。其中,107例(8.587%)妊娠患有SIUFD,双胞胎在子宫内存活。其中,77例(72%)为双胎双胎妊娠,30例(28%)为单胎双胎妊娠。SIUFD的发生率为8.5%。早产是我们研究中观察到的最常见的并发症,在DCDA和MCDA双胞胎中分别有53.5%和58.3%的参与者中发现。分别。在29.2%的SIUFD单绒毛膜双胞胎中发现了存活双胞胎的早期新生儿死亡(生命的24小时内)。妊娠<28周时SIUFD导致存活双胞胎的早期新生儿死亡更多。神经发育障碍(脑瘫,发育迟缓,癫痫)在出生后的人口中为7.5%(n=93)。
    结论:双胎妊娠合并SIUFD的早产发生率增加,增加了幸存的双胞胎的新生儿死亡,和神经发育障碍(脑瘫,发育迟缓,癫痫)。妊娠<28周时的单发性和SIUFD与同胎中新生儿死亡增加有关。神经发育障碍的发病率与绒毛膜不直接相关,但是单绒毛膜组的发育迟缓更为深刻。
    BACKGROUND: Twin pregnancy is associated with an increased risk of perinatal morbidity. Besides, if intrauterine death of a single twin occurs, it increases the morbidity of the surviving co-twin perinatally and postnatally.
    OBJECTIVE:  The objective of this study was to determine the incidence of single intrauterine fetal death (SIUFD) in a twin pregnancy and fetal outcome defined in dimensions according to the complications in the surviving co-twin.
    METHODS: Data on twin pregnancies were collected retrospectively for a period of five years (from 2015 to 2019) from the labour room records of the Central Records Department (CRD) at the Postgraduate Institute of Medical Education and Research, Chandigarh, India. Cases with SIUFD were studied individually and neonatal follow-up was taken post delivery for up to three to eight years. Inclusion criteria were SIUFD in twin pregnancies after 14 weeks gestation, chorionicity pre-defined by early trimester ultrasonography. Exclusion criteria were higher-order pregnancy and monoamniotic twins.
    RESULTS: A total of 1246 (4.273%) twin deliveries were conducted in the study period. Of these, 107 (8.587%) pregnancies had SIUFD with co-twin surviving in utero. Among these, 77 (72%) were dichorionic diamniotic (DCDA) twin pregnancies and 30 (28%) were monochorionic diamniotic (MCDA) twin pregnancies. The incidence of SIUFD was 8.5%. Preterm birth was the most common complication observed in our study and was found in 53.5% and 58.3% of participants in DCDA and MCDA twins, respectively. Early neonatal death (within 24 hours of life) of the surviving twin was found in 29.2% monochorionic twins with SIUFD. SIUFD at < 28 weeks gestation led to a greater number of early neonatal deaths of surviving twins. The incidence of neurodevelopmental disorders (cerebral palsy, developmental delay, epilepsy) in our population after birth was 7.5% (n=93).
    CONCLUSIONS: Twin pregnancies with SIUFD have an increased incidence of preterm labour, increased neonatal death of the surviving twin, and neurodevelopmental disorders (cerebral palsy, developmental delay, epilepsy). Monochorionicity and SIUFD at <28 weeks gestation are associated with increased neonatal deaths in co-twin. The Incidence of neurodevelopmental disorders is not directly associated with chorionicity, but developmental delay is more profoundly seen in the monochorionic group.
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  • 文章类型: Journal Article
    背景:研究COVID-19大流行对围产期死亡风险的影响的人群水平研究结果差异很大。
    目的:使用妊娠队列方法,探讨在大流行之前和期间开始的妊娠中围产期死亡风险的趋势。
    方法:这项次要分析包括艾伯塔省单胎妊娠≥20周的数据,加拿大,从2017年3月5日至2021年3月4日开始。围产期死亡(即死产或新生儿死亡)是考虑的主要结局。此结果的风险是针对妊娠与大流行重叠的妊娠(即没有,0-20周,整个怀孕)。中断的时间序列分析用于进一步确定感兴趣时间段的结果的时间趋势。
    结果:在分析期间有190,853例怀孕。总的来说,围产期死亡的风险随着大流行暴露水平的增加而降低;这一结局以1.0%(95%置信区间[CI]0.9,1.0)出现,0.9%(95%CI0.8,1.1)和0.8%(95%CI0.7,0.9)无重叠妊娠,部分重叠和完全重叠的大流行分别。在大流行期间开始的具有较高的产前风险评分的妊娠与之前开始的妊娠相比,其导致围产期死亡的频率较低;分别为3.3%(95%CI2.7,3.9)和5.7%(95%CI5.0,6.5)。中断的时间序列分析显示,在COVID-19大流行开始前≤40周(即大流行暴露)开始的妊娠围产期死亡呈下降趋势,大流行前>40周开始妊娠的趋势(即没有大流行暴露)。
    结论:我们观察到与艾伯塔省COVID-19大流行重叠的妊娠围产期死亡减少,特别是在这些结果的高风险人群中。在我们的环境中,具体的大流行控制措施和政府应对计划可能促成了这一发现。
    BACKGROUND: Results of population-level studies examining the effect of the COVID-19 pandemic on the risks of perinatal death have varied considerably.
    OBJECTIVE: To explore trends in the risk of perinatal death among pregnancies beginning prior to and during the pandemic using a pregnancy cohort approach.
    METHODS: This secondary analysis included data from singleton pregnancies ≥20 weeks\' gestation in Alberta, Canada, beginning between 5 March 2017 and 4 March 2021. Perinatal death (i.e. stillbirth or neonatal death) was the primary outcome considered. The risk of this outcome was calculated for pregnancies with varying gestational overlap with the pandemic (i.e. none, 0-20 weeks, entire pregnancy). Interrupted time series analysis was used to further determine temporal trends in the outcome by time period of interest.
    RESULTS: There were 190,853 pregnancies during the analysis period. Overall, the risk of perinatal death decreased with increasing levels of pandemic exposure; this outcome was experienced in 1.0% (95% confidence interval [CI] 0.9, 1.0), 0.9% (95% CI 0.8, 1.1) and 0.8% (95% CI 0.7, 0.9) of pregnancies with no overlap, partial overlap and complete pandemic overlap respectively. Pregnancies beginning during the pandemic that had high antepartum risk scores less frequently led to perinatal death compared to those beginning prior; 3.3% (95% CI 2.7, 3.9) versus 5.7% (95% CI 5.0, 6.5) respectively. Interrupted time-series analysis revealed a decreasing temporal trend in perinatal death for pregnancies beginning ≤40 weeks prior to the start of the COVID-19 pandemic (i.e. with pandemic exposure), with no trend for pregnancies beginning >40 weeks pre-pandemic (i.e. no pandemic exposure).
    CONCLUSIONS: We observed a decrease in perinatal death for pregnancies overlapping with the COVID-19 pandemic in Alberta, particularly among those at high risk of these outcomes. Specific pandemic control measures and government response programmes in our setting may have contributed to this finding.
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  • 文章类型: Journal Article
    背景:胎盘植入谱系障碍(PAS)会导致妊娠的主要并发症。虽然与PAS相关的孕产妇发病率是众所周知的,在这种情况下,关于新生儿发病率的信息较少。这项研究的目的是描述新生儿结局(胎儿畸形,新生儿发病率,双胞胎出生,死产,和新生儿死亡),使用国际多中心PAS病例数据库。
    方法:这是一个前瞻性的,基于前瞻性收集病例的多中心队列研究,使用国际PAS协会的国际多中心数据库,2020年1月至2022年6月,由23个有PAS护理经验的中心进行。包括所有PAS病例,无论单胎妊娠还是多胎妊娠,每个中心都根据自己的方案进行管理。数据通过图表审查收集。根据当地政策获得了当地道德委员会的批准和数据使用协议。
    结果:有315例妊娠符合纳入条件,有12个双胞胎怀孕,包括329个胎儿/新生儿;2例由于有关胎儿异常的数据不一致而被排除。为了计算新生儿发病率和死亡率,所有选择性终止妊娠均被排除,因此,分析了311例怀孕和323例新生儿。在我们的队列中,3例新生儿(0.93%)死产;在320例新生儿中,新生儿死亡10例(3.13%)。主要先天畸形的患病率为4.64%(15/323新生儿),最常见的是,心血管,中枢神经系统,胃肠道畸形.妊娠合并PAS的主要新生儿发病率为47/311(15.1%)。没有死胎,新生儿死亡,或报告的双胎妊娠胎儿畸形。
    结论:尽管在我们的队列中某些结果可能太罕见而无法检测到,并且应谨慎解释数据,我们的观察数据支持PAS患者的新生儿结局令人放心.
    BACKGROUND: Placenta accreta spectrum disorders (PAS) lead to major complications in pregnancy. While the maternal morbidity associated with PAS is well known, there is less information regarding neonatal morbidity in this setting. The aim of this study is to describe the neonatal outcomes (fetal malformations, neonatal morbidity, twin births, stillbirth, and neonatal death), using an international multicenter database of PAS cases.
    METHODS: This was a prospective, multicenter cohort study based on prospectively collected cases, using the international multicenter database of the International Society for PAS, carried out between January 2020 and June 2022 by 23 centers with experience in PAS care. All PAS cases were included, regardless of whether singleton or multiple pregnancies and were managed in each center according to their own protocols. Data were collected via chart review. Local Ethical Committee approval and Data Use Agreements were obtained according to local policies.
    RESULTS: There were 315 pregnancies eligible for inclusion, with 12 twin pregnancies, comprising 329 fetuses/newborns; 2 cases were excluded due to inconsistency of data regarding fetal abnormalities. For the calculation of neonatal morbidity and mortality, all elective pregnancy terminations were excluded, hence 311 pregnancies with 323 newborns were analyzed. In our cohort, 3 neonates (0.93%) were stillborn; of the 320 newborns delivered, there were 10 cases (3.13%) of neonatal death. The prevalence of major congenital malformations was 4.64% (15/323 newborns), most commonly, cardiovascular, central nervous system, and gastrointestinal tract malformations. The overall prevalence of major neonatal morbidity in pregnancies complicated by PAS was 47/311 (15.1%). There were no stillbirths, neonatal deaths, or fetal malformations in reported twin gestations.
    CONCLUSIONS: Although some outcomes may be too rare to detect within our cohort and data should be interpreted with caution, our observational data supports reassuring neonatal outcomes for women with PAS.
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  • 文章类型: Journal Article
    This study utilized comprehensive graphical, descriptive and econometric methods to provide empirical answers to the nexus between government health expenditures and neonatal mortality in China. Secondary data from 2000 to 2021 was extracted from the World Development Indicators, after which it was analyzed empirically with the following results; in the past two decades, the incidence of neonatal death has reduced by 85%. Meanwhile, domestic general government health expenditure per capita ranged between $326.2 and $9.4 during the period with a mean value of $138. Average neonatal mortality rate recorded an approximately 10 deaths per 1000 live births, while government health expenditures and neonatal mortality showed a significant negative relationship in China. Therefore, this study confirms that China has been able to meet the SDG 3 with evidence indicating that this may be due to increased government health expenditure.
    Cette étude a utilisé des méthodes graphiques, descriptives et économétriques complètes pour fournir des réponses empiriques au lien entre les dépenses publiques de santé et la mortalité néonatale en Chine. Les données secondaires de 2000 à 2021 ont été extraites des indicateurs de développement dans le monde, après quoi elles ont été analysées empiriquement avec les résultats suivants : au cours des deux dernières décennies, l\'incidence des décès néonatals a diminué de 85 %. Dans le même temps, les dépenses de santé des administrations publiques nationales par habitant ont varié entre 326,2 et 9,4 dollars au cours de la période, avec une valeur moyenne de 138 dollars. Le taux de mortalité néonatale moyen a enregistré environ 10 décès pour 1 000 naissances vivantes, tandis que les dépenses publiques de santé et la mortalité néonatale ont montré une relation négative significative en Chine. Par conséquent, cette étude confirme que la Chine a été en mesure d’atteindre l’ODD 3 avec des preuves indiquant que cela pourrait être dû à l’augmentation des dépenses publiques de santé.
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  • 文章类型: Journal Article
    先天性肺畸形(CLM)是婴儿死亡的主要原因。诊断CLM的临床方法主要依靠计算机断层扫描,磁共振成像,超声检查,和多普勒。然而,新生儿死亡原因的法医鉴定具有挑战性。缺少CLM的明确分类标准,因为其法医鉴定含糊不清。因此,我们旨在分析我们中心的新生儿死亡病例,以帮助识别先天性肺畸形患者。这项回顾性研究确定并分类了2008年1月至2023年4月期间进行尸检的新生儿死亡原因。选择活生生并在28天内死亡且死亡时间明确的病例。法医专家审查了他们的记录.的方式,死因,和其他特点进行了注意和讨论。这项回顾性研究显示,从2008年到2015年,尸检病例稳步增加,这归因于父母同意的改善。提高对尸检重要性的认识,加强医疗资源。然而,随后在2015年后出现下降,可能受到医疗技术和产前检查协议的进步的影响。新生儿死亡的主要原因包括呼吸道疾病,窒息,先天性发育不良,和胎儿窘迫。先天性肺畸形,尤其是支气管肺畸形,构成了很大一部分先天性异常。这项研究强调了标准化尸检和组织病理学检查在诊断和理解CLM中的重要性。未来的研究应集中在扩大病例收集和阐明CLM的遗传基础上,以改善法医管理和结果。
    Congenital lung malformation (CLM) is a leading cause of infant mortality. Clinical methods for diagnosing CLM mainly rely on computed tomography, magnetic resonance imaging, ultrasonography, and Doppler. However, forensic identification of the cause of death in neonates is challenging. Unequivocal classification criteria for CLM are missing as its forensic identification is ambiguous. Therefore, we aimed to analyze neonatal death cases at our center to assist in identifying those with congenital lung malformation. This retrospective study identified and classified the causes of deaths of neonates autopsied between January 2008 and April 2023. All cases born alive and died within 28 days with a clear time of death were selected, and forensic experts reviewed their records. The manner, cause of death, and other characteristics were noted and discussed. This retrospective study reveals a steady increase in autopsy cases from 2008 to 2015, attributed to improved parental consent, heightened awareness of autopsy importance, and enhanced medical resources. However, a subsequent decline post-2015 is observed, potentially influenced by advancements in medical technology and prenatal examination protocols. The top causes of neonatal mortality include respiratory diseases, asphyxia, congenital dysplasia, and fetal distress. Congenital lung malformations, particularly bronchopulmonary malformations, constitute a significant portion of congenital anomalies. This study underscores the importance of standardized autopsies and histopathological examinations in diagnosing and understanding CLM. Future research should focus on expanding case collections and elucidating the genetic basis of CLM to improve forensic management and outcomes.
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  • 文章类型: Journal Article
    目标:COVID-19大流行阻碍了全球常规医疗保健的获取,引起人们对妊娠流产和围产期死亡可能增加的担忧。
    背景:PUDDLES是一项国际合作,探讨COVID-19大流行对七个国家经历妊娠流产和围产期死亡的父母的影响,包括Aotearoa新西兰。
    目的:探讨在新西兰奥特罗阿流感大流行期间失去婴儿后,父母获得医疗保健服务和支持的经验。
    方法:我们进行了深入,对26名失去亲人的父母进行半结构化采访,包括20个分娩母亲,和六个未出生的父母(一个母亲和五个父亲)。损失的类型包括15例死胎,四次晚期流产,还有一个新生儿死亡.参与者种族广泛代表了Aotearoa新西兰的多种族社会。使用模板分析分析数据。
    结果:分析揭示了与流行病对失去亲人的父母经历的影响有关的五个主题。这些是:“远离和非个人护理”;“指导医院规则”;排除非出生父母;“阻碍获得社会支持”;和“关系护理的连续性”。
    结论:COVID-19大流行加剧了失去亲人的父母的孤立,因为医疗保健专业人员感知到了非个人护理,行动限制阻碍了获得社会和文化支持的机会。丧亲后,医疗保健专业人员对规则的同情弯曲和社区产后护理助产士的连续性访问似乎是缓解因素。
    结论:社会隔离对于在大流行期间失去婴儿的父母来说是一个额外的挑战,这可以通过医疗保健专业人员的灵活和富有同情心的护理来缓解,尤其是接生婆的连续性护理。
    OBJECTIVE: The COVID-19 pandemic hindered access to routine healthcare globally, prompting concerns about possible increases in pregnancy loss and perinatal death.
    BACKGROUND: PUDDLES is an international collaboration exploring the impact of the COVID-19 pandemic on parents who experience pregnancy loss and perinatal death in seven countries, including Aotearoa New Zealand.
    OBJECTIVE: To explore parents\' experiences of access to healthcare services and support following baby loss during the COVID-19 pandemic in Aotearoa New Zealand.
    METHODS: We conducted in-depth, semi-structured interviews with 26 bereaved parents, including 20 birthing mothers, and six non-birthing parents (one mother and five fathers). Types of loss included 15 stillbirths, four late miscarriages, and one neonatal death. Participant ethnicities were broadly representative of Aotearoa New Zealand\'s multi-ethnic society. Data were analysed using Template Analysis.
    RESULTS: Analysis revealed five themes relating to pandemic impact on bereaved parent\'s experiences. These were: \'Distanced and Impersonal care\'; \'Navigating Hospital Rules\'; Exclusion of Non-birthing Parents; \'Hindered Access to Social Support\'; and \'Continuity of Relational Care\'.
    CONCLUSIONS: The COVID-19 pandemic exacerbated isolation of bereaved parents through perceived impersonal care by healthcare professionals and restrictions on movement hindered access to social and cultural support. Compassionate bending of the rules by healthcare professionals and community postnatal visits by continuity of care midwives following the bereavement appeared to be mitigating factors.
    CONCLUSIONS: Social isolation is an added challenge for parents experiencing baby loss during a pandemic, which may be mitigated by flexible and compassionate care from healthcare professionals, especially continuity of care midwives.
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  • 文章类型: Journal Article
    正在经历新生儿死亡的父母需要支持来促进和维持他们的父母角色。这包括在生命结束时养育婴儿。床边护士应与父母合作,通过建立有效的沟通,帮助他们维持亲婴关系,建立信任,促进父母的角色。通过这样做,父母将利用这些经历通过意义来处理他们的悲伤。
    Parents who are experiencing neonatal death need support in promoting and maintaining their parental role. This includes parenting their infant during end-of-life. Bedside nurses should partner with parents to help them maintain the parent-infant relationship by establishing effective communication, building trust, and promoting the parental role. By doing so, parents will utilize these experiences to process their grief through meaning-making.
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