Less than 7% of newborn infants displayed clinically significant abnormal issues during postnatal physical examinations

IF 2.1 4区 医学 Q1 PEDIATRICS Acta Paediatrica Pub Date : 2024-09-30 DOI:10.1111/apa.17440
Johanna Soikkeli, Katja Ovaskainen, Päivi Korhonen, Sauli Palmu
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If the child is examined before 24 h of age, it is repeated within a couple of days, because issues such as some congenital heart defects are not detectable immediately after birth.<span><sup>1</sup></span></p><p>This retrospective register study focused on 3729 children born at Tampere University Hospital, one of Finland's largest maternity hospitals, in 2022. They were discharged from the postnatal ward, which only admits infants born at 35 weeks of more and weighing more than 2000 g. Infants admitted to the neonatal intensive care unit were excluded. We assessed the frequency and type of abnormal findings identified during these examinations, which inform discharge decisions and may help to plan neonatal discharge criteria and follow-ups.</p><p>The information on the infants, their medical examination and any International Classification of Diseases, Tenth Revision (ICD-10) diagnoses were collected from their records. 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Also, some studies focused on the first 4 weeks, rather than up to the 48 h in our study, and may have detected later skin manifestations.</p><p>The incidence of congenital heart defects was 0.1%–0.3% in a Swedish study that evaluated congenital heart defect screening.<span><sup>3</sup></span> It highlighted the importance of neonatal physical examinations, as some subjects with negative prenatal screening and postnatal pulse oximetry screening were diagnosed after these. The authors reported that 11% of the heart defects were diagnosed based on early symptoms and 14% by physical examinations after negative pulse oximetry screening. Our study found that 2.6% of our cohort had abnormal cardiovascular system findings and just under 1.0% received an ICD-10 diagnosis related to their cardiovascular system. 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引用次数: 0

Abstract

All Finnish newborn infants are systematically and comprehensively examined by a specialist or trainee paediatrician before discharge, to identify any diseases, deformities and birth injuries. This usually happens at 24–48 h of age. The mother's health and medication during pregnancy, delivery details and the infant's weight and feeding are also evaluated to ensure their safe discharge.1

Early discharge in Finland is defined as <36 h of age. If the child is examined before 24 h of age, it is repeated within a couple of days, because issues such as some congenital heart defects are not detectable immediately after birth.1

This retrospective register study focused on 3729 children born at Tampere University Hospital, one of Finland's largest maternity hospitals, in 2022. They were discharged from the postnatal ward, which only admits infants born at 35 weeks of more and weighing more than 2000 g. Infants admitted to the neonatal intensive care unit were excluded. We assessed the frequency and type of abnormal findings identified during these examinations, which inform discharge decisions and may help to plan neonatal discharge criteria and follow-ups.

The information on the infants, their medical examination and any International Classification of Diseases, Tenth Revision (ICD-10) diagnoses were collected from their records. Abnormal findings were grouped according to body parts and organs. As some newborn infants were examined numerous times after they were discharged, we focused on their last examination in the postnatal ward.

There were 1297 abnormal findings in 20.9% of the newborn infants (Table 1) and 20.0% of these were clinically significant. The most common abnormalities related to skin or colour (13%), head or fontanels (4.0%), hip joints (3.6%) and genitals (2.4%). An ICD-10 diagnosis code other than normal birth was recorded in 37.5% of the children, with 5.5% related to growth, 4.1% to jaundice, 1.1% to respiratory abnormalities and 1.0% to the cardiovascular system. They also included 0.9% with birth injuries and 0.4% with dysmorphism (Table 1).

The median age at discharge was 59 (range: 7–347) h and 5.4% were discharged before 36 h. Most (72.4%) of the examinations were performed on the postnatal ward, with the remainder in outpatient clinics.

The main results were that there were no abnormal findings in two thirds of the newborn infants, most of the abnormalities were related to their skin or colour and the median age at discharge was 59 h.

Skin abnormalities in newborn infants are common and other studies have reported that 57%–99.3% had at least one.2 They were found in 13% of our infants and half of these related to skin colour. Infants are often routinely screened for jaundice before they are discharged, by measuring bilirubin transcutaneously or from serum. The lower frequency in our study may have been due to different classifications, as some findings were grouped by noses and mouths, genitals and heads and fontanels. Also, some studies focused on the first 4 weeks, rather than up to the 48 h in our study, and may have detected later skin manifestations.

The incidence of congenital heart defects was 0.1%–0.3% in a Swedish study that evaluated congenital heart defect screening.3 It highlighted the importance of neonatal physical examinations, as some subjects with negative prenatal screening and postnatal pulse oximetry screening were diagnosed after these. The authors reported that 11% of the heart defects were diagnosed based on early symptoms and 14% by physical examinations after negative pulse oximetry screening. Our study found that 2.6% of our cohort had abnormal cardiovascular system findings and just under 1.0% received an ICD-10 diagnosis related to their cardiovascular system. Our study had a higher diagnosis rate, as it included all cardiovascular system diagnoses.

One study reported that postnatal hospital stays had shortened since the 1970s, especially in developed countries, and that 7.9% of Finnish newborn infants were discharged during the first 2 days in 2008–2015.4 Our study found that hospital stays had shortened even more, as 27.4% of our cohort were discharged during the first 2 days and 5.4% before 36 h. However, we included premature and caesarean section births, so that increase could be even more significant.

The neonatal examinations performed during our study showed that 29.1% of the newborn infants had abnormal findings and 20.0% of these were clinically significant. However, most of them (89.8%) did not have a significant impact on discharge decisions (Table 1). We could not establish if the abnormalities were discovered during the clinical examinations or simply verified and documented at that point. Further studies are needed to assess the role of physical examinations during the discharge process for newborn infants.

Johanna Soikkeli: Investigation; writing – original draft; writing – review and editing; formal analysis. Katja Ovaskainen: Conceptualization; writing – review and editing; supervision. Päivi Korhonen: Conceptualization; writing – review and editing; supervision. Sauli Palmu: Conceptualization; investigation; writing – review and editing; methodology; project administration; supervision; resources.

No conflicts of interest.

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在产后体检中,只有不到 7% 的新生儿表现出明显的临床异常。
所有芬兰新生儿在出院前都由专家或实习儿科医生进行系统和全面的检查,以确定任何疾病、畸形和出生损伤。这通常发生在24-48小时的年龄。还对母亲在怀孕期间的健康和药物、分娩细节以及婴儿的体重和喂养进行评估,以确保他们安全出院。在芬兰,提前出院的定义为36小时。如果孩子在24小时前接受检查,则在几天内重复检查,因为一些先天性心脏缺陷等问题在出生后无法立即检测到。1这项回顾性登记研究的重点是2022年在芬兰最大的妇产医院之一坦佩雷大学医院出生的3729名儿童。他们从产后病房出院,该病房只接纳35周以上出生、体重超过2000克的婴儿。新生儿重症监护病房的婴儿被排除在外。我们评估了在这些检查中发现的异常发现的频率和类型,这为出院决定提供了信息,并可能有助于制定新生儿出院标准和随访。从他们的记录中收集了有关婴儿的信息、他们的医疗检查和任何国际疾病分类第十版(ICD-10)的诊断。异常表现按身体部位和器官分类。由于一些新生儿在出院后进行了多次检查,我们将重点放在他们在产后病房的最后一次检查上。20.9%的新生儿有1297个异常表现(表1),其中20.0%具有临床意义。最常见的异常与皮肤或颜色有关(13%),头部或囟门(4.0%),髋关节(3.6%)和生殖器(2.4%)。37.5%的患儿有非正常出生的ICD-10诊断代码,其中5.5%与生长有关,4.1%与黄疸有关,1.1%与呼吸异常有关,1.0%与心血管系统有关。其中0.9%为出生损伤,0.4%为畸形(表1)。出院时中位年龄为59(范围:7-347)h, 5.4%在36 h前出院。大多数检查(72.4%)在产后病房进行,其余在门诊进行。主要结果是三分之二的新生儿未发现异常,大多数异常与他们的皮肤或颜色有关,出院时中位年龄为59小时。新生儿皮肤异常很常见,其他研究报道57%-99.3%至少有一种皮肤异常在13%的婴儿中发现了这些缺陷,其中一半与肤色有关。婴儿通常在出院前例行筛查黄疸,通过经皮或血清测量胆红素。在我们的研究中,较低的频率可能是由于不同的分类,因为一些研究结果是根据鼻子和嘴、生殖器、头部和囟门分组的。此外,一些研究集中在前4周,而不是在我们的研究中长达48小时,并且可能发现了后期的皮肤表现。在瑞典一项评估先天性心脏缺陷筛查的研究中,先天性心脏缺陷的发生率为0.1%-0.3%它强调了新生儿体格检查的重要性,因为一些产前筛查和产后脉搏血氧仪筛查阴性的受试者在这些检查后被诊断出来。作者报告说,11%的心脏缺陷是根据早期症状诊断出来的,14%是通过脉搏氧饱和度阴性筛查后的身体检查诊断出来的。我们的研究发现,我们的队列中有2.6%的人有心血管系统异常,不到1.0%的人接受了与心血管系统相关的ICD-10诊断。我们的研究有更高的诊断率,因为它包括了所有心血管系统的诊断。一项研究报告称,自20世纪70年代以来,产后住院时间缩短,特别是在发达国家,2008 - 2015年,7.9%的芬兰新生儿在前2天出院。我们的研究发现,住院时间缩短得更多,我们的队列中有27.4%在前2天出院,5.4%在36小时前出院。然而,我们把早产和剖腹产也算在内,所以这一增长可能更为显著。在我们的研究中进行的新生儿检查显示,29.1%的新生儿有异常发现,其中20.0%有临床意义。然而,其中大多数(89.8%)对出院决定没有显著影响(表1)。我们无法确定这些异常是在临床检查中发现的,还是在那时简单地验证和记录。需要进一步的研究来评估体格检查在新生儿出院过程中的作用。Johanna Soikkeli:调查;写作——原稿;写作——审阅和编辑;正式的分析。 Katja Ovaskainen:概念化;写作——审阅和编辑;监督。Päivi Korhonen:概念化;写作——审阅和编辑;监督。Sauli Palmu:概念化;调查;写作——审阅和编辑;方法;项目管理;监督;资源。没有利益冲突。
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来源期刊
Acta Paediatrica
Acta Paediatrica 医学-小儿科
CiteScore
6.50
自引率
5.30%
发文量
384
审稿时长
2-4 weeks
期刊介绍: Acta Paediatrica is a peer-reviewed monthly journal at the forefront of international pediatric research. It covers both clinical and experimental research in all areas of pediatrics including: neonatal medicine developmental medicine adolescent medicine child health and environment psychosomatic pediatrics child health in developing countries
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