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全国极低出生体重儿迟发性溶血的调查。

Nationwide survey of late-onset hemolysis in very low birthweight infants.

机构信息

Departments of, Department of, Child Health, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.

Department of, Pediatrics, University of Tsukuba Hospital, Tsukuba, Japan.

出版信息

Pediatr Int. 2021 Feb;63(2):172-176. doi: 10.1111/ped.14493. Epub 2021 Feb 6.

Abstract

BACKGROUND

In Japan, some cases of late-onset acute hemolysis in very low birthweight (VLBW) infants have been reported. These cases had common features but the cause of hemolysis was unknown. The incidence and prognosis of this disease are also unknown. However, there are only few reports of such hemolytic episodes in countries other than Japan. Thus, this study aimed to examine the incidence and clinical course of late-onset acute hemolysis and to establish it as a new disease concept.

METHODS

A nationwide prospective survey was conducted from 2011 to 2015 as a rare disease surveillance project of the Japan Society for Neonatal Health and Development.

RESULTS

Twenty-four cases were confirmed. The median (range) gestational age, birthweight, and onset of hemolytic episodes were 26 weeks and 2 days (23 weeks and 4 days-31 weeks and 2 days), 898 g (627-1,416 g), and 19 days after birth (9-33 days), respectively. Phototherapy, blood transfusion, and exchange transfusion were required in 22 (96%), 24 (100%), and 7 (29%) cases, respectively. During the observation period, no recurrence of the hemolytic episode occurred. All patients survived; however, one case developed kernicterus and suffered severe neurological sequelae.

CONCLUSIONS

In this study, at least 1 out of 1,259 VLBW infants developed hemolysis at 9-33 days after birth in Japan. Owing to the risk of kernicterus, this disease should be recognized as among the important pathological conditions of VLBW infants, suggesting the need to manage jaundice and anemia until 5 weeks after birth.

摘要

背景

在日本,有一些极低出生体重儿(VLBW)发生迟发性急性溶血的病例报告。这些病例具有共同特征,但溶血的原因尚不清楚。该病的发病率和预后也不清楚。然而,除日本以外的其他国家仅有少数此类溶血发作的报告。因此,本研究旨在探讨迟发性急性溶血的发病率和临床过程,并将其确立为一种新的疾病概念。

方法

作为日本新生儿健康与发展学会罕见病监测项目,于 2011 年至 2015 年进行了全国性前瞻性调查。

结果

共确诊 24 例。中位(范围)胎龄、出生体重和溶血性发作的起始时间分别为 26 周 2 天(23 周 4 天至 31 周 2 天)、898g(627-1416g)和出生后 19 天(9-33 天)。22 例(96%)需要光疗、输血和换血,分别为 24 例(100%)和 7 例(29%)。在观察期间,无溶血发作复发。所有患者均存活;然而,1 例发生核黄疸,伴有严重的神经后遗症。

结论

在本研究中,日本至少有 1/1259 例 VLBW 婴儿在出生后 9-33 天发生溶血。由于存在核黄疸的风险,应将该病视为 VLBW 婴儿重要的病理情况之一,这表明需要管理黄疸和贫血至出生后 5 周。

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The Free Radical Diseases of Prematurity: From Cellular Mechanisms to Bedside.早产儿自由基疾病:从细胞机制到床边。
Oxid Med Cell Longev. 2018 Jul 24;2018:7483062. doi: 10.1155/2018/7483062. eCollection 2018.
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Oxidative injury in neonatal erythrocytes.新生儿红细胞中的氧化损伤。
J Matern Fetal Neonatal Med. 2012 Oct;25(Suppl 5):104-8. doi: 10.3109/14767058.2012.715471.

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