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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.
2
A 12-Day-Old Boy with Methemoglobinemia After Circumcision with Local Anesthesia (Lidocaine/Prilocaine).一名12日龄男婴在局部麻醉(利多卡因/丙胺卡因)下行包皮环切术后发生高铁血红蛋白血症
Drug Saf Case Rep. 2016 Dec;3(1):12. doi: 10.1007/s40800-016-0033-9.
3
The Preterm Infant: A High-Risk Situation for Neonatal Hyperbilirubinemia Due to Glucose-6-Phosphate Dehydrogenase Deficiency.早产儿:因葡萄糖-6-磷酸脱氢酶缺乏导致新生儿高胆红素血症的高危情况。
Clin Perinatol. 2016 Jun;43(2):325-40. doi: 10.1016/j.clp.2016.01.008. Epub 2016 Feb 28.
4
Transcutaneous bilirubin monitoring predicts unexplained late-onset hemolysis in a very low birthweight infant.经皮胆红素监测可预测极低出生体重儿不明原因的迟发性溶血。
BMC Res Notes. 2016 Mar 10;9:153. doi: 10.1186/s13104-016-1970-1.
5
Current incidence of clinical kernicterus in preterm infants in Japan.日本早产儿临床核黄疸的当前发病率。
Pediatr Int. 2015 Jun;57(3):494-7. doi: 10.1111/ped.12651.
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Bilateral cataracts associated with glucose-6-phosphate dehydrogenase deficiency.双侧白内障与葡萄糖-6-磷酸脱氢酶缺乏症相关。
J Perinatol. 2013 Jul;33(7):574-5. doi: 10.1038/jp.2012.148.
7
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.
8
Unexplained late-onset hemolysis and methemoglobinemia in a preterm infant.一名早产儿出现不明原因的迟发性溶血和高铁血红蛋白血症。
Pediatr Int. 2011 Dec;53(6):1084-7. doi: 10.1111/j.1442-200X.2011.03389.x.
9
Methaemoglobinaemia with G6PD deficiency: rare cause of persistently low saturations in neonates.高铁血红蛋白血症合并 G6PD 缺乏症:新生儿持续低饱和度的罕见病因。
Acta Paediatr. 2011 Jul;100(7):e47-8. doi: 10.1111/j.1651-2227.2011.02278.x.
10
Severe hyperbilirubinemia in a glucose-6-phosphate dehydrogenase-deficient preterm neonate: could prematurity be the main responsible factor?一名葡萄糖-6-磷酸脱氢酶缺乏的早产儿发生严重高胆红素血症:早产可能是主要责任因素吗?
Fetal Diagn Ther. 2008;24(4):440-3. doi: 10.1159/000174571. Epub 2008 Nov 20.

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.

DOI:10.1111/ped.14493
PMID:33012035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7986906/
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。