• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

与生长受限和炎症相关的围产期状况与支气管肺发育不良风险增加有关。

Perinatal conditions related to growth restriction and inflammation are associated with an increased risk of bronchopulmonary dysplasia.

作者信息

Eriksson Lena, Haglund Bengt, Odlind Viveca, Altman Maria, Ewald Uwe, Kieler Helle

机构信息

Centre for Pharmacoepidemiology and Unit of Clinical Epidemiology, Department of Medicine, Solna Karolinska Institutet, Stockholm, Sweden; Medical Products Agency, Uppsala, Sweden.

出版信息

Acta Paediatr. 2015 Mar;104(3):259-63. doi: 10.1111/apa.12888. Epub 2015 Jan 30.

DOI:10.1111/apa.12888
PMID:25469645
Abstract

AIM

Bronchopulmonary dysplasia (BPD) is a frequent chronic lung disease in preterm infants, and we aimed to identify factors associated with this condition in infants with respiratory distress syndrome (RDS).

METHODS

This case-control study, using national Swedish data, included 2255 preterm infants, born before 33 gestational weeks. The 667 BPD cases were oxygen dependent at 36 weeks' postmenstrual age, and the 1558 controls only had RDS. Comparisons included perinatal conditions and pharmacological treatments. Adjusted odds ratios with 95% confidence intervals were calculated in a conditional logistic regression model, with gestational age as the conditioning term.

RESULTS

An increased risk of BPD was associated with prelabour preterm rupture of membranes of more than 1 week (3.35, 2.16-5.19), small for gestational age (2.73, 2.11-3.55), low Apgar score (1.37, 1.05-1.81), patent ductus arteriosus (1.70, 1.33-2.18), persistent pulmonary hypertension (5.80, 3.21-10.50), pulmonary interstitial emphysema (2.78, 1.37-5.64), pneumothorax (2.95, 1.85-4.72), late onset infections (2.69, 1.82-3.98), intubation (1.56, 1.20-2.03), chest compressions (2.05, 1.15-3.66) and mechanical ventilation (2.16, 1.69-2.77), but not antenatal corticosteroids.

CONCLUSION

Growth restriction and inflammation increased the risk of BPD in preterm infants and prelabour preterm rupture of membranes, small for gestational age, low Apgar score or need for resuscitation should raise clinical suspicions.

摘要

目的

支气管肺发育不良(BPD)是早产儿常见的慢性肺部疾病,我们旨在确定呼吸窘迫综合征(RDS)患儿中与该疾病相关的因素。

方法

本病例对照研究使用瑞典全国数据,纳入2255例孕周小于33周的早产儿。667例BPD病例在孕龄36周时仍需吸氧,1558例对照仅患有RDS。比较内容包括围产期情况和药物治疗。在以胎龄为条件项的条件逻辑回归模型中计算调整后的比值比及95%置信区间。

结果

BPD风险增加与胎膜早破超过1周(3.35,2.16 - 5.19)、小于胎龄儿(2.73,2.11 - 3.55)、阿氏评分低(1.37,1.05 - 1.81)、动脉导管未闭(1.70,1.33 - 2.18)、持续性肺动脉高压(5.80,3.21 - 10.50)、肺间质气肿(2.78,1.37 - 5.64)、气胸(2.95,1.85 - 4.72)、晚发性感染(2.69,1.82 - 3.98)、插管(1.56,1.20 - 2.03)、胸外按压(2.05,1.15 - 3.66)和机械通气(2.16,1.69 - 2.77)相关,但与产前使用糖皮质激素无关。

结论

生长受限和炎症增加了早产儿患BPD的风险,胎膜早破、小于胎龄儿、阿氏评分低或需要复苏应引起临床怀疑。

相似文献

1
Perinatal conditions related to growth restriction and inflammation are associated with an increased risk of bronchopulmonary dysplasia.与生长受限和炎症相关的围产期状况与支气管肺发育不良风险增加有关。
Acta Paediatr. 2015 Mar;104(3):259-63. doi: 10.1111/apa.12888. Epub 2015 Jan 30.
2
Role of antioxidant nutrients and lipid peroxidation in premature infants with respiratory distress syndrome and bronchopulmonary dysplasia.抗氧化营养素和脂质过氧化在呼吸窘迫综合征和支气管肺发育不良早产儿中的作用。
Am J Perinatol. 2003 Feb;20(2):97-107. doi: 10.1055/s-2003-38315.
3
Prenatal inflammatory risk factors for development of bronchopulmonary dysplasia.支气管肺发育不良发生的产前炎症危险因素。
Pediatr Pulmonol. 2014 Jul;49(7):665-72. doi: 10.1002/ppul.22881. Epub 2013 Sep 4.
4
[Risk factors, frequency and severity of bronchopulmonary dysplasia (BPD) diagnosed according to the new disease definition in preterm neonates].[根据早产儿支气管肺发育不良(BPD)新疾病定义诊断的危险因素、发生率及严重程度]
Med Wieku Rozwoj. 2008 Oct-Dec;12(4 Pt 1):933-41.
5
[Risk factors and short-term prognosis of early pulmonary hypertension in preterm infants].[早产儿早期肺动脉高压的危险因素及短期预后]
Zhonghua Er Ke Za Zhi. 2022 Jul 2;60(7):682-687. doi: 10.3760/cma.j.cn112140-20211222-01068.
6
Hospital variation and risk factors for bronchopulmonary dysplasia in a population-based cohort.基于人群的队列研究中医院变异与支气管肺发育不良的危险因素。
JAMA Pediatr. 2015 Feb;169(2):e143676. doi: 10.1001/jamapediatrics.2014.3676. Epub 2015 Feb 2.
7
Bronchopulmonary dysplasia in very and extremely low birth weight infants - analysis of selected risk factors.极低和超低出生体重儿的支气管肺发育不良——部分危险因素分析
Pol Merkur Lekarski. 2017 Feb 20;42(248):71-75.
8
Neonatal outcome of small for gestational age preterm infants.小于胎龄早产儿的新生儿结局
Eur J Pediatr. 2017 Aug;176(8):1083-1088. doi: 10.1007/s00431-017-2957-1. Epub 2017 Jun 28.
9
Association of Chorioamnionitis With Bronchopulmonary Dysplasia Among Preterm Infants: A Systematic Review, Meta-analysis, and Metaregression.绒毛膜羊膜炎与早产儿支气管肺发育不良的相关性:系统评价、荟萃分析和元回归。
JAMA Netw Open. 2019 Nov 1;2(11):e1914611. doi: 10.1001/jamanetworkopen.2019.14611.
10
Pepsin, a marker of gastric contents, is increased in tracheal aspirates from preterm infants who develop bronchopulmonary dysplasia.胃蛋白酶是胃内容物的一种标志物,在发生支气管肺发育不良的早产儿的气管吸出物中含量会升高。
Pediatrics. 2008 Feb;121(2):e253-9. doi: 10.1542/peds.2007-0056.

引用本文的文献

1
Diagnosis, Prevention, and Management of Fetal Growth Restriction (FGR).胎儿生长受限(FGR)的诊断、预防与管理
J Pers Med. 2024 Jun 28;14(7):698. doi: 10.3390/jpm14070698.
2
Mesenchymal stromal cell extracellular vesicles improve lung development in mechanically ventilated preterm lambs.间质基质细胞细胞外囊泡改善机械通气早产儿羊的肺发育。
Am J Physiol Lung Cell Mol Physiol. 2024 Jun 1;326(6):L770-L785. doi: 10.1152/ajplung.00349.2023. Epub 2024 Apr 2.
3
Effect of Donated Premature Milk in the Prevention of Bronchopulmonary Dysplasia.
捐赠早产儿母乳对预防支气管肺发育不良的影响。
Nutrients. 2024 Mar 15;16(6):859. doi: 10.3390/nu16060859.
4
A nomogram for predicting the risk of Bronchopulmonary dysplasia in premature infants.一种用于预测早产儿支气管肺发育不良风险的列线图。
Heliyon. 2023 Aug 9;9(8):e18964. doi: 10.1016/j.heliyon.2023.e18964. eCollection 2023 Aug.
5
Phthalate exposure in the neonatal intensive care unit is associated with development of bronchopulmonary dysplasia.在新生儿重症监护病房中接触邻苯二甲酸盐与支气管肺发育不良的发生有关。
Environ Int. 2023 Aug;178:108117. doi: 10.1016/j.envint.2023.108117. Epub 2023 Jul 26.
6
Genetic analysis of potential biomarkers and therapeutic targets associated with ferroptosis from bronchopulmonary dysplasia.从支气管肺发育不良中与铁死亡相关的潜在生物标志物和治疗靶点的遗传分析。
Medicine (Baltimore). 2023 Jul 21;102(29):e34371. doi: 10.1097/MD.0000000000034371.
7
The eNAMPT/TLR4 inflammatory cascade drives the severity of intra-amniotic inflammation in pregnancy and predicts infant outcomes.eNAMPT/TLR4炎症级联反应驱动孕期羊膜内炎症的严重程度,并预测婴儿预后。
Front Physiol. 2023 Jun 20;14:1129413. doi: 10.3389/fphys.2023.1129413. eCollection 2023.
8
Early Origins of Chronic Obstructive Pulmonary Disease: Prenatal and Early Life Risk Factors.慢性阻塞性肺疾病的早期起源:产前和生命早期的危险因素。
Int J Environ Res Public Health. 2023 Jan 27;20(3):2294. doi: 10.3390/ijerph20032294.
9
Something Smells Fishy: How Lipid Mediators Impact the Maternal-Fetal Interface and Neonatal Development.有些可疑:脂质介质如何影响母胎界面和新生儿发育。
Biomedicines. 2023 Jan 10;11(1):171. doi: 10.3390/biomedicines11010171.
10
Headway and the remaining hurdles of mesenchymal stem cells therapy for bronchopulmonary dysplasia.支气管肺发育不良的间充质干细胞治疗的进展和剩余障碍。
Clin Respir J. 2022 Oct;16(10):629-645. doi: 10.1111/crj.13540. Epub 2022 Sep 2.