• 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

支气管肺发育不良:定义和长期呼吸系统结局。

Bronchopulmonary dysplasia: definitions and long-term respiratory outcome.

机构信息

Unit of Respiratory Medicine and Allergy, Department of Pediatrics, University of Padova, Via Giustiniani 3, 35128 Padova, Italy.

出版信息

Early Hum Dev. 2009 Oct;85(10 Suppl):S1-3. doi: 10.1016/j.earlhumdev.2009.08.002. Epub 2009 Sep 29.

DOI:10.1016/j.earlhumdev.2009.08.002
PMID:19793629
Abstract

Bronchopulmonary dysplasia (BPD) is a chronic respiratory disease that develops as a consequence of perinatal/neonatal lung injury, and it is one of the most important sequelae of premature birth. In this article we discuss recent changes in the definition of BPD, the main differences between the old and the new form and we summarize recent data on long-term respiratory outcome. The diagnosis of BPD is currently based on the need for supplemental oxygen for at least 28 days after birth, and its severity is graded according to the respiratory support required at 36 postmenstrual weeks. The "new BPD" is mainly a developmental disorder in which the immature lung fails to reach its full structural complexity. Longitudinal studies on children with BPD identified, at all ages, a greater need to use inhaled asthma medication and a significant airflow obstruction. Whether survivors of BPD and prematurity have a risk of developing a COPD-like phenotype with aging is a question that only lung function studies extended to middle-age and beyond will answer.

摘要

支气管肺发育不良(BPD)是一种慢性呼吸系统疾病,是围产期/新生儿肺损伤的后果,也是早产儿最重要的后遗症之一。本文讨论了 BPD 定义的最新变化、新旧形式的主要区别,并总结了关于长期呼吸结局的最新数据。BPD 的诊断目前基于出生后至少 28 天需要补充氧气的需求,并根据 36 孕周时所需的呼吸支持来分级。“新 BPD”主要是一种发育障碍,不成熟的肺部未能达到其充分的结构复杂性。对 BPD 患儿的纵向研究发现,在所有年龄段,都需要更多地使用吸入性哮喘药物,并存在明显的气流阻塞。BPD 和早产儿幸存者随着年龄的增长是否有发展为类似 COPD 表型的风险,这是一个只有通过将肺功能研究延长到中年及以后才能回答的问题。

相似文献

1
Bronchopulmonary dysplasia: definitions and long-term respiratory outcome.支气管肺发育不良:定义和长期呼吸系统结局。
Early Hum Dev. 2009 Oct;85(10 Suppl):S1-3. doi: 10.1016/j.earlhumdev.2009.08.002. Epub 2009 Sep 29.
2
Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia.美国国立卫生研究院支气管肺发育不良共识定义的验证
Pediatrics. 2005 Dec;116(6):1353-60. doi: 10.1542/peds.2005-0249.
3
Is the new definition of bronchopulmonary dysplasia more useful?支气管肺发育不良的新定义更有用吗?
J Perinatol. 2005 Jan;25(1):41-6. doi: 10.1038/sj.jp.7211210.
4
[Prevalence and risk factors of bronchopulmonary dysplasia among extremely low birth weight newborns of regional birth cohort of south-east Poland].[波兰东南部地区出生队列中极低出生体重新生儿支气管肺发育不良的患病率及危险因素]
Przegl Lek. 2009;66(1-2):14-20.
5
Definitions and diagnostic criteria for bronchopulmonary dysplasia.支气管肺发育不良的定义和诊断标准。
Semin Perinatol. 2006 Aug;30(4):164-70. doi: 10.1053/j.semperi.2006.05.002.
6
Pulmonary outcomes in bronchopulmonary dysplasia.支气管肺发育不良的肺部转归
Semin Perinatol. 2006 Aug;30(4):219-26. doi: 10.1053/j.semperi.2006.05.009.
7
Populations at risk for developing respiratory syncytial virus and risk factors for respiratory syncytial virus severity: infants with predisposing conditions.患呼吸道合胞病毒的高危人群及呼吸道合胞病毒严重程度的危险因素:有易患因素的婴儿。
Pediatr Infect Dis J. 2003 Feb;22(2 Suppl):S33-7; discussion S37-9. doi: 10.1097/01.inf.0000053883.08663.e5.
8
Evaluating "old" definitions for the "new" bronchopulmonary dysplasia.评估“新”支气管肺发育不良的“旧”定义。
J Pediatr. 2002 May;140(5):555-60. doi: 10.1067/mpd.2002.123291.
9
Impact of a physiologic definition on bronchopulmonary dysplasia rates.生理定义对支气管肺发育不良发生率的影响。
Pediatrics. 2004 Nov;114(5):1305-11. doi: 10.1542/peds.2004-0204.
10
[Bronchopulmonary dysplasia and prematurity. Short-and long-term respiratory changes].[支气管肺发育不良与早产。短期和长期呼吸变化]
An Pediatr (Barc). 2010 Jan;72(1):79.e1-16. doi: 10.1016/j.anpedi.2009.09.010. Epub 2009 Dec 8.

引用本文的文献

1
Kidney complications in children with bronchopulmonary dysplasia.支气管肺发育不良患儿的肾脏并发症
Pediatr Res. 2024 Oct 24. doi: 10.1038/s41390-024-03638-x.
2
Morphological and molecular aspects of lung development.肺发育的形态学和分子学方面
Histol Histopathol. 2025 Apr;40(4):411-430. doi: 10.14670/HH-18-807. Epub 2024 Sep 4.
3
Lung ultrasound in early prediction of bronchopulmonary dysplasia in pre-term babies.肺超声在早产儿支气管肺发育不良的早期预测中的应用。
J Ultrasound. 2024 Sep;27(3):653-662. doi: 10.1007/s40477-024-00913-9. Epub 2024 Jun 22.
4
Premature infants born <28 weeks with acute kidney injury have increased bronchopulmonary dysplasia rates.出生时胎龄<28 周且伴有急性肾损伤的早产儿支气管肺发育不良发生率增加。
Pediatr Res. 2023 Aug;94(2):676-682. doi: 10.1038/s41390-023-02514-4. Epub 2023 Feb 9.
5
Anakinra Pilot - a clinical trial to demonstrate safety, feasibility and pharmacokinetics of interleukin 1 receptor antagonist in preterm infants.阿那白滞素先导临床试验——一项旨在证明白介素 1 受体拮抗剂在早产儿中的安全性、可行性和药代动力学的临床试验。
Front Immunol. 2022 Oct 27;13:1022104. doi: 10.3389/fimmu.2022.1022104. eCollection 2022.
6
CPAP-induced airway hyper-reactivity in mice is modulated by hyaluronan synthase-3.透明质酸合酶-3 调节 CPAP 诱导的小鼠气道高反应性。
Pediatr Res. 2022 Sep;92(3):685-693. doi: 10.1038/s41390-021-01695-0. Epub 2021 Nov 8.
7
Low-dose hyperoxia primes airways for fibrosis in mice after influenza A infection.低剂量高氧预处理可增强甲型流感病毒感染后小鼠气道的纤维化。
Am J Physiol Lung Cell Mol Physiol. 2021 Oct 1;321(4):L750-L763. doi: 10.1152/ajplung.00289.2020. Epub 2021 Jul 29.
8
Early Changes and Indicators Characterizing Lung Aging in Neonatal Chronic Lung Disease.新生儿慢性肺疾病中肺老化的早期变化及特征指标
Front Med (Lausanne). 2021 May 31;8:665152. doi: 10.3389/fmed.2021.665152. eCollection 2021.
9
Calcium-sensing receptor and CPAP-induced neonatal airway hyperreactivity in mice.钙敏感受体与 CPAP 诱导的新生小鼠气道高反应性
Pediatr Res. 2022 May;91(6):1391-1398. doi: 10.1038/s41390-021-01540-4. Epub 2021 May 6.
10
Neutrophilic inflammation during lung development disrupts elastin assembly and predisposes adult mice to COPD.肺发育过程中的中性粒细胞炎症会破坏弹性蛋白的组装,使成年小鼠易患 COPD。
J Clin Invest. 2021 Jan 4;131(1). doi: 10.1172/JCI139481.