• 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

新生儿护理中极早产儿在 36 孕周后(postmenstrual age)的死亡率:生长障碍和支气管肺发育不良的影响。

Mortality after 36 weeks postmenstrual age of extremely preterm infants in neonatal care: The impact of growth impairment and bronchopulmonary dysplasia.

机构信息

Neonatal Intensive Care Centre, King's College Hospital NHS Foundation Trust, London, United Kingdom; Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.

Department of Women and Children's Health, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.

出版信息

Early Hum Dev. 2022 Aug;171:105618. doi: 10.1016/j.earlhumdev.2022.105618. Epub 2022 Jun 24.

DOI:10.1016/j.earlhumdev.2022.105618
PMID:35759944
Abstract

BACKGROUND

A small group of extremely preterm infants survive to 36 weeks postmenstrual age (PMA), but die before discharge from neonatal care.

AIMS

To investigate which epidemiological and clinical parameters were related to death after 36 weeks PMA in extremely preterm infants.

STUDY DESIGN

Retrospective whole-population study.

SUBJECTS

All infants born <28 weeks of gestation admitted to a neonatal unit in England between 2014 and 2018.

OUTCOME MEASURES

Mortality after 36 weeks PMA and before discharge from neonatal care. Bronchopulmonary dysplasia (BPD) defined as any respiratory support at 36 weeks PMA.

RESULTS

Death after 36 weeks PMA occurred in 156 of a total of 11.747 included infants (1.3 %) and at a median (IQR) age of 130 (93-164) days. A lower gestational age [Odds Ratio: 0.82, 95 % CI:0.72-0.94, adjusted p = 0.005], lower birth weight z-score [Odds Ratio: 0.45, 95 % CI:0.36-0.56, adjusted p < 0.001], greater absolute difference in weight z-score from birth to 36 weeks PMA [Odds Ratio: 0.46, 95 % CI:0.38-0.56, adjusted p < 0.001] were independently associated with death after 36 weeks PMA. A diagnosis of BPD [Odds Ratio: 4.57, 95 % CI:2.19-9.54, adjusted p < 0.001] and of necrotising enterocolitis requiring surgery [Odds Ratio: 2.81, 95 % CI:1.82-4.34, adjusted p < 0.001] were also independently associated with death after 36 weeks PMA.

CONCLUSIONS

Mortality of extremely preterm infants after 36 weeks postmenstrual age is associated with lower gestational age and more impaired growth. The diagnoses of bronchopulmonary dysplasia and necrotising enterocolitis were associated with a higher risk of death after 36 weeks postmenstrual age and before discharge from neonatal care.

摘要

背景

一小部分极早产儿能存活至胎龄 36 周(PMA),但在新生儿护理出院前死亡。

目的

研究哪些流行病学和临床参数与极早产儿胎龄 36 周后死亡相关。

研究设计

回顾性全人群研究。

研究对象

2014 年至 2018 年在英国一家新生儿病房收治的所有胎龄<28 周的婴儿。

结局指标

胎龄 36 周 PMA 后至新生儿护理出院前的死亡率。胎龄 36 周 PMA 时存在任何呼吸支持的支气管肺发育不良(BPD)。

结果

在总共纳入的 11747 名婴儿中,有 156 名(1.3%)在胎龄 36 周 PMA 后死亡,中位(IQR)年龄为 130(93-164)天。较低的胎龄[比值比:0.82,95%置信区间:0.72-0.94,调整后 p=0.005]、较低的出生体重 z 评分[比值比:0.45,95%置信区间:0.36-0.56,调整后 p<0.001]、胎龄 36 周 PMA 时体重 z 评分的绝对差值较大[比值比:0.46,95%置信区间:0.38-0.56,调整后 p<0.001]与胎龄 36 周 PMA 后死亡独立相关。BPD 诊断[比值比:4.57,95%置信区间:2.19-9.54,调整后 p<0.001]和需要手术治疗的坏死性小肠结肠炎[比值比:2.81,95%置信区间:1.82-4.34,调整后 p<0.001]也与胎龄 36 周 PMA 后死亡独立相关。

结论

胎龄 36 周后极早产儿的死亡率与较低的胎龄和更严重的生长障碍有关。BPD 和坏死性小肠结肠炎的诊断与胎龄 36 周 PMA 后和新生儿护理出院前的死亡风险增加相关。

相似文献

1
Mortality after 36 weeks postmenstrual age of extremely preterm infants in neonatal care: The impact of growth impairment and bronchopulmonary dysplasia.新生儿护理中极早产儿在 36 孕周后(postmenstrual age)的死亡率:生长障碍和支气管肺发育不良的影响。
Early Hum Dev. 2022 Aug;171:105618. doi: 10.1016/j.earlhumdev.2022.105618. Epub 2022 Jun 24.
2
Bronchopulmonary dysplasia and postnatal growth following extremely preterm birth.支气管肺发育不良与极早早产儿的产后生长
Arch Dis Child Fetal Neonatal Ed. 2021 Jul;106(4):386-391. doi: 10.1136/archdischild-2020-320816. Epub 2020 Dec 17.
3
Intermediate vs. High Oxygen Saturation Targets in Preterm Infants: A National Cohort Study.早产儿中等氧饱和度目标与高氧饱和度目标对比:一项全国队列研究
Neonatology. 2025;122(1):106-113. doi: 10.1159/000540278. Epub 2024 Aug 5.
4
Neonatal hematological parameters and the risk of moderate-severe bronchopulmonary dysplasia in extremely premature infants.新生儿血液学参数与极早产儿中重度支气管肺发育不良的风险。
BMC Pediatr. 2019 Apr 30;19(1):138. doi: 10.1186/s12887-019-1515-6.
5
Revisiting the Definition of Bronchopulmonary Dysplasia: Effect of Changing Panoply of Respiratory Support for Preterm Neonates.重新审视支气管肺发育不良的定义:改变早产儿呼吸支持方式的影响。
JAMA Pediatr. 2017 Mar 1;171(3):271-279. doi: 10.1001/jamapediatrics.2016.4141.
6
Inositol in preterm infants at risk for or having respiratory distress syndrome.患有或有患呼吸窘迫综合征风险的早产儿体内的肌醇
Cochrane Database Syst Rev. 2019 Jul 8;7(7):CD000366. doi: 10.1002/14651858.CD000366.pub4.
7
Trends in Care Practices, Morbidity, and Mortality of Extremely Preterm Neonates, 1993-2012.1993 - 2012年极早产儿的护理实践、发病率及死亡率趋势
JAMA. 2015 Sep 8;314(10):1039-51. doi: 10.1001/jama.2015.10244.
8
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.
9
Prevalence, Severity Patterns and Risk Factors of Bronchopulmonary Dysplasia in Preterm Infants Younger than 32 Weeks of Gestation in a Tertiary Centre in Oman.阿曼一家三级中心胎龄小于 32 周的早产儿支气管肺发育不良的患病率、严重程度模式和危险因素。
Sultan Qaboos Univ Med J. 2024 May;24(2):259-267. doi: 10.18295/squmj.3.2024.017. Epub 2024 May 27.
10
Effect of Hydrocortisone Therapy Initiated 7 to 14 Days After Birth on Mortality or Bronchopulmonary Dysplasia Among Very Preterm Infants Receiving Mechanical Ventilation: A Randomized Clinical Trial.出生后 7 至 14 天开始给予氢化可的松治疗对接受机械通气的极早产儿死亡率或支气管肺发育不良的影响:一项随机临床试验。
JAMA. 2019 Jan 29;321(4):354-363. doi: 10.1001/jama.2018.21443.

引用本文的文献

1
Sodium propionate protects against bronchopulmonary dysplasia by inhibiting IL-17-mediated apoptosis of alveolar epithelial cells.丙酸钠通过抑制白细胞介素-17介导的肺泡上皮细胞凋亡来预防支气管肺发育不良。
Sci Rep. 2025 Apr 5;15(1):11722. doi: 10.1038/s41598-025-94794-5.
2
[Prognosis of bronchopulmonary dysplasia].[支气管肺发育不良的预后]
Zhongguo Dang Dai Er Ke Za Zhi. 2025 Jan 15;27(1):115-120. doi: 10.7499/j.issn.1008-8830.2406004.
3
First-year outcomes of very low birth weight preterm singleton infants with hypoxemic respiratory failure treated with milrinone and inhaled nitric oxide (iNO) compared to iNO alone: A nationwide retrospective study.
与单独使用吸入性一氧化氮(iNO)相比,米力农联合 iNO 治疗伴有低氧性呼吸衰竭的极低出生体重早产儿的首年结局:一项全国性回顾性研究。
PLoS One. 2024 May 9;19(5):e0297137. doi: 10.1371/journal.pone.0297137. eCollection 2024.