• 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

对初发产后高血压高危患者的纵向血压轨迹进行特征分析:一项随机对照试验的二次分析。

Characterizing longitudinal blood pressure trajectories in patients at high risk for de novo postpartum hypertension: A randomized controlled trial secondary analysis.

作者信息

Emeruwa Ukachi N, Sarker Minhazur R, Bello Natalie, Jacobs Marni, Laurent Louise C, Teal E Nicole, Wen Timothy, Miller Russell S, Gyamfi-Bannerman Cynthia

机构信息

Division of Maternal-Fetal Medicine, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California San Diego School of Medicine, UC San Diego Health, La Jolla, CA, USA.

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California San Diego School of Medicine, UC San Diego Health, La Jolla, CA, USA.

出版信息

Pregnancy (Hoboken). 2025 May;1(3). doi: 10.1002/pmf2.70012. Epub 2025 Apr 24.

DOI:10.1002/pmf2.70012
PMID:40959508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12435528/
Abstract

INTRODUCTION

De novo postpartum hypertension (dnPPHTN), defined as new-onset high blood pressure (BP) after delivery in individuals who were normotensive through pregnancy and delivery, accounts for up to two-thirds of postpartum hypertension cases. Despite its prevalence, there is limited knowledge of BP trends in the postpartum period, hindering opportunities for early detection and timely intervention for dnPPHTN. This study aimed to characterize longitudinal postpartum BP patterns in patients at high risk for dnPPHTN.

METHODS

This secondary analysis utilized data from a negative randomized controlled trial (PMID: 38641089) involving 82 normotensive patients at high risk for dnPPHTN, who were randomized to receive either a 5-day course of 20 mg oral furosemide or placebo starting from postpartum day 1. BPs were monitored every 4-8 h from delivery to discharge, and subsequently via Bluetooth-enabled remote monitoring twice daily for 6 weeks. The primary goal of this secondary analysis was to characterize distinct patterns of longitudinal BP trajectories in the placebo group. Secondary goals included exploring differences in early postpartum BP trends between those who developed dnPPHTN and those who remained normotensive, as well as identifying the timing of peak BPs. Trends were assessed graphically using local polynomial regression fitting. Linear mixed-effects models were used to examine temporal BP trajectories, including random intercepts and slopes, with an interaction term for the time trend and dnPPHTN diagnosis to explore differential impacts.

RESULTS

A total of 40 participants from the placebo arm of the parent trial were included, contributing a total of 2235 postpartum BP measurements. Both systolic BP (SBP) and diastolic BP (DBP) increased until postpartum days 9 and 12, respectively, before subsequently declining. Significant differences in BP trajectories were observed between participants who developed dnPPHTN ( = 3; 167 BP readings) and those who remained normotensive ( = 37; 2068 BP measurements). Those with dnPPHTN had a significantly steeper rise in SBP preceding the diagnosis, which occurred at a median of 5 days (IQR 5-5.5 days). SBP rose by 1.6 mmHg more per day until its peak at postpartum day 9 in those with dnPPHTN, compared to normotensive participants ( < 0.001). DBP rose by 0.3 mmHg more per day and peaked later (postpartum day 14 in those with dnPPHTN vs. day 12 in those who remained normotensive; < 0.001).

CONCLUSION

Using remote monitoring technology, we characterized distinct postpartum BP trajectories in patients at risk for dnPPHTN, revealing a prolonged rise into the second postpartum week and trends that distinguish physiologic from pathophysiologic BP changes. These findings suggest that extended postpartum BP monitoring may be important for timely identification and intervention in patients developing dnPPHTN.

摘要

引言

新发产后高血压(dnPPHTN)定义为在整个孕期和分娩过程中血压正常的个体在产后出现的新发高血压,占产后高血压病例的三分之二。尽管其患病率较高,但对产后血压趋势的了解有限,这阻碍了对dnPPHTN进行早期检测和及时干预的机会。本研究旨在描述dnPPHTN高危患者产后血压的纵向模式。

方法

这项二次分析利用了一项阴性随机对照试验(PMID:38641089)的数据,该试验涉及82名dnPPHTN高危的血压正常患者,他们从产后第1天开始被随机分配接受为期5天的20毫克口服速尿疗程或安慰剂。从分娩到出院,每4 - 8小时监测一次血压,随后通过蓝牙远程监测,每天两次,持续6周。这项二次分析的主要目标是描述安慰剂组中不同的纵向血压轨迹模式。次要目标包括探讨发生dnPPHTN的患者与血压仍正常的患者在产后早期血压趋势的差异,以及确定血压峰值出现的时间。使用局部多项式回归拟合以图形方式评估趋势。使用线性混合效应模型来检查血压的时间轨迹,包括随机截距和斜率,并使用时间趋势和dnPPHTN诊断的交互项来探索差异影响。

结果

来自母试验安慰剂组的40名参与者被纳入,共提供了2235次产后血压测量数据。收缩压(SBP)和舒张压(DBP)分别在产后第9天和第12天之前升高,随后下降。在发生dnPPHTN的参与者(n = 3;167次血压读数)和血压仍正常的参与者(n = 37;2068次血压测量)之间观察到血压轨迹的显著差异。发生dnPPHTN的患者在诊断前SBP上升明显更陡,诊断中位时间为5天(四分位间距5 - 5.5天)。与血压正常的参与者相比,发生dnPPHTN的患者在产后第9天达到峰值之前,SBP每天升高幅度多1.6 mmHg(P < 0.001)。DBP每天升高幅度多0.3 mmHg,且峰值出现时间更晚(发生dnPPHTN的患者在产后第14天,而血压正常的患者在产后第12天;P < 0.001)。

结论

使用远程监测技术,我们描述了dnPPHTN高危患者不同的产后血压轨迹,揭示了血压在产后第二周仍持续升高以及生理血压变化与病理生理血压变化的不同趋势。这些发现表明,延长产后血压监测对于及时识别和干预发生dnPPHTN的患者可能很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/849bdbf933d6/nihms-2109109-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/faeff3fa13ff/nihms-2109109-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/9f4b848e9076/nihms-2109109-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/8aa925d26b62/nihms-2109109-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/849bdbf933d6/nihms-2109109-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/faeff3fa13ff/nihms-2109109-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/9f4b848e9076/nihms-2109109-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/8aa925d26b62/nihms-2109109-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/884e/12435528/849bdbf933d6/nihms-2109109-f0004.jpg

相似文献

1
Characterizing longitudinal blood pressure trajectories in patients at high risk for de novo postpartum hypertension: A randomized controlled trial secondary analysis.对初发产后高血压高危患者的纵向血压轨迹进行特征分析:一项随机对照试验的二次分析。
Pregnancy (Hoboken). 2025 May;1(3). doi: 10.1002/pmf2.70012. Epub 2025 Apr 24.
2
Prescription of Controlled Substances: Benefits and Risks管制药品的处方:益处与风险
3
Post-pandemic planning for maternity care for local, regional, and national maternity systems across the four nations: a mixed-methods study.针对四个地区的地方、区域和国家孕产妇保健系统的疫情后规划:一项混合方法研究。
Health Soc Care Deliv Res. 2025 Sep;13(35):1-25. doi: 10.3310/HHTE6611.
4
Incidence and Risk Factors of De Novo Postpartum Hypertension: Understanding Links to Long-Term Cardiovascular Risk.新发产后高血压的发病率及危险因素:理解与长期心血管风险的关联
JACC Adv. 2025 Jun;4(6 Pt 1):101756. doi: 10.1016/j.jacadv.2025.101756. Epub 2025 May 2.
5
Altered dietary salt intake for preventing diabetic kidney disease and its progression.改变膳食盐摄入量以预防糖尿病肾病及其进展。
Cochrane Database Syst Rev. 2023 Jan 16;1(1):CD006763. doi: 10.1002/14651858.CD006763.pub3.
6
The Black Book of Psychotropic Dosing and Monitoring.《精神药物剂量与监测黑皮书》
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.
7
Sertindole for schizophrenia.用于治疗精神分裂症的舍吲哚。
Cochrane Database Syst Rev. 2005 Jul 20;2005(3):CD001715. doi: 10.1002/14651858.CD001715.pub2.
8
Intravenous magnesium sulphate and sotalol for prevention of atrial fibrillation after coronary artery bypass surgery: a systematic review and economic evaluation.静脉注射硫酸镁和索他洛尔预防冠状动脉搭桥术后房颤:系统评价与经济学评估
Health Technol Assess. 2008 Jun;12(28):iii-iv, ix-95. doi: 10.3310/hta12280.
9
A rapid mixed-methods evaluation of remote home monitoring models during the COVID-19 pandemic in England.英格兰 COVID-19 大流行期间远程家庭监护模式的快速混合方法评估。
Health Soc Care Deliv Res. 2023 Jul;11(13):1-151. doi: 10.3310/FVQW4410.
10
Blood pressure lowering efficacy of partial agonist beta blocker monotherapy for primary hypertension.部分激动剂β受体阻滞剂单药治疗原发性高血压的降压疗效
Cochrane Database Syst Rev. 2014 Nov 27;2014(11):CD007450. doi: 10.1002/14651858.CD007450.pub2.

本文引用的文献

1
Blood pressure changes in gestational hypertension, preeclampsia, and chronic hypertension from preconception to 42-day postpartum.从孕前到产后42天,妊娠期高血压、子痫前期和慢性高血压患者的血压变化。
Pregnancy Hypertens. 2023 Mar;31:25-31. doi: 10.1016/j.preghy.2022.11.009. Epub 2022 Dec 5.
2
Early Pregnancy Blood Pressure Patterns Identify Risk of Hypertensive Disorders of Pregnancy Among Racial and Ethnic Groups.早期妊娠血压模式可识别不同种族和族裔群体妊娠高血压疾病的风险。
Hypertension. 2022 Mar;79(3):599-613. doi: 10.1161/HYPERTENSIONAHA.121.18568. Epub 2021 Dec 29.
3
Longitudinal blood pressure patterns of women with hypertensive disorders of pregnancy: preconception through postpartum.
妊娠高血压疾病女性的纵向血压模式:从孕前到产后。
J Matern Fetal Neonatal Med. 2022 Dec;35(25):9023-9030. doi: 10.1080/14767058.2021.2012650. Epub 2021 Dec 12.
4
Historical and Recent Changes in Maternal Mortality Due to Hypertensive Disorders in the United States, 1979 to 2018.美国 1979 年至 2018 年因高血压疾病导致的孕产妇死亡率的历史和近期变化。
Hypertension. 2021 Nov;78(5):1414-1422. doi: 10.1161/HYPERTENSIONAHA.121.17661. Epub 2021 Sep 13.
5
Postpartum-Specific Vital Sign Reference Ranges.产后特定生命体征参考范围。
Obstet Gynecol. 2021 Feb 1;137(2):295-304. doi: 10.1097/AOG.0000000000004239.
6
Racial Differences in Postpartum Blood Pressure Trajectories Among Women After a Hypertensive Disorder of Pregnancy.妊娠高血压疾病后女性产后血压轨迹的种族差异。
JAMA Netw Open. 2020 Dec 1;3(12):e2030815. doi: 10.1001/jamanetworkopen.2020.30815.
7
Postpartum blood pressure trends are impacted by race and BMI.产后血压趋势受种族和 BMI 的影响。
Pregnancy Hypertens. 2020 Apr;20:14-18. doi: 10.1016/j.preghy.2020.02.006. Epub 2020 Feb 26.
8
Vital Signs: Pregnancy-Related Deaths, United States, 2011-2015, and Strategies for Prevention, 13 States, 2013-2017.生命体征:2011-2015 年美国与妊娠相关的死亡情况,以及 2013-2017 年 13 个州的预防策略。
MMWR Morb Mortal Wkly Rep. 2019 May 10;68(18):423-429. doi: 10.15585/mmwr.mm6818e1.
9
ACOG Committee Opinion No. 743: Low-Dose Aspirin Use During Pregnancy.美国妇产科医师学会委员会意见 No.743:孕期低剂量阿司匹林的应用。
Obstet Gynecol. 2018 Jul;132(1):e44-e52. doi: 10.1097/AOG.0000000000002708.
10
Epidemiology of maternal morbidity and mortality.孕产妇发病率和死亡率的流行病学。
Semin Perinatol. 2017 Oct;41(6):332-337. doi: 10.1053/j.semperi.2017.07.007. Epub 2017 Aug 18.