ISSN 3080-7611(Print)
ISSN 3080-762X(Online)
版权信息 · Copyright

     加入编委 / 副主编 / 同行评议专家
ISSN 3080-7611(Print)
ISSN 3080-762X(Online)

CODEN:ZLYABX
国际标准连续出版物标识符·全球唯一标识符
分配机构:美国化学文摘社(CAS)
DOI前缀:
https://doi.org/10.66106/zlyabx
国图集团 CIBTC
进口备案刊号:G015Z110

索引 检索 存档(Global Indexing)
本刊入选以下全球权威数据库,致力于研究成果的全球化无障碍传播。
DOI
ICI 哥白尼索引(波兰)
EuroPub 欧洲学术出版中心数据库(英国)
Academia 学术界(美国)
CJWK 长江文库(中国)
OALib 开放存取资源图书馆(美国)
Baidu Scholar 百度学术(中国)
Baidu Baike 百度百科(中国)
Google Scholar 谷歌学术(美国)
Microsoft Bing 微软学术(美国)
SPI-Hub 范德比尔特大学医学中心(美国)
Naver 搜遍(韩国)
Yahoo! Search(美国)
ESJI 欧亚科学期刊索引(哈萨克斯坦)
ASCI 亚洲科学引文索引(美国)
ResearchBib 研究者索引(日本)
KIND CONGRESS(阿塞拜疆)
Sci Online 科学在线(中国澳门)
SJIF 科学期刊索引(印度)
RJIF 研究期刊影响因子
SCRIBD 数字图书馆(美国)
CiteFactor 指标与信任索引(印度)
LivRe 巴西国家核能委员会CIN(巴西)
RCCSE 中国学术期刊收录(武汉大学)
Semantic Scholar 语义学者(美国)
OAJ 全球OA期刊索引(中国)
Portico 数字保存库(美国)
Scite(美国)
EBSCO(美国)
MDPI scilit(瑞士)
Crossref 交叉引用(美国)
ProQuest 科睿唯安(美国)
ResearchGate 研究之门(德国)
COAJ 开放获取期刊数据(中国)
DOAJ 开放获取期刊目录(瑞典)
J-Gate 开放获取期刊门户(印度)
WorldCat 全球联机编目数据库(美国)
J-STAGE 学术信息电子期刊库(日本)
arXiv 学术论文预印本平台(美国)
PubMed 医学检索库(美国)
PubMed Central 医学全文库(美国)
The Lens 透镜学术(澳大利亚)
Scopus 爱思唯尔·斯高帕斯(荷兰)
ChatGPT OpenAI在线服务(美国)
EZB 电子期刊图书馆(德国)

Editing and Publishing
Quest Press Limited
Address
Unit D, 7th Floor, No. 19, Rua de Pa̍k-chiông Vai, Macau
Telephone
+853 6881 9699
Email
QuestPress@hotmail.com
Web site
https://zwlc.scionline2025.com
  往期阅览 · All Issues-> 2025年 · 2025  
中外临床医学2025年第1卷第1期第36-40页,pISSN 3080-7611、eISSN 3080-762X 发布者:Quest Press 发布日期:2025/10/9
Open Access 下载2 浏览297

 

Swan-Ganz导管监测下血管活性药物优化对心脏重症患者血流动力学及预后的影响


饶晓丽,刘超

吉林心脏病医院,吉林长春,130117

摘要:目的? 本研究旨在探讨在Swan-Ganz导管监测下,以米力农、多巴酚丁胺及去甲肾上腺素为核心的血管活性药物优化策略对心脏重症患者血流动力学参数及预后的影响,以期为心脏重症患者的规范化治疗提供高级别循证证据,推动从“经验治疗”向“目标导向治疗”的临床模式转变。方法? 本研究为回顾性队列研究,数据来源于某三级医院心脏重症监护病房(CICU)2018年1月至2023年12月收治的连续住院患者。纳入标准包括年龄≥18岁,诊断为急性心力衰竭、心源性休克或心脏术后低心排综合征,置入Swan-Ganz导管并持续监测≥48小时,以及使用米力农、多巴酚丁胺或去甲肾上腺素中的≥2种药物联合治疗≥24小时。排除标准包括终末期肾病、严重主动脉瓣狭窄、妊娠期或产后1周内患者,以及存在Swan-Ganz导管禁忌症的患者。最终纳入126例患者,按用药策略分为优化组(n=68)与对照组(n=58)。优化组基于Swan-Ganz导管实时监测数据调整药物剂量,对照组则依据临床经验及常规生命体征调整用药。主要观察指标包括血流动力学指标(心指数CI、肺动脉楔压PAWP、外周血管阻力指数SVRI、右心房压力RAP)、预后指标(28天死亡率、ICU停留时间、急性肾损伤AKI发生率)及药物使用强度(血管活性药物评分VIS)。结果? 优化组患者用药后48小时CI显著提升23%(P<0.01),PAWP显著下降18%(P=0.02),SVRI下降12.6%(P<0.05)。优化组28天死亡率为12.7%,显著低于对照组的25.9%(P=0.03),且Cox回归分析确认优化用药是降低死亡风险的独立保护因素(HR=0.41,95%CI?0.22-0.78,P=0.006)。此外,优化组ICU平均停留时间显著短于对照组(7.2±2.1天?vs.?9.8±3.4天,P<0.01),AKI发生率也显著降低(22.1%?vs.?39.7%,P=0.02)。优化组VIS评分显著低于对照组(25.6±8.2?vs.?34.1±9.7,P<0.01),且去甲肾上腺素使用剂量中位数显著低于对照组(0.15?vs.?0.28?μg/kg/min,P=0.002)。亚组分析显示,优化用药策略在急性心力衰竭、心源性休克及心脏术后低心排综合征亚组中均表现出一致的血流动力学改善及预后优势。结论? 本研究表明,在Swan-Ganz导管监测下,以米力农、多巴酚丁胺及去甲肾上腺素为核心的血管活性药物优化策略,可显著改善心脏重症患者的血流动力学参数,降低28天死亡率及并发症发生率,缩短ICU停留时间,并减少血管活性药物的使用总量。该策略通过精准调控药物剂量,实现了血流动力学状态的优化,为心脏重症患者的规范化治疗提供了有力证据。

关健词:Swan-Ganz导管;血管活性药物优化;血流动力学监测;心脏重症;预后改善
Impact of Vasoactive Drug Optimization Under Swan-Ganz Catheter Monitoring on Hemodynamics and Prognosis in Critically Ill Cardiac Patients

Xiaoli Rao,Chao Liu

Jilin Heart Disease Hospital,Changchun Jilin 130117, China

Abstract:Objective This study aimed to investigate the effects of a vasoactive drug optimization strategy, centered on milrinone, dobutamine, and norepinephrine, guided by Swan-Ganz catheter monitoring, on hemodynamic parameters and prognosis in critically ill cardiac patients. The goal was to provide high-level evidence for standardized treatment in this population and promote a clinical shift from “empirical therapy” to “goal-directed therapy.”Methods A retrospective cohort study was conducted using data from consecutive hospitalized patients admitted to the cardiac intensive care unit (CICU) of a tertiary hospital between January 2018 and December 2023. Inclusion criteria were: age ≥18 years, diagnosis of acute heart failure, cardiogenic shock, or postoperative low cardiac output syndrome, Swan-Ganz catheter placement with continuous monitoring ≥48 hours, and combination therapy with ≥2 of the following drugs (milrinone, dobutamine, or norepinephrine) for ≥24 hours. Exclusion criteria included end-stage renal disease, severe aortic stenosis, pregnancy/postpartum status within 1 week, or contraindications to Swan-Ganz catheters. A total of 126 patients were enrolled and divided into an optimization group (n=68) and a control group (n=58). The optimization group adjusted drug dosages based on real-time Swan-Ganz catheter data, while the control group relied on clinical experience and routine vital signs. Primary outcomes included hemodynamic indices (cardiac index [CI], pulmonary artery wedge pressure [PAWP], systemic vascular resistance index [SVRI], right atrial pressure [RAP]), prognostic indicators (28-day mortality, ICU length of stay, incidence of acute kidney injury [AKI]), and vasoactive drug intensity (vasoactive-inotropic score [VIS]).Results In the optimization group, CI increased signiffcantly by 23% at 48 hours post-intervention (P<0.01), PAWP decreased by 18% (P=0.02), and SVRI decreased by 12.6% (P<0.01), with a median norepinephrine dose reduction (0.15 vs. 0.28 μg/kg/min, P=0.002). Subgroup analyses demonstrated consistent hemodynamic improvements and prognostic beneffts across acute heart failure, cardiogenic shock, and postoperative low cardiac output syndrome subgroups. Conclusion This study demonstrates that a Swan-Ganz catheter-guided optimization strategy for vasoactive drugs (milrinone, dobutamine, and norepinephrine) signiffcantly improves hemodynamic parameters, reduces 28-day mortality and complication rates, shortens ICU stays, and lowers overall vasoactive drug usage in critically ill cardiac patients. By precisely titrating drug doses, this approach optimizes hemodynamic status and provides robust evidence for standardized care in this population.


Keywords : Swan-Ganz catheter; vasoactive drug optimization; hemodynamic monitoring; critical cardiac care; prognostic im-provement
论文收录证明 / 文献检索报告
Document Retrieval Certificate / Proof of Publication Indexing
作者贡献声明 / 贡献确认书
Author Contribution Statement / Certificate of Authorship Contribution
同行评审报告 / 评审意见
Peer Review Report / Peer Review Comments
利益冲突
Conflict of Interest
作者声明不存在任何利益冲突。
The author declares no conflict of interest.
版权声明
Copyright Statement
本文采用知识共享“署名 4.0 国际”许可 (CC BY 4.0) 进行许可。许可协议详情请访问: https://creativecommons.org/licenses/by/4.0/
This article is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). For details of the license, please visit:https://creativecommons.org/licenses/by/4.0/.

 
Peer Review
同行评审
Editorial Services
编辑服务
Research Ethics Policy
研究伦理政策
Contributorship & Authorship
贡献者与署名
Quest Press / Macau Sino-Foreign Medical Publishing Ltd.
关于 Quest Press / Macau Sino-Foreign Medical Publishing Ltd.
Global Indexing
全球索引
Copyright Licensing
版权许可
Data Sharing Policy
数据共享政策
Appeal/Correction/Retraction
申诉/更正/撤回
Online Submission
线上投稿
To the Librarian
致图书馆员
Open Access Statement
开放获取声明
Misconduct Handling Policy
处理不端行为政策
Content Licensing
内容许可
Guidelines for Reviewers
审稿人指南
Quality Control Mechanism
质量把控机制
Academic Misconduct Screening Policy
学术不端筛查政策
Advertising Policy
广告政策
Article Processing Charge (APC)
文章处理费
Publication Ethics Policy
出版伦理政策
Joining the Editorial Board, Associate Editors, Peer Reviewers, and Editor-in-Chief
加入编委、副主编、同行评审专家及主编
Quest Press
Bridging Research to a Global Stage.
academia
© 2025-2026 Quest Press Ltd.
Address: Unit D, 7th Floor, No. 19, Rua de Pa̍k-chiông Vai, Macau
Tel: +853 6881 9699 / Email: QuestPress@hotmail.com
The QUEST PRESS publishes articles under the following open access license.
Quest Press
is a member of the following organizations.