• 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

未纳入急性肺损伤临床试验的原因。

Reasons for nonenrollment in a clinical trial of acute lung injury.

作者信息

Glassberg Andrea E, Luce John M, Matthay Michael A

机构信息

Permanente Medical Group, Fremont, San Francisco, San Francisco, CA.

University of California, San Francisco, San Francisco, CA.

出版信息

Chest. 2008 Oct;134(4):719-723. doi: 10.1378/chest.08-0633. Epub 2008 Aug 8.

DOI:10.1378/chest.08-0633
PMID:18689583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2789486/
Abstract

BACKGROUND

Enrolling critically ill patients in clinical trials is challenging. We observed that eligible patients at San Francisco General Hospital (SFGH), a public hospital that cares largely for indigent patients, were less likely to be enrolled in a clinical trial of acute lung injury (ALI) than eligible patients at the University of California, San Francisco (UCSF), a university referral center. We examined the reasons for nonenrollment and the impact of the availability of a surrogate decision maker on critical care clinical trials enrollment.

METHODS

Data collected from the ARDS Network trial of lower vs traditional tidal volume ventilation for patients with ALI was analyzed. Patient demographics and reasons for nonenrollment were analyzed among 531 consecutively screened patients at the two hospitals: UCSF and SFGH.

RESULTS

At UCSF, 1% of screened patients were not enrolled because they lacked surrogates, whereas 18% of screened patients were not enrolled at SFGH because they lacked surrogates. Lack of surrogate was the most common reason for nonenrollment among eligible patients at SFGH.

CONCLUSIONS

Critically ill patients with ALI at a public hospital were less likely to be enrolled in a clinical trial than patients at a university hospital primarily because they lacked surrogates. Lack of a surrogate also was a major factor in nonenrollment in other ARDS Network hospitals. In order to provide all affected patients an opportunity to participate in research, innovative strategies for increasing enrollment in critical care research without compromising protection from research risks are needed.

摘要

背景

将重症患者纳入临床试验具有挑战性。我们观察到,旧金山总医院(SFGH)主要收治贫困患者,与大学转诊中心加州大学旧金山分校(UCSF)的合格患者相比,SFGH的合格患者参加急性肺损伤(ALI)临床试验的可能性较小。我们研究了未入组的原因以及替代决策者的可获得性对重症监护临床试验入组的影响。

方法

分析了急性呼吸窘迫综合征网络(ARDS Network)针对ALI患者进行低潮气量通气与传统潮气量通气试验所收集的数据。对UCSF和SFGH这两家医院连续筛查的531例患者的人口统计学数据和未入组原因进行了分析。

结果

在UCSF,1%的筛查患者因缺乏替代决策者而未入组,而在SFGH,18%的筛查患者因缺乏替代决策者而未入组。缺乏替代决策者是SFGH合格患者中最常见的未入组原因。

结论

公立医院的ALI重症患者比大学医院的患者参加临床试验的可能性小,主要原因是他们缺乏替代决策者。缺乏替代决策者也是其他ARDS Network医院未入组的主要因素。为了让所有受影响的患者都有机会参与研究,需要采取创新策略来增加重症监护研究的入组人数,同时又不影响对研究风险的防范。

相似文献

1
Reasons for nonenrollment in a clinical trial of acute lung injury.未纳入急性肺损伤临床试验的原因。
Chest. 2008 Oct;134(4):719-723. doi: 10.1378/chest.08-0633. Epub 2008 Aug 8.
2
Study protocol: The Improving Care of Acute Lung Injury Patients (ICAP) study.研究方案:急性肺损伤患者改善护理(ICAP)研究。
Crit Care. 2006 Feb;10(1):R9. doi: 10.1186/cc3948.
3
[Characteristics and outcome of 70 ventilated COVID-19 patients : Summary after the first wave at a university center].70例接受机械通气的新冠肺炎患者的特征与预后:某大学中心第一波疫情后的总结
Anaesthesist. 2021 Jul;70(7):573-581. doi: 10.1007/s00101-020-00906-3. Epub 2020 Dec 28.
4
Pressure-controlled versus volume-controlled ventilation for acute respiratory failure due to acute lung injury (ALI) or acute respiratory distress syndrome (ARDS).压力控制通气与容量控制通气用于急性肺损伤(ALI)或急性呼吸窘迫综合征(ARDS)所致急性呼吸衰竭的比较。
Cochrane Database Syst Rev. 2015 Jan 14;1(1):CD008807. doi: 10.1002/14651858.CD008807.pub2.
5
Barriers and Facilitators of Surrogates Providing Consent for Critically Ill Patients in Clinical Trials: A Qualitative Study.代表重病患者参与临床试验时的同意书提供:定性研究中的障碍和促进因素。
Chest. 2024 Aug;166(2):304-310. doi: 10.1016/j.chest.2024.02.027. Epub 2024 Feb 20.
6
Characteristics and Outcomes of Eligible Nonenrolled Patients in a Mechanical Ventilation Trial of Acute Respiratory Distress Syndrome.急性呼吸窘迫综合征机械通气试验中合格未入组患者的特征和结局。
Am J Respir Crit Care Med. 2015 Dec 1;192(11):1306-13. doi: 10.1164/rccm.201501-0172OC.
7
PReVENT--protective ventilation in patients without ARDS at start of ventilation: study protocol for a randomized controlled trial.PReVENT——通气开始时非ARDS患者的保护性通气:一项随机对照试验的研究方案
Trials. 2015 May 24;16:226. doi: 10.1186/s13063-015-0759-1.
8
Clinician Recognition of the Acute Respiratory Distress Syndrome: Risk Factors for Under-Recognition and Trends Over Time.临床医师对急性呼吸窘迫综合征的识别:识别不足的危险因素及随时间的变化趋势。
Crit Care Med. 2020 Jun;48(6):830-837. doi: 10.1097/CCM.0000000000004328.
9
Plasma levels of surfactant protein D and KL-6 for evaluation of lung injury in critically ill mechanically ventilated patients.严重机械通气患者肺损伤评估中表面活性蛋白 D 和 KL-6 的血浆水平。
BMC Pulm Med. 2010 Feb 16;10:6. doi: 10.1186/1471-2466-10-6.
10
Effects of tidal volume on work of breathing during lung-protective ventilation in patients with acute lung injury and acute respiratory distress syndrome.潮气量对急性肺损伤和急性呼吸窘迫综合征患者肺保护性通气期间呼吸功的影响。
Crit Care Med. 2006 Jan;34(1):8-14. doi: 10.1097/01.ccm.0000194538.32158.af.

引用本文的文献

1
Alternative Tobacco Product Use in Critically Ill Patients.危重症患者使用另类烟草产品。
Int J Environ Res Public Health. 2020 Nov 24;17(23):8707. doi: 10.3390/ijerph17238707.
2
Detailed systematic analysis of recruitment strategies in randomised controlled trials in patients with an unscheduled admission to hospital.对非计划入院患者的随机对照试验中的招募策略进行详细的系统分析。
BMJ Open. 2018 Feb 2;8(2):e018581. doi: 10.1136/bmjopen-2017-018581.
3
Enrollment Challenges in Critical Care Nursing Research.重症护理研究中的招募挑战。
Am J Crit Care. 2017 Sep;26(5):395-400. doi: 10.4037/ajcc2017511.
4
Strategies to Maximize Enrollment in a Prospective Study of Comatose Children in the PICU.提高儿科重症监护病房昏迷儿童前瞻性研究入组率的策略。
Pediatr Crit Care Med. 2016 Mar;17(3):246-50. doi: 10.1097/PCC.0000000000000642.
5
Perspectives of Decisional Surrogates and Patients Regarding Critical Illness Genetic Research.决策代理人与患者对危重病基因研究的看法
AJOB Empir Bioeth. 2016 Jan 1;7(1):39-47. doi: 10.1080/23294515.2015.1039148. Epub 2015 May 1.
6
Does difficulty functioning in the surrogate role equate to vulnerability in critical illness research? Use of path analysis to examine the relationship between difficulty providing substituted judgment and receptivity to critical illness research participation.在替代角色中发挥功能的困难是否等同于危重病研究中的脆弱性?运用路径分析来检验提供替代判断的困难与接受危重病研究参与之间的关系。
J Crit Care. 2015 Dec;30(6):1310-6. doi: 10.1016/j.jcrc.2015.07.016. Epub 2015 Jul 26.
7
Surrogate receptivity to participation in critical illness genetic research: aligning research oversight and stakeholder concerns.替代者参与危重病遗传研究的接受度:协调研究监督与利益相关者的关切
Chest. 2015 Apr;147(4):979-988. doi: 10.1378/chest.14-0797.
8
Prevalence and impact of active and passive cigarette smoking in acute respiratory distress syndrome.急性呼吸窘迫综合征中主动和被动吸烟的患病率及影响
Crit Care Med. 2014 Sep;42(9):2058-68. doi: 10.1097/CCM.0000000000000418.
9
Critical illness in homeless persons is poorly studied: a systematic review of the literature.对无家可归者的危重病研究不足:文献系统综述
Intensive Care Med. 2014 Jan;40(1):123-5. doi: 10.1007/s00134-013-3124-4. Epub 2013 Oct 15.
10
Optimal duration of a sustained inflation recruitment maneuver in ARDS patients.最佳持续时间的肺复张手法在急性呼吸窘迫综合征患者。
Intensive Care Med. 2011 Oct;37(10):1588-94. doi: 10.1007/s00134-011-2323-0. Epub 2011 Aug 20.

本文引用的文献

1
Informed consent, confidentiality, and subject rights in clinical trials.临床试验中的知情同意、保密及受试者权利。
Proc Am Thorac Soc. 2007 May;4(2):189-93; discussion 193. doi: 10.1513/pats.200701-008GC.
2
A change in the Dutch Directive on Medical Research Involving Human Subjects strongly increases the number of eligible intensive care patients: an observational study.荷兰关于涉及人类受试者的医学研究指令的一项变更显著增加了符合条件的重症监护患者数量:一项观察性研究。
Intensive Care Med. 2006 Nov;32(11):1845-50. doi: 10.1007/s00134-006-0384-2.
3
A paradigm for inpatient resuscitation research with an exception from informed consent.一种无需知情同意的住院患者复苏研究范例。
Crit Care Med. 2006 Oct;34(10):2567-75. doi: 10.1097/01.CCM.0000239115.76603.55.
4
Does the emergency exception from informed consent process protect research subjects?知情同意程序的紧急例外情况是否能保护研究对象?
Acad Emerg Med. 2005 Nov;12(11):1056-9. doi: 10.1197/j.aem.2005.07.001.
5
Incidence and outcomes of acute lung injury.急性肺损伤的发病率及转归
N Engl J Med. 2005 Oct 20;353(16):1685-93. doi: 10.1056/NEJMoa050333.
6
Ethical considerations for research in critically ill patients.危重症患者研究的伦理考量
Crit Care Med. 2003 Mar;31(3 Suppl):S178-81. doi: 10.1097/01.CCM.0000064518.50241.fa.
7
Is the concept of informed consent applicable to clinical research involving critically ill patients?知情同意的概念是否适用于涉及重症患者的临床研究?
Crit Care Med. 2003 Mar;31(3 Suppl):S153-60. doi: 10.1097/01.CCM.0000054901.80339.01.
8
Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome.与传统潮气量相比,采用较低潮气量对急性肺损伤和急性呼吸窘迫综合征进行通气治疗。
N Engl J Med. 2000 May 4;342(18):1301-8. doi: 10.1056/NEJM200005043421801.
9
Ethical considerations of ensuring an informed and autonomous consent in research involving critically ill patients.在涉及重症患者的研究中确保知情且自主同意的伦理考量。
Am J Respir Crit Care Med. 1996 Sep;154(3 Pt 1):582-6. doi: 10.1164/ajrccm.154.3.8810590.
10
Report of the American-European Consensus conference on acute respiratory distress syndrome: definitions, mechanisms, relevant outcomes, and clinical trial coordination. Consensus Committee.欧美急性呼吸窘迫综合征共识会议报告:定义、机制、相关结局及临床试验协调。共识委员会
J Crit Care. 1994 Mar;9(1):72-81. doi: 10.1016/0883-9441(94)90033-7.