Practice of Fluid and Vasopressor Therapy in Critically Ill Invasively Ventilated Patients (PRoFLUID)-study protocol for an international multicenter observational cohort study.

4区 医学 Annals of translational medicine Pub Date : 2024-10-20 Epub Date: 2024-09-12 DOI:10.21037/atm-23-1957
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Abstract

Background: The practice of intravenous fluid and vasopressor therapy in intensive care unit (ICU) patients, particularly in those who receive invasive ventilation, has been subject to change. Traditional approaches of 'early and liberal fluid administration' and 'late and restrictive vasopressor use' have been challenged, leading to recommendations for giving less fluids and earlier administration of vasopressors. Recommendations for fluid deresuscitation-active fluid removal-are absent. The global approach to fluid and vasopressor therapy in invasively ventilated patients is currently unclear. Our aim is to explore the practice of intravenous fluid and vasopressor therapy in invasively ventilated ICU patients in a study named 'Practice of Fluid and Vasopressor Therapy in Critically Ill Invasively Ventilated Patients' (PRoFLUID).

Methods: PRoFLUID is an international, multicenter, observational cohort study in critically ill adult patients that are invasively ventilated for more than 24 hours. The outcomes include various aspects of fluid and vasopressor therapy, urine output and cumulative fluid balances. We will also collect duration of ventilation, lengths of stay and mortality in ICU and hospital. We expect to collect granular data on fluid and vasopressor therapy in a sample of at least 2,500 patients.

Discussion: PRoFLUID will provide useful insights into the practice of fluid and vasopressor therapy in invasively ventilated critically ill patients. PRoFLUID also allows us to determine whether geo-economic differences in management of intravenous fluid and vasopressor therapy exist, and allows for analyses of associations of aspects of fluid and vasopressor therapy with outcomes. Last but not least, its findings could feed sample size calculations of future randomized clinical trials of fluid and vasopressor therapy. In conclusion, PRoFLUID will collect data on fluid and vasopressor therapy in invasively ventilated ICU patients worldwide, providing insights that will guide future clinical decisions and randomized trial designs.

Trial registration: ClinicalTrials.gov NCT05968066. Registered on August 1, 2023.

Keywords: Intensive care; invasive ventilation; fluid therapy; fluid management; vasopressor.

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重症无创通气患者的液体和血管加压疗法实践(PRoFLUID)--一项国际多中心观察性队列研究的研究方案。
背景:重症监护病房(ICU)患者,尤其是接受有创通气的患者的静脉输液和血管加压疗法一直在不断变化。传统的 "早期和自由输液 "和 "晚期和限制性使用血管加压素 "的方法受到了挑战,这导致了减少输液和提早使用血管加压素的建议。目前还没有关于液体复苏--主动清除液体--的建议。目前,有创通气患者液体和血管加压疗法的全球方法尚不明确。我们的目的是在一项名为 "重症无创通气患者液体和血管加压疗法实践"(PRoFLUID)的研究中,探索无创通气 ICU 患者静脉输液和血管加压疗法的实践:PRoFLUID 是一项国际多中心观察性队列研究,研究对象是有创通气时间超过 24 小时的成年重症患者。研究结果包括液体和血管加压疗法、尿量和累积液体平衡的各个方面。我们还将收集患者在重症监护室和医院的通气时间、住院时间和死亡率。我们预计将收集至少 2,500 例患者的输液和血管加压疗法的详细数据:讨论:PRoFLUID 将为有创通气重症患者的输液和血管加压疗法提供有用的见解。PRoFLUID 还能让我们确定在静脉输液和血管加压疗法的管理方面是否存在地域经济差异,并能分析输液和血管加压疗法与预后的关联。最后但并非最不重要的一点是,它的研究结果可以为未来的输液和血管加压疗法随机临床试验的样本量计算提供参考。总之,PRoFLUID 将收集全球无创通气 ICU 患者的液体和血管加压疗法数据,为未来的临床决策和随机试验设计提供指导:试验注册:ClinicalTrials.gov NCT05968066。注册日期:2023 年 8 月 1 日.关键词:重症监护;有创通气:重症监护;有创通气;液体疗法;液体管理;血管加压素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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期刊介绍: The Annals of Translational Medicine (Ann Transl Med; ATM; Print ISSN 2305-5839; Online ISSN 2305-5847) is an international, peer-reviewed Open Access journal featuring original and observational investigations in the broad fields of laboratory, clinical, and public health research, aiming to provide practical up-to-date information in significant research from all subspecialties of medicine and to broaden the readers’ vision and horizon from bench to bed and bed to bench. It is published quarterly (April 2013- Dec. 2013), monthly (Jan. 2014 - Feb. 2015), biweekly (March 2015-) and openly distributed worldwide. Annals of Translational Medicine is indexed in PubMed in Sept 2014 and in SCIE in 2018. Specific areas of interest include, but not limited to, multimodality therapy, epidemiology, biomarkers, imaging, biology, pathology, and technical advances related to medicine. Submissions describing preclinical research with potential for application to human disease, and studies describing research obtained from preliminary human experimentation with potential to further the understanding of biological mechanism underlying disease are encouraged. Also warmly welcome are studies describing public health research pertinent to clinic, disease diagnosis and prevention, or healthcare policy.
 With a focus on interdisciplinary academic cooperation, ATM aims to expedite the translation of scientific discovery into new or improved standards of management and health outcomes practice.
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