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临床试验/NCT02523872
NCT02523872Unknown不适用

Description of Fluid Balance in Patients With Acute Respiratory Failure

Smiths Medical, ASD, Inc.1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2015年8月最近更新:
适应症

试验速览

阶段
不适用
入组人数
50
试验地点
1
主要终点
Sequential Organ Failure Assessment (SOFA)

研究概览

简要总结

The specific aim of this study is to gather data on fluid balance, intravenous medication administration, electrolyte balance, and diuretic and dialysis use in patients with acute respiratory failure who might benefit from a strategy designed to limit fluid administration.

详细描述

Disruption of fluid balance is common in critical illness. Many critical illnesses are inflammatory in nature and associated with capillary leak and swelling of tissues. While fluid administration may be necessary for the immediate resuscitation of a patient in shock, in the long term it may worsen survival and lead to complications. This is especially true in acute respiratory failure, where excess fluid can lead to a longer duration of mechanical ventilation, longer time in the ICU, and a greater need for dialysis. There is also evidence that conservative fluid administration can prevent complications. Fluid overload is associated with increased healthcare resource utilization and cost.

Much of the fluid administered to patients while in the adult ICU in the United States is administered as medications via large volume infusion pumps. This is a descriptive study to gather data on fluid balance, intravenous medication administration, electrolyte balance, and diuretic and dialysis use in patients with acute respiratory failure who might benefit from a strategy designed to limit fluid administration. The information will be used to design an interventional trial of small volume medication infusion.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Intubation and mechanical ventilation for ≤ 7 days
  • An underlying condition associated with acute respiratory failure (e.g. pneumonia, ARDS, sepsis, asthma, COPD exacerbation)
  • If in shock (MAP < 60, fluid bolus ≥30 ml/Kg or 4 L crystalloid or equivalent, vasopressors except for dopamine ≤ 5 mcg/kg/min or low-dose (≤ 0.04 IU/min) vasopressin) there should be no fluid bolus (1000 mL crystalloid or equivalent) for at least 12 hours

排除标准

  • Intubation or mechanical ventilation for > 7 days
  • Respiratory failure (requirement for positive pressure ventilation) in past 30 days
  • Shock (MAP < 60, fluid bolus ≥30 ml/Kg or 4 L crystalloid or equivalent, vasopressors except for dopamine ≤ 5 mcg/kg/min or low-dose vasopressin) requiring fluid bolus (1000 mL crystalloid or equivalent) within past 12 hours
  • Presence of a condition making it unlikely that the patient will be liberated from mechanical ventilation within the next 28 days (e.g. quadriplegia, end-stage lung disease, massive stroke, etc.)
  • Prognosis from underlying condition ≤ 28 days (estimated 28 day mortality from underlying condition >50%)
  • Likely intention (>50% probability) to withhold or withdraw life-supportive care within next 28 days

结局指标

主要结局

Sequential Organ Failure Assessment (SOFA)

时间窗: 28 Days

Mean and highest scores after T=0

Dialysis use

时间窗: 28 Days

Use of intermittent hemodialysis, continuous renal replacement therapy (CvvH, CvvHD), ultrafiltration (intermittent or SCUF), or aquapheresis (Aquadex™)

Ventilator-free days

时间窗: 28 Days

Number of days of being alive and unassisted breathing by 28 days after time=0

ICU-free days

时间窗: 28 Days

Number of days alive and out of ICU-level care by 28 days after time=0

Mortality

时间窗: 28 Days

Discharged from hospital alive or expired

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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