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临床试验/NCT02978300
NCT02978300已完成不适用

High-Flow Nasal Cannula Oxygen Therapy (HFNC) Alone or Associated With Noninvasive Ventilation (NIV) for Immunocompromised Patients Admitted to Intensive Care Unit for Acute Respiratory Failure : FLORALI-Immunodéprimés

Poitiers University Hospital2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2017年1月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
300
试验地点
2
主要终点
mortality rates

研究概览

简要总结

Acute respiratory failure is the leading cause of ICU admission of immunocompromized patients. In this subgroup of patients, the need for intubation and invasive mechanical ventilation occurs in about 50% of cases and is associated with very a high mortality rate, reaching 70% of cases. Therefore, noninvasive oxygenation strategies have been developed to avoid intubation.

More than 15 years ago, 2 trials have suggested that NIV could decrease intubation and mortality rates of immunocompromized patients as compared to standard oxygen through a mask. However these results have not been confirmed in a recent large trial.

HFNC is a recent and well-tolerated oxygenation technique. In a recent trial, HFNC alone could decrease mortality and intubation rates in patients with ARF as compared to NIV. Similar findings have been reported in a post-hoc analysis on immunocompromized patients excluding those with profound neutropenia. Likewise in a retrospective monocentric cohort of immunocompromized patients, we reported better outcomes with HFNC than with NIV.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Admission to ICU for acute respiratory failure defined by all of the following criteria:
  • Dyspnea at rest with RR ≥ 25 breaths/min
  • PaCO2 ≤ 50 mm Hg
  • PaO2/FiO2 ≤ 300 mm Hg under oxygen ≥ 10 l/min through a mask or HFNC or NIV (for patients under oxygen FiO2 will be calculated using the following formula: oxygen flow in liters per minute x 3 + 21)
  • Immunosuppresion defined by 1 of the following criteria:
  • Hematological malignancy (active or remitting < 5 years)
  • Allogenic stem cell transplantation < 5 years
  • Solid cancer (active)
  • Leucopenia < 1 G/l or neutropenia ≤ 0.5 G/l after chemotherapy
  • Solid organ transplantation
  • AIDS (not only HIV)
  • Treatment with immunosuppressive or immunomodulatory drugs
  • Systemic steroids ≥ 0.5 mg/kg/d of prednisone-equivalent for ≥ 3 weeks
  • Non opposition to participate obtained from the patient or their legally acceptable representative.

排除标准

  • Contraindication of NIV (patient refusal, cardiac arrest, coma, not drained pneumothorax, unresolving vomiting, upper airways obstruction, hematemesis, severe facial trauma)
  • Chronic respiratory failure with altered pulmonary function tests
  • Overt cardiogenic pulmonary edema
  • Urgent need for intubation
  • Severe shock (vasopressors > 0.3 µg/kg/min to maintain SAP > 90 mm Hg)
  • Impaired consciousness (Glasgow coma scale score ≤ 12) or agitation
  • Surgery under general anesthesia < 7 days
  • Previously included in the trial
  • Do-not-intubate order
  • Pregnancy or breastfeeding
  • Persons benefiting from enhanced protection, namely minors, persons deprived of their liberty by a judicial or administrative decision, persons staying in a health or social institution, adults under legal protection

研究组 & 干预措施

NIV/HFNC group

Active Comparator

Continuous NIV for at least 4 hours until clinical improvement then intermittent 1-hour sessions for a minimal duration of 12 hours a day. Between NIV sessions HFNC will be delivered as in the HFNC group.

干预措施: NIV/HFNC (Device)

HFNC group

Experimental

Continuous HFNC alone 24h/24 until weaning or intubation.

干预措施: HFNC (Device)

结局指标

主要结局

mortality rates

时间窗: day 28

Mortality rates at day 28 after randomization will be compared between the 2 groups

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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