Trauma Clinical Trial
Official title:
Restrictive vs. Liberal Oxygen Therapy for Trauma Patients. PILOT: The TRAUMOX Trial
The objective of this trial is to investigate whether treatment with oxygen in the early phases after a trauma plays a role in recovery.
Oxygen is probably the most frequently used drug both in the prehospital and emergency
setting. It is cheap, easily administered, and, at least for shorter time frames, widely
believed to be without any risk of harm.
Treatment with oxygen is indicated in the state of hypoxemia in order to prevent hypoxic
organ damage, however, oxygen is administered in many other situations too, sometimes in a
non-consistent manner and very often without even being prescribed.
Notably, administration of un-titrated oxygen, introduces a risk of hyperoxia which has been
associated with serious adverse effects.
Retrospective studies on patients with cardiac arrest, myocardial infarction (MI) and
traumatic brain injury have found hyperoxia to be associated with increased mortality and ICU
length of stays.
A randomized trial also found an increased rate of recurrent myocardial infarction in a
high-concentration oxygen group. Furthermore, in patients undergoing surgery, high
intraoperative FiO2 has been associated with major respiratory complications and with 30-day
mortality. In ICU patients, an observational study as well as a randomized trial found high
levels of oxygen to be associated with higher mortality compared to conservative oxygen
treatment. In particular, the randomized trial found that patients with PaO2 between 70 and
100 mmHg had a mortality of 11.6% compared to 20.2% in patients managed in accordance with
standard ICU practice (which allows PaO2 up to 150mmHg) (p=0.01).
For people between the ages of 5 and 44 years, trauma is one of the top three causes of
death. Almost twice as many men as women die as a result of trauma.
Victims of trauma are often healthy individuals prior to the incident, but acquire numerous
complications including sepsis and pulmonary complications as well as long-term complications
and diminished quality of life after the trauma. Understanding the reasons behind these
complications and poor outcomes and optimizing care is therefore essential to increase
survival rates and quality of life.
In the trauma population, oxygen administration is often standard of care. However, the
evidence supporting oxygen administration in this population appears to be extremely limited.
Nevertheless, absorption atelectases have been shown to develop within minutes under an
oxygen fraction of 1.0, and are strongly related to the development of pneumonia. Indeed, a
recent retrospective study found hyperoxemia to be an independent risk factor for ventilator
associated pneumonia (VAP). As the incidences of hyperoxemia in mechanically ventilated
patients range from 16-50% and the incidence of pneumonia in general in the Intensive Care
Unit (ICU) is close to 26%, and reported to be up to twice as high in the trauma population,
studies are warranted to establish the impact of a restricted, but sufficient, oxygen
strategy vs a liberal oxygen strategy in the trauma population.
The primary objective of this trial is to evaluate whether the maintenance of pragmatic
normoxia, avoiding both hyperoxic and hypoxic phases, is feasible within the first 24 hours
after trauma, as it may result in a reduction of 30-day mortality and major respiratory
complications within 30 days (respiratory failure, pulmonary edema, and pneumonia).
The investigators will therefore conduct a pilot study, where 40 evaluable patients are
randomized to 24 hours of:
- A. Restrictive, but sufficient oxygen treatment:
o Lowest oxygen delivery that obtains a saturation of ≥ 94% (within the low limits of
standard of care and does thus not put patients at risk of receiving worse treatment.
Hypoxic phases will be avoided.)
- B. Liberal oxygen treatment:
- 15 L/min oxygen flow initially/ FiO2 ≥0.8. (Considered as close as possible to the
standard of care. As no precise guidelines on oxygen delivery for trauma patients
within the first 24 hours exist, this will however inevitably vary in practice. We
have therefore set the delivery to be in the high end of the varying standard of
care.)
The investigators hypothesize that hospitalized trauma patients treated with liberal oxygen
therapy during the first 24 hours after trauma will have a greater risk of death and major
respiratory complications compared to trauma patients treated with restrictive oxygen. The
investigators realize that this cannot be assessed in this pilot study, but it is crucial to
know if the study is feasible before doing a large and adequately powered trial.
Composite Primary Outcomes:
• 30-day mortality and major respiratory complications within 30 days (pneumonia, acute
respiratory distress syndrome (ARDS), acute lung injury (ALI)).
Secondary Outcomes
- Intensive Care Unit length of stay (ICU LOS)
- Hospital length of Stay
- Days on ventilator
- 30 days post-trauma (through telephone follow-up if discharged)
- Glasgow Outcome Scale Extended (GOSE)
- Pneumonia
;
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