key: cord-0011230-wilnnd36
authors: Perner, Anders; De Jong, Audrey; Shankar-Hari, Manu
title: Trials on oxygen supplementation in sepsis: better late than never
date: 2019-11-26
journal: Intensive Care Med
DOI: 10.1007/s00134-019-05874-w
sha: 44deb1e65f245f3f66f5e2bc0ed3e19afb5a8336
doc_id: 11230
cord_uid: wilnnd36

nan

Oxygen supplementation is one of the most frequently used interventions in critically ill patients. In addition, most ICU patients with sepsis receive oxygen supplementation irrespective of the presence or absence of hypoxia [1] . In the 2016 iteration of the Surviving Sepsis Campaign (SSC) guideline [2] , there was no guidance on the use of supplementary oxygen or on oxygenation targets for these patients, alongside recommendations for further research [3] .

To our knowledge, at least one randomised trial has been conducted on oxygen therapy in sepsis, the Hyper2S-trial [4] . This two-by-two factorial, multicentre, randomised trial allocated mechanically ventilated patients with septic shock to an FiO 2 at 1.0 (hyperoxia) vs. an FiO 2 targeting an oxygen saturation of 88-95% (normoxia) during the first 24 h. The other allocation was to isotonic vs. hypertonic saline infusion. The trial was stopped prematurely for safety reasons when 442 of the planned 800 patients had been enrolled. The primary outcome, 28-day mortality, had occurred in 43% in the hyperoxia group vs. 35% in the normoxia group (hazard ratio 1.27, 95% CI 0.94-1.72; p = 0.12). The incidence of serious adverse events, including atelectasis and intensive care unit-acquired weakness, appeared to be higher in the hyperoxia vs. the normoxia group. While this caused some concern, the use of FiO 2 at 1.0 in clinical care of patients with sepsis appeared to be quite rare; the baseline FiO 2 in two sepsis trials combined (n = 1770) was reported to be 0.51 (inter-quartile range 0.40-0.70) [1] .

The results of the Hyper2S trial did support the notion of harm from more liberal use of oxygen as observed in observational studies in general ICU patients [5, 6] and in those with sepsis [1] . A post hoc analysis of Hyper2Strial highlighted potential harm only in patients meeting the sepsis-3 defined septic shock, which is hypotension requiring vasopressor therapy and raised lactate concentrations. The implication being harmful effects of oxygen may be exaggerated in sepsis patients with evidence of cellular and metabolic abnormalities [7] , likely to be mediated by reactive oxygen species, in the context of impaired mitochondrial function and lower antioxidant concentrations seen in sepsis [8] . The other larger trial done in ICU patients, the OXYGEN-ICU trial [9] , included 480 adult ICU patients expected to stay at least 72 h, among whom 40% had documented infection at baseline. Again, the results suggested that higher use of oxygen caused harm, but the single-center design and the stopping of the trial after an unplanned interim analysis hamper the interpretation.

On that background, it is more than welcome to read the publication of the sub-group of patients with sepsis from the ICU-ROX trial in Intensive Care Medicine [10] . The ICU-ROX trial was a multicentre randomized trial allocating 1000 adult ICU patients who were expected to be mechanically ventilated for > 24 h to receive conservative or usual oxygen therapy. In the conservativeoxygen group, the upper limit of SpO 2 was 97%; FiO 2 was decreased to 0.21 if the SpO 2 > 90%. In the usualoxygen group, there were no specific measures limiting the FiO 2 or the SpO 2 . In the full trial cohort, there was no difference in the number of ventilator-free days, which was the primary outcome. There were four predefined subgroup analysis, among which patients with suspected hypoxic-ischemic encephalopathy appeared to have worse outcome with usual oxygen therapy. The present study is a post hoc sub-group analysis of 251 patients adjudicated to have sepsis at baseline. There was no statistically significant treatment effect heterogeneity ; p value for interaction = 0.35 for sepsis vs. non-sepsis). None of the secondary outcomes differed between group, but all point estimates favoured usual-care oxygen. The investigators conclude that clinically important harm is possible with conservative oxygen therapy in patients with sepsis, but benefit cannot be excluded. The interpretation of these findings is hampered by the post hoc design, the lack of stratification for sepsis at allocation, in fact many of the patients presented had to identified in registers post hoc, the small samples size as acknowledged by the investigators and use of 90-day mortality as the outcome instead of the primary outcome of ventilator-free days used in the ICU-ROX trial.

Clearly these results call for more trials on oxygen in this patient group as suggested by the ICU-ROX investigators. There are several ongoing randomized trial enrolling ICU patients to different oxygenation strategies ( Table 1) ; several of these trials are likely enrolling at fair number of patients with sepsis. However, none of the trials are focused specifically on sepsis; the enrol patients with acute hypoxia, systemic inflammatory response syndrome or ARDS (Table 1) . And none of the ongoing trials are likely to provide a large sub-group of patients with sepsis to substantially increase the certain of the effect estimates observed in the ICU-ROX sub-group; the HOT-ICU trial is the only large trial ongoing, but the presence of sepsis is not registered at baseline in that trial [11] . A large subgroup of patients with sepsis will likely be included in the MEGA-ROX trial planned by the ICU-ROX investigators. When finalised, MEGA-ROX will have enrolled 40,000 ICU patients and likely provide reliable estimates on the effects of conservative oxygen therapy in sepsis.

Oxygen is a drug-as such it has beneficial effects and side-effects. The balance between the benefit and harm of higher vs. lower targets for oxygen supplementation in patients with sepsis is still unknown. Until we have better evidence from large randomized trials, a strategy that avoids both hypoxia and hyperoxia may be aimed for. Such a strategy was recommended in a recent clinical practice guideline on oxygen therapy in acutely ill medical patients. The strong recommendation was to aim for peripheral capillary oxygen saturation (SpO 2 ) of ≤ 96%, for acutely ill medical patients receiving oxygen therapy. The authors also highlight that it is reasonable to aim for a target range of 90-94% in most patients [12] . 

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Variability in targeted arterial oxygenation levels in patients with severe sepsis or septic shock

The Surviving Sepsis Campaign bundles and outcome: results from the International Multicentre Prevalence Study on Sepsis (the IMPreSS study)

Surviving sepsis campaign: research priorities for sepsis and septic shock

Hyperoxia and hypertonic saline in patients with septic shock (HYPERS2S): a two-by-two factorial, multicentre, randomised, clinical trial

Effectiveness and clinical outcomes of a two-step implementation of conservative oxygenation targets in critically ill patients: a before and after trial

Association between administered oxygen, arterial partial oxygen pressure and mortality in mechanically ventilated intensive care unit patients

Hyperoxia toxicity in septic shock patients according to the Sepsis-3 criteria: a post hoc analysis of the HYPER2S trial

Association between mitochondrial dysfunction and severity and outcome of septic shock

Effect of conservative vs conventional oxygen therapy on mortality among patients in an intensive care unit: the oxygen-ICU randomized clinical trial

Conservative oxygen therapy for mechanically ventilated adults with sepsis: a post hoc analysis of data from the intensive care unit randomized trial comparing two approaches to oxygen therapy (ICU-ROX)

Handling Oxygenation Targets in the Intensive Care Unit (HOT-ICU)-Protocol for a randomised clinical trial comparing a lower vs a higher oxygenation target in adults with acute hypoxaemic respiratory failure

Oxygen therapy for acutely ill medical patients: a clinical practice guideline