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Oxygen targets and 6-month outcome after out of hospital cardiac arrest: a pre-planned sub-analysis of the targeted hypothermia versus targeted normothermia after Out-of-Hospital Cardiac Arrest (TTM2) trial



Optimal oxygen targets in patients resuscitated after cardiac arrest are uncertain. The primary aim of this study was to describe the values of partial pressure of oxygen values (PaO2) and the episodes of hypoxemia and hyperoxemia occurring within the first 72 h of mechanical ventilation in out of hospital cardiac arrest (OHCA) patients. The secondary aim was to evaluate the association of PaO2 with patients’ outcome.


Preplanned secondary analysis of the targeted hypothermia versus targeted normothermia after OHCA (TTM2) trial. Arterial blood gases values were collected from randomization every 4 h for the first 32 h, and then, every 8 h until day 3. Hypoxemia was defined as PaO2 < 60 mmHg and severe hyperoxemia as PaO2 > 300 mmHg. Mortality and poor neurological outcome (defined according to modified Rankin scale) were collected at 6 months.


1418 patients were included in the analysis. The mean age was 64 ± 14 years, and 292 patients (20.6%) were female. 24.9% of patients had at least one episode of hypoxemia, and 7.6% of patients had at least one episode of severe hyperoxemia. Both hypoxemia and hyperoxemia were independently associated with 6-month mortality, but not with poor neurological outcome. The best cutoff point associated with 6-month mortality for hypoxemia was 69 mmHg (Risk Ratio, RR = 1.009, 95% CI 0.93–1.09), and for hyperoxemia was 195 mmHg (RR = 1.006, 95% CI 0.95–1.06). The time exposure, i.e., the area under the curve (PaO2-AUC), for hyperoxemia was significantly associated with mortality (p = 0.003).


In OHCA patients, both hypoxemia and hyperoxemia are associated with 6-months mortality, with an effect mediated by the timing exposure to high values of oxygen. Precise titration of oxygen levels should be considered in this group of patients.

Trial registration: NCT02908308, Registered September 20, 2016.


Cardiac arrest is a major cause of mortality and morbidity, and over the last years [1, 2], attention has risen toward the levels of oxygenation to achieve as an essential determinant of secondary brain injury and worsened outcomes [3]. Mechanical ventilation is commonly required to avoid hypoxemia [4], which is a well-known cause of anoxic brain injury promoting secondary brain and reperfusion-related damage [5, 6]. Recent literature has also focused on the role of hyperoxemia in critically ill patients [7,8,9,10]. Supplemental oxygen can correct hypoxemia, thereby supporting cell function, metabolism, and limiting organ dysfunction. However, it might have detrimental effects on patients’ outcomes through different pathophysiological mechanisms, such as the production of reactive oxygen species and free radicals yielding secondary damage due to reperfusion injury [11,12,13,14,15,16,17]. Studies exploring the role of hypo- and hyperoxemia after cardiac arrest are not conclusive. They present several heterogeneities in terms of study design, sample size and outcome definition, as well as inconsistent results, especially when compared to the preclinical cardiac arrest models [8, 18,19,20,21].

We therefore performed a secondary analysis of the Targeted Hypothermia versus Targeted Normothermia after Out-of-Hospital Cardiac Arrest (TTM2) trial that included Out-of-Hospital Cardiac Arrest (OHCA) patients. The aim was to assess the oxygen targets, the incidence of episodes of hypoxemia and hyperoxemia in the first 72 h of mechanical ventilation, and their association with patients’ 6-months outcome (mortality and neurological status).


This was a pre-planned secondary analysis of the TTM2 trial, which was an international, multicenter randomized controlled trial comparing the effects of normothermia (temperature ≤ 37.5 °C), versus hypothermia (target 33 °C until 28 h after randomization, and then rewarming to 37 °C) [22, 23]. This sub-analysis was conducted according to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guidelines [24] (Additional file 1: Table S1). Ethical approval was obtained in the coordinating center and in each participating center as well as informed consent according to local regulations. This sub-study was conducted in accordance with the principles of the Declaration of Helsinki, and the Medical Research Involving Human Subjects Act (WMO) and was approved on the 23rd of February 2017 by the TTM2 steering committee ( The protocol of the analysis was published [22]. No further ethical approval was necessary for the development of this study.

Objectives and definitions

The primary aim was to describe the arterial partial pressure of oxygen (PaO2) values observed in OHCA patients in the first 72 h of mechanical ventilation and the occurrence of episodes of hypo/hyperoxemia. As previous studies have considered arterial oxygen thresholds of < 60 mmHg and > 300 mmHg when evaluating associations between oxygen exposure and outcome [7, 8, 18, 25], we pre-specified that we would initially evaluate the same thresholds, and then, we aimed to calculate the “best” threshold of hypo/hyperoxemia associated with poor outcome. For primary analysis, three patients’ groups according to conventional thresholds were defined: (1) hypoxemia with one or more episodes of PaO2 levels < 60 mmHg; (2) normoxemia (including mild-moderate hyperoxemia, with PaO2 levels between 60 and 300 mmHg; and (3) severe hyperoxemia with one or more PaO2 levels > 300 mmHg. The secondary objectives were to assess: (1) the association between hypo/hyperoxemia during the first 72 h of mechanical ventilation with mortality and neurological outcome at 6-months; (2) the best threshold of hypo/hyperoxemia associated with mortality and poor neurological outcome; (3) the cumulative effect of the “dose” (oxygen exposure over time, PaO2-Area Under the Curve, AUC) of hypo/hyperoxemia on mortality and poor neurological outcome at 6-months; 4) the effect of PaO2 on outcome according to randomization in the normothermia versus hypothermia group.

Inclusion and exclusion criteria

Inclusion criteria of the TTM2 trial were patients 18 years of age or older admitted to the hospital after OHCA of non-traumatic or unknown cause with a return of spontaneous circulation (ROSC) requiring ICU admission and mechanical ventilation. Exclusion criteria were the following: unwitnessed OHCA with an initial rhythm of asystole, an interval from ROSC to screening over 180 min, temperature on admission < 30 °C, obvious or suspected pregnancy, intracranial bleeding at admission [22, 23]. For this sub-analysis, we further excluded patients who had no available data on PaO2 in the first 24 h from hospital admission.

Data management and collection

Details on the study procedure and patients’ clinical management have been previously described [22, 23]. Ventilatory management was performed according to local practice. Patients’ data were collected at hospital admission, during the intensive care unit (ICU)-stay, at ICU-discharge, at hospital-discharge, and at 6-month follow-up [22, 23]. Data collected included patients’ demographic characteristics, pre-cardiac arrest comorbidities (including Charlson comorbidity index [26]), location, timing, type and management of cardiac arrest, clinical presentation (presence of shock, ST-elevation myocardial infarction—STEMI), data on ventilator settings/parameters (tidal volume—VT, positive end-expiratory pressure—PEEP, respiratory rate—RR, fraction of inspired oxygen—FiO2, plateau pressure—Pplat, peak pressure—Ppeak, compliance of respiratory system—Crs), and arterial blood gases (ABG) values (pHa, PaO2, partial pressure of carbon dioxide—PaCO2, base excess) and clinical outcomes. Ventilatory settings and ABG values were collected from randomization every 4 h for the first 32 h, and then, every 8 h until day 3 (72 h).

Clinical outcome measures

Clinical outcome measures were mortality and patients’ neurological outcome at 6-month follow-up, the latter evaluated through the Modified Rankin Scale (mRS). The mRS score for neurologic disability is a 7 categories scoring system, ranging from no symptoms (score 0) to patient’s death (score 6), where poor neurological outcome is defined as a score ranging from 4 to 6. Follow-up data were obtained by study participants through telephone interview, postal questionnaire, or a face-to-face visit. Responses were obtained from patients or from a next of kin in cases of impaired cognitive capacity, which could prevent patient interview.

Statistical analysis

At baseline, data on patient characteristics, ventilator settings, and ABG were presented as means ± standard deviation, or medians [interquartile range (IQR)] for continuous variables, or as percentages for the categorical ones. The comparisons of means, medians, and frequencies among the three categories for PaO2 were carried out using one-way ANOVA, Kruskal–Wallis' test, and chi-square test, respectively. When building a regression model, the process of variable selection comprised an initial model with: (1) patients’ clinical characteristics (age, sex, body mass index—BMI, height, Charlson comorbidity index, state of shock at admission, and STEMI diagnosis on admission); (2) onsite-related cardiopulmonary resuscitation (CPR) related variables (ROSC time, bystander CPR, OHCA physical location, initial cardiac rhythm, witnessed OHCA); (3) treatment variables from the original trial (randomization arm and tympanic temperature at admission); and (4) ABG values and (5) ventilatory settings parameters. From this initial set of covariates, a more parsimonious model was developed by backward elimination using a multivariable fractional polynomial (FP) procedure [27]. The linearity assumption of continuous variables was tested, and the variable transformed with the appropriate FP when the assumption was not met. Risk estimates from the Cox regression and logistic regression models were expressed as hazard ratios (HRs) and Odds ratios (ORs) with 95% confidence intervals (95% CI), respectively. If PaO2/PaO2-AUC (as continuous) were modeled with a FP, their association with the endpoint was instead depicted through a graph where the HR/OR on the y-scale is plotted against the continuum of the marker.

The independent association between baseline PaO2 (or PaO2 groups-PaO2_class) with 6-months mortality was evaluated with Cox regression analysis. As a sensitivity analysis, the area under the receiving operator curve (ROC) curve of all PaO2 values (PaO2-AUC) was calculated for each patient and tested in a Cox regression for mortality, which was built considering the repeated measures of PaO2 as a single time point representing the numerical integration of PaO2 values and the time between measurements. Therefore, PaO2-AUC represents a sequential (cumulative) integration over time of all PaO2 preceding values obtained during the first 72 h since ICU admission. Because we were interested exploring the prognostic value of PaO2-AUC on hypoxemia and hyperoxemia, an interaction with PaO2_class was included in the Cox regression model.

A 2-sided p value of < 0.05 was the threshold used for significance in all analyses. Stata 16.1 was used for data clean-up, preparation, and statistical analysis. Further details on statistical methods are presented in the Additional file 1.


Characteristics of the patients in the whole population

From a total of 1861 patients included in the TTM2 trial, 443 patients were excluded due to missing values in PaO2 in the first 24 h, leaving a sample of 1418 patients (Table 1, Additional file 1: Tables S2, S3). The median age was 65 [IQR = 55–74] years, and 292 (20.6%) were female. At 6-month follow-up, 696 (49.1%) patients were dead, and 740 (55.9%) had poor neurological outcome. Additional file 1: Table S2 and S3 present patients’ clinical characteristics, outcome measures, and ventilator settings, respectively, and according to the different classes of PaO2.

Table 1 Baseline patients’ characteristics, comorbidities, pre-hospital settings/interventions of the overall population and stratified according to oxygen values

PaO2 distribution and the occurrence of episodes of hypo/hyperoxemia

At admission, the median PaO2 value in the overall population was 108 mmHg [IQR = 83–163]. Seventy-nine patients (5.6%) presented a PaO2 < 60 mmHg (median PaO2 = 51 mmHg [IQR = 39.7–56.2]); 100 (7.1%) patients a PaO2 > 300 mmHg (median PaO2 = 363 mmHg [IQR = 330–433]); and 1239 (87.4%) patients had a PaO2 between 60 and 300 mmHg (median PaO2 = 108 mmHg [IQR = 85.5–148.5]). PaO2 trajectories over the 72 h study period are shown in Additional file 1: Figure S1. Over the study period, 24.9% of patients had at least one episode of PaO2 < 60 mmHg and 7.6% of patients had at least one episode of PaO2 > 300 mmHg, Fig. 1. In most cases, patients had 1 or 2 episodes over the first 72 h, whereas more than 2 episodes were less frequent. The incidence rates (number of episodes per person in the 72 h follow-up) for PaO2 < 60 mmHg and PaO2 > 300 mmHg were 0.42 (95% CI 0.39–0.45) and 0.08 (95% CI 0.07–0.10), respectively.

Fig. 1
figure 1

Frequency distribution of arterial partial pressure of oxygen (PaO2) classes (conventional thresholds). Number of hypoxemia (PaO2 < 60 mmHg) or severe hyperoxemia (PaO2 > 300 mmHg) episodes per patient during the first 72 h after intensive care unit admission. This figure was based on all patients included in the cohort, with a percent distribution as follow: Episodes of Hypoxemia = 0 (n = 1372 (75.01%), 1 (n = 304 (16.62%), 2 (n = 88 (4.81%), 3 (n = 39 (2.13%), 4 + (n = 26 (1.42%). Episodes of Hyperoxemia = 0 (n = 1689 (92.35%), 1 (n = 130 (7.11%), 2 (n = 9 (0.49%), 4 (n = 1 (0.05%)

The association between hypo- and hyperoxemia with 6-months mortality

Figure 2 presents the adjusted PaO2 trajectories according to survival status. PaO2 values decreased significantly until the 40th hour and then, leveled-off afterward both in survivors and non-survivors. The differences between the two trajectories according to survival status were statistically significant up to the first 32 h of measurement (omnibus p value = 0.007). Higher PaO2 values were associated with better survival. The Kaplan–Meier curve (Additional file 1: Figure S2) suggested a trend toward better survival in the normoxemia group, compared to both the hypoxemia and severe hyperoxemia groups, although not statistically significant. At multivariable Cox regression, PaO2 followed a U-shape risk profile, demonstrating that both hypo- and hyperoxemia were independently associated with higher mortality rates (omnibus p value = 0.0006; Fig. 3).

Fig. 2
figure 2

Adjusted hourly trajectories of partial pressure of oxygen according to 6-month survival status. Left panel shows the predicted partial pressure of oxygen (PaO2) trajectories according to survival status. Right panel shows the PaO2 differences between survivors and non-survivors at each time point. For this analysis, mixed regression model included a random intercept on patients ID and a random coefficient on the time variable (time elapsed between measurements). These predicted trajectories were adjusted for TTM2 randomization arms, age (year), gender, Charlson comorbidity index, state of shock at admission, return to spontaneous circulation-ROSC- time, initial cardiac rhythm (shockable vs non-shockable), witnesses of cardiac arrest, respiratory rate (breath/min), plateau pressure (cmH2O),positive end expiratory pressure (cmH2O), arterial partial pressure of carbon dioxide, PaCO2 (mmHg), pH, Base excess (mEq/L), and fraction of inspired O2 (%). Right panel confirmed that the differences between these two trajectories (survivors/non-survivors) are statistically significant up to the first 32 h of measurement (omnibus p value = 0.0074). ICU, Intensive Care Unit

Fig. 3
figure 3

Arterial partial pressure of oxygen (PaO2) mortality risk profile. In this Cox regression, PaO2 was modeled with a fractional polynomial (FP) of second degree FP [0–1], and included the following covariates: TTM2 randomization group, tympanic temperature at admission, age (years), gender, Charlson comorbidity index, cardiac arrest witnessed, time to return to spontaneous circulation, ROSC (min), bystander performed cardiopulmonary resuscitation, CPR, shockable rhythm, cardiac arrest location (home, public place, other), shock diagnosis on admission, ST-Elevated myocardial infarction (STEMI) diagnosis on admission, respiratory rate (breath/min), positive end-expiratory pressure, arterial partial pressure of carbon dioxide (PaCO2) (mmHg), pHa, and Base excess (mEq/L), Driving pressure (cmH20), and mechanical power (J/min). Along the PaO2 continuum, values before and after its median (108.7 mmHg and used as reference—see vertical line in red) were statistically associated with mortality if the 95% confidence interval (CI) did not cover the y-line of 1 (horizontal line in red)

Definition of the “best” threshold of hypoxemia and hyperoxemia associated with 6-months mortality

Figure 4 shows the “best” threshold of hypoxemia and hyperoxemia for the prediction of 6-month mortality in our cohort. The best cut-off point for hypoxemia was a PaO2 of 69 mmHg (Risk Ratio = 1.009, 95% CI 0.93–1.09) and for hyperoxemia was a PaO2 of 195 mmHg (Risk Ratio = 1.006, 95% CI 0.95–1.06). The characteristics of the patients according to the best thresholds calculated are shown in Additional file 1: Table S4–S6. At admission, 165 patients (11.6%) presented with hypoxemia (median value 60 mmHg [IQR = 51.7–65.2]), 263 (18.5%) with hyperoxemia (273 mmHg [IQR = 231.7–342.7]), and 990 patients (69.8%) with normoxemia (105 mmHg [IQR = 87–133]). Over the study period, 55.9% of patients had at least one episode of hypoxemia and 21.7% had at least one episode of hyperoxemia, and in most cases patients experienced only 1 or 2 episodes of hypoxemia and/or hyperoxemia over the first 72 h of mechanical ventilation. The incidence (number episodes per person in the 72 h follow-up) for hypoxemia and hyperoxemia considering the best thresholds was 1.34 (95% CI 1.29–1.40) and 0.26 (95% CI 0.24–0.29), respectively (Fig. 5).

Fig. 4
figure 4

Relative distribution analysis for the definition of the best cut-off of arterial partial pressure of oxygen (PaO2) associated with mortality. Best cutoff point along the continuum of the marker that separated survivors versus non-survivors at the end of the follow-up. In this analysis, the quantile (or proportion) distribution of the marker survivors (plotted on the x-axis plus the corresponding marker values at the top) is plotted against the proportion ratio of the marker distribution for non-survivors

Fig. 5
figure 5

Frequency distribution of arterial partial pressure of oxygen (PaO2) classes (according to best threshold). Numbers of hypoxemia/hyperoxemia episodes per patient during the first 72 of mechanical ventilation. This figure was based on all patients included in the cohort, with a percent distribution as follow: Episodes of Hypoxemia = 0 (n = 805 (44.01%), 1 (n = 439 (24.00%), 2 (n = 239 (13.07%), 3 (n = 142 (7.76%), 4 + (n = 204 (11.05%). Episodes of Hyperoxemia = 0 (n = 1431 (76.90%), 1 (n = 339 (18.53%), 2 (n = 43 (2.35%), 3 (n = 10 (0.55%), 4 + (n = 6 (0.33%)

Dose of oxygen and interaction between oxygen values and TTM2-arms.

Additional file 1: Figure S3 shows the hypoxemia and hyperoxemia mortality risk difference considering the exposure over time or “dose” of oxygen defined as PaO2-AUC. PaO2-AUC for hyperoxemia showed to be associated with higher mortality risk as compared to normoxemia (interaction p value = 0.0039).

Additional file 1: Figure S4 shows the interaction between PaO2 and TTM2-arms (hypothermia versus normothermia). No difference was observed on the effect of PaO2 on mortality between the TTM2-randomization groups (interaction p value = 0.997). HRs of hypoxemia and hyperoxemia on mortality for the hypothermia group were 1.07 (95% CI 0.58–1.98; p = 0.82), and 1.38 (95% CI 0.82–2.32; p = 0.22), respectively.

The association between hypo- and hyperoxemia with neurological outcome

No differences were observed in the trajectories of PaO2 values in the first 72 h according to poor and good neurological status (omnibus value p = 0.35). Also, the distribution of the mRS score was not different among PaO2 classes (Additional file 1: Figure S5, p = 0.55). At multivariate analysis, no significative association with poor neurological outcome (mRS = 4–6) was observed (omnibus value, p = 0.63), even considering separately mRS 4 and 5 (Additional file 1: Figure S6). Accordingly, we were not able to find a best cut-off point for neurological outcome (Additional file 1: Figure S7).


In a large cohort of OHCA patients included in an international multicenter randomized clinical trial, we found that: (1) hypoxemia and severe hyperoxemia events are uncommon after OHCA, considering the conventional thresholds suggested in the literature; (2) the “best” cutoff values of oxygen associated with the risk for mortality were a PaO2 below 69 mmHg and above 195 mmHg; with the use of these cut-offs, the incidence of episodes of hypoxemia and hyperoxemia markedly increased; (3) hypoxemia and hyperoxemia are independently associated with 6-months mortality but not with neurological outcome; the time-exposure (or “dose”) of hyperoxemia was associated with 6-months mortality; and 4) these results were consistent across the group of randomization (normothermia or hypothermia).

To the best of our knowledge, this is the largest prospective study exploring the targets of oxygen as well as the association of hypoxemia and hyperoxemia with outcome in a homogeneous population of OHCA patients. We believe that our results are relevant and confirm not only the important effects of hypoxemia but also of hyperoxemia on 6-months mortality. In addition, we identified new thresholds of PaO2 which are at risk for poor outcome.

Several studies highlighted the importance of maintaining appropriate ventilation targets and levels of PaO2 in OHCA patients [27]. Post-cardiac arrest syndrome includes a number of pathophysiological mechanisms such as brain edema, reperfusion injury and oxidative stress, which can lead to neuronal damage and brain injury [28]. Hypoxemia caused by cardiac arrest yields to an alteration of cerebral metabolism, neuronal cell injury and death [7, 29].

The occurrence of hypoxemia and hyperoxemia is variable in the literature, with overall incidence of about 19% for hypoxemia [7] and between 3 and 60% for hyperoxemia [7, 25, 30]. Considering the conventional thresholds, the incidences of episodes of hypoxemia and severe hyperoxemia in our study were compatible with previous literature. The use of new “best” thresholds for oxygenation compared to traditional ones led to a marked increase in the number of patients exposed to at least one episode of hypoxemia or hyperoxemia.

The PaO2 threshold responsible for the onset of hypoxic neuronal damage is not completely defined, and it is generally considered at 60 mmHg [31,32,33,34]. This value could underestimate the risk of hypoxemia in the OHCA population as the “best” lower threshold associated with increased mortality was found at PaO2 of 69 mmHg.

Although recommendations suggest to give the maximum feasible inspired oxygen during CPR [8, 18, 35] to avoid hypoxemia [36, 37], recent evidence suggests a possible harmful effect also of hyperoxemia after OHCA [38]. A systematic review reported higher mortality in hyperoxemic compared to normoxemic patients with cardiac arrest and extracorporeal life support, but not in other groups of patients [39]. Another recent meta-analysis of observational studies [40] showed that severe hyperoxemia (PaO2 > 300 mmHg) was associated with worse outcome, especially if hyperoxemia occurred during the first 36 h after cardiac arrest. However, high heterogeneity was found among the studies included in the meta-analysis, regarding the threshold of oxygen adopted, patient selection, the use of TTM, outcome measurement, methods of analyzing blood gas and often lack a pre-defined sampling protocol [20, 21, 41]. Many studies just considered PaO2 values in the very early phases from ROSC [42], did not evaluate the duration of hyperoxemia (the dose), had limited sample sizes, or had retrospective designs or prospective design with a post hoc analysis [7, 8, 18, 43]. In the present preplanned study, both hypoxemia and hyperoxemia as well as the dose (AUC) of hyperoxemia over time were associated with mortality. This implies that the pathophysiological effect of hyperoxemia importantly depends not only on the intensity, but also on the duration of the exposure to high oxygen values. Also, the best upper threshold of PaO2 associated with the risk for mortality was above 195 mmHg. This point is of critical importance and makes our results unique, potentially explaining why in previous studies using the conventional threshold of 300 mmHg a non-consistent association with outcome was found [41, 44,45,46]. We hypothesize that the risk for hyperoxemia might have been underestimated considering the traditional thresholds, and that in the post-ROSC phase clinicians should pay attention in the titration of oxygen to lower levels than thought before.

Different oxygen targets have been proposed by trials on oxygen [47,48,49], and the recent BOX trial [49], which compared 2 targets of PaO2 68–75 mmHg vs 98–105 mmHg, showed similar incidence of death or severe disability or coma among groups, suggesting that question remains especially about the higher target of oxygen to be applied in this population, which requires further investigation.

When splitting the patients according to the use of hypothermia and normothermia, no statistically differences were found in outcome between the two groups, thus suggesting that temperature 33 °C does not improve oxygen tolerance and could further explain the lack of protective effect of hypothermia [23]. The fact that hypoxemia and hyperoxemia were not associated with poor neurological outcome (mRS 4 and 5) might be explained by different factors. Firstly, the scale used to evaluate neurological disability does not specifically account for specific cognitive dysfunction; further, neurological outcome may be affected by many different post-acute factors such as systemic complications or secondary brain damage during the ICU stay, in the hospital, or during rehabilitation. In particular, despite we used a robust statistical model which took in consideration several confounding factors, oxygen derangements might be a marker for systemic clinical events that can lead to an increase in mortality, i.e., pneumonia, sepsis, without a definitive effect on neurological outcome.


This study has several limitations. Firstly, although this was a preplanned secondary analysis of the TTM2 trial, this is an observational study, and our results should be regarded as hypothesis-generating, and we cannot make any causality statements from our results. A randomized clinical trial will be in fact necessary to confirm our findings, with the aim to explore the effect of oxygen more deeply on neurological outcome and the interaction of oxygen derangements with systemic factors.

Secondly, we hypothesized that oxygen pressure in-between PaO2 measurement was linear, and we were not able to account for short-term variations of PaO2. Nevertheless, the present study includes the highest number of available data on PaO2 measures with serial measurements. Third, although this was a preplanned study, some information is lacking in eCRF, and some data are missing in the database. Finally, the conventional thresholds used in this analysis were adopted according to robust observational studies, but these values present important heterogeneity in the literature [18, 25, 47], with no definitive conclusions regarding the optimal oxygen targets, especially for the higher threshold of oxygen. The ongoing Mega-ROX trial [48] is exploring two different levels of oxygen mainly based on SpO2 and a recently published RCT [49], compared 2 targets of PaO2 with higher target of 98–105 mmHg. Our results can pave the way to the definition of further RCTs and better define the best thresholds of oxygenation to be applied in this population.


In mechanically ventilated patients after out of hospital cardiac arrest, we found novel “best” cutoff values of oxygen associated with the risk for mortality at PaO2 below 69 mmHg and above 195 mmHg; with the use of these cut-offs, episodes of hypoxemia and hyperoxemia are common in this population. Both hypoxemia and hyperoxemia are associated with higher 6-months mortality, and this may be mediated by the timing exposure to high values of oxygen. More cautious titration of oxygen levels should be considered in this group of patients until stronger evidence is available.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available but are available from the corresponding author on reasonable request.



Arterial blood gas


Area under curve


Body mass index


Confidence interval

CO2 :

Carbon dioxide


Respiratory system compliance


Electronic case record form


Cardiopulmonary resuscitation

FiO2 :

Fraction of inspired oxygen


Fractional polynomial


Hazard ratio


Intensive care unit


Interquartile range


Length of stay


Modified Rankin Scale


Out of hospital cardiac arrest


Odds ratio

PaCO2 :

Arterial partial pressure of CO2

PaO2 :

Arterial partial pressure of oxygen


Positive end-expiratory pressure


Arterial pH


Principal investigator


Peak pressure


Plateau pressure


Return of spontaneous circulation


Respiratory rate


ST elevation myocardial infarction


STrengthening the Reporting of OBservational studies in Epidemiology


Target temperature management 2 Trial

VT :

Tidal volume


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We would like to thank Prof Eduardo Nunez for the support with the statistical analysis.

TTM2 Trial collaborators


Niklas Nielsen, Jan Bělohlávek, Clifton Callaway, Alain Cariou, Tobias Cronberg, Josef Dankiewicz, Glenn Eastwood, David Erlinge, Hans Friberg, Jan Hovdenes, Janus Christian Jakobsen, Michael Joannidis, Hans Kirkegaard, Helena Levin, Gisela Lilja, Matt P. G. Morgan, Alistair D. Nichol, Per Nordberg, Mauro Oddo, Paolo Pelosi, Christian Rylander, Manoj Saxena, Christian Storm, Fabio S. Taccone, Susann Ullén, Matt P. Wise, Paul J. Young


Kathy Rowan, David Harrison, Paul Mouncey, Manu Shankar-Hari, Duncan Young


Susann Ullén, Theis Lange, Karolina Palmér


Core management group: Niklas Nielsen, Josef Dankiewicz, Tobias Cronberg, Hans Friberg, Gisela Lilja, Helena Levin

Clinical Trial Manager: Janus Christian Jakobsen, Susann Ullén

Trial financial management: Ulla-Britt Karlsson, Simon Heissler

Manoj Saxena, Frances Bass, Naomi Hammond, John Myburgh, Colman Taylor

Alain Cariou, Adele Bellino


Marwa Abel-all, Ben Finfer, Carolyn Koch, Yang Li, Anne O’Connor, Julia Pilowsky, Tina Schneider, Anna Tippett, Bridget Ady, Tessa Broadley, Amanda Brown, Liz Melgaard, Mimi Morgan, Vanessa Singh, Rebecca Symons, Kathrin Becker, Nathalie Van Sante, Vendula Saleova, Silvie Zerzanova, Helena Levin. France: Clinical Research Unit, Paris Descartes Necker Cochin, Paris: Samia Sefir-Kribel. Germany: Charité Universitätsmedizin, Berlin: Ute Lübeck. Italy: Mario Negri Institute for Pharmacological Research, Milan: Martina Carrara. New Zealand: Medical Research Institute of New Zealand (MRINZ), Wellington: Kathryn Fernando, Diane Mackle, Leanlove Navarra, Judith Riley. Norway: Oslo University Hospital, Oslo: Elin Westerheim; Haukeland University Hospital, Bergen: Marianne Flatebø. Sweden: Helsingborg Hospital, Helsingborg: Ameldina Ceric, Zana Haxhija, Lovisa Terling; Skåne University Hospital, Lund: Lena Bossmar, Liz Jergle, Helén Holm Månsson. Switzerland: Lausanne University Hospital (CHUV), Lausanne: Samia Abed Maillard, Andreja Vujicic Zagar; Cantonal Hospital St. Gallen, St. Gallen: Christina Jodlauk. United Kingdom: University Hospital of Wales, Cardiff: Helen Hill; Niche Science & Technology, Richmond: Jennifer Scrivens; The HRB Irish Critical Care- Clinical Trials Network (ICC-CTN), Dublin, Ireland: Kate Ainscough, Ciara Fahey.


Australia: Austin Hospital, Melbourne: Rinaldo Bellomo (PI), Glenn Eastwood, Leah Peck, Helen Young; Concord Repatriation General Hospital, Sydney: Winston Cheung (PI), Rosalba Cross, Michael Hayes, Nitin Jain, Mark Kol, Asim Shah, Atul Wagh, Helen Wong; John Hunter Hospital, Newcastle: F. Eduardo Martinez (PI), Gail Brinkerhoff, Dustin Bush; Liverpool Hospital, Sydney: Antony Stewart (PI), Anders Aneman, Lien Lombardo, Peter McCanny, James Penketh; Nepean Hospital, Sydney: Ian Seppelt (PI), Rebecca Gresham, Julie Lowrey, Kristy Masters, Christina Whitehead; Princess Alexandra Hospital, Brisbane: James Walsham (PI), Meg Harward, Josephine Mackay, Jason Meyer, Emma Saylor, Ellen Venz, Krista Wetzig; Royal North Shore Hospital, Sydney: Wade Stedman (PI), Angela Ashelford, Frances Bass, Naomi Hammond, Sharon Mar, Julia Pilowsky, Miyuki Tokumitsu, Elizabeth Yarad; St Vincent's Hospital, Sydney: Hergen Buscher (PI), Claire Reynolds; The Alfred Hospital, Melbourne: Andrew Udy (PI), Aidan Burrell, Jasmin Collins, Dashiell Gantner, Victoria Emma-Leah Martin, Phoebe Mccracken, Vinodh Nanjayya, AlistairNichol, Alexander Sacha Richardson, Meredith Young; The Northern Hospital, Melbourne: Angaj Ghosh (PI), Simone Said.

Austria: Medical University Innsbruck, Innsbruck: Michael Joannidis (PI), Ronny Beer, Frank Hartig, Raimund Helbok, Sebastian Klein, Andreas Peer.

Belgium: Erasme University Hospital, Brussels: Fabio S. Taccone (PI), Jacques Creteur, Dominique Durand; Ziekenhuis Oost-Limburg, Genk: Matthias Dupont (PI), Sigrid Christiaens, Carola Claes, Sebastiaan Deckx, Bert Ferdinande, Sanne Lenaerts, Wilifred Mullens, Sarah Stroobants, Evi Theunissen, David Verhaert.

Czech Republic: General University Hospital, Prague: Ondřej Šmíd (PI), Marek Flaksa, David Kemlink, Jan Malík, Michal Otáhal, Jan Rulíšek, Michal Šíranec, Zdeněk Stach, Anna Valeriánová, Petra Zavadilova; University Hospital Hradec Králové, Hradec Králové: Miroslav Solař (PI), Róber Bánszky, Jana Červená, Renata Černá Pařízková, Libor Šimůnek, Filip Varhaník; Regional Hospital Liberec, Liberec: Jiří Karásek (PI), Matěj Strýček.

Denmark: Aarhus University Hospital, Aarhus: Anders Grejs (PI), Steffen Christensen, Peter Juhl-Olsen, Ida Katrine Thomsen, Lisa Gregersen Østergaard.

France: Cochin University Hospital (APHP), Paris: Alain Cariou (PI), Albert Cao, Pierre Dupland, Ariane Gavaud, Paul Jaubert, Mathieu Jozwiak, Nathalie Marin, Guillaume Savary; Lariboisiere University Hospital (APHP), Paris: Nicolas Deye (PI), Bruno Megarbane, Pierre Mora, Laetitia Sutterlin; Centre Hospitalier de Versailles, Le Chesnay: Stephane Legriel (PI), Hugo Bellut, Alexis Ferre, Guillaume Lacave, Marine Paul; CHU de Nantes, Nantes: Jean-Baptiste Lascarrou (PI), Emmanuel Canet, Charlotte Garret, Arnaud Felix Miaihle, Jean Reignier; Dupuytren Teaching Hospital, Limoges: Philippe Vignon (PI), Thomas Daix, Arnaud Desachy, Bruno Evrard, Bruno Francois, Anne-Laure Fedou, Marine Goudelin.

Germany: Charité Universitätsmedizin, Berlin: Christian Storm (PI), Gabriele Kress, Christoph Leithner, Jens Nee, Kaspar Josche Streitberger.

Italy: San Martino Policlinico Hospital, Genoa: Iole Brunetti (PI), Lorenzo Ball, Denise Battaglini, Giulia Bonatti, Iacopo Firpo, Paolo Frisoni, Arianna Iachi, Simona Maiani, Maura Mandelli, Chiara Robba, Fabio Tarantino; Civil Hospital, Baggiovara, Modena: Alberto Barbieri (PI), Elisabetta Bertellini, Enrico Giuliani, Gabriele Melegari; University of Trieste, Trieste: Erik Roman-Pognuz (PI), Giorgio Berlot, Umberto Lucangelo, Elisabetta Macchini.

Norway: Oslo University Hospital, Rikshospitalet, Oslo: Jan Hovdenes (PI), Vibeke Aune, Tomas Drægni, Simon Jacobsen, Søren Pieschke, Åse Rasmussen, Gro Ringstad Akselsen; St. Olav’s University Hospital, Trondheim: Halvor Langeland (PI), Daniel Bergum, Therese M. Erbe, Pål Klepstad, Helle M. Næss; Sorlandet Hospital, Arendal: Roy Bjørkholt Olsen (PI), Lena Eriksen Skjelnes, Marius Holen, Joakim Iver Post; Haukeland University Hospital, Bergen: Rune Fanebust (PI), Linda Hårteig Sørensen, Ken Åge Kårstad, Carsten Fredrik Wickman.

New Zealand: Wellington Regional Hospital, Wellington: Paul Young (PI), Colin Barnes, Ben Barry, Nina Beehre, Dick Dinsdale, Sam Edney, Anna Hunt, Harriet Judd, Charlotte Latimer-Bell, Cassie Lawrence, James Moore, Shaanti Olatunji, Alex Psirides, Chelsea Robinson, Kate Tietjens, Jason Wright; Christchurch Hospital, Christchurch: David Knight (PI), Brandon Birker, David Bowie, Tara Burke, David Closey, Rosalind Crombie, Neil Davidson, Seton Henderson, Louise Hitchings, James McKay, Jan Mehrtens, Emmeline Minto, Stacey Morgan, Anna Morris, Jay Ritzemar-Carter, Jessica Roberts, Geoffrey Shaw, Katherine Townend, Kymbalee Vander Heyden.

Sweden: Sahlgrenska University Hospital, Gothenburg: Christian Rylander (PI), Marita Ahlqvist, Roman Desta Lindgren, Ingrid Eiving, Andreas Lundin, Patrik Martner, Elisabeth Myhrman, Birgitta Ryding; Skåne University Hospital, Malmö: Joachim Düring (PI), Mattias Bergström, Mattias Bohm, Ingrid Didriksson, Petrea Frid, Katarina Heimburg, Marina Larsson, Oscar Lundberg, Stefan Olsson Hau, Simon Schmidbauer; Skåne University Hospital, Lund: Ola Borgquist (PI), Anne Adolfsson, Anna Bjärnroos, Erik Blennow-Nordström, Irina Dragancea, Thomas Kander, Anna Lybeck, Gustav Mattiasson, Olof Persson, Malin Rundgren, Susann Schrey, Erik Westhall; Helsingborg Hospital, Helsingborg: Martin Annborn (PI), Sara Andertun, Florian Ebner, Nerida Gustavsson, Lisa Hassel, Jesper Johnsson, Marie Nelderup, Heléne Petersson, Jörgen Petersson, Frideriki Stafilidou; Hallands Hospital, Halmstad: Johan Undén (PI), Frida Antonsson, Git Bergman, Jörgen Gamroth, Maria Meirik, Katarina Rudolfsson, Helena Sandberg, Martin Thorsson; Karlstad Central Hospital, Karlstad: Kristin Savolainen (PI), Maria Hansbo, Malin Helliksson, Björne Nödtveidt, Johan Sanner, Victoria Sem, Camilla Sund Lindquist; Södersjukhuset, Karolinska Institute, Stockholm: Per Nordberg (PI), Akil Awad, Anna-Sofia Börjesson, Malin Hedberg, Mia Henning, Jacob Hollenberg; Northern Älvsborg County Hospital, Trollhättan: Per Petersen (PI), Emelia Dahlberg, Johan Forshammar, Veronica Svensson; Capio S:t Görans Hospital, Stockholm: Michael Wanecek (PI), Håkan Eskilsson; Skaraborg Hospital, Skövde: Daniel Rodriguez-Santos (PI), Åsa Appelqvist, Henrietta Jidbratt, Elisabeth Johansson, Lars Kiszakiewicz, Åsa Nilsson, Sinnika Olsson, Anders Paulsson, Urszula Stempel, Andreas Thoren; Örebro University Hospital, Örebro: Stefan Persson (PI), Ida Berglund, Eric Bergström, Cathrine Törnqvist, Ingela Östman; Uppsala University Hospital, Uppsala: Sten Rubertsson (PI), Ing-Marie Larsson, Elin Söderman, Ewa Wallin, Joanna Wessbergh; Linköping University Hospital, Linköping: Thomas Halliday (PI), Filippa Engvall.

Switzerland: Lausanne University Hospital (CHUV), Lausanne: Mauro Oddo (PI), Nawfel Ben-Hamouda, Adriano Bernini, Pierre-Nicolas Carron, Philippe Eckert, Eva Favre, John-Paul Miroz, Paola Morelli, Olivier Muller, Jan Novi, Andrea Rosseti, Madeleine Schnorf; Bern University Hospital, Bern: Matthias Haenggi (PI), Anja Levis, Sandra Nansoz, Marianne Roth & Team, Nicole Söll; Cantonal Hospital St. Gallen, St.Gallen: Claudia Schrag (PI), Mensur Alicajic, Philipp Baier, Joel Dütschler, Dominique Flügel, Edith Fässler, Ruth Gamio-Veis, Marc Güpfert, Yvonne Hilpertshauser, Stefan Hägele-Link, Gian-Reto Kleger, Peter Krähenmann, Maria Elisabeth Mair, Nadja Schai, Christoph Strohmaier, Peter Tangl, Dominik Zieglgänsberger; University Hospital Zurich, Zurich: Marco Maggiorini (PI), Gabriele Claus, Gabi Consani-Vogel, Lukas Imbach, Samira Kaiser, Eva-Maria Kleinert, Pedro David Wendel Garcia; Cardiocentro Ticino, Lugano: Tiziano Cassina (PI), Pamela Agazzi, Bruno Capelli, Gabriele Casso, Martino Regazzi, Hervé Schlotterbeck, Gabriele Via, Michele Villa.

United Kingdom: University Hospital of Wales, Cardiff: Matt P. Wise (PI), Jenny Brooks, Eve Cocks, Jade Cole, Jacqueline Curtin, Michelle Davies, Rhys Davies, Stephen Fernandez, Julie Highfield, Helen Hill, Matt P. G. Morgan, Lydia Pennant, Sofia Rose, Emma Thomas, Angharad Williams; Royal Victoria Hospital, Belfast: Peter McGuigan (PI), Stephen Haffey, Aisling O'Neill, Kathryn Ward; Bristol Royal Infirmary, Bristol: Matthew Thomas (PI), Jeremy Bewley, Anna Chillingworth, Julie Cloake, Libby Cole, Hilary Galvin, Zoe Garland, Lisa Grimmer, Bethany Gumbrill, Lucy Howie, Rebekah Johnson, Chloe Searles, Agnieszka Skorko, Katie Sweet, Victoria Taylor, Denise Webster; Essex Cardiothoracic Centre, Basildon: Thomas Keeble (PI), Gill Adams, Rajesh K Aggarwal, Jo-Anne Cartwright, Steven Church, Gerald J Clesham, John R Davies, Kelly Farrell, Reto Gamma, Jane Harding, Rohan Jagathesan, Alamgir Kabir, Paul A Kelly, Lauren Kittridge, Maria Maccaroni, Gracie Maloney, Marco Mion, Naveen Nain, Raghunath Nalgirkar, Gyanesh Namjoshi, Stacey Pepper, Emily Redman, Nicholas M Robinson, Jeremy Sayer, Amanda Solesbury, Kare H Tang, Sali Urovi, Kunal Waghmare, Noel Watson, Teresa Webber; University Hospitals Birmingham NHS Foundation Trust, Birmingham: Peter Isherwood (PI), Conor Bentley, Colin Bergin, Ronald Carrera, Amy Clark, Lauren Cooper, Liesl Despy, Natalie Dooley, Karen Ellis, Emma Fellows, Stephanie Goundry, Samantha Harkett, Christopher McGhee, Aoife Neal, Hazel Smith, Catherine Snelson, Elaine Spruce, Tony Whitehouse, Kamal Yakoub; Royal Berkshire Hospital, Reading: Andrew Walden (PI), Shauna Bartley, Parminder Bhuie, Matthew Frise, Nicola Jacques, Liza Keating; Queen Alexandra Hospital, Portsmouth: David Pogson (PI), Zoe Daly, Steve Rose; Manchester Royal Infirmary, Manchester: Jonathan Bannard-Smith (PI), Rachael Quayle; Royal Bournemouth Hospital, Bournemouth: Nigel Chee (PI), Nina Barratt, Katie Bowman, Debbie Branney, Elizabeth Howe, Maria Letts, Sally Pitts, Luke Vamplew.

USA: University of Pittsburgh, Pittsburgh PA: Clifton W. Callaway (PI), Sara Difiore Sprouse, Ankur A. Doshi; Mayo Clinic, Rochester MN: Jennifer Fugate (PI), Amy M. Headlee, Eelco F.M.Wijdicks.

PI—Principal Investigator


Copenhagen Trial Unit, Copenhagen, Denmark; Clinical Studies Sweden – Forum South, Skåne University Hospital, Lund, Sweden; The George Institute for Global Health, Sydney, Australia; Australian and New Zealand Intensive Care Research Centre, Monash University, Melbourne, Australia; Medical Research Institute of New Zealand - (MRINZ), Wellington, New Zealand; Clinical Research Unit, Paris Descartes Necker Cochin, Paris, France; Scandinavian Critical Care Trials Group (SCCTG); The HRB Irish Critical Care- Clinical Trials Network (ICC-CTN); The ANZICS Clinical Trials Group (CTG); Spiral Software, Wellington, New Zealand; Allianz Global Corporate & Specialty SE, Copenhagen, Denmark; IBBL (Integrated BioBank of Luxembourg), Dudelange, Luxembourg.


The TTM2 trial was supported by independent research grants from nonprofit or governmental agencies (the Swedish Research Council [Veten-skapsrådet], Swedish Heart–Lung Foundation, Stig and Ragna Gorthon Foundation, Knutsson Foundation, Laerdal Founda-tion, Hans-Gabriel and Alice Trolle-Wachtmeister Foundation for Medical Research, and Regional Research Support in Region Skåne) and by governmental funding of clinical research within the Swedish National Health Service. No further fundings were requested for this sub-analysis.

Author information

Authors and Affiliations




CR and RB contributed to conception of the work, participation in data analysis and interpretation, drafting the manuscript, critical revision of the manuscript, final approval of the version to be published. All the authors contributed to conception of the work, critical revision of the manuscript, final approval of the version to be published. NN and PP contributed to conception of the work, participation in data analysis and interpretation, critical revision of the manuscript, final approval of the version to be published. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Chiara Robba.

Ethics declarations

Ethics approval and consent to participate

Ethical approval was obtained in the coordinating center and in each participating centers as well as informed consent according to local regulations. This sub-study was approved on the 23rd of February 2017 by the TTM2 steering committee ( The protocol of the analysis was previously approved by the TTM2 steering committee and then published. No further ethical approval was necessary for the development of this study.

Consent for publication

Not applicable.

Competing interests

Dr. Saxena is receiving consulting fees from Bard Medical; Dr. Young is receiving lecture fees from Bard Medical; Dr. Taccone is receiving grant support from Bard Medical and ZOLL Medical; Dr. Nichol is receiving grant support, paid to University College Dublin, from AM Pharma and grant sup-port, paid to Monash University, from Baxter Healthcare; Dr. Chew is receiving lecture fees from Edwards Lifesciences; Dr. Friberg is receiving fees for academic advising from TEQCool; and Dr. Nielsen is receiving lecture fees from Bard Medical and consulting fees from BrainCool. Dr Badenes is supported by INCLIVA. Dr Robba received fees for lectures from Masimo, and GE. Dr. Battaglini received fees for lectures from Baxter. No other potential conflict of interest relevant to this article was reported.

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Collaborators of the TTM2 Trial are listed at the end of the manuscript.

Supplementary Information

Additional file 1:

 Additional statistical analysis of subgroups population and association with outcome.

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Robba, C., Badenes, R., Battaglini, D. et al. Oxygen targets and 6-month outcome after out of hospital cardiac arrest: a pre-planned sub-analysis of the targeted hypothermia versus targeted normothermia after Out-of-Hospital Cardiac Arrest (TTM2) trial. Crit Care 26, 323 (2022).

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