Arterial hyperoxia and in-hospital mortality after resuscitation from cardiac arrest
© Bellomo et al.; licensee BioMed Central Ltd. 2011
Received: 3 November 2010
Accepted: 8 March 2011
Published: 8 March 2011
Hyperoxia has recently been reported as an independent risk factor for mortality in patients resuscitated from cardiac arrest. We examined the independent relationship between hyperoxia and outcomes in such patients.
We divided patients resuscitated from nontraumatic cardiac arrest from 125 intensive care units (ICUs) into three groups according to worst PaO2 level or alveolar-arterial O2 gradient in the first 24 hours after admission. We defined 'hyperoxia' as PaO2 of 300 mmHg or greater, 'hypoxia/poor O2 transfer' as either PaO2 < 60 mmHg or ratio of PaO2 to fraction of inspired oxygen (FiO2 ) < 300, 'normoxia' as any value between hypoxia and hyperoxia and 'isolated hypoxemia' as PaO2 < 60 mmHg regardless of FiO2. Mortality at hospital discharge was the main outcome measure.
Of 12,108 total patients, 1,285 (10.6%) had hyperoxia, 8,904 (73.5%) had hypoxia/poor O2 transfer, 1,919 (15.9%) had normoxia and 1,168 (9.7%) had isolated hypoxemia (PaO2 < 60 mmHg). The hyperoxia group had higher mortality (754 (59%) of 1,285 patients; 95% confidence interval (95% CI), 56% to 61%) than the normoxia group (911 (47%) of 1,919 patients; 95% CI, 45% to 50%) with a proportional difference of 11% (95% CI, 8% to 15%), but not higher than the hypoxia group (5,303 (60%) of 8,904 patients; 95% CI, 59% to 61%). In a multivariable model controlling for some potential confounders, including illness severity, hyperoxia had an odds ratio for hospital death of 1.2 (95% CI, 1.1 to 1.6). However, once we applied Cox proportional hazards modelling of survival, sensitivity analyses using deciles of hypoxemia, time period matching and hyperoxia defined as PaO2 > 400 mmHg, hyperoxia had no independent association with mortality. Importantly, after adjustment for FiO2 and the relevant covariates, PaO2 was no longer predictive of hospital mortality (P = 0.21).
Among patients admitted to the ICU after cardiac arrest, hyperoxia did not have a robust or consistently reproducible association with mortality. We urge caution in implementing policies of deliberate decreases in FiO2 in these patients.
The majority of patients who experience cardiac arrest die at the time of the event [1, 2]. Even after response to resuscitation efforts and survival to intensive care unit (ICU) admission, such patients have a short-term mortality of approximately 60% [1, 2]. These dismal outcomes suggest the need for strategies to attenuate postresuscitation injury. Such injury is currently mostly attributed to cerebral, myocardial and global ischemia-reperfusion injury . Accordingly, postresuscitation therapy has focused on finding ways to diminish the intensity and consequences of ischemia-reperfusion injury.
The rapid application of therapeutic hypothermia can modify the outcomes of patients after resuscitation from cardiac arrest [4, 5]. The success associated with this intervention suggests that other aspects of patient care, which may influence the course of reperfusion injury, should also be logical targets for therapeutic manipulation.
In pursuit of potential therapeutic targets, investigators from the Emergency Medicine Shock Research Network (EMShockNet) recently explored the association between hyperoxia and in-hospital outcome in a retrospective, multicentre study . They found that hyperoxia occurred in almost one-fifth of patients, that patients with hyperoxia had greater in-hospital mortality than patients with normoxia or hypoxia and that, after controlling for some confounders, hyperoxia carried a clear independent association with mortality (odds ratio (OR), 1.8). Unfortunately, these investigators used only the first set of arterial blood gases in the ICU to assess oxygenation, excluded close to 30% of patients because of lack of arterial blood gas data and did not adjust for standard illness severity scores. Their conclusion that hyperoxia is a robust predictor of mortality in patients after resuscitation form cardiac arrest was therefore potentially affected by selection bias and by insufficient adjustment for major confounders. Thus, their results are of uncertain significance and require confirmation.
The Australian and New Zealand (ANZ) Adult Patient Database (ANZ-APD) is a high-quality database  of all admissions to most Australian and New Zealand ICUs. Patients admitted after resuscitation from nontraumatic cardiac arrest are coded as such. The database records contain Acute Physiology and Chronic Health Evaluation II (APACHE II) and APACHE III scores as well as demographic, diagnostic and outcome factors . Given the potential clinical importance of hyperoxia following cardiac arrest, we used this larger and more detailed database specifically to confirm or refute the initial findings of the EMShockNet investigators .
Materials and methods
We extracted data from the ANZ Intensive Care Society (ANZICS)-APD. We used exactly same inclusion criteria as the EMShockNet investigators  for patients admitted at a participating centre between 2000 and 2009 after resuscitation from an out-of-hospital or in-hospital cardiac arrest. We excluded readmissions and patients for whom arterial blood gas analysis or vital status at discharge was not available. The ANZICS Centre for Outcomes and Resource Evaluation (CORE) Management Committee granted us access to the data in accordance with standing protocols. Data were collected under the Quality Assurance Legislation of the Commonwealth of Australia (Part VC Health Insurance Act 1973, Commonwealth of Australia) with government support and funding. Each hospital gives ethics approval and allows the data to be used for appropriate research, which is governed by the ANZICS CORE terms of reference and waives the need for informed consent.
Data collection for oxygen values
All arterial blood gases during the first 24 hours of ICU admission were collected and entered into a standardized data collection system which automatically selects the appropriate high and low simultaneous fraction of inspired oxygen (FiO2) and partial pressure of arterial oxygen (PaO2) measurements and deletes other oxygenation data. Using the APACHE II and III methodology for intubated patients with FiO2 ≥0.5, the PaO2 associated with the arterial blood gas with the highest alveolar-arterial (A-a) gradient is selected as the index of worst oxygenation. For nonintubated patients or intubated patients with FiO2 < 0.5, the lowest arterial blood gas PaO2 level is recorded. The ratio of PaO2 to FiO2 (P/F ratio) is also used as an index of illness severity.
We recorded the sizes, types and locations of the hospitals. At the patient level, we extracted the following variables: demographics, comorbidities according to APACHE II and III classifications, hospital and ICU admission source, intubation, treatment limitation, year of admission, physiological and arterial blood gas parameters over the first 24 hours in the ICU, vital status at hospital discharge, hospital discharge destination and an APACHE III risk of death score . As a marker of severity of illness independent of arterial oxygenation, we calculated an adjusted APACHE III index of illness severity (AP3no-ox), in which the oxygen component of the APACHE III scoring system was removed.
All analyses were performed using SAS version 9.2 (SAS Institute Inc., Cary, NC, USA). Continuous data are presented as means ± standard deviations or as medians with interquartile ranges (IQRs), depending on the underlying data distribution. Categorical data are reported as proportions. We categorized oxygenation levels into the same three groups as in the EMShockNet study , defined by the worst PaO2 and P/F ratio obtained in the first 24 hours of ICU admission. Thus, we divided patients into three groups according to worst PaO2 or A-a O2 gradient in the first 24 hours after admission. We defined 'hyperoxia' as a PaO2 300 mmHg or greater, 'hypoxia/poor O2 transfer' as either PaO2 < 60 mmHg or a P/F ratio <300, 'normoxia' as any value between hypoxia and hyperoxia and 'isolated hypoxemia' as PaO2 < 60 mmHg regardless of FiO2 level.
The primary outcome measures were in-hospital mortality and survival time, which are reported as ORs (95% confidence interval (95% CI)) or hazard ratios (HRs) (95% CI), respectively. To determine functional recovery, we also considered discharge to home as a secondary outcome. We compared outcomes between groups using the χ2 test with the Bonferroni correction. We conducted multivariate analysis using logistic regression for mortality and Cox proportional hazards regression for survival time, with models constructed using both stepwise selection and backwards elimination procedures. To increase robustness and model validity, we used a P value of 0.01 for variable inclusion. We applied several models to the statistical analysis of the independent relationship between oxygenation and patient outcome. We constructed an initial model for mortality in accordance with the EMShockNet model (see Additional file 1, Statistical appendix, Model 1) . We then applied a second model to improve discriminatory power using AP3no-ox as a marker of severity (see Additional file 1, Statistical appendix, Model cluster 2). Finally, we conducted further sensitivity analysis inclusive of propensity analysis , Cox proportional hazards modelling, testing of different cutoff points for hyperoxia, analysis of subgroups contemporaneous with the EMShockNet cohort and assessment of PaO2 according to deciles (Additional file 1, Statistical appendix, Model cluster 3).
As our database contained only the worst recorded oxygenation in the first 24 hours after ICU admission, we explored its relationship with that of the first PaO2 measurement after ICU admission (as in the EMShockNet study) and the mean oxygenation on ICU admission days 1, 2 and 3 by selecting 100 of the database patients and obtaining additional data from all of their hospital arterial blood gas records during their ICU stay (see Additional file 1, Statistical appendix, Model cluster 3).
Statistical power considerations
The proportion of living patients with hyperoxia (PaO2 > 400) was 5% (n = 280). Comprising 5,140 patients who lived and 6,968 patients who died, this study had 93% power to detect a change of 1.5% (5% versus 6.5%) in the proportion of patients with hyperoxia (PaO2 > 400) with a two-sided P value of 0.05.
There were 625 patients in the data set with hyperoxia (PaO2 > 400). Comprising 11,483 patients without hyperoxia, this study had 90% power to detect a difference in mortality of 7% (55% versus 62%) between groups with a two-sided P value of 0.05. Given an observed difference of 14% (55% versus 69%) in the EMShockNet study between hyperoxic patients (PaO2 > 400) and nonhyperoxic patients, we felt that this study was adequately powered to detect a relationship between mortality and PaO2 > 400. In our study, the mortality rate in the hyperoxia group (PaO2 > 400) was only 0.5% higher than that in the nonhyperoxia group (54.7% versus 55.2%, P = 0.22).
There were 531 hyperoxia survivors (PaO2 > 300). With 4,609 nonhyperoxia survivors, this study had 80% power to detect a difference between groups of 6% (64% versus 58%) regarding the proportion discharged to home with a two-sided P value of 0.05. Given an observed difference of 6% (38% versus 44%) in the EMShockNet study between hyperoxic survivors (PaO2 > 300) discharged to home and discharged nonhyperoxic survivors, we again felt that this study was adequately powered to detect a relationship between hyperoxia and discharge to home. In our study, there was no observed difference in the proportion of patients who were discharged to home between the hyperoxia and nonhyperoxia groups.
Baseline characteristics of the study patientsa
Mean age, yr (±SD)
Male sex, n (%)
Indigenous Australians, n (%)
Hospital admission source from home, n (%)
Acute renal failure, n (%)
Chronic comorbidities, n (%)
Cardiovascular disease, n (%)
Liver disease, n (%)
Renal disease, n (%)
Respiratory disease, n (%)
Cirrhosis, n (%)
Hepatic failure, n (%)
Immune suppression, n (%)
Cancer, n (%)
Markers of severity
Median APACHE III risk of death (IQR)
66% (36 to 84)
69% (40 to 86)
50% (20 to 73)
66% (36 to 84)
Median APACHE III risk of death (no oxygen)b (IQR)
58% (27 to 79)
60% (29 to 80)
47% (18 to 71)
58% (29 to 80)
ICU admission source, n (%)
Baseline characteristics of the study hospitals
Hospital characteristics, n(%)
Hypoxia/poor O2 exchange
Small to medium (≤300 beds)
Large (301 to 500 beds)
Extra large (>500 beds)
Hospital type and location
The average age of patients was 64 years (SD ± 16), and 64% (7,802) were male. A total of 8,175 patients (68%) were at home prior to hospital admission and 5,756 patients (48%) were admitted to the ICU directly from the Emergency Department. One-third (3,978) of the patients had preexisting chronic comorbidities. The median APACHE III risk of death was 66% (IQR, 36%-84%). Most patients (8,904, 73.5%) had 'hypoxia/poor O2 transfer', while 1,285 (10.6%) were hyperoxic and 1,919 (15.9%) were normoxic. Isolated hypoxemia (PaO2 < 60 mmHg) was present in 1,168 patients (9.7%).
Abnormal vital signs in the first 24 hours in intensive care unit and interventions
Vital signs (means ± SD)
Hypoxia/poor O2 exchange
Highest body temperature
Lowest body temperature
Highest heart rate, beats/min
Highest respiratory rate, breaths/min
Lowest systolic blood pressure, mmHg
Lowest mean arterial pressure, mmHg
Lowest glucose level first 24 hours
Body temperature, n (%)
Highest temperature <34°C
Lowest temperature <34°C
Outcomes of study patients
Hypoxia/poor O2 exchange
In-hospital mortalitya, n (%) (95% CI)
6,968 (58) (57 to 58)
5,303 (60) (59 to 61)
911 (47) (45 to 50)
754 (59) (56 to 61)
Discharge destination for survivors, n
Home a, n (%) (95% CI)
3,341 (28) (27 to 28)
2,350 (26) (25 to 27)
649 (34) (32 to 36)
342 (27) (24 to 29)
Transfer to another hospital
Multiple logistic regression model with in-hospital mortality as dependent variable using EMShockNet model variablesa
Acute renal failure
3.3 (2.9 to 3.7)
Hypotension in first 24 hoursb
1.9 (1.7 to 2.0)
1.1 (1.1 to 1.1)
Emergency department origin
1.6 (1.4 to 1.7)
High heart ratec
1.5 (1.3 to 1.6)
Hypoxia/poor O2 exchange versus normoxia
1.4 (1.3 to 1.6)
Hyperoxia versus normoxia
1.5 (1.3 to 1.8)
2.0 (1.5 to 2.5)
2.2 (1.5 to 3.1)
1.2 (1.1 to 1.3)
1.4 (1.1 to 1.6)
Chronic respiratory disease
1.3 (1.1 to 1.5)
2.7 (1.3 to 5.9)
Multiple regression models for in-hospital mortality and survival time using an APACHE III-based marker of severitya
OR (95% CI)
Time to death
HR (95% CI)
1.5 (1.5 to 1.6)
1.2 (1.2 to 1.2)
5.3 (3.8 to 7.2)
1.7 (1.5 to 1.8)
Year of admission
0.9 (0.9 to 0.9)
0.97 (0.96 to 0.98)
Lowest glucose in first 24 hours
1.1 (1.1 to 1.1)
1.02 (1.02 to 1.03)
Hospital admission from home
1.3 (1.1 to 1.4)
1.1 (1.0 to 1.1)
Hypoxia/poor O2 exchange versus normoxia
1.2 (1.1 to 1.4)
1.1 (1.0 to 1.2)
Hyperoxia versus normoxia
1.2 (1.0 to 1.5)
1.1 (1.0 to 1.2)
Propensity analysis (see Additional file 1, Statistical appendix, Model cluster 3) did not alter this risk or the significance of hyperoxia. However, when the secondary outcome of discharge to home was considered, oxygenation status was no longer a statistically significant predictor (P = 0.64). Using a Cox proportional hazards regression model, we found both hyperoxia and hypoxia/poor O2 transfer to increase the hazard of death in comparison to the normoxia group (HR 1.3 (95% CI, 1.1 to 1.4), P < 0.001, and HR 1.3 (95% CI, 1.2 to 1.4), P < 0.0001, respectively). After adjustment for the covariates described in Additional file 1, Statistical appendix, Model cluster 2, however, oxygenation status was no longer statistically significant (hyperoxia: OR 1.1 (95% CI, 1.0 to 1.2), P = 0.20; hypoxia: OR 1.1 (95% CI, 1.0 to 1.2), P = 0.01) (Table 6).
When a PaO2 of 200 mmHg or greater was used to define hyperoxia, after adjustment (Additional file 1, Statistical appendix, Model cluster 2), oxygenation status was a statistically significant predictor of outcome (P = 0.002) (hyperoxia: OR 1.3 (95% CI, 1.1 to 1.5), P = 0.01; hypoxia: OR 1.3 (95% CI, 1.1 to 1.5), P = 0.001). When a PaO2 of 400 mmHg or greater was used in sensitivity analysis after adjustment, however (Additional file 1, Statistical appendix, Model cluster 2), oxygenation status was no longer statistically significant (P = 0.06) (hyperoxia: OR 1.0 (95% CI, 0.8 to 1.2), P = 0.71; hypoxia: OR 1.1 (95% CI, 1.0 to 1.3), P = 0.04).
When the corresponding time period used by the EMShockNet study group  (2001 to 2005) was considered, after adjustment (Additional file 1, Statistical appendix, Model cluster 2), oxygenation was not predictive of mortality (P = 0.16) (hyperoxia: OR 1.3 (95% CI, 0.9 to 1.8), P = 0.16; hypoxia: OR 1.3 (95% CI, 1.0 to 1.6), P = 0.06). When more detailed information was obtained from a random sample of 100 patients, the worst PaO2 value over the first 24 hours was significantly more representative of mean PaO2 than the first PaO2 value measured upon admission used by the EMShockNet study group . This was true for the first 24 hours (Pearson's r = 0.70 versus Pearson's r = 0.50, P < 0.0001), the first 48 hours (Pearson's r = 0.63 versus Pearson's r = 0.38, P < 0.0001) and the first 72 hours (Pearson's r = 0.60 versus Pearson's r = 0.34, P < 0.0001).
We conducted a large, multicentre, cohort study of patients admitted to ICUs in ANZ after resuscitation from cardiac arrest to examine the relationship between hyperoxia and patient outcome. We initially found that hyperoxia was relatively uncommon and had only a weak relationship with risk of death. This relationship was significantly reduced by the addition of illness severity scores. In addition, once Cox proportional hazards modelling of survival, sensitivity analyses using deciles of hypoxemia, time period matching and defining hyperoxia in keeping with experimental studies [10–13] as PaO2 > 400 mmHg, hyperoxia had no independent association with mortality. Finally, after adjustment for FiO2 and relevant covariates, PaO2 was no longer predictive of hospital mortality. Thus, hyperoxia was relatively uncommon, and it had no robust and consistently reproducible independent relationship with mortality.
Comparison with other studies
Until very recently, concerns about the possible risks associated with hyperoxia during and after recovery from cardiac arrest were based on animal experiments [10–13]. In this regard, several experimental studies have suggested that hyperoxia can increase oxidative stress , induce more severe histopathological changes  and worsen neurological injury . On the other hand, two studies have failed to confirm such findings [16, 17], and two other often-quoted major studies did not actually assess animals after cardiac arrest [10, 12]. Nonetheless, despite the lack of human data, the International Liaison Committee on Resuscitation moved to advocate the avoidance of arterial hyperoxia. The committee instead advocated the targeting of arterial oxygen saturation not exceeding 94% to 96% . In response to these issues, in June 2010, the EMShockNet investigators reported that, in a cohort of 6,326 USA patients who had survived nontraumatic cardiac arrest and were admitted to the ICU, hyperoxia was independently associated with increased risk (OR 1.6) of in-hospital mortality. This was the largest clinical study to date of the association between hyperoxia after cardiac arrest and mortality. Our findings should therefore be evaluated in direct comparison to the EMShockNet study and have been specifically configured to facilitate such comparison.
Several important observations emerge from such comparison. First, the baseline characteristics of the U.S. and ANZ patients appear almost identical, although no information was available on the APACHE scores for the USA cohort. Despite such similarities, there were striking differences in the lowest body temperatures recorded (ANZ 34.9°C, USA 36°C). These differences may reflect greater uptake of therapeutic hypothermia in ANZ and make the observations from our cohort more relevant to current recommended practice [4, 5]. However, we cannot determine whether greater use of therapeutic hypothermia accounts for the difference in the proportion of survivors discharged to home (65% in ANZ as compared to 44% in the USA, approximately a 50% relative increase in favourable outcome).
In the ANZ cohort, hyperoxia occurred in only 10.6% of patients as compared with 18% in the USA, and mortality in the hyperoxic group was identical to that in the hypoxia/poor O2 transfer group, instead of being much greater. Importantly, the relationship between hyperoxia and in-hospital mortality appeared much weaker using the same modelling used by the EMShockNet investigators. Even more importantly, this relationship could not be confirmed when a different threshold for hyperoxia was applied which mimicked that reported in experimental studies [11–13] (rather than using a seemingly arbitrary cutoff point of 300 mmHg), when a Cox proportional hazards model was used, when PaO2 was split into deciles, when FiO2 was taken into account or when the same time period (2000 to 2005) was used for analysis. In the aggregate, these observations suggest that the relationship between hyperoxia and mortality is dependent on the individual healthcare system, the statistical model used, the time period examined and the definitions used. Such features are not consistent with a robust and reproducible biological phenomenon.
Our findings imply that it is incorrect and premature to conclude that hyperoxia is an independent risk factor for mortality in patients resuscitated from nontraumatic cardiac arrest. In particular, we contend that hyperoxia implies the administration of high FiO2 fractions, making it more likely for hyperoxia to actually be a marker of illness severity than a biological toxin. This notion is supported by the significant decrease in ORs for mortality once APACHE scores were added to the model and the disappearance of significant ORs once FiO2 was added to the model. Moreover, the definition of 'hypoxia' used by the EMShockNet investigators (reproduced here to facilitate comparison under the term 'hypoxia/poor O2 transfer') included patients with a P/F ratio <300, together with patients with PaO2 < 60 mmHg. This approach conflates physiologically relevant lack of oxygen at the tissue level (true hypoxia) with a gas transfer problem. When we examined isolated hypoxemia (PaO2 < 60 mmHg), we found that it was nearly as frequent as hyperoxia. The risks of cerebral injury associated with hypoxemia are well known [19–21], and hypoxemic patients in our cohort had particularly poor outcomes. Importantly, after adjustment for FiO2 and relevant covariates, PaO2 was no longer predictive of hospital mortality. These observations suggest that the association seen in the models that do not include FiO2 may simply reflect the fact that hyperoxia is an indirect marker of higher FiO2 (that is, the higher the FiO2, the greater the PaO2) and that a higher FiO2 is a marker of illness severity (that is, the sicker the patient is perceived to be, the greater the FiO2 administered in an emergency situation). However, the link between FiO2 and outcome is independent of APACHE score. Thus, FiO2 cannot be considered simply a marker of disease severity. The physician can lower PaO2 and FiO2 levels at the same time and avoid inducing hyperoxia. Only interventional studies can clarify whether the association between oxygenation and outcome is truly a causal relationship.
All the above observations have potential clinical relevance. For example, emergency responders may not have access to pulse oximetry or blood gas analysis, or such techniques may be unreliable immediately following cardiac arrest because of decreased peripheral perfusion. If fear of hyperoxia led emergency responders, in the absence of adequate monitoring, to limit FiO2 levels, logically more people would likely be exposed to the risk of hypoxemia. In our study, >40% of patients with hypoxemia might have had correction of their hypoxemia had a higher FiO2 level been induced. Thus, if concerns about the alleged ill effects of hyperoxia or high FiO2 administration were taken into the clinical arena to avoid a condition whose association with mortality is uncertain, more patients might be exposed to a condition whose adverse cerebral effects are well established. Given our findings, we counsel against implementing policies of deliberately induced decreases in FiO2 unless accurate continuous pulse oximetry monitoring is in place. Importantly, in no way do we advocate, promote or justify hyperoxia in this setting. However, lowering FiO2 is justified only if good transcutaneous or arterial oxygenation monitoring is available.
Strengths and limitations
This study has several strengths. It involved more than 12,000 patients from 125 ICUs in two countries, making it the largest study of its type conducted so far and making its findings reflective of all ICUs in ANZ [22, 23]. It included a multifaceted assessment of the independent relationship between hyperoxia and outcome using multiple models and adjusting for illness severity. However, like other studies of association using a large database, it is limited by the nature of the data available and by the fact that no causal inferences can be drawn. The assessment of oxygenation status in the first 24 hours was based on the 'worst' possible arterial blood gas result, while the EMShockNet study used the 'first' ICU arterial blood gas measurement for evaluation. Thus, patients may have been exposed to hyperoxia and may not have been identified in our study. However, using a random sample of 100 patients, we found that the measurement used in our study was more closely representative of overall mean oxygenation status in ICU patients during the first 24 to 48 hours after admission (when reperfusion injury occurs) than the first set of blood gas measurements obtained in the ICU. In our study, data were missing for only 5.4% of patients compared with 27.6% in the EM ShockNet study, making selection bias in our study less likely. One-third of patients had a lowest body temperature <34°C. Clinical knowledge (confirmed by the EMShockNet data) that such severe spontaneous hypothermia is uncommon suggests that many patients were therefore treated with induced hypothermia as is common in ANZ [24–28]. This finding distinguishes our study from the US investigation because it is in keeping with current recommendations. Unfortunately, however, our database does not enable us to identify which patients had induced versus spontaneous hypothermia. Finally, we are unable to comment on the causes of death or consider other potential confounding variables that were not collected as part of the ANZICS-APD.
More investigations appear necessary, perhaps using other national databases . Prospective investigations with focused data collection are also needed. If such studies confirmed a postive association, interventional strategies should be tested; if not, interventional studies would not seem justified.
In a large, multicentre, cohort study of patients admitted to the ICU after resuscitation from cardiac arrest, we found that hyperoxia was relatively uncommon. On the basis of initial multivariable analysis, it had only a weak independent relationship with mortality. This relationship could not be confirmed on the basis of sensitivity analysis, adjusted Cox proportional hazards modelling, after taking FiO2 into account or after adjusting for time period, making it unlikely that it represents a reproducible biological phenomenon. Our findings support arguments against implementing policies of deliberate decreases in FiO2 unless accurate and reliable pulse oximetry monitoring is available.
When the worst set of arterial blood gases is used for assessment, hyperoxia is uncommon in the first 24 hours after ICU admission in patients resuscitated from cardiac arrest.
Using the same approach, isolated hypoxemia is just as common.
Hyperoxia in these patients has a weak, model-dependent and nonreproducible association with mortality.
Unless accurate and reliable pulse oximetry is available to prevent hypoxemia, a policy of reducing FiO2 to avoid possible hyperoxia is not justified and may not be prudent.
Australia and New Zealand
Australian and New Zealand Intensive Care Society
- APACHE III:
Acute Physiology and Chronic Health Evaluation III
Centre for Outcomes and Resource Evaluation
inspired fraction of oxygen
arterial oxygen tension.
We thank all data collectors in the 125 participating ICUs in Australia and New Zealand for their collection of high-quality data that made this study possible. Three of the investigators (MB, RB, DJC) are supported in part by an enabling grant from the Australian National Health and Medical Research Council.
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