Article
Hyperoxia is dose-dependently associated with an increase of mortality in ventilated patients with aneurysmal subarachnoid heamorrhage – a retrospective cohort-study
Hyperoxie ist dosisabhängig mit einem Anstieg der Mortalität bei beatmeten Patienten mit aneurysmatischer Subarachnoidalblutung assoziiert – eine retrospektive Kohortenstudie
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Published: | May 25, 2022 |
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Objective: Adequate oxygenation in patients with aneurysmal subarachnoid hemorrhage (SAH) is imperative. However, hyperoxia increases formation of reactive oxygen species and may be associated with a dose-dependent toxicity. We hypothesized a threshold for oxygen partial pressures (paO2) above which toxicity effects precipitate and sought to study the effects on 30-day mortality, favorable outcome at discharge, and delayed cerebral ischemia (DCI) in an exploratory retrospective single-center cohort study.
Methods: In this retrospective single-center cohort study patients with SAH and mechanical ventilation > 72h were included. Oxygen integrals were calculated above thresholds: 80, 100, 120, and 150mmHg and time-weighted mean paO2 for the first 24h after admission as the hyper-acute phase (d1), from admission to day 3 (d3), and admission to day 14 (d14). Finally, we conducted multivariable logistic regression analyses adjusted for age, sex, duration of ventilation, and Hunt&Hess grade. Favorable outcome was defined as Glasgow Outcome Scale 4 and 5.
Results: From 11/2010 until 02/2021 259 out of 549 patients fulfilled the inclusion criteria. For mortality, no significant association for integrals or mean paO2 on d1 and d3 was found. At d14, odds ratios for mortality increased dose-dependently and were 1.074 (95% confidence intervals: 1.03;1.12; p=0.001) for each 1mmHg per day over 14 days above 80mmHg, 1.183 (1.078;1.298) above 100mmHg, 1.411 (1.176;1.693) above 120mmHg, 1.691 (1.267;2.257) above 150mmHg (all p<0.001), and 1.047 (1.017;1.079) for mean paO2 (p=0.002). No significant association was found for favorable outcome or DCI neither on d1, d3 and d14.
Conclusion: Integrals above defined thresholds were dose-dependently associated with an increase in mortality. Because any hyperoxia above 80mmHg was associated with an increase of mortality, these ranges, otherwise defined as normoxia, should be evaluated in future prospective trials.