A Comprehensive Evaluation of Hyperbaric Oxygen Therapy in Resuscitation Medicine - a Pilot Study (HOT-RESUS 1 Trial)

Cardiac arrest (CA) necessitating cardiopulmonary resuscitation (CPR) currently results in a survival rate of around 8% in Europe. The much lower percentage of patients being discharged from hospital with a favourable neurological outcome or with a satisfactory degree of quality of daily life still shows room for improvement in post CA care. The so- called post-CA syndrome after return of spontaneous circulation (ROSC) requires a multidisciplinary management in a coordinated fashion. Despite steady advances in this very specific field of intensive care medicine, both neurologic and psychologic disability after CA still remain dismal with hypoxic brain injury as the main determinant (primary cause of death in 68 % of in-hospital CA and 23 % of out-of-hospital CA [OHCA]), and the optimal treatment approach might still be missing additional beneficial therapeutic options. The neuropathology of anoxic brain injury includes neural toxicity, intracellular calcium accumulation, oxygen free radicals, excitatory amino acid release, reperfusion injury and endothelial dysfunction, with a clinical presentation through impairment of visual, perceptive, expressive, cognitive, and motor functions, or psychological distress. As voiced by former patients and relatives, those functional outcomes are of utmost importance. Therefore, the Core Outcome Set for Cardiac Arrest (COSCA) was developed.

Hyperoxia vs. hyperbaric oxygenation therapy: It seems intuitive that a hypoxic or anoxic state such as CA necessitates a hyperoxic environment for convalescence. However, hyperoxia has been proven to be harmful, mostly through systemically accumulating reactive oxygen species (ROS), inducing oxidative stress in cellular structures, contributing to deleterious cell dysfunction and apoptosis induction, and finally leading to unfavourable neurological outcomes. Hyperoxia is advised against in current guidelines, but not defined or described in detail, leaving clinicians without a clear recommendation. In parallel, hyperbaric oxygen therapy (HBOT) was in its beginnings thought to facilitate similar effects. However, HBOT was then slowly researched in more detail, leading to a paradoxon: On the one side, the described harmful effects of hyperoxia are known, on the other side HBOT was shown to provide antioxidant effects, balancing out the negative features. HBOT has thus been described as safe due to its balance between oxidation and antioxidation. Key molecular changes following HBOT include a preservation of mitochondrial properties (e.g., through upregulation of ATP production), a reduction of neuroinflammatory processes (e.g., through reduced cytokine secretion), an upregulation of angiogenesis (e.g., through an upregulation of cerebral blood flow and vascular endothelial growth factor [VEGF], or downregulation of metalloproteinases), suppression of neutrophil-endothelial adhesion, and the mentioned upregulation of both ROS and antioxidants. HBOT has been shown to restore and increase perfusion and oxygenation of at-risk tissue, to enhance cerebral microcirculation and stabilize the blood-brain barrier through metalloprotease regulation, and to decrease intracranial pressure and cerebral edema. Moreover, it has been linked to several pathways leading to a preservation of neural tissue and a reduction of apoptosis, for instance shown via reduced levels of hypoxia-inducable factor 1 alpha (HIF1α). HBOT has also been linked to anti-inflammatory effects, for instance through a decrease in tumor necrosis factor alpha (TNFα) or an inhibition of the accumulation of leukocytes in ischemic areas. Mentionable other beneficial results of HBOT include improvement of left ventricular function, or the induction of significant senolytic effects including increasing telomere length and clearance of senescent cells. HBOT has in the past been used quite successfully in animal and human ischemic stroke patients for stimulation of a hyperoxic environment during ischemic and reperfusion periods, for instance leading to a reduced infarction area and neuronal death reduction. It was even demonstrated that cognitive function could be improved, and it was hypothesized that it could signal-induce the (re-)growth of grey and white cerebral matter. Moreover, HBOT might have the potential to re-gain suppressed psychological properties such as memories through a complex mechanism of increased cerebral tissue oxygenation, or even to induce an enhanced multitasking performance in healthy volunteers. A recent review on the impact of HBOT on cognitive functions yielded controversial results, concluding with a call for more standardized outcome evaluation.

So far, only four studies and one case report assessed HBOT around CA: In 1952, Koch et al. described a case of CA and cerebral edema being treated with HBOT "successfully". However, the given information lacks detail and is highly out-dated. In 1982, Kapp et al. subjected cats to CA and HBOT, observing a beneficial modification of functional impairment and metabolic derangements. Rosenthal et al. showed in 2003 that HBOT could inhibit neuronal death and improve neurologic outcomes after CPR in a canine model, concluding that HBOT has the potential of overcoming postresuscitative delivery-dependent cerebral ischemia. Of utmost importance, the authors could demonstrate that only one exposure to hyperbaric conditions was sufficient to show an effect, and they proved that HBOT is also beneficial in a globally ischemic model as opposed to a vessel-occluded model such as in the majority of studies covering stroke patients. Van Meter et al. assessed HBOT during CA (and ongoing cardiopulmonary resuscitation) in a porcine model, and concluded that the rate of sustained ROSC was higher in a high-dose HBOT regimen than in a low-dose one or in controls. The same authors even hypothesized HBOT to be potentially feasible for a more widespread use in CA patients in the future. Hadanny et al. investigated eleven human CA survivors receiving HBOT in 2015, and found that the treatment significantly improved memory, attention and executive functions evaluated via NeuroTrax®, a validated psychologic test series. The findings correlated with increased activities in the respective brain areas in imaging. Further research was recommended, but never conducted. Apart from these data, cases on HBOT after CA due to carbon monoxide poisoning exist, but focus on the treatment of this intoxication per se and not on other effects. Interestingly, HBOT was also shown to be stimulating the regeneration of peripheral nerval function after brain injury, potentially inhibiting the development of polyneuropathy and/or improving motor function after CA.

Assessing HBOT effects: In terms of assessing the effects of HBOT, apart from the mentioned psychological function tests, several ways of measuring the proposed molecular therapeutic effects come to mind. For instance, several biomarkers have been suggested, such as metalloproteases, VEGF, HIF1α, laminin-5, or interleukins. Moreover, a general heterogeneity and differences of regional cerebral oxygenation (rSO2) must be taken into account. Techniques such as near-infrared spectroscopy (NIRS) have in the past shown the ability to detect oxygenation responses of the brain during an after CA and CPR. It is not yet known whether NIRS can depict HBOT effects, but a hypothesis of "selective neuronal vulnerability" could be assessed through it. Lastly, endothelial dysfunction that has been reported to be occurring in CA patients, could be assessed via non-invasive function tests and biomarkers of endothelial function in order to depict the potential ameliorating effect of HBOT.

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