Paradigms of Oxygen Therapy in Critically Ill Patients

Marta Carvalho1, Maria Soares1 and Humberto S Machado1,2

1Serviço de Anestesiologia, Centro Hospitalar Universitário do Porto, Portugal

2Instituto de Ciências biomédicas Abel Salazar, Universidade do Porto, Portugal

*Corresponding Author:
Humberto S Machado
MD, M.Sc.. PhD, Serviço de Anestesiologia
Centro Hospitalar Universitário do Porto
Largo Professor Abel Salazar
4099-001 Porto,Portugal.
Tel:
351935848475
E-mail:
[email protected]

Received date: December 09, 2016; Accepted date: December 20, 2016; Published date: December 27, 2016

Citation: Carvalho M, Soares M, Machado HS. Paradigms of Oxygen Therapy in Critically Ill Patients. J Intensive & Crit Care 2017, 3:1.

 
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Abstract

Oxygen administration to patients has potential advantages and some evident drawbacks. Several clinical settings, mainly critical scenarios, demand high oxygen inspired fractions (FiO2) in order to assure safe reserve margins for an eventual arterial desaturation (for example before tracheal intubation in operating room). On the other end some evidence shows that maintain high FiO2 during surgical procedures and/or controlled ventilation in the intensive care units might be more harmful than beneficial. The aim of this revision was to show what type of decision clinicians may make, regarding the amount of oxygen that should be given to patients, with a special focus on the pros and cons of its liberal utilization.

Keywords

Oxygen toxicity; Oxygen therapy; Atelectasis.

Introduction

Oxygen has been present in the atmosphere for 5 billion years. At the beginning, it was present in a low concentration, but nowadays is the second most common gas (≈21%), preceded only by nitrogen (≈78%). It is well known that oxygen is necessary for life maintenance. Oxygen acts as final electron acceptor in the production of adenosine triphosphate (ATP), which is the main source of energy in our body [1].

It was in 1772 that Scheele discovered oxygen although Priestley has published his findings first, in 1775. Priestley was the first to suggest that oxygen could have adverse effects. Later in 1878, Bert described oxygen neurotoxicity when noticed that high-pressure oxygen caused convulsions in larks. Smith observed that rats developed pneumonia after being exposed to high concentration of oxygen for 4 days [2]. Oxygen toxicity has been studied for many years and two mechanisms by which oxygen may cause its adverse effects have been proposed: The production of free radicals, which lead to the disequilibrium between oxidative and anti-oxidative species; and cell metabolism modification and enzymatic inhibition [3].

We know that oxygen is essential for survival but it can be toxic if it is used in excess. This raises the question: How much oxygen can we use without inducing lesion? Many factors should be considered in order to respond to this question. In this review, we describe and discuss the pros and cons of using supplementary oxygen.

Pros

The use of high fraction of oxygen inspired ( FiO2) augments the tolerance time to apnea. In anesthesia practice this is important especially during the induction and emergence of anesthesia. The aim of pre-oxygenation is to replace all the nitrogen in the function residual capacity (FRC) for oxygen. This increases the oxygen stores available and, therefore, increases tolerance to apnea time [4]. In addition, it is important to maintain airway patency and exposure to high FiO2 to permit the oxygen diffusion to the alveoli during the anesthesia induction. This phenomenon is called apneic oxygenation [5, 6]. Edmark et al. [7] evaluated atelectasis formation and time to desaturation in patients exposed do FiO2 of 60%, 80% and 100% during anesthesia induction. They concluded that induction with 80% FiO2 causes minimal atelectasis but the time to desaturation was significantly shortened compared to 100% FiO2.

It has been proposed that high FiO2 reduces incidence of surgical wound infection [8-10]. Surgical-wound infections (SWI) are common and can be a serious problem with implications in morbidity and mortality. The oxidative process is essential in the defense against pathogens. Greif et al. [8] included 500 patients proposed to colorectal surgery and showed that exposure to 80 FiO2 % during anesthesia and 2 h post op reduce the incidence of SWI when compared to exposure of 30% FiO2 .

In 2009, a meta-analysis supported these results by showing that supplemental perioperative oxygenation is beneficial in preventing SWI in patients undergoing colorectal surgery [9]. More studies may be needed to determine if the use of supplemental oxygen is beneficial for patients undergoing other types of surgery. The use of 100% FiO2 during perioperative period seems to increase antimicrobial and pro-inflammatory responses of the alveolar macrophages during anesthesia.

Kotai et al. [11] suggested that these alterations may be beneficial for immune defense in lung tissue.

The effect of high concentration of FiO2 on postoperative nausea and vomiting (PONV) is still not clarified as previous studies had divergent results. In 2013, a meta-analysis including 11 studies regarding the impact of high FiO2 and PONV showed a weak beneficial effect on nausea [10].

Despite the increase of atelectasis formation with exposure to high FiO2 , there are studies showing that this have no impact in pulmonary function. Besides that, it has been suggested that there is no difference in the incidence of pulmonary complications between those who were exposed to high FiO2 and low FiO2 during perioperative period [12].

Finally, the work of Lambertsen and his colleagues at the University of Pennsylvania has shown the relationship between inspired oxygen partial pressures and the time for the appearance of pulmonary and central nervous system toxicity symptoms. It seems that neurologic toxicity occurs only when oxygen exposure happens at high pressure and pulmonary toxicity appears when exposure to high FiO2 oxygen is prolonged in time [13].

Cons

It is very important to carefully decide on the level of inspired fraction that should be used during Oxygen is needed in order to assure patient safety in critical moments, but excessive amounts of oxygen inspired fractions might induce physiologic lesions. It is well recognized and confirmed by recent publications that hyperoxia may induce pulmonary toxicity and cell damage mediated by radical oxygen species (ROS). High doses of oxygen have also been associated to target-organ damage, mainly brain and heart, decreased cerebral and coronary blood flow, systemic vasoconstriction and decreased cardiac output.

High oxygen inspired fractions have been correlated with pulmonary toxicity induced by several mechanisms, including increased inter-cellular adhesion molecules, neutrophil recruitment, 8-iso PGF2 alpha, nitrous oxide, and synthesis of collagen-I and monocyte chemotactic protein 1 [14, 15].

Davis et al. [16] evaluated early reversible changes in human alveolar structures induced by hyperoxia. The authors evaluated 14 normal subjects by broncho alveolar lavage before and immediately after they had breathed more than 95% oxygen for 16.7 ± 1.1 h. They concluded that although some of the effects of oxygen exposure for 17 h were reversible, hyperoxia for this short time period can decrease the structural or functional barriers that normally prevent alveolar-capillary leak and induce processes that may culminate in fibrosis of the alveolar wall.

Regarding toxicity induced by oxygen, Machado et al. [17] conducted an experimental prospective randomized study to evaluate lung inflammation with oxygen supplementation in tracheotomized spontaneously breathing rabbits. Rabbits were randomly assigned to 4 groups: groups 1 and 2 were submitted to 0.5 L/min oxygen supplementation, for 20 or 75 min, respectively; groups 3 and 4 were left at room air for 20 or 75 min. The results showed that oxygen supplementation in spontaneous breathing is associated with an increased inflammatory response when compared to breathing normal room air, and this inflammatory response was mainly constituted by polymorphonuclear cells [17].

Another physiologic change that can be induced by high oxygen inspired fraction is the development of absorption atelectasis. Atelectasis may develop with pre-oxygenation with 100% FiO2 [18]. This is a major issue and needs a special intervention, namely the use of positive end expiratory pressure (PEEP) to maintain the lungs open [18] as even recent investigation has shown that if this is not instituted to the patient, the lung will certainly be poorly aerated [19].

Hedenstierna [20] has shown that patients whose anesthesia was induced during pre-oxygenation with 100% O2 for 3 min had atelectasis, on average, in 10% of the lung area (corresponding to 15-20% of lung tissue). Pre-oxygenation with 80% O2 for a similar time caused much less atelectasis, with a mean of 2%. Reducing inspired oxygen to 60% during pre-oxygenation almost eliminated atelectasis and nothing was observed with 30% O2 . Also, the duration of pre-oxygenation with 100% oxygen can affect the amount of atelectasis that is produced. Thus, preoxygenation with 100% O2 for 6 min resulted in a mean of 6% atelectasis, whereas 100% O2 for shorter time of ventilation (3 min) resulted in a little more than 2%. Finally, 30% oxygen for 3 min resulted in barely visible atelectasis of around 0.3-0.4%. The focus anesthetic regime should be to deliver a patient with no atelectasis to the postoperative ward and to keep the lung open.

In Stroke Patients

Few studies have addressed supplemental oxygen therapy in stroke patients and the results are controversial. Rønning et al. [21] performed a study involving 550 stroke patients who were randomly assigned between two groups: to a group that received supplemental oxygen treatment (100% atmospheres, 3 L/min) for 24 h (n=292) or to a control group, which did not receive additional oxygen. Results showed that there was no statistically significant difference in one year survival between groups, but patients with less severe strokes (Scandinavian Stroke Scale >40) had a higher and significant survival rate in the control group (OR 0.45; 95% CI 0.23 to 0.90; p=0.023).

More recently, Roffe et al. [22] conducted a randomized clinical trial in 289 patients who suffered a stroke and were given supplemental oxygen therapy for 72 h after admission on the local stroke unit. They found a slight short-term improvement in the oxygen group regarding NIHSS at end of one week, but their findings may have been biased by the imbalance of stroke severity between the two groups.

Finally, The Stroke Oxygen Pilot Study did not find long-term significant differences in outcome among stroke patients submitted to supplemental oxygen therapy compared to standard of care [23].

There is a general consensus in what concerns the need for larger studies in this field, but the best current evidence states that oxygen therapy should not routinely be used in stroke patients and it might be deleterious in patients with minor strokes.

In Resuscitation Following Cardiac Arrest

A primary contributor to death and disability in resuscitated patients is the anoxic brain injury that typically follows a severe ischemia/reperfusion insult. To date, therapeutic hypothermia is the only proven treatment for anoxic brain injury after cardiac arrest [24-26]. However, recent evidence suggests that, in addition to body temperature, the amount of oxygen delivered to the brain after reperfusion may represent an important and modifiable factor in post resuscitation care. It is common to deliver supplemental oxygen in maximum concentrations during the resuscitative period, but this strategy may not be innocuous. Numerous laboratory investigations have identified a paradox relative to oxygen delivery to the injured brain. One large-scale clinical study has examined the relationship between excessive supplemental oxygen and outcome in post resuscitation patients [27]. Post resuscitation hyperoxemia exposure, defined as a partial pressure of arterial oxygen (PaO2) 300 mm Hg, was found to be an independent predictor of in-hospital death. The mortality in patients with hyperoxemia was even higher than the mortality for patients with hypoxemia. Furthermore, hyperoxemia was associated with lower likelihood of independent functional status among patients who survived to hospital discharge [27].

Kilgannon et al. [28] designed a multicenter cohort study using the Project IMPACT database (intensive care units at 120 US hospitals) to better define the relationship between supranormal oxygen tension and outcome in post resuscitation patients. The proportion of in- hospital deaths was 41% for patients with a PaO2 in the range of 60 to 99 mm Hg and rose to 65% for patients with a PaO2 in the range 400 mm Hg. The authors observed no clear single threshold of increased risk of death over ascending PaO2 ranges. In addition, they found a significant linear trend for the increase in mortality rates over ascending PaO2 ranges (p<0.0001). The results of this multicenter study showed a linear dose-dependent relationship between supranormal oxygen tension and relative risk of in-hospital mortality, but no evidence supporting a single threshold for harm from supranormal oxygen tension [28].

Acute Myocardial Infarction

Oxygen is widely used in people with acute myocardial infarction (AMI) although evidence of its benefit is controversial. Many systematic reviews have concluded that there is insufficient evidence to know whether oxygen reduces increases or does not have an effect on heart ischemia or infarct size.

The rationale for supplemental oxygen in AMI is that it may improve the oxygenation of the ischemic myocardial tissue and reduce ischemic infarct size, morbidity and mortality. However, potentially harmful mechanisms include the paradoxical effect of oxygen in reducing coronary artery blood flow and increasing coronary vascular resistance [29, 30] reducing stroke volume and cardiac output and the consequent reperfusion injury from increased oxygen free radicals [31, 32].

In 2013, a Cochrane meta-analysis reviewed 4 articles where oxygen supplemental therapy was used in over 400 non-hypoxic patients. When the data were pooled, twice as many people on oxygen died when compared to the group that was given air. Meta-analysis for mortality in participants with confirmed AMI: risk ratio (RR) 2.11 (95% confidence interval (CI) 0.78 to 5.68); meta-analysis for mortality in an intention-to-treat population (including those who did not have AMI): RR 2.05 (0.75 to 5.58) [33].

However, due to the low number of deaths in all four studies (17 in total), the authors recognized that evidence is lacking power and results may have been influenced by chance. As of such, current evidence does not support or clearly refutes the use of supplemental oxygen therapy in non-hypoxic AMI patients.

Neonatal Resuscitation

Up to 10% of newborns require some degree of resuscitation, ranging from simple stimulation to assisted ventilation [34]. The aim of resuscitation is to prevent not only neonatal death but also the adverse long-term neurodevelopmental squeals associated with birth asphyxia [35].

Recommendations point out 100% oxygen as the gas to use during neonatal resuscitation. Nonetheless, many experts challenge this practice on the basis that little evidence exists to support it [35]. Increasing work of breathing and the increased generation of oxygen free radicals are amongst the potential adverse effects of supplemental oxygen [36].

Cochrane meta-analyses of five studies comparing 100% oxygen versus room air in neonatal resuscitation showed a reduction in mortality in the room air group, with no increase in future complications (including long-term neurodevelopmental outcome) [35]. However, long-term follow-up (18-24 months) was only obtained in one study and the proportion of eligible patients was under 70%. Also, up to 25% of patients assigned to the room air group received back-up 100% oxygen therapy. The authors concluded that there is no evidence to recommend using room air over 100% oxygen or vice versa and that future research is required in this field.

In Critical Care

Oxygen administration is the most widely prescribed therapy in critically ill patients and frequently represents a life-saving intervention. Clinical data regarding the relationship between arterial hyperoxia and outcome are contradictory. The question whether exposure to supranormal arterial O2 tensions (PaO2) is safe in critically ill patients remains unanswered.

In 2014, Damiani et al. performed a systematic review and metaanalysis of studies describing the relationship between arterial hyperoxia and mortality in critically ill patients [37]. The majority of studies that have explored the relationship between arterial hyperoxia and mortality in critically ill patients are retrospective observational investigations, with only one prospective beforeafter study, which supported the use of a more conservative strategy. The authors concluded that hyperoxia exposure may be associated with mortality in patient subsets (post-cardiac arrest, stroke and traumatic brain injury). However, they referred that these results must be interpreted carefully given the heterogeneity in criteria used for defining hyperoxia exposure and a significant inconsistency between study findings.

Panwar et al. conducted a multicenter randomized controlled trial to determine whether a conservative oxygenation strategy is a feasible alternative to a liberal oxygenation strategy among ICU patients requiring invasive mechanical ventilation (IMV). At four multidisciplinary ICUs, 103 adult patients deemed likely to require IMV for ≥ 24 h were randomly allocated to either a conservative oxygenation strategy with target SpO2 of 88-92% or a liberal oxygenation strategy with target SpO2 of ≥ 96%. The study findings support the feasibility of delivering conservative oxygen therapy in patients on invasive MV as alternative to the usual oxygenation strategy, while being effective in reducing exposure to hyperoxia [38, 39].

There is still insufficient evidence regarding the safety of arterial hyperoxia in critically ill patients. Most of the existing studies are observational investigations with highly heterogeneous characteristics and inconsistent results. Randomized controlled trials are lacking.

Arterial hyperoxia may be associated with higher mortality in some critically ill patient subsets (post-cardiac arrest, stroke and traumatic brain injury).

While a liberal use of oxygen may provide a margin of safety against hypoxia, a more conservative approach might reduce potentially harmful exposure to excessive FiO2, hyperoxemia and tissue hyperoxia.

Conclusion

The selection of optimum arterial oxygenation goals is essential if cellular hypoxia and unnecessarily excessive oxygenation (and ventilation) are to be avoided. It is imperative to balance the risks associated with hypoxemia and hyperoxemia forms during daily assessment of patients.

The traditional clinical approach to oxygen therapy has been to prioritize the avoidance of hypoxemia while being relatively tolerant of hyperoxemia. The possibility that “too much” oxygen may be as harmful as “not enough” should lead to a pragmatic rethinking of the practice of oxygen administration.

Perhaps, the most prudent and advisable practice when oxygen needs to be used, will be to think of it as a lifesaving drug with its undeniable advantages and uses, and at the same time, a gas that has to be handle with special care, thought that hypoxia may be managed by several means (PEEP, recruitment maneuvers) before the decision of a high- inspired fractions of oxygen should be always in our minds.

Given the widespread use of O2 therapy in critical care, clinicians should be aware of the potentially deleterious effects of excessive O2 administration.

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