Out of Sight, Out of Mind, Right? Not in COVID-19 Shock or Anaerobic and Exhaustive Shock versus Septic Shock Dilemma That Means to Live or Die. Emergency Attention and a Necessity of Trials

Background: COVID-19 brought challenges that did not end after a two-year pandemic. From more straightforward changes in habits to studying to understand the enigmatic parasite-host relationship, we can better manage the patient infected with SARS-CoV-2 even with a vaccine full of doubts and antivirals that do not correctly cover the viral period. SARS-CoV-2 brought the chronic inflammation now called “The Long COVID-19 Syndrome” (LCS), something still little talked about, but we already see deaths due to non-identification of this inflammatory syndrome that can lead to shock. Theory: LCS Shock is due to a long period of metabolic stress, reflecting the shift from inflammation to oxidative stress and innate immunity, and does not respond to antimicrobials, as its main component is inflammatory, although there may be conjoined bacterial translocation. Thus, we are losing patients to a new syndrome confused with sepsis and septic shock. While septic shock (SS) responds to antimicrobials, Inflammatory Shock (ISc) does not respond to antimicrobials alone, requiring high doses of corticosteroids. Review: This study shows that we need to differentiate SS and ISC, as the treatment is different. The review shows that Lactate, LDH and the presence of new/recent cardiac changes and bradycardia in the face of a status where there should be tachycardia as the usual response can differ ISC from SS. Maybe the main responsible for high LDH is Warburg Effect. Conclusion: We have a dilemma that requires clinical studies that routinely match high doses of corticosteroids (until there is something better to be done) and bring How to cite this paper: D’Elia Zanella, L.G.F. de A.B. (2022) Out of Sight, Out of Mind, Right? Not in COVID-19 Shock or Anaerobic and Exhaustive Shock versus Septic Shock Dilemma That Means to Live or Die. Emergency Attention and a Necessity of Trials. Open Journal of Emergency Medicine, 10, 19-47. https://doi.org/10.4236/ojem.2022.101003 Received: December 12, 2021 Accepted: February 21, 2022 Published: February 24, 2022 Copyright © 2022 by author(s) and Scientific Research Publishing Inc. This work is licensed under the Creative Commons Attribution International License (CC BY 4.0). http://creativecommons.org/licenses/by/4.0/


Introduction
Children present with post-COVID- 19  In the appendix there is a proposal for criteria for differential diagnosis between shock by COVID-19 and shock septic, based on the author's review and experience.

Inclusion Criteria for Articles
The review was performed by searching for scientific articles on the PubMed platform using the descriptors "COVID-19" and "SHOCK". A total of 4007 articles were found between the years 2019 and 2021. It was established that the first 50 articles would be evaluated, and those that addressed multisystem inflammation in children would be discarded. Articles must be written in English.

The evaluation criteria followed what is proposed by the Task Force of Academic
Medicine and the GEA-RIME Committee APPENDIX 1, Academic Medicine: September 2001 -Volume 76 -Issue 9 -p 958-959.
Google Scholar was used to complement the study. More than 23 articles were added, totaling and articles. Most articles found addressed chronic inflammation in children. For populations over 18 years of age, there is still a rarity of publica-transforming growth factor β (TGFβ) is considered critical for the differentiation into Th17 cells. IL-21 and IL-23 pathways are involved in IL-6-programmed Th-17 cell differentiation. Various cytokines regulate th17 differentiation. TGF-β and IL-6 induced th17 differentiation in mice, and IL-1β but not TGF-β has been shown to participate in the development of Th17 cells together with IL-6 in humans [5] [6] [7] [8].
The development of Th17 cells is negatively regulated by IFN-γ, IL-27, and IL-2, the signals of which are dependent on Stat1 (IFN-γ and IL-27) and Stat5 (IL-2), respectively. The orphan nuclear receptors, retinoid-related orphan receptor γ (RORγ) and RORα have been identified as the key transcription factors that determine the differentiation of Th17 lineage. AhR is involved in the differentiation of Th17 cells by regulating Stat1 activation, which suppresses Th17 cell differentiation under Th17-polarizing conditions ( Figure 2). Cellular changes in adipose tissue in young and aged mice. Young adipose tissue is highly enriched with iNKT cells, which support M2 macrophage and Treg expansion by production of IL-10 and IL-2, respectively. As mice age, iNKT cells are gradually replaced by a population of IL-17A-secreting γδ T cells that support Tregs by a stromal cell-IL-33 axis. Lower figure. Nonredundant actions of iNKT and γδ T cells promote adipose tissue homeostasis. Top panel, Adipose iNKT cells expand Tregs via production of IL-2 and M2 macrophages via production of IL-10. Furthermore, activation of adipose iNKT cells induces weight loss and thermogenesis through an FGF21-dependent mechanism. Bottom panel, IL-17A-producing γδ T cells in adipose tissue drive Treg expansion by inducing stromal cells to produce IL-33. Additionally, a γδ IL-17A axis in adipose tissue is critical for maintenance of body temperature at thermoneutrality and upon cold challenge. iNKT cells and γδ cells, two innate T lymphocytes, have emerged as key regulators of immune homeostasis in visceral adipose tissue, as well as rheostats controlling body temperature in response to environmental fluctuations in sc and brown adipose depots ( Figure 2). iNKT cells control adipose Tregs and macrophage frequencies through IL-2 and IL-10 production, respectively, whereas T cells influence stromal cell expression of IL-33 through IL-17A production, and this in turn affects ST2+ Treg numbers in visceral adipose tissue. By producing different sets of cytokines, iNKT and T cells are both able to support adipose Tregs at adolescence and with age, respectively. Note that some studies found that adipose iNKT cells drive proinflammatory, pathogenic immune responses during obesity. These differences have not been reconciled but identifying the mechanisms behind them may reveal further insights into iNKT cell biology and how tissue-specific cues can drive different cell phenotypes [3] [4] [9] [10] [11] [12] [13].

The Long COVID-19 Syndrome (in Adults)
About 5% and 10% of patients infected with coronavirus, two severe acute respiratory syndromes (SARS-CoV-2) require admission to the Intensive Care Unit (ICU), with up to 67% developing shock, which was implicated as the leading cause of death in 7% of coronavirus disease cases in 2019 (COVID-19) and contributed to an additional 33%. All four types of shock-distributive, cardiogenic, obstructive, and hypovolemic shock-have been observed in patients with COVID-19 [1] [2] [5].
These data presented are related to patients in the acute phase of the disease.
However, there are no data available regarding inflammatory shock in patients who developed CSF after hospital discharge.
LCS has been gradually identified as a different condition from sepsis but is still closely related to the classic management of septic shock. It is the closest reference for management, considering the similarities of these two nosological entities. However, the similarity has been a brake on the decision of an adequate treatment, which is based on the inflammatory blockade using high doses of corticosteroids [14] [15]. New-onset biventricular failure and vasoplegia progressed to shock with multiorgan dysfunction. All patients had a hyperinflammatory profile associated with vasoplegia and heart failure. Moreover, lymphopenia (and potentially high SARS-CoV-2 Ab titters) could be an indicator of a dysregulated immune system, augmenting the inflammatory cascade and tissue injury. Although SARS-CoV-2 Abs are presumed to have protective and neutralizing properties, the elevated levels of Ab could have played a pathogenic role in the observed hyperinflam-Open Journal of Emergency Medicine matory response. In SARS-CoV-2, non-neutralizing antibodies could cause an inflammatory cascade and enhance viral entry via an antibody-dependent mechanism enhancement. Alternatively, these cases may represent a new phenomenon in analogous adults to those recently described in the paediatric population. Several patients did have nonspecific rashes and other overlapping features though none had clinical vasculitis on coronary angiograms, and some patients had mild nonspecific late gadolinium enhancement on cardiac magnetic resonance imaging (Figure 1 and Figure 2).
The cause of LCS is multifactorial, but with increasing evidence focusing on acute Tryptophan and Phenylalanine deficiency due to ACE-2 internalization, it has brought light to the dark tunnel dug by SARS-CoV-2. This virus promotes metabolic changes in the body and damage to the organs where it passes during the acute phase of infection. These metabolic changes seem to be related to enzymatic mechanisms related to intracellular aerobic respiration. The shift from the Metabolic Try axis to the production of Kynurenine at the expense of the production of serotonin (5-HT) and Vitamin B3 (NAD/NADH+) seems to be Figure 1. Faget's sign. Faget's sign is bradycardia concerning fever when the usual thing is tachycardia due to temperature elevations. It so happens that the pathophysiology behind this phenomenon is still controversial. Given the studies in COVID-19, the possibility arises that this phenomenon is related to the production of Adenosine (ADA) in the face of severe hypoxia that occurs in SARS-COV-2 infection. Adenosine plays an essential role against cell damage, has an anti-inflammatory/immunosuppressive role in addition to causing psychiatric phenomena that are very prevalent in COVID-19. However, this adaptation to cellular damage can become a sign of physical and metabolic exhaustion in the face of such intense inflammation resulting in Bradycardia with a risk of cardiorespiratory arrest due to the amount of serum adenosine and hypoxemia resulting from COVID-19. This situation also appears in other diseases that progress with severity and tissue hypoxia due to disseminated intravascular coagulation, causing cell damage due to lack of tissue oxygen. Open Journal of Emergency Medicine is an essential amino acid required for protein biosynthesis. It is also a biochemical precursor of metabolites that significantly affect mammalian physiology, including gastrointestinal functions, immunity, metabolism, and the nervous system. In the gastrointestinal tract L-Try metabolism can follow three significant pathways, all of which are influenced by the gut microbiota: 1) the kynurenine pathway (KP) in both immune and epithelial cells, 2) the serotonin (5-hydroxytryptamine, 5-HT; production pathway in enterochromaffin cells (ECCs), a specialized subtype of intestinal epithelial cell, and 3) direct transformation by the gutbiota of L-Try into several molecules, including ligands of the aryl hydrocarbon receptor (AhR). In mammalian cells, most L-Trp is metabolized via the KP, while the remainder is utilized in the synthesis of 5-HT and melatonin (MT). In KP, L-Trp is catabolized into the unstable derivative N-formyl-L-kynurenine (NFK) by rate-limiting enzymes tryptophan 2,3-dioxygenase (TDO) and indoleamine 2,3-dioxygenases (IDO1/IDO2). Globally, the enzymes of KP are expressed in a tissue-specific manner.
TDO is expressed in the liver, whereas IDO1 is expressed in many cell types and tissues and is inducible by cytokines NFK is rapidly metabolized by kynurenine formamidase (expressed in liver, kidney, and brain) to form L-kynurenine (L-kyn). L-kyn is a crucial metabolite with potent immunoregulatory functions through its binding to AhR. L-kyn is mainly metabolized by kynurenine monooxygenase (KMO) to form 3-hydroxykynurenine (3-HK). 3-HK is then degraded to 3-hydroxyanthranilic acid (3-HAA) by kynureninase (KYNU). KYNU is subsequently metabolized to 2-amino-3-carboxymuconic 6-semialdehyde (ACMS) by 3-hydroxyanthranilic acid 3,4-dioxygenase (3-HAO). The former is expressed in the liver, kidney, central nervous system (CNS), and placenta, while the latter has a broad tissue distribution. ACMS can be cyclized to quinolinic acid (QUIN) or metabolized by the enzyme 2-amino-3-carboxymuconate-semialdehyde decarboxylase (ACMSD), found mainly in the kidney and to a lesser extent in the liver, and responsible for the synthesis of 2-aminomuconic-6-semialdehyde (AMS). AMS is either metabolized by 2-aminomuconic semialdehyde dehydrogenase (AMSD) to result in acetyl-CoA or cyclized nonenzymatically to form picolinic acid (PICA). In the CNS, QUIN is mainly produced by microglia. It acts as a neurotoxic agent on astrocytes mainly by its selective agonist effect on ionotropic glutamate glutamatergic N-methyl-D-aspartate (NMDA) receptors. However, mechanisms determining the engagement of KP in its synthesis remain undetermined. QUIN is also a precursor for the de novo synthesis pathway for NAD via the enzyme quinolinate phosphoribosyltransferase (QPRT) expressed mainly in the liver and kidney. NAD is a cofactor for numerous enzymes involved in cellular energy metabolism, adaptive responses of cells to bioenergetic and oxidative stress, and genome stability. Its deficiency affects tissues that need high cellular energy, such as the brain, gut, and skin, causing pellagra. Finally, PICA is a neuroprotective molecule whose concentration is reduced in the serum of patients with autism, and plasma and cerebros- one of the most critical pathways that sustain inflammation for months, contributing to generalized metabolic wastage with the emergence of neuropsychiatric symptoms and symptoms related to organ-specific inflammation, such as heart failure, renal failure, dermatological lesions.
Try generates 5-HT with a vasoconstrictor action when in homeostasis; when in inflammation, the Try starts to have its vasoconstrictor action blocked by IDO-1, which has a vasodilator action.
With improved pulmonary lesions caused by the coronavirus in acute illness, the gas exchange mechanisms return to normality; that is, oximetry will indicate adequate haemoglobin saturation. However, the patient complains of tiredness, shortness of breath, symptoms that seem to be dissociated from the improving lung or with few sequelae and a still good heart. It turns out that respiratory failure exists and appears to be due to an intracellular enzyme deficit. The lack of NAD/NADH+ and the shift from inflammation to oxidative stress underlie the pathophysiology of LCS [13].
LCS seems to be caused by the intense anaerobic mechanism of energy production since the aerobic pathway was compromised, especially in severe and critical patients. However, people with a mild, oligosymptomatic disease and even people who considered themselves not infected before in the pandemic complained of LCS signals and symptoms. There is a need for us to be aware that the virus is highly transmissible and that the way it acts in people's bodies can prevent the formation of adequate antibody titres so that, even if produced, they are not identified by the available analytical methods. Thus, we have two critical aggravating factors in the diagnostic search: negative serology does not exclude the disease, and respiratory failure is not seen in monitoring, as its essence is intracellular and not haemoglobin saturation.
Once the patient progresses to CSF with an inflammatory shift to oxidative stress, there is depletion of hormones and neurotransmitters that are important in maintaining the mechanisms of vasodilation and vasoconstriction. Metabolic stress constantly activates the adrenal to produce cortisol and stimulate the production of catecholamines. However, there is little substrate for the formation of catecholamines due to the low absorption of Phe, further accentuating the exhaustion of these molecules required by oxidative stress (Figure 1).
The pathophysiology behind the chronic symptoms in LCS may be related to the virus interfering with the RIG1-MAVS pathway to decrease type I interferon (IFN) production. SARS-CoV-2 infection of white blood cells leads to elevated glycolysis, increased mitochondrial reactive oxygen species (mtROS) production, and dysregulated mitochondrial bioenergetics. Two potent antioxidants reduced viral load and proinflammatory cytokines. Elevated levels of lactate dehydrogenase (LDH) were also reported in COVID-19, which could reflect mitochondrial dysfunction, causing inflammation is by activating the NLRP3 inflammasome in immune cells. The NLRP3 inflammasome participates in the processing and releasing inflammatory cytokines, such as IL-1β and IL-18.
To distinguish the patients with confirmed COVID-19 who may worsen while treated, we justified the following threshold values of the laboratory tests done on admission: lymphocyte count < 2.59 × 10 9 /L, and the upper levels for total bilirubin 11.9 μmol/L, ALT  Lactate is considered an essential substrate for mitochondria in the muscles, heart and brain during exercise and is the primary gluconeogenetic precursor in the liver and kidneys. Median whole blood lactate levels in hospitalized patients were d1 = 3.3, d7 = 2.6, d14 = 2.2, d28 = 1.9 mmol, and in ambulatory patients, d1 = 1.4, d14 = 1.4, d28 = 1.5 mmol. Whole blood lactate decreased significantly during the clinical course and recovery in hospitalized patients (p = 0.008). The blood lactate levels were significantly higher in hospitalized patients than ambulatory patients (day 1: hospitalized versus ambulatory patients (p = 0.002); day 28: hospitalized versus ambulatory patients P ≤ 0.0001). Elevated blood lactate is strongly associated with mortality in septic patients. Lactate seems unrelated to tissue hypoxia but is likely to reflect mitochondrial dysfunction and high adrenergic stimulation. Near-normal blood lactate, indicating preserved mitochondrial function, despite a systemic hyperinflammatory state similar to sepsis. A study Median whole blood lactate levels in hospitalized patients were d1 = 3.3, d7 = 2.6, d14 = 2.2, d28 = 1.9 mmol, and in ambulatory patients, d1 = 1.4, d14 = 1.4, d28 = 1.5 mmol. Whole blood lactate decreased significantly during the clinical course and recovery in hospitalized patients (p = 0.008). Lactate levels were significantly higher in hospitalized patients than ambulatory patients (day 1: hospitalized versus ambulatory patients (p = 0.002); day 28: versus hospitalized ambulatory patients P ≤ 0.0001). These data show a long time of illness in some patients, which elevated lactate in D28 after the onset of symptoms [3].
Another study evaluated a comparison between Lactate and Renin. Area under (area under the receiver operating characteristics curve, 0.682; 95% CI, 0.503 -0.836; (p = 0.05), but initial lactate could not (area under the receiver operating characteristics curve, 0.615; 95% CI, 0.413 -0.803; p = 0.27). Peak renin (area under the receiver operating characteristics curve, 0.728; 95% CI, 0.547 -0.888; (p = 0.01) and peak lactate (area under the receiver operating characteristics curve, 0.746; 95% CI, 0.584 -0.876; p = 0.01) demonstrated moderate discrimination. There was no significant difference in discriminative ability between initial or peak renin and lactate concentration. At each study time point, a higher proportion of renin values exceeded the threshold of normal (40 pg/mL) in nonsurvivors than in survivors, but this association was not significant for lactate [1].
According to the above, there is a rarity on the subject of "chronic inflammation" or "inflammatory shock" in COVID-19 patients, as most data refer to the disease in the acute phase. However, analysing the data found, it is possible to establish that tests such as LDH and Lactate can assess the patient COVID-19 in shock, which can differentiate classic septic shock from inflammatory shock caused by COVID-19. Furthermore, myocardial damage seems to be prevalent in the chronic phase of LCS, helping in the differential diagnosis.
From March 1 through March 10, 2020, the incidence of MIS-C in New York State among people younger than 21 years was 2 per 100,000 individuals vs 322 per 100,000 individuals with laboratory-confirmed SARS-CoV-2 infection. Third, there may be a diversity of phenotypes of MIS not only between individual cases but across age groups. In MIS-C, mucocutaneous manifestations were more common in the younger cohort, while in older children, myocarditis and gastrointestinal symptoms were more frequently reported. 4 In fact, in the adult cases of MIS identified by Davogustto et al., 612 of 15 patients with MIS-A (80.0%) had gastrointestinal complications. As we learn more about MIS-A, we are likely to uncover additional aspects of its spectrum. Lastly, evidence for an optimal treatment strategy for MIS-A is lacking, and for now, therapy may depend on supportive medical management. In children, MIS-C therapy frequently includes intravenous immunoglobulins and glucocorticoids, which are extrapolated from the management strategies of Kawasaki disease. Further research will be needed to decide whether these same treatments can be applied to adult cases. However, initially, the mitochondrial component appears to be preserved in the acute phase of the disease, reflecting low serum lactate titers. The chronic phase appears to reflect the spoliation of enzymes necessary for the metabolic pathway of aerobic cellular respiration to be carried out correctly. Thus, hypoxemia resulting from deficient intracellular respiration despite haematosis preserved by the structural improvement of the lungs, whose acute injury by SARS-CoV-2 triggered respiratory failure. Thus, the patient may present in chronic disease with adequate O 2 saturation, with signs and symptoms of respiratory failure in progress, especially if the patient presents acute deterioration evolving to inflammatory shock [1] [21].
However, recent studies are beginning to challenge the centrality of cytokine storms in severe COVID-19 cases. For instance, a study demonstrated that inflammatory cytokine elevations in patients with severe and critical COVID-19, including elevations of IL-6, are profoundly lower than those reported in patients with comparable conditions such as acute respiratory distress syndrome (ARDS), which is unrelated to COVID-19 and sepsis. In the same study, several non-cytokine biomarkers, including D-dimer, C-reactive protein, and ferritin, were elevated to a similar or greater extent in COVID-19 patients than in patients with sepsis or ARDS. No statistically significant differences were observed in baseline levels of multiple cytokines between COVID-19 and sepsis patients. The COVID-19 complications are now mainly associated with immunosuppression, especially lymphopenia rather than cytokine storm. Increased T lymphopenia, particularlyCD4+ and CD8+ T cells, have been shown to decrease markedly in COVID-19 patients, implying damage of lymphocytes by the SARS-CoV-2 virus. Moreover, unlike episodic cytokine storm, lymphopenia is continuous in critically ill COVID-19 patients and leads to increased secondary infections.

Changes in the Glycolytic Pathway and Adenosine Production
Many viruses alter host cell metabolism similarly to the Warburg effect, increasing glycolysis and producing rapid energy and substrates for nucleotide replication and specific protein synthesis. Increased aerobic glycolysis has been demonstrated in Zika virus (ZIKV) with up-regulation of glycolytic genes, including membrane glucose transporter 1 (GLUT1), various glycolysis enzymes, and MCT4, the transporter that expels lactate out of cells. In intestinal cells, the coronavirus transmissible gastroenteritis virus (TGEV) increases glucose uptake via the apical transporters of Naþ-dependent glucose transporter 1 (SGLT1) and basal glucose transporter 2 (GLUT2), and uptake stimulated by Epidermal growth factor receptor (EGFR) Host cell metabolism and activation of signalling pathways are reprogrammed by viral proteins, as shown in adenovirus-E4-ORF1. The two main signalling pathways-PI3/AKT/mTOR and MAPK/ERK-promote replication of the Middle East Respiratory Syndrome coronavirus (MERS-CoV), enterovirus 71 (EV71) and ZIKA. In MERS-CoV, PI3/AKT/mTOR and MAPK/ERK inhibitors (including rapamycin) inhibit virus replication in vitro, regardless of whether the inhibitors are introduced before or after viral infection. Thus, considering that SARS-CoV-2 and MERS-CoV are beta-coronaviruses that share numerous similarities, we hypothesize that SARS-CoV-2 replication is supported in airway cells by the Warburg effect promoted by PI3 pathways./AKT/mTOR and MAPK/ERK. Studies need to prioritize the following considerations: That metabolism may be cell type dependent. The Warburg effect can be activated independently of the infection itself (e.g., in response to hypoxia).
Moreover, the virus could promote alternative pathways (glutaminolysis) to adapt nutrient conditions to biosynthetic or bioenergetic demands.
The energy consumption of metabolic activities in normal cells depends mainly on mitochondrial oxidative phosphorylation (OXPHOS), which is efficient and generates more adenosine triphosphate (ATP) than glycolysis. COVID-19 causes severe hypoxia due to lung damage and interference with tryptophan metabolism. Hypoxemia generates large production of adenosine, but not only in acute infection.
Although the lungs can recover, or the patient can adapt to the sequelae caused in the acute phase of the disease, dysmetabolism generated with the possibility of chronic inflammation due to the internalization of ACE-2 and interference in the tryptophan cycle, changing the NAD/NADH+. Therefore, it promotes the deflection of aerobic respiration to beta-oxidation of fatty acids and creates an environment for oxidative stress and its consequences, such as insulin resistance and atheroma.
Two primary nutrients captured and utilized by cancer cells are glucose and glutamine. These two nutrients contribute to most cellular carbon sources used for biogenesis. Glucose catabolism generates ATP, NADPH and other biomasses for reductant biosynthesis and ROS detoxification. In association with the TCA cycle, glutamine metabolism provides not only a carbon source but also NADH, NH3+ and other essential intermediates for lipid biosynthesis, amino acid synthesis, and cellular acid detoxification. Monocytes enter sites of microbial or sterile inflammation as the first line of defense of the immune system and initiate pro-inflammatory effector mechanisms. We show that activation with bacterial lipopolysaccharide (LPS) induces them to undergo a metabolic shift toward aerobic glycolysis, similar to the Warburg effect observed in cancer cells. Monocytes, macrophages and dendritic cells [22] [23] undergo a switch from oxidative phosphorylation to glycolysis in response to toll-like receptor 4 activation by LPS, the so-called Warburg effect [24] [25].
Glycolysis supplies metabolic intermediates for other biosynthetic pathways necessary for cellular growth and differentiation during the glycolytic switch. In addition to glycolysis, the pentose phosphate pathway (PPP), the hexosamine pathway and the glutaminolysis are increased upon activation. There is a compensatory increase in anaerobic glycolysis to maintain the cell energy sources. Consequently, intracellular glycogen stores are rapidly depleted, and lactic acid accumulates, leading to decreased activity of many cellular enzymes (due to decreased pH levels). In addition, new evidence revealed that the upregulation of glycolysis is not just for ATP synthesis but also for the synthesis of biomass such as ribonucleotides and amino acids as well as reduced nicotinamide adenine dinucleotide phosphate (NADPH) production, which can remove reactive oxygen species (ROS) generated by cancer cells' accelerated metabolism under hypoxic conditions.
Metabolic syndrome, diabetes, obesity, hypertension, cardiovascular disorders and chronic nephropathy are frequently observed in patients with COVID-19. These conditions promote the occurrence of a low-grade inflammatory state, a condition that increases with ageing. The chronic state of inflammation impairs endothelial function, immune response and antioxidant defence while increasing the development of cancers. Ageing increases the Warburg effect on cells via oxidative stress and the production of reactive oxygen species (ROS), promoting the activation of HIF-1a; Mitochondrial senescence, decreased oxidative phosphorylation (OXPHOS), dysfunction of the AMPK and p53 pathways conspire to promote aerobic glycolysis in elderly patients.
Glycolysis orchestrates the behaviour of inflammatory cells. Upon inflammation, immune cells are reprogrammed towards glycolysis, enhancing this pathway at the expense of OXPHOS and, in macrophages, imbalance [24] [26] in the TCA cycle. Consequently, glycolysis and broken TCA cycle-released metabolites such as lactate, citrate or succinate accumulate in immune cells, promoting signalling, post-translational and epigenetic modifications that drive the inflammatory response. Moreover, glycolytic intermediates fuel other pathways such as the PPP, which provides biosynthetic molecules, and the hexosamine one generates UDP-GlcNAc for glycation reactions.
The pentose phosphate pathway (PPP). The PPP branches after the first step of glycolysis and goes back to fructose 6-phosphate and glyceraldehyde 3-phosphate in the glycolytic and gluconeogenic pathway. The PPP produces R5P and NADPH for biosynthesis and redox regulation. NADPH from the PPP converts oxidized glutathione (GSSG) to reduced glutathione (GSH). GSH elicits insulin granule exocytosis via SENP1. However, NADPH might inhibit insulin secretion by promoting NADPH oxidases (NOXs). Hyperglycemia decreases G6PD activity by activating protein kinase A (PKA) and increasing intracellular oxidative stress, leading to chronic kidney injury and diabetic kidney disease (DKD). β-oxidation is the catabolic process by which fatty acid molecules are broken down to generate acetyl-CoA and NADH and FADH2, which are used in the electron transport chain to produce ATP. However, β-oxidation occurs at two sites, the peroxisome in the cytosol and the mitochondrion using long-chain fatty acids and medium-chain fatty acids, respectively.
Carnitine shuttle is a rate-limiting step of fatty acid oxidation in mitochondria, and therefore fatty acid oxidation can be regulated in this step [23] [24] [25] [26] [27].
Malonyl CoA, a fatty acid synthesis intermediate, presents in the cytosol, is an inhibitor of carnitine acyltransferase I. This indicates that when fatty acid synthesis is in progress, fatty acid oxidation cannot coincide as the carnitine shuttle is impaired by inhibition of carnitine acyltransferase I.
Oxidation of fatty acids is also regulated by the ratio of acetyl CoA to CoA: as the ratio increases, the thiolase reaction that requires CoA (the enzyme that participates in β-oxidation) decreases.
When the [NADH]/[NAD+] ratio increases, the β-hydroxy acyl-CoA dehydrogenase enzyme is inhibited. The Warburg effect is the regeneration of NAD + NADH in the pyruvate-to-lactate step that completes the aerobic glycolysis. In this scenario, NADH produced by glyceraldehyde phosphate dehydrogenase (GAPDH) must be consumed to regenerate NAD+ and keep glycolysis active. This high rate of glycolysis allows supply lines to remain open, such as siphon 3-phosphoglycerate (3PG) to serine for one-carbon metabolism mediated production of NADPH nucleotides. A possible hypothesis is that by significantly decreasing NAD+ (both by consumption and deficit of tryptophane), the Warburg effect is activated to increase the NAD/NADH+ ratio.
One of the possibilities that LDH is a good reference for diagnosing inflammation in COVID-19, both in the acute phase and in LCS, is to consider that, due to the Warburg Effect and the intensification of the glycolytic pathway, there is a greater need for LDH expression. However, due to the Tryptophane deficit, there is little substrate to guarantee the formation of NAD, generating a deficiency in the NAD/NADH+ balance for adequate aerobic cell respiration [22] [23] [24].
LDH ((S)-lactate: NAD+ oxidoreductase; EC 1.1.1.27) is a family of NAD+dependent enzymes that catalyse the inter-conversion between pyruvate and lactate, with concomitant oxidation/reduction of the cofactor (NAD+/NADH). LDH simultaneously regenerates NAD+ molecules is certainly the most important step required for glycolysis to proceed and release cellular energy. LDHA is located mainly in the cytoplasm, but it has also been found to bind single-stranded DNA in the nucleus, although its involvement in DNA metabolism is not well understood. LDHA has been acknowledged as a valuable predictive and prognostic marker; its overexpression is associated with cancer invasiveness; elevated serum lactate levels correlate with poor prognosis and resistance to chemo-and radiotherapy LDHA expression is regulated by c-My and HIF-1. Moreover, tyrosine phosphorylation by the oncogenic FGFR1 receptor was found to activate LDHA, thereby promoting the Warburg effect in cancer cells.
BCAAs and fatty acids can participate in the TCA cycle and glycolysis. The catabolism of BCAAs and fatty acids can interplay through these metabolites and ultimately impact mitochondrial ATP production. Enhanced fatty acid oxidation increased the ratio of mitochondrial acetyl-CoA/CoA and NADH/NAD+, leading to the inactivation of pyruvate dehydrogenase. Increased the intracellular level of citrate, thereby inhibiting the accumulation of phosphofructokinase and glucose-6-phosphate, which hindered the normal progress of glycolysis.
Under normal oxygenated conditions, the rate of ATP catabolism and anabolism are equal, and the concentration of ATP is maintained at a much higher level (at least 10 times higher) than that of ADP. Under conditions of tissue stress or trauma, such as ischemia or hypoxia, however, the oxygen supply is inadequate for oxidative phosphorylation of ADP to regenerate ATP, and the ATP/ADP ratio is compromised. The increasing concentration of ADP results in an increase in the concentration of AMP, which in turn is hydrolyzed to adenosine. The most important source of adenosine quantitatively is the AMP-selective cytosolic 5'-nucleotidase (c-NI), which has been suggested to be responsible for approximately 76% of adenosine production in mammalian cells. Another essential enzyme responsible for the production of adenosine via hydrolysis of AMP is ecto-5'-nucleotidase (e-N), a glycoprotein found primarily in the plasma membrane of eukaryotic cells. In addition to these two enzymes, adenosine can also be produced from S-adenosylhomocysteine (SAH) via SAH-hydrolase [28] [29] [30].
Adenosine is a vital signalling nucleoside that orchestrates cell and tissue adaptation under energy depletion and ischemic/hypoxic conditions by activating four G protein-coupled receptors (GPCR). The regulation and generation of extracellular adenosine in response to stress is critical in tissue protection. Studies in rats and humans have reported that extracellular adenosine signalling plays a beneficial role during acute states.
Adenosine is ubiquitously produced in almost every cell in our body under physiological conditions and subsequently produced under hypoxia or energy depletion conditions. As a critical building block and intermediate metabolite of nucleic acids, adenosine is a key signalling molecule that orchestrates the cellular response to hypoxia, energy depletion and tissue damage, activating its G protein-coupled receptors (GPCR) in various types of cells. Under normal physiological conditions, adenosine extracellular and intracellular levels are in the nanomolar range. However, under stressful conditions, ATP is released from damaged cells, such as endothelial cells, neutrophils, and glial cells, through transmembrane protein channels, including pannexins or connexins, and subsequently dephosphorylated to extracellular adenosine by ectonucleotidases including CD39, which converts ATP to ADP/AMP and CD73 which converts AMP to adenosine.
Adenosine is well known to be induced under hypoxic conditions, and patients with FD are in a chronic state of hypoxia. Elevated plasma adenosine through activation of the ADORA2B receptor in the erythrocyte leads to sick-ling, haemolysis, and damage to various erythrocyte tissues in transgenic mice with sickle cells (Figure 3)

Organizing Pneumonia and COVID-19 Chronic Sequelae
Organizing pneumonia appears as a complication of the late phase of COVID-19.
Corticosteroids are standard therapy for organizing pneumonia, but the question of whether a high-dose corticosteroid approach would be beneficial for patients with organizing pneumonia secondary to COVID-19 remains unanswered.
Patients undergoing chest computed tomography due to maintenance of hypoxemia, which presented a pattern compatible with organizing pneumonia. Patients were treated with high-dose corticosteroids (1 mg/kg VO prednisone), with marked clinical improvement and decreased oxygen flow rate demand.
They were discharged after an average length of stay of 6.3 days.
OP usually appears in hypotheses with the activation of inflammation via IL-6, so it can appear in any situation where there is a cytokine storm with this cytokine pattern. That is, OP is not pathognomonic of COVID-19 [32] [33] [34] [35] [36] (Figure 4).

Discussion
The review used for this article shows that CLS is more easily recognized in paediatric patients than in adult patients and this fact remains a great mystery to be deciphered for the author of this text. LCS (MISc) is treated with corticosteroids and immunoglobulin, while LCS (MIS-A) is still neglected as a nosological entity and is not treated.
In the author's view, LCS is an inflammatory entity caused by SARS-CoV-2 infection due to the internalization of ACE-2 and mainly by the shift from the aerobic axis of cellular respiration to the oxidative stress axis due to the enzyme and intracellular antioxidant deficit, intensifying insulin resistance, initial hypercortisolism and shifting the immune response to innate immunity, which signals the rarity of the disease, as stated in an article already submitted for publication. Furthermore, bradycardia in the presence of fever or hyperthermia may result from cell damage with subsequent production of adenosine, justifying the pathophysiology of the Faget's signal (Figure 1).
It is essential to consider that in ISC, due to its chronic status, the alveoli may already be recovered, or there was an adaptation to the sequelae condition after COVID-19; for this reason, haemoglobin saturation may be normal on pulse oximetry or arterial blood gases. The defect that leads the patient to respiratory failure is intracellular and makes the diagnosis more complicated but not impossible since LDH, elevated triglycerides and cholesterol may indicate that the inflammatory axis is on oxidative stress due to the enzymatic failure necessary for adequate aerobic respiration. Computed tomography images show patients hospitalized in the same period in Hospital do Server Estadual ward. These patients have extensive investigation for tuberculosis and fungi. Negatives. Epidemiology, at a time of SARS-CoV-2 pandemic, the images are not coincidences but are part of the progression to organizing pneumonia, which is not pathognomonic of COVID-19, but is very prevalent when the disease progresses to inflammatory syndrome multisystem. Otherwise, the most common sequelae are laminar atelectasis, mosaic infiltrates and consolidations that resemble calcified nodules.
LCS has a chronic inflammatory status that leads the post-COVID-19 patient to physical and metabolic exhaustion, leading the patient to vasoplegic shock due to exhaustion of catecholamines, since with the internalization of ACE-2, there is less intestinal absorption of amino acids essential as Phenylalanine (Phe) and Tryptophan (Try), with serotonergic involvement as well.
The Kynurenine pathway is initiated by converting L-tryptophan (Try) by either the enzymes tryptophan-2,3-dioxygenase or indoleamine 2,3-dioxygenase forming formyl-kynurenine, which is then further degraded to kynurenine, the precursor of several bioactive compounds, including kynurenic acid, quinolinic acid, picolinic acid, and 3-hydroxyanthranilic acid. The pathway is responsible for over 90% of tryptophan metabolism in the periphery.
Kynureninase is a pyridoxal phosphate-dependent enzyme inhibited by oestrogen and metabolites, with vitamin B6 deficiency and inhibition. There is an increase in Kyn, HK, XA, and Hal and a decrease in KA and AA because of the available vitamin B-6 deficiency simulation in which the activities of the enzymes were not wholly reduced [12] [13].
The development of Th17 cells is negatively regulated by IFN-γ, IL-27, and IL-2, the signals of which are dependent on Stat1 (IFN-γ and IL-27) and Stat5 (IL-2), respectively. The orphan nuclear receptors, retinoid-related orphan receptor γ (RORγ) and RORα have been identified as the key transcription factors that determine the differentiation of Th17 lineage. AhR is involved in the differentiation of Th17 cells by regulating Stat1 activation, which suppresses Th17 cell differentiation under Th17-polarizing conditions ( Figure 2). Cellular damage from hypoxemia produces too much adenosine (ADA) in response to injury. ADA performs negative feedback for multiple pathways of intracellular aerobiosis and stimulates bradycardia when in excess, which can cause cardiorespiratory arrest. Adenosine limits the degree of vascular injury during ischemia and reperfusion by inhibition of oxygen radical release from activated neutrophils, thereby preventing endothelial cell damage, and by inhibition of platelet aggregation. These effects help to preserve endothelial cell function and microvascular perfusion. Long-term exposure to adenosine may also induce coronary angiogenesis [37]- [42].
Due to the need for ATP, the pentose pathway is linked to compensate for the energy deficit through oxidative phosphorylation. However, the citric acid pathway is enzymatically blocked, leaving the cell to carry out the Warburg effect, facilitating oncogenes and protooncogenes to be activated, orchestrating a status of tolerance and immunosuppression. With the activation of the Warburg effect, innate immune cells can produce ATP in a medium nourished by Glucose, while in hypoglycaemic or normoglycemic status, the oxidative phosphorylation pathway is preferred. For this reason, it is necessary to maintain glycaemic control in severe COVID-19 patients, tending to form ATP through a non-injurious and tumorigenic pathway. Elevated LDH shows intense glycolytic activity, thus the need to provide substrates to maintain the citric acid pathway and oxidative phosphorylation patent.
Regarding sepsis and Septic Shock, we have an acute event that, if left untreated, leads to death. Aerobic breathing pathways are not impeded, but tissue perfusion may be impaired, causing an increase in lactate with low LDH. In ISC, however, the DHL is very high due to tissue damage and blockage of the aerobic intracellular respiration pathway (Figure 3).

Conclusion
Post-COVID-19 Inflammatory Syndrome is well recognized in children, and we must recognize that it is part of the pathophysiology of the disease in adults as well. Ignoring the differential diagnosis between classic septic shock and inflammatory vasoplegic shock is a life-or-death condition for the patient. We must carry out trials identifying features that facilitate the diagnosis. Based on the survey carried out in this article, I consider LDH, Lactate, C-Reactive Protein, bradycardia (in situations in which the body demands compensatory tachycardia) to be essential tests to make this difference. Multisystem Inflammatory Syndrome in adults or what this article calls ISC (Inflammatory Shock after COVID-19) should be treated with high doses of corticosteroids or immunoglobulins. ISC is the same or similar entity as the MISc, an inflammatory status that has been seen in paediatric patients. LDH shows a magnitude of the Warburg effect and may indicate that COVID-19 patients are in LCS and chronic inflammation. LDH shows a magnitude of Warburg effect and may indicate that patients with COVID-19 are in LCS and chronic inflammation. Normalizing blood glucose is a way of forcing ATP production by oxidizing phosphorylation. Open Journal of Emergency Medicine volume to maintain a pH greater than or equal to 7.25 and pCO 2 as close to physiological as possible. Avoid permissive hypercapnia.

A3. Pulse of Methylprednisolone [14] [15] [43] [44] [45] [46]
It is indicated for both non-shock and shock associated LCS patients.  Always, if possible, start treatment before the cytokine storm, preferably between D6 and D8 of the onset of symptoms with C-reactive protein (CRP) less than or equal to 10 mg/dL, that is, before the cytokine storm, as the desired effect the storm blocks.
Prescribe Ivermectin 6 mg 2 tablets to be taken as a single dose. Inform that if there is a worsening or if saturation drops to O 2 Saturation (SatO 2 ) value less than or equal to 95%, supplementation should be started at home or the hospital.
Complete rest for 15 days and resume small activities without forcing O 2 demand to perform physical activities.
Request return within 5 days for outpatient reassessment. Lowering FiO 2 too much causes a shift from inflammation to oxidative stress. It is important that clinical trials are carried out to verify that FIO 2 does not cause lung damage, much less falls short of what should be provided to the patient during weaning. Hypoxia causes agitation due to the toxic products of Kynurenine.