Coronavirus disease 2019 (COVID-19) is an unfamiliar illness with potentially devastating consequences. The pandemic is unfolding at different rates with wide geographic separation and seemingly erratic expression. There is well-justified urgency to describe the inconsistently expressed features of this new viral disease and implement strategies to avoid and treat it [1,2,3,4].
Because COVID-19-related illness is caused by a single virus, it seems reasonable to assume a degree of uniformity across populations. Yet, some observations are universal while others apparently conflict. In this urgent situation, we feel impelled to skip steps in the traditional methodology of first making careful observations and then conducting evidence-building research to inform rational management. We have been down this road before of needing to act while not fully understanding a new pathogen variant. But this SARS-CoV-2/COVID-19 seems different. This time around, the disease may infect anyone and most organ systems and is readily and rapidly transmitted. We have a right to be frightened of this novel virus.
Mastering the entirety of medicine is impossible; practicing doctors are trained to diagnose (label) by interpreting observations using their prior education and experience, and then manage on that basis. We have a natural tendency to ‘force-fit’ newly encountered fragments of unfamiliar information into our existing constructs and understandings. (In psychology, this is known as the Barnum effect .) Although usually a functional approach to decision-making when dealing with too little information, we may unintentionally make errors when the disease seems as alien and multifaceted as COVID-19.
The acute respiratory distress syndrome (ARDS) that figures so prominently in severe cases of COVID infection may seem familiar but has historically predisposed to such logical missteps . ARDS itself was originally perceived as a high permeability edema and low lung compliance condition that disrupted function of all alveolar units and resulted primarily from surfactant deficiency . Cause and histologic manifestations went hand-in-hand. This simple perception provided for adult patients a convenient explanation that paralleled that of the infant respiratory distress syndrome, a condition for which the root cause mechanism had already been confirmed . Indeed, for some years after its initial description, the designation of ‘Adult Respiratory Distress’ reflected this flawed theory of cause and effect.
More recently, considerations of lung compliance and underlying pathology have yielded to a broader definition of ARDS based on a relatively acute onset of a known precipitant that impairs oxygenation and produces otherwise unexplained multi-lobar infiltrates . Airspace flooding, collapse, and consolidation are envisioned to parallel (more or less) the severity of oxygenation impairment [9, 10]. Most often, this view serves reasonably well. As pathologic severity increases, key definitional features of ARDS (extensive infiltrates, hypoxemia) usually proceed in synch, serving to guide clinical treatment and prognosis by gas exchange criteria. Accordingly, choices for positive end-expiratory pressure (PEEP), tidal volume, and prone positioning are made with the intention of improving oxygenation and recruiting lung units while avoiding ventilator-induced lung injury (VILI). Clinical trials and guideline tables for mechanical ventilation in ARDS are, for better or worse, keyed to the severity of oxygenation deficit . At the bedside, VILI risk is indexed by plateau pressure, driving pressure, and more recently by mechanical power .
Certain features of COVID-19-associated ARDS (what has been termed “CARDS”) seem to challenge that useful conceptual framework. Specifically, lung compliance may be well preserved in the early and mild stages of CARDS (at least in a subpopulation of these patients), because severe hypoxemia may not originate at first primarily from airspace filling and lung unit drop-out—though these do occur to some modest extent—but rather from a microvascular attack that dysregulates ventilation/perfusion matching in well-ventilated lung units and increases dead space . When simpler measures fail, the familiar initial response is to improve oxygenation—use higher PEEP and lower tidal volumes, offsetting any hemodynamic consequences. Yet, it stands to reason (though still unproven) that because these lungs are initially gas filled and unexpectedly flexible for the severity of hypoxemia, such actions might needlessly accentuate the underlying problem and increase iatrogenic risk without proportionate benefit [13, 14]. In more severe cases and at a later stage, however, those same actions become quite appropriate. In summary, it is not yet known whether standard evidence-based approaches to ARDS management apply equally well at all stages and severities of CARDS. Progress in understanding the biological mechanisms of COVID-19 has been quite rapid, but there remain many unknowns regarding its expression and management.
In confronting COVID-19, there have been shared experiences and points of agreement (Table 1), but the varied and puzzling expressions of COVID-19 have challenged the uniformity of our perceptions and in some cases stimulated brisk controversy [15,16,17,18]. For example, we argue: Does intense, sepsis-like cytokine release drive shock? . Should we manage CARDS as routine ARDS? . The basis of such disagreements may lie less with the soundness of the observations among reports and more with patient vulnerability to attack by COVID-19 and its rapidly evolving pathophysiology. The validity of any given observation and inference for management may depend strongly, for instance, on when in the course of the encounter the observation was made (Fig. 1).
In a sense, with COVID-19, we intensivists are like the blind people of an ancient Indian parable who stumble upon an unfamiliar animal, an elephant. Each individual forms a different image of the unseen beast from the part his or her own hands happen to fall upon that resembles the familiar. The individual tactile sensations are undeniable, and each interpretation and extrapolation to characterize the elephant is understandable—but ultimately, incomplete.
So it may be with COVID-19. Well-meaning authors may advocate for individual interpretations, but our current views of the entire problem are obscured and our answers half-finished. Although pathogenesis is becoming progressively clear and many clinical trials of promising treatments and vaccines have been initiated, we are still at the stage of gathering fundamental observations from which a unified theory of pathogenesis might be constructed, and around which logical and effective treatment approaches might coalesce. The scientific process is self-correcting; over time, varied high-quality scientific and clinical observations will eventually be drawn together into a coherent, unified entity. Although urgency demands that we test especially promising and logical treatment options, for the present time, it seems prudent for the medical community to collate valid observations and experiences from all quarters, form the right image of a dynamic entity, and then devise an appropriate strategy to modify supportive care as we proceed to develop effective counter-measures. As the Rajah said to the bickering blind men when advising them to humbly reflect before drawing conclusions: “The elephant is a very large and rather strange animal. Each man touched only one part. Perhaps if you put the parts together, you will eventually see the truth.”
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Conflicts of interest
Dr. Brodie receives research support from ALung Technologies; he was previously on their medical advisory board. He has been on the medical advisory boards for Baxter, BREETHE, Xenios and Hemovent. JJM and RPD report no conflicts of interest.
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Marini, J.J., Dellinger, R.P. & Brodie, D. Integrating the evidence: confronting the COVID-19 elephant. Intensive Care Med 46, 1904–1907 (2020). https://doi.org/10.1007/s00134-020-06195-z