The “Third Wave”: impending cognitive and functional decline in COVID-19 survivors

Abstract

The novel coronavirus, SARS-CoV-2, was initially discovered in November 2019 in Wuhan, China. The associated human disease, Coronavirus Disease 2019 (COVID-19), rapidly became a global pandemic. 1 By March 2020, the US began to experience its first wave of infections, with New York City at the epicenter. In the hardest hit areas, healthcare facilities were overwhelmed. Critically ill patients exceeded the capacity of intensive care units (ICUs), operating rooms (ORs) were converted to makeshift ICUs, and temporary satellite hospitals were erected to divert care for non-critically ill patients. 2 With the introduction of social distancing, contact tracing, mandatory masks and similar public health measures, New York City and the surrounding area were ultimately able to “flatten the curve” 3 . Months later, as other US cities and states began to relax their stay-at-home restrictions and people across the US optimistically prepared to resume their former lives, cases began to rise again at an alarming rate, especially in Southern and Western states 4 . Although there is debate among epidemiologists whether the recent rise in cases constitutes a “second wave” or an ongoing first wave, the overriding consensus is that the COVID-19 pandemic is far from over 5 . Thus, we have become accustomed to social distancing, mask regulations and quarantine measures, the “new normal”. These measures will likely remain in place until the development and widespread administration of a SARS-CoV-2 vaccine. Several companies including Moderna and the National Institute of Allergy and Infectious Diseases in the US and University of Oxford and AstraZeneca in the UK have entered phase 3 trials for a SARS-CoV-2 vaccine and plan on having results by early 2021. With the growing number of infected people there is a simultaneous rise in the number of recovered patients with chronic needs, so-called “long-haulers”. People who have cleared their SARS-CoV-2 infections are not all symptom-free. Many report continued fatigue, joint and bone pain, palpitations, headaches, dizziness, and insomnia. There is also concern for irreversible pulmonary scarring and dysfunction, especially in patients with severe pulmonary disease 6 . Given that the virus has only been known for a matter of months, long-term studies simply do not exist yet, and the outlook for these patients remains completely unknown. There are likely to be many chronic consequences of COVID-19 beyond the initial wave of acute infections that will be uncovered in the coming months and years. One long-term impact of COVID-19 that is becoming increasingly apparent is its effect on cognitive function, even in those with mild symptoms. One third of COVID-19 patients report neurological symptoms, and there have been anecdotal accounts of “COVID-19 delirium”, manifesting as paranoid hallucinations, confusion and agitation in over 20% of hospitalised patients 7 , 8 . A small study from the UK reported delirium in 42% of COVID-19 patients 9 . One of the highest-risk groups for severe manifestations of COVID-19, patients over 65 yr old, often have underlying mild cognitive impairment (MCI) and are already at increased risk of delirium due to underlying “neurocognitive frailty” 10 , 11 . COVID-19-related inflammation also increases susceptibility to silent infarcts, blood-brain barrier permeability, thrombosis and coagulopathy, all of which may further propagate neurological injury 12 . Moreover, the clinical management of these patients, including patient isolation, lack of personal protective equipment (PPE) resulting in reduced staff contact, lack of family/visitors, and long-term ventilation/sedation, not only places them at high risk for delirium and subsequent cognitive deficits, but also likely under-diagnosis of delirium. Taken together, there is growing evidence that a patient’s COVID-19 risk factors, pathology, and treatment course can independently and synergistically contribute to development of long-term cognitive and functional decline (Figure 1 ). In addition to poor outcomes for patients, the severe agitation associated with delirium in many COVID-19 patients in ICU creates difficulties for staff and compounds the stress of caring for these extremely sick patients. Figure 1 Wheel of factors contributing to long-term cognitive and functional decline in COVID-19 survivors. Figure 1 COVID-19 risk factors and underlying neurocognitive frailty Risk factors for severe COVID-19 infection include advanced age 13 , medical comorbidities, most commonly hypertension (40-60%), diabetes mellitus (20-40%), and obesity (40-50%) 14 , and smoking 15 . This population overlaps significantly with at-risk groups for mild cognitive impairment (MCI) and cognitive decline, which include advanced age, traumatic brain injury, obesity, hypertension, current smoking, and diabetes mellitus 16 . Together, such risk factors represent a baseline neurocognitive frailty that can increase susceptibility to cognitive complications during and following inflammatory states 17 , similar to perioperative neurocognitive disorders associated with surgery and anaesthesia 11 . Thus, the highest risk individuals for severe COVID-19 infection may also represent the most inherently susceptible population for cognitive decline in the setting of COVID-19 inflammation. The multisystemic role of COVID-19 Inflammation in cognitive decline Pulmonary: hypoxaemia Pulmonary dysfunction in COVID-19 is propagated by SARS-CoV-2 infection of ciliated bronchial epithelial cells and type-II pneumocytes. The virus gains entry into these cells by binding to the angiotensin-converting enzyme 2 (ACE2) receptor, triggering viral endocytosis. Subsequently, the viral surface spike (S) glycoprotein is cleaved by the transmembrane protease serine 2 (TMPRSS2) causing release of viral contents and propagation of the infection 18 . The lung damage and resulting hypoxaemia caused by COVID-19 likely contribute in directly to neuronal injury and subsequent cognitive decline. Cognitive impairment is frequently seen in patients with chronic hypoxaemia, including chronic obstructive pulmonary disease (COPD) and obstructive sleep apnoea 19 , 20 . Similarly, patients with COVID-19 acute respiratory distress syndrome (ARDS) can exhibit severe hypoxaemia despite relatively well-preserved lung mechanics 21 . This “silent hypoxaemia” has been described in COVID-19 patients as “oxygen levels incompatible with life without dyspnoea” 22 . In critically ill patients with COVID-19, the resulting hypoxaemia has largely necessitated tracheal intubation and prolonged mechanical ventilation to address the ensuing chronic hypoxaemic state. Vascular: coagulopathy and thrombosis SARS-CoV-2 has also been found to invade endothelial cells, leading to vascular inflammation and a high rate of superimposed arteriovenous thrombotic complications 23 . SARS-CoV-2 can also cause a systemic vasculitis and cytokine storm that can damage a range of organ systems, with renal, hepatic, dermatological, and cardiac manifestations. Cardiac complications are among the most severe in COVID-19 infection, ranging from fulminant myocarditis to heart failure and cardiac arrest 24 . The hypercoagulable and hyperinflammatory states seen in severe COVID-19 may contribute to delirium and future cognitive decline, as inflammation and coagulopathy are independently associated with an increased risk of delirium and poor outcomes in critically-ill patients 12 . Moreover, SARS-CoV-2 infection can cause susceptibility to silent infarcts and thromboses via microemboli. Neurological: blood-brain barrier breakdown, microglial activation and direct neuronal injury Neuroinflammation can cause cognitive dysfunction by compromising the blood-brain barrier (BBB) 10 . In both animals and humans, inflammatory insults can cause upregulation of pro-inflammatory cytokines and inflammatory mediators in the serum and central nervous system (CNS) 11 . Peripheral pro-inflammatory cytokines such as interleukin-1 (IL-1), IL-6, and tumour necrosis factor alpha (TNF-α) compromise BBB permeability via cyclooxygenase-2 (COX-2) upregulation and matrix metalloprotease (MMP) activation. Once the BBB is disrupted, cytokines can enter the CNS and cause microglial activation and oxidative stress, leading to synergistic cognitive impairment. The resulting neuroinflammation can contribute to delirium in the short term and severe long-term cognitive deficits 25 . Iatrogenic factors and hospital delirium In addition to the baseline cognitive susceptibility of high-risk patients and the neurological effects of COVID-19 inflammation, patients affected with COVID-19 often have hospital courses that can further contribute to cognitive decline. Acute mental status changes, such as delirium, are common in hospitalised COVID-19 patients. Delirium itself is associated with subsequent cognitive decline 26 , and is a common occurrence in ICU patients, as observed in ARDS 27 . Despite the known iatrogenic contributors to cognitive decline in COVID-19 patients, many COVID-19 patients were denied typical precautions and interventions for cognitive health because of the transmissibility of SARS-CoV-2 and the increased load of critically ill patients in the first wave. Our experience in a New York City hospital reflects this course: Patients were intubated early in their disease progression, often with limited family contact. These mechanically ventilated patients experienced prolonged periods of “iatrogenic hypoxaemia”, as it is common to maintain PaO2 values as low as 55 mmHg (7.3 kPa) or SaO2 levels as low as 88% in ARDS management 28 . Ventilated patients were commonly agitated and required prolonged sedation with multiple agents to prevent self or staff harm. While arousal and auditory functions such as a patient hearing their name spoken by a familiar voice are some of the most effective measures for emergence from disorders of consciousness 29 , simple measures like this are difficult to implement due to pandemic precautions. Both short- and medium-term neurological deficits are already being observed in both critically ill and non-critically ill COVID-19 survivors, although long-term studies are yet to be completed. In fact, the fourth most common presenting symptom of COVID-19 is confusion or altered consciousness, suggesting both direct and indirect early neurological consequences. These data raise serious concerns regarding subsequent development of cognitive and functional decline in these patients, as cognitive decline is largely an insidious process following a heralding neurological or neurocognitive insult. Moreover, cognitive decline does not occur in isolation; rather it manifests in reduced quality of life and impaired ability to perform activities of daily living (ADLs) and instrumental activities of daily living (IADLs). Cognitive decline is often undiagnosed until it is more advanced and accompanied by moderate to severe functional deficits. It may benefit our cumulative research efforts to consider the long-term effects of COVID-19 in alignment with anaesthesia and surgery, which are known precipitants of inflammation-related cognitive and functional decline. Given the overlapping inflammatory response to injury for both, this may allow us to pre-empt poor cognitive and functional outcomes for COVID-19 patients, and work to implement preventive interventions or treatments that may alleviate long-term consequences of COVID-19. Drawing on the vast body of literature addressing perioperative neurocognitive disorders, which have a similar inflammatory component, may facilitate advances in strategies for both, as well as other neurological injuries, in a relatively short timeframe. In summary, COVID-19 risk factors, pathology, hospital course and patient factors comprise a multiple neurological insults that likely predispose patients to long-term cognitive dysfunction and functional decline. It is critical that we assess and monitor COVID-19 survivors for cognitive impairment, poor psychosocial outcomes and functional decline. Research addressing the neurological sequelae of COVID-19, anaesthesia and surgery and other inflammatory disorders are imperative to reduce or prevent these poor outcomes for COVID-19 survivors, as well as for other inflammatory disease-related neurological insults. Authors' contributions HAB wrote the first draft of the manuscript and prepared the figure. SAS co-wrote the manuscript, provided accounts of clinical care for COVID-19 survivors, and assisted in figure preparation. LAE conceived the idea and edited the manuscript. Declaration of interests The authors have no relevant financial conflicts of interest to disclose. Funding HAB is supported by a Medical Scientist Training Program grant (T32 GM007739) from the US National Institute of General Medical Sciences to the Weill Cornell/Rockefeller/Sloan-Kettering Tri-Institutional MD-PhD Program. SAS is supported by a Medical Research Training Grant (MRTG-02-15-2019-Safavynia) from the Foundation for Anesthesia Education and Research.