key: cord-0742460-h0o5oq3p authors: Rajkumar Tripathi, Awatansh Kumar; Pinto, Lancelot Mark title: Long COVID: “And the fire rages on” date: 2021-10-26 journal: Lung India DOI: 10.4103/lungindia.lungindia_980_20 sha: c2bdd49fcfede716500b83f09f7953b47ecdfe3b doc_id: 742460 cord_uid: h0o5oq3p With the increasing cohort of COVID-19 survivors worldwide, we now realize the proportionate rise in post-COVID-19 syndrome. In this review article, we try to define, summarize, and classify this syndrome systematically. This would help clinicians to identify and manage this condition more efficiently. We propose a tool kit that might be useful in recording follow-up data of COVID-19 survivors. The first case of COVID-19 in India was reported on January 31, 2020. Since then, most of the resources (financial, political, medical research, health infrastructure, etc.,) have been primarily focused on arresting the spread of the disease and treating patients with the disease, i.e. interventions at primary and secondary care level. With these strategies, India has presently achieved over 90% recovery. [1] 9.5 million cases recovered out of 10 million reported as of December 19, 2020 . [2] However as the cohort of survivors expands, it is now being realized that a parallel epidemic of the post-COVID syndrome/long COVID is emerging. This can be regarded as a syndrome encompassing the chronic noncommunicable, often debilitating sequelae of COVID-19. The available literature suggests that up to 88% of COVID-19 survivors may have this syndrome. Understanding the causes, natural history, and how best to intervene are all crucial to the management of the syndrome and will help the health-care system gear up to provide tertiary prevention that may be needed as a consequence. survivors due to the use of high-dose steroids. Similarly, the incidence of pulmonary fibrosis was reported to be 38%-50% post-SARS CoV-1, 33% with MERS (Middle East Respiratory Syndrome), 10% with swine flu (H1N1), and 19% with avian flu (H7N9). However, the progression of pulmonary fibrosis was relatively uncommon with SARS, H1N1, and H7N9 whereas 13% progression was reported with host mass pulmonary fibrosis. [4] [5] [6] [7] [8] The post-COVID syndrome encompasses multiple organ systems. A summary of the organ systems involved can be found in Table 1 . The discussion will focus on the various organ systems, clinical manifestations, and sequelae that have been reported in the past year of the pandemic. Pulmonary sequelae of COVID-19 include persistent symptoms, residual radiographic changes, and impairment in pulmonary function. In a study done in Italy, 143 COVID-19 survivors were followed up for an average of 2 months. It was found that close to 43% of these patients had persistent dyspnea, which after fatigue (reported by 53% of these patients), was the most common persisting symptom. [9] Similar results were replicated in various studies which observed survivors for 4 weeks-3 months. This duration of symptom persistence is greater than what has been reported among those who recover from community-acquired pneumonia. [10, 11] Residual radiographic abnormalities In a retrospective multicenter study from China, 55 COVID-19 survivors were followed for 3-month postdischarge. This study reported radiographic abnormalities in about 71% of individuals. [11] There have been case reports of new-onset bronchiectasis and organizing pneumonia among COVID-19 survivors. [12, 13] Residual pulmonary dysfunction In another cross-sectional analysis, done in 110 COVID survivors, an abnormal diffusion capacity of the lung (DL CO ) was reported in 47% of individuals. [14] There was a decline in DL CO even when adjusted for alveolar volume (DL CO /V A ), suggesting that the loss of diffusion capacity was out of proportion to the loss of vital capacity. Systemic corticosteroids used in moderate-severe COVID-19 pneumonia are known to cause muscle atrophy. Besides, infection with SARS-CoV-2 is now recognized as an independent cause of respiratory muscle strength impairment. In a Chinese study, 49.1% and 22.8% had P i max and P e max values <80% of the predicted value independent of the use of corticosteroids. [15] These findings suggest that a large proportion of recovered COVID-19 patients will need pulmonary rehabilitation and close follow-up. [16] The posthospitalization COVID-19 study (PHOSP-COVID) conducted by a consortium of leading researchers and clinicians from across the UK is recruiting patients to create an evidence base for long COVID. COVID-19 survivors with a residual pulmonary impairment will be followed up for at least 36 months to assess the clinical course of the disease. [16] Table 2 below summarizes the key studies done among post-COVID-19 patients. [9, [17] [18] [19] [20] [21] The incidence of myocardial injury during active COVID-19 infection has been reported to be 14%-19%. [22, 23] Various mechanisms have been postulated such as direct myocardial injury, downregulation of angiotensin-converting enzyme 2 (ACE2) receptors severe inflammation, and hypoxic damage secondary to severe SARS-CoV-2 pneumonia. [24, 25] However, such post-COVID myocardial dysfunction does not appear to be limited to severely infected patients. A cohort of 100 individuals who had recovered from COVID-19 was followed at University Hospital Frankfurt in Germany. [26] Most of these patients (67%) were presymptomatic and were treated at home, and none of them had a history of previous cardiac illness. At an average of 71 days, the incidence of cardiac anomalies as evident on cardiac magnetic resonance imaging was 78%, while active myocardial inflammation was present in 60% of the patients. Arrhythmias have also been reported and are a cause of concern. Metabolic abnormalities dyslipidemia and impaired glucose metabolism are relatively common months after GGOs: Ground-glass opacities, DL CO : Diffusion capacity of the lung discharge, caused by direct effects of disease and adverse effects of corticosteroids used during treatment. [25] H y p e r c o a g u l a b i l i t y i s w e l l r e c o g n i z e d i n COVID-19 patients. [27] A serum d-dimer level has been identified as one of the important predictors of adverse outcomes among hospitalized patients with COVID-19. [28] SARS-CoV-2-induced coagulopathy is postulated to be due to ACE2 receptor-mediated endotheliitis, hypoxia-induced lung injury, cytokine-mediated hemophagocytic lymphohistiocytosis-like syndrome, [29] and neutrophil extracellular trap. [29] These pathophysiological changes can have long-term implications in COVID-19 survivors. Around 60% of recovered patients are at high risk of developing venous thromboembolic events (VTEs) up to 90 days after discharge, [30] odds ratio (OR) of hospital-associated -VTE within 42-day postdischarge has been reported as high as 1.6, [31] while the incidence of symptomatic VTEs can be as high as 0.6%. [32, 33] The current guidelines recommend continuing thromboprophylaxis up to 45 after discharge. [34] The uncertainty and unpredictability in the natural history of the disease, discrimination and stigmatization associated with the diagnosis, adverse effects of social isolation, and influence of an atmosphere of fear created by lockdowns and reporting of the illness in the media have possibly contributed to an increase in the incidence of psychiatric illness among COVID survivors. [34, 35] The burden of corticosteroid-induced neuropsychiatric effects in the current pandemic has not been quantified. The previous SARS epidemic resulted in an incidence as high as 0.7%. [36] HCWs have been at a high risk of developing psychiatric illnesses. The burden of psychiatric illness on HCW was studied in a systematic review and meta-analysis, which included 13 cross-sectional studies comprising 33,062 HCW with post-COVID status. It found that incident anxiety, depression, and posttraumatic stress disorder were reported in up to 20%-25% HCWs, with the highest prevalence among females and nursing staff. [37] In a survey led by a patient on a digital platform, a significant proportion of individuals who had recovered from COVID had persistent symptoms, which were independent of the severity of the illness. [38] Symptoms reported included "brain fog," hallucinations, delirium, short-term memory loss, and strange vibration sense. The pathophysiology of these symptoms remained unexplained. There are various postulated mechanisms proposed to explain these symptoms, one of which has been offered by Akiko Iwasaki, an immunologist at Yale. [39] According to this postulate, a patient may have latent virus or fragments of its genetic material in various body tissues postrecovery. These latent particles may cause a persistent immune activation, or an immunological reactivation responsible for the symptoms. Another postulate by David Putrino, Director of rehabilitation innovation at Mount Sinai suggests that patients with long COVID develop neurological dysautonomia, which could affect up to 15% of all COVID-19 survivors. [40] However, these hypotheses are still to be validated by studies. Post-COVID-19 neurological syndrome encompasses all the neurological disorders that are observed in the convalescence phase of COVID-19 infection. Neurotropism of coronaviruses has been previously demonstrated in various studies. [41, 42] The clinical features associated with novel coronavirus-19 infection are consistent with the previous observation that such viruses have a broad spectrum of neurological presentations. Headaches, anosmia, meningoencephalitis, acute ischemic stroke, several post/para-infectious syndromes, and psychiatric disorder are neurotropic symptoms independent of primary respiratory pathophysiology. [43] The most common proposed mode of central nervous system penetration is through the olfactory bulb during the early stages and through blood during the phase of viremia. [44] Persistent anosmia is one of the most common post-COVID symptoms which is caused by the [45] The phenomenon of molecular mimicry between coronaviruses and myelin sheath [46, 47] can cause T-cell-mediated cross-reactivity, and subsequent autoimmune disease, even after viral clearance. A follow-up study was conducted among 2113 COVID-19 recovered patients, most of whom (2001 out of 2113) were not hospitalized and were mildly symptomatic. After an average of 71 days from illness onset, the incidence of self-reported headache was 76%, muscular pain 64%, ageusia 42%, anosmia 40%, and hot flushes in 25% of patients. [10] Apart from these manifestations, case reports are highlighting severe and morbid neurological outcomes in COVID patients such as meningoencephalitis, acute necrotizing encephalopathy, acute disseminated encephalomyelitis, and acute flaccid paralysis. [43] More recently neurologists in the city of Mumbai have reported 24 cases of Guillain-Barre syndrome and few cases of Bell's palsy in COVID survivors. [48, 49] This disturbing observation is still to be evaluated for its temporal and causal relationship with active COVID-19 infection. The presentation of COVID-19 with cerebrovascular accidents has been described fairly commonly, [50, 51] and the consequent residual neurodeficits and psychological effects of such loss of function would also be part of the sequelae of the disease that we are likely to face often. Coronaviruses affecting the gastrointestinal (GI) tract are common. In the studies, evaluating the incidence of GI symptoms in MERS-CoV-infected patients, diarrhea was reported in 12%-23%, vomiting in 21%-33%, and abdominal pain in 27%-40% of patients. [52, 53] In a recent meta-analysis including 4243 COVID patients from 60 studies, the pooled prevalence of GI symptoms was 17.6%. Anorexia was the most common symptom followed by nausea/vomiting and diarrhea. Stool samples were positive for viral RNA in 48% of patients of which one-third of the samples were collected after respiratory samples were tested negative. [54] This persistence of fecal viral shedding in COVID patients has been correlated with high levels of fecal calprotectin (up to 80% of patients with GI symptoms) caused by injury to GI epithelium which is rich in ACE2 receptor. [55] Similarly, liver injury among COVID-19 patients with GI symptoms can be as high as 17%. [56] These patients may have a high risk for an adverse disease outcome and are not eligible for the administration of remdesvir, which is the only antiviral drug with some evidence on efficacy against COVID-19. [57] In a recent meta-analysis, the pooled estimate of the prevalence of acute kidney injury (AKI) in patients with severe COVID-19 was 28%. [58] The development of AKI is an indicator for a high mortality OR of death being as high as 9%. [59] The estimated OR for the incidence of AKI in deceased versus survivor COVID-19 patients is 15.4. [58] Renal disease related to COVID-19 can also manifest up to 6-month postdischarge in patients who had no kidney injury during the active phase of viral infection. In a cohort study that followed up, 1733 COVID-19 patients for an average of 186-day postdischarge found 107 patients with no AKI, and normal estimated glomerular filtration rate (eGFR) during the acute phase had eGFR <90 mL/min/1·73 m 2 at follow-up. [21] Autopsy studies have concluded that acute tubular necrosis is the most common mode of renal injury followed by nonspecific infiltration. [60, 61] The proposed mechanisms for the development of AKI in COVID patients are hypoxemia and hypercapnia, hypotension, endothelitis, rhabdomyolysis, and direct viral injury. Suggesting treatment for long COVID in the absence of understanding the natural history of the disease would be unscientific, and patients should be enrolled in clinical trials when feasible. For example, the role of antifibrotic medications for post-COVID fibrosis is being investigated. [62] Screening for (and consequently treating) underlying cardiac and lung disease, metabolic abnormalities, vitamin deficiencies, electrolyte imbalances, hormonal dysregulation would all be part of optimizing the recovery process. Physiotherapy, including pulmonary rehabilitation [63] when indicated, along with dietary modifications should not be ignored. In the absence of any large trials for pulmonary rehabilitation for post-COVID states, it would be prudent to follow the guidelines for pulmonary rehabilitation in other lung diseases that manifest with fibrotic interstitial. [64, 65] The principles of rehabilitation would include exercise training (both resistance and aerobic), energy conservation techniques, dietary and lifestyle changes, with a structured approach to ensure adherence and incremental gains. Facilitating smoking cessation, screening for obstructive sleep apnea, and treating it would also be part of rehabilitating individuals for long COVID. Several lacunae in the knowledge and understanding of long COVID still exist: we do not yet know whether long COVID manifestations are attributable to the virus or a dysregulated immune system. The long-term trajectory of these effects remains unknown, as does the probability of success of interventions attempting to alter the course. The first step toward understanding any disease is collecting data to understand the natural history of the disease and attempting to understand predictors of severity. With this aim, all recovered patients must be followed up after their initial illness, and protocols for doing so have been published. [16, [66] [67] [68] Follow-up can be virtual on a digital platform or in-person as per the social restrictions and patient's comfort. We propose a simple and comprehensive tool kit [ Table 3 ] for post-COVID-19 follow-up assessment. Such a toolkit is intended to be a framework to cover the most commonly reported symptoms. However, one may need to add more questions to cover other domains (such as sleep) or may need to contextualize this to the local lexicon ("weakness" vs. "fatigue" vs. "lack of energy" vs. "feeling low"). A review of the available literature makes it evident that of those who survived COVID-19 illness; a significant proportion (nearly 60%-80%) is likely to experience a post-COVID syndrome up to 6 months after the active infective illness. Despite SARS-CoV-2 predominantly being a respiratory pathogen and COVID-19 a respiratory pandemic, post-COVID effects among survivors encompass a broad spectrum. This spectrum includes pulmonary, cardiovascular, neuromuscular, neuropsychiatric systems, and some yet-understood atypical features. It is also important for clinicians to keep in mind that the severity and duration of post-COVID symptoms may not necessarily correlate with the severity of the acute COVID illness. Individuals who present with features of long COVID must be followed up closely and enrolled in longitudinal studies so that we can better comprehend the disease and conduct research on potential therapies to its natural history. Toolkits, which cover the commonly reported symptoms, and can be modified to local contexts could be invaluable. As the number of patients with the disease continues to rise, we must do our best to not only just focus on hospitalizations and treatment but also focus on an increasingly reported incidence of long COVID. Financial support and sponsorship Nil. 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