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The coronavirus pandemic has changed the priorities of the whole medical society. During the clinical course of COVID-19, it has been observed that hepatic injury occurs in a significant proportion of patients, particularly in those with severe or critical illness. In this literature review, we summarize the most recent studies, which covered the pathophysiology of COVID-19 induced liver injury including; hepatic pathological findings, therapy related liver damage, and the effects of the viral infection on pre-existing liver diseasesin context of the most recent recommendations. Conclusions: This review sheds light on the impact of COVID-19 infection on the liver, as well as the prognostic effect of liver laboratory markers on disease outcome. Temporal variations in liver parameters during disease course as well as different patterns of derangement are depicted. More intensive surveillance and individualized therapeutic approaches should be tailored for immunocompromised patients with advanced liver disease, hepatocellular carcinoma, and liver transplant patients. Despite the limited studies on COVID-19 infected patients with preexisting liver disease, this comprehensive overview provides a perspective on the management of liver disease during COVID-19.
Haimovich A, Warner F, Young H.P, et al. Patient factors associated with SARS-CoV-2 in an admitted emergency department population. J Am Coll Emerg Physicians Open202;1–9.
]. Coronavirus disease 2019 (COVID-19) has a wide range of clinical presentations, varying from asymptomatic carrier state to viral pneumonia in addition to various extra-pulmonary manifestations, including liver affection [
]. COVID-19 associated liver injury usually occurs as a result of disease progression, or iatrogenic drug reactions from COVID-19 drug trials, regardless of the presence or absence of a pre-existing liver condition [
]. Till now, the etiological mechanisms for COVID-19 induced hepatic damage are unclear but may have significant consequences in the management and prognosis of the disease. Given the great burden of chronic liver disease globally [
], this pandemic can further disrupt the care of these patients as a result of the failure of the screening, and follow-up. Therefore, the interaction between pre-existing liver illness and COVID-19 requires additional studies. In this review we summarized the most recent studies, which have addressed the pathophysiology of COVID-19-induced liver injury including; the adverse reactions linked to the medications used in treatment, the hepatic pathological findings in COVID-19 patients, and the effect of this infection on the course of pre-existing liver diseases.
1. Pathophysiology of COVID-induced liver injury
Several mechanisms are proposed to explain hepatic injury during COVID-19 infections (Fig. 1). Hypoxia and cardiac failure in critically affected COVID-19 cases can predispose to hypoxic hepatitis [
]. Likewise, the use of high levels of positive end-expiratory pressure (PEEP) may cause hepatic congestion by increasing right atrial pressure and hindering venous return. However, these mechanisms alone cannot explain liver affection in all patients, as liver laboratory test abnormalities are commonly encountered in stable patients who did not require mechanical ventilation. Furthermore, the pattern of aminotransferase rise in this set of patients is not consistent with that of hypoxic hepatitis [
ACE2 receptors, found on many cells including the lungs, heart, liver, kidney, and blood vessels, interact with SARS-CoV-2 by inducing direct cytopathic effects [
]. Recently, the single-cell RNA-seq data in healthy human hepatic samples suggest that ACE2 expression by cholangiocytes (59.7%) is considerably higher than its expression by hepatocytes(2.6%) [
]. Despite this major difference in ACE2 expression, a cholestatic pattern of injury is not a common feature of COVID-19 disease, also ALP and bilirubin were only elevated in a minority of cases [
. Although some studies found GGT, a potential diagnostic marker for cholangiocyte injury, levels were increased by up to 72% in severely infected COVID-19 patients [
] using the ultrastructural examination of postpartum liver tissue biopsies of two deceased COVID-19 patients, detected typical coronavirus particles with their spikes in the cytoplasm of hepatocytes. Virus-related hepatocyte damage was recognized as mitochondrial swelling, endoplasmic reticulum dilatation, and cell membrane dysfunction. Moreover, this study had documented viral ability to replicate in hepatocytes. This is the first study to report SARS-CoV-2 cytopathic liver cell affection as a cause of liver function derangement.
Discordances of ACE2 level of expression in SARS-CoV affected organs are noted [
]. The affinity of SARS-CoV-2 to affect the liver cannot only be explained by the localization of ACE2 receptors. There is a likelihood that the expression levels of ACE2 in hepatocytes may be up-regulated upon viral entry. Another possibility is that extra- ACE2 receptors or co-receptors might exist [
]. In female tissue, ACE2 hepatic expression was markedly elevated, which may explain the better prognosis observed in COVID-19 infected females compared to males [
. Also, TMPRSS2, a SARS-CoV2-interacting host receptor, which is expressed in cholangiocytes and hepatocytes, is essential for proteolytic activation and spread of virus particles [
TMPRSS2 and furin are both essential for proteolytic activation and spread of SARS-CoV-2 in human airway epithelial cells and provide promising drug targets.
]. Further studies are needed to explain why COVID-19-induced liver function abnormalities are mainly manifested as an elevation of serum aminotransferases, rather than increased alkaline phosphatase and bilirubin.
Moreover, a hyper-inflammatory reaction to COVID-19 may add to liver injury. Laboratory tests reveal an increase in plasma cytokines and other inflammatory reactants, such as IL-1, IL-6, and tumor necrosis factor leading to the development of cytokine storm in some patients. This results in hepatocellular immune-mediated damage due to viral-induced cytotoxic (CD8) T cells, and the induction of a dysregulated innate immune response [
]. Another proposed mechanism is attributed to the gut vascular barrier and microbiota alterations. Additional studies are needed to prove the existence of a causal role played by the liver in COVID-19 disease pathogenesis by affecting the release of cytokines and coagulation factors, given the prothrombotic state in severe COVID-19 infections [
Morphological studies concerning the description and interpretation of liver parenchymal alterations associated with COVID-19 infection are completely lacking, and most are post-mortem autopsies. Xu et al. performed the first post-mortem liver autopsy specimen examinations, which showed a moderate degree of microvesicular steatosis and both mild lobular and portal activity. This liver injury could be caused by either SARS-CoV-2 infection or drug-related liver injury [
]. A preliminary study, which included forty-nine COVID-19 positive patients, revealed widespread vascular involvement of portal intrahepatic system in the form of acute (thrombosis and luminal ectasia) or chronic changes (fibrous thickening of the vascular wall), with an abnormal configuration of intrahepatic blood vessels. These findings suggest that coagulation dysfunction or endothelial damage could be the main triggering mechanism in the pathogenesis of COVID-19 liver-related damage [
Sonzogni A, Previtali G, Seghezzi M, et al. Liver and COVID 19 infection: a very preliminary lesson learnt from histological post-mortem findings in 48 patients. Preprints.org2020.
3. Abnormal liver functions during COVID-19 infection
Abnormal liver blood tests have been found in almost one-half of patients, throughout the SARS-CoV-2 infection course. A large systematic review of 11 studies evaluating the liver laboratory parameters of 2541 patients infected with SARS CoV-2, showed the following results; elevated AST and/or ALT (25%), increased LDH (20%), elevated bilirubin (3%), and normal ALP in almost all cases [
] which may indicate limited direct virus-related liver injury due to the overexpression pattern of ACE2 on cholangiocytes. The largest published study to date, which included 5700 patients found that AST and ALT were both commonly elevated (58.4% and 39.0% of patients, respectively) [
]. Other causes for transaminitis should be evaluated including myositis, ischemia, and cytokine release syndrome, as it is not always exclusively originating from the liver [
Another large preprint meta-analysis that covers 20 retrospective studies with 3428 COVID-19 infected patients revealed that higher levels of ALT, AST, and bilirubin were associated with a significant increase in the severity of COVID-19 infection [
]. A large study estimated that the occurrence of liver injury during COVID-19 infection is associated with a 9-fold greater risk of severe infection [
Epidemiological, demographic, and clinical characteristics of 47 cases of Middle East respiratory syndrome coronavirus disease from Saudi Arabia: a descriptive study.
], and it was the first marker found to be elevated upon hospital admission. A recent study by Guan et al., which enrolled nearly 1100 Chinese patients, demonstrated that elevated serum AST and ALT levels were observed in nearly 18% and 29% of patients with non-severe COVID-19 infection, compared to 56% and 28% of patients with severe COVID-19 disease respectively [
]. The previous findings suggest the critical role of immune-mediated systemic inflammation in liver impairment associated with severe cases of COVID-19 infection [
]. Recently Gordon et al. suggested the possibility of direct interaction of mitochondrial proteins with the virus, providing a probable mechanistic reason for the elevated AST-dominant liver profile [
]. A recent study by Wang et al. reported that liver enzyme abnormalities were associated with; disease severity, higher radiology scores as well as higher alveolar-arterial oxygen partial pressure difference, higher GGT, higher ferritin, lower albumin and decreased CD4+ T cells and B lymphocytes [
]. Cai et al. reported that in patients with abnormal liver markers of hepatocellular type or mixed, upon admission had greater odds of progressing to severe disease [
A recent meta-analysis revealed that, among 15,407 COVID-19 patients, the pooled incidence of elevated liver enzymes in COVID-19 was 23.1% at early presentation and 24.4%throughout the course of illness [
]. Another new study by Q Wang which described temporal variations during COVID-19 disease course showed that, the percentage of the patients with both elevated ALT and AST was 12.6% in mild cases vs. 46.2% in severe cases. The majority of the patients experienced ALT elevations between days 4 and 17 of their hospitalization, with a mean of (7.3 and 10.7 days) in severe and mild cases respectively. During treatment, 19% of patients had elevated liver function parameters but most patients had only mild and isolated elevations in ALT and AST. Most of the patients were discharged with normal liver markers [
]. Elevated serum levels of ferritin, IL-6, CRP, and procalcitonin have been described with a non-favorable course of liver injury in COVID-19 positive patients. The simultaneous increase in ferritin, IL-6, and ALT levels in addition to decreased albumin concentration and platelet count suggests more significant liver involvement in the course of COVID-19 [
. Common factors associated with elevated indicators of liver affection include; declined lymphocyte count, neutrophil count increase, and male gender [
]. The degree of pulmonary lesions on CT imaging may be a predictor of liver damage. Thus, patients with aggressive pulmonary lesions need to undergo close monitoring of liver function to allow early identification of any liver insult [
]. AASLD recommends that all COVID-19 patients with abnormal liver functions should be screened for HCV and HBV, and unnecessary imaging should be avoided [
It was postulated that liver impairment in COVID-19 patients could also be drug-related, and this theory was supported by the detection of moderate microvesicular steatosis with mild hepatic inflammation in those patients [
]. Cai et al. showed that more than 10% of those patients experienced increased levels of liver enzymes during hospitalization, which could be attributed to the used medications [
]. For this reason, whenever any liver test abnormality occurs in COVID-19 patients, the drug-induced liver injury should first be confirmed or ruled out [
]. It was noticed that many patients suffering from COVID19 had a history of antipyretic use, commonly paracetamol, overdose of which is a well-established etiology for liver injury. Hydroxychloroquine (an anti-malarial drug) is one of the medications proposed for COVID-19 treatment regimens, relying on sparse evidence in small clinical settings [
]. Such reactions may be attributed to hypersensitivity. However, there is no cross-reactivity between hydroxychloroquine and chloroquine, and it is reasonable to switch between them in case of hypersensitivity. Hydroxychloroquine should be used cautiously in patients with pre-existing liver diseases as it can concentrate in the liver [
AGA institute rapid review of the gi and liver manifestations of COVID-19, meta-analysis of international data, and recommendations for the consultative management of patients with COVID-19.
Azithromycin (a macrolide antibiotic) is used in combined therapy with hydroxychloroquine, with little evidence to support its use. The azithromycin-induced liver injury occurs in rare cases within 1 to 3 weeks after azithromycin initiation. It is predominantly of a hepatocellular pattern, and most patients recover completely [
]. There is limited data available on the use of remdesivir (anti-Ebola drug), as phase III trials are still underway. In a paper describing the first 12 patients with COVID-19 in the United States, the three hospitalized patients, who received remdesivir at the time of clinical worsening, reported elevated liver enzymes [
]. In a case series (n = 53) which studied the use of remdesivir in COVID-19 treatment, 23% of patients had developed elevations in liver enzymes which resulted in premature discontinuation of treatment [
]. Another randomized, double-blind, placebo-controlled, multicenter study showed elevated serum bilirubin in 10% and elevated aminotransferases in 5% of the remdesivir group [
In the study conducted by Cao B and colleagues, lopinavir/ritonavir (anti-HIV medications) used for COVID-19 treatment, showed no significant increase in hepatotoxicity compared to the control group [
An exploratory randomized, controlled study on the efficacy and safety of lopinavir/ritonavir or arbidol treating adult patients hospitalized with mild/moderate COVID-19 (ELACOI).
AGA institute rapid review of the gi and liver manifestations of COVID-19, meta-analysis of international data, and recommendations for the consultative management of patients with COVID-19.
Epidemiological and clinical features of 291 cases with coronavirus disease 2019 in areas adjacent to Hubei, China: a double-center observational study.
]on favipiravir usage for COVID-19 patients showed elevated liver enzymes in 7.6% and 2.6% respectively. Certain drugs are used to control cytokine immune storm like methylprednisolone, however, it increases the risk of spontaneous bacterial peritonitis in patients with decompensated liver cirrhosis, also the risk of HBV reactivation should be taken into consideration. Tocilizumab (Humanized mAb targeting interleukin-6 receptor), showed frequent ALT elevation, but jaundice seems to be rare, and therefore, it should not be used in decompensated cirrhosis [
]. Liver functions should be monitored especially for those receiving lopinavir/ritonavir, remdesivir, or tocilizumab. The presence of abnormal liver biochemistries should not be a contraindication to using these drugs, although AST or ALT levels >5x ULN may exclude patients from investigational drugs [
Several studies have reported obesity as a significant predicting factor for mortality in COVID-19 patients. BMI was significantly higher in patients with severe COVID-19 infection. Moreover, obesity was correlated with the need for mechanical ventilation and overall survival [
. The level of ACE2 expression in adipose tissue is higher than that of lung tissue. This finding may justify the vulnerability of adipose tissue to the COVID-19 invasion [
]. Obese patients are at high risk for NAFLD, which in turn have a higher risk of developing severe COVID-19, a higher likelihood of abnormal liver function from admission to discharge, and a longer viral shedding time. NAFLD was found to be associated with COVID-19 progression (defined by worsening respiratory distress or lung CT findings during hospitalization) [
NAFLD patients may suffer from comorbidities such as diabetes and hypertension, which increases the risk of severe COVID-19 infections. On the other hand, the synergistic effect of NAFLD on COVID-19 severity in young patients with no other co-morbidities was established by a multi-center study [
]. In NAFLD patients, the polarization states of macrophage might be skewed, thus affecting host inflammatory or tolerance response to SARS-CoV-2 signals generated from the gut-liver axis. Also, an imbalance between inflammation-promoting M1 macrophages and inflammation-suppressing M2 macrophages in NAFLD, will lead to the progression of COVID-19 [
NAFLD patients often present with elevated cytokine levels, making them more vulnerable to exaggerated cytokine production associated with COVID-19. Moreover, ACE2 expression was shown to increase in chronic liver damage and experimental diet-induced NAFLD [
]. It has also been demonstrated that patients suffering from COVID-19 exhibited increased serum levels of monocyte chemoattractant protein-1, which is a chemokine known to exacerbate steatohepatitis. Thus the virus may increase NAFLD progression to NASH in the long-term [
]. In short, identification and monitoring of patients with NAFLD who are infected with COVID-19 are advisable.
6. COVID-19 in patients with preexisting chronic hepatitis or cirrhosis
Chronic liver disease represents a major disease burden globally. Generally, patients with pre-existing chronic liver disease may be more susceptible to liver damage from SARS-CoV-2 [
]. A meta-analysis of 11 observational studies enrolling 2043 COVID-19 positive patients, showed that the prevalence of the chronic liver disease among them ranged between 3% and 11% [
. Oyelade et al. conducted a meta-analysis revealing that patients with a pre-existing hepatic disease have increased risk for severe COVID-19 infection (57.33%), and higher mortality (17.65%) [
]. This may be due to cirrhosis-associated immune dysfunction; so strict precautions against SARS-CoV-2 infection should be exerted in that set of patients [
. Regarding viral hepatitis treatment in patients co-infected with COVID-19, AASLD recommends continuing treatment for hepatitis B and hepatitis C if already initiated before acquiring COVID-19, and to consider initiating hepatitis B treatment in case of suspicion of hepatitis B flare; however, not enough studies are available. Initiating hepatitis C treatment in a patient with COVID-19 is not routinely warranted. Regarding patients with autoimmune liver disease, immunosuppressive therapy makes those patients at greater risk for severe infection and should be prioritized for early testing. If AIH patients infected with COVID-19 developed elevated liver enzymes, disease flare should not be presumed without confirmation by biopsy [
]. European Association for the Study of the Liver (EASL) currently advises against reducing immunosuppressive therapy in those patients. Reductions, particularly for antimetabolites, should only be considered after consultation of an expert and under special circumstances (e.g. in case of severe COVID-19 with medication-induced lymphopenia, or bacterial/fungal superinfection) [
Cirrhotic patients are at potentially increased risk for SARS-CoV-2 infection, higher risk for severe disease, and increased risk for hepatic decompensation [
]. Stress and sepsis are particularly problematic in patients with decompensated liver cirrhosis, as either can trigger acute-on-chronic liver failure [
]. A large multicenter cohort showed that hepatic decompensation was strongly associated with COVID-19 infection, increasing the risk of death from 26.2% to 63.2%. Remarkably, 24.3% of patients with new hepatic decompensation had no respiratory symptoms of COVID-19 at the time of diagnosis [
High mortality Rates for SARS-CoV-2 infection in patients with pre-existing chronic liver disease and cirrhosis: preliminary results from an international registry.
]. COVID-19 is characterized by significant cytokine activation, which induces hepatocyte apoptosis and necrosis, which in the setting of the diminished liver reserve, may lead to hepatic decompensation [
Comparison of mortality risk in patients with cirrhosis and COVID-19 compared with patients with cirrhosis alone and COVID-19 alone: multicentre matched cohort.
], found that patients with cirrhosis plus COVID-19 had similar mortality compared to those suffering from cirrhosis alone, but higher than patients with COVID-19 alone. Moreover, a recent work by Hashemi et al. proposed the presence of cirrhosis as an independent predictor of mortality [
EASL recommends that care should be maintained according to guidelines with minimal exposure to medical staff; telemedicine is the preferred method. Listing for liver transplantation should be restricted only to patients with poor short-term prognosis. Guidelines on prophylaxis of spontaneous bacterial peritonitis and hepatic encephalopathy should be followed closely to prevent decompensation and the need for the hospital admission. Testing for SARS-CoV-2 is advisable in patients with acute decompensation or ACLF [
]. American Association for the Study of Liver Diseases (AASLD) recommends in-person new patient visits only for those with significant liver diseases, such as jaundice, elevated transaminases of >500 U/L, or recent decompensation [
]. COVID-19 infection increases the risk of hepatic decompensation, and it reschedules screening for both varices and HCC in cirrhotic patients. On the other hand, pre-existing cirrhosis increases the risk of COVID-19 infection and is associated with higher severity and mortality. The impact of COVID-19 infection on cirrhosis and vice versa is shown in (Fig. 2).
Fig. 2The impact of COVID-19 infection on cirrhosis and vice versa (COVID −19 – cirrhosis interrelationship).
During the pandemic of COVID-19, patients suffering from any malignancy are at an increased risk of infection and more prone to developing more severe clinical outcomes [
] on 28 cancer patients, two of them (7%) with HCC, infected with COVID-19, reported that patients suffering from different malignancies had poorer outcomes when compared to the general population. This was attributed to the age of these patients in addition to the associated comorbidities and underlying cirrhosis. Furthermore, these patients have anemia and hypoproteinemia associated with poor nutritional status, which compromises their immunity, making them more vulnerable to severe infection. According to a prospective nationwide cohort study in China, researchers identified that 1% of patients had both, COVID-19 and a history of cancer. These patients were more vulnerable to severe disease and had an increased chance of mortality, as well as ICU admission. Recent chemotherapy within 1 month also increased the risk of severe disease [
], based on EASL guidelines, recommended the use of telemedicine to replace clinic visits, as well as to replace multidisciplinary team meetings to decrease the risk of spread of COVID-19. The indications of liver transplantation (LT) and locoregional therapy (LRT) in HCC patients have not changed according to these recommendations, but they reserved LT for highly progressive cases because of the shortage of ICU beds and decline in the number of donors. They used LRT as a salvage procedure to decrease the risk of HCC progression during the waiting period. Boettler et al. [
] stated that stereotactic body radiotherapy (SBRT) is another alternative ablative option that can be offered to patients eligible for TACE, especially those with lesions near vascular structures, whom their procedures have been canceled because of COVID-19 [
] also recommends restricting healthcare facility visits but at the same time stressed the importance of continuing surveillance imaging of HCC patients with an acceptable delay of a maximum of 2 months. All local ablative therapies are advised to be done without any delay for eligible patients. Regarding TACE, short term use of corticosteroids is recommended to manage post embolization syndrome to minimize hospital stay, even in patients proven to have COVID-19 except if there is any other contraindication. TACE was preferred over SBRT as the latter requires separate workup and treatment visits while TACE sessions can be separated by intervals ranging from 4 to 12 weeks, according to the response and characteristics of the lesion. For patients with resectable BCLC stage HCC whose surgical procedures have been canceled, transarterial therapies as a bridge to definitive treatment are recommended [
]. EASL recommendations suggest that immunotherapy with nivolumab might have to be temporarily suspended to avoid exposure to COVID-19 at the infusion center [
There is a need for an international consensus on liver transplantation protocols during pandemics, due to the shortage of resources and the increased need for liver transplantation. Little is known on the transmission of the virus from donor to recipient but if this happens, it depends on the level and duration of donor viremia, as well as the incubation period and viability of the virus in different organs [
]. Liver transplant recipients are in an immune-compromised state, which makes them at higher risk of contracting COVID-19 infection. This makes them a source of dissemination of infection to others (super spreaders), especially healthcare workers [
There were some reported cases of liver transplant recipients confirmed to have COVID-19 pneumonia and required hospital admission. All of the cases showed improvement by symptomatic treatment, together with the reduction or withdrawal of their immune-suppression therapy, except for one case who received a single dose of tocilizumab [
]. A Swiss Transplant Cohort prospective observational multicenter Study (STCS), which included 21 solid organ transplant patients, 5 of which had LT, concluded that the only treatment intervention was temporary discontinuation or reduction of anti-metabolite drugs, and maintaining the same doses of steroids and calcineurin inhibitors. They concluded that the clinical course and degree of severity of COVID-19 among organ transplant recipients do not differ from the general population [
] concluded that the majority of the centers adopted a “sickest first” strategy, otherwise a case by case is discussed. Almost all centers advised for COVID-19 screening for donor and recipient. Donors with positive contact history, or compromising respiratory tract disease, were excluded by most centers. The survey revealed that transplantation protocols did not change at the beginning of the pandemic except in Singapore. Due to their experience with SARS-CoV in 2003, Singapore restricted liver transplantation to medically urgent living donor liver transplant (LDLT), and deceased donor liver transplant (DDLT). After the WHO declaration of the viral pandemic, 10 out of the 17 centers limited their transplantation activity.
AASLD recommends against delaying LT wherever possible depending on local availability of resources such as ICU beds, ventilators, and blood donations [
]. It also recommends COVID-19 screening for both donors and recipients listed for liver transplantation, emphasizing that negative results do not exclude infection. All consents for the procedure should include the possible risk of nosocomial COVID-19. After transplantation, they discourage the reduction of immunosuppressive therapy, except in severe cases of bacterial or fungal infections superadded to COVID-19, or associated lymphopenia [
. Drug levels of CNI and mammalian Target Of Rapamycin (mTOR) inhibitors, should be closely monitored when they are administered together with other drugs, such as hydroxychloroquine or azithromycin [
Upper endoscopy is an aerosol-generating procedure that carries a high risk of transmission of infection to medical personnel. In the first case of COVID-19 in the USA, the virus RNA was detected in the patient's stool on the 7th day of illness suggesting a possible feco-oral transmission making the upper endoscopy or colonoscopy a high-risk procedure [
. An Italian multi-center survey included 41 endoscopy units aimed to investigate the burden of COVID-19 on endoscopy units, and to assess the possibility of viral transmission from these units. Most of the centers limited their activity to urgent and high-risk patients, such as gastrointestinal bleeding and bacterial cholangitis. In their survey, there were no reported cases of healthcare staff infection associated with endoscopic procedures performed to COVID-19 positive patients. Most of the units provided protective personal equipment (PPE) for both endoscopy unit personnel and patients [
For variceal screening, EASL recommends risk assessments, such as applying the Baveno VI criteria, whereas AASLD even suggested primary prophylaxis with beta-blockers as an alternative for screening endoscopy, in those with clinically significant portal hypertension or those at risk of decompensation [
]. The Asian Pacific Society for Digestive Endoscopy (APSDE) advised performing upper endoscopy in negative pressure rooms if the patient is suspected to be COVID-19 positive [
]. As regards to liver biopsy, the EASL recommends deferring it for NAFLD, chronic viral hepatitis, and only to perform it for strongly elevated transaminases of unknown etiology, and liver masses suspicious of malignancy [
This review sheds light on the impact of COVID-19 infection on the liver, as well as the prognostic effect of liver laboratory markers on disease outcome. Further studies are needed to elucidate the mechanisms of COVID-19 infection and drug-induced hepatic pathologies. More intensive surveillance and individualized therapeutic approaches should be tailored for those immunocompromised patients with advanced liver disease, HCC, and liver transplant patients. Despite the current lack of knowledge regarding the effect of COVID-19 in patients with preexisting liver disease, this review introduces a comprehensive overview, providing a perspective on the management of liver disease during COVID-19. Improving care pathways for chronic liver disease patients infected with SARS-CoV-2, will be of great importance to improve disease outcomes of both liver disease and COVID-19.
Author's contribution
Marwa Ibrahim Metawea: Conception and design, drafting of the article.
Walid Ibrahim Yousif: Collection of data, analysis, interpretation of data and drafting of the article.
Islam Moheb: Editing and reviewing of the article.
Conflict of Interest
None declared.
References
Huang C.
Wang Y.
Li X.
et al.
Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China.
Haimovich A, Warner F, Young H.P, et al. Patient factors associated with SARS-CoV-2 in an admitted emergency department population. J Am Coll Emerg Physicians Open202;1–9.
TMPRSS2 and furin are both essential for proteolytic activation and spread of SARS-CoV-2 in human airway epithelial cells and provide promising drug targets.
Sonzogni A, Previtali G, Seghezzi M, et al. Liver and COVID 19 infection: a very preliminary lesson learnt from histological post-mortem findings in 48 patients. Preprints.org2020.
Epidemiological, demographic, and clinical characteristics of 47 cases of Middle East respiratory syndrome coronavirus disease from Saudi Arabia: a descriptive study.
AGA institute rapid review of the gi and liver manifestations of COVID-19, meta-analysis of international data, and recommendations for the consultative management of patients with COVID-19.
An exploratory randomized, controlled study on the efficacy and safety of lopinavir/ritonavir or arbidol treating adult patients hospitalized with mild/moderate COVID-19 (ELACOI).
Epidemiological and clinical features of 291 cases with coronavirus disease 2019 in areas adjacent to Hubei, China: a double-center observational study.
High mortality Rates for SARS-CoV-2 infection in patients with pre-existing chronic liver disease and cirrhosis: preliminary results from an international registry.
Comparison of mortality risk in patients with cirrhosis and COVID-19 compared with patients with cirrhosis alone and COVID-19 alone: multicentre matched cohort.
A recent review paper by Metawea et al. in the Digestive and Liver Disease summarizes pathophysiological mechanisms about coronavirus disease 2019 (COVID-19) associated liver injury [1]. Despite a high incidence of liver injury in COVID-19 patients [2], acute liver failure (ALF) or subacute liver failure (SALF), which often manifests as jaundice, coagulopathy, hepatic encephalopathy (HE), and even progression to multiple organ failure [3], are rarely recognized. Considering that ALF is life-threatening with a high mortality [3], we attempted to analyze the characteristics and in-hospital outcomes of COVID-19 patients with ALF/SALF.
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