Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1
Nicolò Brandi
 -- 5279 2023-03-24 10:24:34 |
2 format
Jason Zhu
 Meta information modification 5279 2023-03-27 05:27:35 |

Video Upload Options

We provide professional Video Production Services to translate complex research into visually appealing presentations. Would you like to try it?
No, upload directly Yes

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Brandi, N.; Spinelli, D.; Granito, A.; Tovoli, F.; Piscaglia, F.; Golfieri, R.; Renzulli, M. COVID-19 in Patients with Chronic Liver Disease. Encyclopedia. Available online: https://encyclopedia.pub/entry/42508 (accessed on 21 December 2024).
Brandi N, Spinelli D, Granito A, Tovoli F, Piscaglia F, Golfieri R, et al. COVID-19 in Patients with Chronic Liver Disease. Encyclopedia. Available at: https://encyclopedia.pub/entry/42508. Accessed December 21, 2024.
Brandi, Nicolò, Daniele Spinelli, Alessandro Granito, Francesco Tovoli, Fabio Piscaglia, Rita Golfieri, Matteo Renzulli. "COVID-19 in Patients with Chronic Liver Disease" Encyclopedia, https://encyclopedia.pub/entry/42508 (accessed December 21, 2024).
Brandi, N., Spinelli, D., Granito, A., Tovoli, F., Piscaglia, F., Golfieri, R., & Renzulli, M. (2023, March 24). COVID-19 in Patients with Chronic Liver Disease. In Encyclopedia. https://encyclopedia.pub/entry/42508
Brandi, Nicolò, et al. "COVID-19 in Patients with Chronic Liver Disease." Encyclopedia. Web. 24 March, 2023.
COVID-19 in Patients with Chronic Liver Disease
Edit
This entry is adapted from the peer-reviewed paper 10.3390/ijms24021091

The liver is a secondary and often collateral target of COVID-19 disease but can lead to important consequences. COVID-19 might directly cause a high number of complications in patients with pre-existing chronic liver disease, increasing their risk of hepatic decompensation. Moreover, it also determines indirect consequences in the management of patients with liver disease, especially in those suffering from decompensated cirrhosis and HCC, as well as in the execution of their follow-up and the availability of all therapeutic possibilities. Liver imaging in COVID-19 patients proved to be highly nonspecific, but it can still be useful for identifying the complications that derive from the infection.

COVID-19 liver hepatocellular carcinoma chronic liver disease

1. Introduction

Although it has been more than 2 years since the first outbreak, the coronavirus disease 2019 (COVID-19) pandemic is still having a profound and devastating impact on global healthcare systems. COVID-19 has a wide range of clinical presentations, varying from asymptomatic or mildly symptomatic infection to severe bilateral pneumonia, with a high risk of developing acute respiratory distress syndrome (ARDS) (20–67%) and thus the need for mechanical ventilation and Intensive Care Unit (ICU) admission.
Despite viral pneumonia representing the most common serious manifestation of COVID-19, extrapulmonary manifestations of COVID-19 have progressively gained attention due to their links to clinical outcomes and their potential long-term sequelae, especially in critically ill patients [1]. Vascular complications, myocardial dysfunction, acute kidney injury, gastrointestinal symptoms, neurologic complications, and dermatologic conditions are among the reported extrapulmonary complications [2][3]. Furthermore, recent studies have suggested that COVID-19 could also have a serious impact on the reproductive system, altering male sperm parameters and increasing the rate of female gestational disorders, such as preeclampsia [4][5]. However, whether COVID-19 could also directly affect the liver has been debated, and the literature regarding hepatic involvement in COVID-19 patients is heterogenous, due to variability in the definitions of liver dysfunction and differences in the clinical presentation and disease severity [6].
According to the current data, liver dysfunction or injury, defined as liver test abnormalities, has been reported with a prevalence of approximately 25% in COVID-19 patients, ranging from approximately 3% to 60% [6][7][8]. In particular, several studies demonstrated that patients with COVID-19 who develop liver dysfunction are mostly male, elderly, and obese [9][10][11][12]. Furthermore, hepatic dysfunction is significantly higher in critically ill patients, reaching up to 45% of cases, and is associated with a poor outcome, underlining its importance in clinical settings [13][14]. In those patients with already impaired liver function, SARS-CoV-2 infection may be responsible for the worsening of underlying chronic liver disease [15]. On top of that, COVID-19 may also exert an indirect effect on these patients, disrupting their care as a result of the failure of the screening, treatment, and follow-up [16].
Despite all the evidence, the pathophysiological and immunological mechanisms of liver injury in patients with COVID-19 are still poorly understood, as well as their long-term sequelae. Moreover, the consequences of its indirect effects on the management of patients with chronic liver disease are still emerging. Therefore, with the now inevitable certainty of having to live with this virus and its new variants at least for the next few years, clinicians must pay high attention to the most exposed and fragile patients and continuously search for new strategies that can be implemented in this new pandemic setting.

2. Hepatic Manifestations in COVID-19 Patients

Currently, there is no standardized definition of COVID-19-related liver injury, and the diagnostic time point (admission or during disease progression) is not always reported [17]. In fact, despite some researchers having defined liver injury in COVID-19 patients as any liver function parameter above the upper limit of normal [18][19], others have introduced different threshold values (an increase in liver enzymes higher than 2 or 3 times the normal values) [13] and even further classified different liver injury patterns (hepatocellular type, cholangiocytes type, and mixed type) [14][20]. Because of the different criteria considered, researchers may have overestimated or underestimated COVID-19-related liver damage, partially explaining the mixed results so far and jeopardizing the generalizability of the conclusions and the practical clinical implications derived from these studies. Therefore, an international consensus in this regard is urgently needed.
Abnormal liver function tests in patients with COVID-19 were first reported in a cohort of 99 patients in Wuhan [21]. In particular, nearly all patients (98%) presented with decreased albumin levels, whereas 28% and 35% of them showed a moderate increase in alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels, respectively. In the countless following studies, abnormal liver function tests were commonly reported in COVID-19 patients [22], mainly in the form of a hepatocellular injury pattern rather than cholestatic [23][24]. In fact, a transient increase in aminotransferases is frequent in patients with COVID-19, along with an elevation of lactate dehydrogenase levels, followed by a significant decrease in albumin later in the course of the disease [25][26]; in contrast, alkaline phosphatase and gamma-glutamyl transferase, representatives of bile duct injury, do not increase significantly, and jaundice is uncommon [15][19][27]. In particular, the elevation of AST levels seems to be more frequent and significant than the increase in ALT [28].
The incidence of these abnormal liver tests is reported to be significantly higher in patients with severe COVID-19 compared with those with mild disease [29][30]. For example, in a recent meta-analysis, aminotransferases elevation was observed in 23% of the patients with mild symptoms, whereas hypoalbuminemia was observed in 61%, percentages that increased to 40% and 76%, respectively, in severe patients [6]. Similarly, increased AST was observed in 62% of patients with COVID-19 in the intensive care unit (ICU) compared to 25% in non-ICU patients [15].
Other studies have demonstrated that liver enzyme levels could be used as important clinical markers, since their elevation is associated with a higher risk of in-hospital mortality, a longer hospital stay, and other adverse clinical outcomes, such as the need for vasopressor drugs and mechanical ventilation [28][31][32]. Underlying the important mutual relation between the liver and COVID-19 disease, a recent study demonstrated that liver test abnormalities upon hospital admission, in particular, elevated ALT or AST, can be used to predict the severity of COVID-19 [13]. Therefore, even if non-specific and equally reported also in non-COVID patients [6], these parameters should be always monitored during hospitalization due to their prognostic value.
COVID-19-related liver injury is usually mild and transient, and liver failure is exceedingly rare, being reported only as anecdotical case reports in the setting of a severe disease with sepsis and coagulopathy requiring the administration of multiple drugs. Therefore, whether this drastic derangement of liver function is secondary to true viral damage rather than a bystander to the multiorgan pathophysiology of critical illness or rather the result of the hepatotoxic potential of high doses of antiviral drugs requires further discussion [33][34].
Finally, as previously stated, in addition to systemic inflammation, liver dysfunction could be partially mediated by COVID-19-related coagulopathy and intrahepatic microvascular thrombosis [35][36][37]. This theory is also supported by laboratory findings, as demonstrated by a recent study that found an independent association between higher D-dimer levels and elevation of ALT [38]. Similarly, the abnormally high levels of transaminases detected in COVID-19 patients whose liver samples were analyzed post-mortem showed aspects of intravascular thrombosis, further suggesting possible liver damage linked to impaired coagulation [39].

3. The Role of Imaging in COVID-19-Related Liver Injury

During the early phases of the pandemic, when viral tests were not available or were scarce, imaging provided considerable help in the diagnosis of COVID-19 pneumonia [40]. At present, following the advancement in diagnostic laboratory techniques, its role has evolved, and now imaging is pivotal to the detection and monitoring of COVID-19 complications, both pulmonary and visceral, the evolution of which may be heterogeneous and unpredictable [41][42][43].
To date, no specific hepatic imaging findings related to COVID-19 have been reported in the medical literature [44]. However, some studies have reported non-specific changes in the appearance of the liver on imaging following COVID-19 infection, namely features of hepatic steatosis, suggesting a possible association between these two conditions [45]. On ultrasound (US), in patients after COVID-19, the liver may appear “brighter” due to an increase in echogenicity compared to the renal cortex or spleen, with the loss of physiological hyperechogenicity of the portal branches walls and posterior attenuation of the ultrasonic beam and the consequent failure to visualize the diaphragm [46]. These changes have been also documented in a recent study with Multiparametric US (mpUS), where the sonographic evaluation of liver parenchyma in individuals after COVID-19 revealed significantly more frequent liver steatosis compared to the clinically healthy control group but also increased stiffness (fibrosis) and viscosity (inflammation) values, both indicative of liver injury. However, despite these mpUS features being correlated with an increase in biochemical markers of liver injury, they were not associated with correspondent CT or MR findings [47]. On the other hand, several studies have reported a considerably greater frequency of hepatic steatosis by Computed Tomography (CT) scans in confirmed COVID-19 cases compared to controls, defined as a hepatic attenuation of at least 10 Hounsfield Units (HU) compared to the density of the spleen or absolute liver attenuation of less than 40 HU [48][49]. Moreover, hepatic steatosis resulted more prevalent in patients with laboratory liver dysfunction (approximately 19% vs. 8%) and in those with severe pneumonia (approximately 73% vs. 27%), being similarly reported in patients with and without fatty liver disease [50][51][52]. Furthermore, it seems that hepatic steatosis is only a transient change in COVID-19 patients, as it has been demonstrated to gradually recover on follow-up CT scans, either due to the concomitant improvement of the viral infection or the development of hepatic fibrosis [52].
Currently, only one study has evaluated the Magnetic Resonance Imaging (MRI) liver features following COVID-19 infection [53]. According to the authors, the patients who recovered from COVID-19 presented a lower hepatic T1 relaxation time in the 3-month follow-up compared with the control group of normal volunteers, suggesting that this result might be attributed either to hepatic steatosis and/or iron deposition secondary to hepatocyte impairment and reduce the production of hepcidin. Moreover, higher diffusion/perfusion parameters were also found in the 3-month follow-up group of recovered COVID-19 patients, which may be the result of the inflammation-induced interstitial edema and focal hepatic necrosis. During the 1-year follow-up, all these MRI findings showed mild recovery, indicating that the liver impairment after infection was relieved over time via liver regeneration.
In any case, all these hepatic imaging alterations are highly non-specific, more likely representing the “collateral” consequences of a multisystemic hyperinflammation process and/or the result of multidrug treatments rather than evidence of a direct SARS-CoV-2 invasion of the liver.

4. COVID-19 in Patients with Pre-Existing Chronic Liver Disease

Patients with chronic liver disease are frequently immunocompromised and, as already stated, may exhibit an increased expression of ACE2 in hepatocytes as an injury response to liver fibrosis [54]. Therefore, theoretically, these patients might be more susceptible to SARS-CoV-2 infection [55][56][57]. Nonetheless, based on currently available evidence, patients with chronic liver disease do not appear to be at a higher risk of infection compared to other individuals in the general population [58][59][60].
However, the risk of mortality from COVID-19 was significantly increased in these patients (with a risk ratio of 3) [61], as also confirmed in a large survey including more than 17 million cases [56], especially in those with cirrhosis (where the risk ratio reaches up to 4.6), even in the absence of respiratory symptoms at the time of diagnosis [62][63][64].
In addition to this direct effect, given the great burden of health system reorganization and lockdown strategies, the care of patients with pre-existing chronic liver disease has been widely disrupted during the pandemic, leading to failure of the screening and follow-up, a higher prevalence of related complications (including variceal bleeding, hepatic encephalopathy, liver failure, and hepatocellular carcinoma development), and delayed access to treatments and liver transplantation [16][65]. On top of that, social distancing has further induced and aggravated alcohol use disorders, facilitating the relapse of alcohol addiction, while also favoring the consumption of processed food and the adoption of a sedentary lifestyle, which are well-known risk factors for morbidity and mortality [66][67]. The future long-term consequence of these modifications and delays in management and treatment options are still to be realized and will presumably lead to a transformation of the curable into the incurable [68].

4.1. COVID-19 in Patients with Non-Alcoholic Fat Liver Disease (NAFLD)

Individuals with a poorer prognosis of COVID-19 are typically older (>60 years old) with metabolic co-morbidities such as obesity and diabetes, a profile that is similar to those at increased risk of NAFLD [61][69]. Therefore, it is not surprising that patients with NAFLD have a higher risk of progression to a severe form of COVID-19 (45% vs. 7%) and a likelihood of abnormal liver function tests from admission to discharge (70% vs. 11%) compared to those without NAFLD, even in younger patients without other comorbidities [70]. Moreover, this subgroup of patients tends to present a longer period of viral replication and dispersion [20][71].
However, recent observations suggest the association between NAFLD and severe COVID-19 disease might be confounded by other metabolic perturbations underlying NAFLD, such as obesity, diabetes, and hypertension, which are all well-known factors that increase the risk of all severe infections. In particular, it seems that obesity might represent the most important metabolic perturbation associated with severe COVID-19, and some researchers suggest that it is likely the only causal risk for progression to severe pneumonia, even after adjusting for co-morbidities including NAFLD [72]. As confirmation of this, despite obesity having also been associated with a greater risk of hospitalizations, mechanical ventilation, extensive coagulopathy, and death, the same does not apply to hepatic steatosis [73][74][75].
Similar to NAFLD, in fact, the adipose tissue of obese patients induces a low-grade chronic inflammation with increased serum levels of pro-inflammatory cytokines and is thought to express high levels of ACE2, thus potentially functioning as a SARS-CoV-2 reservoir with prolonged viral shedding time [76]. Moreover, there is no evidence of increased liver uptake of SARS-CoV-2 in NAFLD patients [77], whereas SARS-CoV-2 mRNA has been detected in adipocytes, especially those of visceral fat [78]. Therefore, despite the clear interlink between NAFLD and obesity, whether hepatic steatosis simply represents a concomitant metabolic dysfunction in obese COVID-19 patients or rather an active factor for pneumonia progression is still debated, and further evidence is needed.
Finally, it is fundamental to stress the sneaky and collateral effect of the pandemic on NAFLD patients, whose daily routine has been severely impacted by lockdowns and social isolation, with subsequently more sedentary and unhealthy lifestyles. Therefore, COVID-19 will presumably be an indirect cause of the expansion of the NAFLD epidemic in the next few years [79].

4.2. COVID-19 in Patients with Cirrhosis

Similar to other patients with pre-existing chronic liver disease, cirrhotic patients showed an increased risk of COVID-19-related liver injury and mortality [80][81]. Moreover, recent data appear to indicate a three-fold increased risk of death among cirrhotic patients compared to patients with other chronic liver diseases, and this increases with the stage of cirrhosis, the Child-Turcotte-Pugh class, or the Model for End-Stage Liver Disease (MELD) score [56][82][83].
The greater mortality of this subgroup of patients could be related to cirrhosis-associated immune dysfunction, which would lead to an aberrant inflammatory response during infection with the reduction of complement components, activation of macrophages, and impairment of lymphocyte and neutrophil function [84]. Moreover, COVID-19 cytokine activation may induce hepatocyte apoptosis and necrosis, which, in the setting of a diminished liver reserve, may trigger acute-on-chronic liver failure [85]. A large multi-center cohort, in fact, showed that hepatic decompensation was strongly associated with COVID-19 infection, increasing the risk of death from 26.2% to 63.2% [86]. Similarly, another study found that liver function in cirrhotic patients with COVID-19 upon hospital admission declined compared to the last visit before SARS-CoV-2 infection [63]. Interestingly, the mortality of cirrhotic patients with and without COVID-19 is reported to be similar, whereas the mortality of cirrhotic patients with COVID-19 is higher compared to those suffering from COVID-19 alone [87]. However, sarcopenia is a frequent complication in end-stage liver disease [88][89] and, since it has also been associated with poor clinical outcomes in COVID-19 patients [90], it could be interesting to evaluate whether its presence might influence both morbidity and mortality risk in cirrhotic patients since these data are lacking. Moreover, COVID-19 is now considered a risk factor for the onset and progression of sarcopenia, thus data regarding the relationship between cirrhosis and sarcopenia during the pandemic outbreak deserve to be collected and analyzed.
However, the main cause of death in most cirrhotic patients with COVID-19 is still represented by pulmonary disease rather than the progression of the underlying liver disease [84]. Therefore, it is plausible that pulmonary thromboembolism, a hallmark of critical COVID-19, has a contributory role given the additional hypercoagulable state associated with cirrhosis [91].
Finally, as testified by the drastic reduction in hospitalization for cirrhosis following the onset of the pandemic, delays in both follow-up and treatment have occurred, leading to more frequent and advanced cirrhosis-related complications. For example, acute variceal hemorrhage developed in patients who had not undergone timely endoscopic surveillance, whereas postponed routine elective paracentesis for tense ascites was converted into one requiring emergency hospitalization [92]. Therefore, the recognition that patients with cirrhosis are particularly vulnerable to the severe complications of COVID-19 is paramount. and consideration of early admission for these patients is encouraged. This careful attention should also be maintained following the availability of COVID-19 vaccines since recent data seem to suggest a decreased efficacy and durability of protection in patients with cirrhosis [93].

4.3. COVID-19 in Patients with Viral Hepatitis

Whether chronic viral hepatitis specifically affects the COVID-19 course remains unknown. Some researchers argue that there might be an immune response overlap between chronic viral hepatitis and COVID-19, in which a baseline inflammatory status could be further potentiated following SARS-CoV-2 infection [94].
Some studies suggest that patients with chronic hepatitis B are more vulnerable to COVID-19 [95] but others revealed that these patients do not appear to have a more severe course of the disease [96][97].
Similarly, little is known about the clinical course of COVID-19 in hepatitis C patients, but the current few studies available do not suggest an increased mortality or ICU admission rate compared to patients without HCV infection [98]. However, it recently emerged that patients with active HCV infection have a significantly higher risk of severe COVID-19 and increased mortality compared to the non-active HCV group [99].
Glucocorticoids or immunosuppression therapies are widely used in patients with severe COVID-19, therefore there is an urgent need for data from various populations to inform the risk stratification and management of those who are at elevated risk of HBV and HCV reactivation [100]. A recent systematic review, however, demonstrated a small risk of HBV reactivation overall following Tocilizumab administration (approximately 3%) and an even lower risk for HCV flare [101].
Nonetheless, what appears certain is that, as a consequence of this pandemic, most viral hepatitis elimination programs have diminished or stopped altogether [81]. Recent estimates have calculated that a 1-year delay in viral hepatitis diagnosis and treatment will result in an additional 44,800 hepatocellular carcinoma cases and 72,300 deaths from HCV globally in the next 10 years, thus the collateral burden of the COVID-19 pandemic on patients with viral hepatitis will become clear in the next few years [102].

4.4. COVID-19 in Patients with Alcohol-Associated Liver Disease (ALD)

The consumption of alcohol has increased in the present pandemic due to various reasons such as social isolation, job insecurity, and higher anxiety and depression [103]. Furthermore, the unavailability of professional help and support groups such as Alcoholics Anonymous may have led to psychological decompensation, alcohol abuse, and relapse of alcohol addiction [79]. This trend, coupled with the ubiquitous availability of inexpensive alcohol, determined a worldwide increase in alcoholic beverages. For example, as stay-at-home orders began, alcohol sales increased by up to 55% in the United States during March 2020, along with an alarming 262% increase in online sales compared to 2019 [104]. Similarly, in Canada, there was a 38% relative increase in monthly alcohol sales in March 2020 compared with March 2019 [105]. The same results were reported also in China and France, where 32% and 25% of regular alcohol drinkers reported an increase in their usage amount during the pandemic, respectively [106][107].
The increased consumption of alcohol has inevitably induced and aggravated alcohol-related disorders, in particular alcohol-associated liver disorder (ALD), which may predispose individuals to worse outcomes from COVID-19 [66]. In fact, despite the fact that there are very limited data on the effect of COVID-19 in patients with ALD, the few studies currently available showed that these patients had an increased risk of COVID-19-related complications. The first reason for this is that alcohol use and ALD disrupt the innate and adaptive immune systems by affecting the survival and function of immune cells important in mounting a defense against viral infections. Second, patients with ALD often have other comorbidities, including obesity, diabetes mellitus, chronic kidney disease, and tobacco use, which have been all independently associated with severe COVID-19 outcomes [103][105]. Additionally, a recent study, after adjusting for potential confounders such as sex, disease severity, and other comorbidities, reported that patients with ALD have a higher risk of mortality for COVID-19 even compared to patients with cirrhosis due to other etiologies [80].
On top of that, an interesting study found evidence of a substantial and rising burden of ALD, particularly regarding liver transplantation [108]. In fact, during the COVID-19 era, the percentage of ALD on the liver transplant waiting list significantly increased (approximately 3%), surpassing that of HCV and NASH combined for the first time.
In consideration of this, clinicians and hepatologists should be carefully focused on the prevention of infection by following strict epidemiologic recommendations, as well as on the prevention of alcohol abuse and relapse of alcohol addiction by implementing vigorous social and psychiatric care via alternative telephone or online resources.

4.5. COVID-19 in Patients with Autoimmune Hepatitis (AIH)

Regarding patients with AIH, it has been hypothesized that their immunosuppressive state can predispose them to SARS-CoV-2 infection and a greater risk for severe disease. In particular, the SARS-CoV-2 virus may trigger autoimmune mechanisms in genetically predisposed subjects, hyperstimulating the immune system and exposing foreign peptides homologous to human peptides (molecular mimicry), thus leading to the development of autoantibodies [109]. However, there are scarce reports of AIH triggered by COVID-19 infection, and several confounding factors were always present [110].
Most of the current studies agree that AIH patients under immunosuppression, despite the theoretically suspected susceptibility, have the same prevalence of COVID-19 infection compared to the general population [111][112][113] and a similar disease course [114][115]. Therefore, there is growing evidence suggesting that immunosuppression may provide some protection from lung damage in patients with COVID-19 or at least counterbalance COVID-19-driven hyperinflammatory status.
Since the outcome was favorable in most cases, the most important association for the study of the liver currently advises against reducing immunosuppressive therapy in these patients, except in special circumstances such as severe COVID-19, bacterial/fungal superinfections, or lymphopenia [116][117].

4.6. COVID-19 in Patients with Hepatocellular Carcinoma (HCC)

Patients with both COVID-19 and a history of cancer are more vulnerable to severe disease and have an increased chance of mortality, as well as ICU admission, especially if they have received chemotherapy within 1 month [118]. Since most patients with Hepatocellular Carcinoma (HCC) have pre-existing chronic liver disease, it is possible to assume that this subgroup of patients is even more susceptible to the effects of COVID-19 compared to other patients with cancers.
The COVID-19 pandemic has had a tremendous impact on both the management and treatment of patients with HCC, causing the rescheduling of screening exams and the shift of liver cancer therapy toward nonsurgical procedures.
Several studies reported a significant decrease in the number of new HCCs diagnosed (up to 37%) during the pandemic, which is in marked contrast to the steady increases in previous years and suggests that incident cases went undiagnosed during this period [119][120]. In addition, HCCs diagnosed following the COVID-19 outbreak were significantly larger and more frequently associated with lymphadenopathy and extrahepatic disease, with a consequent shift toward a higher tumor burden at diagnosis. Similarly, symptomatic presentation for HCC moved from being the least common mode of presentation to the most common, accounting for approximately 40% of all cases (vs. 24% in the pre-pandemic era), as demonstrated by the high rate of spontaneous hemorrhages. Furthermore, tumor progression occurred more rapidly and aggressively in HCC patients during the pandemic due to delayed or discontinued follow-up and treatment [121]. To overcome the restrictions in diagnostic procedures due to reduced radiologic capacity during the pandemic, both the American and the European association for the study of the liver recommend continuing surveillance imaging of HCC patients and high-risk cirrhotic patients with a reasonable delay of a maximum of 2–3 months, which is considered safe, possibly prioritizing those at increased risk if resources are limited. Moreover, the increasingly widespread possibility to revise diagnostic images and conduct multidisciplinary meetings online, also known as telemedicine, should be encouraged [116][122].
Elective hospital admissions were also delayed at the peak of the COVID-19 pandemic due to low hospital capacity and the fear of viral spread. As recently reported, this led to delayed treatment in a significant percentage of HCC patients (21–26%) for 1–2 months or longer [123][124]. Despite the fact that indications of surgery, locoregional therapy, and liver transplantation in HCC patients have not changed following the COVID-19 outbreak, a significant difference in the modification of the treatment strategy was noted. In particular, surgical resection and liver transplantation were the most affected due to a shortage of anesthetists and other medical personnel, the shortage of ICU beds, and a decline in the number of donors [125]. Therefore, locoregional procedures such as transarterial chemoembolization (TACE) and radiofrequency ablation became the most important tools in treating patients with HCC, as they acted as a salvage procedure to decrease the risk of cancer progression during the waiting period. Moreover, in addition to a good outcome in oncological terms, nonsurgical treatments are characterized by a lower complication rate and shorter hospital stay, which reduce the patient’s risk of contracting the virus during hospitalization [126][127].
Systemic therapy in advanced HCC should be maintained according to guidelines, and sorafenib administration should be continued without any change in its dose. Conversely, immune-checkpoint inhibitor therapy in HCC patients with severe COVID-19 should be temporarily withdrawn, whereas the decision on whether to continue or reduce its dose in non-severe patients should be taken on a case-by-case basis. Moreover, it is generally recommended to reduce the exposure of patients at the infusion center, which represents a hotspot for COVID-19 infection, through the implementation of home blood sampling and drug delivery, as well as video calls to manage common adverse events [128][129].
In conclusion, the pandemic has led to a rapid and prompt reorganization of activities in order to minimize its effect on patient outcomes and reduce the risk of exposure to SARS-CoV-2 as much as possible. In particular, the adoption of telemedicine together with the optimization of protocols and the implementation of both intra- and postprocedural workflows seems to be the right path to follow [130].

4.7. COVID-19 and Liver Transplantation

The COVID-19 pandemic has substantially impacted solid organ transplantation, including the temporary inactivation of waitlist candidates who tested positive for SARS-CoV-2 infection with a consequent suspension of transplant activity, except for extremely super-urgent cases [131][132]. The first pandemic wave caused a reduction in organ donation compared to the same period in the previous year, as demonstrated by the 25% decrease in liver transplants reported by the United Network for Organ Sharing (UNOS) [133] and also later confirmed in a large population-based study across 22 countries worldwide, which showed an overall reduction in liver transplants of 11% [134]. Moreover, in most countries, transplantation activity only slowly recovered in the following months, due to the occurrence of subsequent pandemic waves [135].
Early studies, in fact, suggested increased perioperative mortality and morbidity in patients with COVID-19 undergoing an elective and emergent general surgery procedure, leading transplant centers to defer liver transplantation in patients with active COVID-19 infection [136][137][138]. Moreover, a further challenge was related to the staff involved in the surgical procedures, who cannot be easily replaced if testing positive [79]. Therefore, both European and American Liver Associations advised prioritizing patients who have a poor short-term prognosis, considering living-donor transplantations on a case-by-case basis, thus leading to an inevitable reduction of transplant activity [115][122].
Nonetheless, more recent studies suggested that liver transplant recipients with COVID-19 infection have a similar risk of mortality compared to the general population and that transplantation is not independently associated with hospitalization or death from COVID-19 [139][140]. An interesting study even surprisingly reported a lower mortality rate in liver transplant patients diagnosed with COVID-19 compared to the complementary general population [140]. This evidence led to the hypothesis that immunosuppression might have favorable effects in transplanted patients by disabling cytokine release syndrome and thus protecting these patients from hyperinflammation and ARDS development in COVID-19 [141][142][143]. Additionally, waitlist mortality among those with end-stage liver disease remains high, and it is unknown whether the risk of COVID-related mortality after transplant outweighs the risk of waitlist mortality [139].
Furthermore, clinicians agree with delaying liver transplantation wherever possible, depending on the local availability of resources such as ICU beds, ventilators, and blood donations. 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 [116][122].
Currently, the use of liver grafts from donors testing positive for COVID-19 is still contraindicated, therefore screening of both donors (living and deceased) and recipients listed for liver transplantation is required [116][122]. To date, in fact, little is known about the transmission of the virus from donor to recipient. Moreover, liver transplant recipients are in an immune-compromised state, which puts them at higher risk of contracting COVID-19 infection and being a source of dissemination of infection to others (super-spreaders) [144].
However, recent studies found that recipient outcomes with the use of SARS-CoV-2-positive donor organs are similar to outcomes with negative testing, and patients receiving grafts from COVID-19-positive donors showed equivalent survival to those receiving grafts from COVID-19-negative donors [145][146]. Moreover, to date, there have been no reports of recognized transmissions of SARS-CoV-2 following blood transfusion, even in immunosuppressed patients [147][148]. Therefore, although, the number of transplants reported from positive SARS-CoV-2 donors is still relatively small, there is no clear evidence of additional risk to allograft survival [149].
Nonetheless, despite transplantation from donors with COVID-19 appearing feasible, especially in selected patients with imminently life-threatening organ failure, evidence is still lacking, and further studies are needed [148][149][150]. Furthermore, the impossibility of clearly defining the risk of transmission prevents the recipient from providing adequate informed consent and the exposure of healthcare workers during organ procurement remains a concern [135].
There have also been few reports of successful liver transplantation in individuals with asymptomatic or mild symptomatic COVID-19 infection without developing postoperative COVID-19 symptoms [151][152][153][154]. However, the decision to proceed with transplantation in this high-risk population must be balanced by the urgency of the procedure against potential COVID-19-associated perioperative risks; therefore, ideally, transplantation should always be deferred until acute COVID-19 infection is resolved.

5. COVID-19 Vaccination and the Liver

Following the development and widespread distribution of COVID-19 vaccines across the globe, sporadic cases of thrombotic events in young women after the vaccination with the Oxford-AstraZeneca vaccine have been reported [155], as well as anecdotal cases of different types of autoimmunity triggered by vaccines, including subacute cutaneous lupus erythematosus and Graves’ disease [156][157].
Similarly, rare case reports of hepatic complications mimicking autoimmune hepatitis (AIH) have been described in recipients of various vaccines, including the adenovirus-based vaccine of Oxford-AstraZeneca and the mRNA vaccines of Pfizer-BioNTech and Moderna, suggesting that these adverse events may be independent of the vaccine mechanisms [158][159][160][161][162]. Only association, but not causality, was suggested between COVID-19 vaccination and AIH due to the presence of other confounding factors, including other autoimmune diseases or concomitant treatment with drugs linked to the induction of autoimmune conditions. The majority of these cases were described in females and had a short latency time from vaccination to the onset of symptoms, which are still generally mild. Moreover, patients were treated with immunosuppressive therapy with remission within 5–6 months.
Despite the current data appearing to suggest a potential role of vaccines in unmasking AIH in predisposed individuals, whether there exists a causal relationship between COVID-19 vaccination and the development of autoimmune hepatitis remains to be determined. Although new variants of SARS-CoV-2 are emerging, vaccination remains an effective and reliable way to reduce disease severity, hospitalization requirement, and more importantly, mortality.

References

  1. Brandi, N.; Ciccarese, F.; Rimondi, M.R.; Balacchi, C.; Modolon, C.; Sportoletti, C.; Renzulli, M.; Coppola, F.; Golfieri, R. An Imaging Overview of COVID-19 ARDS in ICU Patients and Its Complications: A Pictorial Review. Diagnostics 2022, 12, 846.
  2. Gupta, A.; Madhavan, M.V.; Sehgal, K.; Nair, N.; Mahajan, S.; Sehrawat, T.S.; Bikdeli, B.; Ahluwalia, N.; Ausiello, J.C.; Wan, E.Y.; et al. Extrapulmonary manifestations of COVID-19. Nat. Med. 2020, 26, 1017–1032.
  3. Marshall, M. How COVID-19 can damage the brain. Nature 2020, 585, 342–343.
  4. Delli Muti, N.; Finocchi, F.; Tossetta, G.; Salvio, G.; Cutini, M.; Marzioni, D.; Balercia, G. Could SARS-CoV-2 infection affect male fertility and sexuality? APMIS 2022, 130, 243–252.
  5. Tossetta, G.; Fantone, S.; Delli Muti, N.; Balercia, G.; Ciavattini, A.; Giannubilo, S.R.; Marzioni, D. Preeclampsia and severe acute respiratory syndrome coronavirus 2 infection: A systematic review. J. Hypertens. 2022, 40, 1629–1638.
  6. Kumar-M, P.; Mishra, S.; Jha, D.K.; Shukla, J.; Choudhury, A.; Mohindra, R.; Mandavdhare, H.S.; Dutta, U.; Sharma, V. Coronavirus disease (COVID-19) and the liver: A comprehensive systematic review and meta-analysis. Hepatol. Int. 2020, 14, 711–722.
  7. Li, D.; Ding, X.; Xie, M.; Tian, D.; Xia, L. COVID-19-associated liver injury: From bedside to bench. J. Gastroenterol. 2021, 56, 218–230.
  8. Wang, M.K.; Yu, X.L.; Zhou, L.Y.; Si, H.M.; Hui, J.F.; Hou, D.Y.; Li, W.P.; Yang, J.S. COVID-19 and liver dysfunction: What nutritionists need to know. World J. Gastroenterol. 2022, 28, 1526–1535.
  9. Merola, E.; Pravadelli, C.; de Pretis, G. Prevalence of liver injury in patients with coronavirus disease 2019 (COVID-19): A systematic review and meta-analysis. Acta Gastro-Enterol. Belg. 2020, 83, 454–460.
  10. Phipps, M.M.; Barraza, L.H.; LaSota, E.D.; Sobieszczyk, M.E.; Pereira, M.R.; Zheng, E.X.; Fox, A.N.; Zucker, J.; Verna, E.C. Acute Liver Injury in COVID-19: Prevalence and Association with Clinical Outcomes in a Large U.S. Cohort. Hepatology 2020, 72, 807–817.
  11. Jothimani, D.; Venugopal, R.; Abedin, M.F.; Kaliamoorthy, I.; Rela, M. COVID-19 and the liver. J. Hepatol. 2020, 73, 1231–1240.
  12. Kaushik, A.; Wani, S.N.; Baba, M.A.; Agarwal, A.K. Prevalence of Abnormal Liver Function Tests in COVID-19 Patients at a Tertiary Care Centre. J. Assoc. Physicians India 2020, 68, 73–75.
  13. Cai, Q.; Huang, D.; Yu, H.; Zhu, Z.; Xia, Z.; Su, Y.; Li, Z.; Zhou, G.; Gou, J.; Qu, J.; et al. COVID-19: Abnormal liver function tests. J. Hepatol. 2020, 73, 566–574.
  14. Zhang, Y.; Zheng, L.; Liu, L.; Zhao, M.; Xiao, J.; Zhao, Q. Liver impairment in COVID-19 patients: A retrospective analysis of 115 cases from a single centre in Wuhan city, China. Liver Int. 2020, 40, 2095–2103.
  15. D’Ardes, D.; Boccatonda, A.; Cocco, G.; Fabiani, S.; Rossi, I.; Bucci, M.; Guagnano, M.T.; Schiavone, C.; Cipollone, F. Impaired coagulation, liver dysfunction and COVID-19: Discovering an intriguing relationship. World J. Gastroenterol. 2022, 28, 1102–1112.
  16. Toyoda, H.; Huang, D.Q.; Le, M.H.; Nguyen, M.H. Liver Care and Surveillance: The Global Impact of the COVID-19 Pandemic. Hepatol. Commun. 2020, 4, 1751–1757.
  17. Sun, J.; Aghemo, A.; Forner, A.; Valenti, L. COVID-19 and liver disease. Liver Int. 2020, 40, 1278–1281.
  18. Fan, Z.; Chen, L.; Li, J.; Cheng, X.; Yang, J.; Tian, C.; Zhang, Y.; Huang, S.; Liu, Z.; Cheng, J. Clinical Features of COVID-19-Related Liver Functional Abnormality. Clin. Gastroenterol. Hepatol. 2020, 18, 1561–1566.
  19. Xie, H.; Zhao, J.; Lian, N.; Lin, S.; Xie, Q.; Zhuo, H. Clinical characteristics of non-ICU hospitalized patients with coronavirus disease 2019 and liver injury: A retrospective study. Liver Int. 2020, 40, 1321–1326.
  20. Ji, D.; Qin, E.; Xu, J.; Zhang, D.; Cheng, G.; Wang, Y.; Lau, G. Non-alcoholic fatty liver diseases in patients with COVID-19: A retrospective study. J. Hepatol. 2020, 73, 451–453.
  21. Chen, N.; Zhou, M.; Dong, X.; Qu, J.; Gong, F.; Han, Y.; Qiu, Y.; Wang, J.; Liu, Y.; Wei, Y.; et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: A descriptive study. Lancet 2020, 395, 507–513.
  22. Sultan, S.; Altayar, O.; Siddique, S.M.; Davitkov, P.; Feuerstein, J.D.; Lim, J.K.; Falck-Ytter, Y.; El-Serag, H.B.; AGA Institute. Electronic address: . AGA Institute Rapid Review of the Gastrointestinal and Liver Manifestations of COVID-19, Meta-Analysis of International Data, and Recommendations for the Consultative Management of Patients with COVID-19. Gastroenterology 2020, 159, 320–334.e27.
  23. Wijarnpreecha, K.; Ungprasert, P.; Panjawatanan, P.; Harnois, D.M.; Zaver, H.B.; Ahmed, A.; Kim, D. COVID-19 and liver injury: A meta-analysis. Eur. J. Gastroenterol. Hepatol. 2021, 33, 990–995.
  24. Wu, Y.; Li, H.; Guo, X.; Yoshida, E.M.; Mendez-Sanchez, N.; Levi Sandri, G.B.; Teschke, R.; Romeiro, F.G.; Shukla, A.; Qi, X. Incidence, risk factors, and prognosis of abnormal liver biochemical tests in COVID-19 patients: A systematic review and meta-analysis. Hepatol. Int. 2020, 14, 621–637.
  25. Herta, T.; Berg, T. COVID-19 and the liver—Lessons learned. Liver Int. 2021, 41 (Suppl. 1), 1–8.
  26. Bernal-Monterde, V.; Casas-Deza, D.; Letona-Giménez, L.; de la Llama-Celis, N.; Calmarza, P.; Sierra-Gabarda, O.; Betoré-Glaria, E.; Martínez-de Lagos, M.; Martínez-Barredo, L.; Espinosa-Pérez, M.; et al. SARS-CoV-2 Infection Induces a Dual Response in Liver Function Tests: Association with Mortality during Hospitalization. Biomedicines 2020, 8, 328.
  27. Yang, R.X.; Zheng, R.D.; Fan, J.G. Etiology and management of liver injury in patients with COVID-19. World J. Gastroenterol. 2020, 26, 4753–4762.
  28. Lei, F.; Liu, Y.M.; Zhou, F.; Qin, J.J.; Zhang, P.; Zhu, L.; Zhang, X.J.; Cai, J.; Lin, L.; Ouyang, S.; et al. Longitudinal Association Between Markers of Liver Injury and Mortality in COVID-19 in China. Hepatology 2020, 72, 389–398.
  29. Mao, R.; Qiu, Y.; He, J.S.; Tan, J.Y.; Li, X.H.; Liang, J.; Shen, J.; Zhu, L.R.; Chen, Y.; Iacucci, M.; et al. Manifestations and prognosis of gastrointestinal and liver involvement in patients with COVID-19: A systematic review and meta-analysis. Lancet Gastroenterol. Hepatol. 2020, 5, 667–678.
  30. Chen, T.; Wu, D.; Chen, H.; Yan, W.; Yang, D.; Chen, G.; Ma, K.; Xu, D.; Yu, H.; Wang, H.; et al. Clinical characteristics of 113 deceased patients with coronavirus disease 2019: Retrospective study. BMJ 2020, 368, m1091.
  31. Bloom, P.P.; Meyerowitz, E.A.; Reinus, Z.; Daidone, M.; Gustafson, J.; Kim, A.Y.; Schaefer, E.; Chung, R.T. Liver Biochemistries in Hospitalized Patients With COVID-19. Hepatology 2021, 73, 890–900.
  32. Krishnan, A.; Prichett, L.; Tao, X.; Alqahtani, S.A.; Hamilton, J.P.; Mezey, E.; Strauss, A.T.; Kim, A.; Potter, J.J.; Chen, P.H.; et al. Abnormal liver chemistries as a predictor of COVID-19 severity and clinical outcomes in hospitalized patients. World J. Gastroenterol. 2022, 28, 570–587.
  33. Weber, S.; Mayerle, J.; Irlbeck, M.; Gerbes, A.L. Severe liver failure during SARS-CoV-2 infection. Gut 2020, 69, 1365–1367.
  34. Revzin, M.V.; Raza, S.; Srivastava, N.C.; Warshawsky, R.; D’Agostino, C.; Malhotra, A.; Bader, A.S.; Patel, R.D.; Chen, K.; Kyriakakos, C.; et al. Multisystem Imaging Manifestations of COVID-19, Part 2: From Cardiac Complications to Pediatric Manifestations. Radiographics 2020, 40, 1866–1892.
  35. Ierardi, A.M.; Coppola, A.; Tortora, S.; Valconi, E.; Piacentino, F.; Fontana, F.; Stellato, E.; Cogliati, C.B.; Torzillo, D.; Giampalma, E.; et al. Gastrointestinal Bleeding in Patients with SARS-CoV-2 Infection Managed by Interventional Radiology. J. Clin. Med. 2021, 10, 4758.
  36. Marasco, G.; Maida, M.; Morreale, G.C.; Licata, M.; Renzulli, M.; Cremon, C.; Stanghellini, V.; Barbara, G. Gastrointestinal Bleeding in COVID-19 Patients: A Systematic Review with Meta-Analysis. Can. J. Gastroenterol. Hepatol. 2021, 2021, 2534975.
  37. Ierardi, A.M.; Del Giudice, C.; Coppola, A.; Carnevale, A.; Giganti, M.; Renzulli, M.; Tacher, V.; Urbano, J.; Kobeiter, H.; Loffroy, R.; et al. Gastrointestinal Hemorrhages in Patients With COVID-19 Managed With Transarterial Embolization. Am. J. Gastroenterol. 2021, 116, 838–840.
  38. Tsutsumi, T.; Saito, M.; Nagai, H.; Yamamoto, S.; Ikeuchi, K.; Lim, L.A.; Adachi, E.; Koga, M.; Okushin, K.; Akai, H.; et al. Association of coagulopathy with liver dysfunction in patients with COVID-19. Hepatol. Res. 2021, 51, 227–232.
  39. Sonzogni, A.; Previtali, G.; Seghezzi, M.; Grazia Alessio, M.; Gianatti, A.; Licini, L.; Morotti, D.; Zerbi, P.; Carsana, L.; Rossi, R.; et al. Liver histopathology in severe COVID 19 respiratory failure is suggestive of vascular alterations. Liver Int. 2020, 40, 2110–2116.
  40. Brandi, N.; Ciccarese, F.; Balacchi, C.; Rimondi, M.R.; Modolon, C.; Sportoletti, C.; Capozzi, C.; Renzulli, M.; Paccapelo, A.; Castelli, A.; et al. Co-Infections and Superinfections in COVID-19 Critically Ill Patients Are Associated with CT Imaging Abnormalities and the Worst Outcomes. Diagnostics 2022, 12, 1617.
  41. Balacchi, C.; Brandi, N.; Ciccarese, F.; Coppola, F.; Lucidi, V.; Bartalena, L.; Parmeggiani, A.; Paccapelo, A.; Golfieri, R. Comparing the first and the second waves of COVID-19 in Italy: Differences in epidemiological features and CT findings using a semi-quantitative score. Emerg Radiol. 2021, 28, 1055–1061.
  42. Gabelloni, M.; Faggioni, L.; Cioni, D.; Mendola, V.; Falaschi, Z.; Coppola, S.; Corradi, F.; Isirdi, A.; Brandi, N.; Coppola, F.; et al. Extracorporeal membrane oxygenation (ECMO) in COVID-19 patients: A pocket guide for radiologists. Radiol. Med. 2022, 127, 369–382.
  43. Spagnoli, L.; Morrone, M.F.; Giampieri, E.; Paolani, G.; Santoro, M.; Curti, N.; Coppola, F.; Ciccarese, F.; Vara, G.; Brandi, N.; et al. Outcome Prediction for SARS-CoV-2 Patients Using Machine Learning Modeling of Clinical, Radiological, and Radiomic Features Derived from Chest CT Images. Appl. Sci. 2022, 12, 4493.
  44. Caruso, D.; Zerunian, M.; Pucciarelli, F.; Lucertini, E.; Bracci, B.; Polidori, T.; Guido, G.; Polici, M.; Rucci, C.; Iannicelli, E.; et al. Imaging of abdominal complications of COVID-19 infection. BJR Open 2021, 2, 20200052.
  45. Behzad, S.; Aghaghazvini, L.; Radmard, A.R.; Gholamrezanezhad, A. Extrapulmonary manifestations of COVID-19: Radiologic and clinical overview. Clin. Imaging 2020, 66, 35–41.
  46. Bhayana, R.; Som, A.; Li, M.D.; Carey, D.E.; Anderson, M.A.; Blake, M.A.; Catalano, O.; Gee, M.S.; Hahn, P.F.; Harisinghani, M.; et al. Abdominal Imaging Findings in COVID-19: Preliminary Observations. Radiology 2020, 297, E207–E215.
  47. Radzina, M.; Putrins, D.S.; Micena, A.; Vanaga, I.; Kolesova, O.; Platkajis, A.; Viksna, L. Post-COVID-19 Liver Injury: Comprehensive Imaging With Multiparametric Ultrasound. J. Ultrasound Med. 2022, 41, 935–949.
  48. Boraschi, P.; Giugliano, L.; Mercogliano, G.; Donati, F.; Romano, S.; Neri, E. Abdominal and gastrointestinal manifestations in COVID-19 patients: Is imaging useful? World J. Gastroenterol. 2021, 27, 4143–4159.
  49. Renzulli, M.; Brandi, N.; Argalia, G.; Brocchi, S.; Farolfi, A.; Fanti, S.; Golfieri, R. Morphological, dynamic and functional characteristics of liver pseudolesions and benign lesions. Radiol. Med. 2022, 127, 129–144.
  50. Fataftah, J.Z.; Tayyem, R.; Qandeel, H.; Baydoun, H.A.; Al Manasra, A.R.A.; Tahboub, A.; Al-Dwairy, S.Y.; Al-Mousa, A. The Effect of COVID 19 on Liver Parenchyma Detected and measured by CT scan Hounsfield Units. J. Res. Med. Sci. 2022, 27, 26.
  51. Ali, A.; Hasan, M.; Hamed, S.; Elhamy, A. Hepatic steatosis: A risk factor for increased COVID-19 prevalence and severity-a computed tomography study. Egypt. Liver J. 2021, 11, 61.
  52. Chen, F.; Chen, W.; Chen, J.; Xu, D.; Xie, W.; Wang, X.; Xie, Y. Clinical features and risk factors of COVID-19-associated liver injury and function: A retrospective analysis of 830 cases. Ann. Hepatol. 2021, 21, 100267.
  53. Han, Q.; Lu, Y.; Wang, D.; Zhao, Y.; Li, X.; Mei, N.; Zhu, Y.; Xiao, A.; Yin, B. Assessment of dynamic hepatic and renal imaging changes in COVID-19 survivors using T1 mapping and IVIM-DWI. Abdom. Radiol. 2022, 47, 1817–1827.
  54. Zhang, W.; Li, C.; Liu, B.; Wu, R.; Zou, N.; Xu, Y.Z.; Yang, Y.Y.; Zhang, F.; Zhou, H.M.; Wan, K.Q.; et al. Pioglitazone upregulates hepatic angiotensin converting enzyme 2 expression in rats with steatohepatitis. Ann. Hepatol. 2013, 12, 892–900.
  55. Paizis, G.; Tikellis, C.; Cooper, M.E.; Schembri, J.M.; Lew, R.A.; Smith, A.I.; Shaw, T.; Warner, F.J.; Zuilli, A.; Burrell, L.M.; et al. Chronic liver injury in rats and humans upregulates the novel enzyme angiotensin converting enzyme 2. Gut 2005, 54, 1790–1796.
  56. Singh, S.; Khan, A. Clinical Characteristics and Outcomes of Coronavirus Disease 2019 Among Patients With Preexisting Liver Disease in the United States: A Multicenter Research Network Study. Gastroenterology 2020, 159, 768–771.e3.
  57. Meijnikman, A.S.; Bruin, S.; Groen, A.K.; Nieuwdorp, M.; Herrema, H. Increased expression of key SARS-CoV-2 entry points in multiple tissues in individuals with NAFLD. J. Hepatol. 2021, 74, 748–749.
  58. Bertolini, A.; van de Peppel, I.P.; Bodewes, F.A.J.A.; Moshage, H.; Fantin, A.; Farinati, F.; Fiorotto, R.; Jonker, J.W.; Strazzabosco, M.; Verkade, H.J.; et al. Abnormal Liver Function Tests in Patients With COVID-19: Relevance and Potential Pathogenesis. Hepatology 2020, 72, 1864–1872.
  59. Pawlotsky, J.M. COVID-19 and the liver-related deaths to come. Nat. Rev. Gastroenterol. Hepatol. 2020, 17, 523–525.
  60. Docherty, A.B.; Harrison, E.M.; Green, C.A.; Hardwick, H.E.; Pius, R.; Norman, L.; Holden, K.A.; Read, J.M.; Dondelinger, F.; Carson, G.; et al. Features of 20 133 UK patients in hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: Prospective observational cohort study. BMJ 2020, 369, m1985.
  61. Williamson, E.J.; Walker, A.J.; Bhaskaran, K.; Bacon, S.; Bates, C.; Morton, C.E.; Curtis, H.J.; Mehrkar, A.; Evans, D.; Inglesby, P.; et al. Factors associated with COVID-19-related death using OpenSAFELY. Nature 2020, 584, 430–436.
  62. Qi, X.; Wang, J.; Li, X.; Wang, Z.; Liu, Y.; Yang, H.; Li, X.; Shi, J.; Xiang, H.; Liu, T.; et al. Clinical course of COVID-19 in patients with pre-existing decompensated cirrhosis: Initial report from China. Hepatol. Int. 2020, 14, 478–482.
  63. Iavarone, M.; D’Ambrosio, R.; Soria, A.; Triolo, M.; Pugliese, N.; Del Poggio, P.; Perricone, G.; Massironi, S.; Spinetti, A.; Buscarini, E.; et al. High rates of 30-day mortality in patients with cirrhosis and COVID-19. J. Hepatol. 2020, 73, 1063–1071.
  64. Sarin, S.K.; Choudhury, A.; Lau, G.K.; Zheng, M.H.; Ji, D.; Abd-Elsalam, S.; Hwang, J.; Qi, X.; Cua, I.H.; Suh, J.I.; et al. Pre-existing liver disease is associated with poor outcome in patients with SARS CoV2 infection; The APCOLIS Study (APASL COVID-19 Liver Injury Spectrum Study). Hepatol. Int. 2020, 14, 690–700.
  65. Vashishtha, C.; Bhardwaj, A.; Diwaker, A.; Sharma, S.; Sharma, M.K.; Sarin, S. Collateral Impact on Patients of Liver Diseases in the Second COVID-19 Wave: A Retrospective Cohort Study. Cureus 2022, 14, e25542.
  66. Saviano, A.; Wrensch, F.; Ghany, M.G.; Baumert, T.F. Liver Disease and Coronavirus Disease 2019: From Pathogenesis to Clinical Care. Hepatology 2021, 74, 1088–1100.
  67. Kim, D.; Alshuwaykh, O.; Dennis, B.B.; Cholankeril, G.; Ahmed, A. Trends in Etiology-based Mortality from Chronic Liver Disease before and during COVID-19 Pandemic in the United States. Clin. Gastroenterol. Hepatol. 2022, 20, 2307–2316.e3.
  68. Tapper, E.B.; Asrani, S.K. The COVID-19 pandemic will have a long-lasting impact on the quality of cirrhosis care. J. Hepatol. 2020, 73, 441–445.
  69. Napodano, C.; Pocino, K.; Stefanile, A.; Marino, M.; Miele, L.; Gulli, F.; Basile, V.; Pandolfi, F.; Gasbarrini, A.; Rapaccini, G.L.; et al. COVID-19 and hepatic involvement: The liver as a main actor of the pandemic novel. Scand. J. Immunol. 2021, 93, e12977.
  70. Zhou, Y.J.; Zheng, K.I.; Wang, X.B.; Yan, H.D.; Sun, Q.F.; Pan, K.H.; Wang, T.Y.; Ma, H.L.; Chen, Y.P.; George, J.; et al. Younger patients with MAFLD are at increased risk of severe COVID-19 illness: A multicenter preliminary analysis. J. Hepatol. 2020, 73, 719–721.
  71. Gao, F.; Zheng, K.I.; Wang, X.B.; Yan, H.D.; Sun, Q.F.; Pan, K.H.; Wang, T.Y.; Chen, Y.P.; George, J.; Zheng, M.H. Metabolic associated fatty liver disease increases coronavirus disease 2019 disease severity in nondiabetic patients. J. Gastroenterol. Hepatol. 2021, 36, 204–207.
  72. Li, J.; Tian, A.; Zhu, H.; Chen, L.; Wen, J.; Liu, W.; Chen, P. Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19. Clin. Gastroenterol. Hepatol. 2022, 20, 1553–1560.e78.
  73. Kassir, R. Risk of COVID-19 for patients with obesity. Obes. Rev. 2020, 21, e13034.
  74. Lavie, C.J.; Sanchis-Gomar, F.; Henry, B.M.; Lippi, G. COVID-19 and obesity: Links and risks. Expert Rev. Endocrinol. Metab. 2020, 15, 215–216.
  75. Caussy, C.; Wallet, F.; Laville, M.; Disse, E. Obesity is Associated with Severe Forms of COVID-19. Obesity 2020, 28, 1175.
  76. Pasquarelli-do-Nascimento, G.; Braz-de-Melo, H.A.; Faria, S.S.; Santos, I.O.; Kobinger, G.P.; Magalhães, K.G. Hypercoagulopathy and Adipose Tissue Exacerbated Inflammation May Explain Higher Mortality in COVID-19 Patients With Obesity. Front. Endocrinol. 2020, 11, 530.
  77. Biquard, L.; Valla, D.; Rautou, P.E. No evidence for an increased liver uptake of SARS-CoV-2 in metabolic-associated fatty liver disease. J. Hepatol. 2020, 73, 717–718.
  78. Cordeiro, A.; Ribamar, A.; Ramalho, A. Adipose tissue dysfunction and MAFLD in obesity on the scene of COVID-19. Clin. Res. Hepatol. Gastroenterol. 2022, 46, 101807.
  79. Mikolasevic, I.; Bozic, D.; Pavić, T.; Ruzic, A.; Hauser, G.; Radic, M.; Radic-Kristo, D.; Razov-Radas, M.; Puljiz, Z.; Milic, S. Liver disease in the era of COVID-19: Is the worst yet to come? World J. Gastroenterol. 2021, 27, 6039–6052.
  80. Marjot, T.; Moon, A.M.; Cook, J.A.; Abd-Elsalam, S.; Aloman, C.; Armstrong, M.J.; Pose, E.; Brenner, E.J.; Cargill, T.; Catana, M.A.; et al. Outcomes following SARS-CoV-2 infection in patients with chronic liver disease: An international registry study. J. Hepatol. 2021, 74, 567–577.
  81. Moreau, R.; Jalan, R.; Gines, P.; Pavesi, M.; Angeli, P.; Cordoba, J.; Durand, F.; Gustot, T.; Saliba, F.; Domenicali, M.; et al. Acute-on-chronic liver failure is a distinct syndrome that develops in patients with acute decompensation of cirrhosis. Gastroenterology 2013, 144, 1426–1437.
  82. Hunt, R.H.; East, J.E.; Lanas, A.; Malfertheiner, P.; Satsangi, J.; Scarpignato, C.; Webb, G.J. COVID-19 and Gastrointestinal Disease: Implications for the Gastroenterologist. Dig. Dis. 2021, 39, 119–139.
  83. Ge, J.; Pletcher, M.J.; Lai, J.C.; N3C Consortium. Outcomes of SARS-CoV-2 Infection in Patients with Chronic Liver Disease and Cirrhosis: A N3C Study. medRxiv 2021, 161, 1487–1501.e5.
  84. Qi, X.; Liu, Y.; Wang, J.; Fallowfield, J.A.; Wang, J.; Li, X.; Shi, J.; Pan, H.; Zou, S.; Zhang, H.; et al. Clinical course and risk factors for mortality of COVID-19 patients with pre-existing cirrhosis: A multicentre cohort study. Gut 2021, 70, 433–436.
  85. Strnad, P.; Tacke, F.; Koch, A.; Trautwein, C. Liver—Guardian, modifier and target of sepsis. Nat. Rev. Gastroenterol. Hepatol. 2017, 14, 55–66.
  86. Bonnel, A.R.; Bunchorntavakul, C.; Reddy, K.R. Immune dysfunction and infections in patients with cirrhosis. Clin. Gastroenterol. Hepatol. 2011, 9, 727–738.
  87. Bajaj, J.S.; Garcia-Tsao, G.; Biggins, S.W.; Kamath, P.S.; Wong, F.; McGeorge, S.; Shaw, J.; Pearson, M.; Chew, M.; Fagan, A.; et al. Comparison of mortality risk in patients with cirrhosis and COVID-19 compared with patients with cirrhosis alone and COVID-19 alone: Multicentre matched cohort. Gut 2021, 70, 531–536.
  88. Marasco, G.; Serenari, M.; Renzulli, M.; Alemanni, L.V.; Rossini, B.; Pettinari, I.; Dajti, E.; Ravaioli, F.; Golfieri, R.; Cescon, M.; et al. Clinical impact of sarcopenia assessment in patients with hepatocellular carcinoma undergoing treatments. J. Gastroenterol. 2020, 55, 927–943.
  89. Marasco, G.; Dajti, E.; Serenari, M.; Alemanni, L.V.; Ravaioli, F.; Ravaioli, M.; Vestito, A.; Vara, G.; Festi, D.; Golfieri, R.; et al. Sarcopenia Predicts Major Complications after Resection for Primary Hepatocellular Carcinoma in Compensated Cirrhosis. Cancers 2022, 14, 1935.
  90. Wang, P.Y.; Li, Y.; Wang, Q. Sarcopenia: An underlying treatment target during the COVID-19 pandemic. Nutrition 2021, 84, 111104.
  91. Marjot, T.; Webb, G.J.; Barritt, A.S., IV; Moon, A.M.; Stamataki, Z.; Wong, V.W.; Barnes, E. COVID-19 and liver disease: Mechanistic and clinical perspectives. Nat. Rev. Gastroenterol. Hepatol. 2021, 18, 348–364.
  92. Li, J.; Liu, D.; Yan, J.; Tan, Y. Reductions in liver cirrhosis hospitalizations during the COVID-19 pandemic. Hepatol. Int. 2021, 15, 213–214.
  93. Luo, M.; Ballester, M.P.; Soffientini, U.; Jalan, R.; Mehta, G. SARS-CoV-2 infection and liver involvement. Hepatol. Int. 2022, 16, 755–774.
  94. Ronderos, D.; Omar, A.M.S.; Abbas, H.; Makker, J.; Baiomi, A.; Sun, H.; Mantri, N.; Choi, Y.; Fortuzi, K.; Shin, D.; et al. Chronic hepatitis-C infection in COVID-19 patients is associated with in-hospital mortality. World J. Clin. Cases 2021, 9, 8749–8762.
  95. Chen, X.; Jiang, Q.; Ma, Z.; Ling, J.; Hu, W.; Cao, Q.; Mo, P.; Yao, L.; Yang, R.; Gao, S.; et al. Clinical Characteristics of Hospitalized Patients with SARS-CoV-2 and Hepatitis B Virus Co-infection. Virol. Sin. 2020, 35, 842–845.
  96. Zhang, C.; Shi, L.; Wang, F.S. Liver injury in COVID-19: Management and challenges. Lancet Gastroenterol. Hepatol. 2020, 5, 428–430.
  97. Yip, T.C.; Wong, V.W.; Lui, G.C.; Chow, V.C.; Tse, Y.K.; Hui, V.W.; Liang, L.Y.; Chan, H.L.; Hui, D.S.; Wong, G.L. Current and Past Infections of HBV Do Not Increase Mortality in Patients With COVID-19. Hepatology 2021, 74, 1750–1765.
  98. Butt, A.A.; Yan, P.; Chotani, R.A.; Shaikh, O.S. Mortality is not increased in SARS-CoV-2 infected persons with hepatitis C virus infection. Liver Int. 2021, 41, 1824–1831.
  99. Cerbu, B.; Pantea, S.; Bratosin, F.; Vidican, I.; Turaiche, M.; Frent, S.; Borsi, E.; Marincu, I. Liver Impairment and Hematological Changes in Patients with Chronic Hepatitis C and COVID-19: A Retrospective Study after One Year of Pandemic. Medicina 2021, 57, 597.
  100. Xiang, T.D.; Zheng, X. Interaction between hepatitis B virus and SARS-CoV-2 infections. World J. Gastroenterol. 2021, 27, 782–793.
  101. Campbell, C.; Andersson, M.I.; Ansari, M.A.; Moswela, O.; Misbah, S.A.; Klenerman, P.; Matthews, P.C. Risk of Reactivation of Hepatitis B Virus (HBV) and Tuberculosis (TB) and Complications of Hepatitis C Virus (HCV) Following Tocilizumab Therapy: A Systematic Review to Inform Risk Assessment in the COVID-19 Era. Front. Med. 2021, 8, 706482.
  102. Blach, S.; Kondili, L.A.; Aghemo, A.; Cai, Z.; Dugan, E.; Estes, C.; Gamkrelidze, I.; Ma, S.; Pawlotsky, J.M.; Razavi-Shearer, D.; et al. Impact of COVID-19 on global HCV elimination efforts. J. Hepatol. 2021, 74, 31–36.
  103. Sharma, P.; Kumar, A.; Anikhindi, S.; Bansal, N.; Singla, V.; Shivam, K.; Arora, A. Effect of COVID-19 on Pre-existing Liver disease: What Hepatologist Should Know? J. Clin. Exp. Hepatol. 2021, 11, 484–493.
  104. Pollard, M.S.; Tucker, J.S.; Green, H.D., Jr. Changes in Adult Alcohol Use and Consequences During the COVID-19 Pandemic in the US. JAMA Netw. Open 2020, 3, e2022942.
  105. Moon, A.M.; Curtis, B.; Mandrekar, P.; Singal, A.K.; Verna, E.C.; Fix, O.K. Alcohol-Associated Liver Disease Before and After COVID-19-An Overview and Call for Ongoing Investigation. Hepatol. Commun. 2021, 5, 1616–1621.
  106. Sun, Y.; Li, Y.; Bao, Y.; Meng, S.; Sun, Y.; Schumann, G.; Kosten, T.; Strang, J.; Lu, L.; Shi, J. Brief Report: Increased Addictive Internet and Substance Use Behavior During the COVID-19 Pandemic in China. Am. J. Addict. 2020, 29, 268–270.
  107. Rolland, B.; Haesebaert, F.; Zante, E.; Benyamina, A.; Haesebaert, J.; Franck, N. Global Changes and Factors of Increase in Caloric/Salty Food Intake, Screen Use, and Substance Use During the Early COVID-19 Containment Phase in the General Population in France: Survey Study. JMIR Public Health Surveill. 2020, 6, e19630.
  108. Cholankeril, G.; Goli, K.; Rana, A.; Hernaez, R.; Podboy, A.; Jalal, P.; Da, B.L.; Satapathy, S.K.; Kim, D.; Ahmed, A.; et al. Impact of COVID-19 Pandemic on Liver Transplantation and Alcohol-Associated Liver Disease in the USA. Hepatology 2021, 74, 3316–3329.
  109. Floreani, A.; De Martin, S. COVID-19 and Autoimmune Liver Diseases. J. Clin. Med. 2022, 11, 2681.
  110. Singh, B.; Kaur, P.; Maroules, M. Autoimmune Hepatitis-Primary Biliary Cholangitis Overlap Syndrome Triggered by COVID-19. Eur. J. Case Rep. Intern. Med. 2021, 8, 002264.
  111. Di Giorgio, A.; Nicastro, E.; Speziani, C.; De Giorgio, M.; Pasulo, L.; Magro, B.; Fagiuoli, S.; D’Antiga, L. Health status of patients with autoimmune liver disease during SARS-CoV-2 outbreak in northern Italy. J. Hepatol. 2020, 73, 702–705.
  112. Murtas, R.; Andreano, A.; Gervasi, F.; Guido, D.; Consolazio, D.; Tunesi, S.; Andreoni, L.; Greco, M.T.; Gattoni, M.E.; Sandrini, M.; et al. Association between autoimmune diseases and COVID-19 as assessed in both a test-negative case-control and population case-control design. Autoimmun. Highlights 2020, 11, 15.
  113. Verhelst, X.; Somers, N.; Geerts, A.; Degroote, H.; Van Vlierberghe, H. Health status of patients with autoimmune hepatitis is not affected by the SARS-CoV-2 outbreak in Flanders, Belgium. J. Hepatol. 2021, 74, 240–241.
  114. Gerussi, A.; Rigamonti, C.; Elia, C.; Cazzagon, N.; Floreani, A.; Pozzi, R.; Pozzoni, P.; Claar, E.; Pasulo, L.; Fagiuoli, S.; et al. Coronavirus Disease 2019 in Autoimmune Hepatitis: A Lesson From Immunosuppressed Patients. Hepatol. Commun. 2020, 4, 1257–1262.
  115. Efe, C.; Dhanasekaran, R.; Lammert, C.; Ebik, B.; Higuera-de la Tijera, F.; Aloman, C.; Rıza Calışkan, A.; Peralta, M.; Gerussi, A.; Massoumi, H.; et al. Outcome of COVID-19 in Patients With Autoimmune Hepatitis: An International Multicenter Study. Hepatology 2021, 73, 2099–2109.
  116. Boettler, T.; Newsome, P.N.; Mondelli, M.U.; Maticic, M.; Cordero, E.; Cornberg, M.; Berg, T. Care of patients with liver disease during the COVID-19 pandemic: EASL-ESCMID position paper. JHEP Rep. 2020, 2, 100113.
  117. APASL Covid-19 Task Force; Lau, G.; Sharma, M. Clinical practice guidance for hepatology and liver transplant providers during the COVID-19 pandemic: APASL expert panel consensus recommendations. Hepatol. Int. 2020, 14, 415–428.
  118. Liang, W.; Guan, W.; Chen, R.; Wang, W.; Li, J.; Xu, K.; Li, C.; Ai, Q.; Lu, W.; Liang, H.; et al. Cancer patients in SARS-CoV-2 infection: A nationwide analysis in China. Lancet Oncol. 2020, 21, 335–337.
  119. Gandhi, M.; Ling, W.H.; Chen, C.H.; Lee, J.H.; Kudo, M.; Chanwat, R.; Strasser, S.I.; Xu, Z.; Lai, S.H.; Chow, P.K. Impact of COVID-19 on Hepatocellular Carcinoma Management: A Multicountry and Region Study. J. Hepatocell. Carcinoma 2021, 8, 1159–1167.
  120. Muñoz-Martínez, S.; Sapena, V.; Forner, A.; Bruix, J.; Sanduzzi-Zamparelli, M.; Ríos, J.; Bouattour, M.; El-Kassas, M.; Leal, C.R.G.; Mocan, T.; et al. Outcome of liver cancer patients with SARS-CoV-2 infection: An International, Multicentre, Cohort Study. Liver Int. 2022, 42, 1891–1901.
  121. Carissimi, F.; Scotti, M.A.; Ciulli, C.; Fogliati, A.; Uggeri, F.; Chiarelli, M.; Braga, M.; Romano, F.; Garancini, M. COVID-19 and Liver Surgery: How the Pandemic Affected an Italian Medium-Volume HBP Center. Front. Surg. 2022, 9, 918348.
  122. Fix, O.K.; Hameed, B.; Fontana, R.J.; Kwok, R.M.; McGuire, B.M.; Mulligan, D.C.; Pratt, D.S.; Russo, M.W.; Schilsky, M.L.; Verna, E.C.; et al. Clinical Best Practice Advice for Hepatology and Liver Transplant Providers During the COVID-19 Pandemic: AASLD Expert Panel Consensus Statement. Hepatology 2020, 72, 287–304.
  123. Iavarone, M.; Sangiovanni, A.; Carrafiello, G.; Rossi, G.; Lampertico, P. Management of hepatocellular carcinoma in the time of COVID-19. Ann. Oncol. 2020, 31, 1084–1085.
  124. Amaddeo, G.; Brustia, R.; Allaire, M.; Lequoy, M.; Hollande, C.; Regnault, H.; Blaise, L.; Ganne-Carrié, N.; Séror, O.; Larrey, E.; et al. Impact of COVID-19 on the management of hepatocellular carcinoma in a high-prevalence area. JHEP Rep. 2021, 3, 100199.
  125. Wong, G.L.; Wong, V.W.; Thompson, A.; Jia, J.; Hou, J.; Lesmana, C.R.A.; Susilo, A.; Tanaka, Y.; Chan, W.K.; Gane, E.; et al. Management of patients with liver derangement during the COVID-19 pandemic: An Asia-Pacific position statement. Lancet Gastroenterol. Hepatol. 2020, 5, 776–787.
  126. Denys, A.; Guiu, B.; Chevallier, P.; Digklia, A.; de Kerviler, E.; de Baere, T. Interventional oncology at the time of COVID-19 pandemic: Problems and solutions. Diagn. Interv. Imaging 2020, 101, 347–353.
  127. Bollipo, S.; Kapuria, D.; Rabiee, A.; Ben-Yakov, G.; Lui, R.N.; Lee, H.W.; Kumar, G.; Siau, K.; Turnes, J.; Dhanasekaran, R. One world, one pandemic, many guidelines: Management of liver diseases during COVID-19. Gut 2020, 69, 1369–1372.
  128. Farinati, F.; Vanin, V.; Giacomin, A.; Pozzan, C.; Cillo, U.; Vitale, A.; Di Nolfo, A.M.; Del Poggio, P.; Benvegnu’, L.; Rapaccini, G.; et al. BCLC stage B hepatocellular carcinoma and transcatheter arterial chemoembolization: A 20-year survey by the Italian Liver Cancer group. Liver Int. 2015, 35, 223–231.
  129. Pecorelli, A.; Lenzi, B.; Gramenzi, A.; Garuti, F.; Farinati, F.; Giannini, E.G.; Ciccarese, F.; Piscaglia, F.; Rapaccini, G.L.; Di Marco, M.; et al. Curative therapies are superior to standard of care (transarterial chemoembolization) for intermediate stage hepatocellular carcinoma. Liver Int. 2017, 37, 423–433.
  130. Renzulli, M.; Gentilini, M.; Marasco, G.; Brandi, N.; Granito, A.; Lo Monaco, S.; Ierardi, A.M.; De Cinque, A.; Tovoli, F.; Bartalena, L.; et al. The duration of the conventional chemoembolization for hepatocellular carcinoma: Factors affecting the procedural time. Hepatoma Res. 2022, 8, 27.
  131. Anjum, M.R.; Chalmers, J.; Hamid, R.; Rajoriya, N. COVID-19: Effect on gastroenterology and hepatology service provision and training: Lessons learnt and planning for the future. World J. Gastroenterol. 2021, 27, 7625–7648.
  132. Aghemo, A.; Masarone, M.; Montagnese, S.; Petta, S.; Ponziani, F.R.; Russo, F.P.; Associazione Italiana Studio Fegato (AISF). Assessing the impact of COVID-19 on the management of patients with liver diseases: A national survey by the Italian association for the study of the Liver. Dig. Liver Dis. 2020, 52, 937–941.
  133. Merola, J.; Schilsky, M.L.; Mulligan, D.C. The Impact of COVID-19 on Organ Donation, Procurement, and Liver Transplantation in the United States. Hepatol. Commun. 2020, 5, 5–11.
  134. Aubert, O.; Yoo, D.; Zielinski, D.; Cozzi, E.; Cardillo, M.; Dürr, M.; Domínguez-Gil, B.; Coll, E.; Da Silva, M.I.; Sallinen, V.; et al. COVID-19 pandemic and worldwide organ transplantation: A population-based study. Lancet Public Health 2021, 6, e709–e719.
  135. De Carlis, R.; Vella, I.; Incarbone, N.; Centonze, L.; Buscemi, V.; Lauterio, A.; De Carlis, L. Impact of the COVID-19 pandemic on liver donation and transplantation: A review of the literature. World J. Gastroenterol. 2021, 27, 928–938.
  136. COVIDSurg Collaborative; GlobalSurg Collaborative. Timing of surgery following SARS-CoV-2 infection: An international prospective cohort study. Anaesthesia 2021, 76, 748–758.
  137. Deng, J.Z.; Chan, J.S.; Potter, A.L.; Chen, Y.W.; Sandhu, H.S.; Panda, N.; Chang, D.C.; Yang, C.J. The Risk of Postoperative Complications After Major Elective Surgery in Active or Resolved COVID-19 in the United States. Ann. Surg. 2022, 275, 242–246.
  138. Haffner, M.R.; Le, H.V.; Saiz, A.M., Jr.; Han, G.; Fine, J.; Wolinsky, P.; Klineberg, E.O. Postoperative In-Hospital Morbidity and Mortality of Patients With COVID-19 Infection Compared With Patients Without COVID-19 Infection. JAMA Netw. Open 2021, 4, e215697.
  139. Webb, G.J.; Marjot, T.; Cook, J.A.; Aloman, C.; Armstrong, M.J.; Brenner, E.J.; Catana, M.A.; Cargill, T.; Dhanasekaran, R.; García-Juárez, I.; et al. Outcomes following SARS-CoV-2 infection in liver transplant recipients: An international registry study. Lancet Gastroenterol. Hepatol. 2020, 5, 1008–1016.
  140. Colmenero, J.; Rodríguez-Perálvarez, M.; Salcedo, M.; Arias-Milla, A.; Muñoz-Serrano, A.; Graus, J.; Nuño, J.; Gastaca, M.; Bustamante-Schneider, J.; Cachero, A.; et al. Epidemiological pattern, incidence, and outcomes of COVID-19 in liver transplant patients. J. Hepatol. 2021, 74, 148–155.
  141. Ridruejo, E.; Soza, A. The liver in times of COVID-19: What hepatologists should know. Ann. Hepatol. 2020, 19, 353–358.
  142. Merli, M.; Perricone, G.; Lauterio, A.; Prosperi, M.; Travi, G.; Roselli, E.; Petrò, L.; De Carlis, L.; Belli, L.; Puoti, M. Coronaviruses and Immunosuppressed Patients: The Facts During the Third Epidemic. Liver Transpl. 2020, 26, 1543–1544.
  143. Miarons, M.; Larrosa-García, M.; García-García, S.; Los-Arcos, I.; Moreso, F.; Berastegui, C.; Castells, L.; Pérez-Hoyos, S.; Varela, J.; Pau-Parra, A.; et al. COVID-19 in Solid Organ Transplantation: A Matched Retrospective Cohort Study and Evaluation of Immunosuppression Management. Transplantation 2021, 105, 138–150.
  144. Saigal, S.; Gupta, S.; Sudhindran, S.; Goyal, N.; Rastogi, A.; Jacob, M.; Raja, K.; Ramamurthy, A.; Asthana, S.; Dhiman, R.K.; et al. Liver transplantation and COVID-19 (Coronavirus) infection: Guidelines of the liver transplant Society of India (LTSI). Hepatol. Int. 2020, 14, 429–431.
  145. Domínguez-Gil, B.; Fernández-Ruiz, M.; Hernández, D.; Crespo, M.; Colmenero, J.; Coll, E.; Rubio, J.J. Organ Donation and Transplantation During the COVID-19 Pandemic: A Summary of the Spanish Experience. Transplantation 2021, 105, 29–36.
  146. Hong, H.L.; Kim, S.H.; Choi, D.L.; Kwon, H.H. A case of coronavirus disease 2019-infected liver transplant donor. Am. J. Transplant. 2020, 20, 2938–2941.
  147. Cho, H.J.; Koo, J.W.; Roh, S.K.; Kim, Y.K.; Suh, J.S.; Moon, J.H.; Sohn, S.K.; Baek, D.W. COVID-19 transmission and blood transfusion: A case report. J. Infect. Public Health 2020, 13, 1678–1679.
  148. Kates, O.S.; Fisher, C.E.; Rakita, R.M.; Reyes, J.D.; Limaye, A.P. Emerging evidence to support not always “just saying no” to SARS-CoV-2 positive donors. Am. J. Transplant. 2020, 20, 3261–3262.
  149. Schold, J.D.; Koval, C.E.; Wee, A.; Eltemamy, M.; Poggio, E.D. Utilization and outcomes of deceased donor SARS-CoV-2-positive organs for solid organ transplantation in the United States. Am. J. Transplant. 2022, 22, 2217–2227.
  150. Bock, M.J.; Vaughn, G.R.; Chau, P.; Berumen, J.A.; Nigro, J.J.; Ingulli, E.G. Organ transplantation using COVID-19-positive deceased donors. Am. J. Transplant. 2022, 22, 2203–2216.
  151. Mazzola, A.; Kerbaul, F.; Atif, M.; Monsel, A.; Malaquin, G.; Pourcher, V.; Scatton, O.; Conti, F. The impact of Coronavirus 19 disease on liver transplantation in France: The sickest first approach? Clin. Res. Hepatol. Gastroenterol. 2020, 44, e81–e83.
  152. Mouch, C.A.; Alexopoulos, S.P.; LaRue, R.W.; Kim, H.P. Successful liver transplantation in patients with active SARS-CoV-2 infection. Am. J. Transplant. 2022, 22, 2694–2696.
  153. Kidson, K.M.; Park, J.; Charles, M.K.; Omar, M.; Krajden, M.; Wright, A.J.; Hussaini, T.; Kim, P.T.W.; Chung, S.W.; Yoshida, E.M. Successful Liver Transplantation in a Patient With Acute COVID-19 Infection and Acute Liver Failure: A Case Report. Transplant. Direct 2021, 7, e747.
  154. Jacob, R.; Liu, K.; Marinelli, T. Successful liver transplantation for hepatitis B-related acute liver failure in a patient with active COVID-19. Transpl. Infect. Dis. 2022, 24, e13889.
  155. Yohanathan, L.; Campioli, C.C.; Mousa, O.Y.; Watt, K.; Friedman, D.Z.P.; Shah, V.; Ramkissoon, R.; Hines, A.S.; Kamath, P.S.; Razonable, R.R.; et al. Liver transplantation for acute liver failure in a SARS-CoV-2 PCR-positive patient. Am. J. Transplant. 2021, 21, 2890–2894.
  156. Parums, D.V. Editorial: SARS-CoV-2 mRNA Vaccines and the Possible Mechanism of Vaccine-Induced Immune Thrombotic Thrombocytopenia (VITT). Med. Sci. Monit. 2021, 27, e932899.
  157. Vera-Lastra, O.; Ordinola Navarro, A.; Cruz Domiguez, M.P.; Medina, G.; Sánchez Valadez, T.I.; Jara, L.J. Two Cases of Graves’ Disease Following SARS-CoV-2 Vaccination: An Autoimmune/Inflammatory Syndrome Induced by Adjuvants. Thyroid 2021, 31, 1436–1439.
  158. Kreuter, A.; Licciardi-Fernandez, M.J.; Burmann, S.N.; Burkert, B.; Oellig, F.; Michalowitz, A.L. Induction and exacerbation of subacute cutaneous lupus erythematosus following mRNA-based or adenoviral vector-based SARS-CoV-2 vaccination. Clin. Exp. Dermatol. 2022, 47, 161–163.
  159. Ghielmetti, M.; Schaufelberger, H.D.; Mieli-Vergani, G.; Cerny, A.; Dayer, E.; Vergani, D.; Terziroli Beretta-Piccoli, B. Acute autoimmune-like hepatitis with atypical anti-mitochondrial antibody after mRNA COVID-19 vaccination: A novel clinical entity? J. Autoimmun. 2021, 123, 102706.
  160. Avci, E.; Abasiyanik, F. Autoimmune hepatitis after SARS-CoV-2 vaccine: New-onset or flare-up? J. Autoimmun. 2021, 125, 102745.
  161. Bril, F.; Al Diffalha, S.; Dean, M.; Fettig, D.M. Autoimmune hepatitis developing after coronavirus disease 2019 (COVID-19) vaccine: Causality or casualty? J. Hepatol. 2021, 75, 222–224.
  162. Camacho-Domínguez, L.; Rodríguez, Y.; Polo, F.; Restrepo Gutierrez, J.C.; Zapata, E.; Rojas, M.; Anaya, J.M. COVID-19 vaccine and autoimmunity. A new case of autoimmune hepatitis and review of the literature. J. Transl. Autoimmun. 2022, 5, 100140.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Gastroenterology & Hepatology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Nicolò Brandi
,
Daniele Spinelli
,
Alessandro Granito
,
Francesco Tovoli
,
Fabio Piscaglia
,
Rita Golfieri
,
Matteo Renzulli
View Times: 374
Revisions: 2 times (View History)
Update Date: 27 Mar 2023
Table of Contents
    1000/1000
    Hot Most Recent
    Video Production Service
    Feedback