key: cord-0843076-znoflibj
authors: Menon, Trishala; Sharma, Rohit; Kataria, Saurabh; Sardar, Sundus; Adhikari, Ramesh; Tousif, Sohaib; Khan, Hira; Rathore, Sawai Singh; Singh, Romil; Ahmed, Zahoor
title: The Association of Acute Kidney Injury With Disease Severity and Mortality in COVID-19: A Systematic Review and Meta-Analysis
date: 2021-03-15
journal: Cureus
DOI: 10.7759/cureus.13894
sha: bb13cfc2eb4e6ab62c70b68bfda55942a0be1273
doc_id: 843076
cord_uid: znoflibj

Background and objective The coronavirus disease 2019 (COVID-19) pandemic has become a global healthcare emergency. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, has a wide range of clinical manifestations ranging from subclinical infection to multi-organ failure. In addition to the respiratory system, COVID-19 also adversely affects the kidneys. In this study, we aimed to measure the prevalence of acute kidney injury (AKI) in COVID-19 and its association with the disease severity and mortality in COVID-19 patients. Materials and methods We conducted our study by following the Preferred Reporting Items for Systematic Review and Meta-analyses (PRISMA) guidelines. A comprehensive literature search using four databases (PubMed, EMBASE, Google Scholar, and clinicaltrial.gov) was performed. Our initial search returned 2,771 articles. After excluding review articles, duplicates, and non-relevant studies, we included 20 articles that reported an association between COVID-19 and AKI. We subsequently performed a random effect analysis to find the pooled prevalence, pooled odds ratio (OR) estimates, and 95% confidence intervals for severe COVID-19 and mortality outcomes in AKI using Cochrane RevMan (version 5.4) and R programming language (version 4.16-2). Results A total of 14,415 patients from various countries were included. Among the 20 cohorts, the median age was 55.8 ±8.39 years (range: 43-72 years), and 43.78% of the subjects were female. Out of a total of 14,415 patients, 3,820 developed AKI with a pooled prevalence of 11% (95% CI: 0.07-0.15; p<0.01; I(2)=98%). AKI was found to have a significant association with severe COVID-19 disease, with a pooled OR of 8.45 (95% CI: 5.56-12.56; p<0.00001; I(2)=0%). AKI was associated with significantly higher mortality in patients with COVID-19 with an OR of 13.52 (95% CI: 5.43-33.67; p<0.00001; I(2)=88%). Conclusion AKI manifests as a common COVID-19 complication, and COVID-19 patients with AKI generally have poor outcomes in terms of disease severity and mortality.

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of coronavirus disease 2019 . The World Health Organization declared a COVID-19 pandemic in December 2019. COVID-19 generally affects the respiratory system, and the patients predominantly manifest fever, myalgia, cough, dyspnea, and flu-like symptoms. The clinical course of the COVID-19 is highly variable, ranging from asymptomatic infection to respiratory failure, multi-organ dysfunction, and mortality. Apart from the respiratory system, COVID-19 is also associated with hazardous effects on other body systems [1, 2] . 1 2 3, 4 2 5, 6 Several studies have underlined that older patients and patients with comorbidities are more susceptible to COVID-19, its more serious complications, and progression to severe disease. Recent literature has revealed renal involvement in COVID-19 patients as well [3] . Organ dysfunction such as those involving lungs and kidneys are associated with a high mortality rate [4] . During the SARS-CoV and the Middle East Respiratory Syndrome coronavirus (MERS-CoV) epidemics, a close relationship between coronavirus infection and acute kidney injury (AKI) was observed [4] . A recent study by Chu et al. reported that 5-15% of coronavirus patients tend to develop AKI [5] . Viral entry and replication into the target cells induce systemic inflammatory responses leading to multi-organ dysfunction. AKI in these patients might be due to hypoxemia, dehydration, underlying disease, or adverse effects of administered drugs [6] .

In clinical practice, COVID-19 has had a significant impact on nephrology. Our study aimed to evaluate the association of AKI with COVID-19 and the outcomes related to the disease severity and prognosis of SARS-CoV-2 patients with AKI.

By following the Preferred Reporting Items for Systematic Review and Meta-analyses (PRISMA) guidelines, we performed a comprehensive literature search using four databases (EMBASE, PubMed, Google Scholar, clinicaltrial.gov) ( Figure 1 ). Our search stratagem relied on the use of the Medical Subject Headings (MeSH) term and keywords for "SARS-CoV-2" and "acute kidney injury" from the date of COVID-19's inception to November 2020. Our initial search returned 2,771 articles. We were left with 75 full-length studies after excluding case reports, animal studies, duplicates, review articles, and irrelevant studies. We finally included 20 articles that reported an association between COVID-19 and AKI after carefully applying the inclusion and exclusion criteria. 

We exported all studies to EndNote (version 8.0). We screened 669 studies, and 20 articles met our inclusion criteria. Initially, we screened articles by titles and abstract, assessing for relevance. Language restrictions were not imposed. Review articles were excluded. The studies with specialized populations such as cancer and pediatric patients and patients with chronic kidney disease (CKD) and end-stage renal disease (ESRD) were also excluded. We also excluded case reports and randomized clinical trials for drugs. In the beginning, we included full-length articles and then screened each cohort for inclusion criteria. We had prospective and retrospective studies reporting severe COVID-19 and AKI and studies with a more generalized population and detailed extractable AKI-related data. Three authors screened all the articles and assessed full-length studies for inclusion and exclusion criteria. We resolved the disagreements through consensus.

We extracted the clinical information and relevant data using a standard Excel sheet. We reported age, gender ratio, publication year, and country where the study was conducted. We also tabulated outcomes, including AKI incidence ( Table 1) . In our study, the primary outcomes of interest were severe disease and death. We assessed the quality of studies using the Newcastle-Ottawa Scale (NOS) for quality assessment (Appendices). We also evaluated for the selection bias and small study effects using a random effect funnel plot model. 

We finally included 20 studies from various countries. We performed a random effect analysis to find the pooled prevalence, pooled odds ratio (OR) estimates, and 95% confidence intervals for severe COVID-19 and mortality outcomes in AKI using the 'meta' package by Schwarzer et al. in the R programming language (version 4.16-2), and Cochrane RevMan (version 5.4). The inter-study heterogeneity among the studies was assessed using the Q statistic proposed by Cochrane and the I 2 index introduced by Higgins and Thompson. We interpreted the values greater than 50% and 70% to be of moderate and high heterogeneity, respectively. The funnel plot was used to explore the publication bias.

In our study, a total of 2,771 articles were screened, of which 75 full-length studies were further assessed for eligibility, and 20 articles ultimately met the inclusion criteria. These articles involved 14 Twelve studies provided sufficient data in their stated outcomes to measure the association of AKI with the severity of COVID-19. AKI was found to have a significant association with severe COVID-19, with a pooled OR of 8.45 (95% CI: 5.56-12.86) compared with patients with the nonsevere disease ( Figure 3) . The results were significant (p<0.00001), and heterogeneity was negligible (I 2 =0%). The funnel plot showing the association between AKI and severe COVID-19 is presented in Figure 4 . Eight studies provided enough data on mortality in COVID-19 patients with AKI. AKI was associated with significantly higher mortality in patients with COVID-19 with an OR of 13.52 (95% CI: 5.43-33.67). The results were statistically significant (p<0.00001), and heterogeneity was high (I 2 =88%) ( Figure 5 ).

AKI: acute kidney injury; COVID-19: coronavirus disease 2019

Although respiratory system involvement is the most prevalent feature of SARS-CoV-2, the infection is generally mild; however, severe infection can lead to severe pneumonia, acute respiratory distress syndrome (ARDS), and multi-organ dysfunction, including that affecting the kidneys. Kidney dysfunction is generally mild; however, it is significantly worse in patients with pneumonia. Generally, kidney dysfunction is characterized by hematuria, proteinuria, and elevated serum creatinine and blood urea nitrogen (BUN) levels. BUN and serum creatinine levels, being significant AKI indicators, have been reportedly higher in patients with nonsevere COVID-19 than in patients with pneumonia [5] . This analysis provides evidence of COVID-19 prevalence and association of AKI with the severity and mortality in COVID-19 patients. Our study reported a more potent association between AKI and severe COVID-19 with a pooled prevalence of p<0.00001; I 2 =88%). Patients with COVID-19 coupled with AKI have a poor prognosis, and it serves as an independent risk factor for all-cause in-hospital deaths in COVID-19 patients.

Since the emergence of the COVID-19 pandemic, several studies have reported on the prevalence, severity, and prognosis of COVID-19 combined with AKI. A recent study reported a 3% incidence of AKI in hospitalized patients, and this incidence rate increased to 19% when patients with severe disease were included [24] . Moreover, Potere et al. have revealed that the prevalence of AKI was reported to be 6% in hospitalized patients [25] . Lim et al. have reported increased disease severity and mortality in patients with AKI, and the need for ICU care in COVID-19 patients with AKI [26] . Furthermore, in a study by Ali et al., severe AKI was associated with high mortality (relative risk: 3.08; 95% CI: 1.54-6.19) [27] . AKI in COVID-19 is measured as a key marker of severity and has a negative impact on patient survival [2] . We cannot estimate the real burden of AKI in COVID-19 because the serum creatinine value might not reflect the valid preadmission values, and previous serum creatinine values might not be available at that time [21] .

Many recent studies have revealed that AKI has a remarkable prevalence in COVID-19 patients, especially those in ICU. The confirmed proportion of AKI in COVID-19 is variable; however, as per the available data, AKI has a prevalence of more than 20% in hospitalized patients and more than 50% in ICU patients [2, 17, 20, 21] . A recent study by Wang et al. reported a significant association between AKI and severe COVID-19 (OR: 11.88; 95% CI: 9. 29-15.19) and also reported high mortality in COVID-19 patients (OR: 30.46; 95% CI: 18.33-50-59) [28] . Our study also observed a similar trend, revealing a higher association between AKI and severe SARC-CoV-2 infection (p<0.00001) and increased mortality in AKI patients (p<0.00001). Early detection of AKI and appropriate therapeutic measures are essential to limit morbidity and mortality.

The pathophysiology of AKI in COVID-19 patients is yet to be determined. Several mechanisms have been proposed, including chronic medical conditions such as arterial hypertension, chronic kidney disease, diabetes mellitus, hypovolemic conditions, contrast media, and nephrotoxic drugs. Angiotensin-converting enzyme 2 (ACE2) receptors are the key mediator of viral entry and replication in the host cell. These receptors in multiple organs enable the involvement of different systems, including kidneys and respiratory, nervous, and gastrointestinal systems. In kidneys, ACE2 receptors are expressed in podocytes and apical brush borders of proximal convoluted tubules. ACE2 receptors mediate the viral attachment and entry into the kidney and are responsible for replicating SARS-CoV-2 in the host cells [29] . SARS-CoV-2 also induces an imbalanced activation of the renin-angiotensin-aldosterone system (RAAS), resulting in the downregulation of ACE2 receptors, thereby leading to an increase in angiotensin II. Unprovoked RAAS activation results in a cytokine storm, inflammation, arterial constriction, and fibrosis, and thrombosis at the nephron level [5, 24] . Gabarre et al. have proposed that cytopathic activity, cytokine storm, hypoperfusion, and microvascular and intravascular coagulation lead to AKI development in COVID-19 patients [30] . The patients with severe COVID-19 have a high level of inflammatory cytokines, leading to the development of AKI.

Our study has several limitations. We have not included any randomized clinical trials, and all the studies were retrospective or prospective in nature. The individual patient data from each article could not be assessed; thus, we could not make our adjustments. Another limitation is the presence of publication bias, as negative studies were less likely to be published. Also, data on COVID-19 patients is rapidly growing, and many cohorts had a comparatively short follow-up duration and presence of limitations in their detailed description. Moreover, this rapidly emerging data make the retrieval of complete evidence on the subject difficult. We have not included the preprint of the studies, as well as abstracts. AKI after COVID-19 has a significant impact on disease severity and mortality. Our study reported a steady association between AKI and unfavorable outcomes, such as mortality. Given the extent of AKI's impact on COVID-19, emerging literature must provide more comprehensive data on the extent and severity of kidney injury to allow for a proper understanding of the disease prognosis and a comprehensive, resourceful strategy to be adopted during this pandemic.

There is a growing body of evidence to show that AKI develops in a considerable number of COVID-19 patients, and the condition is significantly associated with adverse outcomes in patients with COVID-19. Thus, it is imperative to exercise extraordinary caution while monitoring the kidney functions of patients regardless of comorbidities and initiating supportive interventions that are surely protective for renal functions in the early stages of SARS-CoV-2 infection. We believe this study will contribute to the physician's essential preparation, which is of utmost significance to managing kidney injury. The only possible way to limit the succeeding AKI in COVID-19 and further progression to more severe stages is to recognize the kidney involvement in COVID-19 at early stages and use preventive and therapeutic measures to reduce morbidity and mortality. Further high-quality data from studies to explore the potential mechanism of the association of AKI with COVID-19 and the underlying cause of mortality are warranted.

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Human subjects: Consent was obtained or waived by all participants in this study. Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.