key: cord-0759811-u13eqme3
authors: Sabaghian, Tahereh; Kharazmi, Amir Behnam; Ansari, Ali; Omidi, Fatemeh; Kazemi, Seyyedeh Neda; Hajikhani, Bahareh; Vaziri-Harami, Roya; Tajbakhsh, Ardeshir; Omidi, Sajjad; Haddadi, Sara; Shahidi Bonjar, Amir Hashem; Nasiri, Mohammad Javad; Mirsaeidi, Mehdi
title: COVID-19 and Acute Kidney Injury: A Systematic Review
date: 2022-04-04
journal: Front Med (Lausanne)
DOI: 10.3389/fmed.2022.705908
sha: f499f93aa5fee7edda0df0ae746fa7dfc8937cde
doc_id: 759811
cord_uid: u13eqme3

INTRODUCTION: Acute kidney injury (AKI) has been associated with an increased mortality rate among hospitalized patients with Coronavirus disease 2019 (COVID-19). The current review aimed to evaluate the symptoms, complications, and treatments performed to manage AKI in patients with COVID-19. METHODS: We searched PubMed/Medline, Web of Science, and Embase for the relevant scientific literature published up to February 1, 2022. The following keywords were used: “COVID-19”, “SARS-CoV-2”, and “Acute kidney injury”. RESULTS: Forty-four studies with a total number of 114 COVID-19 patients with AKI (Mean age: 53.6 years) were included in our systematic review. The most common comorbidities in patients with COVID-19 suffering from AKI were the history of diabetes, hypertension, and hyperlipidemia. Twelve out of the 44 included studies reported a history of chronic kidney disease (CKD) in this group of patients. Focal segmental glomerulosclerosis (FSGS) and acute tubular necrosis (ATN) were the most common pathological evidence. The average length of hospital stay was 19 days, and the average duration of need for mechanical ventilation was 3 days. CONCLUSIONS: The current systematic review shows that AKI frequently complicates the course of COVID-19 hospitalizations and is associated with increased severity of illness, prolonged duration of hospitalization, and poor prognosis. Given the extent of the adverse impact of AKI, early detection of comorbidities and renal complications is essential to improve the outcomes of COVID-19 patients.

Acute kidney injury (AKI) has been associated with an increased mortality rate among hospitalized patients with Coronavirus disease 2019 (COVID- 19 ). An incidence rate of around 10% was reported in these patients. This incidence could be associated with age, disease severity, and ethnicity. Studies have shown that AKI could be closely related to the effect of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which is the causative agent of COVID-19, on the kidney rather than any side effect of experimental drugs for COVID-19 such as remdesivir (1) .

According to a recent meta-analysis incidence of AKI in COVID-19 was 8.9% (2) . This was close to the incidence rate of AKI in patients with community-acquired pneumonia. However, there was statistical heterogeneity among the studies (2) . Other meta-analysis studies have shown that males have higher mortality among COVID-19 patients (3) . Another systematic review and meta-analysis revealed that being male and diabetic in COVID-19 patients were associated with developing AKI (4) . Studies from the USA and Europe presented a pooled incidence of 28.6% and 7.7% for AKI, respectively (5) . AKI has also been detected as a predictor of fatality and severe COVID-19 infection (5) .

Due to the importance of this issue, the current study aimed to evaluate the symptoms, complications, and treatments performed to manage AKI in patients with COVID-19 as a comprehensive systematic review.

This review conforms to the "Preferred Reporting Items for Systematic Reviews and Meta-Analyses" (PRISMA) statement (6) .

We searched PubMed/Medline, Web of Science, and Embase for relevant studies, published up to February 1, 2022.

The following terms were used in the search strategy: COVID-19, severe acute respiratory syndrome coronavirus 2, SARS-CoV-2, and acute kidney injury. Only studies written in English were selected.

The records found through database searching were merged, and the duplicates were removed using EndNote X7 (Thomson Reuters, Toronto, ON, Canada). Two reviewers (TS and FO) independently screened the records by title/abstract and full text to exclude those unrelated to the study objectives. Included studies met the following criteria: (1) COVID-19 patients diagnosed with reference standard test; (2) AKI defined according to the Kidney Disease Improving Global Outcomes (KDIGO) guidelines (7) . The KDIGO guidelines define AKI as follows: increase in serum creatinine by ≥0.3 mg/dL (≥26.5 micromol/L) within 48 hours, or increase in serum creatinine to ≥1.5 times baseline, which is known or presumed to have occurred within the prior seven days, or Urine volume <0.5 mL/kg/h for 6 hours. Furthermore, different stages of AKI was defined as follows: Stage 1; increase in serum creatinine to 1.5-1.9 times baseline, or increase in serum creatinine by ≥0.3 mg/dL (≥26.5 micromol/L), or reduction in urine output to <0.5 mL/kg/h for 6-12 h. Stage 2; increase serum creatinine to 2.0-2.9 times baseline, or reduce urine output to <0.5 mL/kg/h for ≥12 hours. Stage 3; increase in serum creatinine to 3.0 times baseline, or increase in serum creatinine to ≥4.0 mg/dL (≥353.6 micromol/L), or reduction in urine output to <0.3 mL/kg/h for ≥24 h, or anuria for ≥12 h, or the initiation of kidney replacement therapy, or, in patients <18 years, decrease in estimated glomerular filtration rate (eGFR) to <35 mL/min/1.73 m 2 .

Two reviewers (TS and FO) designed a data extraction form and extracted data from all eligible studies, with differences being resolved by consensus. Data such as country of origin, the number of patients with AKI, the number of patients with confirmed COVID-19, clinical symptoms, laboratory findings, outcomes, diagnostic methods, and treatment were extracted from the selected articles.

A total of 784 records were found in the initial search; after removing duplicate articles, the titles and abstracts of 506 references were screened (Figure 1 ). Of these, 89 articles were selected for a full-text review. After the full-text review, 44 articles met the inclusion criteria.

The KDIGO criteria were used in all selected papers to define AKI. A total of 114 COVID-19 patients with AKI (Mean age: 53.6 years) were included in the current study ( Table 1) .

Stages of AKI in patients with COVID-19 are presented in Table 2 .

As shown in Table 3 , AKI in admission was reported in 35 of 64 studied patients (56.2%), while 38 out of 51 patients (75.5%) showed AKI after admission.

BMI of patients with COVID-19 suffering from AKI was studied in 21 publications. The results showed that most patients (31/44) had a BMI in the range of 18.5-24.9 ( Table 3) .

The most common comorbidities were the history of diabetes, hypertension, and hyperlipidemia which were present in 40/100 (40%), 59/96 (61.4%), and 12/21 (57.1%) of patients with COVID-19 and AKI, respectively. According to the results of the included studies, 64.7% of patients received angiotensinconverting inhibitor/angiotensin receptor blocker (ACE/ARB), and 62.5% received diuretics. Also, 93.3% of the studied patients were taking oral diabetes medications. A history of chronic kidney disease (CKD) were reported in 12 out of the 54 evaluated patients (22.2%) . More information about reported comorbidities in patients with COVID-19 and AKI can be found in Table 3 .

Fever (91.5%), dyspnea (84.6%), shortness of breath (76%), cough (66%), hypotension (55.5%), loss of smell and taste (50%), and diarrhea (46.6%) were the most common symptoms. Based on the results of the included studies, 34 out of 37 patients (91.8%) showed a blood oxygen saturation level of less than 93%. However, ten other studies showed that 84.6% of patients had oxygen saturation levels higher than 93% ( Table 3) .

Imaging results from 9 studies demonstrated lung involvement in more than 50% of evaluated patients (71.4%). Computed tomography (CT) scans revealed that consolidation was another common finding in 72.2% of patients ( Table 3) .

Focal segmental glomerulosclerosis (FSGS) and acute tubular necrosis (ATN) were the most common pathological evidence ( Table 3) .

In terms of prognosis, intensive care unit (ICU) hospitalization and the need for a ventilator were reported in most of the involved patients ( Table 3) .

The average length of hospital stay was 19 days, and the average duration of need for mechanical ventilation was 3 days.

Most studies reported significant laboratory findings in patients with COVID-19 and AKI. 7/9 (77.7%), 4/4 (100%), and 13/18 (72.2%) of patients showed leukopenia, leukocytosis, and lymphopenia, respectively. High C-reactive protein (CRP) and low albumin were reported in 38/41 (92.7%) and 6/6 (100) of COVID-19 patients with AKI, respectively. Fifteen studies reported proteinuria, according to which 97.4% of patients (38/39) had this problem. Hematuria was seen in 21/34 (61.8%) patients from 11 studies. High creatine phosphokinase (CPK) was also reported in 8 studies ( Table 4) .

As shown in Table 5 , remdesivir, was the most frequently used antiviral agent. Intubation was also reported as the most common non-pharmacological treatment strategy. Furthermore, 33 out of 38 evaluated patients (86.8%) required hemodialysis.

In this systematic review, a total of 114 COVID-19 patients with AKI were identified. In prior studies, the prevalence of AKI in COVID-19 patients has been reported widely ranged from 0.5% in China by Guan et al. (51) to 80% in critically ill COVID-19 patients in France by Rubin et al. (52) . Xu et al. reported that AKI incidence in COVID-19 patients was 10% and increased to 26% in the ICU-admitted subgroup of patients (1) . Silver et al. demonstrated that AKI occurred in 30% of COVID-19 hospitalized patients and that the risk increased to more than 45% in patients requiring ICU admission. The heterogeneity in the reports of AKI incidence between studies could be explained by: (1) variation of the definition of "severe" disease, (2) the differences in admission criteria and hospital care, (3) genetic predisposition to kidney involvement, (4) differences in the frequency of kidney function measurement, and (5) kidney replacement therapy (KRT) resource limitations (53, 54) . In recent studies, kidney tissue sample analysis shed some light on potential pathophysiological mechanisms responsible for COVID-19 related AKI. Commonly cited hypotheses include: (1) tubular epithelial and podocyte damage due to highly expressed angiotensin-converting enzyme-2 (ACE2) in proximal tubular epithelial cells and podocytes, which serves as an entrance door for SARS-COVID-19, causing ATN (55-57), (2) direct infection of glomerular endothelia, causing FSGS (58), (3) COVID-19 related hypovolemia which leads to pre-renal AKI (59), (4) complement activation, cytokine storm, hypercoagulability and microangiopathy which can lead to multiple organ damage especially acute cardiac and lung injury and subsequent AKI via hypoxia and hypotension (55, 60, 61) , (5) nephrotoxic drugs or contrast media (59) , and (6) comorbidities like diabetes mellitus and hypertension which confer renal vulnerability to AKI (59).

As mentioned above, ATN and FSGS were the most common pathological findings in COVID-19 positive AKI in the current study. FSGS was pathologically investigated in all patients evaluated in the related studies (100%). Likewise, the pathological findings of ATN were also observed in 93.7% of patients. The most common comorbidities reported in this systematic review, including the history of diabetes mellitus, hypertension, hyperlipidemia, and CKD, were present in 40%, 61.4%, 57.1%, and 22.2% of patients with COVID-19 and AKI, respectively. Based on the growing consensus and evidence, factors including older age, diabetes, hypertension, cardiovascular disease, high BMI, CKD, immunosuppression for any reason, and smoking are the potential risk factors for COVID-19 AKI (62) (63) (64) . Some laboratory factors including leukocytosis, lymphopenia, elevated CRP, elevated ferritin (62), haematuria and proteinuria (65, 66) were also associated with COVID-19 AKI; which are reported 100, 72.2, 92.7, 88.9, 61.8 and 97.4%, respectively. In terms of prognosis, ICU hospitalization and the need for assisted ventilation were commonly reported in 86.7 and 87.5% of involved patients, respectively. In patients with COVID-19 and AKI, the overall hospital mortality was 66.2%, comparable with early reports (67, 68) .

AKI is considered an independent risk factor for increased mortality in critically ill patients of any disease, including COVID-19 (69) . Kidney involvement has also been reported as an indicator of poor prognosis regardless of initial COVID-19 severity (68), which makes early detection and treatment of renal abnormalities improve the vital prognosis of COVID-19 patients.

According to the previous studies, the burden of CKD following COVID-19-related AKI may be substantial, and AKI has been linked to an increased risk of CKD in individuals with previously normal renal function (70, 71) . It is essential to say that pre-existing CKD and AKI have been described as predictors of severe and critical illness in patients with COVID-19, with a higher mortality rate than patients without kidney deficiency.

The lack of effective treatments for patients with COVID-19 and AKI has required repurposing several drugs, including remdesivir. The current systematic review indicated that remdesivir, was the most frequently used antiviral agent. These compounds may induce AKI and are not recommended in patients with poor renal function. Thus, early detection and specific therapy of renal changes, including adequate hemodynamic support and avoidance of nephrotoxic drugs, may help to improve critically ill patients with COVID-19.

Our systematic review has some limitations. First, since included studies were case reports articles with a low number of patients, the generalizability of our findings may be limited. Second, detailed information on patient characteristics was lacking in the published articles, and the potential influence of pre-existing conditions could not be investigated. Furthermore, studies' variability and different patients' characteristics were other limitations.

In conclusion, this systematic review shows that AKI frequently complicates the course of COVID-19 hospitalizations and is associated with increased severity of illness, prolonged duration of hospitalization, and poor prognosis. Given the extent of the adverse impact of AKI, it is imperative that early detection of comorbidities and renal complications is essential to improve the outcomes of COVID-19 patients. Further research on large scales is warranted to improve our understanding of this disease and design clinical approaches to managing COVID-19 related AKI.

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s. 

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Conflict of Interest: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest