Assessment of Kidney Involvement in COVID-19 Patient – Cureus

Background and aim: Physicians need to be aware of the difficulties that SARS-CoV-2 infection brings to other regions of the body, such as the kidneys, even though the key emphasis is on pulmonary characteristics.The most frequent kidney complication among COVID-19 hospitalized patients is considered acute kidney injury (AKI). This study aimed to describe overall different aspects of acute kidney injury (AKI) in COVID-19 patients admitted to JLNMCH during the COVID-19 pandemic and to determine the prevalence of AKI among COVID-19 hospitalized patients.

Methods and materials: All adult patients (over the age of 18 years) who screened positive for COVID-19 in a swab specimen from areas ofnasopharyngealby reverse transcriptase polymerase chain reactionand then hospitalized were included in the study. Information was gathered on the patient's demographics, general medical history, and drugs prescribed. From past medical information, associated comorbiditiesand home pharmaceuticals were identified. We gathered hospitalization information, such as duration of stay in ICU, details about the application ofmechanical ventilation, information regardingextracorporeal membrane aeration, details of the use ofvasopressor administration, and baselineresults of laboratory test along withbaseline clinical information during 48 hours of hospitalization.

Results: The percentage of patients with no history of AKI requiring traumatic mechanical ventilation was 79.4%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 11.5%. The difference was relevant statistically (p<0.001). The percentage of patients with AKI of any stage requiring traumatic mechanical ventilation was 22.8%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 76.8%. The difference was relevant statistically (p<0.022).

Conclusion: We discovered that AKI was a rather typical finding among hospitalized COVID-19 patients. Patients hospitalized for COVID-19 had a poor prognosis if they developed AKI.

The COVID-19 virus has spread globally. The reason there have been so many confirmed cases is that the virus spreads through close contact between people who coughand sneeze while exchanging droplets or aerosols. Engaging on infected surfaces and subsequently touching transmission points like the areas ofmouth, areas ofeyes, and areas ofnose can also result in infection [1,2]. The completerespiratory organ system isthe principal organ systemaffected by COVID-19 infection, which inextreme situations manifests as conditions of pneumonia, hypoxemia, and acute respiratory distress syndrome. Physicians need to be aware of the difficulties that SARS-CoV-2 infection brings to other regions of the body, such as the kidneys, even though the key emphasis is on pulmonary characteristics.The most frequent kidney complication among COVID-19 hospitalized patients is acute kidney injury considered asAKI [3,4].

SARS-CoV-2 is usually anRNA virus that spreads through mouth and nasal secretions, as well as through tiny droplets created by coughing. The reverse transcriptase-polymerase chain reaction (RT-PCR) conductedon respiratory samples acquired by making a swab ofthe areas of nasopharynxis the usual method of diagnosis. Diverse clinical presentations are possible, including multi-organ failure, mortality, moderate upper respiratory tract disease symptoms, and catastrophic acute breathing distress condition [5,6]. SARS-CoV-2 exploits angiotensin-converting enzyme-2 (ACE-2) to attack numerous organs outside the lungs. One of COVID-19's primary targets in the human bodyis the kidney.AKIis regarded as a measure of the severity of diseaseand a poor prognostic variableforpatients' survival inCOVID-19 conditions [7,8]. Patients who were diagnosed with severe AKI, which was defined as stage 3 or greater in accordance with the recommendations of Kidney Disease Improving Global Outcomes (KDIGO), showed a larger likelihood of passing away than those who were diagnosed with AKI stages 1 and 3 in COVID-19 patients who were impacted by AKI. An increased risk of AKI may occur in individuals who have chronic diseases of the kidney, particularly those suffering from diabetic nephropathy, due to an already present increasedregulation of enzymeACE and reducedregulation ofACE-2 [9].

We saw an incredible amount of patients who experiencedAKI, at a significantly higher frequencythan those reported from China, when we managed patients suffering fromCOVID-19. According to early data from China and Italy, the rate of AKI can range between 0.5% and29%, with many of these estimates falling between these two extremes [10,11].

Clinical data includeonly critically ill ICU patients showingan overall19%risk of AKI. Variationscould be a consequence of the differentpopulations investigated and the criteria of AKI used. Beyond the rate, there hasn't been much written about AKI in COVID-19; for instance, there aren't many details of the chronology, urine tests, connection tofailure of respiratory system, in-depth analyses of the needs for renal replacement therapy for renal replacement, risk variables, or consequences afterAKI [12,13].

In this research, we wanted to describe overall different aspects of the experience of AKI in this population of COVID-19patients and to determine the prevalence of AKI among COVID-19 hospitalized patients.

This was a retrospective study conducted at Jawaharlal Nehru Medical College and Hospital during the COVID-19 epidemic, where Jawaharlal Nehru Medical College and Hospital Review Board ethical approval with IRB number JLNMCH/2021/134 was taken. The hospital health record provided the information for this investigation. All adult patients (over the age of 18 years) who screened positive for COVID-19 in a swab specimen from areas of nasopharyngeal by RT-PCRand thenhospitalized were included in the study.Transfers of patients among institutions within the same health system were handled as a single hospital engagement.

Patients were disqualified if they had undergone a kidney transplant in the past, had suffered fromend-stage renal failure, were relocated to hospitals outside the healthcare system, or had serumlevels of serum creatinine that were below 2 at the time of admission. Before the study began, the study protocol was approved by the institutional review board.We obtainedpreliminary data on AKI as well as renal replacement therapy(RRT) from8000 COVID-19 patients who died or were discharged from our hospital.

KDIGO guidelineswere used to define AKI in the following manner: stage 1 involves an elevationincreatinine level in serumof 0.3 mg/dl during 48 hor even a 1.5-foldto 1.9-fold elevation from values at baseline underseven days, stage 2 involves a 2.9-fold increase under seven days, and stage 3 involves an increment of three-foldor greaterwithin seven days or the start of RRT. Participants were divided into groups based on the maximum AKI stage they had reached while in the hospital.

By using creatinine equation developed by the ChronicDisease of KidneyEpidemiology Consortium, the estimated rate ofglomerular filtration was determined. Additionally, we gathered the findings of computerized microscopy urine analysisand urine electrolytes tests that were performed within 24 hor 48 hfollowing the onset of AKI. There was no way for this investigation to determine if a urethral catheter was in place.

The emergence of AKI was the main outcome. Hospital disposition includingdischarge of the patient from hospitalor death and the requirement for RRT were secondary results. In our healthcare system, individuals with AKI could choose between interrupted hemodialysis and continuous CRRT as their RRT options.

We gathered information on the patient's demographics, general medical history, andprescribed drugs. From past medical information, associated comorbiditiesand home pharmaceuticals were identified. We gathered hospitalization information, such as duration of stay in ICU, details about the application ofmechanical ventilation, information regardingextracorporeal membrane aeration, details of the use ofvasopressor administration, and baselineresults of laboratory test along withbaseline clinical information during 48 hof hospitalization. Numerous extra ICUs were built in unconventional hospital sections and units as a result of the COVID-19 epidemic. Therefore, an ICU stay was determined as the requirement for intrusive mechanical breathing, the requirement for vasopressorsupport, the requirement for assistance from an ICU provider, or the requirement for treatment in a designated ICU location.

For continuous variables with a normally distributed distribution, we calculated means and standard deviations (SD) for without normal distribution variables, medians and interquartile ranges (IQR), and for explanatory data, the percentagewas used. Fisher's exact tests were used to compare categorical parametersbetween individuals with AKIand without AKI, and the nonparametric Kruskal-Wallis test was used to evaluate continuous variables. We used the Kruskal-Wallis test to evaluate the clinical traits of individuals with various stages of AKI.

We used logistic regression analysis with accounting for risk factors that were different between individuals who got AKI compared to those who did not in order to determine risk factors related to the onset of AKI. Whenever the level of the risk factor was less than 0.15, variables were added to the models utilizing a stepwise construction process. A p-value of 0.05 or less was regarded as statistically significant for all two-sided statistical tests.

The mean age of study participants having no AKI was 60.3 0.05 years. The mean age of study participants having AKI of any stage was 70.1 0.13 years. Study participants having AKI stage 1 was 70.8 0.20 years, AKI stage 2 was 71.2 0.31, and AKI stage 3 was 68.1 0.24 years. The percentage of male in study participants having no AKI was 61.3%, having AKI any stage was 64.8%, having AKI stage 1 was 61.1%, having AKI stage 2 was 61.7%, and having AKI stage 3 was 71.5%. The percentage of female in study participants having no AKI was 41.9%, having AKI any stage was 37.4%, having AKI stage 1 was 41.1%, having AKI stage 2 was 42.6% and having AKI stage 3 was 26.8%(Table 1). AKI was significantly associated with old age and the male gender(Table 1).

The percentage of COVID-19 study participants with history of hypertension was as follows: no AKI (51.5%), AKI any stage (65.8%), AKI stage 1 (68.3%), AKI stage 2 (65.2%), and AKI stage 3 (62.6%). The percentage of COVID-19 study participants with history of coronary artery disease was as follows: no AKI (10.0%), AKI any stage (15.5%), AKI stage 1 (15.7%), AKI stage 2 (17.1%), and AKI stage 3 (14.1%). The percentage of COVID-19 study participants with history of heart failure was as follows: no AKI (5.1%), AKI any stage (11.4%), AKI stage 1 (13.1%), AKI stage 2 (11.5%), and AKI stage 3 (8.9%). The percentage of COVID-19 study participants with history of peripheral, vascular disease was as follows: no AKI (2.1%), AKI any stage (4.1%), AKI stage 1 (3.4%), AKI stage 2 (5.0%), and AKI stage 3 (4.4%).The percentage of COVID-19 study participants with history of diabetes was as follows: no AKI (31.2%), AKI any stage (43.7%), AKI stage 1 (41.8%), AKI stage 2 (42.3%), and AKI stage 3 (45.6%).The percentage of COVID-19 study participants with history of HIV was as follows: no AKI (0.9%), AKI any stage (0.7%), AKI stage 1 (0.8%), AKI stage 2 (1.1%), and AKI stage 3 (0.4%).The percentage of COVID-19 study participants with history of chronic obstructive pulmonary disease was as follows: no AKI (4.5%), AKI any stage (8.7%), AKI stage 1 (10.2%), AKI stage 2 (9.3%), and AKI stage 3 (8.2%)(Table 2).

The values of SCr in mg/dl at the time of admission in different categories of COVID-19 patients were as follows: no AKI (0.97), AKI any stage (1.36), AKI stage 1 (1.38), AKI stage 2 (1.33), and AKI stage 3 (1.32). The values of SCr in mg/dl at the time of discharge in different categories of COVID-19 patients were as follows: no AKI (0.92), AKI any stage (1.52), AKI stage 1 (1.23), AKI stage 2 (1.59), and AKI stage 3 (4.46). The values of peak SCr in mg/dl in different categories of COVID-19 patients were as follows: no AKI (1.20), AKI any stage (2.61), AKI stage 1 (1.72), AKI stage 2 (2.35), and AKI stage 3 (5.42). The values of median SCr in mg/dl in different categories of COVID-19 patients were as follows: no AKI (0.97), AKI any stage (1.31), AKI stage 1 (1.15), AKI stage 2 (1.21), and AKI stage 3 (2.16).The values of eGFR at admission expressed in ml/min/1.73 m2 in different categories of COVID-19 patients were as follows: no AKI (83.6), AKI any stage (57.1), AKI stage 1 (55.3), AKI stage 2 (54.2), and AKI stage 3 (63.1). The values of eGFR at discharge was expressed in ml/min/1.73 m2 in different categories of COVID-19 patients were as follows: no AKI (95.1), AKI any stage (46.1), AKI stage 1 (70.1), AKI stage 2 (51.0), and AKI stage 3 (15.1) (Table 3).

There was an analysis regarding the need for invasive mechanical ventilation in different categories of COVID -19 patients. The percentage of patients with no history of AKI requiring traumatic mechanical ventilation was 79.4%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 11.5%. The difference was statistically relevant (p<0.001). The percentage of patients with AKI of any stage requiring traumatic mechanical ventilation was 22.8%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 76.8%. The difference was statistically relevant (p<0.022). The percentage of patients with AKI stage 1 requiring traumatic mechanical ventilation was 16.4%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 24.4%. The difference was not statistically relevant (p<0.062). The percentage of patients with AKI stage 2 requiring traumatic mechanical ventilation was 4.3%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 22.0%. The difference was statistically relevant (p<0.052). The percentage of patients with AKI stage 3 requiring traumatic mechanical ventilation was 2.7%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 44.6%. The difference was statistically relevant(p<0.001). The percentage of patients with renal replacement therapy requiring traumatic mechanical ventilation was 0.3%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 24.3%. The difference was statistically relevant (p<0.001)(Table 4).

When there was analysis regarding factors associated with AKI in patients with COVID-19 then it was found that factors like old age, male gender, history of diabetes, hypertension, cardiovascular disease, mechanical ventilation, use of vasoactive medication, and use of angiotensin-converting enzyme-1 (ACE-1) or angiotensin receptor blocker (ARB) were associated with AKI significantly(Table 5).

When we treated COVID-19 patients, we observed a staggering number of patients who had AKI, at a frequency that was noticeably higher than those reported from China. The rate of AKI can range from 0.5%to 29%, with many of these estimates falling between these two extremes, according to early data from China and Italy. Only critically sick ICU patients are included in clinical data, and the total risk of AKI is 19%. Variations may result from the many populations examined and the various AKI criteria applied [14,15].Except for the rate, not much has been written about AKI in COVID-19; for example, there are few details about the chronology, urine tests, connection to respiratory system failure, in-depth analyses of the needs for renal replacement therapy for renal replacement, risk factors, or consequences after AKI [16,17].

We aimed to find out the prevalence of AKI among hospitalized COVID-19 patients and describe the various general characteristics of AKI experience in this cohort of patients. KDIGO guidelineswere used to define AKI in the following manner: stage 1 involves an elevationincreatinine level in serumof 0.3 mg/dl during 48 hor even a 1.5-foldto 1.9-fold elevation from values at baseline underseven days, stage 2 involves a 2.9-fold increase under seven days, and stage 3 involves an increment of three-foldor greaterwithin seven days or the start of RRT. Participants were divided into groups based on the maximum AKI stage they had reached while in the hospital.

Thirty-four patients with AKI/CKD were admitted to JLNMCH, Bhagalpur, during the COVID-19 pandemic. Out of 8000 patients with COVID-19 admitted in JLNMCH, 460 patients were admitted to ICU of which we had 34 patients who went for renal dialysis. Seven patients were of AKI and the rest was CKD. In patients with AKI, serum creatinine levels were found between seven and 16, while in patients with CKD, the level was between five and 12. Patients usually had a history of diabetes and hypertension in CKD while anuria was the major complaint of AKI. Hemoglobin level was markedly reduced in patients with CKD.

When there was analysis regarding factors associated with AKI in patients with COVID-19 then it was found that factors like old age, male gender, history of diabetes, hypertension, cardiovascular disease, mechanical ventilation, use of vasoactive medication and use of ACE-1 or ARB were associated with AKI significantly.

In this study, the mean age of participants having no AKI was 60.3 0.05 years, participants having AKI of any stage was 70.1 0.13 years, participants having AKI stage 1 was 70.8 0.20 years, participants having AKI stage 2 was 71.2 0.31, and participants having AKI stage 3 was 68.1 0.24 years. The percentage of male study participants having no AKI was 61.3%, having AKI of any stage was 64.8%, having AKI stage 1 was 61.1%, having AKI stage 2 was 61.7%, and having AKI stage 3 was 71.5%. The percentage of female study participants having no AKI was 41.9%, having AKI any stage was 37.4%, having AKI stage 1 was 41.1%, having AKI stage 2 was 42.6%, and having AKI stage 3 was 26.8%(Table 1). AKI was significantly associated with old age and male gender.

In this study, there was an analysis regarding the need for invasive mechanical ventilation in different categories of COVID-19 patients. The percentage of patients with no history of AKI requiring traumatic mechanical ventilation was 79.4%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 11.5%. The difference was relevant statistically (p<0.001). The percentage of patients with AKI of any stage requiring traumatic mechanical ventilation was 22.8%, while the percentage of patients with no history of AKI not requiring traumatic mechanical ventilation was 76.8%. The difference was relevant statistically (p<0.022).

SARS-CoV-2 is typically an RNA virus that spreads by secretions from the mouth and nose as well as via microscopic droplets produced while coughing. The standard procedure for diagnosis uses RT-PCR on respiratory samples obtained by taking a swab from the nasopharynx. Multiple organ failure, death, mild upper respiratory tract disease symptoms, and severe acute breathing distress are just a few examples of the various clinical presentations that could occur [18,19]. SARS-CoV-2 attacks a variety of organs outside the lungs by taking advantage of the angiotensin-converting enzyme-2 (ACE-2). The kidney is one of COVID-19's main targets in the human body. In the COVID-19 illness, AKI is viewed as a marker of disease severity and a poor predictor of patient survival [20,21]. According to KDIGO recommendations, patients with severe AKIdefined as stage 3 or aboveshowed a higher death rate than those with AKI stage 1 and AKI stage 3 in COVID-19 afflicted individuals with AKI. Due to an already existing elevated regulation of enzyme ACE and reduced regulation of enzyme ACE-2, patients with chronic illnesses of the kidney, particularly those suffering from diabetic nephropathy, may be at an increased risk of developing AKI [22,23].

Participants in the COVID-19 research who had a history of hypertension were more likely to have no AKI (51.5%), any stage of AKI (65.8%), stage 1 AKI (68.3%), stage 2 AKI (65.2%), and stage 3 AKI (62.6%). The percentage of COVID-19 study participants with history of coronary artery disease was as follows: no AKI (10.0%), AKI any stage (15.5%), AKI stage 1 (15.7%), AKI stage 2 (17.1%), and AKI stage 3 (14.1%). The percentage of COVID-19 study participants with history of heart failure was as follows: no AKI (5.1%), AKI any stage (11.4%), AKI stage 1 (13.1%), AKI stage 2 (11.5%), and AKI stage 3 (8.9%).

Every nation now has the COVID-19 virus. The virus spreads through close contact between people who cough, sneeze, or speak while exchanging droplets or aerosols, which is why there have been so many confirmed cases. Infection can also occur by interacting with infected surfaces and then touching transmission points like the mouth, eyes, and nose. The primary organ system impacted by COVID-19 infection is the respiratory system as a whole. In severe cases, this infection can cause pneumonia, hypoxemia, and acute respiratory distress syndrome [24,25]. Even though the pulmonary characteristics of SARS-CoV-2 infection are the main focus, doctors need to be mindful of the challenges that illness brings to other parts of the body, such as the kidneys. Acute kidney injury (AKI), often known as AKI, is the kidney symptom that hospitalized COVID-19 patients experience the most frequently [26].

Our study offers some advantages. This cohort of COVID-19 patients that are hospitalized and have an emphasis on AKI is now by far the largest. There are restrictions on this study. First, because itis observational research, we are unable to draw conclusions about the causal links between various levels ofexposure to AKI. Second, despite the fact that we have made adjustments for possible confounders, there can still be unmeasured confounders.

In conclusion, we discovered that AKI was a rather typical finding among hospitalized COVID-19 patients. It was a rare condition when COVID-19 individualsdid not need ventilation and were closely related to the incidence of respiratory failure. Hospitalized COVID-19 patients had a poor prognosis if they developed AKI. To further comprehend the causes of AKI including patient outcomes, more research will be required.

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Assessment of Kidney Involvement in COVID-19 Patient - Cureus