SARS-CoV-2 infection in children with chronic kidney disease

Abstract

Background

Information on the course of SARS-CoV-2 infection in children with chronic kidney disease (CKD) is limited.

Methods

We retrospectively reviewed the presentation and outcomes of SARS-CoV-2 infection in patients with CKD followed at any of the four pediatric nephrology centers in New Delhi from April 2020 to June 2021. Outcomes, including cardiopulmonary and renal complications, were reported in relation to underlying disease category and illness severity at presentation.

Results

Underlying illness in 88 patients included nephrotic syndrome (50%), other CKD stages 1–4 (18.2%), CKD 5D (17%), and CKD 5T (14.8%). Thirty-two of 61 patients with symptomatic COVID-19 and 9/27 asymptomatic patients were admitted for median 10 (interquartile range 7–15) days. Seventeen (19.3%) patients developed moderate or severe COVID-19. Systemic complications, observed in 30 (34.1%), included acute kidney injury (AKI, 34.2%), COVID-19 pneumonia (15.9%), unrelated pulmonary disease (2.3%), and shock (4.5%). Nineteen (21.6%) had severe complications (AKI stage 2–3, encephalopathy, respiratory failure, shock). Eight (11%) of twelve (16.4%) patients with severe AKI required dialysis. Three (3.4%) patients, two with steroid-resistant nephrotic syndrome in relapse and one with CKD 1–4, died due to respiratory failure. Univariate logistic regression indicated that patients presenting with nephrotic syndrome in relapse or moderate to severe COVID-19 were at risk of AKI (respective odds ratio, 95%CI: 3.62, 1.01–12.99; 4.58, 1.06–19.86) and/or severe complications (respective odds ratio, 95%CI: 5.92, 1.99–17.66; 61.2, 6.99–536.01).

Conclusions

Children with CKD presenting with moderate-to-severe COVID-19 or in nephrotic syndrome relapse are at risk of severe complications, including severe AKI and mortality.

Graphical abstract

A higher resolution version of the Graphical abstract is available as Supplementary information

Supplementary Information

The online version contains supplementary material available at 10.1007/s00467-021-05218-1.

Introduction

The pandemic of coronavirus disease (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is considered to be less widespread and serious in children [1, 2]. With the exception of multisystem inflammatory syndrome with shock, the disease in childhood is typically milder with lower case fatality than in adult patients [3]. Systematic reviews indicate that patients with chronic kidney disease (CKD) are affected more often, and are at high risk of respiratory morbidity as well as mortality [4]. Information on COVID-19 in children with underlying CKD is presently limited to seven reports on 152 patients, chiefly from Europe and the US [5–11]. Information on children with CKD outside these regions is limited to 38 patients, in a survey by the International Pediatric Nephrology Association during March–July 2020 [8]. However, South Asia was likely under-represented because the pandemic affected the region several weeks later than China, Europe and North America. Two distinct waves of the pandemic were observed in India during 2020–21, with cases peaking in September 2020 and May 2021 (Supplementary Fig. 1). Preliminary reports of COVID-19 in Indian children show that the features are similar to those reported elsewhere [12]. We describe here the clinical features and outcomes of consecutive children with CKD who were diagnosed with SARS-CoV-2 infection at four academic centers in New Delhi from April 2020 to June 2021.

Methods

We reviewed the case records of consecutive patients ≤ 18 years old with pre-existing CKD and laboratory confirmed SARS-CoV-2 infection, detected at any of four pediatric nephrology centers in New Delhi during the pandemic. Indications for testing patients for SARS-CoV-2 infection included: (i) clinical features suggestive of COVID-19 (fever, cough, dyspnea, rhinorrhea, sore throat, diarrhea, myalgia, anosmia or ageusia); (ii) close contact (within 6-ft of an infected person for 15 min or longer) with an individual diagnosed with SARS-CoV-2 infection [13]; or (iii) admission for management of underlying disease. Patients with SARS-CoV-2 infection who developed AKI during hospital stay, but lacked evidence of pre-existing kidney disease, were excluded. Institutional review boards at participating centers approved the study and waived the need for parental or patient consent.

Testing for SARS-CoV-2 infection was performed on nasal and oropharyngeal swabs using reverse transcriptase polymerase chain reaction (RT-PCR) or rapid antigen test (Standard Q COVID-19 Ag kit, SD Biosensor, Gyeonggi-do, Korea), as recommended by the Indian Council of Medical Research (ICMR) [14] and Centers for Disease Control [15]. Given the low sensitivity (85.0%; 95%CI 78.3–90.2%) and high specificity (98.9%; 95%CI 98.3–99.4%) of the antigen test, patients with negative, but not positive, test results underwent retesting by RT-PCR. Retesting for SARS-CoV-2 by RT-PCR, after at least 3 days of confirmed infection, was restricted to patients in whom there was a proposed change in immunosuppressive therapy, or transfer to another hospital for hemodialysis, or were being considered for discharge but isolation at home was not possible. COVID-19 case definition and its categorization into mild, moderate, or severe disease followed the national guidelines (Supplementary Table 1) [16]. Indications for hospital admission were (i) symptomatic infection, particularly in an immunosuppressed host, (ii) management of the underlying illness, and (iii) inability to ensure home isolation. These patients were managed in separate COVID-19 facilities as per current standard of care [16]. Shock, sepsis, acute respiratory distress syndrome (ARDS), and acute kidney injury (AKI) were diagnosed and managed using standard guidelines [16–18]. The prevalence of AKI, severe AKI (KDIGO stages 2 and 3), and kidney replacement therapy (KRT) [18, 19] is reported for patients not already on maintenance dialysis. Hemodialysis was provided at two centers dedicated to patients with SARS-CoV-2 infection, following standard recommendations [20, 21]. The effluent of peritoneal dialysis was discarded as per International Society of Peritoneal Dialysis recommendations [22].

Following detection of SARS-CoV-2 infection and for 2 weeks afterwards, immunosuppressive therapy was modified, with minor variations, as follows: (i) if on corticosteroids currently or within the last year, prednisolone was administered at a dose of 0.5 mg/kg daily for 1 week, (ii) dose of mycophenolate mofetil was reduced by 25–33%; (iii) cyclophosphamide administration was stopped; and (iv) therapy with calcineurin inhibitors (CNI, cyclosporine or tacrolimus) was continued [23]. Therapy with angiotensin converting enzyme inhibitor or angiotensin receptor blocker was continued, except in the presence of AKI. Policies on therapy for COVID-19 varied over time, with non-uniform use of hydroxychloroquine, azithromycin, ivermectin, remdesivir, tocilizumab, and convalescent plasma.

Data on clinical and laboratory findings were reviewed from medical records for details of pre-planned parameters viz. underlying disease, severity of COVID-19 and associated complications, testing methods for SARS-CoV-2 virus and duration of RT-PCR positivity, therapy received and duration of hospital stay. Underlying CKD was categorised as nephrotic syndrome, other kidney diseases with CKD stage 1–4, CKD 5D, and CKD 5T. In patients with nephrotic syndrome, the presence of nephrotic-range proteinuria at evaluation at onset, relapse or following non-response to immunosuppression, was considered as ‘relapse’.

Patients were followed up until discharge, death or 4weeks after diagnosis of COVID-19, whichever was earlier. Hypertension was defined using standard guidelines [24]. Estimated glomerular filtration rate (eGFR) was calculated using the modified Schwartz formula [25]. Data is summarized as median (interquartile range, IQR) and proportions (95% confidence interval, CI) using Stata software, version 14.2 (Stata Corp., College Station, TX). Univariate logistic regression was performed post hoc to examine the association between baseline features and occurrence of AKI or severe complications (AKI stages 2–3, shock, respiratory distress requiring invasive or non-invasive ventilation, encephalopathy, or death).

Results

We report 88 patients (67 boys) with CKD and median age 10 (IQR 6–15) years, who presented between 21 April 2020 and 11 June 2021 (Table 1, Supplementary Fig. 1). Over half the cases were managed at one center; eight patients required inter-hospital transfer for hemodialysis at facilities dedicated for patients with COVID-19. SARS-CoV-2 infection was identified by RT-PCR in 83 patients and rapid antigen test in 5 patients. Twenty-seven asymptomatic patients were detected on screening performed at hospital admission for reasons apparently unrelated to COVID-19 (n = 9), low-risk contact with infected individual at hemodialysis facility (n = 7), or high-risk contact with family member (n = 11). Symptoms, in 61 patients, included fever (59.1%), cough (38.6%), respiratory distress (15.9%) and diarrhea (10.2%). At onset, the illness was categorized as mild, moderate and severe in 51, eight and two patients, respectively (Table 1). Nephrotic syndrome was the most common underlying diagnosis (n = 44), with 24 (54.5%) of them in relapse, and 27 (61.4%) having steroid-sensitive illness. Twenty-eight patients were on KRT, including 14 patients on maintenance hemodialysis, one on automated peritoneal dialysis and 13 recipients of kidney transplantation. Supplementary Table 1 and Supplementary Figs. 2 and 3 provide details of underlying disease in relation to COVID-19 severity at presentation.

Table 1.

Baseline characteristics of patients with kidney disease and SARS-CoV-2 infection (n = 88)

Parameter	N (%)
Boys	67 (76.1)
Age, years	10 (6–15)
Presentation
Asymptomatic	27 (30.7)
Symptomatic	61 (69.3)
Fever	52 (59.1)
Cough	34 (38.6)
Respiratory distress	14 (15.9)
Diarrhea	9 (10.2)
Clinical severity of COVID-19 [16]
Asymptomatic	27 (30.7)
Mild	51 (57.9)
Moderate	8 (9.1)
Severe	2 (2.3)
Underlying disease
Patients not on kidney replacement therapy	60 (68.2)
Nephrotic syndrome (relapse/remission)	44 (24/20)
Steroid sensitive (relapse/remission)	27 (14/13)
Steroid resistant (relapse/remission)	17 (10/7)
CAKUT (Reflux nephropathy/pelviureteric junction obstruction/PUV)	5 (2/2/1)
Others (HUS, cystic kidneys, Lowe syndrome, Takayasu aortoarteritis, lupus)	11 (3/3/2/2/1)
Patients on kidney replacement therapy	28 (31.8)
Chronic kidney disease 5D (CAKUT/HUS/FSGS/IgA nephropathy/unknown)	15 (5/3/2/2/3)
Chronic kidney disease 5 T (CAKUT/neurogenic bladder/chronic GN/familial hypomagnesemia hypercalciuria and nephrocalcinosis / unknown)	13 (5/2/2/1/3)
Current immunosuppression	50 (56.8)
Prednisolone	40
Mycophenolate mofetil	17
Calcineurin inhibitors (< 3 months back)	25
Cyclophosphamide (< 4 weeks back)	3
IV rituximab (< 6 months back)	2
Estimated glomerular filtration rate (eGFR), ml/minute per 1.73 m2*	81.9 [39.8–104.1]

Data is shown as n (%) or median [interquartile range]; CAKUT congenital anomalies of the kidney and urinary tract; FSGS, focal segmental glomerulosclerosis; GN, glomerulonephritis; HUS, hemolytic uremic syndrome; IV, intravenous; PUV, posterior urethral valves

^*Excluding 15 patients already on dialysis; eGFR at presentation calculated using modified Schwartz formula based on serum creatinine at diagnosis of SARS-CoV-2 infection

Fifty (56.8%) patients were either receiving, or had recently discontinued immunosuppressive drugs (Table 1). Medications included prednisolone (n = 40), CNI (n = 25), or mycophenolate mofetil (n = 17); three patients had discontinued therapy with CNI < 2 months back (Supplementary Table 2). Patients included 32 with nephrotic syndrome and 13 allograft recipients, transplanted more than 1 year previously and on stable immunosuppression (Supplementary Table 2). Two of three patients with anti-factor H associated hemolytic uremic syndrome on hemodialysis were receiving oral prednisolone and IV cyclophosphamide, while the third was on maintenance oral prednisolone and mycophenolate mofetil. One patient with steroid-resistant nephrotic syndrome on maintenance hemodialysis had received rituximab 4 months prior for desensitization in preparation for living related kidney transplantation. One patient with severe flare of lupus, while on therapy with mycophenolate mofetil and prednisolone, had received high dose methylprednisolone, intravenous immunoglobulin (IVIG) and one dose of rituximab (750 mg/m²) 2 weeks prior to admission. Seven patients treated with IV rituximab 2–4 years prior were not deemed immunosuppressed.

Course and complications

Twenty-nine patients with COVID-19 symptoms and 18 asymptomatic patients were managed at home (Supplementary Figs. 2 and 3). Thirty-two patients were admitted for monitoring of symptomatic COVID-19 and nine were admitted for complications of the underlying illness, including five patients with nephrotic syndrome and anasarca, and two patients each with severe anemia and asymptomatic allograft dysfunction. Admission to the intensive care unit was indicated in 18 patients for moderate to severe COVID-19 (n = 8), monitoring for AKI (n = 6) or anasarca (n = 3), and respiratory distress due to pulmonary tuberculosis (n = 1). Five of the eight patients who presented with moderate to severe COVID-19 and admitted to the intensive care unit had underlying CKD 1–4, while two were kidney allograft recipients and one patient had relapse of steroid-dependent nephrotic syndrome. Seven patients with nephrotic syndrome in relapse were admitted with asymptomatic or mild COVID-19 and evolved to moderate or severe COVID-19 during hospital stay (Supplementary Figs. 3–4; Supplementary Tables 1 and 3).

Pulmonary, hemodynamic, and/or renal complications were observed in 30 (34.1%) patients. Pulmonary disease, observed in 16 (18.2%) cases, included 14 patients with COVID pneumonia; 7 of whom were in relapse of nephrotic syndrome with five requiring mechanical ventilation and two non-invasive ventilation, 3 were CKD 1–4 with one each receiving invasive and non-invasive ventilation and face mask oxygen, 2 were CKD 5T on non-invasive ventilation and 2 patients with CKD 5D managed on supplemental oxygen (Table 2, Supplementary Table 3 and Supplementary Fig. 4b). One patient with steroid-dependent nephrotic syndrome with severe AKI and fluid overload was mechanically ventilated for pulmonary edema while another with CKD 5D and pulmonary tuberculosis received supplemental oxygen. Although they were SARS-CoV-2 positive, the respiratory worsening appeared unrelated to COVID-19.

Table 2.

Outcomes of children with kidney diseases affected by COVID-19 (n = 88)

Parameter	N (%)
Hospital admission#	41 (46.6)
Admission to intensive care unit	18 (20.4)
Maximal clinical severity of COVID-19
Asymptomatic	25 (28.4)
Mild	46 (52.3)
Moderate	9 (10.2)
Severe	8 (9.1)
Maximal respiratory support required
Oxygen by face mask	5
High flow nasal cannula	5
Mechanical ventilation	6
Vasopressor support	4 (4.5)
Acute kidney injury^	25 (34.2)
Stage 1	13$
Stage 2	2
Stage 3	10
Need for kidney replacement therapy	8
Outcome
Discharge; well at home (not admitted)	38; 48
Death	3 (3.4)
Re-admission	2
Duration of hospital stay, days	10 (7–15)
Outcomes in patients with AKI n = 25)
Continued need for kidney replacement therapy	2
Estimated GFR*, ml/min/1.73 m2	65.6 [40–84.3]
Hypertension; proteinuria (new onset)@	2; 2
Retesting for clearance of infection	33
Time to negative test result, days	15 (8–24)
Persistent positive for  > 14 days	18 (54.5)
Persistent positive for  > 21 days	11 (33.3)
Persistent positive for  > 6 weeks	3 (9.1)

Data reported as n (%) or median [interquartile range]

^#Included 9 admissions for problems apparently unrelated to COVID-19 (anasarca in 5 patients with nephrotic syndrome; asymptomatic allograft dysfunction and severe anemia in two patients each); ^{^}assessed only in patients not already on dialysis; ^$4 patients were not admitted and recovered with oral hydration at home; *eGFR calculated using modified Schwartz formula [25] based on serum creatinine at discharge in patients not on dialysis; ^@hypertension defined as per clinical practice guidelines of the American Academy of Pediatrics 2017 [24]

Shock was noted in four patients, including three with nephrotic syndrome in relapse and one with CKD 4. A 6-year-old patient with steroid-dependent nephrotic syndrome presented with seizures and encephalopathy and developed shock within 6 h of admission; shock recovered and sensorium improved following aggressive inotropic support, mechanical ventilation and antibiotics. Two patients with steroid-resistant nephrotic syndrome and with persistent viral shedding developed refractory shock on days 7 and 66 of hospital stay and died within hours; shock was considered secondary to fulminant bacterial sepsis in the latter patient. A 15-year-old girl with CKD 4 secondary to reflux nephropathy was mechanically ventilated at presentation with severe ARDS and shock; the child died 6 days later due to ARDS and refractory shock.

AKI was present in 25 children, 21 of whom were admitted. Sixteen children had AKI at admission, including seven patients with nephrotic syndrome in relapse, four patients with CKD 1–4 and five transplant recipients. Four patients, including two each with steroid-sensitive nephrotic syndrome in relapse and CKD 1–4, developed AKI after a median 3 (IQR 2.75–3.5) days of hospital stay; one patient with steroid-resistant nephrotic syndrome developed AKI 6 weeks after admission secondary to bacterial sepsis and multiorgan dysfunction. Two transplant recipients and two patients with steroid-resistant nephrotic syndrome who were isolated at home developed stage 1 AKI, which resolved spontaneously. Supplementary Fig. 4c and Supplementary Table 4 indicate the evolution of AKI based on disease category and disease severity at presentation. Twelve patients had severe AKI (stages 2–3), including seven patients with relapse of nephrotic syndrome, and five with CKD 1–4 (Table 2, Supplementary Table 4). Eight of these 12 patients required KRT (seven hemodialysis, one peritoneal dialysis). For patients not already on dialysis, the prevalence (95% CI) of AKI, severe AKI and KRT were estimated at 34.2% (24.4–45.7%), 16.4% (9.7–26.6%), and 11% (5.7–20.2%), respectively. Similarly, the prevalence (95% CI) of AKI, severe AKI and KRT for patients admitted to the intensive care unit were 83.3% (60.8–94.2%), 55.6% (33.7–75.4%), and 38.9% (20.3–61.4%), respectively.

Immunosuppression and specific management

Immunosuppression was modified for 30 patients, including stress dosing of corticosteroids (n = 23), reduction or discontinuation of mycophenolate mofetil (n = 6), stopping therapy with calcineurin inhibitors (n = 4), and cyclophosphamide (n = 3). Thirty-six patients received empiric therapy for SARS-CoV-2 infection, including azithromycin (n = 28), ivermectin (n = 7), remdesivir (n = 5), hydroxychloroquine (n = 3), and convalescent plasma and IV tocilizumab (one each).

Outcomes

Three out of 88 patients, two with steroid-resistant nephrotic syndrome in relapse and one with CKD 1–4, died, leading to an estimated mortality of 3.4% (95% CI 1.2–9.6%) (Supplementary Fig. 4d). Death was attributed to ARDS due to COVID-19 in two children; the third patient, in addition to being SARS-CoV-2 positive until death, had superadded bacterial sepsis. The remaining 38 patients were discharged after median stay of 10 (7–15) days without any cardiopulmonary sequelae (Supplementary Figs. 2–4 and Supplementary Tables 3–4). Of the 47 patients isolated at home, four developed AKI stage 1, which resolved spontaneously; others recovered without complications.

The median time to SARS-CoV-2 RT-PCR negative test result, in 33 patients, was 15 (8–24) days. Eleven patients, four with relapse of steroid-resistant nephrotic syndrome, three each with CKD 5D and CKD 5T, and one with Lowe syndrome showed viral shedding beyond 3 weeks; eight of these were immunosuppressed. Persistent viral shedding beyond 6 weeks was seen in one patient each with steroid-resistant nephrotic syndrome, CKD 5T and CKD 5D; the latter was not on immunosuppression. Two patients with steroid-resistant nephrotic syndrome were readmitted for anasarca and severe AKI with positive RT-PCR; while one had tested negative by RT-PCR at prior discharge on day 14, the test was persistently positive in the other patient until his death on day 66.

For admitted patients not already on dialysis, the eGFR increased from 81.9 (39.8–104.1) ml/min/1.73 m² at presentation to 90.2 (56.3–109.4) ml/min/1.73 m² at last follow-up (P = 0.008) (Table 1). Similarly, the eGFR in patients with AKI increased from 33.3 (25.5–56.5) to 65.6 (40–84.3) ml/min/1.73 m² at last follow-up (P = 0.0001) (Table 2). Six of 8 patients who required KRT during admission could discontinue dialysis; two patients died while on dialysis.

Determinants of outcomes

The duration of hospital stay (n = 41) and viral shedding (n = 33) were unrelated to sex, age, COVID-19 symptoms, underlying disease, immunosuppression or presence of complications. Univariate logistic regression suggested that presentation with moderate to severe COVID-19 or in relapse of nephrotic syndrome were associated with occurrence of AKI and severe complications (Table 3).

Table 3.

Risk factors for AKI and severe complications (severe acute kidney injury, invasive/non-invasive ventilation, encephalopathy, shock or death)

Baseline variable	Univariate logistic regression
Outcome: AKI (n/N = 25/73)*	Odds ratio	95% CI	P
Age, years	0.91	0.81, 1.04	0.16
Sex, boys	0.56	0.11, 2.85	0.49
Nephrotic syndrome in relapse	3.62	1.01, 12.99	0.048
Estimated glomerular filtration rate, ml/min per 1.73 m2^	1.00	0.99, 1.02	0.66
Recent or current immunosuppression	0.49	0.14, 1.70	0.47
Moderate or severe COVID-19	4.58	1.06, 19.86	0.042
Outcome: Severe complications (n/N = 19/88)	Odds ratio	95% CI	P
Age, years	0.96	0.87, 1.06	0.43
Sex, boys	0.82	0.24, 2.79	0.75
Nephrotic syndrome in relapse	5.92	1.99, 17.66	0.001
Estimated glomerular filtration rate, ml/min per 1.73 m2^	1.00	0.98, 1.02	0.81
Recent or current immunosuppression	1.87	0.64, 5.50	0.25
Moderate or severe COVID-19	61.2	6.99, 536.01	< 0.001

^*Patients with CKD 5D were excluded from analysis

^Pre-illness, in last < 3 months

Discussion

We describe the presentation and outcomes of SARS-CoV-2 infection in 88 pediatric patients with CKD managed at four academic centers in New Delhi over a period of 14 months. The incidence of cases corresponded to the peaks of the two waves of the pandemic in 2020 and 2021 (Supplementary Fig. 1). The chief underlying illness was nephrotic syndrome in half the patients and included children in remission as well as relapse. Half the patients were immunosuppressed and one third were either receiving chronic dialysis or had received a kidney allograft in the past. Two thirds of patients were symptomatic, chiefly with fever or respiratory symptoms, and one-fifth required respiratory support. Although one-third of patients not already on maintenance dialysis developed AKI, only one-third of those who developed AKI required KRT. While the majority of patients with CKD recovered from SARS-CoV-2 infection, three patients died, secondary to multiorgan failure and systemic sepsis. Our findings suggest that patients with CKD who present with moderate to severe COVID-19 or with relapse of nephrotic syndrome were at risk of severe complications, including AKI and mortality.

Systematic reviews describe more severe COVID-19 disease and higher rates of adverse outcomes, including AKI and mortality, in adult patients with CKD [4, 24–27]. In contrast, studies in children with CKD, summarized in Table 4, indicate a relatively milder course of illness [5–11]. These children, predominantly boys (49–74%) had median age of 9–12 years, and the most common underlying diagnosis was nephrotic syndrome. Kidney allograft recipients and patients on dialysis constituted 11–100% and 14–47% cases, respectively. The rates of symptomatic COVID-19 (8–81%) and hospitalization (31–60%) were similar to those in population-based studies [28–30]; severe respiratory illness (9–12%) and mortality (3.5–4%) were also infrequent. Since previous reports chiefly included children from Europe, UK, and North America, this report from India underscores the similarities in severity of SARS-CoV-2 infection and disease presentation in patients with CKD across geographic regions.

Table 4.

Findings in studies on children with kidney diseases and SARS-CoV-2 infection

Author [ref]	Marlais [8]	Marlais [5]	Melgosa [7]	Schwierzeck [11]	Plumb [6]	Mastrangelo [10]	Basalely [9]	Present work
N (countries)	113 (30)	18* (11)	16 (Spain)	13 (Germany)	5 (UK)	3 (Italy)	2 (USA)	88 (India)
Boys, %	49	61	56.3	NA	80	NA	100	76.1
Median age, years	11	11.5	12.3	~ 10	11	NA	1, NA	10
Underlying disease, %					NA
Nephrotic syndrome (% in relapse)	27 (NA)	17 (NA)	31.3 (12.5)	0		0	50 (NA)	50 (52.3)
Other glomerular CKD	23.9	17	50	0		33.3	0	4.5
Non-glomerular CKD	2.6	0	50	0		66.7	0	13.6
CKD 5D	10.6^	6	18.8	100		0	50	17
CKD 5T	47	61	18.8	0		0	0	14.8
Immunosuppressed, %	100	100	56.3	NA	NA	33.3	0	56.8
Symptoms of COVID-19, %	81.4	NA	81.3	7.7	NA	66.7	100	68.2
Admitted, %	60.2	61	50	NA	NA	NA	100	46.6
Respiratory support, %	22.1	17	0	NA	NA	0	50	18.2
Acute kidney injury, %	NA	NA	18.8	NA	NA	0	0	34.2
Death, %	3.5	NA	0	0	NA	0	0	3.4
Predictors of severe complications	None#1	NA	NA	NA	NA	NA	NA	Reported#2

NA not available

^*These patients were also included in the study in column 1

^{^}Includes children with glomerular or non-glomerular CKD or CKD5T on dialysis

^#1All 4 deaths were reported in low-n-income countries; ^#2Risk factors included moderate or severe COVID-19; nephrotic syndrome in relapse

Available reports emphasize the relatively low incidence of SARS-CoV-2 infection in immunosuppressed patients [8, 10, 31, 32]. Our experience was similar, although patient contact has been limited and chiefly through teleconsultations. Regular teleconsultations at one center, over 14 months, resulted in documentation of SARS-CoV-2 infection in thirteen of 80 allograft recipients, ten of ~ 350 patients with nephrotic syndrome administered rituximab previously, and seventeen of almost 800 patients with nephrotic syndrome enrolled in longitudinal cohorts or in randomized studies. However, the limitations imposed by such consultations and lack of opportunities for viral testing might have underestimated the prevalence of SARS-CoV-2 infection in these patients. In the absence of high mortality or morbidity, continuing immunosuppression in standard doses appears rational. In view of concerns of intense immunosuppression, we have refrained from using IV rituximab since the beginning of the pandemic [33]. Similar to the course in a patient with granulomatosis with polyangiitis [34], one patient with lupus nephritis in the present report developed severe COVID-19 following therapy with rituximab, but improved rapidly. While biologicals might favorably influence the interplay of infectious and inflammatory mechanisms [35, 36], the trends of higher respiratory morbidity and mortality [37–39] emphasize that such therapies be used cautiously.

The experience with COVID-19 in immunosuppressed recipients or solid organ transplants is varied [40–42]. A systematic review including 1,500 kidney transplants among 2,772 solid organ recipients, indicated high rates of admission to intensive care units (29%) and higher mortality (18.6%) [42]. In contrast, outcomes in pediatric transplant recipients appear satisfactory [8, 10], with low rates of symptomatic infections [10], mild symptoms, few complications, and similar time to viral clearance as non-immunosuppressed children [7, 8]. Persistent viral excretion in 11 patients in the present report was unrelated to ongoing immunosuppression but was related to COVID-19 severity, as was reported previously [43].

Systematic reviews suggest that AKI affects 11% of patients admitted with COVID-19 and that 6.8% of admitted patients require KRT [4]. Furthermore, severe AKI and the need for KRT are reported to be more frequent in patients with CKD [26, 27]. Unsurprisingly, therefore, AKI was the chief extrapulmonary complication of SARS-CoV-2 infection in the present series, and affected 40% patients who were previously not on KRT. The presence of nephrotic syndrome in relapse appears to be associated with an almost five-fold risk of severe AKI, perhaps due to associated hypovolemia and/or use of diuretics, ACE-inhibitors and other nephrotoxic medications [44]. Similarly, patients with nephrotic syndrome in relapse have higher risk of mechanical ventilation and mortality probably due to edema and respiratory distress. While presentation with moderate to severe COVID-19 and relapse of nephrotic syndrome might be associated with severe complications and death, the wide confidence intervals of these estimates and inability to demonstrate independent association or causality, caution against over-emphasizing these risks. More data is required to explore these findings further.

The present report is one of the larger studies of the impact of COVID-19 on children with CKD, and the first from a developing country. Strengths of the study were the inclusion of consecutive patients diagnosed at four centers in New Delhi, robust diagnosis relying chiefly on RT-PCR, and information on course and complications during a minimum follow-up of 4 weeks. However, the extent of evaluation varied based on whether patients were admitted or isolated at home, and there was heterogeneity in policies on management and documentation of viral clearance. As guidelines for retesting evolved, it was not performed in all patients. Finally, contributions of stress dosing of steroids, ongoing hydroxychloroquine intake, relapse of nephrotic syndrome and cytokine responses in certain population groups on disease course are unclear. While these findings replicate the experience from other regions, patients presenting with moderate to severe COVID-19 or with relapse of nephrotic syndrome appear to be at risk of complicated COVID-19, indicating the need for close monitoring.

Supplementary Information

Below is the link to the electronic supplementary material.

Author contribution

SK, MM, KM, KK, MK, SS, SS, AS, and PK collated the data from patients’ case records; MB and RG performed microbiological studies; SK, AS, PH and AB designed the study, analyzed the data and wrote the first draft; all authors refined the manuscript draft and approved the final manuscript.

Data availability

Anonymized data will be shared if requested.

Declarations

Ethics approval

The Ethics committees at the four centers waived the need for patient and parental consent.

Consent to participate

The Ethics committees at the four centers waived the need for patient and parental consent to participate in the study.

Consent to publication

All authors agree with the content of the manuscript, are responsible for the correctness of the statements provided in the manuscript and have consented to submit it for publication. All authors have obtained consent from the responsible authorities at the four Institutes where the work has been carried out, before submission for consideration for publication.

Competing interests

The authors declare no competing interests.