COVİD-19 infection in a membranous nephropathy patient treated with rituximab

Abstract

While COVID-19 pandemic continues to affect our country and most countries in the world, we have to make some changes both in our social life and our approach to healthcare. We have to struggle with the pandemic on one hand and also try to follow up and treat our patients with chronic diseases in the most appropriate way. In this period, one of our group of patients who are challenging us for follow-up and treatment are those who should start or continue to use immunosuppressive therapy. In order to contribute to the accumulation of knowledge in this area, we wanted to report a patient who was followed up with the diagnosis of COVID-19 and had been administered rituximab very recently due to a nephrotic syndrome caused by membranous nephropathy.

Introduction

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-related coronavirus disease-19 (COVID-19) cases, which emerged in Wuhan [1], China in December 2019 and soon became a pandemic [2], started to appear in our country in March 2020. Membranous nephropathy (MN) is one of the most important causes of nephrotic syndrome (NS) in adults [3]. For treatment of MN, either cyclophosphamide or cyclosporin-A has been used in combination with glucocorticoids for many years. However, recently, rituximab has started to come to the fore [4]. There is insufficient data about COVID-19’s course in immunocompromised patients, especially in NS patients using immunosuppressive agents. As far as we know, COVID-19 has not been reported in glomerulonephritis patients who use immunosuppressives. Herein, a case of COVID-19 who was recently treated with rituximab for MN is presented.

Case presentation

A 48-year old male who was admitted to the emergency clinic with cough, high fever and headache for 4 days was hospitalized on March 15, 2020 with a pre-diagnosis of COVID 19 pneumonia. He is non smoker and not use alcohol, and working as a parking guard. At the latest outpatient visit on March 04, there were no signs or symptoms of infection. His past medical history included type 2 diabetes since 2013. Hemoglobin A1C of 5.8% on March 04, 2020. There was no evidence of retinopathy in the ocular examination and no neuropathy. A renal biopsy performed due to nephrotic syndrome (proteinuria: 8330 mg/day) in May 2019 revelaed MN. At the time of diagnosis, serum albumin and creatinine was 2.4 g/dL and 0.7 mg/dL, respectively. Secondary MN causes were eliminated and primary MN was diagnosed after M-type anti-phospholipase A2 receptor antibodies were positive (715 RU/mL). The patient was started on valsartan and furosemide for proteinuria and edema, and continued to use gliclazide and metformin. There was no significant decrease in proteinuria, 1 g rituximab was administered for 2 times (day 0 and 15) in January and February 2020. On the last follow-up, the patient was not in any kind of remission. Physical examination at presentation to the emergency room revealed that he was febrile (38.5 °C) and normotensive (110/70 mmHg), his pulse was 96 min and rhythmic, and oxygen saturation was 96% while breathing ambient air. On auscultation breath sounds were rough. No crepitations or rhonci were detected. He was empirically administered oseltamivir 75 mg BID and moxifloxacin 400 mg QD on March 15. Microbiological assessment was negative for viral, bacterial or fungal infections, including aspergillosis, pneumocystis, and mycobacteria. Laboratory parameters throughout the follow-up are shown in Table 1, and pneumonic infiltration on computed tomography (CT) is shown in Fig. 1a–d. Nasopharyngeal swab sample was negative for influenza. However, swabs for SARS-CoV 2 by real-time reverse-transcriptase–polymerase-chain-reaction (rRT-PCR) assay were found positive. Due to persistent high fevers, hydroxychloroquine (400 mg BID for 24 h, afterwards 200 mg BID; oral) was added to his treatment on March 19, and on March 21, moxifloxacin was discontinued and azithromycin was given for 5 days. There was no QT prolongation in the control electrocardiogram. C-reactive protein significantly increased to 116 mg/L (23 March). On March 26, lopinavir/ritonavir 200/50 mg 2*2 for 10 days and ascorbic acid 25,000 mg/50 mL QD for 7 days were added to the treatment regimen. As of March 29, his fever returned to normal and never increased again. Control swabs for SARS CoV-2 by rRT-PCR assay were reported as negative twice. During the follow-up, he just needed nasal oxygen and did not need intensive care. Serum creatinine decreased to 0.7 mg/dL from 1.6 mg/dL with proper hydration. During his follow-up, his blood sugar remained stable. No significant increase was observed. Enoxaparin sodium was given as an anticoagulant during hospital stay. Although his second chest CT (Fig. 1e–h) showed more severe pneumonia, he was decided to be discharged because of clinical and laboratory improvement on April 05. The clinical course of the patient is shown in Table 2.

Table 1.

Laboratory parameters throughout the follow-up

Date	15/03/20	18/03/20	21/03/20	23/03/20	26/03/20	29/03/20	01/04/20	03/04/20	13/05/20
Test
WBC (4500–11,000/μL)	5610	2960	5160	6490	5510	4950	7210	7810	6890
Neu (1500–7500/μL)	2930	1690	4060	5340	4880	3720	5700	6200	4070
Lym (600–3400 μ/L)	2180	890	780	990	490	930	940	1060	1950
Hb (13–17 g/dL)	10.9	10.3	10.2	9.6	8.8	9.5	7.9	9.1	11.7
PLT (142–424,000 μ/L)	222,000	173,000	273,000	287,000	334,000	299,000	396,000	442,000	278,000
CRP (0–5 mg/L)	31.7	12.8		116.4		85.7	42.3	19	0.99
Procalcitonin (0–0.5 ng/mL)	0.85					0.89	0.5	0.25
ESR (0–20 mm/h)	70		106			124	140	140	48
Ferritin (22–274 ng/mL)			586.9			1692		727	143
Glukoz (70–100 mg/dL)	159	165		130		152		168	153
Urea (19–44 mg/dL)	57	37	43	35		32	27	23	39
Cr (0.7–1.25 mg/dL)	1.6	1.2	1.26	1.24		1.03	0.87	0.76	1.27
eGFR (> 90 mL/dk/1.73 m2)	49	70	67	68		85	101	107	66
AST (5–34 U/L)	55	32	31	27		39	16	16	15
ALT (0–55 U/L)	26	20	19	19		24	17	14	10
ALP (40/150 U/L)	46					40		46
GGT (12–64 U/L)	22					18		16
LDH (125–220 U/L)	513	468	460	476		483	347	313
CK (30–200 U/L)		516	253	256		233		135
Ca (8.5–10.5 mg/dL)	7.3			8.4		8.3	8.5	8.7
Mg (1.6–2.6 mg/dL)				1.8
Na (135–145 mmol/L)	139	139	135	137		138	137	142	138
K (3.5–5.1 mmol/L)	2.66	3.3	3.1	2.9		3.2	3.45	4.2	4.2
Total protein (6.2–8 g/dL)	4.6							4.7
Albumin (3.5–5 g/dL)	1.9							2.1
PT (12–16.8 s)	16.8							16.2
aPTT (24–42 s)	37.3							35
Serum IgG (540–1822 mg/dL)		545				638
Serum IgA (63–484 mg/dL)		240				251
Serum IgM (22–240 mg/dL)		37				41

ALP alkaline phosphatase, ALT alanine aminotransferase, AST aspartate aminotransferase, Ca calcium, CK creatine kinase, Cr creatinine, CRP c-reactive protein, eGFR estimated glomerular filtration rate, ESR erytrocyte sedimantation rate, GGT gamma glutamyl transferase, Hb hemoglobin, K potassium, LDH lactate dehydrogenase, Lym lymphocyte, Mg magnesium, Na sodium, Neu neutrophil, PLT platelet, PT protrombin time, WBC white blood cell

Fig. 1.

a–d Chest CT shows diffuse areas of diffuse ground-glass infiltrates in both lungs, scattered in a patchy style on March 15, 2020, after symptom onset. e–h Chest CT on March 31, 2020; In a comparative evaluation with CT of 15.03.2020, there is progression in pneumonic consolidations in both lungs. Interlobuler septal thickening in both lungs and pleural effusion increases reaching 10 mm on the left and 3 mm on the right in both hemithorax were observed as new findings

Table 2.

The clinical course of the patient

Discussion

According to World Health Organization data on June 18, 2020, there have been 8,242,999 cases of COVID-19 and 445,535 death in the whole world and 182,727 cases with 4861 deaths in Turkey [5]. According to these data, the average mortality is 5.4% in all over the World and 2.6% in Turkey. The most frequent symptoms are high fever, cough, myalgia and fatigue. More rarely, sputum, headache and diarrhea can be seen. Average incubation period is 5.2 days [6]. According to a meta-analysis, approximately 30% of patients require intensive care caused by acute respiratory distress syndrome, and case fatality rate is 6.8% [7]. Patients who need intensive care and result with mortality are mostly over 65 years of age or have additional comorbidities such as hypertension, chronic obstructive pulmonary disease and diabetes. Some patients have leukocytosis but more of them have leukopenia and lymphopenia, high CRP, LDH and erythrocyte sedimentation rate. CT generally shows bilateral pneumonic infiltration. The most common pattern is ground glass appearance [7]. Opportunistic infections are common in immunocompromised patients [8] and symptoms often become blurred even in typical infectious diseases in these patients. Also, the disease course tends to be heavier in these patients compared to healthy population [9]. We see this situation most frequently in patients with kidney transplants and glomerulonephritis, to whom we administer immunosuppressive therapy. Chronic kidney disease (CKD) patients, especially in end stage, are also considered to be severely immunocompromised [10]. COVID-19 is also expected to be severe in our patients on immunosuppressive therapy. However, our data on this issue is limited. Alberici et al. reported that 5 of 20 patients with kidney transplants diagnosed with COVID-19 died, and four required intensive care. Five of 21 hemodialysis patients died. Mean duration of hospital stay in discharged patients was 12–13 days. Two of the five patients with CKD died [11]. Also, several recovered COVID-19 patients with kidney transplants and a patient with liver transplant have also been reported [9, 12, 13]. In these cases, mycophenolate mofetil, tacrolimus and everolimus were temporarily discontinued in patients with kidney transplantation. In one case, tacrolimus was maintained with a low trough level aiming at 2–4.5 ng/mL [12]. While hydroxychloroquine, oseltamivir, azithromycin or moxifloxacin are generally used in treatment, corticosteroids, tocilizumab, intravenous immunoglobulin, remdecivir and favipravir are used for severe disease [14]. Different treatment protocols are applied in different countries. Although there have not been previously reported glomerulonephritis with COVID-19, patients who use immunosuppressive therapy due to rheumatological diseases may show similarity to our patients with NS. Monti et al. reported eight COVID-19 patients in a series of 320 cases diagnosed with rheumatoid arthritis and spondyloarthropathy. These patients had taken immunosuppressive drugs such as etanercept, abatacept, tofacitinib, baricitinib, methotrexate and leflunomide. Four of them had taken low-dose glucocorticoids and three of them hydroxychloroquine. Only a 65-year old patient needed oxygen and was hospitalized. No one died. Immunosuppressive treatments of all patients were discontinued from the onset of symptoms [15]. Again, it is recommended not to stop the immunosuppressive drugs used for rheumatological diseases during the COVID-19 pandemic by rheumatology specialists from Italy [16]. If the high mortality in kidney transplant and chronic dialysis patients is remembered, it can be understand how difficult this decision is about our patients. Coronavirus uses ACE2, an angiotensin I-converting enzyme (ACE) homologue, which is a cell surface receptor, to enter the cells. While this receptor is slightly expressed in endothelium and kidney, is particularly expressed in airways and heart [17]. Therefore, use of ACE inhibitors (ACEi) and angiotensin receptor blockers (ARBs) has been widely discussed since the beginning of the pandemic. However, clinical studies have shown that ACEi or ARBs do not increase morbidity or mortality in COVID-19 patients [18–20]. Our patient continued to use valsartan. Our patient with bilateral COVID-19 pneumonia who had severe NS due to MN and had received rituximab 1 month ago did not develop severe hypoxemia and did not need intensive care. However, high fever remained for a long time. Hospital stay was well above average (21 days). Combination of hydroxychloroquine, moxifloxacin and azithromycin, oseltamivir, and lopinavir/ritonavir were used at different times for treatment. Our experience in the monitoring and treatment of COVID-19 is increasing day by day. Recently, we have started to use hydroxychloroquine and azithromycin or moxifloxacin in the early onset of pneumonia. When hypoxemia starts to develop, we choose to start patients on favipiravir in order to avoid the need for intensive care. We give prophylactic anticoagulants to all inpatients. We believe that this treatment approach is associated with low mortality in our country [14]. In nephrology practice, there are situations where we cannot stop immunosuppressive treatment such as kidney transplantation and vasculitis leading to rapidly progressive glomerulonephritis. On the other hand, we have patients with NS, in whom immunosuppressive therapy can be delayed for a while. Some of them were started on immunosuppressive agents before the pandemic. Some of our patients which have NS also have an indication for immunosuppressive therapy during the pandemic. We are undecided about temporarily discontinuing the treatment of our patients currently on immunosuppressives agents or postponing the treatment of our patients in need for treatment. According to our observations, we concluded that the use of rituximab should be preferred in patients with absolute indication. Because, we did not observe any significant side effects or increase in mortality due to rituximab. As a result, we make individual decisions on a case-by-case basis. In order to make more accurate decisions, more data on this issue should be collected. Therefore, we thought that it was appropriate to report this case to contribute to this accumulating data.

Compliance with ethical standards

Conflict of interest

The authors have declared that no conflict of interest exists.

Informed consent

Informed consent was obtained from the patient included in the study.