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Clinical Institute of Urology and Renal Transplantation, Cluj-Napoca, RomaniaDepartment of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania
Clinical Institute of Urology and Renal Transplantation, Cluj-Napoca, RomaniaDepartment of Anesthesiology, University of Medicine and Pharmacy, Cluj-Napoca, Romania
Clinical Institute of Urology and Renal Transplantation, Cluj-Napoca, RomaniaDepartment of Urology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, RomaniaBiomed Data Analytics SRL, Cluj-Napoca, Romania
The Transplant Institute, Sahlgrenska University Hospital, Gothenburg, SwedenInstitute for Clinical Sciences, Department of Surgery, Sahlgrenska Academy, University of Gothenburg, Sweden
Studies on remdesivir as COVID-19 therapy excluded patients with poor renal function
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Kidney transplant recipients frequently have impaired renal function
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No negative effect on the renal function was seen after 5 days of remdesivir
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Remdesivir significantly improved intensive care survival
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Remdesivir did not seem to reduce overall mortality
Abstract
Objectives
The aim of the study was to evaluate the impact of remdesivir on overall mortality, ICU mortality, and renal functional outcome in hospitalized patients with COVID-19 who received kidney transplant.
Methods
We reviewed 165 patients with KTx hospitalized owing to COVID-19 between March 1, 2020, and May 31, 2021. A total of 38 patients with KTx received a 5-day RDV treatment, whereas 127 received standard of care (SOC). Overall and ICU mortality along with functional outcome were assessed.
Results
The 2 groups had similar baseline characteristics. RDV treatment was completed in all patients without any adverse effects attributable to RDV. In terms of overall mortality, there was no difference between the RDV and SOC groups (18% vs 23%, p >0.05), but the ICU mortality was significantly reduced in the RDV group (39% vs 83%, p <0.05). RDV seems to have no nephrotoxic effect on patients with KTx because there was no difference in the incidence of AKI between RDV and SOC groups (50% vs 43%, p >0.05), and the discharge eGFR values significantly improved in the RDV group compared with the admission values (57 ± 23 vs 44 ± 22, p <0.05).
Conclusion
Five-day RDV treatment appears safe in KTx recipients, and without obvious nephrotoxic effects. Also, RDV may decrease ICU mortality attributed to COVID-19.
Lifelong immunosuppression and the burden of comorbidities put organ transplant recipients at risk for unfavorable outcome after SARS-CoV-2 infection (
). The initial lack of knowledge concerning this new and puzzling disease as well as the absence of targeted and effective antiviral interventions during the early phases of the pandemic resulted in a mortality of kidney transplant (KTx) recipients exceeding 25% (
). However, rapidly accumulating information, evolving guidelines, and several experimental treatments seem to have improved the outcomes following COVID-19 both in transplanted patients and the general population (
UW Covid-19 SOT Study Team Changing Trends in Mortality Among Solid Organ Transplant Recipients Hospitalized for Covid-19 During the Course of the Pandemic.
Spanish Society of Nephrology COVID-19 Group. Predictors of severe COVID-19 in kidney transplant recipients in the different epidemic waves: Analysis of the Spanish Registry.
), remains to be one of the few evidence-based targeted antiviral interventions available to date.
The urgency required in the development and review of several new anti-COVID-19 compounds, including RDV, has led to the exclusion of several risk groups from the trials conducted during 2020, such as patients with poor liver and kidney function (creatinine clearance less than 30 or 50 mL/min) (
GS-US-540-5774 Investigators. Effect of Remdesivir vs Standard Care on Clinical Status at 11 Days in Patients With Moderate COVID-19: A Randomized Clinical Trial.
). This caution was largely justified by concerns related to previously known side effects such as potential nephrotoxicity of RDV or its inactive ingredient, the solubility enhancer sulfobutylether-β-cyclodextrin (SBECD), which can accumulate in patients with impaired renal function (
). Unfortunately, this has also resulted in a knowledge gap about the safety, optimal dosing, and efficacy of RDV in patients with reduced renal function. Hence, the impact of RDV on COVID-19 outcome in KTx recipients, who frequently have impaired renal function, is poorly known.
There are very few reports on the use of RDV in KTx recipients with COVID-19 (
). This limited body of evidence generated from widely different geographic areas during various pandemic phases could not discern significant side effects and suggests that RDV was well tolerated and safe in KTx recipients with COVID-19. However, its impact on the overall outcomes and comparison with patients receiving the standard of care (SOC) is essentially missing, and only one small study attempted to balance its findings (outcome, biochemistry) against a control group of KTx with COVID-19 not receiving RDV (
). Here, we comparatively analyzed a cohort of KTx recipients with COVID-19 and receiving RDV or not during the same time period at a transplant center in Eastern Europe. The main readouts of this study were overall mortality, ICU mortality, and functional outcome.
Patients and methods
We performed a retrospective cohort single center study of all KTx recipients who underwent transplantation at the Clinical Institute of Urology and Renal Transplantation (CIURT) in Cluj-Napoca, Romania, and who diagnosed with COVID-19 between March 1st, 2020 and May 31st, 2021. We comparatively analyzed hospitalized kidney transplant recipients with COVID-19 receiving RDV versus hospitalized KTx recipients with COVID-19, receiving standard of care (SOC) during the same time period. For the purpose of this study, 2 patient groups were defined: all KTx recipients receiving RDV (RDV group) and all the other hospitalized KTx irrespective of COVID-19 treatment (standard of care group [SOC]). SARS-CoV-2 infection was defined as a positive result for SARS-CoV-2 RNA on a real-time polymerase chain reaction assay of a nasopharyngeal swab. Both asymptomatic KTx recipients and patients presenting with typical symptoms such as fever (>38°C), respiratory, gastrointestinal, neurological, or general symptoms were included. Patients managed entirely on an outpatient basis and patients receiving antiviral therapy other than RDV were excluded from the analysis. The study was performed in accordance with Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement (
STROBE Initiative The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.
) and was approved by the Institutional Review Board of the Clinical Institute of Urology and Renal Transplantation ( 01/2021).
Patient Management
The COVID-19 treatment protocol recommended in Romania in the early phase of the pandemic (March–July 2020) was based on hydroxychloroquine (HCQ) and antiretrovirals. HCQ was started with a loading dose of 400 mg orally twice daily for 1 day and then continued at 200 mg orally twice daily for 7–10 days. Antiretrovirals (Lopinavir/Ritonavir, darunavir/ritonavir, or darunavir/cobicistat) were added in patients with mild and moderate forms and adequate renal function (estimated glomerular filtration rate [eGFR] >30 mL/min/1.73 m2). From mid-July 2020, RDV was added to the treatment protocol in more severe cases, whereas HCQ and antiretrovirals were no longer recommended. When available, RDV (Veklury, Gilead Pharma) was administered in moderate and severe cases applying the five-day European Medicines Agency protocol (
). Low eGFR and AKI were not considered as contraindications. RDV was started at a dose of 200 mg/day on the first day, followed by 100 mg/day over the next 4 days, given as an intravenous infusion. Dexamethasone and antibiotics were also given at the discretion of the medical teams attending the patients. Anticoagulation using low-molecular-weight heparin (LMWH) was recommended in all hospitalized patients from mid-April 2020 onward.
Antibiotics were given at the discretion of the attending medical teams. Immunosuppression was managed through contacts with the transplant nephrologists from CIURT. Immunosuppression was frequently reduced by pausing the antimetabolite (mycophenolate mofetil or mycophenolic acid) with or without adjusting calcineurin inhibitors. Tacrolimus was withdrawn in all patients receiving antiretrovirals and adjusted to maintain a trough level of 4–6 ng/mL in the other patients. Steroids were either kept at the maintenance dose or converted to IV for stress dosing. Other therapies like tocilizumab were given as per the local availability and severity of COVID-19.
Data collection
The following data were recorded as baseline characteristics of the 3 groups: sex, age, weight, body mass index (BMI), comorbidities (hypertension, cardiovascular disease, diabetes, and malignancy), baseline and hospital admission renal function (estimated glomerular filtration rate (eGFR) using the CKD-EPI formula; baseline eGFR was collected during the last 12 months before COVID-19), Charlson comorbidity index (CCI) as previously described (
), time from transplant, baseline immunosuppression, and treatment administered for COVID-19 management. The following data were recorded as outcomes: overall mortality, ICU mortality, COVID-19 severity (classified from mild to critical using the NIH criteria [
, ICU admission, oxygen therapy, mechanical ventilation, acute kidney injury (AKI) incidence during hospitalization (defined as an increase in serum creatinine by 0.3 mg/dl or more within 48 hours or as an increase of 1.5 times or more from baseline), and discharge eGFR.
Data analysis
Demographic, baseline characteristics and outcomes were assessed as counts and percentages for categorical values and as a mean (± standard deviation) or median (± range) for continuous variables. Fisher exact test was used to assess the proportions of categorical variables. Continuous variables were assessed using the Mann-Whitney U test. Kaplan-Meier and the log-rank test were used to calculate and compare survival.
Age, sex, comorbidities, chronic kidney disease grade 4–5 (baseline eGFR <30 ml/min/1.73m2), time from transplantation, and BMI were chosen as potential risk factors based on hypotheses and/or previous studies showing a relationship with COVID-19 mortality. Analyses were performed using GraphPad Prism v.9.3. (GraphPad Software, San Diego, CA)
Results
Baseline patient characteristics
At the start of the pandemic (March 1st, 2020), 1467 KTx recipients were alive and in followed-up at the Institute of Urology and Renal Transplantation in Cluj-Napoca, Romania. Furthermore, 51 patients were transplanted during the study period, resulting in a total of 1518 KTx recipients at risk for developing COVID-19 who were included in this study. During the 15 months of the study, there were 234 KTx recipients diagnosed with COVID-19 (15, 7%). A total of 59 patients (25%) were managed entirely on an outpatient basis and were excluded from the analysis. Further, 10 patients received Favipiravir and were excluded from the analysis. The remaining 165 hospitalized patients formed the basis for the current report: 38 (23%) patients received RDV as part of their COVID-19 management, whereas 127 (77%) did not (SOC group) (Table 1).
Table 1Baseline characteristics of Remdesivir (RDV) and standard of care (SOC) groups.
Data are reported as number /total number of available observations and (percent), or median and interquartile range (Q1-Q3). CCI – Charlson comorbidity index, CNI – calcineurin inhibitors, CRRT – continuous renal replacement therapy, HCQ - hydroxychloroquine, LMWH – low molecular weight heparin, MMF – mycophenolate mofetil, NOAC – Non-Vitamin K antagonist oral anticoagulants.
Patients in the two groups were largely similar in terms of age, time from transplantation, frequency of obesity, and comorbidities (Table 1). However, the RDV group included fewer male subjects (55% vs 70%, p <0.05), more patients with grade G3a kidney disease (37 vs 17%, p <0.05), more patients with diabetes (47% vs 24%, p <0.05), and malignancies (7.9% vs 0.8%, p <0.05) (Table 1). In terms of baseline immunosuppression, the RDV group had more patients on rapamycin (11% vs 2%, p <0.05) (Table 1). In terms of COVID-19 management, the RDV group had less mycophenolate mofetil reduction or withdrawal (37% vs 58%, p <0.05) and administration of low-molecular-weight heparin and nonvitamin K antagonist (84% vs 86%, p<0.01), whereas more patients were administered tocilizumab and dexamethasone (11% vs 2%, p<0.05, and 84% vs 41%, p<0.05, respectively) (Table 1).
Outcomes
In terms of overall mortality, there was no difference between the RDV and SOC groups (18% vs 23%, p >0.05) (Table 2, Figure 1A and B), but the ICU mortality was significantly reduced in the RDV group (39% vs 83%, p <0.05) (Table 2, Figure 1 C and D). The proportion of patients with severe COVID-19 was higher in the RDV group (42 % vs 14%, p <0.05), whereas the proportion of patients with mild COVID-19 disease was lower in the RDV group (8% vs 36 %, p <0.05) (Table 2, Figure 2A). In addition, the proportion of patients requiring ICU admission was significantly higher in the RDV group than patients receiving SOC (47% vs 27%, p <0.05).
Table 2Outcomes of Remdesivir (RDV) and standard of care (SOC) groups
Figure 1A) Overall mortality of Remdesivir (RDV) and standard of care (SOC) groups. B) Kaplan–Meier overall survival analysis for RDV and SOC groups. C) Intensive care unit (ICU) mortality for RDV and SOC groups. D) Kaplan–Meier ICU survival for RDV and SOC groups.
Figure 2A) COVID 19 severity for Remdesivir (RDV) and standard of care (SOC) groups. B) Violin plot with mean and standard deviation representation of discharge estimated glomerular filtration rate (eGFR) for RDV and SOC groups. C) Violin plot with mean and standard deviation representation of baseline and discharge eGFR for RDV group.
Univariate analysis for mortality showed significant differences between survivors and nonsurvivors for the following confounding factors: the number of patients aged over 65 (HR: 2.51 [1.11–5.14], p <0.05), CCI (HR 1.81 [1.06–1.6], p <0.05), recent transplant (<12 months) (HR 2.4 [0.96–5.21], p <0.05), and stage 4–5 chronic kidney disease at baseline (HR 3.81 [1.96–7.35], p <0.05). In multivariate Cox regression, the following confounding factors reached statistical significance for association with shorter survival: recent transplant (<12 months) [HR 3.14 [1.07–8.77], p <0.05), stage 4–5 chronic kidney disease at baseline (HR 7.49 [3.25–17.9], p <0.05) and COVID-19 severity (HR 8.12 [4.32–18.2], p <0.05).
Supplemental oxygen was required significantly more often in patients receiving RDV than patients receiving SOC (84% vs 44%, p <0.05), and there was no difference in the proportion of patients requiring mechanical ventilation (21% vs 24%, p >0.05) (Table 2).
Toxicity and renal function
No serious adverse effects attributable to RDV were noted, and the 5-day RDV treatment was completed in all patients.
At hospital discharge, there was no sign of RDV nephrotoxicity, with no difference in the incidence of AKI between RDV and SOC groups (50% vs 43%, p>0.05); whereas, the admission eGFR values significantly improved in the RDV group compared to the discharge values (44±22 vs 57±23, p<0.05) (Table 2, Figure 2C). There was no difference in the discharge eGFR between RDV and SOC groups (57 ± 23 vs 62 ± 28 ml/min/1.73 m2, p >0.05) (Table 2, Figure 2B).
Discussion
This study reports the outcomes of hospitalized kidney transplant recipients with COVID-19 treated with RDV compared with patients receiving SOC alone. The results suggest that RDV has a positive impact on COVID-19 patients in terms of ICU mortality and that the drug is not associated with significant nephrotoxicity. Consequently, these results suggest that recommendations on RDV use in the normal populations could be extended to KTx recipients.
The landmark paper of Beigel et al has provided essential knowledge about optimal dosing and timing, adverse effects, and outcomes of RDV (
). Currently, RDV is recommended in hospitalized patients requiring supplementary oxygen (i.e., severe disease forms) but not mechanical ventilation, with or without dexamethasone, as a 5- or 10-day treatment protocol, administered as soon as possible after the onset of symptoms and preferably, within the first week. However, because severe COVID-19 typically begins to manifest 8–12 days after symptom onset, it is possible that in some patients, including patients in this study, RDV administration was initiated late in the course of the disease. Hence, the window of opportunity in the first days after infection, when intense viral replication occurs, can easily be missed. The median time from onset of symptoms and diagnosis and treatment start was within this time frame, and although several patients received RDV after more than 10 days from the first symptoms, they all survived.
This study suggests that RDV significantly decreased ICU mortality, possibly limiting disease progression. This finding is in line with several much larger studies in nontransplanted patients, where RDV reduced the odds of death during the study and shortened the time to clinical recovery, particularly in hospitalized patients requiring oxygen supplementation but who were not in very critical condition (intubated or on extracorporeal membrane oxygenation) (
Impaired renal function following RDV treatment has been the main concern because of the potential accumulation, and renal tubule toxicity of RDV's active metabolite or its inactive ingredient, SBECD, used to improve its aqueous solubility (
). Consequently, all initial studies on RDV have excluded patients with kidney impairment (eGFR <30–50 ml/min/1.73 m2), an exclusion criterion that has led to a gap of knowledge in terms of efficacy and safety of RDV in this vulnerable patient group, especially KTx patients
In this study, there was no difference in terms of AKI incidence for RDV and SOC groups (50% vs 43%, p >0.05). Similar to previous reports, the short RDV course applied in this study did not add to the other causes of renal impairment, such as dehydration, viral tropism, endothelial dysfunction, coagulopathy, or systemic inflammation (
). Moreover, there was an improvement in renal function during the hospitalization, the discharge eGFR being significantly increased compared to baseline (Figure 2C). This apparent improvement, likely owing to several factors such as the decrease or discontinuation of calcineurin inhibitors, rehydration, and resolution of the disease, did not seem to be negatively affected by RDV.
RDV is metabolized by the cytochrome P450 3A4, similar with tacrolimus. Although no apparent drug-drug interactions (DDI) are expected between RDV and Tacrolimus (
) , which may theoretically result in supratherapeutic levels of both RDV and tacrolimus. In contrast with Lopinavir/Ritonavir (Kaletra), which has been frequently used during the first months of the pandemic and where DDI between it and numerous drugs, including Tacrolimus, are well known, this concern has been largely theoretical during the use of RDV (
Pharmacologic Treatment of Transplant Recipients Infected With SARS-CoV-2: Considerations Regarding Therapeutic Drug Monitoring and Drug-Drug Interactions.
). In addition, in patients with severe and critical disease, in whom the “cytokine storm” could have developed, tacrolimus administration was frequently reduced or even discontinued (
This study has several significant limitations. Until October 2020, the length of hospitalization for individuals infected with SARS-CoV-2 in Romania was regulated through a governmental ordinance to at least 10 days of hospitalization or 14 days from the start of symptoms, even if the patients have recovered completely. Unfortunately, this ambitious measure that aimed at ensuring optimal isolation during and after COVID-19 also turned the length of hospital stay into an irrelevant outcome measure for over half of the study period.
The relatively small size, unequal distribution between groups, and the retrospective design preclude solid conclusions, and the results need to be interpreted cautiously. Some relevant clinical or laboratory data (notably daily creatinine or liver function tests) could not be reliably assessed and compared because its availability was inconsistent between the 2 study groups. Kidney function and injury were assessed based only on serum creatinine, a widely available yet coarse parameter. In addition, although the groups were largely similar in terms of demographics, comorbidities, and immunosuppression, we found several significant differences in terms of kidney graft function, diabetes, and malignancies, which may have reflected a certain selection bias. However, this selection bias did not favor the RDV group, which had worse baseline eGFR and more patients with diabetes and malignancies (Table 1). Despite these circumstances, these patients had better ICU survival, which may suggest a certain benefit of RDV.
Despite these limitations, this analysis also has several strengths—notably, the presence of a contemporary control group and the use of the same RDV treatment protocol throughout the study. The study population matched well with other larger studies or meta-analyses in terms of patient age, comorbidity burden, and overall results (ICU admission rate, mortality) (
Incidence of Mortality, Acute Kidney Injury and Graft Loss in Adult Kidney Transplant Recipients with Coronavirus Disease 2019: Systematic Review and Meta-Analysis.
). Although the study period stretched over 3 pandemic waves and presents an evolutionary experience where COVID-treatment protocols have changed over time (
Spanish Society of Nephrology COVID-19 Group. Predictors of severe COVID-19 in kidney transplant recipients in the different epidemic waves: Analysis of the Spanish Registry.
), patients in the 2 study groups received simultaneously, albeit not randomized, either RDV or SOC, according to the recommendation at that point in time.
In conclusion, this study indicates that RDV was safe and well tolerated in KTx recipients with COVID-19. Its administration did not appear to negatively impact the renal outcome of KTx. Although the ability of RDV to improve the overall mortality remains unclear, there may be a certain patient subgroup with noncritical disease that may benefit from RDV treatment.
Acknowledgements
We thank the “Research in Urology Association” support for publishing this paper.
Conflict of interest
The authors have no conflicts of interests to declare.
Ethical considerations
The study was reviewed and approved by the Ethical Review Committee of the Clinical Institute for Urology and Renal Transplantation (01/2021).
Funding
There is no funding source to be reported.
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