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1.
Contrib Nephrol ; 199: 229-243, 2021.
Article in English | MEDLINE | ID: covidwho-1338891

ABSTRACT

Clinical Background: The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) rapidly spread globally from late 2019, reaching pandemic proportions. Epidemiology: The related disease, COVID-19, exacerbates and progresses due to patients' abnormal inflammatory/immune responses, widespread endothelial damage, and complement-induced blood clotting with microangiopathy. COVID-19 manifests mainly as a respiratory illness. In cases of severe viral pneumonia, it may lead to acute respiratory distress syndrome, respiratory failure, and death. Challenges: Many extrapulmonary manifestations commonly occur, and a substantial proportion of patients with severe COVID-19 exhibit signs of kidney damage. Clinically, kidney involvement ranges from mild/moderate proteinuria and hematuria to acute kidney injury (AKI) requiring renal replacement therapy (RRT). The pathophysiologic mechanisms of kidney damage and AKI in patients with COVID-19 remain unclear but are known to be multifactorial. Current knowledge implies direct SARS-CoV-2-dependent effects on kidney cells (tubular epithelial cells and podocytes) and indirect mechanisms through the systemic effect of viral infection secondary to the critical pulmonary illness and its management. Prevention and Treatment: Standard-of-care strategies apply, as there is no specific evidence to suggest that COVID-19 AKI should be managed differently from other types in severely ill patients. If conservative management fails, RRT should be considered. The choice of RRT approaches and sequential extracorporeal therapies depends on local availability, resources, and expertise. The focus should now be on the long-term follow-up of COVID-19 patients, especially those who developed kidney injury and dysfunction. This represents an opportunity for integrated multidisciplinary research to clarify the natural history of COVID-19 renal sequelae and the best therapeutic interventions to mitigate them.


Subject(s)
Acute Kidney Injury/therapy , Acute Kidney Injury/virology , COVID-19/complications , COVID-19/therapy , COVID-19/epidemiology , Hematuria/virology , Humans , Nephrologists , Proteinuria/virology , Renal Replacement Therapy , SARS-CoV-2
2.
Kidney Blood Press Res ; 45(6): 1018-1032, 2020.
Article in English | MEDLINE | ID: covidwho-917826

ABSTRACT

INTRODUCTION: Acute kidney injury (AKI) is strongly associated with poor outcomes in hospitalized patients with coronavirus disease 2019 (COVID-19), but data on the association of proteinuria and hematuria are limited to non-US populations. In addition, admission and in-hospital measures for kidney abnormalities have not been studied separately. METHODS: This retrospective cohort study aimed to analyze these associations in 321 patients sequentially admitted between March 7, 2020 and April 1, 2020 at Stony Brook University Medical Center, New York. We investigated the association of proteinuria, hematuria, and AKI with outcomes of inflammation, intensive care unit (ICU) admission, invasive mechanical ventilation (IMV), and in-hospital death. We used ANOVA, t test, χ2 test, and Fisher's exact test for bivariate analyses and logistic regression for multivariable analysis. RESULTS: Three hundred patients met the inclusion criteria for the study cohort. Multivariable analysis demonstrated that admission proteinuria was significantly associated with risk of in-hospital AKI (OR 4.71, 95% CI 1.28-17.38), while admission hematuria was associated with ICU admission (OR 4.56, 95% CI 1.12-18.64), IMV (OR 8.79, 95% CI 2.08-37.00), and death (OR 18.03, 95% CI 2.84-114.57). During hospitalization, de novo proteinuria was significantly associated with increased risk of death (OR 8.94, 95% CI 1.19-114.4, p = 0.04). In-hospital AKI increased (OR 27.14, 95% CI 4.44-240.17) while recovery from in-hospital AKI decreased the risk of death (OR 0.001, 95% CI 0.001-0.06). CONCLUSION: Proteinuria and hematuria both at the time of admission and during hospitalization are associated with adverse clinical outcomes in hospitalized patients with COVID-19.


Subject(s)
Acute Kidney Injury/urine , Acute Kidney Injury/virology , COVID-19/urine , Hematuria/virology , Proteinuria/virology , Acute Kidney Injury/mortality , Aged , COVID-19/mortality , COVID-19/virology , Cohort Studies , Female , Hematuria/mortality , Humans , Male , Middle Aged , New York/epidemiology , Proteinuria/mortality , Retrospective Studies , SARS-CoV-2/isolation & purification , Survival Analysis
3.
Clin J Am Soc Nephrol ; 15(11): 1549-1556, 2020 11 06.
Article in English | MEDLINE | ID: covidwho-781834

ABSTRACT

BACKGROUND AND OBJECTIVES: Coronavirus disease 2019 is spreading rapidly across the world. This study aimed to assess the characteristics of kidney injury and its association with disease progression and death of patients with coronavirus disease 2019. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: This is a retrospective study. Two representative cohorts were included. Cohort 1 involved severe and critical patients with coronavirus disease 2019 from Wuhan, China. Cohort 2 was all patients with coronavirus disease 2019 in Shenzhen city (Guangdong province, China). Any kidney injury was defined as the presence of any of the following: hematuria, proteinuria, in-hospital AKI, or prehospital AKI. AKI was defined according to the Kidney Disease Improving Global Outcomes (KDIGO) creatinine criteria. The primary outcome was death at the end of follow-up. The secondary outcome was progression to critical illness during the study period. RESULTS: A total of 555 patients were enrolled; 42% of the cases (229 of 549) were detected with any kidney injury, 33% of the cases (174 of 520) were detected with proteinuria, 22% of the cases (112 of 520) were detected with hematuria, and 6% of the cases (29 of 520) were detected with AKI. Of the 29 patients with AKI, 21 cases were recognized as in-hospital AKI, and eight were recognized as prehospital AKI. Altogether, 27 (5%) patients died at the end of follow-up. The death rate was 11% (20 of 174) in patients with proteinuria, 16% (18 of 112) in patients with hematuria, and 41% (12 of 29) in the AKI settings. Multivariable Cox regression analysis showed that proteinuria (hazard ratio, 4.42; 95% confidence interval, 1.22 to 15.94), hematuria (hazard ratio, 4.71; 95% confidence interval, 1.61 to 13.81), and in-hospital AKI (hazard ratio, 6.84; 95% confidence interval, 2.42 to 19.31) were associated with death. Among the 520 patients with noncritical illness at admission, proteinuria (hazard ratio, 2.61; 95% confidence interval, 1.22 to 5.56) and hematuria (hazard ratio, 2.50; 95% confidence interval, 1.23 to 5.08) were found to be associated with progression to critical illness during the study period. CONCLUSIONS: Kidney injury is common in coronavirus disease 2019, and it is associated with poor clinical outcomes. PODCAST: This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2020_09_18_CJN04780420.mp3.


Subject(s)
Acute Kidney Injury/epidemiology , Coronavirus Infections/complications , Hematuria/epidemiology , Pneumonia, Viral/complications , Proteinuria/epidemiology , Acute Kidney Injury/mortality , Acute Kidney Injury/virology , Adult , Aged , Betacoronavirus , COVID-19 , China/epidemiology , Critical Illness , Disease Progression , Female , Hematuria/mortality , Hematuria/virology , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Pandemics , Prevalence , Proportional Hazards Models , Proteinuria/mortality , Proteinuria/virology , Retrospective Studies , SARS-CoV-2 , Survival Rate
4.
J Card Surg ; 35(11): 3202-3204, 2020 Nov.
Article in English | MEDLINE | ID: covidwho-713504

ABSTRACT

Patients with durable left ventricular assist devices pose special problems for management in the setting of COVID-19 infection. We describe the successful management of a 44-year-old man with severe COVID-19 infection and HeartMate 3 left ventricular assist device. His course was complicated by cytokine storm and COVID-19-associated coagulopathy. We describe our institutional protocol for managing COVID-19 infection in patients on mechanical circulatory support, focusing on the need for a thoughtful, multidisciplinary approach.


Subject(s)
COVID-19/complications , Heart-Assist Devices , Hematoma , Thrombosis , Adult , Anticoagulants/therapeutic use , Aspirin/therapeutic use , Biomarkers/blood , Blood Transfusion , Cytokine Release Syndrome/virology , Fibrin Fibrinogen Degradation Products/analysis , Fibrinogen/analysis , Hematoma/therapy , Hematoma/virology , Hematuria/therapy , Hematuria/virology , Hemorrhage/therapy , Hemorrhage/virology , Heparin/therapeutic use , Humans , Male , Platelet Aggregation Inhibitors/therapeutic use , Retroperitoneal Space , Thrombocytopenia/therapy , Thrombocytopenia/virology , Thrombosis/therapy , Thrombosis/virology
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