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      Call for Papers: Epidemiology of CKD and its Complications

      Submit here by August 31, 2024

      About Kidney and Blood Pressure Research: 2.3 Impact Factor I 4.8 CiteScore I 0.674 Scimago Journal & Country Rank (SJR)

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      Endothelial Biomarkers in Critically Ill COVID-19 Patients: Potential Predictors of the Need for Dialysis

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      a , b , c , a , c , b , a , b , a , c , c , c , d , e , f , * , b , a , b , a , b , e , f , b , f , a
      Kidney and Blood Pressure Research
      S. Karger AG
      COVID-19, Dialysis, Endothelium, Biomarkers, ICU, Prognosis

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          Abstract

          Introduction: The aim of this was to evaluate the function of vascular biomarkers to predict the need for hemodialysis in critically ill patients with COVID-19. Methods: This is a prospective study with 58 critically ill patients due to COVID-19 infection. Laboratory tests in general and vascular biomarkers, such as VCAM-1, syndecan-1, angiopoietin-1, and angiopoietin-2, were quantified on intensive care unit (ICU) admission. Results: There was a 40% death rate. VCAM and Ang-2/Ang-1 ratio on ICU admission were associated with the need for hemodialysis. Vascular biomarkers (VCAM-1, syndecan-1, angiopoietin-2/angiopoietin-1 ratio) were predictors of death and their cutoff values were useful to stratify patients with a worse prognosis. In the multivariate cox regression analysis with adjusted models, VCAM-1 (OR 1.13 [CI 95%: 1.01–1.27]; p = 0.034) and Ang-2/Ang-1 ratio (OR 4.87 [CI 95%: 1.732–13.719]; p = 0.003) were associated with the need for dialysis. Conclusion: Vascular biomarkers, mostly VCAM-1 and Ang-2/Ang-1 ratio, showed better efficiency to predict the need for hemodialysis in critically ill COVID-19 patients.

          Plain Language Summary

          This study reports the use of endothelial biomarkers as useful tools to predict the first dialysis requirement during the ICU stay in patients with severe COVID-19. Endothelial dysfunction is an important mechanism to explain the pathophysiology of acute kidney injury caused by severe acute respiratory syndrome coronavirus 2 infection.

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          Most cited references40

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          A Novel Coronavirus from Patients with Pneumonia in China, 2019

          Summary In December 2019, a cluster of patients with pneumonia of unknown cause was linked to a seafood wholesale market in Wuhan, China. A previously unknown betacoronavirus was discovered through the use of unbiased sequencing in samples from patients with pneumonia. Human airway epithelial cells were used to isolate a novel coronavirus, named 2019-nCoV, which formed a clade within the subgenus sarbecovirus, Orthocoronavirinae subfamily. Different from both MERS-CoV and SARS-CoV, 2019-nCoV is the seventh member of the family of coronaviruses that infect humans. Enhanced surveillance and further investigation are ongoing. (Funded by the National Key Research and Development Program of China and the National Major Project for Control and Prevention of Infectious Disease in China.)
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            Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study

            Summary Background An ongoing outbreak of pneumonia associated with the severe acute respiratory coronavirus 2 (SARS-CoV-2) started in December, 2019, in Wuhan, China. Information about critically ill patients with SARS-CoV-2 infection is scarce. We aimed to describe the clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia. Methods In this single-centered, retrospective, observational study, we enrolled 52 critically ill adult patients with SARS-CoV-2 pneumonia who were admitted to the intensive care unit (ICU) of Wuhan Jin Yin-tan hospital (Wuhan, China) between late December, 2019, and Jan 26, 2020. Demographic data, symptoms, laboratory values, comorbidities, treatments, and clinical outcomes were all collected. Data were compared between survivors and non-survivors. The primary outcome was 28-day mortality, as of Feb 9, 2020. Secondary outcomes included incidence of SARS-CoV-2-related acute respiratory distress syndrome (ARDS) and the proportion of patients requiring mechanical ventilation. Findings Of 710 patients with SARS-CoV-2 pneumonia, 52 critically ill adult patients were included. The mean age of the 52 patients was 59·7 (SD 13·3) years, 35 (67%) were men, 21 (40%) had chronic illness, 51 (98%) had fever. 32 (61·5%) patients had died at 28 days, and the median duration from admission to the intensive care unit (ICU) to death was 7 (IQR 3–11) days for non-survivors. Compared with survivors, non-survivors were older (64·6 years [11·2] vs 51·9 years [12·9]), more likely to develop ARDS (26 [81%] patients vs 9 [45%] patients), and more likely to receive mechanical ventilation (30 [94%] patients vs 7 [35%] patients), either invasively or non-invasively. Most patients had organ function damage, including 35 (67%) with ARDS, 15 (29%) with acute kidney injury, 12 (23%) with cardiac injury, 15 (29%) with liver dysfunction, and one (2%) with pneumothorax. 37 (71%) patients required mechanical ventilation. Hospital-acquired infection occurred in seven (13·5%) patients. Interpretation The mortality of critically ill patients with SARS-CoV-2 pneumonia is considerable. The survival time of the non-survivors is likely to be within 1–2 weeks after ICU admission. Older patients (>65 years) with comorbidities and ARDS are at increased risk of death. The severity of SARS-CoV-2 pneumonia poses great strain on critical care resources in hospitals, especially if they are not adequately staffed or resourced. Funding None.
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              The pathogenesis and treatment of the `Cytokine Storm' in COVID-19

              Summary Cytokine storm is an excessive immune response to external stimuli. The pathogenesis of the cytokine storm is complex. The disease progresses rapidly, and the mortality is high. Certain evidence shows that, during the coronavirus disease 2019 (COVID-19) epidemic, the severe deterioration of some patients has been closely related to the cytokine storm in their bodies. This article reviews the occurrence mechanism and treatment strategies of the COVID-19 virus-induced inflammatory storm in attempt to provide valuable medication guidance for clinical treatment.
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                Author and article information

                Journal
                KBR
                Kidney Blood Press Res
                10.1159/issn.1420-4096
                Kidney and Blood Pressure Research
                Kidney Blood Press Res
                S. Karger AG
                1420-4096
                1423-0143
                2024
                January – December 2024 2024
                28 November 2023
                : 49
                : 1
                : 27-37
                Affiliations
                [a ]Medical Sciences Postgraduate Program, Department of Internal Medicine, School of Medicine, Universidade Federal do Ceará, Fortaleza, Brazil
                [b ]Instituto José Frota (IJF) Hospital, Fortaleza, Brazil
                [c ]Clinical and Toxicological Analysis Department, School of Pharmacy, Federal University of Ceará, Fortaleza, Brazil
                [d ]School of Medicine, Universidade Federal do Ceará, Fortaleza, Brazil
                [e ]Public Health Postgraduate Program, School of Medicine, Health Sciences Center, Universidade de Fortaleza, Fortaleza, Brazil
                [f ]School of Medicine, Health Sciences Center, Universidade de Fortaleza, Fortaleza, Brazil
                Author notes
                *Gdayllon Cavalcante Meneses, gdayllon@yahoo.com.br
                Article
                535035 Kidney Blood Press Res 2024;49:27–37
                10.1159/000535035
                38016435
                c6017126-385e-492b-a789-2edece500e15
                © 2023 The Author(s). Published by S. Karger AG, Basel
                History
                : 26 April 2023
                : 30 October 2023
                Page count
                Figures: 3, Tables: 3, Pages: 11
                Funding
                Brazilian Coordination of Postgraduation – Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) supported this study through grants given to the co-authors (PLMMA). Number of the process: 88882.306447/2018-01.Brazilian Coordination of Postgraduation – Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) supported the materials used. Number of process support 1: 88881.505364/2020-01. Number of process support 2: 88881.507066/2020-01.Edson Queiroz Foundation/University of Fortaleza for the financial support.
                Categories
                Research Article

                Medicine
                COVID-19,Dialysis,Endothelium,Biomarkers,ICU,Prognosis
                Medicine
                COVID-19, Dialysis, Endothelium, Biomarkers, ICU, Prognosis

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