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      The association between acid–base status and clinical outcome in critically ill COVID-19 patients admitted to intensive care unit with an emphasis on high anion gap metabolic acidosis

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          Abstract

          Objective

          The aim of this study was to identify arterial blood gas (ABG) abnormalities, with a focus on a high anion gap (AG) metabolic acidosis and evaluate outcomes in coronavirus disease 2019 (COVID-19) patients admitted to the ICU.

          Methods

          A retrospective, observational study was conducted in a tertiary hospital in Cape Town during the first and second COVID-19 waves. Age, gender, sodium (Na), potassium (K), chloride (Cl), bicarbonate (HCO 3std), pH, partial pressure of carbon dioxide (pCO 2), creatinine, estimated glomerular filtration rate (eGFR), lactate levels and ABG results were obtained. The Pearson χ2 test or Fisher exact test and the Wilcoxon rank-sum test were used to compare mortality and survival. To identify factors associated with non-survival, a multivariable model was developed.

          Results

          This study included 465 patients, 226 (48%) of whom were female. The sample population’s median (IQR) age was 54.2 (46.1–61.3) years, and 63% of the patients died. ABG analyses found that 283 (61%) of the 465 patients had alkalosis (pH ≥ 7.45), 65 (14%) had acidosis (pH ≤ 7.35) and 117 (25%) had normal pH (7.35–7.45). In the group with alkalosis, 199 (70.3%) had a metabolic alkalosis and in the group with acidosis, 42 (64%) had a metabolic acidosis with an increased AG of more than 17. Non-survivors were older than survivors (56.4 years versus 50.3 years, p < .001).

          Conclusion

          Most of the COVID-19 patients admitted to the ICU had an alkalosis, and those with acidosis had a much worse prognosis. Higher AG metabolic acidosis was not associated with patients’ characteristics.

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          Most cited references25

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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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            Management of acute kidney injury in patients with COVID-19

            Summary The outbreak of coronavirus disease 2019 (COVID-19) has rapidly evolved into a global pandemic. Most patients with COVID-19 have mild symptoms, but about 5% develop severe symptoms, which can include acute respiratory distress syndrome, septic shock, and multiple organ failure. Kidney involvement is frequent, with clinical presentation ranging from mild proteinuria to progressive acute kidney injury (AKI) necessitating renal replacement therapy (RRT). An understanding of the pathophysiology and mechanisms of kidney damage and AKI in the setting of critical illness and COVID-19 is emerging, although further research is needed to identify patients at risk of AKI and to guide management strategies. As no specific treatment options exist for AKI secondary to COVID-19, intensive care is largely supportive. Current approaches to prevention and management of AKI, and identification of potential indications for use of RRT and sequential extracorporeal therapies, are based mainly on clinical experience, and AKI strategies are adapted empirically to patients with COVID-19. International collaborative and cross-disciplinary research is needed to obtain adequate evidence to support current clinical approaches and to develop new approaches to management.
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              Clinical profile and outcomes in COVID-19 patients with diabetic ketoacidosis: A systematic review of literature

              Background and aim To perform a systematic literature review and analyze the demographic/biochemical parameters and clinical outcomes of COVID-19 patients with diabetic ketoacidosis (DKA) and combined DKA/HHS (hyperglycemic hyperosmolar syndrome). Methods PubMed, Scopus, Embase, and Google Scholar databases were systematically searched till August 3, 2020 to identify studies reporting COVID-19 patients with DKA and combined DKA/HHS. A total of 19 articles reporting 110 patients met the eligibility criteria. Results Of the 110 patients, 91 (83%) patients had isolated DKA while 19 (17%) had DKA/HHS. The majority of the patients were male (63%) and belonged to black ethnicity (36%). The median age at presentation ranged from 45.5 to 59.0 years. Most of the patients (77%) had pre-existing type 2 diabetes mellitus. Only 10% of the patients had newly diagnosed diabetes mellitus. The median blood glucose at presentation ranged from 486.0 to 568.5 mg/dl, being higher in patients with DKA/HHS compared to isolated DKA. The volume of fluid replaced in the first 24 h was higher in patients with DKA/HHS in contrast to patients with DKA alone. The in-hospital mortality rate was 45%, with higher mortality in the DKA/HHS group than in the isolated DKA group (67% vs. 29%). pH was lower in patients who had died compared to those who were discharged. Conclusion DKA in COVID-19 patients portends a poor prognosis with a mortality rate approaching 50%. Differentiating isolated DKA from combined DKA/HHS is essential as the latter represents around one-fifth of the DKA cases and tends to have higher mortality than DKA alone.
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                Author and article information

                Journal
                Ann Clin Biochem
                Ann Clin Biochem
                spacb
                ACB
                Annals of Clinical Biochemistry
                SAGE Publications (Sage UK: London, England )
                0004-5632
                1758-1001
                7 November 2022
                7 November 2022
                : 00045632221134687
                Affiliations
                [1 ]Division of Chemical Pathology, Department of Pathology, Ringgold 26697, universityFaculty of Medicine & Health Sciences, Stellenbosch University ; university& NHLS Tygerberg Hospital; , Cape Town, South Africa
                [2 ]Division of Epidemiology and Biostatistics, Department of Global Health, Ringgold 26697, universityFaculty of Medicine & Health Sciences, Stellenbosch University; , Cape Town, South Africa
                [3 ]Division of Haematological Pathology, Department of Pathology, Ringgold 26697, universityFaculty of Medicine & Health Sciences, Stellenbosch University ; university& NHLS Tygerberg Hospital; , Cape Town, South Africa
                [4 ]Division of Pulmonology, Department of Medicine, Ringgold 26697, universityFaculty of Medicine & Health Sciences, Stellenbosch University ; university& Tygerberg Hospital; , Cape Town, South Africa
                [5 ]Department of Biomedical Sciences, Ringgold 146301, universityCape Peninsula University of Technology; , Bellville Campus, Cape Town
                [6 ]Sefako Makgatho Health Sciences universityUniversity,; Ga-Rankuwa, universityPretoria, ; universitySouth Africa;
                [7 ]Division of Infection and Immunity, Centre for Clinical Microbiology, Ringgold 159057, universityUniversity College London Royal Free Campus; , London, UK; universityNIHR Biomedical Research Centre; , universityUCL Hospitals NHS Foundation Trust; , London, UK
                [8 ]Division of Epidemiology and Biostatistics, School of Public Health, universityUniversity of the Witwatersrand; , Johannesburg, South Africa
                Author notes
                [*]Peter S Nyasulu, Division of Epidemiology and Biostatistics, Department of Global Health, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa. Email: pnyasulu@ 123456sun.ac.za
                Author information
                https://orcid.org/0000-0001-7621-4679
                https://orcid.org/0000-0003-1070-1962
                Article
                10.1177_00045632221134687
                10.1177/00045632221134687
                9643107
                36220779
                722fbe8f-723a-4636-92a9-3a242c1c0970
                © The Author(s) 2022

                This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.

                History
                : 6 October 2022
                Funding
                Funded by: The COVID-19 Africa Rapid Grant Fund;
                Categories
                Research Article
                Custom metadata
                corrected-proof
                ts10

                Biochemistry
                covid-19,sars-cov-2,acid–base,arterial blood gas,intensive care unit
                Biochemistry
                covid-19, sars-cov-2, acid–base, arterial blood gas, intensive care unit

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