9 research outputs found

    Hypokalemia as a sensitive biomarker of disease severity and the requirement for invasive mechanical ventilation requirement in COVID-19 pneumonia: A case series of 306 Mediterranean patients

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    Objectives: Serum levels of potassium (K+) appear to be significantly lower in severe cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the clinical significance of this is unknown. The objective was to investigate whether hypokalemia acts as a biomarker of severity in coronavirus disease 2019 (COVID-19) pneumonia and is associated with major clinical outcomes.Methods: A retrospective cohort study of inpatients with COVID-19 pneumonia (March 3 to May 2, 2020) was performed. Patients were categorized according to nadir levels of K+ in the first 72 h of admission: hypokalemia (K+ ≤3.5 mmol/l) and normokalemia (K+ >3.5 mmol/l). The main outcomes were all-cause mortality and the need for invasive mechanical ventilation (IMV); these were analyzed by multiple logistic regression (odds ratio (OR), 95% confidence interval (CI)).Results: Three hundred and six patients were enrolled. Ninety-four patients (30.7%) had hypokalemia and these patients showed significantly higher comorbidity (Charlson comorbidity index ≥3, 30.0% vs 16.3%; p = 0.02) and CURB65 scores (median (interquartile range): 1.5 (0.0-3.0) vs 1.0 (0.0-2.0); p = 0.04), as well as higher levels of some inflammatory parameters at baseline. After adjustment for confounders, hypokalemia was independently associated with requiring IMV during the admission (OR 8.98, 95% CI 2.54-31.74). Mortality was 15.0% (n = 46) and was not influenced by low K+. Hypokalemia was associated with longer hospital and ICU stays.Conclusions: Hypokalemia is prevalent in patients with COVID-19 pneumonia. Hypokalemia is an independent predictor of IMV requirement and seems to be a sensitive biomarker of severe progression of COVID-19

    Post-acute COVID-19 syndrome. Incidence and risk factors: A Mediterranean cohort study

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    Objectives: This study aims to analyze the incidence of Post-acute COVID-19 syndrome (PCS) and its components, and to evaluate the acute infection phase associated risk factors.Methods: A prospective cohort study of adult patients who had recovered from COVID-19 (27th February to 29th April 2020) confirmed by PCR or subsequent seroconversion, with a systematic assessment 10-14 weeks after disease onset. PCS was defined as the persistence of at least one clinically relevant symptom, or abnormalities in spirometry or chest radiology. Outcome predictors were analyzed by multiple logistic regression (OR; 95%CI).Results: Two hundred seventy seven patients recovered from mild (34.3%) or severe (65.7%) forms of SARS-CoV-2 infection were evaluated 77 days (IQR 72-85) after disease onset. PCS was detected in 141 patients (50.9%; 95%CI 45.0-56.7%). Symptoms were mostly mild. Alterations in spirometry were noted in 25/269 (9.3%), while in radiographs in 51/277 (18.9%). No baseline clinical features behaved as independent predictors of PCS development.Conclusions: A Post-acute COVID-19 syndrome was detected in a half of COVID19 survivors. Radiological and spirometric changes were mild and observed in less than 25% of patients. No baseline clinical features behaved as independent predictors of Post-acute COVID-19 syndrome development

    Spread of a SARS-CoV-2 variant through Europe in the summer of 2020

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    [EN] Following its emergence in late 2019, the spread of SARS-CoV-21,2 has been tracked by phylogenetic analysis of viral genome sequences in unprecedented detail3,4,5. Although the virus spread globally in early 2020 before borders closed, intercontinental travel has since been greatly reduced. However, travel within Europe resumed in the summer of 2020. Here we report on a SARS-CoV-2 variant, 20E (EU1), that was identified in Spain in early summer 2020 and subsequently spread across Europe. We find no evidence that this variant has increased transmissibility, but instead demonstrate how rising incidence in Spain, resumption of travel, and lack of effective screening and containment may explain the variant’s success. Despite travel restrictions, we estimate that 20E (EU1) was introduced hundreds of times to European countries by summertime travellers, which is likely to have undermined local efforts to minimize infection with SARS-CoV-2. Our results illustrate how a variant can rapidly become dominant even in the absence of a substantial transmission advantage in favourable epidemiological settings. Genomic surveillance is critical for understanding how travel can affect transmission of SARS-CoV-2, and thus for informing future containment strategies as travel resumes.S

    Reducing the environmental impact of surgery on a global scale: systematic review and co-prioritization with healthcare workers in 132 countries

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    Abstract Background Healthcare cannot achieve net-zero carbon without addressing operating theatres. The aim of this study was to prioritize feasible interventions to reduce the environmental impact of operating theatres. Methods This study adopted a four-phase Delphi consensus co-prioritization methodology. In phase 1, a systematic review of published interventions and global consultation of perioperative healthcare professionals were used to longlist interventions. In phase 2, iterative thematic analysis consolidated comparable interventions into a shortlist. In phase 3, the shortlist was co-prioritized based on patient and clinician views on acceptability, feasibility, and safety. In phase 4, ranked lists of interventions were presented by their relevance to high-income countries and low–middle-income countries. Results In phase 1, 43 interventions were identified, which had low uptake in practice according to 3042 professionals globally. In phase 2, a shortlist of 15 intervention domains was generated. In phase 3, interventions were deemed acceptable for more than 90 per cent of patients except for reducing general anaesthesia (84 per cent) and re-sterilization of ‘single-use’ consumables (86 per cent). In phase 4, the top three shortlisted interventions for high-income countries were: introducing recycling; reducing use of anaesthetic gases; and appropriate clinical waste processing. In phase 4, the top three shortlisted interventions for low–middle-income countries were: introducing reusable surgical devices; reducing use of consumables; and reducing the use of general anaesthesia. Conclusion This is a step toward environmentally sustainable operating environments with actionable interventions applicable to both high– and low–middle–income countries

    Uso de heptapéptidos para el control de la hipertensión

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    La presente invención se refiere a heptapéptidos inhibidores de la enzima conversora de angiotensina (ECA). También se refiere al proceso de producción de los péptidos de la invención mediante estrategias biotecnológicas, por lo que además se refiere al ácido nucleico, al cassette de expresión y al vector que los codifican, así como a la célula hospedadora que los comprende. Así mismo también se refiere al uso de los péptidos para la prevención y/o el tratamiento de la hipertensión así como a la composición farmacéutica que los comprende.Peer reviewedConsejo Superior de Investigaciones Científicas (España), Fundación para la Investigación del Hospital la Fe de ValenciaA1 Solicitud de patente con informe sobre el estado de la técnic

    Heptapéptidos y su uso para el control de la hipertensión

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    [EN] The present invention relates to angiotensin-converting-enzyme (ACE) inhibitor heptapeptides. The invention also relates to the process for producing the peptides of the invention by means of biotechnological strategies and therefore, furthermore, relates to the nucleic acid, the expression cassette and the vector that encodes said peptides, and also to the host cell that comprises said peptides. Moreover, the invention also relates to the use of the peptides for preventing and/or treating hypertension and also to the pharmaceutical composition that comprises said peptides.[ES] La presente invención se refiere a heptapéptídos inhibidores de la enzima conversora de angiotensina (ECA). También se refiere al proceso de producción de los péptidos de la invención mediante estrategias biotecnológicas, por lo que además se refiere al ácido nucleico, al cassette de expresión y al vector que los codifican, así como a la célula hospedadora que los comprende. Así mismo también se refiere al uso de los péptidos para la prevención y/o el tratamiento de la hipertensión así como a la composición farmacéutica que los comprende.Peer reviewedConsejo Superior de Investigaciones Científicas (España), Fundación para la Investigación del Hospital la Fe de ValenciaA1 Solicitud de patente con informe sobre el estado de la técnic

    Fracción de bajo peso molecular de un hidrolizado de lactoferrina para el tratamiento de la hipertensión

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    [EN] The invention relates to a method for obtaining the lactoferrin hydrolysate fraction with a molecular weight of less than 3000 Da, comprising several peptides. The invention also relates to the lactoferrin hydrolysate fraction that can be obtained by said method and sorne of the peptides that it includes. The invention further relates to the use of said fraction and peptides for producing medicaments for the prevention and/or treatment of hypertension, and food or food supplements.[ES] La invención se refiere a un método para obtener la fracción de paso molecular inferior a 3000 Da de un hidrolizado de lactoferrina, el cual comprende diversos péptidos. La invención también engloba la fracción del hidrolizado de lactoferrina obtenible por dicho método y algunos de los peptidos que incluye, asi como al uso de dicha fracción y péptidos para la elaboración de medicamentos para la prevención y/o el tratamiento de la hipertensión, asi como alimentos o suplementos alimenticios.Peer reviewedConsejo Superior de Investigaciones Científicas, Fundación para la Invetigación del Hospital la Fe de ValenciaA1 Solicitud de patente con informe sobre el estado de la técnic

    Prediction of early mortality in patients with cancer-associated thrombosis in the RIETE Database

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    Patient-Level, Institutional, and Temporal Variations in Use of Imaging Modalities to Confirm Pulmonary Embolism

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    International audienceBackground: The choice of the imaging modality for diagnosis of pulmonary embolism (PE) could be influenced by provider, patient or hospital characteristics, or over time. However, little is known about the choice of the diagnostic modalities in practice. The aim of this study was to evaluate the variations in the use of imaging modalities for patients with acute PE. Methods: Using the data from Registro Informatizado Enfermedad TromboEmbolica (RIETE), a prospective international registry of patients with venous thromboembolism (March 2001–January 2019), we explored the imaging modalities used in patients with acute PE. The imaging modalities included computed tomography pulmonary angiography, ventilation/perfusion scanning, pulmonary angiography, a combination of these tests, or PE signs and symptoms plus imaging-confirmed proximal deep vein thrombosis but no chest imaging. Results: Among 38 025 patients with confirmed PE (53.1% female, age: 67.3±17 years), computed tomography pulmonary angiography was the dominant modality of diagnosis in all RIETE enrollees (78.2% [99% CI, 77.6–78.7]); including pregnant patients (58.9% [99% CI, 47.7%–69.4%]) and patients with severe renal insufficiency (62.5% [99% CI, 59.9–65.0]). A greater proportion of patients underwent ventilation/perfusion scanning in larger hospitals compared with smaller hospitals (13.1% versus 7.3%, P <0.001). The use of computed tomography pulmonary angiography varied between 13.3% and 98.3% across the countries, and its use increased over time (46.5% in 2002 to 91.7% in 2018, P <0.001). Conclusions: In a large multinational PE registry, variations were observed in the use of imaging modalities according to patient or institutional factors and over time. However, computed tomography pulmonary angiography was the dominant modality of diagnosis, even in pregnancy and severe renal insufficiency. The safety, costs, and downstream effects of these tests on PE-related and non-PE-related outcomes warrant further investigation
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