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1.
J Crit Care ; 78: 154382, 2023 12.
Article in English | MEDLINE | ID: mdl-37516091

ABSTRACT

BACKGROUND: Acute kidney injury (AKI) is associated with high morbidity and mortality rates in the intensive care unit (ICU). In low- and middle-income countries (LMICs), epidemiological information about this condition is still scarce. Our main objective was to characterize its epidemiology, prognosis, and its treatment. METHODS: This multicenter prospective cohort study included 1466 patients from 35 ICUs during 6 months in Argentina in 2018. Risk factors and outcomes in patients with and without AKI, and between AKI on admission (AKIadm) and that developed during hospitalization (AKIhosp) were analyzed. RESULTS: AKI occurred in 61.3% of patients (900/1466); 72.6% were AKIadm and 27.3% AKIhosp. Risk factors were age, BMI, arterial hypertension, cardiovascular diseases, diabetes, SOFA, APACHE II, dehydration, sepsis, vasopressor use, radiocontrast, diuresis/h and mechanical ventilation. Independent predictors for AKI were sepsis, diabetes, dehydration, vasopressors on admission, APACHE II and radiocontrast use. Renal replacement therapies (RRT) requirement in AKI patients was 14.8%. Hospital mortality in AKI vs. non-AKI was 38.7% and 23.3% (p < 0.001); and in AKIadm vs. AKIhosp, 41.2% and 37.8% (p = 0.53). CONCLUSIONS: ICU-acquired AKI has high incidence, complications and mortality. Risk factors for AKI and RRT utilization were similar to those described in other epidemiological studies. AKIadm was more frequent than AKIhosp, but had equal prognosis.


Subject(s)
Acute Kidney Injury , Sepsis , Humans , Prospective Studies , Critical Illness/epidemiology , Argentina/epidemiology , Dehydration/complications , Prognosis , Intensive Care Units , Risk Factors , Acute Kidney Injury/epidemiology , Acute Kidney Injury/therapy , Acute Kidney Injury/etiology , Retrospective Studies
2.
Mol Ther ; 18(10): 1885-90, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20606647

ABSTRACT

The ocular environment has been shown to induce tolerance to locally administered antigens. We therefore investigated whether there was a systemic immune response against adenoviral vectors injected into the vitreous of retinoblastoma patients enrolled in a phase 1 clinical trial of adenoviral-mediated thymidine kinase gene transfer. Sections of enucleated eyes were immunostained with antibodies against inflammatory cells. A trend toward increasing numbers of plasma cells, T cells, macrophages, and antigen-presenting cells was observed in the injected subjects' eyes, but systemically, there was no significant increase in the number of adenovirus-specific cytotoxic T lymphocytes (CTLs) or in adenovirus neutralizing antibodies. Therefore, in contrast to studies showing significant immunogenicity of Ad-RSVtk following injection into extraocular tumors, injection into the eye produces only a mild local inflammatory response without evidence of systemic cellular or humoral immune responses to adenovirus.


Subject(s)
Adenoviridae/genetics , Adenoviridae/immunology , Genetic Vectors/genetics , Genetic Vectors/immunology , Retinoblastoma/immunology , Retinoblastoma/therapy , Antigen-Presenting Cells/immunology , Eye/immunology , Eye/metabolism , Genetic Therapy/methods , Humans , Immunohistochemistry , In Vitro Techniques , Macrophages/immunology , Retinoblastoma/genetics , Retinoblastoma/metabolism , T-Lymphocytes/immunology , Thymidine Kinase/genetics , Thymidine Kinase/metabolism
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