24 research outputs found

    Severe cutaneous reactions to drugs in the setting of a general hospital

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    Abstract: BACKGROUND: Cutaneous drug reactions are frequently found. Assessing the clinical and epidemiological profile of severe forms is extremely relevant for their better recognition and management. Few studies have assessed the severe forms of cutaneous drug reactions in patients hospitalized in our setting. OBJECTIVES: To assess the clinical and epidemiological aspects of severe cutaneous adverse reactions to drugs in a tertiary hospital in Porto Alegre, Brazil. METHODS: All cases of severe cutaneous adverse reactions to drugs in patients hospitalized from January/2005 to December/2010 were retrospectively analyzed for clinical and epidemiological variables. Cases of Stevens- Johnson Syndrome, Toxic Epidermal Necrolysis, drug hypersensitivity syndrome or Drug Reaction with Eosinophilia and Systemic Symptoms and acute generalized exanthematous pustulosis were included. RESULTS: An occurrence rate of 1 serious reaction for every 3,048 inpatients was found (total of 173,767 inpatients admitted in the period). Drug Reaction with Eosinophilia and Systemic Symptoms was the most frequent presentation. The drugs most frequently involved were anticonvulsants (40.4%), antibiotics (26.3%), and analgesics/anti-inflammatory drugs (10.5%). Thirty seven patients (64.9%) were admitted to hospital because of the cutaneous drug reaction. Ten patients (17.5%) died and in most of those (60%), the drug causing the reaction could not be determined. CONCLUSIONS: The frequency of severe cutaneous adverse reactions to drugs in our setting is significant. Drug Reaction with Eosinophilia and Systemic Symptoms seems to be the most frequent presentation of severe cutaneous drug reactions. Most patients developed cutaneous drug reactions outside the hospital. Mortality rates were higher for Toxic Epidermal Necrolysis and this presentation significantly affected older people. Not knowing the drug causing the reaction was related to mortality

    The desmosome and pemphigus

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    Desmosomes are patch-like intercellular adhering junctions (“maculae adherentes”), which, in concert with the related adherens junctions, provide the mechanical strength to intercellular adhesion. Therefore, it is not surprising that desmosomes are abundant in tissues subjected to significant mechanical stress such as stratified epithelia and myocardium. Desmosomal adhesion is based on the Ca2+-dependent, homo- and heterophilic transinteraction of cadherin-type adhesion molecules. Desmosomal cadherins are anchored to the intermediate filament cytoskeleton by adaptor proteins of the armadillo and plakin families. Desmosomes are dynamic structures subjected to regulation and are therefore targets of signalling pathways, which control their molecular composition and adhesive properties. Moreover, evidence is emerging that desmosomal components themselves take part in outside-in signalling under physiologic and pathologic conditions. Disturbed desmosomal adhesion contributes to the pathogenesis of a number of diseases such as pemphigus, which is caused by autoantibodies against desmosomal cadherins. Beside pemphigus, desmosome-associated diseases are caused by other mechanisms such as genetic defects or bacterial toxins. Because most of these diseases affect the skin, desmosomes are interesting not only for cell biologists who are inspired by their complex structure and molecular composition, but also for clinical physicians who are confronted with patients suffering from severe blistering skin diseases such as pemphigus. To develop disease-specific therapeutic approaches, more insights into the molecular composition and regulation of desmosomes are required

    A922 Sequential measurement of 1 hour creatinine clearance (1-CRCL) in critically ill patients at risk of acute kidney injury (AKI)

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    Effect of sodium hypochlorite on primary dentin - A scanning electron microscopy (SEM) evaluation

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    Objective: The aim of this study was to evaluate the alterations of etched deciduous dentin when submitted to different time and concentrations of sodium hypochlorite (NaOCl), using scanning electron microscopy (SEM). Material and methods: Forty deciduous anterior teeth were selected, cleaned and ground until expose a flat dentin area on the buccal surface. The specimens were randomly distributed into eight groups (n = 5), according to dentin surface treatment (35% phosphoric acid etching for 7 s-AE and/or NaOCl application), NaOCl solution concentration (5% or 10%), and time of application (0, 30, 60, and 120 s), as follows: G1: control (without AE and NaOCl); G2: only AE; G3, G4, and G5: AE + 5% NaOCl for 30, 60, and 120 s, respectively; G6, G7, and G8: AE + 10% NaOCl for 30, 60, and 120 s, respectively. All specimens were prepared for SEM analysis and the photomicrographs (three for each specimen) were classified according to a score as follow: 0: presence of smear layer (SL); 1: absence of SL + non-altered collagen fibrils; 2: absence of SL + collagen fibrils slightly altered; 3: absence of SL + collagen fibrils severely altered; and 4: absence of SL and absence of collagen fibrils. Data were submitted to Kruskal-Wallis and Mann-Whitney tests (p < 0.05). Results: All groups treated with NaOCl solution were significant different from G1 and G2, and showed alterations on the collagen fibrils network. Collagen complete removal was only observed when a 5% NaOCI solution was applied for 120 s and 10% NaOCI solution for 30, 60, and 120 s. Conclusions: The NaOCl action produced significant changes in the etched deciduous dentin. The higher NaOCl concentration, the lower the time required to completely removing the collagen fibrils network in deciduous dentin. (c) 2005 Published by Elsevier Ltd.34745445
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