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      How to manage aspergillosis in non-neutropenic intensive care unit patients

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          Abstract

          Invasive aspergillosis has been mainly reported among immunocompromised patients during prolonged periods of neutropenia. Recently, however, non-neutropenic patients in the ICU population have shown an increasing risk profile for aspergillosis. Associations with chronic obstructive pulmonary disease and corticosteroid therapy have been frequently documented in this cohort. Difficulties in achieving a timely diagnosis of aspergillosis in non-neutropenic patients is related to the non-specificity of symptoms and to lower yields with microbiological tests compared to neutropenic patients. Since high mortality rates are typical of invasive aspergillosis in critically ill patients, a high level of suspicion and prompt initiation of adequate antifungal treatment are mandatory. Epidemiology, risk factors, diagnostic algorithms, and different approaches in antifungal therapy for invasive aspergillosis in non-neutropenic patients are reviewed.

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          Most cited references98

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          Treatment of aspergillosis: clinical practice guidelines of the Infectious Diseases Society of America.

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            Invasive aspergillosis.

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              Glucocorticoids and invasive fungal infections.

              Since the 1990s, opportunistic fungal infections have emerged as a substantial cause of morbidity and mortality in profoundly immunocompromised patients. Hypercortisolaemic patients, both those with endogenous Cushing's syndrome and, much more frequently, those receiving exogenous glucocorticoid therapy, are especially at risk of such infections. This vulnerability is attributed to the complex dysregulation of immunity caused by glucocorticoids. We critically review the spectrum and presentation of invasive fungal infections that arise in the setting of hypercortisolism, and the ways in which glucocorticoids contribute to their pathogenesis. A better knowledge of the interplay between glucocorticoid-induced immunosuppression and invasive fungal infections should assist in earlier recognition and treatment of such infections. Efforts to decrease the intensity of glucocorticoid therapy should help to improve outcomes of opportunistic fungal infections.
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                Author and article information

                Contributors
                Journal
                Crit Care
                Crit Care
                Critical Care
                BioMed Central
                1364-8535
                1466-609X
                2014
                25 July 2014
                : 18
                : 4
                : 458
                Affiliations
                [1 ]Infectious Diseases Division, Santa Maria Misericordia University Hospital, Udine, 33100, Italy
                [2 ]Istituto di Anestesiologia e Rianimazione, Università Cattolica-Policlinico Universitario A.Gemelli, Roma, 00100, Italy
                [3 ]Department of Health Sciences, Anesthesiology and Intensive Care Section, University of Florence, Firenze, 50100, Italy
                [4 ]Anesthesia, Analgesia and Intensive Care Division, P.Giaccone University Hospital, School of Medicine DiBiMef-University of Palermo, Palermo, 90100, Italy
                [5 ]Department of Health Sciences - Section of Clinical Pharmacology and Oncology, University of Florence, Firenze, 50100, Italy
                [6 ]Department of Health Sciences, Università degli Studi di Milano, Milano, 20100, Italy
                [7 ]Second Division, Lazzaro Spallanzani National Institute for Infectious Diseases, Roma, 00100, Italy
                [8 ]Department of Bio-medical Sciences, University of Catania, Catania, 95100, Italy
                Article
                s13054-014-0458-4
                10.1186/s13054-014-0458-4
                4220091
                25167934
                56e2bc44-4011-4c5e-b5f9-6861e8c0e36f
                Copyright © 2014 Bassetti et al., licensee BioMed Central Ltd.

                The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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                Review

                Emergency medicine & Trauma
                Emergency medicine & Trauma

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