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Diagnosis of severe respiratory infections in immunocompromised patients

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  • Diagnosis of severe respiratory infections in immunocompromised patients


    Intensive Care Med. 2020 Feb 7. doi: 10.1007/s00134-019-05906-5. [Epub ahead of print] Diagnosis of severe respiratory infections in immunocompromised patients.

    Azoulay E1,2, Russell L3, Van de Louw A4, Metaxa V5, Bauer P6, Povoa P7, Montero JG8, Loeches IM9, Mehta S10, Puxty K11, Schellongowski P12, Rello J13,14, Mokart D15, Lemiale V16, Mirouse A16,17; Nine-i Investigators.
    Author information

    Abstract

    An increasing number of critically ill patients are immunocompromised. Acute hypoxemic respiratory failure (ARF), chiefly due to pulmonary infection, is the leading reason for ICU admission. Identifying the cause of ARF increases the chances of survival, but may be extremely challenging, as the underlying disease, treatments, and infection combine to create complex clinical pictures. In addition, there may be more than one infectious agent, and the pulmonary manifestations may be related to both infectious and non-infectious insults. Clinically or microbiologically documented bacterial pneumonia accounts for one-third of cases of ARF in immunocompromised patients. Early antibiotic therapy is recommended but decreases the chances of identifying the causative organism(s) to about 50%. Viruses are the second most common cause of severe respiratory infections. Positive tests for a virus in respiratory samples do not necessarily indicate a role for the virus in the current acute illness. Invasive fungal infections (Aspergillus, Mucorales, and Pneumocystis jirovecii) account for about 15% of severe respiratory infections, whereas parasites rarely cause severe acute infections in immunocompromised patients. This review focuses on the diagnosis of severe respiratory infections in immunocompromised patients. Special attention is given to newly validated diagnostic tests designed to be used on non-invasive samples or bronchoalveolar lavage fluid and capable of increasing the likelihood of an early etiological diagnosis.


    KEYWORDS:

    Aspergillosis; Cytomegalovirus; Influenza; Mucormycosis; Pneumocystis pneumonia; Toxoplasmosis

    PMID: 32034433 DOI: 10.1007/s00134-019-05906-5

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