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      Comprehensive Molecular Testing for Respiratory Pathogens in Community-Acquired Pneumonia

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          Abstract

          This is the first time a comprehensive, multipathogen, quantitative and qualitative molecular approach for respiratory bacteria and viruses has been compared with traditional diagnostic methods on a large hospitalized pneumonia cohort, with estimation of potential effects on antibiotic prescribing.

          Abstract

          Background.  The frequent lack of a microbiological diagnosis in community-acquired pneumonia (CAP) impairs pathogen-directed antimicrobial therapy. This study assessed the use of comprehensive multibacterial, multiviral molecular testing, including quantification, in adults hospitalized with CAP.

          Methods.  Clinical and laboratory data were collected for 323 adults with radiologically-confirmed CAP admitted to 2 UK tertiary care hospitals. Sputum (96%) or endotracheal aspirate (4%) specimens were cultured as per routine practice and also tested with fast multiplex real-time polymerase-chain reaction (PCR) assays for 26 respiratory bacteria and viruses. Bacterial loads were also calculated for 8 bacterial pathogens. Appropriate pathogen-directed therapy was retrospectively assessed using national guidelines adapted for local antimicrobial susceptibility patterns.

          Results.  Comprehensive molecular testing of single lower respiratory tract (LRT) specimens achieved pathogen detection in 87% of CAP patients compared with 39% with culture-based methods. Haemophilus influenzae and Streptococcus pneumoniae were the main agents detected, along with a wide variety of typical and atypical pathogens. Viruses were present in 30% of cases; 82% of these were codetections with bacteria. Most (85%) patients had received antimicrobials in the 72 hours before admission. Of these, 78% had a bacterial pathogen detected by PCR but only 32% were culture-positive ( P < .0001). Molecular testing had the potential to enable de-escalation in number and/or spectrum of antimicrobials in 77% of patients.

          Conclusions.  Comprehensive molecular testing significantly improves pathogen detection in CAP, particularly in antimicrobial-exposed patients, and requires only a single LRT specimen. It also has the potential to enable early de-escalation from broad-spectrum empirical antimicrobials to pathogen-directed therapy.

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          Most cited references37

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          Community-acquired pneumonia requiring hospitalization among U.S. children.

          Incidence estimates of hospitalizations for community-acquired pneumonia among children in the United States that are based on prospective data collection are limited. Updated estimates of pneumonia that has been confirmed radiographically and with the use of current laboratory diagnostic tests are needed.
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            BTS guidelines for the management of community acquired pneumonia in adults: update 2009.

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Rapid and quantitative detection of human adenovirus DNA by real-time PCR.

              Rapid diagnosis of human adenovirus (HAdV) infections was achieved by PCR in the recent years. However, conventional PCR has the risk of carry-over contamination due to open handling with its products, and results are only qualitative. Therefore, a quantitative "real-time" PCR with consensus primer and probe (dual fluorescence labelled, "TaqMan") sequences for a conserved region of the hexon gene was designed and evaluated. Real-time PCR detected all 51 HAdV prototypes. Sensitivity of the assay was
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                Author and article information

                Journal
                Clin Infect Dis
                Clin. Infect. Dis
                cid
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press
                1058-4838
                1537-6591
                01 April 2016
                07 January 2016
                07 January 2016
                : 62
                : 7
                : 817-823
                Affiliations
                [1 ]Medical Microbiology, Department of Laboratory Medicine, Royal Infirmary of Edinburgh
                [2 ]College of Medicine and Veterinary Medicine, University of Edinburgh
                [3 ]Department of Anaesthesia, University of Cambridge
                [4 ]Respiratory Medicine, Royal Infirmary of Edinburgh , United Kingdom
                Author notes
                Correspondence: N. J Gadsby, Medical Microbiology, Department Laboratory Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK EH16 4SA ( naomi.gadsby@ 123456luht.scot.nhs.uk ).
                Article
                civ1214
                10.1093/cid/civ1214
                4787606
                26747825
                34aa002b-2cdc-42c1-bd76-8e3a04cc6f35
                © The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, contact journals.permissions@ 123456oup.com .

                History
                : 27 August 2015
                : 24 November 2015
                Funding
                Funded by: Chief Scientist Office http://dx.doi.org/10.13039/501100000589
                Award ID: ETM/250
                Categories
                Articles and Commentaries

                Infectious disease & Microbiology
                community-acquired pneumonia,bacterial load,viral,molecular testing,pcr

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