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High negative predictive value diagnostic strategies for the reevaluation of early antifungal treatment: A multicenter prospective trial in patients at risk for invasive fungal infections

Authors :
Sophie Cassaing
Olivier Cointault
Bernard Georges
V. Mondain
Eric Rosenthal
Florence Robert-Gangneux
Stanislas Nimubona
Pierre Tattevin
Pierre Marty
Hervé Hyvernat
Laurence Lavayssière
Anne Sirvent
Jean-Pierre Gangneux
Sophie de Guibert
Antoine Berry
Lilia Hasseine
Matthieu Revest
Judith Fillaux
Service de Parasitologie et Mycologie
CHU Toulouse [Toulouse]-Institut Fédératif de Biologie (IFB) - Hôpital Purpan
Hôpital Purpan [Toulouse]
CHU Toulouse [Toulouse]-CHU Toulouse [Toulouse]-Hôpital Purpan [Toulouse]
CHU Toulouse [Toulouse]
Service de Parasitologie-Mycologie [Rennes]
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes]
Institut de recherche en santé, environnement et travail (Irset)
Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )-Institut National de la Santé et de la Recherche Médicale (INSERM)-École des Hautes Études en Santé Publique [EHESP] (EHESP)-Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Université d'Angers (UA)
Centre méditerranéen de médecine moléculaire (C3M)
Université Nice Sophia Antipolis (... - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Université Côte d'Azur (UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Service de Parasitologie-Mycologie
Centre Hospitalier Universitaire de Nice
Centre Hospitalier Universitaire de Nice (CHU Nice)-Centre Hospitalier Universitaire de Nice (CHU Nice)
Service de Parasitologie et Mycologie [CHU Toulouse]
Institut Fédératif de Biologie (IFB)
Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Pôle Biologie [CHU Toulouse]
Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)
Université de Rennes (UR)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes]
Université d'Angers (UA)-Université de Rennes (UR)-École des Hautes Études en Santé Publique [EHESP] (EHESP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
Université Nice Sophia Antipolis (1965 - 2019) (UNS)
COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Côte d'Azur (UCA)
Centre Hospitalier Universitaire de Nice (CHU Nice)
Source :
Journal of Infection, Journal of Infection, WB Saunders, 2015, 71 (2), pp.258-265. ⟨10.1016/j.jinf.2015.04.005⟩, Journal of Infection, 2015, 71 (2), pp.258-265. ⟨10.1016/j.jinf.2015.04.005⟩
Publication Year :
2014

Abstract

International audience; Early antifungal therapeutic strategies are proposed during invasive fungal infection (IFI), but antifungal stewardship programs should institute a systematic reevaluation of prescriptions, particularly in the context of empirical treatment. Here, we aimed to evaluate the performances and particularly the negative predictive value (NPV) of diagnostic strategies, including a whole blood panfungal quantitative PCR assay (PF-qPCR) in a high risk population for IFI. The first step was to standardize and optimize a new PF- rtPCR targeting ITS2 region. Then, this method was evaluated in a multicenter prospective study including 313 patients with suspected IFI for whom an early antifungal treatment was prescribed. All patients enrolled at day 0 of their treatment benefited from serum Aspergillus galactomannan (GM) antigen detection twice a week, weekly PF-qPCR assay, and when indicated and feasible, CT-scan and mycological sampling. In total, 125 of 313 patients were diagnosed with IFI: 68 invasive aspergillosis (eight proven, 48 probable and 12 possible), one fusariosis, 47 candidemia, three disseminated candidiasis and six cryptococcosis. Globally, the sensitivity of the PF-qPCR assay was only 40%, but the specificity, PPV and NPV were 96%, 88% and 69%, respectively. In the population of patients at high risk for invasive aspergillosis who also benefited from Aspergillus GM detection, the sensitivity and the NPV of the combined detection reached to 78% and 84%, respectively. Even higher NPV were obtained when combining negative PF-qPCR and CT scan (95%) as well as negative GM and CT scan (93%), thus allowing to rationalize and re-evaluate the prescription of empirical treatment in such highly selected population.

Details

ISSN :
15322742 and 01634453
Volume :
71
Issue :
2
Database :
OpenAIRE
Journal :
The Journal of infection
Accession number :
edsair.doi.dedup.....9c41902473df1568dd87ac712c6134e6