Literature DB >> 29608752

T2MR contributes to the very early diagnosis of complicated candidaemia. A prospective study.

Patricia Muñoz1,2,3,4, Antonio Vena1,2,4,5, Marina Machado1,2,4, María Carmen Martínez-Jiménez1, Francesca Gioia6, Elia Gómez6, Julia Origüen7, María Ángeles Orellana7, Francisco López-Medrano7, María-Jesús Pérez-Granda1, José María Aguado7, Jesús Fortún6, Emilio Bouza1,2,3,4.   

Abstract

Objectives: Diagnosis of complicated candidaemia represents a challenge for clinicians since early clinical manifestations may be non-specific and difficult to identify, thus precluding an appropriate treatment. Patients and methods: This was a multicentre prospective study for predicting complicated episodes in patients with bloodstream infection caused by Candida species, while assessing the value of follow-up blood cultures (BCs) and the persistence of positive results for T2Candida MR (T2MR) and blood β-d-glucan (BDG) tests. Immediately after the first positive BC yielding Candida species, samples were obtained on days 0, +2, +4, +7 and +14, to simultaneously perform follow-up BC, T2MR and BDG. An episode of candidaemia was defined as 'complicated' when (i) it caused septic metastasis; and/or (ii) it was the cause of the patient's death.
Results: From January to June 2017, 30 patients were enrolled in the study. Of these, nine (30%) had complicated candidaemia. Values of persistently positive samples for the prediction of complicated episodes for BCs, T2MR and BDG, respectively, were as follows: sensitivity (44.4%, 100%, 100%); specificity (76.1%, 76.1%, 38.9%); positive predictive value (PPV) (44.4%, 64.2%, 40.9%) and negative predictive value (NPV) (76.1%, 100%, 100%). In multivariate analysis, having a positive T2MR within the first 5 days was associated with an almost 37-fold higher risk of developing complicated candidaemia. Conclusions: The T2MR test performed in patients with proven candidaemia may be a better marker of complicated infection than follow-up BCs or BDG. It is possible that this test may change current clinical practice, influencing the length and type of antifungal therapy in this population.

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Year:  2018        PMID: 29608752     DOI: 10.1093/jac/dky048

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  6 in total

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Journal:  J Clin Microbiol       Date:  2022-09-07       Impact factor: 11.677

3.  Noninvasive Testing and Surrogate Markers in Invasive Fungal Diseases.

Authors:  George R Thompson; David R Boulware; Nathan C Bahr; Cornelius J Clancy; Thomas S Harrison; Carol A Kauffman; Thuy Le; Marisa H Miceli; Eleftherios Mylonakis; M Hong Nguyen; Luis Ostrosky-Zeichner; Thomas F Patterson; John R Perfect; Andrej Spec; Dimitrios P Kontoyiannis; Peter G Pappas
Journal:  Open Forum Infect Dis       Date:  2022-03-04       Impact factor: 4.423

Review 4.  T2Candida for the Diagnosis and Management of Invasive Candida Infections.

Authors:  Lea M Monday; Tommy Parraga Acosta; George Alangaden
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5.  Intensive Care Antifungal Stewardship Programme Based on T2Candida PCR and Candida Mannan Antigen: A Prospective Study.

Authors:  Jannik Helweg-Larsen; Morten Steensen; Finn Møller Pedersen; Pia Bredahl Jensen; Michael Perch; Kirsten Møller; Birthe Riis Olesen; Mathias Søderlund; Maiken Cavling Arendrup
Journal:  J Fungi (Basel)       Date:  2021-12-06

6.  Role of the T2Dx magnetic resonance assay in patients with suspected bloodstream infection: a single-centre real-world experience.

Authors:  Angela Quirino; Vincenzo Scaglione; Nadia Marascio; Maria Mazzitelli; Eugenio Garofalo; Francesca Divenuto; Francesca Serapide; Andrea Bruni; Rosaria Lionello; Grazia Pavia; Chiara Costa; Aida Giancotti; Cinzia Peronace; Federico Longhini; Alessandro Russo; Maria Carla Liberto; Giovanni Matera; Carlo Torti; Enrico Maria Trecarichi
Journal:  BMC Infect Dis       Date:  2022-02-01       Impact factor: 3.090

  6 in total

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