Aspergillus specific nested PCR from the site of infection is superior to testing concurrent blood samples in immunocompromised patients with suspected invasive aspergillosis.


Journal

Mycoses
ISSN: 1439-0507
Titre abrégé: Mycoses
Pays: Germany
ID NLM: 8805008

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 05 03 2019
revised: 29 07 2019
accepted: 30 07 2019
pubmed: 14 8 2019
medline: 25 2 2020
entrez: 13 8 2019
Statut: ppublish

Résumé

Invasive aspergillosis (IA) is a severe complication in immunocompromised patients. Early diagnosis is crucial to decrease its high mortality, yet the diagnostic gold standard (histopathology and culture) is time-consuming and cannot offer early confirmation of IA. Detection of IA by polymerase chain reaction (PCR) shows promising potential. Various studies have analysed its diagnostic performance in different clinical settings, especially addressing optimal specimen selection. However, direct comparison of different types of specimens in individual patients though essential, is rarely reported. We systematically assessed the diagnostic performance of an Aspergillus-specific nested PCR by investigating specimens from the site of infection and comparing it with concurrent blood samples in individual patients (pts) with IA. In a retrospective multicenter analysis PCR was performed on clinical specimens (n = 138) of immunocompromised high-risk pts (n = 133) from the site of infection together with concurrent blood samples. 38 pts were classified as proven/probable, 67 as possible and 28 as no IA according to 2008 European Organization for Research and Treatment of Cancer/Mycoses Study Group consensus definitions. A considerably superior performance of PCR from the site of infection was observed particularly in pts during antifungal prophylaxis (AFP)/antifungal therapy (AFT). Besides a specificity of 85%, sensitivity varied markedly in BAL (64%), CSF (100%), tissue samples (67%) as opposed to concurrent blood samples (8%). Our results further emphasise the need for investigating clinical samples from the site of infection in case of suspected IA to further establish or rule out the diagnosis.

Identifiants

pubmed: 31402465
doi: 10.1111/myc.12983
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1035-1042

Informations de copyright

© 2019 The Authors. Mycoses published by Blackwell Verlag GmbH.

Références

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Auteurs

Tobias Boch (T)

University Hospital Mannheim, Heidelberg University, Mannheim, Germany.

Birgit Spiess (B)

University Hospital Mannheim, Heidelberg University, Mannheim, Germany.

Werner Heinz (W)

Würzburg University Hospital, Würzburg, Germany.

Oliver A Cornely (OA)

First Department of Internal Medicine and ZKS Köln, BMBF 01KN1106, University Hospital Cologne, Deutsches Zentrum für Infektionsforschung, Cologne, Germany.

Rainer Schwerdtfeger (R)

Helios Klinikum Buch, Berlin, Germany.

Joachim Hahn (J)

Regensburg University Hospital, Regensburg, Germany.

Stefan W Krause (SW)

Erlangen University Hospital, Erlangen, Germany.

Matthias Duerken (M)

Department of Pediatric Hematology, Mannheim University Hospital, Mannheim, Germany.

Hartmut Bertz (H)

Freiburg University Hospital, Freiburg, Germany.

Stefan Reuter (S)

Klinikum Leverkusen, Leverkusen, Germany.

Michael Kiehl (M)

Klinikum Frankfurt/Oder, Frankfurt/Oder, Germany.

Bernd Claus (B)

Ludwigshafen General Hospital, Ludwigshafen, Germany.

Peter Markus Deckert (PM)

Brandenburg Medical School Theodor Fontane, Brandenburg an der Havel, Germany.

Wolf-Karsten Hofmann (WK)

University Hospital Mannheim, Heidelberg University, Mannheim, Germany.

Dieter Buchheidt (D)

University Hospital Mannheim, Heidelberg University, Mannheim, Germany.

Mark Reinwald (M)

Brandenburg Medical School Theodor Fontane, Brandenburg an der Havel, Germany.

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