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When to change treatment of acute invasive aspergillosis: an expert viewpoint

Authors :
Francisco M. Marty
Paul E. Verweij
Monica A. Slavin
J. Peter Donnelly
P. Lewis White
Catherine Cordonnier
Emma Harvey
Yee-Chun Chen
Olivier Lortholary
Ruth Hargreaves
Manuel Cuenca-Estrella
Bart J. A. Rijnders
Andreas H. Groll
Marcio Nucci
Johan Maertens
Oliver A. Cornely
George Richard Thompson
John H. Rex
F2G (UK)
Internal Medicine
Source :
The Journal of antimicrobial chemotherapy, 77(1), 16-23. Oxford University Press, Repisalud, Instituto de Salud Carlos III (ISCIII), Journal of Antimicrobial Chemotherapy, The Journal of antimicrobial chemotherapy, vol 77, iss 1
Publication Year :
2021
Publisher :
Oxford University Press, 2021.

Abstract

Invasive aspergillosis (IA) is an acute infection affecting patients who are immunocompromised, as a result of receiving chemotherapy for malignancy, or immunosuppressant agents for transplantation or autoimmune disease. Whilst criteria exist to define the probability of infection for clinical trials, there is little evidence in the literature or clinical guidelines on when to change antifungal treatment in patients who are receiving prophylaxis or treatment for IA. To try and address this significant gap, an advisory board of experts was convened to develop criteria for the management of IA for use in designing clinical trials, which could also be used in clinical practice. For primary treatment failure, a change in antifungal therapy should be made: (i) when mycological susceptibility testing identifies an organism from a confirmed site of infection, which is resistant to the antifungal given for primary therapy, or a resistance mutation is identified by molecular testing; (ii) at, or after, 8 days of primary antifungal treatment if there is increasing serum galactomannan, or galactomannan positivity in serum, or bronchoalveolar lavage fluid when the antigen was previously undetectable, or there is sudden clinical deterioration, or a new clearly distinct site of infection is detected; and (iii) at, or after, 15 days of primary antifungal treatment if the patient is clinically stable but with ≥2 serum galactomannan measurements persistently elevated compared with baseline or increasing, or if the original lesions on CT or other imaging, show progression by >25% in size in the context of no apparent change in immune status. F2G Ltd funded the advisory board, provided travel and accommodation costs, as well as providing an honorarium according to global, national and local regulations for the time spent at the workshop and for completing the pre- and post-meeting questionnaires. None of the authors was paid for writing or reviewing this paper. Sí

Details

Language :
English
ISSN :
03057453
Database :
OpenAIRE
Journal :
The Journal of antimicrobial chemotherapy, 77(1), 16-23. Oxford University Press, Repisalud, Instituto de Salud Carlos III (ISCIII), Journal of Antimicrobial Chemotherapy, The Journal of antimicrobial chemotherapy, vol 77, iss 1
Accession number :
edsair.doi.dedup.....01b586e3068c6ab0c187065e352b5520