A randomized, double-blind, placebo-controlled clinical trial of fluconazole as early empiric treatment of coccidioidomycosis pneumonia (Valley Fever) in adults presenting with community-acquired pneumonia in endemic areas (FLEET-Valley Fever).

dc.contributor.author

Messina, Julia A

dc.contributor.author

Maziarz, Eileen K

dc.contributor.author

Galgiani, John

dc.contributor.author

Truong, Jonathan T

dc.contributor.author

Htoo, Aung K

dc.contributor.author

Heidari, Arash

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Johnson, Royce H

dc.contributor.author

Narang, Aneesh T

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Donovan, Fariba M

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Ewell, Marion

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Catanzaro, Antonino

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Thompson, George R

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Ampel, Neil M

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Perfect, John R

dc.contributor.author

Naggie, Susanna

dc.contributor.author

Walter, Emmanuel B

dc.date.accessioned

2021-11-16T02:35:08Z

dc.date.available

2021-11-16T02:35:08Z

dc.date.issued

2021-12

dc.date.updated

2021-11-16T02:35:06Z

dc.description.abstract

Introduction: Coccidioidomycosis is a fungal infection endemic in the southwestern United States (US). Primary pulmonary coccidioidomycosis (PPC) is a leading cause of community-acquired pneumonia (CAP) in this region, although its diagnosis is often delayed, leading to lag in antifungal treatment and subsequent morbidity. The impact of early empiric antifungal therapy as part of treatment for CAP in endemic areas on clinical outcomes is unknown. Methods: Phase IV randomized, double-blind, placebo-controlled trial in individuals aged 18 years or older with CAP who met all eligibility criteria in Coccidioides endemic regions in the US. Eligible participants with CAP were randomized to receive either fluconazole (400 mg daily) or matching placebo for 42 days and were subsequently monitored for clinical resolution of their illness. Objectives: The primary objective was to assess the clinical response of early empiric antifungal therapy with fluconazole through Day 22 in subjects with PPC who were adherent to the study intervention. Secondary objectives included: assessments of the impact of early empiric antifungal therapy with fluconazole through Day 22 and 43 in subjects with PPC regardless of adherence, comparisons of the clinical response and its individual components over time by treatment group in subjects with PPC, assessments of days lost from work or school, hospitalization, and all-cause mortality. Discussion: This trial was halted early due to slow enrollment (72 participants in one year, 33 received fluconazole and 39 received placebo). Of those enrolled, eight (11%) met the study definition of PPC. The study design and challenges are discussed.

dc.identifier

S2451-8654(21)00151-4

dc.identifier.issn

2451-8654

dc.identifier.issn

2451-8654

dc.identifier.uri

https://hdl.handle.net/10161/23985

dc.language

eng

dc.publisher

Elsevier BV

dc.relation.ispartof

Contemp Clin Trials Commun

dc.relation.isversionof

10.1016/j.conctc.2021.100851

dc.subject

Coccidioidomycosis

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Community-acquired pneumonia

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Valley fever

dc.title

A randomized, double-blind, placebo-controlled clinical trial of fluconazole as early empiric treatment of coccidioidomycosis pneumonia (Valley Fever) in adults presenting with community-acquired pneumonia in endemic areas (FLEET-Valley Fever).

dc.type

Journal article

duke.contributor.orcid

Messina, Julia A|0000-0001-6411-198X

duke.contributor.orcid

Maziarz, Eileen K|0000-0001-7779-9605

duke.contributor.orcid

Perfect, John R|0000-0002-6606-9460|0000-0003-3465-5518

duke.contributor.orcid

Naggie, Susanna|0000-0001-7721-6975

pubs.begin-page

100851

pubs.organisational-group

School of Medicine

pubs.organisational-group

Medicine, Infectious Diseases

pubs.organisational-group

Duke

pubs.organisational-group

Medicine

pubs.organisational-group

Clinical Science Departments

pubs.publication-status

Published online

pubs.volume

24

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