Evidence map›Paper›PMID 42919407›Full record

ArticleCritical care (London, England)2026

Mucormycosis in critically ill patients: a 9-year multicenter cohort study of clinical features, management, and 90-day outcomes.

Frank Bidar, Samy Maamcha, Pauline Tirard-Collet, Jean-Christophe Richard, Arnaud Friggeri, Jean-Luc Fellahi, Matthias Jacquet-Lagrèze, Frederic Aubrun, Laurent Argaud, Frederic Dailler and 4 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Critical care (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Frank BidarDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Louis Pradel, Hospices Civils de Lyon, Bron, France. frankbidar@gmail.com.ORCID https://orcid.org/0000-0003-1406-4067
Samy MaamchaDepartment of Anesthesiology and Intensive Care Medicine, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
Pauline Tirard-ColletDepartment of Mycology and Parasitology, Institute of Infectious Agents, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Jean-Christophe RichardMedical Intensive Care Unit, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Arnaud FriggeriDepartment of Anesthesiology and Intensive Care Medicine, Lyon Sud Hospital, Hospices Civils de Lyon, Pierre-Bénite, France.
Jean-Luc FellahiCarMeN Laboratory, INSERM UMR 1060, Claude Bernard Lyon 1 University, Lyon, France.
Matthias Jacquet-LagrèzeDepartment of Anesthesiology and Intensive Care Medicine, University Hospital Louis Pradel, Hospices Civils de Lyon, Bron, France.
Frederic AubrunDepartment of Anesthesiology and Intensive Care Medicine, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Laurent ArgaudMedical Intensive Care Unit, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
Frederic DaillerDepartment of Anesthesiology and Intensive Care Medicine, Pierre Wertheimer Hospital, Hospices Civils de Lyon, Bron, France.
Fabienne VenetImmunology Laboratory, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.
Florent ValourDepartment of Infectious Diseases, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Florence PersatDepartment of Mycology and Parasitology, Institute of Infectious Agents, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Thomas RimmeléDepartment of Anesthesiology and Intensive Care Medicine, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucormycosis is a rare but life-threatening invasive fungal infection that primarily affects immunocompromised patients. Data on its presentation, management, and prognosis in the intensive care unit setting remain scarce. We aimed to evaluate 90-day mortality and to explore clinical, microbiological, therapeutic, and immunological factors associated with outcome in critically ill patients with mucormycosis.

methodsThis retrospective multicenter cohort study included patients diagnosed with mucormycosis and admitted to the ICUs of the Hospices Civils de Lyon between January 2014 and July 2023. Patients were identified through mycological records and hospital discharge codes. Univariable analysis and multivariable Cox model were performed to identify factors associated with 90-day mortality.

resultsAmong 43 patients included, hematological malignancy and trauma were the most common underlying conditions (26% each), followed by solid organ transplantation (21%), and burns (16%). Cutaneous forms (49%) predominated, especially among trauma and burn patients, while pulmonary and rhinocerebral forms were mostly observed in previously immunocompromised individuals. The number of mucormycosis diagnoses increased nearly threefold over the study period, paralleling the implementation of Mucorales-specific polymerase chain reaction. Antifungal therapy was initiated in 39 patients (91%); first-line treatment was liposomal amphotericin B in 32 (74%), at a median maximum dose of 7.5 [3.5-9.4] mg/kg/day, and 12 (28%) received a combination therapy. The 90-day mortality was 47%. In the multivariable Cox model, older age, hematological malignancy, and a higher Sequential Organ Failure Assessment score at diagnosis were independently associated with mortality, while lower liposomal amphotericin B dosing was associated with mortality in univariable analysis. In eight patients without previous immunosuppression and uncontrolled disease, immune monitoring was performed and revealed decreased monocyte HLA-DR expression at 4556 [4194-6936] Ab/c, in favor of injury-induced immunosuppression. Among them, six patients received interferon-gamma as immunotherapy; four responded immunologically and survived.

conclusionsMucormycosis in critically ill patients is associated with high mortality, particularly in those with hematological malignancies. Polymerase chain reaction-based diagnostics may allow earlier detection, and immune monitoring could help identify high-risk patients, particularly in trauma and burn settings.

Indexed as

MucormycosisAdultAgedAmphotericin BAntifungal AgentsCohort StudiesCritical IllnessFemaleFranceHumansIntensive Care UnitsMaleMiddle AgedProportional Hazards ModelsRetrospective StudiesAmphotericin BAntifungal AgentsImmunosuppressionIntensive care unitLiposomal amphotericin BMucormycosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.