Tato stránka byla automaticky přeložena a přesnost překladu není zaručena. Podívejte se prosím na anglická verze pro zdrojový text.

Derivation and Validation of the Fungal Pneumonia Assessment and Likelihood Predictor Score (FUNGAL-P)

26. června 2026 aktualizováno: Peiman Nazerian, Azienda Ospedaliero-Universitaria Careggi

The FUNGAL-P study is a single-center observational study designed to derive and validate a clinical prediction score for the early identification of fungal pneumonia in adult patients presenting with pneumonia.

The study includes a retrospective derivation cohort and a prospective validation cohort of patients undergoing microbiological evaluation of lower respiratory tract samples. Clinical, laboratory, radiological, microbiological, and treatment-related variables associated with fungal pneumonia will be analyzed to identify independent predictors of fungal infection. These predictors will be combined to develop the FUNGAL-P score.

The derived score will subsequently be evaluated in a prospective validation cohort to assess its diagnostic performance, calibration, and clinical utility. The ultimate goal is to facilitate earlier recognition of fungal pneumonia and support timely diagnostic testing and antifungal treatment in patients presenting to the Emergency Department or hospital with pneumonia.

Přehled studie

Postavení

Nábor

Podmínky

Intervence / Léčba

Detailní popis

Fungal pneumonia is an increasingly recognized cause of severe respiratory infection and is associated with substantial morbidity and mortality. Early diagnosis remains challenging because clinical manifestations are often nonspecific and conventional diagnostic criteria may not be readily applicable in emergency care settings. Delayed recognition may result in delayed diagnostic investigations and initiation of targeted antifungal therapy.

The FUNGAL-P study is a no-profit, single-center observational study conducted at Careggi University Hospital (Florence, Italy). The study was designed to derive and validate a clinical prediction rule for the early identification of fungal pneumonia or fungal-bacterial coinfection among adult patients presenting with pneumonia.

The study consists of two sequential phases.

Retrospective derivation phase

The derivation cohort includes adult patients with microbiologically confirmed pneumonia diagnosed between January 1, 2022 and December 31, 2023. Eligible patients underwent bronchoalveolar lavage (BAL), bronchial aspirate, or endotracheal aspirate collection within 48 hours of hospital presentation. Microbiological investigations included fungal and bacterial cultures, galactomannan testing, molecular assays for Aspergillus species and Pneumocystis jirovecii, and multiplex molecular respiratory pathogen testing.

Patients with microbiologically confirmed fungal pneumonia constituted the study group, whereas patients with bacterial or viral pneumonia served as controls. Cases of fungal-bacterial coinfection were classified as fungal pneumonia. Patients without microbiological identification of a pathogen were excluded.

Prospective validation phase

The validation cohort includes consecutive adult patients with pneumonia enrolled between January 1, 2024 and December 31, 2024. Patients underwent routine microbiological investigations according to standard clinical practice. The performance of the derived FUNGAL-P score was evaluated prospectively without influencing clinical decision-making.

Outcome definition

The primary study outcome is fungal pneumonia, including infections caused by Aspergillus species, Pneumocystis jirovecii, and other fungal pathogens, as well as fungal-bacterial coinfections. Diagnosis is based on an integrated assessment of clinical presentation, radiological findings, microbiological results, fungal biomarkers, and molecular testing results. Final case adjudication includes review of clinical follow-up data, imaging studies, microbiological findings, and treatment decisions.

Data collection

Demographic characteristics, medical history, comorbidities, fungal infection risk factors, vital signs, laboratory findings, radiological data, microbiological results, administered treatments, and clinical outcomes are collected for all participants.

Statistical analysis

Independent predictors of fungal pneumonia are identified using multivariable logistic regression. Candidate variables are selected based on prior evidence and univariable analyses. Predictors retained in the final model are incorporated into the FUNGAL-P score. Diagnostic performance is evaluated using sensitivity, specificity, predictive values, likelihood ratios, receiver operating characteristic (ROC) curves, and area under the ROC curve (AUROC). Calibration is assessed using calibration plots and the Hosmer-Lemeshow test. Internal validation is performed using bootstrap resampling, and clinical utility is evaluated through decision curve analysis.

Primary Objective

To derive a clinical prediction score for fungal pneumonia or fungal-bacterial coinfection in adult patients presenting with pneumonia.

Secondary Objectives

To prospectively validate the FUNGAL-P score. To assess score calibration and discrimination. To determine sensitivity, specificity, positive predictive value, and negative predictive value.

To evaluate the clinical utility of the score for identifying patients at increased risk of fungal pneumonia.

Typ studie

Pozorovací

Zápis (Odhadovaný)

400

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Studijní záloha kontaktů

Studijní místa

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ne

Metoda odběru vzorků

Vzorek nepravděpodobnosti

Studijní populace

Adult patients presenting with pneumonia at Careggi University Hospital who underwent microbiological evaluation of lower respiratory tract samples, including bronchoalveolar lavage, bronchial aspirate, or endotracheal aspirate, within 48 hours of hospital presentation. The study population includes patients with microbiologically confirmed fungal, bacterial, or viral pneumonia enrolled in retrospective and prospective cohorts for derivation and validation of the FUNGAL-P clinical prediction score.

Popis

Inclusion Criteria:

  • Age ≥18 years and ≤90 years.
  • Presentation to the Emergency Department or hospital with pneumonia.
  • Pneumonia defined according to IDSA/ATS criteria as the presence of at least two clinical signs or symptoms of lower respiratory tract infection (temperature <36.0°C or >38.0°C, respiratory rate >20 breaths/min, oxygen saturation <90% on room air, arterial PaO₂ <60 mmHg, cough, sputum production, white blood cell count <4,000/μL or >10,000/μL, or bandemia >10%) together with radiographic evidence of a new pulmonary infiltrate or cavitary lesion.
  • Bronchoalveolar lavage (BAL), bronchial aspirate (BAS), or endotracheal aspirate (ETA) performed within 48 hours of hospital presentation.
  • Modified Rankin Scale score <5.
  • Availability of microbiological investigations for identification of fungal, bacterial, or viral pathogens.
  • Provision of informed consent, when required by applicable regulations and ethics committee approval.

Exclusion Criteria:

  • Refusal or withdrawal of informed consent.
  • Age <18 years or >90 years.
  • Pregnancy.
  • Expected life expectancy <3 months.
  • Hospital-acquired pneumonia with onset >48 hours after hospital admission.
  • Modified Rankin Scale score ≥5.
  • Absence of microbiological diagnostic evaluation.
  • No identified bacterial, fungal, or viral pathogen after microbiological investigations.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

Kohorty a intervence

Skupina / kohorta
Intervence / Léčba
Retrospective Derivation Cohort
Adult patients with microbiologically confirmed pneumonia enrolled at Careggi University Hospital between January 1, 2022 and December 31, 2023. Clinical, laboratory, radiological, microbiological, treatment, and outcome data were collected to identify independent predictors of fungal pneumonia and to derive the FUNGAL-P clinical prediction score.
Jiný: FUNGAL-P Score Assessment
Observational assessment of clinical, laboratory, radiological, and microbiological variables used to derive and validate the FUNGAL-P clinical prediction score for fungal pneumonia. No study-specific intervention was performed and patient management was not influenced by the study.
Prospective Validation Cohort
Consecutive adult patients with pneumonia enrolled at Careggi University Hospital between 13 nov, 2025 and December 31, 2030. The cohort was used to prospectively evaluate the diagnostic performance, calibration, and clinical utility of the derived FUNGAL-P score without influencing clinical management.
Jiný: FUNGAL-P Score Assessment
Observational assessment of clinical, laboratory, radiological, and microbiological variables used to derive and validate the FUNGAL-P clinical prediction score for fungal pneumonia. No study-specific intervention was performed and patient management was not influenced by the study.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Area under the receiver operating characteristic curve (AUROC) of the FUNGAL-P score
Časové okno: At completion of study analysis (30 days)
Evaluation of the discriminative ability of the FUNGAL-P score for identifying fungal pneumonia.
At completion of study analysis (30 days)

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Area under the receiver operating characteristic curve (AUROC) of the FUNGAL-P score
Časové okno: At completion of study analysis (30 days)
Evaluation of the discriminative ability of the FUNGAL-P score for identifying fungal pneumonia.
At completion of study analysis (30 days)
Sensitivity and specificity of the FUNGAL-P score
Časové okno: At completion of study analysis (30 days)
Assessment of sensitivity, specificity, positive predictive value, and negative predictive value of the FUNGAL-P score at predefined score thresholds.
At completion of study analysis (30 days)
Calibration of the FUNGAL-P score
Časové okno: At completion of study analysis (30 days)
Assessment of agreement between predicted and observed probabilities of fungal pneumonia using calibration plots and the Hosmer-Lemeshow test.
At completion of study analysis (30 days)
Clinical utility of the FUNGAL-P score
Časové okno: At completion of study analysis (30 days)
Evaluation of the net clinical benefit of the FUNGAL-P score using Decision Curve Analysis.
At completion of study analysis (30 days)

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Sponzor

Azienda Ospedaliero-Universitaria Careggi

Vyšetřovatelé

  • Vrchní vyšetřovatel: Lorenzo Pelagatti, MD, PhD, University of Florence

Publikace a užitečné odkazy

Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.

Obecné publikace

  • 1. Esandi M, Magnasco L, Farina EC, et al. Early diagnosis of candidiasis in non-neutropenic critically ill patients: prospective study. Intensive Care Med. 2003;29(9):1534-1540. doi:10.1007/s00134-003-1825-3 2. Wang K, Wang Y, Liu M, et al. Retrospective evaluation of risk factors for invasive Candida infections in a medical ICU. Medicine (Baltimore). 2024;103(14):e38338. doi:10.1097/MD.0000000000038338 3. Kullberg BJ, Arendrup MC. Invasive candidiasis. N Engl J Med. 2015;373(15):1445-1456. doi:10.1056/NEJMra1315399 4. Playford EG, Eggimann P, Calandra T, et al. Epidemiology of invasive candidiasis in non-neutropenic critically ill patients. Lancet Infect Dis. 2010;10(12):775-784. doi:10.1016/S1473-3099(10)70267-7 5. Leroy G, Lambiotte F, Thévenin D, et al. Risk factors of invasive fungal disease in critically ill adult patients: a systematic review. Crit Care. 2012;16(5):R242. doi:10.1186/cc11844 6. Aguilar C, Kumar D, Humar A, et al. Risk factors for invasive fungal infections in lung transplant recipients: a systematic review and meta-analysis. Clin Transplant. 2021;35(4):e14232. doi:10.1111/ctr.14232 7. Li Y, Wang J, Zhang H, et al. A novel scoring system to predict invasive candidiasis in immunocompetent critically ill patients. Front Microbiol. 2023;14:1097574. doi:10.3389/fmicb.2023.1097574 8. Bougnoux ME, Kac G, Aegerter P, et al. Candidemia and Candida colonization in critically ill patients: incidence and risk factors. Intensive Care Med. 2008;34(11):1955-1961. doi:10.1007/s00134-008-1197-4 9. Bassetti M, Righi E, Ansaldi F, et al. A multicenter study of candidemia in intensive care units in Italy. Intensive Care Med. 2006;32(10):1523-1529. doi:10.1007/s00134-006-0298-8 10. Blot SI, Taccone FS, Van den Abeele AM, et al. A clinical algorithm to diagnose invasive pulmonary aspergillosis in critically ill patients. Intensive Care Med. 2012;38(9):1294-1303. doi:10.1007/s00134-012-2600-5 11. Lu LY, Cheng Y, Wang H, et al. Risk factors and outcomes of influenza

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Aktuální)

13. listopadu 2025

Primární dokončení (Odhadovaný)

13. listopadu 2030

Dokončení studie (Odhadovaný)

13. listopadu 2031

Termíny zápisu do studia

První předloženo

26. června 2026

První předloženo, které splnilo kritéria kontroly kvality

26. června 2026

První zveřejněno (Aktuální)

2. července 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

2. července 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

26. června 2026

Naposledy ověřeno

1. června 2026

Více informací

Termíny související s touto studií

Klíčová slova

Další relevantní podmínky MeSH

Další identifikační čísla studie

  • CEAVC 29602

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NEROZHODNÝ

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

Klinické studie na FUNGAL-P Score Assessment

Prohledejte podobné pokusy

Sponzoři a spolupracovníci

Zdravotní podmínky

Drogové intervence

CROs by country

CROs in Slovakia

Podmínky

Vzácné nemoci

Drogové intervence

Doplňky stravy

Sponzor / Spolupracovníci

Místa

3
Předplatit