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Non-invasive Tools to Diagnose Invasive Aspergillosis Infections in ICU Patients With COVID-19 and Other Conditions. (BM-ASP-ICU)

Primary Purpose

Invasive Pulmonary Aspergillosis

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
respiratory sample
blood sample
Sponsored by
Centre Hospitalier Universitaire de Besancon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Invasive Pulmonary Aspergillosis focused on measuring ICU patients, Covid-19

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. ICU adult patient (age > 18 years old at inclusion)
  2. Patient with respiratory distress (fever refractory to > 3 days of antibiotherapy, pleuritic chest pain, hemoptysis) or Patient with sign of infection on thoracic scan or Patient with positive culture for Aspergillus sp on any respiratory sample
  3. Informed consent signed by the patient or proxy
  4. Patient with health insurance

Exclusion Criteria:

  1. Minor patient (age < 18 years old at inclusion)
  2. Known risk of immunodepression as defined by EORTC/MSG:

    • Recent history neutropenia (< 500 neutrophils/mm3 for > 10 days)
    • Haematological malignancy
    • Receipt of an allogenic stem cell transplant
    • Receipt of a solid organ transplant
    • Prolonged use of corticosteroids (excluding among patients with allergic bronchopulmonary aspergillosis) at a therapeutic dose of ≥0·3 mg/kg corticosteroids for ≥3 weeks in the past 60 days
    • Treatment with recognized T-cell immunosuppressant for more than 90 days (such as calcineurin inhibitors, TNF blockers, lymphocyte-specific monoclonal antibodies, and immunosuppressive nucleoside analogues)
    • Treatment with recognized inhibitors of B-cell receptor pathway (e. g, ibrutinib), possibly BCL2 inhibitors (e. g, venetoclax)
    • Inherited severe immunodeficiency (e. g, chronic granulomatous disease, STAT3 deficiency, or severe combined immunodeficiency)
    • Acute graft-versus-host disease grade III or IV, involving the gut, lungs, or liver, that is refractory to first-line treatment with steroids
  3. Patient under legal protection (e. g, tutorship)
  4. Patients without health insurance
  5. Pregnancy

Sites / Locations

  • CHU BesançonRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

biological sample

Arm Description

respiratory and blood sample

Outcomes

Primary Outcome Measures

Performance indicators of the algorithm
sensitivity, specificity, positive and negative predictive values, and likelihood ratios.

Secondary Outcome Measures

Full Information

First Posted
November 17, 2021
Last Updated
April 20, 2023
Sponsor
Centre Hospitalier Universitaire de Besancon
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1. Study Identification

Unique Protocol Identification Number
NCT05138666
Brief Title
Non-invasive Tools to Diagnose Invasive Aspergillosis Infections in ICU Patients With COVID-19 and Other Conditions.
Acronym
BM-ASP-ICU
Official Title
Non-invasive Tools to Better Diagnose Invasive Aspergillosis Infections in ICU Patients With COVID-19 and Other Non-immunosuppressive Conditions.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 16, 2022 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
March 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Besancon

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Invasive aspergillosis (IA) are difficult to diagnose in the ICU population, as the patients often do not present the conventional risks factors of immunocompromised patients (EORTC/MSG criteria). In the ICU population, patients often present other risk factors, such as cirrhosis, COPD, influenza and currently SARS-Cov2. The clinicians are thus currently missing precise criteria to distinguish colonization from IA in these patients, while they need to decide if an antifungal treatment is necessary or not. A new algorithm, entitled BM ASP ICU, based on investigators field experience and the scientific literature, which takes into account both EORTC/MSG criteria and a combination of fungal biomarkers, was proposed recently by Haman et al, Annals Intensive Care, 2021. Additional serological assays (immunoprecipitation and ELISA) showed since their interest, especially concerning SARS-Cov2 patients, a new population at risk of IA in the ICU, which emerged in the past months. The present study aims at prospectively implementing the BM ASP ICU algorithm during two years in the routine practice of six ICU units distributed in general and teaching hospitals situated northeast of France. The BM ASP ICU algorithm would be completed by serological assays aiming at assessing a sensitization towards Aspergillus fumigatus. The investigators plan to include 400 ICU patients at risk of IA; SARS-Cov2 patients will be part of the cohort. A weekly screening including culture of respiratory samples, galactomannan antigen, fungal qPCRS (targeting A. fumigatus), and A. fumigatus serology will be applied for all included patients. The performance (sensitivity and specificity, likelihood ratios) of each fungal biomarkers, alone and in combination with others, will be assessed, for all patients, and also within subgroups of patients with specific risk factors (such as SARS-Cov2 for example). These results should lead to solid understanding of which combination of tests is optimal to diagnose IA and thus to initiate appropriate antifungal treatment. the investigators hope that this study will result in improved survival rate of ICU patients with IA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Invasive Pulmonary Aspergillosis
Keywords
ICU patients, Covid-19

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
363 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
biological sample
Arm Type
Experimental
Arm Description
respiratory and blood sample
Intervention Type
Biological
Intervention Name(s)
respiratory sample
Intervention Description
tracheal aspirate or sputum if the patient is not intubated
Intervention Type
Biological
Intervention Name(s)
blood sample
Intervention Description
Blood sampling drawn from an existing arterial line twice a week
Primary Outcome Measure Information:
Title
Performance indicators of the algorithm
Description
sensitivity, specificity, positive and negative predictive values, and likelihood ratios.
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ICU adult patient (age > 18 years old at inclusion) Patient with respiratory distress (fever refractory to > 3 days of antibiotherapy, pleuritic chest pain, hemoptysis) or Patient with sign of infection on thoracic scan or Patient with positive culture for Aspergillus sp on any respiratory sample Informed consent signed by the patient or proxy Patient with health insurance Exclusion Criteria: Minor patient (age < 18 years old at inclusion) Known risk of immunodepression as defined by EORTC/MSG: Recent history neutropenia (< 500 neutrophils/mm3 for > 10 days) Haematological malignancy Receipt of an allogenic stem cell transplant Receipt of a solid organ transplant Prolonged use of corticosteroids (excluding among patients with allergic bronchopulmonary aspergillosis) at a therapeutic dose of ≥0·3 mg/kg corticosteroids for ≥3 weeks in the past 60 days Treatment with recognized T-cell immunosuppressant for more than 90 days (such as calcineurin inhibitors, TNF blockers, lymphocyte-specific monoclonal antibodies, and immunosuppressive nucleoside analogues) Treatment with recognized inhibitors of B-cell receptor pathway (e. g, ibrutinib), possibly BCL2 inhibitors (e. g, venetoclax) Inherited severe immunodeficiency (e. g, chronic granulomatous disease, STAT3 deficiency, or severe combined immunodeficiency) Acute graft-versus-host disease grade III or IV, involving the gut, lungs, or liver, that is refractory to first-line treatment with steroids Patient under legal protection (e. g, tutorship) Patients without health insurance Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Laurence MILLON, MD
Phone
0370632353
Email
lmillon@chu-besancon.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Jean-Chrisptophe NAVELLOU, MD
Phone
0381668212
Email
jcnavellou@chu-besancon.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Chrisptophe NAVELLOU, MD
Organizational Affiliation
CHU Besançon
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Besançon
City
Besançon
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurence MILLON, PU-PH

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Non-invasive Tools to Diagnose Invasive Aspergillosis Infections in ICU Patients With COVID-19 and Other Conditions.

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