Invasive fungal infection: Difference between revisions

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(added classification)
(: cleaned up list of criteria)
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* The classification is based on a combination of patient risk factors (host factors), imaging, and mycology [[CiteRef::de pauw2008re]]
 
* The classification is based on a combination of patient risk factors (host factors), imaging, and mycology [[CiteRef::de pauw2008re]]
* Host factors:
+
* '''Host factors'''
** Recent history of neutropenia (<0.5 × 109 neutrophils/L [<500 neutrophils/mm3] for >10 days) temporally related to the onset of fungal disease
+
** Recent history of neutropenia (<0.5 × 109 neutrophils/L for >10 days) temporally related to the onset of fungal disease
 
** Receipt of an allogeneic stem cell transplant
 
** Receipt of an allogeneic stem cell transplant
** Prolonged use of corticosteroids (excluding among patients with allergic bronchopulmonary aspergillosis) at a mean minimum dose of 0.3 mg/kg/day of prednisone equivalent for >3 weeks
+
** Prolonged use of corticosteroids (excluding [[ABPA]]) at a mean minimum dose of 0.3 mg/kg/day of prednisone equivalent for >3 weeks
** Treatment with other recognized T cell immunosuppressants, such as cyclosporine, TNF-α blockers, specific monoclonal antibodies (such as alemtuzumab), or nucleoside analogues during the past 90 days
+
** Treatment with other recognized T cell immunosuppressants, such as [[cyclosporine]], TNF-α blockers, specific monoclonal antibodies (such as alemtuzumab), or nucleoside analogues during the past 90 days
** Inherited severe immunodeficiency (such as chronic granulomatous disease or severe combined immunodeficiency)
+
** Inherited severe immunodeficiency (such as [[chronic granulomatous disease]] or [[severe combined immunodeficiency]])
* Clinical criteria:
+
* '''Clinical criteria'''
** Lower respiratory tract fungal disease
+
** Lower respiratory tract fungal disease: the presence of 1 of the following 3 signs on CT
 
*** Dense, well-circumscribed lesions(s) with or without a halo sign
*** The presence of 1 of the following 3 signs on CT:
 
 
*** Air-crescent sign
**** Dense, well-circumscribed lesions(s) with or without a halo sign
 
 
*** Cavity
**** Air-crescent sign
 
 
** Tracheobronchitis: tracheobronchial ulceration, nodule, pseudomembrane, plaque, or eschar seen on bronchoscopic analysis
**** Cavity
 
 
** Sinonasal infection: imaging showing sinusitis plus at least 1 of the following 3 signs:
** Tracheobronchitis
 
 
*** Acute localized pain (including pain radiating to the eye)
*** Tracheobronchial ulceration, nodule, pseudomembrane, plaque, or eschar seen on bronchoscopic analysis
 
 
*** Nasal ulcer with black eschar
** Sinonasal infection
 
 
*** Extension from the paranasal sinus across bony barriers, including into the orbit
*** Imaging showing sinusitis plus at least 1 of the following 3 signs:
 
 
** CNS infection: 1 of the following 2 signs
**** Acute localized pain (including pain radiating to the eye)
 
 
*** Focal lesions on imaging
**** Nasal ulcer with black eschar
 
 
*** Meningeal enhancement on MRI or CT
**** Extension from the paranasal sinus across bony barriers, including into the orbit
 
 
** Disseminated candidiasis: At least 1 of the following 2 entities after an episode of candidemia within the previous 2 weeks:
** CNS infection
 
 
*** Small, target-like abscesses (bull's-eye lesions) in liver or spleen
*** 1 of the following 2 signs:
 
 
*** Progressive retinal exudates on ophthalmologic examination
**** Focal lesions on imaging
 
 
* '''Mycological criteria'''
**** Meningeal enhancement on MRI or CT
 
** Disseminated candidiasis
 
*** At least 1 of the following 2 entities after an episode of candidemia within the previous 2 weeks:
 
**** Small, target-like abscesses (bull's-eye lesions) in liver or spleen
 
**** Progressive retinal exudates on ophthalmologic examination
 
* Mycological criteria
 
 
** Direct test (cytology, direct microscopy, or culture)
 
** Direct test (cytology, direct microscopy, or culture)
 
*** Mold in sputum, bronchoalveolar lavage fluid, bronchial brush, or sinus aspirate samples, indicated by 1 of the following:
 
*** Mold in sputum, bronchoalveolar lavage fluid, bronchial brush, or sinus aspirate samples, indicated by 1 of the following:
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*** Recovery by culture of a mold (e.g., Aspergillus, Fusarium, Zygomycetes, or Scedosporium species)
 
*** Recovery by culture of a mold (e.g., Aspergillus, Fusarium, Zygomycetes, or Scedosporium species)
 
** Indirect tests (detection of antigen or cell-wall constituents)
 
** Indirect tests (detection of antigen or cell-wall constituents)
 
*** Aspergillosis: Galactomannan antigen detected in plasma, serum, bronchoalveolar lavage fluid, or CSF
*** Aspergillosis
 
 
*** Invasive fungal disease other than cryptococcosis and zygomycoses: β-d-glucan detected in serum
**** Galactomannan antigen detected in plasma, serum, bronchoalveolar lavage fluid, or CSF
 
*** Invasive fungal disease other than cryptococcosis and zygomycoses
 
**** β-d-glucan detected in serum
 
   
 
=== Proven ===
 
=== Proven ===

Revision as of 17:03, 22 September 2019

Microbiology

Epidemiology

  • Among patients on posaconazole for a hematologic malignancy or bone marrow transplant, there is an approximately 2% rate of breakthrough infection 1

Classification

  • The classification is based on a combination of patient risk factors (host factors), imaging, and mycology 2
  • Host factors
    • Recent history of neutropenia (<0.5 × 109 neutrophils/L for >10 days) temporally related to the onset of fungal disease
    • Receipt of an allogeneic stem cell transplant
    • Prolonged use of corticosteroids (excluding ABPA) at a mean minimum dose of 0.3 mg/kg/day of prednisone equivalent for >3 weeks
    •  Treatment with other recognized T cell immunosuppressants, such as cyclosporine, TNF-α blockers, specific monoclonal antibodies (such as alemtuzumab), or nucleoside analogues during the past 90 days
    • Inherited severe immunodeficiency (such as chronic granulomatous disease or severe combined immunodeficiency)
  • Clinical criteria
    •  Lower respiratory tract fungal disease: the presence of 1 of the following 3 signs on CT
      • Dense, well-circumscribed lesions(s) with or without a halo sign
      • Air-crescent sign
      • Cavity
    • Tracheobronchitis: tracheobronchial ulceration, nodule, pseudomembrane, plaque, or eschar seen on bronchoscopic analysis
    •  Sinonasal infection: imaging showing sinusitis plus at least 1 of the following 3 signs:
      •  Acute localized pain (including pain radiating to the eye)
      •  Nasal ulcer with black eschar
      •  Extension from the paranasal sinus across bony barriers, including into the orbit
    •  CNS infection: 1 of the following 2 signs
      •  Focal lesions on imaging
      •  Meningeal enhancement on MRI or CT
    •  Disseminated candidiasis: At least 1 of the following 2 entities after an episode of candidemia within the previous 2 weeks:
      •  Small, target-like abscesses (bull's-eye lesions) in liver or spleen
      •  Progressive retinal exudates on ophthalmologic examination
  • Mycological criteria
    •  Direct test (cytology, direct microscopy, or culture)
      •  Mold in sputum, bronchoalveolar lavage fluid, bronchial brush, or sinus aspirate samples, indicated by 1 of the following:
      •  Presence of fungal elements indicating a mold
      •  Recovery by culture of a mold (e.g., Aspergillus, Fusarium, Zygomycetes, or Scedosporium species)
    •  Indirect tests (detection of antigen or cell-wall constituents)
      •  Aspergillosis: Galactomannan antigen detected in plasma, serum, bronchoalveolar lavage fluid, or CSF
      •  Invasive fungal disease other than cryptococcosis and zygomycoses: β-d-glucan detected in serum

Proven

Probable

  • Requires a susceptible host, clinical/radiographic features, and mycological evidence

Possible

  • Only cases with the appropriate host factors and with sufficient clinical/radiographic evidence without supporting mycological evidence
  • Not used for endemic fungi

References

  1. ^  Oliver A. Cornely, Johan Maertens, Drew J. Winston, John Perfect, Andrew J. Ullmann, Thomas J. Walsh, David Helfgott, Jerzy Holowiecki, Dick Stockelberg, Yeow-Tee Goh, Mario Petrini, Cathy Hardalo, Ramachandran Suresh, David Angulo-Gonzalez. Posaconazole vs. Fluconazole or Itraconazole Prophylaxis in Patients with Neutropenia. New England Journal of Medicine. 2007;356(4):348-359. doi:10.1056/nejmoa061094.
  2. ^  Ben De Pauw, Thomas J. Walsh, J. Peter Donnelly, David A. Stevens, John E. Edwards, Thierry Calandra, Peter G. Pappas, Johan Maertens, Olivier Lortholary, Carol A. Kauffman, David W. Denning, Thomas F. Patterson, Georg Maschmeyer, Jacques Bille, William E. Dismukes, Raoul Herbrecht, William W. Hope, Christopher C. Kibbler, Bart Jan Kullberg, Kieren A. Marr, Patricia Muñoz, Frank C. Odds, John R. Perfect, Angela Restrepo, Markus Ruhnke, Brahm H. Segal, Jack D. Sobel, Tania C. Sorrell, Claudio Viscoli, John R. Wingard, Theoklis Zaoutis, John E. Bennett. Revised Definitions of Invasive Fungal Disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group. Clinical Infectious Diseases. 2008;46(12):1813-1821. doi:10.1086/588660.