Invasive fungal infections
Invasive
fungal infections occur in both immunocompetent and immunocompromised patients.
Endemic Fungal Infections
Endemic
fungal infections can affect both healthy and immunocompromised patients.
Species
|
Remark(s)
|
Histoplasmosis
|
§ Endemic
to Southeast Asian rivers
§ Itraconazole
is used as monotherapy for mild and chronic pulmonary disease.
§
Amphotericin B (AmB) with itraconazole is
recommended for moderate-to-severe histoplasmosis.
|
Blastomycosis
|
§ Extrapulmonary
dissemination involving the skin occurs in up to 40% of cases.
§
Treatment includes itraconazole for
mild-to-moderate disease and liposomal AmB (L-AmB) followed by itraconazole
for life-threatening pulmonary infections.
|
Sporotrichosis
|
§ Sporothrix
schenckii is globally located and not isolated to certain
regions.
§ Infection
results primarily from cutaneous contact with sporotrichosis.
§
Mild-to-moderate pulmonary disease requires
itraconazole, whereas AmB followed by itraconazole is recommended for severe
disease.
|
Coccidioido-mycosis
|
§ Presentation
as community-acquired pneumonia in endemic areas.
§ Immunocompetent
infected hosts may not require treatment.
§ Immunocompromised
patients are treated with fluconazole or itraconazole.
§
In serious pulmonary disease, treatment with
AmB is initiated, followed by an azole.
|
Opportunistic Fungal Infections
Opportunistic fungal infections primarily
cause infections in patients who tend to be immunocompromised.
Species
|
Remark(s)
|
Aspergillosis
|
§ Primary
treatment for invasive pulmonary aspergillosis (IPA) is voriconazole.
§ Alternatives
include lipid-based AmB formulations, echinocandins, and posaconazole.
§ Data
to support combination therapy are currently lacking; therefore, combination
therapy is not recommended.
|
Cryptococcosis
|
§ Immunocompetent
patients are typically asymptomatic, which results in a dormant infection.
§ Because
cryptococcosis is associated with a high risk of mortality secondary to
dissemination, immediate identification and treatment are necessary to avoid
dissemination to the central nervous system.
§ For
those exhibiting mild-to-moderate symptoms, fluconazole therapy is recommended.
§ An
AmB formulation with or without flucytosine, followed by oral fluconazole, is
the primary recommendation for severe symptomatic pulmonary cryptococcosis.
|
Candidiasis
|
§ Pulmonary
pneumonia infection due to Candida species
is rare and diagnosis can be difficult.
§ Colonization
of the lung parenchyma with Candida species
is common, yet usually will be dormant in immunocompetent person.
§ Many
critically ill patients are empirically treated with broad-spectrum antibiotics.
Further clinical deterioration and lack of improvement in these cases suggest
the initiation of empiric antifungal therapy.
§ Because
triazole antifungals and echinocandins exhibit excellent lung penetration,
they—in addition to AmB formulations—are effective for treating pulmonary
candidiasis, despite the lack of specific studies regarding the treatment of Candida pneumonia.
|
Mucormycosis
|
§ Uncommon.
§ Occurs
in patients with diabetes mellitus, organ or hematopoietic stem cell
transplant, neutropenia, or malignancy.
§ Pulmonary
mucormycosis is primarily observed in patients with a predisposing condition
of neutropenia or corticosteroid use.
§ Treatment
should include control of the predisposing problem, débridement of necrotic
tissue, and antifungal therapy.
§ Current
recommendations for efficacious treatment of mucormycosis include AmB
formulations, posaconazole, and iron chelation therapy.
§ Because
of the lack of literature regarding combination therapy, its use in
mucormycosis is not recommended.
|
Pneumocystis jirovecii
Pneumonia (PCP) |
§ Originally
considered a parasite, PCP is currently categorized as a fungus based on
molecular similarities to fungal RNA.
§ Infection
occurs through the inhalation of airborne spores, with further maturation
occurring in the lungs.
§ PCP
is extremely resistant to common antifungal therapy, including AmB
formulations and triazole antifungals.
§ Trimethoprim/sulfamethoxazole
remains the mainstay for PCP treatment and prophylaxis.
§ If
clinical improvement is not noted, failure of the first-line treatment should
be considered and a second-line agent should be initiated.
§ Second-line
agents indicated for the treatment of PCP include primaquine plus
clindamycin, atovaquone, or IV pentamidine.
|
Reference:
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[Accessed
on 21 Dec 2018]
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