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CHAPTER 11: ANTI-FUNGAL AGENTS oContraindications – Hepatic /renal

FUNGUS dysfunction, pregnancy and lactation


o Composed of a rigid cell wall made up of chitin o Adverse effect- Liver toxicity, tetrogenic
and various polysaccharides, and a cell effects and bone marrow supression
membrane containing ergosterol o Drug-to–Drug Interaction- Cyclosporine
o Protective layers of the fungal cell make the AMPHOTERICIN B
organism resistant to antibiotics o Indications – Very potent – reserved for
PATIENTS SUSCEPTIBLE TO FUNGAL progressive potential fatal fungal infections
INFECTIONS o Pharmacokinetics - IV form only,
o Patients with AIDS and AIDS-related metabolism not well understood, excreted in
complex (ARC) the urine
o Patients taking immunosuppressant drugs o Contraindications – Pregnancy, lactation
o Patients who have undergone transplantation and renal impairment
surgery or cancer treatment o Adverse Effect - related to their toxic
o Members of growing elderly population no effects on the liver and kidneys, severe renal
longer protected from environmental fungi impairment and bone marrow suppression
CULTURE o Drug-to-drug Interaction- Nephrotoxic
o A culture should be obtained prior to antibiotics or antineoplastics, cyclosporine,
prescribing anti-fungal agents. or corticosteroids
o Patients on antifungal agents are typically FLUCYTOSINE
immunosuppressed and should not be placed o Indications – Prevent the fungal cells from
at additional risks for incorrect agent and reproducing by altering the cell membrane
toxic effects. o Pharmacokinetics – IV form only,
MOST COMMON SYSTEMIC ANTIFUNGAL metabolism not well understood, excreted in
AGENTS the urine
o Caspofungin (Cancidas) (IV) o Contraindications – Pregnancy, lactation
o Approved for the treatment of invasive and renal impairment
aspergillosis in patients who are o Adverse Effect – Toxic effects on the liver
refractory to other treatments and kidneys and bone marrow suppression
o Flucytosine (Ancobon) (Oral) o Drug-to-drug Interaction- Nephrotoxic
o Less toxic drug used for the treatment antibiotics or antineoplastics, cyclosporine,
of systemic infections caused by or corticosteroids
Candida or Cryptococcus TOPICAL ANTIFUNGAL AGENTS
o Nystatin (Mycostatin, Nilstat) (Oral) o Indication- Work to alter the cell
o Used for the treatment of intestinal permeability of the fungus, causing
candidiasis; also available in a number prevention of replication and fungal death,
of topical preparations indicated only for local treatment of
AZOLES mycoses, including tinea infections
o Indications - Newer class of drugs used to o Pharmacokinetics- Not systemic
treat systemic fungal infections, less toxic o Contraindications- Limited to known
than amphotericin B but also less effective, allergy to any of these drugs
bind to sterols and can cause cell death, o Adverse Reactions- Irritation, burning,
inhibit glucan synthesis rash, and swelling at the site
o Pharmacokinetics – Absorbed rapidly from o Drug-to-drug Interactions: Unknown
the GI tract, metabolized in the liver and
excreted in urine and feces
o Contraindications – Hepatic and renal
dysfunction, pregnancy and lactation and
drugs that prolong the QTc interval
o Adverse effect- Liver toxicity and
tetrogenic effects
o Drug-to–Drug Interaction- Many

ECHINOCANDIN ANTIFUNGALS
o Indications – Another group of antifungals,
inhibit glucan synthesis leading to death of
the cell wall
o Pharmacokinetics – Given IV, rapid onset,
metabolized degradation and excreted in
feces
NURSING CONSIDERATIONS
1. SYSTEMIC
o Assess:
o History of allergy to antifungal
o Physical status
o Culture of the infected area
o Renal and hepatic function tests and
CBC
2. TOPICAL
o Assess:
o Known allergy to any topical antifungal
agent
o Physical status
o Culture and sensitivity testing
o Area of application for color,
temperature, and evidence of lesions

SITE OF ACTION OF ANTIFUNGALS

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