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By
M.D.
Fungi are eukaryotic, heterotrophic (not
self sustaining) organisms that live as
saprobes or parasites.
They are complex organisms in
comparison to bacteria.
Fungal infections are also called as
mycoses.
Classification
Superficial
1-Dermatophytes
2-Candida
3-TVC
Deep:
1-Candiadiasis
2-Aspergillosis
3-Histoplasmosis
4-Coccidiomycosis
Ideal Antifungal
1-Potent activity against different fungal
pathogens
2-Flexibility to oral and parenteral route
3-Favourable pharmacokinetics
4-Few adverse effects
5-Low cost
What are the targets for antifungal
therapy?
Cell membrane
Fungi use principally
ergosterol instead of
cholesterol
Cell Wall
Unlike mammalian
cells, fungi have a
cell wall
DNA Synthesis
Some compounds may be
selectively activated by
fungi, arresting DNA
synthesis
Site of action
At the nuclear level
1-Flucytosine
2-Griseofulvin
At the cell membrane level
1-polyenes
2-Imidazoles
3-Triazoles
4-Allylamines
Squaline epoxidase
14-alpha sterol demthylase
Effect Mechanism Antifungals Involved Suggested clinical
management
Decreased serum
concentration of azole
Antacids
H2 Receptor
antagonism
Proton Pump
Inhibitors
Sulcrafate
Didanosine (oral)
Decreased
dissolution/absorption
of solid dosage form
Ketoconazole,
itraconazole
(capsules),
Use solution
formulation of
itraconazole or other
azole if indicated (i.e.
voriconazole)
Avoid taking antacids
within 2 hours of oral
azole therapy
Increased metabolism
of azole
Isoniazid
Rifampin
Phenytoin
Carbamazepine
Phenobarbital
Barbiturates
Induction of
mammalian
cytochrome-P450
mediated metabolism of
azole
Ketoconazole,
itraconazole,
Griseofulvin
fluconazole,
voriconazole,
posaconazole
Avoid concomitant use
of these agents if
possible. May require
switch to amphotericin
B formulation or
echinocandin
Drug interactions
Increased serum
concentration of co-
administered drug or
metabolite
Oral hypoglycemics
warfarin
Cyclosporin
Phenytoin
Carbamezepine
Triazolam,
midazolam
Diltiazem
Lovastatin
Isoniazid
Rifampin
Quinidine
Busulfan
Vincristine
Cyclophosphamide
Digoxin
Loratidine
Inhibition of
cytochrome P450,
P-gp, or both
Ketoconazole,
itraconazole,
voriconazole >
fluconazole (usual
doses)
Avoid concomitant
use if possible.
Severity of possible
interaction is drug-
dependent. Consult
prescribing
information of each
drug to address
interaction severity
Drug interactions
Griseofulvin: OCP, warfarin, cyclosporin
Fluconazole: OCP
Itraconazole: OCP
Lamisil: Non
Decreased level of other drugs
Clinical uses
TVC:
Topical: lotion, cream, shampoo
Systemic: Curative and prophylactic
Clinical uses
Tinea Capitis
Topical: lotion, cream, shampoo
Systemic: Curative and prophylactic
Griseofulvin versus other antifungals
Trichophyton species: similar efficacy &
much shorter duration of treatment.
Microsporum species: Griseofulvin is
better, but needs longer duration
Treatment protocols should therefore
reflect local epidemiology and be based on
the most likely culprit organism. A
prolonged course or a change of agent may
be required in cases of treatment Failures.
Treatment failures
-Wrong diagnosis
-Lack of compliance – especially in long TTT
-Suboptimal absorption of drug
-Relative insensitivity of the organism
-Reinfection
Clinical uses
Tinea Corporis/cruris/axillaris
Topical: lotion, cream, gel
Systemic: indications and doses
Clinical uses
Tinea pedis: Inflammatory & Non
Topical: lotion, cream, gel
Systemic: indications and doses
Clinical uses
Onychomycosis
Topical: Amorolfine 5%, ciclopirox
8% & tioconazole 28%
Systemic: indications and doses
Pulse & continous
Treatment of onychomycosis
Treatment of toe onychomycosis
Clinical applications
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
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Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
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Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
Antifungal treatment
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Antifungal treatment
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Antifungal treatment

  • 1.
  • 3. Fungi are eukaryotic, heterotrophic (not self sustaining) organisms that live as saprobes or parasites. They are complex organisms in comparison to bacteria. Fungal infections are also called as mycoses.
  • 5. Ideal Antifungal 1-Potent activity against different fungal pathogens 2-Flexibility to oral and parenteral route 3-Favourable pharmacokinetics 4-Few adverse effects 5-Low cost
  • 6. What are the targets for antifungal therapy? Cell membrane Fungi use principally ergosterol instead of cholesterol Cell Wall Unlike mammalian cells, fungi have a cell wall DNA Synthesis Some compounds may be selectively activated by fungi, arresting DNA synthesis
  • 7. Site of action At the nuclear level 1-Flucytosine 2-Griseofulvin At the cell membrane level 1-polyenes 2-Imidazoles 3-Triazoles 4-Allylamines
  • 9.
  • 10.
  • 11. Effect Mechanism Antifungals Involved Suggested clinical management Decreased serum concentration of azole Antacids H2 Receptor antagonism Proton Pump Inhibitors Sulcrafate Didanosine (oral) Decreased dissolution/absorption of solid dosage form Ketoconazole, itraconazole (capsules), Use solution formulation of itraconazole or other azole if indicated (i.e. voriconazole) Avoid taking antacids within 2 hours of oral azole therapy Increased metabolism of azole Isoniazid Rifampin Phenytoin Carbamazepine Phenobarbital Barbiturates Induction of mammalian cytochrome-P450 mediated metabolism of azole Ketoconazole, itraconazole, Griseofulvin fluconazole, voriconazole, posaconazole Avoid concomitant use of these agents if possible. May require switch to amphotericin B formulation or echinocandin Drug interactions
  • 12. Increased serum concentration of co- administered drug or metabolite Oral hypoglycemics warfarin Cyclosporin Phenytoin Carbamezepine Triazolam, midazolam Diltiazem Lovastatin Isoniazid Rifampin Quinidine Busulfan Vincristine Cyclophosphamide Digoxin Loratidine Inhibition of cytochrome P450, P-gp, or both Ketoconazole, itraconazole, voriconazole > fluconazole (usual doses) Avoid concomitant use if possible. Severity of possible interaction is drug- dependent. Consult prescribing information of each drug to address interaction severity Drug interactions
  • 13. Griseofulvin: OCP, warfarin, cyclosporin Fluconazole: OCP Itraconazole: OCP Lamisil: Non Decreased level of other drugs
  • 14.
  • 15. Clinical uses TVC: Topical: lotion, cream, shampoo Systemic: Curative and prophylactic
  • 16. Clinical uses Tinea Capitis Topical: lotion, cream, shampoo Systemic: Curative and prophylactic
  • 17.
  • 18.
  • 19.
  • 20. Griseofulvin versus other antifungals Trichophyton species: similar efficacy & much shorter duration of treatment. Microsporum species: Griseofulvin is better, but needs longer duration
  • 21. Treatment protocols should therefore reflect local epidemiology and be based on the most likely culprit organism. A prolonged course or a change of agent may be required in cases of treatment Failures.
  • 22. Treatment failures -Wrong diagnosis -Lack of compliance – especially in long TTT -Suboptimal absorption of drug -Relative insensitivity of the organism -Reinfection
  • 23. Clinical uses Tinea Corporis/cruris/axillaris Topical: lotion, cream, gel Systemic: indications and doses
  • 24.
  • 25. Clinical uses Tinea pedis: Inflammatory & Non Topical: lotion, cream, gel Systemic: indications and doses
  • 26. Clinical uses Onychomycosis Topical: Amorolfine 5%, ciclopirox 8% & tioconazole 28% Systemic: indications and doses Pulse & continous
  • 28. Treatment of toe onychomycosis