Antifungal Flashcards

1
Q

What organisms live as saprobes or parasites, have a rigid cell wall made of chitin and have ergosterol in their cell membranes instead of cholesterol?

A

Fungi

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2
Q

What are the two kinds of fungal infections?

A

1-Superficial

2-Systemic

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3
Q

What are the main 3 mechanisms that anti fungal drugs target?

A

1-Fungal cell membrane
2-Cell wall synthesis
3-Nucleic acid synthesis (DNA and RNA)

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4
Q

What are the 3 main groups of drugs used to treat systemic fungal infection?

A

Amphotericin B
Azoles
Echinocandins

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5
Q

Which drug family bind ergosterol in fungal cell membranes?

A

Polyenes (Amphotericin-B and Nystatin)

*Form pores in the cell membrane

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6
Q

Which drug family inhibits 14-a-sterol demthylase to prevent ergosterol synthesis?

A

Imidazoles and triazoles

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7
Q

Which drug family inhibits squalene epoxies and prevents ergosterol synthesis?

A

Allylamines

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8
Q

Which drug family inhibits fungal cell wall synthesis by inhibiting glucan synthesis?

A

Echinocandins

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9
Q

Which drug is effective against most serious systemic fungal infections(1st line for candidemia), is administered parenterally only, and can cause renal or neurotoxicity?

A

Amphotericin-B

*Can also be used for aspergillus but is not the drug of choice

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10
Q

Which drug is similar to amphotericin B but is only used topically because it has a high toxicity, is used for oral, esophageal or vaginal candidiasis and can have a disulfiram like reaction?

A

Nystatin

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11
Q

What are the two main groups of broad spectrum fungistatic azoles?

A

Imidazoles (2 nitrogens)

Triazoles (3 nitrogens)

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12
Q

Which group of antifungals increase membrane fluiditiy by inhibiting ergosterol synthesis, are used topically or systemically and are contraindicated for pregnant, lactating or hepatic dysfunction patients?

A

Azoles

*lack selectivity and also inhibit human gonadal and steroid synthesis. Also rarely causes hepatotoxicity

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13
Q

Which azole is the most commonly prescribed systemic anti fungal, is the drug of choice for candidiasis, is effective agains fungal cryptococcal meningitis in AIDs and is highly teratogenic?

A

Fluconazole

*widest therapeutic index

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14
Q

Which azole was the first azole used for systemic and topical therapy?

A

Ketoconazole

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15
Q

Which azole requires lo pH for absorption, does not inhibit steroidogenesis, and is more toxic than fluconazole?

A

Itraconazole

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16
Q

Which two azoles are used topically only for vulvovaginal candidiasis, oral candidiasis, athletes foot and jock rash?

A

Clotrimazole and Mitconazole

17
Q

Which azole is the 1st line treatment for aspergillis?

A

Vorconizole

18
Q

Which drug should not be taken with amphotericin B because it reduces the fungicidal action?

A

Ketoconazole

19
Q

Which drug inhibits both DNA and RNA synthesis, is used for systemic fungal infections, is synergistic with amphotericin B for cryptococcal meningitis but may cause bone marrow suppression?

A

Flucytosine

20
Q

Which drugs are the penicillins of the antifungals are fungicidal agains some candida, fungistatic against some aspergillis and is embryo toxic (Cat C)?

A

Echinocandins

*used against azole resistant candida or 2nd line against refractory aspergillosis

21
Q

Which echinocandin blocks B-glucan synthase, is used against aspergillis and candida and should be avoided in pregnant patients?

A

Caspofungin

22
Q

Which drug is fungistatic by disrupting microtubule function, has a local action increases metabolism of other drugs is teratogenic, carcinogenic and causes severe headaches?

A

Griseofulvin

23
Q

Which drug inhibits squalene epoxidase to inhibit ergosterol synthesis, is used to treat dermatophytes, and has replaced griseofulvin for treatment of onychomycosis?

A

Allylamine antifungals (Terbinafine)

24
Q

How should normal immune systems vs. immunocompromised be treated for candidiasis?

A

Normal: topical
Compromised: Sytemic