Chapter 23 deck 3 Flashcards

(42 cards)

1
Q

Oxalodinones name

A

Nlinezolid

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2
Q

Oxalodinones pharmacodynamics. Action, what is it effective against

A

Inhibitors of bacterial ribosomal protein synthesis

Most effective against aerobic gram-positive bacteria
Resistance emerging

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3
Q

Oxalodinones pharmacokinetics

A

Well absorbed orally

Does not use CYP450 enzymes

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4
Q

Oxalodinones ADR

A

Diarrhea, headache, nausea

Myelosuppression has been reported; resolves with discontinuation of drug

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5
Q

Linezolid (oxalodinone) clincial use

A

MRSA pneumonia
Uncomplicated skin infections
Use less expensive drugs first

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6
Q

Oxalodinone linezolid can be used in

A

vancomycin resistant enterocacus.

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7
Q

Vancomycin is

A

exepensive, but oral form is less expensive than IV

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8
Q

Sulfonamides block

A

folic acid synthesis

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9
Q

trimethoprim inhibits

A

dna synthesis

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10
Q

nitrofurantoin may inhibit

A

acetyl coenzymes

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11
Q

Sulfonamides, trimethoprim, nitrofurantoin and fosfomycin all

A

inhibit both gram-positive and gram negative bacteria

. coli, S. pyogenes, S. pneumoniae, H. influenzae, and some protozoa

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12
Q

What is an issue with sulfonamides, trimethoprim, nitrofurantoin, and fosfomycin

A

resistance

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13
Q

Sulfonimide example

A

bactrim

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14
Q

ADR for Sulfonamides, Trimethoprim, Nitrofurantoin, and Fosfomycin

A

ADRs: GI – anorexia, n/v, diarrhea, stomatitis; rashes, increased hypersensitivity reactions, photosensitivity; CNS – headache, dizziness, drug interactions
Avoid in glucose-6-phosphate dehydrogenase (G6PD) deficiency
Use cautiously in renal impairment

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15
Q

Clinical use for Sulfonamides, Trimethoprim, Nitrofurantoin, and Fosfomycin

A

Most commonly used in UTI infections

MRSA is susceptible in some areas

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16
Q

Sulfonamides, Trimethoprim, Nitrofurantoin, and Fosfomycin rational for drug selection

A

Low-cost alternative in children older than 2 months and in those with PCN allergies

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17
Q

Monitoring for Sulfonamides, Trimethoprim, Nitrofurantoin, and Fosfomycin

A

Control and status if treating UTI
Long-term use: check complete blood count (CBC)
Chest x-ray in patients who develop a cough when on nitrofurantoin

18
Q

Chest x-ray in patients who develop a cough when on

A

nitrofurantoin

19
Q

Tetracyclines and Doxycycline drug class

20
Q

Tetracycline pharmacodynamics

A

Bind reversibly to the 30S subunit of the bacterial ribosome

21
Q

What decreases absorbtion with tetracycline

A

food

especially milk and calcium. Don’t take a multivitamin with it

22
Q

Precautions and contraindications

Tetracyclines

A

Do not prescribe to pregnant women (category D), lactating women, or children age less than 8 years.
Drug interactions: many

23
Q

Tetracyclines

Clinical use and dosing

A

Doxycycline is considered first-line therapy for C. trachomatis and Ureaplasma urealyticum.
Tetracycline and minocycline are used to treat P. acnes

24
Q

Tetracyclines

Rational drug selection

A

Doxycycline and minocycline can be taken with food. still no calcium

25
Tetracyclines | Patient education
Administration, ADRs, avoiding pregnancy
26
Glycopeptides name
Vancomycin
27
Vancomycin pharmacodynamics
Vancomycin, telavancin (Vibativ), dalbavancin (Zeven) Used for severe gram-positive infections, such as MRSA resistant to first-line antibiotics Inhibits cell wall synthesis
28
Pharmacokinetics | Vancomycin
Poor oral absorption, given IV
29
Vancomycin ADR
Ototoxicity (transient or permanent) Nephrotocity “Red Man” syndrome if infused too fast ******
30
Vancomycin Clinical use and dosing
Serious gram-positive infections resistant to other medications Oral vancomycin is used to treat C. difficile infection
31
Vancomycin monitoring
``` Monitoring Hearing and renal function Patient education Administration ADRs ```
32
Mycobacteria
Grow slowly and are relatively resistant to drugs that are largely dependent on how rapidly cells are dividing Have a lipid-rich cell wall relatively impermeable to many drugs Are usually intracellular and inaccessible to drugs that do not have good intracellular penetration Have the ability to go into a dormant state Easily develop resistance to any single drug
33
Antimycobacterials | Names
Isoniazid Rifampin Ethambutol
34
Isoniazid action
(INH) and ethambutol inhibit synthesis of mycolic acids.
35
Rifampin action
binds to the beta subunit of mycobacterial DNA–dependent RNA polymerase and inhibits RNA synthesis.
36
Ethambutol action
inhibits synthesis of arabinogalactan, an essential component of mycobacteria cell walls.
37
Pharmacokinetics Antimycobacterials
Well absorbed orally | Metabolism of isoniazid highly variable and dependent on acetylator status
38
Antimycobacterials ADRS
INH: peripheral neuropathy INH, rifampin, and pyrazinamide: hepatotoxicity Ethambutol: optic neuritis Streptomycin and capreomycin: ototoxicity Rifabutin: neutropenia and thrombocytopenia
39
Antimycobacterials Drug Interactions
Many drug interactions | Rifampin: an inducer of CYP450 enzyme
40
Take home of antimycobacterials
Used to treat a tougher bacteria. ADRs. Well absorbed orally, but genetics can have an impact Used to treat TB
41
Antimycobacterials | Clinical use and dosing
Follow Centers for Disease Control and Prevention (CDC) guidelines. Active TB requires four-drug therapy. Preventive therapy includes INH.
42
Antimycobacterials Rational and monitoring
Rational drug selection Follow CDC guidelines. Monitoring Directly observed therapy