Tuberculosis Flashcards

0
Q

Multi Drug Resistant TB

A

So prevalent, it might be the primary infection, resistant to IRPE therapy, and added ABXs, may require up to 7 drugs per day

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1
Q

First line of drugs to give

A

RIPE: Rifampin, INH, PZA, Ethambutol for 2 months, then for the next 4-7 months continue with only INH and Rifampin

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2
Q

Isoniazid (INH): class and agent

A

Antitubercular; primary agent for treatment and prophylaxis

Highly selective for mycobacteria (Taken by all individuals infected with INH sensitive strains of M tuberculosis)

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3
Q

(INH) MOA?

A

Inhibits the synthesis of mycolic acid, bacteriocidal for rapidly diving organisms, bacteriostatic for dormant mycobacteria

IF RESISTANCE OCCURS THEN REGIME NEEDS TO CHANGE

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4
Q

INH administration and pharmokinetics:

A

PO or IM (alone in latent TB, with other abx in active TB)
Metabolized by the liver
Excreted in the urine

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5
Q

INH adverse effects:

A

Neurotoxicity: primary adverse effect; causes peripheral neuropathy where the pt will complain of numbness, tingling, burning, if they experience this they should come off of it.

Hepatotoxicity: PT SHOULD NOT DRINK

Inhibits vit B 6 so patient needs a supplement

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6
Q

Rifampin

A

Brother to INH * one of the most effective

Antitubercular, broad spectrum ABX

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7
Q

Rifampin MOA

A

Inhibits DNA dependent polymerase, decreases tubercle bacilli replication (Bactericidal)

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8
Q

Rifampin Pharmokinetics

A
Absorbed well on empty stomach
Eliminated primarily by the liver (20% leaves in urine)
Take in AM same time everyday
DOC for pulmonary of disseminated TB
ALWAYS used in combo to avoid RESISTANCE
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9
Q

Rifampin Adverse Effects

A

Hepatotoxicity
Discoloration of body fluids
(Yellow contact lenses)

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10
Q

What drugs are contraindicated with Rifampin?

A

Oral Contraception (need other contraception)
HIV meds
Oral hypoglycemic

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11
Q

Pyrazinamide (PZA) class

A

Antitubercular

Bactericidal to TB

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12
Q

PZA MOA?

A

Interferes with lipid nucleic acid biosynthesis

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13
Q

PZA Pharmacokinetics

A

Well absorbed orally
Metabolized by the liver
Excreted in urine

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14
Q

PZA Adverse Effects:

A

Hepatotoxic (NO ALCOHOL)
Photosensitivity
Hyperurecemia
Arthralgias

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15
Q

Ethambutol class

A

Antitubercular

16
Q

Ethambutol MOA

A

Inhibits RNA synthesis, decreases tubercle bacilli replication

17
Q

Ethambutol Adverse Effects

A

**Optic Neuritis: Blurred vision, constriction of the visual field, disturbance of color discrimination. Usually resolves once med is stopped.

Pruritis
GI upset
confusion
acute gouty arthritis

18
Q

Ethambutol Nursing Implications

A

ALWAYS given in combination to avoid resistance!!

NEEDS to be given 2 hours prior to antiacids bc antiacids decrease the effects of ethambutol

19
Q

Streptomycin Class

A

Aminoglycoside Antibiotic

Second line agent

20
Q

Streptomycin MOA

A

Causes bacterial death by interfering with protein synthesis

21
Q

Streptomycin Administration

A

MUST BE IM/IV

NOT ABSORBED BY GI TRACT

22
Q

Streptomycin peak:

A

20-30 mins after IM, trough levels drawn hrs later

23
Q

Streptomycin Adverse Effects

A

Toxicity to the 8th cranial nerve
Neprhotoxic
Ototoxic
Neurotoxic

24
Q

General TB therapy Nursing Implications

A

Pt Education is critical!!! **
Therapy may last up to 24 months
Take med exactly as ordered, same time every day
Emphasize the importance of strict adherence to regimen for improvement of condition or cure

25
Q

Which lab tests are important in TB drug therapy

A

Liver and Kidney: especially in INH and Rifampin
NO alchohol!
Recommended on an empty stomach (unless GI upset)

26
Q

TB implications continued

A

Monitor for therapeutic effects:
decrease in symptoms such as cough and fever
Lab studies (C/S tests) and CXR should confirm clinical findings
WATCH FOR LACK OF CLINICAL RESPONSE TO THERAPY, INDICATING POSSIBLE DRUG RESISTANCE