Anti-Mycobacterial Therapy Flashcards

1
Q

What is the general idea in drug therapy of TB?

A

Multiple drugs are used

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2
Q

Isoniazid HCl MOA

A
  • Isoniazid is a “prodrug” that is activated by catalase peroxidase, which is regulated by the TB katG gene
  • Targets the TB inhA gene product – enoyl- reductase – and therefore inhibits synthesis of mycolic acid in the TB cell wall
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3
Q

Isoniazid HCl Resistance Mechanisms

A
  • Mutations in katG gene result in inactivation of catalase-peroxidase
  • Mutation in regulatory region of inhA gene, which is involved in mycolic acid synthesis
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4
Q

Isoniazid HCl Metabolism

A

INH acetylation in liver by N-acetyltransferase - rate is dependent upon genetics

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5
Q

Does INH cross the BBB?

A

Yes - CSF levels 20% plasma levels but may equal

plasma levels with meningeal inflammation

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6
Q

Isoniazid HCl SE

A
  • Hepatotoxicity
  • Neurotoxicity
  • Hypersensitivity Reactions
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7
Q

How is a diagnosis of TB made?

A
  • PPD skin test is shown to be positive
  • The Hx will then be reviewed for any signs of risk factors
  • Presence of risk factors will prompt a CXR
  • Abnormal CXR will lead to AFB of the sputum for mycobacteria
  • Positive AFB will the lead to the NAAT test for TB
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8
Q

What are the drug interactions of INH?

A

• INH + rifampin increases occurrence of hepatitis

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9
Q

Rifampin MOA

A

Inhibits DNA-dependent RNA polymerase encoded by the rpoB gene

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10
Q

Rifampin Resistance Mechanisms

A

Mutations in the rpoB gene will grant resistance

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11
Q

Does rifampin cross the BBB into the CNS?

A

Yes it penetrates well

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12
Q

Rifampin SE

A
  • Hepatotoxicity increased with other hepatotoxic drugs like INH
  • Red discoloration of body fluids – urine, tears, soft contacts
  • Acute renal failure, interstitial nephritis
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13
Q

What are the drug interactions of rifampin?

A

Induces hepatic microsomal enzymes - interacts with hundreds of drugs

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14
Q

What is the clinical use of ethambutol?

A

A “helper” drug that inhibits resistance to other drugs

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15
Q

Ethambutol MOA

A

Inhibits synthesis mycobacterial arabinosyl transferase encoded by embB which affects wall synthesis

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16
Q

Does ethambutol cross the BBB into the CNS?

A

No - very poorly even with inflammation

17
Q

Ethambutol SE

A
  • Optic neuritis

- Peripheral neuropathy

18
Q

What is the clinical use of pyrazinamide?

A

First line TB drug – for the 1st two months of therapy - increases the cure rate and reduces the likelihood of relapse

19
Q

Pyrazinamide MOA

A

A “prodrug” activated by TB pyrazinamidase, encoded by pncA

20
Q

Does pyrazinamide cross the BBB into the CNS?

A

Distribution is good, including in the CSF in tuberculous meningitis

21
Q

Pyrazinamide SE

A
  • Hepatitis, worse in patients with preexisting liver disease
  • Skin rash and gastrointestinal intolerance
  • Increased serum uric acid levels, but acute gout is uncommon
22
Q

What is the clinical use of streptomycin in TB?

A

Second line TB drug

23
Q

Streptomycin MOA

A

Inhibits protein synthesis by binding to ribosome

24
Q

Streptomycin SE

A
  • Ototoxicity

- Nephrotoxicity

25
What is primary TB resistance?
Infection by a source case with drug-resistant TB - acquired with the infection
26
What is secondary TB resistance?
From ineffective therapy causing resistance to develop during treatment
27
Why is multi drug therapy used in cases of TB?
Risk of evolution of resistance to two drugs is the product of the risk of the development of resistance to each drug - FAR lower
28
What is multi-drug resistant TB?
Resistance to both INH and rifampin - more common in those with HIV
29
What is extensively drug resistant TB?
* Resistance to INH and Rifampin * Resistance to a fluoroquinolone antibiotic * Resistance to one of three injectable antibiotics (amikacin, kanamycin, capreomycin)
30
What is the problem with therapy in MDR-TB?
Requires therapy for at least 18-24 months because rifampin resistance eliminates the short course therapy
31
What is the 6 month TB treatment regimen?
* 4-drug regimen (“RIPE” therapy = Rifampin-INH-PZA-Ethambutol) * Initial phase: RIPE * Continuation phase: RI (Note: Emb not needed if pan-suceptible)
32
How is intermittent treatment of TB administered (2-3 times a week)?
Directly Observed Therapy
33
Why is rifampin resistance so important clinically?
Loss of rifampin from the regimen means loss of the option for short-course (6 month) TB therapy
34
What are some of the treatments for latent TB infection?
- INH monotherapy for 9 months is highly effective | - Rifampin – 4 month, daily therapy
35
What are the drugs that are unique to NTM treatment?
- Clarithromycin | - Azithromycin
36
What drugs are used for both TB and NTM?
- Rifampin - Ethambutol - FQs - AGs
37
Is the treatment of leprosy different than that of TB?
Yes. Leprosy treatment is different treatment from TB treatment.
38
Paucibacillary Leprosy Treatment
Rifampin + dapsone daily for 12 months
39
Multibacillary Leprosy Treatment
Rifampin + dapsone + clofazimine daily for 24 months