tb chemotherapy & susc Flashcards

1
Q

First line

A
Streptomycin (STR)
Isoniazid (INH)
Rifampin (RIF)
Ethambutol (EMB)
Pyrazinamide (PZA)
initial treatment phase recommends treatment with 4 or 5 drugs
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2
Q

monoresistant

A

any one TB drug

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3
Q

poly-resistant

A

any two drugs

but not both Rifampin, and Isoniazid

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4
Q

MDR TB

A

at least isoniazid and rifampin

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5
Q

XDR TB

A

isoniazid and rifampin

and any flouroquinolone and at least 1 of 3 injectable second-line drugs (kanamycin, capreomycin, amikacin)

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6
Q

Chemotherapy

A

follow-up for patients with positive smears is done weekly until two negative smears are obtained
follow up for culture conversion is done on a monthly basis until two sputum cultures are neg

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7
Q

INH

A

inhibits mycolic acid synthase
blocks action of fatty acid synthase
used for prophylaxis
not used for high prevalence of INH-resistance
certain parts of OC INH resistance as high as 21%

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8
Q

Rifampin

A

complexes with RNA polymerase
semi-synthetic
good absorption kills intracellular orgaisms
orange eyes

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9
Q

Ethambutol

A

inhibits mycolic acid synthase
INH-resistant MTB
loss of visual acuity

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10
Q

Pyrazinamide

A
exact target unknown (energy metabolism plasma membrane)
synthetic drug
short course
best for actively multiplying organisms
used during initial phase
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11
Q

Drug-resistant TB

A

treatest with 4 drugs for 6 months

MDR- treatment continued until chest x-ray clears- followed by 12 months additional treatment

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12
Q

susceptibility testing

A

performed on first MTB isolate

if still culture + repeated 2 months

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13
Q

followup treatment

A

smears- weekly until 2 negative smears
sputum cultures monitored mothly until negative
patient monitored monthly for anorexia, nausea
monthly chemistry panel
INH causes mild abnormal liver function

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14
Q

DOT

A

direct observed therapy
ensures patient adherence
all OC cases

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15
Q

critical concentration

A

amount of drug that inhibits growth of most of the cells (95%)

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16
Q

Absolute Concentration

A

standard inoculum is placed on control quadrant and quadrants with graded concentration of the drug
LOWEST CONCENTRATION THAT INHIBITS GROWTH

17
Q

Resistance Ration Method

A

compares resistance of unknown MTB to a known standard strain
two-fold dilution of drugs
R = MIC Test Strain/ MIC Std. Strain
MIC- lowest conc of drug that prevents visible growth

18
Q

Agar Proportion Method

A

most commonly used
calculate precise quantitation of the proportion of mutants resistant to a given drug
when 1% of population becomes resistant to critical concentration that drug is not useful for treatment

19
Q

Agar proportion direct

A

more representative of actual bacterial population
but subject to more variability (contamination)
results only vaiid if MTBC is identified

20
Q

Agar proportion method media

A

7H10, 7H11 with 4 quadrant
one is drug free
other three have different drugs or different concentrations
0.1 ml seeded onto each quadrant

21
Q

susceptibility interpretation

A
>500 4+
200-500 3+
100-200 2+
50-100 1+
<50 record number of colonies
atleast one of the control quadratns of the set of should have minimum of 50 colonies
22
Q

BACTEC susceptibility

A

same principle as conventiaonl agar

growth monitored radiometrically

23
Q

BACTEC SUSC PROCEDURE

A

inoculum in control is diluted 1:100
rate of growth in control vial is compared to drug
growth index is read daily and delta gi is calculated
final reading when control vial reach GI of 30 or more

24
Q

PZA susceptibility

A
requires media to be slightly acidic
drug active only at lower ph
modified 7H12 pH = 6.0
gi must reach 200
11% resistant
25
Q

bactec sucs adv.

A

ideal condition for mtb growth, rapid testsing

automated, direct and indirect

26
Q

bactec susc disadv,

A

contamination, mixed cultures can yield false resistance

27
Q

MGIT susceptibility

A

non-radiometic

28
Q

E-test

A

epsilometer test
MIC- point at which ellipse meets the strip gives you MIC
0.5 McF suspension plated onto 7H10 or 7H11

29
Q

MRD strain in presence of drugs

A

THRIVE
growth on control quadrant may notoped colonies, but drug quadrant will have profuse growth
vials with drugs may have gi >999

30
Q

Second LIne Drug Susceptibility Testing

A

considered if
patient has had prior therapy
contact of paitents with MDR-TB
from a country with endemic MDR-TB
isolate resistant to rifampin or other first line-drugs
positive cultue 3 months or more after therapy

31
Q

Luciferase Indirect Quantativie TEst

A

based on viability of MTB after exposure to a particular drug
vial mycobacteria are vulnerable to infection with mycobacteriophages with firefly luciferase gene
infected cells synthesize & translate mRNA to make luciferase
addition of substrate makes the surviving drug-resistant cells glow

32
Q

Flow cytometry

A

viable MTB hydrolyze fluorescein diacetate (FDA) and detect fluorescent mycobacteria
does not require multiplication

33
Q

Atypical susceptibility

A

M. Kansasii, M. szulgai, M. marinum
normally susceptible to rifampin and ehtambutol
M. szulgai & M. kansasii- conventional method m. marinum - Mueller hinton agar enriched with OADC

34
Q

Atypical susceptibility of rapid growers

A

M. fortuiutm, M. chelonae, M. abscessus are resistant to primary drugs
normally susceptible to aminoglycosides
can cause traumatic infections & have been implicated in infections after surgical procedures
E-test

35
Q

M. fortuitum & M. chelonae resistance

A

m. chelonae stubborn or resistant to most, m. fortuitum is generally susceptible

36
Q

M. avium complex resistance

A

resistant to most drugs used for TB

major pathogen in HIV patients, but finding a drug to treat MAC is difficult (considerable mutation)