TB Treatment
TB Treatment
TB Treatment
DRUGS
Dr Ndayisaba Corneille
Introduction
Mycobacteria are intrinsically resistant to
most antibiotics & they grow slowly
compared with other bacteria.
Thus antibiotics that are most active
against growing cells are relatively
ineffective.
Mycobacterial cells can also be dormant &
thus completely resistant to many drugs or
Dr Ndayisaba Corneille
Dr Ndayisaba Corneille
Mycobacteria have ability to develop
resistance.
Combinations of 2 or more drugs is
required to overcome emergence of
resistance during course of therapy.
The response to chemotherapy is slow &
Rx must be administered for months to
years, depending on which drugs are used.
Dr Ndayisaba Corneille
FIRST LINE DRUGS USED IN TB RX
1st line agents
Isoniazid (H)
Rifampin (R)
Pyrazinamide(P)
Ethambutol (E)
Streptomycin (S)
Thiacetazone (T)
Dr Ndayisaba Corneille
Isoniazid & rifampin are the most active
drugs.
In practice, therapy is initiated with a four-
drug regimen of 2HERZ/6EH OR
2HERZ/4RH after pts are diagnosed of TB.
Prevalence of isoniazid resistance among
US clinical isolates is approx 10%.
Prevalence of resistance to both H&R
(multiple drug resistance) is about 3%.
Dr Ndayisaba Corneille
Isoniazid (H) or (INH)
Most active drug for Rx of TB cozed by susceptible
strains.
Has structural similarity to pyridoxine
Its bactericidal for actively growing tubercle bacilli.
It is less effective against atypical mycobacterial
species.
It penetrates into macrophages & is active against
both extracellular & intracellular organisms.
Dr Ndayisaba Corneille
Mechanism of Action
Inhibits synthesis of mycolic acids, which are
essential components of mycobacterial cell walls.
Blocks mycolic acid synthesis & kills the cell.
Basis of Resistance
Mutations in certain genes controlling synthesis of
mycolic acids
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Mutants are readily selected out if isoniazid or any
is usually less
Dr Ndayisaba Corneille
Thus, at least two or more active agents
shld always be used to Rx active TB to
prevent emergence of resistance during
therapy.
Pharmacokinetics
mg/kg/d)
Clinical Uses
Dr Ndayisaba Corneille
Adverse Reactions
The incidence & severity of unwanted effects to
isoniazid are related to dosage & duration of
administration.
Immunologic reactions
Fever
skin rashes.
Drug-induced systemic lupus erythematosus has
been reported. Dr Ndayisaba Corneille
Direct toxicity
Isoniazid-induced hepatitis
Most common major toxic effect.
Liver aminotransferases increase 3- 4 times
normal.
This does not require cessation of drug if pt is
asymptomatic
This is seen in 10–20% of pts.
Dr Ndayisaba Corneille
Clinical hepatitis with;loss of appetite, nausea,
vomiting, jaundice & right upper quadrant pain
occurs in 1% of (H) recipients & can be fatal,
particularly if drug is not discontinued promptly.
There is histologic evidence of hepatocellular
damage & necrosis is present
Dr Ndayisaba Corneille
Pts at high risk of Isoniazid hepatitis;
Age >50 years
Alcoholics
Pregnant women
Postpartum mothers
Dev’t of (H) hepatitis contraindicates its further
use.
Dr Ndayisaba Corneille
Peripheral neuropathy
Observed in 10–20% of pts given dosages >5
mg/kg/d
Infrequently seen with standard 300 mg adult
dose.
Patients at risk of neuropathy
Slow acetylators
Those with predisposing conditions like AIDS,
malnutrition, alcoholism, DM, & uremia.
Dr Ndayisaba Corneille
Pyridoxine, 25–50 mg/d, is recommended
for those with conditions predisposing to
neuropathy
Neuropathy is due to a relative pyridoxine
deficiency as (H) promotes excretion of
pyridoxine
Dr Ndayisaba Corneille
CNS toxicity;
less common
Memory loss,
Psychosis &
Seizures.
These may also respond to pyridoxine.
Dr Ndayisaba Corneille
Miscellaneous adverse effects
Hematologic abnormalities
Provocation of pyridoxine deficiency anemia.
Tinnitus
GI discomfort
Reduced metabolism of phenytoin, increasing its
blood level & toxicity
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Rifampin
A semisynthetic derivative of rifamycin, an
antibiotic produced by Streptomyces mediterranei.
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Pharmacokinetics
Dosage is usually 600 mg/d (10 mg/kg/d)
Given PO & well absorbed frm GIT with wide
distribution in body fluids & tissues.
Relatively highly protein-bound & adequate [CSF]s
are achieved only in presence of meningeal
inflammation.
Dr Ndayisaba Corneille
Readily penetrates most tissues &
phagocytic cells.
Kills organisms that are inaccessible to
many drugs, such as intracellular organisms
& those sequestered in abscesses + lung
cavities.
Excreted mainly thru liver into bile. Then
undergoes enterohepatic recirculation, with
the bulk excreted as a deacylated metabolite
in feces & a small amount in urine.
Dr Ndayisaba Corneille
Dose reduction in liver & renal insufficiency are not
required
Resistance
Results frm any one of several possible point
mutations in rpoB, the gene for the subunit of RNA
polymerase.
This result in reduced binding of rifampin to RNA
polymerase.
Dr Ndayisaba Corneille
Clinical uses
1) Mycobacterial infections like
TB
Atypical mycobacterial infections
Leprosy.
Alternative to (H) prophylaxis for pts with latent
TB only who are unable to take isoniazid.
Dr Ndayisaba Corneille
2) Other indications
Elimination of meningococcal carriage
Prophylaxis for haemophilus influenzae type b
disease in contacts of children.
Eradication of staphylococcal carriage whn
combined with a 2nd agent .
Rx of serious staphylococcal infections such as
osteomyelitis & prosthetic valve endocarditis whn
used in combination therapy
Dr Ndayisaba Corneille
Adverse Reactions
Imparts a harmless orange color to urine, sweat,
tears & contact lenses (soft lenses may be
permanently stained).
Dr Ndayisaba Corneille
ETHAMBUTOL
Synthetic, water-soluble, heat-stable compound
Mechanism of action
Inhibit mycobacterial cell wall synthesis
Inhibits mycobacterial arabinosyl transferases,
which are encoded by embCAB operon.
Dr Ndayisaba Corneille
Arabinosyl transferases are involved in
polymerization reaction of arabinoglycan, an
essential component of mycobacterial cell wall.
Resistance
Resistance to ethambutol is due to mutations
resulting in overexpression of emb gene pdts or
within the embB structural gene.
Dr Ndayisaba Corneille
As with all other anticocks, resistance to emerges
rapidly whn drug is used alone.
Pharmacokinetics
Given PO & well absorbed frm the gut
Dosage is 15–25 mg/kg/d ,usually given as a
single daily dose in combination with other drugs.
Dr Ndayisaba Corneille
It crosses BBB only if meninges are
inflamed with highly variable [CSF]s of drug,
(4% to 64%) of serum levels in the setting of
meningeal inflammation.
About 20% of drug is excreted in feces &
50% in urine in unchanged form.
It accumulates in renal failure.
Dose shld be reduced by half if creatinine
clearance is < 10 mL/min.
Dr Ndayisaba Corneille
Clinical Use
Rx of active TB
Dr Ndayisaba Corneille
Adverse Reactions
Hypersensitivity; Is rare.
Retrobulbar neuritis, resulting in loss of visual
acuity & red-green color blindness.
Most common serious adverse event
This dose-related S/E, more likely to occur at
doses of 25 mg/kg/d continued for several months.
Dr Ndayisaba Corneille
At 15 mg/kg/d or less, visual disturbances are very
rare.
Periodic visual acuity testing is desirable if 25
mg/kg/d dosage is used.
Contraindications
Relatively contraindicated in children too young to
permit assessment of visual acuity & red-green
color discrimination.
Dr Ndayisaba Corneille
PYRAZINAMIDE
A relative of nicotinamide.
Stable & slightly soluble in water.
An important front-line drug used in conjunction
with H&R in short-course (ie, 6-month) regimens
as a "sterilizing" agent active against residual
intracellular organisms that may cause relapse.
Dr Ndayisaba Corneille
Mechanism of action
The drug target & mechanism of action are
unknown.
Pyrazinamide is converted to pyrazinoic acid the
active form of the drug—by mycobacterial
pyrazinamidase, which is encoded by pncA.
The drug is taken up by macrophages & exerts its
activity against mycobacteria residing within acidic
environ’t of lysosomes.
Dr Ndayisaba Corneille
Resistance
Resistance may be due to impaired uptake of drug
Mutations in pncA that impair conversion of
pyrazinamide to its active form.
Tubercle bacilli develop resistance to it fairly
readily.
No cross-resistance with other anti-cocks.
Dr Ndayisaba Corneille
Pharmacokinetics
Given PO
Dose of 25 mg/kg/d.
Half-life is 8–11 hours.
Dr Ndayisaba Corneille
Parent compound is metabolized by liver, but
metabolites are renally cleared.
Thus doses shld be lowered in renal insufficiency.
In pts with normal renal function, a dose of 40–50
mg/kg is used for thrice-wkly or twice-wkly Rx
regimens.
Dr Ndayisaba Corneille
Adverse Reactions ;
Major adverse effects include
Hepatotoxicity (1–5% of pts),
Nausea
Vomiting
Drug fever occurs uniformly & is not a reason to
halt therapy.
Hyperuricemia. May provoke acute gouty
arthritis.
Dr Ndayisaba Corneille
Streptomycin
o Isolated frm a strain of Streptomyces griseus.
o The antimicrobial activity is typical of that of other
aminoglycosides, as are the mechanisms of
resistance.
Dr Ndayisaba Corneille
Spectrum of activity against in mycobacteria
M.tuberculosis spp
Mycobacterium avium complex (MAC)
Mycobacterium kansasii
Rest of the Spp of mycobacterium are resistant .
Resistance
All large popns of tubercle bacilli contain some
streptomycin-resistant mutants.
Dr Ndayisaba Corneille
Resistance is due to a point mutation in either the
rpsL gene encoding the S12 ribosomal protein
gene or the rrs gene encoding 16S ribosomal
rRNA, which alters the ribosomal binding site.
Ribosomal resistance develops readily, limiting its
role as a single agent.
Dr Ndayisaba Corneille
Pharmacokinetics
Given IM or IV
Typical adult dosage is 1g/day (15 mg/kg/d )daily
for adults & 7.5–15 mg/kg/d for children
It penetrates into cells poorly & is active mainly
against extracellular tubercle bacilli.
It crosses BBB & achieves [therapeutic]s with
inflamed meninges.
Dr Ndayisaba Corneille
Clinical Uses
1. Mycobacterial infections
Used when an injectable drug is needed or
desirable
2nd -line agent for Rx of MDR-TB with other agents.
Severe & possibly life-threatening forms of TB eg,
TBM & disseminated disease
Dr Ndayisaba Corneille
Adverse Reactions
Hypersensitivity
Fever
skin rashes & other allergic
manifestations.
Occurs most frequently with prolonged
contact with drug either in pts who
receive a prolonged course of Rx or in
medical personnel who handle the drug.
Dr Ndayisaba Corneille
Pain at the injection site
o Common but usually not severe
Disturbance of vestibular function.
o Most serious toxic effect & manifest by
Vertigo &
Loss of balance.
Dr Ndayisaba Corneille
Ototoxicity
Nephrotoxicity
Contraindications
o Pregnancy, can cause deafness in the newborn
o Renal failure
o Vestibular disorders
Dr Ndayisaba Corneille
Thiacetazone
Is bacteriostatic
With a low potency
Dosage is 2.5mg/day
Is the only essential anti-TB drug that can not be
given intermittently e.g. 2 timely weekly
Dr Ndayisaba Corneille
Has a narrow therapeutic range thus margin btn
therapeutic & toxic dose is very small
Some countries still use it in combination with
Isoniazid during continuation phase of Rx
Known ISS pts shld not be put on this drug bcoz of
its severe skin reactions thus Ethambutol shld
replace this drug in areas where HIV is common
Dr Ndayisaba Corneille
Side effects
Common
Skin rash often involving mucous membrane &
some times blistering
Others
Agranulocytosis
Hepatitis
Dr Ndayisaba Corneille
END
BY
DR NDAYISABA CORNEILLE
MBChB,DCM,BCSIT,CCNA,Cyber Security
contact: [email protected] ,
[email protected]