TUBERCULOSIS : - PowerPoint PPT Presentation

1 / 21
About This Presentation
Title:

TUBERCULOSIS :

Description:

Hyperuricemia, leading to attack of gout. Ethambutol (EMB) ... Other forms of treatments being implemented to cure the XDR and MDR forms of TB ... – PowerPoint PPT presentation

Number of Views:107
Avg rating:3.0/5.0
Slides: 22
Provided by: asCla
Category:

less

Transcript and Presenter's Notes

Title: TUBERCULOSIS :


1
  • TUBERCULOSIS
  • BACKGROUND, CAUSES TREATMENTS
  • By Hardik Modi

2
What is TB?
  • TB is an infectious airborne disease the germs
    (Mycobacterium tuberculosis) are transferred from
    person to person.
  • Spreads via air, exchanging same air with a TB
    patient gives rise to a latent TB infection
  • It is believed to have spread from Cows
    (Mycobacterium bovis) to Humans (Mycobacterium
    tuberculosis)

3
Initial Body defense
  • Initially Macrophages try to attack the bacteria.
  • Phagocytosis, chemotaxis, etc.
  • If bacteria not killed, latent TB infection
    develops
  • Gives rise to active form, as the immune system
    weakens

4
  • Bodies defense system walls the clumps of
    bacteria into the lumps of scar tissues, the
    tubercles.
  • The mixture of dead and latent bacteria and the
    macrophages in the tubercle is called caseous.

http//commons.wikimedia.org/wiki/ImageTuberculou
s_caseous_granuloma_(2)_TBLB.jpg
5
Harmful effects of Mycobacteria tuberculosis
  • The bacteria slowly eats away the healthy lung
    tissue
  • Ulcer-like cavities full of pus, form in the
    sponge-like portion of the lungs
  • Coughs increase
  • A one inch cavity may contain 1million of these
    remorseless bacteria
  • http//www.lung.ca/tb/tbtoday/tbdiagnosis/xrays.ht
    ml

6
  • Abscesses and deformities of the shoulders, hips,
    legs or spine
  • Cause harm to the kidneys
  • Infection of the GI tract, cause devastating
    diarrhea

7
Spread of the disease
  • For centuries the symptoms of the disease were
    known, not the spread
  • Weight loss, weakness and prolonged sickness
  • It was thought to be a hereditary disease
  • Robert Koch suggested that it spreads via air.
  • He had observed the similarities between
    Mycobacteria bovis and Mycobacteria tuberculosis
  • The sputum could be obtained and it became easy
    to diagnose the disease

8
Previously Practiced Treatments
  • Pneumothorax treatment (air in the chest)
  • First invented by Giorgio Baglivi
  • Collapsing the lungs some how cured TB
  • Thoracoplasty ribs on one side were taken off,
    to collapse the lung
  • Ping pong balls, heavy thick oil were inserted to
    keep lungs collapsed

9
Introduction of Vaccine
  • Calmette and Geurin invented BCG vaccine after
    231 transfers
  • 14 million people received this vaccine between
    1948 and 1951
  • Problems with this vaccine TB bacteria
    naturally mutated
  • BCG strains may vary from one batch to another
    and one lab to another.
  • No methods were present for assessing the potency
  • Did not know what strain of vaccine was being
    used or what its characteristics were.

10
Discovery of Rifampin
  • Dr. Sensi and his collegue Parenti discovered
    Rifampin in the early 1960s
  • Found Nocardia mediterranei as antibiotic
    agianst mycobacteria family
  • RIF inhibits gene transcription, by interacting
    with the beta subunit of the RNA polymerase
    enzyme.
  • Bactericidal against dividing mycobacteria
  • Some activity against non-dividing bacilli

11
Rifampicin
  • It could be given via IV
  • In blood, it is bound to plamsa protein
  • Distributes into body tissues and fluids,
    including cerebrospinal fluid and breast milk.
  • Side effects
  • Diverse alteration in the GI tract, skin, kidney
    and nervous system.
  • Red-orange coloration of the body fluids.

12
Isoniazid (INH)
  • It is a pro-drug
  • It becomes active in the cell by the activation
    of catalse-peroxidase (KatG) enzyme
  • INH acts by inhibiting the biosynthesis of
    mycolic acids, important components of
    mycobacterial cell wall.

13
  • INH is metabolized in the liver
  • It is acetylated into various metabolites
  • INH concentrations are lower in rapid acetylators
    than slow acetylators
  • Slow acetylators have higher risk of developing
    adverse effects
  • About 10-20 may develop transient increase in
    liver enzymes and sometimes develop hepatic
    damage.

14
Pyrazinamide (PZA)
  • It is also a pro-drug, it needs to be converted
    into pyrazinoic acid by pyrazinamidases.
  • It is active against persisting and non- dividing
    bacilli
  • Even against those located intracellularly
  • The use of PZA into treatment regimens for TB has
    reduced the duration of such regimens to six
    months

15
Adverse effects
  • Patients may develop liver alterations, such as
    transient increase in enzymes, hepatomegaly,
    splenomegaly and jaundice.
  • Hyperuricemia, leading to attack of gout

16
Ethambutol (EMB)
  • EMB is a bacteriostatic drug, only active against
    dividing mycobacteria
  • It affects the biosynthesis of the cell wall
  • Increases susceptibility of M. tuberculosis to
    other drugs

17
Adverse effects
  • EMB causes reduction in visual acuity
  • Green-red color blindness
  • Constriction of the central or peripheral
    scomata

18
Streptomycin
  • It was the first drug used in the treatment of TB
  • It is an aminoglycoside
  • Administered by intramuscular injection

http//www.alanwood.net/pesticides/streptomycin.ht
ml
19
Periods in which these drugs are used
  • INH, RIF, PZA, EMB and SM are the first line
    drugs
  • usually isoniazid, rifampicin, pyrazinamide and
    ethambutol or streptomycin are used for first two
    months
  • From the next 4-7 months usually INH and RIF are
    used
  • Second line drugs are aminoglycosides kanamycin
    and amikacin, the polypeptide capreomycin, PAS,
    cycloserine, the thioamides ethionamide and
    prothionamide

20
TB in recent years
  • XDR- TB, extremely drug resistant and MDR-TB have
    recently developed
  • Second line drugs are said to be used for the
    treatment
  • But the drugs are expensive, and toxic and have
    more side effects
  • It has mainly risen in regions of Asia and South
    Africa

21
Further research
  • Drug target interactions
  • Drug drug interactions
  • How the first line drugs interact with other
    drugs and inhibit their effectiveness
  • Second-line drugs
  • Treatments for the side effects
  • Dosage of each of the drugs
  • Other forms of treatments being implemented to
    cure the XDR and MDR forms of TB
Write a Comment
User Comments (0)
About PowerShow.com