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Leprosy
introduction
 Leprosy is a rare disease in US but a small number
of cases reported each year. Worldwide it is a
much larger problem.
 Approximately, 70% of all cases in world are
located in india.
Treatment
 Bacilli from skin lesion or nasal discharge of
infected patients enter susceptible individuals via
abraded skin or the respiratory tract.
 The WHO recommends the triple-drug regimen of
Dapsone, Clofazimine, and Rifampin for 6 to 24
months.
Drugs used in leprosy
Dapsone
 Inhibits folate synthesis via dihydropteroate
synthetase inhibition.
 Well absorbed orally,widely distributed .
 Half-life 1-2 days,tends to be retained in
skin,muscle,liver and kidney.
 Excreted into bile and reabsorbed in the intestine.
 Excreted in urine as acetylated.
 It is well tolerated.
Clinical uses
 Tuberculoid leprosy. (Tuberculoid leprosy is a skin
condition characterized by solitary skin lesions that are
asymmetrically distributed.)
 Lepromatous leprosy (Lepromatous leprosy is a skin
condition consisting of pale macules) in combination with
rifampin & clofazimine.
 To prevent & treat Pneumocystis pneumonia in
AIDS caused by Pneumocystis jiroveci (
Pneumocystis carinii).
Adverse effects
 Haemolytic anaemia
 Methemoglobinemia
 Gastrointestinal intolerance
 Fever,pruritus,rashes.
 Erythema nodosum leprosum (is an inflammatory condition
characterised by inflammation of the fat cells under the skin, resulting in tender
red nodules or lumps that are usually seen on both shins.)
Clofazimine
 It is a phenazine dye.
 Antiinflammatory effect.
 Absorption from the gut is variable.
 Given orally , once daily.
 Excreted mainly in feces.
 Stored mainly in reticuloendothelial tissues and skin.
 Half-life 2 months.
 Delayed onset of action (6 weeks).
Mechanism of Action
 It binds to DNA and prevent it from serving as
template for future DNA replication.
 Its redox properties may lead to generation of
cytotoxic oxygen radical that are also toxic to
bacteria.
 It is bactericidal drug.
Clinical uses
 Multidrug resistance TB.
 Lepromatous leprosy
 Tuberculoid leprosy in :
 patients intolerant to sulfones
 dapsone-resistant bacilli.
 Chronic skin ulcers caused by M.ulcerans.
Adverse effects
 Skin discoloration ranging from red-brown to black.
 Gastrointestinal intolerance.
 Red colour urine.
 Eosinophilic enteritis

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leprosy.pptx

  • 2. introduction  Leprosy is a rare disease in US but a small number of cases reported each year. Worldwide it is a much larger problem.  Approximately, 70% of all cases in world are located in india.
  • 3. Treatment  Bacilli from skin lesion or nasal discharge of infected patients enter susceptible individuals via abraded skin or the respiratory tract.  The WHO recommends the triple-drug regimen of Dapsone, Clofazimine, and Rifampin for 6 to 24 months.
  • 4. Drugs used in leprosy Dapsone  Inhibits folate synthesis via dihydropteroate synthetase inhibition.  Well absorbed orally,widely distributed .  Half-life 1-2 days,tends to be retained in skin,muscle,liver and kidney.  Excreted into bile and reabsorbed in the intestine.  Excreted in urine as acetylated.  It is well tolerated.
  • 5. Clinical uses  Tuberculoid leprosy. (Tuberculoid leprosy is a skin condition characterized by solitary skin lesions that are asymmetrically distributed.)  Lepromatous leprosy (Lepromatous leprosy is a skin condition consisting of pale macules) in combination with rifampin & clofazimine.  To prevent & treat Pneumocystis pneumonia in AIDS caused by Pneumocystis jiroveci ( Pneumocystis carinii).
  • 6. Adverse effects  Haemolytic anaemia  Methemoglobinemia  Gastrointestinal intolerance  Fever,pruritus,rashes.  Erythema nodosum leprosum (is an inflammatory condition characterised by inflammation of the fat cells under the skin, resulting in tender red nodules or lumps that are usually seen on both shins.)
  • 7. Clofazimine  It is a phenazine dye.  Antiinflammatory effect.  Absorption from the gut is variable.  Given orally , once daily.  Excreted mainly in feces.  Stored mainly in reticuloendothelial tissues and skin.  Half-life 2 months.  Delayed onset of action (6 weeks).
  • 8. Mechanism of Action  It binds to DNA and prevent it from serving as template for future DNA replication.  Its redox properties may lead to generation of cytotoxic oxygen radical that are also toxic to bacteria.  It is bactericidal drug.
  • 9. Clinical uses  Multidrug resistance TB.  Lepromatous leprosy  Tuberculoid leprosy in :  patients intolerant to sulfones  dapsone-resistant bacilli.  Chronic skin ulcers caused by M.ulcerans.
  • 10. Adverse effects  Skin discoloration ranging from red-brown to black.  Gastrointestinal intolerance.  Red colour urine.  Eosinophilic enteritis