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KUSHAL KUMAR
before/during/after
•Not
Type I
•Change in host CMI
•Seen in borderlines
•Skin and nerve lesions
Type II
•Antigen antibody
•Seen in LL & BL leprosy
•Skin, nerve & systemic
involvement
Erythema Nodosum Leprosum(ENL)
 Erythematous.Tender .Subcutaneous.
 Resolve in 7 to 10 days.
 Associated with fever & joint pains.
 May be vesicular, pustular & may ulcerate
 Treatment:with CLOFAZIMINE
Treat ‘Reaction’ as a Medical Emergency:
Rest & Analgesics
DOC-Prednisolone(40-60 mg)
Taper gradually over 12-16 wks.
All need a detailed Neuromuscular assessment by a
physiotherapist.
ADVERVE EFFECT OF ANTI-LEPROTIC DRUGS:
DRUGS MINOR MAJOR
1. RIFAMPICIN RED URINE JAUNDICE
GIT UPSET HEPATITIS
FLU LIKE SYNDROME SHOCK
2. DAPSONE GIT UPSET DAPSONE SYNDROME
DRUG RASH AGRANULOCYTOSIS
ANAEMIA HEMOLYTICANAEMIA
3. CLOFAZIMINE GIT UPSET ACUTE PAINABDOMEN
DISCOLOURATIONOF SKIN
ICHTHYOSIS
DISABILITIES
Specific deformities:
facies
leprosa
Paralytic deformities
3)Anesthetic deformity :
WHO Grade 0 Grade 1 Grade 2
EYES Normal
vision,lid
gap,blinking.
Corneal reflex
weak
Reduced
vision,lagopht
halmos.
HANDS Normal
sensation &
m.power.
Loss of feeling
in the palm
Visible
damage:woun
ds,claw
hand,loss of
tissue etc.
FEET Normal
sensation &
m.power.
Loss of feeling
in the sole
Visible
damage:woun
d,foot drop,loss
of tissue.
Peripheral nerves
Sensory Motor Autonomic
Hypoaestesia / anaestesia Muscle paralysis Lack of sweating & sebum
Ulcers Ulnar nerve Claw hand
Radial nerve Wrist drop
Lt. popliteal Foot drop
Post. tibial Claw toes
Facial lagophthalmous
Dry skin
Cracked skin
Ulcers
COMPLICATIONS OF
EYE
Involvment of the ophthalmic division of the (5th.) trigeminal nerve
Corneal sensation imparment
Patients ignore injuries
keratitis, conjunctivitis and ulcers
Involvment of zygomatic & temporal braches of the (7th.) facial nerve.
Lagophthalmos
Unable to close the eye (unbliking stare)
Care of eyes
PSYCHO- SOCIAL PROBLEMS
Rehabilitation
MILESTONES OF
NLEP IN INDIA
National Leprosy Eradication Program
• Started in 1955 as NLCP with the objective of early detection of
cases and treatment with Dapsone monotherapy
• It was made a centrally sponsored programme in 1980
• With the advent of Multi DrugTherapy (MDT) for
leprosy the cure rates increased
It was changed into eradication programme in 1983
with the objective of eradicating the disease by the
end of 2000
The ‘elimination’ was defined as attaining a prevalence Rate
(PR) of less than 1 case per 10,000 population
Milestones of leprosy Eradication
phase I
phase II
Conclusion
•Fortunately, modern medicine has cured most
of the world of Leprosy
•People with Leprosy are being more accepted
by communities around the world
•Leprosy still Remains a problem in
undeveloped countries
• The World Health Organization is putting a stop to
this
• If they reach their goal, Leprosy should be eliminated
from the world within 20 years
COMPLICATIONS  OF  LEPROSY  & ITS MANAGEMENT

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COMPLICATIONS OF LEPROSY & ITS MANAGEMENT

  • 2.
  • 3.
  • 4.
  • 5.
  • 6. before/during/after •Not Type I •Change in host CMI •Seen in borderlines •Skin and nerve lesions Type II •Antigen antibody •Seen in LL & BL leprosy •Skin, nerve & systemic involvement
  • 7. Erythema Nodosum Leprosum(ENL)  Erythematous.Tender .Subcutaneous.  Resolve in 7 to 10 days.  Associated with fever & joint pains.  May be vesicular, pustular & may ulcerate  Treatment:with CLOFAZIMINE Treat ‘Reaction’ as a Medical Emergency: Rest & Analgesics DOC-Prednisolone(40-60 mg) Taper gradually over 12-16 wks. All need a detailed Neuromuscular assessment by a physiotherapist.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12. ADVERVE EFFECT OF ANTI-LEPROTIC DRUGS: DRUGS MINOR MAJOR 1. RIFAMPICIN RED URINE JAUNDICE GIT UPSET HEPATITIS FLU LIKE SYNDROME SHOCK 2. DAPSONE GIT UPSET DAPSONE SYNDROME DRUG RASH AGRANULOCYTOSIS ANAEMIA HEMOLYTICANAEMIA 3. CLOFAZIMINE GIT UPSET ACUTE PAINABDOMEN DISCOLOURATIONOF SKIN ICHTHYOSIS
  • 17. WHO Grade 0 Grade 1 Grade 2 EYES Normal vision,lid gap,blinking. Corneal reflex weak Reduced vision,lagopht halmos. HANDS Normal sensation & m.power. Loss of feeling in the palm Visible damage:woun ds,claw hand,loss of tissue etc. FEET Normal sensation & m.power. Loss of feeling in the sole Visible damage:woun d,foot drop,loss of tissue.
  • 18. Peripheral nerves Sensory Motor Autonomic Hypoaestesia / anaestesia Muscle paralysis Lack of sweating & sebum Ulcers Ulnar nerve Claw hand Radial nerve Wrist drop Lt. popliteal Foot drop Post. tibial Claw toes Facial lagophthalmous Dry skin Cracked skin Ulcers
  • 19.
  • 20.
  • 21.
  • 23. Involvment of the ophthalmic division of the (5th.) trigeminal nerve Corneal sensation imparment Patients ignore injuries keratitis, conjunctivitis and ulcers Involvment of zygomatic & temporal braches of the (7th.) facial nerve. Lagophthalmos Unable to close the eye (unbliking stare)
  • 24.
  • 27.
  • 28.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 36. National Leprosy Eradication Program • Started in 1955 as NLCP with the objective of early detection of cases and treatment with Dapsone monotherapy • It was made a centrally sponsored programme in 1980 • With the advent of Multi DrugTherapy (MDT) for leprosy the cure rates increased It was changed into eradication programme in 1983 with the objective of eradicating the disease by the end of 2000 The ‘elimination’ was defined as attaining a prevalence Rate (PR) of less than 1 case per 10,000 population
  • 37. Milestones of leprosy Eradication phase I phase II
  • 38.
  • 39.
  • 40.
  • 41.
  • 42.
  • 43.
  • 44.
  • 45.
  • 46.
  • 47. Conclusion •Fortunately, modern medicine has cured most of the world of Leprosy •People with Leprosy are being more accepted by communities around the world •Leprosy still Remains a problem in undeveloped countries • The World Health Organization is putting a stop to this • If they reach their goal, Leprosy should be eliminated from the world within 20 years