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LEISHMANIASIS
Mr. Kuldeep Vyas
M.Sc. Community Health Nursing
1Kuldeep Vyas M.Sc. N. CHN
Leishmaniasis
2Kuldeep Vyas M.Sc. N. CHN
 It’s a communicable disease.
 Leishmaniasis are a group of protozoal diseases caused
by parasites of genus “ Leishmania”.
 Genus Leishmania is named after Sir William Leishman,
who discovered the flagellate protozoa causing Kala-azar,
the Indian visceral leishmaniasis.
 Majority of leishmaniasis are zoonoses involving wild/
domestic mammals (rodents , canines).
Kala-Azar/Dum-Dum fever in India 3Kuldeep Vyas M.Sc. N. CHN
 Various syndromes in humans
1. Kala-azar/visceral leishmaniasis (V.L)
2. Cutaneous leishmaniasis (C.L)
3. Muco-cutaneous leishmaniasis (M.C.L)
4. Anthroponotic or urban cutaneous leishmaniasis(A.C.L)
5. Zoonotic or rural cutaneous leishmaniasis (Z.C.L)
6. Post-Kala-azar dermal leishmaniasis (P.K.D.L)
• Kala-azar=black sickness
4Kuldeep Vyas M.Sc. N. CHN
5Kuldeep Vyas M.Sc. N. CHN
• Visceral leishmaniasis or Kala-azar is a major public health problem in
many parts of world.
• According to WHO, 5,00,000 cases of visceral leishmaniasis occur
every year.
• Of these new cases, 90% are found in the Indian subcontinent and
Sudan and Brazil.
• The disease occurs in endemic, epidemic, or sporadic forms. Major
Problem Statement
6Kuldeep Vyas M.Sc. N. CHN
7Kuldeep Vyas M.Sc. N. CHN
• The resurgence of Kala-azar in India, beginning in the mid1970s
assumed epidemic proportions in 1977 and involved over 1,10,000 cases
in humans.
• Initially, the disease was confined to Bihar. Since then, the cases are
increasing and involving newer areas.
• The epidemic extended to West Bengal and first outbreak occurred in
1980 in Malda district.
• At present, the disease has established its endemicity in 31 districts in
Bihar, 11 districts in West Bengal, 5 districts in Jharkhand, and 3
districts in Uttar Pradesh. Sporadic cases have been reported from Tamil
Problem Statement- India
8Kuldeep Vyas M.Sc. N. CHN
9Kuldeep Vyas M.Sc. N. CHN
 Epidemiological determinants
1. Agent factors
The causative organisms are
• L.donovani for V.L
• L.tropica for C.L
• L.braziliensis for M.C.L
Reservoir-animals: Dogs,
Jackals,
Foxes and Rodents.
10Kuldeep Vyas M.Sc. N. CHN
11Kuldeep Vyas M.Sc. N. CHN
2. Host –Factors
• Age: Peak age incidence 5 to 9 years.
• Sex: Males are affected twice to females.
• Population movement: From endemic to non-endemic areas.
• Socio-economic status: Strikes poorest of poor.
• Occupation: Workers of forestry, mining, fishing
• Immunity: Gives lasting immunity. 12Kuldeep Vyas M.Sc. N. CHN
3. Environmental Factors
Altitude: Confined to plains.
Season: During and after rains(peak in November and april).
Rural areas: Suitable for breeding of sand fly.
Vectors: Phlebotomus argentipes for V.L
P.papatasi
P.sergenti
Development Projects: Cultivation projects, Colonization, migrants
} C.L
13Kuldeep Vyas M.Sc. N. CHN
14Kuldeep Vyas M.Sc. N. CHN
 Mode of transmission
•By bite and contact when insect is crushed during act
of feeding.
•Transmission also takes place through contaminated
blood transfusion.
• Extrinsic incubation period is 6-9 days.
• Incubation period is about 1-4 months.
15Kuldeep Vyas M.Sc. N. CHN
1
6
5
4
3
2
16Kuldeep Vyas M.Sc. N. CHN
17Kuldeep Vyas M.Sc. N. CHN
Clinical features
• VL:
1. Fever
2. Splenomegaly
3. Hepatomegaly
4. Anaemia
5. Weight loss
6. Darkening of skin of face,
hand, feet, abdomen
7. Lymphadenopathy
• PKDL: Multiple nodular infiltration
of skin without ulceration.
18Kuldeep Vyas M.Sc. N. CHN
19Kuldeep Vyas M.Sc. N. CHN
20Kuldeep Vyas M.Sc. N. CHN
• CL: characterized by painful ulcers.
These are restricted to skin. (DD- leprosy)
Variant – diffuse C.L.
• MCL: Similar to CL but appears around margin of mouth and nose
21Kuldeep Vyas M.Sc. N. CHN
22Kuldeep Vyas M.Sc. N. CHN
23Kuldeep Vyas M.Sc. N. CHN
24Kuldeep Vyas M.Sc. N. CHN
25Kuldeep Vyas M.Sc. N. CHN
Tapir nose
26Kuldeep Vyas M.Sc. N. CHN
27Kuldeep Vyas M.Sc. N. CHN
28Kuldeep Vyas M.Sc. N. CHN
1) Parasitological diagnosis: Demonstration of LD
Bodies in the aspirations of spleen, liver, bone
marrow, lymph nodes or in the skin.
2) Aldehyde test of Napier: Used for diagnosis of VL.
1-2 ml of serum from a patient of VL and a
drop or 2 drops of 40% formalin is added.
+ve test→Jellification to milk
-It becomes positive 2-3 months after on
set of disease and reverse to negative 6months after
cure.
-It also positive in reversed Ab/Gb ratio.
29Kuldeep Vyas M.Sc. N. CHN
3) Serological test : DAT, ELISA,IFAT
ELISA used for diagnosis as well as
epidemiological field survey.
4) Leishmanin(montengro) test: It’s a skin
test.
Induration of 5mm or more is positive.
Usually positive after 4-6 weeks after onset
of case of C.L and M.C.L.
-ve in active phase of V.L and becomes +ve
in 75% of people after recovery.
5) Hematological findings: Progressive
leucopenia, anaemia, reversed Ab/Gb ratio.
E.S.R is increased.
30Kuldeep Vyas M.Sc. N. CHN
MONTENIGRO TEST
31Kuldeep Vyas M.Sc. N. CHN
1
2
3
5
4
32Kuldeep Vyas M.Sc. N. CHN
 Control measures
1)control of reservoir: Active and passive case
detection and treatment.
House to house visits and mass surveys.
Treatment: Pentavalent antimony compounds
are used.
Recommended schedule: Sodium stibogluconate
20mg/KG daily for 20 days.
Second line drug: Pentamidine isethionate
3mg/KG for 10 days.
Amphoterecin B 1mg/KG for 20 days.
Milteforsine 2.5mg/KG for 4 weeks.
Animal reservoir: Dogs & rodent control
programme
33Kuldeep Vyas M.Sc. N. CHN
2) Sand fly control:
• DDT is first choice of insecticide.
• BHC is used for resistance cases.
• Sanitation measures: Elimination of
breeding places and location of
cattle shed at a far distance.
34Kuldeep Vyas M.Sc. N. CHN
3)Personal prophylaxis
• Health education.
• Individual protect measures like
1. Avoiding sleeping on the
floor.
2.Using fine mesh nets.
• Insect repellants for temporary
protection.
• Keeping environment clean.
35Kuldeep Vyas M.Sc. N. CHN
Thank you
36Kuldeep Vyas M.Sc. N. CHN
Assessing your understanding of
Leishmaniasis
37Kuldeep Vyas M.Sc. N. CHN
38Kuldeep Vyas M.Sc. N. CHN
39Kuldeep Vyas M.Sc. N. CHN

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Leshmaniasis kala azar

  • 1. LEISHMANIASIS Mr. Kuldeep Vyas M.Sc. Community Health Nursing 1Kuldeep Vyas M.Sc. N. CHN
  • 3.  It’s a communicable disease.  Leishmaniasis are a group of protozoal diseases caused by parasites of genus “ Leishmania”.  Genus Leishmania is named after Sir William Leishman, who discovered the flagellate protozoa causing Kala-azar, the Indian visceral leishmaniasis.  Majority of leishmaniasis are zoonoses involving wild/ domestic mammals (rodents , canines). Kala-Azar/Dum-Dum fever in India 3Kuldeep Vyas M.Sc. N. CHN
  • 4.  Various syndromes in humans 1. Kala-azar/visceral leishmaniasis (V.L) 2. Cutaneous leishmaniasis (C.L) 3. Muco-cutaneous leishmaniasis (M.C.L) 4. Anthroponotic or urban cutaneous leishmaniasis(A.C.L) 5. Zoonotic or rural cutaneous leishmaniasis (Z.C.L) 6. Post-Kala-azar dermal leishmaniasis (P.K.D.L) • Kala-azar=black sickness 4Kuldeep Vyas M.Sc. N. CHN
  • 6. • Visceral leishmaniasis or Kala-azar is a major public health problem in many parts of world. • According to WHO, 5,00,000 cases of visceral leishmaniasis occur every year. • Of these new cases, 90% are found in the Indian subcontinent and Sudan and Brazil. • The disease occurs in endemic, epidemic, or sporadic forms. Major Problem Statement 6Kuldeep Vyas M.Sc. N. CHN
  • 8. • The resurgence of Kala-azar in India, beginning in the mid1970s assumed epidemic proportions in 1977 and involved over 1,10,000 cases in humans. • Initially, the disease was confined to Bihar. Since then, the cases are increasing and involving newer areas. • The epidemic extended to West Bengal and first outbreak occurred in 1980 in Malda district. • At present, the disease has established its endemicity in 31 districts in Bihar, 11 districts in West Bengal, 5 districts in Jharkhand, and 3 districts in Uttar Pradesh. Sporadic cases have been reported from Tamil Problem Statement- India 8Kuldeep Vyas M.Sc. N. CHN
  • 10.  Epidemiological determinants 1. Agent factors The causative organisms are • L.donovani for V.L • L.tropica for C.L • L.braziliensis for M.C.L Reservoir-animals: Dogs, Jackals, Foxes and Rodents. 10Kuldeep Vyas M.Sc. N. CHN
  • 12. 2. Host –Factors • Age: Peak age incidence 5 to 9 years. • Sex: Males are affected twice to females. • Population movement: From endemic to non-endemic areas. • Socio-economic status: Strikes poorest of poor. • Occupation: Workers of forestry, mining, fishing • Immunity: Gives lasting immunity. 12Kuldeep Vyas M.Sc. N. CHN
  • 13. 3. Environmental Factors Altitude: Confined to plains. Season: During and after rains(peak in November and april). Rural areas: Suitable for breeding of sand fly. Vectors: Phlebotomus argentipes for V.L P.papatasi P.sergenti Development Projects: Cultivation projects, Colonization, migrants } C.L 13Kuldeep Vyas M.Sc. N. CHN
  • 15.  Mode of transmission •By bite and contact when insect is crushed during act of feeding. •Transmission also takes place through contaminated blood transfusion. • Extrinsic incubation period is 6-9 days. • Incubation period is about 1-4 months. 15Kuldeep Vyas M.Sc. N. CHN
  • 18. Clinical features • VL: 1. Fever 2. Splenomegaly 3. Hepatomegaly 4. Anaemia 5. Weight loss 6. Darkening of skin of face, hand, feet, abdomen 7. Lymphadenopathy • PKDL: Multiple nodular infiltration of skin without ulceration. 18Kuldeep Vyas M.Sc. N. CHN
  • 21. • CL: characterized by painful ulcers. These are restricted to skin. (DD- leprosy) Variant – diffuse C.L. • MCL: Similar to CL but appears around margin of mouth and nose 21Kuldeep Vyas M.Sc. N. CHN
  • 29. 1) Parasitological diagnosis: Demonstration of LD Bodies in the aspirations of spleen, liver, bone marrow, lymph nodes or in the skin. 2) Aldehyde test of Napier: Used for diagnosis of VL. 1-2 ml of serum from a patient of VL and a drop or 2 drops of 40% formalin is added. +ve test→Jellification to milk -It becomes positive 2-3 months after on set of disease and reverse to negative 6months after cure. -It also positive in reversed Ab/Gb ratio. 29Kuldeep Vyas M.Sc. N. CHN
  • 30. 3) Serological test : DAT, ELISA,IFAT ELISA used for diagnosis as well as epidemiological field survey. 4) Leishmanin(montengro) test: It’s a skin test. Induration of 5mm or more is positive. Usually positive after 4-6 weeks after onset of case of C.L and M.C.L. -ve in active phase of V.L and becomes +ve in 75% of people after recovery. 5) Hematological findings: Progressive leucopenia, anaemia, reversed Ab/Gb ratio. E.S.R is increased. 30Kuldeep Vyas M.Sc. N. CHN
  • 33.  Control measures 1)control of reservoir: Active and passive case detection and treatment. House to house visits and mass surveys. Treatment: Pentavalent antimony compounds are used. Recommended schedule: Sodium stibogluconate 20mg/KG daily for 20 days. Second line drug: Pentamidine isethionate 3mg/KG for 10 days. Amphoterecin B 1mg/KG for 20 days. Milteforsine 2.5mg/KG for 4 weeks. Animal reservoir: Dogs & rodent control programme 33Kuldeep Vyas M.Sc. N. CHN
  • 34. 2) Sand fly control: • DDT is first choice of insecticide. • BHC is used for resistance cases. • Sanitation measures: Elimination of breeding places and location of cattle shed at a far distance. 34Kuldeep Vyas M.Sc. N. CHN
  • 35. 3)Personal prophylaxis • Health education. • Individual protect measures like 1. Avoiding sleeping on the floor. 2.Using fine mesh nets. • Insect repellants for temporary protection. • Keeping environment clean. 35Kuldeep Vyas M.Sc. N. CHN
  • 36. Thank you 36Kuldeep Vyas M.Sc. N. CHN
  • 37. Assessing your understanding of Leishmaniasis 37Kuldeep Vyas M.Sc. N. CHN