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RABIES 
 Primarily a Zoonotic disease of warm 
blooded animal 
 such as :- 
 Dogs, 
wild cats, 
 Jackals, 
wolves etc. 
 It is caused by the Neurotropic RNA virus belongs to 
Rhabdoviridae type I (LYSSAVIRUS type I) is Bullet 
shaped virus
 It is an acute 
 Highly fatal viral dis: of CNS 
Transmitted to man by: 
 Bites 
OR 
 Licks of rabid animals
Rabies virus structure 
Envelope 
Matrix protein 
Glycoprotein 
Nucleocapsid protein 
Source: http://www.cdc.gov
History of Rabies Virus 
Man described the disease in 2300 B.C. 
The origin “rabhas”, meaning “to do violence” 
comes from ancient Indian Sanskrit dating 3000 
B.C.
History of the Rabies Virus 
Since Roman times, man established the link between 
the infectivity of a rabid dogs saliva and the spread of 
the disease. 
Because there is no cure for rabies, those that had been 
bitten by a rabid dog would commonly commit suicide to 
avoid the painful death that would inevitably follow.
History of the Rabies Virus 
 Louis Pasteur was the first person to 
diagnose that rabies targeted the CNS. 
 Also determined that nervous tissue of an 
infected human or animal also contained 
the virus. 
 In 1890 created the rabies vaccine and 
saved 9 year old child after he had been bit 
by a rabid dog.
Epidemiology 
87 countries contain Rabies, but more 
cases are reported in Asia. 
In Indo-Pakistan rabies is a major 
public health problem mainly due to 
presence of a large no: of stray dogs. 
More than 30,000 people died of 
Rabies every year in Asia. Every year 
10 million people require treatment 
and protection from Rabies which is 
great Financial loss.
RESERVOIR OF INFECTION 
1) URBAN RABIES: 
From Dogs and 
cats.
2) WILD LIFE RABIES: 
From jackals and foxes.
3) BAT RABIES: 
Vampire bats which live on the blood of animals and men. 
These are one of the main causes of the death of bovine, around 0.5 
to 1 million per year.
Source of Infection 
 Saliva of Rabid animal
Host Factors 
 All warm blooded animals including man. 
 Rabies in man is a dead-end infection.
Mode of Transmission 
1. ANIMAL BITES 
2. LICKS 
3. AEROSOL 
4. PERSON TO PERSON
INCUBATION PERIOD: 
 normally it is 3 - 8 wks 
may be short that is 4 days 
 or may be prolonged for years.
CLINICAL PICTURE 
1. Prodromal symptoms 
Headache, malaise, sore throat, low 
fever, pain at the site of bite 
2. Excitation Symptoms 
sensory sys: involvement 
Aero phobia, excitation of N.S. 
Motor sys: inv: 
increase reflexes, muscle spasm, 
Symp:inv: dilatation of Pupils. increase 
perspiration, salivation, and Lacrimation,
Mental changes: fear of death, anger, 
irritability and depression 
Hydrophobia ( Fear of water) 
sight or sound of water may produce 
spasm of degulation 
the duration of illness is 2-3 days may be 
prolonged to 5-6 days 
Stage of paralysis & coma 
DEATH / Recovery
Clinical forms of rabies 
 encephalitic = furious 
 ~ 80% 
 paralytic = dumb 
 ~ 20%
Encephalitic rabies 
 prodromal symptoms 
 paresthesias/pain/pruritus at site of bite 
 episodes of generalized arousal or 
hyperexcitability separated by lucid 
periods 
 autonomic dysfunction 
 hydrophobia
Paralytic rabies 
 paresthesias/pain/pruritus at site of bite 
 early flaccid muscle weakness 
 often begins in bitten extremity 
 progresses to produce quadriparesis 
 bilateral facial weakness 
 sensory examination is usually normal 
 sphincter involvement 
 fatal outcome 
 often misdiagnosed as Guillain - Barré syndrome
DIAGNOSIS 
1. History 
2. Sign and symptom 
3. Examination 
4. Detection of Antigen by taking Skin 
Biopsy using Immunofluorescence 
by virus isolation from Saliva & 
other secretions.
Control Measures 
 Notification 
 Isolation 
 Disinfection 
 Immunization
Prevention of human rabies 
post Exposure prophylaxis 
1. General consideration:- Aim is to neutralize virus before entering CNS 
2. LOCAL WOUND TREATMENT 
a, Cleansing of wound(soap & water) 
b, Chemical treatment: 
 Either Alcohol 400-700 ml /liter 
 Tincture Iodine
c, Suturing not recommended 
d, Anti Rabies Serum 
e, Antibiotic and ATS 
f, Observe the animal for 10 days
 3, Immunization 
 1,NERVOUS TISSUE VACCINE (NTV 
2, Human diploid cell vaccine 
(HDCV)
Rabies postexposure guide: 
exposure to dogs, cats, and ferrets 
Evaluation of Animal Recommendation 
Healthy and available for 
10 days observation 
No treatment unless 
animal develops clinical 
signs of rabies 
Rabid or suspected rabid Immediate treatment* 
Unknown (e.g., escaped) Consult local 
public health 
department 
*Discontinue treatment if tests on animal prove negative.
Vaccines for immunization 
Definition: 
it is fluid or dried preparation of 
Rabies “Fixed” virus grown in the 
Neural tissue of 
Rabbits, 
Sheep, 
Goats, 
Mice or Rats 
OR in embryonated duck eggs 
OR in cell culture
Nervous Tissue 
vaccine 
Duck embryo 
vaccine 
Cell culture 
vaccine 
preparation From fixed virus grown in 
brain of sheep or other 
animals 
potency Low or variable Eliminate Neuroparalytic 
factors 
More potent 
more safer 
Doses Large nos: are required Fewer doses of small 
volume 
Side effects Severe & fatal reactions Allergic risks Fewer 
Uses Exposed subjects Used in UK,USA in past 1, (HDC) safe, potent 
Pre & post 
expos:Immunization 
Suckling mouse brain V 
Devoid of Neuroparalytic 
effect 
Used in Latin America 
Improvement over adult 
animal nervous tissue V 
Now purified DEV 
developed 
Improvement over adult 
animal nervous tissue V 
Not available in India & 
Pakistan 
2Tissue culture 2nd G 
(Non-human) 
Potent, low cost 
WHO recommendatio
Type of Vaccine 
NERVOUS TISSUE VACCINE (NTV) 
a. Derived from adult animal nervous 
tissue eg. Sheep 
b. Derived from suckling mouse brain 
Type: Killed viral vaccine 
Dose: 2.5 ml S/C (Ant. 
Abdominal wall) 
Schedule: 14 doses
Type of Vaccine (conti) 
Duck Embryo Vaccine (DEV) 
Type: Killed viral vaccine 
Dose: 1 ml S/C ( Ant. Abdominal wall) 
Schedule: 14 doses OD 
not available in Pakistan
Type of Vaccine (conti) 
CELL CULTURE VACCINES 
a. Human diploid cell vaccine (HDCV) 
b. Second generation tissue culture 
vaccine (non- Human) 
Type: Killed viral vaccine 
Dose: 1 ml IM 
Schedule: on 0, 3, 7, 14, 28 day, 
booster on day 90
Adverse Reactions to Rabies Vaccines 
Most common side-effects of rabies vaccines: 
 Systemic reactions such as headache, 
myalgia, malaise (5-40%) 
 Mild to moderate local reactions at injection 
site (30-74%)
PASSIVE IMMUNIZATION 
 Horse Anti Rabies serum: 40 iu / kg at 
0 day 
 Human rabies immunoglobin (HRIG): 
20 iu / kg around the wound and rest 
in IM on 0 day 
 Booster doses are essential whenever 
anti rabies serum is given with the 
vaccine
IMMUNITY 
 Duration of Immunity is upto 06 
month 
 If again bite by rapid animal than 
dose according to blood titre 
if more than 0.5 i.u. / ml than only two 
dose 0, 3 day 
if less than 0.5 i.u. / ml than 0, 3, 7 
day
General measures 
 Regist:,licensing & taxation of dog. 
 Muzzling of dogs 
 Yearly mass vaccination of dog 
 Destruction of stray dogs 
 Facilities for diagnosis of rabies in dogs 
 Destruction of wildlife where the animals are 
known to be the reservoir of infection. 
 Publicity
Preexposure rabies prophylaxis 
 3 doses of rabies vaccine (days 0, 7, and 21 
or 28) 
 May check rabies antibody titre periodically – 
want >0.5 IU/mL 
 after a rabies exposure: 
 2 doses of IM rabies vaccine (days 0 and 3) 
 no HRIG
Pre-exposure rabies prophylaxis 
Tissue culture vaccine: 1 dose IM or 0.1 ml ID 
Day 0 7 21 28
Rabies prevention - Summary 
 Rabies is a preventable disease. 
 Failure to recognize a risk of infection results 
in human deaths. 
 Increased awareness of sources and routes 
of virus transmission could save lives. 
 Pre-exposure vaccination should be used 
widely. 
 Post-exposure treatment is urgent. 
 For previously vaccinated people post 
-exposure treatment is simpler, cheaper and 
more effective.
rabies ppt

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rabies ppt

  • 1.
  • 2. RABIES  Primarily a Zoonotic disease of warm blooded animal  such as :-  Dogs, wild cats,  Jackals, wolves etc.  It is caused by the Neurotropic RNA virus belongs to Rhabdoviridae type I (LYSSAVIRUS type I) is Bullet shaped virus
  • 3.  It is an acute  Highly fatal viral dis: of CNS Transmitted to man by:  Bites OR  Licks of rabid animals
  • 4.
  • 5. Rabies virus structure Envelope Matrix protein Glycoprotein Nucleocapsid protein Source: http://www.cdc.gov
  • 6. History of Rabies Virus Man described the disease in 2300 B.C. The origin “rabhas”, meaning “to do violence” comes from ancient Indian Sanskrit dating 3000 B.C.
  • 7. History of the Rabies Virus Since Roman times, man established the link between the infectivity of a rabid dogs saliva and the spread of the disease. Because there is no cure for rabies, those that had been bitten by a rabid dog would commonly commit suicide to avoid the painful death that would inevitably follow.
  • 8. History of the Rabies Virus  Louis Pasteur was the first person to diagnose that rabies targeted the CNS.  Also determined that nervous tissue of an infected human or animal also contained the virus.  In 1890 created the rabies vaccine and saved 9 year old child after he had been bit by a rabid dog.
  • 9. Epidemiology 87 countries contain Rabies, but more cases are reported in Asia. In Indo-Pakistan rabies is a major public health problem mainly due to presence of a large no: of stray dogs. More than 30,000 people died of Rabies every year in Asia. Every year 10 million people require treatment and protection from Rabies which is great Financial loss.
  • 10. RESERVOIR OF INFECTION 1) URBAN RABIES: From Dogs and cats.
  • 11. 2) WILD LIFE RABIES: From jackals and foxes.
  • 12. 3) BAT RABIES: Vampire bats which live on the blood of animals and men. These are one of the main causes of the death of bovine, around 0.5 to 1 million per year.
  • 13. Source of Infection  Saliva of Rabid animal
  • 14. Host Factors  All warm blooded animals including man.  Rabies in man is a dead-end infection.
  • 15. Mode of Transmission 1. ANIMAL BITES 2. LICKS 3. AEROSOL 4. PERSON TO PERSON
  • 16. INCUBATION PERIOD:  normally it is 3 - 8 wks may be short that is 4 days  or may be prolonged for years.
  • 17. CLINICAL PICTURE 1. Prodromal symptoms Headache, malaise, sore throat, low fever, pain at the site of bite 2. Excitation Symptoms sensory sys: involvement Aero phobia, excitation of N.S. Motor sys: inv: increase reflexes, muscle spasm, Symp:inv: dilatation of Pupils. increase perspiration, salivation, and Lacrimation,
  • 18. Mental changes: fear of death, anger, irritability and depression Hydrophobia ( Fear of water) sight or sound of water may produce spasm of degulation the duration of illness is 2-3 days may be prolonged to 5-6 days Stage of paralysis & coma DEATH / Recovery
  • 19.
  • 20. Clinical forms of rabies  encephalitic = furious  ~ 80%  paralytic = dumb  ~ 20%
  • 21. Encephalitic rabies  prodromal symptoms  paresthesias/pain/pruritus at site of bite  episodes of generalized arousal or hyperexcitability separated by lucid periods  autonomic dysfunction  hydrophobia
  • 22. Paralytic rabies  paresthesias/pain/pruritus at site of bite  early flaccid muscle weakness  often begins in bitten extremity  progresses to produce quadriparesis  bilateral facial weakness  sensory examination is usually normal  sphincter involvement  fatal outcome  often misdiagnosed as Guillain - Barré syndrome
  • 23. DIAGNOSIS 1. History 2. Sign and symptom 3. Examination 4. Detection of Antigen by taking Skin Biopsy using Immunofluorescence by virus isolation from Saliva & other secretions.
  • 24. Control Measures  Notification  Isolation  Disinfection  Immunization
  • 25. Prevention of human rabies post Exposure prophylaxis 1. General consideration:- Aim is to neutralize virus before entering CNS 2. LOCAL WOUND TREATMENT a, Cleansing of wound(soap & water) b, Chemical treatment:  Either Alcohol 400-700 ml /liter  Tincture Iodine
  • 26. c, Suturing not recommended d, Anti Rabies Serum e, Antibiotic and ATS f, Observe the animal for 10 days
  • 27.  3, Immunization  1,NERVOUS TISSUE VACCINE (NTV 2, Human diploid cell vaccine (HDCV)
  • 28. Rabies postexposure guide: exposure to dogs, cats, and ferrets Evaluation of Animal Recommendation Healthy and available for 10 days observation No treatment unless animal develops clinical signs of rabies Rabid or suspected rabid Immediate treatment* Unknown (e.g., escaped) Consult local public health department *Discontinue treatment if tests on animal prove negative.
  • 29. Vaccines for immunization Definition: it is fluid or dried preparation of Rabies “Fixed” virus grown in the Neural tissue of Rabbits, Sheep, Goats, Mice or Rats OR in embryonated duck eggs OR in cell culture
  • 30. Nervous Tissue vaccine Duck embryo vaccine Cell culture vaccine preparation From fixed virus grown in brain of sheep or other animals potency Low or variable Eliminate Neuroparalytic factors More potent more safer Doses Large nos: are required Fewer doses of small volume Side effects Severe & fatal reactions Allergic risks Fewer Uses Exposed subjects Used in UK,USA in past 1, (HDC) safe, potent Pre & post expos:Immunization Suckling mouse brain V Devoid of Neuroparalytic effect Used in Latin America Improvement over adult animal nervous tissue V Now purified DEV developed Improvement over adult animal nervous tissue V Not available in India & Pakistan 2Tissue culture 2nd G (Non-human) Potent, low cost WHO recommendatio
  • 31. Type of Vaccine NERVOUS TISSUE VACCINE (NTV) a. Derived from adult animal nervous tissue eg. Sheep b. Derived from suckling mouse brain Type: Killed viral vaccine Dose: 2.5 ml S/C (Ant. Abdominal wall) Schedule: 14 doses
  • 32. Type of Vaccine (conti) Duck Embryo Vaccine (DEV) Type: Killed viral vaccine Dose: 1 ml S/C ( Ant. Abdominal wall) Schedule: 14 doses OD not available in Pakistan
  • 33. Type of Vaccine (conti) CELL CULTURE VACCINES a. Human diploid cell vaccine (HDCV) b. Second generation tissue culture vaccine (non- Human) Type: Killed viral vaccine Dose: 1 ml IM Schedule: on 0, 3, 7, 14, 28 day, booster on day 90
  • 34. Adverse Reactions to Rabies Vaccines Most common side-effects of rabies vaccines:  Systemic reactions such as headache, myalgia, malaise (5-40%)  Mild to moderate local reactions at injection site (30-74%)
  • 35. PASSIVE IMMUNIZATION  Horse Anti Rabies serum: 40 iu / kg at 0 day  Human rabies immunoglobin (HRIG): 20 iu / kg around the wound and rest in IM on 0 day  Booster doses are essential whenever anti rabies serum is given with the vaccine
  • 36. IMMUNITY  Duration of Immunity is upto 06 month  If again bite by rapid animal than dose according to blood titre if more than 0.5 i.u. / ml than only two dose 0, 3 day if less than 0.5 i.u. / ml than 0, 3, 7 day
  • 37. General measures  Regist:,licensing & taxation of dog.  Muzzling of dogs  Yearly mass vaccination of dog  Destruction of stray dogs  Facilities for diagnosis of rabies in dogs  Destruction of wildlife where the animals are known to be the reservoir of infection.  Publicity
  • 38. Preexposure rabies prophylaxis  3 doses of rabies vaccine (days 0, 7, and 21 or 28)  May check rabies antibody titre periodically – want >0.5 IU/mL  after a rabies exposure:  2 doses of IM rabies vaccine (days 0 and 3)  no HRIG
  • 39. Pre-exposure rabies prophylaxis Tissue culture vaccine: 1 dose IM or 0.1 ml ID Day 0 7 21 28
  • 40. Rabies prevention - Summary  Rabies is a preventable disease.  Failure to recognize a risk of infection results in human deaths.  Increased awareness of sources and routes of virus transmission could save lives.  Pre-exposure vaccination should be used widely.  Post-exposure treatment is urgent.  For previously vaccinated people post -exposure treatment is simpler, cheaper and more effective.

Editor's Notes

  1. Autonomic features: hypersalivation, gooseflesh, cardiac arrhythmias, and priapism in males.
  2. SLIDE 61 OTHER ADVERSE REACTIONS TO US LICENSED RABIES VACCINES FOR HUMANS Most vaccine-related adverse events following administration of rabies vaccines for human use licensed by the FDA are transient mild to moderate responses, involving either local reactions at the injection site, or systemic symptoms such as headache, muscle pain, or fatigue. Severe neurologic or anaphylactic reactions are very rare; fewer than 1 per 1,000,000 doses of US-licensed vaccines have been reported.