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Amjad Khan Afridi
In the 19th century, rabies was often referred to as “Hydrophobia,” as depicted
in this 1826 illustration, by T.L. Busby, entitled “Rabid Dog in Town.” A few
years later, in 1831, Pasteur was a schoolboy who observed an outbreak of
rabies in Arbois, France. Image online via the National Library of Medicine.
Amjad Khan Afridi
Lecturer,
Department of Health & Biological Sciences
Abasyn University Peshawar
In the 19th century, rabies was often referred to as “Hydrophobia,” as depicted
in this 1826 illustration, by T.L. Busby, entitled “Rabid Dog in Town.” A few
years later, in 1831, Pasteur was a schoolboy who observed an outbreak of
rabies in Arbois, France. Image online via the National Library of Medicine.
• Rabies, also known as hydrophobia, is a highly
fatal viral disease that causes inflammation of
the brain in humans and other mammals.
• It is caused by Lyssavirus type 1.
• Transmission of Rabies tohuman;
• Bites (95%),
• Scratches &
• Licks from infected animals.
It is a zoonotic disease of warm blooded animals
such as – dogs, skunk, cats, jackals, bats and
wolves.
History of Rabies
• Man described the disease in 2300 B.C.
• The word ‘Rabies’ originated from “rabhas”,
meaning “to do violence”.
• 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, those that had been bitten
by a rabid dog would commonly commit suicide to
avoid the painful death that would inevitably follow.
• Louis Pasteur
(a French biologist,
microbiologist and
chemist) was the first
person to diagnose
that rabies targets the
Central Nervous
System (CNS)
• In 1890 created the rabies vaccine and saved 9
year old Joseph Meister after he had been bit by a
rabid dog
Global Burden
• Avery wide distribution- Human rabies is present in 150 countries and
territories and on all continents, except forAntarctica.
EPIDEMIOLOGY
AGENT
 Rhabdovirus
 Lyssavirus type 1
 Bullet shaped virus
 Has a lipoprotein envelope
 Knob like spikes or glycoprotein G.
 Matrix protein layer
 Genome –unsegmented ,linear,
negative sense RNA.
TYPES OF RABIES VIRUS
STREET VIRUS FIXED VIRUS
The virus recovered from
naturally occurring cases of
rabies is called street virus.
The virus which has a short,
fixed and reproducible
incubation period is called
fixed virus.
SOURCES It is naturally occurring virus . It
is found in saliva of infected
animal
It is prepared by repeated culture
in brain of rabbit such that its IP
is reduced and fixed.
FEATURES 1. It produce negri bodies
2. Incubation period is 20 to
60 days.
3. It is pathogenic for
all mammals
4. Cannot be usedfor
preparation of
vaccine
1. It does not formnegri
bodies
2. Incubation period is
constant between 4-6
days.
3. It can be pathogenic
for humans under
certain conditions.
4. It is used to prepare
anti- rabies vaccine.
RESERVIOUR OF INFECTION
• URBAN RABIES:
1. 99% cases in Asia is from dogs andcats.
2. A single infected dog capable of transmitting over an areaof
40 km.
• WILD LIFE RABIES :
1. Foxes, jackals, hyenas , skunks etc.
2. Transmit infection among themselves and to dogs andman.
• BATRABIES:
1. Latin American countries ,USA
2. Vampire bats feed on blood of humans and animals.
3. Cause havoc to cattle population
4. Transmission by bite and aerosols.
HOST FACTORS
• All warm blooded animals including man.
• Rabies in man is a dead end infection
• People at risk-lab workers, veterinarians, dog
handlers , hunters etc
PATHOGENESIS
RABIES IN MAN
• Know as hydrophobia (fear of water)
• Duration of disease: 2-3 days prolonged to 5-6 days (exceptional
cases)
• Prodromal symptoms (3-4 days)
• Headache
• Malaise
• Sore throat
• slight fever
• Followed by excitation and stimulation off all parts ofnervous
system
• Sensory system
• Nervous system
• Motor system
• Sympathetic system
• Mental system
• Patient becomes intolerant to noise, bright light, cold draught ofair
(sensory).
• Aerophobia (fear of air ) may be present.
• Increased reflexes and muscle spasms (motor).
• Increased perspiration , salivation. sympathetic).
• Fear of death , irritability , anger and depression (mentalchanges).
• Patient dies abruptly due to convulsions or pass to comaand
paralysis.
18th May, 2022
DIAGNOSIS
• On basis of clinical history of bite by rabid animal
• Characteristic signs and symptoms
• Confirmatory tests
• Antigen detection by immunofluroscence (skinbiopsy).
• Virus isolation (saliva and other secretions)
• Immunofluroscence of corneal impression smears proven
unreliable.
TREATMENT
• No specific treatment
• Case management
– Isolation in a quiet room protected as far as possiblefrom
external stimuli to prevent spasms and convulsions
– Relieve anxiety and pain by use of sedatives
– Morphia 30-54mg
– If spastic muscle contractions present use drugs with curare like
action
– Ensure hydration and diuresis ( Kidneys Filter)
– Intensive therapy in the form of respiratory andcardiac
support
• Patients with rabies are highly infectious virus is present inall
secretions like saliva , tears, vomits, urine, and other body
fluids.
• Nursing personnel should be warned of risks and protect
themselves with PPE
• Persons with open wounds and cut should not attend the
patients
• In places where rabies cases are encountered frequentlypre
exposure prophylaxis (2-3 doses HDC vaccine )
recommended.
PREVENTION OF HUMAN RABIES
This may be considered under 3 heads
1. Post-exposure prophylaxis.
2. Pre-exposure prophylaxis.
3. Post-exposure treatment of persons who
have been vaccinated previously
Post-exposure Prophylaxi
1. General consideration
2. Local treatment of
wound
(a)Cleansing
(b)Chemical treatment
(c)Suturing
(d)Antibiotics and anti-tetanus
measure
3.Immunization
Immunization
• Rabies vaccines prequalified by WHO do
not contain preservatives such as
thimerosal.
• The shelf-life 3 years
• Stored at +2°C to +8°C and protected from
sunlight.
• Following reconstitution with the accompanying
sterile diluents, the vaccines should be used
immediately, or within 6-8 hours if kept at the
correct temperature.
•
Immunization of immunocompromised
individuals
• In immunocompromised individuals including
patients with HIV/AIDS, a complete series of 5 doses
of intramuscular CCEEV in combination with
comprehensive wound management and local
infiltration with human rabies immunoglobulin is
required for patients with category II and III
exposures.
RABIES IN DOGS
RABIES IN DOGS
• INCUBATION PERIOD : Ranges from 3-8 weeks but it
may be as short as 10 days or as long as 1 year.
• CLINICAL PICTURE:
It manifest in 2 forms : Furious rabies and
dumb rabies.
• FURIOUS RABIES : Typical mad-dog
syndrome.
CHANGE IN BEHAVIOUR
Loses its fear of bites people , aggressive,
unusual objects- stick , straw and mud.
• RUNNINGAMUCK:
Tendency to run away from home
and wander.
• CHANGE IN VOICE: Barks and growls in a
hoarse voice or unable to bark
• EXCESSIVE SALIVATION: Foaming at
the angle of mouth
• PARALYTIC STAGE: Later stage paralysis of
• DUMB RABIES: Exciting and irritating stage is
lacking .
• Its predominantly paralytic.
• Dog withdraws from being
seen and disturbed.
• Dies in about 3 days.
LAB DIAGNOSIS :
• FLUROSCENT ANTIBODY TEST:Highly
reliable and
best single test for rabies antigen detection.
• If brain is negative by FRA test , person need notbe
treated.
• MICROSCOPIC EXAINATION: Negri bodies
identifies 75-90% of cases.
Rabies Infection.pptx

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Rabies Infection.pptx

  • 1. Amjad Khan Afridi In the 19th century, rabies was often referred to as “Hydrophobia,” as depicted in this 1826 illustration, by T.L. Busby, entitled “Rabid Dog in Town.” A few years later, in 1831, Pasteur was a schoolboy who observed an outbreak of rabies in Arbois, France. Image online via the National Library of Medicine. Amjad Khan Afridi Lecturer, Department of Health & Biological Sciences Abasyn University Peshawar In the 19th century, rabies was often referred to as “Hydrophobia,” as depicted in this 1826 illustration, by T.L. Busby, entitled “Rabid Dog in Town.” A few years later, in 1831, Pasteur was a schoolboy who observed an outbreak of rabies in Arbois, France. Image online via the National Library of Medicine.
  • 2.
  • 3. • Rabies, also known as hydrophobia, is a highly fatal viral disease that causes inflammation of the brain in humans and other mammals. • It is caused by Lyssavirus type 1. • Transmission of Rabies tohuman; • Bites (95%), • Scratches & • Licks from infected animals.
  • 4. It is a zoonotic disease of warm blooded animals such as – dogs, skunk, cats, jackals, bats and wolves.
  • 5. History of Rabies • Man described the disease in 2300 B.C. • The word ‘Rabies’ originated from “rabhas”, meaning “to do violence”. • 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, those that had been bitten by a rabid dog would commonly commit suicide to avoid the painful death that would inevitably follow.
  • 6. • Louis Pasteur (a French biologist, microbiologist and chemist) was the first person to diagnose that rabies targets the Central Nervous System (CNS) • In 1890 created the rabies vaccine and saved 9 year old Joseph Meister after he had been bit by a rabid dog
  • 7. Global Burden • Avery wide distribution- Human rabies is present in 150 countries and territories and on all continents, except forAntarctica.
  • 9. AGENT  Rhabdovirus  Lyssavirus type 1  Bullet shaped virus  Has a lipoprotein envelope  Knob like spikes or glycoprotein G.  Matrix protein layer  Genome –unsegmented ,linear, negative sense RNA.
  • 10. TYPES OF RABIES VIRUS STREET VIRUS FIXED VIRUS The virus recovered from naturally occurring cases of rabies is called street virus. The virus which has a short, fixed and reproducible incubation period is called fixed virus. SOURCES It is naturally occurring virus . It is found in saliva of infected animal It is prepared by repeated culture in brain of rabbit such that its IP is reduced and fixed. FEATURES 1. It produce negri bodies 2. Incubation period is 20 to 60 days. 3. It is pathogenic for all mammals 4. Cannot be usedfor preparation of vaccine 1. It does not formnegri bodies 2. Incubation period is constant between 4-6 days. 3. It can be pathogenic for humans under certain conditions. 4. It is used to prepare anti- rabies vaccine.
  • 11. RESERVIOUR OF INFECTION • URBAN RABIES: 1. 99% cases in Asia is from dogs andcats. 2. A single infected dog capable of transmitting over an areaof 40 km. • WILD LIFE RABIES : 1. Foxes, jackals, hyenas , skunks etc. 2. Transmit infection among themselves and to dogs andman.
  • 12. • BATRABIES: 1. Latin American countries ,USA 2. Vampire bats feed on blood of humans and animals. 3. Cause havoc to cattle population 4. Transmission by bite and aerosols.
  • 13. HOST FACTORS • All warm blooded animals including man. • Rabies in man is a dead end infection • People at risk-lab workers, veterinarians, dog handlers , hunters etc
  • 15.
  • 17. • Know as hydrophobia (fear of water) • Duration of disease: 2-3 days prolonged to 5-6 days (exceptional cases) • Prodromal symptoms (3-4 days) • Headache • Malaise • Sore throat • slight fever • Followed by excitation and stimulation off all parts ofnervous system • Sensory system • Nervous system • Motor system • Sympathetic system • Mental system
  • 18. • Patient becomes intolerant to noise, bright light, cold draught ofair (sensory). • Aerophobia (fear of air ) may be present. • Increased reflexes and muscle spasms (motor). • Increased perspiration , salivation. sympathetic). • Fear of death , irritability , anger and depression (mentalchanges). • Patient dies abruptly due to convulsions or pass to comaand paralysis.
  • 20. DIAGNOSIS • On basis of clinical history of bite by rabid animal • Characteristic signs and symptoms • Confirmatory tests • Antigen detection by immunofluroscence (skinbiopsy). • Virus isolation (saliva and other secretions) • Immunofluroscence of corneal impression smears proven unreliable.
  • 21. TREATMENT • No specific treatment • Case management – Isolation in a quiet room protected as far as possiblefrom external stimuli to prevent spasms and convulsions – Relieve anxiety and pain by use of sedatives – Morphia 30-54mg – If spastic muscle contractions present use drugs with curare like action – Ensure hydration and diuresis ( Kidneys Filter) – Intensive therapy in the form of respiratory andcardiac support
  • 22. • Patients with rabies are highly infectious virus is present inall secretions like saliva , tears, vomits, urine, and other body fluids. • Nursing personnel should be warned of risks and protect themselves with PPE • Persons with open wounds and cut should not attend the patients • In places where rabies cases are encountered frequentlypre exposure prophylaxis (2-3 doses HDC vaccine ) recommended.
  • 23. PREVENTION OF HUMAN RABIES This may be considered under 3 heads 1. Post-exposure prophylaxis. 2. Pre-exposure prophylaxis. 3. Post-exposure treatment of persons who have been vaccinated previously
  • 24. Post-exposure Prophylaxi 1. General consideration 2. Local treatment of wound (a)Cleansing (b)Chemical treatment (c)Suturing (d)Antibiotics and anti-tetanus measure 3.Immunization
  • 25. Immunization • Rabies vaccines prequalified by WHO do not contain preservatives such as thimerosal. • The shelf-life 3 years • Stored at +2°C to +8°C and protected from sunlight. • Following reconstitution with the accompanying sterile diluents, the vaccines should be used immediately, or within 6-8 hours if kept at the correct temperature. •
  • 26. Immunization of immunocompromised individuals • In immunocompromised individuals including patients with HIV/AIDS, a complete series of 5 doses of intramuscular CCEEV in combination with comprehensive wound management and local infiltration with human rabies immunoglobulin is required for patients with category II and III exposures.
  • 28. RABIES IN DOGS • INCUBATION PERIOD : Ranges from 3-8 weeks but it may be as short as 10 days or as long as 1 year. • CLINICAL PICTURE: It manifest in 2 forms : Furious rabies and dumb rabies. • FURIOUS RABIES : Typical mad-dog syndrome.
  • 29. CHANGE IN BEHAVIOUR Loses its fear of bites people , aggressive, unusual objects- stick , straw and mud. • RUNNINGAMUCK: Tendency to run away from home and wander. • CHANGE IN VOICE: Barks and growls in a hoarse voice or unable to bark • EXCESSIVE SALIVATION: Foaming at the angle of mouth • PARALYTIC STAGE: Later stage paralysis of
  • 30. • DUMB RABIES: Exciting and irritating stage is lacking . • Its predominantly paralytic. • Dog withdraws from being seen and disturbed. • Dies in about 3 days. LAB DIAGNOSIS : • FLUROSCENT ANTIBODY TEST:Highly reliable and best single test for rabies antigen detection. • If brain is negative by FRA test , person need notbe treated. • MICROSCOPIC EXAINATION: Negri bodies identifies 75-90% of cases.

Notas del editor

  1. https://www.youtube.com/watch?v=9BE_vOAqxRM&ab_channel=JustinEyck
  2. Hydrophobia is the result of late-stage rabies that spreads from the initial wound through the central nervous system.
  3. Constant sources of infection to man and animals
  4.  the immunofluorescent staining of material obtained from the corneas of patients suspected of having the disease. Negri bodies may vary in size from 0.25 to 27 µm. They are found most frequently in the pyramidal cells of Ammon's horn, and the Purkinje cells of the cerebellum. They are also found in the cells of the medulla and various other ganglia. The American pathologist Anna Wessels William
  5. Sedatives are a type of prescription medication that slows down your brain activity. ey're typically used to make you feel more relaxed. Doctors commonly prescribe sedatives to treat conditions like anxiety and sleep disorders.  Spasticity is abnormal muscle tightness due to prolonged muscle contraction. It is a symptom associated with damage to the brain, spinal cord or motor nerves, and is seen in individuals with neurological conditions, such as: Cerebral palsy (CP) Multiple sclerosis (MS)
  6. A prophylactic is a medication or a treatment designed and used to prevent a disease from occurring Human diploid cell 
  7. Thimerosal is a mercury-containing organic compound preserve biological drug CCEEVs
  8. chicken embryo cell vaccines