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ο‚–
INTRODUCTION
ο‚–
ο‚™Rabies or hydrophobia is an
acute, highly fatal viral disease
of the central nervous system,
caused by Lyssavirus
DEFINITION
ο‚–
ο‚™ In India, about 15 million people are bitten by animals
ο‚™ In india 25,000–30,000 human deaths from rabies
annually.
INCIDENCE
ο‚–
ο‚™ Lyssavirus is a bullet shaped RNA virus.
ο‚™ It belongs to the family rabdoviridae
AGENT FACTORS
ο‚–
Lassa virus
ο‚–
3 epidemiological forms
1. Urban rabies
2. Wild life rabies
3. Bat rabies
RESERVOIRS OF
INFECTION
ο‚–
ο‚™ The transfer of infection from wild life to domestic dogs
results in the creation of urban cycle and is responsible for
99% of human cases in India
Urban rabies
ο‚–
ο‚™ The wild life is perpetuated by the jackal, fox and other
wild life carriers.
Wild life rabies
ο‚–
ο‚™ In Latin American countries and U.S.A vampire bat
is an important host and vector of rabies
Bat rabies
ο‚–
ο‚™Source of infection to man is the
saliva of rabid animal. In dogs and cats,
the virus may be present in the saliva for
3-4 days before the onset of clinical
symptoms and during the course of
illness till death.
SOURCE OF
INFECTION
ο‚–
ο‚™All warm blooded animals including
man are susceptible to rabies. Laboratory
staff working with rabies virus,
veterinarians, dog handlers, hunters
faces higher risk of rabies than general
public.
HOST FACTORS
ο‚–
1.Animal bites
2.Licks
3.Aerosols
4.Person-to-person
MODE OF
TRANSMISSION
ο‚–
ο‚™ In India most of the human rabies cases have resulted
from dog-bites. Transmission to man is particularly
through rabid dog bites. As a prerequisite for
transmission, the saliva of the dog must contain the virus
at the time of bite. It may also occur from other animals
beside dog like cat, sheep, goat, monkey, horse.
Animal bites
ο‚–
ο‚™Dogs have the habit of licking.
Licks on abraded skin and mucosa
can transmit the disease.
Licks
ο‚–
ο‚™ Aerosol or respiratory transmission is found only in
certain caves harbouring rabies infected bats.
Aerosols
ο‚–
ο‚™ Man to man transmission, although rare is possible.
ο‚™ A case of a child biting his parent is in record
ο‚™ There is also reports of transmission of rabies by corneal
and organ transplants.
Person-to-person
ο‚–
ο‚™ 3-8 weeks
ο‚™ The incubation period in man is highly variable,
commonly 3-8 weeks, but may vary from 4 days to
many years.
INCUBATION PERIOD
ο‚–
Bite
Entryof rabies virus in man
Virus replicate in muscle or connective tissue cells at the site of introduction
Virus attaches to nerve endings
PATHOPHYSIOLOGY
ο‚–
Enters peripheral nerves
Spreads centripetally via peripheral nerves towards CNS
Infects CNS
Virus spreads centrifugally in peripheral nerves to many tissues
Invades skeletal, myocardial muscle, adrenal glands, skin
Contd..
ο‚–
ο‚™ Duration of illness 2-3 days rarely 5-6 days
ο‚™ PRODROMAL SYMPTOMS
ο‚™ Headache
ο‚™ Malaise
ο‚™ Sore throat
ο‚™ Slight fever lasting for 3-4 days
ο‚™ Pain and tingling at the site of bite
CLINICAL FEATURES
ο‚–
ο‚™ widespread excitation and stimulation of all parts of nervous
system
1. Intolerance to noise
2. Intolerance to bright light
3. Intolerance to cold draught of air
4. Aerophobia
5. Increased reflexes
6. Muscle spasms
7. Dilatation of pupils
8. Increased perspiration
SPECIFIC SYMPTOMS
ο‚–
1. Salivation
2. Lacrimation
3. Mental changes due to fear of death, anger, irritability
and depression
4. Symptoms progressively aggravate
5. All attempts at swallowing liquid become unsuccessful
6. Mere sight or sound of water provoke spasm of muscles
of deglutination- hydrophobia
7. Patient may die abruptly during one of the convulsion or
may pass on to the stage of paralysis or coma
Contd…
ο‚–
ο‚™ History of bite by a rabid animal
ο‚™ Signs and symptoms
ο‚™ Detection of rabies antigen
ο‚™ Using immunofluroscence of skin biopsy
ο‚™ Virus neutralizing antibodies appear in CSF and
serum after 7-10 days of illness
ο‚™ Virus isolation from saliva, CSF and other secretions
DIAGNOSIS
ο‚–
ο‚™ Nervous tissue vaccines
ο‚™ Duck embryo vaccine
ο‚™ Cell culture vaccines
ο‚™ Human diploid cell vaccine (HDCV)
Non- human origin-second generation vaccines
TREATMENT
ο‚–
Intramuscular schedule
ο‚™
VACCINE
ADMINISTRATION
οƒ˜ Schedule consist of 6 doses (1 ml each) on days 0, 3,7,14 and 28 and a booster dose on
day 90.
οƒ˜ Injections are given IM on deltoid and must not be given to buttocks
Dose: one dose, IM dose into deltoid (1ml)
Day 0 3 7 14 28
ο‚–
 2 site ID method
0.5 ml of Purified Vero Cell Vaccine (PVRV)
1 ml of Purified Chick Embryo Cell Vaccine (PCECV)
1 ml of Purified Duck Embryo Vaccine (PDEV)
Volume of ID dose is one-fifth of IM dose per site. ie if IM dose is 0.5 ml, ID dose is 0.1
ml.
Dose: 1, ID dose = one fifth of IM dose
Day 0 3 7 28 90
Sites X2 X2 X2 X1 X1
Intradermal schedule
ο‚–
 8 site ID method
Human Diploid Cell Vaccine (HDCV) and Purified Chick Embryo Cell Vaccine
(PCECV)
On day 0--- 0.1 ml of reconstituted vaccine is given at each of 8 sites.
Sites are deltoid, lateral thigh, supra scapular region and lower quadrant of abdomen
On day 7--- 0.1 ml of vaccine is given at each of 4 sites over deltoid and thighs.
On days 28 and 90--- 0.1 ml of vaccine is given at one site, over deltoid
Dose 0.1ml ID per site
Day 0 7 28 90
Sites X8 X4 X1 X1
8 site ID method
ο‚–
ο‚™ The patient should be isolated in quiet room protected as far as
possible from external stimuli such as bright light, noise or cold
draughts which may precipitate spasms or convulsions
ο‚™ Relieve anxiety and pain by liberal use of sedatives.
ο‚™ Ensure hydration and diuresis
ο‚™ Intensive therapy in the form of respiratory and cardiac support may
be given
ο‚™ Nursing personnel attending rabid patient should be warned against
possible risk of contamination and should wear face masks, gloves,
goggles and aprons to protect themselves
ο‚™ Pre- exposure prophylaxis with 2-3 doses of HDC vaccine is reco
GENERAL
MANAGEMENT
ο‚–
ο‚™ POST- EXPOSURE PROPHYLAXIS
ο‚™ Local treatment of wound
ο‚™ 1. Cleansing
ο‚™ 2. Chemical treatment
ο‚™ 3. Suturing
ο‚™ 4. Anti rabies serum
ο‚™ 5. Antibiotics and anti tetanus measure
ο‚™ 6. Observe the animal for 10 days
PREVENTION
ο‚–
ο‚™ 1. Horse anti rabies serum
ο‚™ 2. Human rabies immunoglobulin
ANTI RABIES SERUM
ο‚–
ο‚™ laboratory staff working with rabies virus,
veterinarians, animal handlers and wild- life officers
ο‚™ 1ml cell culture vaccine, IM on days 0, 7 and 28
PRE-EXPOSURE
PROPHYLAXIS
ο‚–
ο‚™ 1 ml, IM doses of human diploid cell vaccine on days
0, 3 and 7.
POST EXPOSURE
PROPHYLAXIS
ο‚–
ASSESSMENT
ο‚™ ask for a history of bite by an animal
ο‚™ - assess whether he has undergone immediate
prophylactic measures
ο‚™ - assess for characteristics like photophobia,
hydrophobia etc
ο‚™ - check for the presence of antigen
NURSING
MANAGEMENT
ο‚–
ο‚™ 1. Hyperthermia related to infectious process as
evidenced by elevated body temperature more than
100 degree farenheit
ο‚™ 2. Acute pain related to tissue injury at the site of
bite as evidenced by pain scale score more than 7
ο‚™ 3. Fatigue related to bacterial invasion of central
nervous system as evidenced by inability to perform
ADLs
ο‚™ 4. Risk for injury related to confusion
NURSING DIAGNOSIS
ο‚–
Malaria
ο‚–
ο‚™ Malaria is a protozoal disease caused by infection
with parasites of the genus Plasmodium and
transmitted to man by infected female Anopheles
mosquito
DEFINITION
ο‚–
Female anophelous
mosquito
ο‚–
ο‚™ 300-500 million clinical cases each year.
INCIDENCE
ο‚–
1. P.vivax,
2. P. falciparum
3. P. malariae,
4. P. ovale.
AGENT FACTORS
ο‚–
ο‚™ Age- malaria affects all ages
ο‚™ Gender- males are more frequently affected because of the
outdoor life they lead
ο‚™ Pregnancy-pregnancy increases risk of malaria in women.
Malaria during pregnancy may cause intrauterine death
of foetus, premature labour or abortion
ο‚™ Socio-economic development- poor socioeconomic status
contributes to malaria
ο‚™ Occupation - It is predominantly a rural disease and is
related to
HOST FACTORS
ο‚–
ο‚™ Season – it is a seasonal disease and has maximum
prevalence from July to November.
ο‚™ Temperature – malarial parasite develops at the
temperature of 20-30 degree celcius
ο‚™ Humidity – a relative humidity of 60% is considered
necessary for mosquitoes to live
ο‚™ Rainfall – rainfall provides opportunities for breeding of
mosquitoes and increases epidemics
ο‚™ Man-made malaria – burrow pits, garden pools,
irrigation channels, engineering projects led to breeding
of mosquitoes.
ENVIRONMENTAL
FACTORS
ο‚–
ο‚™ VECTOR TRANSMISSION
ο‚™ DIRECT TRANSMISSION
ο‚™ CONGENITAL MALARIA
MODE OF
TRANSMISSION
ο‚–
ο‚™ Usually less than 10 days
ο‚™ falciparum malaria it is 9-14days
ο‚™ quarten malaria it is 18-40 days
ο‚™ vivax it is 8-17
ο‚™ ovale it is 16-18
INCUBATION PERIOD
ο‚–
ο‚™ COLD STAGE
ο‚™ HOT STAGE
ο‚™ SWEATING STAGE
CLINICAL FEATURES
ο‚–
ο‚™ Demonstration of parasite in blood
ο‚™ Dipstick (antigen capture) assay for detection of
plasmodium falciparum
DIAGNOSIS
ο‚–
 Presumptive Treatment
 Radical Treatment
 Treatment of resistant infection
 Severe and Complicated Malaria
ο‚–
ο‚™ NURSING DIAGNOSIS
ο‚™ 1. Acute pain related to inflammatory process as
evidenced by pain scale score above 7
ο‚™ 2. Hyperthermia related to infectious process as
evidenced by elevated body temperature
ο‚™ 3. Fatigue related to bacterial invasion as evidenced
by inability to perform ADLs
NURSING
MANAGEMENT
ο‚–
EVIDENCE BASED
PRACTICE
ο‚–
SUMMARY
ο‚–
CONCLUSION
ο‚–
BIBLIOGRAPHY
ο‚–
Thank you

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Rabies: A Deadly Zoonotic Disease

  • 1.
  • 3. ο‚– ο‚™Rabies or hydrophobia is an acute, highly fatal viral disease of the central nervous system, caused by Lyssavirus DEFINITION
  • 4. ο‚– ο‚™ In India, about 15 million people are bitten by animals ο‚™ In india 25,000–30,000 human deaths from rabies annually. INCIDENCE
  • 5. ο‚– ο‚™ Lyssavirus is a bullet shaped RNA virus. ο‚™ It belongs to the family rabdoviridae AGENT FACTORS
  • 7. ο‚– 3 epidemiological forms 1. Urban rabies 2. Wild life rabies 3. Bat rabies RESERVOIRS OF INFECTION
  • 8. ο‚– ο‚™ The transfer of infection from wild life to domestic dogs results in the creation of urban cycle and is responsible for 99% of human cases in India Urban rabies
  • 9. ο‚– ο‚™ The wild life is perpetuated by the jackal, fox and other wild life carriers. Wild life rabies
  • 10. ο‚– ο‚™ In Latin American countries and U.S.A vampire bat is an important host and vector of rabies Bat rabies
  • 11. ο‚– ο‚™Source of infection to man is the saliva of rabid animal. In dogs and cats, the virus may be present in the saliva for 3-4 days before the onset of clinical symptoms and during the course of illness till death. SOURCE OF INFECTION
  • 12. ο‚– ο‚™All warm blooded animals including man are susceptible to rabies. Laboratory staff working with rabies virus, veterinarians, dog handlers, hunters faces higher risk of rabies than general public. HOST FACTORS
  • 14. ο‚– ο‚™ In India most of the human rabies cases have resulted from dog-bites. Transmission to man is particularly through rabid dog bites. As a prerequisite for transmission, the saliva of the dog must contain the virus at the time of bite. It may also occur from other animals beside dog like cat, sheep, goat, monkey, horse. Animal bites
  • 15. ο‚– ο‚™Dogs have the habit of licking. Licks on abraded skin and mucosa can transmit the disease. Licks
  • 16. ο‚– ο‚™ Aerosol or respiratory transmission is found only in certain caves harbouring rabies infected bats. Aerosols
  • 17. ο‚– ο‚™ Man to man transmission, although rare is possible. ο‚™ A case of a child biting his parent is in record ο‚™ There is also reports of transmission of rabies by corneal and organ transplants. Person-to-person
  • 18. ο‚– ο‚™ 3-8 weeks ο‚™ The incubation period in man is highly variable, commonly 3-8 weeks, but may vary from 4 days to many years. INCUBATION PERIOD
  • 19. ο‚– Bite Entryof rabies virus in man Virus replicate in muscle or connective tissue cells at the site of introduction Virus attaches to nerve endings PATHOPHYSIOLOGY
  • 20. ο‚– Enters peripheral nerves Spreads centripetally via peripheral nerves towards CNS Infects CNS Virus spreads centrifugally in peripheral nerves to many tissues Invades skeletal, myocardial muscle, adrenal glands, skin Contd..
  • 21. ο‚– ο‚™ Duration of illness 2-3 days rarely 5-6 days ο‚™ PRODROMAL SYMPTOMS ο‚™ Headache ο‚™ Malaise ο‚™ Sore throat ο‚™ Slight fever lasting for 3-4 days ο‚™ Pain and tingling at the site of bite CLINICAL FEATURES
  • 22. ο‚– ο‚™ widespread excitation and stimulation of all parts of nervous system 1. Intolerance to noise 2. Intolerance to bright light 3. Intolerance to cold draught of air 4. Aerophobia 5. Increased reflexes 6. Muscle spasms 7. Dilatation of pupils 8. Increased perspiration SPECIFIC SYMPTOMS
  • 23. ο‚– 1. Salivation 2. Lacrimation 3. Mental changes due to fear of death, anger, irritability and depression 4. Symptoms progressively aggravate 5. All attempts at swallowing liquid become unsuccessful 6. Mere sight or sound of water provoke spasm of muscles of deglutination- hydrophobia 7. Patient may die abruptly during one of the convulsion or may pass on to the stage of paralysis or coma Contd…
  • 24. ο‚– ο‚™ History of bite by a rabid animal ο‚™ Signs and symptoms ο‚™ Detection of rabies antigen ο‚™ Using immunofluroscence of skin biopsy ο‚™ Virus neutralizing antibodies appear in CSF and serum after 7-10 days of illness ο‚™ Virus isolation from saliva, CSF and other secretions DIAGNOSIS
  • 25. ο‚– ο‚™ Nervous tissue vaccines ο‚™ Duck embryo vaccine ο‚™ Cell culture vaccines ο‚™ Human diploid cell vaccine (HDCV) Non- human origin-second generation vaccines TREATMENT
  • 26. ο‚– Intramuscular schedule ο‚™ VACCINE ADMINISTRATION οƒ˜ Schedule consist of 6 doses (1 ml each) on days 0, 3,7,14 and 28 and a booster dose on day 90. οƒ˜ Injections are given IM on deltoid and must not be given to buttocks Dose: one dose, IM dose into deltoid (1ml) Day 0 3 7 14 28
  • 27. ο‚–  2 site ID method 0.5 ml of Purified Vero Cell Vaccine (PVRV) 1 ml of Purified Chick Embryo Cell Vaccine (PCECV) 1 ml of Purified Duck Embryo Vaccine (PDEV) Volume of ID dose is one-fifth of IM dose per site. ie if IM dose is 0.5 ml, ID dose is 0.1 ml. Dose: 1, ID dose = one fifth of IM dose Day 0 3 7 28 90 Sites X2 X2 X2 X1 X1 Intradermal schedule
  • 28. ο‚–  8 site ID method Human Diploid Cell Vaccine (HDCV) and Purified Chick Embryo Cell Vaccine (PCECV) On day 0--- 0.1 ml of reconstituted vaccine is given at each of 8 sites. Sites are deltoid, lateral thigh, supra scapular region and lower quadrant of abdomen On day 7--- 0.1 ml of vaccine is given at each of 4 sites over deltoid and thighs. On days 28 and 90--- 0.1 ml of vaccine is given at one site, over deltoid Dose 0.1ml ID per site Day 0 7 28 90 Sites X8 X4 X1 X1 8 site ID method
  • 29. ο‚– ο‚™ The patient should be isolated in quiet room protected as far as possible from external stimuli such as bright light, noise or cold draughts which may precipitate spasms or convulsions ο‚™ Relieve anxiety and pain by liberal use of sedatives. ο‚™ Ensure hydration and diuresis ο‚™ Intensive therapy in the form of respiratory and cardiac support may be given ο‚™ Nursing personnel attending rabid patient should be warned against possible risk of contamination and should wear face masks, gloves, goggles and aprons to protect themselves ο‚™ Pre- exposure prophylaxis with 2-3 doses of HDC vaccine is reco GENERAL MANAGEMENT
  • 30. ο‚– ο‚™ POST- EXPOSURE PROPHYLAXIS ο‚™ Local treatment of wound ο‚™ 1. Cleansing ο‚™ 2. Chemical treatment ο‚™ 3. Suturing ο‚™ 4. Anti rabies serum ο‚™ 5. Antibiotics and anti tetanus measure ο‚™ 6. Observe the animal for 10 days PREVENTION
  • 31. ο‚– ο‚™ 1. Horse anti rabies serum ο‚™ 2. Human rabies immunoglobulin ANTI RABIES SERUM
  • 32. ο‚– ο‚™ laboratory staff working with rabies virus, veterinarians, animal handlers and wild- life officers ο‚™ 1ml cell culture vaccine, IM on days 0, 7 and 28 PRE-EXPOSURE PROPHYLAXIS
  • 33. ο‚– ο‚™ 1 ml, IM doses of human diploid cell vaccine on days 0, 3 and 7. POST EXPOSURE PROPHYLAXIS
  • 34. ο‚– ASSESSMENT ο‚™ ask for a history of bite by an animal ο‚™ - assess whether he has undergone immediate prophylactic measures ο‚™ - assess for characteristics like photophobia, hydrophobia etc ο‚™ - check for the presence of antigen NURSING MANAGEMENT
  • 35. ο‚– ο‚™ 1. Hyperthermia related to infectious process as evidenced by elevated body temperature more than 100 degree farenheit ο‚™ 2. Acute pain related to tissue injury at the site of bite as evidenced by pain scale score more than 7 ο‚™ 3. Fatigue related to bacterial invasion of central nervous system as evidenced by inability to perform ADLs ο‚™ 4. Risk for injury related to confusion NURSING DIAGNOSIS
  • 37. ο‚– ο‚™ Malaria is a protozoal disease caused by infection with parasites of the genus Plasmodium and transmitted to man by infected female Anopheles mosquito DEFINITION
  • 39. ο‚– ο‚™ 300-500 million clinical cases each year. INCIDENCE
  • 40. ο‚– 1. P.vivax, 2. P. falciparum 3. P. malariae, 4. P. ovale. AGENT FACTORS
  • 41. ο‚– ο‚™ Age- malaria affects all ages ο‚™ Gender- males are more frequently affected because of the outdoor life they lead ο‚™ Pregnancy-pregnancy increases risk of malaria in women. Malaria during pregnancy may cause intrauterine death of foetus, premature labour or abortion ο‚™ Socio-economic development- poor socioeconomic status contributes to malaria ο‚™ Occupation - It is predominantly a rural disease and is related to HOST FACTORS
  • 42. ο‚– ο‚™ Season – it is a seasonal disease and has maximum prevalence from July to November. ο‚™ Temperature – malarial parasite develops at the temperature of 20-30 degree celcius ο‚™ Humidity – a relative humidity of 60% is considered necessary for mosquitoes to live ο‚™ Rainfall – rainfall provides opportunities for breeding of mosquitoes and increases epidemics ο‚™ Man-made malaria – burrow pits, garden pools, irrigation channels, engineering projects led to breeding of mosquitoes. ENVIRONMENTAL FACTORS
  • 43. ο‚– ο‚™ VECTOR TRANSMISSION ο‚™ DIRECT TRANSMISSION ο‚™ CONGENITAL MALARIA MODE OF TRANSMISSION
  • 44. ο‚– ο‚™ Usually less than 10 days ο‚™ falciparum malaria it is 9-14days ο‚™ quarten malaria it is 18-40 days ο‚™ vivax it is 8-17 ο‚™ ovale it is 16-18 INCUBATION PERIOD
  • 45. ο‚– ο‚™ COLD STAGE ο‚™ HOT STAGE ο‚™ SWEATING STAGE CLINICAL FEATURES
  • 46. ο‚– ο‚™ Demonstration of parasite in blood ο‚™ Dipstick (antigen capture) assay for detection of plasmodium falciparum DIAGNOSIS
  • 47. ο‚–  Presumptive Treatment  Radical Treatment  Treatment of resistant infection  Severe and Complicated Malaria
  • 48. ο‚– ο‚™ NURSING DIAGNOSIS ο‚™ 1. Acute pain related to inflammatory process as evidenced by pain scale score above 7 ο‚™ 2. Hyperthermia related to infectious process as evidenced by elevated body temperature ο‚™ 3. Fatigue related to bacterial invasion as evidenced by inability to perform ADLs NURSING MANAGEMENT