tetanus and anthrax Flashcards

1
Q

Tetanus MB

A

gram + rod motile drum stick appearance on microscope , they are spore forming rods

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2
Q

how to we acquire tetanus

A

The bacteria are usually found in soil, dust, and manure and enter the body through breaks in the skin — usually cuts or puncture wounds caused by contaminated objects.

through the soil
deep wound and will be able to survive as long as conditions are anaerobic
object contaminated with spores

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3
Q

virulence factor of tetanus

A

tetanolysin- destroys blood cells
tetanospasmin (increases excitability of neurones leading to parlaysiis ) it is a neurotoxin . it blocks the inhibitory neurones meaning the production of ACH is uncontrolled due to less gaba produced

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4
Q

symptoms of tetanus

A

first symptom is usally pain around the site

trismus ( jaw lock)
rises sardinicus due to spasm of facial muscles
opisthotonus
very severe spasms that can even cause bone fractures
spasms are painful
fever , tachy, hypertentsion

difficulty swallowing
s.o.b

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5
Q

treatment tetanus

A

penicillin

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6
Q

prophylaxis

A

DPT vaccine which includes toxoids of sipstheira and tetanus and killed pertussis or angins of pertussis (double check)

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7
Q

who’s at risk for tetanus

A

neonates via the umbilical stump and very fatal >90%, caused by when the mother did not pass protective ab’s to baby , babies will have optihstonun

foreign body in wound

exposure to soil or manure

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8
Q

types o tetanus

A
  1. descending type - most common has a shorter incubation period and worser prognosis
  2. ascending type - opposite
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9
Q

spores of tetanus

A

remain viable soil for many years, they are heat stable to kill them you need to autoclave them at 121 for 15 mins . however the vegetative forms are heat liable

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10
Q

diagnosis of tetanus

A

wound exudates

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11
Q

prognosis of tetanus

A

ortality is high once the stage of lock- jaw has been reached.

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12
Q

types of patients you will meet

A

Patients who were immunized as a child and re- ceived periodic boosters but the last shot was more than 10 years ago. These patients are given another booster.
2) Patients who have never been immunized. Not only do these patients need a booster, but they should also receive preformed antibodies to the tetanus toxin called human tetanus immune globulins.
3) Patients who come to the hospital having already developed tetanus. The big picture is to clear the toxin and the toxin-producing bacteria and to keep the pa- tient alive until the toxin has cleared. This is accom- plished in the following 5 steps of therapy:
a) Neutralize circulating toxin with human tetanus immune globulins.
b) Give an immunization booster to stimulate the patient’s own immune system to develop anti- tetanus toxin antibodies.
c) Clean the wound, excising any devitalized tis- sue, to remove any remaining source of Clostridium tetani.
d) Antibiotics (penicillin) may help to clear the remaining toxin-producing bacteria.
e) Provide intensive supportive therapy until the toxin is cleared. Muscle relaxants may have to be
administered, and the patient may have to be placed on a ventilator.

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13
Q

what type of disease is bacillus anthrosis

A

a zoonoses affects humans and animals such as herbivores sheep and cows and horses . it mainly affects animals!

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14
Q

mb anthrax

A

the same as tetanus gram + rod
has a capsule - the only bacteria with a protein capsule and has spores but is an adobe unlike clostridium

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15
Q

why is anthrax so important

A

because it can be used a weapon for terrorism bio in 2001 spores sent on letter s in the US , because of its small size (enough to inhale) stability in environment and 100% fatality in pulmonary hemorrage . it was used by the japense army

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16
Q

SPORES. of bacillus

A

just like tetanus they survive for years and only destroyed by autoclaving but vegetative forms are heat labile

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17
Q

how do humans catch anthrax

A

direct contact with spores in soil
alimentary route - contaminated meat
respiratory route
skin - has to be a break into the skin
handling contaminated animal products like fur and wool

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18
Q

forms of anthrax

A

skin- most common erythema (BLACK) without tx up to 20% can die but with tx rarely fatal
pulmonary - hemorragic pneumonia (most sever) by inhalation of spores
intestinal - eating contaminated meat
septic - complications of. above

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19
Q

diagnosis anthrax

A

microscopy: bamboos stick appearance
culture from respiratory sections, cutaneous
pcr , elisa

20
Q

vaccine for anthrax

A

live vaccine but controversial
animals obligatory vaccination

its not typically available to the general public but for people at increased risk

21
Q

tx anthrax

A

penicillin its still sensitive too
doxycycline

22
Q

virulence factors of anthrax

A

The exotoxin contains 3 separate proteins, which by themselves are nontoxic but together produce the systemic effects of anthrax:
edema facto
lethal factor
protective factor

23
Q

can anthrax spread from person to person s

A

Inhalation (lung) anthrax is not spread from person to person. Even if you develop symptoms of inhalation anthrax, you are not contagious to other persons. If you develop cutaneous (skin) anthrax, the drainage from an open sore presents a low risk of infection to others. The only way cutaneous (skin) anthrax can be transmitted is by direct contact with the drainage from an open sore.rare cases reported. Anthrax is not spread from person to person by casual contact, sharing office space or by coughing and sneezing.

24
Q

spores definition

A

A spore is a dormant form that certain bacteria take when they have no food supply. Spores can grow and cause disease when better conditions are present, as in the human body

25
Q

where is bacillus naturally found

A

in the soil like tetanus

26
Q

anthrax in history

A

Robert Koch uses anthrax to develop his famous Koch Postulates - demonstrate a causal relationship between a specific microorganism and a disease.

later

1881 - Louis Pasteur creates the first vaccine for anthrax

27
Q

epi on anthraz

A

sub Saharan africa

28
Q

anthrax in Bulgaria

A

On 21 July 2015, Bulgaria reported a fatal case of Bacillus anthracis infection in a 53-year-old breeder of sheep and cows;
He died on 17 July in Varna after having slaughtered a sick cow. Further investigations revealed that a meat processing plant used contaminated meat from the sick animal to prepare sausages.
Bulgarian authorities implemented control measures, minimizing the risk of further spread of the infection.
Exposure to the infected animal or its meat occurred only at a local level, and there were no reports of international distribution of possibly contaminated meat.
The event was rated as a negligible risk for other EU/EEA countries.

29
Q

how do animals get affected with anthrax

A

by spores in the soil,

30
Q

IP period of anthrax

A

usually 5-7 days

31
Q

new form of anthrax

A

Since 2009, anthrax has emerged among heroin users in Europe, presenting a novel clinical manifestation, ‘injectional anthrax’, which has been attributed to contaminated heroin.
Before 2009, only one such case had been reported.
In 2009–2010, Scotland experienced the largest ever outbreak of injectional anthrax, with 119 cases identified. A few cases, most likely linked to the same contaminated batch of heroin, were also reported in Germany and the UK.

32
Q

vaccination of anthrax schedule

A

for those at high risk Five IM injections - at day 0, week 4, months 6, 12, and 18.
After the 6 month dose (3 doses), the vaccine recipient is considered protected and can work in areas where there is a risk of exposure to anthrax.
Annual booster - are recommended for ongoing protection.

33
Q

contact persons

A

Anthrax vaccine is also recommended for unvaccinated people who have been exposed to anthrax.
The vaccine has not been studied or used in children less than 18 years of age (informed consent from parents).
These people should get 3 doses of vaccine together with recommended antimicrobial drugs (doxycycline, ciprofloxacin, levofloxacin):
-the first vaccine dose as soon after exposure as possible,
-the remaining doses 2 and 4 weeks after the first.

34
Q

people at risk for anthrax

A

veterinarian
military personnel
livestock handlers

35
Q

what to do if you suspect a dead animal

A

Report to authorities - In animal farms, owners or workers should report any unexplained fever or new skin lesions to their health care provider and describe any recent contact with suspected sick animals.
Quarantine the area - Make sure there is minimal contact with the carcass by establishing a quarantine area, generally for 21 days after the last anthrax death.
Do not open carcass
Minimize contact
Wear protective clothing
Latex gloves, face mask
Vaccination of susceptible animals

Burn or bury carcasses, bedding, other materials
Decontaminate soil - with 5% lye or quicklime (anhydrous calcium oxide), hydrogen peroxide, peracetic acid or gluteraldehyde
Remove organic material and disinfect structures
In all these cases - Protective clothing should be worn!!!

36
Q

final disinfection in th case of anthrax

A

For final disinfection, one of the following disinfectants should be applied at a rate of 0.4 liters per square meter for an exposure time of at least 2 hours:
10% formaldehyde (approximately 30% formalin);
4% glutaraldehyde (pH );
3% hydrogen peroxide;
1% peracetic acid.
Hydrogen peroxide and peracetic acid are not appropriate if blood is present. When using glutaraldehyde, hydrogen peroxide or peracetic acid, the surface should be treated twice with an interval of at least one hour between applications. Formaldehyde and glutaraldehyde should not be used at temperatures below 10°C.
After the final disinfection, closed spaces such as rooms or animal houses should be well ventilated before use. The effectiveness of the disinfection procedure cannot be assumed and attempts should be made to confirm it has been adequate by means of swabs and culture.

37
Q

IP tetanus

A

around 8 days

38
Q

correlation to IP and nervous system

A

In general the further the injury site is from the central nervous system, the longer is the incubation period.
-Shorter incubation periods are associated with a higher chance of death.

39
Q

clinical forms of tetanus

A

cephalic (rare)- occasionally occurring with otitis media in which C. tetani is present in the flora of the middle ear, or following injuries to the head. difficulty swallowing and rigidity o abdominal muscles

local

generalised: descending type, causing truisms and commonly involves cranial nerves espaiclly fo the face

40
Q

the immunity of tetanus

A

People who recover from tetanus do not have natural immunity and can be infected again and therefore need to be immunized!!!!

Active immunization with tetanus toxoid should begin or continue as soon as the person’s condition has stabilized.

41
Q

vaccination for tetanus

A

6 doses (3 primary plus 3 booster doses) of tetanus-toxoid-containing vaccines (TTCV) through routine immunization!!!

42
Q

diagnosis of tetanus

A

C. tetani is recovered from the wound in only 30% of cases and can be isolated from patients who do not have Tetanus.

The diagnosis is entirely clinical and does not depend upon bacteriologic confirmation.

43
Q

toxid vaccine

A

There are two types of toxoid available:
- adsorbed (aluminum salt precipitated) toxoid
fluid toxoid.
Although the rates of seroconversion are about equal, the adsorbed toxoid is preferred because the antitoxin response reaches higher titers and is longer lasting than that following the fluid toxoid.

44
Q

boosters for teteanus

A

Antitoxin levels decrease with time. While some persons may be protected for life, by 10 years after the last dose, most persons have antitoxin levels that only approach the minimal protective level. As a result, routine boosters are recommended every 10 years.

45
Q

prevent neonatal tetanus

A

Neonatal tetanus can be prevented by immunizing women of reproductive age with TTCV, either during pregnancy or outside of pregnancy.

and using clean instruments on umbilicus