Biodefense and antibiotics Flashcards

1
Q

What are the labs that we need?

A
  1. Plasma proteins–> C reactive protein and erythrocyte sedimentation
  2. Leukocytosis
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2
Q

Tell me about C-reactive protein

A

Lab value should be < 1.0
Predictor for CV events Hi risk >3.0
Does not rise with viral infections
Used to dx bacterial infections inflamm, d/o’s such as RA

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3
Q

Tell me about erythrocyte sedimentation rate

A

Non-Specific
Indirect measure of inflammation
As auto immune disease worsens it increases, falls with in improvement
Acute phase lab finding=inflammation response

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4
Q

Tell me about leukocytosis

A

WBC’s greater than 10,000

Will look at different types of WBC’s

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5
Q

What is IgE?

A

Principal antibodies in allergic response and parasitic infection

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6
Q

What is a hypersensitivity reaction? How are they broken down?

A

A reaction that can occur quickly or hours to days after re- exposure
types 1,2,3 require antibodies
type 4 require T cells
(you can’t have an allergic rxn unless you have been exposed to it before)

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7
Q

describe anaphylaxis

A

a severe reaction after RE-EXPOSURE
Most serious allergic reaction to antimicrobials
Symptoms include hives, edema, choking sensation, chest pain, SOB, No
tx Includes epinephrine SQ

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8
Q

What is a type 1 reaction?

A
IgE mediated
Immediate <1hr onset 
Anaphylaxis and or hypotension
Penicillin most common 
Larger # of IgE produced in response to allergens Get mast cell degranulation, histamine release, leukotrienes
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9
Q

What is a type 2 Reaction?

A

A tissue specific reaction
think blood transfusions, The more blood transfusions that someone has the more antibodies they get, It’s harder to find a match

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10
Q

What is a type 4 reaction?

A

A localized reactionSuch as poison ivy TX Oral prednisone

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11
Q

Describe pathogenic defense mechanisms

A
  1. Compete with normal flora
  2. produce toxins/enzymes
  3. avoid opsonization
  4. destroy CT
  5. Avoid lysis
  6. stop complement cascade by degrading complement protein
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12
Q

What are viruses?

A

Are intracellular parasites, do you not have organelles necessary for reproduction
Replicate by taking over host self

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13
Q

Factors that influence development of infection

A
  1. Entry portal (spread is easy through blood and lymph)
  2. MOA (How does the damage cells)
  3. Infectivity (Ability to enter and replicate)
  4. Pathogenicity (Ability to produce disease)
  5. Virulence (Speed of replication)
  6. Toxigenicity (Production of toxins)
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14
Q

What are the four stages of infection?

A
  1. Incubation (from initial exposure to the onset of the first signs and symptom)
  2. Prodromal (Initial symptoms which are often very mild)
  3. Invasion (Immune in inflammatory responses are triggered and symptoms of pathogen replication)
  4. Convalescence (Either successful termination of the infectious disease or latency phase with potential for reactivation)
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15
Q

What are the clinical manifestations of infectious disease?

A

Variable depending on the pathogen, organ system affected, and severity
Fatigue, weakness, LOC, Generalize aching, Loss of appetite, Fever
Leukocytosis (Increase white blood cell)

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16
Q

What is the hallmark of most infectious disease this?

A

Fever, resetting of the hypothalamus

17
Q

What is bacteremia?

A

Presence of bacteria in the blood due to a failure of the body’s defense magnesium
You can have bacteremia and not septicemia

18
Q

What is septicemia?

A

Secondary clinical manifestations blood infection, septic shock, very virulent bacteremia

19
Q

What are antibacterials?

A

Chemicals that killed or suppress the growth of a micro organisms
Known as antimicrobials/antibiotics
also Antivirals antifungal’s antiparasites

20
Q

What is the MOA of antimicrobials?

A

Gain access to target sites,
bactericidal drugs: cause death to the organism
bacteriostatic drugs: prevent pathogen from growing and dividing
some have both

21
Q

Principles of treatment

A

Right antimicrobial for the pathogen
Try to get cultures and sensitivities
Most treatment is empiric based start with broad spectrum

22
Q

Antibiotic resistance occurs when

A

Antimicrobial is unable to reach the potential target sight of its action
Microbe produces an enzyme beta-lactamase (destroys PCN)
host defense mechanisms

23
Q

Super infection

A

Secondary infection, occurs during antimicrobial therapy
Normal organisms destroyed
Ex: getting treated for pneumonia and then get a UTI

24
Q

What factors increase risk for getting super infection?

A

Large doses, more than one antibiotic, broad spectrum drugs

25
Q

Super infection management

A

Discontinue drug being given or replace it
Culture that suspected infected area
Possibly administer an anti-microbial affective against aa new microbe

26
Q

Nursing management for super infections

A

Monitor clients response
Ask about rash, diarrhea?
Educate: Take full course of meds, do not share, do not take leftover for new illnesses

27
Q

Contraindication for live vaccines

A

Fever, diarrhea

28
Q

What are viruses?

A

Non-living agents that contain no cellular organs, Intracellular parasites