Module 2: infection Med Surg readings Flashcards

1
Q

PPT: clinical presentation of infection. how does it differ from inflammation

A
Redness
Swelling
Pain
Warmth
Exudate

On the slides inflammation does not have exudate

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

are all infectious diseases communicable?

A

no.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

an infectious disease is…

A

any disease caused by the growth of pathogenic microbes in the body

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

?components of chain of infection

A
  1. causative organism
  2. reservoir
  3. mode of exit (portal of exit)
  4. route of transmission
  5. susceptible host
  6. portal of entry
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

infection definition

A

a condition in which the host interact physiologicaly and immunologically with a microorganism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

whats the primary source of info about bacterial infections?

A

lab reports

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

clinical evidence of infection

A

redness, heat, pain and lab evidence of WBCs on the wound specimen smear.

Infection is recognized by the host reaction as well as the lab evidence

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

?when the host interacts immunologically with an organism but doesnt have symptoms do they have an infectious disease?

A

no. Infectious disease is the state in which the infected host displays a “decline in wellness” due to infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

colonization=

A

microorganisms present without host interference or interaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

as markers for the likelihood of infection what markers generally provide the most helpful information and why?? not lab tests but part of microbiology report

A

the smear and the stain because they describe the mix of cells present at the anatomic site at the time of specimen collection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

3 components of microbiology report

A

the smear the stain
antimicrobial sensitivity
the culture and organism identification

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

?when to wash hands instead of using ABHR

A

visibly soiled
after toilet
norovirus
C diff

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

?Airborne precautions used for

A
  • Chickenpox
  • TB
  • Measles
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

?what type of organism do you use contact precautions for?

A

c. difficile

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

?antibiotic resistant organisms examples

A
MRSE, 
VRE, 
C DIFF also 
extended spectrum beta lactamase 
carbapenemase producers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

?C difficile

A

C difficile
o Spore forming bacterium-freq cause of HA diarrhea.
o Usually preceded by antibiotic use that disrupts the usual intestinal flora
o Spread fecal-oral
o Treat w vancomycin often. Or new fecal transplants

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

?MrSA

A
MRSA
o	Resistant to methicillin
o	Healthcare assoc and community assoc
o	Fear its becoming VRSA
treat w vanomycin or linezolid
18
Q

?VRE

A

VRE
o Gram positive bacteria that live in the GI tract and commonly found in env
o May be colonized but not have symptoms considered infected once symptoms present
o Tx with penicillin formulation

19
Q

without running tests, what can you assess to gain info to determine if the pt has an infection?

A

health history and physical exam

20
Q

when taking health hx what type of questions do you ask to obtain information about possible infection? (17)

A
  • vaccinations
  • occupation
  • hobbies
  • travelling
  • sex hx
  • substance use hx
  • insects/animals/farms
  • past hx of infectious disease
  • fever
  • cough
  • TB? tests exposure etc
  • pain
  • edema
  • dirrhea, vomiting, abdominal pain
  • rash
  • exposure to others
  • meds-antibiotics-corticosteroids, immunosuppressants-chemo
21
Q

?generalized signs of chronic infection may include

A

-significant weight loss or pallor asso w anemia of chronic diseases

22
Q

acute infection may manifest w

A

fever
chills
lymphadenopathy
rash

23
Q

potential complications from infection

A
septicemia, bacteremia, sepsis
septic shock
dehydration
abscess formation
endocarditis
infectious disease related cancers
infertility
congenital abnormalities
24
Q

nurses role in teaching about the infectious process

A
  • encourage immunizations to parents, immunocompromised, older adults over 65, disabled or chronically ill, those in nursing homes
  • may be duty to report cases of infection to public health agencies
  • get vaccinated
  • teach to take accurate fever measurements
  • educate about prevention
25
Q

how should you monitor fever?

A

graph it to see the trends, it gives clues to infection severity, and whether it responds to therapy

26
Q

?what should you be alert for in the vital signs of someone with septic shock
what other 4 things should you monitor

A
fever, tachycardia, tachypnea, evidence of dec perfusion or dysfunction of vital organs in the form of 
1-change in mental status 
2. hypoxemia (ABG)
3. elevated lactate levels
4. urine output less than 30ml/hr
27
Q

? who should you teach endocarditis prevention to (inflammation of the endocardium)

A
pts with:
-valvular disease
-congenital heart disease
-intracardiac prosthesis
-previous endocarditis
(these people are at risk of seeding of the cardiac valves during procedures that can cause bacteremia)
28
Q

when is it best to give antibiotics

A

as early as possible

29
Q

?sepsis=

A

Sepsis is a potentially life-threatening complication of an infection. Sepsis occurs when chemicals released into the bloodstream to fight the infection trigger inflammatory responses throughout the body.

30
Q

?symptoms of sepsis

A

the patient typically develops fever, tachycardia, tachypnea, and leukocytosis.

31
Q

Procalcitonin=

how is it used?

A

Procalcitonin (PCT) is a peptide precursor of the hormone calcitonin.Procalcitonin (PCT) is a highly specific marker for the diagnosis of clinically relevant bacterial infections and sepsis. It doesnt elevate significantly with viral infections. If elevated more than 2 nanograms/ml it should be sepsis.

32
Q

diagnostics for inflammation

A
  • c-reactive protein
  • WBC differential
  • WBC count
33
Q

diagnostics for infection

A
White blood cell count
Differential
C-Reactive Protein
Procalcitonin
Identification of an organism
Gram stain
Culture
34
Q

describe culture and sensitivity

A

Culture and Sensitivity. A culture is done to find out what kind of organism (usually bacteria) is causing an illness or infection by looking at size, shape, and color using gram stain and microscope. Culturing can also enable a bacterial count to be made, which can assist in deciding whether a wound is colonised or infected.
A sensitivity test checks to see what kind of medicine, such as an antibiotic, will work best to treat the illness or infection. If the organism grows up to a disc it is resistant to that antibiotic; if there is a clear zone around the disc it is susceptible. This can confirm a patient is on the correct treatment or not and can further help with identification e.g. methicillin-resistant Staphylococcus aureus (MRSA).

35
Q

WBC differential

A

Differential:Neutrophils
pyogenic infections

Eosinophils
allergic disorders & parasitic inf’ns

Basophils
parasitic inf’ns &
some allergic disorders

Lymphocytes
viral infections

Monocyte
severe infections (phagocytosis)
36
Q

PPT:WBC count

A

Complete count is both diagnostic and prognostic. It will be elevated in infection, inflammation, tissue necrosis, and (leukemic neoplasia). If very decreased indicates bone marrow failure.
Lifespan of WBC is 13-20 days
Destroyed by lymphatic system, excreted in feces

37
Q

neutrophils inc in

A

Neutrophils

pyogenic infections

38
Q

eosinophils inc in

A

Eosinophils

allergic disorders & parasitic inf’ns

39
Q

\Basophils inc in

A

Basophils
parasitic inf’ns &
some allergic disorders

40
Q

lymphocytes inc in

A

Lymphocytes

viral infections

41
Q

monocytes inc in

A
Monocyte
severe infections (phagocytosis)