Week 4 Hospital Acquired Infections/ adaptive immunity Flashcards

1
Q

Name some common viral HCAI?

A

Blood borne viruses- hep B, C, HIV
Norovirus- winter D&V
Influenza
Chicken pox

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2
Q

Name some examples of bacterial HCAI?

A
Staphylococcus aureus - MRSA_ resistant to wide range of ABs
Clostridium difficile 
Escherichia coli
Klebsiella pneumoniae 
Pseudomonas aeruginosa
TB
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3
Q

What are healthcare infection and what characteristics define one

A

Infections that arise as a consequence of providing healthcare
- can be bacteria, virus, fungi, parasites
In hospital onset at least 48hrs after admission- less that this will have been incubating when admitted.
Eg. C diff takes 72hrs

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4
Q

What pt factors predispose people to HCAI?

A

Extremes of age
- premature babies- receive essential antibodies from mother in last 4 weeks of development, poor skin quality, incubation- invasive instruments

Obesity, diabetes, cancer, immunosuppresed, smokers, surgical patient, emergency admission as no prepared.

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5
Q

Describe some pt interventions to prevent HCAI for themselves and spreading to others?

A

Optimise pt condition- stop smoking, treat diabetes well,
Antimicrobial prophylaxis
Hand hygiene

Isolate infected individuals, protect susceptible pts

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6
Q

Describe some healthcare worker interventions to prevent HCAI?

A

Healthy themselves- disease free, vaccinated

Good practice- sterile non touch,Chandigarh hygiene, PPE, Antimicrobial prescribing

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7
Q

In relation to the infection model where can infection prevention intervention occur?

A

Preventing pathogen
Preventing interaction with pt
Preventing spread to others by recognising infection

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8
Q

What are the 4 P’s of infection prevention and how do they apply to hospital acquired infections?

A
  1. Patient- risk factors, interaction with other pts, hc workers and visitors
  2. pathogen- virulence factors- toxins, ecological interactions- other bacteria, ABs
  3. practice- general and specific activities of HC workers, policies, structure,
  4. place- fixed features- where deliver healthcare- no of individual rooms, toilets per pt, variable features- bedding, curtain types
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9
Q

Describe some environmental interventions to prevent HCAI?

A

Space, layout

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10
Q

Describe the use of PPE?

A

Personal protective equipment- gloves, apron, full suit- tailor to suspected infection

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11
Q

What are the characteristics of Clostridium difficile, it’s pathogenesis and management?

A

Gram +ve bacilli,
Opportunistic pathogen- if antibiotic therapy disrupt normal balance of gut flora c.diff dominate causing infection.
Diarrhoea- transported fecal oral route
Possess AB resistance and because of spore forming AB treatment is difficult

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12
Q

What are the characteristics of Staphylococcus aureus with regards to hospital acquired infections and drug resistance?

A

Gram positive cocci
Frequently found in resp tract and skin infections
Methicillin resistant staph aureus is a strain that developed resistance to beta lactam ABs including penicillins and cephalosporins

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13
Q

What are the characteristics of Norovirus?

A

Commonly known as winter vomiting bug - D&V
Most common cause of gastroenteritis
Transmitted by fecally contaminated food or water, by person to person contact or aerosols
Usually self limiting within a few days and not severe

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14
Q

Describe the need for APC’s?

A

T cells cannot recognise pathogens and therefore needs APCs to capture, modify and present pathogens to them in order for T cells to become active - do this by recognising PAMPs

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15
Q

What are some common types of health care associated infections (HCAI)?

A
Gastro intestinal 21%
UTI 20%
Pneumonia 14%
Surgical wound infections 14%
Other 14%
Skin and soft tissue 10%
Primary bloodstream 7%
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18
Q

Describe MHC molecules in relation to microbe presentation?

A

Major histocompatibility complex on APC or HLA in humans

  • this is what the T cell sees, have 6- 3 from each parent
  • present microbe peptides to T cells
  • type 1 found on all nucleated cells
  • type 2 found on dendritic cells, macrophage and B cells and also express type 1
20
Q

Decrease T cells and their role in infection?

A
Produced in bone marrow, mature in thymus 
-CD4+ MHC class 2 activate T helper cell 1 resulting in B cell activation and antibody production alongside macrophage activation leading to phagocytic activity 

-CD8+ MHC class 1 active Cytotoxic T lymphocytes which targets and destroys microbe

21
Q

Describe some features of APCs?

A

Strategic location- for B and T cell interactions
- skin, mucous membranes, lymphoid organs, blood circulation

Pathogen capture- sense and detect what is harmful and not- phagocytosis

Diversity in pathogen sensors - PRR
- intracellular and extracellular pathogens

22
Q

What is the difference between intracellular and extracellular microbes and what response to each generate?

A

Intracellular- viruses = cell pendant immunity- cytotoxic T cells, macrophage and antibodies
Extracellular- bacteria= humoral immunity- antibodies and complement

22
Q

Name some types of antigen presenting cells?

A
  • Dendritic cells- in lymph nodes, mucous membranes, blood- present to T and B cells
  • langerhans cells- on skin, present to T cells
  • macrophages- various locations- present to T cells
  • B cells- in lymphoid tissue- present to T cells
    • to produce different antibodies, without T cells only have IgM, with have IgG
22
Q

Which MHC class is involved with intracellular and extracellular microbes?

A
Intracellular- viruses- class 1 MHC
Extracellular- bacteria- class 2
22
Q

Which T cells response to MHC class 1 and 2?l

A

Class 1 - CD8+ T cells

Class 2- CD4+ T cells

22
Q

Name some clinical problems associated with MHC molecules?

A

Major cause of organ transplant rejection- HLA molecules mismatch, graft vs host reaction

HLA associated and autoimmune disease
- diabetes

Cross reactivity between microbial and host antigens
- rheumatic heart disease, type 1 DM

23
Q

What are the immune functions of the following antibodies-

IgG, IgM, IgA, IgE?

A

IgG- phagocytosis, complement activation, neonatal immunity
IgM- complement activation
IgA- mucosal immunity- prevent attachment
IgE- immunity agains helminth, mast cell degranulation- allergies