Miscellaneous Flashcards

1
Q

Name 3 risk factors for a BSI

A

1) Age
2) Immunocompromised
3) Number of procedures
4) Malnutrition
5) Multiple underlying conditions

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2
Q

What are two common sources of VADA BSI?

A

1) Colonization of the VAD
2) Colonization of the fluid through the VAD

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3
Q

Name three of the four ways extrinsic microorganisms gain access to a sterile space in the body.

A

1) Contaminated fluid injected
2) Skin flora at injection site
3) Catheter hub (part where meds are plugged into)
4) Intrinsically - infections elsewhere in the body can travel through the blood to the site of the VAD

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4
Q

Name three of the 4 most likely pathogens that cause pneumonia.

A

1) Staph aureus
2) Strep Pnemo
3) H-Flu
4) Moraxella

Other less common: Legionella, Chlamydia, Mycroplasm. TB can mimic pneumonia.

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5
Q

3 Risk factors for MDRO Colonization

A

1) hospitalization for >=5 days
2) immunocompromised
3) Antimicrobial therapy in preceding 90days
4) Risk factors for HCAP
5) High frequency of antibiotic resistance in community

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6
Q

3 ways to prevent atypical pneumonia? (not cause by the 4 main microorganisms)

A

1) Avoid endotrachael intubation
2) Subglottic secretion drainage
3) Reduced usage of nasogastric tubes
4) Enteral feeding 24-48hrs after intubation

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7
Q

3 risk factors for VAP

A

1) Head not elevated
2) Poor oral hygiene
3) Emergent intubation
4) Route or intubation - endotrachael is a risk factor)
5) Etomidate - short acting anesthesia

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8
Q

CDC classification of SSIs: Name the three types of cut location and describe them

A

1) Superficial incisional- skin + subcutaneous
2) Deep Incisional - Muscle + Fascia
3) Organ - organs

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9
Q

CDC classification of SSIs: Name the four types of wounds and describe.

A

Class 1 - Clean (C)
- uninfected wound
- resp, alimentary, genital or urinary tract are not entered
Class 2 - Clean Contaminated (CC)
- resp, alimentary, genital or urinary tract were entered. No unusual contamination
Class 3 - Contaminated (CO)
- Open, fresh, accidental wounds
Class 4 - Dirty Infected (D)
- old traumatic wounds with devitalized tissue and those that involve an existing clinical infection or perforated viscera

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10
Q

Required documentation for an IPCP

A

1) A documented IPCP
2) at least one trained IP
3) antibiotic stewardship program
4) QAPI program

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11
Q

3 of the 5 attributes outlined by the US National Patient Safety Foundation for all healthcare organizations to strive to implement

A

1) All HCP accept responsibility for safety
2) Safety priority over financial and operational goals
3) Org encourages/rewards identification of safety issues
4) Learning from accidents
5) Money allocated to maintain effective safety systems

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12
Q

Name the two subtypes of skill-based errors.

A

1) Slip - external failure (reduced intentionality)
2) Lapse - internal failure (memory failure)

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13
Q

How often should a risk assessment be performed?

A

Annually and whenever new risks arise.

Annual summary should also be shared and go over cost savings and outcomes. This should also be reviewed as part of the QAPI program

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14
Q

Name 5 vulnerable populations

A

1) immunocompromised
2) pregnant
3) dialysis
4) pediatric
5) elderly

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15
Q

4 common types of dialysis-associated infections

A

1) access site infections
2) bacteremia
3) peritonitis
4) BBP - HBV, HCV, HIV

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16
Q

Toddlers younger than 2 have a ________ immunity response to ________, putting them at increased risk to what 3 pathogens?

A

Decreased
Polysaccharide Antigens

Strep pneumonia
H-Flu
Nisseria meningitidis

17
Q

When would someone typically have low granulocytes (granulocytopenia)?

A

Cancer treatment, bone marrow condition

18
Q

What is the difference between cell-mediated immunity and humoral immunity?

A

Humoral immunity involves antibodies primarily driven by B-cells.

Cell-mediated is driven by T-cells, macrophages, and cytokines.

19
Q

Name 3 Medical treatments or medical conditions that may result in impaired immunocompetence.

A

1) Active treatment of tumor or hematologic malignancies (blood cancer)
2) Hematologic malignancies (leukemia, lymphoma)
3) Receipt of organ transplant and taking immunosuppressive therapy
4) Receipt of T-cell therapy or stem cell transplant within 2 years
5) Moderate or severe immunodeficiency
6) Advanced or untreated HIV/Aids (CD4 cell count <200cells/mm3)
7) Active treatment with high-dose corticosteroids, chemo treatment, tumor necrosis factor blockers.

20
Q

Are participation of QAPI programs based in one institution or not limited to one institution?

A

Based in one institution, but national scale is possible.

Implementation science is not limited to one institution and often is national.