finale Flashcards

(34 cards)

1
Q

Shock

A

Inadequate cellular energy production caused either by poor oxygen delivery or increased cellular oxygen consumption.

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2
Q

Decreased oxygen delivery (DO2)

A

Diminished tissue perfusion

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3
Q

Increased oxygen consumption (VO2)

A

Increased cellular metabolism (heat stroke, sepsis, seizures/ tremors, etc.)

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4
Q

Why does energy production decrease?

A

No O2 = shift to anaerobic metabolism.

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5
Q

Determinants of DO2?

A
Cardiac output (HR+SV) x
CaO2 (Hgb,SaO2,PaO2)
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6
Q

Shock Classifications

know about each – causes and clinical examples

A
Cardiogenic
Hypovolemic
Obstructive
Distributive/ Vasogenic
(“Call Help or Die”)
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7
Q

Shock Stages

know about each – clinical signs and outcome

A

Compensatory
Early Decompensatory
Decompensatory (Terminal)

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8
Q

How do Cats Differ?

A

Bradycardia, hypothermia, hypoglycemia, hypotension. Smaller blood volume than dogs.

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9
Q

Overall approach to shock?

A

Must identify and treat the underlying cause, and support patient to treat or prevent SIRS/ other complications.

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10
Q
Where are the following useful for shock treatment?
Pressors
Chronotropes
Fluids
Vasodilators
Contractility
RBC Transfusion
Oxygen therapy
A
Pressors – Increase SVR
Chronotropes – Increase heart rate
Fluids – Increase preload
Vasodilators – Reduce afterload
Contractility – Increase strength of contraction
RBC Transfusion – Increase hemoglobin
Oxygen therapy – Increase dissolved O2
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11
Q

List monitoring parameters for shock (in order of clinical applicability)

A
Mentation
MM color
CRT
Heart rate
Pulse quality
Blood pressure
Urine output
CVP
Acid-base
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12
Q

Upper limits for shock dose of crystalloid and colloid? Know indications for each, and how to adjust if crystalloid and colloid are both used?

A
Crystalloid:
Dogs 80-90 ml/kg, cats 50-60 ml/kg
Colloid: Up to 20 ml/kg
Administer ~25% of dose, reevaluate to treat to end points
Hypertonic Saline: 4 ml/kg
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13
Q

Major drugs for inotropic and pressor support?

A

Dobutamine – Inotrope
Dopamine – Inotrope (lower dose) or pressor (higher dose)
Both given IV CRI

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14
Q

Define Systemic Inflammatory Response (SIRS)

A

A local problem causing systemic inflammation (infectious and non-infectious causes – be able to provide examples). Essentially, an overreaction to inflammation.

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15
Q

What are the major cytokines in SIRS?

A

IL1, IL6, IL8, TNF-alpha, Platelet activating factor

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16
Q

How is multiple organ dysfunction caused?

A

Animal with SIRS has damage to vascular endothelium from activation of coagulation, complement pathways, PGs and LTs

17
Q

Which are the target cells for SIRS

A

WBC, Platelets, Endothelial cells

18
Q

Define multiple organ dysfunction syndrome (MODS)

A

Severe, acquired dysfunction of 2 or more organ systems for > 24-48 hours not due to primary illness

19
Q

What are SIRS criteria

A
Hyperthermia or hypothermia
Tachycardia
Tachypnea
Respiratory alkalosis (low PaCO2)
Leukocytosis or leukopenia, left shift
20
Q

SIRS treatment?

A

Antibiotics
Gastric protectants and nutrition (to avoid gastric barrier breakdown)
Positive pressure ventilation (ARDS)
Anticipate and avoid complications
Critically ill – require 24-hour care facility and monitoring

21
Q

Zoonosis vs. Anthropozoonosis

A

Zoonosis: Found in animals, transmissible to people
Anthropozoonosis: Found in people, transmissible to animals

22
Q

Methcillin-resistant Staph aureus (MRSA)

A

One member of a group of bacteria which are highly resistant to common classes of antibiotics. Also includes MRSPseudintermedius. Zoonotic and anthropozoonotic. Therefore, infection can be harbored and cause re-infection.

23
Q

Biosecurity

A

Active steps to prevent introduction of hazardous threats (biological, chemical, etc.) into an environment.

24
Q

Identify 2 sources discussed in class of free, online resources available to veterinarians to develop sound infection control practices

A

National Association of State Public Health Veterinarians website (Model infection control document) and Canadian Committee on Antimicrobial Resistance (Infection Prevention and Control Best Practices document)

25
Identify and describe 3 levels of infection control in an infection control plan
Engineering controls: Physical facility design to facilitate hygiene/ prevent human error Administrative controls: Written policies/ procedures developed to address various aspects of infection control Personal protective equipment: Contains, but does not eliminate, a hazard
26
What is the role of the Infection Control Practitioner?
Addresses all aspects of the infection control plan, alters the plan to address changes in infection landscape, and enforces adherence to institutional policy.
27
In a 2008 survey of veterinarians, what risk was identified for respondents without a written infection control policy (ICP)?
Lack of a written ICP = poor infection control practice.
28
What is the single most important infection prevention tool?
Appropriate hand hygiene (hand washing, alcohol-based hand sanitizer use)
29
What is the cardinal rule of disinfection?
Organic matter must be cleaned from the environment before disinfection can work.
30
What is a nosocomial infection?
Infection that is not present or incubating at the time of admission to a healthcare facility
31
What is the difference between active and passive surveillance?
Passive surveillance: Ongoing assessment tool to identify nosocomial populations and detect serious threats by reviewing medically indicated test results. Active surveillance: Proactive protocol of performing testing to identify specific bacterial threats or evaluate hygiene programs
32
Tentorium herniation | Loss brain fn progression
Ro➡️Ca: CPPDR ``` Consciousness Posture/tone Pupils Dolls eye Respiration ```
33
Stage tentorium herniation
DMPM Dienceph Midbrain: 👀 CN 3 Pons: 🚫 dolls eye Medulla ➡️ foramen magnum ☠️
34
Head trauma tx
🚫 GCC ✅sedate: ace/opiates/diazepam ✅hypertonic saline ✅mannitol