Path - Inflammation (Ischemia, Infarcts, Shock, & Atrophy) Flashcards

Pg. 221-22 in First Aid 2014 Sections include: -Ischemia: susceptible areas -Infarcts: red vs. pale -Shock -Atrophy

1
Q

What areas in the brain are susceptible to hypoxia/ischemia and infarction?

A

ACA/MCA/PCA boundary areas;

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2
Q

Explain the general blood supply of watershed areas. What are these areas protected from versus susceptible to in terms of hypoxia/ischemia and infarction? Give 2 organs and specific areas within them to which the concept of watershed areas applies.

A

Watershed areas (border zones) receive dual blood supply from most distal branches of 2 arteries, which protects these areas from single-vessel focal blockage. However, these areas are susceptible to ishcemia from systemic hypoperfusion; (1) Brain - ACA/MCA/PCA boundary areas (2) Colon - Splenic flexure, rectum

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3
Q

What is HIE, and what cells/regions does it affect?

A

Hypoxic ischemic encephalopathy (HIE) affects pyramidal cells of hippocampus and Purkinje cells of cerebellum

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4
Q

What area in the heart is susceptible to hypoxia/ischemia and infarction?

A

Subendocardium (LV)

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5
Q

What 2 areas in the Kidney are susceptible to hypoxia/ischemia and infarction?

A

(1) Straight segment of proximal tubule (medulla) (2) Thick ascending limb (medulla)

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6
Q

What area in the liver is susceptible to hypoxia/ischemia and infarction? Both describe/define and name this area.

A

Area around central vein (zone III)

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7
Q

What 2 areas in the Colon are susceptible to hypoxia/ischemia and infarction?

A

(1) Splenic flexure (2) Rectum

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8
Q

What causes reperfusion injury?

A

Reperfusion injury is due to damage by free radicals

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9
Q

What is another name for red infarcts? In what setting/context do they occur? Give 3 examples of such organs.

A

Red (hemorrhagic) infarcts occur in loose tissues with multiple blood supplies, such as liver, lungs, and intestine; Think: “REd = REperfusion”

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10
Q

In what setting/context do pale infarcts occur? Give 3 examples of such organs.

A

Pale infarcts occur in solid tissues with a single blood supply, such as heart, kidney, and spleen

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11
Q

What is the first sign of shock?

A

First sign of shock is tachycardia

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12
Q

What kind of presentation involving shock would suggest an etiology of sepsis?

A

Shock in the setting of DIC secondary to trauma is likely due to sepsis

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13
Q

What are 3 types of distributive shock?

A

Distributive shock includes septic, neurogenic, and anaphylactic shock

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14
Q

Compare/contract the output failure in Distributive versus Hypovolemic/Cardiogenic shock. Give the change in relevant variables in each case.

A

DISTRIBUTIVE: High-output failure (low TPR, high CO, high venous return); HYPOVOLEMIC/CARDIOGENIC: Low-output failure (high TPR, low CO, low venous return)

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15
Q

Compare/contract the PCWP in Distributive versus Hypovolemic/Cardiogenic shock.

A

DISTRIBUTIVE: Low PCWP; HYPOVOLEMIC/CARDIOGENIC: PCWP high in cardiogenic & low in hypovolemic

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16
Q

Compare/contract the vascular change in Distributive versus Hypovolemic/Cardiogenic shock. Give the relevant clinical presentation/findings in each case.

A

DISTRIBUTIVE: Vasodilation (warm, dry skin); HYPOVOLEMIC/CARDIOGENIC: Vasoconstriction (cold, clammy patient)

17
Q

Compare/contract the use of IV fluids in Distributive versus Hypovolemic/Cardiogenic shock.

A

DISTRIBUTIVE: Failure to increase blood pressure with IV fluids; HYPOVOLEMIC/CARDIOGENIC: Blood pressure restored with IV fluids

18
Q

What is atrophy?

A

Reduction in the size and/or number of cells

19
Q

What are 7 causes of atrophy?

A

Causes include: (1) low endogenous hormones (e.g., post-menopausal ovaries) (2) high exogenous hormones (e.g., factitious thyrotoxicosis, steroid use) (3) low innervation (e.g., motor neuron damage) (4) low blood flow/nutrients (5) low metabolic demand (e.g., prolonged hospitalization, paralysis) (6) high pressure (e.g., nephrolithiasis) (7) Occlusion of secretory ducts (e.g., cystic fibrosis)

20
Q

What hormonal changes cause atrophy? Give at least one example of each change.

A

(1) low endogenous hormones (e.g., post-menopausal ovaries) (2) high exogenous hormones (e.g., factitious thyrotoxicosis, steroid use)

21
Q

What change in innervation causes atrophy? Give an example of this.

A

low innervation (e.g., motor neuron damage)

22
Q

What change in blood flow/nutrients causes atrophy?

A

low blood flow/nutrients

23
Q

What change in metabolic demand causes atrophy? Give 2 examples of this.

A

low metabolic demand (e.g., prolonged hospitalization, paralysis)

24
Q

What change in pressure causes atrophy? Give an example of this.

A

high pressure (e.g., nephrolithiasis)

25
Q

What kind of occlusion causes atrophy? Give an example of this.

A

Occlusion of secretory ducts (e.g., cystic fibrosis)