Cardio part 2.1 Flashcards

1
Q

what is a hTN emergency

A

anything over 180 systolic and 120 or above

pt may have severe HQ , retinal hemorrhage and papilledema

changes in sensorwmun and decreased levels or consciousness and seizure can occur
* go to emergency with any of these findings

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2
Q

what is primary hypertension-

A
  • silent killer
  • (0-95%)
  • HTN with no underlying causes
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3
Q

what causes secondary HTN

A

d.t chronic renal failure and or stenosis of renal arteries

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4
Q

what happens to the kD during HTN

A

increases renin and angiotensin

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5
Q

reasons for 2 HTN

A
There are multiple etiologies for secondary hypertension including but not limited to:
Medications such as NSAIDs
Sleep apnea
Pheochromocytoma
Hyperaldosteronism (Conn's syndrome)
Cushing's syndrome 
Hyperparathyroidism
Acromegaly
Hyperthyroidism/ Hypothyroidism
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6
Q

Reno vascular HTN

A

high blood pressure caused by narrowing of the arteries supplying the kidneys. It is a form of secondary hypertension - a form of hypertension whose cause is identifiable. RAS induces renin secretion that causes the angiotensin conversion, causing aldosterone release and then water retention and potassium depletion.

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7
Q

potential mechanisms for 1 HTN

Na+

A
  • abn NA+ transport d.t defect in or inhibition of the Na-K pump
  • Inc, cellular perm. to Na+
  • net result is an increased intracellular sodium which may make the cell more sen
  • SM contracts stronger
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8
Q

Potential cause of 1 HTN ca+

A

genetic condition inherited as a dominant trait that results in abnormal connective tissue, due to production of abnormal fibrillin-1 protein.
This syndrome is noted in 5–9% of all individuals who develop aortic dissection.
Individuals with Marfan’s syndrome tend to have aneurysms that are localized to the aorta relative to other vessels and are more prone to proximal dissections of the aorta

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9
Q

Potential cause of HTN

renin-angiotension

A

genetic condition inherited as a dominant trait that results in abnormal connective tissue, due to production of abnormal fibrillin-1 protein.
This syndrome is noted in 5–9% of all individuals who develop aortic dissection.
Individuals with Marfan’s syndrome tend to have aneurysms that are localized to the aorta relative to other vessels and are more prone to proximal dissections of the aorta

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10
Q

What is the most common cause of renal disease

the second most common cause

A

HTN

DM

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11
Q

how does renal dz contribute to HTN

A

increased production of renin which results in salt retention and systemic vasoconstriction

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12
Q

HTN is the leading cause of what

A

ischemic heart dz, PVD, cerebrovascular dz, ventricular hypertrophy and CHF

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13
Q

What are the 3 types of hypertension

A

labile, benign, accelerated

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14
Q

Labile HTN

A

BP elevations which are inconsistent. Individuals that have increased Catecholamines form seeing doc “white coat HTN”

-can occur with pheochromocytoma ( usu dramatic event)

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15
Q

how do pt with pheochromocytoma present

A
  • paroxysmal HA, sweats, palpitations, HTN and orthostatic hypotension
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16
Q

what is pheochromocytoma?

A

tumor on the adrenal gland

17
Q

Benign HTN

A
  • potential sequelae of long standing HTN include MI, stroke, renal disease and renal failure, peripheral vascular disease and blindness,
18
Q

What is an Aneurysm

A

ballooning out” of an a vessel wall due to underlying weakness of the wall and/ or the force of increased blood pressure.

19
Q

Where to Aneurysms occur

A
  • in any vessel but arteries more common.
  • aorta and the circle of Willis are vessels in which aneurysm development has the greatest potential for increased morbidity and mortality
20
Q

what is a berry aneurysm

A

occurs where there is a greater degree force compared to the surrounding ares. I.e circle of willis, where there are a lot od branches

21
Q

describe an aortic dissection

A

extremely severe and potentially life threatening comp. HTN
Dissection usu. through the medial tissue layer of the aorta and can affect the ascending aorta, the aortic arch, descending aorta and abdominal aorta.

22
Q

how does a pt with aortic dissection ptc

A

excruciating pain the may be resistant to tx w/ very large morphine

-immediate blood pressure control must be achieved

23
Q

MArfans- diseases

A
  • genetic condition dominant- production of abnormal fibrillin-1 protein.
  • This syndrome is noted in 5–9% of all individuals who develop aortic dissection.
  • tend to have aneurysms that are localized to the aorta relative to other vessels and are more prone to proximal dissections of the aorta
24
Q

Marfans characteristics

A

Marfan’s patients are often very tall individuals with long extremities and especially long digits.
Collagen abnormalities in the vessel wall result in the vessel becoming extremely vulnerable to damage and particularly susceptible to aortic dissection.

25
Q

what are the most serious signs of marinas

A

The most serious signs and symptoms associated with Marfan’s syndrome involve the cardiovascular system and include new onset fatigue, shortness of breath, heart palpitations, tachycardia and new onset murmur.
The signs of regurgitation from prolapse of the mitral or aortic valves can occur as a result of collagen degeneration of the root of these valves.

26
Q

Define CHF

A

condition in which the heart is unable to pump enough blood to meet the body’s metabolic

the heart’s must pump blood coming into the ventricles from the lower pressure venous system against the higher pressure arterial system.

  • you can have forward to backward failure- can’t push blood forward. can get blood out thats coming in
27
Q

what does CHF cause

A

inadequate emptying of blood at the venous side and inadequate blood delivery to both the pulmonary and system circulation

28
Q

LCHF

A

pulmonary edema