HTN Flashcards

1
Q

Definition

A

Constant increase in systolic blood pressure(SBP)and or diastolic blood pressure(DBP) values are both values considered normal for age and sex

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2
Q

Generally over____ by conventional office BP measurement

A

140/90 mmHg

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3
Q

Automated Multiple BP(AOBP)=

A

3-6 meas(>3)/4-7 min

Patient alone in the examination room

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4
Q

Threshold values =

A

135/85 mmHg( 131/85 mmHg - 140/90 mmHg)

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5
Q
  1. Feocromocytoma (1)
A

mechanism: excess and autonomic secretion of catecholamines
⊕ inotropism
↑ PVR
Clinical:
HTA with different patterns (depending on the type and mode of secretion)
Mild chronic sistolo-diastolic HTA
HTA paroxysms on a background of normo/hypertension
!!! orthostatic hTA
Crisis:
can be triggered by lumbar microtraumas, urination, pregnancy, anesthesia, surgery
Symptoms: anxiety, intense headache, palpitations, nonspecific thoracic or even angina attacks
objective: pale, sweaty, arrhythmias

Complications:
acute catecholaminic myocarditis
APE (acute pulmonary oedema)
Arrhythmias
HT encephalopathy or cerebral hemorrhages
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6
Q
  1. Feocromocytoma (2)

Paraclinical

A
paraclinical:
plasma and urinary catecholamine dosing
regitin test
Imaging:
SR glond ultrasound
iv urography
CT/MRI
scintigraphy (meta-I131-benzyl guanidine)
Selective arteriography of SR
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7
Q
  1. Primary hyperaldosteronism
A

mechanism:
1. excess and autonomous secretion of aldosterone
2. retention of Na+ and water
3. iinhibitionR-AT-A

Clinical:

  1. Systolic HTA (mild or moderate)manifestations due to hypoK+:
  2. Arrhythmias
  3. intestinal muscle paralysis (dynamic ileus)
  4. Polyuria
  5. metabolic alkalosis
paraclinical:
1.hipoK+ (<3,5 mEq/L)
2.hiperpotasiuria (> 30 mEq/L)
↑ increased serum and urinary concentration of aldosterone or its metabolites
3.low PRA (plasma renin activity)
4.CT/RMN/Scintigrafie (Scintandren)
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8
Q

VI. Secondary forms of HT

A

Complementary paraclinical explorations
Required in a limited group of hypertensive people, which requires special evaluation for the diagnosis of a secondary HTA:

  1. Patients in whom history, physical examination or common laboratory data, suggest a cause of secondary HT.
  2. Stable HT in young people (under 35–40 years) or adolescents, where the prevalence of secondary HT is particularly high.
  3. HT with poor response or “resistance” to correct treatment.
  4. Accelerating or suddenly worsening HT
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9
Q

History of snoring + daytime sleepiness + morning headache

A

OSA

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10
Q

Repetitive episodes of sweating + pulsating headache + anxiety + palpitations

A

pheochromocytoma

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11
Q

Episodes of muscle weakness and tetany

A

HYPERALDOSTERONISM

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12
Q

secondary HT screening

clinical examination

A

Cushing symptom
acromegaly
pheochromocitoma
myxedema

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13
Q

Palpable abdominal formations

A

polycystic kidneys

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14
Q

reduction/delay/absence of pulse mb

A

coarctation of Ao, aortic disease, BAP

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15
Q

Abdominal breaths

A

stenosis of A.Renal

- Precordial /thoracic sulfels ->coarctation of Ao,aortic disease,stenosis A.subclavie

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16
Q

Arrhythmic heart noises

A

primary hyperaldosteronism with severe hypoK

TA mara differential between the two arms