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An algorithm for the management of
Resistant Hypertension
Is the patient compliant
No Yes
Is the regimen adequate
No Yes
Are drugs interactions possible
An algorithm for the management of
Resistant Hypertension
Are drugs interactions possible
Yes No
Does the patient have pseudohypertension
Yes No
Does the patient have office
hypertension
An algorithm for the management of
Resistant Hypertension
Does the patient have office hypertension
Yes No
Has secondary hypertension been excluded
Yes No
Alter regimen empirically
BP Controlled BP not Controlled
Evaluate mechanisms and alter regimen appropriately
Secondary causes
Renal parenchymal disease
(Polycystic Kidney Disease)
Renovascular hypertension
Primary aldosteronism
Pheochromocytoma
Hypothyroidism
1. Age of onset <20 ; >50
2. Level of BP >180/110
3. Target organ damage
 Fundi Grade II or worse
 Serum Creatinine >1.5mg/dl
 Cardiomegaly or LVF
4. Presence of features suggesting secondary
causes
Unprovoked hypokalemia
 Abdominal bruit
 Variable BP with tachycardia, sweating and
tremor
 Family history of renal disease, proteinuria
5. Poor response to appropriate drug regimen
Clinical clues
 Onset of hypertension < 30 years or > 50 years
 Accelerated or malignant hypertension
 Unexplained deterioration of renal function or
during therapy with ACEI
 Acquired resistance to a previously
antihypertensive regimen
 Presence of systolic/diastolic abdominal bruit
Clinical clues
 Persistent hypokalemia during diuretic therapy
despite concomitant administration of K
sparing agents and or oral KCl
 Resistance to anti-hypertensive therapy
 Obtrusive sleep apnea (OSA)
Biochemical clues
 Spontaneous hypokalemia i.e. serum K <
3.5mEg/L and 24 hour urinary potassium
>30mEq
 Serum K < 3.0mEq/L on conventional diuretic
dosages
 Plasma aldosterone/plasma renin activity
(PRA) >30
Clinical clues
 Symptomatic paroxysms of hypertension with
headache, tachycardia, palpitation and sweating.
 History of labile BP
 Substandard weight or recent weight loss
 A pressor response to antihypertensive drugs or
during induction of anesthesia
 Refractory hypertension
 Occasional occurrence with neurocutaneous
syndrome
 Unusual liability of BP or orthostatic hypotension
 Abnormal glucose tolerance
Biochemical clues
 Elevated plasma metanephrines
 Elevated values of 24 hours urinary NMN + MN
i.e. >1.3mg/24hrs
 Elevated plasma catecholamine i.e.
>2,000pg/ml that is non-suppressible by
clonidine
clinical clues
 Proteinuria, hematuria, renal insufficiency
 Common secondary cause of hypertension not
usually reversible
 Sulfosalycilic acid for light chains
 Spot urine protein/ creatinine ratio 24 hours
quantitative protein
 Renal ultrasound, KUB
clinical clues
HYPERTHYROID
 Hyperdynamic circulation,
SBP
 Exophthalmos
 History of weight loss
HYPOTHYROID
 High prevelance diastolic
hypertension
 Fatigue, constipation
HYPERPARATHYROIDISM
 Most asymphamatic
 Hypercalemia
 Polyuria, polydypsia and
renal calculi
 May occur with MEN
Associated condition
 Smoking
 Increasing obesity
 Sleep Apnea
 Insulin resistance/
hyperinsulinemia
 Ethanol intake >30ml per day
 Anxiety induced
hyperventilation or panic
attack
 Chronic pain
 Intensive vasoconstriction
(arteritis)
 Organic brain syndrome
(memory deficit)
 Patient resistance
 Physician resistance
 Insufficient dosage
 Infrequent administration
 Inadequate physician
education
 Lack of Physician motivation
 Drug interactions
 Excessive salt intake
 Office hypertension
 Secondary causes of
hypertension
 True-drug hypertension
NEUROHORMONAL
ABERRATION
MANAGEMENT
Plasma renin activity (increase
RAAS)
Beta-Blocker ACE I – ARB direct
renin inhibitor
Aldosterone production Spironolactatone Eplerenone
Plasma catecholamines Clonidine Methyldopa Prazocin
HEMODYNAMIC ABERRATION MANAGEMENT
Plasma volume
 Diuretics
 Sodium Restriction
Peripheral resistance
 Vasodilators
 ACES, ARB
 Direct renin inhibitors
 Calcium antagonist
Algorhythm for management of resistant hypertension

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Algorhythm for management of resistant hypertension

  • 1.
  • 2. An algorithm for the management of Resistant Hypertension Is the patient compliant No Yes Is the regimen adequate No Yes Are drugs interactions possible
  • 3. An algorithm for the management of Resistant Hypertension Are drugs interactions possible Yes No Does the patient have pseudohypertension Yes No Does the patient have office hypertension
  • 4. An algorithm for the management of Resistant Hypertension Does the patient have office hypertension Yes No Has secondary hypertension been excluded Yes No Alter regimen empirically BP Controlled BP not Controlled Evaluate mechanisms and alter regimen appropriately
  • 5. Secondary causes Renal parenchymal disease (Polycystic Kidney Disease) Renovascular hypertension Primary aldosteronism Pheochromocytoma Hypothyroidism
  • 6. 1. Age of onset <20 ; >50 2. Level of BP >180/110 3. Target organ damage  Fundi Grade II or worse  Serum Creatinine >1.5mg/dl  Cardiomegaly or LVF
  • 7. 4. Presence of features suggesting secondary causes Unprovoked hypokalemia  Abdominal bruit  Variable BP with tachycardia, sweating and tremor  Family history of renal disease, proteinuria 5. Poor response to appropriate drug regimen
  • 8. Clinical clues  Onset of hypertension < 30 years or > 50 years  Accelerated or malignant hypertension  Unexplained deterioration of renal function or during therapy with ACEI  Acquired resistance to a previously antihypertensive regimen  Presence of systolic/diastolic abdominal bruit
  • 9. Clinical clues  Persistent hypokalemia during diuretic therapy despite concomitant administration of K sparing agents and or oral KCl  Resistance to anti-hypertensive therapy  Obtrusive sleep apnea (OSA)
  • 10. Biochemical clues  Spontaneous hypokalemia i.e. serum K < 3.5mEg/L and 24 hour urinary potassium >30mEq  Serum K < 3.0mEq/L on conventional diuretic dosages  Plasma aldosterone/plasma renin activity (PRA) >30
  • 11. Clinical clues  Symptomatic paroxysms of hypertension with headache, tachycardia, palpitation and sweating.  History of labile BP  Substandard weight or recent weight loss  A pressor response to antihypertensive drugs or during induction of anesthesia  Refractory hypertension  Occasional occurrence with neurocutaneous syndrome  Unusual liability of BP or orthostatic hypotension  Abnormal glucose tolerance
  • 12. Biochemical clues  Elevated plasma metanephrines  Elevated values of 24 hours urinary NMN + MN i.e. >1.3mg/24hrs  Elevated plasma catecholamine i.e. >2,000pg/ml that is non-suppressible by clonidine
  • 13. clinical clues  Proteinuria, hematuria, renal insufficiency  Common secondary cause of hypertension not usually reversible  Sulfosalycilic acid for light chains  Spot urine protein/ creatinine ratio 24 hours quantitative protein  Renal ultrasound, KUB
  • 14. clinical clues HYPERTHYROID  Hyperdynamic circulation, SBP  Exophthalmos  History of weight loss HYPOTHYROID  High prevelance diastolic hypertension  Fatigue, constipation HYPERPARATHYROIDISM  Most asymphamatic  Hypercalemia  Polyuria, polydypsia and renal calculi  May occur with MEN
  • 15. Associated condition  Smoking  Increasing obesity  Sleep Apnea  Insulin resistance/ hyperinsulinemia  Ethanol intake >30ml per day  Anxiety induced hyperventilation or panic attack  Chronic pain  Intensive vasoconstriction (arteritis)  Organic brain syndrome (memory deficit)
  • 16.  Patient resistance  Physician resistance  Insufficient dosage  Infrequent administration  Inadequate physician education  Lack of Physician motivation  Drug interactions  Excessive salt intake  Office hypertension  Secondary causes of hypertension  True-drug hypertension
  • 17. NEUROHORMONAL ABERRATION MANAGEMENT Plasma renin activity (increase RAAS) Beta-Blocker ACE I – ARB direct renin inhibitor Aldosterone production Spironolactatone Eplerenone Plasma catecholamines Clonidine Methyldopa Prazocin
  • 18. HEMODYNAMIC ABERRATION MANAGEMENT Plasma volume  Diuretics  Sodium Restriction Peripheral resistance  Vasodilators  ACES, ARB  Direct renin inhibitors  Calcium antagonist