nuevos conceptos en hta
TRANSCRIPT
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Dr. Christian Amurrio Gonz
Nuevos conceptos en HTA
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Objetivo 1
Diagnostico correcto
Preguntas adicionales:
El paciente toma alguna sustancia que puede infsobre su presion arterial?
Hay otras enfermedades presentes que pueden
tener impacto sobre su riesgo cardiovascular?
Hay evidencia de dao a organo-blanco porhipertension sostenida?
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Table : Prescription medications that elevate blood pressure
Corticosteroids
NSAIDs
Cyclosporine
Tacrolimus
Erythropoietin
Tricyclic antidepressants
Venlafaxine (Effexor)
MAO inhibitors
Oral contraceptives ***
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Table : Classification of blood pressure1
BP Classification
Systolic BP, mm Hg Diastolic BP, mm
Normal 100
Riesgos asociados con HTA
enf. Cardiovascular [aortic aneurysm and aortic dissection
enf. Cerebrovascular
enfermedad renal-terminalinsuficiencia cardiaca congestica
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La curva J
Coronary perfusion occurs during diastole, andthere is concern that as diastolic pressure isbrought to ever lower levels, coronary perfusion willbe compromised and cardiovascular mortality willincrease. INVEST trial
"in view of the uncertainty on this issue, it wouldseem prudent to counsel that in patients with anelevated DBP and occlusive CAD with evidence ofmyocardial ischemia, the BP should be loweredslowly, and caution is advised in inducing falls ofDBP below 60mm HG if the patient has diabetes
"
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Every 5mm Hg increase in diastolic blood pressure andevery 10mm Hg increase in systolic blood pressure is
associated with a 28% increase in the risk of death from
coronary heart disease, even in individuals who are not
classified as hypertensive.
Systolic blood pressure has been shownto be a
stronger predictor
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Objetivo 2Table : Objectives of evaluation of the newly-diagnosed hypertensive
ObjectiveExamples
Identification of other cardiovascular risk
factors Diabetes
Hypercholesterolemia
Tobacco
Positive family historyIdentification of possible secondary
causes Renal artery stenosis
Obstructive sleep apnea
Cushing's disease
Conn's syndromeIdentification of possible target organdamage Left ventricular hypertrophy
Chronic kidney disease
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Table : Physical evidence of target organ damage
Physical finding Comments
Hypertensive retinopathy18 ExamplesArteriovenous nicking
"Copper-wiring"
Retinal hemorrhagesVascular bruits Examples:
Carotid bruits
Renal artery bruits
Femoral artery bruitsLeft ventricular hypertrophy LV heave on physical exam; EKG may sh
evidence of hypertrophy or strain
Left or right ventricular failure Examples:S3 gallop
Pulmonary rales
Elevated JVP
Peripheral edemaDiminished pedal pulses Inquire about intermittent claudication; co
obtaining ankle/brachial indices
Neurologic abnormalities (i.e. stroke) Consider evaluation of cerebrovascular c
T bl 6 C l d d i h l di d h i 1 19
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Table 6: Commonly recommended tests in the newly diagnosed hypertensive1, 19
Test Comment
EKG May demonstrate evidence of LVH, conduction abnormalities, ischemia or in
all of which will demonstrate target organ damage and alter not only the init
of therapy, but also the time course of instituting therapyBasic metabolic panel Demonstrates pre-treatment sodium and potassium, which will affect initial c
therapy along with providing a possible clue to a secondary cause of hyperte
(e.g. hyperaldosteronism). Ca++The BUN and creatinine will demonstrate the presence or absence of targe
damage, and also guide initial choice of therapy (thiazides do not work well
creatinine is above 1.5 -2 mg/dL; a loop diuretic should be considered if a di
needed. ACE-inhibitors do not work well if the creatinine is above 3mg/dL).Guidelines for antihypertensive therapy for diabetics and those with renal d
among the most aggressive; thus the creatinine and glucose provided with t
metabolic panel will alter therapy.Urinalysis Provides evidence of target organ damage that will guide initial managemen
proteinuria).
Lipids Indicated for risk stratification for coronary artery disease. Elevated LDL cho
an independent risk for the development of coronary artery disease, and wil
be evaluated in most individuals diagnosed with hypertensionComplete blood count To exclude polycythemia as a possible cause of hypertension
T bl Lif t l difi ti d i t bl d 1
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Table : Lifestyle modification and impact on blood pressure1
Modification RecommendationsApproximate Systolic
Pressure Reduct
Weight reductionMaintain normal body weight (BMI
18.5-24.9)5-20mm Hg/10kg weig
Adopt DASH eating plan
Consume a diet rich in fruits,
vegetables, and low-fat dairy products
with a reduced content of saturated
and total fat
8-14mm Hg
Dietary sodium
reduction
Reduce dietary sodium intake to no
more that 2.4 g sodium or 6g sodium
chloride
2-8mm Hg
Physical activity
Engage in regular aerobic physical
activity such as brisk walking (30mins,
most days/week)
4-9mm Hg
Moderation of alcoholconsumption
Limit consumption to no more than 2
drinks/day (men) or 1 drink/day(women and lighter weight persons)
2-4mm Hg
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inmediato?
The individual who presents with an elevated bloo
pressure who has no target organ damage or othecardiovascular risks The level of blood pressureelevation will also impact your decision.
Salt restriction lowers blood pressure in patients w
and without hypertension.
In one study, individuals who lost as little as 2.4kghad a 77% reduction in the odds of developinghypertension seven years later.
DASH and TONE
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Objetivo 4 HTA secundaria
Table : Red flags for secondary hypertension
Evaluation component Finding Potential implication
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p g p
History Onset of HTN age 50 Prevalence of secondary causes higher
population
History of well-controlled HTN, now poorly controlled Suggests secondary cause, especially
artery stenosis
Flash pulmonary edema Suggests renal artery stenosis
Episodic hypertension Suggests pheochromocytoma
Daytime somnolence; loud snoring Suggests obstructive sleep apnea
Physical exam Obesity Suggests obstructive sleep apneaThyroid goiter Suggests hyperthyroidism
Moon facies Suggests Cushing's
Dorsal fat pad Suggests Cushing'sPurple striae Suggests Cushing's
Vascular bruits Suggests renal artery stenosis
Abdominal mass Suggests polycystic kidney disease
Decreased pulses in lower extremities Suggests coarctation of the aorta
Isolated systolic hypertension Suggests anemia, hyperthyroidism, aor
insufficiency, arteriovenous fistula, Pag
disease of bone
Labs Hypokalemia Suggests Cushing's, hyperaldosteronis
artery stenosisHypercalcemia Suggests hyperparathyroidism
Metabolic alkalosis Suggests Cushing's, hyperaldosteronis
possibly obstructive sleep apnea
Elevated hematocrit Suggests polycythemia
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HTA resistente y refractaria
History: onset of HTN before 30 or after 50; h/owell controlled HTN now out of control; flashpulmonary edema; episodic HTN; daytimesomnolence, loud snoring; uncontrolled BPdespite 3 meds at or near maximal dose(including a diuretic)
Physical: Obesity; thyroid goiter; moon facies;dorsal fat pad; purple striae; vascular bruits;abdominal mass; decreased pulses lowerextremities
Labs: Hypokalemia; hypercalcemia; metabolicalkalosis; elevated hematocrit
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Figure 1: Considerations in resistant hypertension
Table: Review of causes of secondary hypertension
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Table: Review of causes of secondary hypertensionCause Clues
Renal parenchymal disease Microalbuminuria; proteinuria; nocturia; edema
Renal artery stenosis Flash pulmonary edema; multiple vascular risks
well-controlled hypertension, now poorly contro
vascular bruits; hypokalemia; renal insufficiency
Fibromuscular dysplasia Women between ages 15 and 50; beaded appe
renal angiogram
Obstructive sleep apnea Daytime somnolence; loud snoring; met. alkal
Pheochromocytoma Sustained or episodic hypertension with headac
palpitations, diaphoresis
Hyperaldosteronism ( Conn syndrome) Hypokalemia; metabolic alkalosis
Hypercortisolism (including Cushing syndrome) Dorsal fat pad; moon facies; purple striae; trunc
proximal muscle weakness; metabolic alkalosis
hypokalemia
Hyperparathyroidism Hypercalcemia; "bones, stones, abdominal groa
Hyperthyroidism Systolic hypertension, tachycardia, weight loss,
exophthalmos, goiter, thyroid bruit.
Hypothyroidism Cold intolerance; constipation; mental slowing;
hypertension; lateral thinning of eyebrows; perio
edema; delayed relaxation of reflexes
Table 10: AHA recommendations for blood pressure targets in cardiac d
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Table 10: AHA recommendations for blood pressure targets in cardiac d
Area of concern TargetBP Comments
General CAD prevention 160 of DBP > 100High CAD risk 1
Stable angina
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et vo e camentoadecuado
The single most important aspect in
treating a patient with hypertension is
the level of blood pressure control.
However, the agent(s) chosen to
achieve blood pressure control may
provide additional benefit in specificclinical conditions
ALLHAT
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ALLHAT Men and women aged 55 or older with blood pressure
greater than 140/90 and at least one other cardiovascu
risk factor were randomized to receive treatment witheither a diuretic (chlorthalidone), an alpha-blocker(doxazosin), a calcium channel blocker (amlodipine) oan ACE-inhibitor (lisinopril). Beta blockers were notincluded. Goal blood pressure reduction for all groupswas set at BP
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Clinical outcomes of those patients treated withchlorthalidone were compared to those treated withamlodipine or lisinopril. Chlorthalidone proved superior
the other agents in lowering blood pressure, reducingclinical events, and was better tolerated than the otheragents. As compared to amlodipine, chlorthalidone wasassociated with 25% fewer cases of heart failure,although other clinical outcomes were not statistically
different. As compared to lisinopril, chlorthalidone wasbetter tolerated and resulted in better blood pressurecontrol. In addition, the lisinopril group had a greater risof stroke, heart failure, angina, and coronaryrevascularization as compared to chlorthalidone. Theauthors concluded that "thiazide-type diuretics should bconsidered first for pharmacologic therapy in patients
Table : Indicaciones convincentes
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Table : Indicaciones convincentes
High-risk condition
with compelling
indication
Diuretic
recommen
ded
Beta-blocker
recommende
d
ACEI
recomme
nded
ARB
recomm
ended
CCB
recomm
ended
Aldo
anta
recom
CHF
Post-MI
High CAD risk **
DM
CKD
Recurrent CVA
prevention
**ACCOMPLISH ACE-inhibitor/dihydropyridine CCBbenazepril/amlodipine
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y yp gDiuretics Drug of choice for hypertension without compel
indications for another drugThiazide diuretics may have beneficial effects o
metabolismLow dose diuretics may be of benefit in patients
diabetesThiazide diuretics may precipitate gout
Beta-blockers Drug of choice for preoperative hypertensionIncreasingly useful in cardiovascular risk reduct
cardiac surgeryDrug of choice for hypertension associated with
hyperthyroidismUseful for migraine prophylaxisAcceptable for use during pregnancy (other acc
agents: methydopa; vasodilators)
ACE-inhibitors Absolutely contraindicated in pregnancyA 35% increase in creatinine is acceptable whe
therapy with ACE-inhibitorsMay be less effective for blood pressure control
Americans, who are also more likely to dev
angioedema in response to ACE-I
Angiotensin-receptor blockers (ARBs) Not currently a first line agent; Used when ACEb t t t l t d
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but not toleratedEvidence continues to increase that they are eq
ACE-I in benefits to kidneys in diabeticsAbsolutely contraindicated in pregnancyAs with ACE-I, a 35% increase in creatinine ma
when initiating therapy
Calcium channel blockers May be of particular use when treating isolat
hypertension in the elderlyMay be more effective for blood pressure co
African AmericansMay be used for migraine prophylaxisNon-dihydropyridine CCBs (e.g. verapamil) t
choice in diabetic nephropathy if ACE otolerated55
Non-dihydropyridine CCBs may also delay p
of proteinuria in other causes of chronic
disease 56
In the absence of benefit in specific clinical s
calcium channel blockers are now consi
line agents, after therapy with diuretics, blockers, and/or ACE-inhibitors
Alpha blockers Should not be used as monotherapt t t f h t i
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treatment of hypertension May help treat symptoms in men w
prostatic hypertrophy
Aldosterone antagonists Includes spironolactone and eplere
(brand name Inspra) Defined role in management of CH
Both cause hyperkalemia Spironolactone associated with sex
effects, seen less with eplerenone
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GRACIAS
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