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Cardiovascular Maturing

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  1. Cardiovascular Aging Dorothy D. Sherwood, M.D. Health Core Physician Group Presbyterian Hospital of Dallas Division of Geriatrics July 26th, 2006

  2. Epidemiology • Currently, 12 % of the population is >65 years of age – 35 million people. • In 2030, 20% of the population will be >65 years of age – 71 million people – one in five. • Half of the people > 65 years of age have after tax incomes at the poverty level.

  3. Epidemiology • Cardiovascular disease is the leading cause of death in the population >65 years. • One half to two thirds of the population > 65 years have hypertension. • The leading discharge diagnosis for> 65 years is congestive heart failure.

  4. Epidemiology • Compelling data indicates that aggressive treatment of hypertension, heart failure, coronary artery disease, and hyperlipidemia in those between the ages of 65 and 74 reduces morbidity and mortality. • Few trials have enrolled those over 75 or those with co-morbid conditions.

  5. Pathophysiology • Hallmarks of cardiovascular aging include • Increase in systolic blood pressure • Increase in pulse pressure and pulse wave velocity (PWV) • Increase in left ventricular mass • Increase in CAD • Increase in Atrial fibrillation

  6. Pathophysiology • Aging is associated with a: • Decrease in early left ventricular diastolic filling. • Decrease in maximal heart rate • Decrease in maximal cardiac output • Decrease in maximal aerobic capacity • Decreased exercise induced augmentation of LVEF and heart rate • Decreased vasodilatation in response to beta adrenergic stimulation or endothelial mediated vasodilatation.

  7. Pathophysiology • Cellular, enzymatic, and molecular alterations in the arterial vessel: • Smooth muscle cells (SMC) migrate to the intima, causing intimal thickening. • Metalloproteinases, angiotensin II, transforming growth factor beta, intracellular cell adhesion molecules, result in increased production of collagen, collagen cross linking, fibronectin, calcification, in the media with decrease in elastin in the media – leading to stiff vessel. • Reduced endothelial function due to apoptosis and senescence results in decreased NO • Decreased vasodilatory response to beta adrenergic agonists and alpha adrenergic antagonist

  8. Pathophysiology • This results in arterial dilation with increased arterial stiffness and decreased NO induced vasodilatation.

  9. Pathophysiology • Cellular, enzymatic, and molecular alterations in the Heart: • Similar to those in the arterial wall – with similar enzymatic changes resulting in increased collagen cross linking, increased fibronectin, decrease in elastin • In the atria, decrease in sinus node cells, and alterations in the extracellular matrix results in sinus node dysfunction leading to atrial fibrillation; similar changes occur in the AV node.

  10. Pathophysiology • Reduced, but hypertrophied myocytes result in alteration in calcium channels, leading to • Prolongation of contraction and relaxation of the myocardium with aging.

  11. Pathophysiology • Changes in the intravascular environment with age: • Increase in prothrombotic factors s such as V, VIII, IX, plasminogen, resulting in impaired fibrinolyisis • Increased pro-thrombotic cytokines – especially interleukin 6 • All of these potentiate the development of atherosclerosis

  12. Pathophysiology • Autonomic nervous system • Decreased number of alpha and beta adrenergic cells and decreased function of the cells with aging. • Decreased dopaminergic responsiveness with aging • Decreased vascular response to cholinergics, but increased central nervous system response

  13. Pathophysiology • The combined effect of the changes in the autonomic nervous system results in a decreased baroreceptor response in the elderly and decreased ability to respond to stress.

  14. Pathophysiology • We can impact some of the age related changes: • Exercise increases endothelial function • Exercise decreases arterial wall stiffness • ACEI, ARB, Aldosterone inhibitors, Beta blockers may influence remodeling of the vessels and the myocardium.

  15. Pharmacodynamic effects of aging • Suffice it to say, that elderly are highly sensitive to: • The therapeutic effects of a drug: i.e. a direct vasodilator such a prazocin; the rate effects of beta blockers • The toxic effects of the drug: i.e. digoxin toxicity occurs at a much lower dose in the elderly • The drug-drug interactions: ACEI and NSAID for example –

  16. Pharmacodynamic effects of aging • Elderly patients can not take a joke! • Look up every drug before you give it • If renally cleared – adjust the dose – i.e. beta blockers are renally cleared. • Know the drug-drug interactions • Know the complications • Start low – go slow, and re-address need for drug at every visit.

  17. Hypertension • Measure BP in both arms, supine, sitting, and standing. • Elderly patients are very susceptible to orthostatic hypotension. • The risk of hypertension is greater in the elderly, at least up to age 80, than in the younger population, and the reduction in CAD and heart failure is greater in the elderly with treatment than in the young.

  18. Hypertension • Limited data from placebo controlled trials reveals a decrease in strokes and heart failure in patients over the age of 80 with treated hypertension, but no difference in mortality.

  19. Multiple trials demonstrating benefit of treatment of hypertension in the elderly

  20. Hypertension • Thiazides are as effective as any other drug for first line treatment. • Risk of hyponatremia • Risk of incontinence • Risk of hypokalemia • Never go above 25 mg, start at 6.25 mg

  21. Hypertension • To evaluate the best second line therapy for each patient, take into account their co-morbid conditions, and the drug-drug interactions that will occur. Use • Or JNC 7 to determine the best choice

  22. Hypertension • Postural Hypotension – a fall of 20 mm Hg with standing is associated with a marked increase in falls. • Increases the risk associated with anti-depressants, anti-psychotics, and anti-parkinsonian medications • Increases the risk associated with post-prandiol hypotension • Greatest fall in BP is 1 hour after eating, returning to normal 3 to 4 hours after eating

  23. CAD • Autopsy studies show that > 50% of the men over the age of 60 have significant CAD with increase in the incidence of multi-vessel disease and left main disease • The life time risk for developing CAD is estimated to be 1 in 3 for men and 1 in 4 for women

  24. CAD • By the age of 80, 20 to 30% of men and women have symptomatic CAD. • History is atypical: epigastric discomfort; shoulder pain; back pain; SOB; nausea or no symptoms at all • Symptoms not necessarily related to exertion.

  25. CAD • Testing: • Exercise stress testing has about an 80% sensitivity and 75% specificity • The addition of an echocardiogram or nuclear study improves the validity of the test • In men and women who can not exercise, dobutamine or adenosine can be used. • Due to high levels of calcification in the arteries, CT may not be useful in the elderly.

  26. CAD • Treatment: the same as the younger population, unless there is less than a 2 year life expectancy. • Heart Protection Study showed benefit in patients with disease treated with statins • There is no data regarding statins and primary prevention in patients over the age of 75

  27. CAD • Age is a risk factor for myopathy with statin therapy. Therefore, the lowest effective dose should be used in this population. • Beta blockers, ACEI, and long-acting nitrates should be used. • Avoid Beta blockers in SA or AV nodal disease • Avoid Calcium Channel Blockers

  28. CAD • Revascularization: • BARI study – 109 patients ages 65 to 83. • CABG vs. PTCA • CABG associated with increased early mortality and morbidity, but less angina and less repeat procedures • Stroke was more common after CABG and heart failure after PTCA • 5 year survival was 86% for CABG and 81 % for PTCA • In hospital mortality for CABG in patients over 75 is 6 to 8% and stroke is 3 to 6%

  29. CAD • TIME trial compared re-vasularization to optimal medical therapy. At 6 months, revascularization was favored, but a 1 year there was no difference in outcomes • Data is limited in the use of drug eluting stents and off pump bypass.

  30. CAD • Treatment of acute MI in the elderly with thrombolysis or primary angioplasty is associated with better outcomes, but also, with increased risk of complications including hemorrhage and stroke. • Thin, black, female, prior cva, Bp >160 associated with increased risk of ICH

  31. CAD • Post MI treatment • Beta Blockers, ACEI, ASA, Statins all have been shown to be of benefit in the elderly. • Start with lower doses and titrate carefully

  32. CHF • Five year mortality is 50% for patients with systolic impairment and 25% for patients with diastolic HF • There is a 4 fold increase in mortality in patients with diastolic dysfunction compared to those without HF. • Age is associated with HF with preserved systolic function

  33. CHF • Exercise intolerance is the mark of heart failure • Nocturnal cough, PND, DOE are common signs of heart failure, but may not be recognized • Less than 50% of patients with moderate diastolic HF by doppler had the diagnosis of Hf

  34. CHF • Physical exam in the elderly is not easy – they all have edema; their neck veins are always distended or appear to be; S3 and rales are only present when decompensated. • One must rely on ECHO and BNP to diagnose heart failure at times.

  35. CHF • Treatment • Not good data in the elderly – most CHF studies are with patients with systolic dysfunction. Women and the frail elderly are not included at all.

  36. CHF • Treatment of Systolic Failure • Control BP • Diurese • Control heart rate if in A fib. • ACEI or ARB gently • Beta blocker gently • Exercise

  37. CHF • Diastolic Dysfunction • Diuretics • ACEI or ARB gently • Beta blockers gently • Exercise

  38. Arrhythmia • Up to 90 % of the sinus node cells are lost by the age of 75! • Resting heart rate is not effected by age, but maximal heart rate and beat to beat variability are both reduced. • SN response to beta adrenergic and parasympathetic stimulation is reduced.

  39. Arrhythmia • EKG shows prolonged PR and LAD • Arrhythmias requiring treatment • Bradycardia due to SA or AV nodal dysfunction • A Fib – 8 to 10% of 80 year olds have A fib. • 50% of patients with A fib are > 75 years old

  40. Arrhythmia • A fib • Focus should be on anticoagulation for stroke prevention and rate control. Rarely is rhythm control needed or possible. • Warfarin – INR 2 to 2.5 • Don’t forget – associated with osteoporosis • ASA 325 mg in very elderly or very debilitated.

  41. Summary • CV aging is associated with • Decreased arterial compliance • Decreased cardiac compliance • Decreased maximal heart rate and EF with exercise/stress • Decreased adrenergic sensitivity • Increased systolic hypertension • Increased LV mass • Increased CAD • Increased arrhythmias

  42. Summary • Treatment • Encourage Exercise and: • Monitor orthostatic BP. • Start low, go slow. • Avoid vasodilators if possible. • May have increased sensitivity to bradycardia from beta blockers, calcium channel blockers. • Watch for drug/drug interactions. • Monitor frequently, be careful.