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Title: Chapter%2018%20Alterations%20in%20Cardiac%20Function


1
Chapter 18Alterations in Cardiac Function
2
Coronary Heart Disease
  • CHD is characterized by insufficient delivery of
    oxygenated blood to the myocardium due to
    atherosclerotic coronary arteries (CADs)
  • Sequelae of CHD include
  • Angina pectoris
  • Myocardial infarction
  • Dysrhythmias
  • Heart failure
  • Sudden cardiac death

3
Coronary Heart Disease (Cont.)
  • Etiology of Coronary Heart Disease
  • Known risk factors
  • Atherosclerosis causes narrowing of the arterial
    lumen that can lead to cardiac ischemia through
  • Thrombus formation
  • Coronary vasospasm
  • Endothelial cell dysfunction

4
Coronary Heart Disease (Cont.)
5
Coronary Heart Disease (Cont.)
  • Mechanisms of Coronary Atherosclerosis
  • Lipids are transported via apoproteins
  • Lipoproteins associated with a greater risk of
    atherosclerosis
  • High-density lipoproteins transport cholesterol
    from peripheral tissue back to the liver,
    clearing atheromatous plaque

6
Coronary Heart Disease (Cont.)
7
Coronary Heart Disease (Cont.)
  • Mechanisms of Coronary Atherosclerosis
  • Atherosclerotic plaque formation initiated by
    injury to coronary artery endothelium
  • Endothelium becomes permeable and recruits
    leukocytes
  • LDL insudation occurs with oxidation by
    endothelial cells and macrophages
  • Oxidized lipids are damaging to endothelial and
    smooth muscle cells, and stimulate recruitment of
    macrophages into the vessel

8
Coronary Heart Disease (Cont.)
  • Mechanisms of Coronary Atherosclerosis
  • Macrophages engulf the lipids foam cells release
    inflammatory mediators and growth factors,
    attracting more leukocytes and stimulate smooth
    muscle proliferation
  • Excess lipid and debris accumulate within vessel
    wall and coalesce into lipid core

9
Coronary Heart Disease (Cont.)
  • Mechanisms of Coronary Atherosclerosis
  • Vulnerable plaques may rupture or become eroded,
    which stimulates clot formation on the plaque
  • Vulnerable plaques have
  • Large lipid core
  • Thin cap
  • High shear stress

10
Coronary Heart Disease (Cont.)
11
Coronary Heart Disease (Cont.)
  • Pathophysiology of Ischemia
  • Ischemia occurs when oxygen supply is
    insufficient to meet metabolic demands
  • Critical factors in meeting cellular demands for
    oxygen include
  • Rate of coronary perfusion
  • Myocardial workload

12
Coronary Heart Disease (Cont.)
  • Pathophysiology of Ischemia
  • Coronary perfusion can be altered by
  • Large, stable atherosclerotic plaque
  • Acute platelet aggregation and thrombosis
  • Vasospasm
  • Failure of autoregulation by the microcirculation
  • Poor perfusion pressure

13
Coronary Heart Disease (Cont.)
  • Clinical Features and Management of Coronary
    Syndromes
  • Chronic syndromes with slow progression due to
    chronic obstruction from stable atherosclerotic
    plaques
  • Stable angina pectoris
  • Ischemic cardiomyopathy

14
Coronary Heart Disease (Cont.)
  • Clinical Features and Management of
  • Coronary Syndromes
  • Acute coronary syndrome (ACS) associated with
    acute changes in plaque morphology and thrombosis
  • Unstable angina
  • Myocardial infarction

15
Coronary Heart Disease (Cont.)
  • Angina Pectoris
  • Chest pain associated with intermittent
    myocardial ischemia
  • May result in inefficient cardiac pumping with
    resultant pulmonary congestion and shortness of
    breath
  • Three patterns of angina pectoris
  • Stable or typical angina
  • Prinzmetal or variant angina
  • Unstable or crescendo angina

16
Coronary Heart Disease (Cont.)
  • Acute Coronary Syndrome
  • Chest pain usually more severe and lasts longer
    than typical angina
  • Plaque rupture with acute thrombus development
  • Unstable anginaocclusion is partial
  • MIocclusion is complete
  • ECG and biomarkers used for diagnosis

17
Coronary Heart Disease (Cont.)
18
Coronary Heart Disease (Cont.)
19
Coronary Heart Disease (Cont.)
20
Coronary Heart Disease (Cont.)
  • Acute Coronary Syndrome
  • MI leads to drop in CO, triggering compensatory
    responses including sympathetic activation
  • Sympathetic nervous system activation leads to
    increased myocardial workload by increasing
  • Heart rate
  • Contractility
  • Blood pressure

21
Coronary Heart Disease (Cont.)
22
Coronary Heart Disease (Cont.)
23
Coronary Heart Disease (Cont.)
  • Sudden Cardiac Death
  • Unexpected death from cardiac causes within 1
    hour of symptom onset
  • Use of external defibrillators and CPR has
    increased survival
  • Lethal dysrhythmia (such as ventricular
    fibrillation) is usually the primary cause

24
Coronary Heart Disease (Cont.)
  • Chronic Ischemic Cardiomyopathy
  • Heart failure develops insidiously due to
    progressive ischemic myocardial damage
  • Typically have history of angina or MI
  • More common in older adults

25
Endocardial and Valvular Disease
  • Endocardial and valvular structures may be
    damaged by
  • Inflammation and scarring
  • Calcification
  • Congenital malformations
  • Cause altered hemodynamics of the heart and
    increase myocardial workload

26
Endocardial and Valvular Disease (Cont.)
  • Stenosis failure of the valve to open completely
    results in extra pressure work for the heart
  • Regurgitation inability of a valve to close
    completely results in extra volume work for the
    heart

27
Endocardial and Valvular Disease (Cont.)
  • Mitral Stenosis
  • Blood flow from the left atrium to the left
    ventricle is impaired during ventricular diastole
  • Increased pressure of the left atrium leads to
    atrial chamber enlargement and hypertrophy
  • Can lead to chronic pulmonary hypertension, right
    ventricular hypertrophy, and right-sided heart
    failure
  • Low-pitched, rumbling diastolic murmur

28
Endocardial and Valvular Disease (Cont.)
29
Endocardial and Valvular Disease (Cont.)
  • Mitral Regurgitation
  • Backflow of blood from the left ventricle to the
    left atrium during ventricular systole
  • Left atrium and ventricle dilate and hypertrophy
    due to extra volume
  • May lead to left-sided heart failure
  • High-pitched, pansystolic, blowing murmur

30
Endocardial and Valvular Disease (Cont.)
31
Endocardial and Valvular Disease (Cont.)
  • Mitral Valve Prolapse
  • Displacement of the mitral valve leaflets into
    the left atrium during ventricular systole
  • Typically asymptomatic
  • Complications may include infective endocarditis,
    sudden cardiac death, cerebral embolic events,
    and progression to mitral regurgitation
  • Midsystolic click or systolic murmur

32
Endocardial and Valvular Disease (Cont.)
  • Aortic Stenosis
  • Predominant cause is age-related calcium deposits
    on the aortic cusps
  • Results in obstruction of aortic outflow from the
    left ventricle into the aorta during systole
  • May result in ischemia and left-sided HF
  • Crescendo-decrescendo murmur during ventricular
    systole with prominent S4

33
Endocardial and Valvular Disease (Cont.)
34
Endocardial and Valvular Disease (Cont.)
  • Aortic Regurgitation
  • Incompetent aortic valve allows blood to leak
    back from the aorta into the left ventricle
    during diastole
  • Leads to left ventricle hypertrophy and dilation
    with eventual left-sided HF
  • High-pitched blowing murmur during ventricular
    diastole

35
Endocardial and Valvular Disease (Cont.)
36
Endocardial and Valvular Disease (Cont.)
  • Diseases of the Endocardium
  • Rheumatic heart disease
  • Acute inflammatory disease that follows infection
    with group A ß-hemolytic streptococci
  • Antibodies against the streptococcal antigens
    damage connective tissue in joints, heart, and
    skin
  • Occurs mainly in children

37
Endocardial and Valvular Disease (Cont.)
  • Infective endocarditis
  • Invasion and colonization of endocardial
    structures by microorganisms with resulting
    inflammationvegetations
  • Most common bacteria
  • Streptococcus
  • Staphylococcus
  • Predisposing risk factors typically present

38
Myocardial Diseases
  • Myocarditis inflammatory disorder of the heart
    muscle characterized by necrosis and degeneration
    of myocytes
  • Cardiomyopathy may be genetic or acquired and is
    noninflammatory

39
Myocardial Diseases (Cont.)
  • Myocarditis
  • Causes include microbial agents, immune-mediated
    diseases, physical agents
  • Viral etiology most common
  • Characterized by left ventricular dysfunction and
    general dilation of all four chambers

40
Myocardial Diseases (Cont.)
41
Myocardial Diseases (Cont.)
  • Cardiomyopathy
  • Classified by cause or functional impairment
  • Primary dysfunction of unknown cause
  • Secondary known cause
  • Dilated
  • Hypertrophic
  • Restrictive

42
Myocardial Diseases (Cont.)
  • Dilated Cardiomyopathy
  • Cardiac failure associated with dilation of one
    or both ventricular chambers
  • May be related to
  • Alcohol toxicity
  • Pregnancy
  • Postviral myocarditis
  • Genetic abnormality
  • Slow progression of biventricular heart failure
    with low ejection fraction

43
Myocardial Diseases (Cont.)
44
Myocardial Diseases (Cont.)
  • Hypertrophic Cardiomyopathy
  • Thickened, hyperkinetic ventricular muscle mass
  • Septum may be affected, leading to idiopathic
    hypertrophic subaortic stenosis
  • Genetic abnormality
  • Clinical course is variable, typically slow
    progression

45
Myocardial Diseases (Cont.)
  • Restrictive Cardiomyopathy
  • Rarest form of cardiomyopathy
  • Stiff, fibrotic ventricle with impaired diastolic
    filling
  • Most commonly associated with amyloidosis
  • Decreased cardiac output and left-sided heart
    failure can result

46
Myocardial Diseases (Cont.)
  • Specific Cardiomyopathy
  • Presumed known origin
  • Present functionally as dilated, hypertrophic, or
    restrictive disorders

47
Pericardial Diseases
  • Typically sequelae of other disorders such as
  • Systemic infection
  • Trauma
  • Metabolic derangement
  • Neoplasia

48
Pericardial Diseases (Cont.)
  • Pericardial Effusion
  • Accumulation of noninflammatory fluid in the
    pericardial sac
  • Composition of usual fluids
  • Serous
  • Serosanguineous
  • Chylous
  • Blood

49
Pericardial Diseases (Cont.)
  • Cardiac Tamponade
  • When fluid accumulation in the pericardial sac is
    large/sudden it can lead to external compression
    of the heart chambers such that filling is
    impaired
  • Symptoms include
  • Reduced stroke volume
  • Compensatory increases in heart rate

50
Pericardial Diseases (Cont.)
  • Pericarditis
  • Acute or chronic inflammation of the pericardium
  • Categories
  • Idiopathic
  • Infectious
  • Immune-inflammatory
  • Neoplastic
  • Radiation induced
  • Early postcardiac sx
  • Hemopericardium
  • Trauma
  • Congenital
  • Miscellaneous

51
Pericardial Diseases (Cont.)
  • Acute Pericarditis
  • Most cases idiopathic and presumed viral
  • Uncomplicated form resolves spontaneously
  • Complicated forms involve pericardial effusion,
    or persistent/recurrent inflammation
  • Typically presents as chest pain

52
Pericardial Diseases (Cont.)
  • Chronic Pericarditis
  • Two principal forms
  • Adhesive mediastinopericarditis pericardial sac
    is destroyed and the external aspect of the heart
    adheres to surrounding mediastinal structures
  • Constrictive pericarditispericardial sac becomes
    dense, nonelastic, fibrous, and scarred

53
Congenital Heart Diseases
  • Abnormality of the heart that is present from
    birth
  • Different congenital heart anomalies result in
    two primary pathologic processes
  • Shunting of blood through abnormal pathways in
    the heart or great vessels
  • Obstruction to blood flow because of abnormal
    narrowing

54
Congenital Heart Diseases (Cont.)
  • Embryologic Development
  • Heart defects commonly associated with these
    abnormalities
  • Development of atrial septum
  • Development of the ventricular septum
  • Division of the main outflow tract (truncus
    arteriosus) into the pulmonic and aortic arteries
  • Development of the valves

55
Congenital Heart Diseases (Cont.)
  • Etiology and Incidence of Congenital
  • Heart Disease
  • Congenital heart disease is the most common heart
    disorder in children
  • Overall incidence is 0.8 of all live births
  • May be attributed to
  • Maternal rubella during first trimester of
    pregnancy
  • Exposure to cardiac teratogens
  • Genetic influences

56
Congenital Heart Diseases (Cont.)
57
Congenital Heart Diseases (Cont.)
  • Pathophysiology of Congenital Heart
  • Disease
  • Result in two primary pathologies
  • Shunt abnormal path of blood flow through the
    heart or great vessels
  • Obstruction interference with blood flow leading
    to increased workload of affected chamber

58
Congenital Heart Diseases (Cont.)
  • Acyanotic Congenital Defects
  • Disorders that result in left-to-right shunting
    of blood or obstruction to flow are generally
    acyanotic
  • These disorders include
  • Atrial septal defect
  • Ventricular septal defect
  • Patent ductus arteriosus
  • Coarctation of the aorta
  • Pulmonary and aortic stenosis or atresia

59
Congenital Heart Diseases (Cont.)
  • Atrial Septal Defect
  • Majority of atrial septal defects occur at the
    location of the foramen ovale
  • Long-term increase in pulmonary blood flow may
    eventually lead to pulmonary hypertension, right
    ventricular hypertrophy, and reversal to a
    right-to-left shunt

60
Congenital Heart Diseases (Cont.)
61
Congenital Heart Diseases (Cont.)
  • Ventricular Septal Defect
  • Most common congenital cardiac anomaly
  • Typically located in the membranous septum, near
    the bundle of His
  • Increase in pulmonary blood flow can result in
    pulmonary hypertension, right ventricular
    hypertrophy, and reversal of the shunt

62
Congenital Heart Diseases (Cont.)
63
Congenital Heart Diseases (Cont.)
  • Patent Ductus Arteriosus
  • Conditions that cause low blood oxygen tension
    may contribute to continued patency
  • No clinical significance in early life
  • Continued patency identified by harsh, grinding
    systolic murmur or thrill
  • Results in pulmonary hypertension, and can lead
    to right-sided heart failure

64
Patent Ductus Arteriosus
65
Congenital Heart Diseases
  • Coarctation of the Aorta
  • Narrowing or stricture of the aorta that impedes
    blood flow
  • Commonly located just before or after the ductus
    arteriosus
  • Preductal coarctation usually more severe and
    associated with other anomalies
  • Usually accompanied by systolic murmurs and
    ventricular hypertrophy

66
Coarctation of the Aorta
67
Congenital Heart Diseases
  • Pulmonary Stenosis or Atresia
  • Pulmonary atresiablood must enter the lungs by
    traveling through a septal opening and a patent
    ductus arteriosus
  • Pulmonary stenosisusually due to abnormal fusion
    of the valvular cusps and can lead to right
    ventricular hypertrophy

68
Congenital Heart Diseases (Cont.)
  • Aortic Stenosis or Atresia
  • Aortic atresias are not compatible with survival
  • Aortic stenosis may involve the valvular cusps or
    the subvalvular fibrous ring and results in high
    left ventricular afterload with left ventricular
    hypertrophy

69
Congenital Heart Diseases (Cont.)
  • Cyanotic Congenital Defects
  • Disorders that result in right-to-left shunting
    of blood result in cyanosis
  • These disorders include
  • Tetralogy of Fallot
  • Transposition of the great arteries
  • Truncus arteriosus
  • Tricuspid atresia

70
Congenital Heart Diseases (Cont.)
  • Tetralogy of Fallot
  • Four defining features
  • Ventricular septal defect
  • Aorta positioned above the ventricular septal
    opening
  • Pulmonary stenosis that obstructs right
    ventricular outflow
  • Right ventricular hypertrophy

71
Tetralogy of Fallot
72
Congenital Heart Diseases
  • Transposition of the Great Arteries
  • Aorta arises from the right ventricle and the
    pulmonary artery arises from the left ventricle
  • Results in two separate, noncommunicating
    circulations
  • Incompatible with life unless mixing of blood
    occurs through other defects

73
Transposition of the Great Arteries
74
Congenital Heart Diseases
  • Truncus Arteriosus
  • Failure of the pulmonary artery and aorta to
    separate results in formation of one large
    vessel that receives blood from both the right
    and left ventricles
  • Results in systemic cyanosis
  • High pulmonary blood flow may cause pulmonary
    hypertension and right ventricular hypertrophy

75
Truncus Arteriosus
76
Congenital Heart Diseases
  • Tricuspid Atresia
  • Usually associated with underdevelopment of the
    right ventricle and an atrial septal defect
  • Allows blood to bypass right ventricle
  • A patent ductus arteriosus is required to perfuse
    lungs
  • Cyanosis present at birth, mortality high
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