Cardiovascular
Cardiovascular
Cardiovascular
SYSTEM
CARDIOVASCULAR
SYSTEM
Consists: heart, arteries, veins, capillaries
Functions:
1. circulation of blood
2. delivery of oxygen and other nutrients to tissues
of the body
3. removal of carbon dioxide and other products of
cellular metabolism
CARDIOVASCULAR
SYSTEM
HEART
ANATOMY and PHYSIOLOGY:
A. Heart wall
1. pericardium
a. fibrous pericardium
b. serous pericardium
2. epicardium
3. myocardium
4. endocardium
CARDIOVASCULAR
SYSTEM
B. Chambers
1. Atria a. right
b. left
2. Ventricles a. right
b. left
C. Valves
1. Atrioventricular valves
a. Mitral valve
b. Tricuspid valve
CARDIOVASCULAR
SYSTEM
c. Function:
- permit unidirectional flow of blood from
specific atrium to specific ventricle during
ventricular diastole
- prevent reflux during ventricular systole
- valve leaflets open during ventricular
diastole and close during ventricular systole; valve
closure produces the first heart sounds (S1)
CARDIOVASCULAR
SYSTEM
2. Semilunar valves
a. Pulmonary valve
b. Aortic valve
c. Function:
- permit unidirectional flow of blood from specific
ventricle to arterial vessel during ventricular systole
- prevent reflux during ventricular diastole
- valves open when ventricles contract and close
during ventricular diastole; valve closure produces the
second heart sound (S2)
CARDIOVASCULAR
SYSTEM
D. Conduction System
1. Sinoatrial (SA) node
2. Internodal Tracts
3. Atrioventricular (AV) node
4. Bundle of His
- right bundle branch
- left bundle branch
5. Purkinje fibers
* Electrical activity of heart can be visualized by ECG
CARDIOVASCULAR
SYSTEM
E. Coronary Circulation
1. Arteries
a. right coronary artery
b. left coronary artery
2. Veins
a. coronary sinus veins
b. thebesian veins
CARDIOVASCULAR
SYSTEM
VASCULAR SYSTEM
Function:
a. supply tissues with blood
b. remove wastes
c. carry unoxygenated blood
back to the heart
CARDIOVASCULAR
SYSTEM
TYPES OF BLOOD VESSELS
A. Arteries
B. Arterioles
C. Capillaries: the following exchanges occur:
- oxygen and carbon dioxide
- solutes between the blood and tissues
- fluid volume transfer between the plasma
and interstitial spaces
D. Venules
E. Veins
CARDIOVASCULAR
SYSTEM
ASSESSMENT
HEALTH HISTORY
A. Presenting problem
1. Nonspecific symptoms may include
- fatigue - shortness of breath
- cough - palpitations
- headache - weight loss/gain
- syncope - difficulty sleeping
- dizziness - anorexia
CARDIOVASCULAR
SYSTEM
2. Specific signs and symptoms
a. chest pain
b. dyspnea (shortness of breath)
c. orthopnea / paroxysmal nocturnal dyspnea
d. palpitations: precipitating factors
e. edema
f. cyanosis
B. Lifestyle: occupation, hobbies, financial status,
stressors, exercise, smoking, living conditions
CARDIOVASCULAR
SYSTEM
C. Use of medications: OTC drugs, contraceptives,
cardiac drugs
D. Personality profile: Type A, manic-depressive,
anxieties
E. Nutrition: dietary habits, cholesterol, salt intake,
alcohol consumption
F. Past Medical History
G. Family history: heart disease (congenital, acute,
chronic); risk factors (DM, hypertension, obesity)
CARDIOVASCULAR
SYSTEM
PHYSICAL EXAMINATION
A. Skin and mucous membranes:
- color/texture, temperature, hair distribution on
extremities, atrophy or edema, petechiae
B. Peripheral pulses:
- palpate and rate all arterial pulses (temporal,
carotid, brachial, radial, femoral, popliteal,
dorsalis pedis and posterior tibial) on scale of:
0=absent, 1=palpable, 2=normal, 3=full, 4=full
and bounding
CARDIOVASCULAR
SYSTEM
C. Assess for arterial insufficiency and venous
impairment
D. Measure and record blood pressure
E. Inspect and palpate the neck vessels:
a. jugular veins: note location, characteristics,
jugular venous pressure
b. carotid arteries: location and characteristics
F. Auscultate heartsounds
- normal (S1, S2)
- abnormal (S3, S4)
CARDIOVASCULAR
SYSTEM
LABORATORY / DIAGNOSTIC TESTS
A. Blood Chemistry and electrolyte analysis
1. Cardiac enzymes: in MI
a. Troponin T: detected 3-12 hours after chest
pain
b. Troponin I: detected 3-12 hrs
c. creatine phosphokinase (CPK – MB): 6-12Hrs
d. Aspartate aminotransferase (AST) (SGOT): 24
Hrs after chest pain
e. Lactic dehydrogenase (LDH): 36 Hrs
CARDIOVASCULAR
SYSTEM
2. Electrolytes
a. Sodium (Na) 135-148meq/L
- hyponatremia: fluid excess
- hypernatremia: fluid deficit
b. Potassium (K) 3.5-5 meq/L
- inc. or dec. levels can cause
dysrhythmias
c. Magnesium (Mg) 1.3-2.1 meq/L
- dec. levels can cause dysrhythmias
CARDIOVASCULAR
SYSTEM
d. Calcium (Ca) 4.5-5.3 meq/L:
- nec. For blood clotting and neuromuscular
activity
- dec. levels cause tetany, inc. levels causes
muscle atony
- dec. and inc. levels cause dysrhythmias
3. Serum Lipids
a. Total Cholesterol 150-200mg/dl:
- high levels predispose to atherosclerotic HD
CARDIOVASCULAR
SYSTEM
b. High density lipids (HDL) 30-85 mg/dl
- low levels predispose to CVD
c. Low density lipids (LDL) 50-140 mg/dl:
- high levels predispose to atherosclerotic
plaque formation
d. Triglycerides 10-150 mg/dl:
- high levels increase risk of atherosclerotic
heart disease
CARDIOVASCULAR
SYSTEM
B. Hematologic Studies
1. CBC
2. Coagulation time: 5-15mins; inc. levels indicate
bleeding tendency, used to monitor heparin tx.
3. Prothrombin time (PT) 9.5-12sec.; INR 1.0,
used to monitor warfarin tx.
4. Activated partial thromboplastin time (APTT)
20-45sec; used to monitor heparin therapy
5. Erythrocyte sedimentation rate(ESR)
<20mm/hr; inc. level indicate inflamm. process
CARDIOVASCULAR
SYSTEM
C. Urine Studies (routine U/A)
D. Electrocardiogram (ECG)
1. Noninvasive ECG – a graphic record of the electrical
activity of the heart
2. Portable recorder (Holter monitor) – provides
continuous recording of ECG for up to 24 hrs.
E. Exercise ECG (stress test): the ECG is recorded during
prescribed exercise; may show heart disease when
resting ECG does not
F. Echocardiogram: noninvasive recording of the cardiac
structures using ultrasound
CARDIOVASCULAR
SYSTEM
G. Cardiac catheterization: invasive, but often
definitive test for diagnosis of cardiac disease.
1. A catheter is inserted into the right or left side
of the heart to obtain information
2. Purpose: to measure intracardiac pressures
and oxygen levels in various parts of the heart;
with injection of a dye, it allows visualization of
the heart chambers, blood vessels and blood flow
(angiography)
CARDIOVASCULAR
SYSTEM
3. Nursing care: prior to the test
- informed consent
- any allergies esp. to iodine
- keep client on NPO for 8-12 hrs
- record height, weight, V/S
- inform client that a feeling of warmth
and fluttering sensation as catheter is inserted
CARDIOVASCULAR
SYSTEM
4. Nursing care: post test
- assess circulation to the extremity used for
catheter insertion
- check peripheral pulses, color, sensation of
affected extremity
- if protocol requires, keep affected ext. straight
for approx. 8 hrs.
- observe catheter insertion site for swelling,
bleeding
- assess V/S and report for sig. changes
CARDIOVASCULAR
SYSTEM
H. Coronary arteriography
1. visualization of coronary arteries by
injection of radiopaque contrast dye and
recording on a movie film.
2. Purpose: evaluation of heart disease
and angina, location of areas of infarction and
extent of lesions, ruling out coronary artery
disease in clients with MI.
3. Nursing care: same as cardiac
catheterization
ANALYSIS
Nursing diagnosis for the client with CVD include
A. Fluid volume excess
B. Decreased cardiac output
C. Altered peripheral tissue perfusion
D. Impairment of skin integrity
E. Risk for activity intolerance
F. Pain
G. Ineffective coping
H. Fear
I. Anxiety
PLANNING AND
IMPLEMENTATION
GOALS
A. Fluid imbalance will be resolved, edema minimized
B. Cardiac output will be improved.
C. Cardiopulmonary and peripheral tissue perfusion
will be improved
D. Adequate skin integrity will be maintained
E. Activity intolerance will progressively increase
F. Pain in the chest will be diminished
G. Client’s level of fear and anxiety will be decreased
PLANNING AND
IMPLEMENTATION
INTERVENTIONS
CARDIAC MONITORING
A. ECG
1. strip: small square: 0.04secs.
large square: 0.2secs.
2. P wave: produced by atrial depolarization;
indicates SA node function
PLANNING AND
IMPLEMENTATION
3. P-R interval (N˚= 0.12 - 0.20 secs.)
a. indicates AV conduction time or the time it
takes an impulse to travel from the atria down
and through the AV node
b. measured from beginning of P wave to
beginning of QRS complex
4. QRS complex (N˚= 0.06-0.10 secs.)
a. indicates ventricular depolarization
b. measured from onset of Q wave to end of S
wave
PLANNING AND
IMPLEMENTATION
5. ST segment
a. indicates time interval between complete
depolarization of ventricles and repolarization of
ventricles
b. measured after QRS complex to beginning of T
wave
6. T wave
a. represents ventricular repolarization
b. follows ST segment
PLANNING AND
IMPLEMENTATION
HEMODYNAMIC MONITORING
(Swan Ganz Catheter)
A. A multilumen catheter with a balloon tip that is
advanced through the superior vena cava into the
RA, RV, and PA. When it is wedged it is in the distal
arterial branch of the pulmonary artery.
B. Purpose:
1. Proximal port: measures RA pressure
2. Distal port:
a. measures PA pressure and PCWP
PLANNING AND
IMPLEMENTATION
b. normal values: PA systolic and diastolic
less than 20mmHg; PCWP 4-12mmHg
C. Nursing care
1. a sterile dry dressing should be applied to site
and changed every 24 hours; inspect site daily
and report signs of infection
2. if catheter is inserted via an extremity,
immobilize extremity to prevent catheter
dislodgment or trauma.
PLANNING AND
IMPLEMENTATION
3. Observe catheter site for leakage
4. Ensure that balloon is deflated with a syringe
attached except when PCWP is read
5. Continuously monitor PA systolic and diastolic
pressures and report significant variations
6. Irrigate line before each reading of PCWP
7. Maintain client in same position for each
reading
8. Record PA systolic and diastolic readings at
least every hour and PCWP as ordered.
PLANNING AND
IMPLEMENTATION
CENTRAL VENOUS PRESSURE (CVP)
A. Obtained by inserting a catheter into the external
jugular, antecubital, or femoral vein and
threading it into the vena cava. The catheter is
attached to an IV infusion and H2O manometer
by a three way stopcock
B. Purposes:
1. Reveals RA pressure, reflecting alterations in
the RV pressure
PLANNING AND
IMPLEMENTATION
2. Provides information concerning blood volume
and adequacy of central venous return
3. Provides an IV route for drawing blood
samples, administering fluids or medication, and
possibly inserting a pacing catheter
C. Normal range is 4-10 cmH20;
elevation indicates hypervolemia,
decreased level indicates hypovolemia
D. Nursing care
1. Ensure client is relaxed
PLANNING AND
IMPLEMENTATION
2. Maintain zero point of manometer always at
level of right atrium (midaxillary line)
3. Determine patency of catheter by opening IV
infusion line
4. Turn stopcock to allow IV solution to run into
manometer to a level of 10-20cm above expected
pressure reading
5. Turn stopcock to allow IV solution to flow from
manometer into catheter; fluid level in
manometer fluctuates with respiration
PLANNING AND
IMPLEMENTATION
6. Stop ventilatory assistance during
measurement of CVP
7. After CVP reading, return stopcock to IV
infusion position
8. Record CVP reading and position of client
EVALUATION
DISORDERS OF THE
CARDIOVASCULAR SYSTEM
HEART
CORONARY ARTERY DISEASE (CAD)
A. General Information
1. refers to a variety of pathology that cause
narrowing or obstruction of the coronary arteries,
resulting in decreased blood supply to the
myocardium
2. major causative factor: Atherosclerosis
3. bet 30-50 y.o., men>women
4. may manifest as angina pectoris or MI
CORONARY ARTERY
DISEASE
5. Risk factors:
- family history of CAD - DM
- el. Serum lipoproteins - hypertension
- cigarette smoking - obesity
- el serum uric acid - lifestyle
B. Medical mgt:
1. Drug therapy: nitrates, beta adrenergic blocking
agents, and/or calcium blocking agents, lipid
reducing drugs if cholesterol is elevated
ANGINA PECTORIS
2. Lifestyle modification
3. Surgery: coronary bypass surgery
C. Assessment Findings:
1. Pain: substernal with possible radiation to the
neck, jaw, back and arms, relieved by REST
2. Palpitations, tachycardia, dyspnea, diaphoresis
3. el. serum lipid levels
ANGINA PECTORIS
4. Diagnostic tests:
- ECG may reveal ST segment depression and T-
wave inversion during chest pain
- Stress test may reveal an abnormal ECG during
exercise
D. Nursing interventions:
1. administer oxygen
2. give prompt pain relief with nitrates or narcotic
analgesics as ordered.
ANGINA PECTORIS
3. Monitor V/S, status of cardiopulmonary
function, monitor ECG
4. place patient in semi-high Fowler’s position
5. provide emotional support, health teachings
and discharge instructions.
6. Instruct client to notify physician immediately if
pain occurs and persists, despite rest and
medication administration.
MYOCARDiAL
INFARCTiON
A. General information:
1. The death of myocardial cells from inadequate
oxygenation, often caused by a sudden complete
blockage of a coronary artery; characterized by
localized formation of necrosis (tissue
destruction) with subsequent healing by scar
formation and fibrosis.
2. Risk factors:
- atherosclerotic CAD - DM
- thrombus formation - hypertension
MYOCARDiAL
INFARCTiON
B. Assessment findings:
1. Pain same as in angina, crushing, viselike with
sudden onset; UNRELIEVED by rest or nitrates
2. nausea/vomiting, dyspnea
3. skin: cool, clammy, ashen
4. elevated temperature
5. initial increase in BP and pulse, with gradual
drop in BP
6. Restlessness
MYOCARDiAL
INFARCTiON
7. Occasional findings: rales or crackles; presence of
S4; pericardial friction rub; split S1, S2
8. Diagnostic tests:
a. elevated WBC, cardiac enzymes (troponin,
CPK-MB, LDH, SGOT)
b. ECG changes (specific changes dependent on
location of myocardial damage and phase of the
MI; inverted T wave and ST segment changes
seen with myocardial ischemia
c. inc. ESR, el. serum cholesterol
MYOCARDiAL
INFARCTiON
C. Nursing interventions:
1. establish a patent IV line
2. provide pain relief; morphine sulfate IV (poor
peripheral perfusion, false + for enzymes)
3. Administer O2 as ordered to relieve dyspnea
and prevent arrhythmias
4. Provide bed rest with semi fowler’s position
5. Monitor ECG and hemodynamic procedures
6. Administer anti-arrhythmias as ordered.
MYOCARDiAL
INFARCTiON
7. Monitor I & O, report if UO <30 ml/hr
8. Maintain full liquid diet with gradual increase to
soft, low salt
9. Maintain quiet environment
10. Administer stool softeners as ordered
11. Relieve anxiety associated with CCU
environment
12. Administer anticoagulants, thrombolytics (tpa
or streptokinase) as ordered and monitor for S/E
MYOCARDiAL
INFARCTiON
13. Provide client teaching and discharge instruction
concerning
- effects of MI, healing process and treatment regimen
- Medication regimen: name, purpose, schedule, dosage,
S/E
- Risk factors with necessary lifestyle modification
- Dietary restrictions: low salt, low cholesterol, avoidance
of caffeine
- Resumption of sexual activity as ordered (usually 4-
6weeks)
MYOCARDiAL
INFARCTiON
- Need to report the ff. symptoms:
* increased persistent chest pain
* pain, dyspnea, weakness, fatigue
* persistence palpitations, light
headedness
- Enrollment of client in a cardiac rehabilitation
program
DYSRHYTHMIAS
An arrhythmia is a disruption in the normal
events of the cardiac cycle. It may take a variety
of forms.
Treatment varies on the type dysrhythmias
SINUS TACHYCARDIA
A. General Information:
1. A heart rate of over 100 beats/min, originating
in the SA node
DYSRHYTHMIAS
2. May be caused by:
- fever - anemia
- apprehension - hyperthyroidism
- physical activity - myocardial ischemia
- caffeine - drugs (epi., theo)
B. Assessment findings:
1. Rate: 100-160 beats /min
2. Rhythm: regular
DYSRHYTHMIAS
3. P wave: precedes each QRS complex with
normal contour
4. P-R interval: normal (0.08 sec)
5. QRS complex: normal (0.06 sec)
C. Treatment;
- correction of underlying cause, elimination of
stimulants, sedatives, propranolol (Inderal)
DYSRHYTHMIAS
SINUS BRADYCARDIA
A. General Information:
1. A slowed heart rate initiated by SA node
2. Caused by:
- excessive vagal or decreased sympathetic tone
- MI - IC tumors
- meningitis - myxedema
- cardiac fibrosis
- normal variation of the heart rate in well trained
athletes
DYSRHYTHMIAS
B. Assessment findings:
1. Rate: <60 beats/min
2. Rhythm: regular
3. P wave: precedes each QRS with a normal
contour
4. P-R interval: normal
5. QRS complex: normal
C. Treatment: usually not needed
- if cardiac output is inadequate: atropine and
isoproterenol; pacemaker
DYSRHYTHMIAS
ATRIAL FIBRILLATION
A. General information
1. An arrhythmia in which ectopic foci cause
rapid, irregular contractions of the heart
2. seen in clients with
- rheumatic mitral stenosis - thyrotoxicosis
- cardiomyopathy - pericarditis
- hypertensive heart disease - CHD
DYSRHYTHMIAS
B. Assessment findings:
1. Rate: atrial: 350-600 beats/min
ventricular: varies bet. 100-160 beats /min
2. Rhythm: atrial and ventricular regularly
irregular
3. P wave: no definite P wave; rapid undulations
called fibrillatory waves
4. P-R interval: not measurable
5. QRS complex: generally normal
DYSRHYTHMIAS
C. Treatment: digitalis preparations, propanolol,
verapamil in conjunction with digitalis; direct
current cardioversion
B. Assessment findings:
1. Rate: varies according to no. of PVC’s
2. Rhythm: irregular because of PVC’s
3. P wave: normal; however, often lost in QRS
complex
DYSRHYTHMIAS
4. P-R interval: often not measurable
5. QRS complex: greater then 0.12secs, wide
C. Treatment:
1. IV push of Lidocaine (50-100mg) followed by
IV drip of lidocaine at rate of 1-4 mg/min
2. Procainamide, quinidine
3. Treatment of underlying cause
DYSRHYTHMIAS
VENTRICULAR TACHYCARDIA
A. General information:
1. 3 or more consecutive PVC’s; occurs from
repetitive firing of an ectopic focus in the
ventricles
2. caused by:
- MI - CAD
- digitalis intoxication - hypokalemia
DYSRHYTHMIAS
B. Assessment findings:
1. Rate: atrial: 60-100 beats/min
ventricular: 110-250 beats/min
2. Rhythm: atrial(regular), ventricular (occly.
irregular)
3. P wave: often lost in QRS complex
4. P-R interval usually not measurable
5. QRS complex: greater than 0.12 secs, wide
DYSRHYTHMIAS
C. Treatment:
1. IV push of lidocaine (50-100mg), then IV drip
of lidocaine 1-4 mg/min
2. Procainamide via IV infusion of 2-6 mg/min
3. direct current cardioversion
4. bretylium, propanolol
PERCUTANEOUS
TRANSLUMINAL CORONARY
ANGIOPLASTY (PTCA)
A. General information:
1. PTCA can be performed instead of coronary
artery bypass graft surgery in various clients with
single vessel CAD.
2. Aim: revascularize the myocardium
decrease angina – increase survival
3. a balloon tipped catheter is inserted into the
stenotic, diseased coronary artery. The balloon is
inflated with a controlled pressure and thereby
decreases the stenosis of the vessel
CORONARY ARTERY
BYPASS SURGERY
A. General information:
1. A coronary artery bypass graft is the surgery of
choice for clients with severe CAD
2. new supply of blood brought to
diseased/occluded coronary artery by bypassing
the obstruction with a graft that is attached to the
aorta proximally and to the coronary artery distally
3. Procedure requires use of extracorporeal
circulation (heart-lung machine, cardiopulmonary
bypass)
CORONARY ARTERY
BYPASS SURGERY
B. Nursing interventions: preoperative
1. Explain anatomy of the heart, function of
coronary arteries, effects of CAD
2. Explain events of the day of surgery
3. Orient to the critical and coronary care units and
introduce to staff
4. Explain equipments to be used (monitors,
hemodynamic procedures, ventilators, ET, etc)
5. Demonstrate activity and exercise
6. Reassure availability of pain medications
CORONARY ARTERY
BYPASS SURGERY
C. Nursing interventions: post-operative
1. Maintain patent airway
2. Promote lung re-expansion
3. monitor cardiac status
4. maintain fluid and electrolyte balance
5. maintain adequate cerebral circulation
6. provide pain relief
7. prevent abdominal distension
CORONARY ARTERY
BYPASS SURGERY
8. Monitor for and prevent the ff. complications:
a. Thrombophlebitis / pulmonary embolism
b. Cardiac tamponade
c. arrhythmias
d. CHF
9. Provide client teaching and discharge planning
concerning:
a. limitation with progressive increase in
activities
CORONARY ARTERY
BYPASS SURGERY
b. sexual intercourse can usually be resumed by
3rd or 4th week post-op
c. medical regimen
d. meal planning with prescribed modifications
e. wound cleansing daily with mild soap and H2O
and report for any signs of infection
f. Symptoms to be reported:
- fever, dyspnea, chest pain with minimal
exertion
CONGESTIVE HEART
FAILURE
A. Gen. Info:
- Inability of the heart to pump an adequate
supply of blood to meet the metabolic needs of
the body
B. Types:
1. Left sided heart failure
2. Right sided heart failure
CONGESTIVE HEART
FAILURE
1. LEFT SIDED HEART FAILURE
a. Left ventricular damage causes blood to back up
through the left atrium and into the pulmonary veins.
Increased pressure causes transudation into the
interstitial tissues of the lungs with resultant pulmonary
congestion
b. Caused by:
- left ventricular damage (MI, CAD)
- hypertension, aortic valve disease (AI, AS)
- mitral stenosis, cardiomyopathy
CONGESTIVE HEART
FAILURE
c. Assessment findings:
Signs:
- easy fatigability, dyspnea on exertion, PND,
orthopnea, cough, nocturia, confusion
Symptoms:
- S3 gallop, tachycardia, tachypnea, rales,
wheezing, pleural effusion
CONGESTIVE HEART
FAILURE
d. Diagnostic tests:
- ECG, chest x-ray (cardiomegaly, pleural
effusion), echocardiography, cardiac
catheterization, dec. PO2, inc. PCO2
c. Assessment findings:
Symptoms:
- easy fatigability, lower extremity swelling, early
satiety, RUQ discomfort
CONGESTIVE HEART
FAILURE
Signs:
- elevated jugular venous pressure,
hepatomegaly, ascites, lower extremity edema
d. Diagnostic tests:
- chest x-ray: reveals cardiac hypertrophy
- echocardiography: indicates inc. size of cardiac
chambers
- elevated CVP, dec. PO2, inc. ALT(SGPT)
CONGESTIVE HEART
FAILURE
C. Medical Management:
1. determination and elimination/control of
underlying cause
2. Drug therapy:
- Diuretics: Furosemide, Spironolactone
- Dilators: ACE inhibitors, nitrates
- Digitalis: digoxin
3. Diet: low salt, low cholesterol
* If medical therapies unsuccessful, mechanical assist devices (intra-aortic
balloon pump), cardiac transplantation or mechanical hearts may be
employed.
CONGESTIVE HEART
FAILURE
D. Nursing Interventions:
1. Monitor respiratory status and provide
adequate ventilation (when CHF progresses to
pulmonary edema)
2. Provide physical and emotional rest
3. Increase cardiac output
4. Reduce/eliminate edema
5. Provide client teaching and discharge planning
CARDIAC ARREST
A. General Info:
- sudden, unexpected cessation of breathing and
adequate circulation of blood by the heart
B. Medical management:
1. Cardiopulmonary resuscitation (CPR)
2. Drug therapy:
a. lidocaine, procainamide, verapamil
b. Dopamine, isoproterenol, Norepinephrine
CARDIAC ARREST
c. Epinephrine to enhance myocardial automaticity,
excitability, conductivity, and contractility
d. Atropine sulfate to reduce vagus nerve’s control over
the heart, thus increasing the heart rate
e. Sodium bicarbonate: administered during first few
moments of a cardiac arrest to correct respiratory and
metabolic acidosis
f. Calcium chloride: calcium ions help the heart beat
more effectively by enhancing the myocardium's contractile
force
3. Defibrillation
CARDIAC ARREST
C. Assessment findings:
- unresponsiveness, cessation of respiration, pallor,
cyanosis, absence of heart rate/ BP/pulses, dilation of
pupils, ventricular fibrillation
D. Nursing interventions:
1. Begin precordial thump and if successful, administer
lidocaine
2. If unsuccessful, defibrillation - CPR
3. Assist with administration of and monitor effects of
emergency drugs
CARDIOPULMONARY
RESUSCITATION
A. General info: process of externally supporting the
circulation and respiration of a person who has
had a cardiac arrest
B. Assessment:
- fever, pericardial friction rub, gallop rhythm
- murmur, signs of heart failure, fatigue, dyspnea
- tachycardia, chest pain
MYOCARDITIS
C. Implementation:
1. Assist client to assume a position of comfort
2. Administer analgesics, salicylates, NSAIDS
3. Administer O2, provide adequate rest periods
4. Limit activities, to dec. workload of heart
5. Treat underlying cause
6. Administer meds. as ordered:
- antibiotics, diuretics, ACE inhibitors, digitalis
7. Monitor complications: thrombus, heart failure,
cardiomyopathy
PERICARDITIS
A. General Info:
1. An inflammation of the visceral and parietal
pericardium
2. caused by bacterial, viral, or fungal infection;
collagen diseases; trauma; acute MI, neoplasms,
uremia, radiation, drugs (procainamide,
hydralazine, Doxorubicin HCL)
PERICARDITIS
B. Medical management:
1. Determination and elimination/control of
underlying cause
2. Drug therapy
a. Medication for pain relief
b. Corticosteroids, *salicylates (aspirin),
indomethacin, to reduce inflammation
3. Specific antibiotic therapy against the causative
organism may be indicated
PERICARDITIS
C. Assessment findings:
1. chest pain with deep inspiration (relieved by
sitting up), cough, hemoptysis, malaise
2. tachycardia, fever, pericardial friction rub,
cyanosis or pallor, jugular vein distension
3. Elevated WBC and ESR, normal or inc. SGOT
4. Diagnostic test:
a. chest x-ray may show increased heart size
b. ECG: ST elevation, T wave inversion
PERICARDITIS
D. Nursing Interventions:
1. Ensure comfort, bed rest with semi- or high
Fowler’s position
2. Monitor hemodynamic parameters
3. Administer medications as ordered and monitor
effects
4. Provide client teaching and discharge planning:
- S/S of pericarditis indicative of recurrence (chest
pain intensified by lying down and relieved when
sitting up; medication regimen
CONGENITAL HEART
DISEASE (CHD)
A. General Info:
1. CHDs are structural defects of the heart, great
vessels, or both that are present from birth
2. 2nd only to prematurity as a cause of death in the
first year of life
1. Pathophysiology
- blood flows from the aorta through the PDA and
back to the pulmonary artery and lungs, causing
inc. LV workload and increase pulmonary vascular
congestion
ACYANOTIC CHD (PDA)
2. Assessment findings:
a. Clinical manifestations:
1. if defect is small, child may be aysmptomatic
2. a loud machine like murmur is characteristic
3. child may have frequent resp. infections
4. child may have CHF with poor feeding, fatigue,
hepatosplenomegaly, poor weight gain, tachypnea
and irritability
5. widened pulse pressure and bounding pulse rate
maybe detected
ACYANOTIC CHD (PDA)
b. Laboratory and diagnostic findings:
1. ECG – normal but may show ventricle enlargement if the
shunt is large
3. Nursing management:
a. Provide family teaching abt. treatment options
- some close spont; others can be closed surgically or nonsurgically
b. In premature infants, PDA sometimes can be
closed using prostaglandin synthetase inhibitors
(Indomethacin) w/c stimulate closure of the ductus arteriosus
ACYANOTIC CHD (ASD)
B. ATRIAL SEPTAL DEFECT
- an abnormal communication between the to
atria; results when the atrial septal tissue does not
fuse properly during embryonic devt.
1. Pathophysiology
a. pressure is higher in the left atrium than the
right, causing blood to shunt from left to right
b. the RV and PA enlarge because they are
handling more blood
ACYANOTIC CHD (ASD)
2. Assessment findings:
a. Clinical manifestations:
- most infants tend to be aysmptomatic until early
childhood and many defects close spont. By 5y.o.
- symptoms vary with the size of the defect,
fatigue and dyspnea on exertion are the mc
- slow weight gain and frequent respiratory
infections may occur
- systolic ejection murmur may be auscultated,
usually most prominent at the 2nd ICS
ACYANOTIC CHD (ASD)
b. Laboratory and diagnostic study findings:
- echocardiography with doppler gen. reveals the enlarged R
side of the heart and the inc. pulmonary circulation
- cardiac catheterization demonstrates the separation of the R
atrial septum and the inc. oxygen saturation in the R atrium
3. Nursing management:
a. Provide family teaching abt. treatment options:
- defects are usually repaired in girls due to possibility of clot formation
during child bearing years
- small ASDs are left open in boys, larger ones are repaired
- surgical closure is performed during the school age years
ACYANOTIC CHD (VSD)
C. VENTRICULAR SEPTAL DEFECT
- the most common CHD, is an abnormal opening
between the right and left ventricles
- the degree of this defect vary from a pinhole
between the R & L ventricles to an absent septum
1. Pathophysiology
a. pressure from the LV causes blood to flow through
the defect to RV, resulting in increased pulmonary
vascular resistance and right heart enlargement
ACYANOTIC CHD (VSD)
b. RV and PA pressures increase, leading eventually
to obstructive pulmonary vascular disease
2. Assessment findings:
- symptoms vary with the size of the defect, age
and amt of resistance, usually the child is asymp.
- failure to thrive, excessive sweating, fatigue
- more susceptible to pulmonary infections
- may exhibit s/s of CHF
ACYANOTIC CHD (VSD)
b. Laboratory and diagnostic study findings:
- Echocardiography with Doppler U/S or MRI
reveals RVH and possible PA dilatation from the inc. blood flow
- ECG shows RVH
3. Nursing management
a. provide family teaching abt treatment options
- some VSDs close spontaneously
- others are closed with a Dacron patch, recommended for large
defects, PA hypertension, CHF, recurrent resp. infxns. FTT
CYANOTIC CHD (TOF)
ACYANOTIC CHD
A. TETRALOGY OF FALLOT (TOF)
- consists of 4 major anomalies:
a. VSDc. PS
b. RVH d. overriding aorta
1. Pathophysiology
a. PS impedes the flow of blood to the lungs, causing
increased pressure in the RV, forcing deoxygenated
blood through the septal defect to the LV
CYANOTIC CHD (TOF)
b. the increased workload on the RV causes hypertrophy.
The overriding aorta receives blood from both right and
left ventricles.
2. Assessment findings:
a. Clinical manifestations: vary, depending on the size
of the VSD and the degree of PS.
1. Acute episodes of cyanosis (“tet spells”) and transient
cerebral ischemia. “Tet spells” are char. By irritability,
pallor, and blackouts or convulsions.
2. Cyanosis occurring at rest (as PS worsens)
CYANOTIC CHD (TOF)
3. Squatting (a char. posture of older children that
serves to decrease the return of poorly oxygenated
venous blood from the lower extremities and to inc.
SVR, w/c increases pulmonary blood flow and eases
respiratory effort)
4. slow weight gain
5. clubbing, exertional dyspnea, fainting, or fatigue
slowness due to hypoxia
6. a pansystolic murmur may be heard at the mid-
lower left sternal border
CYANOTIC CHD (TOF)
b. Laboratory and diagnostic study findings
1. echocardiography and ECG show the enlarged
chambers of the right side of the heart
2. echocardiography also demonstrates the decrease in
the size of the PA and the reduced blood flow through
the lungs
3. cardiac catheterization and angiography allow
definitive evaluation of the extent of the defect,
particularly the PS and the VSD
4. CBC reveals polycythemia, ABG demonstrate
reduced oxygen saturation
CYANOTIC CHD (TOF)
3. Nursing management
a. Provide family teaching about treatment options
1. elective repair is usually performed during
the infant’s 1st year of life, but palliative repairs may
be warranted for infants who cannot undergo primary
repair
2. total repair involves VSD closure,
infundibular stenosis resection, and pericardial patch
to enlarge RV outflow tract
b. Provide preoperative and postoperative care
CYANOTIC CHD (TGV)
B. TRANSPOSITION OF GREAT VESSELS (TGV)
- in TGV, the PA leaves the LV and the aorta exits the
RV, there is no communication between the systemic
and pulmonary circulations
1. Pathophysiology
a. this defect results in two separate circulatory patterns;
the right heart manages systemic circulation and the left
manages pulmonary circulation
b. to sustain life, the child must have an associated
defect.
CYANOTIC CHD (TGV)
Associated defects such as septal defects or a PDA,
permit oxygenated blood into the systemic circulation
but cause increased cardiac workload.
c. Potential complications include CHF, infective
endocarditis, brain abscess, and cerebral vascular
accidents resulting from hypoxia or thrombosis.
2. Assessment findings:
a. Clinical manifestations vary, depending on
associated defects
CYANOTIC CHD (TGV)
1. In infants with minimal communication (no associated
defects), severe respiratory depression and cyanosis, will
be evident at birth
2. In infants with associated defects, there is less cyanosis
but the infant may have symptoms of CHF
3. easily fatigued, FTT
C. TRUNCUS ARTERIOSUS
- failure of normal septation and division of the embryonic
bulbar trunk into the PA and aorta, resulting in a single
vessel that overrides both ventricles
CYANOTIC CHD
1. Pathophysiology
a. blood ejected from the ventricles enters the common
artery and flows either the lungs or aortic arch.
b. pressure in both ventricles is high and blood flow to
the lungs is markedly increased.
2. Assessment findings:
a. neonates with this defect appear normal; however,
as pulmonary vascular resistance decreases after birth,
severe pulmonary edema and CHF commonly develop
CYANOTIC CHD
2. marked cyanosis, especially on exertion; S/S of CHF;
LVH, dyspnea, marked activity intolerance, and
retarded growth
3. loud systolic murmur best heard at the lower left
sternal border and radiating throughout the chest
b. Laboratory and diagnostic study findings:
- echocardiography reveals the defect
4. Nursing management
a. surgical repair is necessary in the 1st few months of
life, the mortality rate associated with surgery is greater
than 10%; w/o surgery, children die w/in 1 yr.
OBSTRUCTIVE CHD (COA)
OBSTRUCTIVE CHD
A. COARCTATION OF AORTA (COA)
- a defect that involves a localized narrowing of the aorta
1. Pathophysiology
a. COA is char. by inc. pressure proximal to the defect
and decreased pressure distal to it
b. restricted blood flow through the narrowed aorta
increases the pressure on the LV and causes dilation of
the proximal aorta and LVH, w/c may lead to LVF
OBSTRUCTIVE CHD (COA)
c. eventually, collateral vessels develop to bypass the
coarctated segment and supply circulation to the LE
2. Assessment findings:
a. Clinical manifestations
1. the child may be asymptomatic or may experience
the classic difference in BP and pulse quality between
the upper and lower ext. – the BP is elevated in the UE
and dec. in the LE while the pulse is bounding in the
UE and dec. or absent in the LE. Thus femoral pulse
are weak or absent
OBSTRUCTIVE CHD (COA)
2. epistaxis, headaches, fainting and lower leg cramps
3. a systolic murmur may be heard over the left anterior
chest and between the scapula posteriorly
4. rib notching may be observed in an older child
b. Laboratory and diagnostic findings
1. ECG, echocardiography, and chest x-ray may reveal
left sided heart enlargement resulting from back pressure
2. the radiograph may also demonstrate rib notching
from enlarged collateral vessels
OBSTRUCTIVE CHD (COA)
3. Nursing management
a. repair involves surgical removal of the stenotic area
b. nonsurgical repair via balloon angioplasty
2. Assessment findings:
a. clinical manifestations:
1. faint pulse, hypotension, tachycardia, and poor
feeding pattern
2. exercise intolerance, chest pain, and dizziness when
standing for long periods
3. a systolic ejection murmur may be heard best at the
2nd ICS
OBSTRUCTIVE CHD (AS)
b. Laboratory and diagnostic study findings:
1. ECG or echocardiography reveals LVH
2. cardiac catheterization demonstrates degree of the
stenosis
3. Nursing management:
a. if the child’s symptoms warrant, surgical aortic
valvulotomy or prosthetic valve replacement is
necessary
b. balloon angioplasty can be used to dilate the narrow
valve
OBSTRUCTIVE CHD (PS)
C. PULMONIC STENOSIS (PS)
- a defect that involves obstruction of blood flow from the
right ventricle
1. Pathophysiology
a. RV pressure increases leading to RVH and eventually RV
failure may occur
2. Assessment findings:
a. Clinical manifestations
1. may be asymptomatic or may have mild cyanosis or CHF
OBSTRUCTIVE CHD (PS)
2. a systolic murmur may be heard over the pulmonic
area; a thrill may be heard if stenosis is severe
3. in severe cases, decreased exercise tolerance,
dyspnea, precordial pain and generalized cyanosis may
occur
Types:
a. Essential (primary, idiopathic): marked by loss of
elastic tissue and arteriosclerotic changes in the aorta
and larger vessels coupled with decreased caliber of the
arterioles
b. Benign: a moderate rise in BP marked by a gradual
onset and prolonged course
HYPERTENSION
c. Malignant: characterized by a rapid onset
and short dramatic course with a DBP of >150mmHg
d. Secondary: elevation of the BP as a result of
another disease such as renal parenchymal disease,
Cushing’s disease, pheochromocytoma, primary
aldosteronism, coarctation of the aorta
B. Medical management:
1. Diet and weight reduction (restricted sodium, kcal,
cholesterol)
2. Lifestyle changes: alcohol moderation, exercise
regimen, cessation of smoking
3. Antihypertensive drug therapy
HYPERTENSION
C. Assessment findings:
1. Pain similar to anginal pain; pain in calves of legs after
ambulation or exercise (intermittent claudication); severe
occipital headaches, particularly in the morning; polyuria;
nocturia; fatigue; dizziness; epistaxis; dyspnea on exertion
2. BP consistently above 140/90, retinal hges and exudates,
edema of extremities
3. Rise in SBP from supine to standing position (indicative of
essential hypertension)
4. Diagnostic tests: elevated serum uric acid, sodium,
cholesterol levels
HYPERTENSION
D. Nursing interventions:
1. Record baseline BP in 3 positions (lying, sitting, standing)
and in both arms
2. Continuously assess BP and report any variables that
relate to changes in BP (positioning, restlessness)
3. Administer antihypertensive agents as ordered; monitor
closely and assess for S/E
4. Monitor intake and hourly output
5. Provide client teaching and discharge planning:
- risk factors, dietary instructions, compliance of
antihypertensive medications, routine follow up w/ MD
ARTERIOSCLEROSIS
OBLITERANS
- a chronic occlusive arterial disease that may affect
the abdominal aorta or the LE. The obstruction to
blood flow with resultant ischemia usually affects
the femoral, popliteal, aortic and iliac arteries
- occurs most often in men ages 50-60
- caused by atherosclerosis
- Risk Factors: cigarette smoking, hyperlipidemia,
hypertension, DM
ARTERIOSCLEROSIS
OBLITERANS
B. Medical management:
1. Drug therapy
a. Vasodilators: papaverine, Isoxsuprine Hcl (Vasodilan),
Nylidrin Hcl (Arlidin), nicotinyl alcohol (Roniacol)
cyclandelate (Cyclospasmol), tolazoline Hcl (priscoline) to
improve arterial circulation; effectiveness questionable
C. Assessment findings:
1. Pain both intermittent claudication and rest pain,
numbness or tingling of the toes
2. Pallor after 1-2 mins. Of elevating feet, and dependent
hyperemia/rubor; diminished or absent dorsalis pedis,
posterior tibial and femoral pulses; shiny, taut skin
with hair loss on lower legs
ARTERIOSCLEROSIS
OBLITERANS
3. Diagnostic tests:
a. Oscillometry may reveal decrease pulse volume
b. Doppler U/S reveals decreased blood flow through
affected vessels
c. Angiography reveals location and extent of
obstructive process
4. Elevated serum triglycerides; sodium
D. Nursing Interventions:
1. Encourage slow, progressive physical activity
ARTERIOSCLEROSIS
OBLITERANS
2. Administer medications as ordered
3. Assist with Buerger-Allen exercises qid
a. client lies with legs elevated above heart for 2-3 mins
b. client sits on edge of bed with legs and feet
dependent and exercises feet and toes – upward and
downward, inward and outward – for 3 mins
c. client lies flat with legs at heart level for 5 mins
4. Assess for sensory function; protect client from injury
5. Provide client teaching and discharge planning: stop
cigarette smoking, diet, drug compliance, exercise
THROMBOANGIITIS
OBLITERANS
(BUERGER’S DISEASE)
- Acute inflammatory disorder affecting medium/smaller
arteries and veins of the LE. Occurs as focal,
obstructive process; results in occlusion of a vessel
with subsequent development of collateral circulation
- Most often affects men ages 25-40; disease is idiopathic;
high incidence among smokers
C. Nursing Interventions:
1. Prepare client for surgery
THROMBOANGIITIS
OBLITERANS
(BUERGER’S DISEASE)
2. Provide client teaching and discharge planning
- drug regimen, avoidance of trauma to the affected
extremity, need to maintain warmth esp. during cold
weathers, importance of stopping smoking
RAYNAUD’S
PHENOMENON
- intermittent episode of arterial spasms, most frequently
involving the fingers; most often affects women
between the teenage years and age 40; cause
unknown
- Predisposing factors: collagen diseases (SLE, RA), trauma
(from typing, playing piano)
C. Nursing interventions
1. provide client teaching concerning:
- importance of stopping smoking; need to maintain warmth;
need to use gloves in handling cold objects; drug regimen
ANEURYSM
- a sac formed by dilation of an artery secondary to
weakness and stretching of an arterial wall. The
dilation may involve one or all layers of the arterial
wall.
Classification
1. Fusiform: uniform spindle shape involving the entire
circumference of the artery
2. Saccular: outpouching on one side only, affecting part of
the arterial circumference
ANEURYSM
3. Dissecting: separation of the arterial wall layers to form a
cavity that fills with blood
4. False: the vessel wall is disrupted, blood escapes into
surrounding area but is held in place by surrounding tissue
A. General info:
1. an aneurysm, usually fusiform or dissecting, in the
descending, ascending, or transverse section of the
thoracic aorta
2. usually occurs in men ages 50-70; caused by arteriosclerosis,
infection, syphilis, hypertension
ANEURYSM
B. Medical management:
1. control of underlying hypertension
2. Surgery: resection of the aneurysm and replacement
with a Teflon/Dacron graft; client will need
extracorporeal circulation
C. Assessment findings:
1. Often asymptomatic; deep, diffuse chest pain;
hoarseness; dysphagia; dyspnea
2. Pallor, diaphoresis, distended neck veins
ANEURYSM
3. Diagnostic tests:
a. Aortography shows exact location of the aneurysm
b. X-rays: chest film reveals abnormal
widening of aorta; abdominal film may show
calcification within walls of aneurysm
2. Surgery
a. Vein ligation and stripping
b. venous thrombectomy: removal of a clot in the
iliofemoral region
c. plication of the inf. vena cava: insertion of an
umbrella-like prosthesis into the lumen of the vena cava
to filter incoming clots
THROMBOPHLEBITIS
C. Assessment findings:
1. Pain in the affected extremity
2. Superficial vein: tenderness, redness, induration along
course of the vein
3. Deep vein: swelling, venous distension of limb, tenderness
over involoved vein, (+) Homan’s sign
4. Elevated WBC and ESR
5. Diagnostic tests:
a. venography (phlebography): inc. uptake of radioactive
material
THROMBOPHLEBITIS
b. Doppler ultrasonography: impairment of blood flow
ahead of thrombus
c. Venous pressure measurements: high in affected
limb until collateral circulation is developed
D. Nursing interventions
1. Provide bed rest, elevating involved extremity
2. Apply continuous warm, moist soaks to dec. lymphatic
congestion
3. Administer anticoagulants as ordered
THROMBOPHLEBITIS
a. Heparin
1. monitor PTT, use infusion pump to administer IV heparin
2. assess for bleeding tendencies (hematuria; hematemesis;
bleeding gums; epistaxis, melena)
3. have antidote ( protamine sulfate) available
b. Warfarin (Coumadin)
1. assess PT daily, advise client to withhold dose and notify
physician immediately if bleeding or signs of bleeding occurs
2. instruct client to use a soft toothbrush and to floss gently,
prepare antidote: Vit. K
THROMBOPHLEBITIS
4. monitor for chest pain or SOB (possible pulmonary
embolism)
5. Provide client teaching and discharge planning:
a. need to avoid standing, sitting for long periods;
constrictive clothing; crossing legs at the knees;
smoking; oral contraceptives
b. importance of adequate hydration
c. use of elastic stockings when ambulatory
d. importance of planned rest with elevation of feet
e. importance of weight reduction and exercise
VARICOSE VEINS
A. General info:
1. Dilated veins that occur most often in the lower extremities
and trunk. As the vessel dilates, the valves become
stretched and incompetent with resultant venous
pooling/edema
2. most common between ages 30-50
3. predisposing factor: congenital weakness of the veins,
thrombophlebitis, pregnancy, obesity, heart disease
D. Nursing interventions:
1. Elevate legs above heart level
VARICOSE VEINS
2. Apply knee length elastic stockings
3. Provide adequate rest
4. Prepare client for vein ligation, if necessary
a. Provide routine pre-op care
b. keep affected extremity elevated above the level of
the heart to prevent edema
c. apply elastic bandages and stockings, which should be
removed every 8hrs for short periods.
d. assist out of bed within 24hrs, ensuring that elastic
stockings are applied.
e. assess for increased bleeding