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Alterations in Cardiovascular
Function in Children
Joy A. Shepard, PhD, RN-C, CNE
Joyce Buck, PhD(c), MSN, RN-C, CNE
1
Learning Outcomes
 Describe anatomy and physiology of
cardiovascular system focusing on blood flow
and action of heart valves
 Contrast pathophysiology associated with
congenital heart defects with increased
pulmonary circulation, decreased pulmonary
circulation, and obstructed systemic blood flow
 Plan the nursing care for an infant with a
congenital heart defect
2
Learning Outcomes (cont’d)
 Plan the nursing care for a child undergoing
open heart surgery
 Recognize signs of congestive heart failure
 Develop a nursing care plan for child with
congestive heart failure
 Differentiate between heart diseases
acquired during childhood and congenital
heart defects
3
Overview of the Cardiovascular
System
4
5
Function of the Heart
 Pulmonary circulation—
Pumps blood to the
lungs for oxygenation
and removal of carbon
dioxide
 Systemic circulation—
Pumps oxygenated
blood to the body
tissues; metabolic
wastes taken away
6
Anatomy of the Heart
 Muscular pump with
four chambers:
 Upper chambers—
atria
 Lower chambers—
ventricles
 Valves, veins, and
arteries connect the
chambers
7
The Heart is Like a House….
 It has:
 Electricity
(power)
and
 Plumbing
(mechanical)
8
Electrical (Conduction) System
 Powers the pump
 Cardiac cycle:
depolarization and
repolarization of the
cardiac muscle
 Conduction pathways:
 Sinoatrial node (SA) —>
 Atrioventricular (AV)
node —>
 Bundle of His —>
 Left and right bundle
branches —>
 Purkinje fibers
9
Pumping System
 Heart—powerful,
muscular pump
 Two pumps: left and
right
 Pressures in the left
much higher than right
 Continuous coordinated
pumping action keeps
the body supplied with
oxygen-rich blood
10
Valves are essential to the
heart's pumping function
 Keeps blood flowing
forward through the
heart
 One-way valve at the
exit of each of the
four chambers:
 Tricuspid
 Pulmonic
 Mitral
 Aortic valves
11
12
Physiology of the Heart
 CO = HR X SV
Heart Rate
 Components of
Stroke Volume:
 Preload
 Afterload
 Contractility
13
Untillateschool-ageandadolescence,cardiacoutputinthechildisRATE
DEPENDENT,notstrokevolumedependent,makingheartratemorerapid.
14
Preload
 Amount of stretch of the myocardial fibers before
contraction
 Measured by central venous pressure (CVP)
15
Afterload
 Amount of resistance against which the heart
(ventricle) pumps
16
Contractility
 “Squeeze”—Strength of muscular contraction
independent of preload (inotropic)
17
Fetal Circulation
(pp. 273-274, Lowdermilk; pp. 569-571 Ball & Bindler)
18
Fetal Circulation
 Fetal circulation
differs from neonatal
circulation in three
ways:
 Gas exchange
 Pressures (systemic
and pulmonary
circulations)
 Structures (shunts,
umbilical cord)
19
Gas Exchange—Placenta; Umbilical
Vein—Oxygenated Blood
 Oxygenation and
removal of carbon
dioxide (gas
exchange) takes
place in the placenta
 Umbilical vein
oxygenated blood to
inferior vena cava
20
Fetal Circulation—Pressure
Differences
 Oxygenated blood flow (from the
placenta) is from right to left
 Oxygenated blood enters right side of
fetal heart
 Blood pressure on the right side of the
heart > blood pressure on the left side
of the heart
21
Fetal Circulation—Pressure
Differences
 High resistance in fetal lungs (arterioles
are constricted, alveoli are filled with
fluid)
 Resistance to blood flow in the lungs
(pulmonary vascular resistance) >
Resistance to blood flow in the body
(systemic vascular resistance)
 Fetal lungs don’t receive much blood
22
Fetal Circulation—1st Shunt
 Ductus venosus—
fetal structure
connecting inferior
vena cava to
umbilical vein
 Most of fetal liver
bypassed (blood
shunted away from
liver)
23
Fetal Circulation— 2nd Shunt
 Inferior vena cava
Right atrium
 Left atrium (by way
of the foramen
ovale)
 Most of lungs
bypassed
 Left ventricle aorta
(supplying heart and
brain)
24
Fetal Circulation—3rd Shunt
 Deoxygenated blood from
the upper body mixes with
oxygenated blood from
the placenta @ the right
atrium
 Ductus arteriosus
descending aorta
(bypassing the lungs)
 Organ systems
 Blood returns to the
placenta (by way of the
two umbilical arteries)
25
26
Transition from Fetal to
Pulmonary Circulation
27
Circulation After Birth—Gas
Exchange
 With the
neonate’s first
breath, gas
exchange is
transferred from
the placenta to
the lungs
  Pa02 levels
  PaC02 levels
28
Circulation After Birth—
Pressure Changes
  Resistance
 Pulmonary
circulation
  Pulmonary blood
flow
  Resistance
 Systemic
circulation
29
Circulation After Birth—
Pressure Changes
 Umbilical cord clamped
  Blood to right heart
 Blood pressure (left side of the
heart) > blood pressure (right side of
heart)
 Systemic vascular resistance >
pulmonary vascular resistance
30
Circulation After Birth—
Pressure Changes
 Lungs inflate with
air, allowing gas
exchange
 Resistance to blood
flow in the lungs
(pulmonary vascular
resistance) decreases
 Much more blood
flows into the lungs
 First breath: alveoli
expand and blood
vessels in the the
lungs open up
31
Circulation After Birth—
Pressure Changes
 Deoxygenated
blood
right heart
lungs
 Oxygenated
blood
left heart
body
32
Circulation After Birth—Shunts
Close
 Fetal shunts close
in response to
pressure changes,
 Pa02 levels, in
the pulmonary
and systemic
circulations
33
To Review…
Normal fetal circulation (lungs and liver bypassed)
Normal circulation after birth (systemic AND
pulmonary circulations; high systemic pressure)
34
Pediatric Cardiac Assessment
35
36
See Video “Pediatric Assessment,” 23:15-24:05
Health History
 Review:
 Table 5-12, p. 141
 Assessment Guide: The Child with a Cardiac Condition,
p. 572
 Congenital heart disease in family
 Maternal illness, infections, medications taken
during pregnancy
 Child’s behavior patterns (playfulness, irritability)
 Medications
37
Health History
 Feeding problems (fatigue or
diaphoresis during feeding; poor weight
gain)
 Respiratory difficulties (tachypnea,
shortness of breath, cyanosis; frequent
respiratory infections)
 Chronic fatigue, exercise intolerance
38
Inspection
 Skin color
 Activity level
 Chest
 Respiratory
pattern
39
Review Question
 An infant who has a cyanotic congenital heart defect
comes into the clinic with complaints of irritability, pallor,
and increased cyanosis that began quickly over the last 30
minutes. As the nurse assesses the infant, the parent asks
why the child’s color is bluish. The best response by the
nurse is, “Skin color is:
A. Related to the time of day.”
B. Related to brain function.”
C. Related to hemoglobin level and oxygen saturation.”
D. Unrelated to your child’s condition.”
40
Auscultation: A(P)TM
 Normal areas of
auscultation
 PMI: 3-4th ICS infants;
4th ICS < 7; 5th ICS > 7
 Heart sounds
 Rhythm: Regular
 S1, S2
 S3 —normal finding in
children
 S4 —cardiac failure
 Murmurs, clicks, friction
rubs
41Auscultate apical pulse with stethoscope for a full 60 seconds
42
Normal Heart Rates for Children of Different Ages
44
Palpation
 Skin temperature
 Pulses
 Blood pressure
 Capillary refill—
normal < 2
seconds
 Chest
45
The sites used to assess the pulses in
children
Significant Findings
 Growth abnormalities
 Cyanosis
 Clubbing of fingers and
toes
 Edema (periorbital,
peripheral)
 Tachypnea
 Pulse alterations (fast,
slow, diminished)
 Hypotension, unequal BP
arms / legs
 Murmurs, bruits, thrills
 Engorged neck veins
 Abdominal distention,
enlarged liver / spleen
47
See “Assessment Guidelines for the Child with a Cardiac Condition,” p. 572
Clubbing of the Fingers
Question
 An infant born at 39 weeks gestation is sent to
the intensive care nursery. The nurse suspects
a possible cardiac anomaly when the admission
assessment reveals:
 A. Projectile vomiting
 B. An irregular respiratory rhythm
 C. Hyperreflexia of the extremities
 D. Unequal peripheral blood pressures
49
Diagnostics
50
Diagnostic Tests / Procedures
 Labs
 EKG
 Chest x-ray
 Echocardiogram
 Cardiac catheterization
51
See Table 21-4: Clinical Interventions for Congenital Heart Defects, p. 574
See Table 21-2: Diagnostic Procedures & Laboratory Tests, p. 571
52
Labs
 Hgb/Hct
 Serum electrolytes
(especially K+,
Mg++, Ca++)
 ABG
 Digoxin level
 Cholesterol
 Triglycerides
 Urine SG
53
Question
 The pediatric nurse practitioner orders a
complete blood workup for a 5-month-old
infant with a cyanotic congenital heart defect.
Because of the infant’s heart disease, the
nurse would expect the report to show:
 A. Polycythemia
 B. Agranulocytosis
 C. Thrombocytopenia
 D. A decreased hematocrit level
54
Pulse Oximetry
 Evaluates degree of
oxygen saturation in the
blood using a small
infrared light probe that
is placed on:
 Finger, toe, earlobe,
bridge of the nose
 Norm: 95 – 100%
 Cyanosis not visible until
sat < 85%
55
12-Lead EKG
 Helps evaluate:
 Cardiac muscle
 Cardiac rate
and rhythm
 Cardiac impulse
conduction
56
Chest X-Ray
 X-ray picture of
heart, organs in
chest cavity
 Provides information
on:
 Size of the heart and
its chambers
 Blood flow to lungs
57
Echocardiogram
 High-frequency sound
waves, noninvasive
 Helps assess:
 Thickness of heart walls
 Size of cardiac chambers
 Motion of valves and septa
(walls) within the heart
 Great vessels and various
cardiac structures
 Defects in structure or
function
58
Cardiac Catheterization
 Provides information on:
 Oxygen levels in cardiac
chambers and great
arteries
 Pressures
 Blood flow
 Cardiac output / stroke
volume
 Anatomic abnormalities
 Cardiac conduction
system
59
Interventional Catheterization
 Corrective treatments
performed by use of
specialized catheters
 Balloon catheters—open
narrowed valves or
arteries
 Balloon/blades—shunt
creations, septostomy
 Device closure—close
extra vessels, “holes” in
heart
60
Cardiac Catheterization—
Nursing Care (p. 573)
 Child must lay still, supine, with affected leg straight
for 4 – 6 hours
 Vital signs, insertion site observed, distal pulses
checked q15 minutes X 1st hour, then q30 minutes
 Observe for bleeding at site; pallor, loss of pulses,
coolness in extremity distal to site
 Push fluids to help flush the dye out of the body
 Observe for reactions to dye (vomiting, rash,
increased creatinine, decreased urinary output)
 Strict I & O
61
Question
 A 3-1/2-year-old child returns to the room after
a cardiac catheterization. Post-procedure
nursing care for the child should include:
 A. Encouraging early ambulation
 B. Monitoring the insertion site for bleeding
 C. Restricting fluids until blood pressure is
stabilized
 D. Comparing blood pressure in affected and
unaffected extremities
62
Heart Disease in Children
63
Heart Disease in Children
 Manifestations in
infants, children:
 Frequent respiratory
infections and dyspnea
 Activity intolerance
 Difficulty and fatigue
during feedings
 Failure to thrive, low
weight
 Pallor, cyanosis, clubbing
64
Manifestation: Respiratory
Difficulties
 Shortness of breath,
difficulty breathing
 Increased respiratory
rate, retractions,
nasal flaring
 Frequent respiratory
infections
 Activity intolerance,
fatigue, delayed
gross motor skills
65
Manifestation: Feeding
Difficulties, Stunted Growth
 Difficulty and
fatigue during
feedings
 Frequent emesis, at
risk for NEC
 Stunted growth
 Low weight
 Failure to thrive
66
Feeding Interventions
 Provide periods of uninterrupted rest
 Neutral thermal environment
 Feed child slowly and more often (q3°
optimal time)
 Frequent, small feedings may be less tiring
 Concentrating formula 24-27 kcal/oz may
increase caloric intake without increasing
infant’s work
67
Feeding Interventions
 Provide relaxed
environment
 Reduce anxiety,
sadness, crying
 Hold infant in upright
position; less
stomach
compression and
improves respiratory
effort
 Place infant on right
side after feeding,
HOB 30 - 45º
68
Feeding Interventions
 Limit bottle feedings to 30 minutes
 If child unable to consume appropriate
amount during 30-minute feeding every
3 hours, consider nasogastric feeding
 Monitor for increased tachypnea,
diaphoresis, or feeding intolerance
(vomiting)
69
Supplemental Feedings
 Infants with cardiac
conditions often
require
supplemental
feedings to provide
sufficient nutrients
for growth and
development
70
Question
 When caring for a 4-month-old infant
with congestive heart failure, the nurse
should:
 A. Force nutritional fluids
 B. Provide small, frequent feedings
 C. Measure the head circumference daily
 D. Position the infant flat on the abdomen
71
Manifestation: Pallor and
Cyanosis
 Bluish discoloration of
skin, nail beds, mucous
membranes
 Hypoxia—tissues are
deprived of adequate
amounts of oxygen (02
sat < 85%)
 Hgb must be at least 5
 Often appears when
child is feeding
 Polycythemia—
compensatory response
to chronic hypoxia
72
Manifestation: Clubbing
 Fingers or toes
 Chronic hypoxemia
 Base of nails
swollen
 Ends of digits
increase in size
 Angle b/n nail and
nailbed  180º
73
Early and Late Clubbing
74
Question
 When attempting to identify the presence of a
congenital heart defect in an infant, the nurse
should understand that:
 A. In the absence of cyanosis, poor sucking is
insignificant
 B. Many infants retain mucous that may interfere
with feeding
 C. Feeding problems are fairly common in infants
during the first year
 D. Poor sucking and swallowing may be early
indications of heart defects
75
Pediatric Congestive Heart
Failure
76
Pediatric Congestive Heart
Failure (p. 591)
 Pump is insufficient to meet the metabolic
demands of the body
 Heart becomes overloaded and unable to
deliver adequate cardiac output
 Most commonly caused by congenital heart
defects
 Acquired conditions: rheumatic heart disease,
endocarditis, myocarditis, cardiomyopathies,
severe dysrhythmias
77
Pediatric Congestive Heart
Failure
 Infants have a
greater risk of heart
failure than older
children because the
immature heart is
more sensitive to
volume or pressure
overload (Figure 21-7, p. 594)
78
Pediatric Congestive Heart
Failure—Right-Sided Failure
 Right-sided heart failure:
Periorbital and facial
edema, enlarged liver or
spleen, ascites, wheezing,
neck vein distension
  CVP (pooling of venous
blood)
  CO
 Causes: Left-to-right
shunts (VSD, ASD)
79
80
Pediatric Congestive Heart
Failure—Left-Sided Failure
 Left-sided heart
failure: Tachypnea,
dyspnea, crackles,
intercostal / sternal
retractions,
wheezing
 Pulmonary edema
 Causes: Right-to-
left shunts; PDA,
COA
81
82
83
Pediatric Congestive Heart
Failure—Both
 Most children with CHF have a
combination of left and right
 Both: Tachycardia, cardiomegaly,
decreased CO, gallop rhythm (S4),
decreased peripheral perfusion, excessive
diaphoresis, weight gain
 Blood diverted to vital organs and away
from GI tract—at risk for necrotizing
enterocolitis (NEC)
84
Pediatric Congestive Heart
Failure—Manifestations
 Difficulty eating or
sleeping, fussy,
underweight
 Nasal flaring, grunting,
retractions
 Sudden weight gain
(fluid retention)
 Crackles
 Dry, hacking cough
 Decreased urinary
output
85
Pediatric CHF—Nursing
Diagnoses
 Review CP, pp. 595-598
 Decreased Cardiac Output r/t decreased
myocardial function
 Ineffective Tissue Perfusion r/t increased
cardiac workload
 Excess Fluid Volume r/t left and right
ventricular overload and ineffective
pumping
86
Pediatric CHF—Nursing
Diagnoses
 Review CP, pp. 595-598
 Ineffective Breathing Pattern r/t
pulmonary congestion
 Imbalanced Nutrition: Less than Body
Requirements r/t increased energy
expenditure
 Deficient Knowledge r/t unfamiliarity with
disease process, treatment, interventions,
and home care
87
Three early signs of CHF in
infants/children…
 Tachypnea
 Poor feeding
 Diaphoresis
during feeding
88
Question
 A 4-month-old who has a congenital heart
defect develops congestive heart failure and is
exhibiting marked dyspnea at rest. This finding
is attributed to:
 A. Anemia
 B. Hypovolemia
 C. Pulmonary edema
 D. Metabolic acidosis
89
Medications for Pediatric Heart
Failure
 Aim of medications:
 Decrease cardiac
workload
 Improve cardiac
output
 Types of
medications:
 Positive inotropes
 Diuretics
 Afterload-reducing drugs
90
See “Medications Used to Treat Congestive Heart Failure,” p. 593
Digoxin (Lanoxin)
 IV, PO
 Slows and
strengthens the
heart
 Positive inotropic
agent (Increases the
contractility of the
myocardium)
 Monitor: Dig level, K+,
Mg++, Ca++
 Signs of toxicity:
 Nausea, vomiting,
anorexia,
bradycardia,
dysrhythmia
91
Digoxin—Parent Teaching
 Safety Alert: Administering Digoxin, p. 594
 Count apical heart rate for one full minute
before giving
 Call for physician’s advice before giving if HR <
100 BPM infant/toddler, < 70 children
 Give at same time each day, with doses
equally spaced apart (morning, evening)
 If the dosage is spit up or vomited, do not
repeat
92
Digoxin—Parent Teaching
 Don’t use teaspoon, eye dropper—draw up in
syringe or calibrated dropper
 Always remove the cap before administering
the medication into the child's mouth
 Notify physician: nausea, vomiting,
listlessness, anorexia
 Keep medications out of reach of children
 Refill medicine 1 week before it runs out and
ask for new prescription at doctor’s visit
93
94
Furosemide (Lasix)
 IV / IM / PO
 Loop diuretic that blocks sodium
reabsorption in the ascending loop of
Henle
 Decreases preload by increasing water
excretion
 Side effects: Electrolyte imbalances ( K+,
 Mg++); metabolic alkalosis; hypotension
 Monitor: Electrolytes, urinary output, BP,
daily weights
95
Spironolactone (Aldactone)
 PO
 Potassium-sparing diuretic
 Decreases preload
 Side effects: Hyperkalemia,
hypovolemia, contraindicated in renal
failure
 Monitor: I & O, electrolytes, BP
96
Captopril (ACE Inhibitors)
 PO
 Decreases angiotensin II
 Dilates blood vessels, making it easier for the
heart to pump blood forward into the body
 Reduces afterload (blood pressure)
 Less strain on heart muscle and valves, decreased
myocardial oxygen use
 Monitor blood pressure carefully; monitor renal
function
97
Question
 A toddler is hospitalized with CHF and is
receiving digoxin and Lasix. She has
vomited twice in the past 4 hours. The
nurse’s best action is to:
 A. Increase the child’s fluid intake.
 B. Omit the next dose of Lasix.
 C. Check the child’s blood pressure prior to
the next dose of digoxin.
 D. Get an order to draw a digoxin level.
98
Question
 The mother of a 5-month-old infant with
congestive heart failure questions the necessity
of weighing the infant every morning. The
nurse’s response should be based on the fact
that this daily information is important in
determining:
 A. Renal failure
 B. Fluid retention
 C. Nutritional status
 D. Medication dosage
99
Pediatric Pulmonary
Hypertension
100
Pulmonary Hypertension (PH):
The OTHER Hypertension (p. 599)
 Increased pressure, narrowing:
pulmonary arteries, arterioles
 Elevated mean pulmonary arterial
pressure (PAP) >25 mmHg
 Causes: lung disease, some congenital
heart diseases
 RV failure  Rt heart failure  Lt heart
failure  reduced CO  hypotension
101
Pulmonary Hypertension
102
Signs/ Symptoms & Dx
 Infants: poor appetite, poor growth,
lethargy, tachypnea, tachycardia,
sweating, cyanosis
 Children: fatigue, chest pain, dyspnea,
dizziness, syncope
 Dx: echocardiography, cardiac
catheterization
103
Treatment
 Rapidly lethal – Must treat early while
reversible (to prevent pulmonary vascular
remodeling)
 Treat underlying cause (if known)
 Surgery 3-6 mos: ASD, VSD, AVSD, PDA
 Medications: O2, nitric oxide, calcium channel
blockers (nifedipine), diuretics, sildenafil
(Viagra)
 Lung transplantation: severe cases
104
Heart Disease in Children
105
Heart Disease in Children
 Two types:
 Congenital
 One or more heart structure abnormalities
that develop before birth or persistence of a
fetal structure after birth
 Acquired
 Any cardiac condition that was not present
at birth
106
Congenital Heart Disease
107
Congenital Heart Disease is
associated with….
 Family history of
congenital heart disease
 Fetal exposure to drugs
such as dilantin and
lithium
 Maternal diabetes
mellitus
 Maternal viral infections
such as rubella
 Trisomy 21 (Down
syndrome)
108
Congenital Heart Disease
 Three Types:
 Acyanotic
 Obstructive
 Cyanotic
109
Acyanotic Heart Lesions
(Increase Pulmonary Blood Flow, p. 575)
 Left-to-right shunting
 Ventricular septal defect (VSD)
 Patent ductus arteriosus (PDA)
 Atrial septal defect (ASD)
 Atrioventricular septal defect
(endocardial cushion defect)
110
Acyanotic Heart Lesions—
Manifestations
 Left-to-right shunt
 Systemic pressure >
pulmonic pressure
 Oxygenated blood
backwashing to right side
of heart
 Venous blood does NOT
enter systemic circulation
 ALL of the blood returning
to the right side of the
heart passes through the
lungs
111
Acyanotic Heart Lesions
 NO cyanosis
 Not always apparent at birth
 Excessive pulmonary blood flow
(pulmonary HTN)
 Enlarged heart (right, sometimes
left)
 Congestive heart failure
 Enlarged liver, dyspnea, tachypnea,
intercostal retractions, poor growth,
frequent respiratory infections
112
Ventricular Septal Defect
(VSD)
 Hole or defect in
ventricular septum
(wall)
113
Ventricular Septal Defect
114
Ventricular Septal Defect
(VSD)
  Pulmonary blood flow
 Pulmonary HTN
 Usually not symptomatic
at birth
 Loud, harsh systolic
murmur
 Large defects: CHF,
poor feeding, failure to
thrive
115
VSD—Medical Management
 20-60% close
spontaneously
 CHF—Lanoxin and
Lasix
 Nutritional
supplements
 Antibiotic prophylaxis
to prevent
endocarditis
116
Antibiotic Prophylaxis
 Children with congenital heart defects at risk
for bacterial endocarditis and damage to
heart valves
 Must use antibiotics:
 Before and after dental, oral, and invasive
procedures / surgeries
 Any unexplained fever or malaise within 2
months of procedure may be a sign of
infection
117
Question
 The father of a child with a congenital heart
defect asks the nurse why his daughter has to
take penicillin before she gets her teeth
cleaned by the dentist. The nurse explains that
this is necessary to prevent:
 A. Bacterial endocarditis
 B. Congestive heart failure
 C. Rheumatic fever
 D. Infected gums
118
VSD—Pulmonary Artery (PA)
Banding
 Helps prevent
pulmonary vascular
obstructive disease
 Palliative surgery
 Closed heart surgery—
does not require
cardiopulmonary bypass
 Band placed around
pulmonary artery,
decreasing pulmonary
blood flow
 Used when VSD cannot be
closed (multiple VSD’s, very
small infants with severe
CHF)
 Less frequently done than
corrective surgery
119
VSD—Patch Closure
 Corrective surgery
 Purse-string suture
around small defects
 “Patch” over large
defects
 Open heart surgery
 Requires
cardiopulmonary
bypass
120
Question
 A cardiac catheterization is scheduled for a 5-
year-old with a ventricular septal defect to:
 A. Identify the degree of cardiomegaly present
 B. Demonstrate the exact location of the defect
 C. Confirm the presence of a pansystolic murmur
 D. Establish the presence of ventricular
hypertrophy
121
Patent Ductus Arteriosus
(PDA) (p. 576)
 Opening between aorta
and pulmonary artery
  Pulmonary blood flow
 Back to left atrium/left
ventricle
 Left ventricular
hypertrophy
 CHF (left side)
 Respiratory distress
 Machinery-type murmur
Connection between
pulmonary artery and aorta
122
PDA—Treatment
 CHF: digoxin, lasix
 Medical—
indomethacin
(Indocin)
 Interventional—
cardiac
catheterization
 Surgical—ligation of
ductus (left
thoracotomy)
123
Indomethacin (Indocin)
Ibuprofen
 IV
 NSAID—inhibits the production of prostaglandins
 Promotes closure of PDA; onset of action usually
within minutes
 Closure of PDA in 80% of patients
 Monitor renal function
 Side effects: bleeding (intraventricular
hemorrhages, GI bleeds)
124
Atrial Septal Defect (ASD)
(p. 576)
 Hole or defect in
atrial septum (wall)
125
Atrial Septal Defect
126
Atrial Septal Defect
 Often asymptomatic
 Systolic murmur
 Large defect: CHF,
pulmonary vascular
disease (often 1st
appearing as an
adult)
 Antibiotic prophylaxis
 Treatment: “patch”
127
Atrioventricular Septal Defect (AVSD)
(Endocardial Cushion, AV Canal) (p. 577)
 LARGE hole in center
of heart
 ASD, VSD, and
combined mitral and
tricuspid valves
(common
atrioventricular
opening or “canal”)
 Common with Down
syndrome
128
Atrioventricular Septal Defect
129
Atrioventricular Septal Defect
 Left-to-right shunting:
Backward flow of
oxygenated blood
through both ASD and
VSD to right side of
heart
 Right-sided heart failure
 Pulmonary hypertension
 Systolic murmur
130
Atrioventricular Septal Defect
 Hemodynamic
changes with
untreated cases:
permanent right-to-
left shunting,
cyanosis
 Tachypnea,
tachycardia, poor
growth
http://www.gundluth.org/images/ei_0033.jpg
131
Atrioventricular Septal Defect
 Medical: digoxin, diuretics, and afterload
reduction (ACE)
 Treatment: surgical repair early in infancy (3-4
mos) before the lungs become damaged and
permanent hemodynamic changes occur
 “Patches” over both septal defects and valvular
repair
 Antibiotic prophylaxis
132
Review Question
 A toddler has been diagnosed with an
acyanotic cardiac defect. Which
assessment data would most likely
indicate congestive heart failure?
A. Heart murmur.
B. Cardiac volume overload.
C. Anuria.
D. Excitability.
133
Obstructive/ Stenotic Lesions
 Pulmonary stenosis
 Aortic stenosis
 Coarctation of the aorta
134
Pulmonary Stenosis (p. 582)
 Area where blood
exits the heart's
lower right chamber
is too narrow (right
ventricular outflow
tract obstruction)
 Harsh systolic
murmur
135
Pulmonary Stenosis
 Mild: asymptomatic,
requires only
antibiotic prophylaxis
 Severe or critical:
balloon valvuloplasty
or open-heart
surgical repair
136
Aortic Stenosis (p. 590)
 Obstruction of blood
flow from heart to
body (obstruction to
blood flow leaving left
ventricle)
  Afterload
  Cardiac output
  Systemic blood flow
 Harsh systolic murmur
137
Aortic Stenosis
 Mild: asymptomatic,
exercise fatigue
 Severe or critical:
CHF, left ventricular
hypertrophy, shock
138
Aortic Stenosis
 Mild: continue to
monitor, antibiotic
prophylaxis
 Severe or critical: aortic
balloon valvuloplasty
(cardiac
catheterization), surgical
valvotomy
 May need aortic valve
replacement
139
Coarctation of the Aorta (COA)
(p. 590)
 Obstructive lesion
 Restricts flow of blood
out of the left ventricle
 Aorta is pinched at some
point along its length,
limiting the amount of
oxygen-rich blood that
can reach the rest of the
body
140
Coarctation of the Aorta (COA)
  Afterload
  Cardiac output
  Systemic blood flow
  Pulmonary congestion
(pooling of blood in left
side of heart)
 Enlarged left ventricle;
CHF
 Decreased pulses and
BP in the lower
extremities
 Cold feet, legs
 Epistaxis (nose bleeds),
BP higher in arms
141
COA—Treatment
 Symptomatic CHF: digoxin,
lasix
 Medical: prostaglandin
infusion to keep ductus
arteriosus patent (improve
perfusion to lower body)
 Balloon angioplasty
 Surgical repair: left
thoracotomy with
anastomosis
 Antibiotic prophylaxis for
life
142
Question
 An infant with a left-to-right shunt was
admitted to the hospital in congestive heart
failure. She weighed 3.6 kg yesterday. A
finding that indicates a worsening of her
condition today is:
 A. Weight 3.66 kg.
 B. Urine output of 40 ml in past 8 hours.
 C. Crackles in the lower lobes.
 D. All of the above.
143
Cyanotic Heart Lesions
(Decrease Pulmonary Blood Flow, p. 581)
 Right-to-left
shunting
 Tetralogy of Fallot
(TOF)
 Transposition of the
Great Arteries (TGA)
 Hypoplastic Left
Heart Syndrome
(HLHS)
144
Cyanotic Heart Lesions—
Manifestations
 Right-to-left shunt
 Pulmonic pressure >
than systemic
 Unoxygenated blood
bypasses pulmonary
circulation and goes
directly to the left
side of the heart to
be pumped into the
systemic circulation
145
Cyanotic Heart Lesions—
Manifestations
 “Blue baby”—
Cyanosis
 Symptomatic soon
after birth
 Decreased
pulmonary blood
flow
146
Tetralogy of Fallot (p. 582)
 Defect composed of
four distinct lesions:
1. Ventricular septal
defect
2. Pulmonic stenosis
3. Overriding aorta
4. Right ventricular
hypertrophy
147
Cross-Section of a Normal Heart and
a Heart With Tetralogy of Fallot
148
Tetralogy of Fallot
 Reduced blood flow
to lungs
 Aortic blood (to
body) mainly
oxygen-poor venous
blood
 Severity of cyanosis
depends primarily on
degree of pulmonary
stenosis
149
Tetralogy of Fallot—Signs and
Symptoms
 X-ray: Heart is “Boot-
shaped”
 Cyanosis, difficulty
breathing
 Clubbing of fingers
(because of hypoxemia)
 Systolic murmur,
palpable thrill
 Polycythemia
 Hypercyanotic episodes
150
Hypercyanotic Episode:
“Tet Spell” (p. 585)
151
Hypercyanotic Episode
152
Question
 A child diagnosed with tetralogy of Fallot becomes
upset, crying and thrashing around when a blood
specimen is obtained. The child’s color becomes blue
and the respiratory rate increases to 44
breaths/minute. Which of the following actions would
the nurse do first?
 A. Obtain an order for sedation for the child.
 B. Assess for an irregular heart rate and rhythm.
 C. Explain to the child that it will only hurt for a
short time.
 D. Place the child in a knee-to-chest position.
153
Question
 A newborn with TOF is fed in the semi-Fowler’s
position. After the nurse feeds and burps the infant
and changes the infant’s position, the infant has a
bowel movement and almost immediately becomes
cyanotic, diaphoretic, and limp. These symptoms are
most likely caused by the:
 A. Burping
 B. Formula
 C. Position change
 D. Bowel movement
154
TOF Surgical Repair
 Surgical treatment:
 Palliative—Relieves symptoms by
increasing the blood flow to the
lungs
 Corrective—Repairs the underlying
defects
155
Blalock-Taussig Shunt (p. 586)
 Palliative procedure
 Closed-heart surgery
 Shunt created from aorta
to pulmonary artery
  Blood flow to lungs
 “Buys” time for infant to
grow
  Success of corrective
surgery when done later
156
Question
 The nurse is aware that the aim of
palliative surgery for children with
tetralogy of Fallot is to directly increase
the blood flow to the:
 A. Brain
 B. Lungs
 C. Myocardium
 D. Right ventricle
157
TOF Repaired
 Open-heart surgery
 2 to 4 months
 Pulmonary valve widened
 VSD patched
 No treatment: Displaced
aorta, enlarged rt.
ventricle
 Antibiotic prophylaxis for
life
158
Question
 Parents of a toddler with tetralogy of Fallot
explain that they do not want him to overexert
himself; so they always keep him in his
playpen or crib to limit his mobility. Based on
this information, the most appropriate nursing
diagnosis is:
 A. Activity Intolerance
 B. Risk for Impaired Parenting
 C. Caregiver Role Strain
 D. Risk for Delayed Development
159
Transposition of the Great
Arteries (TGA) (p. 584)
Reversal of aorta and pulmonary artery
160
Transposition of the Great
Arteries (TGA)
 Babies born with
TGA can only survive
if they have one or
more connections
that allow some
oxygenated blood to
go to the body (PDA,
ASD)
161
Prostaglandin E1 (PGE1)
 IV infusion
 Causes the ductus
arteriosus to stay
artificially open (patent)
 For infants with ductal-
dependent cardiac
abnormalities (TGA,
HLHS, severe TOF)
 Ventilator
 Monitor: Respiratory,
cardiovascular status,
bleeding (inhibits
platelet aggregation)
 Side effects: Apnea,
fever, irritability,
flushing, bleeding, third-
spacing
162
Transposition of the Great
Arteries (TGA)
 Balloon atrial
septostomy—tears a
hole in the atrial septum
 Corrective surgery is
performed in the early
days following birth:
 Arterial switch
procedure—aorta and
pulmonary artery
returned to their
normal positions
163
Tiny Baby Survives Open Heart
Surgery
164
Hypoplastic Left Heart
Syndrome (HLHS) (p. 591)
 Inadequate
development of the
left side of the heart
 Only one functional
ventricle
 Aortic valve, mitral
valve, and ascending
aorta may also be
small or hypoplastic
165
HLHS—Signs and Symptoms
 Cyanosis, appears
“gray”
 CHF
 Tachycardia, dyspnea
 Hypotension,
weakness
 Hypoperfusion, shock,
metabolic acidosis
166
HLHS—Treatment
 Comfort care
 Without surgery, fatal within the first 2 weeks of
life
 Medications: PGE1 infusion to keep the
ductus open
 Surgery: 3-staged palliative surgery (ages 1
week, 6 months and 2 years of age)
 Heart transplant—infrequent due to scarcity
of neonatal donor hearts
167
Child With HLHS Who
Received Heart Transplant
http://www.texaschildrenshospital.org/CareCenters/KidsCourageous/Heart_Noah.aspx
168
HLHS—Palliative Surgery
 Three-stage surgical
approach to improve
flow of blood throughout
the body
 The Norwood Procedure
(Stage 1)
 1 week of age
 Provides blood flow from
the right ventricle
directly to the aorta
169
The Norwood Procedure
170
HLHS—Palliative Surgery
 The Bi-Directional Glenn
(Stage 2)
 6 months of age
 The Fontan Procedure
(Stage 3)
 2 years of age
 Re-routes blood flow
around the defective
areas of the heart by
creating new pathways
for blood circulation to
and from the lungs
171
Fontan Procedure
172
HLHS—Prognosis
 4-year survival following
staged repair up to 85%
 Long-term survival
remains to be seen
 Long-term complications
(advanced disease):
ventricular and valvular
dysfunction,
dysrhythmias, low
albumin, pleural
effusions, ascites
173
Question
 Parents of children with congenital heart
problems often experience loss of control when
the child is hospitalized. The nurse who
understands this will:
 A. Encourage parents to participate in their child’s
care.
 B. Explain procedures prior to performing them.
 C. Answer questions honestly.
 D. Do all of the above.
174
175
Cardiac Surgery
176
Cardiac Surgery (p. 578; 580)
 Two types:
 Open-heart surgery:
repair to the
myocardium (heart
muscle); requires
cardiopulmonary bypass
 Closed-heart surgery:
interventions to
structures around the
heart but not the heart
muscle itself; done
without bypass
177
Open-Heart Surgery
 Read pp. 578-580
 Trend: to intervene
at an early age
 Risks: bleeding,
emboli,
dysrhythmias, fluid &
electrolyte
imbalances
178
Post Cardiac Surgery
 STERNAL PRECAUTIONS
 Chest tube, NGT,
ventilator, cardiac
monitor, pulse oximetry
 Encourage cough, IS
 Monitor VS, cardiac,
respiratory, I & O,
electrolytes, chest tube
drainage
 Very painful surgery:
Adequate pain control
very important
179
Acquired Heart Disease
180
Rheumatic Fever (RF) (p. 600)
 Children ages 5 – 15
 Inflammatory autoimmune
response
 Result of “strep throat”
that has not been treated
with antibiotics
 Manifests 1 – 3 weeks
afterwards
 Affects connective tissue
of heart, joints,
subcutaneous tissues,
blood vessels
 Most serious: Cardiac
valvular disease (esp.
scarring of mitral valve)
 Prevention: refer all
children with sore throats
for throat cultures
181
Scarlet Fever
182
Manifestations of
Rheumatic Fever
 Carditis—inflammation of all
parts of the heart (mitral, aortic
valves)
 Murmur
 Polyarthritis—joint pain
 Chorea—involuntary movements
of legs, arm, and face
 Erythema marginatum—red skin
lesions
 Subcutaneous nodules—
nontender lumps located over
the joints
183
RF—Diagnostics / Treatment
 Positive antistreptolysin
O titer (+ ASO)
  SED (erythrocyte
sedimentation) rate
 Positive C-reactive
protein
 EKG changes
 Monitor for cardiac
complications, seizures
 Antiinflammatory
agents (aspirin,
corticosteroids),
analgesics,
antipyretics
 Streptococcal
prophylaxis for many
years
184
Streptococcal Prophylaxis for the
Child with Rheumatic Fever
 Damaged valves can become further
damaged with repeated infections
 Streptococcal prophylaxis is lifelong if
there is actual valve involvement
 Intramuscular penicillin, administered
monthly, is the drug of choice
 Alternatives include oral penicillin twice
daily or oral sulfadiazine once a day
185
Rheumatic Fever—Valvular
Malfunctions
186
Question
 When examining the laboratory work
of a child with the diagnosis of
rheumatic fever, the nurse would
expect the findings to demonstrate:
 A. A negative C-reactive protein
 B. A positive antistreptolysin titer
 C. An elevated reticulocyte count
 D. A decreased erythrocyte sedimentation
rate
187
Kawasaki Disease (KD)
(p. 601)
 Children < 4 years (peak incidence 18 – 24 months)
 Mucocutaneous lymph node syndrome
 Inflammatory autoimmune disease—principle area of
involvement is the heart
 Antibody-antigen complexes
 If caught and treated early the prognosis is usually
very good
 If left untreated or caught too late, it can be fatal or
leave the child with irreversible heart and/or organ
damage
188
Kawasaki Disease (KD)
 May damage the coronary arteries (vasculitis)
and heart muscle
 Most common cause of acquired heart disease
in U.S. children
 Can lead to coronary aneurysms and
myocardial infarctions later in life
 Cause: ??? noncontagious infection; associated
with rug shampooing, dust mites, or proximity
to stagnant water
 Seasonal:  Late winter, early spring
189
KD—Signs and Symptoms
 Affecting children under the
age of 5, diagnostic criteria
include at least:
 5 days of fever (> 39 ° C,
102.2° F), unresponsive to
antibiotics
 Conjunctival eye redness
without discharge
 Red-fissured lips
 Strawberry tongue
 Red rash
 Redness and/or swelling
of palms and soles, and
lymph nodes in the neck
190
KD—Phases and Treatment
 3 phases
 Acute phase: 1 to 2 weeks, with high fever > 5
days
 Nurse needs to closely monitor cardiac status,
VS, observe for CHF
 Echocardiogram, ECG,  SED rate
 Early treatment can dramatically reduce the
likelihood of cardiovascular damage
 High-dose IV Gamma-globulin
 High-dose PO ASA therapy
191
Kawasaki Disease
192
Strawberry Tongue
193
Aspirin (ASA)
 PO, administer with milk or food
 Antiplatelet agent (inhibit platelet function by
making them less sticky)
 High dose therapy (KD): 80-100 mg/kg/day for
the first two weeks to reduce fever, swelling
and inflammation; and to decrease the chance
of blood clots
 Don’t give to children <16 y with chickenpox
or flu-like symptoms (Reye syndrome)
 Side effects: Bleeding
194
195
Review Question
 A toddler with Kawasaki’s disease is ordered to receive
aspirin therapy. Typical administration of aspirin for
Kawasaki’s disease would include which of the
following principles?
A. High doses of aspirin should be given while fever is
high.
B. Aspirin therapy is given to reduce fever.
C. Aspirin dose increases after fever is gone.
D. Aspirin dosage is unrelated to platelet count.
196
Gamma Globulin (IVIG)
 One time dose 2 g/kg
 Administered through an intravenous
(I.V.) line for 10 hours
 If given first 10 days, will dramatically
reduce the risk of damage to the
coronary arteries
 Side effects: Hypotension; facial
flushing; tightness in the chest
197
IVIG—cont’d…
 Monitor BP closely
 Benadryl and acetaminophen: control
side effects
 Epinephrine: anaphylactic reactions
 Vaccines must be delayed for 5 months
months after treatment
198
199
Childhood Hypertension, High
Cholesterol
200
Management of Hypertension
in Children
 Diastolic > 95% percentile
 Not common, but incidence rising
 Kidney disease, obesity
 Weight reduction
 Physical conditioning
 Dietary modification
 Pharmacologic treatment
201
High Cholesterol Risk Factors
 Tobacco use
 Dyslipidemia (elevated LDLs and
cholesterol and decreased HDLs)
 Hypertension
 Decreased physical activity
 Obesity
 NANDA diagnosis: Sedentary Lifestyle
202
203

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Alterations in cardiovascular function in children

  • 1. Alterations in Cardiovascular Function in Children Joy A. Shepard, PhD, RN-C, CNE Joyce Buck, PhD(c), MSN, RN-C, CNE 1
  • 2. Learning Outcomes  Describe anatomy and physiology of cardiovascular system focusing on blood flow and action of heart valves  Contrast pathophysiology associated with congenital heart defects with increased pulmonary circulation, decreased pulmonary circulation, and obstructed systemic blood flow  Plan the nursing care for an infant with a congenital heart defect 2
  • 3. Learning Outcomes (cont’d)  Plan the nursing care for a child undergoing open heart surgery  Recognize signs of congestive heart failure  Develop a nursing care plan for child with congestive heart failure  Differentiate between heart diseases acquired during childhood and congenital heart defects 3
  • 4. Overview of the Cardiovascular System 4
  • 5. 5
  • 6. Function of the Heart  Pulmonary circulation— Pumps blood to the lungs for oxygenation and removal of carbon dioxide  Systemic circulation— Pumps oxygenated blood to the body tissues; metabolic wastes taken away 6
  • 7. Anatomy of the Heart  Muscular pump with four chambers:  Upper chambers— atria  Lower chambers— ventricles  Valves, veins, and arteries connect the chambers 7
  • 8. The Heart is Like a House….  It has:  Electricity (power) and  Plumbing (mechanical) 8
  • 9. Electrical (Conduction) System  Powers the pump  Cardiac cycle: depolarization and repolarization of the cardiac muscle  Conduction pathways:  Sinoatrial node (SA) —>  Atrioventricular (AV) node —>  Bundle of His —>  Left and right bundle branches —>  Purkinje fibers 9
  • 10. Pumping System  Heart—powerful, muscular pump  Two pumps: left and right  Pressures in the left much higher than right  Continuous coordinated pumping action keeps the body supplied with oxygen-rich blood 10
  • 11. Valves are essential to the heart's pumping function  Keeps blood flowing forward through the heart  One-way valve at the exit of each of the four chambers:  Tricuspid  Pulmonic  Mitral  Aortic valves 11
  • 12. 12
  • 13. Physiology of the Heart  CO = HR X SV Heart Rate  Components of Stroke Volume:  Preload  Afterload  Contractility 13 Untillateschool-ageandadolescence,cardiacoutputinthechildisRATE DEPENDENT,notstrokevolumedependent,makingheartratemorerapid.
  • 14. 14
  • 15. Preload  Amount of stretch of the myocardial fibers before contraction  Measured by central venous pressure (CVP) 15
  • 16. Afterload  Amount of resistance against which the heart (ventricle) pumps 16
  • 17. Contractility  “Squeeze”—Strength of muscular contraction independent of preload (inotropic) 17
  • 18. Fetal Circulation (pp. 273-274, Lowdermilk; pp. 569-571 Ball & Bindler) 18
  • 19. Fetal Circulation  Fetal circulation differs from neonatal circulation in three ways:  Gas exchange  Pressures (systemic and pulmonary circulations)  Structures (shunts, umbilical cord) 19
  • 20. Gas Exchange—Placenta; Umbilical Vein—Oxygenated Blood  Oxygenation and removal of carbon dioxide (gas exchange) takes place in the placenta  Umbilical vein oxygenated blood to inferior vena cava 20
  • 21. Fetal Circulation—Pressure Differences  Oxygenated blood flow (from the placenta) is from right to left  Oxygenated blood enters right side of fetal heart  Blood pressure on the right side of the heart > blood pressure on the left side of the heart 21
  • 22. Fetal Circulation—Pressure Differences  High resistance in fetal lungs (arterioles are constricted, alveoli are filled with fluid)  Resistance to blood flow in the lungs (pulmonary vascular resistance) > Resistance to blood flow in the body (systemic vascular resistance)  Fetal lungs don’t receive much blood 22
  • 23. Fetal Circulation—1st Shunt  Ductus venosus— fetal structure connecting inferior vena cava to umbilical vein  Most of fetal liver bypassed (blood shunted away from liver) 23
  • 24. Fetal Circulation— 2nd Shunt  Inferior vena cava Right atrium  Left atrium (by way of the foramen ovale)  Most of lungs bypassed  Left ventricle aorta (supplying heart and brain) 24
  • 25. Fetal Circulation—3rd Shunt  Deoxygenated blood from the upper body mixes with oxygenated blood from the placenta @ the right atrium  Ductus arteriosus descending aorta (bypassing the lungs)  Organ systems  Blood returns to the placenta (by way of the two umbilical arteries) 25
  • 26. 26
  • 27. Transition from Fetal to Pulmonary Circulation 27
  • 28. Circulation After Birth—Gas Exchange  With the neonate’s first breath, gas exchange is transferred from the placenta to the lungs   Pa02 levels   PaC02 levels 28
  • 29. Circulation After Birth— Pressure Changes   Resistance  Pulmonary circulation   Pulmonary blood flow   Resistance  Systemic circulation 29
  • 30. Circulation After Birth— Pressure Changes  Umbilical cord clamped   Blood to right heart  Blood pressure (left side of the heart) > blood pressure (right side of heart)  Systemic vascular resistance > pulmonary vascular resistance 30
  • 31. Circulation After Birth— Pressure Changes  Lungs inflate with air, allowing gas exchange  Resistance to blood flow in the lungs (pulmonary vascular resistance) decreases  Much more blood flows into the lungs  First breath: alveoli expand and blood vessels in the the lungs open up 31
  • 32. Circulation After Birth— Pressure Changes  Deoxygenated blood right heart lungs  Oxygenated blood left heart body 32
  • 33. Circulation After Birth—Shunts Close  Fetal shunts close in response to pressure changes,  Pa02 levels, in the pulmonary and systemic circulations 33
  • 34. To Review… Normal fetal circulation (lungs and liver bypassed) Normal circulation after birth (systemic AND pulmonary circulations; high systemic pressure) 34
  • 36. 36 See Video “Pediatric Assessment,” 23:15-24:05
  • 37. Health History  Review:  Table 5-12, p. 141  Assessment Guide: The Child with a Cardiac Condition, p. 572  Congenital heart disease in family  Maternal illness, infections, medications taken during pregnancy  Child’s behavior patterns (playfulness, irritability)  Medications 37
  • 38. Health History  Feeding problems (fatigue or diaphoresis during feeding; poor weight gain)  Respiratory difficulties (tachypnea, shortness of breath, cyanosis; frequent respiratory infections)  Chronic fatigue, exercise intolerance 38
  • 39. Inspection  Skin color  Activity level  Chest  Respiratory pattern 39
  • 40. Review Question  An infant who has a cyanotic congenital heart defect comes into the clinic with complaints of irritability, pallor, and increased cyanosis that began quickly over the last 30 minutes. As the nurse assesses the infant, the parent asks why the child’s color is bluish. The best response by the nurse is, “Skin color is: A. Related to the time of day.” B. Related to brain function.” C. Related to hemoglobin level and oxygen saturation.” D. Unrelated to your child’s condition.” 40
  • 41. Auscultation: A(P)TM  Normal areas of auscultation  PMI: 3-4th ICS infants; 4th ICS < 7; 5th ICS > 7  Heart sounds  Rhythm: Regular  S1, S2  S3 —normal finding in children  S4 —cardiac failure  Murmurs, clicks, friction rubs 41Auscultate apical pulse with stethoscope for a full 60 seconds
  • 42. 42
  • 43. Normal Heart Rates for Children of Different Ages
  • 44. 44
  • 45. Palpation  Skin temperature  Pulses  Blood pressure  Capillary refill— normal < 2 seconds  Chest 45
  • 46. The sites used to assess the pulses in children
  • 47. Significant Findings  Growth abnormalities  Cyanosis  Clubbing of fingers and toes  Edema (periorbital, peripheral)  Tachypnea  Pulse alterations (fast, slow, diminished)  Hypotension, unequal BP arms / legs  Murmurs, bruits, thrills  Engorged neck veins  Abdominal distention, enlarged liver / spleen 47 See “Assessment Guidelines for the Child with a Cardiac Condition,” p. 572
  • 48. Clubbing of the Fingers
  • 49. Question  An infant born at 39 weeks gestation is sent to the intensive care nursery. The nurse suspects a possible cardiac anomaly when the admission assessment reveals:  A. Projectile vomiting  B. An irregular respiratory rhythm  C. Hyperreflexia of the extremities  D. Unequal peripheral blood pressures 49
  • 51. Diagnostic Tests / Procedures  Labs  EKG  Chest x-ray  Echocardiogram  Cardiac catheterization 51 See Table 21-4: Clinical Interventions for Congenital Heart Defects, p. 574 See Table 21-2: Diagnostic Procedures & Laboratory Tests, p. 571
  • 52. 52
  • 53. Labs  Hgb/Hct  Serum electrolytes (especially K+, Mg++, Ca++)  ABG  Digoxin level  Cholesterol  Triglycerides  Urine SG 53
  • 54. Question  The pediatric nurse practitioner orders a complete blood workup for a 5-month-old infant with a cyanotic congenital heart defect. Because of the infant’s heart disease, the nurse would expect the report to show:  A. Polycythemia  B. Agranulocytosis  C. Thrombocytopenia  D. A decreased hematocrit level 54
  • 55. Pulse Oximetry  Evaluates degree of oxygen saturation in the blood using a small infrared light probe that is placed on:  Finger, toe, earlobe, bridge of the nose  Norm: 95 – 100%  Cyanosis not visible until sat < 85% 55
  • 56. 12-Lead EKG  Helps evaluate:  Cardiac muscle  Cardiac rate and rhythm  Cardiac impulse conduction 56
  • 57. Chest X-Ray  X-ray picture of heart, organs in chest cavity  Provides information on:  Size of the heart and its chambers  Blood flow to lungs 57
  • 58. Echocardiogram  High-frequency sound waves, noninvasive  Helps assess:  Thickness of heart walls  Size of cardiac chambers  Motion of valves and septa (walls) within the heart  Great vessels and various cardiac structures  Defects in structure or function 58
  • 59. Cardiac Catheterization  Provides information on:  Oxygen levels in cardiac chambers and great arteries  Pressures  Blood flow  Cardiac output / stroke volume  Anatomic abnormalities  Cardiac conduction system 59
  • 60. Interventional Catheterization  Corrective treatments performed by use of specialized catheters  Balloon catheters—open narrowed valves or arteries  Balloon/blades—shunt creations, septostomy  Device closure—close extra vessels, “holes” in heart 60
  • 61. Cardiac Catheterization— Nursing Care (p. 573)  Child must lay still, supine, with affected leg straight for 4 – 6 hours  Vital signs, insertion site observed, distal pulses checked q15 minutes X 1st hour, then q30 minutes  Observe for bleeding at site; pallor, loss of pulses, coolness in extremity distal to site  Push fluids to help flush the dye out of the body  Observe for reactions to dye (vomiting, rash, increased creatinine, decreased urinary output)  Strict I & O 61
  • 62. Question  A 3-1/2-year-old child returns to the room after a cardiac catheterization. Post-procedure nursing care for the child should include:  A. Encouraging early ambulation  B. Monitoring the insertion site for bleeding  C. Restricting fluids until blood pressure is stabilized  D. Comparing blood pressure in affected and unaffected extremities 62
  • 63. Heart Disease in Children 63
  • 64. Heart Disease in Children  Manifestations in infants, children:  Frequent respiratory infections and dyspnea  Activity intolerance  Difficulty and fatigue during feedings  Failure to thrive, low weight  Pallor, cyanosis, clubbing 64
  • 65. Manifestation: Respiratory Difficulties  Shortness of breath, difficulty breathing  Increased respiratory rate, retractions, nasal flaring  Frequent respiratory infections  Activity intolerance, fatigue, delayed gross motor skills 65
  • 66. Manifestation: Feeding Difficulties, Stunted Growth  Difficulty and fatigue during feedings  Frequent emesis, at risk for NEC  Stunted growth  Low weight  Failure to thrive 66
  • 67. Feeding Interventions  Provide periods of uninterrupted rest  Neutral thermal environment  Feed child slowly and more often (q3° optimal time)  Frequent, small feedings may be less tiring  Concentrating formula 24-27 kcal/oz may increase caloric intake without increasing infant’s work 67
  • 68. Feeding Interventions  Provide relaxed environment  Reduce anxiety, sadness, crying  Hold infant in upright position; less stomach compression and improves respiratory effort  Place infant on right side after feeding, HOB 30 - 45º 68
  • 69. Feeding Interventions  Limit bottle feedings to 30 minutes  If child unable to consume appropriate amount during 30-minute feeding every 3 hours, consider nasogastric feeding  Monitor for increased tachypnea, diaphoresis, or feeding intolerance (vomiting) 69
  • 70. Supplemental Feedings  Infants with cardiac conditions often require supplemental feedings to provide sufficient nutrients for growth and development 70
  • 71. Question  When caring for a 4-month-old infant with congestive heart failure, the nurse should:  A. Force nutritional fluids  B. Provide small, frequent feedings  C. Measure the head circumference daily  D. Position the infant flat on the abdomen 71
  • 72. Manifestation: Pallor and Cyanosis  Bluish discoloration of skin, nail beds, mucous membranes  Hypoxia—tissues are deprived of adequate amounts of oxygen (02 sat < 85%)  Hgb must be at least 5  Often appears when child is feeding  Polycythemia— compensatory response to chronic hypoxia 72
  • 73. Manifestation: Clubbing  Fingers or toes  Chronic hypoxemia  Base of nails swollen  Ends of digits increase in size  Angle b/n nail and nailbed  180º 73
  • 74. Early and Late Clubbing 74
  • 75. Question  When attempting to identify the presence of a congenital heart defect in an infant, the nurse should understand that:  A. In the absence of cyanosis, poor sucking is insignificant  B. Many infants retain mucous that may interfere with feeding  C. Feeding problems are fairly common in infants during the first year  D. Poor sucking and swallowing may be early indications of heart defects 75
  • 77. Pediatric Congestive Heart Failure (p. 591)  Pump is insufficient to meet the metabolic demands of the body  Heart becomes overloaded and unable to deliver adequate cardiac output  Most commonly caused by congenital heart defects  Acquired conditions: rheumatic heart disease, endocarditis, myocarditis, cardiomyopathies, severe dysrhythmias 77
  • 78. Pediatric Congestive Heart Failure  Infants have a greater risk of heart failure than older children because the immature heart is more sensitive to volume or pressure overload (Figure 21-7, p. 594) 78
  • 79. Pediatric Congestive Heart Failure—Right-Sided Failure  Right-sided heart failure: Periorbital and facial edema, enlarged liver or spleen, ascites, wheezing, neck vein distension   CVP (pooling of venous blood)   CO  Causes: Left-to-right shunts (VSD, ASD) 79
  • 80. 80
  • 81. Pediatric Congestive Heart Failure—Left-Sided Failure  Left-sided heart failure: Tachypnea, dyspnea, crackles, intercostal / sternal retractions, wheezing  Pulmonary edema  Causes: Right-to- left shunts; PDA, COA 81
  • 82. 82
  • 83. 83
  • 84. Pediatric Congestive Heart Failure—Both  Most children with CHF have a combination of left and right  Both: Tachycardia, cardiomegaly, decreased CO, gallop rhythm (S4), decreased peripheral perfusion, excessive diaphoresis, weight gain  Blood diverted to vital organs and away from GI tract—at risk for necrotizing enterocolitis (NEC) 84
  • 85. Pediatric Congestive Heart Failure—Manifestations  Difficulty eating or sleeping, fussy, underweight  Nasal flaring, grunting, retractions  Sudden weight gain (fluid retention)  Crackles  Dry, hacking cough  Decreased urinary output 85
  • 86. Pediatric CHF—Nursing Diagnoses  Review CP, pp. 595-598  Decreased Cardiac Output r/t decreased myocardial function  Ineffective Tissue Perfusion r/t increased cardiac workload  Excess Fluid Volume r/t left and right ventricular overload and ineffective pumping 86
  • 87. Pediatric CHF—Nursing Diagnoses  Review CP, pp. 595-598  Ineffective Breathing Pattern r/t pulmonary congestion  Imbalanced Nutrition: Less than Body Requirements r/t increased energy expenditure  Deficient Knowledge r/t unfamiliarity with disease process, treatment, interventions, and home care 87
  • 88. Three early signs of CHF in infants/children…  Tachypnea  Poor feeding  Diaphoresis during feeding 88
  • 89. Question  A 4-month-old who has a congenital heart defect develops congestive heart failure and is exhibiting marked dyspnea at rest. This finding is attributed to:  A. Anemia  B. Hypovolemia  C. Pulmonary edema  D. Metabolic acidosis 89
  • 90. Medications for Pediatric Heart Failure  Aim of medications:  Decrease cardiac workload  Improve cardiac output  Types of medications:  Positive inotropes  Diuretics  Afterload-reducing drugs 90 See “Medications Used to Treat Congestive Heart Failure,” p. 593
  • 91. Digoxin (Lanoxin)  IV, PO  Slows and strengthens the heart  Positive inotropic agent (Increases the contractility of the myocardium)  Monitor: Dig level, K+, Mg++, Ca++  Signs of toxicity:  Nausea, vomiting, anorexia, bradycardia, dysrhythmia 91
  • 92. Digoxin—Parent Teaching  Safety Alert: Administering Digoxin, p. 594  Count apical heart rate for one full minute before giving  Call for physician’s advice before giving if HR < 100 BPM infant/toddler, < 70 children  Give at same time each day, with doses equally spaced apart (morning, evening)  If the dosage is spit up or vomited, do not repeat 92
  • 93. Digoxin—Parent Teaching  Don’t use teaspoon, eye dropper—draw up in syringe or calibrated dropper  Always remove the cap before administering the medication into the child's mouth  Notify physician: nausea, vomiting, listlessness, anorexia  Keep medications out of reach of children  Refill medicine 1 week before it runs out and ask for new prescription at doctor’s visit 93
  • 94. 94
  • 95. Furosemide (Lasix)  IV / IM / PO  Loop diuretic that blocks sodium reabsorption in the ascending loop of Henle  Decreases preload by increasing water excretion  Side effects: Electrolyte imbalances ( K+,  Mg++); metabolic alkalosis; hypotension  Monitor: Electrolytes, urinary output, BP, daily weights 95
  • 96. Spironolactone (Aldactone)  PO  Potassium-sparing diuretic  Decreases preload  Side effects: Hyperkalemia, hypovolemia, contraindicated in renal failure  Monitor: I & O, electrolytes, BP 96
  • 97. Captopril (ACE Inhibitors)  PO  Decreases angiotensin II  Dilates blood vessels, making it easier for the heart to pump blood forward into the body  Reduces afterload (blood pressure)  Less strain on heart muscle and valves, decreased myocardial oxygen use  Monitor blood pressure carefully; monitor renal function 97
  • 98. Question  A toddler is hospitalized with CHF and is receiving digoxin and Lasix. She has vomited twice in the past 4 hours. The nurse’s best action is to:  A. Increase the child’s fluid intake.  B. Omit the next dose of Lasix.  C. Check the child’s blood pressure prior to the next dose of digoxin.  D. Get an order to draw a digoxin level. 98
  • 99. Question  The mother of a 5-month-old infant with congestive heart failure questions the necessity of weighing the infant every morning. The nurse’s response should be based on the fact that this daily information is important in determining:  A. Renal failure  B. Fluid retention  C. Nutritional status  D. Medication dosage 99
  • 101. Pulmonary Hypertension (PH): The OTHER Hypertension (p. 599)  Increased pressure, narrowing: pulmonary arteries, arterioles  Elevated mean pulmonary arterial pressure (PAP) >25 mmHg  Causes: lung disease, some congenital heart diseases  RV failure  Rt heart failure  Lt heart failure  reduced CO  hypotension 101
  • 103. Signs/ Symptoms & Dx  Infants: poor appetite, poor growth, lethargy, tachypnea, tachycardia, sweating, cyanosis  Children: fatigue, chest pain, dyspnea, dizziness, syncope  Dx: echocardiography, cardiac catheterization 103
  • 104. Treatment  Rapidly lethal – Must treat early while reversible (to prevent pulmonary vascular remodeling)  Treat underlying cause (if known)  Surgery 3-6 mos: ASD, VSD, AVSD, PDA  Medications: O2, nitric oxide, calcium channel blockers (nifedipine), diuretics, sildenafil (Viagra)  Lung transplantation: severe cases 104
  • 105. Heart Disease in Children 105
  • 106. Heart Disease in Children  Two types:  Congenital  One or more heart structure abnormalities that develop before birth or persistence of a fetal structure after birth  Acquired  Any cardiac condition that was not present at birth 106
  • 108. Congenital Heart Disease is associated with….  Family history of congenital heart disease  Fetal exposure to drugs such as dilantin and lithium  Maternal diabetes mellitus  Maternal viral infections such as rubella  Trisomy 21 (Down syndrome) 108
  • 109. Congenital Heart Disease  Three Types:  Acyanotic  Obstructive  Cyanotic 109
  • 110. Acyanotic Heart Lesions (Increase Pulmonary Blood Flow, p. 575)  Left-to-right shunting  Ventricular septal defect (VSD)  Patent ductus arteriosus (PDA)  Atrial septal defect (ASD)  Atrioventricular septal defect (endocardial cushion defect) 110
  • 111. Acyanotic Heart Lesions— Manifestations  Left-to-right shunt  Systemic pressure > pulmonic pressure  Oxygenated blood backwashing to right side of heart  Venous blood does NOT enter systemic circulation  ALL of the blood returning to the right side of the heart passes through the lungs 111
  • 112. Acyanotic Heart Lesions  NO cyanosis  Not always apparent at birth  Excessive pulmonary blood flow (pulmonary HTN)  Enlarged heart (right, sometimes left)  Congestive heart failure  Enlarged liver, dyspnea, tachypnea, intercostal retractions, poor growth, frequent respiratory infections 112
  • 113. Ventricular Septal Defect (VSD)  Hole or defect in ventricular septum (wall) 113
  • 115. Ventricular Septal Defect (VSD)   Pulmonary blood flow  Pulmonary HTN  Usually not symptomatic at birth  Loud, harsh systolic murmur  Large defects: CHF, poor feeding, failure to thrive 115
  • 116. VSD—Medical Management  20-60% close spontaneously  CHF—Lanoxin and Lasix  Nutritional supplements  Antibiotic prophylaxis to prevent endocarditis 116
  • 117. Antibiotic Prophylaxis  Children with congenital heart defects at risk for bacterial endocarditis and damage to heart valves  Must use antibiotics:  Before and after dental, oral, and invasive procedures / surgeries  Any unexplained fever or malaise within 2 months of procedure may be a sign of infection 117
  • 118. Question  The father of a child with a congenital heart defect asks the nurse why his daughter has to take penicillin before she gets her teeth cleaned by the dentist. The nurse explains that this is necessary to prevent:  A. Bacterial endocarditis  B. Congestive heart failure  C. Rheumatic fever  D. Infected gums 118
  • 119. VSD—Pulmonary Artery (PA) Banding  Helps prevent pulmonary vascular obstructive disease  Palliative surgery  Closed heart surgery— does not require cardiopulmonary bypass  Band placed around pulmonary artery, decreasing pulmonary blood flow  Used when VSD cannot be closed (multiple VSD’s, very small infants with severe CHF)  Less frequently done than corrective surgery 119
  • 120. VSD—Patch Closure  Corrective surgery  Purse-string suture around small defects  “Patch” over large defects  Open heart surgery  Requires cardiopulmonary bypass 120
  • 121. Question  A cardiac catheterization is scheduled for a 5- year-old with a ventricular septal defect to:  A. Identify the degree of cardiomegaly present  B. Demonstrate the exact location of the defect  C. Confirm the presence of a pansystolic murmur  D. Establish the presence of ventricular hypertrophy 121
  • 122. Patent Ductus Arteriosus (PDA) (p. 576)  Opening between aorta and pulmonary artery   Pulmonary blood flow  Back to left atrium/left ventricle  Left ventricular hypertrophy  CHF (left side)  Respiratory distress  Machinery-type murmur Connection between pulmonary artery and aorta 122
  • 123. PDA—Treatment  CHF: digoxin, lasix  Medical— indomethacin (Indocin)  Interventional— cardiac catheterization  Surgical—ligation of ductus (left thoracotomy) 123
  • 124. Indomethacin (Indocin) Ibuprofen  IV  NSAID—inhibits the production of prostaglandins  Promotes closure of PDA; onset of action usually within minutes  Closure of PDA in 80% of patients  Monitor renal function  Side effects: bleeding (intraventricular hemorrhages, GI bleeds) 124
  • 125. Atrial Septal Defect (ASD) (p. 576)  Hole or defect in atrial septum (wall) 125
  • 127. Atrial Septal Defect  Often asymptomatic  Systolic murmur  Large defect: CHF, pulmonary vascular disease (often 1st appearing as an adult)  Antibiotic prophylaxis  Treatment: “patch” 127
  • 128. Atrioventricular Septal Defect (AVSD) (Endocardial Cushion, AV Canal) (p. 577)  LARGE hole in center of heart  ASD, VSD, and combined mitral and tricuspid valves (common atrioventricular opening or “canal”)  Common with Down syndrome 128
  • 130. Atrioventricular Septal Defect  Left-to-right shunting: Backward flow of oxygenated blood through both ASD and VSD to right side of heart  Right-sided heart failure  Pulmonary hypertension  Systolic murmur 130
  • 131. Atrioventricular Septal Defect  Hemodynamic changes with untreated cases: permanent right-to- left shunting, cyanosis  Tachypnea, tachycardia, poor growth http://www.gundluth.org/images/ei_0033.jpg 131
  • 132. Atrioventricular Septal Defect  Medical: digoxin, diuretics, and afterload reduction (ACE)  Treatment: surgical repair early in infancy (3-4 mos) before the lungs become damaged and permanent hemodynamic changes occur  “Patches” over both septal defects and valvular repair  Antibiotic prophylaxis 132
  • 133. Review Question  A toddler has been diagnosed with an acyanotic cardiac defect. Which assessment data would most likely indicate congestive heart failure? A. Heart murmur. B. Cardiac volume overload. C. Anuria. D. Excitability. 133
  • 134. Obstructive/ Stenotic Lesions  Pulmonary stenosis  Aortic stenosis  Coarctation of the aorta 134
  • 135. Pulmonary Stenosis (p. 582)  Area where blood exits the heart's lower right chamber is too narrow (right ventricular outflow tract obstruction)  Harsh systolic murmur 135
  • 136. Pulmonary Stenosis  Mild: asymptomatic, requires only antibiotic prophylaxis  Severe or critical: balloon valvuloplasty or open-heart surgical repair 136
  • 137. Aortic Stenosis (p. 590)  Obstruction of blood flow from heart to body (obstruction to blood flow leaving left ventricle)   Afterload   Cardiac output   Systemic blood flow  Harsh systolic murmur 137
  • 138. Aortic Stenosis  Mild: asymptomatic, exercise fatigue  Severe or critical: CHF, left ventricular hypertrophy, shock 138
  • 139. Aortic Stenosis  Mild: continue to monitor, antibiotic prophylaxis  Severe or critical: aortic balloon valvuloplasty (cardiac catheterization), surgical valvotomy  May need aortic valve replacement 139
  • 140. Coarctation of the Aorta (COA) (p. 590)  Obstructive lesion  Restricts flow of blood out of the left ventricle  Aorta is pinched at some point along its length, limiting the amount of oxygen-rich blood that can reach the rest of the body 140
  • 141. Coarctation of the Aorta (COA)   Afterload   Cardiac output   Systemic blood flow   Pulmonary congestion (pooling of blood in left side of heart)  Enlarged left ventricle; CHF  Decreased pulses and BP in the lower extremities  Cold feet, legs  Epistaxis (nose bleeds), BP higher in arms 141
  • 142. COA—Treatment  Symptomatic CHF: digoxin, lasix  Medical: prostaglandin infusion to keep ductus arteriosus patent (improve perfusion to lower body)  Balloon angioplasty  Surgical repair: left thoracotomy with anastomosis  Antibiotic prophylaxis for life 142
  • 143. Question  An infant with a left-to-right shunt was admitted to the hospital in congestive heart failure. She weighed 3.6 kg yesterday. A finding that indicates a worsening of her condition today is:  A. Weight 3.66 kg.  B. Urine output of 40 ml in past 8 hours.  C. Crackles in the lower lobes.  D. All of the above. 143
  • 144. Cyanotic Heart Lesions (Decrease Pulmonary Blood Flow, p. 581)  Right-to-left shunting  Tetralogy of Fallot (TOF)  Transposition of the Great Arteries (TGA)  Hypoplastic Left Heart Syndrome (HLHS) 144
  • 145. Cyanotic Heart Lesions— Manifestations  Right-to-left shunt  Pulmonic pressure > than systemic  Unoxygenated blood bypasses pulmonary circulation and goes directly to the left side of the heart to be pumped into the systemic circulation 145
  • 146. Cyanotic Heart Lesions— Manifestations  “Blue baby”— Cyanosis  Symptomatic soon after birth  Decreased pulmonary blood flow 146
  • 147. Tetralogy of Fallot (p. 582)  Defect composed of four distinct lesions: 1. Ventricular septal defect 2. Pulmonic stenosis 3. Overriding aorta 4. Right ventricular hypertrophy 147
  • 148. Cross-Section of a Normal Heart and a Heart With Tetralogy of Fallot 148
  • 149. Tetralogy of Fallot  Reduced blood flow to lungs  Aortic blood (to body) mainly oxygen-poor venous blood  Severity of cyanosis depends primarily on degree of pulmonary stenosis 149
  • 150. Tetralogy of Fallot—Signs and Symptoms  X-ray: Heart is “Boot- shaped”  Cyanosis, difficulty breathing  Clubbing of fingers (because of hypoxemia)  Systolic murmur, palpable thrill  Polycythemia  Hypercyanotic episodes 150
  • 153. Question  A child diagnosed with tetralogy of Fallot becomes upset, crying and thrashing around when a blood specimen is obtained. The child’s color becomes blue and the respiratory rate increases to 44 breaths/minute. Which of the following actions would the nurse do first?  A. Obtain an order for sedation for the child.  B. Assess for an irregular heart rate and rhythm.  C. Explain to the child that it will only hurt for a short time.  D. Place the child in a knee-to-chest position. 153
  • 154. Question  A newborn with TOF is fed in the semi-Fowler’s position. After the nurse feeds and burps the infant and changes the infant’s position, the infant has a bowel movement and almost immediately becomes cyanotic, diaphoretic, and limp. These symptoms are most likely caused by the:  A. Burping  B. Formula  C. Position change  D. Bowel movement 154
  • 155. TOF Surgical Repair  Surgical treatment:  Palliative—Relieves symptoms by increasing the blood flow to the lungs  Corrective—Repairs the underlying defects 155
  • 156. Blalock-Taussig Shunt (p. 586)  Palliative procedure  Closed-heart surgery  Shunt created from aorta to pulmonary artery   Blood flow to lungs  “Buys” time for infant to grow   Success of corrective surgery when done later 156
  • 157. Question  The nurse is aware that the aim of palliative surgery for children with tetralogy of Fallot is to directly increase the blood flow to the:  A. Brain  B. Lungs  C. Myocardium  D. Right ventricle 157
  • 158. TOF Repaired  Open-heart surgery  2 to 4 months  Pulmonary valve widened  VSD patched  No treatment: Displaced aorta, enlarged rt. ventricle  Antibiotic prophylaxis for life 158
  • 159. Question  Parents of a toddler with tetralogy of Fallot explain that they do not want him to overexert himself; so they always keep him in his playpen or crib to limit his mobility. Based on this information, the most appropriate nursing diagnosis is:  A. Activity Intolerance  B. Risk for Impaired Parenting  C. Caregiver Role Strain  D. Risk for Delayed Development 159
  • 160. Transposition of the Great Arteries (TGA) (p. 584) Reversal of aorta and pulmonary artery 160
  • 161. Transposition of the Great Arteries (TGA)  Babies born with TGA can only survive if they have one or more connections that allow some oxygenated blood to go to the body (PDA, ASD) 161
  • 162. Prostaglandin E1 (PGE1)  IV infusion  Causes the ductus arteriosus to stay artificially open (patent)  For infants with ductal- dependent cardiac abnormalities (TGA, HLHS, severe TOF)  Ventilator  Monitor: Respiratory, cardiovascular status, bleeding (inhibits platelet aggregation)  Side effects: Apnea, fever, irritability, flushing, bleeding, third- spacing 162
  • 163. Transposition of the Great Arteries (TGA)  Balloon atrial septostomy—tears a hole in the atrial septum  Corrective surgery is performed in the early days following birth:  Arterial switch procedure—aorta and pulmonary artery returned to their normal positions 163
  • 164. Tiny Baby Survives Open Heart Surgery 164
  • 165. Hypoplastic Left Heart Syndrome (HLHS) (p. 591)  Inadequate development of the left side of the heart  Only one functional ventricle  Aortic valve, mitral valve, and ascending aorta may also be small or hypoplastic 165
  • 166. HLHS—Signs and Symptoms  Cyanosis, appears “gray”  CHF  Tachycardia, dyspnea  Hypotension, weakness  Hypoperfusion, shock, metabolic acidosis 166
  • 167. HLHS—Treatment  Comfort care  Without surgery, fatal within the first 2 weeks of life  Medications: PGE1 infusion to keep the ductus open  Surgery: 3-staged palliative surgery (ages 1 week, 6 months and 2 years of age)  Heart transplant—infrequent due to scarcity of neonatal donor hearts 167
  • 168. Child With HLHS Who Received Heart Transplant http://www.texaschildrenshospital.org/CareCenters/KidsCourageous/Heart_Noah.aspx 168
  • 169. HLHS—Palliative Surgery  Three-stage surgical approach to improve flow of blood throughout the body  The Norwood Procedure (Stage 1)  1 week of age  Provides blood flow from the right ventricle directly to the aorta 169
  • 171. HLHS—Palliative Surgery  The Bi-Directional Glenn (Stage 2)  6 months of age  The Fontan Procedure (Stage 3)  2 years of age  Re-routes blood flow around the defective areas of the heart by creating new pathways for blood circulation to and from the lungs 171
  • 173. HLHS—Prognosis  4-year survival following staged repair up to 85%  Long-term survival remains to be seen  Long-term complications (advanced disease): ventricular and valvular dysfunction, dysrhythmias, low albumin, pleural effusions, ascites 173
  • 174. Question  Parents of children with congenital heart problems often experience loss of control when the child is hospitalized. The nurse who understands this will:  A. Encourage parents to participate in their child’s care.  B. Explain procedures prior to performing them.  C. Answer questions honestly.  D. Do all of the above. 174
  • 175. 175
  • 177. Cardiac Surgery (p. 578; 580)  Two types:  Open-heart surgery: repair to the myocardium (heart muscle); requires cardiopulmonary bypass  Closed-heart surgery: interventions to structures around the heart but not the heart muscle itself; done without bypass 177
  • 178. Open-Heart Surgery  Read pp. 578-580  Trend: to intervene at an early age  Risks: bleeding, emboli, dysrhythmias, fluid & electrolyte imbalances 178
  • 179. Post Cardiac Surgery  STERNAL PRECAUTIONS  Chest tube, NGT, ventilator, cardiac monitor, pulse oximetry  Encourage cough, IS  Monitor VS, cardiac, respiratory, I & O, electrolytes, chest tube drainage  Very painful surgery: Adequate pain control very important 179
  • 181. Rheumatic Fever (RF) (p. 600)  Children ages 5 – 15  Inflammatory autoimmune response  Result of “strep throat” that has not been treated with antibiotics  Manifests 1 – 3 weeks afterwards  Affects connective tissue of heart, joints, subcutaneous tissues, blood vessels  Most serious: Cardiac valvular disease (esp. scarring of mitral valve)  Prevention: refer all children with sore throats for throat cultures 181
  • 183. Manifestations of Rheumatic Fever  Carditis—inflammation of all parts of the heart (mitral, aortic valves)  Murmur  Polyarthritis—joint pain  Chorea—involuntary movements of legs, arm, and face  Erythema marginatum—red skin lesions  Subcutaneous nodules— nontender lumps located over the joints 183
  • 184. RF—Diagnostics / Treatment  Positive antistreptolysin O titer (+ ASO)   SED (erythrocyte sedimentation) rate  Positive C-reactive protein  EKG changes  Monitor for cardiac complications, seizures  Antiinflammatory agents (aspirin, corticosteroids), analgesics, antipyretics  Streptococcal prophylaxis for many years 184
  • 185. Streptococcal Prophylaxis for the Child with Rheumatic Fever  Damaged valves can become further damaged with repeated infections  Streptococcal prophylaxis is lifelong if there is actual valve involvement  Intramuscular penicillin, administered monthly, is the drug of choice  Alternatives include oral penicillin twice daily or oral sulfadiazine once a day 185
  • 187. Question  When examining the laboratory work of a child with the diagnosis of rheumatic fever, the nurse would expect the findings to demonstrate:  A. A negative C-reactive protein  B. A positive antistreptolysin titer  C. An elevated reticulocyte count  D. A decreased erythrocyte sedimentation rate 187
  • 188. Kawasaki Disease (KD) (p. 601)  Children < 4 years (peak incidence 18 – 24 months)  Mucocutaneous lymph node syndrome  Inflammatory autoimmune disease—principle area of involvement is the heart  Antibody-antigen complexes  If caught and treated early the prognosis is usually very good  If left untreated or caught too late, it can be fatal or leave the child with irreversible heart and/or organ damage 188
  • 189. Kawasaki Disease (KD)  May damage the coronary arteries (vasculitis) and heart muscle  Most common cause of acquired heart disease in U.S. children  Can lead to coronary aneurysms and myocardial infarctions later in life  Cause: ??? noncontagious infection; associated with rug shampooing, dust mites, or proximity to stagnant water  Seasonal:  Late winter, early spring 189
  • 190. KD—Signs and Symptoms  Affecting children under the age of 5, diagnostic criteria include at least:  5 days of fever (> 39 ° C, 102.2° F), unresponsive to antibiotics  Conjunctival eye redness without discharge  Red-fissured lips  Strawberry tongue  Red rash  Redness and/or swelling of palms and soles, and lymph nodes in the neck 190
  • 191. KD—Phases and Treatment  3 phases  Acute phase: 1 to 2 weeks, with high fever > 5 days  Nurse needs to closely monitor cardiac status, VS, observe for CHF  Echocardiogram, ECG,  SED rate  Early treatment can dramatically reduce the likelihood of cardiovascular damage  High-dose IV Gamma-globulin  High-dose PO ASA therapy 191
  • 194. Aspirin (ASA)  PO, administer with milk or food  Antiplatelet agent (inhibit platelet function by making them less sticky)  High dose therapy (KD): 80-100 mg/kg/day for the first two weeks to reduce fever, swelling and inflammation; and to decrease the chance of blood clots  Don’t give to children <16 y with chickenpox or flu-like symptoms (Reye syndrome)  Side effects: Bleeding 194
  • 195. 195
  • 196. Review Question  A toddler with Kawasaki’s disease is ordered to receive aspirin therapy. Typical administration of aspirin for Kawasaki’s disease would include which of the following principles? A. High doses of aspirin should be given while fever is high. B. Aspirin therapy is given to reduce fever. C. Aspirin dose increases after fever is gone. D. Aspirin dosage is unrelated to platelet count. 196
  • 197. Gamma Globulin (IVIG)  One time dose 2 g/kg  Administered through an intravenous (I.V.) line for 10 hours  If given first 10 days, will dramatically reduce the risk of damage to the coronary arteries  Side effects: Hypotension; facial flushing; tightness in the chest 197
  • 198. IVIG—cont’d…  Monitor BP closely  Benadryl and acetaminophen: control side effects  Epinephrine: anaphylactic reactions  Vaccines must be delayed for 5 months months after treatment 198
  • 199. 199
  • 201. Management of Hypertension in Children  Diastolic > 95% percentile  Not common, but incidence rising  Kidney disease, obesity  Weight reduction  Physical conditioning  Dietary modification  Pharmacologic treatment 201
  • 202. High Cholesterol Risk Factors  Tobacco use  Dyslipidemia (elevated LDLs and cholesterol and decreased HDLs)  Hypertension  Decreased physical activity  Obesity  NANDA diagnosis: Sedentary Lifestyle 202
  • 203. 203