Care of the Pediatric Patient with Respiratory Problems
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Transcript Care of the Pediatric Patient with Respiratory Problems
Care of the
Pediatric Patient
with Respiratory
Problems
Elizabeth Allen RN, MSN
Learning Objectives
Describe
Unique Characteristics of
Pediatric Respiratory System
List Respiratory Conditions and Injuries that
Cause Respiratory Distress in Children
Distinguish between Mild, Moderate, and
Severe Respiratory Distress
Differentiate between Signs and
Symptoms of Upper and Lower Airway
Conditions
Differences in A&P
Newborn- 3 months
obligatory nose
breathers
Child’s airway is shorter
and more narrow<6
years breathe with
diaphragm- intercostal
muscles immature
A newborn’s chest is
circular until age 6.
Decreased muscularity is
responsible for the thin
chest wall in infants.
Differences in A&P
Child epiglottis
longer, floppier
Higher oxygen
demand in children
Immature Infant
Respiratory and
Neurologic System
Offers Less-Efficient
Response to Hypoxia
and Elevated PCO2
Pediatric Respiratory Assessment
Noises
Work of Breathing
Stridor
Wheeze
Cough
Grunting
Cry
Rate
Head bobbing
Retractions
Nasal flaring
Pulse Oximetry
Auscultate
Diagnostic Tests
Pulmonary
Radiology
Function
Chest
Neck
Arterial
Blood Gases
Capillary Blood Gases
Pulse oximetry
Respiratory Distress
Can
Lead to Respiratory Failure
Early recognition and intervention vital
Mild
Tachypnea, tachycardia, diaphoresis, mild retractions
Moderate
Flaring, moderate retractions, grunting, wheezing
Anxiety, irritability, confusion, mood changes
Severe
Dyspnea, severe retractions
Bradycardia, bradypnea
Stupor, coma
Cyanosis = late sign
How Long can the
child maintain
that level of effort?
Respiratory Distress
Interventions
Assessment
Oxygen
Airway
positioning
Tripod Position
Medications
Racemic Epinephrine
Beta 2 Agonists/ Bronchodilators
Corticosteroids
Antibiotics
Apparent Life Threatening
Event (ALTE)
1
week to 2 months
Identifying diseases and conditions
GERD, acute respiratory infections,
seizures, Congenital heart defects,
metabolic conditions, child abuse
(Munchausen by proxy)
Lab work
Diagnostic testing
Monitoring
Home Education
Sudden Infant Death
Syndrome (SIDS)
Etiology / Pathophysiology
Genetic
Clinical Manifestation
Cardiopulmonary arrest
Season
Collaborative Care
Back to Sleep
Nursing Management
Safe Sleep Environment
Supportive Care
Safe Sleep Environment
Respiratory Infection
Transmission
Airborne Isolation
Small particles
negative pressure room
Droplet
Large
Isolation
particles- drop 3 feet
Contact
Isolation
Upper Airway
Problems
Strep Throat/
Viral tonsillitis
Tonsillitis
Supportive care
Strep Throat- Streptococcus infection
Fevers, gastritis
Positive rapid strep test or
positive culture
Treat with antibiotics
No longer contagious 24 hrs.
after first antibiotic dose
Upper Airway Problems
Tonsillectomy
and possible
Adenoidectomy
Post Op Care
Pain
management
Maintain hydration
Evaluate for bleeding,
swelling or
airway compromise
Upper Airway Problems
Croup
Upper
airway
illness causing
inflammation in
larynx and
epiglottis
Viral or bacterial
Symptoms:
“Barking” cough
Stridor
Hoarseness
Laryngealtracheobronchitis
Viral
Treatment
Keep
child calm!!!
Cold, humid night air
Corticosteroids
Racemic epinephrine
Albuterol as needed
Upper Airway Treatment
Cool Mist Tent
Upper Airway Problems
Epiglottitis
Inflammation of the
epiglottis – life threatening
Symptoms: 3 D’s
Bacterial
• Dysphagia
• Drooling
• Dysphonia
Hx: Acute fever, sore throat,
dysphonia and dysphagia
Diagnostic testing
Streptococcus
Staphylococcus
Haemophilus influenzae
type B
X-ray?
Treatment/Interventions
Antibiotics
Cephalosporin
Airway management
Evaluation
Upper Airway Problems
Foreign Body
Aspiration
Developmental- older
infants and Toddlers
Usually bronchial
obstruction, R bronchial
Signs
Cough, weak cough
Stridor
Respiratory Distress
Muffled or hoarse voice
Drooling
Anxiety, irritability
Unilateral diminished
breath sounds
Aspiration
Treatment
Keep child calm
Position of comfort
Monitor
cardiorespiratory
status
Airway intervention if
necessary
CXR
Endoscopy
OR
Upper Airway Problems
Otitis Media
Inflammation of
middle ear
84% infants have at
least 1 case before
age 3 years
More common in:
Kids with allergies
Families who smoke
Pacifiers
American Indian
Symptoms
Ear pain/ pulling at
ear
Fever
Vomiting/diarrhea
Irritability
Treatment Guidelines
AAP
Avoid over treatment
with antibiotics
Educate families to
complete courseavoid drug resistance
Figure 19–9 This young child is pulling at the ear and
acting fussy, two important signs of otitis media. Ask the
parents about the presence of fever and night
awakenings, additional signs that are often observed in
children with this condition.
Upper Airway Problems
Otitis Media
Repeated Otitis
Media
Hearing Loss
Speech delay
Tympanostomy
Tubes
Fall
out on own
Drainage
Lower Airway Problems
Bronchitis/
Bronchiolitis
Viral or bacterial
Underlying chronic illness
Bronchiolitis
(bronchioles)
RSV, parainfluenza,
adenovirus
Edema, debris clog and
narrow airway
Clinical
Therapy
Maintain Respiratory
Function
Close monitoring
Keep airways clear!
Oxygen
Humidity
Hydration
Nutrition
Rest
Anxiety
Discharge Planning
Lower Airway Problems
Nursing
Diagnoses
for bronchiolitis?
What’s your
priority?
Breathing
pattern,
ineffective
Ineffective airway
clearance
Fluid volume
deficit, risk for
Anxiety
Lower Airway Problems
Asthma
Etiology/Pathophysiology
Clinical Therapy
Assessment
Peak Expiratory
Flow Rate
Respiratory Distress
Triggers
Interventions
Medications
Maintain
Airway
Patency
Meet Fluid Needs
Pediatric
Considerations
Discharge Planning
Evaluation
Resource
http://www.nhlbi.nih.gov/fil
es/docs/public/lung/asthm
a_actplan.pdf
Lower Airway Problems
Asthma Exacerbation: Across the Room Assessment
LOC
Asthma Exacerbation Video- follow link
Respiratory rate
https://www.youtube.com/watch?v=EK8nzKzdnIM
Retractions
Audible wheezing
Head bobbing
Grunting
Speaking
Then listen for wheezing, diminished breath sounds
Lower Airway Problems
Know
your
Peak Flow
Green
zone: 80%-
100%
Yellow zone: 50%80%
Red zone: below
50%
Lower Airway Problems
Asthma
Severity Scale
Medications
http://www.nhlbi.nih.gov/files/docs/guidelines/asthma_
qrg.pdf
Intermittent asthma to Persistent Asthma requiring daily
medications
Short acting Beta2 agonist
Inhaled corticosteroid
Montelukast
Evaluate control with medications
PFT
Symptom tracking
Lower Airway Problems
(London et. al., 2014)
Lower Airway Problems
(London et. al., 2014)
Lower Airway Problems
(London et. al., 2014)
Lower Airway Problems
(London et. al., 2014)
Lower Airway Problems
Cystic
Fibrosis
Autosomal
recessive disorder
Incidence
Pathophysiology
Defective
chloride secretion and increased
sodium absorption.
Rate of progression varies among children
Clinical
manifestations
Diagnostic Procedures- Sweat Chloride Test
Resource
http://www.cff.org/
Defective chloride-ion
transport
and decreased water
flow
across cell membranes –
excessive
electrolyte loss.
Lower Airway
Problems
Cystic
Assessment
Chest Physiotherapy
Prophylactic antibiotics?
Nutrition
Physiologic
Psychosocial
Developmental
Respiratory Therapy
(including)
Fibrosis
Pancreatic Enzymes
Discharge Planning
Lower Airway Problems
Cystic Fibrosis
Clinical Therapy
Maintain respiratory
function
Manage infection
Optimize nutrition
Prevent
gastrointestinal
blocking
Nursing Diagnoses
Medications
Pancreatic enzymes
Antibiotics- oral and
inhaled
Osmotic
medicationpolyethylene glycol
High calorie formula,
MCT
H2 blocker, PPI
Tracheostomy
Tracheostomy
Care
Suctioning
Routine
Care
Emergency care
Tracheostomy