RESPIRATORY
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Holy Family University *
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Course
433
Subject
Anatomy
Date
Jan 9, 2024
Type
docx
Pages
11
Uploaded by dgraff1926
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Alterations in Respiratory Functions
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Pediatric versus Adult Respiratory System Anatomy and Physiology
Anatomy of upper airway
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A smaller nasopharynx is easily occluded during infections.
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A small oral cavity and a large tongue increase the risk of obstruction
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The large amounts of soft tissue and loosely anchored mucous membranes increase the risk of edema and
obstruction.
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Cartilage around trachea flexible
•
Airway diameter
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Trachea shorter and narrower → increased airway resistance → increased respiratory effort
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Pediatric versus Adult Respiratory System
Anatomy and Physiology
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Position of trachea
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Right bronchus acute angle at bifurcation
→
increased foreign body aspiration
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Pediatric versus Adult Respiratory System
Anatomy and Physiology
Anatomy of lower airway
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Use diaphragm to breathe until 6 years of age
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Immature chest muscles and ribs → retractions
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Suprasternal and intercostal
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https://youtu.be/n66CTtQRf60
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Subcostal and intercostal
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https://youtu.be/FOsxPhJsZrE
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Substernal •
https://youtu.be/TUWk4t_RTq4
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Respiratory Distress and Respiratory Failure
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Respiratory failure
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Partially occluded airway
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Malfunction of the respiratory center
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Fatigued muscles of respiration
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Body can no longer maintain effective gas exchange.
–
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Respiratory Distress and Respiratory Failure
Mild Respiratory Distress: Attempting to Compensate
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Restlessness
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Tachypnea
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Tachycardia
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Diaphoresis
Moderate Respiratory Distress: Early Decompensation
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Nasal flaring
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Retractions
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Grunting
, wheezing
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Anxiety, irritability, mood changes, confusion
Severe Respiratory Distress: Respiratory Failure/Imminent Arrest
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Dyspnea
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Bradycardia
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Cyanosis (note that cyanosis is a late sign)
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Stupor, coma
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Pediatric Emergencies
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Brief resolved unexplained event (B R U E)
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Frightening episode of one of the following: apnea, decreased breathing, cyanosis or pallor, change in muscle tone, and altered level of responsiveness in a child less than 1 year of age.
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Lasts less than 1 minute
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Common causes
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Gastroesophageal reflux
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Seizures
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Lower respiratory disorders
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Cardiac arrhythmias
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Brief resolved unexplained event (B R U E)
Diagnostics
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CBC, electrolytes
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Blood and urine cultures
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EKG
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EEG
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pH study
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MRI
Management
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Treatment is targeted at the underlying condition Nursing Care
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Monitor cardiorespiratory status
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Emergency resuscitation
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Provide emotional support
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Teaching
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Sudden Infant Death Syndrome (S I D S)
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The sudden death during sleep of an infant under 1 year of age that remains unexplained after a thorough investigation
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Most S I D S deaths occur in infants between 2 and 4 months of age.
•
Risk factors
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Maternal smoking during pregnancy
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Secondhand smoke
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Co-sleeping
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Premature, low birth weight
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Prone or side-lying position
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Viral illness
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Soft bedding, pillows
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Low apgar scores
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Sudden Infant Death Syndrome (S I D S)
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Parent education related to prevention
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Back to sleep
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Avoid loose bedding, toys, pillows
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Use a firm, tight mattress in crib
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Discourage co-sleeping
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Use of pacifier during sleep
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Smoking increases risk
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Keep immunizations up to date
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Pediatric Airway Disorders
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Croup syndromes
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Upper airway illnesses that result from inflammation and swelling of the epiglottis and larynx
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Broad classification of upper airway illnesses
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Viral syndromes
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Acute spasmodic laryngitis
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Laryngotracheobronchitis (LTB)
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Bacterial syndromes
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Bacterial tracheitis
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Epiglottitis
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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14
Laryngotracheobronchitis (LTB)
Causes Parainfluenza RSV
Influenza Adenoviruses Enteroviruses Who?
Children 3 months- 3 years old
Manifestations Early
Fever Barking-seal Stridor
Restlessness, irritable Later
Retractions Increased stridor
Cyanosis
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Laryngotracheobronchitis (LTB)
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Monitor for airway obstruction
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Cool mist
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Administer O2 if needed
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Administer corticosteroids (oral dexamethasone) as ordered
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Administer nebulized racemic epinephrine
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Epiglottitis
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Usually caused by Haemophilus Influenzae
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MEDICAL EMERGENCY
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Progresses rapidly → complete airway obstruction
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Absence of cough, drooling
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Tripod position
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Epiglottitis
Management
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Immediate endotracheal intubation
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Supplemental oxygen
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IV antibiotics
Nursing Care
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Protect airway- prepare for intubation
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Monitor continuous oximetry
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Droplet precautions for first 24 hours
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Avoid throat culture
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Bronchiolitis
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Lower respiratory tract illness that causes inflammation and obstruction in bronchioles
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Leading cause of hospitalization in first year of life
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Most common cause: Respiratory syncytial virus (RSV)
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Transmitted through direct respiratory secretions or contaminated surfaces
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Occurs October through March
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RSV Bronchiolitis
Risk factors for severe infection:
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Age- younger the child, the higher the risk
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Immunosuppression
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Very low birth weight
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Lung disease
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Neuromuscular disease
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Congenital heart defects
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RSV Bronchiolitis
How is it tested?
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Nasopharyngeal secretions
What are the symptoms?
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Early
: Runny nose, nasal congestion, sneezing, cough, fever, wheezing
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Progresses to tachypnea, retractions, refusal to feed, dehydration
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Severe: RR > 70/min, listlessness, poor breath sounds, poor air exchange, apneic
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RSV Bronchiolitis
Nursing Care
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Symptom management
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Humidified oxygen
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Maintain airway
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Fluid intake
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Nasal suction as needed
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Provide a private room or cohort the patient. Designated equipment in room.
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Bronchodilators are not recommended
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Steroids are controversial
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Antibiotics for a coexisting bacterial infection
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Pneumonia
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Inflammation or infection of the bronchioles and alveoli
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Occurs most often in infants and young children
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Caused by viruses and bacteria
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> 5 years old Mycoplasma
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Usually preceded by a URI
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Symptoms
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Fever, crackles, wheezes, cough, tachypnea, restlessness, decreased breath sounds, chest pain, retractions, nasal flaring
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Pneumonia
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Diagnostics
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History and Physical
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Nasal swab for influenza and other respiratory viruses
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Chest x-ray
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Blood culture Management
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Airway management
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Antibiotics
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Pneumonia
Nursing Care
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Administer oxygen
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Monitor continuous oximetry
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Administer antipyretics and antibiotics as ordered
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Monitor I & O
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Encourage rest Complications
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Pneumothorax
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Pleural effusion
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Bronchopulmonary Dysplasia
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Chronic lung disease of prematurity
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Defined as the need for supplemental oxygen for at least 28 days after premature birth
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Usually occurs in babies born at less than 28 weeks gestation
Why does it happen?
-Positive pressure ventilation and oxygen injures the immature lungs
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Bronchopulmonary Dysplasia
What are the clinical manifestations
?
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Tachypnea, nasal flaring, grunting,
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Irritability
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Retractions, wheezing
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Failure to thrive
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Barrel Chest
What is the treatment?
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Supplemental oxygen
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Surfactant, corticosteroids, caffeine
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Bronchopulmonary Dysplasia
Complications
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Cognitive delays, cerebral palsy
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Growth failure
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Abnormal lung function
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Severe BPD → Chronic lung disease
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High risk of RSV → Palivizumab given monthly NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Nursing management
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Assess respiratory status
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Ensure adequate nutrition
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Promote growth and development
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Asthma
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Chronic disorder characterized by bronchial constriction, hyperresponsive airways, and airway inflammation
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Triggers
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Allergens
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Exercise
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Cold air
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Infections
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Strong emotions
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Asthma Physical Assessment
Findings
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Dyspnea
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Cough
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Wheezing
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Coarse lung sounds
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Restlessness, irritability
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Use of accessory muscles
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Decreased oxygen saturation
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Asthma
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Four categories
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Intermittent
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Mild persistent
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Moderate persistent
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Severe persistent
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Diagnostics
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Pulmonary function tests
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Most accurate diagnostic test
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Baseline at diagnosis and then routinely
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Peak expiratory flow rate
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Pulmonary Function Test
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Asthma
Treatment
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Bronchodilators
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Watch child for tremors, tachycardia, irritability and vomiting with albuterol
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Observe child for dry mouth with ipratropium
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Anti-inflammatory agents
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Oral steroids can be given for 3 or 10 day course
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Encourage to take with food
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Inhaled steroids can be given daily as preventative
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Rinse mouth after the use of corticosteroid inhaler
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Leukotriene modifiers
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Asthma
Nursing Care
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Respiratory assessment
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Monitor for shortness of breath, dyspnea, and wheezing
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Position the child to maximize ventilation
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Monitor pulse oximeter
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Administer oxygen as prescribed
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Administer medications as ordered
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Asthma Education
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Identify personal triggers and avoid them
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Asthma action plan
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Teach child and family how to use a peak flow meter and keep records
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Teach how to recognize an exacerbation
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Decreased peak flow
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Increased used of rescue inhaler
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Difficulty speaking or eating
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Educate family when to use rescue vs. maintenance meds
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Stress importance of immunizations
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Status asthmaticus
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Life threatening airway obstruction
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Labored breathing, lack of air movement in lungs
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Accessory muscle use
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Risk for cardiac and respiratory arrest
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Treatment
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Magnesium sulfate
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Heliox
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Cystic Fibrosis
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Inherited autosomal recessive respiratory disorder characterized by mucus glands that secrete an increased amount of thick mucus which lead to obstruction of organs
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Affects respiratory, gastrointestinal, reproductive systems
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Median life span mid-40s
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Most common in caucasians
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Cystic Fibrosis Clinical Manifestations
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Respiratory
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Wheezing, cough
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Progress to dyspnea, atelectasis on CXR
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Cyanosis, barrel-shaped chest, clubbing of fingers in advanced disease
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GI
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Large, bulky, greasy, foul smelling stools
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Voracious appetite →
loss of appetite → lose weight
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Meconium ileus is the earliest indication of CF
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Failure to thrive (FTT)
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Deficiency of vitamins A,D,E,K
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Cystic Fibrosis
Other manifestations
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Integumentary
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Sweat, tears and saliva have an excessively high content of sodium and chloride
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Reproductive system
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Viscous cervical mucus
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Decreased or absent sperm
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Cystic Fibrosis
Diagnostic Procedures
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DNA testing
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Sweat chloride test
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–
Device that uses an electrical current to stimulate sweat production
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Collection from two different sites
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Confirmative diagnosis
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Chloride >40 mEq/L infants less than 3 months old
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Chloride >60 mEq/L for all others
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Sodium > 90mEg/L
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PFTs, Sputum culture
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Abdominal x-ray
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Stool analysis
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Cystic Fibrosis Medications
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Respiratory
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Albuterol, ipratropium
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Dornase alfa-decreases the viscosity of mucus
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Antibiotics
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Pulmonary infections
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Pancreatic enzymes
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Treats pancreatic insufficiency
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Given with all meals and snacks
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Swallow or sprinkle capsules on food
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Vitamins
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Cystic Fibrosis
Nursing management
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Assist in airway clearance techniques (ACT)
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Encourage physical exercise
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Administer diet high in protein, fat, calories
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Administer pancreatic enzymes within 30 min of eating
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Encourage oral fluid intake
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Administer vitamin supplements
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Monitor blood glucose levels
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Administer laxatives/softeners as needed for constipation
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Cystic Fibrosis
Nursing education
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Help parents create schedule for medication administration.
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Teach respiratory therapy techniques; create schedule.
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Determine nutritional needs.
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Determine if financial assistance is needed.
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Plan for exercise.
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Promote regular provider visits, emphasize immunizations
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Pneumothorax
Air enters pleural space because of penetrating chest injury or tears in the tracheobronchial tree.
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Open Pneumothorax
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Caused by a penetrating injury
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Sucking sound might be heard
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Symptoms
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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Restlessness, cyanosis
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Treatment
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Water-tight bandage
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Thoracostomy → chest tube
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Pneumothorax
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Closed pneumothorax
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Caused by blunt chest trauma with no evidence of rib fracture
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Following motor vehicle crash or abuse, bicycle, scooter, skateboard, skate accident
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Manifestations
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Breath sounds are decreased on the injured side
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Respiratory distress
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Treatment
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Thoracostomy →
chest tube
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Pneumothorax
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Tension Pneumothorax
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Life threatening emergency
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Air leaks into the chest during inspiration but cannot escape during expiration
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Pressure increases → lung collapse → mediastinal shift → decreased cardiac output
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Manifestations
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Respiratory distress
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Decreased breath sounds
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Paradoxical breathing
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Treatment
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Needle thoracentesis → Chest tube
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Pneumothorax
Nursing Management
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Monitor respiratory status
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Monitor vital signs
•
Assess surgical site
Complications
•
Hemothorax
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Lung tissue injury
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Scarring from poor tube placement
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Alterations in Respiratory Function
Questions???
NUFT 433- PEDS- ALTERATION IN RESPIRATORY FUNCTIONS
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