Week 3: Acute and Chronic Respiratory Conditions in the Pediatric Client
Normal Pediatric Respiratory Anatomy and Physiology
Upper respiratory tract components (as summarized in the transcript): nasal passages, nasopharynx, epiglottis, larynx. These structures contain smooth muscle and mucous glands.
Transient upper airway sounds are heard
Infants aiway cartilage is soft
outh breather
Airway diameter is smaller
Difficult to ausculate due to a narrower airway and the presence of secretions, which can lead to challenges in diagnosing respiratory conditions effectively.
Lower respiratory tract components: trachea, carina, bronchi, bronchioles, alveolar space.
Alveoli: air sacs where oxygenation occurs via capillaries; alveolus structure supports gas exchange.
Visual cues on the slides included a cross-sectional view showing the airway from nasal/oral entry through bronchioles to alveoli; emphasis on airway mucous production and smooth muscle affecting patency.
Infant vs adult anatomy notes (e.g., tongue size and airway considerations) highlighted in the slide sequence; these influence airway patency in pediatrics.
Tongue is larger and can cause obstruction.
Respiratory Assessments and Manifestations
Key assessment domains: Respirations, Oxygenation, Observation, Auscultation.
Early manifestations vs later manifestations of respiratory distress should be differentiated; the dehydration status should be considered during assessment.
Signs of respiratory distress, such as tachypnea, retractions, and nasal flaring, may appear initially, while later signs can include cyanosis, altered mental status, and exhaustion.
Early manifestation: fuzzy or irritative, pallor.
Later: lethargic, tachypnic, and tachycardic, expect adventitious breath sounds, cyanosis.
Also, beware of their position (tripod), head bobbing (super concerning), and nasal flaring.
Higher retractions, more distressed. Shoulder usage.
Assess for skin color, pulse ox, and work of breathing to evaluate the severity of respiratory distress and to guide further intervention.
Children under 3 years of age are not able to blow their nose; therefore, suction is necessary.
First suction, then put them on oxygen in their nares (nasal cannula 4 L max), then if nothing changes, call the provider.
Are they dehydrated? Assessing hydration levels is crucial, as dehydration can exacerbate respiratory conditions and influence the overall clinical picture (such as crying with minimal tears)
Respiratory rate>60 is concerning, and the child would be NPO.
Pulse oximetry is a useful adjunct in infant assessment (image reference in slide).
Rotate sight to prevent skin ulcers.
Retractions and Severity of Respiratory Distress
Retractions: higher retractions denote greater airway compromise; observing and documenting severity is important.
Important nursing note: if an infant is not allowed to eat (NPO) and has a respiratory rate > 60 breaths per minute, this indicates SEVERE distress.
Acute Epiglottitis (Medical Emergency)
Etiology: Bacterial, usually Haemophilus influenzae type b (Hib influenzae).
Health Promotion/Maintenance considerations: Vaccination status relevant (Hib vaccine); Droplet precautions until stabilized.
Age/Onset: typically 2–5 years; progresses rapidly.
Expected findings: stridor, drooling, muffled voice, dysphagia; tripod position; chin protrusion; mouth open; tongue protruding; inflamed, large cherry-red epiglottis; respiratory distress; high fever.
Keep upright, in an undisturbed, comfortable position.
Do not put anything in their mouth or tongue to prevent obstructing their airway. NOTHING IN THEIR MOUTH.
Likely intubated.
No spontaneous cough, as they can’t clear their airway.
Therapeutic procedures/meds: possible endotracheal intubation or tracheostomy in severe cases; lateral neck X-ray; antibiotics; droplet precautions for 24 hours after IV antibiotics; corticosteroids; IV fluids; humidified oxygen.
Nursing interventions:
Do not insert anything in the mouth.
Position the child for comfort; provide calm reassurance to the caregiver and child.
Maintain droplet precautions.
Monitor vital signs and oxygenation status.
Have intubation equipment readily available at the bedside.
Acute Laryngotracheal Bronchitis (Croup)
Etiology: Viral (RSV, influenza A & B), mycoplasma pneumonia, measles, parainfluenza types 1–3.
Health promotion and maintenance, educate the client on vaccines.
Age/Onset: Infants and children <2 years; gradual onset.
Expected findings: inspiratory stridor, barky/brassy cough, hoarseness, restlessness, irritability, retractions, low-grade fever.
Therapeutic procedures/meds: cool air outside or cool mist (shocks the airway); steroids (oral/IV); racemic epinephrine (nebulized); nebulized budesonide.
Nursing interventions: frequent VS monitoring; be alert for airway obstruction/distress; provide reassurance; stay calm; caregiver support; hold child as needed.
Supportive care: oxygenation, fluids, and suctioning.
Hear stridor, give steroids and racemic epenephrine!
Acute Spasmodic Laryngitis
Etiology: Viral, possibly allergy-related.
Age/Onset: 1–3 years.
Pattern: child awakens at night with sudden dyspnea and barking metallic cough; stridor; hoarseness; restlessness; symptoms typically disappear during the day and recur.
Therapeutic procedures/meds: cool mist (shocks the airway); steroids; racemic epinephrine (nebulized); supportive care.
Nursing interventions: Often managed at home; use a cool mist vaporizer; encourage quiet activities at home.
Bronchitis and Bronchiolitis (RSV)
Bronchitis/Bronchiolitis often involves lower respiratory tract infection with cough and airway inflammation.
Bronchitis is common in kids under the age of 2, while bronchiolitis primarily affects infants and young children under 12 months.
Important note: cough suppressants may hinder clearance of secretions; care focuses on supportive management.
Bronchiolitis: Etiology and Assessment
Common etiologies: RSV (most common cause), parainfluenza, adenovirus.
Risk factors: males are more often affected; peak incidence is <7 months; under 2 years; prematurity; crowding; chronic disease; daycare; secondhand smoke exposure.
Expected findings: fever, cough, rhinorrhea/pharyngitis, irritability, respiratory distress, copious secretions, wheezing or crackles; possible eye/ear infections; dehydration signs.
Mental status change, adventitious breath sounds, tachypnea and tachycardia, lethargy.
Diagnostics/Labs: NP viral panel/NP wash; ABGs; electrolytes; rapid antigen testing (IF/ELISA).
Swab their nares for labs.
Therapeutic procedures: bronchodilators are generally not recommended; supportive care; ribavirin (for RSV as indicated); corticosteroids (sometimes); palivizumab (Synagis) for prevention in high-risk groups (premies from getting RSV).
Suction before feeds to prevent aspiration.
Nursing interventions: droplet and contact precautions; suction, repositioning, supplemental oxygen as needed; limit visitors; assign to RN with no other at-risk visitors; encourage fluids; avoid chest physiotherapy (not proven to be effective); education on handwashing, avoiding smoke exposure, suction technique with bulb syringe.
Otitis Media (Acute Otitis Media, AOM)
Contributing factors: age < 24 months; Cleft lip/palate; daycare exposure; passive smoke exposure; bottle propping; recent URI; allergies; enlarged lymph nodes; winter/spring season; incomplete immunizations; Down syndrome.
Expected findings: ear pain, fever, enlarged lymph glands, bulging tympanic membrane, inconsolable crying, poor appetite/sleep, purulent drainage if rupture; transient hearing loss.
Diagnostics/Meds/Therapeutic procedures: otoscopy, acoustic reflectometry, tympanometry; antibiotics (if bacterial infection), antipyretics/analgesics; topical anesthetics; myringotomy with tympanostomy tubes (BMTs) in select cases (to help drain).
Nursing interventions/education: explain pinna rationale; apply heat to affected ear; maintain dry ear with WET ear care; monitor for hearing loss; promote vaccine adherence; avoid bottle propping; avoid passive smoking; encourage breastfeeding; seek care when symptoms occur; BMT care includes keeping water out of the ear and notifying the provider when tubes extrude.
Tonsillitis and Tonsillectomy
Contributing factors: often in younger children.
Due to an underdeveloped immune system.
Expected findings: halitosis, snoring, nasal-sounding voice, mouth breathing, hearing difficulties, throat pain with swallowing, fever, persistent cough, breathing/swallowing difficulties.
Diagnostics/Therapeutics: throat culture; CBC; clotting times; antibiotics if strep positive; antipyretics; antiemetics; topical anesthetics; tonsillectomy if indicated.
Nursing interventions: diet considerations (soft/liquids); cool-mist vaporizer; warm saline gargles.
Tonsillectomy pre-operative care: consent, bleeding risk, URI symptoms, loose teeth; baseline VS.
Take note of CBC and clotting times.
Post-operative care: monitor for excessive bleeding (signs of swallowing difficulty, frequent throat clearing); airway assessment; elevate head of bed; NPO transitioning to clear/soft; around-the-clock analgesia; ice collar; patient education on discharge and when to seek help for bleeding, persistent cough, ear pain, or fever.
Complications: bleeding, pain, and dehydration.
Reposition for drainage.
Monitor for frequent clearing of the throat or swallowing.
If you see a child constantly coughing or clearing their throat, this is alarming and can be a sign of bleeding.
Avoid gargling and vigorous tooth brushing.
Avoid red dyes in their diet.
Pneumonia and Related Considerations
Pneumonia can be viral or bacterial; discuss possible complications and preventive strategies.
Upper respiratory infection
Risk of bacterial infection
Abrupt and suspect viral infection
If bacteria use antibiotics
Hib vaccine is a preventative measure.
In clinical notes, there is emphasis on infection control and monitoring for respiratory status changes.
Chronic Pulmonary Conditions in the Pediatric Client: Asthma and Cystic Fibrosis (CF)
Endocrine dysfuntion
Asthma: Pathophysiology and Course
Pathophysiology: chronic inflammatory process with IgE-mediated responses; involvement of mast cells, eosinophils, and T-lymphocytes leading to vascular congestion; bronchiolar hyperreactivity to irritants; intrinsic vs extrinsic triggers; bronchospasm and mucus production cause air trapping and hypoxemia.
Respiratory failure is the key thing you’re worried about.
Dehydration could be a factor.
Clinical course: exposure to environmental factors provokes airway inflammation; coughing, wheezing, chest tightness, and breathlessness may progress to airway hyper-responsiveness and obstruction, potentially leading to hypoxemia and respiratory failure if severe.
Key concepts: Chronic inflammation, airway remodeling, and variability in symptoms.
Asthma Classification (Four Categories)
Intermittent: Findings frequency 0-2 times per week; nighttime findings none for ages 0–4 years old or none or infrequent for older children; activity limitations none.
Mild Persistent: Frequency greater than intermittently but not daily; nighttime findings 1–2 times per month (0–4 years) or 3–4 times per month (5–11 years); minor activity limitations.
Moderate Persistent: Daily symptoms; nighttime findings more frequent (3–4 times per month for 0–4; frequent for older children); some activity limitations.
Severe Persistent: Continuous symptoms; nighttime findings frequent (more than once/week, but not daily for 0–4; frequent for older children); extreme activity limitations.
Use of Short-Acting Beta-Agonists (SABA) as rescue medication increases with greater severity.
Should not be used daily or multiple times a day. Need steroids to deal with it better.
Triggers of Asthma
Extrinsic triggers (allergens): pollen, dust mites, mold, animal dander, cockroaches, etc.
Know to keep children away from this.
Intrinsic triggers (nonallergic): exercise, cold air, irritants (smoke, strong odors), viral infections, irritants in the environment.
An increase in women due to hormonal changes during menses.
Asthma Expected Findings and Diagnostics
Typical symptoms: dyspnea, cough, inspiratory and/or expiratory wheeze; decreased air movement is a concern even if wheezing is absent.
Diagnostics: age-appropriate assessment plus tests such as chest X-ray, pulmonary function tests (PFTs), Peak Expiratory Flow Rate (PEFR), CBC, and pulse oximetry.
PEFR details: PEFR measures the maximum flow of air that can be forcibly exhaled in one second. Measured using a peak expiratory flow meter (PEFM) in L/min. Each child should establish their personal best, measured over 2-3 weeks when asthma is stable.
A chronic cough with no infection or expiratory wheezing can support a diagnosis.
Therapeutic Procedures / Medications (Asthma)
Bronchodilators:
Short-Acting Beta-2 Agonists (SABA)
Heart and lungs
Tachycardia
Long-Acting Beta-2 Agonists (LABA)
Controllers
Distinguish rescue meds from long-term control meds.
Cholinergic antagonists (anticholinergics).
Allergen control strategies.
Anti-inflammatory agents (e.g., corticosteroids).
Leukotriene modifiers.
Mast cell stabilizers.
Good controllers for allergies.
Monoclonal antibodies.
Combination medications.
Emergency measures: Magnesium sulfate (need to call a rapid response, bolus of fluid needed due to low BP that could happen); Oxygen; IV fluids; ABGs; BMP; high potassium diet (note: referenced in slide as part of emergency management).
Complications to monitor: Status asthmaticus (medical emergency), respiratory failure.
Nursing interventions/education:
Frequent assessments before and after treatments.
Auscultate the heart and respiratory rate before and after treatment.
If the child is very tachycardic, then spread out treatment to address this.
Use of spacers with metered-dose inhalers (MDIs).
Rinse the mouth after inhaled steroids or other inhaled meds to prevent candidiasis.
Review Questions and Clinical Scenarios (Asthma)
Example ER scenario: In a 10-year-old with acute asthma exacerbation, worsening condition is indicated by increased wheezing vs decreased wheezing, among other signs. (Slide prompts to distinguish signs of worsening.)
Poster/presentation review questions address inflammation, airway swelling, and the timing of bronchial narrowing during bronchospasm; most children with chronic asthma have allergies is a common statement in review prompts.
Controller therapy teaching: when a child is instructed after taking controller medication, suggest actions such as rinsing the mouth after inhaler use.
Cystic Fibrosis (CF): Pathophysiology and Systems Involved
CF is a multi-system disease characterized by thick, sticky mucus production due to defective chloride transport in sweat glands and exocrine glands.
Contributed factors: family history, which is seen heavily amongst Caucasian clients.
Higher risk for sepsis!
Decreased immune system, increased chances of infection.
PICC line or VAC for IV antibiotic meds.
Organs affected (cross-sectional view):
Lungs: thick mucus buildup, bacterial infections, widened airways; risk of bronchiectasis, bronchitis, bronchiolitis, pneumonia, atelectasis, pneumothorax, bronchial obstruction due to mucus.
Sinuses: sinusitis, nasal polyps.
Liver: hepatic steatosis, portal hypertension, biliary cirrhosis, neonatal obstructive jaundice, cholelithiasis.
Pancreas: blocked pancreatic ducts leading to malabsorption and fat-soluble vitamin deficiency; pancreatitis; insulin deficiency.
intestines: meconium ileus in newborns, distal intestinal obstruction syndrome, rectal prolapse, malabsorption issues.
Reproductive: infertility (aspermia or absent vas deferens in males; amenorrhea and delayed puberty in females).
Skin: sweat glands produce salty sweat; tears/saliva also high in sodium and chloride.
Growth and nutrition: poor weight gain, failure to thrive due to malabsorption; fat-soluble vitamin deficiencies (A, D, E, K).
CF Diagnostics
Nutritional panel (fat-soluble vitamin levels A, D, E, K)
Sputum culture, chest and abdominal X-rays
DNA testing, Sweat chloride testing
Pulmonary function tests (PFTs)
Stool analysis
CF Therapeutic Procedures and Medications
Respiratory and supportive care:
Oxygen, IV fluids, feeding tube as needed.
High-protein, high-calorie diet.
Chest physiotherapy (CPT) for airway clearance; airway clearance therapy (ACT) 2x daily or more as ordered; CPT is performed to loosen mucus.
May use a vest chest PT, do not eat after use, as there is the chance of emesis.
Vaccines and RSV prevention: Palivizumab.
Pancreatic enzyme replacement within 30 minutes of meals.
Dornase alfa (DNase) to decrease mucus viscosity.
Multivitamins; fat-soluble vitamin supplementation; antibiotics/antifungals.
H2 blockers and PPIs as needed; stool softeners as needed.
Transplant options (lung, heart, pancreas) in end-stage disease; liver transplant in some CF-related situations; also consideration of bowel transplant in select cases.
CF Nursing Interventions
Frequent respiratory assessments; daily weight checks.
Involve the child and caregiver in care planning.
Airway clearance therapy (ACT) 2x daily or more as ordered; CPT as prescribed.
Maintain a high-protein, high-calorie diet with snacks; moderate aerobic exercise.
Monitor glucose for CFRD (CF-related diabetes).
Education and psychosocial support for the patient and family.
Educate the family on having their child meet their caloric needs, the definition of the disease process, and how to react to it (when to give meds, non-therapeutic methods).
Dietary counseling and coordination of care.
CF Complications and General Manifestations
Respiratory: bacterial/fungal colonization, bronchiectasis, recurrent infections, pneumothorax, atelectasis, hemoptysis, bronchiolitis, bronchitis, etc.
Hematologic/vascular: pulmonary hypertension, cor pulmonale in advanced disease.
Liver and biliary: hepatic steatosis, portal hypertension, biliary cirrhosis.
Gastrointestinal and nutrition: meconium ileus in neonates, pancreatic insufficiency with malabsorption, and malnutrition.
Growth and developmental: failure to thrive, growth delays.
Daily weight due to the failure to thrive.
CF Diet and Nutrition Counseling
CF patients require high-calorie, high-protein diets with adequate salt intake to offset salt losses in sweat.
Salt intake considerations: sweat and tears can be salty; ensure electrolyte balance is maintained.
Diet and Education Scenarios (CF Nutrition Question)
Typical exam question: A CF patient should be advised to consume foods high in calories and protein to meet higher energy needs; salt intake should be managed to prevent hyponatremia in sweat-rich states.
Practical Nursing Implications and Distinguishing Features
Early recognition of distress in pediatric respiratory conditions is critical for timely intervention.
Infection control measures (droplet and contact precautions) are essential in epiglottitis, bronchiolitis, and other infectious etiologies.
Family education is central: suction techniques, hand hygiene, vaccination adherence, avoidance of tobacco smoke, and recognition of warning signs of deterioration.
For CF, multi-system involvement requires coordinated care focusing on nutrition, airway clearance, infection control, and monitoring for CFRD and liver/pancreatic complications.