General aspects of respiratory infections
upper respiratory tract
Oronasopharynx, pharynx, larynx, and trachea
Lower respiratory tract
Bronchi, bronchioles, and alveoli
Croup syndromes
Infections of epiglottis, larynx
Infectious Agents
Viruses
RSV
parainfluenza
Others
Group A ß-hemolytic streptococcus
Staphylococci
Chlamydia trachomatis, mycoplasma, pneumococci
Haemophilus influenzae
Age
Infants <6 months: maternal antibodies
3-6 months: infection rate increases
Toddler and preschool ages: high rate of viral infection
>5 yrs: increase in mycoplasma pneumonia and ß-strep infections
Increased immunity with age
Size differences in children
Diameter of airways
Distance between structures is shorter, allowing organisms to rapidly move down
Short Eustachian tubes
Differences in adults and pediatric airways
Give description, detailed, easy to study
Seasonal variations
Most common during winter and spring
Mycoplasmal infections more common in fall and winter
Asthmatic bronchitis more frequent in cold weather
RSV season considered winter and spring
Clinical manifestations
Vary with age
Generalized signs and symptoms and local manifestations differ in young children
Fever
Absent in newborns, peak 3 months to 3 years
Anorexia, vomiting, diarrhea, abdominal pain
Cough, sore throat, nasal blockage or discharge
Respiratory sounds (explain and examples)
Nasal flaring
Color changes
Chest pain
Restlessness, irritability, unexplained sudden confusion
↑HR & RR
clubbing
Retractions—location significant
Suprasternal
Clavicular
Intercostal
Substernal
Subcoastal
Nursing considerations
Assessment
Nursing diagnosis
PlanninG
Implementation
Evaluation
Assessment guideline for child in respiratory distress
Quality of respirations
Quality of pulse
Color
Cough
Behavior change
Signs of dehydration
*Be alert! Children can crash quickly!!
Nursing interventions
Ease respiratory effort
Fever management
Promote rest and comfort
Infection control
Promote hydration and nutrition
Family support and teaching
Prevent spread of infection
Provide support and plan for home care
Upper respiratory tract infections (URI)
Nasopharyngitis—“common cold”
Caused by numerous viruses
RSV, rhinovirus, adenovirus, influenza and parainfluenza viruses
Clinical manifestations
fever—varies with child irritability, restlessness decreased appetite and fluid intake nasal inflammation vomiting and diarrhea
Home management—varies with age
Pharmacological tx for URI
OTC pediatric cold remedies are NOTrecommended for treating “common cold”
Antihistamines ineffective in most cases
Antipyretics for comfort from fever
Cough suppressants for dry cough (caution alcohol content
Decongestant to shrink swollen nasal passages (nose drops more effective than oral administration
Acute streptococcal pharyngitis
GABHS infection of upper airway
At risk for sequelae
Acute rheumatic heart fever
Acute glomerulonephritis
Clinical manifestations
Diagnostics: rapid strep test and/or throat culture
Therapeutic management
Nursing considerations
Pharmacological interventions - strep
Penicillin
Oral
Needs 10 day treatment to decrease risk of rheumatic fever and glomerulonephritis post strep
Issues with medication compliance
IM: Penicillin G Resolves compliance issue (one injection)
Painful injection
Penicillin G Procaine is less painful injection
CANNOT give Penicillin G by IV route
Erythromycin if penicillin allergy
Tonsillitis
Pathophysiology and etiology
Clinical manifestations
Tonsilar edemaobstructs passage of air and food
Difficulty swallowing & breathing
If adenoids swollen, blocks post. nares mouth breather
Therapeutic management
Remove if ≥3 infections/year despite appropriate tx
Nursing considerations
General
postop
Nursing concerns
Airway
Positioning
Bleeding
Observation—frequent swallowing?
Prevention of recurrent bleeding
Maintain quiet environment
Minimize agitation/crying
NO suctioning
Comfort
Influenza = “flu”
3 types: A, B, C
Spread by direct contact or by articles contaminated with NP secretions
More common in winter
People are infectious 24 hrs before and after onset of symptoms
Meds: Zanamivir (A & B) & Rimantadine (A)
Pharmacological intervention for influenza in children
Antivirals for children
Oseltamivir (Tamiflu)
Zanamivir (RELENZA)
Must start within 48 hrs of symptom onset
Avoid aspirin—possible link with Reye syndrome
Otitis Media (OM) - Ear infection
Pathophysiology and etiology
Diagnostics
Therapeutic management
Pharmacologic
Not for initial tx; wait 72 hrs in uncomplicated OM
Surgical: M & T
Nursing considerations
Pain relief, facilitate drainage, prevent complications & recurrence, educate family, emotional support
Prevention of recurrence
Acute otitis media is characterized by abrupt onset, pain, middle ear effusion, and inflammation. Note the injected vessels and altered shape of cone of light.
Otitis media with effusion is noted on otoscopy by fluid line or air bubbles. Pneumatic otoscopy or tympanometry shows a nonmobile tympanic membrane. Note that the light reflex is not in the expected position due to a change in tympanic membrane shape from air bubbles.
Otitis Media—Antibiotic Therapy?
If over age 6 months—”watchful waiting” up to 72 hours for spontaneous resolution
Antibiotics if <2 years with persistent acute symptoms of fever and severe ear pain
Antibiotics if <6 months
Topical relief—heat or cold or benzocaine drops (Rx)
Pharmacologic interventions
First line antibiotics
Amoxicillin PO divided twice daily x 10days
Second-line antibiotics
Amoxicilliln-clavulanate (Augmentin),
Azithromycin
Cephalosporins IM—if highly resistant organism or noncompliant with oral doses
Analgesic-antipyretic drugs
Acetaminophen
Ibuprofen (only if >6 months of age
No steroids, antihistamines, decongestants, antibiotic ear drops
Croup Syndrome
Characterized by hoarseness, “barking” cough, inspiratory stridor, and varying degrees of respiratory distress
Croup syndromes affect larynx, trachea, and bronchi
Epiglottitis, laryngitis, laryngotracheobronchitis (LTB), tracheitis
Acute epiglottitis - a medical emergency
Clinical manifestations
Sore throat, pain, tripod positioning, retractions
Inspiratory stridor, mild hypoxia, distress, drooling, no spontaneous cough
Therapeutic management
Potential for respiratory obstruction
Nursing considerations
Never examine throat without emergency equipment handy
Prevention: Hib vaccine
Signs of increasing respiratory distress in children
RESTLESSNESS
Tachycardia
Tachypnea
Retractions
Substernal
Suprasternal
Intracostal
Acute LTB
LTB = Laryngotracheobronchitis
Most common of the croup syndromes
Generally affects children <5 yrs
Organisms responsible
RSV, parainfluenza virus, Mycoplasma pneumoniae, influenza A and B
Manifestations
Inspiratory stridor
Suprasternal retractions
Barking or “seal-like” cough
Increasing respiratory distress and hypoxia
Can progress to respiratory acidosis, respiratory failure and death
Therapeutic management
Airway management
Maintain hydration—PO or IV
High humidity with cool mist
Nebulizer treatments
Epinephrine
Steroids
Acute Spasmodic Laryngitis
AKA spasmodic croup, midnight croup
Paroxysmal attacks of laryngeal obstruction; viral
Occur chiefly at night
Inflammation: mild or absent
Most often affects children ages 1-3
Therapeutic management
Bacterial tracheitis
Infection of the mucosa of the upper trachea
Distinct entity with features of croup and epiglottitis
Clinical manifestations similar to LTB
May be complication of LTB
Thick, purulent secretions result in respiratory distress
Therapeutic management
Humidified oxygen
Antipyretics
Antibiotics
May require intubation—be prepared for respiratory failure
Infections of the lower airways
Considered the “reactive” portion of the lower respiratory tract
Includes bronchi and bronchioles
Cartilaginous support not fully developed until adolescence
Constriction of airways
Bronchitis
AKA tracheobronchitis
Definitions
Causative agents
Clinical manifestations: persistent dry, hacking cough becoming productive in 2-3 days, tachypnea, low-grade fever
Supportive care
Bronchiolitis
Begins as URI with serous nasal drainage
Mild fever, gradually develops into resp. illness, dyspnea, paroxysmal non- productive cough, tachypnea, nasal flaring, retractions, wheezing
Maybe caused by many viral agents, but RSV is primary agent seen in 80% of cases
RSV - respiratory syncytial virus
Transmission through direct contact with secretions, can live hours on surfaces
Pathophysiology: bronchiole mucosa swell and fills with mucous → obstruction
Therapeutic management: supportive
Prevention of RSV—RSV immune globulin to at risk infants
Nursing considerations
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS- CoV-2): COVID-19
Coronavirus
Clinical Manifestations
Diagnostic Evaluation
Therapeutic Management
COVID-19 vaccination
Nursing Care Management
Multisystem Inflammatory Syndrome in Children (MIS -C)
Post COVID syndrome
Hyper- inflammatory syndrome
Clinical Manifestations
Prognosis
PNEUMONIA
Lobar pneumonia
Bronchopneumonia
Interstitial pneumonia
Pneumonitis
Etiology of Pneumonias
Bacterial Or Viral
Aspiration
Histomycosis, coccidiomycosis, other fungi
“Atypical pneumonias”-
Mycoplasma
May be asymptomatic or cause several symptoms
Etiology and epidemiology
Clinical manifestations
Fever, malaise, rapid respiration, and cough
Chest or abdomen pain, nausea
Diagnostic evaluation
Therapeutic management
Prevention: PCV vaccine
Therapies
Complications
Nursing care management
Foreign body aspiration
Risk for child with feeding difficulties
Prevention of aspiration
Feeding techniques, positioning
Avoid aspiration risks
Oily nose drops
Solvents
Talcum powder
Inhalation injury: smoke and carbon monoxide
Severity depends on nature of substance, environment, and duration of contact
Local injury
Systemic injury
Therapeutic management
Nursing considerations
Passive smoking
Scope of the problem
Impact on children
Nursing considerations
Asthma
Chronic inflammatory disorder of airways
60-80% caused by allergens
Some genetic predisposition
Inflammation causes bronchial hyper- responsiveness to variety of stimuli
Episodic-wheezing, breathlessness, chest tightness, and cough
Limited airflow or obstruction that reverses spontaneously or with treatment
Risk factors of asthma
Age
Atopy
Heredity
Gender
Mother <age 20 years
Smoking (maternal and grandmaternal)
Ethnicity (African Americans at greatest risk)
Previous life-threatening attacks
Lack of access to medical care
Psychologic and psychosocial problems
Pathophysiology
Bronchospasm and obstruction from:
edema and inflammation of mucous membranes
Tenacious secretions
Spasm of smooth muscle of bronchi & bronchioles
Leads to ↓caliber of airways and child
Triggers
Allergy
Irritants
Exercise
Cold air
Changes in weather
Medications
Emotions
Medical conditions
Food additives
Foods
Endocrine factors
Diagnosis
Based on clinical manifestations, history, PE, lab tests
Asthma management
To prevent disability, minimize physical and psychological morbidity, and assist in leading a “normal” life
Allergen control
Stepwise approach
Long-term control medications (prevent)
Quick-relief medications (rescue)
Common medications in asthma
Rescue medications
B-adrenergic
Albuterol
Metaproterenol
Terbutaline
Xopenex
Metabolite of albuterol with less side effects, nebulized only, q 6 hours, expensive
Controller medications
Corticosteroid
Oral or inhaled
Cromolyn
Inhaled NSAID
Leukotriene modifier
Singulair
Accolate
Zyflo
Rarely used medications
Methylxanthines
Theophylline
Toxicity
Must check serum levels
Can be given IM, IV, PO
Anticholinergics
Atropine
Asthma Severity Classification in Children 5 yrs and Older
Step I: mild, intermittent asthma
Step II: mild, persistent asthma
Step III or IV: moderate, persistent asthma
Daily symptoms 3-4 times a month
Step V or VI: severe, persistent asthm
Continual symptoms throughout the day
Frequent nighttime symptoms
Clinical features of each classification
Mild intermittent - step 1
Symptoms: ≤ 2 days/week and ≤ 2 nights/month
No daily medication
Albuterol prn symptoms
Nebulizer
MDI with spacer
Mild Persistent-step 2: sx >2/week, but < 1x/day; > 2 night/month
Daily anti-inflammatory (low-dose)
Leukotriene OR
Nebulizer
Pulmicort
Cromolyn
MDI
Pulmicort
Flovent
Others
Rescue as needed
Moderate Persistent-step 3 or 4
Symptoms daily & > 1 night/week
Daily anti-inflammatory (medium dose)
Nebulizer
MDI
Long-acting bronchodilator
Serevent
Rescue as needed
Severe Persistent-step 5 or 6
Symptoms continual during day and frequent at night
Anti-inflammatory (high-dose)
Nebulizer
MDI
Long-acting bronchodilator
Oral steroids
Asthma interventions
Exercise
Exercised induced asthma-use short- acting bronchodilators (2-3 hours) and long-term bronchodilators (10-12 hours)
Hyposensitization
Prognosis
Other management musts
Peak expiratory flow monitoring used daily
Has 3 zones like stop light
Establish child’s best and uses to compare at later times
Written Action Plan
Signs of SEVERE Respiratory Distress in Children with Asthma
Remains sitting upright, refuses to lie down
Sudden agitation
Agitated child who suddenly becomes quiet
Diaphoresis
Pale
Status asthmaticus
Respiratory distress continues despite vigorous therapeutic measures
Emergency treatment—epinephrine 0.01 mL/kg SQ (max dose 0.3 mL)
IV magnesium sulfate
IV ketamine
IV corticosteroids
Concurrent infection in some cases
Therapeutic intervention
Goals of asthma management
Avoid exacerbation
Avoid allergens
Relieve asthmatic episodes promptly
Relieve bronchospasm
Monitor function with peak flow meter
Self-management of inhalers, devices, and activity regulation
Cystic Fibrosis (CF)
Avoid exacerbation
Avoid allergens
Relieve asthmatic episodes promptly
Relieve bronchospasm
Monitor function with peak flow meter
Self-management of inhalers, devices, and activity regulation
Pathophysiology of CF
Characterized by several unrelated clinical features
Respiratory system
GI system
small intestine, pancreas, bile ducts
Growth patterns
Reproductive system & skin
Pulmonary complications
Increased viscosity of mucous gland secretion
Results in mechanical obstruction
Thick, inspissated mucoprotein accumulates, dilates, precipitates, coagulates to form concretions in glands & ducts
Respiratory tract & pancreas are predominantly affected
EFFECTS OF EXOCRINE GLAND IN CF: (dumb it down and simplify)
Increased Viscosity of Mucous Gland Secretion
Results in mechanical obstruction
Thick mucoprotein accumulates, dilates, precipitates, coagulates to form concretions in glands and ducts
Respiratory tract and pancreas are predominately affected
Increased sweat electrolytes
Basis of the most reliable diagnostic procedure—sweat chloride test
Sodium and chloride will be 2-5 times greater than the controls
Respiratory manifestations
Present in almost all CF patients but onset/extent is variable
Stagnation of mucus and bacterial colonization result in destruction of lung tissue
Tenacious secretions are difficult to expectorate-obstruct
Decreased O2/CO2 exchange
Results in hypoxia, hypercapnea, acidosis
Air gets trapped in small airways → atelectasis
Hyperaeration of alveoli → barrel chest, cyanosis, clubbing
Respiratory progression
Gradual progression follows chronic infection
Bronchial epithelium is destroyed when chronically weakened → pulmonary disease
Infection spreads to peribronchial tissues weakening bronchial walls
Peribronchial fibrosis
Decreased O2/CO2 exchange
Further respiratory progression
Chronic hypoxemia causes contraction/hypertrophy of muscle fibers in pulmonary arteries/arterioles
Compression of pulmonary blood vessels and progressive lung dysfunction lead to pulmonary hypertension, cor pulmonale, respiratory failure, and death
Pneumothorax
Hemoptysis
GI tract
Thick secretions block ducts—cystic dilation — degeneration — diffuse fibrosis
Prevents pancreatic enzymes from reaching duodenum
Impaired digestion/absorption of fat- steatorrhea
Impaired digestion/absorption of protein- azotorrhea
4 F’s of stools: frothy, foul-smelling, fat-containing, float
Endocrine function of pancreas initially stays unchanged
Eventually pancreatic fibrosis occurs; may result in diabetes mellitus
Focal biliary obstruction results in multilobular biliary cirrhosis
Failure to thrive
Increased weight loss despite increased appetite
Clinical manifestations of CF
Pancreatic enzyme deficiency
Progressive COPD associated with infection
Sweat gland dysfunction
Failure to thrive
Increased weight loss despite increased appetite
Gradual respiratory deterioration
Presentation
Wheezing respiration, dry nonproductive cough
Generalized obstructive emphysema
Patchy atelectasis
Cyanosis
Clubbing of fingers and toes
Repeated bronchitis and pneumonia
Meconium ileus
Distal intestinal obstruction syndrome
Excretion of undigested food in stool — increased bulk, frothy, and foul
Wasting of tissues
Prolapse of the rectum
Delayed puberty in females
Sterility in males
Parents report children taste “salty”
Dehydration
Hyponatremic/hypochloremic alkalosis
Infectious agents for cf patients
Pseudomonas aeruginosa
Burkholderia cepacia
Staphylococcus aureus
Haemophilus influenzae
Escherichia coli
Klebsiella pneumoniae
DIAGNOSTIC Evaluation
Quantitative sweat chloride test
Chest x-ray
PFT
Stool fat and/or enzyme analysis
Barium enema
3 Major Presentations of DX:
Meconium ileus, FTT or malabsorption, chronic RESPIRATORY INFECTION
GOALS
Prevent/minimize pulmonary complications
Adequate nutrition for growth
Assist in adapting to chronic illness
Respiratory management
CPT: ThAIRapy vest
Medications
Bronchodilators
Pulmozyme (DNase)
Antibiotics
oxygen
Forced expiration
Burkholderia cepacia issues
Lung transplant
GI management
Replacement of pancreatic enzymes
High protein high calorie diet as much as 150% RDA
Intestinal obstruction
Reduction of rectal prolapse
Salt supplementation
Oral glucose-lowering agents or insulin injections as needed
Replace fat soluble vitamins
Prognosis of CF
Decreased life expectancy for child born with CF
Maximize health potential
Nutrition
Prevention/early aggressive treatment of infection
Pulmonary hygiene
New research → hope for the future
Transplantation
Gene therapy
Bilateral lung transplants
Improved pharmacologic agents
Family support
Coping with emotional needs of child and family
Child requires treatments multiple times/ day
Frequent hospitalization
Implications of genetic transmission of disease
Cardiopulmonary resuscitation (CPR)
Pediatric cardiac arrest frequently represents the terminal event following respiratory failure or progressive shock
Pediatric cardiac arrest rarely results from sudden cardiac collapse, as in adult populations
Why chain of survival is different
Causes of cardiac arrest
Vary with age and underlying chronic medical conditions
Out of hospital causes include: trauma, SIDS, poisoning, choking, severe asthma attack, drowning
In-hospital causes typically due to underlying condition
Standard care
CPR
Pediatric advanced life support (PALS)