respiratory disorders peds
TRANSCRIPT
Respiratory Disorders
Nursing IIILinda Speranza PhD, ARNP-C
Respiratory Assessment Count respiration
for 1 full minute Infants – obligatory
nose breathers Identify signs of
respiratory distressListen to breath
sounds 1st! Stridor- thrill harsh
sound Rhonchi Wheezing
Respiratory Assessment Quality of respirations Quality of pulse Color- pale, cyanotic, mottling Cough- croupy- loose, wet, dry Behavior change- tired of breathing fast?,
restless?, lethargic?, change in LOC Signs of dehydration- low I&O, L skin turgor- check
in abd or sternum, lack of tears in older children,
Respiratory Assessment
Nasal Flaring Widening of the nares during inspirationRepresents an increased effort by the
infant to breathe
Retractions Depth and location of retractions
indicate the severity of distress Intercostal retractions- mild Subcostal - moderate Suprasternal – moderate Supraclavicular- severe Use of accessory muscles- severe
Anatomy is Different!• Development • Airways – shorter and more narrower • Increase in airway resistance in children • Flexible larynx • Tongue is proportionally larger– can cause obstruction
• Obligate nose breathers– plugging can cause respiratory distress
A Child’s Respiratory Anatomy
Respiratory Distress Syndrome Result of a primary
absence, deficiency, or alteration in the production of pulmonary surfactant
Prematurity
Surfactant deficiency disease
Signs & Symptoms of RDS Shortness of breath Grunting Nasal flaring Cyanosis Apneic spells Increased work of
breathing – tachypnea 1st sign of
respiratory distress Retractions
Management/Treatment of RDS Support adequate
ventilation
Surfactant replacement therapy
Monitor for Complications
Nursing Interventions Risk for ineffective breathing pattern
Check prenatal meds Monitor vitals and skin Clear airway prn with bulb syringe Give warm humidified O2
Ineffective thermoregulation Warm all inspired gases. Cold air= more need of O2
and high metabolic rate Respiratory distress can lead to metabolic acidosis.
Check for acrocyanosis, bradycardia, apnea, etc
Altered nutrition: less If there is respiratory distress do not give oral fluids. Start
parenteral nutrition per MD Give calories to prevent metabolic acidosis due to
starvation. TPN is an alternative Risk for fluid vol deficit
Record I& O hourly and daily weights. Circulatory overload= pulmonary edema
Check signs of dehydration: poor skin turgor, pale mucous memb, sunken anterior fontanelle. Specific gravity, etc
Check IV sites for infiltration, infection (edema, and erythema)
Croup Syndrome Broad classification of upper airway illnesses that
result from swelling of the epiglottis and larynx Viral
Spasmodic laryngitis Laryngotracheitis Laryngotracheobronchitis (LTB)
Bacterial Bacterial trachitis Epiglottitis
Laryngotracheobronchitis (LTB) LTB, most common form of croup Usually caused by virus;
Adenovirus, Respiratory Syncytial Virus (RSV) Influenza Virus
Inflammation and narrowing of the laryngeal and tracheal areas.
Clinical Manifestations of LTB Upper respiratory infection (URI) symptoms that
gradually progress to signs of distress. Hoarseness, barky cough Inspiratory stridor Retractions Restlessness and irritability Pallor and cyanosis Sometimes a low grade fever
Potential complication: airway obstruction Difficulty swallowing or drooling= epiglotitis
Treatment/Management of LTB Lateral neck x-ray
confirms diagnosis Maintain Airway
Patency Supplemental
oxygen with humidity
Cool mist tent Meet fluid and
nutritional needs
Treatment/Management of LTBMedication
Racemic epinephrine Bronchodilators – Albuterol
Side tachycardia Steroid therapy- IV or inhaled
Keep calm and comfortableNO Throat cultures or visual
inspections of the mouth Continue to monitor- Respiratory effort,
responsiveness, signs of respiratory distress
Constant attendance
Epiglottitis• An inflammation of the epiglottis, the long
narrow structure that closes off the glottis during swallowing
• A life-threatening condition!!! This is a Medical Emergency
• Bacterial- Caused by strep, staph, and haemophilus influenzae type B • Hib vaccine reduces risk for epiglottitis
Clinical Manifestation of Epiglottitis Sudden onset CARDINAL SIGNS- intense sore
throat/difficulty swallowing/ drooling Cherry red, edematous epiglottis High fever- 102 Dysphonia Dysphagia Inspiratory stridor Respiratory distress Tripod position
Diagnosis of Epiglottitis Diagnosis confirmed by lateral neck films High Oxygenation to reverse hypoxemia Cool mist oxygen
Cools airway and lowers swelling! Antipyretics, ab, & steroids to decrease
inflammation May use a tracheostomy to bypass the problem
Treatment/ Management Epiglottitis Closely Monitor Respiratory status. Do
not attempt to examine the throat. Axillary temp only!
Medications include antibiotics and steroids to decrease inflammation
Minimize fear and anxiety to decrease oxygen consumption
Bronchitis Lower airway disorder
Inflammation of the trachea and bronchi
Cause- mainly viral
Symptoms Fever, dry hacking cough
non productive. Productive in a couple of days
Management Cool, humid air, increase
fluids, antipyretics, cough suppressants
Bronchiolitis Caused when a virus
or bacterium causes inflammation and obstruction (mucus) of the small airways
Occurrence- First 2 years Peak: 6 months
Cause – Respiratory Syncytial Virus (RSV)
Bronchiolitis
Pathophysiology Cell debris- death virus after bursting to
invade Irritation= Swelling/mucus Bronchospasm Inhalation, poor exhalation Wheezing, hypoxemia, respiratory failure
Clinical Manifestation of Bronchiolitis Illness may have been occurring for a few
days- upper respiratory
Lower respiratory
Severe respiratory distress. Thick mucus occludes bronchioles Initial: Rhinitis, cough, low fever, tachypnea,
poor feeding, v & d, dehydration, less playful
Clinical Therapy For Bronchiolitis History and Physical Chest x-ray
Hyperinflation, atelectasis and inflammation Nasal swab- to find bacteria Ribavirin – antiviral for RSV. Used for
immunocompromised Bulb syringe & Saline Isolation Risk Factors – lung disease, low weight,
siblings that go to school, passive smoke, premmie
Treatment/Management Bronchiolitis Rest & elevate HOB to 30 Clear fluids (NPO if resp rate >60)
I& O x 8 h & daily weights, mucous memb Maintain respiratory functions. Use suctioning-
Also before feeding Cool, humidified oxygen Albuterol updrafts Steroids Infants often hospitalized due to feeding
difficulties, increased respirations Hand washing!- RSV is recurrent
Bronchopulmonary Dysplasia (BPD)
Chronic Lung Disease Results from an acute respiratory disorder that
begins during infancy Risk Factors
Prematurity Lung immaturity High inspired oxygenation concentrations, Positive pressure ventilation Patent ductus arteriosus Vitamin A deficiency
Clinical Manifestation of BPD Persistent signs of respiratory distress
Tachypnea Wheezing Crackles Irritability Nasal flaring Grunting Retractions Pulmonary edema FTT- Failure to Thrive- O2 demands ↑ + fatigue Intermittent bronchospasm & mucous plugs
Tracheostomy Keep small toys, dust away from child Careful when bathing! No showers Observe and clean skin daily Suction prn
Only 5 sec, sterile gloves, intermittent suction when withdrawing cath
Notify if secretions increase or turn purulent, or fever Have an emergency bag w extra cath and tubes No smoking O2 away from heat
BPD Diagnoses
Chest x-ray shows hyperexpansion, atelectasis, and interstitial thickening
Air trapping can cause “Barrel Shape” Chest Treatment
Support respiratory function- supplemental O2 w humidity. Chest physiotherapy + meds
Medications Nutrition
Prognosis
Otitis Media Inflammation of
the middle earOccurrence- 6-36
m (winter)Risk FactorsCausative
organisms Streptococcus
pneumoniae H. flu. Moraxella catarrhalis
Otitis Media Etiology – Eustachian tube dysfunction Pathophysiology
Preceding upper respiratory infection Edema Blocked air Air reabsorbed to bloodstream Fluid is pulled from mucosal lining Tympanic membrane becomes infected
Otitis MediaS & Sx
Pulling at the ear Diarrhea, vomiting, & fever Irritability, awakens at night crying
Diagnosis Otoscopic examination- Shows a red,
bulging, non-mobile tympanic membrane
Treatment Antibiotics Myringotomy/Tympanostomy (PE tubes) Pain relief – Tylenol/Ibuprofen, anesthetic
ear drops- verify integrity of tympanic membrane
Tonsillitis Infection or
inflammation of the palatine tonsils
Clinical Manifestations Frequent throat
infection Breathing and
swallowing difficulties Persistent redness Enlargement of cervical
lymph nodes
Tonsillectomy Before surgery
H&P Are tonsils simply large or inflamed w
exudate? Past tonsillar infections and lengh of present
discomfort Free from sore throat, fever, respiratory
infection for week before surgery No aspirin or ibuprofen for 2 weeks Check other home medication
Tonsillectomy
Tonsillectomy After Surgery
May have sore throat for 7-10 days Drink cool fluid and chew gum Give Acetaminophen elixir Apply ice collar around child’s neck Side-lying position- difficult to swallow
Sore throat: cool fluids, chew gum, ice collar, gargle ½ tsp. of each baking soda and salt in water, rinse w viscous lidocaine and swallow. No citrus liquids
Report bright red blood or increased swallowing immediately Avoid red, purple or brown liquids= difficult to
assess for bleeding Normal: white, and odor on back of throat in
the first wk. Report fever 102 F
AsthmaChronic inflammatory disorder of the
airway Airway obstruction Increased airway responsiveness Acute exacerbations or persistent symptoms
Onset- before age 5Causes of asthma & respiratory problems
in children Smoking, pet dander
Pathophysiology of Asthma After exposure to various “triggers”
Bronchospasm Inflammation and edema of the bronchial
mucosa Production of thick mucus
Asthma triggers- perfume
Pathophysiology of Asthma Reactive airway responses Antigen binds to the specific
immunoglobulin E surface on the mucosal mast cell
Histamine is released Intercellular chemical mediators are
released- histamines, prostaglandins, leukotrienes Release cytokines that make permanent
airway remodeling- thickening Result: bronchospasm, mucosal edema, &
mucus secretion
Clinical Manifestations of Asthma
Airway Inflammation Obstruction (narrowing) Hyperreactivity
“Asthma Attack”- sudden cough, wheeze, or SOB
“Silent” asthma- frequent coughing, especially at night (airway is very sensitive)
Clinical Manifestations of Asthma Respirations Appears tired Nasal flaring- 4 wks Intercostal retractions Productive cough Expiratory wheezing Decreased air movement Respiratory fatigue In severe obstruction
Diagnosis of Asthma
4 key elements Symptoms of episodic airflow obstruction
Partial reversal of bronchospasm with bronchodilator treatment
Exclusion of alternative
Diagnosis confirmation by spirometry
Evaluation of Asthma Spirometry
Shows how much a person can exhale- evidence of episodic airflow obstruction and airway hyper-responsiveness. Place mouth covering entire mouth piece… Breathe out as hard as possible and then breathe in deeply
Evaluation of Asthma Peak flow meter (expiratory flow meter)
Blow into it every morning to see if you need treatment like a nebulizer to open up the airway.
Warns of impending attack Green- ok Yellow Red- less than 50%= Warning!
Skin testing- to id triggers Medications
Medications Used for AsthmaShort-acting bronchodilators
Albuterol/ventolin/proventil- drug of choice Terbutaline- not very common
Long & short acting beta agonists Salmeterol- can use for exercise and night sx
Mast cell inhibitor Intal/cromolyn- Can be used in nebulizer Ex Singulair- Minimizes allergies
Corticosteroids Prednisone or solumedrol
Status Asthmaticus
Severe respiratory distress & bronchospasm in an asthmatic
It persists in spite of pharmacologic and supportive interventions
Considered a medical emergency
Without immediate intervention, it will progress to respiratory failure & death
Meds Continuous nebulized albuterol Inhaled inpratropium, iv corticosteroids,
magnesium, aminophylline Check electrolytes Nonivasive positive pressure ventilation intubation
Cystic Fibrosis
Cystic Fibrosis is an autosomal recessive multisystem disorder with dysfunction of the exocrine glands Genetic testing Expected lifespan- 30 years (terminal
disease) Results in physiologic alterations in
several systems
Cystic Fibrosis Abnormal secretion of thick, tenacious mucus
causes obstruction and dysfunction of all body organs with mucous ducts.
This includes the pancreas, lungs, salivary glands, sweat glands, and reproductive organs.
Clinical Manifestations Production of thick sticky mucus Meconium ileus Constipation Chronic moist productive cough Frequent respiratory infections Chronic sinus infections Difficulty gaining & maintaining weight Short stature Clubbing of finger tips & toes
Clubbing of Fingers
Diagnostic & Evaluation of CF 3 presentations
Meconium ileus Malabsorption- steatorrhea Chronic recurrent respiratory infections
The Sweat test is the standard diagnostic test for CF Spirometer Sputum cultures
Treatment & Management Chest physiotherapy (CPT): Can use percussion
to help move secretions downward so they can cough it up. Position: head of baby downward to use gravity
3-4 x day to prevent increase of hospitalizations and infections
Do not perform immediately after eating Give bronchodilator to open bronchi for easier
expectoration before therapy AM Exercise stimulates mucus expectoration Use forced expiratory technique to mobilize
secretion- Huffing
Treatment & Management of CF
Antibiotics (oral, IV, & inhalation) Pancreatic enzymes with meals,
Pancrease or Creon. To help digest food Aerosol bronchiodilators Steroids Diet- high calorie & protein, extra salt in
hot weather, ADEK vitamins Psychosocial concerns
Allergic Reactions Allergy- abnormal or altered reaction to an
antigen Allergens – antigens that cause allergy
Allergic reaction - antigen-antibody reaction that can manifest as anaphylaxis, atopic dermatitis, serum sickness or contact dermatitis
Hypersensitivity response
Allergy Assessment
Physical exam- history of exposure to allergens, itching, tearing, burning of eyes and skin, rashes, nose twitching, stuffiness
Lab X-ray Pulmonary function studies Nasal function Skin testing
Treatment of Allergies
Avoidance
Desensitization
For skin allergies
Allergy alert bracelet
Teaching about allergens in the home
Skin Allergy Testing
Question One: Which of the following respiratory
conditions is always considered a medical emergency? A. Asthma B. Epiglottitis C. Cystic Fibrosis D. Laryngotracheobronchitis
Question Two: In a child with asthma, albuterol is
administered primarily to do which of the following? A. Dilate the bronchioles B. Decrease postnasal drip C. Reduce airway inflammation D. Reduce secondary infections
Question Three: When developing a care plan for a child
diagnosed with cystic fibrosis, which of the following must the nurse keep in mind? A. CF is an autosomal dominant hereditary
disorder B. Pulmonary secretions are abnormally thick. C. Obstruction of the endocrine glands occur D. Elevated levels of K+