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Disorders of Respiratory Function Chapter 31 Respiratory Disorders Acute respiratory infections Extremely common Range from minor to life threatening Most involve viral pathogens Bacterial infections involve: Group A B-hemolytic streptococci Staphylococcus aureus Haemophilus influenza Respiratory Distress Syndrome Etiology RDS, idiopathic respiratory distress syndrome, hyaline membrane disease – severe lung disorder Major cause of morbidity & mortality in neonatal period Deficiency of surfactant Occurs in preterm, low birth weight infant More common in males and C-sections RDS Etiology Predisposing factors Infants of diabetic mothers Asphyxia Maternal hemorrhage Shock Surfactant – reduces the surface tension of fluids that line the alveoli, thereby permitting expansion of the lungs & alveolar inflation Infant unable to keep lungs inflated, alveoli collapse Hypoxia Atelectasis Respiratory acidosis RDS Clinical manifestations Signs & symptoms apparent immediately after birth Nasal flaring Expiratory grunting Intercostal, subcostal, or substernal retractions Dusky color Tachypnea Low body temperature Severe cases – die within hours RDS Diagnostic tests Clinical presentation Radiographic exam Blood gases – degree of respiratory & metabolic acidosis RDS Medical management Supportive Correction of imbalances Oxygen therapy – continually evaluated Neutral thermal environment Adequate oxygenation Prevent hypoxia Prevent toxic effects Nutritional support RDS Medical management Administration of exogenous pulmonary surfactant Has greatly reduced morbidity & mortality Directly into the lungs Corticosteroids – before delivery to increase production of surfactant RDS Nursing/Patient teaching Observing & assessing response to therapy Continuous monitoring – oxygen therapy Respiratory assessments Suctioning as needed – can lead to bronchospasm, airway damage, infection, pneumothorax, hypoxia, & increased ICP Positioning Skin assessments Emotional support for parents RDS Prognosis Self limiting Survive first 96 hours – reasonable chance of recovery Surfactant replacement therapy Improve survival Reduce the severity Bronchopulmonary Dysplasia Etiology Chronic pulmonary disorder that develops in premature infants Associated with: Meconium aspiration RDS High concentrations of oxygen Positive pressure ventilation Endotracheal intubation BPD Etiology Chronic lung changes: Thickening & necrosis of alveolar walls with impairment of O2 diffusion from the alveoli to the capillaries Edema & inflammation of the capillary bed –cause alveoli to collapse, some to hyperinflate, others to rupture Characterized by: Diffuse infiltrates Hyperinflation Chronic pulmonary insufficiency BPD Clinical manifestations Vary widely Evidence of respiratory distress Wheezing, retracting, nasal flaring, irritability, abundant secretions, & cyanosis More prone to upper respiratory infections Frequent hospitalizations – poor respiratory status BPD Diagnostic tests No specific tests Radiographic exam & ABG’s - helpful PFT – degree of lung dysfunction BPD Medical management Prevent RDS & reduce ventilation & O2 requirements Use lowest O2 possible During weaning – bronchodilators used to decrease airway resistance & increase lung compliance Nutritional support BPD Nursing/Patient teaching Rest periods – decrease effort & conserve energy Small frequent feedings – prevent overdistention of the stomach Support parents & encourage them to participate Counsel parents – reduce respiratory infections CPR BPD Prognosis High mortality rate the first year Risk for chronic lung disease Use of surfactant for RDS – greatly reduced incidence of BPD Pneumonia Etiology Acute inflammation of the pulmonary parenchyma, small airways, & alveoli Classified by etiologic agents: Bacterial Viral Mycoplasmal Foreign body aspiration Pneumonia Common throughout childhood More frequently in infants & young children Viral pneumonias are more common than bacterial RSV - largest percentage of infections in infants & young children Bacterial pneumonias – streptococcal, staphylococcal, pneumococcal, or H. Influenzae Pneumonia Clinical manifestations Cough Wheezes or crackles Respiratory distress Chest pain Anorexia Irritability Malaise Lethargy Headache Fever Myalgia Abdominal pain Nasal discharge Pneumonia Diagnostic tests CXR – location & extent Blood tests – elevated WBC Culture & gram stain – causative organism No bacterial microorganism – considered viral Pneumonia Medical management Improving oxygenation Preventing dehydration Treatment includes Antibiotics O2 therapy CPT Suctioning Fluid administration Bronchodilators Antipyretics Pneumonia Medical management Prevention of RSV in premature neonates Monthly infusions of RSV immune globulin Delivered outpatient from November through April Pneumonia Nursing/Patient teaching Respiratory Skin color Cardiovascular Infection control Supportive nursing Observation & assessment Adequate rest periods Maintain hydration Gentle suctioning Encourage parents to participate in care Pneumonia Prognosis Pneumococcal & streptococcal Generally good with rapid resolution Staphylococcal Longer course Effective Sudden Infant Death Syndrome Etiology Sudden, unexpected, and unexplained death of a healthy infant under 1 year of age Postmortem exam fails to establish a cause Peak incidence between 2 and 4 months of age Always occurs during sleep Leading cause of death in infants between 1 month and 1 year of age SIDS Etiology Occurs more in males & siblings of SIDS victims Increased in winter months with peak in January Associated with: Premature birth & low birth weight Low apgar scores Multiple births CNS & respiratory dysfunctions Maternal smoking, drug addiction, & maternal age <20 SIDS Etiology Breast fed infants with lower incidence Cause unknown Numerous theories: Abnormalities of cardiorespiratory regulation Prolonged sleep apnea Depressed ventilatory response Excessive periodoc breathing Sleep positions SIDS Clinical manifestations Diagnostic tests Occurs during sleep with no audible cry or signs of distress Postmortem – pulmonary edema & intrathoracic hemorrhage Medical management Assisting the family SIDS Nursing interventions Initial response – shock & disbelief Guilt & blame Non judgmental Listen to & support the family Grief & mourning SIDS Patient teaching Visit post death to help with feelings of isolation Understand the SIDS phenomenon Assist with siblings’ feelings Refer to Sudden Infant Death Syndrome Alliance Prevention 1992 AAP recommended: Supine or non prone “Back to Sleep” 38% decline in SIDS cases from 1992 to 1996 Acute Pharyngitis (Sore throat) Etiology Inflammation of the pharynx 80% of cases are viral 20% are bacterial – group A B hemolytic streptococci Frequently seen in age group of 4 & 12 years Children < 3 years – usually infected with Haemophilus influenzae – watch for meningitis Acute pharyngitis Clinical manifestations Viral Low grade fever Malaise Anorexia Pharyngeal erythema Throat soreness Headache Cough Hoarseness Rhinitis Conjunctivitis Streptococcal High fever Throat soreness White exudates on the posterior pharynx & tonsillar region Vomiting Abdominal pain Diagnostic tests Throat culture Acute pharyngitis Medical management Viral Treated symptomatically Lozenges, gargles, and acetaminophen Streptococcal 10 day course of antimicrobial therapy Penicillin Other antibiotics Acute Pharyngitis Nursing/Patient teaching Throat discomfort Relieved with saline gargles, lozenges, warm compresses, & acetaminophen Cool liquids Soft bland foods next Follow up for strep infections Instruct the family on antimicrobial therapy Acute Pharyngitis Prognosis Usually excellent Inadequately treated strep infections Rheumatic fever Acute glomerulonephritis Tonsillitis Etiology Tonsils are masses of lymphoid tissue believed to protect the respiratory & alimentary tracts from invasion by pathogenic microorganisms Play a role in antibody formation Usually occurs as a result of pharyngitis Viral or bacterial Tonsillitis Clinical manifestations Viral & bacterial are similar Sore throat Headache Edematous & tender cervical lymph glands Fever Hoarseness Cough Strep Vomiting Muscle aches Difficulty swallowing or breathing Diagnostic tests CBC Throat culture Tonsillitis Medical management Comfort measures Bacterial Described in pharyngitis 10 day course of penicillin Surgical removal Controversial Recommended for children with hypertrophied tonsils that interfere with eating or breathing Tonsillitis Nursing interventions Same as pharyngitis Surgery Prepares child preoperatively Infection Loose teeth Lab data Postoperatively Semi prone position Monitor for excessive bleeding Analgesics as prescribed Fluids (avoid acidic, grape, red, or chocolate) Soft diet follows Tonsillitis Patient teaching Discharge instructions Avoid foods that are irritating Avoid use of gargles Discourage from coughing or clearing the throat Mild analgesics or ice collar for pain Alert that hemorrhage may occur 5 to 10 days after surgery – Any signs of bleeding require immediate attention Tonsillitis Prognosis Usually excellent Inadequately treated strep infections Rheumatic fever Acute glomerulonephritis Croup Acute viral disease of childhood Resonant barking cough Suffocative & difficulty breathing Laryngeal spasm Croup Etiology Laryngotracheobronchitis (LTB) Most common form of croup 3 months to 3 years of age Usually viral Follows an URI that descends Gradual, progressive onset Croup Etiology Acute epiglottitis Severe, potentially life threatening bacterial infection Older children Usually caused by H. Influenzae, type B Inflamed epiglottitis Cherry red & edematous Can lead to total airway obstruction Croup Clinical manifestations LTB Initially Hoarseness Inspiratory stridor Tachypnea Nasal flaring Suprasternal retractions Barking cough Temperature – normal to mildly elevated Croup Clinical manifestations Epiglottitis High fever Muffled voice Drooling Progressive respiratory distress Anxiety Fear Croup Diagnostic tests LTB History of preceding URI CBC with differential Clinical signs & symptoms Physical exam Croup Diagnostic tests Epiglottitis Tentative by signs & symptoms OR/surgery room with emergency equipment Intubation/trach supplies available Visual examination of the pharynx & invasive procedures are done with the child under anesthesia Tracheal secretions are collected for culture & sensitivity Croup Medical management LTB Maintain an open airway High cool mist humidity Low concentration O2 Epinephrine by aerosol – short lived NPO Adequate hydration Never use sedatives Croup Medical management Epiglottitis Artificial airway Humidification Gentle suctioning Epinephrine by aerosol IV antibiotics & fluids Third day – possible extubation Croup Nursing/Patient teaching Respond quickly in a calm manner Support & reassure parents Assess child’s response Fowler’s position Respiratory & cardiac status monitored Keep intubation & trach equipment at bedside Croup Prognosis LTB Relatively mild Recovery 3-7 days Most serious complication – laryngeal obstruction Epiglottitis Prompt diagnosis & treatment Rapid course can cause death within a few hours Bronchitis (Tracheobronchitis) Etiology Inflammation of the large airways, the trachea, and the bronchi Usually follows URI Almost always viral Most common – rhinovirus Others – parainfluenza, adenovirus, RSV Mycoplasma pneumoniae – common cause in children > 6 years Bronchitis Clinical manifestations Onset gradual Cough Coryza Little or no fever 2-3 days Non productive, hacking cough becomes productive Worsens at night Bronchitis Diagnostic tests Severe signs & symptoms CXR Medical management Basically palliative Cough suppressants contraindicated unless sleep significantly affected Acetaminophen for fever Lasts beyond 10 days – possible bacterial infection Bronchitis Patient teaching Cool mist humidifier Fluids Prognosis Self limiting Acute Bronchiolitis Etiology Viral inflammation of the smaller airway passages, the bronchioles, which become inflamed causing edema Accumulation of mucus & exudate can partially or completely obstruct the lumen RSV – majority of cases Peak incidence 6 months of age Bronchiolitis Clinical manifestations URI signs & symptoms Worsening to signs & symptoms of respiratory distress Retractions Tachypnea Nasal flaring Paroxysmal nonproductive cough Wheezing May have: Low grade or very high fever Irritable Fussy Anxious Difficulty eating Progressively more severe during the first 72 hours Bronchiolitis Diagnostic tests Based on age & clinical signs & symptoms CXR Atelectasis Hyperinflation Nasal smears for RSV Bronchiolitis Medical management High humidity via mist tent If hypoxic – O2 therapy recommended IV fluids if unable to tolerate oral feeds Bronchodilators for severe cases Bronchiolitis Nursing/Patient teaching Respiratory isolation precautions Hand washing Promoting: Adequate oxygenation Monitor respiratory status Maintain hydration Support parents Bronchiolitis Prognosis Lasts 3-10 days Generally good Pulmonary Tuberculosis Etiology Chronic, bacterial lung infection Caused by bacillus Mycobacterium tuberculosis Public health problem in the US Inadequate immune response Age or impaired immune system Primary source – infected adult TB Clinical manifestations First infected – do not exhibit signs & symptoms Extremely variable Develop gradually May go unnoticed TB Diagnostic tests Most important screening measure Confirm diagnosis Tuberculin skin testing Positive bacteriologic cultures – M. tuberculosis Best way to obtain sputum sample is by gastric aspiration CXR – presence & extent of active lesions TB Patient teaching Teach parents importance of med compliance Usual course of treatment no less than 12 months 18 to 24 months for serious cases Cystic Fibrosis Etiology Inherited disorder of the exocrine glands Mucus producing glands Characterized by excessive thick mucus - obstructs the lungs & GI tract Multi organ disease Death usually by pulmonary failure Most common fatal genetic disorder Affects both sexes equally CF Etiology Bronchiolar obstruction – predisposes lung to infections, bronchiectasis, & cystic dilations Complications Bronchial & bronchiolar obstruction Pulmonary hypertension Cor pulmonale CF Pancreatic Obstruction leads to dilation & fibrosis Hepatic Decrease in pancreatic enzymes – results in malabsorption Obstruction leads to biliary cirrhosis, portal hypertension, & splenomegaly Elevated sodium chloride concentrations in sweat & saliva – result of abnormal reabsorption of chloride by epithelial cells CF Clinical manifestations Steatorrhea (bulky, foul smelling, fatty stools) Growth failure Protruding abdomen Thin, wasted extremities Rectal prolapse – GI Malabsorption – Vit K deficiency CF Pulmonary Chronic cough Wheezing Sputum production Dyspnea Leads to hypoxia, clubbing of fingers & toes, & cyanosis Barrel chest CF Diagnostic tests Family history Absence of pancreatic enzymes Pulmonary involvement Positive sweat test CF Medical management Goals Good nutrition Prevention & control of respiratory infections Provide a normal lifestyle (as possible) Pulmonary therapy CPT & postural drainage Breathing exercises Inhalation therapy with bronchodilators CF Medical management Pancreatic enzyme replacement Diet high in calories, protein, & salt CF Nursing interventions Improve pulmonary function Facilitate lung clearance Prevent or manage respiratory infections Promote normal growth & development Optimizing nutritional status Education Refer for counseling CF Respiratory treatments Infection control measures Pancreatic enzymes CPT, postural drainage, nebulizers Given before meals and snacks Frequent hospitalizations – need support Positive coping strategies Ctstic Fibrosis Foundation CF Patient teaching Educate on nutrition Coordinate counseling, referrals to community support, and home care services Educate of disease process & management CF Prognosis More then 50% live to adulthood According to the CF Foundation's National Patient Registry, the median age of survival for a person with CF is in the mid-30s Bronchial Asthma Etiology Reversible obstructive respiratory disorder Common chronic illness Familial tendency Frequent cause – allergic hypersensitivity to environmental factors Asthma Common factors Bronchospasm Mucosal edema Increased mucosal secretions Classification based on symptom indicators of disease severity Mild intermittent Mild persistent Moderate persistent Severe persistent Asthma Clinical manifestations Tightness in the chest Audible expiratory wheeze Progresses SOB Inspiratory & expiratory wheezing Tachypnea Dyspnea Coarse breath sounds Prolonged expiration Restlessness Anxiety Deep dark red color to lips Cyanosis Paroxysmal cough Fatigue Diaphoresis Asthma Diagnostic tests Clinical signs & symptoms History Physical exam PFT ABG CBC CXR – rule out other pathology Asthma Medical management Medications Long term control medications – preventive Quick relief medications – rescue Metered dose inhalers Nebulized medications – infants & young children Corticosteroids Cromolyn sodium Nedocromil sodium B adrenergic agonists Leukotriene modifiers Asthma Nursing interventions Monitor VS Adequate hydration High Fowler’s position Provide rest periods Teach breathing exercises Calm environment Educate Asthma Nursing diagnosis Suffocation, risk for Breathing pattern ineffective Patient teaching Nature of the disease & allergens to avoid (once determined) How to use meds Avoid exposure to extremes of weather Self care Asthma Prognosis Outlook varies widely Many lose signs & symptoms at puberty Death rate has been rising steadily – despite improvements in treatment