The Child with a Respiratory Alteration



The Child with a Respiratory Alteration


Learning Objectives


After studying this chapter, you should be able to:



• Describe the differences in the anatomy and physiology of the infant’s or child’s respiratory system that increase the risk for respiratory disease.


• Outline nursing care for a child with allergies to inhalants.


• Discuss the pathophysiology, clinical manifestations, and therapeutic management of common acute and chronic respiratory alterations.


• Identify the nursing care needs of infants and children with acute and chronic respiratory alterations.


• Develop guidelines for the home care of a child with an acute respiratory alteration.


• Identify common triggers of asthma symptoms.


• Apply measures that can be taken to prevent and treat asthma episodes.


• Identify teaching needs for children with asthma and their families.


• Describe the nursing care of the child with cystic fibrosis.


• Discuss measures to maintain adequate oxygenation and provide appropriate developmental stimulation for the child with bronchopulmonary dysplasia.


• Describe the correct method of administering and evaluating tuberculosis skin tests.


• Identify ways to prevent the transmission of tuberculosis and explain the importance of administering antituberculosis medications as prescribed.


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CLINICAL REFERENCE


Review of the Respiratory System


The respiratory system consists of the nose, pharynx, larynx, trachea, bronchi, and lungs. It is further divided into the upper respiratory tract (nose, pharynx, larynx) and the lower respiratory tract (trachea, bronchi, lungs).


The Upper Airway


Air enters the body through the nares, or nostrils, two nasal cavities lined with mucous membrane. In older infants and children, air can also enter through the mouth into the pharynx, or throat. The nasopharynx is located immediately behind the nasal cavity; the oropharynx is located behind the mouth. The laryngeal pharynx lies below the oropharynx and opens into the larynx toward the front and into the esophagus toward the back.


The larynx is located between the pharynx and the trachea. The vocal cords are at the upper end of the larynx. The proximity of the upper esophagus to the upper respiratory system can put an individual at risk for inhaling food or liquids, but the epiglottis covers the larynx during swallowing and helps keep food out of the lower respiratory tract.


Cilia are hairlike processes that move mucus and fluid. Damage to cilia interferes with the removal of mucus from the respiratory tract. Ciliated mucous membranes line the larynx and filter dust and other particles from the air. The particles are then carried to the pharynx to be removed by sneezing, blowing, or coughing. After being filtered, the air that enters the respiratory system is humidified and warmed before proceeding into the lungs.


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Tonsils are located in the posterior oropharynx. The three types of tonsils are the oval palatine tonsils, located on either side of the pharynx; the lingual tonsil, located below the palatine tonsils at the base of the tongue; and the pharyngeal tonsils, or adenoids, located at the nasopharyngeal border. The tonsils are composed mainly of lymphoid tissue. They help filter the circulating lymph of bacteria and other foreign material that enter the body, especially through the mouth and nose.


The Lower Airway


The trachea conducts air between the larynx and the lungs. It divides into right and left main bronchi at its lower end, the carina. The right main bronchus is shorter and wider than the left. The main bronchi divide into lobar bronchi, segmental bronchi, and bronchioles and terminate in alveoli. Mucus-secreting goblet cells line the bronchi and protect the lungs from dust and bacteria.


The lungs are two cone-shaped structures within the thoracic cavity. The right lung has three lobes (upper, middle, and lower); the left has two lobes (upper and lower). The pleura consists of two layers, the parietal pleura and the visceral pleura. The parietal pleura line the entire thoracic cavity; the visceral pleura encase each lung. The pleura help maintain lung stability. Negative pressure within the intrapleural space prevents the lungs from separating from the thorax. Diffusion of gases takes place in the lungs. Terminal bronchioles lack mucus-secreting goblet cells and cilia, and gas exchange does not take place here.


Distal to the terminal bronchioles are the alveoli, where most gas exchange occurs. Thinness of the alveolar walls aids in gas exchange. An almost solid sheet of capillaries is within the alveolar walls, so the alveolar gases are proximate to the capillary blood.


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Prenatal Respiratory Development


The respiratory system must mature before birth for the neonate to survive. The placenta performs oxygenation in utero, but to adapt to extrauterine life the neonate must be able to inflate the lungs, establish continuous breathing, and transfer the gases needed to meet metabolic needs.


Postnatal Respiratory Changes


Postnatal changes in the respiratory system occur as follows:



Gas Exchange and Transport


Two-way diffusion takes place between the walls of the alveoli. In diffusion, molecules move from an area of greater concentration to one of lesser concentration. Blood entering the lung capillaries is somewhat low in oxygen. Oxygen will diffuse from the alveoli, where its concentration is higher, into the blood. Similarly, carbon dioxide moves out of the blood and into the alveoli. Most oxygen that diffuses into the capillary blood in the lungs is bound to the hemoglobin of red blood cells. A small percentage is dissolved in plasma. For oxygen to enter the cells, it must separate from hemoglobin. Carbon dioxide diffuses into the blood from the tissues and is transported to the lungs by the blood. In this activity, hemoglobin is a buffer that enables blood to take up carbon dioxide without altering the blood pH significantly. The uptake and delivery of gases by the blood is a continuous process.


Ventilation occurs through inspiration and expiration. In inspiration, the diaphragm contracts and flattens, expanding the vertical dimension of the chest; the lung volume increases. In expiration, the diaphragm and chest wall relax, decreasing thoracic volume. Intrathoracic pressure increases, and gas flows out of the lungs, taking with it the carbon dioxide that was delivered to the lungs by the blood. Ventilation of the lungs is intermittent. Inspired air is 21% oxygen; end-expired air is 16% oxygen and 35% carbon dioxide.


Diagnostic Tests


In most instances, respiratory tract disorders are diagnosed from the findings on physical examination and the clinical manifestations. Sometimes, however, specific diagnostic tests are needed.


Blood Gas Analysis


Arterial blood gas analysis plays an important role in the investigation of pulmonary function. Arterial blood gas values most frequently determined include the partial arterial oxygen pressure (PaO2), the partial pressure of carbon dioxide in arterial blood (PaCO2), the acid-base balance (pH), and bicarbonate (HCO3). Arterial blood is more reliable than capillary or venous blood for these tests, especially in children with poor peripheral perfusion.



PEDIATRIC DIFFERENCES IN THE RESPIRATORY SYSTEM



• Surfactant is lacking in premature infants. Infants born before 34 weeks of gestation have a higher risk for respiratory distress syndrome (RDS).


• Smaller lower airways and undeveloped supporting cartilage predispose the child to an increased risk for obstruction by mucus, edema, and foreign bodies. The neonate’s airway is 50% smaller than that of adults. A premature infant has a more compliant chest wall and weaker respiratory muscles than a term infant.


• Lung size is proportional to body height. Therefore, lung volumes and capacities do not vary from age to age.


• Infants are obligatory nose breathers; they have difficulty breathing through the mouth. If the infant has nasal congestion, breathing becomes more difficult.


• The diaphragm is the neonate’s major respiratory muscle. Intercostal muscles are not well developed. Retractions are more common in the infant than in older children and adults.


• Brief periods of apnea (10 to 15 seconds) are common in the neonate. The respiratory pattern may be irregular.


• Children’s normal respiratory rate is higher than that of adults.


• An increased metabolic rate increases oxygen needs.


• Alveoli develop from approximately 20 million to 200 million by age 3 years. Alveolar development gradually decreases after age 3 years; few develop after age 8 years.


• The lung surface increases until age 5 to 8 years. Actual lung growth continues into the adolescent years.


• Eustachian tubes are relatively horizontal, which increases the risk for bacteria entering the middle ear.


• Tracheal size approximately triples by adulthood.


• Tonsillar tissue is normally enlarged in early school-age children.


• Infants and children use abdominal muscles to inhale until about age 5 to 6 years.


• The child’s flexible larynx is more susceptible to spasm.



COMMON LABORATORY AND DIAGNOSTIC TESTS FOR RESPIRATORY DISORDERS



























































TEST DESCRIPTION NORMAL FINDINGS INDICATIONS NURSING CONSIDERATIONS
Chest radiography, posterior, anterior and lateral views Shows airways, lungs, heart, great vessels Normal appearance of internal structures of chest To detect respiratory disease of lungs Assist in holding child.
Computed tomography Shows lesions in chest wall, pleural space, mediastinum, and lung parenchyma Normal cross section of lung tissue To image tumors or masses; to evaluate response to therapy aimed at defined lesions Assist with sedation and immobilization of child. Withhold feedings 3-4 hr before the test because of frequent use of contrast medium.
Bronchoscopy Provides viewing of tracheobronchial tree through a scope Normal appearance of tracheobronchial tree or successful removal of foreign body or mucous plugs To view a lesion and obtain biopsy material for culture; to remove foreign body or mucous plugs Rigid bronchoscopy is usually performed with child under general anesthesia.
Fiberoptic flexible bronchoscopy can be performed while child is awake or sedated.
Observe child closely for signs of airway obstruction.
Mist may be given to decrease swelling and edema.
Laryngoscopy Provides direct viewing of larynx with a scope Normal appearance of larynx To identify cause of stridor and local abnormalities Mirror (indirect) laryngoscopy can be performed on children age 4 yr or older. In infants and younger children, direct laryngoscopy or transnasal laryngoscopy with flexible bronchoscope will give much better results.
General anesthesia is usually required; topical anesthesia and mild sedation may be provided for fiberoptic examination.
Fluids and foods are withheld until effects of local anesthetic have worn off and gag reflex has returned.
Cultures Throat, blood, nasopharyngeal, sputum, induced sputum No culture growth or normal flora only To isolate and identify pathogens See Chapter 37 for procedures.
RAST for IgE Measures quantity of IgE antibodies in serum after exposure to specific antigens If the child is not allergic to the antigen, IgE antibody is not detected
A test result is positive in relation to a specific antigen if the value is above 400% of control
To identify specific allergens; systemic reactions to insect venom, drugs, and chemicals; to monitor response to desensitization procedures; also performed at the onset of asthma, hay fever, or dermatitis Prepare child for peripheral blood sample to be drawn.
Determine whether child has undergone any radioisotope tests within past week because such tests may alter the results.
Pilocarpine iontophoresis (sweat test) Measures sweat electrolyte concentration for diagnosis of CF
Sweating is stimulated on the child’s forearm with a small electrical current and pilocarpine; a sweat sample is then collected on preweighed, dry, sterile gauze or filter paper and the amounts of sweat sodium and chloride are measured
Normal chloride: <40 mEq/L
Suggestive of CF: 40 to 60 mEq/L
Positive for CF: >60 mEq/L
To diagnose cystic fibrosis No physical preparation is needed. Offer parents and child support as they face the implications of a positive diagnosis.
Inform child and parents that the test is painless and that it is usually performed twice to ensure accurate results.
Because an adequate amount of sweat is difficult to obtain from infants, the sweat test is usually unreliable in infants younger than 2 wk.
Mantoux test Skin test for TB
PPD, 5 TB units (0.1 mL) is injected intradermally into volar surface of forearm with short, 26- to 27-gauge needle, beveled side up
A wheal 6-10 mm in diameter should appear during injection
The site is checked in 48-72 hr by a health care professional
Results are recorded in millimeters (not simply as positive or negative). The reading is based on induration (hardness), not redness
Positive result: area of induration ≥15 mm (in children 4 yr of age and older); area of induration ≥10 mm in children younger than 4 yr or at high risk for exposure; area of induration ≥5 mm in highest risk group
Negative result: Mantoux test cannot rule out the presence of TB, particularly in young infants
To screen and test individuals suspected of having TB or of having been exposed to TB Test is fairly difficult to administer.
After PPD is injected, withdrawal of needle should be delayed 2-3 sec to minimize leakage of PPD at the puncture site.
In most children, skin testing will elicit positive reaction 3-6 wk after initial infection.
Steroids and immunosuppressants given within 4-6 wk can cause false-negative skin test results.
Positive tuberculin reactivity usually continues for person’s lifetime, even with treatment.


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CF, Cystic fibrosis; IgE, immunoglobulin E; PPD, purified protein derivative; RAST, radioallergosorbent test; TB, tuberculosis.


Arterial blood gas values are used primarily to determine acid-base balance, not oxygen saturation (see Chapter 40).


Pulmonary Function Tests


Probably the most useful measures of ventilatory function are the vital capacity and the expiratory flow rate, both measured by spirometry. Spirometry can be performed at an acceptable level by most preschool-aged children (Gaffin, Shotola, Martin, et al., 2010). Accurate measurements are difficult to obtain in younger children because they are unable to follow commands. Infant pulmonary function testing is now being performed at many institutions with use of conscious sedation. Pulmonary function tests assess the degree of pulmonary disease, the response to therapy, and the presence of restrictive or obstructive disease. They are also done to test the child’s response to bronchodilators should pulmonary function be affected.


The child must be given instruction and practice in blowing, pushing, and holding respirations. The child should become familiar with the mouthpiece and the nose clip to feel comfortable with their use.


Pulse Oximetry


Pulse oximetry is a simple, noninvasive, intermittent or continuous method for measuring oxygen saturation for the purpose of determining the need for or response to oxygen therapy (see Chapter 37). The goal of treatment for most respiratory conditions is an oxygen saturation value greater than 95%. For children with chronic respiratory disease, however, a realistic goal may be slightly lower.


Transcutaneous Monitoring


Transcutaneous monitoring continuously checks oxygen and carbon dioxide concentrations in the body through an electrode placed on the child’s skin. Electrode sites must be changed every 3 to 4 hours to prevent burning the skin, and the machine must be recalibrated each time electrodes are changed. The readings may not be accurate if tissue perfusion is poor.


End-Tidal Carbon Dioxide Monitoring


End-tidal carbon dioxide monitoring, often used in conjunction with pulse oximetry, measures carbon dioxide in the exhaled breath noninvasively. It is useful in verifying endotracheal tube position, in evaluating asthma, and during procedural sedation. It can also be a primary indicator of worsening respiratory distress or impending respiratory failure because results are thought to detect respiratory distress and hypercarbia before changes in pulse oximetry (Walsh, Crotwell, & Restrepo, 2011).


Respiratory Illness in Children


Respiratory alterations are the most common causes of illness in the infant and child. Upper respiratory disorders affect the ears, nose, pharynx, and larynx; lower respiratory disorders include those disorders that involve the trachea, bronchi, and lungs.


Infants and children younger than 3 years are at greater risk than older children and adults for development of respiratory infections because of their immature immune systems, smaller upper and lower airways, and underdeveloped supporting cartilage. Although most respiratory infections are self-limiting, in infants and young children respiratory distress can occur quickly as mucus and edema obstruct their small airways.


Parents should be taught preventive measures, including adequate rest, optimal nutrition, and good hygiene, with an emphasis on hand hygiene. Even with the most careful hygiene and preventive practices, however, most children will have some type of respiratory infection each year. School nurses often see children with respiratory problems in the school health office and may be the primary health care providers for these children.


Most children can be cared for at home by their parents and do not need hospitalization. Those children who are hospitalized are being discharged from the hospital earlier in their recovery than in the past. The current health care environment underlies the need for nurses to teach parents appropriate home care techniques, including careful observation and recognition of signs that indicate the need to contact health care providers. Parents, especially first-time parents, often are frightened by the sudden onset of respiratory symptoms, which may indicate a severe problem. Teaching them the signs and symptoms of serious illness will help them develop appropriate decision-making skills.


Children with chronic conditions have many special needs, and the child with a chronic respiratory disease is no different. Medications and treatments become a way of life for many of these children. Their activity level is often altered, and some may have a shortened life span.


Children with chronic respiratory conditions are now becoming adults with those same conditions. As advances in treatment modalities are made and children with these conditions are living longer, the transition to adult care becomes a necessity.


The nurse plays an important role in the care of the child with a chronic respiratory disease. Beyond giving acute care to the hospitalized child, the nurse must coordinate and facilitate the child’s long-term care. Because of advances being made in the treatment of chronic pediatric respiratory conditions, the treatment and care of children affected by these disorders are constantly changing and improving, requiring the nurse to stay current in these areas.


Allergic Rhinitis


Allergic rhinitis is an inflammatory disorder of the nasal mucosa. It is usually seasonal, recurrent, and triggered by specific allergens (see Chapter 42). It is sometimes referred to as seasonal allergic rhinitis or hay fever. Some children have symptoms year round (perennial allergic rhinitis).


Etiology and Incidence


Agents that commonly cause allergic rhinitis include dust mites; feathers; animal dander; mold spores; and pollens of trees, grasses, and weeds. There is usually a family history, similar to that seen in individuals with atopic dermatitis and asthma. Unlike atopic dermatitis, however, allergic rhinitis does not predispose to the development of asthma.


The onset of allergic rhinitis usually occurs during childhood but rarely before age 2 years. It is estimated that 20% to 40% of children have this type of allergic response (Milgrom & Leung, 2011).



PATHOPHYSIOLOGY


Allergic Rhinitis


Allergens (pollens, molds, spores, dust mites, animal dander) are deposited on the nasal mucosa, causing local inflammation and increased capillary permeability. Local immunoglobulin E (IgE) is produced, and sensitization of the respiratory tissues occurs. Mast cell mediators are released, producing vasodilation, mucosal edema, mucus secretions, stimulation of itch receptors, and a reduced threshold for sneezing.


Manifestations


The classic symptoms of allergic rhinitis are clear rhinorrhea, associated with itching of nose, eyes, ears, and palate, and paroxysmal sneezing. Additional signs and symptoms include the “allergic salute”—an upward rubbing of the nose with the palm of the hand, which can leave a crease below the bridge (Figure 45-1); allergic shiners—dark circles under the eyes from congestion and edema; dry lips from mouth breathing; pale, boggy nasal mucous membranes; and nasal obstruction. Children with allergic rhinitis have symptoms as long as they are exposed to the allergen.



It is important to distinguish allergic rhinitis from viral nasopharyngitis (the common cold), which is usually caused by a rhinovirus and is spread by droplet or by contact with contaminated items. Usually children with nasopharyngitis have the associated symptoms of sore throat, fever, cough, and fatigue. The condition is self-limiting and usually resolves within 2 weeks. The quality of the nasal discharge in children with nasopharyngitis often changes from clear to cloudy or yellow. Management is supportive. Because young infants are obligatory nose breathers, the infant’s blocked nasal passages can be relieved with instillation of normal saline solution drops followed by gentle bulb suction.


Diagnostic Evaluation


A thorough personal and family history usually elicits a description that suggests an allergic rather than infectious pattern. The nasal smear may demonstrate eosinophils. Allergy skin testing is done if signs and symptoms continue after treatment with medication. The radioallergosorbent test (RAST) is used only when skin testing is difficult because of generalized dermatitis, the child is very young, or the child is too ill for skin testing. A complete blood cell count might reveal elevated eosinophils, a finding associated with allergic manifestations.


Therapeutic Management


The treatment of choice is to eliminate the allergen from the child’s environment; however, complete elimination may be difficult in children (Turner & Kemp, 2010). When this is impossible, as in the case of pollen in the air, medication can control symptoms.


Antihistamines or intranasal corticosteroids may be effective in treating allergic rhinitis. Antihistamines are most effective when given before or very early in an allergic episode. Because they can cause drowsiness, they should be given at night. Some of the newer antihistamines (e.g., loratadine, cetirizine, fexofenadine) are long acting, have fewer side effects and require only one or two doses daily. They are prescribed according to the child’s age. Decongestants may be effective in relieving nasal congestion, but are not recommended in children. Decongestants have side-effect profiles that include insomnia, behavior problems, and even cardiac events; therefore, their use is no longer recommended (Turner & Kemp, 2010).


Short-term topical intranasal corticosteroids (e.g., fluticasone, mometasone, and budesonide) are highly effective and may be used as first-line therapy for children with allergic rhinitis (Milgrom & Leung, 2011; Turner & Kemp, 2010). It usually takes several days of treatment before the child feels the effects of topical corticosteroids.


Leukotriene inhibitors (e.g., montelukast [Singulair]) may be used in the treatment of allergic rhinitis, although results may be suboptimal. These medications have a good safety profile and seem to work well for children with both allergic rhinitis and asthma (Turner & Kemp, 2010).


Finally, immunotherapy (allergy shots) may be considered for children whose condition is not responsive to either environmental modification or medication. Immunotherapy involves injecting the child with progressively larger doses of the allergen in an effort to reduce the magnitude of the body’s allergic response. Injections are given once or twice a week until a maintenance dose is reached; monthly maintenance injections can continue for several years.


Nursing Considerations


Nursing care focuses on early identification of clinical signs and symptoms of allergic rhinitis and the therapeutic management of the condition. The nurse assesses and records the applicable history and helps the family identify allergens to which the child is sensitive. Once the allergens are known, the nurse counsels parents regarding administration of medications, environmental control, and immunotherapy as appropriate (see Patient-Centered Teaching: How to Implement Environmental Modifications). Allergies, including allergic rhinitis, can negatively affect quality of life and school performance—not only does allergic rhinitis impair cognitive function, but allergies are also one of the most common reasons for missed school days (Parker, Akinbami, & Woodruff, 2009).



PATIENT-CENTERED TEACHING


How to Implement Environmental Modifications


To reduce your child’s exposure to allergens, take the following measures:


Pollen and Dust



Mold



Dander



For further information, contact: Allergy & Asthma Network/Mothers of Asthmatics, Inc. website: www.aanma.org, a family site that provides information on asthma, products, kits, and books.


Side effects of medications used to treat allergic rhinitis can further impair functioning. Drowsiness, the most common side effect of antihistamines, can usually be alleviated if the child takes the medication at night. Some children may have dry mucous membranes or excitability. Warm water or saline solution irrigations of the nasal passages can be used to moisten mucous membranes, soften crusted secretions, and wash out irritants. Saline solution can be mixed by adding ¼ teaspoon of salt to a cup of warm water. Saline solution nose drops are also available without prescription.


When specific allergens have been identified, they should be eliminated or controlled. During the pollen season, the child should stay indoors as much as possible and the windows should be kept closed if the house is air conditioned. After being outdoors, the child should shower and wash his or her hair to remove pollens from the body. Animals that have been outside may also be a source of contamination.


Receiving immunotherapy can be a traumatic experience for the child. It is often difficult for children to understand how an injection will help them. Allergy injections must be given in a physician’s office because the risk of an anaphylactic reaction to the allergy serum exists. Monitor the child closely (vital sign changes, difficulty breathing) for 20 to 30 minutes after the injection in case anaphylaxis develops. Keep emergency epinephrine ready.


Sinusitis


Sinusitis, although not itself a serious disorder, can lead to life-threatening complications. Inflammation and infection of the sinuses can be acute or chronic.


Etiology and Incidence


Acute sinusitis often follows an upper respiratory tract viral infection. Children with chronic sinusitis often have allergic rhinitis or otitis media with effusion (OME) as well. Hypertrophied adenoids, immune deficiencies, and foreign body obstruction in the nose also predispose one to sinusitis. Children with cystic fibrosis have a high incidence of sinusitis because of highly viscous mucus secretions and nasal polyps. The most common causative organisms are Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staphylococcus aureus (Pappas & Hendley, 2011).


Sinus infections can occur in infancy as well as in childhood and are seen frequently in preschool and school age children as a result of group exposure to upper respiratory infection (Pappas & Hendley, 2011).


Manifestations


Sinusitis is characterized by signs and symptoms of a cold that do not improve after 14 days, low-grade fever, nasal congestion with purulent nasal discharge, halitosis, cough (which usually increases when the child is lying down), and headache, tenderness, and a feeling of fullness over the affected sinuses. Young children may become irritable. Occasionally, children have facial edema. Children with chronic sinusitis have many of the same symptoms except that the cough is chronic and the



PATHOPHYSIOLOGY


Sinusitis


Acute sinusitis occurs when the sinus cavity is invaded by bacteria, causing mucosal inflammation and edema that block narrow sinus channels. The volume of secretions increases, and the affected sinuses fill with purulent material. Inflammation and infection interfere with the protective cleansing action of the cilia covering the sinus mucous membranes. Impaired mucociliary transport leads to stagnation of secretions within the sinuses; the stagnant secretions provide a medium for bacterial growth.


Chronic sinusitis is usually a complication of acute sinusitis. Prolonged or repeated infections result in irreversible changes in the mucosal lining of the sinus. Nasal polyps, a deviated septum, and enlarged adenoids inhibit sinus drainage, which can lead to infections. The frontal and sphenoid sinuses are most often involved in children.


Infection from sinusitis can spread to the middle ear, causing otitis media. Serious complications occur when infection spreads either directly through the bone or along the venous channels of the skull into adjacent structures, such as the orbit or the central nervous system.


headache is recurrent. The child’s sense of taste or smell may be impaired, and the child may be fatigued.


Diagnostic Evaluation


Sinus radiographs show mucosal thickening, opacification, and air-fluid levels in children older than 1 year. Sinus radiographs are of no value in younger children because of their small sinuses. Computed tomography is the diagnostic tool chosen most often for evaluation of sinus disease because it provides detailed anatomic information (Leo, Mori, Incorvaia, et al., 2009). Because of the thick bone of the maxilla in the anterior part of the face and the small size of the sinus, transillumination of the sinuses is not useful.


Therapeutic Management


Most cases of acute sinusitis are self-resolving and do not require antibiotics (Suhaili, Goh, & Gendeh, 2010). When a prescription is required, amoxicillin or amoxicillin–potassium clavulanate (Augmentin) is used most frequently (DeMuri & Wald, 2010). In addition to antibiotics, treatment includes analgesics, hydration, and the application of moist heat. The use of decongestants or antihistamines in the treatment of sinusitis should be avoided in children secondary to inefficacy and potential risks posed to children (DeMuri & Wald, 2010). Antihistamines may be used to treat allergy symptoms associated with chronic sinusitis, but they tend to impair sinus drainage by thickening secretions. Steroid nasal sprays may be used to reduce inflammation while avoiding the rebound effect of decongestant nose drops. Saline nasal washes may also be helpful (DeMuri & Wald, 2010). Surgical correction may be considered for children with chronic sinusitis who have not responded to antibiotic therapy, who have other chronic respiratory disease (e.g., cystic fibrosis), or who have anatomical abnormalities (Wu, Shapiro, & Bhattacharyya, 2009).


If orbital cellulitis develops, the child should be hospitalized immediately and parenteral antibiotic therapy begun (Pappas & Hendley, 2011).


Nursing Considerations


The nurse assesses the location of pain or fullness. Pain can occur in the forehead or over the cheek bones or upper teeth, or it may radiate to the top of the head. Inspect and palpate the face for edema, document any fever, and inspect the nose and throat for purulent discharge. The nasal mucous membranes are inspected for erythema and edema.


Nursing care focuses on teaching the parents antibiotic administration, comfort measures, how to monitor for response to treatment, and how to identify complications. Emphasize the importance of the child’s taking the antibiotics as prescribed. Sinus drainage is facilitated by increasing the child’s intake of clear fluids and by using a bedside humidifier.


Warm, moist compresses applied two or three times daily help decrease swelling and pain. Acetaminophen is given for fever and discomfort. Breathing warm mist in a hot shower or through hot, moist towels can help liquefy and mobilize nasal mucus, as can saline solution nose drops. The nurse teaches the parent to administer nose drops after the nasal passages have been gently cleaned. The amount, color, and consistency of nasal drainage should be noted and evaluated to determine whether the child is responding to treatment.


Carefully evaluate the child’s response to treatment and the development of complications. Advise parents to contact the physician promptly if symptoms become worse, if the child has any periorbital redness or edema, or if the child does not seem to be feeling better after 3 to 4 days.


Otitis Media


Otitis media is one of the most common illnesses of infancy and childhood. The term otitis media refers to effusion (fluid) and infection or blockage of the middle ear. Acute otitis media (AOM) is effusion and inflammation in the middle ear that occurs suddenly and is associated with other signs of illness. Otitis media with effusion (OME) refers to the presence of fluid behind the tympanic membrane without signs of infection. Otitis media with effusion often follows an episode of AOM and usually resolves in 1 to 3 months.


Etiology


The bacterial pathogens that usually cause AOM are S. pneumoniae, H. influenzae, and M. catarrhalis (Coates, Thornton, Langlands, et al., 2008). Although viruses do not cause otitis media, they are thought to predispose the child to ear infection by altering host defenses and contributing to eustachian tube dysfunction. Allergies are also thought to precipitate otitis media.


Attendance at daycare centers may predispose children to otitis media. Infants younger than 1 year who attend daycare have a significant risk for acquiring AOM. Other risk factors include age (highest in 6- to 24-month-olds), ethnicity (higher in Native Americans, Alaskan and Canadian Inuit, and indigenous people of Australia), exposure to household cigarette smoke, pacifier use, and poverty (Kerschner, 2011).


Bottle feeding can contribute to ear infection because of the position of the infant during feeding. Reflux of formula into the eustachian tube from the nasopharynx occurs when the infant swallows while supine. Breastfeeding offers some protection from ear infection by providing maternal antibodies and by decreasing the incidence of allergy; also, the more upright position of the infant while nursing or bottle feeding may be protective against ear infection (Kerschner, 2011).


Incidence


The incidence of otitis media peaks between ages 6 months and 6 years, with most episodes occurring in children younger than 3 years. Most initial episodes occur at about age 6 months, when maternal antibody levels decline. Early onset of AOM (during infancy) increases the risk for recurrent episodes (Lasisi, Olayemi, & Irabor, 2008).


By the end of the third year of life, more than 80% of all children have had at least one episode of AOM (Kerschner, 2011). Most children younger than 5 years of age have two or three episodes of otitis media each year. Boys have a slightly higher incidence of otitis media than girls. The incidence of otitis media is highest in winter and spring and lowest in the summer months.


Manifestations


AOM is characterized by the following:




These signs and symptoms might also be accompanied by irritability, sleep disturbances, persistent crying in infants, fever, vomiting, anorexia, or diarrhea (especially in infants).


OME differs from AOM in that there are no signs of acute infection. The tympanic membrane appears retracted and either dull gray or yellow, and an air-fluid level or air bubbles may be visible through the tympanic membrane. The mobility of the tympanic membrane is decreased, and landmarks are distorted. Associated signs and symptoms can be subtle and can include the following:



AOM is considered to be persistent if the child experiences symptoms while being treated or within 1 month after treatment is complete. AOM is viewed as recurrent if the child




PATHOPHYSIOLOGY


Otitis Media


The immature anatomy of the child’s middle ear and eustachian tube predisposes infants and toddlers to otitis media. When the eustachian tube is obstructed, as frequently occurs with enlarged adenoids or mucosal edema from an upper respiratory tract infection, effective drainage and ventilation of the middle ear cannot occur. Air that is normally present in the middle ear is absorbed by the blood, causing a vacuum or negative pressure in the middle ear. Effusion accumulates within the middle ear space, creating a medium for bacterial growth. After an upper respiratory tract infection, pathogens travel from the nasopharynx to the eustachian tube. In the presence of effusion, negative pressure in the middle ear draws mucus through the eustachian tube whenever the child cries, yawns, or sucks forcefully on a nipple. Purulent fluid accumulates in the middle ear space, causing the pressure and pain of acute otitis media.


If the eustachian tube remains nonfunctional for a prolonged period, the fluid within the middle ear becomes thick and dark (glue ear). Mild temporary conductive hearing loss (see Chapter 55) often occurs in otitis media with effusion because of the decreased mobility of the ossicles and the tympanic membrane. Permanent conductive hearing loss can result from repeated episodes of otitis media and may interfere with the development of language and cognitive skills. Chronic otitis media with effusion is the most common cause of hearing loss in children.


Complications of otitis media include conductive hearing loss and sensorineural hearing loss. The infection of acute otitis media can spread to surrounding tissues, causing mastoiditis or intracranial complications such as meningitis or brain abscess. Inflammation and pressure from otitis media may result in tympanosclerosis (scarring of the tympanic membrane), perforation of the tympanic membrane, and cholesteatoma (a cyst formed from pus and debris in the middle ear).


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experiences more than three episodes over a 6-month period or four episodes in a year (Kotsis, Nikolopoulos, Yiotakis, et al., 2009).


Diagnostic Evaluation


The diagnosis of otitis media is based on the history of signs and symptoms and pneumatic otoscopy. In pneumatic otoscopy, a small puff of air is blown into the ear canal through the otoscope; the examiner can discern the appearance and mobility of the tympanic membrane. In addition to pneumatic otoscopy, tympanometry or tympanography can be used to confirm what was seen with the eye.


Therapeutic Management


The emergence of resistant organisms has created much discussion around the use of antibiotics to treat AOM because spontaneous resolution of the infection occurs in about 80% of children. In 2004, the American Academy of Pediatrics (AAP) issued two policy recommendations regarding identification and management of AOM and OME in healthy children ages 2 months to 12 years (AAP, 2004; AAP Subcommittee on Otitis Media with Effusion, American Academy of Family Physicians, American Academy of Otolaryngology—Head and Neck Surgery, 2004). Recommendations include the following:


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Oct 8, 2016 | Posted by in NURSING | Comments Off on The Child with a Respiratory Alteration

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