NR 602 Quiz Questions and Answers, Quizzes of Nursing

Download NR 602 Quiz Questions and Answers and more Quizzes Nursing in PDF only on Docsity! Chamberlain College of Nursing NR 602 Week 2 Quiz Answers Restrictive Processes Restrictive disease is less common in pediatric patients and is characterized by decreased lung compliance with relatively normal flow rates. Examples of causative factors include neuromuscular weakness, lobar pneumonia, pleural effusion or masses, severe pectus excavatum, or abdominal distention. Key findings of restrictive lung disease are rapid respiratory rate and decreased tidal volume/capacity (Carter and Marshall, 2011). Defense Systems The respiratory defense system includes mechanical and biologic processes. Mechanical defenses include: • Filtering of particles • Warming and humidifying of inspired air • Clearing of airway through mucociliary and coughing actions • Spasm and breathing changes Approximately 75% of inspired air is warmed as it passes through the nose, paranasal sinuses, pharynx, larynx, and upper portion of the trachea. Final warming and humidifying of the airstream take place in the trachea and large bronchi. Heat and moisture are removed during the expiratory phase of respiration. The nose has a large surface area on which particles larger than 5 mm are trapped and filtered to prevent them from entering the lower airways. The trachea and bronchioles are lined with various defensive cells and mucus glands. Goblet cells secrete the mucous layer that lies on the tip of cilia. Particles entering the conducting airway are quickly cleared by the mucociliary defenses. Coughing is a reflex mechanism that has three phases: (1) inspiratory, (2) compressive, and (3) expiratory. Through forceful expiration FBs and other materials can be removed from the airways; coughing propels particles. Young infants and children cannot effectively expectorate mucus, so they swallow it. Loss of the cough reflex leads to aspiration and pneumonia. Temporary breathing cessation, reflex shallow breathing, laryngospasm, and even bronchospasm are compensatory efforts aimed at stopping foreign matter from further entry into the lower respiratory tract. 797However, these respiratory efforts offer limited protection and have significant drawbacks. Biologic processes that protect the respiratory system include: • Phagocytosis • Absorption of noxious gases in the vasculature of the upper airway • Absorption of particles by the lymph system Phagocytosis, aided by the secretory IgA plus interferon, lysozyme, and lactoferrin, is the principal antimicrobial defense. Particles reaching the alveoli can be phagocytized by alveolar macrophages and polymorphonuclear (PMN) cells, cleared from the lung by the mucociliary system, or carried by lymphocytes into regional nodes or the blood. These particles can take days to months to clear. The respiratory defense system is at risk for compromise from numerous environmental factors. Damage to epithelial cells is caused by a variety of substances and gases, such as sulfur, nitrogen dioxide, ozone, chlorine, ammonia, and cigarette smoke. Hypothermia, hyperthermia, morphine, codeine, and hypothyroidism can adversely alter mucociliary defenses. Dry air from mouth breathing during periods of nasal obstruction, tracheostomy placement, or inadequately humidified oxygen therapy results in dryness of the mucous membrane and slowing of the cilia beat. Cold air is also irritating to the lower airways. Phagocytic ability is also reduced by many substances, including ethanol ingestion and cigarette smoke. Hypoxemia, starvation, chilling, corticosteroids, increased oxygen, narcotics, and some anesthetic gases also impair phagocytosis. Recent acute viral infections can reduce antibacterial killing capacity. Damage from infection and chemical irritants may or may not be reversible. Recurrent respiratory infections in children merit investigation for immunodeficiency or other underlying diseases, such as primary ciliary dyskinesia or CF. The mnemonic SPUR (Bush, 2009) can help determine which children need further workup: Severe infection Persistent infection and poor recovery Unusual organisms Recurrent infection Immunodeficiencies should be considered if the child has four or more new ear infections in a year, two or more serious sinus infections, two or more pneumonias in a year, persistent oral candidiasis, failure to thrive, two or more deep seeded skin abscesses, 2 or more months on antibiotics without improvement, and/or the need for intravenous (IV) antibiotics to clear infections. Also consider immunodeficiencies if there is a family history of immunodeficiency or two or more deep skin infections (Modell et al, 2014). Assessment of the Respiratory System The history provides valuable information about the causes, progression, and potential complications of a child's respiratory condition. The physical examination and diagnostic testing allow the provider to determine the extent of respiratory distress. History History of the present illness can be assessed using the mnemonic PQRST: • Promoting, preventing, precipitating, palliating factors • Contacts: Are any family members or close contacts (e.g., day care, school) ill with similar signs and symptoms? • Prevention: Do you give your child any medications or supplements (include any herbs, botanicals, or vitamins) to try to prevent a cold? What are your hand washing practices? Do you encourage fluids when your child has a URI? Are the child's immunizations up to date? • Progression: Are the respiratory signs or symptoms increasing in severity, lessening, or about the same? Is the child easily fatigued, less active, having trouble sleeping, or working harder to breathe? • Treatment: Have any OTC, prescription drugs, herbs, supplements, or botanicals been used? Have any other treatment modalities been used, including folk cures or home remedies? • Quality or quantity • How severe are the symptoms? Is the illness interfering with school attendance or play? Are breathing problems affecting the child's ability to sleep and eat? • Region or radiation • Does the child complain of chest pain? • Severity, setting, simultaneous symptoms or similar illnesses in the past • Key signs and symptoms: Has the child had symptoms or signs of a daytime or nighttime cough, fever, vomiting, malaise, rhinorrhea, sore throat, lesions in the mouth, retractions, cyanosis, dyspnea, or increased respiratory effort? Table 32-1 lists key characteristics and causes of cough. TABLE 32-1 Key Characteristics of Cough, Common Causes, and Questions to Ask in a Pediatric History • How long has it lasted? How has it changed over time? • Family history • Do others in the family have a history of allergies or asthma? 798 • Is there any family history of immunodeficiency, ear-nose-throat, or respiratory problems? • Does anyone in the family have genetic diseases, such as CF or alpha 1-antitrypsin deficiency? • Are other family members ill? • Review of systems • Note any infections, constitutional diseases, or congenital problems that might have a respiratory component. • Environment • Does anyone in the family or in the day care setting smoke? Does the child live or attend school in an urban or industrial area subject to air pollution (e.g., near a major highway, industrial plant, or bus terminal)? Has the child or a family contact traveled recently and where? Physical Examination When determining respiratory distress, think about the total presentation and not just individual isolated findings. Consider the anxiety level, respiratory rate and rhythm, use of accessory muscles, color, breath sounds, grunting, and pulse oximetry results. Information pertinent to the physical examination of a child with suspected respiratory disease includes the following: • Measurement of vital signs and observation of general appearance: • A normal respiratory rate is age dependent and, if elevated, is a key indicator of lower respiratory involvement. • The level of anxiety, nasal flaring, and position of comfort are useful indicators of respiratory distress. 799Changes in skin color may be subtle or obvious, depending on the level of deoxygenation. Grunting is a sign of small airway disease. • Inspection of: • Nose: Look for rhinorrhea—clear, mucoid, mucopurulent; FBs, erosion, polyps, lesions, bleeding, septal position, and color of the mucous membrane. • Throat, pharynx, and tonsils: Look for lesions, vesicles, exudate, enlargement of any structure, or other abnormalities. If epiglottitis is a consideration, do not inspect the mouth or attempt to elicit a gag reflex (see discussion later in this chapter). • Chest: Look at the depth, ease, symmetry, and rhythm of respiration. These are key indicators of lower respiratory tract involvement. The use of accessory muscles and the presence of retractions should be noted. A prolonged expiratory phase is associated with respiratory obstruction in the lower airways. • Palpation or percussion of: • Chest: Percuss for signs of dullness or hyperresonance caused by consolidation, fluid, or air trapping. • Auscultation of the chest: • Upper tract: Pathology frequently causes noisy breathing, snoring, stridor, and musical or wheezing tracheal breath sounds and can be a source of referred breath sounds (Bohadana et al, 2014). • Lower tract: Pathology is suggested by fine crackles, coarse crackles, rhonchus, pleural friction rub, wheezing, and bronchial breath sounds (Bohadana et al, 2014). Upper Respiratory Tract The upper respiratory tract includes the nostrils, nasopharynx, larynx, upper part of the trachea, eustachian tubes, and sinuses. Air is warmed and humidified as it travels through the nasal passages, and coarse nasal hairs filter out particles. The nasal passages are lined with lysozymes, secretory immunoglobulin A (IgA), and immunoglobulin G (IgG) in nasal mucosa to defend against microbial invasion. The nasal mucosa is continuous and similar to the sinus mucosa except that the nasal mucosa is thicker with more glands. A blanket of mucus covers the surface epithelium of the nasal and sinus mucosa. The mucosal lining of the sinuses is composed of pseudostratified, ciliated columnar epithelium interspersed with mucus producing goblet cells (Rose et al, 2013). The mucociliary action of the paranasal epithelium moves secretions from the sinuses to the nasal cavity. The frontal, maxillary, and anterior parts of the ethmoid sinuses drain to the middle meatus of the nose, whereas the sphenoid and posterior parts of the ethmoid sinuses drain to the superior meatus of the nose. Secretions need to be able to move through patent ostia into the nose. The quality of secretions and normally functioning cilia are key factors in the movement of secretions into the nose. Inflammation of nasal mucosa frequently causes edema and disruption of the sinus secretions. If there is significant swelling of the ostia due to a URI or allergic inflammation, or mechanical or local obstruction, ostial obstruction results and obstruction of the sinus secretions occurs. Cilia movement and mucus flow allow the sinuses to be free of pathogens. The maxillary sinuses are present by the second trimester of gestation but are not fully pneumatized until a child is about 4 years old. Ethmoid sinuses develop by the fourth month of gestation and form the thin lateral walls of the orbit of the eye. They are pneumatized at birth and can be visualized on plain radiographs when the child is 1 to 2 years old. The sphenoid sinuses start to form in the first 2 years of life but remain rudimentary until age 6, which is when they become visible on radiographs. By 12 years old, they reach their permanent size, but not shape. As a result, the nasal cavity and paranasal sinuses reach adult proportion by age 12 (Cherry and Shapiro, 2009). The sinuses become clinically significant sites of infection at the following ages: • Maxillary and ethmoid sinuses: As early as late infancy • Sphenoid sinuses: Around 3 and 4 years old • Frontal sinuses: Around 6 to 10 years old The epiglottis deflects swallowed material toward the esophagus to protect the larynx. The vocal cords form a V-shaped opening known as the glottis.The subglottic space is beneath the vocal cords, and its walls converge toward the cricoid ring to form a complete ring of cartilage around the larynx. In children younger than 2 to 3 years old, the cricoid ring is the narrowest part of the airway; in older children and adults, the glottis is narrowest. The rings of tracheal cartilage support the trachea and the mainstem bronchi. 795 The trachea and airways of the infant and young child are more compliant than those of an adult. Hyperextension of the neck can constrict the airway of infants. Consequently, changes in intrapleural pressure lead to greater changes in an infant's or young child's airway compared with the effect that such changes would exert on adult airways, thereby causing an increased risk of airway collapse. Similarly, increased chest wall compliance in young infants makes them more vulnerable to adverse events, and their respiratory muscles cannot effectively handle sustained, intense respiratory workload that occurs during severe pulmonary illnesses. Bronchiolitis Bronchiolitis is also called infectious asthma, asthmatic bronchitis, wheezy bronchitis, or virus-induced asthma. Bronchiolitis is a disease that causes inflammation, necrosis, and edema of the respiratory epithelial cells in the lining of small airways, as well as copious mucus production (Ralston et al, 2014). Bronchiolitis is characterized by the insidious onset of URI symptoms over 2 to 3 days that progresses to lower respiratory symptoms that last as long as 10 days (Da Dalt et al, 2013). It is a communicable disease found primarily in infancy to 2 years old (Teshome et al, 2013) that accounts for 10% of visits to a primary provider the first 2 years of life (Schroeder and Mansbach, 2014). Bronchiolitis is a common diagnosis used for an infant seen with wheezing for the very first time and is the leading cause of hospitalizations for infants. The most common age for severe disease occurs in infants between 2 to 3 months due to the natural postnatal nadir in maternal immunoglobulins received via the placenta during the last trimester (Da Dalt et al, 2013). More than 80% of the cases of bronchiolitis occur in infants younger than 1 year of age with a male-to-female ratio of 1.5 : 1 (Welliver, 2009). In mild cases, symptoms can last for 1 to 3 days. In severe cases, cyanosis, air hunger, retractions, and nasal flaring with symptoms of severe respiratory distress within a few hours may be seen. Apnea can occur with a wide range of prevalence reported (Ralston et al, 2014) and may require mechanical ventilation. Newer understanding of the pathophysiology in bronchiolitis points to airway obstruction as a result of epithelial and inflammatory cellular debris due to infiltration of the virus into the small bronchiole epithelium and alveolar epithelial cells (AEC), types I and II. Membranous pneumatoceles, or AEC type I, are dominant and cover 96% of the respiratory tree. Their role is in gas exchange, whereas AEC type II are important to surfactant production (Chuquimia et al, 2013). It is a disease of the small bronchioles that are 2 mm in size. There is a sparing of basal cells in the bronchiole. The main lesion is epithelial necrosis, which leads to a dense plugging of the bronchial lining. This results in increased airway resistance, atelectasis, hyperinflation, and increased mucus production (Teshome et al, 2013). Bronchiolitis is a viral illness predominantly caused by RSV, especially in outbreaks (Da Dalt et al, 2013; Welliver, 2009). Recent data suggest that up to 30% of infants with severe bronchiolitis are co-infected with two or more viruses (Mansbach et al, 2012). In descending order after RSV, rhinovirus, parainfluenza, adenovirus, and mycoplasma are causes (Teshome et al, 2013). Metapneumovirus was discovered in 2001 and is a cause of bronchiolitis 7% of the time. Human bocavirus is a common co-infecting virus with RSV and is found up to 80% of the time (Teshome et al, 2013). RSV-specific immunoglobulin E (IgE), eosinophils, and chemokines may play a role in the pathogenesis of bronchiolitis (Welliver, 2009). Adenovirus and RSV can cause long-term complications. The incubation period for RSV is 2 to 8 days and typically occurs from November through March with virtually no outbreaks in the summer (Teshome et al, 2013; Welliver, 2009). Fever tends to be higher with adenovirus versus RSV (Teshome et al, 2013). Respiratory viruses are spread by close contact with infected respiratory secretions or fomites and can live on 818surfaces for up to 30 minutes (Teshome et al, 2013). The most frequent mode of transmission is hand carriage of contaminated secretion. The source of infection is an older child or adult family member with a “mild” URI. Older children and adults have larger airways and tolerate the swelling associated with this infection better than infants do. Most cases of bronchiolitis resolve completely, but recurrence of infection is common, and symptoms tend to be mild. Infants who are at higher risk of severe RSV include children with major chronic pulmonary disease, such as CF, neuromuscular disorders, or bronchopulmonary dysplasia; premature birth before 35 weeks of gestational age; and infants with significant hemodynamically difficulties due to congenital heart disease (Teshome et al, 2013). Other risk factors for severe RSV disease are male gender, crowded household, lack of breastfeeding, smoke exposure, day care attendance, having siblings, birth during the winter months, and immunodeficiency (Da Dalt et al, 2013). Clinical Findings History The following are reported: • Initial presentation: Typically the illness begins with URI symptoms of cough, coryza, and rhinorrhea and progresses over 3 to 7 days (Smith, 2011). • Gradual development of respiratory distress marked by noisy, raspy breathing with audible expiratory wheezing. • Low-grade to moderate fever up to 102° F (38.9° C). • Decrease in appetite. • No prodrome in some infants; rather they have apnea as the initial symptom. • Usually the patient's course is the worst by 48 to 72 hours after the wheezing starts and then the patient starts to improve. If the child has a bacterial illness, the child will continue to worsen with a high fever. Physical Examination Findings include the following: • Upper respiratory findings • Coryza • Mild conjunctivitis in 33% (Welliver, 2009) • Progressive stridor or stridor at rest • Apnea • Increasing respiratory rate (sleeping rate of greater than 50 to 60 breaths per minute) • Restlessness, pallor, or cyanosis • Hypoxia recorded by either blood gas (partial pressure of oxygen [PO2] less than 60 mm Hg) or pulse oximetry (less than 92% on room air) • Rising partial pressure of carbon dioxide (PCO2) (recorded by blood gas) • Inability to tolerate oral feedings • Depressed sensorium 820 • Presence of chronic cardiovascular or immunodeficiency disease • Parent unable to manage at home for any reason In-hospital management focuses on supportive care, focusing on suctioning of nares, humidified supplemental oxygen, and elevation of the child to a sitting position at a 30- to 40-degree angle. IV hydration (or in infants nasogastric hydration) is needed when respiratory distress interferes with nursing or bottle feeding. Occasionally a hospitalized child is not able to be quickly weaned back to room air. Home management of these infants requiring oxygen is sometimes difficult and may require a team approach, including involvement of a pediatric health care provider and home care nursing visits. Strict outpatient follow-up is mandatory for as long as the child is receiving home oxygen. Complications The first 48 to 72 hours after the onset of cough are the most critical. Apneic spells are common in infants. The child is ill-appearing and toxic but gradually improves. The fatality rate associated with bronchiolitis is about 1% to 2%. Infants younger than 12 weeks old and those with underlying cardiorespiratory or immunodeficiency are at risk for severe disease. Prolonged apnea, uncompensated respiratory acidosis, and profound dehydration secondary to loss of water from tachypnea and an inability to drink are the factors leading to death in young infants with bronchiolitis. In some children, bronchiolitis can cause minor pulmonary function problems and a tendency for bronchial hyperreactivity that lasts for years. RSV bronchiolitis has been associated with the development of asthma, but its role in the causality of asthma is still debated. Recurrent episodes of wheezing can be seen during childhood in patients with a history of bronchiolitis. This persists into adolescence with 10% of the children still wheezing. However, this figure may not be different from the general population (Welliver, 2009). Prevention Palivizumab (Synagis) is an RSV-specific monoclonal antibody used to provide some protection from severe RSV infection for high-risk infants (see Chapter 24 for guidelines). Educate caregivers about decreasing exposure to and transmission of RSV, especially those with high-risk infants. Advice should include limiting exposure to child care centers whenever possible; use of alcohol-based hand sanitizers if available or hand washing if the alcohol-based hand sanitizer is not available (Ralston et al, 2014); avoiding tobacco smoke exposure; and scheduling RSV prophylaxis vaccination, when indicated. Foreign Body Aspiration The symptoms and physical findings associated with aspiration of an FB depend on the nature of the material aspirated, plus the location and degree of the obstruction. The cough reflex protects the lower airways, and most aspirated material is immediately expelled with coughing. Onset of a sudden episode of coughing without a prodrome or signs of respiratory infection should make the provider suspicious of FB aspiration. Objects that are either too large to be eliminated by the mucociliary system or cannot be expelled by coughing eventually lead to some form of respiratory symptomatology. Obviously a large FB occluding the upper airway can cause suffocation. A small object in the lower respiratory tree may not produce symptoms for days to weeks. Obstruction results from either the FB itself or edema associated with its presence. Hot dogs are one of the most common causes of fatal aspiration. Although toddlers commonly aspirate FBs, aspiration occurs in children of all ages. Laryngeal Foreign Body Clinical Findings History. A rapid onset of hoarseness and the development of a chronic croupy cough with aphonia are reported. Be suspicious of an FB aspiration in children with sudden episode of cough, unilateral wheezing, and or recurrent pneumonia. Physical Examination. The child can present with cough, unilateral wheezing, clinical signs of pneumonia, hemoptysis, dyspnea, and cyanosis. Diagnostic Studies. Expiratory or lateral decubitus chest radiographs should be ordered. Because most FBs are not radiopaque, radiographs may not be useful in the diagnosis. However, if a chest radiograph does not reveal an FB but shows local emphysema—an area that does not inflate or deflate—suspect FB aspiration (Carter and Marshall, 2011). If the history suggests FB aspiration, bronchoscopy must be undertaken. Direct laryngoscopy might reveal the presence of foreign matter. Tracheal Foreign Body Clinically the child has a history of a brassy cough, hoarseness, dyspnea, and possibly cyanosis. The most characteristic signs of tracheal FB aspiration are the homophonic wheeze and the audible slap and palpable thud sound produced by the momentary expiratory effect of the FB at the subglottic level. Bronchial Foreign Body Most objects are aspirated into the right lung. A careful medical history may reveal a forgotten episode of choking. Clinical Findings History. An initial episode of coughing, gagging, and choking is described. Some objects are inhaled with no choking (e.g., a spear of grass). Blood-streaked sputum may be expectorated, but hemoptysis rarely occurs as an early symptom. On rare occasions hemoptysis does occur as an initial symptom months or years after the aspiration event took place. Children aspirating a metallic object often complain of a “metallic taste” in their mouths. 821 Physical Examination. The initial clinical findings are similar to those seen in either tracheal or laryngeal FB aspiration. If the object is nonobstructive and nonirritating, few or no initial symptoms may be seen. The child may have limited chest expansion, decreased vocal fremitus, atelectasis, or emphysema-like changes with resulting hyporesonance or hyperresonance. Diminished breath sounds are often found. A small object can act as a bypass valve, and homophonic wheezes can be heard. Crackles, rhonchi, and wheezes can be present if air movement is adequate. If the acute episode is missed or not appreciated, a latent period of mild “wheezing” or cough may be evident. Diagnostic Studies. Clinical suspicion is the clue to this diagnosis. Inspiratory and forced expiratory chest radiographs and chest fluoroscopy are useful in identifying radiolucent FBs (Fig. 32-1). Management The patient should be referred to a pulmonary specialist for bronchoscopy. If the object is removed via bronchoscopy before permanent damage occurs, recovery is usually complete. Secondary lung infections and bronchospasms should be treated as suggested in the section on management of pneumonia in this chapter and asthma in Chapter 25. Complications If the FB is vegetable matter, vegetal or arachidic bronchitis can occur. This severe condition can be characterized by sepsis-like fever, dyspnea, and cough. If the material has been there for a long time, suppuration can occur. Lobar pneumonia, intractable wheezing, status asthmaticus can develop. Emphysema or atelectasis can also occur as the result of a large obstruction caused by a bronchial FB. Prevention. Anticipatory education regarding prevention of FB aspiration should be part of well-child supervision guidance. Parents should be cautioned about high-risk foods (e.g., whole carrots, nuts, popcorn, and hot dogs). Young children need to be supervised closely as they put small objects into their mouths as well as when they cry, shout, run, and play with food or other objects in their mouths. Nonbacterial and Bacterial Pneumonia Pneumonia is a lower respiratory tract infection associated with fever and respiratory symptoms involving the parenchyma of the lung (Gereige and Laufer, 2013). It can be lobar, interstitial, or bronchopneumonia. Lobar pneumonia involves infection of the alveolar space that results in consolidation; it is described as “typical” pneumonia. Atypical pneumonia describes patterns of consolidation that are not localized. In interstitial pneumonia, cellular infiltrates attack the interstitium, which makes up the walls of the alveoli, the alveolar sacs and ducts, and the bronchioles; this type of pneumonia is typical of acute viral infections but may also be a chronic process. Viral infection affects the lung defenses by altering normal secretions, inhibiting phagocytosis, modifying the normal bacterial flora, and disrupting the epithelial layer. Many childhood viruses set the stage for secondary bacterial infection. Children with immunologic problems or chronic illnesses are prone to primary bacterial pneumonia and experience recurrent pneumonias or fail to clear the initial infection completely. Bronchial pneumonia is associated with bacterial infection 824with multiple areas of consolidation involving one or more pulmonary lobules. Pneumonitis is a general term used to describe lung inflammation that may or may not be associated with consolidation. Community-acquired pneumonia is acquired in the community as opposed to hospital-acquired or nosocomial pneumonia. In neonates, the risk factors for early onset pneumonia include prolonged rupture of membranes, maternal amnionitis, premature delivery, fetal tachycardia, or maternal intrapartum fever. The risk factors for late onset pneumonia include having anomalies of the airway, severe underlying disease, prolonged hospitalization, neurologic impairment, or nosocomial infection from poor hand washing or overcrowding. Risk factors for childhood pneumonia include male gender, coming from a lower socioeconomic class, poor nutrition, lack of breastfeeding, exposure to cigarette smoke (either passive or active), alcohol use, drug use, having underlying cardiopulmonary disease or neuromuscular disease, gastroesophageal reflux, tracheoesophageal fistula, or congenital and acquired immunodeficiency (Gereige and Laufer, 2013). Bacterial pneumonia occurs as a primary infection caused by organisms that spread from the nasopharynx or as a secondary complication of a viral pneumonia (Bradley et al, 2011). Primary bacterial pneumonia is less common in childhood than secondary bacterial infection after a viral infection. S. pneumoniae is the leading cause of bacterial pneumonia in all age groups except newborns (Gereige and Laufer, 2013). Certain bacterial pneumonias have a specific pattern of disease: S. pneumoniae causes a lobar pneumonia, whereas community- Characteristi c Bacterial Viral Mycoplasma pneumonia and Chlamydophi la pneumonia Chlamydia trachomatis Treatment Depends on bacteria and age of child; amoxicillin, penicillin, methicillin, cefuroxime, gentamicin, vancomycin Supportive care Erythromycin Azithromycin Clarithromycin Erythromycin CBC, Complete blood count; RSV, respiratory syncytial virus; URI, upper respiratory infection; WBC, white blood cell. TABLE 32-7 Age Variants in Pneumonia Microorganisms Age Viral Organisms Bacterial Organisms Neonatal Cytomegalovirus (CMV) More common Group B streptococci Gram-negative enteric bacteria Listeria Chlamydia trachomatis Uncommon organisms Streptococcus pneumoniae Group D streptococcus Anaerobes Infants Most common Respiratory syncytial virus (RSV) Parainfluenza Influenza Adenoviruses Metapneumovirus Less common S. pneumoniae Haemophilus influenzae Mycoplasma pneumonia Mycobacterium tuberculosis Bordetella pertussis Pneumocystis jiroveci Preschool children Most common RSV Parainfluenza Influenza Adenoviruses Metapneumovirus Bocavirus role is not clear Less common S. pneumoniae H. influenzae M. pneumoniae M. tuberculosis Chlamydophila pneumoniae Age Viral Organisms Bacterial Organisms School-age children Respiratory viruses as above M. pneumoniae C. pneumoniae S. pneumoniae M. tuberculosis Adapted from Ranganathan SC, Sonnappa S: Pneumonia and other respiratory infections, Pediatr Clin North Am 56(1):140, 2009. Conjugated vaccines, such as Prevnar 13 and HIB vaccine, have decreased the incidence of these bacteria. The introduction of Prevnar 13 has decreased the incidence of pneumococcal pneumonia. Pneumococcal pneumonia occurs most commonly in the late winter and early spring after the cycle of viral URIs. Asymptomatic carriers play a more important role in dissemination of disease than sick contacts. Children younger than 4 years old suffer the highest attack rate. Clinical Findings in Infants and Young Children The hallmark of pneumonia is fever and cough in all age groups. Tachypnea and increased work of breathing may precede coughing. Cough, hypoxia, nasal flaring, rales, retractions, and rhonchus lung sounds are specific but not as sensitive for pneumonia. Viral pneumonia tends to have an insidious onset that is associated with more wheezing than what is typically noted with bacterial pneumonia. In contrast, lobar pneumonia (caused by pneumococcal pneumonia) typically presents with fever, cough, and decreased breath sounds in the area of the pneumonia. However, the child may present with a mixture of symptoms. Pneumonia can cause referred symptoms, such as abdominal pain, which may be present in a child with a diaphragmatic pneumonia or radiating neck pain that may be associated with upper lobe pneumonias. Irritation of the pleura causes the chest pain in children with pneumonia. History The following may be reported (Bradley et al, 2011; Gereige and Laufer, 2013; Iroh Tam, 2013): • Neonate • History of group B streptococcal or C. trachomatis infection in the mother 825 • Prenatal drug use or lack of prenatal care as risk factors for SBI in the neonate • With C. trachomatis, the infant is typically afebrile; prior, concurrent, or no history of inclusion conjunctivitis reported • Infant • Slower onset of respiratory symptoms, cough, wheezing, or stridor with less prominent fever suggests viral pneumonia (bacterial pneumonia is less likely in a wheezing child) • Determine mother's HIV status or infant's exposure to tuberculosis • Child and adolescent • Get immunization history and travel history of the family • Tuberculosis status • Evaluate sick contacts at home • Evaluate for possible FB aspiration • Initial history of a mild URI for a few days—similar for both bacterial and viral • Abrupt high fever with temperatures greater than 103.3° F (39.6° C), chills, cough, and dyspnea suggest bacterial pneumonia • Other manifestations include restlessness, shaking chills, apprehension, shortness of breath, malaise, and pleuritic chest pain; irritation of the pleura causes chest pain Physical Examination The health care provider needs to pay close attention to the general appearance, looking at the work of breathing, assessing for hypoxia, and evaluating tachypnea, which is considered to be the most valuable sign for ruling out pneumonia. Early onset pneumonia in the neonate presents within the first 3 days of life with: • Respiratory distress, apnea, tachycardia, poor perfusion • Tachycardia • No fever, or fever only with subtle or no physical findings Typical findings seen in all types of pneumonia include: • Nasal flaring, grunting, retractions • Tachypnea (may be the only clue), generally more than 60 breaths per minute in infants younger than 2 months old, more than 50 breaths per minute in children 2 to 82611 months old, or more than 40 breaths per minute at rest in children 1 to 5 years old • Tachycardia, air hunger, and cyanosis are significant findings • Fine crackles, dullness, diminished breath sounds • To encourage preschoolers and school-age children to breathe deeply, ask them to blow crumbled papers off your hands or use a phone application that allows them to “blow up a balloon” In bacterial pneumonia: • Fever, hypoxia, lethargy • Splinting the affected side to minimize pleuritic pain or lying on the side in a fetal position helps compensate for decreased air exchange and improves ventilation • Tachypnea and retractions • Progression to delirium, circumoral cyanosis, and posturing • Presence of a pleural effusion and signs of congestive heart failure • Abdominal distention, downward displacement of the liver or spleen In viral pneumonia: • Wheezing • Downward displacement of the liver or spleen In primary atypical bacterial pneumonia (C. trachomatis): • C. trachomatis pneumonia characterized by repetitive, staccato cough with tachypnea, cervical adenopathy, crackles, and rarely wheezing • Conjunctivitis is associated with C. trachomatis in infants (Iroh Tam, 2013) Diagnostic Studies A chest x-ray should not be routinely performed in children with pneumonia (Bradley et al, 2011). However, a chest x-ray is recommended for any child older than 3 months who fails to improve after 72 hours on the standard treatment or who is being admitted. Follow-up films are not needed in patients who have an uneventful recovery. Blood cultures should not be routinely used in outpatient setting unless the child fails to improve or deteriorates on antibiotic therapy. Blood cultures should be done on children who are admitted with moderate to severe pneumonia. Sputum cultures can be used in hospitalized children who can produce sputum. Urine antigen detection tests for S. pneumonia are not recommended, because the false-positive rate is high. 827 Rapid tests for influenza and other respiratory viruses are helpful, whereas a CBC is not recommended in outpatient settings but may be helpful in inpatient settings. Acute phase reactants do not differentiate between viral and bacterial pneumonia and are not recommended for fully immunized children who are being treated as an outpatient. These tests may be useful for more seriously ill patients. Testing for M. pneumonia when the Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* diarrhea, bloody stools, abdominal pain, fever, nausea, vomiting Mild to moderate illness is characteriz ed by watery diarrhea, low-grade fever, and mild abdominal pain wee ks of antib iotic use; can occu r with out bein g asso ciate d with such treat ment or from stool of other coloniz ed or infecte d people by the fecal- oral route positive gross blood, leukocytes; CBC: ↑ WBCs; ESR normal clindamycin , second- and third- generation cephalospor ins). Fluids and electrolyte replacement are usually sufficient. If antibiotic is still needed or illness is severe, treat with oral metronidazo le (drug of choice in children) or vancomycin for 7 to 10 days. Supplement with probiotics. Lactobacillu s GG, Saccha romyces boulardii ar e recommend ed (Jones, 2010; Shane , 2010). Complication s include pseudomem branous colitis, toxic megacolon, colonic perforation, relapse, Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* intractable proctitis, death in debilitated children. Enterohemorrhag ic Escherichi a coli(EHEC) including E. coli O157:H7 and other Shiga toxin– producing E. coli(STEC) 1 to 8 days Severe diarrhea that is often bloody, abdominal pain and vomiting Usually little or no fever More common in children <4 years old 5 to 10 days Underco oked beef, especia lly hambur ger, unpaste urized milk and juice, raw fruits, vegeta bles (e.g., sprouts , spinach , lettuce) , salami (rarely) Contami nated water; petting zoos Stool culture; E. coliO157:H7 requires special media to grow. If E. coliO157:H7 is suspected, specific testing must be requested. Shiga toxin testing may be done using commercial kits; positive isolates should be forwarded to public health laboratories for confirmation and serotyping. Stool grossly positive for blood. Supportive care: Monitor CBC, platelets, and kidney function closely. E. coli O157:H 7 infection is also associated with HUS, which can cause lifelong complicatio ns. Studies indicate that antibiotics may promote the developmen t of HUS. Enterotoxigenic E. coli(ETEC) and enteroadheren t E. coli (frequent cause of 1 to 3 days Watery diarrhea, abdominal cramps, some vomiting; often cause of 3 to >7 days Water or food contam inated with Stool culture. ETEC requires special laboratory techniques for identification. If suspected, Supportive care: Antibiotics are rarely needed except in severe cases. Recommend Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* traveler's diarrhea) mild traveler's diarrhea human feces must request specific testing. ed antibiotics include TMP-SMX and quinolones. See www.cd c.gov/travel. Listeria monocytogen es Variable , rang ing from 1 day to mor e than 3 wee ks Rare, but serious Fever, muscle aches, and nausea or diarrhea Pregnant women may have mild flulike illness, and infection can lead to premature delivery or stillbirth Older adults or immunoco mpromise d patients may have bacteremia or meningitis Infants infected from mother at risk for sepsis or meningitis Variable Thrives in salty and acidic conditi ons, such as fresh soft cheeses , ready- to-eat deli meats, hot dogs; also unpaste urized milk, inadeq uately pasteur ized milk; multipl ies at low temper atures, even in properl y refriger Blood or cerebrospinal fluid cultures. Asymptomatic fecal carriage occurs; therefore, stool culture usually not helpful. Antibody to listeriolysin O may be helpful to identify outbreak retrospectively. Initial therapy with IV ampicillin and an aminoglyco side usually gentamicin, recommend ed for severe infections. Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* vomiting is not usually severe to fecal contam ination of water supplie s or street- vended foods n, or TMP- SMX; if resistance shown to any of those, use IM ceftriaxone, cefotaxime; or azithromyci n or quinolones. A vaccine exists for S. typhi in certain cases. Shigella spp. Varies from 1 to 7 days , but typic ally is 1 to 3 days Abdominal cramps, fever, and diarrhea; Stools may contain blood and mucus Seen most commonly in those 6 months old to 3 years old 4 to 7 days Food or water contam inated with human fecal materia l Usually person- to- person spread, fecal- oral transmi ssion Ready- to-eat foods touche d by infecte d food worker s (e.g., Routine stool cultures; gross blood, leukocytes. CBC: normal or slightly ↑ WBCs with left shift Supportive care: If antibiotics indicated (severe disease, dysentery, immunocom promised), test first for susceptibilit y. Oral ampicillin (amoxicillin less so) or TMP-SMX recommend ed in the United States; for organism resistance, use IM ceftriaxone for 2 to 5 days; PO ciprofloxaci Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* raw vegeta bles, salads, sandwi ches) n; azithromyci n (oral cephalospor ins not useful). If child is at risk of malnutrition , supplement with vitamin A (200,000 international units). No swimming in recreational pools/slides for 1 week after symptoms resolve. Yersinia enterocolytic aand Y. pseudotuberc ulosis Typicall y 4 to 6 days with a rang e of 1 to 14 days Appendicitis -like symptoms (diarrhea and vomiting, fever, and RLQ pain) occur primarily in older children and young adults May have a scarlatinif orm rash or erythema nodosum with Y. 1 to 3 wee ks, usua lly self- limit ing Underco oked pork, unpaste urized milk, tofu, contam inated water Infection has occurre d in infants whose caregiv ers handle d chitterl ings Stool, vomitus, or blood culture. Yersini a requires special medium to grow. If suspected, must request specific testing. Serology is available in research and reference laboratories. Supportive care: If septicemia or other invasive disease occurs, antibiotic therapy with gentamicin or cefotaxime (doxycyclin e and ciprofloxaci n also effective) after susceptibilit Etiology Incubat ion Perio d Signs and Symptoms Duratio n of Illnes s Route of Transmi ssion Laboratory Testing Treatment and Complicatio ns* pseudotub erculosis Seen in all ages y testing is done. Pyloric Stenosis Pyloric stenosis is characterized by hypertrophied pyloric muscle, causing a narrowing of the pyloric sphincter. Pyloric stenosis occurs in 3 per 1000 live births, with a fourfold increase in males compared with females (Hunter and Liacourus, 2011b). It tends to be familial and is seen more commonly in Caucasian first-born males. Clinical Findings History. • Regurgitation and non-projectile vomiting during the first few weeks of life • Projectile vomiting beginning at 2 to 3 weeks old • Insatiable appetite with weight loss, dehydration, and constipation • An association of pyloric stenosis with the administration of erythromycin in the first 2 weeks of life has been demonstrated Physical Examination. • Weight loss • Nonbilious vomitus that can contain blood • A distinct “olive” mass that is often palpated in the epigastrium to the right of midline • Reverse peristalsis visualized across the abdomen Diagnostic Studies. Ultrasound, with measurement of the pyloric muscle thickness, is used in most centers. An upper gastrointestinal series demonstrates a “string sign,” indicating a fine, elongated pyloric canal may be required if ultrasound is unavailable or inconclusive. Management and Prognosis Surgical intervention (pyloromyotomy) is indicated after correction of fluid and electrolyte imbalance. Vomiting can continue for a few days after surgery, although it is not as significant as it was preoperatively; feedings should be introduced gradually. The prognosis is excellent. Hirschsprung Disease (Congenital Aganglionic Megacolon) Hirschsprung disease is an absence of ganglion cells in the bowel wall, most often in the rectosigmoid region, resulting in a portion of the colon having no motility. This disorder occurs in 1 in 5000 births. It is the most common cause of neonatal obstruction of the colon and accounts for approximately 33% of all neonatal obstructions. The disease is familial, affects males four times more commonly than females, and is common in children with trisomy 21. Additional anomalies are sometimes present (Hunter and Liacourus, 2011b). Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* to 14 days weight, stomach cramps, nausea, vomitin g, fatigue, myalgia, low- grade fevers month s (various types of fresh produce [importe d berries, lettuce]) to examine water or food. Entamoeba histolytica Commonl y 2 to 4 weeks (know n to also range from days, month s, to years) ; fecal- oral trans missio n Can be asympto matic with nonspec ific complai nts of diarrhea, lower abdomin al pain In invasive disease (amebic colitis) sympto ms of increasi ng diarrhea, bloody diarrhea, lower abdomin al pain, tenesmu s, weight loss progress over a Weeks to years, depen ding on respon se to treatm ent; no drug is compl etely effecti ve Spread by fecal- oral route Stool examination for trophozoites or cysts; PCR, isoenzyme analysis, monoclonal antibody– based antigen; enzyme immunoassay ; ultrasounds and CT scans to identify suspected liver abscess or other extraintestinal infection. Asymptomati c cyst excreters: Luminal amebicide (iodoquinol , paromomyc in, diloxanide). Mild to moderate or severe involvemen t/liver abscesses: metronidaz ole or tinidazole followed by luminal amebicide. Follow-up stool examinatio n after treatment. Perform stool examinatio ns on household members or Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* 1- to 3- week period; occasion al fever Advanced disease hepatom egaly, liver tenderne ss other suspected contacts. Do not treat with corticostero ids or antimotility drugs. Complicati ons include liver abscess, ameboma. Giardia intestinalis 3 weeks Can include bouts of watery diarrhea ; abdomin al pain, greasy, foul- smelling stools; bloody diarrhea (rare); flatulenc e; abdomin al distentio n; anorexia ; weight loss; FTT; anemia; asympto matic infectio Pending effecti ve treatm ent Fecal-oral or contami nated food or water. Water can be contami nated by Giar dia from dogs, cats, beavers, and other animals. Stool specimens for trophozoites or cysts using staining methods; antigens using enzyme immunoassay ; PCR techniques. Increased sensitivity by obtaining three or more specimens every other day and by rapid examination of stool (can be placed in a fixative). Correct for any dehydration or electrolyte imbalance. Tinidazole, metronidaz ole, nitazoxanid e drugs of choice. Albendazol e, mebendazol e effective also in children with fewer side effects. Consult for those immunoco mpromised. Contact local health department s in cases of outbreaks. Infected individuals Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* n common should not use recreational water sources for swimming until 2 weeks after symptoms resolve. Filtration, boiling, chemical disinfection may be required for drinking water. Some infections are self- limited and treatment is not required. Dehydratio n and electrolyte abnormaliti es can occur and should be corrected. Complication s: Debilitating disease leading to malabsorpti on; anorexia; weight loss; FTT. Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* hygiene, proper handling of underwear and diapers. Ascaris lumbricoides( roundworm) 8 weeks from egg ingesti on to adult egg- laying capaci ty Weight loss, malnutri tion; worms can be seen in vomitus and stools; can cause cough, fever, chest discomf ort if pass through lungs (not a common occurren ce) Children can have large worm burdens Stressful conditio ns (fever, illness) and some anthelmi ntic drugs can cause 12 to 18 month s witho ut treatm ent Fecal-oral from ingestio n of eggs from contami nated food (fruit, vegetabl es) or soil (where incubati on occurs; adult worms live in small intestine and eggs are excreted in feces). Larvae migrate from intestine s via portal blood to liver and lungs, ascend through tracheob Stool/vomitus/nar es: Worms seen via microscopy. CBC: Marked eosinophilia. Have laboratory check for all concurrent worm infestations in order to treat all worms appropriately. Albendazole, mebendazol e, ivermectin; surgical intervention if necessary. Complication s: Impaired nutritional status of children and growth; bowel or biliary obstruction, peritonitis, obstruction of common bile duct (biliary colic, cholangitis, pancreatitis ); Löffler syndrome due to allergic response as larvae migrate to the lungs. Reinfection common. Globally, most common human intestinal nematode. Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* adults to migrate ronchial tree to pharynx, to intestine s again to develop into adults. Found in areas where human feces are used for fertilizer . Taenia (tapewor m) (T. saginata[beef ]; T. solium[pork]) 2 to 3 month s after larvae ingest ed to feces excret ion Worm(s) may be seen in perianal region May be asympto matic or have abdomin al pain, nausea, diarrhea, excessiv e appetite Several years before cystic ercosi s sympt oms eviden t Fecal-oral from ingestio n of water or food contami nated with eggs or from ingested cysts or larvae in inadequ ately cooked pork or beef. Stool microscopy: ova seen. Praziquantel, niclosamide , nitazoxanid e. Complication s: Systemic cysticercosi s from T. solium(visc era, brain, muscle invasion with possible seizures). Etiology Incubatio n Period Signs and Symptom s Duration of Illness Route of Transmis sion Laboratory Testing Treatment* Trichuris trichiura(whi pworm) 12 weeks Asymptoma tic unless infestati on is heavy; abdomin al pain, tenesmu s, bloody diarrhea with mucus; can mimic IBD; growth retardati on Fecal-oral from contami nated soil (where eggs incubate ), water, and/or food (embeds in mucosal lining of large intestine s). Not spread person to person. Stool microscopy or concentration techniques. Mebendazole , albendazole , ivermectin for 3 days; can reexamine stools after 2 weeks to ensure resolution. Complication s: Chronic colitis, rectal prolapse, compromis ed nutritional status, growth retardation. *See Table 33-15 for dosages. CBC, Complete blood count; CT, computed tomography; FTT, failure to thrive; IBD, inflammatory bowel disease; PCR, polymerase chain reaction; TMP-SMX, trimethoprim-sulfamethoxazole. TABLE 33-15 Medications for Treatment of Parasite Infestations* Drug Dosage Albendazole (Albenza): Take with food. The tablet may be crushed or chewed and swallowed with a drink of water. Ascariasis: 1 year old: 200 mg once; >2 years old: 400 mg once Taenia solium: 15 mg/kg/day in 2 doses × 8 to 30 days; can be repeated as necessary (maximum 400 mg per dose) The American Academy of Otolaryngology—Head and Neck Surgery (AAO-HNS) states that 10% of infants younger than 1 year old with regurgitation develop significant complications (GERD) (AAO-HNS, 2011). Risk factors include prematurity, neurologic impairment, obesity, CF, hiatal hernia, and family history of GERD. Clinical Findings Common signs and symptoms by age that should lead the clinician to suspect GERD are found in Table 33- 4; 845although, according to the guidelines, there is no symptom or symptom complex that is diagnostic of GERD or predicts response to therapy. In older children and adolescents, history and physical examination may be sufficient to diagnose GERD. The most common symptom is “heartburn.” Recurrent regurgitation with or without vomiting, weight loss or poor weight gain, ruminative behavior, hematemesis, dysphagia, and respiratory disorders such as, wheezing, stridor, cough, apnea, hoarseness, and recurrent pneumonia are also associated with GERD. TABLE 33-4 Symptoms and Signs that May Be Associated with Gastroesophageal Reflux Symptoms and Signs that Vary by Age Symptoms for All Children Signs for All Children Infancy: Regurgitation; signs of esophagitis (irritability, arching, choking, gagging, feeding aversion); FTT. Usually symptoms resolve between 12 and 24 months of age. Obstructive apnea, stridor, lower airway disease by which reflux complicates a primary airway disease (e.g., bronchopulmonary dysplasia). Otitis media, sinusitis, lymphoid hyperplasia, hoarseness, vocal cord nodules, laryngeal edema. Child and adolescent: Regurgitation during preschool years, complaints of abdominal and chest pain, neck contortions (arching, turning of head), asthma, sinusitis, laryngitis Recurrent regurgitation with/without vomiting Ruminative behavior Heartburn or chest pain Hematemesis Dysphagia, odynophagia Respiratory disorders, such as wheezing, stridor, cough, hoarseness, persistent throat clearing or cough Halitosis Esophagitis Esophageal stricture Barrett esophagus Laryngeal/pharyngeal inflammation Recurrent pneumonia Anemia Dental erosion Apnea spells Apparent life- threatening events Weight loss or poor weight gain FTT, Failure to thrive. Adapted from Vandenplas Y, Rudolph C, Di Lorenzo C, et al: Pediatric gastroesophageal reflux clinical practice guidelines: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN), J Pediatr Gastroenterol Nutr 49(4):498–547, 2009, p 519. History Box 33-4 summarizes the history for GERD that should be collected according to the national guidelines. Warning signs that merit urgent investigation of vomiting are found in Box 33-5. Box 33-4 H i s t or y for t he Ch i l d w i t h Sus pe c t ed G as t r oe s ophage a l Re f l ux Di s e as e Feeding and Dietary History • Amount/frequency (overfeeding) • Preparation of formula • Observe the child during a feeding (clinician) • Recent changes in feeding type or technique • Position during feeding, burping technique and frequency Behavior during Feeding • Choking, gagging, coughing, arching, discomfort, refusal Pattern of Vomiting • Frequency and amount, pain, forceful • Blood or bile • Associated fever, lethargy, diarrhea Medical History • Prematurity and newborn screen results • Growth and development, previous weight and height gain (growth charts) • Past surgery, hospitalizations • Recurrent illnesses, especially croup, pneumonia, asthma • Symptoms of hoarseness, fussiness, hiccups, apnea • Other chronic conditions • Medications: Current, recent, prescription, nonprescription Family Psychosocial History • Sources of stress and/or postpartum depression • Maternal or paternal drug use Family Medical History • Significant illnesses • Family history of gastrointestinal (GI) disorders • Family history of atopy Box 33-5 War n i ng S i gna l s Re qu i r i ng Ur ge nt I nve s t i ga t i on i n I n f ant s w i t h Re gur g i t a t i on or V om i t i ng • Bilious vomiting • Gastrointestinal (GI) bleeding, hematemesis, hematochezia • Consistently forceful vomiting or onset of vomiting after 6 months old • Failure to thrive (FTT) • Recurrent respiratory infections • Feeding problems (uncoordinated swallow, choking or cough associated with feeding) • Diarrhea or constipation • Fever and/or lethargy • Hepatosplenomegaly • Bulging fontanelles, macrocephaly, or microcephaly • Seizures • Abdominal tenderness or distension • Documented or suspected genetic/metabolic syndrome Physical Examination • Review of height, weight, and head circumference • Signs of FTT • Torticollis: Neck arching • Hoarseness • Anemia • Tooth erosion resulting from destruction of enamel by gastric acids caused by frequent vomiting • Rash, recurrent diarrhea, persistent vomiting, or early-morning vomiting (symptoms of other primary disease with GERD as a secondary problem) Diagnostic Studies In most infants with vomiting and in older children with regurgitation and heartburn, a history and physical examination are sufficient to reliably diagnose GERD, recognize 846complications, and initiate treatment. An empiric trial of acid suppression with a PPI for 4 weeks may be used as a diagnostic test in older children and adolescents but is not recommended in infants and young children. Nonradiologic diagnostic tests as indicated: • CBC with differential to rule out anemia and infection • UA and urine culture • Stool for occult blood • Testing for H. pylori The following specialized tests may be obtained following consultation with a physician or a pediatric gastroenterologist. • Esophageal pH monitoring has been the gold standard to diagnose reflux. However, the presence of reflux may not correlate with the severity of illness, and some gastric contents may not be acidic. Transnasal pH placement may be uncomfortable, decrease appetite and activity, and thus underestimate the true incidence of reflux episodes. Typically, patients are asked to discontinue H2 blockers for 72 hours before the test and PPIs for 1 week before the study. • Multichannel intraluminal impedance (MII) measures episodes of reflux independent of the pH of the fluid. It is especially useful for making a diagnosis in children with respiratory events related to reflux, because it can measure multiple indices, such as heart rate, oxygenation, sleep state, and apnea episodes. It can also measure the height of refluxed material and the content and direction of the reflux (liquid, air, or both). It is preferred by many gastroenterologists because it can measure acid and nonacid reflux (50% of reflux in infants is nonacidic). Cost, time to interpret results, and lack of consensus about norms for frequency or length of nonacidic reflux events are disadvantages to this study (Vandenplas et al, 2009). • Wireless pH monitoring is also available. A pH probe is placed transorally, temporarily attached to the esophageal mucosa where it is programmed to record events for 48 hours. The capsule typically sloughs in about 5 days. Failure to attach, chest pain, feeling of foreign body, and premature detachment are negative aspects of this technology. • Endoscopy to obtain a biopsy can help determine severity of reflux esophagitis. It can rule out esophagitis and other pathologic conditions if deemed necessary. It may also be used to re-dilate strictures. • Barium upper GI series should only be used if obstruction or an anatomic abnormality of the upper GI tract is suspected. • Radionuclide scan with scintiscan and esophageal and gastric ultrasonography studies are not recommended for routine evaluation of GERD. • Gastric emptying scan can be used to evaluate for delayed gastric motility associated with GER. • A video swallow study may be necessary if recurrent respiratory infection, persistent cough, or feeding refusal (or difficulty) is present to evaluate for effective esophageal swallow and to rule out aspiration. Medication Pediatric Dosage Famotidine (Pepcid) Infants: 1 to 3 months old: 0.5 mg/kg/dose once daily for up to 8 weeks Infants >3 months old to 1 year old: 0.5 mg/kg/dose twice daily for up to 8 weeks Children and adolescents: Initially 0.25 mg/kg/dose every 12 hours (maximum dose: 20 mg/dose) Nizatidine (Axid) Infants 6 months old to children 11 years old: 5-10 mg/kg/day divided twice daily Children 12 years+: 150 mg once daily Ranitidine (Zantac) Infants >1 month, children, and adolescents <16 years old: 4-8 mg/kg/day divided twice daily (maximum dose: 300 mg) Adolescents >16 years old: 150 mg twice daily or 300 mg once HS Proton Pump Inhibitors Lansoprazole (Prevacid) Children 1 to 11 years old: <30 kg: 15 mg once daily for up to 12 weeks >30 kg: 30 mg once daily for up to 12 weeks Omeprazole (Prilosec) Children > 1 year: 5 to 10 kg: 5 mg once daily for up to 12 weeks 10 to 20 kg: 10 mg once daily for up to 12 weeks >20 kg: 20 mg once daily for up to 12 weeks Rabeprazole (Aciphex) Children 1 to 11 years old: <15 kg: 5 mg once daily for <12 weeks >15 kg: 10 mg once daily for <12 weeks Adult dose: 20 mg once daily for <12 weeks Pantoprazole (Protonix) Infants and children <5 years old: 1.2 mg/kg/day once daily for 4 weeks Children 5 to 11 years old: 20-40 mg once daily for up to 8 weeks Children and adolescents 12 to 16 years old: 20 or 40 mg once daily for up to 8 weeks Esomeprazole (Nexium) Infants: 3 to 5 kg: 2.5 mg once daily for up to 8 weeks 5 to 7.5 kg: 5 mg once daily for up to 8 weeks >7.5 kg: 10 mg once daily for up to 8 weeks Children 1 to 11 years old: <20 kg 10 mg once daily for up to 8 weeks >20 kg: 10-20 mg once daily for up to 8 weeks Children >12 years old: 20-40 mg once daily for up to 8 weeks Contents of capsule may be mixed with 1 tablespoon of applesauce for easier swallowing, if needed. Medication Pediatric Dosage Cytoprotective Agent Sucralfate (Carafate) 40-80 mg/kg/day divided every 6 hours Adult dose 250 mg divided every 6 hours Take on an empty stomach 1 hour before meal and HS Data from Engorn B, Flerage J: The Harriet Lane handbook: a manual for pediatric house officer, ed 20, Philadelphia, 2015, Elsevier; Khan S, Orenstein S: Gastroesophageal reflux disease. In Kliegman RM, Stanton BF, St. Geme JW, et al: Nelson textbook of pediatrics, ed 19, Philadelphia, 2011, Elsevier; Lightdale JR, Gremse DA, Section on Gastroenterology, Hepatology, and Nutrition: Gastroesophageal reflux: management guidance for the pediatrician, Pediatrics 131(5):e1684–e1685, 2013. PPIs are superior to H2RAs in relieving symptoms and promoting mucosal healing and do not result in tolerance as do H2RAs. However H2RAs and buffering agents have a rapid onset of action and are useful in on- demand treatment (Vandenplas et al, 2009). There is insufficient evidence to justify the routine use of prokinetic agents such as cisapride, metoclopramide, domperidone, bethanechol, erythromycin, or baclofen for GERD. Because safe and convenient alternatives are available that are more acceptable to patients, chronic antacid therapy is generally not recommended for patients with GERD (Vandenplas et al, 2009). Nutrition Feeding techniques, volumes, and frequency of feeding should be normalized. A trial of extensively hydrolyzed protein formula may be used for 2 to 4 weeks in formula-fed infants with vomiting. Thickening agents for formula (1 tablespoon rice cereal/ounce formula) reduce regurgitation but not significantly (Hegar et al, 2008). An increase in caloric density may be necessary in infants with FTT (poor weight gain or weight loss). In older children and adolescents, there is no evidence to support specific dietary restrictions to decrease symptoms; however, avoiding eating 847less than 2 hours before bedtime may be helpful. Obesity is related to GERD, so weight management could be helpful. Lifestyle Because prone positioning is associated with increased risk of sudden infant death syndrome (SIDS), supine positioning during sleep in infants is recommended. Positioning infants upright may worsen reflux. There may be some benefit in older children to left-side positioning during sleep or elevation of the head of the bed (elevate the head of the bed and don't add pillows because it may increase abdominal flexion and compression). 848 Surgical Antireflux surgery strategies, such as fundoplication, are used for management of cases that have not responded to less invasive strategies, have life-threatening complications, or will have long-term dependence on medical therapy in which compliance or patient preference precludes ongoing use. However, the surgery is not necessarily curative. For example, in one study of fundoplication in children with cystic fibrosis (CF), 12% had repeat surgery, 48% had recurrent GERD symptoms, and only 28% discontinued GERD medications (Vandenplas et al, 2009). Now that PPI therapy is so successful, fundoplication may become less common (Khan and Orenstein, 2011b). Complications Complications include chronic cough, FTT, irritability, and malnutrition. Esophageal injury secondary to reflux results in bleeding, stricture formation, and Barrett esophagus. GERD is circumstantially associated with significant asthma, recurrent pneumonia, or laryngeal disorders. In the majority of infants with apnea or apparent life-threatening event, GERD is not the cause. However, in the rare case where a relationship is suspected, pH monitoring in combination with polysomnographic recording and precise, synchronous symptom recording may aid in establishing cause and effect (Vandenplas et al, 2009). Red flags in infants are bilious vomiting and/or hematemesis (see Box 33-5). Patient and Family Education • Assure parents of infants that regurgitation is usually self-limited and symptoms improve as the child grows. Parental education and reassurance are recommended for infants with uncomplicated regurgitation. Remind parents that GERD may temporarily worsen during illness. • Review medication information, including dosages and side effects. Urinary Tract Infection and Pyelonephritis There are three kinds of UTI in children: (1) asymptomatic bacteriuria, (2) cystitis, and (3) pyelonephritis. Young children may have limited or unusual symptoms; therefore, a high degree of suspicion must be maintained to diagnose UTI. Inflammation and infection can occur at any point in the urinary tract, so a UTI must be identified according to location. Asymptomatic bacteriuria is bacteria in the urine without other symptoms, is benign, and does not cause renal injury. Cystitis is an infection of the bladder that produces lower tract symptoms but does not cause fever or renal injury (Elder, 2011d). Pyelonephritis is the most severe type of UTI involving the renal parenchyma or kidneys and must be readily identified and treated because of the potential irreversible renal damage that can occur. Clinical signs thought to be consistent with pyelonephritis include fever, irritability, and vomiting in an infant, and urinary symptoms associated with fever, bacteriuria, vomiting, and renal tenderness in older children. UTIs are the most common cause of serious bacterial infection in infants younger than 24 months old with fever without a focus (Elder, 2011d). A complicated UTI is defined as a UTI with fever, toxicity, and dehydration or a UTI occurring in a child younger than 3 to 6 months old. The UTI may be classified based on its association with other structural or functional abnormality, such as VUR, obstruction, dysfunctional voiding, or pregnancy. Additionally, a UTI must be identified as a first occurrence, recurrent (within 2 weeks with the same organism or any reinfection with a different organism), or chronic (ongoing, unresolved, often caused by a structural abnormality or resistant organism). Finally, age and gender of the pediatric patient are important factors in determining the method of evaluation and the course of treatment. The organism most commonly associated with UTI is Escherichia coli (70%), although other organisms (such as, Enterobacter, Klebsiella, Pseudomonas, and Proteus) can cause infection. UTI secondary to group B streptococcus is more common in neonates. Several factors are believed to contribute to the etiology of UTIs. Most UTIs are thought to be ascending (i.e., the infection begins with colonization of the urethral area and ascends the urinary tract). If the infection progresses to the kidney, intrarenal reflux deep into the kidneys can lead to scarring. However, the most important risk factor for the development of pyelonephritis in children is VUR, which can be detected in 10% to 45% of young children who have symptomatic UTIs. Furthermore, reflux of infected urine from the bladder increases the risk of pyelonephritis. This damage to the kidney occurs in the compound papillae, which have wide and gaping 916openings allowing intrarenal reflux. The compound papillae are located in the upper and lower poles of the kidney, which is the usual site of scarring. Simple conical papillae have angled, slit-like openings that resist intrarenal reflux (Fig. 35-2). Neonates Infants Toddlers and Preschoolers School-Age Children and Adolescents Jaundice Malaise, irritability Altered voiding pattern “Classic dysuria” with frequency, urgency, and discomfort Hypothermia Difficulty feeding Malodor Failure to thrive (FTT) Poor weight gain Abdominal/flank pain* Malodor Sepsis Fever* Enuresis Enuresis Vomiting or diarrhea Vomiting or diarrhea Vomiting or diarrhea* Abdominal/flank pain* Cyanosis Malodor Malaise Fever/chills* Abdominal distention Dribbling Fever* Vomiting or diarrhea* Lethargy Abdominal pain/colic Diaper rash Malaise *Findings increase likelihood of pyelonephritis. 917 Diagnostic Studies The method used to collect urine has an effect on the interpretation of results. It is acceptable to collect urine for UA only from a non–toilet-trained child by using a sterile, adhesive bag carefully placed over well-cleaned genitals. If the bagged urine results in a positive leukocyte esterase or nitrite test, a child younger than 24 months old has risk factors, or the patient is symptomatic, additional urine should be collected by sterile catheterization or suprapubic aspiration. Older children, who can void on command, should be able to obtain a clean-catch void. Having the female child sit backward on the toilet separates the labia and decreases contamination. See the Diagnostic Studies section earlier in this chapter for other pertinent information. • Urine culture by standard culture methods is essential to confirm the diagnosis. If the culture shows greater than 100,000 colonies of a single pathogen in a clean catch urine specimen, greater than 50,000 in a catheterized or suprapubic specimen, or if there are 10,000 colonies of a single pathogen and the child is symptomatic, the child is considered to have a UTI (Elder, 2011d; Shaw, 2015) • UA should be used only to raise or lower suspicion. Suspicious findings include foul odor, cloudiness, nitrites, leukocytes, alkaline pH, proteinuria, hematuria, pyuria, and bacteriuria. • Nitrite chemical tests are reliable on urine specimens when gram-negative bacteria are present and when the urine has been in the bladder for 4 hours or longer. False-positive results are rare, whereas false- negative results are common. • Leukocyte esterase chemical tests detect pyuria, but pyuria may arise from causes other than UTI. • Microscopic evaluation of uncentrifuged urine may be helpful if bacteria are seen. • Gram stain may be helpful if bacteria are identified. • Bacterial identification and determination of sensitivities are necessary in patients who appear toxic or could have pyelonephritis, have relapses or recurrent UTI, or are nonresponsive to medication. • Complete blood count (CBC) (elevated WBC count), erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), BUN, and creatinine should be done if the child is younger than 1 year old, appears ill, or if pyelonephritis is suspected. • Serum procalcitonin level of more than 0.5 ng/mL is an accurate and reliable biologic marker for renal involvement during a febrile UTI, pyelonephritis, and with renal scarring, so it may be useful in the clinical diagnosis and treatment of UTIs (Leroy et al, 2011) • Blood culture should be done if sepsis is suspected (see Chapter 24). Differential Diagnosis The differential diagnosis includes urethritis, vaginitis, viral cystitis, foreign body, sexual abuse, dysfunctional voiding, appendicitis, pelvic abscess, and pelvic inflammatory disease. Any child who has acute fever without a focus, FTT, chronic diarrhea, or recurrent abdominal pain should be evaluated for UTI. Management Goals of treatment are to quickly identify the extent and level of infection; to treat appropriately to eradicate infection; to provide symptomatic relief; to find and correct anatomic or functional abnormalities; and to prevent recurrence and new or progressive renal damage (AAP Subcommittee on Urinary Tract Infection, Steering Committee on Quality Improvement and Management, 2011). When deciding on a treatment plan, the child's age, gender, symptoms, the suspected location of the UTI and antibiotic 918resistance patterns in the community must be considered. Figure 35-3 outlines treatment of UTI in the child. Enuresis Enuresis is defined as voluntary or involuntary urination into bed or clothes at an age when toilet training should be complete. Children who have never established control have primary enuresis. Secondary enuresis is present when children have been dry for more than 6 to 12 months and begin wetting. Nocturnal enuresis is incontinence during sleep. If a child has normal daytime elimination with no concerns, then nighttime wetting is called monosymptomatic nocturnal enuresis (MNE). More commonly, children with nocturnal enuresis have BBD symptoms during the day as well; this type of nocturnal enuresis is non-monosymptomatic nocturnal enuresis (NMNE). Diurnal enuresis, daytime wetting, occurs during waking hours. Diagnosing enuresis can be a challenge. According to the ICCS, using ICD-10 and DSM-V, a diagnosis of enuresis requires a minimum age of 5 years old, and one episode a month for a duration of 3 months. The ICCS goes on to state that enuresis is frequent if it occurs four or more times a week and infrequent if it occurs four or less times a month (Austin et al, 2014). It is important to remember that the age at which urinary continence is normally achieved varies greatly and thus children should be evaluated on a case-by-case basis, taking into account the child and family dynamics and developmental stages and the amount of duress the issue is causing. Regardless of the numbers, if the parent or child asks for help, they should receive it. The cause of enuresis varies among children and can be difficult to determine. A number of factors have been found to be associated with enuresis, including the following: • Constipation: It cannot be overemphasized how important it is to determine if constipation or impaction exists before treating nocturnal enuresis. • Familial disposition: Even if there is a presumed genetic predisposition based on parental history, many of these children have constipation; and if that is treated, they have improvement. • Neurologic developmental delay • Behavioral comorbidities (e.g., externalizing behaviors): There appears to be a strong association between enuresis (especially daytime enuresis) and attention-deficit/hyperactivity disorder (ADHD) (von Gontard et al, 2011). • Functional small bladder capacity: In some children, bladder capacity appears normal during the day but is functionally reduced at night (Godbole et al, 2011). • Sleep disorders: Obstructive sleep apnea and disordered sleep patterns are associated with increased incidence of nocturnal enuresis (Godbole et al, 2011). • Stress and family disruptions: Some examples are a divorce, move, or a new family member. • Polyuria: This can be caused by nocturnal drinking as well as caffeine intake (Godbole et al, 2011). • Inappropriate toilet training: This is especially common when parents are overly demanding or punitive of the child. Clinical Findings The goals of assessment are to (1) determine if there are comorbid or underlying conditions that require pediatric urology referral and (2) establish the best approach to treating this particular child's condition. History It is essential to gather the most honest nighttime and daytime history of elimination habits possible, both urine and bowel. Parents should be asked about the following: • Voiding characteristics: • Urgency, dysuria, or dribbling • Are there voiding or stooling postponement behaviors? • Number of voids per day: Is nocturia present? 230 • Cluster voiding: For example, is the child waiting until after school? • Frequency of wetting—day and night • Type of urinary stream • These findings warrant referral to a pediatric urologist (Nevéus et al, 2010): • Weak or interrupted urinary stream • Need to use abdominal pressure to urinate • Daytime incontinence and nocturnal enuresis combined • Fluid intake, how much and when • UTI • History of enuresis, treatment, and age of resolution for other family members, including parents • History of toilet training: What age was toilet training begun? How was it handled? Was the child ever dry? For how long? • Effect of enuresis on child and parents Other drugs are not recommended as first-line treatment. These include anticholinergics (antimuscarinic drugs [also used for treatment of overactive bladder]: oxybutynin, tolterodine, and solifenacin), which can cause constipation and could complicate the problem; botulinum toxin type A (BtA); and imipramine, which should only be used as third-line therapy at tertiary care facilities, if at all, due to its cardiotoxic side effects. Sacral nerve stimulation for children with severe voiding dysfunction that has not responded to aggressive urotherapy and medical interventions is currently being studied. Complications Enuresis contributes to poor self-esteem and disrupted family interactions and threatens the child's ability to 232establish strong peer relationships. Parents of children with nocturnal and diurnal enuresis rate those children as having more problem behaviors than do parents of children without enuresis; these parents also rate their own stress level as higher (De Bruyne et al, 2009); children with enuresis are at risk for child abuse. Effective treatment improves behavior and self-concept, suggesting that enuresis precedes behavior problems. Patient and Family Education Supportive, proactive education of parents and positive reinforcement of children's efforts can help prevent enuresis. For 3- to 5-year-old children, a nonjudgmental attitude of “benign neglect” in the face of accidents is the best approach. For older children with enuresis, aggressive, long-term interventions are appropriate; wetting is a common phenomenon, and parents should be reassured that it rarely indicates disease. Dealing with a child who wets frequently can be frustrating, however, and parents need to know that the provider is committed to working closely with them until the child is dry. Nephritis and Glomerulonephritis Nephritis is a noninfectious, inflammatory response of the kidneys characterized by varied degrees of hypertension, edema, proteinuria, and hematuria that can be either microscopic or macroscopic with dysmorphic RBCs and casts. Nephritis is classified as acute, intermittent, or chronic. Primary GN occurs when the original and predominant structure impaired is the glomerulus. Secondary GN occurs when renal involvement is secondary to systemic disease (e.g., SLE, HSP, primary vasculitis, Goodpasture syndrome, or drug hypersensitivity reactions). Involvement can be in the glomerulus or the interstitium and either localized in one part of the kidney or generalized throughout. GN refers to inflammation primarily in the glomeruli; interstitial nephritis refers to inflammation in the interstitium primarily caused by drug reactions. PSGN is the classic form of GN. Acute nephritis most commonly occurs as PSGN, which is characterized by a history of streptococcal infection within the prior 2 weeks and an acute onset of edema, oliguria, hypertension, and gross hematuria. Consider an alternative diagnosis if the following findings are present: nephrotic levels of protein, lack of evidence for a post- infection mechanism, rapidly deteriorating renal function, or clinical or laboratory findings suggesting other forms of GN (e.g., rash, positive ANA). Intermittent gross hematuria and proteinuria syndromes include the following: • IgA nephropathy, or Berger disease, is the most common chronic GN in children of European Asian descent and is uncommon in African Americans; it has a 2 : 1 male preponderance. It is an immunologic entity causing recurrent gross and microscopic hematuria and often proteinuria. It is present in about one third of persons biopsied for persistent microscopic hematuria. It is often precipitated by viral infections or strenuous exercise, and each episode lasts less than 72 hours. BP is normal, no edema is present, and C3 is normal. Definitive diagnosis is made by biopsy. The prognosis is good in the absence of elevated serum creatinine or nephrotic- range proteinuria, although progression to chronic renal insufficiency can occur. • Hereditary or familial nephritis involves many disorders, but the best known is Alport syndrome. More common and severe in males, with onset before 15 years old in 75% of children, this condition is inherited as an X-linked dominant trait. The initial manifestation is isolated, persistent, microscopic hematuria with intermittent macrohematuria and variable proteinuria, occurring with an upper respiratory infection or exercise. Laboratory abnormalities are variable; biopsy verifies the diagnosis. Extrarenal abnormalities, including neurogenic deafness, ocular abnormalities, and macrothrombocytopenia, are often found. Vision and hearing screening are essential with referral for any abnormalities. Severe forms of the disease can lead to end- stage renal disease, which is often heralded by hypotension. • Familial or benign recurrent nephritis, also known as thin-basement-membrane disease, is a disorder inherited as an autosomal dominant trait with unknown etiology. Episodes are characterized by macroscopic and microscopic hematuria and mild proteinuria, often precipitated by upper respiratory tract infection. Laboratory values other than UA are normal. The diagnosis is confirmed by biopsy, which may not be needed if the disease is mild and confirmed in relatives. In the absence of notable proteinuria, deafness, ocular defects, renal failure, and with normal biopsy findings, the prognosis is excellent. Chronic nephritis is most commonly known as membranoproliferative GN and is distinguished by four types based on biopsy. Chronic nephritis can be found after acute nephritis or when investigating nonspecific complaints, 933such as anorexia, intermittent vomiting, and malaise. It is manifested by diminished renal function that ultimately has detrimental effects on other organ systems. Types I and II may respond to steroids, but the overall prognosis is guarded. Pyelonephritis, discussed earlier in the Pyelonephritis section, is inflammation of the renal parenchyma, calyces, and pelvis caused by bacteria. The inflammatory response of the kidneys results from various causes, such as infection, an immunologic response, a drug or toxin, and vascular or systemic disorders. PSGN is an immune response by the host to a group A beta-hemolytic streptococcal infection, whereas acute postinfectious glomerulonephritis (APGN) can be caused by bacterial, fungal, viral, parasitic, or rickettsial agents. PSGN is the most common form of nephritis in childhood, occurs most often between 5 and 12 years old, occurs more often in males (2 : 1), and is unusual in children younger than 3 years old. The incidence of APGN is difficult to determine because of the large number of patients with subclinical cases (Pan and Avner, 2011a). Clinical Findings History • Streptococcal skin (more likely) or pharyngeal infection within the past 2 to 3 weeks (PSGN). Classically a latent period of 7 to 10 days elapses between infection and the onset of symptoms; if fewer than 5 days or more than 14 days, consider other causes. • Abrupt onset of gross hematuria. • Reduced urine output (with diuresis in 5 to 7 days). • Lethargy, anorexia, nausea, vomiting, abdominal pain. • Chills, fever, backache (pyelonephritis). • Medication taken in the past few weeks. Physical Examination • Hypertension that is transient and resolves in 1 to 2 weeks • Edema, especially periorbital edema, or abrupt onset with weight gain • Circulatory congestion—dyspnea, cough, pallor, pulmonary edema if severe • Ear malformations • Flank or abdominal pain or a mass (in polycystic kidney or malignancy [e.g., Wilms tumor]) • Costovertebral angle tenderness (in pyelonephritis) • Rashes or arthralgias (with SLE, HSP, or impetigo) • Evidence of trauma or abuse Diagnostic Studies • UA with microscopic examination—tea color; elevated specific gravity; macrohematuria and microhematuria; proteinuria not exceeding the amount of hematuria; pyuria in PSGN; granular, hyaline, WBC, or RBC casts; and dysmorphic RBCs • Serum C3 or C4 (low early in disease, returning to normal in 6 to 8 weeks), total protein and albumin (elevated) • CBC, ESR, ASO titer (elevated), streptozyme test (positive), anti–deoxyribonucleic acid (DNA) antibody titer • Electrolytes, BUN, creatinine, and cholesterol • Fluorescent antinuclear antibody (SLE), hepatitis titers, sickle cell or hemoglobin electrophoresis, tuberculin PPD, and fluorescent treponemal antibody absorption (syphilis) Differential Diagnosis Acute nephritis also occurs as part of systemic illnesses, such as SLE, HSP, hemolytic-uremic syndrome, vasculitis, or as a reaction to drugs or irradiation. Management Consultation with a nephrologist is recommended in all cases PSGN treatment is supportive because resolution occurs spontaneously 95% of the time. The course does not seem to be affected by corticosteroids, immunosuppression, or other treatment modalities. During the peak of oliguria and hypertension in the first few days of illness, hospitalization may be required with fluid and sodium limitation and diuretic, antihypertensive, and antibiotic treatment if cultures are positive. Resolution occurs once diuresis begins. Gross hematuria persists for 1 to 2 weeks, urine can be abnormal for 6 to 12 weeks, and microscopic hematuria can persist for up to 2 years. Complement levels return to normal in 6 to 8 weeks (Pan and Avner, 2011a). • Acute nephritis—possible hospitalization with treatment, as described previously. • IgA nephropathy—annual follow-up with BP, UA, and determination of renal function. • Benign familial or hereditary nephritis—perform audiometry and review family medical history. Hereditary markers are being developed for this disease. • Benign recurrent nephritis—monitor UA and renal function every 1 to 2 years. • Chronic nephritis—a team approach is required to adequately provide care. Complications Prolonged oliguria and renal failure can occur if acute nephritis progresses. Hypertensive encephalopathy or congestive heart failure can occur secondary to PSGN. Irreversible parenchymal damage causes hypertension and renal insufficiency. Patient and Family Education, Prevention, and Prognosis Patients with PSGN may have macrohematuria or microhematuria for up to 6 to 12 months, but the long-range outcome is excellent. Thin-basement-membrane disease has a good outcome. IgA nephropathy with severe histologic findings has a poor outcome, especially if the child is African American. Patient education should stress the importance of continued, regular care to monitor renal function. Osgood-Schlatter Disease Osgood-Schlatter disease is caused by microtrauma in the deep fibers of the patellar tendon at its insertion on the tibial tuberosity. The diagnosis is usually based on history and physical examination. The quadriceps femoris muscle inserts on a relatively small area of the tibial tuberosity. Naturally high tension exists at the insertion site. In children, additional stress is placed on the cartilaginous site as a result of vigorous physical activity, leading to traumatic changes at insertion. Osgood-Schlatter disease is often seen in the adolescent years after undergoing a rapid growth spurt the previous year. It occurs more frequently in boys than girls, with a male-to-female ratio of 3 : 1. This difference is probably related to a greater participation in specific risk activities by boys than by girls (Sullivani, 2015). RF, Rheumatoid factor. The underlying cause of most forms of JIA is unclear; however, it is a heterogenous disorder. It is likely environmentally induced in genetically predisposed individual. Human leukocytic antigen (HLA) class I and II alleles have been associated with JIA (Gowdie and Tse, 2012). This linkage points to the involvement of T cells and antigen presentation in the pathophysiology of the disease. An environmental trigger, such as infection or trauma, is also important in the pathogenetic process in JIA. The trigger results in an uncontrolled adaptive and innate response toward the self-antigen, the autoimmune reaction. The presence of autoantigens from cartilage and joint tissue leads to activation of the T cells and results in release of proinflammatory cytokines (Gowdie and Tse, 2012). In contrast, systemic juvenile idiopathic arthritis (SJIA), which does not have HLA gene association, may be the result of an autoinflammatory response from the innate immune system. SJIA is postulated to be the result of uncontrolled activity of the innate immune system, because this type of JIA disease is not associated with 552autoantibodies but rather uncontrolled activity of the phagocytes, including neutrophils, monocytes, and macrophages. The difference in the pathogenic processes may explain the differences in the clinical presentation of the disease. In oligoarticular and rheumatoid factor (RF)-positive polyarticular JIA, there is autoimmunity with involvement of the adaptive immune system. The presence of positive ANAs and RF is associated with HLA genes. The humoral response is responsible for the release of autoantibodies (especially ANAs), an increase in serum immunoglobulins, and the formation of circulating immune complexes and complement activation. The cell-mediated reaction is associated with a T-lymphocyte response that plays a key role in cytokine production, resulting in the release of tumor necrosis factor alpha (TNF-α), IL-1, and IL-6. B lymphocytes are activated by T-helper cells and produce autoantibodies that link to self-antigens. The B lymphocytes infiltrate the synovium with the end result of nonsuppurative chronic inflammation of the synovium that can lead to articular cartilage and joint structure erosion. The chronic arthritides of childhood present unique challenges to the child, family, and the pediatric provider. Approximately 1 in 1000 children are affected with oligoarticular JIA, the most common arthritic subtype. Certain histocompatibility complex antigens are more prevalent in the JIA population. Cytokine production, proliferation of macrophage-like synoviocytes, infiltration with neutrophils and T lymphocytes, and autoimmunity are thought to be the major pathologic processes causing chronic joint inflammation. The rate of JIA is significantly higher in girls than in boys, typically in oligoarticular and pauciarticular JIA. The female to male ratio in systemic onset is equal. The approximate percentage of occurrence and age breakdown for each of the subtypes follows: systemic (10%) occurs at any age; polyarticular (40%) has a late (6 to 12 years old) or early childhood (1 to 4 years old) onset; and oligoarticular (50%) has a late or early onset. Adolescents tend to have more RF-positive disease (Wu et al, 2011). Clinical Findings History The major complaints in all forms of JIA are from the arthritis characterized by: • Pain—generally a mild to moderate aching • Joint stiffness—worse in the morning and after rest; arthralgia may occur during the day • Joint effusion and warmth Systemic symptoms are found more commonly in systemic and polyarticular subtypes and include anemia, anorexia, fever, fatigue, lymphadenopathy, salmon-colored rash (SJIA), and weight loss. Growth abnormalities can result in localized growth disturbances, including premature fusion of the epiphyses, bony overgrowth (rheumatoid nodules), and limb-length discrepancies. Physical Examination Associated features are: • Non-migratory monoarticular or polyarticular involvement of large or proximal interphalangeal joints for more than 3 months • Systemic manifestations—fever, salmon-colored rashes, leukocytosis, serositis, lymphadenopathy, and rheumatoid nodules Less commonly seen are ocular disease (e.g., iridocyclitis, iritis, or uveitis), pleuritis, pericarditis, anemia of chronic disease, fatigue, and growth failure, or leg-length discrepancy if the arthritis is unilateral. Key physical findings are: • Swelling of the joint with effusion or thickening of synovial membrane, or both, noted on palpation of the joint line • Heat over inflamed joint and tenderness along joint line • Loss of joint range of motion and function; child typically holds the affected joints in slight flexion and may walk with limp • Uveitis may be present with ciliary injection and decreased vision. However, it is usually asymptomatic. There are five major types of JIA (Gowdie and Tse, 2012): 1. Oligoarticular pattern: This type of JIA involves four or less joints, typically the weight-bearing joints within the first 6 months of diagnosis. The diagnosis is classified as persistent or extended disease, depending on the number of joints involved. About 50% progress to extended disease where there is involvement of four or more joints after the first 6 months of disease. This involvement primarily is in larger or medium joints, such as the knee, ankle, wrists, and elbow; however, systemic symptoms are rare. The synovitis may be mild and painless with asymmetric joint involvement and unremarkable laboratory values. Uveitis occurs in 30% especially if the child has a positive ANA (Gowdie and Tse, 2012). 2. Polyarticular pattern: This involves five or more joints and is divided into RF-negative and RF-positive disease. Involved joints can be large or small with an acute or insidious onset. RF-negative ANA positive polyarticular JIA is difficult to distinguish from extended oligoarticular pattern disease. Using the number of joints involved and the timing of onset of the arthritis can be helpful. In contrast, RF-positive disease can have chronic pain and symmetric joint swelling, low-grade fever, fatigue, nodules, and anemia of chronic disease. An acute form of uveitis occurs in this subtype. Polyarticular JIA typically involves small joints of the hands, feet, ankles, wrists, knees, and can also involve the cervical spine. Adolescents with this type differ from those with early onset in that they exhibit a positive RF. Adolescents who develop late-onset polyarticular JIA have a course similar to the adult entity. Both forms of the disease are more common in females. 3. SJIA: This is characterized by arthritis in one or more joints for 6 weeks' duration in a child younger than 16 years old with a fever of at least 2 weeks' duration with 553at least 3 days of daily fever. In addition, there is also a fleeting erythematous rash, lymphadenopathy, hepatomegaly, splenomegaly, and serositis (Ringold et al, 2013). Myocarditis with pericardial effusion occurs in approximately 10%. RF is rarely positive and the ANA is only positive in 5% to 10%; however, there may be anemia, thrombocytosis, increased acute phase reactants, and elevated transaminase levels. About 10% of children with SJIA develop a life-threatening macrophage activation syndrome (MAS) with fever, organomegaly, cytopenia, hyperferritinemia (acute phase reactant), hypertriglyceridemia, coagulopathy, and hypofibrinogenemia. 4. Enthesitis-related JIA: This typically entails arthritis of the lower limbs especially the hip and intertarsal joints with the sacroiliac joints involved later in the disease. Enthesitis involves inflammation at the insertion of tendons, ligaments, or joint capsules and is characterized by swelling, tenderness, and warmth. Enthesitis may present with joint or foot pain. There is a risk of anklyosing spondylitis 10 to 15 years later. It tends to occur in late childhood and adolescence and acute symptomatic uveitis occurs in about 7%. 5. Psoriatic arthritis: This is more common between the ages of 2 and 4 and again between 9 to 11 years old. There is usually a family history of psoriasis, or the child has psoriasis; however, the arthritis can precede the psoriasis by years. There can be dactylitis or a sausage-like swelling of the digits; involvement in the small digits is not uncommon. Diagnostic Studies JIA is a diagnosis of exclusion. The diagnosis is based on physical findings and history of arthritis lasting for 6 weeks or longer. There is no diagnostic laboratory test for JIA. Most children with oligoarticular arthritis have negative laboratory markers. Those with polyarticular and systemic-onset typically have elevated acute-phase reactants and anemia of chronic disease. A positive result for RF by latex fixation may be present, but a positive RF occurs in less than 10% of children with JIA and rarely in those with SJIA. ANA may be present in up to 50% of children with oligoarticular disease. A positive ANA helps identify children at higher risk for uveitis. The anti- CCP antibody test can be added to the initial workup of JIA, because citrullinated residues are part of the essential antigenic components that are recognized by autoantibodies in rheumatoid arthritis (Mehta, 2012). The anti-CCP antibodies are associated with more aggressive disease and may be present before the onset of symptoms. The anti-CCP antibody is highly specific, but its precise role has not been established because it is found primarily in children with polyarticular JIA (Mehta, 2012). Useful laboratory tests include a complete blood count (CBC) (to exclude leukemia); ESR, CRP, Lyme titers, and liver function tests. The results may reveal lymphopenia, anemia, elevated transaminases, and hypoalbuminemia; however, laboratory studies may be normal in these children. Imaging studies (MRI) can help in managing joint pathologic conditions. Analysis of synovial fluid is not helpful in the diagnosis of JIA. Differential Diagnosis The various causes of monoarticular arthritis are part of the differential diagnosis. However, Lyme disease must be excluded and other differentials, including tumors, leukemia, cancer, bacterial infections, toxic synovitis, rheumatic fever, SLE, spondyloarthropathies, inflammatory bowel disease, septic arthritis, and chondromalacia patellae, need to be carefully considered. Management A specialist in pediatric rheumatology should follow children with severe involvement. Ophthalmology referral and evaluation is critical in a child with a positive ANA. Uveitis needs immediate ophthalmologic management. It is most common in oligoarticular JIA and is highly associated with a positive ANA. Other pediatric subspecialists, such as orthopedists, pain management specialists, and cardiologists, may be consulted as needed. Therapy depends on the degree of local or systemic involvement. The main treatment goals are to suppress inflammation, preserve and maximize joint function, prevent joint deformities, and prevent blindness. Drug therapy is used to control the inflammation responsible for tissue injury with the goal of preventing permanent tissue changes, which is not always possible. Aggressive early treatment to induce a remission is a key consideration in JIA management in order to prevent deformity and improve outcomes and is now the goal of the practice guidelines for both polyarticular JIA and SJIA (Ringold et al, 2013, 2014). Aspirin therapy has largely been replaced with the use of nonsteroidal anti-inflammatory drugs (NSAIDs). Pharmacologic agents commonly used in the management of JIA include the following (Gowdie and Tse, 2012): • NSAIDs: Children with oligoarthritis generally respond well to NSAIDs (Taketomo et al, 2014). • Ibuprofen: 30 to 40 mg/kg/day three to four divided doses (maximum single dose is 800 mg; maximum daily dose 2400 mg/day) • Tolmetin: 20 to 30 mg/kg/day divided in three to four doses (maximum dose is 1800 mg/day) • Naproxen: 10 mg/kg/day in two divided doses (maximum dose is 1000 mg/day) • Indomethacin: Older than 2 years old, 1 to 2 mg/kg/day divided in two to four doses (maximum dose is 4 mg/kg/day); adults, 25 to 50 mg/dose two or three times/day (maximum dose is 200 mg/day) • Celecoxib: Older than 2 years old and adolescents (≥10 kg to ≤25 kg), 50 mg twice daily; >25 kg, 100 mg twice daily • Oral, parenteral, intraarticular corticosteroids: • Systemic arthritis: Can be used for 2 weeks as initial therapy for SJIA with involvement of more than four joints and a physician global assessment (using the Provider global assessment tool of disease activity) of 554less than 5 or a Provider global score of more than 5 without care about active joint involvement. Corticosteroids can be used as bridging therapy until other medications take effect (Ringold et al, 2013) • All the other types of arthritis: Prednisone in the lowest possible dose with optional intraarticular steroid injection (Ringold et al, 2014) Physical Examination. Findings may include the following: • Antalgic gait with limited hip movement • Trendelenburg gait resulting from pain in the gluteus medius muscle • Muscle spasm • Atrophy of gluteus, quadriceps, and hamstring muscles • Decreased abduction, internal rotation, and extension of the hip • Adduction flexion contracture • Pain on rolling the leg internally Diagnostic Studies. Routine AP pelvis and frog-leg lateral views are used to confirm the diagnosis, stage the disease, and follow disease progression and response to treatment. Radiographic findings can include smaller epiphysis, increased epiphyseal density, subchondral fracture line, lateralization of the femoral head, and other features. Changes in the epiphysis margin are discerned by the orthopedist and radiologist (Fig. 38-10). However, there may be no radiographic findings early in LCPD. Ultrasonography is useful in the preliminary diagnosis; capsular distention can be seen on sonographic images. Bone scans and MRI allow for precise localization of the bone involvement, but changes seen as bone marrow edema and joint effusions are nonspecific. CT is not typically used on a routine basis to evaluate patients with LCPD (Kim and Herring, 2014). Differential Diagnosis Acute and chronic infections, sickle cell disease, toxic synovitis, Gaucher disease, slipped capital femoral epiphysis (SCFE), osteomyelitis, juvenile rheumatoid arthritis, hemophilia, and neoplasm are included in the differential diagnosis. Management • Referral to an orthopedist is necessary. Because age of onset and the severity of LCPD can vary significantly from one child to another, there are various approaches to the management, and treatment remains controversial. Overall, the general approach is guided by the principle of containment of the femoral head within the acetabulum. To be successful, containment must be instituted while the femoral head is still moldable. Non-operative containment can be achieved in a variety of ways and ranges from activity limitation, and protected weight-bearing, use of NSAID and physical therapy to maintain hip motion to bed rest with traction using casts to maintain hip abduction. Surgical approaches involve pelvic and femoral osteotomies of the proximal femur or pelvis. • Support and monitor the child throughout treatment and recovery, including during interruption of school or other activities. Treatment and monitoring of LCPD can last months to years. Complications Osteoarthritis related to femoral head deformity and decreased use of the hip joint may occur, depending on the femoral head remodeling status. Older children have a poorer prognosis owing to the decreased opportunity for femoral head remodeling in the remaining growth period. Females with LCPD also have a poorer prognosis. Prevention The condition is not preventable, but early identification and treatment reduce the long-term complications of the disorder, such as premature degenerative arthritis in early adult life. Idiopathic Scoliosis Adolescent scoliosis can resolve, remain static, or increase. As a result treatment options vary considerably. Treatment decisions are based on the natural history of each curvature. Infantile scoliosis can resolve spontaneously; however, progressive curves require bracing and surgery in an attempt to slow the curve progression and prevent complications (e.g., thoracic insufficiency syndrome). Juvenile scoliosis is found more frequently in girls, and the curves are at high risk for progression and often require surgical intervention. The goal in treatment is to delay spinal fusion, allowing time for the pulmonary system and thoracic cage to have matured and maximum trunk height to be achieved. (See the various surgical procedures described in the following section.) The natural history includes the degree of skeletal maturity or growth remaining, the magnitude of the curve, and any associated diagnoses or medical conditions. Observation is always indicated for curves less than 20 degrees. Bracing or surgery may be indicated for larger curves. Brace treatment may reduce the need for surgery, restore the sagittal profile, and change vertebral rotation. Indications for bracing are a curve more than 30 degrees. Additional indications for brace therapy include skeletally immature patients with curves of 20 to 25 degrees that have shown more than 5 degrees of progression. The efficacy of bracing for adolescent idiopathic scoliosis remains controversial. Some studies show brace treatment to be effective in preventing curvature progression; however, it has been found that the success of the treatment is proportional to the amount of time that the patient wears the brace. Various brace treatment protocols suggest wearing a brace as much as 23 hours per day; therefore, compliance is a significant factor for this treatment modality (Spiegel and Dormans, 2011). Surgical treatment is indicated for children and adolescents who have progressive spinal deformity that do not respond to bracing and for those with curvature exceeding 45 to 50 degrees (Richards et al, 2014). There are various surgical procedures; all aim to control progressive curvatures. In the past, surgery was limited to arthrodesis (surgical fusion) of the spine. In recent years, several procedures have been developed that are designed to postpone and, in some cases, eliminate the need for early spinal fusion and allow for growth. These include the vertical expandable prosthetic titanium rib (VEPTR). This procedure is indicated for children with restricted pulmonary function due to the curvature of their thoracic spine. The surgery involves implanting a prosthesis that serves to enlarge the constricted thorax. The prosthesis can be adjusted approximately every 4 to 6 months, thereby allowing for growth. The “growing rod” surgical procedure has shown success in patients with adolescent idiopathic scoliosis and involves inserting spinal rods that are used to exert distraction forces that are adjusted approximately every 6 months. The rods serve as an internal brace to control the curvature of the spine while allowing skeletal growth. A more recent procedure involves intervertebral spinal stapling or tethering. Unlike the VEPTR and growing rod procedures, intervertebral spinal stapling does not require repeat adjustments and, therefore, eliminates the need for repeat surgical procedures. Research on this technique is limited, and clinical indications have not been universally agreed upon. Further research is necessary and long-term results are yet to be determined. Referral to an orthopedist or a center that specializes in working with infants and children with scoliosis is essential. Support must be given to the child and family 1060through the diagnostic and treatment phases, considering school and peer factors. The primary care provider needs to assist the child with psychological adjustment issues that arise if bracing or surgery is recommended and instituted. Some specific concerns of the child can include self-esteem problems, managing hostility and anger, learning about the disease and its care, wondering about the long-term prognosis, and concerns about clothing and participation in sports and other activities. Croup (Laryngotracheitis and Spasmodic Croup) Croup is an acute, inflammatory disease of the larynx, trachea, and bronchi that clinically presents with a brassy cough that sounds like a bark and is associated with varying degrees of inspiratory stridor, hoarseness, and respiratory distress. Croup (laryngotracheitis and spasmodic croup) causes disease in children younger than 6 years old. The most common form of croup is typically termed laryngotracheitis. A viral infection of the glottic region extending into the subglottic region is called laryngotracheobronchitis (LTB), which is the term reserved for the more severe form of croup. It is an extension of laryngotracheitis occurring 5 to 7 days into the disease and is associated with bacterial superinfection (Roosevelt, 2011). Human parainfluenza types 1 and 2 (less so) are the most common viral agents responsible for fall outbreaks in children 1 to 6 years old, typically in odd numbered years. Other causative agents include other human parainfluenza types (notably HPIV-3), influenza A and B, human coronavirus HL-63, coxsackieviruses, echoviruses, metapneumovirus, adenoviruses, RSV, and rhinovirus (Mejias and Ramilo, 2012). Viral croup is most common in children between 6 and 36 months old (60% are younger than 24 months), and it occurs most often in fall and winter. HPIV-3 is endemic in children younger than 6 months old and occurs in the spring and summer months, less commonly in the autumn if other parainfluenzae viruses are absent (Fox and Christenson, 2014). The incubation period is 2 to 4 days with viral shedding for up to 1 week before the onset of the disease (can shed up to 3 to 4 weeks with HPIV-3) (Mejias and Ramilo, 2012). See Chapter 24 for more discussion about human parainfluenza viruses. Males are affected more often than females. Recurrent croup and recurrent laryngitis can develop in children until they are 6 years old. A positive family history has been noted in a small percentage of children in whom croup develops. Croup lasts approximately 5 days. With growth, the child's laryngeal tracheal airway is less vulnerable to the effects of viral infections and less susceptible to obstruction. Clinical Findings Clinical manifestations depend on the infectious agent responsible for the croup and the extent of the upper airway involvement. History The history typically includes the following: • URI prodromal symptoms (rhinorrhea, conjunctivitis, or both) are sometimes present before stridor • Acute onset of a hoarse, barking-like cough • Mild to severe laryngeal obstruction • Mild to severe inspiratory stridor with dyspnea • Gradual onset of symptoms (2 to 3 days) • Symptoms worse at night (Fox and Christenson, 2014) • May or may not have sore throat • Duration is generally 3 to 5 days for viral croup • The presence of fever without reoccurrence differentiates it from spasmodic croup (Fox and Christenson, 2014) Physical Examination The following can be seen: • Slight dyspnea, tachypnea, and retractions • Mild, brassy, or barking cough (harsh sounding) • Stridor—a high-pitched, harsh sound from turbulent airflow that is generally inspiratory, but may be biphasic • Temperature is typically low grade, but may be elevated to 104° F (40° C) • If visualized on examination of the mouth, the epiglottis will appear normal • Substernal and chest wall retraction in severe cases • Prolonged inspiration • Wheezing and rales may be heard if there is additional lower airway involvement Diagnostic Studies Croup is a clinical diagnosis. Radiography of the soft tissues of the neck and chest displays a classic pattern of subglottic narrowing (“steeple sign”) on posteroanterior views but is usually not done unless there is a question Symptoms and Treatment Mild Moderate Severe Impending Respiratory Failure Agitation and distress Treatment Education of parent X X X X Corticosteroid X X X X Nebulized epinephrine X X Blow-by oxygen X X until intubation Intubation X Data from Alberta Clinical Practice Guidelines Working Group: Guidelines for diagnosis and management of croup, Canada, 2003; Alberta, ON. Indications for Hospitalization Children in distress with respiratory rates between 70 and 90 breaths per minute or exhibiting stridor at rest should be hospitalized. A child with a temperature higher than 102.2° F (39° C) should be carefully evaluated; hospitalization may be necessary if other worrisome symptoms are present. Racemic epinephrine by aerosol may help but should be used in conjunction with corticosteroids to limit rebound swelling (dexamethasone 0.5 to 2 mg/kg/dose every 8 hours IV). Hydration is important (Fox and Christenson, 2014). IV fluids may be needed in patients who cannot tolerate feedings. Complications Increasing obstruction of the airways causes continuous stridor, nasal flaring, and suprasternal, infrasternal, and intercostal retractions. With further obstruction, air hunger and restlessness occur and are quickly followed by hypoxia, weakness, decreased air exchange, decreased stridor, increased pulse rate, and eventual death from hypoventilation. Anything that taxes the child's respiratory efforts, such as crying or feeding, causes more respiratory distress. Examination of the nasopharynx with a tongue depressor may result in sudden respiratory compromise. Severely ill children should be evaluated for acute epiglottitis or bacterial tracheitis. Viral pneumonia complicates about 1% to 2% of croup cases. Respiratory syncytial virus immune globulin RSV-IGIV (RespiGam) Reduces risk of RSV bronchiolitis or pneumonia in high-risk children Provides additional protection against other respiratory viral illnesses; may be preferred over palivizumab in children with immune deficiencies or for premature infants prior to discharge in the RSV season for the first month of prophylaxis Palivizumab, a monoclonal antibody, is generally preferred over RSV- IGIV (see Chapter 32, Bronchiolitis)