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Otitis media is a middle ear infection associated with effusion, rapid

symptom development, and evidence of middle ear inflammation.

Case 104-8 (Questions 1–3)

Options for therapy include antibiotic management and watchful waiting,

the choice of which depends on the age of the child and severity of

disease. Amoxicillin (or amoxicillin/clavulanate) remains the antibiotic of

choice despite the high incidence of penicillin nonsusceptible

Streptococcus pneumoniae.

Acute pharyngitis may be caused by respiratory viruses or bacteria, most

commonly Streptococcus pyogenes. Treatment goals for bacterial

pharyngitis include resolution of symptoms and prevention of rheumatic

heart disease. Amoxicillin is the antibiotic of choice for bacterial

pharyngitis.

Case 104-9 (Questions 1, 2)

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p. 2155

Children represent more than 25% of the population and receive an average of three

prescription medications before 5 years of age. According to the Slone Survey,

between 1998 and 2007, 56% of children younger than 12 years of age had taken at

least one medication in the previous week.

1 Prescription medications accounted for

only 20% of cases; thus, the use of over-the-counter (e.g., nonprescription)

medications was most prevalent. The most predominant over-the-counter medications

used were acetaminophen, pseudoephedrine, ibuprofen, dextromethorphan,

antihistamines, and iron. The most prevalent prescription medications were

amoxicillin and albuterol. The prevalence of chronic medication use for

dyslipidemia, hypertension, type 2 diabetes, and attention deficit hyperactivity

disorder has increased in recent years, illustrating that chronic disease management

is becoming more important in pediatric medicine.

2,3 Given the prevalence of

medication use in children, it is essential that health care providers be prepared to

educate families and children on the appropriate use of over-the-counter and

prescription medications.

ADMINISTERING MEDICATION TO CHILDREN

CASE 104-1

QUESTION 1: M.B., a 16-month-old girl weighing 9 kg, has been diagnosed with an ear infection. She will be

receiving amoxicillin (400 mg/5 mL) 5 mL by mouth every 12 hours. What tips for successfully administering

these medications should be recommended?

Oral Medications

The administration of oral medications to a young child or infant often requires two

adults: one to gently restrain the child while the other rapidly and accurately

administers the medication. If only one adult is available, one can restrain the arms

and legs of the child in a swaddling blanket or large towel as depicted in Figure 104-

1.

Figure 104-1 Administration of oral liquid medication to a young child. (1) Premeasure the medication and have it

within reach. (2) Hold the child in your lap, placing one of the child’s arms behind your back and both of the child’s

legs between your legs. Restrain the child’s other arm securely with your nondominant arm. (3) Tilt the child’s

head back slightly, pressing gently on the child’s cheeks to open the mouth. Using your dominant hand, aim the

dropper or syringe between the rear gum and cheek. Administer small amounts of medication (1–2 mL) at a time,

making sure the baby swallows.

The administration device (syringe, dropper, or dosing spoon) that generally

accompanies a liquid medication product provides the most accurate measurement of

the desired dose. For infants, liquid medications are most easily administered to the

back cheek in 1- to 2-mL amounts with an oral syringe. Household teaspoons should

not be used to measure medications because teaspoons are of variable sizes and hold

3 to 8 mL of a liquid. Other considerations involve the unit of measurement. To

decrease errors and improve precision of drug delivery, it is recommended to use

milliliter-based dosing exclusively while prescribing and administering liquid

products.

4 Regarding unique delivery devices, studies have shown that parents have

more difficulty accurately delivering doses using dosing cups than other devices.

5

In some situations, crushed tablets or capsule contents mixed in small amounts (1–

2 teaspoons) of food (e.g., chocolate pudding, applesauce, ice cream, jelly, and

chocolate syrup) offer an alternative to liquid formulations. The taste of liquid

dosage formulations is generally improved by refrigeration and flavoring agents, and

“chasers” (i.e., popsicle, chocolate syrup, or a flavored drink after a dose) are also

helpful. Although medications can be delivered in small amounts (10–15 mL) of

liquid in a bottle (juice, milk, and formula), doses should not be diluted into an entire

scheduled feeding or prepared ahead of time in batches in anticipation of future

administration. Limiting the volume more likely facilitates delivery of the entire

dose, and adding the medication to a feeding bottle immediately before delivery

minimizes the potential of drug instability. Drug interactions with foods and dairy

products should also be considered before drugs are added to feeding formulas. Most

children are able to swallow tablets at 5 to 8 years of age. Duplicate supplies of

medication should be provided to the caregiver, when midday doses are required for

children who attend school or childcare in the event a dose is dropped. Children of

all ages should be encouraged and praised for their cooperation in taking their

medicine. Rewards and positive reinforcements can be useful to gain cooperation in

an older child.

For M.B.’s amoxicillin, the parents should be given a dosing syringe and shown

how to measure 5 mL. If M.B. is uncooperative with medication administration, she

may need to be restrained and the medication delivered in 1- to 2-mL increments.

The parents should be ready to provide M.B. with something that tastes good

immediately after administering the medication.

Ear, Nose, and Eye Drops

Otic, ophthalmic, and nasal medications usually need to be administered to infants

and young children in a different manner than adults. Otic medications should be

instilled by pulling the auricle down and out in infants and young children, whereas

older children should have the auricle of the ear held up and back to straighten the

ear canal. During the instillation of nose and eye drops, position infants and toddlers

with their head lower than the rest of the body because gravity assists in dispersing

the medication. This can be achieved by laying the infant across a bed with the

shoulders projecting over the edge of the bed. Restraining the infant often is required

during the administration of ophthalmic formulations. When administering the eye

medication (Fig. 104-2), the caregiver must be cautious to avoid injury to the eye

caused by sudden movements of the infant. The technique of placing the hand, which

holds the eye medication on the forehead of the infant during administration, can help

to minimize eye injury because the hand holding the eye dropper will move when the

infant’s head moves.

To minimize fear and improve cooperation during instillation of eye, nose, or ear

drops, the procedure should be explained to the child as simply as possible. It is best

to warm the medication in your hand for a few minutes before administration because

medications can feel cold inside the ears or nose even when stored at room

temperature.

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p. 2156

Figure 104-2 Administering eye drops to a young child. (1) Place the child on a flat surface. Enlist the help of a

second adult to restrain the child or swaddle the child. (2) Holding the child’s head steady, gently pull the eyelids

apart. The hand that is holding the medication dropper can rest on the child’s head while administering the

medication to minimize the potential for injury to the eye if the child’s head moves abruptly. Administer the

medication as directed.

If ear drops were to be administered to M.B., she should be lying down with the

affected ear up. The auricle should be pulled down and out, and the ear drops placed

in the ear canal. She should remain in that position for at least 1 minute.

INFANT CARE

Diaper Rash

ETIOLOGY

Diaper dermatitis is commonly encountered in pediatric practice, occurring in up to

4.

1.

2.

3.

35% of infants at any given time. Although the pathogenesis of diaper dermatitis is

not well defined, a number of factors (e.g., chemical irritants, friction, and bacteria)

have been associated with skin inflammation in the diaper area. In particular, skin

wetness and pH have been implicated in diaper dermatitis, and wetness appears to

have greater influence than that of pH. Overhydration of the skin increases the

permeability of low-molecular-weight compounds and exacerbates the effects of

friction.

6 Cloth diapers covered with plastic pants or disposable diapers with plastic

outer linings decrease air circulation and increase moisture in the diaper area and

should be avoided.

7 Residual chemicals or laundry detergents in the diaper (cloth or

disposable), as well as soaps, medications, or lotions that have been applied directly

to the infant’s skin, also have roles in the development of diaper rash.

CLINICAL PRESENTATION

Four clinical presentations of dermatitis are associated with diaper wear:

A mild, scaling rash in the perianal area

A sharply demarcated confluent erythema

Ulceration distributed through the diaper area

A beefy red confluent erythema with satellite lesions, vesiculopustular lesions, and

diffuse involvement of the genitalia

TREATMENT

CASE 104-2

QUESTION 1: K.G., a 3-month-old infant, has had a severe diaper rash for the last 4 days. The very inflamed

and tender area is confined to the diaper area, and vesicular satellite lesions are present on the periphery of the

erythematous area. K.G.’s mother uses only cloth diapers and has not changed soap or her normal pattern of

diaper care since K.G. was born. What is the likely cause of K.G.’s diaper rash and what treatments are

appropriate?

K.G.’s rash is consistent with a candidal infection, which typically is beefy red

and associated with vesicular satellite lesions. The presence of a rash for longer than

3 days and the diffuse involvement of the genitalia and inguinal folds are also

characteristic of this form of diaper rash. K.G.’s rash can be treated with 1%

clotrimazole or 2% miconazole cream applied to the inflamed area four times daily

until it has resolved. Nystatin (100,000 units/g) ointment can be applied, but often is

not as effective as the imidazole antifungals because of increasing resistance of

Candida species to nystatin.

CASE 104-2, QUESTION 2: What steps would you recommend for K.G.’s mother to treat her diaper rash

and prevent recurrence?

The removal of stool and urine from the diaper area by gentle rinsing with plain

water and more frequent diaper changes often help to alleviate diaper rashes. Wiping

the baby with diaper wipes that contain alcohol can sting, further irritating the



involved area, and should be avoided until the rash has resolved. A good protective

agent containing zinc oxide or petrolatum (e.g., Desitin) can be applied with each

diaper change to create a barrier to irritants and seal out moisture. Powdered

protective agents (e.g., cornstarch and talc) can minimize friction caused by diapers,

but should be used cautiously because the infant can aspirate powder particles and

develop a chemical pneumonia.

8 When used, powders should be shaken into the

diaper or applied close to the body, away from the baby’s face. Other prevention and

treatment measures appropriate for K.G. include the following:

Change the diaper as soon as it is wet or at least every 2 to 4 hours during the day.

Keep the diaper area clean (e.g., nightly baths until resolved).

Use superabsorbent disposable diapers at night.

Expose the diaper area to air as often as possible.

Dry the diaper area completely before a new diaper is put on.

Apply a barrier cream such as zinc oxide or petrolatum after each diaper change.

For cotton diapers, use a bacteriostatic agent in the diaper pail and rinse water or

use a diaper service to ensure that diapers are sterile.

Apply a low-potency, nonfluorinated topical corticosteroid, such as 0.5% to 1%

hydrocortisone, twice daily for no longer than 2 weeks when severe inflammation

is present.

7

Fever

Normal body temperature varies throughout the day, peaking in late afternoon or

early evening. Body temperature can be measured rectally, orally, axillary (under the

arm), temporally (on the forehead), and tympanically. Rectal temperatures are most

reliable in infants younger than 3 months of age. Oral measurements of temperature

are not appropriate in children younger than 3 years of age because it is difficult for

young children to maintain a tight seal around the thermometer.

Although references differ, fever can be defined as an axillary temperature greater

than 37.5°C (99.5°F) or a core temperature

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greater than 38°C (100.4°F).

9 Rectal and tympanic measurements are typically

0.3°C to 0.6°C (0.5°F to 1°F) higher than an oral reading, whereas axillary

measurements are lower by the same amount. (Fahrenheit temperatures can be

converted to or from centigrade temperatures by the formula °F = 1.8°C + 32.)

Children with fevers might not have other signs or symptoms of an illness. Any

child younger than 2 months of age who develops a fever requires a complete

evaluation (e.g., blood culture and urinalysis), because clinical manifestations of a

serious infection often are subtle, nonspecific, and not predictive of the extent or

severity of illness.

10

In this situation, antibiotic therapy is usually initiated while

awaiting laboratory results. Children 3 to 36 months of age with a temperature

greater than or equal to 39°C (102.2°F) and white blood cell counts less than 5,000

μL

–1 or greater than 15,000 μL

–1 are at increased risk for bacteremia.

10 Children of

any age with a temperature greater than 41°C should be evaluated not only for

bacteremia, but also for possible meningitis. Blood cultures, lumbar puncture,

urinalysis, and chest radiograph should be considered on an individual basis to help

determine the etiology of infection. Febrile immunocompromised children and febrile

children with functional or anatomic asplenia are at increased risk for sepsis or

fulminant infections (e.g., Streptococcus pneumoniae, Salmonella species, and

Escherichia coli) and should receive prompt antibiotic therapy.

11

Febrile Seizures

CASE 104-3

QUESTION 1: R.B., a 12-month-old, 10-kg baby boy, was well yesterday until his mother noticed that he felt

warm to her touch later in the afternoon. For the past 24 hours, he has remained warm and is fussy and less

active. A rectal temperature 15 minutes ago was 39°C. Because her other two children experienced febrile

seizures, his mother is concerned R.B.’s temperature will continue to rise and put R.B. at risk for febrile

seizures. Is this a valid concern?

Febrile seizures occur in approximately 2% to 4% of children 6 months to 5 years

of age who have temperature elevations greater than 38°C.

12 The etiology and

pathogenesis are unknown, and there is no evidence that the rate of temperature

increase is important.

13 Genetic predisposition also appears to be a factor because

febrile seizures occur with greater frequency among family members.

12 Febrile

seizures are of two types: simple and complex. Simple febrile seizures last less than

15 minutes and do not have significant focal features. Complex febrile seizures have

a longer duration, occur in series, and are associated with focal changes. Typically,

febrile seizures occur within the first 24 hours of a febrile episode.

12,13 Although R.B.

is in the age group at greatest risk for having a febrile seizure, he has been febrile for

more than 24 hours, and a seizure is unlikely during this illness.

TREATMENT

CASE 104-3, QUESTION 2: How should R.B.’s fever be treated?

Acetaminophen is the most common antipyretic agent used in children. The usual

dose, oral or rectal, is 10 to 15 mg/kg/dose administered every 4 to 6 hours as

needed to a maximum of 75 mg/kg/day.

14

Ibuprofen is administered as 5 to 10

mg/kg/dose orally every 6 to 8 hours as needed to a maximum of 40 mg/kg/day.

Ibuprofen is as effective as acetaminophen as an antipyretic and is similar in safety.

15

Although renal failure has been reported after ibuprofen use in children, the risk of

renal impairment appears greater in children with dehydration, underlying

cardiovascular or renal disease, or other nephrotoxic drugs, and children <6 months

of age.

15

Acetaminophen 100 to 150 mg every 4 to 6 hours as needed or ibuprofen 50 to 100

mg every 6 to 8 hours as needed should be effective in lowering R.B.’s fever.

Acetaminophen typically has been considered to be a first-line drug in children.

Dosing errors have occurred, when teaspoonful quantities of acetaminophen infant

drops (80 mg/0.8 mL) were given instead of the liquid formulation (160 mg/5 mL) or

when regular-strength tablets (325 mg) have been substituted for chewable children’s

tablets (80 and 160 mg). To reduce the risk for dosing errors, in 2011, the Consumer

Healthcare Products Association (a group of leading manufacturers and distributors

of nonprescription medications) voluntarily converted to a single 160 mg/5 mL

acetaminophen concentration. In addition, in 2017 manufacturers began transitioning

to a single strength of children’s chewable acetaminophen tablets (160 mg).

However, providers should continue to question caregivers about the dosage form of

acetaminophen they have at home, concurrent use of any other products containing

acetaminophen, and whether cumulative doses are within the recommended range.

Recent data have suggested that ibuprofen may be a more effective alternative to

acetaminophen for R.B. and should be used first.

16

It is available in two liquid

formulations (infant drops, 40 mg/mL; children’s suspension, 100 mg/5 mL) and a

chewable tablet (100 mg). Adverse effects are limited when ibuprofen is used in

recommended doses for short-term antipyresis. Some data suggest that combination

therapy with acetaminophen every 4 to 6 hours and ibuprofen every 6 to 8 hours may

be more effective in reducing time with fever in the first 24 hours.

16 However,

combination therapy may be associated with medication errors,

15 and recent data

suggest an increased risk of acute kidney injury may occur with this combination.

17

Aspirin therapy is not recommended for treatment of fever in children or adolescents

with chickenpox, gastroenteritis, or respiratory viral infections because of its link

with Reye syndrome.

18,19

Cough and Cold

Another common diagnosis in children is viral upper respiratory infection or the

common cold. Preschool children generally experience between six and eight colds

each year.

20 Children with a cold often present with sore throat, nasal congestion,

rhinorrhea, sneezing, cough, and irritability.

CLINICAL PRESENTATION AND TREATMENT

CASE 104-4

QUESTION 1: J.K. is a 3-month-old, 5.3-kg infant who began having nasal congestion, rhinorrhea, and cough

yesterday. She has had no fever and is eating well, but did not sleep well last evening. J.K.’s mother called her

pediatrician and was told that J.K. most likely has a cold caused by a virus. J.K.’s mother would like to know

which cold medications would be appropriate to manage J.K.’s symptoms.

A cool-mist humidifier can increase the amount of moisture in room air and

decrease irritation in the upper airway when humidity is low. Saline nose drops

followed by bulb suctioning can help to clear the nasal passages in J.K. who is

younger than 6 months of age. It is especially important to do this before feedings. A

decongestant, however, should not be prescribed for J.K. because of her age and the

potential for adverse effects. If J.K. was older and a topical nasal decongestant was

needed, phenylephrine would be preferred over oxymetazoline and xylometazoline

because of its lesser association with toxicity (e.g., sedation, convulsions, insomnia,

and coma) in children younger than 6 years of age.

21,22 Neither antihistamines,

antitussives, nor guaifenesin should be recommended for J.K.

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because there is no evidence of their efficacy, and unintentional overdoses are

common in this age group. Antihistamines are not effective for rhinorrhea caused by

the common cold and should not be recommended. Antitussives are likely not

effective and should not be used if the child’s cough is productive. Expectorants,

such as guaifenesin, are also not effective, and evidence is insufficient to support the

use of vitamin C, zinc, or echinacea in children for treatment or prevention of the

common cold.

Several hundred over-the-counter medications for upper respiratory symptoms are

available, and over 1 billion units of these products are sold each year in the United

States.

23 Nevertheless, the safety and effectiveness of these cough and cold

medications in children have yet to be proved.

24 The Centers for Disease Control and

Prevention (CDC) reported that 1,519 children younger than 2 years of age were

admitted to emergency departments in 2004 to 2005 because of overdoses and other

problems associated with cough and cold medicines. Furthermore, according to the

US Food and Drug Administration (FDA), 54 deaths in children were linked to the

use of decongestants (e.g., pseudoephedrine, phenylephrine, and ephedrine) and 69

deaths to antihistamines (e.g., diphenhydramine, brompheniramine, and

chlorpheniramine) from 1969 to September 13, 2006. Most of these deaths occurred

in children younger than 2 years of age, and some of the fatalities occurred in

children who received overdoses that might have been the result of inadvertent

administration of multiple medications containing the same ingredient.

In 2008, the FDA issued a public health advisory recommending that over-thecounter cough and cold medications not be used in children younger than 2 years of

age.

25 Later that year, the Consumer Healthcare Products Association announced that

many manufacturers would voluntarily modify their labels to exclude

recommendations for children younger than 4 years of age.

26 Owing to reports of

toxicity and death related to over-the-counter cough and cold products, the CDC has

recommended that caregivers avoid giving these products to children younger than 2

years of age unless advised by a clinician.

24

If deemed necessary by a physician for

older children, nonprescription cough and cold medications containing single

ingredients should be selected to minimize the potential for adverse effects and

administration of multiple products with similar ingredients. Of note, parents often

misunderstand labeling of over-the-counter products, placing the child at risk for

dosing errors.

27

It is critical that health care providers educate caregivers on the

proper use and administration of these medications to children. Treatment of J.K.’s

symptoms should include the use of a cool-mist humidifier in the room and saline

nasal drops followed by suctioning before feedings.

Constipation

Chronic constipation is defined as delay or difficulty in stooling for at least 2 weeks’

duration.

28,29

It accounts for 3% of annual visits to pediatrician offices, and up to a

quarter of referrals to gastroenterologists.

30 Beyond the neonatal period, constipation

is most commonly idiopathic or functional and may be related to a diet low in fiber,

lack of time or routine for toileting, or passage of a painful stool resulting in a fear of

defecating. Other causes of constipation include anatomic (fissures), neurogenic

(Hirschsprung disease), hypotonic (cerebral palsy), and endocrine (cystic fibrosis

and hypothyroidism) disorders.

30 Medications such as opioids, antacids, and

anticonvulsants, among others, can also contribute to constipation. It is important that

constipation be managed appropriately because it can have negative effects on

growth and development, has been linked to gastrointestinal distress, and adversely

impacts quality of life.

30

In addition, constipation in childhood can remain a problem

into adulthood.

31

CLINICAL PRESENTATION AND TREATMENT

CASE 104-5

QUESTION 1: R.J., a 2-year-old, 15-kg boy, has had abdominal pain for 4 weeks. On average, he has one

stool weekly, and he cries each time because of pain. R.J. eats regular table food and has two glasses of whole

milk each day. After obtaining a thorough history and performing a physical examination, the physician

determines that R.J. has functional constipation. What treatment measures are appropriate to relieve and

prevent R.J.’s constipation?

Before maintenance therapy can be initiated, disimpaction of the patient is

necessary. Although no controlled studies compare efficacy of the oral and rectal

routes, oral therapy (mineral oil, polyethylene glycol, and bisacodyl) is preferred

because it is less invasive and might lead to better adherence than rectal therapy

(phosphate soda enemas, mineral oil enemas, glycerin suppositories in infants, and

bisacodyl suppositories in older children).

30 After disimpaction, a combination of

behavioral, dietary, and pharmacologic therapies should be initiated to promote

regular stool production and prevent reimpaction. Dietary interventions include

adequate fluid and fiber intake. The impact of cow’s milk on constipation is still

controversial. Some data suggest no link,

30 although other recent literature hints at

causation through an immune-mediated mechanism.

31,32 Medications such as

polyethylene glycol 3350, mineral oil, lactulose, and sorbitol should be titrated to

produce one to two soft stools daily. Stimulant laxatives might be needed

intermittently in certain cases. Although no clear recommendation for one

maintenance medication has been given over others, recent data suggest that

polyethylene glycol may be the most effective and best tolerated in children.

33–37 The

recommended dosing of medications for treatment of constipation is listed in Table

104-1. Appropriate initial therapy for R.J. could include eliminating or limiting milk

intake, behavioral techniques, and polyethylene glycol 0.5 to 1.5 g/kg/day (7.5–15 g).

Practically, this would be half to one 17-g packet administered daily in 4 to 8 ounces

of water or other beverage.

Vomiting and Diarrhea

Vomiting and diarrhea, two commonly encountered complaints in pediatric practice,

are usually self-limiting, but severe cases can result in serious complications such as

dehydration, metabolic disturbances, and even death. Infants and young children are

particularly susceptible to the more severe complications.

PATHOGENESIS AND PRESENTATION OF VOMITING

Vomiting or emesis is defined as forceful expulsion of gastrointestinal (GI) contents

through the mouth or nose, while nonforceful expulsion of GI contents is considered

regurgitation. In newborns, regurgitation of small amounts of breast milk or formula

after feeding, especially when burping, is common. In most cases, regurgitation

usually resolves by 1 to 2 years of age and rarely causes problems.

38 Extensive

evaluation of regurgitation is not needed in a child who is growing well. Other

causes of vomiting during the newborn period include pyloric stenosis,

gastroesophageal reflux (GER), overfeeding, food intolerance, and GI obstruction.

Beyond the neonatal period, the most common cause of vomiting is infection.

Vomiting in infants and children can also be caused by central nervous system (CNS)

disease (e.g., intracranial tumors), metabolic disease (e.g., urea cycle disorder),

inflammatory bowel disease, and ulcers. Conditions causing emesis in older infants

and children range from viral gastroenteritis to more severe illnesses, such as bowel

obstruction or head injury, which require immediate medical attention.

39 Acute

vomiting can also result from medication or toxic ingestions. In teenagers, migraine,

pregnancy, and psychological disorders, such as bulimia, have been associated with

vomiting.

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Table 104-1

Medications for the Treatment of Constipation

28,29

Medication Initial Dosage Comments

Osmotic Agents

Polyethylene glycol 3350 0.2–0.8 g/kg/day 0.5 g/kg initial dose; titrate to effect; do not

exceed 17 g/day

Lactulose 1–2 g/kg/day divided once or twice

daily

1.5–3 mL/kg/day; do not exceed 60 mL/day

Sorbitol 1–3 mL/kg/day once or twice daily Less expensive than lactulose

Barley malt extract 2–10 mL/240 mL of milk or juice daily Useful for infants drinking from a bottle

Magnesium hydroxide 1–3 mL/kg/day using 400 mg/5 mL Infants are at risk for hypermagnesemia

Phosphate enema ≥2 years of age: 6 mL/kg up to 135

mL

Electrolyte abnormalities more common in

children with renal failure or Hirschprung

disease. Avoid in children <2 years

Lubricant

Mineral oil >1 year of age: Disimpaction: 15–30

mL/year of age up to 240 mL daily

Better tolerated if chilled. Avoid in children

<1 year. Lipoid pneumonia may occur if

aspirated

Maintenance: 1–3 mL/kg/day Maximum daily dose: 90 mL/day

Stimulants

Senna 2–6 years of age: 2.5–5 mg/day Not recommended for chronic use

6–12 years of age: 7.5–10 mg/day

>12 years: 15–20 mg/day

Bisacodyl 3–10 years: 5 mg/day Not recommended for chronic use

>10 years: 5–10 mg/day

Glycerin suppositories 2–5 years: 1 pediatric suppository per

dose

Preferred stimulant for children <2 years of

age

≥6 years: 1 adult suppository per dose

PATHOGENESIS AND PRESENTATION OF DIARRHEA

Diarrhea refers to an increase in frequency, volume, or liquidity of stool when

compared with normal bowel movements. In developing countries, diarrhea is a

common cause of death in children younger than 5 years of age. In the United States,

gastroenteritis accounts for approximately 1 to 2 million physician visits, more than

200,000 hospitalizations, and about 300 deaths each year.

40

Acute diarrhea in infants and children is generally abrupt in onset, lasts a few

days, and is most commonly caused by viruses. (see Chapter 69, Infectious Diarrhea

for infectious diarrhea of other origins.) Diarrhea is considered chronic if it is longer

than 2 weeks in duration. Chronic diarrhea can be caused by malabsorption,

inflammatory disease, infection, alteration of intestinal flora, milk or protein

intolerance, drugs, and other causes.

41

Infants and children are at high risk for morbidity and mortality secondary to

diarrhea for several reasons. Dehydration can occur easily because acute net

intestinal fluid losses are relatively much greater in young children than in adults.

This may result from inefficient transport systems in the developing intestine. In

addition, the percentage of total body water in children is higher than in adults; thus,

they are more susceptible to body fluid shifts. Total body water changes from 80% of

total body weight in premature infants to 70% in term infants and 60% in adults.

Finally, the renal capacity to compensate for fluid and electrolyte imbalances in the

infant is limited compared with that of adults.

42

VIRAL GASTROENTERITIS

CASE 104-6

QUESTION 1: J.R., a 15-month-old male 10-kg infant, had one loose stool and began vomiting this morning,

but he has not had a fever. On questioning, you discover that many children attending day care with J.R. are

experiencing vomiting, diarrhea, and low-grade temperatures. How should J.R.’s vomiting be treated?

Routine use of antiemetics for acute vomiting in children is not recommended

because masking of symptoms may delay diagnosis of a treatable illness. In addition,

the safety and efficacy of the antiemetics, including metoclopramide, promethazine,

trimethobenzamide, and dimenhydrinate, have not been demonstrated.

43

In particular,

promethazine is contraindicated in children younger than 2 years of age because of

the risk of fatal respiratory depression. Ondansetron does decrease vomiting,

increases oral intake and decreases the need for intravenous (IV) rehydration;

however, the utility of ondansetron in gastroenteritis needs consideration because this

effect may not be sustained, and the drug has not been shown to decrease consistently

hospital admission.

44–46

Parents should be taught the signs and symptoms of gastroenteritis and vomiting

that are sufficiently serious to warrant medical attention. The child’s primary-care

provider should be contacted if the child is toxic appearing, exhibits unusual

behavior, exhibits signs of an ear infection, experiences abdominal pain or

distension, has red or black vomitus or stool, or if there is a history or suspicion of

toxic ingestion or head trauma. Medical evaluation is also necessary for infants

younger than 6 months of age, when persistent vomiting or high-volume diarrhea is

present, or when

p. 2159

1.

p. 2160

chronic medical conditions or prematurity is involved. Because fever can

accompany vomiting in viral gastroenteritis, any fever occurring in a neonate

warrants medical attention. Fever in older infants and children warrants medical

attention, when it becomes prolonged or changes in pattern.

When communicating with a health care provider about a vomiting child, it is

helpful if the parents have knowledge of the child’s fluid intake, and the frequency

and volume of vomiting and urination. The amount of vomitus can be estimated by the

following rule of thumb: one tablespoon makes a spot 4 inches wide and a quartercup makes a spot approximately 8 inches wide.

Vomiting associated with gastroenteritis usually resolves in 24 to 48 hours. Infants

are particularly susceptible to the development of fluid and electrolyte abnormalities;

therefore, fluid and electrolyte replacements are critically important.

J.R., who is early in the course of gastroenteritis, must receive sufficient fluids to

prevent dehydration. Oral hydration therapy can be successful when given in small

volumes, even if J.R. is still vomiting. For example, 5 to 10 mL can be administered

every 5 to 10 minutes, with gradual increases in volume as tolerated. Volumes equal

to estimated fluid deficit (usually 50–100 mL/kg) should be given over the course of

2 to 4 hours. For each diarrheal stool, an additional 10 mL/kg of oral electrolyte

solution should be given. If diarrhea or vomiting recurs, 10 mL/kg and 2 mL/kg of an

oral rehydration solution (ORS) can be administered for each stool or emesis,

respectively.

46 J.R.’s clinical condition should continue to be monitored by his

caregiver. If stool output exceeds 10 mL/kg/hour, ORS might not be sufficient, and

the health care provider should be contacted. ORS should only be abandoned in

children with intractable vomiting, loss of consciousness, bowel obstruction, or if the

child is in shock. Most infants will tolerate oral hydration when small amounts are

given frequently. As dehydration is corrected, the frequency of vomiting typically

decreases. Once rehydration has been achieved, fluids other than ORS and a diet

appropriate for age may be started.

46 Breast milk or formula should be given as

tolerated.

Assessment of Dehydration

CASE 104-6, QUESTION 2: On the second day of illness, J.R. develops a mild fever and diarrhea that has

increased in frequency and water content. How can the severity of J.R.’s diarrhea be assessed?

To determine the severity of dehydration and whether hospitalization may be

needed, consider the following questions:

Does the child have any of the following signs and symptoms of severe

dehydration: deeply sunken eyes, parched mucous membranes, significantly

prolonged capillary refill; cool, mottled extremities; crying without tears; oliguria

2.

3.

or anuria; weak or thready pulses; lethargy; poor oral intake; deep respirations;

history of seizures or convulsions; a fever without perspiration; or thirst?

Are a large number of copious stools still being produced (>10 mL/kg/hour)? Is

bowel obstruction a possibility?

Is there a risk of dehydration from inadequate monitoring, or is the parent unable to

care for the child? Specific inquiries should be made about the number and

consistency of stools in children with diarrhea.

Estimating the degree of dehydration is particularly valuable in assessing the

patient with diarrhea, and weight loss is a good criterion. A 3% to 9% weight loss is

considered mild to moderate dehydration, whereas more than 9% is considered

severe dehydration.

43

(see Chapter 103, Pediatric Fluid, Electrolytes, and Nutrition,

for information about IV replacement therapy in children with 10% or more

dehydration.)

Oral Replacement Therapy

CASE 104-6, QUESTION 3: J.R. was evaluated by his pediatrician and was not considered to be sufficiently

dehydrated to warrant hospitalization. How might J.R.’s fluids and electrolytes be managed on an outpatient

basis?

The goal of J.R.’s treatment should be focused on the prevention of dehydration

and the restoration and maintenance of adequate fluid and electrolyte balance. Mild

to moderate diarrhea without dehydration is generally managed at home by continued

age-appropriate feeding. Fluid losses in stools can be replaced with a glucosecontaining ORS. Glucose provides calories and enhances salt and water absorption

in the small intestine through mechanisms that are usually unimpaired in many toxininduced diarrheas. Parents formerly were instructed to prepare salt and sugar

solutions at home; however, frequent errors in the preparation of these solutions

resulted in exacerbation of problems with fluid and electrolyte balance.

Commercially available oral glucose–electrolyte formulations, such as Pedialyte, are

designed to enhance glucose and sodium absorption and should be used in infants and

young children. Carbonated beverages and fruit juices do not contain sufficient

sodium to replace diarrheal losses and should not be used. Rehydration and

maintenance solutions can be made more palatable with sugar-free flavorings (e.g.,

Kool-Aid and Crystal Lite).

The World Health Organization (WHO) formerly promoted use of an oral

replacement solution (WHO formula) containing sodium (90 mEq/L), potassium (20

mEq/L), bicarbonate (30 mEq/L), chloride (80 mEq/L), and 2% glucose for the

widespread management of acute diarrhea in third-world countries. The WHO

formula, which had a 90% successful rehydration rate for the management of

diarrhea, contained a high concentration of sodium. Although commercially available

ORS contain less sodium than the WHO formulation, these preparations were equally

effective as the WHO formula, even when used to treat the high-sodium losses

associated with cholera. Furthermore, these lower sodium-containing formulations

were associated with less vomiting, lower stool output, and reduced need for IV

infusions in non–cholera-associated gastroenteritis. As a result, the WHO, in 2002,

promoted a new formulation that consists of 75 mEq/L sodium and a total osmolarity

of 245 mOsm/L.

43,45 Glucose is added to oral electrolyte solutions to enhance

glucose-coupled sodium transport; however, concentrations greater than 3% can

impair sodium absorption because the glucose-coupled sodium transport system

becomes saturated at this concentration and any additional glucose acts as an

osmotically active solute in the bowel lumen. The electrolyte content of commonly

used ORS is provided in Table 104-2. Assuming J.R.’s fluid deficit is 50 to 100

mL/kg, he should receive 500 to 1,000 mL of ORS in the course of approximately 4

hours. In addition, he should receive an extra 100 mL for each diarrheal stool and 20

mL for each emesis that occurs. If stool output continues at a pace that cannot be

matched with oral replacement, or signs and symptoms of severe dehydration occur,

J.R. should be referred to his pediatrician again.

REINSTITUTION OF ORAL FEEDINGS

Previously, feeding during an episode of viral gastroenteritis has been delayed

because of the malabsorption that typically occurs during and after these bouts. The

malabsorption, however, is self-limiting, and substantial amounts of carbohydrate,

protein, and fat can still be absorbed. The reinstitution of a regular diet, therefore,

should not adversely affect mild diarrhea and can be beneficial.

46 Parents are

encouraged to continue feeding their children using age-appropriate diet while

avoiding simple sugars, which can increase osmotic load and worsen diarrhea.

Continuation of oral feeding, despite diarrheal episodes, minimizes the development

of protein and energy deficits, facilitates the maintenance and repair of intestinal

mucosa, promotes recovery of brush border membrane disaccharidases, decreases

the duration of illness, and improves nutritional status.

45,46 Although lactose

intolerance can occur with viral gastroenteritis, most children with mild diarrhea can

tolerate full-strength animal milk, animal milk-based formula, and breast milk. If the

child becomes lactose intolerant during this illness, a lactose-free formula may be

substituted for 2 to 6 weeks until GI lactase production returns to normal. Specific

diets are often recommended during diarrhea (e.g., BRAT [bananas, rice, applesauce,

toast]). Although these diets can be occasionally useful, the nutritional value of these

foods is relatively low, and they do not provide optimal nutrition compared with

complete diets with fats and proteins.

45,46 Once J.R. has been adequately rehydrated,

he may resume his normal diet. However, the caregivers must take care to avoid

juices and other foods with simple sugars, which may worsen diarrhea.

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p. 2161

Table 104-2

Oral Electrolyte Solutions

43

Solution

Compositions

Sodium (mmol/L)

Potassium

(mmol/L)

Carbohydrate

(mmol/L) Osmolality

Rehydration

Rehydralyte 75 20 140 305

WHO formula (1975) 90 20 111 311

WHO formula (2002) 75 20 75 245

Maintenance

Enfalyte 50 25 167 200

Pedialyte 45 20 139 250

Home Remedies

Apple juice 0.4 44 667 730

Gatorade 20 3 255 330

Ginger ale 3 1 500 540

Chicken broth 250 8 500

Cola 1.6 622 730

WHO, World Health Organization.

Drug Therapy

Medications play a minor role in the treatment of acute infantile diarrhea because

most episodes are self-limiting. Antibiotics are recommended when systemic

bacteremia is suspected, when immune defenses are compromised, when a persistent

enteric infection is sensitive to antibiotics, or when Shigella, Campylobacter, Vibrio

cholerae, Clostridium difficile, and certain Escherichia coli strains are isolated.

46,47

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