Basics
Description
- Problems may present in 1 or several of the components of "feeding":
- Getting food into oral cavity: Appetite, food-seeking behavior, ingestion
- Swallowing food: Oral and pharyngeal phases
- Ingestion and absorption: Esophageal swallowing, GI phase
- Acute feeding problems may be a component of acute systemic disease:
- Infection, bowel obstruction
- Chronic feeding problems may result from underlying neuromuscular, cardiovascular, or behavioral issues:
- Cerebral palsy, prematurity, congenital heart disease, chronic neglect
- Minor feeding difficulties reported in 25-50% of normal children:
- Mainly colic, vomiting, slow feeding, and refusal to eat
- More severe problems observed in 40-70% of infants born prematurely or children with chronic medical conditions.
Etiology
- Several distinct areas of pathology-but overlap is common
- Structural abnormalities:
- Naso-oropharynx:
- Cleft lip/palate
- Choanal atresia
- Micrognathia and/or Pierre Robin sequence
- Macroglossia
- Tonsillar hypertrophy
- Retropharyngeal mass or abscess
- Larynx and trachea:
- Laryngeal cleft or cyst
- Subglottic stenosis
- Laryngo- or tracheomalacia
- Tracheoesophageal fistula
- Esophagus:
- Esophageal strictures, stenosis, or web
- Tracheoesophageal compression from vascular ring/sling
- Esophageal mass or tumor
- Foreign body
- Neurologic conditions:
- Cerebral palsy
- Muscular dystrophies
- Mitochondrial disorders
- Arnold-Chiari malformation
- Myasthenia gravis
- Brainstem injury
- Pervasive developmental disorder (autism spectrum disorders)
- Infant botulism
- Brainstem glioma
- Polymyositis/dermatomyositis
- Prematurity
- Immune disorders:
- Allergy
- Eosinophilic esophagitis
- Celiac disease
- Congenital heart disease:
- Precorrection: Fatigue, respiratory compromise, increased metabolic needs
- Postcorrection: Any/all of the above, recurrent laryngeal nerve injury
- Chronic aspiration
- Conditioned dysphagia:
- Gastroesophageal reflux (GER)
- Prolonged tube or parenteral feeding early in life
- Metabolic disorders:
- Hypothyroidism
- Inborn errors of metabolism
- Acute illness or event:
- Sepsis
- Pharyngitis
- Intussusception
- Malrotation
- Shaken baby syndrome
- Behavioral issues:
- Poor environmental stimulation
- Dysfunctional feeder-child interaction
- Selective food refusal
- Rumination
- Phobias
- Conditioned emotional reactions
- Depression
- Poverty (inadequate food available)
Diagnosis
Signs and Symptoms
Common presentations:
- Caregiver concerns regarding feeding or postfeeding behavior
- Poor weight gain/failure to thrive
- Recurrent or chronic respiratory illness
History
- Onset of problem
- Length of meals (often prolonged)
- Food refusal/oral aversion
- Independent feeding (if >8 mo):
- Neuromuscular problems decrease ability to get food to the mouth
- Failure to thrive/poor weight gain
- Recurrent pneumonia/respiratory distress:
- Most aspiration episodes are silent in infants
- Recurrent pneumonia or wheezing may be primary symptoms of chronic aspiration
- Chronic lung disease
- Recurrent vomiting or gagging:
- Diarrhea, rectal bleeding
- Onset of irritability or lethargy during feeding, colic
- Duration of feeding highly variable, especially in breast-fed infants-for all ages, feeding times >30 min on a regular basis is cause for concern:
- Full-term healthy infant usually has 2-3 oz of formula every 2-3 hr.
- Breast-fed baby eats 10-20 min on each breast every 2-3 hr.
- As child gets older, duration and frequency may decrease.
- 1 mo old normally eats 4 oz every 4 hr.
Physical Exam
- Vital signs, including oximetry
- Weight, length, head circumference:
- Comparison with prior measurements; plotting growth curve
- Slow velocity of growth
- Impaired nutritional status. Severe cases may show emaciation, weakness, apathy.
- General physical exam-especially note:
- Affect and social responsiveness
- Dysmorphism (facial asymmetry, tongue and jaw size, etc.)
- ENT-oropharyngeal inflammation, infection, or anatomic abnormality
- Cardiovascular status (murmur, tachycardia, tachypnea, retractions)
- Pulmonary-tachypnea, color change, evidence of aspiration
- Abdominal exam-bowel sounds, distension, tenderness, masses
- Neurologic-tone, coordination, alertness
- Skin: Allergic rash or atopy:
- Loss of subcutaneous fluid or fat is often most apparent around the eyes, which will appear "sunken" in most dehydrated or malnourished infants
- Edema, however, may occur with protein deficiency (kwashiorkor).
- Observation of feeding: Neuromuscular tone, posture, position; patient motivation; oral structure and function; efficiency of oral intake:
- Ability to handle oral secretions
- Pace of feeding
- Noisy airway sounds after swallowing
- Gagging, coughing, or emesis during feeding
- Respiratory distress with feeding
- Oximetry during feeding may be helpful
- Onset of fatigue or irritability
- Duration of feeding
Essential Workup
- A well-hydrated, comfortable child with a normal physical exam and recent history of good weight gain may not need any ED workup beyond assuring good follow-up.
- Children who show evidence of distress, dehydration, discomfort, respiratory distress, or poor weight gain require further evaluation.
Diagnosis Tests & Interpretation
Lab
- Initial assessment if child failing to thrive or appears malnourished:
- CBC, urinalysis, electrolytes, BUN, glucose, erythrocyte sedimentation rate (ESR) and/or CRP, thyroid functions, LFTs, total protein, and albumin
- Cultures of blood, urine, if concern of infection-CSF analysis and culture if concern for meningitis
- Serum NH3, urine for organic acids, and blood for inborn errors or metabolism if concern for metabolic disorders
Imaging
- CXR if suspected cardiopulmonary concerns
- EKG if cardiac disease suspected
- Referral or admission for ultrasound and other imaging studies as indicated. Fiberoptic or videofluoroscopic evaluation of swallowing may be needed.
- MRI if concerns for brainstem, skull base, or spinal problems
Diagnostic Procedures/Surgery
- May need a multidisciplinary evaluation involving speech pathologist, pediatrician, and potentially an otolaryngologist.
- Surgical correction of specific pathology
Differential Diagnosis
Feeding disorder encompasses symptoms observed as a final pathway for many disorders.
Specific clues to the etiology may include:
- Prolonged feeding, fatigue:
- Consider cardiac disease.
- Recurrent pneumonias:
- Consider chronic aspiration.
- Stridor with feeds:
- Consider glottic or subglottic anomalies.
- Suck-swallow-breathing coordination:
- Consider nasal congestion, choanal atresia.
- Vomiting, diarrhea, abdominal pain, colic:
Treatment
Pre-Hospital
- Assess vital signs and hydration; resuscitate as necessary.
- Assess for and treat hypoglycemia.
Initial Stabilization/Therapy
- Cardiovascular/respiratory/fluid resuscitation as needed
- Assess for and treat hypoglycemia if suspected.
- Certain inborn errors of metabolism (glycogen storage diseases) can cause profound hypoglycemia if unable to take PO feeds-if known or suspected, IV dextrose should be started immediately
- Bilious vomiting in a young infant may be a sign of malrotation with volvulus causing intestinal ischemia-this requires emergent surgical consultation.
Ed Treatment/Procedures
- Treat dehydration if present:
- Oral rehydration if practical
- IV if PO contraindicated, not tolerated, or impractical
- Ondansetron for acute vomiting
- Treat respiratory distress if present:
- Nasal suction to clear secretions prior to feeding may be very helpful in young infants with URI/bronchiolitis symptoms
- Oxygen and other interventions as needed
- Treat infection if suspected.
Patients with severe malnutrition are at risk for sepsis AND may have blunted physiologic responses-a high index of suspicion for infection is warranted in severely malnourished patients.
Medication
Ondansetron: 0.1 mg/kg IV or PO q8h PRN nausea or vomiting-min. oral dose 2 mg, max. dose 4 mg:
- Monitor if patient at risk of QT prolongation
- For short-term use (2-3 doses) in patients >6 mo.
- Review FDA black box warning re QT prolongation
Follow-Up
Disposition
Admission Criteria
- Suspected systemic infection
- Inability to maintain hydration
- Sustained hypoxia during feeding
- Significant failure to thrive:
- Particularly in infants <3 mo
- Decompensated cardiopulmonary disease
- Symptomatic anemia or endocrine dysfunction
- Negligent or overwhelmed caretaker
Discharge Criteria
- Demonstrated ability to tolerate oral feedings
- Weight gain if failure to thrive
- Reliable caretaker and follow-up
Issues for Referral
- Specific referrals based on source of problem
- For complex or chronic feeding problems, a multidisciplinary approach is often needed.
- Chronic disease process may interfere with feeding AND increase caloric needs:
- Nonoral nutrition such as percutaneous endoscopic gastrostomy (PEG) tubes are often needed to address these issues.
Follow-Up Recommendations
- When available, a primary provider is the most important resource for follow-up.
- In the case of complex problems, a multidisciplinary approach is often needed-the primary provider is often in the best position to coordinate this.
Pearls and Pitfalls
- Successful feeding in infants requires coordinated, effective interaction of complex physiologic, developmental, and environmental factors.
- The factors are interdependent-disruption of 1 often leads to disruption of others:
- Premature infant gavage fed for immature suck-swallow coordination, misses critical period for developing this reflex-develops aversion to oral stimulus because of recurrent noxious stimuli.
- Feeding problems of recent, acute onset are likely to have a single identifiable cause:
- Gastroenteritis, pyloric stenosis, pharyngitis, sepsis
- In an infant with upper respiratory symptoms the answer may be as simple as vigorously suctioning the nose to effectively clear it immediately before feeding
- More chronic, long-term problems are more likely to have multifactorial and/or subtle causes:
- Feeding is an essential part of the parent-child interaction:
- Dysfunctional interaction may be the cause of or a response to a feeding problem.
- Chronic feeding issues of medical origin may result in continued behavioral feeding difficulties even after the medical problem is corrected.
- Swallowing disorders and aspiration are frequently occult.
Additional Reading
- Arvedson JC. Assessment of pediatric dysphagia and feeding disorders: Clinical and instrumental approaches. Dev Disabil Res Rev. 2008;14(2):118-127.
- Bernard-Bonnin AC. Feeding problems of infants and toddlers. Can Fam Physician. 2006;52(10):1247-1251.
- McDevitt, Barbara E. Vomiting, spitting up, and feeding disorders. In: Baren JM, Rothrock SG, Brennan JA, et al, eds. Pediatric Emergency Medicine. Philadelphia, PA: Saunders-Elsevier; 2008:319-327.
See Also (Topic, Algorithm, Electronic Media Element)
- Failure to Thrive
- Feeding Tube Complications
- Inborn Errors of Metabolism
- Intussusception
- Irritable Infant
- Malrotation
- Pyloric Stenosis
- Vomiting, Pediatric
Codes
ICD9
- 779.31 Feeding problems in newborn
- 783.0 Anorexia
- 783.3 Feeding difficulties and mismanagement
- 787.20 Dysphagia, unspecified
- 307.59 Other disorders of eating
ICD10
- P92.9 Feeding problem of newborn, unspecified
- R63.0 Anorexia
- R63.3 Feeding difficulties
- R13.10 Dysphagia, unspecified
- F50.8 Other eating disorders
SNOMED
- 102609007 Feeding problem in child (finding)
- 161838002 Infant feeding problem (finding)
- 79890006 Loss of appetite (finding)
- 40739000 Dysphagia (disorder)
- 105481005 refusing food (finding)