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DOI: 10.1542/pir.34-12-549
2013;34;549Pediatrics in Review
James A. Phalen
Managing Feeding Problems and Feeding Disorders
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Managing Feeding Problems and Feeding
Disorders
James A. Phalen, MD*
Author Disclosure
Dr Phalen has
disclosed no financial
relationships relevant
to this article. This
commentary does not
contain a discussion of
an unapproved/
investigative use of
a commercial product/
device.
Educational Gap
Up to 50% of typically developing children and up to 80% of those who have develop-
mental disabilities have feeding problems. These may evolve into a feeding disorder, with
potential effects on psychomotor and neurologic development. (1) (2)
Objectives After completing this article, readers should be able to:
1. Understand normal feeding patterns in children.
2. Recognize that feeding problems are common.
3. Prevent or ameliorate feeding problems.
4. Distinguish between feeding problems and feeding disorders.
5. Treat a child who has a feeding disorder.
Introduction
Feeding plays a central role in the parent-infant relationship. The developmental progres-
sion of food selectivity is primarily determined by a childs ability to manipulate, chew, and
swallow food (Table 1). Functional, safe feeding requires coordination of sensorimotor
function, swallowing, and breathing. Children self-regulate and may vary their oral intake
up to 30% per day with no ill effect on growth. Caregivers are responsible for what, when,
and where their children eat; the child is responsible for how much and whether they eat.
Normal feeding depends on the successful interaction of a childs health, development,
temperament, experience, and environment. Altering any of these factors can result in
a feeding problem. (1)
Common Feeding Problems
Symptoms of feeding problems include food refusal, regurgitation, gagging, or swallowing
resistance (Table 2). (1) (3) Although the child maintains adequate growth, the behavior
causes distress for caretakers. Factors that increase a childs risk for feeding problems, par-
ticularly during transition to more advanced textures, are listed in Table 3.
Between 25% and 50% of typically developing children and up to 80% of those with de-
velopmental disabilities have feeding problems. However, these problems are usually transient
and cause no serious outcomes. (1) Feeding problems are thus the norm. Practitioners must
consider cultural and ethnic differences and adjust for prematurity when setting expectations
for feeding. Some fundamental mealtime rules apply to toddlers and older children and can
prevent or resolve many feeding problems (Table 4). If a child is otherwise healthy and grow-
ing well, practitioners can reassure caregivers.
Feeding Disorder
Afeeding disorder is any condition in which a child has an
inability or difculty in eating or drinking sufcient quanti-
ties to maintain optimal nutritional status, regardless of
cause. Growth may be unaffected. Between 3% and 10%
of children are affected. Feeding disorders are multifactorial
and may begin with the child (Table 3), the parents, or the
Abbreviations
BMI: body mass index
CDC: Centers for Disease Control and Prevention
GERD: gastroesophageal reux disease
g-tube: gastrostomy tube
W/L: weight-length ratio
*Developmental Pediatrics, San Antonio Military Pediatric Center, San Antonio, TX; Department of Pediatrics, University of Texas
Health Science Center at San Antonio; Department of Pediatrics, Uniformed Services University of the Health Sciences, Bethesda,
MD.
Article nutrition
Pediatrics in Review Vol.34 No.12 December 2013 549
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environment (Table 5). (2) Regardless of its origins, it
affects the parent-child dyad and often evolves into a be-
havioral problem. Older children may experience low
self-esteem and social isolation.
Evaluation of Feeding Disorders
Initial evaluation of feeding disorders begins with the pri-
mary care practitioner, who should assess parental coping,
mental health, and bonding. Most parents whose children
have feeding disorders describe feeling frustrated and dis-
tressed at mealtime. The growth chart (length, weight,
and weight-length ratio [W/L], or body mass index
[BMI]) should be reviewed. True failure to thrive is a sus-
tained decrease in growth velocity, best dened as a W/L or
BMI below the fth percentile. Failure to thrive usually
results from inadequate energy intake but may reect inad-
equate nutrient absorption or increased energy require-
ments. Although growth charts exist for specic conditions,
the Centers for Disease Control and Prevention (CDC)
recommend that practitioners use the World Health Orga-
nization growth standards to monitor growth for infants
and children ages 0 to 2 years in the United States (avail-
able at http://www.cdc.gov/GrowthCharts/who_charts.
htm) and CDC growth charts to monitor growth for chil-
dren ages 2 to 20 years in the United States (available at
http://www.cdc.gov/GrowthCharts/cdc_charts.htm).
A thorough review of the childs prenatal, birth, and
medical histories should focus on the following key areas:
Table 1. Developmental Progression of Food Selectivity Based on Motor
Skills
Age, mo Food Consistency Fine and Gross Motor Skill Oral Motor Skill
0-4 Liquid Dependent on outside support Suckling present
Head control emerging Protective reflexes
4-6 Infant cereal Sits briefly Suckles more efficiently
Pure
´ed fruits and vegetables Head control improves Sucks foods rather than phasic biting
Brings hands to midline Eats messily from spoon
Clasps bottle but needs help
6-9 Pure
´ed meats Independent sitting Sips messily from cup
Variety of pure
´ed baby food Reaches for food Vertical munching
Begins to finger feed Limited lateral tongue action
Unrefined pincer grasp Clears spoon with upper lip
Holds bottle independently Bite and release pattern
Assists with spoon Breaks off pieces of meltable solids
9-12 Ground and lumpy pure
´es Sits in variety of positions Lip closure for liquids and soft solids
Mashed table foods Refined pincer grasp Spoon clearing more efficient
Soft, dissolvable solids Finger feeding refined Cup drinking with assistance
Grasps spoon with whole hand Begins drinking from
spouted cup
Grasps cup handle Begins to drink through a straw
12-18 Finely chopped table foods Scoops food Lateral tongue action
Chews juicy foods Brings to mouth Diagonal chewing
Bites through crunchy
foods (cookies, crackers)
More independent feeding Begins drinking from straw
Upper teeth clear food from lower lip
18-24 More chewable solids Handles finger foods, spoon,
and cup largely independently
Rotary chewing
Booster chair Cup drinking improved
Minimal food lost during eating
24-36 Tougher solids Total self-feeding Mature chewing for tougher solids
Open cup drinking without spilling
Variety of liquids through straw
Tongue clears food from lips
36 Advanced textures
(meats, fried foods,
whole fruits)
Begins using fork to stab food Open cup independently
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Small for gestational age. Up to 15% of infants born
small for gestational age fail to achieve appropriate
catch-up growth by age 2 years and continue to expe-
rience poor growth throughout childhood. Rapid
catch-up growth before age 2 years in this group in-
creases the risk of developing metabolic disease later
in life. (4) (5) (6) Thus, practitioners must temper at-
tempts to promote catch-up growth against the risks.
It is reasonable to aim for a W/L or BMI between the
10th and 50th percentiles in this population.
Aspiration. Aspiration involves passage of secretions,
drink, or solid food below the true vocal cords. It
may occur before, during, or after swallowing or from
gastroesophageal reux. Signs include coughing,
throat clearing, gurgling voice, noisy breathing, recur-
rent wheezing or stridor, and recurrent lower respira-
tory tract infections. Some children aspirate with no
obvious symptoms; this condition is called silent aspi-
ration and suggests lack of a protective reex. (7) As-
piration suggests oral motor delay or oropharyngeal
dysphagia. Infants and children who have oral motor
delay typically have oral hypotonia and an underdevel-
oped suck-swallow-breathe pattern. Thus, they may
have poor lip closure, drooling after age 12 months,
lack of tongue lateralization, and loss of food from
the mouth (Table 1). Oropharyngeal dysphagia, how-
ever, is pathologic difculty swallowing because of un-
derlying neurologic or structural abnormalities.
Motor disabilities (eg, cerebral palsy and spina bida). Chil-
dren with motor disabilities are less mobile than neurotyp-
ical children and thus have lower energy requirements. A
W/L or BMI greater than the 50th percentile makes hy-
giene, mobility, and transfers (eg, wheelchair to tub) more
challenging and increases the risk of medical complications
of obesity through excessive caloric intake.
Gastroesophageal reux disease (GERD). Signs of
GERD include regurgitation, postprandial emesis,
choking, gagging, food refusal, constant or sudden
crying, irritability, poor sleep patterns, apnea, stridor,
laryngospasm, bronchospasm, and hoarseness. Eosino-
philic esophagitis deserves consideration in any child
presenting with symptoms of GERD in whom a trial
of medical therapy with a proton pump inhibitor fails,
especially in the setting of atopy. Persistent symptoms
and food impaction (food getting stuck in the esoph-
agus) should raise additional concern.
Constipation. Signs and symptoms of constipation in-
clude bulky, painful, or infrequent bowel movements,
failed attempts to stool, bloody stools, anal ssures,
urinary incontinence, and overow incontinence
(encopresis). Parents often confuse the latter with diar-
rhea. Chronic constipation may cause early satiety and
reduced caloric intake. Stool withholding exacerbates
constipation and may have psychosocial consequences.
Medications. Medications that can cause excessive se-
dation or decreased appetite include stimulants, selec-
tive serotonin reuptake inhibitors, and topiramate.
Pica and rumination are more likely to occur in individuals
who have developmental disabilities, psychiatric disorders, or
physiologic conditions (eg, iron deciency and pregnancy).
Table 2. Common Feeding
Problems in Children
Delayed development of oral motor and self-feeding
skills; common in infants and children with hypotonia,
global developmental delay or intellectual disability,
and neurologic disorders
Reluctance or refusal to eat based on sensory issues (eg,
taste, texture, temperature, smell, or appearance)
Food selectivity (eg, personal preference, discomfort with
certain foods because of gastroesophageal reflux
disease, or food allergy)
Decreased appetite for or interest in food
Slow feeding (ie, >30 minutes to finish)
Food pocketing (ie, holding food in cheeks or front of
mouth for prolonged periods) suggests poor oral
transport or refusal
Using feeding behaviors to comfort, self-soothe, or
self-stimulate
Table 3. Pediatric Conditions
Associated With Feeding
Problems and Feeding Disorders
Temperamental traits that complicate feeding and
overwhelm parents
Prematurity (especially neonates who require prolonged
respiratory support or enteral feeds or with delayed
introduction of oral feeds)
Genetic or chromosomal abnormalities (eg, Down
syndrome and inherited neuromuscular disease)
Craniofacial anomalies (eg, Pierre-Robin sequence and
cleft palate)
Acquired brain impairment (eg, cerebral palsy, stroke,
and traumatic brain injury)
Gastrointestinal disorders (eg, gastroesophageal reflux
disease and chronic constipation)
Neurodevelopmental disorders (eg, autism spectrum
disorder, global developmental delay, and intellectual
disability)
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Table 4. Mealtime Rules for Toddlers and Older Children
Feature Rules Benefit
Scheduling Regular meals with planned, low-calorie snacks Prevents “grazing”
Same room, table, and utensils for every meal Enhances sense of hunger and satiety
Limit mealtime to 30 minutes
(ie, “kitchen is open”)
Caregivers maintain control of
feeding schedule
Offer no liquids between meals except plain
water (ie, “kitchen is closed”)
Home is less chaotic
Environment Family sits together at mealtime Focus is on socializing rather than eating
Neutral atmosphere (no forced feeding or
comments regarding intake)
Avoids conflict
Eliminate distractions: turn off all
electronic devices, child sits with
back to open room
Allows child to focus on mealtime
Allow younger child to explore foods by
touching, smelling, and tasting
Mealtime is more pleasant
Allow older child to participate in food
purchase and meal preparation
Never use food as a reward, bribe, or incentive
Praise child for showing interest in food
Allow at least 20 exposures to new foods for
acceptance
Methods Optimal feeding posture: More likely to consume calorically dense foods
Head midline and neck neutral or
slightly flexed
Expands food repertoire
Trunk symmetrical and elongated Promotes independence
Pelvis stable with hips symmetrical in neutral
position
Prevents constipation and anemia from
excessive milk intake
Hips, knees, and ankles each at 90
o
Prevents loose stools and dental caries from
excessive juice intake
Serve food at table for everyone from same
container
Small portions
Small easily chewed bites or long thin
strips child can grasp
Offer liquids only after child begins eating solids
Offer plain, unflavored water as primary beverage
Limit daily intake of low-fat or fat-free white or
flavored milk to:
2 cups for children ages 2 to 3 years
cups for children ages 4 to 8 years
3 cups for those 9 years and older
Do not dilute fruit juice, and limit to
4 to 6 oz per day
Discourage sweetened beverages (soft
drinks and sports or energy drinks)
Encourage self-feeding (eg, finger feeding
and holding spoon)
Food chaining: offer unfamiliar or
nonpreferred foods first and paired with
familiar or preferred foods
Avoid excessive coaxing, threatening, or
forced feeding
Remove food without comment if child
loses interest
Wipe face and clean up only when
meal completed
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Neither should be diagnosed unless symptoms are of an
unusual extent or cause health concerns. (8) (9)
Pica disorder. Pica disorder is the recurring ingestion of
nonfood, nonnutritive substances for at least 1 month in
a child at least 2 years of age, which is inappropriate to
the childs developmental level and sociocultural norms.
Rumination disorder. Rumination disorder is the re-
peated regurgitation of food for at least 1 month. Re-
gurgitated food may be rechewed, reswallowed, or spit
out, most often during or shortly after meals. It is not
associated with nausea or a medical condition. It is vo-
litional, distinguishing it from vomiting and gastro-
esophageal reux.
Feeding History
It is important to have caretakers describe the mealtime en-
vironment (Table 5) and the childs feeding habits (Table 6).
Feeding Observation
If time and resources allow, the practitioner or clinic
nurse may observe (in person or by video) the child feed-
ing. Such observation allows identication of appropriate
child positioning and posture, the childs hunger and sa-
tiety cues, the caretakers response to and interactions
with the child, any delayed oral motor or self-feeding
skills, and difculty managing or tolerating liquids or sol-
ids (eg, oropharyngeal dysphagia).
A complete physical, neurologic, and oral motor ex-
amination must be performed. The oral motor examina-
tion includes evaluating facial symmetry, hard and soft
palate for (submucous) cleft, and dentition; symmetry
and movement of lips and tongue; vocal intensity, pitch,
and quality; and cranial nerves. Prolonged inadequate en-
ergy and nutrient intake may have broad effects beyond
physical growth, with potential effects on psychomotor
and neurologic development. It may also affect the im-
mune, skeletal, and cardiovascular systems.
Practitioners should select diagnostic laboratory stud-
ies based on the history and physical examination nd-
ings. The following are reasonable:
In cases of failure to thrive: complete blood cell count,
urinalysis, blood urea nitrogen, serum electrolytes, and
serologic screening for celiac disease (usually IgA anti-
bodies to tissue transglutaminase).
In cases of pica disorder: serum iron and lead levels.
Classification of Feeding Disorders
The Diagnostic and Statistical Manual of Mental Dis-
orders, Fifth Edition (DSM-5), informed by available
research and extensive discussion of expert clinical expe-
rience and opinion, takes a lifespan approach to how age
and development affect psychiatric diagnoses. Avoidant/
restrictive food intake disorder replaces the previous term
feeding disorder of infancy or early childhood (Table 7).
Other classication systems exist; however, none is uni-
versally accepted, and few are evidence based.
Management of Feeding Disorders
The long-term goals of treatment are to improve nutritional
status, growth, feeding safety, and quality of life. Recognition
and treatment of GERD and constipation are essential. On
the basis of ndings, practitioners may consult the following:
A pediatric speech-language pathologist to perform
a clinical swallowing evaluation coupled with a video
uoroscopic swallow study to evaluate for oral motor
delay and oropharyngeal dysphagia.
A registered pediatric dietitian to assess caloric intake,
nutritional quality, and dietary practices and to coman-
age enteral feeds.
Table 5. Parental and Environmental Factors Associated With Feeding
Disorder
Factor Result
Conditioned aversion Pairing eating with a painful medical condition or procedure (eg, airway suctioning and
intubation)
Lack of opportunity Delayed introduction of breast, bottle, or solids is associated with delayed attainment of
appropriate eating skills
Positive reinforcement Caretakers coax or bribe infant who bats away the spoon, turns the head away, or cries
Negative reinforcement Caretakers terminate meal when child acts out
Forced feeding Results in aversion to meals and evokes inappropriate behavior at future meals
Overly rigid parents Undermines child’s ability to regulate food intake and impairs child’s psychosocial development
Chaotic parents Fail to provide child with appropriate food, support, structure, or opportunity to learn to enjoy
a variety of foods or to master eating-related social patterns
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A pediatric gastroenterologist to evaluate severe recal-
citrant constipation, GERD, and eosinophilic esopha-
gitis and to comanage enteral feeds.
A developmental pediatrician to further evaluate for
contributing causes (eg, global developmental delay,
autism spectrum disorder, and parent-child conict).
An interdisciplinary feeding team that includes some
combination of the above professionals along with
a clinical child and pediatric psychologist.
Oral motor skills usually improve over time but can be
promoted in a more organized and efcient manner with
therapy. Pediatric speech-language pathologists and oc-
cupational therapists generally use noninvasive treat-
ments, such as proper positioning and posture, thickened
liquids, modication of bolus size, oral motor and desen-
sitization exercises, specialized nipples and bottles, and
altering the temperature, texture, or presentation of food.
The evidence base for these interventions is limited. (7)
(10) Transcutaneous neuromuscular electrical stimula-
tion is an emerging therapy for dysphagia in children.
It involves noninvasive, external electrical stimulation
of peripheral motor nerves of the anterior throat to acti-
vate the pharyngeal muscles involved in swallowing.
Dietary interventions aim to establish a balanced,
healthful diet. Because liquids are usually easier than sol-
ids to consume, the tendency is to supplement the diet
with toddler formula. Often formulas come to replace
meals, leading to grazing and inadequate energy and nu-
trient intake, further aggravating the childs nutritional
deciency. Clinicians should thus discourage overreliance
on toddler formulas and other liquid supplements. Reg-
istered dietitians may recommend nutrient- and energy-
dense foods and/or specialized formula.
Behavioral feeding therapy is implemented most ap-
propriately in the context of an interdisciplinary team,
typically including a registered dietitian, speech-language
pathologist, and clinical child and pediatric psychologist.
Effective therapy aims to eliminate factors that reinforce
maladaptive mealtime behavior. (2) Settings include out-
patient, partial day, and inpatient facilities. Treatment
should start with the least intrusive approach, generally
outpatient. The literature does not support pharmaco-
logic treatment with appetite stimulants (eg, megestrol
acetate and cyproheptadine) for behavioral feeding disor-
ders. Caregiver compliance is strongly associated with
skills maintenance and generalization.
Table 6. Components of a Feeding History
Ask Caretakers Clinical Significance
How they prepare infant formula Healthy infants require a concentration of 20 kcal/oz,
whereas those who have medical problems (eg,
cardiac disease) or failure to thrive may require
more concentrated or specialized formula
Whether they add infant cereal, pure
´ed solids, or
proprietary thickeners to formula
Poor tolerance of nonthickened formula may indicate
oral motor delay or oropharyngeal dysphagia;
premature introduction of solids may reflect
cultural practices
About food preferences and nutritional deficits (eg, convenience
foods, inadequate intake of fruits and vegetables, and excessive
juice or milk intake)
May suggest the child’s preferences or that caretakers
have difficulty setting limits
About grazing (eg, overly frequent breastfeeding in older infants;
toddlers and older children eating and drinking throughout the
day); these children may come to your clinic snacking and
drinking.
Grazing may lead to reduced energy intake, increases
the risk for dental caries, and suggests caretakers
have difficulty setting limits
About reliance on dietary supplements (eg, multivitamins,
megavitamins, toddler formula, and breakfast drinks) or appetite
stimulants (eg, megestrol acetate and cyproheptadine)
Indicates caretaker or practitioner concern and may
reveal inappropriate feeding practices
About difficulty chewing, excessive drooling, or food
or liquid leaving the mouth or nose
Indicates delayed oral motor skills
Patient’s age at and difficulty with transitions
from liquids to pure
´es to solids
May indicate delayed oral motor skills or behavioral
preferences
Whether child gags, chokes, coughs, or vomits during feeds or has
disruptions in breathing, apnea, or cyanosis during feeds
Raises concern for oropharyngeal dysphagia
About refusal, tantrums, rumination, pica, avoidance of certain
food textures, temperatures, and colors
Identifies maladaptive mealtime behaviors
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Those who cannot consume sufcient energy and nu-
trients or do so safely by mouth require enteral (ie, tube)
nutrition. Enteral nutrition can be delivered via nasogas-
tric tube, orogastric tube, or gastrostomy tube (g-tube).
For those requiring enteral nutrition for longer than 6
weeks, the latter is preferred. Minimally invasive percuta-
neous endoscopic gastrostomy and laparoscopic gastro-
stomy have largely supplanted the open laparotomy for
placement of g-tubes. To preserve oral activity and feed-
ing habits, along with hunger and satiety cues, oral feeds
(when safe) should precede supplemental tube feeds. En-
teral nutrition is delivered either intermittently or contin-
uously. The preferred method is intermittent bolus
feedings, which is more physiologic; however, if the pa-
tient does not tolerate bolus feeds then continuous feeds,
either intragastric or transpyloric (through a gastrojeju-
nostomy), is reasonable. Although the decision to initiate
enteral nutrition is emotionally challenging for parents, it
eliminates the pressure for oral feeding. It allows the child
to be fed safely and efciently, reducing the risk of aspi-
ration and allowing for catch-up growth. Rapid or volu-
minous feeds may trigger retching or aggravate GERD.
Excessive caloric intake can cause overweight or obe-
sity, leading to problems handling and lifting children
who have physical disabilities. Bypassing the oral route
deprives the child of the experiences associated with feed-
ing, thus delaying oral sensorimotor skills and increasing
the risk for sensory-based food aversions when oral feeds
are reintroduced. The earlier in life that a g-tube is placed,
the more difcult it becomes to wean the child from it
later in life. Finally, continuous feeds are less physiologic
than are bolus feeds, resulting in decreased appetite and
increasing the risk of grazing and reliance on the g-tube.
Tube dependency occurs when the child has the ability to
ingest and digest food but cannot be weaned from tube
feeding, regardless of medical criteria. For these reasons,
children who have g-tubes should be exposed to the
mealtime environment, be encouraged to touch and in-
teract with food without regard to intake, be given bolus
feeds if tolerated, and have oral feeds advanced when pos-
sible. This, along with oral motor and/or behavioral
feeding therapy involving the parents, helps the child
progress to g-tube independence. Children who receive
no feeds, uids, or ushes through their g-tube for 12
months are candidates to have the device removed. Pre-
mature removal may increase the childs risk for compli-
cations, such as failure to thrive.
Table 7. DSM-5 Diagnostic Criteria
for Avoidant/Restrictive Food
Intake Disorder (307.59)
A. An eating or feeding disturbance (eg, apparent lack of
interest in eating or food; avoidance based on the
sensory characteristics of food; concern about
aversive consequences of eating) as manifested by
persistent failure to meet appropriate nutritional and/
or energy needs associated with one (or more) of the
following:
1. Significant weight loss (or failure to achieve
expected weight gain or faltering growth in children)
2. Significant nutritional deficiency
3. Dependence on enteral feeding or oral nutritional
supplements
4. Marked interference with psychosocial functioning
B. The disturbance is not better explained by lack of
available food or by an associated culturally
sanctioned practice.
C. The eating disturbance does not occur exclusively
during the course of anorexia nervosa or bulimia
nervosa, and there is no evidence of a disturbance in
which one’s body weight or shape is experienced.
D. The eating disturbance is attributable to a concurrent
medical condition or better explained by another
mental disorder. When the eating disturbance occurs
in the context of another condition or disorder, the
severity of the eating disturbance exceeds that
routinely associated with the condition or disorder
and warrants additional clinical attention.
Reprinted with permission from the American Psychiatric Association.
Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition.
Washington, DC: American Psychiatric Association; 2013.
Summary
On the basis of strong research evidence, feeding
problems and feeding disorders are common,
especially in children who have developmental
disabilities. (1) (3)
On the basis of strong research evidence, a variety of
prenatal, medical, environmental, behavioral, and
parental factors contribute to childhood feeding
disorders. (1) (3)
On the basis of some research evidence plus
consensus, many feeding problems are preventable or
easily treated.
On the basis of strong research evidence, left
untreated, feeding disorders may result in
complications, including aspiration pneumonitis,
failure to thrive, and parent-child conflict.
On the basis of some research evidence plus consensus,
treatment of feeding disorders improves nutritional
status, growth, feeding safety, and quality of life.
nutrition feeding problems and disorders
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by James Phalen on December 2, 2013http://pedsinreview.aappublications.org/Downloaded from
ACKNOWLEDGMENT. The author acknowledges past
and present members of the Interdisciplinary Feeding
Team at San Antonio Military Pediatric Center for their
clinical expertise and guidance, without which this article
would not be possible.
(The views expressed are those of the author and do not
reect the ofcial policy or position of the US Air Force, De-
partment of Defense or the US Government.)
Suggested Reading
American Speech-Language-Hearing Association. Swallowing and
Feeding Disorders. Available at http://www.asha.org/slp/
clinical/dysphagia/. Accessed October 29, 2013
Ellyn Satter Associates. Available at http://www.EllynSatter.com.
Accessed October 29, 2013
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Cochrane Database Syst Rev. 2012;10:CD009456
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1. A previously well 7-month-old infant is developing normally. She sits and holds her bottle independently,
reaches for food, and finger feeds herself. What is the most appropriate food choice for this infant?
A. Chewable solids.
B. Finely chopped table foods.
C. Mashed table foods.
D. Pureed meats.
E. Whole fruits.
The vignette below will be used for questions 2 and 3.
2. A healthy 14-month-old boy refuses solids at mealtime and prefers milk and juice. He has grown and
developed normally. He has no siblings. His mother is frustrated and concerned because nothing has worked to
change the behavior. His physical examination findings are unremarkable. What is the first step in treatment?
A. Ordering a comprehensive metabolic panel.
B. Prescribing a proton pump inhibitor.
C. Reassuring the mother.
D. Referring to a gastroenterologist.
E. Referring to an occupational therapist.
nutrition feeding problems and disorders
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3. The mother of the 14-month-old boy asks for some healthful behavior-shaping tips. In response you would
have her:
A. Arrange special mealtimes for her son.
B. Encourage him to self-feed.
C. Make the child sit alone at the table until his plate is clean.
D. Offer a cup of diluted juice if he eats some solids.
E. Permit the boy to watch videos during mealtime.
4. Which of the following 14-month-old boys who are growing normally has a feeding disorder rather than just
a feeding problem?
A. Drools constantly and dribbles food from mouth.
B. Feeds slowly but finishes most meals.
C. Pockets foods in mouth he does not like.
D. Refuses solids but loves milk and juice.
E. Spits out lima beans and broccoli.
5. A 14-month-old girl has severe oropharyngeal dysphagia related to hypoxic-ischemic brain injury secondary to
abruptio placentae. She now requires enteral feeding to provide adequate nutrition. Assuming the gut works
normally, the child is exposed to the family mealtime environment, and the child is encouraged to touch food
without regard to intake, optimal management would include:
A. Continuous gastrostomy tube feeding.
B. Continuous gastrojejunostomy tube feeding.
C. Continuous nasogastric tube feeding.
D. Intermittent bolus gastrostomy tube feeding.
E. Intermittent bolus nasogastric tube feeding.
Parent Resources From the AAP at HealthyChildren.org
English: http://www.healthychildren.org/English/ages-stages/baby/feeding-nutrition/Pages/Signs-of-Feeding-
Difficulties.aspx
Spanish: http://www.healthychildren.org/spanish/ages-stages/baby/feeding-nutrition/paginas/signs-of-feeding-
difficulties.aspx
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DOI: 10.1542/pir.34-12-549
2013;34;549Pediatrics in Review
James A. Phalen
Managing Feeding Problems and Feeding Disorders
Services
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References http://pedsinreview.aappublications.org/content/34/12/549#BIBL
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... Research indicates that breastfeeding positively affects the acceptance of new, unfamiliar foods in infants. It has also been hypothesised that the timing of the initiation of complementary feeding or the introduction of more textured foods may be necessary for the later acceptance of different food tastes and textures [41,43]. In a study by Coulthard et al., children who were introduced to lumpy foods at 10 months were more likely to have feeding difficulties, consume inadequate amounts of food, and be fussy eaters and refuse to eat at seven years of age compared to children who were introduced to pureed foods with lumps at the recommended time [44]. ...
Article
Full-text available
Food neophobia is standard behaviour in child development. It is a complex process and occurs to varying degrees. The symptoms of neophobia can be variable depending on the individual. Food neophobia is a fear of new foods, whereby difficulties in eating and trying unfamiliar foods follow. It is one of the more vital determinants of the number of meals consumed at a young age. Such a process is not a disorder in itself but can lead to one. The highest severity of neophobia occurs between the ages of two and six, but in some children, it lasts beyond age 6. This study aimed to assess the prevalence of food neophobia among children aged 2–7 years, taking into account the method of complementary feeding, the length of breastfeeding, exclusive breastfeeding, the period of introduction of complementary foods, and the use of the BLW method during the period of dietary expansion. Materials and methods: The study used an anonymous survey questionnaire consisting of five parts as the research tool. The first part of the questionnaire was a metric and concerned the socio-demographic data of the parent/guardian and their child. A standardised questionnaire assessing food neophobia among children was used to assess food neophobia: the Food Neophobia Scale—Children (FNSC). Results: In the study group, 171 children (29.23%) had a low risk of food neophobia according to the FNSC, 182 children (31.11%) had a medium risk of neophobia, and 232 children (39.66%) had a high risk of neophobia. A correlation was observed between the age and the risk of food neophobia (p = 0.0002). Statistically significant differences were found between children aged 2 and 4 (p = 0.003) and children aged 2 and 5 years (p = 0.049). We observed no correlation between gagging (p = 0.88557), choking (p = 0.17597), and needing medical intervention (p = 0.61427) and the risk of associated neophobia. Conclusion: In the study group of children, the highest risk of food neophobia was characterized by children aged 4, 5, and 7 years. The length of breastfeeding and exclusive breastfeeding did not affect the risk of food neophobia. In the month in which complementary feeding (CF) was introduced, the children were fed using the baby-led weaning method (BLW method), and introducing puree and puree with lump food into the children’s diet also did not affect the risk of food neophobia. It was shown, however, that children whose mothers observed difficulties during CF and whose children had a vomiting reflex and spat food out of their mouths during CF were more likely to develop food neophobia at the preschool age.
... Caregivers should be asked to describe the mealtime environment and the child's feeding habits. The assessment should identify components of the feeding problem, clarify the family's treatment objectives, and determine whether the family's goals are appropriate and achievable [30]. A specialized feeding assessment of patients with complex feeding disorders often includes a review of medical records, a clinical interview, caregiver-completed questionnaires, and mealtime observation [31]. ...
Article
Full-text available
Feeding disorders are increasingly common in children, especially as medical advancements improve the life expectancy of children born with prematurity and complex medical conditions. The most common symptoms include malnutrition, refusal to eat and drink, food pocketing, disruptive feeding behavior, slow feeding, food selectivity or rigid food preferences, limited appetite, and delayed feeding milestones. A unifying diagnostic definition of pediatric feeding disorder has been proposed by a panel of experts to improve the quality of health care and advance research. Referral to specialized care should be considered when feeding problems are complex or difficult to resolve. In this review, we provide an overview of the evaluation and management of pediatric feeding disorders and information that may be useful when considering whether referral to specialized care may be beneficial.
... Timely treatment may be particularly important for a child with ARFID as the consequences of the disorder can be serious and even potentially life threatening. Furthermore, children with ARFID who do not receive quick access to treatment might require enteral feedings, which requires surgery, and opens the door to several other challenges (i.e., dependency on tube feedings and limited exposure to oral feedings; Phalen, 2013). Identifying processes that lead to a decreased time requirement to conduct an FA of IMTB may be an important direction for research. ...
Article
Full-text available
Visual inspection is the traditional method behavior analysts use to interpret functional‐analysis results. Limitations of visual inspection include lack of standardized rules, subjectivity, and inconsistent interrater reliability (Fisch, 1998). To address these limitations, researchers have developed, evaluated, and refined structured criteria to aid interpretation of functional analyses of destructive behavior (Hagopian et al., 1997; Roane et al., 2013; Saini et al., 2018). The current study applied the structured criteria Saini et al. (2018) described to functional analyses of inappropriate mealtime behavior. We assessed its predictive validity and evaluated its efficiency relative to 3 post hoc visual inspection procedures. Validity metrics were lower than those in Saini et al. however, ongoing visual inspection increased the efficiency of functional analyses by more than 30%. We discuss these findings relative to the procedural differences between functional analyses of destructive behavior and inappropriate mealtime behavior.
Article
Full-text available
Stunting is a condition where a child fails to optimally grow and develop his/her bodily organs. Due to the high rate of stunting case in Indonesia, particularly in South Sumatra, this study aimed to determine the causes of stunting in children of 0 yr to 5 yr old as the dependent variable. Independent variables of infection, birth weight, gender, and age were studied accordingly. The purposive sampling method selected 100 babies and toddlers in Sungai Rengit Murni, Banyuasin, South Sumatra, Indonesia. The cross-sectional design applied univariate, bivariate (chi-square test), and multivariate (multiple logistic regression and backward regression tests) analyses. The result showed that while age was insignificant (0.649, P > 0.25) and infection was less significant (0.077, P > 0.05), low birth weight (0.044, P < 0.05) and gender (0.045, P < 0.05) are significant in affecting stunting.Being 61 % accurate, the independent variables of this study covered 15.1 % of known stunting cause.
Article
Full-text available
Objective: Pediatric feeding disorder (PFD) is defined as impaired oral intake, associated with dysfunction in at least one of four domains: medical, nutritional, feeding skill, and/or psychosocial. The pediatric aerodigestive patient presents with conditions impacting airway, breathing, feeding, swallowing, or growth. The objective of the study was to determine the prevalence of PFD and dysfunctional domain, in the aerodigestive patient presenting to a tertiary aerodigestive clinic. Methods: Twenty-five charts from patients enrolled in Mayo Clinic Children's Center Aerodigestive Program were retrospectively reviewed for documentation of dysfunction within the four feeding disorder domains. Results from the aerodigestive triple scope, functional endoscopic evaluation of swallow (FEES), and videofluoroscopic swallow study (VFSS) were recorded. Height and weight z-scores were compared between the initial assessment and 6-12 months later. Results: Median age was 20 months (range 2-81 months). Of the patients, 100% (n = 25) had dysfunction in at least one PFD domain. The domain identified most frequently was medical dysfunction (96%; n = 24). Feeding dysfunction was observed in 76% (n = 19). Psychosocial dysfunction was observed in 76% (n = 19). Nutritional dysfunction was observed in 60% (n = 15). Dysfunction in three or greater domains was seen in 80% (n = 20). Weight z-score increased in 76% (n = 19) of patients 6 to 12 months after the initial aerodigestive evaluation. Conclusion: Aerodigestive patients frequently have PFD and utilizing the consensus definition of PFD at intake may enhance clinical assessment and therapeutic evaluation, and provide a framework to measure outcomes in this heterogeneous patient population.
Article
Objectives: To compare institutional practice patterns for gastrostomy tube placement in neonates with duodenal atresia (DA) and trisomy 21. Methods: A retrospective review of the Pediatric Health Information System (PHIS) from 2015-2018 identified infants <10 days old with ICD-10 diagnostic codes for DA and trisomy 21, in addition to procedure codes for an intestinal bypass or duodenoduodenostomy. This cohort was then queried for gastrostomy tube procedure codes and diagnostic codes for associated co-morbidities. Results: 209 infants were identified with DA, trisomy 21, and an intestinal bypass. 57 (27%) underwent gastrostomy placement. Baseline characteristics of those with and without gastrostomy tubes were similar. Patients from 16 hospitals that placed no gastrostomy tubes (No-G-tube-Hospitals) were compared to children from 30 hospitals that placed at least one gastrostomy tube (G-tube-Hospitals). Open atresia repairs occurred more frequently at G-tube-Hospitals, but patients were otherwise similar. There was no difference in readmission at 12 months for gastrostomy placement between children from No-G-tube-Hospitals and those from G-tube-Hospitals that did not undergo gastrostomy during their index admission. Conclusions: One third of institutions in this study did not place gastrostomy tubes during index admissions for neonates with trisomy 21 and DA, yet this did not negatively impact length of stay or incidence of subsequent gastrostomy placement as a result. Future research is needed to determine factors that predispose patients to failure without gastrostomy, as well as best practices for post-operative management in these patients to reduce unnecessary tube placement.
Article
Full-text available
Feeding aversion in children may progress to severe feeding difficulties. While oral-motor and sensory issues are usually the leading causes, organic etiologies should be considered. This study aimed to assess the prevalence of gastrointestinal conditions in children with severe feeding difficulties. We conducted a retrospective study of 93 children requiring an intensive feeding program. The medical records, radiologic and diagnostic tests, use of gastric tube feedings, preexisting medical conditions, and medications were reviewed. Fifty-two percent (52%) had esophagitis, 26.2% gastritis, and 40.7% lactase deficiency in upper endoscopy. In those who underwent an upper endoscopy, 26% of patients that were also tested for small intestinal bacterial overgrowth were found to be positive. Allergy testing was abnormal in 56.6% of those tested, while 27.5% and 75% had abnormal gastric emptying times and pH impedance results, respectively. Constipation was present in 76.3%. Thirteen of 32 were weaned off tube feedings. We conclude that gastrointestinal conditions are common in children with feeding disorders and should be investigated prior to feeding therapy.
Article
Full-text available
Pediatric feeding disorders lack a universally accepted definition. Feeding disorders require comprehensive assessment and treatment of four closely-related, complementary domains (medical, psychosocial, and feeding skill-based systems and associated nutritional complications). However, previous diagnostic paradigms have typically defined feeding disorders using the lens of a single professional discipline and fail to characterize associated functional limitations that are critical to plan appropriate interventions and improve quality of life. Using the framework of the World Health Organization (WHO) International Classification of Functioning, Disability, and Health (ICF), a unifying diagnostic term is proposed: "Pediatric Feeding Disorder" (PFD), defined as impaired oral intake that is not age-appropriate, and is associated with medical, nutritional, feeding skill, and/or psychosocial dysfunction. By incorporating associated functional limitations, the proposed diagnostic criteria for PFD should enable practitioners and researchers to better characterize the needs of heterogeneous patient populations, facilitate inclusion of all relevant disciplines in treatment planning, and promote the use of common, precise, terminology necessary to advance clinical practice, research, and health-care policy.This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0. Full Text accessible online: https://journals.lww.com/jpgn/Abstract/publishahead/Pediatric_Feeding_Disorder__Consensus_Definition.96648.aspx
Article
CASE: David is a 22-month-old boy who is new to your practice. He recently moved from a rural area in the Midwest. His father is in the United States Air Force, and his mother works as a full-time homemaker. Their household includes 5 older siblings. The family moves every year because of the father's Air Force placement. David was born full-term in Virginia, with no reported pregnancy complications and no alcohol, tobacco, or drug exposure. He was delivered vaginally, with Apgar scores of 7 and 9, respectively and no respiratory issues. In the newborn nursery, his nurse noted that he was floppy, with generalized low muscle tone. Laboratory work performed included normal thyroid studies and a chromosomal microarray. Because of persistent hypotonia, he was seen by a pediatric neurologist at 9 months of age. A magnetic resonance imaging was performed and was normal, with no structural deficits noted. He was referred to Early Intervention at 6 months, when he was not yet rolling over. He received physical therapy for a few months before the family moved again for his father's next placement. David presents in your office as a sweet nondysmorphic toddler who maintains steady eye contact and smiles responsively. His height, head circumference, and weight are at the 50th percentile. His physical examination is notable for generalized hypotonia, with intact upper and lower deep tendon reflexes. He spontaneously says about 20 words. He turns his head when his name is called and can follow a simple command, such as “clap, clap.” He reaches his whole hand toward desired objects and will look at his parents if they are out of reach. He can grasp a block, bang, and transfer objects. He demonstrates an immature pincer grasp. He can roll over and sit independently and is just beginning to pull to a stand. His parents report he has recently restarted Early Intervention, where he is receiving physical, speech, and occupational therapy. His audiology examination is normal. His parents' primary concern today is regarding feeding. David is a picky eater. He has difficulty with new foods and textures. The parents noticed a regression in his tolerance for new foods around the recent move. He eats baby puffs, stage 2 to 3 baby foods, and fruit and vegetable pouches. He does not like soft, sticky foods. He is also reported to have other sensory sensitivities. He does not tolerate loud noises and is bothered by tags in his clothing. You wonder, what further work-up would be helpful for David? How can his feeding issues be addressed?
Article
CASE: Kendra is a 4-year-old girl with autism spectrum disorder (ASD) who presents for follow-up of feeding problems to her pediatric clinician. She is an only child in a family where both parents are scientists. Feeding concerns date to infancy, when she was diagnosed with Gastroesophageal Reflux Disease (GERD) associated with persistent bottle refusal and the acceptance of few pureed foods. At 13 months, milk and peanut allergies were diagnosed. Following a feeding clinic evaluation at 24 months, she was prescribed a soy milk supplement and an H2 blocker. There was no concern for oral-motor dysfunction. She was also referred to early intervention for feeding therapy. However, her parents terminated participation after 6 months because she became anxious and had tantrum prior to treatment groups. She was seen in another feeding program at 3 years; zinc, folate, thyroid, and a celiac panel were normal, and an endoscopy was negative for eosinophilic esophagitis. She began individual feeding therapy, where concerns for rigidity, difficulty transitioning, and limited peer interactions led to a neuropsychological evaluation. Kendra was diagnosed with an ASD and avoidant/restrictive food intake disorder (ARFID). Her cognitive skills were average, and expressive and receptive language skills were low average. Her diet consisted of French fries, Ritz crackers, pretzels, and 32 ounces of soy formula daily. She had stopped accepting Cheerios and saltines 2 months prior. She controlled other aspects of feeding, insisting on a specific parking spot at a fast food restaurant and drinking from a particular sippy cup. Her parents accepted these demands with concern about her caloric intake, which they tracked daily. Following diagnosis with ARFID, she resumed feeding therapy using a systematic desensitization approach with rewards. At the first session, she kissed and licked 2 new foods without gagging. Her mother appeared receptive to recommendations that included continuing the “food game” at home, replacing 1 ounce of soy formula by offering water each day, limiting between-meal grazing, and refusing specific feeding demands. Currently, her parents plan to discontinue feeding therapy with concerns that the treatment was “too harsh.” Her father produces logs of her caloric and micronutrient intake as evidence that she did not replace missed formula with other foods and reports that she subsequently became more difficult to manage behaviorally. Her father now demands to see randomized controlled trials of feeding therapy approaches. Her weight is stable, but she has now limited her pretzel intake to a specific brand. How would you approach her continued care?
Article
Full-text available
Abstract: Early identification and management of aspiration associated with oral intake will help contribute to the best possible outcome for infants and children who have airway protection issues with swallowing. Though the incidence and prevalence of aspiration specifically related to swallowing dysfunction across medical conditions in the pediatric population is unknown, there is accumulating evidence of swallowing-related aspiration in infants and children with diagnoses that include structural abnormalities of the upper airway, central nervous system abnormalities, and progressive neurological disease. Chronic aspiration is associated with compromised respiratory health, progressive lung disease, bronchiectasis, and respiratory failure; thus, early detection and appropriate management is crucial. Determining the etiology and effect of aspiration is complex, and multiple evaluations are often required. This article will focus on instrumental studies of swallowing physiology used in the diagnosis and management of swallowing dysfunction and aspiration. Therapeutic strategies to improve airway protection during swallowing will also be described.
Article
Oropharyngeal dysphagia encompasses problems with the oral preparatory phase of swallowing (chewing and preparing the food), oral phase (moving the food or fluid posteriorly through the oral cavity with the tongue into the back of the throat) and pharyngeal phase (swallowing the food or fluid and moving it through the pharynx to the oesophagus). Populations of children with neurological impairment who commonly experience dysphagia include, but are not limited to, those with acquired brain impairment (for example, cerebral palsy, traumatic brain injury, stroke), genetic syndromes (for example, Down syndrome, Rett syndrome) and degenerative conditions (for example, myotonic dystrophy). To examine the effectiveness of interventions for oropharyngeal dysphagia in children with neurological impairment. We searched the following electronic databases in October 2011: CENTRAL 2011(3), MEDLINE (1948 to September Week 4 2011), EMBASE (1980 to 2011 Week 40)
, CINAHL (1937 to current)
, ERIC (1966 to current), PsycINFO (1806 to October Week 1 2011), Science Citation Index (1970 to 7 October 2011), Social Science Citation Index (1970 to 7 October 2011), Cochrane Database of Systematic Reviews, 2011(3), DARE 2011(3), Current Controlled Trials (ISRCTN Register) (15 October 2011), ClinicalTrials.gov (15 October 2011) and WHO ICTRP (15 October 2011). We searched for dissertations and theses using Networked Digital Library of Theses and Dissertations, Australasian Digital Theses Program and DART-Europe E-theses Portal (11 October 2011). Finally, additional references were also obtained from reference lists from articles. The review included randomised controlled trials and quasi-randomised controlled trials for children with oropharyngeal dysphagia and neurological impairment. All three review authors (AM, PD and EW) independently screened titles and abstracts for inclusion and discussed results. In cases of uncertainty over whether an abstract met inclusion criterion, review authors obtained the full-text article and independently evaluated each paper for inclusion. The data were categorised for comparisons depending on the nature of the control group (for example, oral sensorimotor treatment versus no treatment). Effectiveness of the oropharyngeal dysphagia intervention was assessed by considering primary outcomes of physiological functions of the oropharyngeal mechanism for swallowing (for example, lip seal maintenance), the presence of chest infection and pneumonia, and diet consistency a child is able to consume. Secondary outcomes were changes in growth, child's level of participation in the mealtime routine and the level of parent or carer stress associated with feeding. Three studies met the inclusion criteria for the review. Two studies were based on oral sensorimotor interventions for participants with cerebral palsy compared to standard care and a third study trialled lip strengthening exercises for children with myotonic dystrophy type 1 compared to no treatment (Sjogreen 2010). A meta-analysis combining results across the three studies was not possible because one of the studies had participants with a different condition, and the remaining two, although using oral sensorimotor treatments, used vastly different approaches with different intensities and durations. The decision not to combine these was in line with our protocol. In this review, we present the results from individual studies for four outcomes: physiological functions of the oropharyngeal mechanism for swallowing, the presence of chest infection and pneumonia, diet consistency, and changes in growth. However, it is not possible to reach definitive conclusions on the effectiveness of particular interventions for oropharyngeal dysphagia based on these studies. One study had a high risk of attrition bias owing to missing data, had statistically significant differences (in weight) across experimental and control groups at baseline, and did not describe other aspects of the trial sufficiently to enable assessment of other potential risks of bias. Another study was at high risk of detection bias as some outcomes were assessed by parents who knew whether their child was in the intervention or control group. The third study overall seemed to be at low risk of bias, but like the other two studies, suffered from a small sample size. The review demonstrates that there is currently insufficient high-quality evidence from randomised controlled trials or quasi-randomised controlled trials to provide conclusive results about the effectiveness of any particular type of oral-motor therapy for children with neurological impairment. There is an urgent need for larger-scale (appropriately statistically powered), randomised trials to evaluate the efficacy of interventions for oropharyngeal dysphagia.
Article
Current classification of eating disorders is failing to classify most clinical presentations; ignores continuities between child, adolescent and adult manifestations; and requires frequent changes of diagnosis to accommodate the natural course of these disorders. The classification is divorced from clinical practice, and investigators of clinical trials have felt compelled to introduce unsystematic modifications. Classification of feeding and eating disorders in ICD-11 requires substantial changes to remediate the shortcomings. We review evidence on the developmental and cross-cultural differences and continuities, course and distinctive features of feeding and eating disorders. We make the following recommendations: a) feeding and eating disorders should be merged into a single grouping with categories applicable across age groups; b) the category of anorexia nervosa should be broadened through dropping the requirement for amenorrhoea, extending the weight criterion to any significant underweight, and extending the cognitive criterion to include developmentally and culturally relevant presentations; c) a severity qualifier "with dangerously low body weight" should distinguish the severe cases of anorexia nervosa that carry the riskiest prognosis; d) bulimia nervosa should be extended to include subjective binge eating; e) binge eating disorder should be included as a specific category defined by subjective or objective binge eating in the absence of regular compensatory behaviour; f) combined eating disorder should classify subjects who sequentially or concurrently fulfil criteria for both anorexia and bulimia nervosa; g) avoidant/restrictive food intake disorder should classify restricted food intake in children or adults that is not accompanied by body weight and shape related psychopathology; h) a uniform minimum duration criterion of four weeks should apply.
Article
A systematic review of the literature regarding treatment of pediatric feeding disorders was conducted. Articles in peer-reviewed scientific journals (1970-2010) evaluating treatment of severe food refusal or selectivity were identified. Studies demonstrating strict experimental control were selected and analyzed. Forty-eight single-case research studies reporting outcomes for 96 participants were included in the review. Most children presented with complex medical and developmental concerns and were treated at multidisciplinary feeding disorders programs. All studies involved behavioral intervention; no well-controlled studies evaluating feeding interventions by other theoretical perspectives or clinical disciplines met inclusion criteria. Results indicated that behavioral intervention was associated with significant improvements in feeding behavior. Clinical and research implications are discussed, including movement toward the identification of key behavioral antecedents and consequences that promote appropriate mealtime performance, as well as the need to better document outcomes beyond behavioral improvements, such as changes in anthropometric parameters, generalization of treatment gains to caregivers, and improvements in nutritional status.
Article
To review the literature related to the current DSM-IV-TR diagnostic criteria for feeding disorder of infancy or early childhood; pica; rumination disorder; and other childhood presentations that are characterized by avoidance of food or restricted food intake, with the purpose of informing options for DSM-V. Articles were identified by computerized and manual searches and reviewed to evaluate the evidence supporting possible options for revision of criteria. The study of childhood feeding and eating disturbances has been hampered by inconsistencies in classification and use of terminology. Greater clarity around subtypes of feeding and eating problems in children would benefit clinicians and patients alike. A number of suggestions supported by existing evidence are made that provide clearer descriptions of subtypes to improve clinical utility and to promote research.
Article
The association between obesity and morbidity resulting from chronic diseases is well known. This systematic review addresses studies of the role of rapid growth in infancy and childhood as possible determinants of overweight and obesity later in the life course. We reviewed MEDLINE for studies reporting on growth in infancy and childhood, as well as measures of weight or adiposity in later childhood, adolescence or adulthood. The methodological quality of the papers was assessed using the criteria suggested by Downs and Black. Sixteen articles that fulfilled review criteria were located. There was wide variability in the indicators used for defining rapid growth as well as overweight or obesity. The age range in which weight or adiposity was measured ranged from 3 to 70 years. In spite of differences in definitions used, 13 articles that reported on early rapid growth found significant associations with later overweight or adiposity. Efforts should be made to standardize the definition of rapid growth, as well as that of overweight and obesity in children and adolescents. The most frequent definition for rapid growth in this review was a Z-score change greater than 0.67 in weight for age between two different ages in childhood. Regarding obesity, the definition proposed by the International Obesity Task Force also appears to be most appropriate. The present results indicate that early growth is indeed associated with the prevalence of obesity later in the life course.
Article
To assess the association between infant size or growth and subsequent obesity and to determine if any association has been stable over time. Systematic review. Medline, Embase, bibliographies of included studies, contact with first authors of included studies and other experts. Studies that assessed the relation between infant size or growth during the first two years of life and subsequent obesity. Obesity at any age after infancy. 24 studies met the inclusion criteria (22 cohort and two case-control studies). Of these, 18 assessed the relation between infant size and subsequent obesity, most showing that infants who were defined as "obese" or who were at the highest end of the distribution for weight or body mass index were at increased risk of obesity. Compared with non-obese infants, in those who had been obese odds ratios or relative risks for subsequent obesity ranged from 1.35 to 9.38. Ten studies assessed the relation of infant growth with subsequent obesity and most showed that infants who grew more rapidly were at increased risk of obesity. Compared with other infants, in infants with rapid growth odds ratios and relative risks of later obesity ranged from 1.17 to 5.70. Associations were consistent for obesity at different ages and for people born over a period from 1927 to 1994. Infants who are at the highest end of the distribution for weight or body mass index or who grow rapidly during infancy are at increased risk of subsequent obesity.
Article
Unlabelled: In a systematic review, we identified 21 separate studies with data on the association between rapid infancy weight gain, up to age 2 y, and subsequent obesity risk. Uniformly all studies reported significant positive associations. We transformed the reported effect sizes to a standard infancy weight gain exposure, and found that further differences in study design accounted for much of the variation in risk. An accompanying paper by Melinda Yeung reminds us that there are benefits of postnatal catch-up growth in certain populations, and suggests that genetic and nutritional factors could moderate the unhealthy translation of rapid infancy weight gain to visceral fat and insulin resistance. Further evidence is needed, and we will need to rigorously test the benefits and risks of any interventions. However, the concept of "healthy" rapid catch-up infancy growth is an attractive prospect. Conclusion: Rapid infancy weight gain is consistently associated with increased subsequent obesity risk, but the predictive ability of different weight gain cut-offs needs to be tested.
Feeding and its disorders
  • Eicher