Gastroesophageal Reflux What Is Gastroesophageal Reflux?
Gastroesophageal Reflux What Is Gastroesophageal Reflux?
GASTROESOPHAGEAL REFLUX
Gastroesophageal reflux is the bringing up of stomach contents or acid into the esophagus
(the swallowing tube). Almost everyone refluxes at some point during the day especially
after meals. What distinguishes normal reflux from pathologic or abnormal reflux is how
often reflux occurs and if it causes symptoms or damage to the esophagus. Reflux is
being increasingly recognized in children and adolescents. Although the symptoms in
teenagers may be similar to those seen in adults, the symptoms in infants and younger
children may differ enough so that they are not recognized as being due to reflux.
Almost all infants reflux or regurgitate a portion of their feeding at one time or another.
What distinguishes normal regurgitation from abnormal regurgitation is how often the
reflux occurs, if it is associated with discomfort, and if it results in other complications.
These complications include poor weight gain known as “failure to thrive”, breathing
difficulties such as infrequent breaths or apnea, asthma symptoms such as wheezing, or a
hoarse voice or cry. Other complications of reflux are aspiration, which is when the
refluxed stomach contents reach the lungs, pneumonia due to aspiration, or inflammation
of the esophagus called esophagitis. Spitting up blood or material that looks like old
“coffee grounds” is rarely seen and requires evaluation by a physician.
Reflux symptoms in infants tend to get better as they get older, usually by 12 to 15
months. This is because as infants get older their stomach is able to empty quicker and
their esophagus lengthens, therefore there is less material in the stomach to regurgitate.
Infants who reflux or regurgitate will not necessarily have problems with reflux as they
get older or as adults.
There are a number of reasons, other than reflux, that a baby may vomit. Babies may be
allergic to the milk or soy protein that they are getting in their formula and this can result
in irritability, vomiting, poor weight gain and blood in the bowel movements. This is
treated with a change to a specialized formula where the proteins are broken down to
make them less allergenic (allergy causing). Babies can be born with problems where the
Between 4-8 weeks of age infants can develop a condition known as pyloric stenosis.
This results in significant and forceful vomiting and is usually associated with poor
weight gain and possibly weight loss. Parents of infants with this problem describe their
child's vomiting as projectile. Pyloric stenosis is currently treated with surgery. There are
other non-gastrointestinal causes of vomiting in infants and young children including
hormonal problems, kidney problems and problems with increased pressure on the brain.
These are unusual conditions but patients should be tested for these problems if their
physician feels that their symptoms are not typical or they are not responding to
medications.
Reflux is usually diagnosed based on symptoms and physical examination. X-rays are
generally not helpful in diagnosing abnormal reflux although they are often used to
exclude other problems that may mimic reflux. Performing an upper intestinal endoscopy
with biopsies can be helpful to determine if inflammation of the esophagus is present.
The test currently considered most helpful in making the diagnosis of acid reflux is a pH
probe. This probe is a small tube inserted through the nose into the esophagus that
continuously measures how often acid is being regurgitated into the esophagus. There are
normal expected values for children and adults.
What are treatment choices for children and adolescents with gastroesophageal
reflux?
LACTOSE INTOLERANCE
Lactose is the sugar found in milk and dairy products such as cheese and yogurt. After
eating dairy products that contain this sugar, lactase a digestive enzyme of the small
intestine, helps to breakdown this complex sugar into two simple sugars. Normally
lactase breaks down lactose into two components, glucose and galactose. These simple
sugars are then absorbed in the small intestine and ultimately reach the blood stream
where they act as nutrients. The enzyme lactase is located in the lining of the small
intestine known as the intestinal villi.
Lactose is also the sugar found in breast milk and standard infant formulas. Therefore
almost all babies are able to digest and absorb this sugar and it serves as their primary
dietary sugar.
In addition to milk and dairy products such as ice cream, yogurt and cheese, lactose can
be found in bread and baked goods, processed breakfast cereals, instant potatoes, some
soups and non-kosher lunch meats, candies, dressings and mixes for pancakes and
biscuits.
A cause of temporary lactose intolerance in infants and young children is infection. Older
infants and young children will commonly be infected by a virus known as rotavirus.
Most children will have had at least one episode of this type of infection by the age of
five years, with the majority of cases occurring before two years of age. The symptoms of
rotavirus infection include vomiting, diarrhea (frequent watery stools), and fever. This
type of viral infection commonly causes damage to the lining of the small intestine.
Because this is where the enzyme lactase is located, rotavirus infection often results in
lactose intolerance. This type of lactose intolerance is transient or temporary, however,
and when the lining of the intestine returns to normal within three to four weeks, the
lactose intolerance usually goes away. Another type of infection that causes temporary
lactose intolerance is giardia infection. Giardia is a parasite that is found in well water
and fresh water from lakes and streams and also causes damage to the surface of the
small intestine resulting in temporary lactose intolerance. Treatment of the giardia with
antibiotics will resolve the lactose intolerance.
Many individuals acquire lactose intolerance as they get older. It is estimated that
approximately one half of adults in the United States have acquired lactase deficiency.
This condition is due to a normal decline in the amount of the enzyme lactase present in
the small intestine as we age. Although lactose is an important part of the diet in infants
and young children it represents only 10% of the carbohydrate (sugar) intake in adults.
However, individuals who are lactose intolerant may not be able to tolerate even small
amounts of this sugar in their diet.
Lactose intolerance occurs more frequently in certain families. One of the most important
factors affecting the rate of developing lactose intolerance is an individual's ethnic
background. Approximately 15% of adult Caucasians, and 85% of adult African
Americans in the United States are lactose intolerant. The rate of lactose intolerance is
also very high in individuals of Asian descent, Hispanic descent, Native Americans and
Jewish individuals.
The symptoms of lactose intolerance can start during childhood or adolescence and tend
to get worse with age. The severity of symptoms is usually proportional to the amount of
the milk sugar ingested with more symptoms following a meal with higher milk sugar
content. The symptoms of lactose intolerance are abdominal distension and pain, excess
Although eating lactose containing products will result in discomfort for someone who is
lactose intolerant, they will not be harmed by eating lactose. There are no long term
concerns for someone who is lactose intolerant of developing more serious intestinal
disease because of this. The only exception to this would be for babies who are born with
primary lactase deficiency or children with secondary lactase deficiency as discussed
above. These children may have poor growth as a result of chronic diarrhea and
malnutrition if they are not switched to a lactose free diet or supplemented with the
lactase enzyme (commercially available).
Because lactose is not digested properly in the small intestine in individuals who are
lactose intolerant, it passes whole into the large intestine or colon. Upon reaching the
colon it is broken down by the normal colon bacteria. This breakdown results in the
production of carbon dioxide and hydrogen gases and short chain fatty acids. The carbon
dioxide and short chain fatty acids produced in the colon result in the symptoms of
lactose intolerance. The hydrogen is absorbed and ultimately excreted in the breath as
described below.
Lactose intolerance is diagnosed by a simple test called a breath hydrogen test. After a
period of fasting from midnight the night before the test, an individual drinks a specified
amount of the milk sugar as a syrup. In adults this corresponds to the amount of milk
sugar in a quart of milk. They then breathe into a test bag every fifteen minutes for
approximately two hours. The breath that they exhale into the bag is analyzed to
determine its hydrogen content. During the course of the test individuals who are lactose
intolerant will have an increase in the amount of hydrogen that they exhale. If the values
for hydrogen increase above a certain value the diagnosis of lactose intolerance is made.
Patients who are lactose intolerant may also develop their typical symptoms during the
test.
There are several conditions in older children, adolescents and adults that can cause
temporary lactose intolerance. The lactose intolerance usually resolves with treatment.
These diseases include acute diarrhea due to an infection, celiac sprue which is an
intolerance to wheat products, Crohn’s disease of the small intestine discussed below, and
other causes of malnutrition.
Ulcerative colitis and Crohn's disease differ primarily in the portions of the bowel that
they each involve and also the layers of the bowel wall that are involved. Ulcerative
colitis involves only the large bowel. It can involve a part of the large bowel only or the
entire large bowel but it does not have “skip” areas. Skip areas are areas of the intestine
Both ulcerative colitis and Crohn’s disease are relatively uncommon problems in both
children and adults. The incidence or number of new cases occurring each year appears to
be increasing more for Crohn’s disease than for ulcerative colitis. In a group of
approximately 100,000 children age 15 years or younger, it is estimated that
approximately 2 or 3 of them will develop Crohn’s disease each year. However in a
group of 100,000 children age 15-19, the rate of developing Crohn’s disease increases to
16 new cases per year. The chance of developing ulcerative colitis in childhood and
adolescence is less than the chance of developing Crohn’s disease, with an incidence of 2
to 10 new cases per 100,000 population per year. The teenage years are one of the most
likely times for inflammatory bowel disease to be diagnosed. The other most common
time is between 30-40 years of age.
Both ulcerative colitis and Crohn’s disease are more common in certain families. In large
studies it has been shown that if someone has either ulcerative colitis or Crohn’s and all
of their close family members (parents, grandparents, brothers, sisters and children) are
followed for a period of thirty years there is a one in three chance of another family
member developing either ulcerative colitis or Crohn’s disease. If the original family
member has ulcerative colitis the relative is likely to develop ulcerative colitis and if they
have Crohns disease the relative is likely to develop Crohns. Neither ulcerative colitis nor
Crohn’s disease are contagious, which means that you cannot catch it from your family
member. The reason for family members being more likely to develop these diseases is
probably due to inheriting a gene that makes an individual more susceptible to develop
this type of inflammation of the bowel. In addition to being more common in certain
families, both ulcerative colitis and Crohn’s disease are more common in certain ethnic
groups, especially Jewish individuals of eastern European descent.
The most common symptoms of ulcerative colitis in children and teenagers are diarrhea,
blood in the bowel movements and pain in the abdomen. Patients with this condition may
The symptoms of Crohn’s disease may be subtler than those of ulcerative colitis or may
be dramatic. Abdominal pain, diarrhea and weight loss are the most common symptoms
occurring in 65-75% of patients. Poor growth is also common and a very important sign
of pediatric Crohn’s disease. A child who is usually amongst the tallest in their class who
becomes amongst the smallest, especially around the time of puberty may have Crohn’s
disease. The average time between the first symptoms of Crohn’s disease and the
diagnosis of Crohn’s disease may be up to a year in some studies, due to the subtle first
symptoms of Crohns disease. Fatigue or being tired due to anemia is common as is blood
in the bowel movements, although less common than in ulcerative colitis. Up to 25% of
patients will have disease around their bottom or anus; this may go unrecognized in a
teenager who is uncomfortable discussing bowel issues with their parents or doctors. This
includes extra folds of skin, which may become inflamed and can be painful, drainage of
pus from small openings in the skin known as fistulas and fissures or cracks in the skin
around the anus that may be painful.
After a careful history and physical examination your doctor can order blood work to
screen for ulcerative colitis or Crohn’s disease. Blood work that would be abnormal in
these conditions can include a blood count demonstrating anemia, especially if the iron
level is low, an increased white blood cell count which may indicate inflammation or
infection, an increased platelet count (the part of the blood that is responsible for helping
blood clot), decreased blood levels of proteins such as albumin and an elevated
sedimentation rate, a nonspecific marker of inflammation. There are new additional blood
tests available that detect certain antibodies found more commonly in patients with
inflammatory bowel disease. However testing positive or negative for these antibodies
does not establish or rule out the diagnosis of inflammatory bowel disease and therefore
expert interpretation of these blood tests is required.
An x-ray called an upper GI with small bowel follow through can be obtained to look for
irregularity in the small intestine. This is particularly helpful in pediatric patients, as the
terminal ileum, which is the end of the small intestine, is the site most commonly
abnormal in children with Crohn’s disease.
Although the stomach, small intestine and colon are the areas of the body that are most
commonly involved with inflammatory bowel disease, patients can develop symptoms
outside of the GI tract that are due to their inflammatory bowel disease. How severe the
symptoms are may in some cases be related to how severe the bowel disease is or may be
independent of the bowel symptoms. These symptoms are generally not due to
medications administered for the bowel disease. The table below indicates some of the
most common extraintestinal manifestations of inflammatory bowel disease.
What are the treatment options for Ulcerative colitis and Crohn’s disease?
There are a variety of medications available to treat both ulcerative colitis and Crohn’s
disease. Important pediatric considerations for medical therapy include long term side
effects of the medications especially with regards to growth, bone disease such as
osteoporosis (decreased calcium in the bone), development of cataracts in the eyes from
medications such as steroids and a small risk of developing certain types of cancer with
some medications or as a result of having chronic inflammatory bowel disease over a
long period of time.
There are a variety of nutritional options also available for patients with Crohn’s disease
and it has been shown that disease activity appears to decrease if patients are able to
significantly increase their caloric intake through the use of standard or specialized diets.
Supplementation with folic acid, calcium and Vitamin D in patients with decreased bone
calcium is also helpful in patients with inflammatory bowel disease.
Surgery is curative for ulcerative colitis, but not for Crohn’s disease. Surgery is usually
performed for disease that does not get better despite medications, if severe medication
side effects develop or for other complications of the underlying inflammatory bowel
disease. Children undergoing removal of their colon for ulcerative colitis can have a
pouch fashioned of small intestine that serves as a reservoir for stool and takes the place
of the rectum. Children undergoing surgery for Crohn's disease generally do so for
development of a specific complication of their disease or their medication. Because
Crohn’s disease always comes back following surgery patients are usually continued on
maintenance medications following surgery to cut down how quickly or how severely the
disease comes back. Also the amount of bowel removed is limited in patients with
Crohns disease in order to prevent additional problems with absorption of nutrients after
surgery. Patients still require regular follow up with their pediatric gastroenterologist or
their gastroenterologist after surgery for either ulcerative colitis or Crohn’s disease.
DIARRHEA
Diarrhea is a very common problem in children younger than age five. In developing or
non-industrialized countries, multiple episodes of diarrhea can lead to serious problems
such as malnutrition (poor nutrition). In the United States and Canada, young children
have an average of two episodes of diarrhea per year.
Acute diarrhea often called acute gastroenteritis by physicians is when stools are softer
and more frequent then normal, (usually more than three bowel movements each day for
less than 3 weeks total). Diarrhea may be due to infections with bacteria, viruses or
parasites. Diarrhea is more common in children attending day care and is usually due to a
virus. While cases of diarrhea due to infection are usually mild and go away on their own,
it is important to avoid becoming dehydrated from loss of body fluid in diarrheal stools.
What is dehydration and how can I tell if my child is starting to develop this?
Dehydration is when someone is unable to take in sufficient fluid orally to meet their
daily requirements and compensate for losses in their stools. Physicians can determine if
someone is dehydrated and how severely they are dehydrated by examining them. Parents
can watch for signs of dehydration by checking how often their child is passing urine,
determining if they are able to cry with tears, or have dry lips. Figuring out how much a
child is urinating may be difficult if an infant is in diapers, and the urine is mixed with
loose bowel movements. Children often become fussy with decreased energy level.
Diarrhea due to acute infection (acute gastroenteritis) usually does not require tests. In
some cases doctors will order blood tests to determine if a child is dehydrated. Collection
of stool samples (stool cultures) can be done to identify the specific cause of the diarrhea
in some children, especially if they have blood in stools. Stool cultures can take from 2 to
5 days before a result is available. Stool studies can also be done to look for parasites
including giardia.
Children with mild dehydration can be treated outside of the hospital with special oral
rehydration solutions (ORS) that can be purchased at the pharmacy or grocery store. Oral
rehydration solutions are the best way to rehydrate a child who is able to drink and is not
vomiting. Although other drinks such as juices, colas and sports drinks are frequently
used, they are not a good substitute for ORS, and can actually worsen the diarrhea.
Patients with more severe diarrhea, vomiting and dehydration may require intravenous
fluids (fluids given through a vein in the arm) in the hospital.
In a child who is otherwise healthy, it is very important to start feeding them their regular
diet as soon as possible. Breast fed infants should be nursed normally during episodes of
acute gastroenteritis. Formula fed infants can continue their regular diet and older
children should be re-introduced to their regular diet as soon as possible. Older children
may avoid dairy initially and try a bland diet consisting of bananas, apple sauce, rice, and
toast. Careful hand washing should be practiced by all family members especially after
diaper changes. Rarely, antibiotics are prescribed for children with specific bacterial or
When diarrhea lasts longer than three weeks it is considered to be chronic. There are
many causes of chronic diarrhea. Usually chronic diarrhea is due to a disease that causes
inflammation of the bowel, but diarrhea may also be due to other causes such as
malabsorption of nutrients. Common causes of chronic diarrhea are shown below:
The diagnosis of these conditions usually requires confirmatory tests. Chronic non-
specific diarrhea is seen in toddlers and is usually dietary in origin, such as from drinking
too much juice. It resolves by simply limiting the amount of juice intake. Celiac disease
is mostly seen in Caucasian children and usually presents with chronic symptoms
including diarrhea, poor weight gain, decreased energy, and abdominal distension. A
child can be screened for this condition by a blood test. Inflammatory bowel disease is
discussed above. Irritable bowel syndrome is a common cause of diarrhea in teenagers,
although many patients will present with abdominal pain and diarrhea that alternates with
constipation. Irritable bowel syndrome and diarrhea are discussed elsewhere in this web-
book. Antibiotic associated diarrhea is seen after antibiotic use and is thought to be due to
an imbalance between the ‘good and bad’ bacteria in the intestine. One such bacterium is
called clostridium difficile, which can be tested for in stool samples. Establishing the
exact cause of chronic diarrhea may require several different tests, some of which are
listed below:
Blood tests
Stool tests
X-ray studies
Endoscopy with biopsy (EGD)
Colonoscopy with biopsy
Lactose breath hydrogen test
Colonoscopy is usually indicated when stool studies have not identified an infection and
diarrhea persists. It is most useful in distinguishing acute inflammation of the colon that
CONSTIPATION
What is constipation?
Infants
The first bowel movement usually occurs within 36 hours after birth in term babies
(babies born within two weeks of their expected due date). Regular or normal bowel
movements can vary significantly among children, especially among infants. Breast fed
infants usually have more frequent bowel movements than formula fed babies.
Children
Most children have from 3 bowel movements per day to 3 per week.
Any change in a child's normal routine including a change in diet, a change in activity
level or a different bathroom can cause constipation. Although it can start without any
clear cause, there are certain times when a child is more likely to become constipated:
Whenever bowel movements become hard, passing them becomes a painful and
unpleasant experience. The child then usually tries to avoid passing bowel movements by
It is slightly more common in boys than girls. About 25-50% of children with
constipation will have a family member with similar problems. Children whose
development is delayed and those born with problems affecting the anus or rectum are
more likely to suffer from chronic constipation, as do those with attention deficit
disorder.
Constipation may be associated with stomachaches or pain in other parts of the abdomen.
Constipation can result in tears of the anus called anal fissures. These cause blood in the
bowel movements. Because stools may be painful to pass over an anal tear, children who
have these tears may develop withholding behavior as described above. Withholding can
result in chronic constipation, soiling of the underwear with stool and even difficulty
walking. Soiling is usually an indication of rectal impaction with stool. It often occurs
when the child is relaxed such as in a warm bathtub or sleeping and is not withholding.
Soft, ‘clay-like’ stool then leaks around the ball of impacted stool in the rectum. Children
who are withholding their bowel movements often have a decreased appetite and activity
level.
In over 90% of children, constipation is not associated with other diseases. There are
however certain 'red flags' or worrisome characteristics that should alert the physician
that another underlying disease should be considered and tested for. Diseases that can
have constipation as one of their symptoms include:
Hirschsprung's disease - a condition where the nerves of the large intestine (colon) are
not properly formed at birth
Thyroid problems- usually underactive thyroid
Celiac disease- a severe wheat intolerance
Lead poisoning
Hormonal problems that cause abnormal blood calcium levels
Constipation can also be a side effect of a medicine that the child is taking for another
condition.
If constipation does not go away or does not get better after the treatment that your
pediatrician prescribes, seeing a pediatric gastroenterologist can be helpful. These
specialists will obtain a detailed history and perform a physical examination to
distinguish constipation that is due to withholding behavior or from constipation due to
an underlying disease. While most children do not need any tests, your physician is the
best judge to decide which test if any is necessary and to provide the most information
about the cause of your child’s constipation.
What types of tests might my child have to determine what is causing their
constipation?
Your doctor may suggest one or more of the following special tests for constipation:
This is a single or set of x-rays that can give your physician a rough idea if
there is a lot of stool present. It may also indicate if the colon is dilated.
This type of x-ray is also obtained prior to a barium enema which is
described below.
This test determines if the nerves and muscles responsible for passing a
bowel movement are working together. It is performed by inserting a very
small balloon at the end of a catheter into the rectum and blowing up the
balloon. The response to inflating the balloon determines if the nerves and
muscles are working together properly. This test is used to diagnose
Hirschsprung’s disease. Normal relaxation of the anal muscles, known as
the anal sphincter, after inflation of the balloon means that a patient does
not have Hirschsprung's disease.
Barium enema
This is a test where a small (pinch) biopsy is performed from the lining of
the rectum to determine if normal nerve cells are present in its walls. The
sample of tissue that is obtained is examined under the microscope. This
test is being used less frequently than it has been in previous years because
of the availability of anorectal manometry testing.
Colonoscopy
This is a scope test. This test is usually not indicated for the evaluation of
routine constipation in children. This test may be helpful if children have
blood in their bowel movements not due to a fissure or straining or for
placing a colonic manometry catheter (see below).
Colonic manometry
Bran
Fresh fruits: apricots, apples, pears, melons
Fresh vegetables: asparagus, beans, broccoli, carrots, beets, cauliflower,
other greens
Whole wheat products: cereals, breads, and pasta.
Fiber supplements are available if parents find their children will not eat more fiber in
their diet. There is little information to recommend one product over another. A patient
may have to try several before finding one that is acceptable and that they are willing to
take regularly. Fiber supplements are given two times a day and must be taken with a
sufficient amount of water. Some patients may notice increased passage of gas while on
fiber supplements. Increasing a patient’s physical activity is also helpful to promote
regular bowel movements.
If constipation does not get better with dietary and behavior modifications, stool softeners
are indicated. The two most common stool softeners used in children are Miralax and
lactulose.
Miralax (polyethylene glycol) has become the most widely used medication for treating
constipation in children. It is a white powder that can be dissolved in juice or water and
does not get absorbed. It is tasteless, safe and non-habit forming. They have soft, more
frequent stools on this medication.
Lactulose is a laxative that is made of a sugar that is not absorbed by the intestine. It
works by pulling water into the bowel movements that helps to keep them soft. Because it
is not absorbed, lactulose is not associated with side effects except for increased gassiness
and diarrhea if the dose of the medicine is too high. Lactulose is not a stimulant and
therefore the bowel does not become dependent on it.
Mineral oil, which is given mixed with juice or milk, acts as a lubricant to allow bowel
movements to pass easier. This type of medication is particularly useful in toddlers who
withhold their bowel movements. Older children may have leakage of the oil in their
underwear that may not be acceptable. This problem usually goes away with decreasing
the dose of mineral oil. Mineral oil should not be given to children with neurologic
problems who are at high risk for aspiration. Flavored forms of mineral oil are also
available.
Stimulant laxatives, such as senna or bisacodyl (dulcolax), that cause the colon to have
strong contractions, are not popular with pediatricians due to the concerns that they may
damage the intestinal nerves, if given over prolonged periods.
Surgery is rarely needed for constipation. The exception to this is Hirschsprung’s disease,
which is treated with surgical removal of the portion of the bowel where there are no
normal nerves. Also, there are rare cases when children develop a dilated and floppy
colon that has no normal contractions, a condition called pseudo-obstruction. These
children also may benefit from removing the affected colon surgically. Recently special
surgical procedures, such as cecostomy (opening between the bowel and skin which
allows drainage of stool), have been devised to help children with spinal cord
abnormalities that have severe problems with constipation.