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Marsha Kay, M.D. and Vasundhara Tolia, M.D.
Department of Pediatric Gastroenterology and Nutrition, The
Cleveland Clinic Foundation and Division of Gastroenterology,
Childrens Hospital Of Michigan
GASTROESOPHAGEAL REFLUX
What is 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.
Is it normal if my infant spits up?
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.
Is vomiting in my baby always due to gastroesophageal reflux?
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 intestine is not formed or
positioned properly or is blocked. These types of problems
are usually found in the immediate newborn period but can
present later in some infants. A combination of x-rays and
or endoscopy (looking at the lining of the stomach and upper
intestines and/or colon with a long tube with a video camera
at the tip) is usually helpful to make this diagnosis.
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.
What are the symptoms of reflux in older children and adolescents?
Reflux symptoms in children are variable. Children may be
unable to communicate typical heartburn symptoms. They may
complain of generalized stomachaches, frequently around the
area of the belly button and on occasion may complain of
chest pain. Often children will report a feeling that they
need to throw up and on occasion will describe that they
get a taste in their mouth as if they have thrown up. Other
children will report that they feel that the food is coming
back up and that they then re-swallow it. Occasionally they
will report a feeling that food is not going down correctly
or feels like it is getting stuck. Some patients may complain
of asthma symptoms such as cough or wheezing that are worsened
by reflux. Even though children may not relate reflux symptoms
to eating, obtaining a dietary history for foods and medicines
that trigger reflux is important.
How is the diagnosis of reflux made?
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?
There are many medications available to treat gastroesophageal
reflux. Many of these medications have been used successfully
to treat children. Dosages of medication must be modified
for a child's weight. Also they require monitoring
to reduce possible long-term side effects. Diet is an important
part of reflux management and children and teenagers with
reflux should avoid the products listed below. Medications
such as aspirin, ibuprofen and alcohol based products should
be avoided if possible in children with reflux. Rarely a
surgical procedure called a fundoplication (or wrap) is required
for severe reflux. This procedure is usually reserved for
patients with severe symptoms or complications of reflux
that do not respond to standard medications and dietary treatment.
Foods to avoid if you have reflux
Spicy, acidic or tomato based foods
Fatty foods
Citrus products including citrus juices
Apple juice (apples are fine)
Caffeinated drinks- cola, tea, coffee, hot chocolate
Chocolate and licorice
LACTOSE INTOLERANCE
What is 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.
What are other sources of lactose?
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.
Who gets lactose intolerance?
Rarely babies may be born with a deficiency or absence of
the enzyme lactase. This condition is very rare and is known
as primary lactase deficiency. Babies inherit this condition
by getting one gene that causes this problem from each of
their parents, even though both parents may be lactose tolerant.
Babies who lack this enzyme may have severe feeding problems
with diarrhea, vomiting and poor growth starting in early
infancy. These babies require a specialized formula with
another type of sugar such as sucrose (present in table sugar),
which they are able to digest. The majority of infants who
have feeding problems however are not lactose intolerant.
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.
What are the symptoms of lactose intolerance?
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 burping, loud bowel
sounds, excess gas and diarrhea following ingestion of lactose.
An individual who is lactose intolerant may have very watery
and explosive bowel movements. Individuals who are lactose
intolerant may feel a sense of urgency with bowel movements.
This means that they feel that they have to get to the bathroom
immediately or they will have an accident. If someone who
is lactose intolerant does not eat lactose they will not
have the symptoms noted above.
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).
What causes the symptoms of lactose intolerance?
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.
How is lactose intolerance diagnosed?
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.
What can be done to treat or manage lactose intolerance?
The best treatment of the symptoms of lactose intolerance
is a combination of dietary modification and taking a supplement
to aid in digestion of lactose. Individuals who are lactose
intolerant should meet with a dietician to review the sources
of lactose in their diet. Some reduction in the daily lactose
consumption is usually required. When an individual is going
to be eating a food that contains lactose they should take
a commercially available non prescription lactase supplement
at the time of lactose ingestion. This type of supplement
can be taken throughout the day whenever lactose is ingested.
Some individuals will be less lactose intolerant and therefore
will be able to tolerate comparatively larger amounts of
lactose. Alternatives to milk for lactose intolerant individuals
include products such as soy milk. If an individual is restricting
their milk/ dairy intake it is important to ensure adequate
supplementation of calcium in the diet. This is especially
important for pediatric patients and women.
Recommended daily calcium intakes
| 1-3 years of age |
500 mg |
| 4-8 years of age |
800 mg |
| 9-24 years of age |
1300 mg |
| Age 25 and above |
800-1000 mg |
| Pregnant and nursing women |
1200 mg |
Is it possible to become temporarily lactose intolerant?
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.
INFLAMMATORY BOWEL DISEASE
What is inflammatory bowel disease?
Inflammatory bowel disease refers to a chronic (long term/
lifelong) inflammation or irritation of the stomach, small
intestine and/or colon (large bowel). Inflammatory bowel
disease should not be confused with irritable bowel syndrome
which is discussed elsewhere in the web book. There are two
types or categories of inflammatory bowel disease, Ulcerative
Colitis and Crohn's disease. Patients can have either
type but not both. Occasionally one type of inflammatory
bowel disease is diagnosed and with further testing or time
the disease may be re-diagnosed as the other type.
What is the difference between Ulcerative colitis and Crohn's
disease?
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 that are normal with abnormal areas on either
side of them. Ulcerative colitis only involves the innermost
layer of the bowel (the lining of the bowel) known as the
mucosa. It does not involve deeper layers of the bowel. Crohn’s
disease on the other hand can involve any area of the gastrointestinal
tract from the mouth to the rectum (the last portion of the
colon) and the anus. Crohn’s disease involves not only
the lining of the bowel, but can and usually does involve
the deeper layers of the bowel. Even though Crohn’s
disease can involve any portion of the gastrointestinal tract
it typically does not involve every portion of the gastrointestinal
tract. The most common sites of involvement are the end of
the small intestine known as the terminal ileum, involved
in up to 80% of patients, involvement in the colon in approximately
50% of patients, with approximately 5% of patients having
disease in their stomach or first part of the small intestine
known as the duodenum.
How common is ulcerative colitis and Crohn’s
disease in pediatric patients?
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.
What are the symptoms of Ulcerative Colitis in children
and teenagers?
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
have pain prior to a bowel movement that improves after a
bowel movement, and frequent bowel movements up to 10 times
per day or more. Patients may also feel that they need to
have a bowel movement immediately or they are going to have
an accident. Having bowel movements at night is not uncommon
in patients with ulcerative colitis, especially when the
colon is more inflamed. Other symptoms in children can include
anemia (a low blood count), weight loss and poor growth,
although the later two are more common with longstanding
disease and more likely to occur with Crohn’s disease.
What are the symptoms of Crohn’s disease in
children and teenagers?
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.
How is the diagnosis made of ulcerative colitis
or Crohn’s
disease?
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.
Endoscopy with biopsy (taking samples of tissue) also known
as performing a scope test is the definitive way to diagnose
inflammatory bowel disease and also to determine how much
of the colon is involved. Endoscopy can also be performed
of the stomach and first part of the small intestine in patients
suspected of having Crohn’s disease. Medications are
given during the procedure to sedate the patient and increase
the comfort of the procedure.
What does my gastroenterologist mean when he talks
about “extra
intestinal manifestations” of Crohn’s disease
or ulcerative colitis?
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.
| Symptom |
Crohn’s disease |
Ulcerative colitis |
| Joint swelling or pain/arthritis |
yes |
yes |
| Skin rashes |
yes |
yes |
| Mouth sores |
yes |
no |
| Inflammation of the eye |
yes |
yes, but less common |
| Clotting problems |
yes |
yes |
| Kidney stones |
yes |
no |
| Abnormal liver function tests |
yes |
yes |
| Inflammation of the pancreas |
yes |
uncommon except with meds |
| Bone disease |
yes |
yes, but less common |
| Anemia |
yes |
yes |
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.
Medications used for pediatric patients with inflammatory
bowel disease include the following:
| Types |
How it is given |
| Aminosalicylate or 5-ASA products |
by mouth, as a suppository or an enema |
| Steroids |
by mouth, in the vein, or as an enema |
| Immunosuppressants (Imuran, 6-MP) |
by mouth |
| Immunosuppressants (Methotrexate) |
by mouth or by injection |
| Immunosuppressants (Cyclosporine) |
by mouth or in the vein |
| Antibiotics |
by mouth, in the vein |
| Immune-modulators (Infliximab) |
in the vein |
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.
Can surgery cure ulcerative colitis or Crohn’s
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.
What is acute diarrhea? 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.
What testing should my child have if they are having diarrhea?
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.
What can I do to treat my child’s diarrhea
and dehydration?
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 parasitic illnesses, although
in most cases antibiotics do not change how long the diarrhea
lasts or its severity. While oral rehydration solutions can
prevent dehydration, they do not decrease the number of stools
or how long the diarrhea lasts. Medicines which slow down
bowel movements are not recommended in children with acute
diarrhea.
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:
Diarrhea following infection (post infectious diarrhea)
Chronic nonspecific diarrhea
Celiac disease (wheat intolerance)
Inflammatory bowel disease (ulcerative colitis and Crohn’s
disease)
Lactose intolerance
Irritable bowel syndrome
Diarrhea after antibiotic use (antibiotic associated colitis)
Food allergies
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:
Common tests for chronic diarrhea
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 gets better on its own, known as acute self limited
colitis, from chronic inflammation of the bowel known as
chronic colitis. Colonoscopy does not usually help to find
the cause of diarrhea due to infection with the exception
of diarrhea that follows antibiotic use. Colonoscopy is invaluable
in making the diagnosis of inflammatory bowel disease and
figuring out what portion of the colon is involved with the
inflammation. Your physician can assist you in choosing the
best treatment after determining the cause of your child’s
diarrhea.
CONSTIPATION
What is constipation?
Constipation is defined as infrequent bowel movements, hard
bowel movements, and difficulty in passing bowel movements
or painful bowel movements. It is a very common problem but
not always easy to treat. Children may not complain of this
problem to their parents. Parents may be reluctant to talk
about this problem with their family members or physicians.
It is one of the most frequent reasons that children are
sent to see a pediatric gastroenterologist.
What is considered a normal bowel pattern?
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.
What causes constipation?
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:
When solid foods are introduced as an infant
During toilet training
At the start of school
Birth of a sibling
Parents separating or divorcing
Move to a new place
Whenever bowel movements become hard, passing them becomes
a painful and unpleasant experience. The child then usually
tries to avoid passing bowel movements by holding it. This
may eventually lead to larger, harder stools that worsen
the situation. The children may cross their legs, stand on
toes, or squeeze their buttocks together to try to avoid
passing a bowel movement. Many times parents misinterpret
these behaviors as straining to pass stools when in reality
the children are trying not to have a bowel movement. These
behaviors are called retentive withholding.
Who is likely to develop chronic constipation?
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.
What happens when my child is constipated?
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.
Is my child's constipation a sign that they
have another disease?
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.
When should my child see a specialist about their constipation?
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:
Plain x-ray of the abdomen (also known as a KUB)
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.
Anorectal manometry or motility test
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 an x-ray test where barium or another type of
contrast is inserted via a catheter into the rectum and
x-rays of
the abdomen are taken. The test may or may not require
a special bowel preparation to clean out the bowel before
the test. This test is used to diagnose a blockage in
the intestine or an area that may be narrowed or abnormal.
It is also used in the diagnosis of Hirschsprung’s
disease. This test is being used less frequently to diagnose
Hirschsprung’s disease than it has been in previous
years because of the availability of other simpler types
of tests such as anorectal manometry that is described
above.
Rectal biopsy
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.
Transit study or marker study
This test is performed to determine if the reason
for constipation is due to slow movement throughout
the
colon or just in
the last part of the colon known as the rectum. Plastic
markers, which can be seen on x-ray, are swallowed
and then several x-rays are performed over the next
4-7 days
to determine how long it takes them to pass through
the GI tract. Patients with normal motility pass
the majority
(>80%) of the markers within 5 days. If the markers
are not passed but are found to remain throughout the
colon, this suggests slowing of the entire colon. If
the markers
do not pass and are clustered in the rectum, this may
indicate a problem in the rectum only.
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
This is a specialized test done in children
who have continued problems with intractable
constipation despite adequate
medical therapy. It involves placing a catheter at the
time of colonoscopy to determine whether there are normal
contractions in all parts of the colon. The test requires
a period of prolonged monitoring of the contractions
of the colon after placement of the catheter.
This test is
used to establish the diagnosis of colonic pseudo-obstruction
in children, a very rare condition.
How is constipation treated in children?
The best way to treat constipation is a combination of education,
behavioral modification, dietary modification and non-habit
forming medications. If there is an impaction of stool, which
means a very large amount of stool in the rectum, it needs
to be evacuated first either by an enema or by a medication
given by mouth. Patients are then started on a maintenance
medication for a few months to soften the stools, and a program
of bowel retraining is started. The child is advised to sit
on the potty after every major meal for 5-10 minutes and
try to have a bowel movement. Positive reinforcement (reward)
is provided if the child has a stool in the potty. Behavioral
modification may be needed in some patients. Some children,
especially boys, tend to get so involved in sports or playing
video games that they ignore the ‘urge’ to have
a bowel movement. Postponing the event makes things worse
in the long run. The goal of treatment is to make having
a bowel movement pain free for the child by softening the
stools. Consistency in treatment is crucial for success.
Dietary and lifestyle changes may be helpful in improving
a patient’s symptoms. Increasing dietary fiber over
1 to 2 weeks is often helpful, by increasing bulk that then
stimulates colon contractions. This strategy may take a while
to work and should not be tried in children with severe constipation
as it may make it worse. High fiber foods include:
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.
What types of medications are used in children?
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.
Milk of Magnesia is a mild stimulant laxative that may be
used at bedtime in children with mild constipation. It is
available over the counter without a prescription. The major
limiting factor in its use in children is its taste, even
though it is now available in different flavors.
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.
Is surgery ever performed for treatment of constipation?
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.
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