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Intestinal Obstructions

Definition

Intestinal obstructions are a partial or complete blockage of the small or large intestine, resulting in failure of the contents of the intestine to pass through the bowel normally.

Description

Intestinal obstructions can occur in children as a result of congenital defects, with symptoms appearing any time between birth and adulthood. Abdominal pain and vomiting are the most frequent symptoms and a common cause of admission to emergency rooms. It is difficult for doctors to predict at birth which infants will suffer intestinal obstructions.

Intestinal obstructions can be mechanical or nonmechanical. Mechanical obstruction is the physical blockage of the intestine by a tumor, scar tissue, or another type of blockage that prevents intestinal contents from getting past the point of obstruction. One type of mechanical obstruction is caused by the bowel twisting on itself (volvulus) or telescoping into itself (intussusception). Mechanical obstruction can also result from hernias, fecal impaction, abnormal tissue growth, the presence of foreign bodies in the intestines, or inflammatory bowel disease (Crohn's disease). Non-mechanical obstruction occurs when the normal wavelike muscular contractions of the intestinal walls (peristalsis), which ordinarily move the waste products of digestion through the digestive tract, are disrupted (as in spastic ileus, dysmotility syndrome, or psuedo-obstruction) or stopped altogether as in paralysis of the bowel walls (paralytic ileus).

Mechanical obstruction in infants under one year of age can be caused by meconium ileus, volvulus, intussusception, and hernias. Meconium ileus is a disorder that occurs in newborns in which the meconium, the neonate's first fecal excretion after birth, is abnormally thick and stringy, rather than the collection of mucus and bile that is normally passed. The abnormal meconium blocks the intestines and must be removed with an enema or through surgery. This condition is due to a deficiency of the enzyme trypsin and other digestive enzymes produced in the pancreas. It can be an early clue that the infant may have cystic fibrosis. Intussusception commonly follows an infection that causes increased lymph node size in the gut, which acts as the point of folding for the intussusception.

Hirschsprung's disease (congenital megacolon), which may involve meconium ileus, is a motility disorder that is responsible for 25 percent of newborn non-mechanical intestinal obstructions, though symptoms may not develop until late in infancy or in childhood, delaying diagnosis. Children diagnosed with Hirschsprung's disease lack nerve cells (ganglia) in the large intestine, severely affecting the wavelike movements that propel material through the colon. In most affected infants, the first sign is failure to pass a stool (meconium) within 24 to 48 hours after birth. Between birth and age two, these children will likely develop other symptoms, such as chronic constipation, small watery stools, a distended abdomen, vomiting, poor appetite, slow weight gain, and failure to thrive. Most children will require surgery to remove the affected part of the colon. Surgery can be performed at age six months or as soon as diagnosed in an older infant or child. Symptoms can be removed in at least 90 percent of children born with Hirschsprung's disease. The disease is sometimes associated with other congenital conditions, such as Down syndrome.

Volvulus is the twisting of the small or large bowel around itself (malrotation). Volvulus of the large bowel is rare in infants and children; when it does occur it is usually in the sigmoid (sigmoid volvulus) in the lower colon. Duodenal volvulus occurs when the duodenum, the portion of small intestine that connects the stomach and jejunum, is twisted. Twisting of any portion of the intestines may cut off the supply of blood to a loop of bowel (strangulation), reducing the flow of oxygen to bowel tissue (ischemia) and leading to tissue death (gangrene). Strangulation occurs in about 25 percent of bowel obstruction cases and is a serious condition that can progress to gangrene within six to 12 hours.

Intussusception is a condition in which the bowel telescopes into itself like a radio antenna folding up. Intussusception is the most common cause of intestinal obstruction in children between the ages of three months and six years. Boys are twice as likely as girls to suffer intussusception.

Hernias are weaknesses in the abdominal wall that can trap a portion of intestine (incarceration) and cut off the passage of food and waste through the digestive tract. In 1–5 percent of children, a hernia results when a feature of fetal anatomy in the inguinal area of the groin (processus vaginalis, the space through which the testis or ovaries descend) fails to close normally after birth. These inguinal hernias easily become incarcerated, trapping the bowel and causing obstruction. They are sometimes found on both sides (bilateral hernia) and they occur nine times more often in boys than girls. Parents may see a bulge in the groin area when an inguinal hernia is present. Incarceration occurs only rarely after eight years of age. In most cases, the incarcerated hernias are corrected manually rather than surgically by pushing the incarcerated bowel back up into the abdominal cavity.

Congenital adhesions or post-surgical adhesions can also cause intestinal obstruction in children. Adhesions are bands of fibrous tissue that can bind the loops of intestine to each other or to abdominal organs, narrowing the space between the intestinal walls or pulling sections of the intestines out of place, blocking the passage of food and waste. In adults, adhesions are most often caused by repeat surgery; children who have a history of abdominal surgery can also develop adhesions that can obstruct the intestines. It is not known precisely what causes the abnormal growth of fibrous tissue in congenital adhesions.

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