Abdominal Pain and Vomiting in the Infant
Casey Grover, MD, Stanford/Kaiser Emergency Medicine Residency, Stanford, CA.
Ewen Wang, MD, Associate Professor of Surgery/Emergency Medicine, Associate Director, Pediatric Emergency Medicine, Stanford School of Medicine, Stanford, CA.
Nick Erbrich, MD, FAAP, Department of Emergency Medicine, St. Christopher's Hospital for Children, Philadelphia, PA.
Abdominal pain with vomiting is a common presenting complaint to the emergency department (ED) in infants. In the majority of cases, the patient's symptoms come from a benign cause such as gastroenteritis. However, it remains essential for the emergency physician (EP) to thoroughly understand the differential diagnosis of abdominal pain and vomiting in infants, particularly identifying those causes requiring surgical intervention.1-3 This article will discuss seven key causes of abdominal pain and vomiting in infants: malrotation with volvulus, necrotizing enterocolitis, Hirschsprung's disease, pyloric stenosis, intussusception, appendicitis, and acute gastroenteritis. A summary of the presenting age and frequency of each condition is displayed in Table 1 for quick reference.
Table 1. Presenting Age and Frequency of Conditions Causing Abdominal Pain and Vomiting in Infants
3rd - 8th week of life
2-4 per 1000 births
3rd month - 5th year of life (most common in 1st year of life)
18-56 per 100,000 births
1st - 10th day of life
12% of babies under 1500 g
10% of all cases in term
Malrotation with volvulus
80% within first month of life
Malrotation: 1 per 500 births; malrotation with volvulus: 1 per 5000 births
3.7 million physician visits in the United States annually
First days of life
1 per 5000 births
Any age; < 5% younger than 5 years, most frequent in 2nd decade of life
86 per 100,000 patients per year
A review of gastrointestinal (GI) tract development is essential to understand the pathophysiology of acute abdominal processes occurring in the infant. At approximately the fourth to fifth week of development, the midgut begins to develop, extending from the anterior intestinal portal to the yolk sac. As the gut develops, it initially extrudes into the umbilical cord between weeks five and 10. The bowel then rotates counter-clockwise through a path of 270 degrees around the superior mesenteric artery, ultimately attaching to the posterior abdominal wall at about the fourth to fifth month of development. The ascending and descending colon normally attach and anchor to the right and left abdominal gutters, respectively. It is during this period that failure of the normal process of rotation and fixation of the intestine can lead to malrotation and predispose to volvulus in infancy. In such cases, the colon develops abnormal attachments to the right side of the retroperitoneum, commonly referred to as Ladd's bands, which may cause duodenal obstruction and also allow for the bowel to twist upon its mesentery.5-7 Furthermore, during the first trimester of development, neural crest cells migrate distally from the central neurologic structures toward the anal end of the intestinal tract. Enteric nervous system precursor cells ultimately develop from these neural crest cells, allowing for the development of the enteric nervous system. Failure of this migration of neural crest cells can cause Hirschsprung's disease in infancy.8
Malrotation with Volvulus
Etiology. Malrotation represents any failure during development of the normal rotation pattern, leading to a congenitally abnormal position of the bowel within the abdomen. Subsequently, the poorly attached intestine is at an increased risk of twisting, producing a volvulus, which can lead to obstruction. It is important to recognize that malrotation itself is not a condition requiring emergent surgical management; it is only when patients develop acute intestinal obstruction from volvulus that emergency surgery is needed.3-7,9
Malrotation can occur as an isolated phenomenon; however, it is also associated with a number of congenital syndromes, such as Cornelia de Lange syndrome, cat-eye syndrome, or Marfan syndrome. This condition also frequently occurs with other gastrointestinal abnormalities, such as duodenal stenosis or atresia, Hirschsprung's disease, omphalocele, and gastroschesis.9
Epidemiology. Malrotation occurs in approximately one in every 500 births, with one in every 5000 births developing volvulus and becoming symptomatic. While infants may present any time, approximately 80% of cases of malrotation with volvulus occur within the first month of life. Of infants who develop this condition within the first month of life, the majority will present within the first week of life.7
Presentation. The classic presentation is one of a sudden onset of vomiting, apparent abdominal pain, and difficulty feeding. As a result of the intestinal obstruction, infants develop bilious vomiting, which is a hallmark feature of malrotation with volvulus. Other symptoms that may be seen include diarrhea, constipation, and hematochezia. In infants with advanced disease, signs and symptoms of peritonitis may be present, as well as hemodynamic compromise.3,7
Laboratory Studies and Diagnostic Imaging. Routine laboratory studies are often sent, such as a complete blood count, basic metabolic panel, and type and screen. However, these tests are not helpful in making the diagnosis of malrotation with volvulus. Routine abdominal radiographs also may not be helpful. In confirmed cases of malrotation with volvulus, plain abdominal X-rays may demonstrate a variety of findings, from obstruction to a normal bowel gas pattern.3 Findings on radiograph that increase concern for malrotation are those that suggest an abnormal anatomical location of the bowel, such as the "double bubble" sign when duodenal dilation is present.7
The upper GI series is the imaging reference standard for the diagnosis of malrotation with or without volvulus, with sensitivities as high as 93-100%. Malrotation with volvulus is suspected when there are signs of proximal intestinal obstruction such as an abrupt end to the contrast material within the bowel and an abnormal location of the duodenal junction. At the point of obstruction, one may see a "beaked" or "corkscrew" appearance. Other signs indicating proximal intestinal obstruction may include a Z-shaped configuration of the duodenum secondary to obstructing peritoneal bands.3,7,9 (See Figure 1.)
Figure 1. Malrotation with Volvulus
Two images from an upper GI study demonstrating lack of transit of contrast from the stomach and duodenal bulb into the proximal small bowel with corkscrew configuration of the proximal duodenum consistent with malrotation with volvulus. Images courtesy of Casey Grover, MD.
In the event that the upper GI series is inconclusive, other imaging studies may be used. If an ultrasound is performed, special attention should be paid to the relationship between the superior mesenteric vein and mesenteric artery. Normally, the vein is to the right of the artery. In malrotation, the vein is to the left of the artery or rotates around the artery as a result of the bowel twisting on its axis. Additionally, a volvulus may appear as a "whirled" appearance of vasculature entering and within the volvulus, referred to as the "whirlpool" sign. Computed tomography may be used in challenging cases and can be helpful in evaluating malposition of the bowel as well as the relationship between the superior mesenteric vein and arteries.3,7
Treatment. Malrotation with volvulus is a surgical emergency. When the diagnosis is either suspected based on a history of bilious vomiting or confirmed via imaging studies, infants should be aggressively resuscitated. Pediatric surgical consultation should be obtained emergently, even prior to definitive imaging, since volvulus can result in necrotic bowel within hours. Intra-operatively, the volvulus is untwisted, and any necrotic sections of bowel are resected. Furthermore, any obstructing bands within the abdomen are lysed, and the bowel is fixed in an appropriate location. As the appendix is commonly in an abnormal position in patients with malrotation, appendectomy is frequently performed during this procedure as well.5,10
Etiology. While the exact predisposing cause of necrotizing enterocolitis (NEC) is not known, this condition is characterized by an inflammatory process of the neonatal bowel wall that often involves necrosis. In term infants, NEC is nearly always associated with a precipitating event, such as asphyxia, congenital heart disease, abdominal wall defects, neural tube defects, polycythemia, and anoxia, to name a few. This condition is characterized by a necrotic section of intestine, leading to accumulation of gas in the submucosa of the bowel. NEC may present at any point within the neonatal gastrointestinal system, but is most commonly seen involving the jejunum, ileum, and cecum, leading to a presentation of disease in the right lower quadrant.1,11-13
The marked intestinal inflammation leads to disruption of the function of intracellular tight junctions in the intestinal epithelium. As a result, infants with this condition are at high risk for third-spacing fluid in the abdomen and intra-abdominal sepsis.13
Epidemiology. NEC is a disease in neonates associated with prematurity and hypoxia, occurring in up to 12% of infants weighing less than 1500 grams. This condition is much less common in term infants, with only 10% of cases being in babies born at term. NEC is the most common gastrointestinal emergency in premature and newborn infants, and while it is largely a disease seen and managed in the neonatal intensive care unit (NICU). The fact that it can occur in term infants makes this an important condition for emergency physicians to understand. When seen in term infants, it most commonly presents within the first 10 days of life, but in rare cases can present in infants up to several months of age.1,11-13
Presentation. The first signs of NEC are nonspecific and, thus, subtle, and include poor feeding tolerance and abdominal distension. As the disease progresses, the abdomen may become tender to palpation, suggestive of peritonitis. As a result of the inflammation of the gastrointestinal tract, motility is decreased, leading to vomiting, which may be bilious in severe cases. Stools, while normal in the majority of cases, may demonstrate occult blood in early cases and frank blood in more advanced cases.1,11,12
Laboratory Studies and Diagnostic Imaging. Laboratory findings that are more common in NEC include elevated C-reactive protein, thrombocytopenia, elevated or decreased white blood cell count (WBC), and acidosis.14 However, none of these tests are of high enough sensitivity or specificity to confirm the diagnosis.
Radiologic studies are the best modality for making the diagnosis. Plain X-ray films of the abdomen are the first and best imaging study, with dilated bowel loops suggestive of this condition, and pneumatosis intestinalis (air in the bowel wall) pathognomonic for NEC. (See Figure 2.) In severe cases in which there has been perforation, pneumoperitoneum may be present.
Figure 2. Necrotizing Enterocolitis
Plain film of the abdomen demonstrating intramural air (pneumatosis intestinalis) in the right lower abdomen, consistent with necrotizing enterocolitis. Image courtesy of Casey Grover, MD.
Ultrasonography has limited utility in necrotizing enterocolitis. Ascites and hyperemia of the bowel are most suggestive of this condition, but may be non-specific findings. In advanced cases, ultrasound may demonstrate intra-abdominal fluid with debris consistent with perforation.15
Treatment. Necrotizing enterocolitis requires aggressive treatment, including fluid resuscitation and bowel rest. Enteral feeds should be stopped, and gastric decompression with a nasogastric or orogastric tube should be performed. As injury to the bowel lumen predisposes the patient to bacterial translocation across the injured bowel wall with subsequent infection, broad-spectrum antibiotics should be initiated. In infants who deteriorate with medical management, surgical intervention is needed. Specific signs that indicate the need for surgical management include intestinal gangrene, clinical deterioration, abdominal wall edema or erythema, worsening pneumatosis intestinalis or portal venous gas, or worsening acidosis.1,11,12
Hirschsprung's Disease/Intestinal Aganglionosis
Etiology. Hirschsprung's disease (HD) is characterized by a lack of normal migration of ganglion cells in the myenteric and submucosal plexus of the intestine. As a result of this deficit of intestinal neurons, colonic motility is markedly impaired, leading to obstruction. In approximately 75% of cases, the extent of neural crest cells is near normal, and only the rectum is affected. While HD is generally confined to the colon, in rare cases the small bowel and even the entire gut may be affected.8,16
Down syndrome increases the risk of Hirschsprung's disease by 100-fold as compared to the general population.17 Variability exists in the length of gut affected in this condition, with total colonic aganglionosis (TCA) being the most severe form. TCA is estimated to occur in 5% to 15% of all cases of Hirschsprung's disease.18
Epidemiology. HD is the most common congenital disorder of intestinal motility, and is estimated to occur in one out of every 5,000 births. Approximately 80-90% present in the neonatal period. This discussion will only focus on presentation in neonates. Hirschsprung's disease is more common in male infants, and appears to have differential incidence based on ethnic heritage, occurring less frequently in Hispanic and white patients and more frequently in African-American and Asian patients.17
Presentation. Initial symptoms may include constipation, abdominal distention, and vomiting. The cardinal presenting symptom in HD is delayed passage of meconium. Nearly all normal infants will pass stool within the first 24 hours of life. By comparison, more than 90% of patients with HD will fail to pass meconium within the first 24 hours of life. A rectal examination may reveal a tight anus and may also allow for the passage of meconium in an infant with HD.8,16,19
Between 5% and 44% of patients may develop Hirschsprung-associated enterocolitis, which is characterized by foul-smelling diarrhea, abdominal distension, and fever. This condition should be recognized quickly, as in severe cases, infants may develop toxic megacolon. Signs of toxic megacolon include marked abdominal distension, bile-stained vomit, fever, and shock.8,19
Laboratory Studies and Diagnostic Imaging. As with many of the conditions producing abdominal pain in infants, basic laboratory studies are not specific for making the diagnosis. Plain abdominal radiographs can be obtained initially and may demonstrate gaseous colonic dilation with an undilated rectum. Contrast enema also may be used in the initial work-up, predominantly to differentiate HD from other causes of lower intestinal obstruction. Findings on contrast enema that are suggestive of this disease include an abrupt change in caliber of bowel size from the normal-sized aganglionic segment to the dilated colon proximal to the aganglionic segment. Contrast enema is estimated to have a 76% sensitivity and 97% specificity for the diagnosis of HD.8,19
A definitive diagnosis of Hirschsprung's disease requires more specific testing. Anorectal manometry allows for the measurement of pressures of the anorectal region and, thus, of the functioning of the sphincters of the intestine. Furthermore, this test can be used to look for the presence of the rectoanal inhibitory reflex (RAIR), a finding that is absent in infants with HD.8,19
Finally, histopathologic analysis of rectal tissue to evaluate for presence or absence of intestinal ganglionic cells remains the gold standard in the diagnosis of Hirschsprung's disease.8,19
Treatment. In patients with Hirschsprung-associated enterocolitis, infants should receive immediate fluid resuscitation and antibiotics should be started. A pediatric surgeon should be emergently consulted, and the intestine should be decompressed.
Treatment of Hirschsprung's disease is surgical. Initially, a diverting ostomy is done to bypass the aganglionic segment causing obstruction. A second operation is performed later, in which the affected bowel is removed with anastomosis of functional bowel to the anus.8,19
Etiology. This condition results from hypertrophy of the pyloric muscle at the distal end of the stomach. The muscular enlargement causes narrowing of the pyloric channel, which leads to gastric outlet obstruction. While the exact etiology of this disease has not been elucidated, there are several factors that have been implicated in the development of pyloric stenosis. First, there appears to be a genetic predisposition for this condition. While pyloric stenosis has been associated with specific genetic syndromes such as Cornelia de Lange syndrome, no specific gene has been isolated. One extrinsic factor that has been implicated in the development of pyloric stenosis is exposure to erythromycin. Infants exposed to erythromycin in the first two weeks of life carry up to a 10-fold higher risk of pyloric stenosis, and there is some evidence that maternal exposure to erythromycin during pregnancy and breastfeeding may also increase the risk of this condition.20-23
Epidemiology. Pyloric stenosis is a relatively rare condition, with approximately 2-4 cases per 1000 births. It is more common in males, with a four- to five-fold greater risk of developing pyloric stenosis in males relative to females. Furthermore, this condition is more common in first-born children as compared to later-born children. There is also an increased risk in infants with a family history of this disease.20,21
Presentation. Pyloric stenosis typically presents between the third and eighth week of life with projectile vomiting. Vomiting tends to occur within 30 minutes of feeding and is non-bilious. The physical examination typically demonstrates a child who appears hungry and eager to feed, even after an episode of vomiting. The abdominal examination is classically described as having a palpable "olive" in the mid-epigastric region of the abdomen, representing the hypertrophied muscle. However, this may be a difficult finding to appreciate in an active and awake infant. In the early stages of disease, infants may appear well; however, as the disease progresses and patients are unable to maintain hydration secondary to vomiting, infants will develop moderate to severe dehydration.3,20
Laboratory Studies and Diagnostic Imaging. Routine laboratory studies, such as a complete blood count and basic metabolic panel, are not commonly helpful. However, they may demonstrate hypokalemic, hypochloremic, or metabolic alkalosis from vomiting.3,24
The diagnosis of pyloric stenosis may be made by one of two different diagnostic imaging studies. First, an upper GI contrast study may be used to make the diagnosis. A positive study will demonstrate a narrowed pyloric channel, often referred to as the "string sign." Advantages to this modality are that it is relatively operator-independent and it has a sensitivity of 96% and a specificity of 100% in the hands of an experienced radiologist. The disadvantages of this modality are that it is relatively invasive and exposes the child to ionizing radiation.1,25 Second, an abdominal ultrasound may be used to make the diagnosis of pyloric stenosis, with a positive study demonstrating pyloric muscle thickness of greater than or equal to 4 mm or length of the pyloric canal being greater than or equal to 14 mm. (See Figure 3.) This modality boasts a sensitivity of 98% and a specificity of 100%, with no radiation exposure to the child. The disadvantage of this study is that, as with all ultrasound, it is somewhat operator-dependent. Generally speaking, due to the less invasive nature of ultrasound and the lack of radiation exposure, ultrasound is the first-line imaging study in the evaluation of the infant with possible pyloric stenosis.1,3,25
Figure 3. Pyloric Stenosis
Treatment. Infants with pyloric stenosis should receive fluid resuscitation intravenously to correct dehydration and provide maintenance fluid needs. Affected patients should be made NPO, and pediatric surgical consultation should be obtained. Definitive treatment consists of surgical pyloromyotomy. This procedure is well tolerated and is associated with a low incidence of morbidity and mortality.21
Etiology. Intussusception is the result of prolapse of one part of the intestine into the lumen of an adjacent portion. While the vast majority of cases in children are idiopathic, certain conditions may act as a "lead point" for intussusception. Such conditions include lymphoma, Meckel's diverticulum, and Henoch-Schonlein purpura. When one portion of the intestine prolapses into another, this results in compression of the lumen with subsequent obstruction of venous return. This, in turn, leads to edema, increased pressure on the bowel, and, ultimately, obstruction to arterial flow with gangrene and perforation of the bowel as manifestations of end-stage disease.1,26
Epidemiology. Approximately 18-56 cases of intussusception occur per 100,000 births. While it may be seen any time between the ages of 3 months and 5 years, it is most common in the first year of life. Peak incidence is between 6 and 11 months of age, with a male predominance.1,24
Presentation. The clinical presentation of intussusception may be variable. Common symptoms include irritability and intermittent crying. Features seen in more advanced cases include bloody stool, often referred to as "currant jelly stool." Parents may describe the pain as intermittent, in which the child draws his or her knees up to the chest for up to five minutes at a time, only to be followed by an asymptomatic period of up to 20 minutes. Lethargy remains another common presentation of intussusception.
On physical examination, the child may appear uncomfortable or lethargic. The abdomen may appear distended and tender, and one may appreciate a mass on the right side of the abdomen, most commonly in the right upper quadrant. A rectal examination classically demonstrates grossly bloody stool, which usually is a late finding.1,26 Early on, there may be a normal-appearing stool that may be positive for occult blood.
Laboratory Studies and Diagnostic Imaging. There are no laboratory studies that are specific for the diagnosis of intussusception.1
Imaging studies are essential in the diagnosis of intussusception. Plain abdominal radiography is often the initial imaging study and may demonstrate a mass in the right upper quadrant, reduced air in the small intestine, or small bowel obstruction. (See Figure 4.) Studies of the accuracy of plain abdominal radiography in the diagnosis of intussusception have demonstrated high sensitivity but only moderate specificity.27,28
Figure 4. Intussusception
Ultrasonography has proven to be an outstanding imaging modality for the evaluation of this condition. A technique of graded compression is used, yielding a sensitivity of 98-100% and a specificity of more than 90%. A positive examination demonstrates an intussusception mass, usually a complex structure greater than 5 cm with a hypoechoic region surrounding an echogenic center often described as resembling a target or doughnut. (See Figure 5.) When viewed on ultrasound in long axis, the hypoechoic layers on each side of the echogenic center may resemble a kidney, creating an appearance often referred to as the "pseudokidney" sign. In addition to the increased sensitivity and specificity of ultrasound over plain abdominal radiography, ultrasound may also be able to identify the lead point of the intussusception.28
Figure 5. Small Bowel Intussusception
Ultrasound of the abdomen demonstrating a target sign (white arrow) consistent with a small bowel intussusception. Image courtesy of Casey Grover, MD.
Treatment. To prevent ischemia, necrosis, and subsequent perforation of intestine, the intussusception must be reduced. Barium, water-soluble contrast, and air have all been used as enemas for the reduction of intussusception. While the barium enema has previously been the gold standard for the diagnosis and treatment of this condition (see Figure 6), air enemas have become the more commonly used technique, with a higher rate of successful reduction. Air enemas are preferred because they eliminate the possibility of barium peritonitis in the case of colonic perforation during reduction. In addition, they impart a lower radiation dose to the child. Recurrence of intussusception after air reduction may occur in 5-20% of cases. As such, all children with intussusception must be admitted to the hospital so that additional efforts at enema reduction or surgical intervention may be made if the condition recurs.1,26,29
Figure 6. Intussusception
The most feared complication of enema reduction of intussusception is intestinal perforation, which may occur in up to 1% of all cases of attempted reduction with enema. For this reason, all cases of intussusception ideally should be evaluated by a pediatric surgeon prior to enema reduction, so as to facilitate swift operative intervention should a perforation occur.1,26
Etiology. Appendicitis may be described as a disease process that occurs in five stages, usually progressing over a 24-36 hour period. The process begins with obstruction of the appendiceal lumen, usually from a fecalith or lymphoid hyperplasia. More unusual inciting causes include foreign bodies, malignancy, and parasites. As a result of this obstruction, the appendiceal lumen becomes unable to drain and dilates. This distension leads to the second stage of disease, in which the eighth through 10th visceral afferent thoracic nerves are stimulated by the increasing appendiceal distension. During this second phase, patients experience peri-umbilical pain. With increasing distension of the appendix, perfusion to the luminal wall of the appendix decreases, producing the third stage of acute appendicitis. Decreased perfusion allows for bacterial invasion of the appendiceal lumen, creating the fourth stage, consisting of inflammation of the wall of the appendix. Finally, inflammation spreads outside of the appendix and into the peritoneum, leading to the fifth and final stage of appendicitis. During this period, as a result of the irritation of parietal peritoneum, patients experience pain in the right lower quadrant.17,30
Epidemiology. Appendicitis is the most common surgical cause of abdominal pain in pediatric patients presenting to the ED, with a worldwide incidence of appendicitis estimated to be 86 cases per 100,000 patients per year. It is estimated that there are 70,000 hospital discharges each year for acute pediatric appendicitis, with approximately one-third of all children developing rupture of the appendix prior to surgical intervention. Rates of rupture increase in an inverse relationship to patient age, with perforation rates as high as 82% in children younger than 5 years old and 100% in children younger than 1 year old.17,30,31
Presentation. Abdominal pain remains one of the most common presentations of acute appendicitis in children. However, this symptom may be challenging to elicit. Fever is also commonly present in infants with acute appendicitis, but is not universally present. As a result of the intra-abdominal inflammation and discomfort, infants with acute appendicitis may also develop poor feeding (a manifestation of anorexia or nausea) and vomiting. However, it remains important to remember that infants with appendicitis often present with atypical symptoms, making acute appendicitis a very difficult diagnosis to determine based on history alone. A review of a large number of studies on acute appendicitis in the pediatric population identified fever as the most predictive symptom of appendicitis, with a positive likelihood ratio of 3.4. However, being a relatively common symptom, fever is of low specificity for the diagnosis of acute appendicitis, making it of limited utility in detecting this condition.31,32
The physical examination for appendicitis may be challenging in infants due to their inability to communicate and lack of cooperation. The examination should focus on trying to determine the location of pain and assessing whether or not signs of peritoneal inflammation, such as rebound tenderness or guarding, are present. When performing the abdominal examination, it is important to remember that voluntary and involuntary guarding are very different. While voluntary guarding is a state of contraction of the abdominal musculature due to fear or pain, which can be overcome by distraction, involuntary guarding is spasm of the abdominal musculature secondary to peritoneal inflammation, which remains constant despite distraction or relaxation. Furthermore, rebound tenderness is a physical exam finding that is suggestive of peritoneal irritation, but may be difficult to elicit in infants. Rebound tenderness is defined as increasing pain with release of pressure on the abdomen rather than with compression of the abdomen.
When assessing an infant with suspected appendicitis, the focus of the examiner's gaze should be on the patient's face to look for grimacing or increased crying with palpation in a particular area. While classically tenderness to palpation in the right lower quadrant of the abdomen is strongly suggestive of acute appendicitis, a review of studies of the physical examination in appendicitis has shown rebound tenderness to be most predictive of appendicitis, with a positive likelihood ratio of 3.0. This same review found signs of diffuse peritoneal irritation on abdominal examination, younger age, and higher temperature elevation as predictive of ruptured appendicitis rather than unperforated appendicitis. In children who are able to ambulate, asking them to walk or jump can be an excellent screening test to look for peritonitis. As a result of the intra-abdominal inflammation in peritonitis, any movement causes pain, and so affected patients will be unwilling to walk or jump. A similar technique may be used in non-ambulatory infants. Asking the caretaker to bounce the child up and down on their lap will cause pain if peritonitis is present, and will induce crying or fussiness.1,31,32
In the majority of cases, the appendix lies in the right lower quadrant of the abdomen. When the appendix lies in the retrocecal position, it may produce pain in the right upper quadrant or persistent pain in the epigastrium. The psoas sign can be used in cooperative children to detect retrocecal appendicitis. A positive psoas sign occurs when pain is elicited in the right lower quadrant with passive extension of the hip.33,34
One key point to remember about acute appendicitis is that it is commonly mistaken for gastroenteritis. As such, the diagnosis of acute appendicitis should be strongly considered in patients who have previously been diagnosed with gastroenteritis who return to the ED with vomiting and abdominal pain. Additionally, any patient with vomiting and abdominal pain who has abdominal tenderness should be evaluated for appendicitis, as gastroenteritis generally does not produce abdominal tenderness on examination.1,3
Laboratory Studies and Diagnostic Imaging. As acute appendicitis is a condition of infection and inflammation, many clinicians obtain a C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and complete blood count, specifically looking for an elevated white blood cell count. The predictive value of each is dependent on the threshold value used to decide whether or not a patient is likely to have acute appendicitis. A summary of the predictive values of laboratory tests used in the diagnosis of acute appendicitis is presented in Table 2. It is important to recognize that any individual laboratory study lacks adequate sensitivity, specificity, or predictive value to be used to determine whether or not the patient being evaluated has acute appendicitis.31
Table 2. Likelihood Ratios for Laboratory Tests in Appendicitis37
White blood cell count (WBC)
Over 10,000: + LR 2.0
Under 10,000: - LR 0.22
Over 15,000: + LR 3.4
C reactive protein (CRP)
Over 25: + LR 5.2
Under 10: - LR 0.45
Erythrocyte sedimentation rate (ESR)
Over 20: + LR 3.8
Under 20: - LR 0.68
While previously appendicitis was a clinical diagnosis, imaging has become the mainstay of confirming or excluding the diagnosis. As there is no ionizing radiation associated with it, ultrasound is becoming the first-line radiologic study. This study consists of graded compression in the right lower quadrant to displace loops of bowel and visualize the appendix. A positive study consists of a non-compressible, fluid-filled tubular appendix, with a diameter of greater than 6 mm. One may also see hyperemia of the appendix or an appendicolith. Ultrasound has been extensively studied for its use in the diagnosis of acute appendicitis, with estimated sensitivity of 78-94% and specificity 89-98% in the pediatric population. (See Figure 7.) The main limitation of ultrasound is the fact that it is operator-dependent, and visualization of the appendix can be impaired by a number of patient factors, most notably obesity and bowel gas. As adults tend to have more abdominal adipose tissue than children, ultrasound for the detection of appendicitis is generally reserved for pediatric patients.17
Figure 7. Ultrasound of Appendicitis
Computed tomography (CT) of the abdomen has become the gold standard for the diagnosis of acute appendicitis. (See Figure 8.) A positive study demonstrates an appendix with a diameter greater than 6 mm, and demonstrates inflammatory changes of the appendix, including thickening of the appendiceal wall, contrast enhancement of the appendiceal wall, and fat stranding around the appendix. Studies evaluating the performance of CT in diagnosing appendicitis in the pediatric population purport sensitivities of 88% to 97% and specificities of 94% to 97%. The majority of studies on the topic have found sensitivities greater than 95%. The main limitations of CT include the fact that children may require sedation or restraint to lie still for the study, IV contrast is required at most centers, and that CT exposes children to ionizing radiation, which may increase the risk of malignancy in the future.17
Figure 8. CT of Appendicitis
Although ultrasound is an excellent modality for the evaluation of suspected appendicitis, the sensitivity of ultrasound in detecting acute appendicitis is less than that of CT. To minimize the amount of radiation and also to address the imperfect sensitivity of ultrasound, a staged ultrasound and CT pathway may be used. In such a protocol, ultrasound is used as the initial imaging study, with CT only performed if the ultrasound is equivocal. Research on such protocols has demonstrated that half of patients may be managed with ultrasound alone, with a rate of missed appendicitis less than 0.5%. Furthermore, this approach has a sensitivity of 99% with a specificity of 91% and reduces radiation exposure from CT scans.35,36
While currently used only infrequently in pediatric patients, magnetic resonance imaging (MRI) is a technology that may be used more in the future, as it provides outstanding image detail and carries no risk of radiation.37
Treatment. In infants with acute appendicitis, treatment should primarily focus on stabilizing and correcting metabolic derangements. IV access should be obtained, patients should be rehydrated, if necessary, with IV fluids, and pediatric surgical consultation should be obtained. In non-perforated appendicitis, patients may be started on a single agent, with cefoxitin, cefotetan, piperacillin/tazobactam, or ampicillin/sulbactam being frequently used agents. For perforated appendicitis, many surgeons elect to use "triple" therapy, such as with ampicillin, gentamycin, and metronidazole, or other combination regimens such as ceftriaxone and metronidazole. However, a review of the literature on this topic has demonstrated that single-agent, broad-spectrum antibiotics may be used for both perforated and non-perforated appendicitis, with piperacillin/tazobactam being a commonly used antimicrobial for both situations. In patients with non-perforated appendicitis, appendectomy should be performed, most commonly via the laparoscopic approach. Recent research on the topic has shown that the risk of perforation is not increased if appendectomy is delayed for 12-24 hours, suggesting that appendectomy may be performed on a semi-urgent basis. In tune with this evidence, nearly 70% of pediatric surgeons perform appendectomies on non-perforated appendicitis on a semi-urgent basis.38,39
Management of perforated appendicitis is somewhat controversial, with some surgeons preferring to operate immediately, while others prefer a non-operative approach consisting of initially treating the patient with intravenous antibiotics followed by an interval appendectomy in two to three months after initial hospital discharge. In cases in which a discrete abscess has formed, patients may be managed initially with intravenous antibiotics and percutaneous drainage. It is important to recognize that the non-operative approach to appendicitis should be used only in non-toxic infants; any infant with significant toxicity likely deserves surgical intervention.38,39
Etiology. While viral gastroenteritis may be caused by a number of different viral pathogens, the two most common causes are rotavirus and norovirus. In the United States, norovirus accounts for more than 90% of all outbreaks of viral gastroenteritis and is the most common cause of gastroenteritis worldwide. Rotavirus, in comparison, is the leading cause of viral gastroenteritis in children younger than 5 years old. Fortunately, vaccines are available against rotavirus, and have been shown to decrease both incidence of disease and severity of symptoms.40-43
Both agents are primarily transmitted by the fecal-oral route, although viral particles may be spread by respiratory droplets as well. Interpersonal transmission may be rapid, leading to outbreaks of these infections in groups of people in close proximity, such as on cruise ships, in nursing homes, and in daycare centers.40,41
Epidemiology. Viral gastroenteritis is an extremely frequent entity in children, accounting for 150,000 hospitalizations and 3.7 million physician visits annually in the United States. It is also estimated to be the cause of up to 10% of all hospitalizations in the United States in children younger than 5 years of age. With good access to medical care and rehydration, deaths from gastroenteritis in developed nations are relatively uncommon. Globally, gastroenteritis is a major problem as a result of poor access to adequate rehydration and is estimated to cause up to 870,000 deaths per year.40,42,44
Presentation. Gastroenteritis can be defined as a syndrome of vomiting, diarrhea, or the combination of both. Viral infections account for approximately 70% of all cases of acute gastroenteritis, and generally present with nausea, vomiting, and watery diarrhea. Affected individuals generally also have low-grade fevers, abdominal pain, cramping, and some degree of malaise. Blood or mucus seen in vomitus or stool is unusual in viral gastroenteritis and is suggestive of an invasive bacterial pathogen. Viral gastroenteritis is a self-limited disease, usually lasting anywhere from 24-60 hours in immunocompetent hosts. In immunocompromised patients and patients at the extremes of age, symptoms may be more severe and prolonged.40,41
Infants with abdominal pain, vomiting, and diarrhea may also be suffering from bacterial or even protozoal gastroenteritis. Many of these conditions produce vomiting, abdominal pain, and diarrhea in a manner that is very difficult to distinguish clinically from viral infections.40
Laboratory Studies and Diagnostic Imaging. Viral gastroenteritis is a clinical diagnosis. Routine laboratory studies, such as a complete blood count or basic metabolic panel, are largely unhelpful when trying to determine the etiologic pathogen in a patient with vomiting and diarrhea. Urinalysis may also be helpful in assessing a patient's level of dehydration.40 Plain X-rays of the abdomen should only be obtained if another etiology of the patient's symptoms is suspected.
PCR studies of vomitus or stool are the best tests to isolate the viral pathogen causing a patient's symptoms. However, such tests are not available in all clinical laboratories. As viral gastroenteritis is a self-limiting condition, the utility of PCR testing is limited; a patient's symptoms may have already resolved prior to the results of the test being available. Stool studies, such as a stool culture, are only performed when there is concern for a non-viral cause of vomiting or diarrhea, such when symptoms last longer than two weeks or there is blood or mucus in the stool. A stool white blood cell can also be performed to look for intestinal inflammation, but is of poor sensitivity and specificity and does not indicate the cause of inflammation.40,41
Treatment. No specific treatment exists for viral gastroenteritis. However, the fluid losses from vomiting and diarrhea, in combination with poor oral intake from nausea, can lead to dehydration. Treatment of this condition, thus, is focused on rehydration. The first step in managing patients with viral gastroenteritis is to assess their level of dehydration. Signs and symptoms of moderate dehydration include: decreased urine output, capillary refill greater than two seconds, decreased skin turgor, and tachypnea. Tachycardia also is frequently a sign of mild to moderate dehydration. Laboratory abnormalities that suggest dehydration include low serum bicarbonate, hypokalemia, and hypoglycemia. In infants with mild to moderate dehydration, oral rehydration remains first-line therapy. Oral intake can be increased with the use of the antiemetic ondansetron. Infants unable to adequately hydrate orally should receive intravenous hydration. Indications for admission to the hospital include moderate to severe dehydration with inability to tolerate oral fluids, intractable emesis, marked electrolyte disturbances, and poor social situation, including lack of parental reliability.41,44-46
Other Conditions in the Differential Diagnosis of Abdominal Pain and Vomiting
The above listed conditions, while essential to understand when approaching an infant with vomiting and abdominal pain, only represent a very small number of the possible causes of abdominal pain and vomiting. Infants are particularly prone to vomiting, and may vomit for any number of infectious causes, including urinary tract infections, otitis, pneumonia, pharyngitis, hepatitis, sepsis, and upper respiratory infections. Furthermore, infants with metabolic conditions such as diabetic ketoacidosis, adrenal insufficiency, and inborn errors of metabolism may present with abdominal pain and vomiting. One should also consider additional intra-abdominal pathology, such as small bowel obstruction, incarcerated hernia, and gonadal torsion.2,47
Abdominal pain and vomiting in the infant patient remains a challenging complaint to evaluate. A solid understanding of the differential diagnosis, combined with a thorough history and physical examination, provide an excellent start to the evaluation of this presentation. Use of appropriate laboratory testing and imaging studies aids in the confirmation of surgical causes of abdominal pain and vomiting, and can guide appropriate and timely surgical consultation when necessary.
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