Continuing Medical Education

Functional Abdominal Pain in Children

by Miguel Saps, MD, Ashish Chogle, MD, MPH

Educational objectives

At the conclusion of this activity, participants will be able to:

  • Identify pain-predominant functional gastrointestinal disorders in children
  • Explain proposed pathophysiology of functional gastrointestinal disorders
  • Formulate a comprehensive treatment plan and effectively counsel patients and parents about functional gastrointestinal disorders

CME credit

This is an article from The Child's Doctor, Fall/Winter 2009 issue. You must read all five articles and complete each related quiz before receiving 2 Category 1 credits for the Fall/Winter 2009 issue.

Author disclosures

Dr. Saps has no industry relationships to report and does not refer to products that are still investigational or not labeled for the use in discussion.

Dr. Chogle has no industry relationships to disclose and does not refer to products that are still investigational or not labeled for the use in discussion.


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Pediatricians frequently see patients with chronic abdominal pain. In most children, chronic abdominal pain is functional, that is, without demonstrable evidence of an underlying pathologic condition, such as an anatomic, infectious, inflammatory, metabolic, or neoplastic disorder. The pain-predominant functional gastrointestinal disorders (PP-FGIDs) include functional dyspepsia, irritable bowel syndrome (IBS), abdominal migraine, childhood functional abdominal pain and childhood functional abdominal pain syndrome. A child with PP-FGID is usually in distress, the parents are troubled with the recurrent symptoms, and the physician is concerned about ordering investigations to avoid missing serious disease. Managing these conditions also can present considerable challenges in terms of explaining the etiology and lack of proven therapy. This article will review the current understanding of PP-FGIDs to help pediatricians counsel families and guide treatment decisions.

Definition

Five decades ago, Apley and Naish described children who presented with at least 3 abdominal pain episodes interfering with their daily functioning over at least 3 months as having recurrent abdominal pain (RAP).[1] Later studies showed that this was a "waste basket" term. RAP is a symptom rather than a diagnosis. Although 90% of the patients with RAP have a functional gastrointestinal disorder (FGID), some of these children have an organic condition requiring different diagnostic and therapeutic approaches.

Currently, the Rome II criteria define FGIDs in children as chronic gastrointestinal conditions without clinical evidence of anatomical or structural abnormalities. The latest edition of the Rome criteria defines 5 pain-predominant FGIDs (PP-FGIDs): functional dyspepsia, IBS, abdominal migraine, childhood functional abdominal pain and childhood functional abdominal pain syndrome (Table 1).[2-4]

Importance

PP-FGIDs are very common in children. These disorders represent 2% to 4% all of pediatric office visits.[5] Approximately 38% of school children complain of abdominal pain weekly.[6] Six percent of middle school students and 14% percent of high school students have IBS symptoms.[7] Furthermore, studies at the doctor's office misrepresent the enormity of the problem, as only 3% of all children complaining of abdominal pain at the community level seek consultation.[8] Abdominal pain is associated with worse quality of life, school absenteeism, and higher anxiety and depression scores.[9] Children with a history of PP-FGID also have higher prevalence of psychiatric conditions, socialization problems and use of medications as adults.[10] The estimated financial burden of chronic abdominal pain is substantial, with the expenses associated with treatment of IBS alone ranging between $8 billion to $30 billion per year in adult patients.

Pathophysiology

Although the pathophysiology of PP-FGIDs remains unclear, recent developments have contributed to the understanding of these conditions. Pathophysiology of PP-FGIDs is thought to involve abnormalities at multiple levels of the enteric nervous system (ENS) or the "little brain in the gut," and the central nervous system (CNS). Dysregulation of the bidirectional communication between ENS and CNS plays a key role in the pathogenesis of PP-FGIDs. Although some patients with PP-FGIDs present with gastrointestinal motor abnormalities, these are rarely related temporally with the pain episode or not severe enough to account for the patients' symptoms.

Research suggests that children with PP-FGIDs may have an abnormal reaction to different physiologic and pathologic stimuli affecting the gut: distension, meals, hormonal changes, inflammatory processes, as well as psychological stressors such as anxiety or problems with parents and school.[11] Evidence also suggests that PP-FGIDs may be associated with visceral hyperalgesia, including hypersensitivity (lower threshold to pain) and allodynia (a painful response to a usually non-painful stimulus). Adult studies in patients with IBS show abnormal processing of pain, with amplification of pain, failure to down-regulate pain and involvement of emotional and stress related areas in response to painful gut stimuli.[12]

Some studies have linked bacterial and viral infections to the onset of IBS in children and adults.[13,14] The associated mucosal inflammatory processes may cause afferent nerve sensitization that leads to visceral hyperalgesia.

The concept of visceral hyperalgesia can be explained to patients and family members by comparing it to skin sensitization after a burn. Even mild stimuli, such as contact with clothes, may be painful for a long time after a burn.

Children also may be predisposed to develop a PP-FGID. Twin studies seem to indicate that there is a genetic predisposition, but at this time no gene has been isolated that could explain most of the cases of PP-FGIDs.[15] Predisposition also could be due to early sensitization or other unknown reasons.

The most accepted framework to explain PP-FGIDs is the biopsychosocial model. It proposes that there is no single etiology for these conditions. PP-FGIDs result from the interplay of different factors including biological, psychological and social. This is an important concept, not only to explain the pathogenesis of these conditions, but also to select an appropriate treatment modality for each individual patient.

Diagnosis

Functional abdominal pain is the most common cause of chronic abdominal pain. PP-FGIDs are clinically diagnosed based on parent and child's reports of symptoms using the Rome criteria (Table 1). No tests will provide elements for diagnosis as there are no biological markers to characterize a functional condition.

However, it is generally accepted that a limited battery of tests could be conducted for reassurance, especially if the pain is severely affecting the quality of life of the patient and family. If any alarm symptoms (Table 2) are present, selected testing to rule out anatomic, infectious, inflammatory or metabolic conditions is indicated.

When tests are ordered, parents should be told that negative results are expected. A negative result does not mean that more testing is needed, but instead confirms the diagnosis of PP-FGIDs. Extensive or repeated testing frequently confuses parents and may provide an impression that the practitioner is lost in the diagnostic process.

Providing reassurance

Managing chronic painful conditions is challenging. It requires extensive patience and time. Counseling and reassurance play an important role in management of PP-FGIDs. Parents are frequently frustrated and many times disappointed with past investigations and treatments. They frequently change physicians to get a satisfactory answer about their child's medical condition.

It is important to regain the parents' trust. The practitioner can give families more confidence by discussing with them the proposed pathogenesis of PP-FGIDs and criteria for the diagnosis. One effective strategy is to show parents the Rome criteria and ask them to verify whether the child's symptoms correspond to any of the diagnoses listed. Naming the condition brings comfort to worried parents who are concerned that the child "may have something bad." Parents need to be reassured that PP-FGID is one of the most common conditions in children.

Providing education on the chronic but benign nature of the condition is important, since parents are frequently worried and may have misconceptions. A frequent concern is whether the child will always have abdominal pain. Pediatricians can explain to parents that similar to asthma, the child has a predisposition for this condition and that he/she may be prone to episodes of abdominal pain, although these may not happen again in the near future.

Children and parents are often worried that nobody believes the symptoms or understands what they are going through. It is essential to let the child know that you as a doctor believe the symptoms are real. Physicians have to show empathy and understanding, reassuring the family that the symptoms are not just in the child's head.

It also is important to reassure parents about the adequacy of earlier investigations by prior physicians. It helps to affirm that if the previous doctor did not find anything with the extensive battery of tests, you too will not find anything new by repeating or ordering any other tests. PP-FGID can be compared to a bad migraine, in that the pain can be extreme and debilitating, but no tests, not even brain CT scans, will provide any valuable information.

Biopsychosocial model of care

The child with functional abdominal pain should be treated in the context of a biopsychosocial model of care. The model proposes that this condition may result from an interaction of multiple factors, and therefore care may also require multiple types of treatments. Treatment should be tailored to individual needs and cases. The nature of the condition may require a multidisciplinary and personalized approach.

It is important to discuss the prognosis and agree on the goals of treatment. Goals should be realistic, focused on decreasing pain and improving quality of life. Setting the goal to abolish pain may result in failure and loss of trust if a new episode of pain occurs. Setting unrealistic goals may lead to disappointment even in the case of good outcomes, such as achieving a lower degree of pain to the level that does not affect the patient's daily function.

At the same time, the physician should explain that the resolution of the condition will not be achieved without the cooperation of the patient and family, and that it is very important that the patient take responsibility for the process of healing. Patients who are currently missing school should be encouraged to return to school. School attendance is not part of the problem and in fact is part of the solution. Distraction from pain is a useful strategy. While in school, children are distracted and less focused on pain or other ailments. Adequate social interaction also facilitates healing. School re-entry may occur in stages. To build confidence, the child may go only for 2 hours on the first day, 4 hours on the second day, and so on. Parents should be made aware that they might be reinforcing the symptoms by allowing the child to obtain secondary gains, such as staying home from school.

The role of the brain-gut axis and stressors in the pathophysiology of symptoms should be explained to the family. The physician should focus on understanding whether any stressful situations may be present in the child's life. These may include family distress, abnormal family dynamics, problems with peers or in school. If present, psychological or social problems need to be addressed.

However, proposing that anxiety or any other psychological condition might be involved in causing the pain may result in the patient and family becoming defensive and losing trust. If anxiety is perceived, it is useful to validate the condition, since some degree of anxiety is expected, considering the amount of suffering the patient is experiencing.

When anxiety impairs daily functioning, patients should be referred to a mental health professional. Once the patient or parents agree that having pain and missing daily activities can cause anxiety, it is usually easy to refer. If a patient is referred to a mental health professional, contacting the specialist in advance is frequently helpful. It is very common to receive a letter from a specialist stating that the patient does not have a psychological condition according to the DSM IV-R. Patients with functional abdominal pain usually do not have a psychological condition. The goal of the mental health referral is to help the patient cope with the condition through cognitive-behavioral therapy.

Treatment

There is a paucity of evidence-based recommendations for most of the medications used in the treatment of PP-FGIDs in children. Most of the medication treatments are based on anecdotal experience or adult data. Therefore, the physician should be judicious in prescribing medications for PP-FGIDs. Medications should be part of a multifaceted, individualized approach aimed at relieving symptoms and disability.

Patients with pain associated with dyspepsia may benefit from the use of acid-reduction therapy. Although there are no pediatric data that justify their use, the use of antispasmodic agents and smooth muscle relaxants is common. Non-stimulating laxatives or antidiarrheals may be used for associated symptoms (altered bowel pattern), as they do not relieve pain. Non-steroidal anti-inflammatory drugs (NSAIDs) are not effective in treating PP-FGIDs.

A clinical trial of enteric-coated peppermint oil has shown that this herbal therapy could be beneficial in the treatment of functional abdominal pain in children.[16] However, enteric-coated peppermint oil is difficult to obtain in pharmacies, expensive and not covered by insurance companies. Non-enteric coated preparations may lead to esophagitis and mild rectal irritation.

A recent double-blind placebo-controlled trial found cyproheptadine efficacious for the treatment of PP-FGIDs in children.[17]

Data show conflicting results about the benefit of low-dose tricyclic antidepressants in treating PP-FGIDs in children. One double-blind placebo-controlled study found significant improvement with amitriptyline in adolescents with IBS. However, recently published large, randomized, placebo-controlled multicenter studies of amitriptyline showed that it was equally effective as placebo in children with IBS, functional dyspepsia and functional abdominal pain.[18,19] These studies showed a very substantial placebo effect, which underscores the importance of the physician-patient-family relationship.

Data in adults suggests that selective serotonin reuptake inhibitor (SSRI) antidepressants do not have any advantage over tricyclic antidepressants for managing functional abdominal pain.[20] A clinical trial of SS RIs for children with PP-FGIDs is underway.

Dietary interventions including fiber supplements, lactose-free diets or lactobacillus supplementation have not been proven to be beneficial in treating children with PP-FGIDs.[21] Parents often link the onset of symptoms with the ingestion of dairy products. There is no evidence to support that lactose ingestion results in worsening symptoms of PP-FGIDs.[22] Although some studies have shown improvement in bloating and pain in response to probiotics, their benefit in the treatment of abdominal pain is controversial.[23]

As mentioned earlier, cognitive-behavioral therapy may be a useful intervention for children with PP-FGIDs. There also is increasing scientific evidence for the benefit of some complementary treatments, including hypnotherapy and guided imagery.

A 3-month clinical trial of hypnotherapy in the treatment of functional abdominal pain in children has proven this technique to be beneficial. The study randomized children to 6 sessions of either hypnotherapy or supportive "traditional" medical care. Hypnotherapy was superior to the supportive medical therapy at all times, even after discontinuation of therapy.[24]

Guided imagery with progressive muscle relaxation is a technique that uses the patient's imagination to achieve improvement of symptoms.[25] This is a simple, noninvasive therapy with potential benefit for treating children with PP-FGIDs.[26-28]

However, the utilization of alternative and complementary therapies is sometimes difficult. Some patients may be reluctant to use these therapies while in other cases, insurance or geographical limitations may preclude their use.

Conclusion

PP-FGIDs continue to be challenging medical conditions for the patient, family and physician alike. The biopsychosocial model provides the conceptual basis for the understanding of FGIDs. Accordingly, a comprehensive tailored treatment plan can be offered to the patient and the family. Parents are often confused about the exact pathogenesis of FGIDs. Effective explanation of the various theories will help to educate parents about these conditions and alleviate their anxiety.

References

[1.] Apley J. The child with recurrent abdominal pain. Pediatr Clin North Am 1967;14(1):63-72.

[2.] Hyman PE, et al. Childhood functional gastrointestinal disorders: Neonate/toddler. Gastroenterology 2006;130(5):1519-1526.

[3.] Rasquin A, et al. Childhood functional gastrointestinal disorders: Child/adolescent. Gastroenterology 2006;130(5):1527-1537.

[4.] Veereman-Wauters G. The quest for light in the misty frontierland of pediatric functional gastrointestinal disorders: Act II: Rome III criteria. J Pediatr Gastroenterol Nutr 2006;43(2):156-157.

[5.] Starfield B, et al. Who provides healthcare to children and adolescents in the United States? Pediatrics 1984;74(6):991-997.

[6.] Saps M, et al. A prospective school-based study of abdominal pain and other common somatic complaints in children. J Pediatr 2008 Nov. Epub ahead of print.

[7.] Hyams JS, et al. Abdominal pain and irritable bowel syndrome in adolescents: A community-based study. J Pediatr 1996;129(2):220-226.

[8.] Saps M, Li BU. Chronic abdominal pain of functional origin in children. Pediatr Ann 2006;35(4):246, 249-256.

[9.] Greco LA, Freeman KE, Dufton L. Overt and relational victimization among children with frequent abdominal pain: Links to social skills, academic functioning, and health service use. J Pediatr Psychol 2007;32(3):319-329.

[10.] Campo JV, et al. Adult outcomes of pediatric recurrent abdominal pain: Do they just grow out of it? Pediatrics 2001;108(1):E1.

[11.] American Academy of Pediatrics, North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition. Clinical Report: Chronic abdominal pain in children. Pediatrics 2005;115(3):812-815.

[12.] Mertz H. Role of the brain and sensory pathways in gastrointestinal sensory disorders in humans. Gut 2002;51 Suppl 1:i29-33.

[13.] Marshall JK, et al. Postinfectious irritable bowel syndrome after a food-borne outbreak of acute gastroenteritis attributed to a viral pathogen. Clin Gastroenterol Hepatol 2007;5(4):457-460.

[14.] Saps M, et al. Post-infectious functional gastrointestinal disorders in children. J Pediatr 2008;152(6):812-816.

[15.] Lembo A, et al. Influence of genetics on irritable bowel syndrome, gastro-oesophageal reflux and dyspepsia: A twin study. Aliment Pharmacol Ther 2007;25(11):1343-1350.

[16.] Kline RM, et al. Enteric-coated, pH-dependent peppermint oil capsules for the treatment of irritable bowel syndrome in children. J Pediatr 2001;138(1):125-128.

[17.] Sadeghian M, et al. Cyproheptadine for the treatment of functional abdominal pain in childhood: A double-blinded randomized placebo-controlled trial. Minerva Pediatr 2008;60(6):1367-1374.

[18.] Bahar RJ, et al. Double-blind placebo-controlled trial of amitriptyline for the treatment of irritable bowel syndrome in adolescents. J Pediatr 2008;152(5):685-689.

[19.] Saps M, et al. Multicenter, randomized, placebo-controlled trial of amitriptyline in children with functional gastrointestinal disorders. Gastroenterology 2009;137(4):1261-1269.

[20.] Talley NJ, et al. Antidepressant therapy (imipramine and citalopram) for irritable bowel syndrome: A double-blind, randomized, placebo-controlled trial. Dig Dis Sci 2008;53(1):108-115.

[21.] Huertas-Ceballos AA, et al. Dietary interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood. Cochrane Database Syst Rev 2009;(1):CD003019.

[22.] Fernandez-Banares F, et al. Sugar malabsorption in functional bowel disease: Clinical implications. Am J Gastroenterol 1993;88(12):2044-2050.

[23.] Saps M, Di Lorenzo C. Probiotics for abdominal pain disorders in children--safe to use but are they helpful? Nat Clin Pract Gastroenterol Hepatol 2007;4(8):430-431.

[24.] Vlieger AM, et al. Hypnotherapy for children with functional abdominal pain or irritable bowel syndrome: A randomized controlled trial. Gastroenterology 2007;133(5):1430-1436.

[25.] Huertas-Ceballos A, et al. Psychosocial interventions for recurrent abdominal pain (RAP) and irritable bowel syndrome (IBS) in childhood. Cochrane Database Syst Rev 2008;(1):CD003014.

[26.] Weydert JA, et al. Evaluation of guided imagery as treatment for recurrent abdominal pain in children: A randomized controlled trial. BMC Pediatr 2006;6:29.

[27.] Youssef NN, et al. Treatment of functional abdominal pain in childhood with cognitive behavioral strategies. J Pediatr Gastroenterol Nutr 2004;39(2):192-196.

[28.] Ball TM, et al. A pilot study of the use of guided imagery for the treatment of recurrent abdominal pain in children. Clin Pediatr (Phila) 2003;42(6):527-532.


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Miguel Saps, MD
Director of Gastrointestinal Motility and Functional Bowel Disorders Program; Attending physician, Gastroenterology, Children's Memorial Hospital; Assistant professor of Pediatrics, Northwestern University's Feinberg School of Medicine
Read short biography

Ashish Chogle, MD, MPH
Fellow, Gastroenterology, Hepatology and Nutrition, Children's Memorial Hospital