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review article

Indian Pediatr 2009;46: 389-399

Recurrent Abdominal Pain in Children


Niranga Manjuri Devanarayana, Shaman Rajindrajith and H Janaka de Silva

From the Department of Physiology, Department of Pediatrics and Department of Medicine, Faculty of Medicine, University of Kelaniya, Sri Lanka.

Correspondence to: Niranga M Devanarayana, Department of Physiology, Faculty of Medicine, University of Kelaniya, Thalagolla Road, Ragama, Sri Lanka. E-mail: [email protected] 
 

Abstract

Context: Recurrent abdominal pain is one of the commonest gastrointestinal complaints in children, affecting approximately 10% of school aged children and adolescents. There is no consensus with regards to etiology, investigation and management of this common problem. This review addresses some of the issues related to epidemiology, etiology, management and prognosis of recurrent abdominal pain.

Evidence acquisition: We reviewed current literature on this broad subject, specially concentrating on epidemiology, etiology and, basic and advanced management strategies, from 1958 to date, using PubMed, Embase, Cochrane database and cross references.

Results: The majority of the affected children have functional gastrointestinal diseases. The exact cause of pain remains obscure. New evidence suggests that emotional stress, visceral hypersensitivity and gastrointestinal motility disorders may play a vital part in its origin. Pharmacological treatments are commonly used in an effort to manage symptoms, despite the lack of data supporting their efficacy.

Conclusions: Most children with recurrent abdominal pain have functional gastrointestinal diseases and a detailed history, examination and basic stool, urine and hematological investigations are sufficient to exclude organic pathology in them. Despite the magnitude of the problem, knowledge on the effective management options is poor.

Key words: Abdominal pain, Adolescent, Children, Emotional stress, Functional gastrointestinal disorder, Helicobacter pylori, Gastrointestinal motility, Visceral hypersensitivity. 


Abdominal pain is perhaps the most common painful health problem in school-aged children. J Apley, a British pediatrician, studied abdominal pain among children extensively and observed that approximately 10% of school aged children get recurrent episodes of abdominal pain. He named this symptom complex as recurrent abdominal pain (RAP) syndrome and defined it as "at least three episodes of abdominal pain, severe enough to affect their activities over a period longer than three months"(1). His findings formed the main guidelines for the practising pediatricians and researchers dealing with this problem. Even though, the term chronic is used when referring to RAP, each episode of pain is distinct and separated by periods of well-being.

Epidemiology

RAP is reported in 10-12% of school aged children in developed countries(1,2). Epidemiological studies in Asia have reported similar prevalence. Boey and his colleagues studied RAP among school children in Malaysia and found a prevalence of 10.2% (urban 8.2-9.6%, rural 12.4%)(3,4). Similarly, Rasul and Khan reported RAP in 11.5% of Bangladesh school children(5). Prevalence of RAP in Sri Lanka is 10.5% (6). In the majority of studies, girls are more affected than boys(1,3-6).

Clinical Profile

It is generally agreed that the complaint of pain made by children with RAP is genuine, and not simply social modelling, imitation of parental pain, or a means to avoid an unwanted experience (e.g. school phobia). The commonest presentation is periumbilical pain associated with autonomic and functional symptoms like nausea, vomiting, pallor and other painful conditions like headache and limb pains(1,5,6). Thus, on initial presentation, RAP may mimic any acute abdominal disorder, and may prompt extensive evaluation and unnecessary invasive investigation.

Often there is a family history of RAP among first-degree relatives(1,2,4-6). Similar associations have been found in functional bowel disorders causing abdominal pain, like irritable bowel syndrome(7). This may be due to genetic or environment vulnerability and further studies are needed to detect a definite genetic predisposition.

Etiology

The origin of abdominal pain is complex and does not lend itself to a single model of causation. Apley and Naish suggested that organic pathology cannot be identified in 90% of children suffering from this problem(1). During the last half century, new diagnostic methods have broadened the investigation of these children, and have contributed to improved knowledge of the pathophysiology of RAP. In some of the subsequent studies, the percentage of children with organic RAP was found to be higher than initially reported by Apley(8-11). The majority of these studies were carried out in secondary and tertiary care hospitals where patients were highly selected and it was therefore more likely that an organic pathology was found(8-11). In some of these studies, the percentage of organic RAP was found to be as high as 82%(11). A recent epidemiological study in Sri Lanka has reported organic diseases in 23.6% of affected children(12).

Organic diseases causing RAP

Numerous organic disorders lead to abdominal pain; in most, the pathophysiology is related to infection (e.g. urinary tract infection), inflammation (e.g. Crohn’s disease) or distension or obstruction of a hollow viscous (e.g. obstructive uropathy). Table I demonstrates common causes for RAP among children(13,14). Several etiological studies in India have recognised intestinal parasitic infections, including giadiasis, as the leading cause for RAP(8,9,11), while in Sri Lanka, commonest organic aetiology is constipation(12). In many developed countries, the common organic causes include chronic constipation and gastroesophageal reflux disease(10).

Table I



Causes of Recurrent Abdominal Pain
Gastrointestinal   Urinary tract
Chronic constipation Hepatitis Urinary tract infection
Inflammatory bowel disease Gall bladder calculi Urinary calculi
Parasitic infection (e.g. ameba, giardia) Chronic appendicitis Pelvi-ureteric junction obstruction
Dietary intolerance (e.g. lactose) Chronic pancreatitis
Gastro-esophageal reflux disease Functional dyspepsia Gynecological
Helicobacter pylori infection Irritable bowel syndrome Ovarian cyst
Celiac disease Functional abdominal pain/syndrome Endometriosis
Peptic ulcer Abdominal migraine Pelvic inflammatory disease
Gastritis Aerophagia Miscellaneous
    Abdominal epilepsy
    Physical, emotional and sexual abuse

Few studies have demonstrated a contributory role of lactose malabsorption in the symptoms of RAP(15). In contrast to this, a large number of subsequent studies have neither demonstrated an association between RAP and lactose malabsorption nor a significant improvement in symptoms following lactose free diet(16,17). Lactase deficiency is reported to be very high (70%) in Asian children with RAP but no causal association was found between the two conditions(17). Therefore, the diagnostic value of investigating Asian children with RAP for lactase deficiency is doubtful. The role of Helicobacter pylori in the aetiology of childhood RAP is controversial. Many researchers have shown an association between Helicobacter pylori infection and RAP(18-20), while several others contradict this finding(12,21-24).

Identifying organic abnormalities by comprehen-sive investigations does not necessarily mean that the explanation for the symptoms is found. It is also important to realize that the organic and non organic causes for RAP can co-exist in some patients.

Functional gastrointestinal disorders causing RAP

Until a decade ago ‘functional gastrointestinal disorder’ was a label used for the conditions with uncertain etiology, and was a diagnosis of exclusion. When Rome criteria were defined to diagnose functional gastrointestinal disorders (FGID), it became an important positive diagnosis. According to Rome II criteria, abdominal pain related conditions in children were classified into five categories; functional dyspepsia, irritable bowel syndrome, abdominal migraine, aerophagia and functional abdominal pain(25). Validation of pediatric Rome II criteria was done by Caplan, et al.(26). They found that more than half the patients classified as having functional problems met at least one pediatric Rome II criteria for FGID. Another study by Saps and Di Lorenzo reported low interobserver reliability (45-47%) for Rome II criteria among pediatric gastroenterologists and fellows(27).

Even though functional bowel diseases are considered as a cause of RAP in children(14), so far very few studies have been done to detect their prevalence among affected children(12,28,29). Walker, et al.(28) found that 73% of patients with RAP fulfilled Rome II criteria for FGID, and most of them had irritable bowel syndrome (44.9%). Using the same criteria, Schurman, et al.(29) found FGID in 84-89% of RAP children attending a tertiary care center. In this study, functional dyspepsia was the commonest diagnosis (35-47%). Similarly, another study in Sri Lanka has reported FGID in 79% patients with functional RAP. Of them, 31% had functional abdominal pain(12). Unfortunately, 11-27% of the children with non-organic RAP could not be classified under any one of the FGID using Rome II criteria(12,28,29).

To overcome drawbacks in Rome II criteria, they were revised and modified in 2006, and Rome III criteria were developed(30). Table II summarizes the Rome III criteria for pediatric FGID. Validity and reliability of Rome III criteria in diagnosing pediatric FGID have yet to be studied. Using Rome III criteria, a recent study in Sri Lanka has reported FGID in 93% of patients with non-organic RAP. Of them, 45.2% had functional abdominal pain(12). Therefore, it is important to consider FGID in the differential diagnosis of RAP early in the evaluation.

Table II



Rome III Diagnostic Criteria for Pediatric Functional Bowel Disorders 
H2a. Diagnostic criteria* for functional dyspepsia

Must include all of the following:

1. Persistent of recurrent pain or discomfort centered in the upper abdomen (above the umbilicus).

2. Not relieved by defecation or associated with the onset of a change in stool frequency or stool form (i.e., not
                irritable bowel syndrome).

3. No evidence of an inflammatory, anatomic, metabolic, or neoplastic process that explains the subject’s
                symptoms.

H2b. Diagnostic criteria* for irritable bowel syndrome

Must include all of the following:

1. Abdominal discomfort (an uncomfortable sensation not described as pain) or pain associated with 2 or more
                of the following at least 25% of the time: 

(a) Improved with defecation

(b) Onset associated with a change in frequency of stool; and

(c)  Onset associated with a change in from (appearance) of stool.

2. No evidence of an inflammatory, anatomic, metabolic, or neoplastic process that explains the subject’s
                symptoms.

H2c. Diagnostic criteria†for abdominal migraine

Must include all of the following:

1. Paroxysmal episodes of intense acute periumbilical pain that lasts for 1 hours or more.

2. Intervening periods of usual health lasting weeks to months.

3. the pain interferes with normal activities.

4. The pain is associated with 2 or more of the following: anorexia, nausea, vomiting, headache, photophobia,
                pallor.

5.             No evidence of an inflammatory, anatomic, metabolic, or neoplastic process that  explains the subject’s
                symptoms.

H2d. Diagnostic criteria* for childhood functional abdominal pain

Must include all of the following:

1. Episodic or continuous abdominal pain.

2. insufficient criteria for other functional gastrointestinal disorders.

3. No evidence of an inflammatory, anatomic, metabolic, or neoplastic process that explains the subject’s 
                symptoms.

H2d1. Diagnostic criteria*for childhood functional abdominal pain syndrome

Must include childhood functional abdominal pain at least 25% of the time and 1 or more of the following:

1.    Some loss of daily functioning

2.    Additional somatic symptoms such as headache, limb pain, or difficulty in sleeping

H1c. Diagnostic criteria* for aerophagia

Must include at least 2 of the following:

1. Air swallowing.

2. Abdominal distension due to intraluminal air.

3. Repetitive belching and/or increased flatus.

* Criteria fulfilled at least once per week for at least 2 months before diagnosis; †Criteria fulfilled 2 or more times in the preceding 12 months.

Classification of non-organic RAP into the appropriate functional bowel disorder helps to let the child and the parents know that the symptoms they are feeling are real but not dangerous or life threatening, and also helps to direct the treatment appropriately. Once the diagnosis is made, a simple explanation of the condition and reassurance is usually enough to alleviate anxiety in the child and the family.

RAP and emotional stress

Many previous researchers have demonstrated a significant association between exposure to stressful life events and RAP(1,5,6,31). Patients can sometimes date the onset of pain to a specific stressful event, such as change in school, birth of a sibling or separation of parents. Boey and his colleagues have shown a significant association between recurrent abdominal pain and lower family income(3,4). Even though sibling rivalry is regarded as a predisposing factor for RAP, according to available data, family size, birth order and being an only child are not associated with RAP(2-4,6). Some case-control studies have shown higher levels of anxiety and depression in patients with RAP than in healthy children(32). In contrast to this, some other studies have failed to demonstrate significant differences in psychological distress between children with functional RAP (non organic RAP) and those with demonstrable organic cause for their pain(12,33).

RAP and gastrointestinal motility

Even though altered gastrointestinal motility is considered as underlying cause for RAP, to date only few studies were done to detect this association. A study done in 1988 reported abnormalities in migrating motor complexes (fasting contractions) in the affected children(34). More recent studies have reported impaired gastric myoelectrical activity, hypomotility of proximal and distal stomach and delayed gastric emptying in children with functional RAP(35,36). The exact cause of abnormal gastro-intestinal motility is not clear. High levels of emotional stress and abnormalities in autonomic nervous system which regulate gastrointestinal motility probably contribute to this. Stress related changes have been reported in patients with FGID(37). Some studies have reported disturbances in the autonomic nervous system in children with RAP(38), while others contradict this(39).

RAP and visceral hypersensitivity

The most current theory on origin of pain in these patients is based on the "visceral hypersensitivity or hyperalgesia". This means that the intensity of the signals from the gastrointestinal system, which travel by nerves to the brain, is exaggerated. This may occur following illnesses that cause inflammation in the intestine (e.g. viral gastro-enteritis), or after psychologically traumatic events that "sensitize" the brain to stimuli. Previous studies in children with RAP and FGID have demonstrated visceral hyperalgesia of the gastrointestinal tract(40). In these children, the site of hyperalgesia varies with predominant symptom. For example; patients with irritable bowel syndrome shows predominantly rectal hypersensitivity while in those with RAP it is mainly in the stomach(40).

Management

RAP should not require an exhaustive series of diagnostic tests to rule out organic causes of pain. Excessive testing may increase parental anxiety and put the child through unnecessary stress. On the other hand, uncertainty about the diagnosis and the recurrent nature of the problem also tend to corrode the trust between clinician and the parents. Therefore, it is crucial from both child-parent’s end and the clinician’s end to come to a reasonable clinical diagnosis at initial consultation. A thorough analysis of the complain and the other components of the history, meticulous examination and ordering a judicious set of investigations will not only give a good insight to the clinician but also reassure the child and parents that their concerns are seriously taken in to consideration.

There are no studies that have evaluated the nature, location, severity and duration of the pain to differentiate between organic and functional disorders. However it had been noted that children with RAP are more likely than children without RAP to have headache, joint pain, anorexia, vomiting, nausea, excessive gas and altered bowel habits, although there is insufficient evidence to state that they can discriminate between functional and organic disorders(12). Similarly, no studies have critically evaluated the value of physical signs in identifying organic diseases in patients with RAP. The ‘red flag’ signs have long been used by clinicians to guide themselves to identify children who need further investigations and the salient ones on history and examination are noted in Table III(13,14).

TABLE III



“Red flags” in History and Examination of Recurrent Abdominal Pain
“Red flags” on history “Red flags” on physical examination
Localized pain away from the umbilicus Loss of weight or growth retardation
Pain awakening the child at night Organomegaly
Pain associated with changes in bowel habits, dysuria, rash, arthritis Localized abdominal tenderness, particularly away from the umbilicus
Occult bleeding Joint swelling, tenderness or heat
Repeated vomiting, especially bilious Pallor, rash, hernias of the abdominal wall
Constitutional symptoms like recurrent fever, loss of  
appetite, lethargy  

Only basic urine, stool and blood examinations are recommended to exclude organic causes in the diagnosis of RAP (Table IV)(13,14). Ultrasound scanning, extensive radiographic evaluation and invasive investigations like endoscopy in these children are rarely diagnostic or cost-effective(41,42). It is also important to realize that the presence of an abnormal test result alone does not pinpoint to a diagnosis unless it is clinically relevant.

TABLE IV



Investigations in Recurrent Abdominal Pain
Basic investigations (1st line investigations)

Full blood count

Erythrocyte sedimentation rate/C-reactive protein

Urine analysis

Urine culture

Stool for ova, cysts and parasites

Second line investigations

Plain X-ray abdomen

Liver function tests

Renal function tests

Abdominal ultrasound

Breath hydrogen test for lactose intolerance

Tests for Helicobacter pylori

Barium follow through

Esophageal manometry and pH-metry

Upper and lower gastrointestinal endoscopy

Intravenous urogram/micturition cystourethrogram

The recommendation for treating children with non-organic RAP includes support and empathy for the family, with reassurance that no serious disease is present. The guidelines outlined by Rappaport and Leichtner in 1993 are still valid in the management of these children (Box)(43). With this approach, approximately 30% to 60% of children have resolution of their pain(44,45). However, the remainder continue to exhibit symptoms and go on to be adults with abdominal pain, anxiety, or other somatic disorders(46). Pharmacological treatments are commonly used in an effort to manage symptoms despite the lack of data supporting their efficacy. In fact, there are few randomized controlled medication trials in children with RAP, and conclusive evidence on the efficacy of any single treatment is lacking.

Box: Guidelines for Management of Recurrent Abdominal Pain
  1. Explain and reassure. Carefully explain to the family and the child the concepts and reasoning behind all
    
    investigations. Ask the parents about any particular concerns or diseases they believe to be the culprit of the 
    
    child’s pain. Once organic cause has been systematically ruled out, reassure the patient and family that no 
    
    major illness is present.
  2. Identify red flags. Make sure that the parents fully understand objective changes and provide guidelines for 
    
    what to do if they occur.
  3. Avoid psychological “labelling”. Unless evidence supports the contrary, do not suggest that the child’s pain 
    
    is psychological or that the child may be malingering. 
  4. Allow normal activity. Encourage normal activity between times of pain.
  5. Watch out for withdrawal. If the child begins to withdraw from normal activity, psychological referral should
    
    be considered over escalating pain management.
  6. Establish regular follow-up. Establish a system of regular return visits to monitor the symptoms.
  7. Be available. Assure parents that you are available to see the child if changes occur or the parents become
    
    anxious. Allow appropriate time, in an unrushed environment, for them to be seen.
  8. Beware the placebo response. Avoid making an immediate diagnosis based on a therapeutic response. 
    
    Placebo effects, particularly involving the gastrointestinal tract, can be misleading.
  9. Make judicious use of “second opinions”. Be open to requests for second opinions, particularly for anxious 
    
    patients and families. Assure the parents that you will continue to help manage their child’s problem even after 
    
    a second opinion is obtained. 

Pharmacological management

According to a clinical trial performed, famotidine (an H2-receptor antagonist) is effective in children with RAP who have predominantly dyspeptic symptoms. Pizotifen, a serotonin antagonist, has been found to be effective when used prophylactically in children with abdominal migraine(47). Their effects on the majority of RAP patients with typical periumbilical pain are still not clear.

Local remedies

Many local remedies are used to alleviate symptoms in children with RAP, but to date there are very few treatment trials to asses their effect on the affected children. One study evaluated the therapeutic value of peppermint oil in the treatment of irritable bowel syndrome in children. Improvement in symptoms was reported in 71% of the peppermint oil group versus 43% in the placebo group(48).

Dietary modifications

There is a lack of high quality evidence on the effectiveness of dietary interventions on childhood RAP. According to the systematic reviews available, the treatment trials of fibre supplements and lactose restricting diets are inconclusive(49). Feldman, et al.(50) and Christiansen(51) studied the effect of dietary fibre on the symptoms of RAP. Feldman, et al.(50) reported a significant benefit for the children in the fibre group. The percentage of those with the fibre intervention having at least a 50% decrease of pain episodes was 50% compared with only 27% in the placebo group (P<0.05). Less severe pain was also noted in the fiber group(50). Although not mentioned in the original study, it was recently reported that the P value was calculated from a 1-sided statistic. Reanalysis of the same data found no difference between the 2 treatment groups(49). Christiansen(51) also failed to find a difference in the number of pain episodes reported by parents following fibre supplementation versus placebo. Liebman(15) studied lactose malabsorption in children with RAP and reported significant or total pain relief following a lactose elimination diet for 4 week. In contrast to this, Wald, et al.(16) and Boey(17) did not find significant improvement of symptoms in RAP children following periods of lactose free diet.

Low fat diet is suggested as a possible treatment option in FGID, including functional dyspepsia and irritable bowel syndrome(52), but to date no studies have evaluated the value of this in children with RAP.

Cognitive behavior therapy

Cognitive behavior therapies have been tried in patients with RAP, and some have demonstrated significant effects. They have been used with the idea that pain behaviors produce secondary gain (special attention, school avoidance, etc.) that in future reinforces the pain behaviors. Robins, et al.(54) has reported significant improvement of symptoms and fewer school absences in children with RAP following a short period of cognitive-behavioral family treatment. In agreement with this, a study by Youssef, et al.(54) also demonstrated significant improvement in symptoms in children with chronic abdominal pain following two cognitive behavior techniques; guided imagery and progressive relaxation.

Combined treatment options

Humphreys and Gevirtz have analyzed the effect of four treatment protocols: (i) fiber only, (ii) fiber and biofeedback, (iii) fiber, biofeedback and cognitive behavior therapy, (iv) fibre, biofeedback, cognitive behavior therapy and parental support, on outcome of RAP(55). In this study, all groups showed improvement in self-reported pain. However, the active treatment groups showed significantly more improvement than the fiber-only group. In contrast to Robins, et al.(53) and Youssef, et al.(54), who showed significant effect of cognitive behavior therapy in management of RAP, in the study done by Humphreys and Gevirtz(55), the cognitive and parental support components did not seem to independently increase treatment effectiveness.

Health Care Utilization of Children with RAP

There have been relatively few studies on health care utilization among children with RAP. In 2000, Huang, et al.(2) showed a health care consultation rate of 34.0% among Australian children. Two studies done in Malaysia have shown health care consultation rates of 45.5% among urban and 48.4%, among rural school children(56,57). Recent study has reported health care consultation of 70% in Sri Lankan school children(6). It was significantly associated with age of the affected child, age at onset of symptoms, severity, frequency and duration of pain, school absenteeism, interruption of sleep and presence of vomiting(6,56,57).

RAP and Education

Although RAP does occur in preschool children, it is rare in children below 5 years and above 15 years(1). It is most frequently encountered in school aged children; this might be a result of psychological difficulties these children experience during school. Irish pediatrician O’Donnell observed that RAP almost never occurs during summer holidays and many children got symptoms on return to school after vacation(58). This was compatible with a study done by William, et al.(59), which showed that the admission of children to British hospitals with non-specific abdominal pain was significantly higher during the school term compared with school holidays.

Very few studies have been done so far to detect the impact of RAP on education and schooling of affected children. Some studies have shown that the majority of children with RAP do not attend schools regularly, and school absenteeism is significantly higher among these children(5,6). Even though, general consensus regarding RAP is that it is most common among the high academic achievers; research data available up to date failed to show any association between RAP and school academic performance(1,6,58) or the child’s participation in sports(6).

Prognosis

Two long-term studies done by Apley and Hale(44) and Christensen and Mortensen(45) reported that nearly half of the children with functional RAP experience pain as adults. According to Christensen and Mortensen, offspring do not have a significant risk of RAP. Other studies have reported development of irritable bowel syndrome in 25-29% of them in later life(8,60).

Contributors: NMD and SR equally contributed to concept, design, literature search, drafting, editing and review. JDS critically analyzed the manuscript.

Funding: None.

Competing interests: None stated.

References

1. Apley J, Naish N. Recurrent abdominal pain: A field survey of 1000 school children. Arch Dis Child 1958; 33: 165-170.

2. Huang RC, Plamer LJ, Forbes DA. Prevalence and pattern of childhood abdominal pain in an Australian general practice. J Paediatr Child Health 2000; 36: 349-353.

3. Boey CC, Yap S, Goh KL. The prevalence of recurrent abdominal pain in 11- to 16-year-old Malaysian schoolchildren. J Paediatr Child Health 2000; 36: 114-116.

4. Boey CC, Goh KL. Predictors of recurrent abdominal pain among 9 to 15-year-old urban school-children in Malaysia. Acta Paediatr 2001; 90: 353-355.

5. Rasul CH, Khan MAD. Recurrent abdominal pain in school children in Bangladesh. J Ceylon Coll Phys 2000; 33: 110-114.

6. Devanarayana NM, de Silva DGH, de Silva HJ. Recurrent abdominal pain syndrome in a cohort of Sri Lankan children and adolescents. J Trop Pediatr 2008; 54: 178-183.

7. Pace F, Zuin G, Di Gianomo S, Molteni P, Casini V, Fontana M, et al. Family history of irritable bowel syndrome is the major determinant of persistent abdominal complaints in young adults with a history of pediatric recurrent abdominal pain. World J Gastroenterol 2006; 12: 3874-3877.

8. Dutta S, Mehta M, Verma IC. Recurrent abdominal pain in Indian children and its relation with school and family environment. Indian Pediatr 1999; 36: 917-920.

9. Balani B, Patwari AK, Bajaj P, Diwan N, Anand VK. Recurrent abdominal pain - a reappraisal. Indian Pediatr 2000; 37: 876-881.

10. Stordal K, Nygaard EA, Bentsen B. Organic abnormalities in recurrent abdominal pain in children. Acta Paediatr 2001; 90: 1-5.

11. Buch NA, Ahmad SM, Ahmad SZ, Ali SW, Charoo BA, Hussan MU. Recurrent abdominal pain in children. Indian Pediatr 2002; 39: 830-834.

12. Devanarayana NM, de Silva GDH, de Silva HJ. Aetiology of recurrent abdominal pain in a cohort of Sri Lankan children. J Paediatr Child Health 2008; 44: 195-200.

13. Pearl RH, Irish MS, Caty MG, Glick PL. The approach to common abdominal diagnosis in infants and children. Part II. Pediatr Clin North Am 1998; 45: 1287-1326.

14. Thiessen PN. Recurrent abdominal pain. Pediatr Rev 2002; 23: 39-46.

15. Liebman WM. Recurrent abdominal pain in children: lactose and sucrose intolerance, a prospective study. Pediatrics 1979; 64: 43-45.

16. Wald A, Chandra R, Fisher SE, Gartner JC, Zitelli B. Lactose malabsorption in recurrent abdominal pain in childhood. J Pediatr 1982; 100: 65-68.

17. Boey CC. Lactose deficiency among Malaysian children with recurrent abdominal pain. J Paediatr Child Health 2001; 37: 157-160.

18. Das BK, Kakkar S, Dixit VK, Kumar M, Nath G, Mishra OP. Helicobacter pylori infection and recurrent abdominal pain in children. J Trop Pediatr 2003; 49: 250-252.

19. Frank F, Stricker T, Stallmach T, Braegger CP. Helicobacter pylori infection in recurrent abdominal pain. J Pediatr Gastroenterol Nutr 2000; 31: 424-427.

20. Ozen H, Dinler G, Akyon Y, Kocak N, Yuce A, Gurakan F. Helicobacter pylori infection and recurrent abdominal pain in Turkish children. Helicobacter 2001; 6: 234-238.

21. Hardikar W, Feekery C, Smith A, Oberklaid F, Grimwood K. Helicobacter pylori and recurrent abdominal pain in children. J Pediatr Gastroenterol Nutr 1996; 22: 148-152.

22. Bansal D, Patwari AK, Malhotra VL, Malhotra V, Anand VK. Helicobacter pylori infection in recurrent abdominal pain. Indian Pediatr 1998; 35: 329-335.

23. Macarthur C, Saunders N, Feldman W, Ipp M, Winders-Lee P, Roberts S, et al. Helicobacter pylori and childhood recurrent abdominal pain: Community based case-control study. BMJ 1999; 319: 822-823.

24. Wewer V, Anderson LP, Paerregaard A, Gernow A, Hansen JPH, Matzen P, et al. Treatment of Helicobacter pylori in children with recurrent abdominal pain. Helicobacter 2001; 6: 244-248.

25. Rasquin-Weber A, Hyman PE, Cucchiara S, Fleisher DR, Hyams JS, Milla PJ, et al. Childhood functional gastrointestinal disorders. Gut 1999; 45(Supplement 2): ii60-ii68.

26. Caplan A, Walker L, Rasquin A. Validation of the Pediatric Rome II criteria for functional gastrointestinal disorders using the questionnaire on pediatric gastrointestinal symptoms. J Pediatr Gastroenterol Nutr 2005; 41: 305-316.

27. Saps M, Di Lorenzo C. Interobserver and intraobsever reliability of the Rome II criteria in children. Am J Gastroenterol 2005; 100: 2079-2082.

28. Walker LS, Lipani TA, Greene JW, Caines K, Stutts J, Polk DB, et al. Recurrent Abdominal Pain: Symptom Subtypes Based on the Rome II Criteria for Pediatric Functional Gastrointestinal Disorders. J Pediatr Gastroenterol Nutr 2004; 38: 187-191.

29. Schurman JV, Friesen CA, Danda CE, Andre L, Welchert E, Lavenbarg T, et al. Diagnosing functional abdominal pain with the Rome II criteria: parent, child, and clinician agreement. J Pediatr Gastroenterol Nutr 2005; 41: 291-295.

30. Rasquin A, Lorenzo CD, Forbes D, Guiraldes E, Hyams JS, Staiano A, et al. Childhood functional gastrointestinal disorders: child/adolescent. Gastroenterology 2006; 130: 1527-1537.

31. Boey CC, Goh KL. Stressful life events and recurrent abdominal pain in children in a rural district in Malaysia. Eur J Pediatr 2001; 13: 401-404.

32. Dorn LD, Campo JC, Thato S, Dahl RE, Lewin D, Chandra R, et al. Psychological comorbidity and stress reactivity in children and adolescents with recurrent abdominal pain and anxiety disorders. J Am Acad Child Adolesc Psychiatry 2003; 42: 66-75.

33. Walker LS, Green JW. Children with recurrent abdominal pain and their parents: More somatic complaints, anxiety, depression than other patient families? J Pediatr Psychol 1989; 14: 231-243.

34. Pineiro-Carrero VM, Andres JM, Davis RH, Mathias JR. Abnormal gastroduodenal motility in children and adolescents with recurrent functional abdominal pain. J Pediatr 1988; 113: 820-825.

35. Olafsdottir E, Gilja OH, Aslaksen A, Berstad A, Fluge G. Impaired accommodation of the proximal stomach in children with recurrent abdominal pain. J Pediatr Gastroenterol Nutr 2000; 30: 157-163.

36. Devanarayana NM, de Silva DGH, de Silva HJ. Gastric myoelectrical and motor abnormalities in children and adolescents with functional recurrent abdominal pain. J Gastroenterol Hepatol 2009 [In press].

37. Monnikes H, Tebbe JJ, Hilderbrandt M, Arck P, Osmanoglou E, Rose M, et al. Role of stress in functional gastrointestinal disorders. Evidence for stress-induced alterations in gastrointestinal motility and sensitivity. Dig Dis 2001; 19: 201-211.

38. Chelimsky G, Boyle JT, Tusing L, Chelimsky TC. Autonomic abnormalities in children with functional abdominal pain: coincidence or etiology? J Pediatr Gastroenterol Nutr 2001; 33: 47-53.

39. Olafsdottir E, Ellertsen B, Berstad A, Fluge G. Personality profiles and heart rate variability (vagal tone) in children with recurrent abdominal pain. Acta Paediatr 2001; 90: 632-637.

40. Di Lorenzo C. Youssef NN, Sigurdsson L, Scharff L, Griffiths J, Wald A. Visceral hyperalgesia in children with functional abdominal pain. J Pediatr 2001; 139: 838-843.

41. Shannon A, Martin DJ, Feldman W. Ultrasonographic studies in the management of recurrent abdominal pain. Pediatrics 1990; 86: 35-38.

42. Boey CC, Goh KL, Hassall E, Maqiod M. Endoscopy in children with recurrent abdominal pain. Gastrointest Endosc 2001; 53: 142-143.

43. Rappaport LA, Leichtner AM. Recurrent abdominal pain. In: Schechter NL, Berde CB, Yaster M editors. Pain in Infants, Children, and Adolescents. Baltimore: Williams and Wilkins, 1993. p. 561-569.

44. Apley J, Hale B. Children with recurrent abdominal pain: how do they grow up? BMJ 1973; 3: 7-9.

45. Christensen MF, Mortensen O. Long-term prognosis in children with recurrent abdominal pain. Arch Dis Child 1975; 50: 110-114.

46. Campo JV, Di Lorenzo C, Chiappetta L, Bridge J, Colborn DK, Gartner J, et al. Adult outcomes of pediatric recurrent abdominal pain: do they just grow out of it? Pediatrics 2001; 108: E1.

47. Huertas-Ceballos A, Macarthur C, Logan S. Pharmacological interventions for recurrent abdominal pain (RAP) in childhood. Cochrane Database Syst Rev 2004; 1: CD 003017.

48. Kline RM, Kline JJ, Di Palma J, Barbero G. Enteric coated, pH dependent peppermint oil capsules for the treatment of irritable bowel syndrome in children. J Pediatr 2001; 138: 125-128

49. Huertas-Ceballos A, Macarthur C, Logan S. Dietary interventions for recurrent abdominal pain (RAP) in childhood. Cochrane Database Syst. Rev 2004; 1: CD003019.

50. Feldman W, McGrath P, Hodgeson C, Ritter H, Shipman RT. The use of dietary fiber in the management of simple, childhood, idiopathic, recurrent abdominal pain. Results in a prospective, double-blind, randomized, controlled trial. Am J Dis Child 1985; 139: 1216-1218.

51. Christensen MF. Recurrent abdominal pain and dietary fiber. Am J Dis Child 1986; 140: 738-739.

52. Feinle-Bisset C, Horowitz M. Dietary factors in functional dyspepsia. Neurogastroenterol Motil 2006; 18: 608-618.

53. Robins PM, Smith SM, Glutting JJ, Bishop CT. A randomized controlled trial of a cognitive-behavioural family intervention for paediatric recurrent abdominal pain. J Pediatr Psychol 2005; 30: 397-408.

54. Youssef NN, Rosh JR, Loughran M, Schuckalo SG, Cotter AN, Verga BG, et al. Treatment of functional abdominal pain in childhood with cognitive behavioural therapy. J Pediatr Gastroenterol Nutr 2004; 39: 192-196.

55. Humphreys, PA, Gevirtz RN. Treatment of recurrent abdominal pain: components analysis for four treatment protocols. J Pediatr Gastroenterol Nutr 2000; 31: 47-51.

56. Boey CC, Goh KL. Predictors of health-care consultation for recurrent abdominal pain among urban school children in Malaysia. J Gastroenterol Hepatol 2001; 16: 154-159.

57. Boey CC, Goh KL. Recurrent abdominal pain and consulting behaviour among children in a rural community in Malaysia. Digest Liver Dis 2001; 33: 140-144.

58. O’Donnell B. Outcome based on personal experience: Two small series. In: O’Donnell B, editor. Abdominal Pain in Children. Worcester: Blackswell Scientific Publications, 1985. p.106-13.

59. Williams N, Jackson D, Lambert PC, Johnstone M. Incidence of non-specific abdominal pain in children during school term: Population survey based on discharge diagnosis. BMJ 1999; 318: 1455.

60. Jarrett M, Heitkemper M, Czyzewski DI, Shulman R. Recurrent abdominal pain in children: forerunner for adult irritable bowel syndrome? JSPN 2003; 8: 81-89.

 

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