Diagnostic outcomes following childhood non-specific abdominal pain: a record-linkage study

G C D Thornton1, M J Goldacre2, R Goldacre2

  • 1Department of Paediatric Gastroenterology, Oxford University Hospitals Trust, Oxford, UK.

Insights

Children diagnosed with non-specific abdominal pain (NSAP) face an increased risk of subsequent bowel conditions, including Crohn's disease and irritable bowel syndrome (IBS). This elevated risk for bowel pathology persists for up to 10 years following the initial NSAP diagnosis.

Area of Science:

  • Pediatric Gastroenterology
  • Clinical Epidemiology

Background:

  • Non-specific abdominal pain (NSAP) is a frequent discharge diagnosis for pediatric abdominal pain admissions.
  • Understanding long-term risks following NSAP is crucial for effective patient management.

Purpose of the Study:

  • To determine the risk of subsequent hospital diagnoses of organic and functional gastrointestinal conditions after an initial NSAP diagnosis in children.
  • To assess the duration and persistence of this risk.

Main Methods:

  • A large cohort of 268,623 children diagnosed with NSAP (aged 0-16) was established using English Hospital Episode Statistics (1999-2011).
  • A control cohort of 1,684,923 children hospitalized for unrelated conditions was used for comparison.
  • Standardized rate ratios were calculated for clinically relevant outcomes.

Main Results:

  • Children with NSAP had a significantly higher risk of later hospitalization for bowel pathology (5.8%) and functional disorders (5%).
  • Specific increased risks included Crohn's disease (4.84 times), acute appendicitis (4.23 times), and irritable bowel syndrome (IBS) (7.22 times).
  • Elevated risks for inflammatory bowel disease (IBD), IBS, and functional disorders persisted up to 10 years post-NSAP diagnosis, except in children under 2.

Conclusions:

  • While a small percentage of children with NSAP develop underlying bowel pathology, their risk is notably increased.
  • The heightened risk for bowel conditions following NSAP extends up to a decade.
  • Refining diagnostic strategies and implementing active surveillance for children with NSAP are recommended.
Abstract

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