Assessment of abdominal pain through global outcomes and recent FDA recommendations in children: are we ready for change?

J Pediatr Gastroenterol Nutr. 2014 Jan;58(1):46-50. doi: 10.1097/MPG.0b013e3182a20764.

Abstract

Objectives: Irritable bowel syndrome is a multisymptom construct, with abdominal pain (AP) acting as the driving symptom of patient-reported severity. The Food and Drug Administration considers a >30% decrease in AP as satisfactory improvement, but this has not been validated in children. We investigated the correspondence of 2 measures for AP assessment, ≥30% improvement in AP and global assessment of improvement.

Methods: Secondary analysis of data from 72 children who completed a randomized clinical trial for abdominal pain-associated functional gastrointestinal disorders. Children completed daily assessment of AP intensity, functional disability inventory (FDI), question regarding pain's interference with activities, and 2 global assessment questions. We measured the extent to which ≥30% improvement of AP and global assessment questions correlated with each other and with disability.

Results: The global questions correlated with each other (r=0.74; P<0.0001) and with a ≥30% improvement in AP (P<0.01). Global outcomes were satisfaction with treatment was inversely related to the child's report of interference with activities (P<0.01) and symptom relief was positively associated with ≥30% improvement in FDI scores (P<0.009). A 30% change in FDI scores was associated with global questions of symptom relief (P=0.009) but not with satisfaction with treatment (P=0.07). The association of AP improvement with interference with activities (P=0.14) or change in FDI scores (P=0.27) did not reach significance.

Conclusions: Currently used global assessments are significantly associated with decreased pain intensity, decreased interference with daily activities, and a ≥30% change in FDI scores, whereas recommended 30% improvement in pain intensity is not as comprehensive.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Validation Study

MeSH terms

  • Abdominal Pain / drug therapy*
  • Abdominal Pain / etiology
  • Activities of Daily Living*
  • Adolescent
  • Amitriptyline / therapeutic use
  • Analgesics, Non-Narcotic / therapeutic use
  • Child
  • Disability Evaluation*
  • Female
  • Humans
  • Irritable Bowel Syndrome / complications
  • Irritable Bowel Syndrome / drug therapy*
  • Irritable Bowel Syndrome / pathology
  • Male
  • Outcome Assessment, Health Care / standards*
  • Patient Satisfaction*
  • Practice Guidelines as Topic
  • Severity of Illness Index*
  • Surveys and Questionnaires
  • United States
  • United States Food and Drug Administration

Substances

  • Analgesics, Non-Narcotic
  • Amitriptyline