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Quality of life in children with Crohn disease
1University of Queensland, Children's Nutrition Research Centre, Discipline of Paediatrics and Child Health, Australia. rj.hill@uq.edu.au
Insights
Children with Crohn disease (CD) diagnosed within 6 months have lower quality of life (QOL) than those diagnosed later. Regular QOL assessments are recommended for these patients and those with significant disease activity or complications.
Area of Science:
- Pediatric Gastroenterology
- Inflammatory Bowel Disease Research
- Quality of Life Studies
Background:
- Quality of life (QOL) is a critical outcome measure in pediatric chronic diseases.
- Children with Crohn disease (CD) often experience impaired QOL, particularly early in their disease course.
Purpose of the Study:
- To evaluate QOL in Australian children with CD.
- To analyze the relationship between QOL, disease duration, disease activity, and treatment in pediatric CD patients.
Main Methods:
- Utilized the IMPACT-III questionnaire to assess QOL in 41 children with CD.
- Employed the Pediatric Crohn's Disease Activity Index (PCDAI) to measure disease activity.
- Collected 186 paired measurements of QOL and disease activity.
Main Results:
- QOL was significantly lower in patients within 6 months of diagnosis compared to those diagnosed longer ago.
- Higher disease activity correlated with poorer QOL (r = -0.51, P = 0.00).
- The PCDAI and its clinical components were significant predictors of QOL; disease duration, age, and sex were not significant predictors.
Conclusions:
- Children diagnosed with CD within 6 months exhibit impaired QOL.
- Regular QOL assessments are beneficial for children with CD, especially those with growth issues, high disease activity, or complications.
Objectives:
: Quality of life (QOL) is reportedly poor in children with Crohn disease (CD) but improves with increasing disease duration. This article aims to detail QOL in a cohort of Australian children with CD in relation to disease duration, disease activity, and treatment.
Materials And Methods:
: QOL, assessed using the IMPACT-III questionnaire, and disease activity measures, assessed using the Pediatric Crohn's Disease Activity Index (PCDAI), were available in 41 children with CD. For this cohort, a total of 186 measurements of both parameters were available.
Results:
: QOL was found to be significantly lower, and disease activity significantly higher (F = 31.1, P = 0.00), in patients within 6 months of their diagnosis compared with those up to 2.5 years, up to 5 years, and beyond 5 years since diagnosis. Higher disease activity was associated with poorer QOL (r = -0.51, P = 0.00). Total QOL was highest in children on nil medications and lowest in children on enteral nutrition. The PCDAI (t = -6.0, P = 0.00) was a significant predictor of QOL, with the clinical history (t = -6.9, P = 0.00) and examination (t = -2.9, P = 0.01) sections of the PCDAI significantly predicting QOL. Disease duration, age, or sex was neither related to nor significant predictors of QOL, but height z score and type of treatment approached significance.
Conclusions:
: Children with CD within 6 months of their diagnosis have impaired QOL compared with those diagnosed beyond 6 months. These patients, along with those with growth impairment, ongoing elevated disease activity with abdominal pain, diarrhoea and/or perirectal and extraintestinal complications, may benefit from regular assessments of QOL as part of their clinical treatment.
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