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Pharmacologic treatment in pediatric functional abdominal pain disorders: a systematic review
Judith J Korterink1, Juliette M T M Rutten1, Leonie Venmans2
1Department of Pediatric Gastroenterology and Nutrition, Emma's Children's Hospital Academic Medical Center, Amsterdam, The Netherlands.
Insights
Limited high-quality studies exist for pharmacologic treatments in pediatric functional abdominal pain disorders (AP-FGIDs). Peppermint oil, cyproheptadine, and famotidine show potential, but more research is needed to support routine use.
Area of Science:
- Pediatric Gastroenterology
- Pharmacology
- Evidence-Based Medicine
Background:
- Abdominal pain-related functional gastrointestinal disorders (AP-FGIDs) are common in children.
- Pharmacologic treatments are frequently used, but their efficacy and safety in this population require systematic evaluation.
Purpose of the Study:
- To systematically review the existing literature on the efficacy and safety of pharmacologic treatments for AP-FGIDs in children.
- To assess the quality of evidence for various drug classes used in pediatric AP-FGIDs.
Main Methods:
- Searched MEDLINE and Cochrane Database for systematic reviews and randomized controlled trials (RCTs) in children aged 4-18 years.
- Assessed the quality of evidence using the Grades of Recommendation, Assessment, Development and Evaluation (GRADE) approach.
- Included 6 studies evaluating antispasmodics, antidepressants, antireflux agents, antihistamines, and laxatives.
Main Results:
- Overall quality of evidence was very low.
- Peppermint oil showed potential for symptom improvement (OR 3.3).
- Cyproheptadine reduced pain frequency (RR 2.43) and intensity (RR 3.03).
- Amitriptyline improved quality of life (15% increase).
- Famotidine showed benefit in global symptom improvement (OR 11.0).
- Polyethylene glycol with tegaserod decreased pain intensity compared to PEG alone.
- No serious adverse effects were reported. No studies on antidiarrheals, antibiotics, or pain medications were found.
Conclusions:
- High-quality RCTs are lacking for pharmacologic treatments in pediatric AP-FGIDs.
- There is insufficient evidence to support the routine use of any pharmacologic therapy.
- Peppermint oil, cyproheptadine, and famotidine may be potential interventions, warranting further investigation in well-designed RCTs.
Objective:
To systematically review literature assessing efficacy and safety of pharmacologic treatments in children with abdominal pain-related functional gastrointestinal disorders (AP-FGIDs).
Study Design:
MEDLINE and Cochrane Database were searched for systematic reviews and randomized controlled trials investigating efficacy and safety of pharmacologic agents in children aged 4-18 years with AP-FGIDs. Quality of evidence was assessed using Grades of Recommendation, Assessment, Development and Evaluation approach.
Results:
We included 6 studies with 275 children (aged 4.5-18 years) evaluating antispasmodic, antidepressant, antireflux, antihistaminic, and laxative agents. Overall quality of evidence was very low. Compared with placebo, some evidence was found for peppermint oil in improving symptoms (OR 3.3 (95% CI 0.9-12.0) and for cyproheptadine in reducing pain frequency (relative risk [RR] 2.43, 95% CI 1.17-5.04) and pain intensity (RR 3.03, 95% CI 1.29-7.11). Compared with placebo, amitriptyline showed 15% improvement in overall quality of life score (P = .007) and famotidine only provides benefit in global symptom improvement (OR 11.0; 95% CI 1.6-75.5; P = .02). Polyethylene glycol with tegaserod significantly decreased pain intensity compared with polyethylene glycol only (RR 3.60, 95% CI 1.54-8.40). No serious adverse effects were reported. No studies were found concerning antidiarrheal agents, antibiotics, pain medication, anti-emetics, or antimigraine agents.
Conclusions:
Because of the lack of high-quality, placebo-controlled trials of pharmacologic treatment for pediatric AP-FGIDs, there is no evidence to support routine use of any pharmacologic therapy. Peppermint oil, cyproheptadine, and famotidine might be potential interventions, but well-designed randomized controlled trials are needed.
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