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Published on: June 2, 2014
Functional gastrointestinal disorders in migrainous children: efficacy of flunarizine
G Boccia1, E Del Giudice, A F Crisanti
1Department of Paediatrics, University of Naples Federico II, Naples, Italy.
Insights
Most children with migraine experience functional gastrointestinal disorders (FGIDs), which are linked to delayed gastric emptying. Flunarizine treatment effectively reduced FGIDs and migraine symptoms in pediatric patients.
Area of Science:
- Pediatric Gastroenterology
- Neurology
- Pharmacology
Background:
- Functional gastrointestinal disorders (FGIDs) are common in children with migraine headaches.
- Delayed gastric emptying is a potential contributing factor to FGIDs in this population.
Purpose of the Study:
- To determine the prevalence of FGIDs in pediatric migraine patients.
- To investigate the impact of flunarizine on gastrointestinal manifestations and migraine symptoms.
Main Methods:
- Utilized structured questionnaires to diagnose FGIDs in 50 pediatric migraine patients.
- Measured total gastric emptying time (TGEt) using ultrasonography at baseline and after flunarizine treatment.
- Assessed symptom frequency and duration before and during flunarizine therapy in a subset of patients.
Main Results:
- 70% of pediatric migraine patients exhibited FGIDs, with significantly prolonged TGEt compared to controls.
- Flunarizine treatment led to a significant reduction in TGEt at 1 and 2 months.
- Flunarizine decreased the frequency of abdominal pain, vomiting, and headache, and reduced headache duration.
Conclusions:
- FGIDs are highly prevalent in children with migraine and associated with delayed gastric emptying.
- Flunarizine is effective in improving both gastrointestinal symptoms and migraine characteristics in pediatric patients.
Abstract:
The aim of this study was to evaluate the prevalence of functional gastrointestinal disorders (FGIDs) in children with migraine headache and the effects of flunarizine on gastrointestinal manifestations. We studied 50 migrainous children (mean age 8.63 years). The clinical pattern and the diagnosis of FGIDs were obtained from structured questionnaires. All subjects underwent measurement of total gastric emptying time (TGEt) performed by real-time ultrasonography of the gastric antrum at baseline (T0). In the second part of the study, we evaluated 10 migrainous children (mean age 9.8 years) with associated FGIDs. In these 10 patients, repeated TGEt evaluation together with a detailed symptom history was obtained after 1 (T1) and 2 months (T2) of treatment with flunarizine. Control groups were composed of 10 migrainous children without FGIDs (mean age 9.2 years) and nine sex- and age-matched healthy children. Gastrointestinal disorders were present in 70% of the patients. Migrainous children with FGIDs had significantly (P < 0.01) more prolonged TGEt than subjects without FGIDs. Prior to therapy, all migrainous children with FGIDs had prolongation of TGEt compared with controls (P < 0.05). Patients on flunarizine had a significant decrease in TGEt at both 1 (P < 0.01) and 2 months (P = 0.002) of therapy. The mean frequency of abdominal pain per month was significantly (P < 0.001) reduced at T1 compared with T0. The mean frequency of vomiting per month was significantly decreased at T1 (P < 0.05) and even more so at T2 (P < 0.01). Finally, the mean frequency of headache per month was significantly reduced only at T2 (P < 0.05), whereas the mean duration of headache was significantly decreased at T1 (P < 0.01) with no difference between T1 and T2. Most children with migraine report FGIDs, associated with a delayed gastric emptying. Flunarizine decreases the frequency and duration of migrainous episodes as well as the gastrointestinal symptoms.
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