Boccia G, Del Giudice E, Crisanti A F, Strisciuglio C, Romano A, Staiano A
Department of Paediatrics, University of Naples Federico II, Naples, Italy.
Cephalalgia. 2006 Oct;26(10):1214-9. doi: 10.1111/j.1468-2982.2006.01196.x.
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.
本研究旨在评估偏头痛儿童中功能性胃肠疾病(FGIDs)的患病率以及氟桂利嗪对胃肠道表现的影响。我们研究了50名偏头痛儿童(平均年龄8.63岁)。FGIDs的临床模式和诊断通过结构化问卷获得。所有受试者在基线时(T0)通过胃窦实时超声测量总胃排空时间(TGEt)。在研究的第二部分,我们评估了10名伴有FGIDs的偏头痛儿童(平均年龄9.8岁)。在这10名患者中,在接受氟桂利嗪治疗1个月(T1)和2个月(T2)后,重复进行TGEt评估并获取详细的症状病史。对照组由10名无FGIDs的偏头痛儿童(平均年龄9.2岁)和9名性别及年龄匹配的健康儿童组成。70%的患者存在胃肠疾病。患有FGIDs的偏头痛儿童的TGEt显著延长(P < 0.01),比无FGIDs的受试者更明显。治疗前,所有患有FGIDs的偏头痛儿童与对照组相比TGEt均延长(P < 0.05)。接受氟桂利嗪治疗的患者在治疗1个月(P < 0.01)和2个月(P = 0.002)时TGEt均显著降低。与T0相比,T1时每月腹痛的平均频率显著降低(P < 0.001)。每月呕吐的平均频率在T1时显著降低(P < 0.05),在T2时更是如此(P < 0.01)。最后,每月头痛的平均频率仅在T2时显著降低(P < 0.05),而头痛的平均持续时间在T1时显著缩短(P < 0.01),T1和T2之间无差异。大多数偏头痛儿童报告有FGIDs,伴有胃排空延迟。氟桂利嗪可降低偏头痛发作的频率和持续时间以及胃肠道症状。