Cadranel S, Di Lorenzo C, Rodesch P
Pharmatherapeutica. 1987;5(1):9-15.
A series of studies was carried out in infants and children suffering from gastro-oesophageal reflux to assess the therapeutic efficacy and tolerability of alizapride, a recently developed dopaminergic-receptor blocker. Investigational techniques such as manometry, pH monitoring, endoscopy and scintigraphy were used to evaluate a prokinetic activity of the drug and its effects on oesophageal and gastric motility when given by the intravenous and oral routes. Preliminary findings indicate that alizapride had a significant effect on lower oesophageal sphincter pressure and peristaltic wave amplitude, but the evidence for an effect on gastric motility was less clear. Long-term treatment with oral alizapride (usually in a dosage of 5 mg/kg/day) suggests that it produced marked symptomatic improvement and was very well tolerated in the majority of the patients studied. A double-blind controlled trial is now in progress to provide more objective evidence of the usefulness of alizapride in the management of digestive tract motor disorders in paediatric patients.
对患有胃食管反流的婴幼儿和儿童进行了一系列研究,以评估最近研制的多巴胺能受体阻滞剂阿立必利的治疗效果和耐受性。采用诸如测压法、pH监测、内窥镜检查和闪烁扫描术等研究技术,来评估该药物的促动力活性及其静脉内和口服给药时对食管和胃动力的影响。初步研究结果表明,阿立必利对食管下括约肌压力和蠕动波幅度有显著影响,但对胃动力的影响证据尚不太明确。口服阿立必利长期治疗(通常剂量为5毫克/千克/天)表明,它能使症状明显改善,且在大多数研究患者中耐受性良好。目前正在进行一项双盲对照试验,以提供更客观的证据,证明阿立必利在治疗小儿患者消化道运动障碍方面的有效性。