Thomas V E, O'Connell F, Harrison A J, Fuller R W
Department of Clinical Pharmacology, Royal Postgraduate Medical School, London.
Br J Clin Pharmacol. 1992 Sep;34(3):266-8. doi: 10.1111/j.1365-2125.1992.tb04135.x.
A randomised placebo-controlled cross-over group study was conducted to ascertain the occurrence and duration of xerostomia induced by 240 micrograms (high dose) and 120 micrograms (low dose) of ipratropium bromide (IPB) delivered by metered dose inhaler (MDI) into the mouth in normal subjects. Salivary output was higher with both doses of IPB than with placebo though the differences were not statistically significant. IPB was less palatable than placebo as indicated on visual analogue scale (VAS) and the taste of the drug may have caused a reflex increase in salivary output from the major salivary glands which would have masked any possible local effect of the drug on the smaller submucosal glands of the mouth. IPB delivered into the oral cavity by MDI is therefore not a suitable treatment for hypersalivation.
进行了一项随机、安慰剂对照的交叉组研究,以确定在正常受试者中,通过定量吸入器(MDI)将240微克(高剂量)和120微克(低剂量)的异丙托溴铵(IPB)送入口腔所诱发的口干的发生率和持续时间。两种剂量的IPB的唾液分泌量均高于安慰剂,尽管差异无统计学意义。视觉模拟量表(VAS)显示,IPB的口感不如安慰剂,药物的味道可能导致主要唾液腺的唾液分泌反射性增加,这可能掩盖了药物对口腔较小的黏膜下腺的任何可能的局部作用。因此,通过MDI将IPB送入口腔不是治疗唾液分泌过多的合适方法。