[Clinical and instrumental evaluation by multiple colonic manometry of tiropramide, trimebutine and octylonium bromide in irritable colon. II. Repeated oral administration].

Pharmatherapeutica Pub Date : 1986-01-01
M Galeone, E Benazzi, M Bossi, G Moise, A Riva, F Stock
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Abstract

Sixty out-patients with acute or sub-acute irritable colon were randomly allocated to receive 3 daily doses of 100 mg tiropramide, 150 mg trimebutine maleate or 20 mg octilonium bromide, orally during 5 consecutive days. Before and after treatment, multiple colonic manometry was performed, monitoring tonus, intensity and frequency of sinusoid contraction waves, transitories and vibrations, as well as the voluntary contraction capacity. Before treatment and after 2 and 5 days, the specific symptoms were also monitored, scored and recorded. Significant variations in tonus were not observed with any drug, but while tiropramide left unmodified the voluntary contractile ability, a significant inhibition was observed with trimebutine and, mainly, with octilonium. The overall power of spontaneous colonic contractions did not vary significantly with any drug. However, while with tiropramide a significant redistribution of muscular power was observed so as to increase propulsion waves and to decrease the ineffective transitory and vibrational contractions, with octilonium and trimebutine no clinically relevant redistribution of the power wasted in transient spasms was observed. Based on these observations, tiropramide was considered to be at least as effective an antispasmodic as octilonium and at least as effective a synchronizer as trimebutine, but was different from both reference drugs because it was the only one to act simultanously as both an antispasmodic and a synchronizer. The three drugs produced an improvement in each and all monitored symptoms as well as in the overall symptom intensity. Tiropramide, however, produced an improvement significantly faster, more progressively and to a greater extent than either reference drug.(ABSTRACT TRUNCATED AT 250 WORDS)

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替罗普胺、曲美布汀和溴化辛溴铵在肠易激性中的临床及仪器评价。2反复口服]。
60例急性或亚急性结肠易激症门诊患者随机分为3组,每日口服替罗普胺100 mg、马来酸曲美布汀150 mg或溴化奥替溴铵20 mg,连续5天。治疗前后行多次结肠测压,监测张力、正弦收缩波强度、频率、瞬缩、振动、自主收缩能力。治疗前、治疗后2、5天对具体症状进行监测、评分和记录。任何药物均未观察到张力的显著变化,但替罗普胺未改变自愿收缩能力,而曲美布汀和奥替溴铵则观察到明显的抑制作用。自发结肠收缩的总功率与任何药物没有显着变化。然而,使用替罗普胺可以观察到肌肉力量的显著重新分配,从而增加推进波,减少无效的短暂性和振动性收缩,而使用奥替溴铵和曲美布汀则没有观察到短暂性痉挛中浪费的能量的临床相关重新分配。基于这些观察,替罗普胺被认为是至少与奥替溴铵一样有效的抗痉挛药,至少与曲美布汀一样有效的同步剂,但与这两种参考药物不同,因为它是唯一一种同时作为抗痉挛药和同步剂的药物。这三种药物在每个和所有监测症状以及总体症状强度方面都有改善。然而,替罗普胺比任何一种参比药物更快、更渐进、更大程度地产生改善。(摘要删节250字)
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