Abdulsalam Aliyu, Neele Dellschaft, Caroline Hoad, Hannah Williams, Emily Gaudoin, Sarah Sulaiman, Colin Crooks, Penny Gowland, Alexia Aran, Robert Lange, Beatrice Bois De Fer, Maura Corsetti, Luca Marciani, Robin Spiller
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Secondary endpoints included: small bowel water content, whole gut transit time (WGTT), colonic volumes, stool frequency, and consistency using Bristol Stool Form Score (BSFS). Exploratory endpoints: changes in the serial segmental volumes were quantified from the number of \"mass movements\" defined as episodes when segmental volume change from the previous scan was > 20% of baseline volume. We also measure the time to defecate after dosing. After 3 days of bisacodyl, ascending colon water content (T1) was 62% greater than after placebo, mean difference T1 AUC<sub>300-450 minutes</sub> 50.2 (61.0) sec.min, 95% CI (9.2, 91.2), P = 0.02, while after a single dose difference was only 11% (P = 0.58). Both single and repeated doses shortened WGTT (P < 0.049) and time to defecate (P 0.01). Only repeated doses significantly increased small bowel water content (P < 0.03), the number of \"mass movements\" (P = 0.048), bowel frequency (P = 0.006), and BSFS (P = 0.03). 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引用次数: 0
摘要
Bisacodyl是一种广泛使用的泻药,可以刺激运动和分泌。我们的目的是利用MRI的独特能力来定义比沙代的作用模式。进行了两项安慰剂对照交叉试验,其中一项使用单剂量5毫克的比沙代,而另一项使用连续3天的每日剂量。每75分钟做一次MRI。主要终点:T1AC AUC300-450分钟评估的升结肠水分含量。次要终点包括:小肠含水量、全肠运输时间(WGTT)、结肠体积、大便频率和布里斯托大便形式评分(BSFS)一致性。探索性终点:连续节段容积的变化通过“肿块运动”的次数来量化,“肿块运动”定义为前一次扫描时节段容积变化为基线容积的20%。我们也测量服药后排便的时间。给药3天后,结肠升水含量(T1)比安慰剂组高62%,平均T1差AUC300-450分钟50.2 (61.0)sec.min, 95% CI (9.2, 91.2), P = 0.02,而单次给药后差异仅为11% (P = 0.58)。单次和多次给药均能缩短WGTT (P
Magnetic Resonance Imaging Reveals Novel Insights into the Dual Mode of Action of Bisacodyl: A Randomized, Placebo-controlled Trial in Constipation.
Bisacodyl is a widely used laxative that stimulates both motility and secretion. Our aim was to exploit the unique capabilities of MRI to define bisacodyl's mode of action. Two placebo-controlled cross-over trials were performed, one using a single dose of Bisacodyl 5 mg while the second dosed daily for 3 consecutive days. Serial MRI was performed every 75 minutes. Primary endpoint: ascending colon water content as assessed by T1AC AUC300-450 minutes. Secondary endpoints included: small bowel water content, whole gut transit time (WGTT), colonic volumes, stool frequency, and consistency using Bristol Stool Form Score (BSFS). Exploratory endpoints: changes in the serial segmental volumes were quantified from the number of "mass movements" defined as episodes when segmental volume change from the previous scan was > 20% of baseline volume. We also measure the time to defecate after dosing. After 3 days of bisacodyl, ascending colon water content (T1) was 62% greater than after placebo, mean difference T1 AUC300-450 minutes 50.2 (61.0) sec.min, 95% CI (9.2, 91.2), P = 0.02, while after a single dose difference was only 11% (P = 0.58). Both single and repeated doses shortened WGTT (P < 0.049) and time to defecate (P 0.01). Only repeated doses significantly increased small bowel water content (P < 0.03), the number of "mass movements" (P = 0.048), bowel frequency (P = 0.006), and BSFS (P = 0.03). Repeated, compared to single dosing of Bisacodyl, additionally increases small bowel and colon water content and increases the number of "mass movements" thereby increasing its laxative effect. MRI is a non-invasive, patient-acceptable technique for evaluating drugs which alter secretion and/or motility.
期刊介绍:
Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.