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Bisacodyl plus split 2-L polyethylene glycol-citrate-simethicone improves quality of bowel preparation before screening colonoscopy 被引量:10
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作者 Flavio Valiante Angelo Bellumat +1 位作者 Manuela De Bona Michele De Boni 《World Journal of Gastroenterology》 SCIE CAS 2013年第33期5493-5499,共7页
AIM:To compare the bowel cleansing efficacy,tolerability and acceptability of split 2-L polyethylene glycol(PEG)-citrate-simethicone(PEG-CS)plus bisacodyl(BIS)vs 4-L PEG for fecal occult blood test-positive screening ... AIM:To compare the bowel cleansing efficacy,tolerability and acceptability of split 2-L polyethylene glycol(PEG)-citrate-simethicone(PEG-CS)plus bisacodyl(BIS)vs 4-L PEG for fecal occult blood test-positive screening colonoscopy.METHODS:This was a randomised,observer-blind comparative study.Two hundred and sixty-four subjects underwent screening colonoscopy(mean age 62.5±7.4years,male 61.7%).The primary objective of the study was to compare the bowel cleansing efficacy of the two preparations.Interventions:BIS plus PEG-CS:3 tablets of 5-mg BIS at 16:00,PEG-CS 1-L at 19:00 and 1-L at7:00,4-L PEG:3-L at 17:00,and 1-L at 7:00.Colonoscopy was carried out after 11:00,at least 3 h after the completion of bowel preparation.Bowel cleansing was evaluated using the Harefield Cleansing Scale.RESULTS:Bowel preparation was successful for 92.8%of subjects in the PEG-CS group and for 92.1%of subjects in the 4-L PEG(RR=1.01;95%CI:0.94-1.08).BIS+PEG-CS was better tolerated than 4-L PEG.A greater rate of patients in the BIS+PEG-CS group had no difficulty and/or were willing to repeat the same preparation compared to split-dose 4-L PEG group.Subjects in the BIS+PEG-CS group rated the prep as good or satisfactory in 90.6%as compared to 77%in the 4-L PEG(P=0.003).Subjects receiving BIS+PEGCS stated they fully adhered to instructions drinking all the 2-L solution in 97.1%compared with 87.3%in the4-L PEG(P=0.003).CONCLUSION:BIS plus split 2-L PEG-CS was as effective as but better tolerated and accepted than split4-L PEG for screening colonoscopy.This new procedure may increase the positive attitude and participation to colorectal cancer screening colonoscopy. 展开更多
关键词 COLONOSCOPY Colon CLEANSING Bowel preparations Polyethylene GLYCOL SIMETHICONE bisacodyl
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Same-day colonoscopy preparation with Senna alkaloids and bisacodyl tablets:A pilot study 被引量:7
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作者 Erdinc Yenidogan Ismail Okan +5 位作者 Huseyin Ayhan Kayaoglu Gokhan Giray Akgul Mufit Sansal Servet Tali Zeki Ozsoy Mustafa Sahin 《World Journal of Gastroenterology》 SCIE CAS 2014年第41期15382-15386,共5页
AIM:To evaluate the efficacy of same-day bowel preparation with Senna alkaloids combined with bisacodyl tablets in routine colonoscopy procedures.METHODS:Between March and June 2013,a sameday bowel preparation was imp... AIM:To evaluate the efficacy of same-day bowel preparation with Senna alkaloids combined with bisacodyl tablets in routine colonoscopy procedures.METHODS:Between March and June 2013,a sameday bowel preparation was implemented in our endoscopy unit.The preparation consisted of a semi-liquid,fiber-free diet one day prior to the procedure,with two bisacodyl tablets after lunch and dinner,and 250 mL of Senna alkaloid with 1.5 L of drinking water at 6 am the day of the procedure.The quality control parameters of colonoscopy were evaluated and implemented according to the guidelines of the American Society for Gastrointestinal Endoscopy.The pre-procedure,duringprocedure and post-procedure patient data were collected and analyzed:(1) pre-procedure(age,gender,comorbid diseases,colonoscopy indications,complete lack of compliance with the bowel preparation protocol);(2) during-procedure(sedation dose,duration of colonoscopy,withdrawal time,cecal intubation rate,polyp detection rate,Boston Bowel Preparation Scores and presence of foam and clear liquid); and(3) postprocedure(visual analogue scale score,pain during the procedure,patient satisfaction and premature withdrawal due to the insufficient bowel preparation).RESULTS:A total of 75 patients were included in this study with a mean age of 54.64 ± 13.29 years; 53.3%(40/75) were female and 46.7%(35/75) were male.A complete lack of compliance with the bowel preparation protocol was seen in 6.7% of patients(5/75).The mean total duration of colonoscopy was 16.12 ± 6.51 min,and the mean withdrawal time was 8.89 ± 4.07 min.The cecal intubation rate was 93.8%(61/64) and the polyp detection rate was 40%(30/75).The mean Boston Bowel Preparation Score was 7.38 ± 1.81,with the following distribution:right colon,2.34 ± 0.89; transverse colon,2.52 ± 0.67; left colon,2.52 ± 0.63.The mean visual analogue scale score was 4.59 ± 1.57.Due to insufficient bowel preparation,seven patients(7/75; 9.3%) were asked to repeat the procedure.Of these,five patients had poor or modest compliance with the protocol,and two patients reported constipation.Premature withdrawal due to insufficient bowel preparation was 2.7%(2/75).The overall satisfaction with the protocol was 86.7%(65/75),with patients reporting they would prefer the same protocol in a repeat procedure.CONCLUSION:The same-day administration of Senna alkaloids appears to be a safe and effective bowel cleansing protocol for colonoscopy procedures. 展开更多
关键词 bisacodyl Bowel PREPARATION COLONOSCOPY Same-day p
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Pilot study on efficacy of reduced cathartic bowel preparation with polyethylene glycol and bisacodyl 被引量:3
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作者 Zhi-Yuan Chen He-Song Shen +6 位作者 Ming-Yue Luo Chai-Jie Duan Wen-Li Cai Hong-Bing Lu Guo-Peng Zhang Yang Liu Jerome Z Liang 《World Journal of Gastroenterology》 SCIE CAS 2013年第4期561-568,共8页
AIM:To evaluate the efficacy of reduced cathartic bowel preparation with 2 L polyethylene glycol(PEG)-4000 electrolyte solution and 10 mg bisacodyl enteric-coated tablets for computed tomographic colonography(CTC).MET... AIM:To evaluate the efficacy of reduced cathartic bowel preparation with 2 L polyethylene glycol(PEG)-4000 electrolyte solution and 10 mg bisacodyl enteric-coated tablets for computed tomographic colonography(CTC).METHODS:Sixty subjects who gave informed consent were randomly assigned to study group A,study group B or the control group.On the day prior to CTC,subjects in study group A were given 20 mL 40% wt/vol barium sulfate suspension before 3 mealtimes,60 mL 60% diatrizoate meglumine diluted in 250 mL water after supper,and 10 mg bisacodyl enteric-coated tablets 1 h before oral administration of 2 L PEG-4000 electrolyte solution.Subjects in study group B were treated identically to those in study group A,with the exception of bisacodyl which was given 1 h after oral PEG-4000.Subjects in the control group were managed using the same strategy as the subjects in study group A,but without administration of bisacodyl.Residual stool and fluid scores,the attenuation value of residual fluid,and discomfort during bowel preparation in the three groups were analyzed statistically.RESULTS:The mean scores for residual stool and fluid in study group A were lower than those in study group B,but the differences were not statistically significant.Subjects in study group A showed greater stool and fluid cleansing ability than the subjects in study group B.The mean scores for residual stool and fluid in study groups A and B were lower than those in the control group,and were significantly different.There was no significant difference in the mean attenuation value of residual fluid between study group A,study group B and the control group.The total discomfort index during bowel preparation was 46,45 and 45 in the three groups,respectively,with no significant difference.CONCLUSION:Administration of 10 mg bisacodyl enteric-coated tablets prior to or after oral administration of 2 L PEG-4000 electrolyte solution enhances stool and fluid cleansing ability,and has no impact on the attenuation value of residual fluid or the discomfort index.The former is an excellent alternative for CTC colorectum 展开更多
关键词 COLORECTAL cancer Screening COMPUTED tomographic COLONOGRAPHY POLYETHYLENE GLYCOL bisacodyl
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Bisacodyl and Sodium Picosulfate Improve Bowel Function and Quality of Life in Patients with Chronic Constipation—Analysis of Pooled Data from Two Randomized Controlled Trials 被引量:1
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作者 Stefan Müller-Lissner Erika Richter +3 位作者 Marion Eberlin Harald Weigmann Tobias Mück Michael A. Kamm 《Open Journal of Gastroenterology》 2017年第1期32-43,共12页
Background: Quality of life (QoL) is impaired in chronic constipation. Among nonprescription laxatives QoL data out of randomized controlled trials are available only for bisacodyl and sodium picosulfate (SPS). Method... Background: Quality of life (QoL) is impaired in chronic constipation. Among nonprescription laxatives QoL data out of randomized controlled trials are available only for bisacodyl and sodium picosulfate (SPS). Methods: In two randomized, double-blind, placebo-controlled, parallel-group trials, the efficacy and safety of treatment with either bisacodyl or SPS, respectively, were assessed. After a 2-week baseline period patients with functional constipation were randomized to a 4-week treatment with either bisacodyl (2 tablets = 10 mg), SPS (18 drops = 10 mg), or matching placebo in a ratio of active drug to placebo of 2:1. Dose reduction as well as resuming the original dose was permitted. Patients who did not experience a bowel movement for more than 72 h were allowed to use a bisacodyl suppository. The primary endpoint was the mean number of Complete Spontaneous Bowel Movements (CSBMs) per week during the trial. QoL was assessed using the Patient Assessment of Constipation (PAC)-QoL questionnaire. Results: Active treatment led to a greater improvement of PAC-QoL scores for every domain. Active treatment was also superior to placebo for all individual questions of the questionnaire. Of note, SPS or bisacodyl not only improved satisfaction with stool patterns (“quite a bit/extremely satisfied” in 12.8% of patients on placebo and 50.3% on active treatment) but bloating was also considerably ameliorated (“not at all feeling bloated” in 24.5% on placebo and 41.4% on active treatment). Conclusion: Bisacodyl and SPS not only improve stool variables but also quality of life in patients with chronic functional constipation. (EudraCT Nos. 2007-001991-34 and 2007-002087-10). 展开更多
关键词 CONSTIPATION LAXATIVE bisacodyl SODIUM Picosulfate Quality of Life
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益气活血灌肠方联合比沙可啶治疗老年排便障碍型便秘的临床疗效及机制探讨 被引量:2
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作者 孙健 陆金根 +2 位作者 林晖 张宸 丁超 《老年医学与保健》 CAS 2023年第2期390-397,共8页
目的 观察益气活血灌肠方联合比沙可啶治疗排便障碍型便秘气虚证的临床疗效及对肛门动力学的影响。方法 将2018年11月—2021年5月在上海市长宁区天山中医医院肛肠科门诊及病房就诊的排便障碍型便秘气虚证的80例患者采用随机数字表法分... 目的 观察益气活血灌肠方联合比沙可啶治疗排便障碍型便秘气虚证的临床疗效及对肛门动力学的影响。方法 将2018年11月—2021年5月在上海市长宁区天山中医医院肛肠科门诊及病房就诊的排便障碍型便秘气虚证的80例患者采用随机数字表法分为观察组、对照组,每组40例。观察组采用益气活血灌肠方保留灌肠配合口服比沙可啶,对照组采用口服比沙可啶,2组均治疗14 d。观察2组患者在肛门动力学方面的变化情况、临床疗效、便秘主要症状积分及PAC-QOL评分。结果 (1)最终完成试验者77例,其中观察组39例、对照组38例。(2)观察组的总有效率(92.31%)高于对照组(73.68%)(P<0.05)。(3)治疗前后组内比较,2组便秘症状各项积分、PAC-QOL四个维度方面的分值均较治疗前降低(P<0.05);组间治疗后比较,观察组的便秘症状积分及PAC-QOL分值均低于对照组(P<0.05)。(4)在肛门动力学方面,观察组在治疗后FSV、DSV、MTV等直肠阈感觉得到改善(P<0.05);肛管最大收缩压与治疗前相比有提升(P<0.05);直肠肛管抑制反射的例数较治疗前增加(P<0.05)、矛盾收缩的例数较治疗前减少(P<0.05)。而对照组治疗前后各项肛门动力学指标之间无显著性差异(P>0.05)。结论 益气活血灌肠方联合比沙可啶能明显改善排便障碍型便秘患者的临床症状,其机制可能与通过中医灌肠技术改善患者的直肠阈感觉、增加肛管收缩力,改善直肠肛门括约肌的不协调运动有关。 展开更多
关键词 老年 中药保留灌肠 肛门动力学 便秘 益气活血方 比沙可啶
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腹部穴位按摩治疗老年人功能性便秘疗效观察 被引量:22
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作者 刘雯霞 刘占举 《胃肠病学》 2017年第6期367-369,共3页
背景:老年人功能性便秘(FC)患病率高,寻找简单、安全、有效的治疗方案具有重要意义。目的:观察腹部穴位按摩治疗老年人FC的疗效和安全性。方法:151例老年FC患者纳入研究,随机分为3组,分别接受比沙可啶5 mg qd口服、每日3次按摩关元、中... 背景:老年人功能性便秘(FC)患病率高,寻找简单、安全、有效的治疗方案具有重要意义。目的:观察腹部穴位按摩治疗老年人FC的疗效和安全性。方法:151例老年FC患者纳入研究,随机分为3组,分别接受比沙可啶5 mg qd口服、每日3次按摩关元、中脘、天枢穴和两种方法联合治疗,疗程4周。记录每周排便次数,行便秘患者症状自评量表(PAC-SYM)评分。结果:三组患者基线情况无明显差异(P>0.05)。治疗1、2、4周后,三组每周排便次数、PAC-SYM总分和各维度评分均较治疗前显著改善(P<0.05)。比沙可啶对排便次数、粪便性状、直肠症状的改善作用优于穴位按摩(P<0.05),穴位按摩对腹部症状的改善作用优于比沙可啶(P<0.05)。比沙可啶不良反应轻微,穴位按摩无不良反应发生。结论:腹部穴位按摩可安全、有效地改善老年FC患者的排便次数和便秘症状,尤其是腹痛、腹胀等腹部症状。 展开更多
关键词 穴位按压 比沙可啶 功能性便秘 老年人
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高效液相色谱法测定便秘糖衣丸中3种有效成分的含量 被引量:3
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作者 徐文峰 金鹏飞 +4 位作者 徐硕 姜文清 吴学军 邝咏梅 徐巧玲 《中南药学》 CAS 2019年第9期1525-1528,共4页
目的建立高效液相色谱法测定便秘糖衣丸中比沙可啶、番泻苷A和番泻苷B的含量。方法采用Alltima C18色谱柱(150 mm×4.6 mm,5μm),乙腈-30 mmol·L^-1磷酸二氢铵溶液为流动相,流速为1.0m L·min^-1,比沙可啶的检测波长为265 ... 目的建立高效液相色谱法测定便秘糖衣丸中比沙可啶、番泻苷A和番泻苷B的含量。方法采用Alltima C18色谱柱(150 mm×4.6 mm,5μm),乙腈-30 mmol·L^-1磷酸二氢铵溶液为流动相,流速为1.0m L·min^-1,比沙可啶的检测波长为265 nm,番泻苷A和番泻苷B的检测波长为340 nm。结果比沙可啶、番泻苷A与番泻苷B的线性范围分别为26.23~419.68μg·mL^-1、9.72~194.44μg·m L^-1、9.54~190.72μg·m L^-1,相关系数分别为0.9998、0.9997、0.9993,上述3种化学成分平均加样回收率分别为98.6%、97.5%、97.2%,RSD均小于3%。结论该方法可用于测定便秘糖衣丸中比沙可啶、番泻苷A和番泻苷B的含量。 展开更多
关键词 便秘糖衣丸 比沙可啶 番泻苷A 番泻苷B 含量测定
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聚乙二醇4000联合比沙可啶对帕金森病患者便秘症状及相关生活质量的影响 被引量:9
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作者 朱敏 刘高飞 李达文 《临床军医杂志》 CAS 2014年第8期783-785,共3页
目的探讨聚乙二醇4000联合比沙可啶对帕金森病患者便秘症状及相关生活质量的影响。方法将98例明确诊断为帕金森病便秘的患者随机分为试验组49例和对照组49例,其中对照组予以聚乙二醇4000口服,治疗组在对照组方案基础上联合比沙可啶肠溶... 目的探讨聚乙二醇4000联合比沙可啶对帕金森病患者便秘症状及相关生活质量的影响。方法将98例明确诊断为帕金森病便秘的患者随机分为试验组49例和对照组49例,其中对照组予以聚乙二醇4000口服,治疗组在对照组方案基础上联合比沙可啶肠溶片口服,疗程均为2周,观察比较两组患者的大便频率、形状等便秘相关症状及其相关生活质量的变化。结果完成本研究试验者共87例,其中对照组44例,治疗后排便频率和粪便性状均有明显改善(P<0.05),治疗组43例患者在排便频率、粪便性状及费力程度等相关症状方面均较治疗前显著改善(P<0.05),组间比较:治疗组优于对照组(P<0.05);两组患者治疗后生活质量评分均有降低(P<0.05),且组间比较治疗组明显优于对照组,差异有统计学意义(P<0.05)。结论聚乙二醇4000联合比沙可啶对有效改善帕金森病患者便秘相关症状、提高其生活质量具有重要作用。 展开更多
关键词 联合疗法 帕金森病 便秘 聚乙二醇4000 比沙可啶
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比沙可啶的研究概况及临床应用 被引量:3
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作者 黄敏 陈继红 +2 位作者 谭诗云 罗和生 Jan DHuizinga 《胃肠病学和肝病学杂志》 CAS 2017年第2期227-230,共4页
结肠动力障碍性疾病如慢性便秘是一种临床常见疾病,治疗药物种类繁多,其中刺激性泻剂比沙可啶(Bisacodyl)历史悠久,有较好的治疗效果。随着人结肠测压技术的进展,其作用不仅限于治疗,还可作为诊断结肠动力异常尤其是神经性损伤的生物标... 结肠动力障碍性疾病如慢性便秘是一种临床常见疾病,治疗药物种类繁多,其中刺激性泻剂比沙可啶(Bisacodyl)历史悠久,有较好的治疗效果。随着人结肠测压技术的进展,其作用不仅限于治疗,还可作为诊断结肠动力异常尤其是神经性损伤的生物标记物之一,使其在研究领域和临床上褒贬不一。至今,Bisacodyl的主要作用机制尤其是结肠动力方面尚不明确,本文就Bisacodyl对结肠影响、作用机制及结肠测压中的应用作一概述。 展开更多
关键词 比沙可啶 便秘 结肠动力 人结肠测压
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RP-HPLC法测定比沙可啶片剂含量及有关物质 被引量:11
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作者 王卉 杜春波 +1 位作者 沈立 刘文英 《药学进展》 CAS 2005年第12期565-568,共4页
目的建立RP-HPLC法测定比沙可啶片剂含量及有关物质。方法色谱柱为Hypersil ODS C18(300mm×4mm,5μm),以乙腈-水(45∶55)为流动相,流速为1.0mL/min,进样量为10μL,检测波长为265nm。结果比沙可啶浓度在0.115~1.150g/L范围内,色谱... 目的建立RP-HPLC法测定比沙可啶片剂含量及有关物质。方法色谱柱为Hypersil ODS C18(300mm×4mm,5μm),以乙腈-水(45∶55)为流动相,流速为1.0mL/min,进样量为10μL,检测波长为265nm。结果比沙可啶浓度在0.115~1.150g/L范围内,色谱峰面积与浓度线性关系良好,r=0.9999;线性范围内3个浓度的平均回收率(n=3)分别为99.2%(RSD=0.68%)、99.3%(RSD=0.21%)和99.1%(RSD=0.87%)。样品中有关物质检查符合质量要求。结论该方法简便、快速、准确、重现性好,可用于比沙可啶片剂的含量测定和有关物质检查。 展开更多
关键词 反相高效液相色谱法 比沙可啶片剂 含量测定 有关物质
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发酵方竹笋对蒙脱石散诱导便秘的预防效果研究 被引量:1
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作者 李贵节 徐廷祥 +4 位作者 张腾辉 邓刚 梁宇 罗德跃 赵欣 《西南师范大学学报(自然科学版)》 CAS 北大核心 2015年第4期36-41,共6页
通过动物实验对发酵方竹笋对蒙脱石散诱导小鼠便秘的预防效果进行了研究.建立便秘动物模型,观察饲喂发酵方竹笋对便秘小鼠的影响.结果显示发酵方竹笋喂养组小鼠的体质量变化接近正常小鼠,高于对照组小鼠.发酵方竹笋喂养组小鼠排出首粒... 通过动物实验对发酵方竹笋对蒙脱石散诱导小鼠便秘的预防效果进行了研究.建立便秘动物模型,观察饲喂发酵方竹笋对便秘小鼠的影响.结果显示发酵方竹笋喂养组小鼠的体质量变化接近正常小鼠,高于对照组小鼠.发酵方竹笋喂养组小鼠排出首粒黑便的时间(104min)低于对照组(185min)和未发酵方竹笋喂养组(122min),高于正常组(68min)和比沙可啶治疗组(90min).活性炭在发酵方竹笋喂养组小鼠(68.7%)小肠中的推进率也高于对照组(38.3%)和未发酵方竹笋喂养组(50.4%),低于正常组(98.3%)和比沙可啶治疗组(79.3%).发酵方竹笋喂养组小鼠血清的胃动素(MTL)、内皮素-1(ET-1)、血管活性肠肽(VIP)和乙酰胆碱酯酶(AchE)水平也显著高于对照组和方竹笋喂养组,低于正常组和比沙可啶治疗组.通过显微镜观察发现,发酵方竹笋纤维品质比未发酵方竹笋更好,有利于预防便秘.发酵方竹笋是一种具有良好抑制便秘作用的健康食品. 展开更多
关键词 方竹笋 发酵 蒙脱石散 便秘 比沙可啶
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HPLC法测定比沙可啶肠溶片的有关物质 被引量:6
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作者 袁志江 李晓红 《中国药事》 CAS 2009年第8期799-800,785,共3页
目的建立测定比沙可啶肠溶片有关物质的高效液相色谱法。方法采用色谱柱:Kromasil C18柱;流动相:甲醇-水-冰醋酸(65:35:0.1);流速:1mL·min^-1;检测波长:263nm;进样量:20μL;柱温:室温。结果比沙可啶肠在2~10μg&#... 目的建立测定比沙可啶肠溶片有关物质的高效液相色谱法。方法采用色谱柱:Kromasil C18柱;流动相:甲醇-水-冰醋酸(65:35:0.1);流速:1mL·min^-1;检测波长:263nm;进样量:20μL;柱温:室温。结果比沙可啶肠在2~10μg·mL^-1(r=0.9999)范围内线性关系良好。结论实验表明,该方法准确、可靠、重现性好,可用于测定比沙可啶肠溶片的有关物质。 展开更多
关键词 比沙可啶肠溶片 有关物质 HPLC法
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比沙可啶合成工艺研究 被引量:3
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作者 张奕华 侯秀清 黄赐福 《中国药师》 CAS 1999年第1期7-8,共2页
比沙可啶是国外广泛应用的一种理想的缓泻药。参照文献方法并加以改进和创新,合成了该药。以α-皮考啉为起始原料,经氧化、加成、缩合和酸化反应,获得目的物,总收率为14.7%(文献收率8.64%)。
关键词 比沙可啶 合成 工艺
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比沙可啶对照品的建立 被引量:1
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作者 王卉 叶小敏 +1 位作者 蔡振利 王强 《中国药师》 CAS 2009年第7期860-862,共3页
目的:建立供含量测定用的比沙可啶对照品。方法:将比沙可啶原料药精制后获得比沙可啶精制品,通过UV、IR、DSC等手段进行鉴别,并用TLC、HPLC、DSC、电位滴定等多种方法进行纯度分析及含量测定。结果:TLC法表明其有关物质的量低于1%;HPLC... 目的:建立供含量测定用的比沙可啶对照品。方法:将比沙可啶原料药精制后获得比沙可啶精制品,通过UV、IR、DSC等手段进行鉴别,并用TLC、HPLC、DSC、电位滴定等多种方法进行纯度分析及含量测定。结果:TLC法表明其有关物质的量低于1%;HPLC、DSC法、电位滴定法测得的比沙可啶精制品的绝对含量分别为99.6%、99.5%、100.6%。结论:比沙可啶精制品的纯度符合供含量测定用对照品的要求。 展开更多
关键词 比沙可啶 对照品 含量测定
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比沙可啶栓剂与片剂治疗便秘的临床比较 被引量:1
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作者 沈立 梅师祖 +5 位作者 韩光曙 徐兆明 周亚夫 殷凯生 杨美兰 洪立基 《药学进展》 CAS 1997年第4期237-240,共4页
218例便秘患者,其中111例使用比沙可啶栓剂治疗,107例使用比沙可啶片剂治疗,两组间进行比较,结果总有效率:栓剂100%,片剂96.3%;显效率:栓剂94.6%,片剂76.6%;平均起效时间:栓剂1.77h,片剂... 218例便秘患者,其中111例使用比沙可啶栓剂治疗,107例使用比沙可啶片剂治疗,两组间进行比较,结果总有效率:栓剂100%,片剂96.3%;显效率:栓剂94.6%,片剂76.6%;平均起效时间:栓剂1.77h,片剂11.45h.两组均无明显毒副作用。 展开更多
关键词 比沙可啶 便秘 栓剂 片剂 疗效
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Efficacy and tolerability of high and low-volume bowel preparation compared:A real-life single-blinded large-population study 被引量:4
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作者 Vincenzo Occhipinti Paola Soriani +8 位作者 Francesco Bagolini Valentina Milani Emanuele Rondonotti Maria Laura Annunziata Flaminia Cavallaro Sara Vavassori Maurizio Vecchi Luca Pastorelli Gian Eugenio Tontini 《World Journal of Gastrointestinal Endoscopy》 2021年第12期659-672,共14页
BACKGROUND Low-volume preparations for colonoscopy have shown similar efficacy compared to high-volume ones in randomized controlled trials(RCT).However,most RCTs do not provide data about clinical outcomes including ... BACKGROUND Low-volume preparations for colonoscopy have shown similar efficacy compared to high-volume ones in randomized controlled trials(RCT).However,most RCTs do not provide data about clinical outcomes including lesions detection rate.Moreover,real-life comparisons are lacking.AIM To compare efficacy(both in terms of adequate bowel preparation and detection of colorectal lesions)and tolerability of a high-volume(HV:4 L polyethylene glycol,PEG)and a low-volume(LV:2 L PEG plus bisacodyl)bowel preparation in a real-life setting.METHODS Consecutive outpatients referred for colonoscopy were prospectively enrolled between 1 December 2014 and 31 December 2016.Patients could choose either LV or HV preparation,with a day-before schedule for morning colonoscopies and a split-dose for afternoon procedures.Adequate bowel preparation according to Boston Bowel Preparation Scale(BBPS),clinical outcomes including polyp detection rate(PDR),adenoma detection rate(ADR),advanced adenoma detection rate(AADR),sessile/serrated lesion detection rate(SDR)and cancer detection rate and self-reported tolerability of HV and LV were blindly assessed.RESULTS Total 2040 patients were enrolled and 1815(mean age 60.6 years,50.2%men)finally included.LV was chosen by 52%of patients(50.8%of men,54.9%of women).Split-dose schedule was more common with HV(44.7%vs 38.2%,P=0.005).High-definition scopes were used in 33.4%of patients,without difference in the two groups(P=0.605).HV and LV preparations showed similar adequate bowel preparation rates(89.2%vs 86.6%,P=0.098),also considering the two different schedules(HV split-dose 93.8%vs LV split-dose 93.6%,P=1;HV daybefore 85.5%vs LV day-before 82.3%,P=0.182).Mean global BBPS score was higher for HV preparations(7.1±1.7 vs 6.8±1.6,P<0.001).After adjustment for sex,age and indications for colonoscopy,HV preparation resulted higher in PDR[Odds ratio(OR)1.32,95%CI:1.07-1.63,P=0.011]and ADR(OR 1.29,95%CI 1.02–1.63,P=0.038)and comparable to LV in AADR(OR 1.51,95%CI 0.97-2.35,P=0.069),SDR and cancer detection rate.The use of standard-definition colonoscopes was associated to lower PDR(adjusted OR 1.59,95%CI:1.22-2.08,P<0.001),ADR(adjusted OR 1.71,95%CI:1.26–2.30,P<0.001)and AADR(adjusted OR 1.97,95%CI:1.09-3.56,P=0.025)in patients receiving LV preparation.Mean Visual Analogue Scale tolerability scored equally(7,P=0.627)but a≥75%dose intake was more frequent with LV(94.6%vs 92.1%,P=0.003).CONCLUSION In a real-life setting,PEG-based low-volume preparation with bisacodyl showed similar efficacy and tolerability compared to standard HV preparation.However,with higher PDR and ADR,HV should still be considered as the reference standard for clinical trials and the preferred option in screening colonoscopy,especially when colonoscopy is performed with standard resolution imaging. 展开更多
关键词 Bowel preparation volume Polyethylene glycol bisacodyl COLONOSCOPY Colonic adenomas TOLERABILITY
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Colonic preparation before colonoscopy in constipated and non-constipated patients:A randomized study 被引量:1
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作者 Lisandro Pereyra Daniel Cimmino +7 位作者 Carlos González Malla Mariano Laporte Nicolás Rotholtz Carlos Peczan Sandra Lencinas Silvia Pedreira Hugo Catalano Luis Boerr 《World Journal of Gastroenterology》 SCIE CAS 2013年第31期5103-5110,共8页
AIM: To compare the efficacy of different doses of sodium phosphate(NaP) and polyethylenglicol(PEG) alone or with bisacodyl for colonic cleansing in constipated and non-constipated patients.METHODS: Three hundred and ... AIM: To compare the efficacy of different doses of sodium phosphate(NaP) and polyethylenglicol(PEG) alone or with bisacodyl for colonic cleansing in constipated and non-constipated patients.METHODS: Three hundred and forty-nine patients,older than 18 years old,with low risk for renal damage and who were scheduled for outpatient colonoscopy were randomized to receive one of the following preparations(prep): 90 mL of NaP(prep 1);45 mL of NaP + 20 mg of bisacodyl(prep 2);4 L of PEG(prep 3) or 2 L of PEG + 20 mg of bisacodyl(prep 4).Randomization was stratified by constipation.Patients,endoscopists,endoscopists' assistants and data analysts were blinded.A blinding challenge was performed to endoscopist in order to reassure blinding.The primary outcome was the efficacy of colonic cleansing using a previous reported scale.Secondary outcomes were tolerability,compliance,side effects,endoscopist perception about the necessity to repeat the study due to an inadequate colonic preparation and patient overall perceptions.RESULTS: Information about the primary outcome was obtained from 324 patients(93%).There were no significant differences regarding the preparation quality among different groups in the overall analysis.Compliance was higher in the NaP preparations being even higher in half-dose with bisacodyl: 94%(prep 1),100%(prep 2),81%(prep 3) and 87%(prep 4)(2 vs 1,3 and 4,P < 0.01;1 vs 3,4,P < 0.05).The combination of bisacodyl with NaP was associated with insomnia(P = 0.04).In non-constipated patients the preparation quality was also similar between different groups,but endoscopist appraisal about the need to repeat the study was more frequent in the half-dose PEG plus bisacodyl than in whole dose NaP preparation: 11%(prep 4) vs 2%(prep 1)(P < 0.05).Compliance in this group was also higher with the NaP preparations: 95%(prep 1),100%(prep2) vs 80%(prep 3)(P < 0.05).Bisacodyl was associated with abdominal pain: 13%(prep 1),31%(prep 2),21%(prep 3) and 29%(prep 4),(2,4 vs 1,2,P < 0.05).In constipated patients the combination of NaP plus bisacodyl presented higher rates of satisfactory colonic cleansing than whole those PEG: 95%(prep 2) vs 66%(prep 3)(P = 0.03).Preparations containing bisacodyl were not associated with adverse effects in constipated patients.CONCLUSION: In non-constipated patients,compliance is higher with NaP preparations,and bisacodyl is related to adverse effects.In constipated patients NaP plus bisacodyl is the most effective preparation. 展开更多
关键词 COLONIC CLEANSING Sodium phosphate Polyethylenglicol bisacodyl CONSTIPATION COLONOSCOPY
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中药导入气流弥散法治疗便秘的疗效观察 被引量:5
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作者 赵璟 《中医学报》 CAS 2011年第6期742-743,共2页
目的:比较中药导入气流弥散法治疗便秘和口服西药治疗便秘的临床疗效。方法:选择2008年9月至2010年9月门诊治疗的便秘患者82例,分为气弥组56例(中药导入气流弥散法治疗);西药组26例(口服西药比沙可啶片治疗),分别记录临床症状,经统计学... 目的:比较中药导入气流弥散法治疗便秘和口服西药治疗便秘的临床疗效。方法:选择2008年9月至2010年9月门诊治疗的便秘患者82例,分为气弥组56例(中药导入气流弥散法治疗);西药组26例(口服西药比沙可啶片治疗),分别记录临床症状,经统计学处理比较两种方法治疗便秘的有效率和复发率。结果:两种方法治疗便秘的有效率和复发率经统计学检验有显着性差异(P<0.05)。结论:中药导入气流弥散法治疗便秘疗效明显优于口服西药治疗便秘,且疗效确切,治疗方法无痛苦,值得广泛应用。 展开更多
关键词 便秘 中药导入气流弥散法 芪黄肠康液 沙可啶片
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Development of triple-layered tablets containing laxatives with a hydrophilic polymer
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作者 Woo Heon Song Jin Seob Oh +1 位作者 Kyung Soo Lee Jun Sang Park 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2016年第1期134-135,共2页
Constipation is a common functional gastrointestinal disorder which has caused much discomfort affecting the quality of life. The prevalence of constipation in the general population is approximately 20%(1)Various kin... Constipation is a common functional gastrointestinal disorder which has caused much discomfort affecting the quality of life. The prevalence of constipation in the general population is approximately 20%(1)Various kinds of laxatives were introduced such as bulking agent, stool softener, stimulant, and osmotic agent (2)Fixed dose combination with bisacodyl as a stimulant and docusate sodium as a stool softener, Ducolax STM, was developed as enteric coated tablets targeting colon. 展开更多
关键词 HYDROPHILIC polymer Sodium CARBOXYMETHYLCELLULOSE bisacodyl Triple-layered tablet
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口服复方聚乙二醇-4000前吞服比沙可啶对简化CT结肠镜肠道清洁准备的作用 被引量:2
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作者 陈志远 沈合松 +6 位作者 罗明月 段侪杰 卢虹冰 张国鹏 刘洋 Wen-Li CAI Jerome Z LIANG 《中国医学影像技术》 CSCD 北大核心 2013年第4期577-581,共5页
目的探讨口服复方聚乙二醇-4000前吞服比沙可啶对简化CT结肠镜肠道清洁准备的作用。方法将40例接收CT结肠镜检查的患者随机均分成试验组、对照组。检查前1天,试验组三餐前口服40%W/V硫酸钡20ml,晚餐后将60%泛影葡胺20ml溶于250ml水并服... 目的探讨口服复方聚乙二醇-4000前吞服比沙可啶对简化CT结肠镜肠道清洁准备的作用。方法将40例接收CT结肠镜检查的患者随机均分成试验组、对照组。检查前1天,试验组三餐前口服40%W/V硫酸钡20ml,晚餐后将60%泛影葡胺20ml溶于250ml水并服完,口服2L复方聚乙二醇-4000电解质液之前1h吞服10mg比沙可啶肠溶片;对照组不吞服比沙可啶,其余同试验组。统计分析两组结直肠存留肠液评分、存留肠液CT值及存留粪块评分。结果试验组存留肠液平均评分(1.50±0.06)低于对照组(1.78±0.08),差异有统计学意义(P=0.024)。试验组、对照组存留肠液平均CT值分别为(729±29)HU、(597±27)HU,差异无统计学意义(P>0.05)。试验组存留粪块评分(1.96±0.11)低于对照组(2.63±0.12),差异有统计学意义(P=0.001)。结论口服复方聚乙二醇-4000前吞服比沙可啶既可增强对肠液的清洁能力,又不影响存留肠液CT值,同时可增强对肠道粪块的清洁能力,较单独口服复方聚乙二醇-4000的肠道清洁效果好,是CT结肠镜前较好的简化肠道准备方法。 展开更多
关键词 结肠肿瘤 筛查 聚乙烯二醇类 比沙可啶
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