Laxative

泻药
  • 文章类型: Journal Article
    自古以来,植物已被用作治疗多种疾病的药物。植物的药理特性是由于次级代谢产物如萜类化合物的存在,黄酮类化合物,生物碱,等。蒽醌代表在各种植物物种中大量发现的一组天然存在的醌。蒽醌由于其在治疗多种疾病中的报道功效而引起大量关注。它们复杂的化学结构,结合固有的药用特性,强调了它们作为治疗药物的潜力。他们展示了几种治疗特性,如泻药,抗肿瘤,抗疟药,抗菌,抗真菌药,抗氧化剂,等。蒽醌在植物中以不同的形式(衍生物)被发现,由于它们的结构和化学性质,它们表现出各种药用特性。高等植物中蒽醌生物合成的前体是通过不同的途径提供的,例如质体半类2-C-甲基-D-erthriol4-磷酸酯(MEP),甲羟戊酸(MVA),异氯酸盐合成酶和聚酮。通过对科学文献进行彻底的分析,这篇综述提供了对蒽醌生物合成及其对人类健康的广泛贡献之间复杂相互作用的见解。
    Since ancient times, plants have been used as a remedy for numerous diseases. The pharmacological properties of plants are due to the presence of secondary metabolites like terpenoids, flavonoids, alkaloids, etc. Anthraquinones represent a group of naturally occurring quinones found generously across various plant species. Anthraquinones attract a significant amount of attention due to their reported efficacy in treating a wide range of diseases. Their complex chemical structures, combined with inherent medicinal properties, underscore their potential as agents for therapy. They demonstrate several therapeutic properties such as laxative, antitumor, antimalarial, antibacterial, antifungal, antioxidant, etc. Anthraquinones are found in different forms (derivatives) in plants, and they exhibit various medicinal properties due to their structure and chemical nature. The precursors for the biosynthesis of anthraquinones in higher plants are provided by different pathways such as plastidic hemiterpenoid 2-C-methyl-D-erthriol4-phosphate (MEP), mevalonate (MVA), isochorismate synthase and polyketide. By conducting a thorough analysis of scientific literature, this review provides insights into the intricate interplay between anthraquinone biosynthesis and its broad-ranging contributions to human health.
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  • 文章类型: Journal Article
    背景:便秘在全球范围内引起大量发病率。方法:这项调查使用日本版本的肠易激综合征生活质量(IBS-QOL-J)工具评估了日本的便秘相关因素。我们还检查了泻药类型之间的关系,布里斯托尔凳子表格量表(BSFS)得分,和治疗费用。最后,我们根据泻药类型检查了满意度得分的差异,治疗类型,治疗费用,和BSFS得分。结果:服用盐和/或刺激性泻药的人中IBS-QOL-J较高。那些支付>5000日元(50.00美元)的IBS-QOL-J最低。在BSFS评分为1或2(严重便秘)的人群中,IBS-QOL-J明显较低。结论:这项研究的结果表明,各种因素,包括治疗类型和费用,与排便满意度有关。那些有硬凳子的人,使用多种泻药,或花更多的治疗不太满意。未来的策略应针对不需要多种泻药且治疗成本较低的疗法。以最低的成本使用少量适当的泻药进行适当的排便似乎可以提高排便满意度。需要确定适当的泻药并改善饮食习惯和锻炼程序。还必须停止盲目增加泻药的使用,并正确诊断便秘障碍,例如功能性便秘以外的解剖学异常。
    Background: Constipation causes substantial morbidity worldwide. Methods: This survey assessed constipation-related factors in Japan using the Japanese version of the Irritable Bowel Syndrome Quality of Life (IBS-QOL-J) instrument. We also examined the relationship among laxative type, Bristol Stool Form Scale (BSFS) scores, and treatment cost. Finally, we examined differences in satisfaction scores according to laxative type, treatment type, treatment cost, and BSFS score. Results: IBS-QOL-J was higher among those taking salt and/or irritation laxatives. Those paying >JPY 5000 (USD 50.00) had the lowest IBS-QOL-J. IBS-QOL-J was significantly lower among those with a BSFS score of 1 or 2 (severe constipation). Conclusions: This study\'s findings suggest that a variety of factors, including treatment type and cost, are associated with defecation satisfaction. Those who had hard stools, used multiple laxatives, or spent more on treatment were less satisfied. Future strategies should target therapies that do not require multiple laxatives with lower treatment costs. Adequate defecation with a small number of appropriate laxatives at minimal cost appears to improve defecation satisfaction. It is desirable to identify appropriate laxatives and improve dietary habits and exercise routines. It is also necessary to stop blindly increasing laxative usage and properly diagnose constipation disorders such as anatomical abnormalities other than functional constipation.
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  • 文章类型: Journal Article
    背景:掌叶大黄,R.tangutum,和R.officinale,大黄属的整体种,在全球温带和亚热带地区广泛使用。这些物种被纳入功能性食品中,药物,和化妆品,它们大量的生物活性成分。
    目的:这篇综述旨在综合2014年至2023年有关植物学特征的发展,民族药理学,营养价值,化学成分,药理活性,行动机制,和这些物种的毒性。
    方法:三种大黄的数据来自对同行评审文章的全面回顾,专利,以及通过PubMed获得的临床试验,谷歌学者,WebofScience,和CNKI。
    结果:地上部分营养丰富,提供必需氨基酸,脂肪酸,矿物,适合用作保健食品或补充剂。研究已经确定了143种化合物,包括蒽醌,anthrones,黄酮类化合物,和色原,这有助于它们广泛的药理特性,如泻药,抗腹泻,神经保护,保肝,心血管,抗糖尿病药,抗肿瘤,抗炎,抗病毒,和抗菌作用。值得注意的是,通过评估不同治疗环境中的生物活性化合物,材料科学方法增强了对其药用能力的理解。
    结论:作为具有药用和经济意义的草本植物,大黄物种提供可食用的地上部分和提供实质性健康益处的药用地下成分。这些特点为开发营养成分和治疗产品提供了新的机会,支持食品和制药行业。
    BACKGROUND: Rheum palmatum, R. tanguticum, and R. officinale, integral species of the genus Rheum, are widely used across global temperate and subtropical regions. These species are incorporated in functional foods, medicines, and cosmetics, recognized for their substantial bioactive components.
    OBJECTIVE: This review aims to synthesize developments from 2014 to 2023 concerning the botanical characteristics, ethnopharmacology, nutritional values, chemical compositions, pharmacological activities, mechanisms of action, and toxicity of these species.
    METHODS: Data on the three Rheum species were gathered from a comprehensive review of peer-reviewed articles, patents, and clinical trials accessed through PubMed, Google Scholar, Web of Science, and CNKI.
    RESULTS: The aerial parts are nutritionally rich, providing essential amino acids, fatty acids, and minerals, suitable for use as health foods or supplements. Studies have identified 143 chemical compounds, including anthraquinones, anthrones, flavonoids, and chromones, which contribute to their broad pharmacological properties such as laxative, anti-diarrheal, neuroprotective, hepatoprotective, cardiovascular, antidiabetic, antitumor, anti-inflammatory, antiviral, and antibacterial effects. Notably, the materials science approach has enhanced understanding of their medicinal capabilities through the evaluation of bioactive compounds in different therapeutic contexts.
    CONCLUSIONS: As medicinal and economically significant herb species, Rheum species provide both edible aerial parts and medicinal underground components that offer substantial health benefits. These characteristics present new opportunities for developing nutritional ingredients and therapeutic products, bolstering the food and pharmaceutical industries.
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  • 文章类型: Journal Article
    人们经常抱怨长期便秘。使用现代药物治疗便秘的成本是巨大的,并且遇到副作用的可能性非常高。这些限制限制了它们在治疗中的有效性,仍未解决,并强调需要研究替代治疗方法。蒿属植物已用于治疗便秘。因此,这项研究的目的是评估水的A.abysicia叶和茎提取物对小鼠的泻药作用。
    使用三种模型评估了深参叶和茎提取物的泻药活性:泻药活性,胃肠蠕动,和胃肠分泌。在这项研究中,比沙可啶被用作标准泻药,洛哌丁胺被用于诱发便秘。
    在泻药试验中,200(P<0.05)和400mg/kg(p<0.01)剂量的植物提取物显着增加了粪便含水量的百分比。此外,最高剂量的提取物增加了12h后排便的频率(p<0.05)。在剩下的两个模型中,实验计划还显示出明显更高的胃肠蠕动和明显的肠液积累。
    这项研究的结果表明,A.abysinica的水性叶和茎提取物具有通便作用。
    UNASSIGNED: People frequently complain of long-term constipation. The cost associated with using modern medications to treat constipation is significant, and the probability of encountering side effects is notably high. These limitations restrict their effectiveness in therapy, remain unresolved, and underscore the need for research on alternative therapeutic approaches. Plants of the genus Artemisia have been used to treat constipation. Therefore, the aim of this study was to evaluate the laxative effects of aqueous A. abyssinica leaf and stem extracts of Artemisia abyssinica in mice.
    UNASSIGNED: The laxative activity of A. abyssinica leaf and stem extracts was evaluated using three models: laxative activity, gastrointestinal motility, and gastrointestinal secretion. In this study, bisacodyl was used as a standard laxative and loperamide was used to induce constipation.
    UNASSIGNED: In the laxative test, 200 (P<0.05) and 400 mg/kg (p<0.01) doses of plant extract significantly increased the percentage of fecal water content. Moreover, the highest dose of extract increased the frequency of defecation after 12 h (p<0.05). In the remaining two models, the experimental plans also showed significantly higher gastrointestinal motility and noticeable accumulation of intestinal fluid.
    UNASSIGNED: The results of this study indicate that aqueous leaf and stem extracts of A. abyssinica have laxative effects.
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  • 文章类型: Journal Article
    除了众所周知的阿片类药物的不良反应外,比如便秘,越来越多的证据也支持潜在的免疫抑制作用。
    在这项研究中,我们对阿片类药物抑制免疫系统的临床前和临床证据以及治疗的可能考虑因素进行了叙述性综述.
    体外和动物研究表明,阿片类药物对炎性细胞因子表达有明确的影响,免疫细胞活性,和病原体易感性。迄今为止,人类的观察数据支持临床前发现,在各种阿片类药物使用情况下,有多个感染率上升的报告。然而,与阿片类药物使用相关的其他风险因素相比,阿片类药物对免疫系统的影响导致这种风险的程度仍不确定.考虑到显示免疫抑制和阿片类药物感染风险增加的数据,需要持续接受阿片类药物治疗的患者需要采取措施来降低这种风险.在临床前研究中,阿片受体拮抗剂的给药阻断了阿片类药物的免疫调节作用。
    作为外周阿片受体的选择性拮抗剂,外周作用的μ阿片受体(MOR)拮抗剂可能能够防止免疫损伤,同时仍允许阿片类药物镇痛。未来的研究有必要进一步研究阿片类药物与感染风险之间的关系,以及外周作用MOR拮抗剂在抵消这些风险方面的潜在应用。
    UNASSIGNED: In addition to the more well-known adverse effects of opioids, such as constipation, mounting evidence supports underlying immunosuppressive effects as well.
    UNASSIGNED: In this study, we provide a narrative review of preclinical and clinical evidence of opioid suppression of the immune system as well as possible considerations for therapies.
    UNASSIGNED: In vitro and animal studies have shown clear effects of opioids on inflammatory cytokine expression, immune cell activity, and pathogen susceptibility. Observational data in humans have so far supported preclinical findings, with multiple reports of increased rates of infections in various settings of opioid use. However, the extent to which this risk is due to the impact of opioids on the immune system compared with other risk factors associated with opioid use remains uncertain. Considering the data showing immunosuppression and increased risk of infection with opioid use, measures are needed to mitigate this risk in patients who require ongoing treatment with opioids. In preclinical studies, administration of opioid receptor antagonists blocked the immunomodulatory effects of opioids.
    UNASSIGNED: As selective antagonists of peripheral opioid receptors, peripherally acting mu-opioid receptor (MOR) antagonists may be able to protect against immune impairment while still allowing for opioid analgesia. Future research is warranted to further investigate the relationship between opioids and infection risk as well as the potential application of peripherally acting MOR antagonists to counteract these risks.
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  • 文章类型: Journal Article
    关于药物引起的便秘(DIC)的详细临床信息有限。本研究旨在调查DIC的实际情况。
    这项回顾性研究使用了2014年至2021年注册的日本索赔数据库的数据。便秘队列包括至少有一个治疗便秘记录的受试者,而非便秘队列是通过随机分层抽样方法选择的,按性别匹配便秘队列。使用倾向评分将具有至少一个已知致病药物(CD)病史的研究人群和对照进行1:1匹配。潜在DIC(PDIC)的比例,PDIC的诊断时机,计算了CD和泻药按药物类别划分的处方比例,同时进行logistic回归分析以探讨其他相关因素.
    在4533905个科目中,178852在研究人群和对照中均合格。pDIC组包括19485名患者,占所有治疗便秘受试者的10.9%,而非便秘型CD组有10430名受试者。记录的CD处方和治疗的便秘之间的中位持续时间为38.0天。最常用的CD是心血管药物(47.9%)。所有CD类,作为男性,一些合并症与pDIC的发生有关。
    pDIC受试者占所有治疗便秘病例的约11%。由于与其他便秘类型相比,DIC需要不同的治疗方案,医生应该认识到为患者提供优化的治疗方法。
    UNASSIGNED: Detailed clinical information regarding drug-induced constipation (DIC) is limited. This study aimed to investigate the real-world situation of DIC.
    UNASSIGNED: This retrospective study used data from a Japanese claims database registered from 2014 to 2021. The constipation cohort included subjects with at least one record of treated constipation, while the non-constipation cohort was selected through random stratified sampling method, to match the constipation cohort by gender. The study population and control with at least one history of a known causative drug (CD) were matched 1:1 using propensity scores. The proportion of potential DIC (pDIC), the timing of diagnosis for pDIC, and the proportion of prescriptions by drug class for both the CDs and the laxatives were calculated, while logistic regression analysis was performed to explore additional associated factors.
    UNASSIGNED: Of the 4 533 905 subjects, 178 852 were eligible in both the study population and the control. The pDIC group comprised of 19 485 patients, which accounted for 10.9% of all treated constipation subjects, while the non-constipation with CD group had 10 430 subjects. The median duration between the recorded CD prescription and treated constipation was 38.0 days. The most frequently prescribed CD was cardiovascular drugs (47.9%). All CD classes, being male, and some comorbidities were associated with the occurrence of pDIC.
    UNASSIGNED: The pDIC subjects accounted for about 11% of all treated constipation cases. Since DIC requires different treatment regimens compared to other constipation types, physicians should be cognizant to provide patients with optimized treatments.
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  • 文章类型: Journal Article
    库拉索芦荟磨坊。在中医史中有着悠久的药用历史,在那里它赢得了相当大的声誉。其多方面的治疗特性,其特点是抗炎和抗菌属性,除了其作为泻药的既定功效外,已被广泛记录。这篇综述从术语的探索开始,基本特征,库拉索芦荟的主要成分。负责其泻药作用。随后,我们深入研究了库拉索芦荟的分子机制。\的泻药特性,便秘治疗的类型,市售制剂,关于毒性的考虑,及其临床应用。这篇综述旨在作为医疗保健专业人员和研究人员的全面参考点,增进对库拉索芦荟最佳利用的了解。在便秘的治疗中。
    Aloe barbadensis Mill. has a long history of medicinal use in the annals of traditional Chinese medicine, wherein it has garnered considerable renown. Its multifaceted therapeutic properties, characterized by its anti-inflammatory and antibacterial attributes, alongside its established efficacy as a laxative agent, have been extensively documented. This review commences with an exploration of the nomenclature, fundamental characteristics, and principal constituents of Aloe barbadensis Mill. responsible for its laxative effects. Subsequently, we delve into an extensive examination of the molecular mechanisms underlying Aloe barbadensis Mill.\'s laxative properties, types of constipation treatments, commercially available preparations, considerations pertaining to toxicity, and its clinical applications. This review aims to serve as a comprehensive reference point for healthcare professionals and researchers, fostering an enhanced understanding of the optimal utilization of Aloe barbadensis Mill. in the treatment of constipation.
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  • 文章类型: Journal Article
    该意见涉及赤藓糖醇(E968)作为食品添加剂的重新评估,以及根据法规(EU)No1169/2011对其免除泻药警告标签要求的申请。赤藓糖醇是一种多元醇,它是通过用传粉念珠菌BC或巨大念珠菌KW3-6发酵,然后纯化和干燥而获得的。赤藓糖醇在人体中容易且剂量依赖性地吸收,并且可以在很小的程度上代谢为红呢。然后赤藓糖醇在尿液中排泄不变。它不会引起对遗传毒性的担忧。评估的数据集由人类介入研究组成。小组认为赤藓糖醇有可能导致人类腹泻,这被认为是不利的,因为它可能与电解质和水的不平衡有关。对于0.5g/kg体重(bw)的腹泻,未观察到的不良反应水平(NOAEL)范围的下限被确定为参考点。小组认为在参考点水平上设定可接受的每日摄入量(ADI)是适当的。专家小组认为每天0.5g/kgbw的ADI可保护即时泻药效应和潜在的慢性效应。继发于腹泻。儿童(742mg/kgbw/天)和青少年(1532mg/kgbw/天)的平均和第95百分位数慢性暴露最高。第99百分位儿童的急性暴露量最大为每餐3531mg/kgbw。总的来说,专家组认为这两种饮食暴露评估都是高估.小组的结论是,赤藓糖醇的急性和慢性膳食暴露(E968)的暴露估计值均高于ADI,这表明高摄入量的个体在单次和重复暴露后可能有经历不良反应的风险。关于新的申请,小组的结论是,现有数据不支持豁免建议。
    This opinion addresses the re-evaluation of erythritol (E 968) as food additive and an application for its exemption from the laxative warning label requirement as established under Regulation (EU) No 1169/2011. Erythritol is a polyol obtained by fermentation with Moniliella pollinis BC or Moniliella megachiliensis KW3-6, followed by purifications and drying. Erythritol is readily and dose-dependently absorbed in humans and can be metabolised to erythronate to a small extent. Erythritol is then excreted unchanged in the urine. It does not raise concerns regarding genotoxicity. The dataset evaluated consisted of human interventional studies. The Panel considered that erythritol has the potential to cause diarrhoea in humans, which was considered adverse because its potential association with electrolyte and water imbalance. The lower bound of the range of no observed adverse effect levels (NOAELs) for diarrhoea of 0.5 g/kg body weight (bw) was identified as reference point. The Panel considered appropriate to set a numerical acceptable daily intake (ADI) at the level of the reference point. An ADI of 0.5 g/kg bw per day was considered by the Panel to be protective for the immediate laxative effect as well as potential chronic effects, secondary to diarrhoea. The highest mean and 95th percentile chronic exposure was in children (742 mg/kg bw per day) and adolescents (1532 mg/kg bw per day). Acute exposure was maximally 3531 mg/kg bw per meal for children at the 99th percentile. Overall, the Panel considered both dietary exposure assessments an overestimation. The Panel concluded that the exposure estimates for both acute and chronic dietary exposure to erythritol (E 968) were above the ADI, indicating that individuals with high intake may be at risk of experiencing adverse effects after single and repeated exposure. Concerning the new application, the Panel concluded that the available data do not support the proposal for exemption.
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  • 文章类型: Clinical Trial, Phase II
    背景:肠道准备的可接受性和耐受性对于克服患者在接受结肠癌筛查和结肠镜检查时的犹豫至关重要。为了改善患者体验,开发了一种含有聚乙二醇(PEG)和硫酸盐(FPSS)的新型运动饮料风味肠道制剂,以提供与通常使用但未获得美国食品和药物管理局(FDA)批准的PEG和运动饮料肠道制剂(PEG-SD)相似的体验。同时也达到改善清洁功效。
    方法:此FPSS准备,2023年6月获得FDA批准,在一项非随机2期研究中进行了评估,其中40例需要结肠镜检查的患者使用FPSS准备,20例使用PEG-SD准备.
    结果:基于非盲局部内窥镜评估(93%)和盲中心读数(97%),FPSS的总体清洁成功率很高,超过PEG-SD,成功率为84%(本地阅读),74%和68%(盲化中央读段)。如局部内窥镜医师所评估的,对于结肠段的出色准备和清洁成功,也看到了有利于FPSS的类似差异。两种制剂的耐受性都很好,93%的FPSS患者将他们的制剂评为可耐受非常容易食用,与100%的PEG-SD相比。先前进行结肠镜检查准备的患者发现FPSS和PEG-SD优于先前的准备(73%和70%,分别),几乎所有人都会在将来再次要求他们分配的研究准备。大约三分之二的FPSS患者同意该制剂的味道类似于运动饮料。
    结论:新型运动饮料风味制剂与PEG-SD相比,在肠道清洁功效方面具有优势,同时达到相似的患者满意度。该研究已在www上注册。
    结果:gov(NCT03328507)于2017年01月11日。
    BACKGROUND: Acceptability and tolerance of bowel preparation is critical to overcome patient hesitancy in undergoing colon cancer screening and surveillance colonoscopy. To improve patient experience, a new sports drink-flavored bowel preparation containing polyethylene glycol (PEG) and sulfate salts (FPSS) was developed to provide a similar experience to a commonly used but not United States Food and Drug Administration (FDA) approved PEG and sports drink bowel preparation (PEG-SD), while also achieving improved cleansing efficacy.
    METHODS: This FPSS preparation, approved by the FDA in June 2023, was evaluated in a non-randomized Phase 2 study in which 40 patients requiring colonoscopy were prepared with FPSS and 20 with PEG-SD.
    RESULTS: Overall cleansing success was high with FPSS based on unblinded local endoscopist assessment (93%) and blinded central reading (97%), exceeding PEG-SD which achieved success rates of 84% (local read), 74% and 68% (blinded central reads). Similar differences favoring FPSS were seen for excellent preparations and cleansing success by colon segment as rated by local endoscopists. Both preparations were well-tolerated, with 93% of FPSS patients rating their preparation as Tolerable to Very Easy to consume, compared to 100% of PEG-SD. Patients who had previously taken a preparation for colonoscopy found FPSS and PEG-SD better than their prior preparation (73% and 70%, respectively) and nearly all would request their assigned study preparation again in the future. About two thirds of FPSS patients agreed that the preparation tasted similar to a sports drink.
    CONCLUSIONS: The new sports drink-like flavored preparation compares favorably to PEG-SD for bowel cleansing efficacy while achieving similar patient satisfaction. The study was registered at www.
    RESULTS: gov (NCT03328507) on 01/11/2017.
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  • 文章类型: Observational Study
    Naldemedine用于治疗阿片类药物引起的便秘(OIC),但是关于其预防OIC功效的报道很少。因此,我们回顾性调查了影响纳地米定同步处方治疗OIC疗效的因素.开始服用羟考酮10mg/d的癌症门诊患者纳入研究。医生将符合条件的患者分为以下三组:A组在引入羟考酮之前使用常规泻药,并在羟考酮给药的同时开始纳地定治疗。B组在引入羟考酮之前不服用泻药,并在羟考酮给药的同时开始纳地米定,和C组在引入羟考酮之前一直定期服用泻药,并且不与羟考酮同时服用纳迪米定。支持团队评估时间表日文版便秘评分,排便频率,布里斯托尔凳子表格秤,感觉不完全的直肠排空,比较三组在羟考酮给药前后排便紧张的发展或恶化。B组,除了不完全的直肠排空感之外,四个参数都显着恶化,而A组和C组未出现任何变化。在逻辑回归分析中,体重≥51.8kg是显着降低纳地米定对OIC的预防作用的因素,定期使用泻药是显着增加纳地米定对OIC的预防作用的因素。因此,应根据体重和定期使用泻药考虑开始使用纳地米定。
    Naldemedine is indicated for the treatment of opioid-induced constipation (OIC), but reports on its efficacy in preventing OIC are few. Therefore, we retrospectively investigated factors affecting the efficacy of concurrent prescription of naldemedine on OIC. Outpatients with cancer who were started on oxycodone 10 mg/d were included in the study. The eligible patients were classified by their physicians into the following three groups: Group A used regular laxatives before the introduction of oxycodone and initiated naldemedine treatment simultaneously with oxycodone administration, Group B did not take laxatives before the introduction of oxycodone and started naldemedine simultaneously with oxycodone administration, and Group C had been administering regular laxatives before the introduction of oxycodone and were not prescribed naldemedine simultaneously with oxycodone treatment. The Support Team Assessment Schedule Japanese edition score for constipation, frequency of defecation, Bristol Stool Form Scale, sense of incomplete rectal evacuation, and development or worsening of straining to pass bowel movements were compared among the three groups before and after oxycodone administration. In Group B, there was significant worsening of the four parameters except for the sense of incomplete rectal evacuation, whereas Groups A and C did not present any changes. In logistic regression analysis, body weight ≥51.8 kg was a factor significantly decreasing the preventive effect of naldemedine on OIC, and regular use of laxatives was a factor significantly increasing the preventive effect of naldemedine on OIC. Thus, the initiation of naldemedine should be considered depending on the body weight and regular laxative use.
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