Amoxicillin

阿莫西林
  • 文章类型: Journal Article
    携带新德里金属β-内酰胺酶编码基因的IncX3质粒,blaNDM-5在人类和动物中迅速传播。鉴于碳青霉烯被列入WHOAWaRe观察小组,禁止在动物中使用,携带blaNDM-5-IncX3质粒的耐碳青霉烯类肠杆菌(CRE)成功传播的驱动因素仍然未知.我们观察到携带blaNDM-5-IncX3的大肠杆菌可以在阿莫西林给药的情况下在鸡肠中持续存在,用于牲畜的最大的兽用β-内酰胺之一,或者没有任何抗生素压力。因此,我们表征了blaNDM-5-IncX3质粒并鉴定了转录调节因子,VirBR,与调节基因actX的启动子结合,增强IV型分泌系统(T4SS)的转录;从而,促进IncX3质粒的缀合,增加菌毛粘附能力并增强blaNDM-5-IncX3转结合体在动物消化道中的定植。我们的机制和体内研究确定VirBR是blaNDM-5-IncX3在单健康AMR部门成功传播的主要因素。此外,VirBR通过铜和锌离子的存在增强质粒接合和T4SS表达,从而对通用动物饲料的使用产生了深远的影响。
    IncX3 plasmids carrying the New Delhi metallo-β-lactamase-encoding gene, blaNDM-5, are rapidly spreading globally in both humans and animals. Given that carbapenems are listed on the WHO AWaRe watch group and are prohibited for use in animals, the drivers for the successful dissemination of Carbapenem-Resistant Enterobacterales (CRE) carrying blaNDM-5-IncX3 plasmids still remain unknown. We observe that E. coli carrying blaNDM-5-IncX3 can persist in chicken intestines either under the administration of amoxicillin, one of the largest veterinary β-lactams used in livestock, or without any antibiotic pressure. We therefore characterise the blaNDM-5-IncX3 plasmid and identify a transcription regulator, VirBR, that binds to the promoter of the regulator gene actX enhancing the transcription of Type IV secretion systems (T4SS); thereby, promoting conjugation of IncX3 plasmids, increasing pili adhesion capacity and enhancing the colonisation of blaNDM-5-IncX3 transconjugants in animal digestive tracts. Our mechanistic and in-vivo studies identify VirBR as a major factor in the successful spread of blaNDM-5-IncX3 across one-health AMR sectors. Furthermore, VirBR enhances the plasmid conjugation and T4SS expression by the presence of copper and zinc ions, thereby having profound ramifications on the use of universal animal feeds.
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  • 文章类型: Journal Article
    SolarFenton是一种重要且广泛使用的高级氧化工艺(AOP),用于降解药物污染物。本研究的目的是评估混合污染物(阿莫西林,对乙酰氨基酚,和环丙沙星)用于使用太阳能Fenton工艺的水溶液。操作参数,如pH,铁剂量,H2O2剂量,污染物浓度,研究了时间。从实验结果来看,获得了去除混合污染物的理想条件,如pH3,Fe2+0.04mM,H2O24mM,混合污染物的浓度为5mg/L,太阳辐射400W/m2,时间10分钟,分别。利用伪一级动力学研究了混合污染物的降解效率。研究结果表明,混合污染物的降解效率>99%。观察到最大63%的矿化,和羟基自由基清除剂的效果进行了研究。最佳条件用于评估加标废水(市政废水(MWW)和医院废水(HWW))。AMX的最高消除率,ACET,和CIP为65%,89%,MWW占85%,76%,92%,HWW占80%,分别。通过LC-ESI-MS在水基质(水溶液和加标废水)中检测降解的副产物,并对转化产物进行了ECOSAR分析。研究得出的结论是,太阳能Fenton技术对于去除水基质中的混合污染物是有前途且有效的。
    Solar Fenton is an important and extensively used advanced oxidation process (AOP) to degrade pharmaceutical pollutants. The objective of this study was to evaluate the performance of simultaneous degradation of the mixed pollutants (amoxicillin, acetaminophen, and ciprofloxacin) for an aqueous solution using the solar Fenton process. Operating parameters such as pH, iron doses, H2O2 doses, pollutant concentrations, and time were studied. From the experimental results, the ideal conditions were obtained for the removal of mixed pollutants such as pH 3, Fe2+ 0.04 mM, H2O2 4 mM, the concentration of the mixed pollutants 5 mg/L, solar radiation 400 W/m2, and time 10 min, respectively. The pseudo-first-order kinetics were utilized to investigate the degradation efficacy of the mixed pollutants. The result of the study indicates that the degradation efficiency was > 99% for the mixed pollutants. A maximum of 63% mineralization was observed, and hydroxyl radical scavenger effects were studied. The best optimal conditions were applied to assess the spiked wastewater (municipal wastewater (MWW) and hospital wastewater (HWW)). The highest elimination rates for AMX, ACET, and CIP were observed as 65%, 89%, and 85% for MWW and 76%, 92%, and 80% for HWW, respectively. The degraded by-products were detected by LC-ESI-MS in the water matrix (aqueous solution and spiked wastewater), and ECOSAR analysis was performed for the transformed products. The study concluded that the solar Fenton technique is promising and effective for the removal of mixed pollutants from the water matrix.
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  • 文章类型: Journal Article
    背景:难治性幽门螺杆菌(H.pylori)感染不可避免地增加了药物选择的难度。这里,我们描述了我们使用针对幽门螺杆菌的新型四价IgY治疗难治性幽门螺杆菌感染患者的经验.
    方法:患者被随机分配接受标准四联疗法(阿莫西林,克拉霉素,奥美拉唑和柠檬酸铋钾)2周或口服250mg禽多克隆IgY,每天两次,共4周。通过蛋白质印迹13检测IgY与幽门螺杆菌抗原的结合功效。进行尿素呼气试验以评估根除治疗的疗效。通过各种常规试验评价IgY的副作用。采用问卷收集临床症状和不良反应。
    结果:蛋白质印迹分析显示,四价IgY同时与VacA结合,Hpaa,幽门螺杆菌的CagA和UreB。四价IgY在难治性幽门螺杆菌患者中的根除率为50.74%,对13C-尿素的DOB的抑制率为50.04%(相对于基线的δ)。34例有临床症状的患者症状缓解率为61.76%,四价IgY治疗期间未见不良反应。
    结论:多克隆禽类四价IgY可减少幽门螺杆菌感染,在难治性幽门螺杆菌感染患者的治疗中表现出良好的疗效和安全性,这代表了难治性幽门螺杆菌感染患者的有效治疗选择。
    BACKGROUND: Refractory Helicobacter pylori (H. pylori) infection inevitably increase the difficulty of drug selection. Here, we described our experience with the use of a novel tetravalent IgY against H. pylori for the treatment of patients with refractory H. pylori infection.
    METHODS: Patients were randomly assigned to receive the standard quadruple therapy (amoxicillin, clarithromycin, omeprazole and bismuth potassium citrate ) for 2 weeks or 250 mg of avian polyclonal IgY orally twice a day for 4 weeks. The binding efficacy of IgY to H. pylori antigens was detected by western blotting13. C-urea breath test was performed to evaluate the eradication therap\'s efficacy. The side effects of IgY were evaluated via various routine tests. The questionnaire was used to gather clinical symptoms and adverse reactions.
    RESULTS: Western blot analysis showed that tetravalent IgY simultaneously bind to VacA, HpaA, CagA and UreB of H. pylori. Tetravalent IgY had an eradication rate of 50.74% in patients with refractory H. pylori and an inhibition rate of 50.04% against DOB (delta over baseline) of 13C-urea. The symptom relief rate was 61.76% in thirty-four patients with clinical symptoms, and no adverse reactions were observed during tetravalent IgY treatment period.
    CONCLUSIONS: Polyclonal avian tetravalent IgY reduced H. pylori infection, and showed good efficacy and safety in the treatment of refractory H. pylori infection patients, which represented an effective therapeutic option of choice for patients with refractory H. pylori infection.
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  • 文章类型: Journal Article
    目的:甲氧苄啶-磺胺甲恶唑(TMP-SMX)可能会增加地高辛浓度,治疗指数狭窄的药物。地高辛浓度的微小变化可能使个体容易发生毒性风险。
    目的:研究TMP-SMX联合处方与阿莫西林联合处方后服用地高辛的老年人发生地高辛毒性的风险。
    方法:安大略省基于人群的回顾性队列研究,加拿大(2002-2020年)使用关联医疗保健数据。参与者包括47,961名服用地高辛的老年人(58%为女性;中位年龄80岁[四分位数范围74-86]),他们新接受TMP-SMX治疗(n=10,273),而新接受阿莫西林治疗的人(n=37,688)。
    方法:TMP-SMX与阿莫西林在老年人同时服用地高辛的联合处方。
    方法:主要结果是住院(即,入院或急诊科就诊)在抗生素处方后30天内出现地高辛毒性。使用倾向评分上的治疗加权的逆概率来平衡基线健康指标上的比较组。使用改进的Poisson回归获得加权风险比(RR),并使用二项回归获得加权风险差(RD)。伤害所需的数量(NNH)计算为1/RD。
    结果:TMP-SMX治疗的49/10,273(0.48%)患者与阿莫西林治疗的32/37,688(0.08%)患者(加权RR,5.71[95%置信区间(CI),3.19至10.24];加权RD,0.39%[95%CI,0.25%至0.53%];NNH256[95%CI,233至400])。
    结论:在服用地高辛的老年人中,与阿莫西林相比,共同处方的TMP-SMX在医院遇到地高辛毒性的30天风险高出近6倍,尽管绝对风险差异较低(0.4%).医生应在临床上适当时开一种替代抗生素。如果TMP-SMX必须与地高辛共同处方(如果认为益处大于风险),地高辛应该在个体基础上减少剂量。
    OBJECTIVE: Trimethoprim-sulfamethoxazole (TMP-SMX) may increase digoxin concentration, a medication with a narrow therapeutic index. Small changes in digoxin concentration could predispose individuals to the risk of toxicity.
    OBJECTIVE: To characterize the risk of digoxin toxicity in older adults taking digoxin following co-prescription of TMP-SMX compared with co-prescription of amoxicillin.
    METHODS: Retrospective population-based cohort study in Ontario, Canada (2002-2020) using linked health care data. Participants comprised 47,961 older adults taking digoxin (58% women; median age 80 years [interquartile range 74-86]) who were newly treated with TMP-SMX (n = 10,273) compared with those newly treated with amoxicillin (n = 37,688).
    METHODS: Co-prescription of TMP-SMX versus amoxicillin in older adults concurrently taking digoxin.
    METHODS: The primary outcome was a hospital encounter (i.e., hospital admission or emergency department visit) with digoxin toxicity within 30 days of the antibiotic prescription. Inverse probability of treatment weighting on the propensity score was used to balance comparison groups on indicators of baseline health. Weighted risk ratios (RR) were obtained using modified Poisson regression and weighted risk differences (RD) using binomial regression. The number needed to harm (NNH) was calculated as 1/RD.
    RESULTS: A hospital encounter with digoxin toxicity occurred in 49/10,273 (0.48%) patients treated with TMP-SMX versus 32/37,688 (0.08%) in those treated with amoxicillin (weighted RR, 5.71 [95% confidence interval (CI), 3.19 to 10.24]; weighted RD, 0.39% [95% CI, 0.25% to 0.53%]; NNH 256 [95% CI, 233 to 400]).
    CONCLUSIONS: In older adults taking digoxin, the 30-day risk of a hospital encounter with digoxin toxicity was nearly 6 times higher in those co-prescribed TMP-SMX versus amoxicillin, although the absolute risk difference was low (0.4%). Physicians should prescribe an alternative antibiotic when clinically appropriate. If TMP-SMX must be co-prescribed with digoxin (if the benefit is believed to outweigh the risk), digoxin should be dose-reduced on an individual basis.
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  • 文章类型: Journal Article
    牙周机械清创是治疗牙周炎最常见的疗法。然而,根据疾病的严重程度,机械清创已被推荐与全身抗生素联合使用.在这项研究中,我们使用Epistemonikos(FRISBEE)方法对机械清创联合阿莫西林和甲硝唑治疗慢性牙周炎的有效性和安全性进行了系统评价。我们对Epidemonikos数据库进行了系统的搜索,从10项系统评价中提取数据,并重新分析23项主要研究的数据,以生成结果总结(SoF)表.我们使用RevMan5.3和GRADepro进行数据分析和数据呈现。分析了以下结果:探查深度(平均差异(MD):0.07mm);临床附着水平(MD:0.04mm);探查出血(MD:5.06%);和化脓(MD:0.31%)。在所研究的牙周结局中,与单独的牙周机械清创疗法相比,没有证据表明牙周机械清创疗法联合阿莫西林和甲硝唑治疗慢性牙周炎的临床相关益处。
    Periodontal mechanical debridement is the most common therapy for the treatment of periodontitis. However, depending on the severity of the disease, mechanical debridement has been recommended in combination with systemic antibiotics. In this study, we performed an overview of systematic reviews using the Friendly Summaries of Body of Evidence using Epistemonikos (FRISBEE) methodology on the effectiveness and safety of mechanical debridement combined with amoxicillin and metronidazole compared to mechanical debridement alone for the treatment of chronic periodontitis. We conducted a systematic search of the Epistemonikos database, extracted data from 10 systematic reviews and re-analyzed data from 23 primary studies to generate a summary of findings (SoF) table. We used RevMan 5.3 and GRADEpro for data analysis and data presentation. The following outcomes were analyzed: probing depth (mean difference (MD): 0.07 mm); clinical attachment level (MD: 0.04 mm); bleeding on probing (MD: 5.06%); and suppuration (MD: 0.31%). There was no evidence of a clinically relevant benefit of periodontal mechanical debridement therapy combined with amoxicillin and metronidazole compared to periodontal mechanical debridement therapy alone for the treatment of chronic periodontitis in the studied periodontal outcomes.
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  • 文章类型: Journal Article
    细菌中的抗生素耐药性被认为是导致治疗失败的主要因素。在这项研究中,我们的目的是研究巴勒斯坦幽门螺杆菌对抗生素的耐药性.我们招募了91名消化不良患者,包括49名女性和42名男性。这些参与者接受了食管胃十二指肠镜检查和胃活检。随后对这些活组织检查进行微生物学评估,并测试其对各种抗微生物药物的敏感性。在91名患者中,38例(41.7%)表现出幽门螺杆菌的存在。值得注意的是,环丙沙星对幽门螺杆菌的疗效最高,其次是左氧氟沙星,莫西沙星,和阿莫西林,耐药率为0%,0%,2.6%,和18.4%,分别。相反,甲硝唑和克拉霉素的有效性最低,电阻百分比为100%和47.4%,分别。这项研究的结果强调,巴勒斯坦患者组中的幽门螺杆菌菌株对传统的一线抗生素如克拉霉素和甲硝唑表现出实质性的耐药性。然而,替代药物如氟喹诺酮和阿莫西林仍然是有效的选择.因此,我们建议支持以喹诺酮为基础的幽门螺杆菌感染治疗方案,并在巴勒斯坦人群中采用更明智的抗生素使用方法.
    Antibiotic resistance among bacteria is recognized as the primary factor contributing to the failure of treatment. In this research, our objective was to examine the prevalence of antibiotic resistance in H. pylori bacteria in Palestine. We enlisted 91 individuals suffering from dyspepsia, comprising 49 females and 42 males. These participants underwent esophagogastroduodenoscopy procedures with gastric biopsies. These biopsies were subsequently subjected to microbiological assessments and tested for their susceptibility to various antimicrobial drugs. Among the 91 patients, 38 (41.7%) exhibited the presence of H. pylori. Notably, Ciprofloxacin displayed the highest efficacy against H. pylori, followed by Levofloxacin, Moxifloxacin, and Amoxicillin, with resistance rates of 0%, 0%, 2.6%, and 18.4%, respectively. On the contrary, Metronidazole and Clarithromycin demonstrated the lowest effectiveness, with resistance percentages of 100% and 47.4%, respectively. The outcomes of this investigation emphasize that H. pylori strains within the Palestinian patient group exhibit substantial resistance to conventional first-line antibiotics like clarithromycin and metronidazole. However, alternative agents such as fluoroquinolones and amoxicillin remain efficacious choices. Consequently, we recommend favoring quinolone-based treatment regimens for H. pylori infections and adopting a more judicious approach to antibiotic usage among the Palestinian population.
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  • 文章类型: Journal Article
    幽门螺杆菌引起的胃并发症的挑战不断升级,在抗生素耐药性上升和持续癌症风险的推动下,强调对创新治疗策略的需求。这项研究通过开发定制的半互穿聚合物网络(semi-IPN)作为阿莫西林(AMOX)的胃滞留基质来解决这一紧迫性。它们是可生物降解的,吸收大量模拟胃液(溶胀指数>360%),并表现出超多孔微结构,显著的粘膜粘附,和浮力。调查包括在pH1.2下进行评估,以便与之前的研究进行比较分析,特别是,在pH5.0时,反映了幽门螺杆菌感染胃中的酸性环境。半IPN表现出凝胶状结构,在整个24小时控释研究中保持完整性,并在完成其预期功能时解体。评价胃滞留给药系统的性能,AMOX在pH1.2和pH5.0超过24小时释放(10%-100%)采用实验设计方法,阐明主要的释放机制。他们的粘膜粘着剂,浮力,三维脚手架稳定性,和胃的生物降解性使得它们非常适合容纳大量的AMOX。此外,探索将钾竞争性酸阻滞剂(P-CAB)vonoprazan(VONO)纳入负载AMOX的制剂中显示出精确有效的药物递送前景。这种创新的方法有可能对抗幽门螺杆菌感染,从而防止这种病原体诱发的胃癌。
    The escalating challenges of Helicobacter pylori-induced gastric complications, driven by rising antibiotic resistance and persistent cancer risks, underscore the demand for innovative therapeutic strategies. This study addresses this urgency through the development of tailored semi-interpenetrating polymer networks (semi-IPN) serving as gastroretentive matrices for amoxicillin (AMOX). They are biodegradable, absorb significant volume of simulated gastric fluid (swelling index > 360 %) and exhibit superporous microstructures, remarkable mucoadhesion, and buoyancy. The investigation includes assessment at pH 1.2 for comparative analysis with prior studies and, notably, at pH 5.0, reflecting the acidic environment in H. pylori-infected stomachs. The semi-IPN demonstrated gel-like structures, maintaining integrity throughout the 24-hour controlled release study, and disintegrating upon completing their intended function. Evaluated in gastroretentive drug delivery system performance, AMOX release at pH 1.2 and pH 5.0 over 24 h (10 %-100 %) employed experimental design methodology, elucidating dominant release mechanisms. Their mucoadhesive, buoyant, three-dimensional scaffold stability, and gastric biodegradability make them ideal for accommodating substantial AMOX quantities. Furthermore, exploring the inclusion of the potassium-competitive acid blocker (P-CAB) vonoprazan (VONO) in AMOX-loaded formulations shows promise for precise and effective drug delivery. This innovative approach has the potential to combat H. pylori infections, thereby preventing the gastric cancer induced by this pathogen.
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  • 文章类型: English Abstract
    OBJECTIVE: Was to determine the presence of an amoxicillin-based antibiotic in bone implant biopsies by Raman spectroscopy in an experiment.
    METHODS: Experimental animals (n=10, a miniature pig of the Svetlogorsk breed) were divided into 2 groups of 5 animals. Groups 1 and 2 were injected with amoxicillin 2 ml per 20 kg of body weight 30 minutes before dental implantation surgery, then group 2 was additionally injected with 1 ml per 20 kg of body weight for 5 days. Each animal has 6 implants installed. On the 1st, 3rd, 7th, 14th day, an implant-bone biopsy was removed from each animal, micro-preparations were made and Raman spectroscopy was performed to assess the peak matching of the Raman spectrum.
    RESULTS: In animals of the 1st and 2nd groups, the main peak of the Raman spectrum, which is closest to the values of the antibiotic spectrum of interest to us, is located closer to 1448 cm-1 and 1446 cm-1, respectively. At the same time, in both observations, the peaks relate to the spectrum of bone tissue, which cannot indicate the content of an antibiotic in the drug.
    CONCLUSIONS: No scattering spectra corresponding to the antibiotic molecule were found in any animal from both groups, regardless of the mode of administration and dosage of amoxicillin. The detected peaks corresponded to bone tissue without an antibiotic.
    UNASSIGNED: Определить наличие антибиотика на основе амоксициллина в имплантато-костных биоптатах методом рамановской спектроскопии в эксперименте.
    UNASSIGNED: Экспериментальные животные (n=10, миниатюрная свинья светлогорской породы) были разделены на 2 группы по 5 животных. 1-й и 2-й группе за 30 минут до операции дентальной имплантации вводили амоксициллин 2 мл на 20 кг массы тела, затем 2-й группе дополнительно вводили 1 мл на 20 кг массы тела в течение 5 дней. Каждому животному установлено по 6 имплантатов. На 1-й, 3-й, 7-й, 14-й день, у каждого животного изымали имплантато-костный биоптат, изготавливали микропрепараты и проводили рамановскую спектроскопию с оценкой пикового соответствия спектра комбинационного рассеяния.
    UNASSIGNED: У животных 1-й и 2-й группы основной пик спектра комбинационного рассеяния, наиболее близкий к интересующим нас значениям спектра антибиотика, расположен ближе к 1448 см–1 и 1446 см–1 соответственно. При этом в обоих наблюдениях пики относятся к спектру костной ткани, который не может указывать на содержание антибиотика в препарате.
    UNASSIGNED: Ни у одного животного из обеих групп вне зависимости от режима приема и дозирования амоксициллина спектров рассеивания, соответствующих молекуле антибиотика, обнаружено не было. Обнаруженные пики соответствовали костной ткани без антибиотика.
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  • 文章类型: Journal Article
    本研究旨在比较三种牙髓封闭剂(AHPlus,矿物三氧化物集料[MTA]Fillapex,和BioRootRCS)有和没有阿莫西林对粪肠球菌。
    阿莫西林,相当于密封剂总重量的10%,与密封剂混合。在没有阿莫西林的情况下制备另一批。使用直接接触试验(DCT)和琼脂扩散试验来评估抗菌效果。使用单向方差分析(ANOVA)分析结果,F检验,还有Kruskal-Wallis测试.
    AHPlus在DCT中没有添加阿莫西林的情况下显着抑制粪肠球菌(p=0.011),而在琼脂扩散试验中,BioRootRCS具有比对照更大的抑制区(p<0.001)。当阿莫西林添加到密封剂中时,AHPlus(p=0.003)和MTAFillapex(p=0.042)降低了粪肠球菌的生长。相比之下,所有三种密封剂均显示出比对照更大的抑制区(p=0.001),AHPlus显示出比MTAFillapex(p=0.042)和BioRootRCS(p=0.032)更大的抑制区。
    由此得出结论,向牙髓封闭剂中添加阿莫西林增强了它们对粪肠球菌的抗微生物活性。
    UNASSIGNED: This study aimed to compare the antimicrobial effect of three endodontic sealers (AH Plus, Mineral trioxide aggregate [MTA] Fillapex, and BioRoot RCS) with and without amoxicillin against E. faecalis.
    UNASSIGNED: Amoxicillin, equivalent to 10% of the sealers\' total weight, was mixed with the sealers. Another batch was prepared without amoxicillin. The direct contact test (DCT) and the agar diffusion test were used to assess the antibacterial effect. Results were analysed using one-way analysis of variance (ANOVA), the F-test, and the Kruskal-Wallis test.
    UNASSIGNED: AH Plus significantly suppressed E. faecalis without the addition of amoxicillin in the DCT (p = 0.011), while in the agar diffusion test, BioRoot RCS had a larger inhibition zone than the control (p < 0.001). When amoxicillin was added to the sealers, AH Plus (p = 0.003) and MTA Fillapex (p = 0.042) reduced E. faecalis growth. In contrast, all three sealers showed larger inhibition zones than the control (p = 0.001), with AH Plus displaying a larger inhibition zone than MTA Fillapex (p = 0.042) and BioRoot RCS (p = 0.032).
    UNASSIGNED: It was thus concluded that the addition of amoxicillin to endodontic sealers enhances their antimicrobial activity against E. faecalis.
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  • 文章类型: Systematic Review
    背景:在根除幽门螺杆菌的双重疗法中使用的阿莫西林剂量在不同的研究中存在差异,并且对于基于vonoprazan的双重疗法的最佳阿莫西林剂量仍不清楚。我们旨在研究低和高剂量阿莫西林在伏诺拉赞-阿莫西林双重治疗中的疗效和安全性。
    方法:通过搜索数据库从开始到2023年10月进行了全面的系统评价。包括所有评价沃诺拉赞-阿莫西林双重疗法根除幽门螺杆菌的有效性和安全性的试验。汇集根除率,不良事件的发生率,相对风险,并给出了95%的置信区间。
    结果:18项研究包括12个低剂量阿莫西林(VLA)和13个高剂量阿莫西林(VHA)组。VLA治疗的合并根除率分别为82.4%和86.8%,通过意向治疗和符合方案分析,VHA治疗占86.0%和90.9%,分别。在按持续时间分层的亚组分析中,7天内达到的根除率,10天,VLA和VHA双重疗法治疗14天的比例为80.8%,84.2%,83.1%,和67.3%,88.8%,87.5%,分别。在直接比较VLA和VHA双重疗法的四项随机对照试验中,意向治疗的疗效无统计学差异(76.9%vs81.4%,p=0.337)和每个协议(81.6%vs84.0%,p=0.166)分析。此外,两组的不良事件发生率(p=0.965)和依从性(p=0.994)相似.
    结论:VLA治疗与VHA治疗具有相当的疗效和安全性,以及地区差异。适当延长的治疗持续时间对于优化vonoprazan-阿莫西林治疗的治疗效果至关重要。
    BACKGROUND: The amoxicillin dose used in dual therapy to eradicate Helicobacter pylori varies across studies and the optimal amoxicillin dose for vonoprazan-based dual therapies remains unclear. We aimed to investigate the efficacy and safety of low- and high-dose amoxicillin in vonoprazan-amoxicillin dual therapy.
    METHODS: A comprehensive systematic review was conducted by searching databases from inception to October 2023. All trials that evaluated the effectiveness and safety of vonoprazan-amoxicillin dual therapy for eradicating H. pylori were included. Pooled eradication rate, incidence of adverse events, relative risks, and 95% confidence intervals are presented.
    RESULTS: Eighteen studies with 12 low-dose amoxicillin (VLA) and 13 high-dose amoxicillin (VHA) arms were included. The pooled eradication rates were 82.4% and 86.8% for VLA therapy, and 86.0% and 90.9% for VHA therapy by the intention-to-treat and per-protocol analyses, respectively. In the subgroup analysis stratified by duration, the eradication rates achieved in 7 days, 10 days, and 14 days treatments with VLA and VHA dual therapies were 80.8%, 84.2%, 83.1%, and 67.3%, 88.8%, 87.5%, respectively. In the four randomized controlled trials that directly compared VLA and VHA dual therapies, the efficacy was not statistically different in the intention-to-treat (76.9% vs 81.4%, p = 0.337) and per-protocol (81.6% vs 84.0%, p = 0.166) analyses. Additionally, the incidence of adverse events (p = 0.965) and compliance (p = 0.994) were similar in both groups.
    CONCLUSIONS: VLA therapy demonstrated comparable efficacy and safety to VHA therapy, along with regional differences. An appropriately extended treatment duration may be critical for therapeutic optimization of vonoprazan-amoxicillin treatment.
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