H

Richter综合征
  • 文章类型: Case Reports
    被称为“Mott细胞”的浆细胞存在称为“罗素体”的免疫球蛋白的不可分泌积累。它的存在与血液肿瘤有关,但它可以出现在慢性炎症过程中。消化道内最常见的是与幽门螺杆菌感染相关的胃窦。我们的患者增加了罕见的胃外病例,其中与幽门螺杆菌的关联不一致。我们发现了与这些病例相关的下消化道和泌尿系统肿瘤的频繁出现,肿瘤区域循环细胞因子的表达导致浆细胞过度活化。这种可能的关联可能使我们了解有关肿瘤环境的数据,并为我们的早期诊断或未来的治疗目标服务。
    Plasma cells known as \"Mott cells\" present non-secretable accumulations of immunoglobulins called \"Russell bodies\". Its presence is related to hematological neoplasms, but it can appear in chronic inflammatory processes. The most common occurrence within the digestive tract is the gastric antrum associated with H. pylori infection. Our patient is added the rare extragastric cases where the association with H. pylori is inconsistent. We have found a frequent appearance of lower digestive and urological neoplasms in relation to these cases, justified by the expression of circulating cytokines in the tumor area that lead to the overactivation of plasma cells. This possible association could lead us to know data about the tumor environment and serve us for early diagnosis or future therapeutic targets.
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  • 文章类型: Journal Article
    由于透析治疗的高成本,在美国(US),终末期肾病(ESRD)的患病率增加代表了相当大的经济负担。这篇综述研究了来自现实世界研究的数据,以确定成本驱动因素并探索可以降低透析成本的领域。
    我们从MEDLINE的全面文献检索中确定并综合了2016-2023年发布的报告美国成年患者直接透析费用的证据,Embase,和灰色文献来源(例如,美国肾脏数据系统报告)。
    与医疗保险支出相关的大多数识别数据。2020年的总体医疗保险支出为29B用于血液透析,28亿美元用于腹膜透析(PD)。透析费用占ESRD受益人医疗保险总支出的近80%。私人保险付款人一贯为透析支付更多费用;例如,私人保险公司在门诊透析上的每人每月支出估计为10,149美元,而Medicare支出为3,364美元。特定高危患者组的透析费用较高(例如,2型糖尿病,丙型肝炎)。血液透析的支出高于PD,但是PD和血液透析之间的支出差距正在缩小。血管通路费用占透析费用的很大比例。
    确定的研究细节不足,特别是与门诊费用有关,限制了确定关键驱动因素的机会。测量透析成本的方法研究之间的差异使这些结果的概括变得困难。
    这些研究结果表明,预防或延迟发展到ESRD可以为医疗保险和私人付款人节省大量成本,特别是在2型糖尿病等高风险患者中。需要更有效地利用资源,包括低成本的药物治疗,为了改善临床结果和降低总成本,尤其是高危人群。在安全和适当的地方扩大对PD的访问可能有助于降低透析成本。
    以前的论文研究了肾衰竭需要透析的患者的治疗费用。我们审查了这些成本并寻找模式。透析是治疗患有肾脏疾病的人最昂贵的部分。使用私人保险进行透析比使用Medicare要昂贵得多。糖尿病患者的透析费用高于无糖尿病患者。在医院透析比在家里透析花费更多。有机会降低透析费用,应该进一步探索,例如,更多使用可以防止肾脏疾病恶化并减少透析需求的低成本药物。
    UNASSIGNED: The increasing prevalence of end-stage renal disease (ESRD) in the United States (US) represents a considerable economic burden due to the high cost of dialysis treatment. This review examines data from real-world studies to identify cost drivers and explore areas where dialysis costs could be reduced.
    UNASSIGNED: We identified and synthesized evidence published from 2016-2023 reporting direct dialysis costs in adult US patients from a comprehensive literature search of MEDLINE, Embase, and grey literature sources (e.g. US Renal Data System reports).
    UNASSIGNED: Most identified data related to Medicare expenditures. Overall Medicare spending in 2020 was $29B for hemodialysis and $2.8B for peritoneal dialysis (PD). Dialysis costs accounted for almost 80% of total Medicare expenditures on ESRD beneficiaries. Private insurance payers consistently pay more for dialysis; for example, per person per month spending by private insurers on outpatient dialysis was estimated at $10,149 compared with Medicare spending of $3,364. Dialysis costs were higher in specific high-risk patient groups (e.g. type 2 diabetes, hepatitis C). Spending on hemodialysis was higher than on PD, but the gap in spending between PD and hemodialysis is closing. Vascular access costs accounted for a substantial proportion of dialysis costs.
    UNASSIGNED: Insufficient detail in the identified studies, especially related to outpatient costs, limits opportunities to identify key drivers. Differences between the studies in methods of measuring dialysis costs make generalization of these results difficult.
    UNASSIGNED: These findings indicate that prevention of or delay in progression to ESRD could have considerable cost savings for Medicare and private payers, particularly in patients with high-risk conditions such as type 2 diabetes. More efficient use of resources is needed, including low-cost medication, to improve clinical outcomes and lower overall costs, especially in high-risk groups. Widening access to PD where it is safe and appropriate may help to reduce dialysis costs.
    Previous papers have studied the cost of treating patients who need dialysis for kidney failure. We reviewed these costs and looked for patterns. Dialysis was the most expensive part of treatment for people with kidney disease who have Medicare. Dialysis with private insurance was much more expensive than with Medicare. People with diabetes experienced higher costs of dialysis than those without diabetes. Dialysis in a hospital costs more than dialysis at home. There are opportunities to reduce the cost of dialysis that should be explored further, such as more use of low-cost medication that can prevent the worsening of kidney disease and reduce the need for dialysis.
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  • 文章类型: Journal Article
    研究人员和政策制定者之间正在就如何使透明度成为医疗保健系统的强大工具进行辩论。这项研究探讨了有关普通人群的医疗服务信息的可用性和可及性如何影响俄罗斯的医疗保健结果。根据系统审查和荟萃分析(PRISMA)指南的首选报告项目进行系统审查和报告。还审查了世界上最有效的医疗保健系统中使用的卫生设施的透明度指标。尽管提高俄罗斯医疗系统的透明度被认为是提高效率的工具,在提高实际透明度方面做得很少。俄罗斯医疗保健系统的现有制度细节对可接受的透明度水平施加了严重限制。在回顾的俄罗斯实证研究中,透明度通常被简单地视为医疗机构网站上提供的信息或与强制性医疗统计报告的可访问指标数量有关的问题。这项研究的新颖之处在于(a)审查有关该主题的最新研究,以及(b)在分析中包括俄语研究。我们详细阐述了改善俄罗斯医疗系统透明度驱动成果的一般和具体政策含义。
    There is an ongoing debate among researchers and policy-makers on how to make transparency a powerful tool of healthcare systems. This study addresses how the availability and accessibility of information about medical services to the general population affects healthcare outcomes in Russia. A systematic review was conducted and reported according to the Preferred Reporting Items for Systematic Reviewing and Meta-Analysis (PRISMA) guidelines. Transparency indicators of health facilities used in the world\'s most efficient healthcare systems are also reviewed. Although the increase of transparency in the Russian healthcare system is considered as a tool for improving its efficiency, very little has been done to improve the actual level of transparency. The existing institutional specifics of the Russian healthcare system impose serious restrictions on acceptable levels of transparency. In the reviewed empirical Russian studies, transparency is often viewed simplistically as either information available on the websites of medical organizations or issues related to the amount of accessible indicators of compulsory medical statistical reporting. The novelty of this study consists in (a) reviewing the most recent studies on the topic and (b) including studies in Russian in the analysis. We elaborate on general and specific policy implications for improving transparency-driven outcomes in the Russian healthcare system.
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  • 文章类型: Journal Article
    这项研究的目的是比较A型肉毒杆菌毒素(BoNT-A)治疗小儿上肢痉挛的临床和成本效益,包括AbobotulinumtoxinA(aboBoNT-A)和OnabotulinumtoxinA(onaBoNT-A)。
    对报告疗效和安全性结果的随机对照试验进行系统文献回顾和间接治疗比较。疗效通过改良的Ashworth量表(MAS)和Ashworth量表(AS)表征,直至注射后16周。结果用于为1年时间范围的成本效益模型提供信息,从英国的角度来看,将应答率与健康相关生活质量(HRQoL)结果和成本联系起来。成本效益模型中包括的其他数据来源是药品单位成本,基于英国医生调查的医疗保健资源利用情况,与口服抗痉挛疗法相关的不良事件的HRQoL影响。结果被表征为每个质量调整生命年的成本和每个响应者的成本。
    六项研究被纳入证据综合。aboBoNT-A有更高的反应率的趋势,这导致与onaBoNT-A相比改善了HRQoL并降低了年度成本。BoNT-A疗法的安全性结果相似。在成本效益分析中,aboBoNT-A在每质量调整生命年的成本方面是一种经济上占优势的治疗方法。aboBoNT-A与1年的每位响应者的成本估计为39,056英镑。£54,831用于onaBoNT-A。
    根据观察到的安全性和有效性数据,aboBoNT-A估计会导致更高的治疗反应,从而提高生活质量和降低成本,vs.儿童上肢痉挛的onaBoNT-A。本研究的局限性包括可用于onaBoNT-A研究的研究异质性有限细节(例如使用物理治疗),以及响应者数据的有限可用性。如果需要假设,他们被要求对abBoN-A保守。
    UNASSIGNED: The objective of this study was to compare clinical- and cost-effectiveness of type A botulinum toxin (BoNT-A) therapies for management of pediatric upper limb spasticity, including AbobotulinumtoxinA (aboBoNT-A) and Onabotulinumtoxin A (onaBoNT-A).
    UNASSIGNED: Systematic literature review and indirect treatment comparisons were conducted of randomized controlled trials reporting efficacy and safety outcomes. Efficacy was characterized by Modified Ashworth Scale (MAS) and Ashworth Scale (AS) up to 16-weeks post-injection. Results were used to inform a cost-effectiveness model with a 1-year time horizon, linking response rates with health-related quality-of-life (HRQoL) outcomes and costs from a UK perspective. Other data sources included in the cost-effectiveness model were drug unit costs, health care resource utilization based on UK physician survey, and HRQoL impacts of adverse events associated with oral anti-spasticity therapies. Results were characterized as cost per quality-adjusted life year and cost per responder.
    UNASSIGNED: Six studies were included in evidence syntheses. There was a trend towards greater response rate for aboBoNT-A which resulted in improved HRQoL and lower annual costs compared with onaBoNT-A. Safety outcomes were similar across BoNT-A therapies. In cost-effectiveness analysis, aboBoNT-A was an economically dominant therapy with respect to cost per quality-adjusted life year. The cost per responder at 1 year was estimated to be £39,056 for aboBoNT-A vs. £54,831 for onaBoNT-A.
    UNASSIGNED: Based on observed safety and efficacy data, aboBoNT-A is estimated to result in higher treatment response and consequently increased quality-of-life and reduced costs, vs. onaBoNT-A in children with upper limb spasticity. Limitations to the study include study heterogeneity limited details available for onaBoNT-A studies (e.g. use of physical therapy), and limited availability of responder data. Where assumptions were required, they were made to be conservative towards aboBoN-A.
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  • 文章类型: Journal Article
    UNASSIGNED: Here, we aimed to compare early hepatectomy (EH) with delayed hepatectomy (DH) as a treatment for spontaneously ruptured hepatocellular carcinoma (HCC).
    UNASSIGNED: Several databases were systematically searched for eligible studies that compared DH with EH for spontaneously ruptured HCC treatment. Studies that met the inclusion criteria were reviewed systematically, and the reported data were aggregated statistically, using the RevMan v5.3 software.
    UNASSIGNED: Seven studies were included, with a total of 385 patients, comprising of 224 EH cases and 161 DH cases. Compared with the EH group, incidence of intraoperative bleeding [mean difference (MD), 353.93; 95% CI, 230.04-447.83; P < 0.00001], volume of intraoperative blood transfusion (MD, 420.61; 95% CI, 354.40-486.81, P < 0.00001), and 30-day mortality rate (OR, 14.94; 95% CI, 1.76-126.66; P = 0.01) were significantly lower in the DH group. Furthermore, the 1-, 2-, and 3-year survival rates were significantly higher in the DH group [1-year:hazard ratio (HR), 1.76; 95% CI, 1.06-2.94; P = 0.03; 2-year:HR, 1.52; 95% CI, 1.02-2.25; P = 0.04; 3-year: HR, 1.53; 95% CI, 1.06-2.21; P = 0.02]. There was no difference between the groups in the 5-year survival rate (HR, 1.40; 95% CI, 0.92-2.11; P = 0.11).
    UNASSIGNED: For resectable spontaneously ruptured HCC, DH could reduce intraoperative bleeding, intraoperative blood transfusion volume, and 30-day mortality rate and increase the 1-, 2-, and 3-year survival rates, endowing the patients with greater short- and long-term benefits during and following the surgery.
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  • 文章类型: Journal Article
    调查了烷烃灵活性在确定液晶行为中的作用的最新发现。随着了解烷烃构象问题的建立,最近的模型依赖(1)HNMR的工作将在取得进展的地方进行审查,但最终需要规避模型变得明显。仔细观察烷烃的刚性基本单元将提供前进的方向,表明溶解在液晶中的这些分子的取向有序和各向异性势彼此缩放。一旦这种关系建立起来,将涵盖一系列使用各向异性和各向同性(1)HNMR光谱研究烷烃构象统计的工作,其中气体的影响,将描述各向同性凝聚相和各向异性凝聚相。
    Recent discoveries of the role of alkane flexibility in determining liquid-crystal behaviour are surveyed. With the impetus for understanding the alkane conformational problem established, recent model dependent (1)H NMR work on the topic will be reviewed where progress is made but the need to circumvent models eventually becomes evident. A closer look at the rigid basic units of alkanes will provide the way forward where it is shown that the orientational ordering and anisotropic potentials of these molecules dissolved in liquid crystals scale with each other. Once this relationship is established, a series of works using anisotropic and isotropic (1)H NMR spectroscopy to study alkane conformational statistics will be covered, wherein the influence of the gas, isotropic condensed and anisotropic condensed phases will be described.
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  • 文章类型: Journal Article
    我们尝试使用负指数模型量化退出后中风风险的下降,采用以前用于IHD的方法。我们确定了22个RRs区块(来自13项研究),比较了目前的吸烟者,以前吸烟者(按时间戒烟)和从不吸烟者。相应的伪数的病例和对照/风险形成了用于模型拟合的数据。我们试图估计半衰期(H,自戒烟以来的时间,当每个街区的超额风险变为持续吸烟者的一半时)。该方法未能在当前吸烟者RR<1.40的9个块中收敛或产生非常可变的H估计。拒绝这些,在一项模型拟合中出现问题的研究中,按烟熏量组合块,最终分析使用了11个块。每个块的拟合度都足够了,H的综合估计值为4.78(95CI2.17-10.50)年。然而,存在相当大的异质性,任何研究的因素都无法解释,随机效应估计为3.08(1.32-7.16)。敏感性分析允许反向因果关系或最终戒烟期的不同假设时间给出了类似的结果。中风和IHD的H估计值相似,和个人估计类似异质。拟合模型更难中风,由于它与吸烟的联系较弱。
    We attempted to quantify the decline in stroke risk following quitting using the negative exponential model, with methodology previously employed for IHD. We identified 22 blocks of RRs (from 13 studies) comparing current smokers, former smokers (by time quit) and never smokers. Corresponding pseudo-numbers of cases and controls/at risk formed the data for model-fitting. We tried to estimate the half-life (H, time since quit when the excess risk becomes half that for a continuing smoker) for each block. The method failed to converge or produced very variable estimates of H in nine blocks with a current smoker RR <1.40. Rejecting these, and combining blocks by amount smoked in one study where problems arose in model-fitting, the final analyses used 11 blocks. Goodness-of-fit was adequate for each block, the combined estimate of H being 4.78(95%CI 2.17-10.50) years. However, considerable heterogeneity existed, unexplained by any factor studied, with the random-effects estimate 3.08(1.32-7.16). Sensitivity analyses allowing for reverse causation or differing assumed times for the final quitting period gave similar results. The estimates of H are similar for stroke and IHD, and the individual estimates similarly heterogeneous. Fitting the model is harder for stroke, due to its weaker association with smoking.
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