innovative

创新
  • 文章类型: Journal Article
    背景:新的治疗方法不适合需要的患者,没有实现他们的目标。医院的药物和治疗委员会通过合理的理由编制处方来确保与患者接触。不断发展的创新分子景观挑战了国家报销后及时的配方适应。目的将国家报销报告整合到医院的评估中,从而促进患者毫不拖延地进入。方法2019年,根特大学医院新分子的基本原理,比利时,与国家健康和残疾保险研究所的公共评估报告进行了比较,在制造商提出报销要求后,评估特定适应症的药物。回顾性比较两个数据库(国家和医院)中匹配药物之间的决策标准(治疗价值和成本)[无(%),平均值(SD)]。结果分析了200份公开报告和30份处方决定(抗肿瘤和免疫调节是最普遍的类别:41.0%。36.7%)。国家决定通常涉及仅在医院使用的药物(89;44.5%),而没有患者自付费用(101;50.5%)。在13种匹配的药物(相同的适应症)中,国家决定和处方组入院之间的时间延迟平均为3.1个月(SD2.3).比较分析表明,两个委员会的评估主要基于随机对照试验的疗效终点。医院评估中使用的文献最近发表日期:0.78(SD2.2)年。使用公共报告作为地平线扫描可以快速识别新的适应症。结论为了加快患者进入,国家报销报告的科学证据可用于医院处方集决策。
    Background New therapies that do not reach patients in need, have not achieved their goal. Drug and Therapeutics Committees in hospitals ensure access to patients by compiling a formulary on rational grounds. An evolving landscape of innovative molecules challenges timely formulary adaptation after national reimbursement. Aim To integrate national reimbursement reports in the hospital\'s appraisal, thereby promoting access for patients without delay. Method For 2019, the rationale for new molecules at Ghent University Hospital, Belgium, was compared with the public assessment report of the National Institute for Health and Disability Insurance, assessing a medicine in a specific indication following a reimbursement request by the manufacturer. Decision criteria (therapeutic value and cost) between matching medicines in both databases (national & hospital) were retrospectively compared [no (%), mean (SD)]. Results Two-hundred public reports and 30 formulary decisions were analysed (with antineoplastic & immunomodulating as most prevalent class: 41.0% resp. 36.7%). National decision often concerned hospital-only medicines (89; 44.5%) without patient co-payment (101; 50.5%). Of 13 matched medicines (same indication), time delay between national decision and formulary admission was on average 3.1 (SD 2.3) months. Comparative analysis showed that assessment in both committees was mostly based on the efficacy endpoints of Randomised Controlled Trials. Literature used in hospital appraisals was of more recent publication date: + 0.78 (SD 2.2) years. Using public reports as a horizon scan could enable quick identification of new indications. Conclusion To speed up patient access, the scientific evidence of national reimbursement reports can be used for the purpose of hospital formulary decisions.
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  • 文章类型: Case Reports
    大规模(或危及生命)咯血是医生遇到的时间敏感的紧急情况,需要跨学科,合作努力迅速及时地阻止出血。放置支气管内渡边龙头(EWS)以阻止咯血是一种相对较新的技术,其在气道病理学中的广泛应用。随着目前其用途扩展到支气管出血。然而,由于无法立即获得EWS,因此需要对常规外科手术中使用的日常材料进行创新,并且在资源有限的环境中可用,可以起到龙头的作用。在这份报告中,我们揭露了一个危及生命的案例,隐源性咯血是通过一种新的技术来管理的,该技术使用花生纱作为龙头,导致成功的支气管内填塞。
    Massive (or life-threatening) haemoptysis is a time-sensitive emergency encountered by a physician that requires an interdisciplinary, collaborative effort to arrest the bleeding in a prompt and timely manner. Placement of an endobronchial Watanabe spigot (EWS) to halt haemoptysis is a relatively recent technique finding its wide application in airway pathology, with the current extension of its use to bronchial bleeding. However, the lack of immediate access to EWS gives rise to the need to innovate with day-to-day materials used in routine surgical practice and available in resource-limited settings, which may serve the purpose of a spigot. In this report, we bring to light a case of life-threatening, cryptogenic haemoptysis that was managed by a novel technique of using peanut gauze as a spigot resulting in a successful endobronchial tamponade.
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  • 文章类型: Journal Article
    OBJECTIVE: A common concern in the use of a roundabout is providing adequately for the pedestrian. This unique roundabout layout, which introduces raised crosswalks directly at the roundabout entrance, as opposed to at a car length back, aims at improving safety and convenience for pedestrians at roundabouts.
    METHODS: A preliminary evaluation of the layout was undertaken to establish its effectiveness in meeting study objectives. A quasi-experimental before-and-after study design was used to compare speeds on approach and immediately prior to the crossing to ascertain potential impact speed and implications for pedestrian safety. Compliance to crossing and crossing time were also compared in relation to safety and convenience outcomes. A questionnaire assessed pedestrian perception of the safety and convenience at the roundabout before and after treatment.
    RESULTS: Results from this case study indicate that mean approach speeds (free speeds 30 m from crossing) reduced from 32.7 to 30.7 km/h and immediately prior to crossing, mean speeds reduced from 19.1 to 16.3 km/h. There was also a marked reduction in proportions of vehicles traveling at speeds that could elevate risk to pedestrians. Total crossing time after treatment reduced by around 4 s, and crossing compliance increased from approximately half to approximately 90 percent. Survey of pedestrians indicated positive response to the perceived safety and convenience posttreatment.
    CONCLUSIONS: Preliminary results of the case study suggest positive safety and convenience outcomes. Implications for pedestrian safety include less exposure to traffic and lower risk of serious injury, particularly for elderly pedestrians; convenience outcomes include shorter waiting times to cross and greater compliance to the crossing. A larger study is required to substantiate the findings.
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