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Clinical pharmacy and telemedicine: an opportunity to improve epilepsy management. 临床药学和远程医疗:改善癫痫管理的契机。
IF 0.4 Q4 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-22 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3095
Rossella Moscogiuri

Clinical pharmacy, as defined by the European Society of Clinical Pharmacy, is a comprehensive professional practice encompassing all pharmacist profiles regardless of the setting. It focuses on promoting optimal drug utilization for patient-centric clinical outcomes. Telemedicine leverages information and communication technologies for remote healthcare delivery, bridging geographical gaps. The integration of clinical pharmacy and telemedicine is crucial in modern healthcare paradigms, especially for patients with chronic illnesses. In 2021, marketing authorization was granted for cenobamate as adjunctive treatment for focal-onset seizures with or without secondary generalization in adults with epilepsy who have not been adequately controlled despite a history of treatment with at least two antiepileptic medicinal products. This review emphasizes the synergistic role of clinical pharmacists and neurologists in utilizing telemedicine for patient counselling, drug information dissemination, adverse drug reaction surveillance, and personalized medication management within the context of epilepsy care. This integration could enhance patient safety, therapeutic outcomes and address socio-economic challenges faced by chronic patients.

根据欧洲临床药剂学协会的定义,临床药剂学是一项综合性的专业实践,涵盖了所有药剂师的工作内容,与工作环境无关。其重点是促进药物的最佳利用,以达到以患者为中心的临床效果。远程医疗利用信息和通信技术提供远程医疗服务,缩小了地域差距。临床药学与远程医疗的整合在现代医疗保健模式中至关重要,尤其是对慢性病患者而言。2021 年,塞诺巴马特获得了上市许可,可用于辅助治疗成人癫痫患者的局灶性癫痫发作(伴有或不伴有继发性全身化),尽管这些患者曾接受过至少两种抗癫痫药物的治疗,但病情仍未得到充分控制。本综述强调了临床药剂师和神经科医生在利用远程医疗进行患者咨询、药物信息传播、药物不良反应监测以及癫痫护理中的个性化用药管理方面的协同作用。这种整合可以加强患者安全、提高治疗效果并应对慢性病患者面临的社会经济挑战。
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引用次数: 0
Valutazione dell’innovatività e negoziazione di prezzi e rimborso dei farmaci: raccomandazioni da un panel di esperti. 评估创新性以及药品定价和报销谈判:专家小组的建议。
IF 0.4 Q4 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-15 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3107
Claudio Jommi, Francesca Patarnello, Cosetta Bianchi, Giuliano Buzzetti
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引用次数: 0
Exploring the administrative burden faced by hematologists: a comprehensive study in Italy. 探索血液科医生面临的行政负担:意大利的一项综合研究。
IF 0.4 Q4 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-03 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3042
Davide Petruzzelli, Marco Vignetti, Stefania Trasarti, Paolo Sportoletti, Silvia Della Torre, Roberto Cairoli, Francesca Pia Chiara Leone, Giuseppe Pompilio, Marco Gullì, Eva Brown Hajdukova, Davide Integlia

Background: Administrative burdens have been identified as a major issue impacting patient care, professional practice, and the overall efficiency of healthcare systems. The aim of this study is to assess the administrative burden faced by Italian hematologists.

Methods: A cross-sectional survey that included both closed-ended quantitative questions and open-ended free text answer options was administered to 1,570 hematologists working with malignancies and members of Italian GIMEMA Foundation - Franco Mandelli ONLUS and the Italian Linfomi Foundation (FIL). The survey was conducted online from May 24 to June 30, 2023. Descriptive statistics were computed for the quantitative data to clearly summarize the responses and descriptive analysis of free text responses was carried out.

Results: Surveyed hematologists spend an average of 47.07% of their time on administrative tasks, with 63.22% (n = 110) of respondents reporting spending at least half of their time on these activities. More than half (57.47%, n = 100) reported that "Patient care" is the medical task most affected by a lack of time. Additionally, 55.17% (n = 96) reported experiencing burnout in the past 6 months, with filling out "Forms" being identified as the top contributing administrative task by 27.59% (n = 48) of respondents, followed by "Scheduling" (24.71%, n = 43) and "Managing IT system failures" (21.84%, n = 38). Nearly half of the surveyed hematologists (45.40%, n  =  = 79) identified patient care as the top priority requiring more time.

Conclusions: The study confirms that the administrative workload of hematologists has a significant impact on patient care, communication, and burnout risk, reducing the time available for patient care, leading to exhaustion and concern about clinical errors.

背景:行政负担已被认为是影响患者护理、专业实践和医疗系统整体效率的主要问题。本研究旨在评估意大利血液科医生所面临的行政负担:方法:对 1570 名从事恶性肿瘤治疗的血液科医生以及意大利 GIMEMA 基金会 - Franco Mandelli ONLUS 和意大利 Linfomi 基金会 (FIL) 的成员进行了横向调查,其中包括封闭式定量问题和开放式自由文本答案选项。调查于 2023 年 5 月 24 日至 6 月 30 日在线进行。对定量数据进行了描述性统计,以清楚地概括答复内容,并对自由文本答复进行了描述性分析:接受调查的血液学专家平均花费 47.07% 的时间在行政工作上,其中 63.22% 的受访者(n = 110)表示至少花费一半的时间在这些活动上。超过一半的受访者(57.47%,n = 100)表示,"患者护理 "是受时间不足影响最大的医疗任务。此外,55.17%(n = 96)的受访者表示在过去 6 个月中出现过职业倦怠,27.59%(n = 48)的受访者认为填写 "表格 "是导致职业倦怠的首要行政任务,其次是 "日程安排"(24.71%,n = 43)和 "管理 IT 系统故障"(21.84%,n = 38)。近一半的受访血液科医生(45.40%,n = = 79)认为病人护理是需要更多时间的首要任务:研究证实,血液科医生的行政工作量对患者护理、沟通和职业倦怠风险有重大影响,减少了可用于患者护理的时间,导致疲惫和对临床错误的担忧。
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引用次数: 0
Cabozantinib use in second or subsequent line of treatment in renal cell carcinoma: an analysis of Italian administrative databases. 在肾细胞癌二线或后续治疗中使用卡博替尼:意大利行政数据库分析。
IF 0.4 Q4 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-03 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.2892
Cristian Lolli, Antonio Verde, Luca Degli Esposti, Valentina Acciai, Alessia Brigido, Emanuela Proietti, Sarah Scagliarini

Background: Cabozantinib use in everyday clinical practice for advanced or metastatic renal cell carcinoma (RCC) is relatively recent, and real-world data on treatment persistence, adherence and sequencing are still limited.

Methods: We conducted an analysis based on an integrated administrative database, covering around 6.9 million health-assisted Italian individuals, to explore the use of cabozantinib for RCC. Patients with at least one prescription for cabozantinib during 2017-2020 were searched. These were characterized during all available period (i.e. from 2010 onwards) before the index date and were observed after inclusion.

Results: A total of 113 patients treated with cabozantinib in second or subsequent line were included, and their demographic, clinical and treatment characteristics were described. About half of these RCC patients were aged >65 years (47.8%). Sixty patients (53.1%) were highly adherent to cabozantinib therapy, and the median cabozantinib treatment duration of use was 8.7 months (95% confidence interval: 5.8-11.1). During the first year of follow-up, the average total cost per patient was €32,508.

Conclusions: We described second or subsequent line cabozantinib treatment for RCC in a real-world setting and the economic burden of disease in Italy, taking advantage of large, integrated administrative databases.

背景:卡博替尼用于晚期或转移性肾细胞癌(RCC)的日常临床实践相对较晚,有关治疗持续性、依从性和排序的真实世界数据仍然有限:我们基于一个综合行政数据库进行了一项分析,该数据库涵盖了约 690 万名接受医疗援助的意大利人,旨在探讨卡博替尼(cabozantinib)治疗 RCC 的使用情况。我们搜索了在 2017-2020 年间至少开过一次卡博替尼处方的患者。这些患者在索引日期之前的所有可用期间(即从 2010 年起)都有特征,并在纳入后进行了观察:共纳入了113例接受卡博替尼二线或后续治疗的患者,并对其人口统计学、临床和治疗特征进行了描述。这些RCC患者中约有一半年龄大于65岁(47.8%)。60名患者(53.1%)高度坚持卡博替尼治疗,中位卡博替尼治疗持续时间为8.7个月(95%置信区间:5.8-11.1)。在第一年的随访中,每位患者的平均总费用为32,508欧元:我们利用大型综合行政数据库,描述了在真实世界环境中卡博替尼对RCC的二线或后续治疗,以及意大利的疾病经济负担。
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引用次数: 0
Accesso precoce ai farmaci: una proposta di riforma per il Servizio Sanitario Nazionale. 尽早获得药品:国民健康服务改革建议》。
IF 0.4 Pub Date : 2024-06-17 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3098
Patrizia Popoli, Giovanni Giuliani, Arturo Cavaliere, Claudio Jommi
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引用次数: 0
Differenze di genere e ipercolesterolemia: evidenze real-world dallo studio WECARE (Women Effective CArdiovascular Risk Evaluation). 性别差异与高胆固醇血症:来自 WECARE(女性有效心血管风险评估)研究的实际证据。
IF 0.5 Pub Date : 2024-06-11 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.2731
Valentina Perrone, Gerardo Medea, Stefano Urbinati, Diego Sangiorgi, Luca Degli Esposti
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引用次数: 0
Quale efficacia degli strumenti di governance prescrittiva? Risultati dall’applicazione delle note AIFA. 规范性治理工具的有效性如何?应用 AIFA 说明的结果。
IF 0.5 Pub Date : 2024-06-10 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3027
Giaele Moretti, Benedetta Dal Canto, Francesco Attanasio, Alma Martelli, Francesca Ferrè
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引用次数: 0
Determining value in the treatment of activated PI3Kδ syndrome in Spain: a multicriteria decision analysis from the perspective of key stakeholders. 确定西班牙活化 PI3Kδ 综合征的治疗价值:从主要利益相关者的角度进行多标准决策分析。
IF 0.5 Pub Date : 2024-05-22 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3041
María Reyes Abad, Carmen Alerany, Laia Alsina, Eduardo López Granados, Olaf Neth, Jose Luis Poveda, Jacques G Rivière, Carlos Rodríguez-Gallego, Joanne B Tutein Nolthenius, Raquel Figueiredo, Silvia Subías Labazuy, Alicia Gil

Introduction: Activated phosphoinositide 3-kinase (PI3K)δ syndrome (APDS) is an ultra-rare inborn error of immunity (IEI) combining immunodeficiency and immune dysregulation. This study determined what represents value in APDS in Spain from a multidisciplinary perspective applying multicriteria decision analysis (MCDA) methodology.

Methods: A multidisciplinary committee of nine experts scored the evidence matrix. A specific framework for orphan drug evaluation in Spain and the weights assigned by a panel of 98 evaluators and decision-makers was used. Re-evaluation of scores was performed.

Results: APDS is considered a very severe disease with important unmet needs, including misdiagnosis and diagnostic delay. Current management is limited to treatment of symptoms with off-label use of therapies supported by limited evidence. Therapeutic benefit is partial, resulting in limited disease control. Haematopoietic stem cell transplantation (HSCT), the only potential curative alternative, is restricted to a reduced patient population and without evidence of long-term efficacy or safety. All options present a limited safety profile. Data on patients' quality of life are lacking. APDS is associated with high pharmacological, medical and indirect costs.

Conclusions: APDS is considered a severe disease, with limited understanding by key stakeholders of how treatment success is assessed in clinical practice, the serious impact that has on patients and the associated high economic burden. This study brings to light how MCDA methodology could represent a useful tool to complement current clinical and decision-making methods used by APDS experts and evaluators.

简介活化磷酸肌酸 3- 激酶(PI3K)δ 综合征(APDS)是一种极其罕见的先天性免疫错误(IEI),集免疫缺陷和免疫失调于一身。本研究采用多标准决策分析(MCDA)方法,从多学科角度确定了西班牙 APDS 的价值所在:由九位专家组成的多学科委员会对证据矩阵进行了评分。方法:一个由九名专家组成的多学科委员会对证据矩阵进行评分,并使用西班牙孤儿药评估的特定框架以及由 98 名评估员和决策者组成的小组分配的权重。结果:结果:APDS 被认为是一种非常严重的疾病,有很多需求尚未得到满足,包括误诊和诊断延迟。目前的治疗方法仅限于治疗症状,并在标签外使用证据有限的疗法。治疗效果不佳,导致疾病控制有限。造血干细胞移植(HSCT)是唯一可能治愈疾病的替代方法,但仅限于少数患者,而且没有证据表明其具有长期疗效或安全性。所有方案的安全性都很有限。有关患者生活质量的数据也很缺乏。APDS与高昂的药物、医疗和间接成本相关:APDS 被认为是一种严重的疾病,主要利益相关者对临床实践中如何评估治疗成功率、对患者造成的严重影响以及相关的高经济负担了解有限。本研究揭示了 MCDA 方法如何成为一种有用的工具,以补充 APDS 专家和评估人员目前使用的临床和决策方法。
{"title":"Determining value in the treatment of activated PI3Kδ syndrome in Spain: a multicriteria decision analysis from the perspective of key stakeholders.","authors":"María Reyes Abad, Carmen Alerany, Laia Alsina, Eduardo López Granados, Olaf Neth, Jose Luis Poveda, Jacques G Rivière, Carlos Rodríguez-Gallego, Joanne B Tutein Nolthenius, Raquel Figueiredo, Silvia Subías Labazuy, Alicia Gil","doi":"10.33393/grhta.2024.3041","DOIUrl":"10.33393/grhta.2024.3041","url":null,"abstract":"<p><strong>Introduction: </strong>Activated phosphoinositide 3-kinase (PI3K)δ syndrome (APDS) is an ultra-rare inborn error of immunity (IEI) combining immunodeficiency and immune dysregulation. This study determined what represents value in APDS in Spain from a multidisciplinary perspective applying multicriteria decision analysis (MCDA) methodology.</p><p><strong>Methods: </strong>A multidisciplinary committee of nine experts scored the evidence matrix. A specific framework for orphan drug evaluation in Spain and the weights assigned by a panel of 98 evaluators and decision-makers was used. Re-evaluation of scores was performed.</p><p><strong>Results: </strong>APDS is considered a very severe disease with important unmet needs, including misdiagnosis and diagnostic delay. Current management is limited to treatment of symptoms with off-label use of therapies supported by limited evidence. Therapeutic benefit is partial, resulting in limited disease control. Haematopoietic stem cell transplantation (HSCT), the only potential curative alternative, is restricted to a reduced patient population and without evidence of long-term efficacy or safety. All options present a limited safety profile. Data on patients' quality of life are lacking. APDS is associated with high pharmacological, medical and indirect costs.</p><p><strong>Conclusions: </strong>APDS is considered a severe disease, with limited understanding by key stakeholders of how treatment success is assessed in clinical practice, the serious impact that has on patients and the associated high economic burden. This study brings to light how MCDA methodology could represent a useful tool to complement current clinical and decision-making methods used by APDS experts and evaluators.</p>","PeriodicalId":12627,"journal":{"name":"Global & Regional Health Technology Assessment","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11113520/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141087373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Patient-reported outcomes in epilepsy: a case study exploring their usage and impact. 癫痫患者报告结果:探索其用途和影响的案例研究。
IF 0.5 Pub Date : 2024-05-03 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3020
Simona Lattanzi, Angela La Neve

Background: This study aimed to obtain insights from epilepsy specialists on the use of Patient-Reported Outcome (PRO) measures and how they can affect the management of people with epilepsy and healthcare resource utilization.

Methods: The heads of two referral units for people with epilepsy at one tertiary care hospital were invited to respond to a structured survey.

Results: Paper-based questionnaires and face-to-face interviews were the main modalities used to measure the quality of life of people with epilepsy. The Quality of Life in Epilepsy Inventory-31 (QOLIE-31), the Adverse Event Profile (adult centre), the Generalized Anxiety Disorder-7, Short-Form Health Survey 36, PSY-Flex, SAFA and Child Behavior Checklist (paediatric centre) were the most used scales. There was consensus about the favourable impact of PRO upon patient management, disease management and measurement of the success of a treatment. Both respondents considered the PRO as important as other main indicators like efficacy and tolerability of the treatment. Lack of time, personnel and economic resources was identified as a barrier on the use of PRO. The PRO could reduce the number of visits, exams and treatments, and increase the time spent on each patient and the number of neuropsychological, psychological and rehabilitation services. The standardized use of PRO was considered useful and the increase in human resources was considered a priority to achieve this goal.

Conclusions: Despite the heterogeneity in the actual collection of PRO, there was a uniform perception about their role to optimize the care of people with epilepsy.

背景:本研究旨在了解癫痫专家对患者报告结果(PRO)测量方法的使用情况,以及这些方法如何影响癫痫患者的管理和医疗资源的利用:本研究旨在了解癫痫专家对患者报告结果(PRO)测量方法的使用情况,以及这些方法如何影响癫痫患者的管理和医疗资源的利用:方法:邀请一家三甲医院的两个癫痫患者转诊科室的负责人对一项结构化调查做出答复:结果:纸质问卷和面对面访谈是衡量癫痫患者生活质量的主要方式。使用最多的量表是癫痫生活质量量表-31(QOLIE-31)、不良事件档案(成人中心)、广泛性焦虑症-7、短式健康调查 36、PSY-Flex、SAFA 和儿童行为检查表(儿科中心)。人们一致认为,PRO 对病人管理、疾病管理和衡量治疗成功与否都有积极影响。两个受访者都认为 PRO 与其他主要指标(如疗效和耐受性)一样重要。缺乏时间、人力和经济资源被认为是使用 PRO 的障碍。PRO 可以减少就诊、检查和治疗的次数,增加花在每个病人身上的时间以及神经心理、心理和康复服务的次数。标准化使用 PRO 被认为是有益的,而增加人力资源被认为是实现这一目标的优先事项:尽管在实际收集 PRO 方面存在差异,但人们对 PRO 在优化癫痫患者护理方面的作用有着一致的认识。
{"title":"Patient-reported outcomes in epilepsy: a case study exploring their usage and impact.","authors":"Simona Lattanzi, Angela La Neve","doi":"10.33393/grhta.2024.3020","DOIUrl":"10.33393/grhta.2024.3020","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to obtain insights from epilepsy specialists on the use of Patient-Reported Outcome (PRO) measures and how they can affect the management of people with epilepsy and healthcare resource utilization.</p><p><strong>Methods: </strong>The heads of two referral units for people with epilepsy at one tertiary care hospital were invited to respond to a structured survey.</p><p><strong>Results: </strong>Paper-based questionnaires and face-to-face interviews were the main modalities used to measure the quality of life of people with epilepsy. The Quality of Life in Epilepsy Inventory-31 (QOLIE-31), the Adverse Event Profile (adult centre), the Generalized Anxiety Disorder-7, Short-Form Health Survey 36, PSY-Flex, SAFA and Child Behavior Checklist (paediatric centre) were the most used scales. There was consensus about the favourable impact of PRO upon patient management, disease management and measurement of the success of a treatment. Both respondents considered the PRO as important as other main indicators like efficacy and tolerability of the treatment. Lack of time, personnel and economic resources was identified as a barrier on the use of PRO. The PRO could reduce the number of visits, exams and treatments, and increase the time spent on each patient and the number of neuropsychological, psychological and rehabilitation services. The standardized use of PRO was considered useful and the increase in human resources was considered a priority to achieve this goal.</p><p><strong>Conclusions: </strong>Despite the heterogeneity in the actual collection of PRO, there was a uniform perception about their role to optimize the care of people with epilepsy.</p>","PeriodicalId":12627,"journal":{"name":"Global & Regional Health Technology Assessment","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11074701/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140876252","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Costs and benefits in patients with NYHA class III heart failure treated with CardioMEMS in Italy. 意大利 NYHA III 级心力衰竭患者接受 CardioMEMS 治疗的成本和收益。
IF 0.5 Pub Date : 2024-05-02 eCollection Date: 2024-01-01 DOI: 10.33393/grhta.2024.3018
Andrea Messori, Maria Rita Romeo, Valeria Fadda, Francesca Collini, Sabrina Trippoli

Background: CardioMEMS is a device suitable for telemedicine that is currently being evaluated by the Regional Health Technology Assessment (HTA) Committee of Tuscany. Two detailed HTA reports are available in the specialized literature, the results of which need to be transferred to our regional setting. These decisions in Tuscany are made by the so-called Centro Operativo HTA.

Aim: To validate, with local cost-effectiveness data, the decision on CardioMEMS that will be made in the Tuscany region.

Methods: Two detailed international HTA reports were rearranged and adapted to our regional setting to generate a simplified analysis that could form the basis of our decision. Two willingness-to-pay (WTP) thresholds of €20,000/quality-adjusted life year (QALY) and €50,000/QALY were considered.

Results: Based on epidemiological and regulatory information, the target population in Tuscany for this device is 166 cases. The value-based price of CardioMEMS is estimated to be €4,332 and €16,662 at WTP thresholds of 20,000/QALY and 50,000/QALY, respectively. Its current price in Italy is €12,000.

Conclusion: In our region, the introduction of CardioMEMS is likely to be gradual, around 50 patients/year (or €0.60 million/year at current price). This example highlights the need to adapt the information published in the international literature to the local context in which the approval decision is made. In this context, simplified analyses are easier to apply than complex Markov models.

背景介绍CardioMEMS 是一种适用于远程医疗的设备,托斯卡纳地区卫生技术评估 (HTA) 委员会目前正在对其进行评估。专业文献中已有两份详细的 HTA 报告,其结果需要移植到我们的地区环境中。托斯卡纳的这些决定由所谓的 Centro Operativo HTA 做出。目的:利用当地的成本效益数据,验证托斯卡纳地区将做出的关于 CardioMEMS 的决定:对两份详细的国际 HTA 报告进行了重新编排,并根据我们的地区环境进行了调整,以生成一份简化的分析报告,作为我们决策的基础。我们考虑了两个支付意愿(WTP)阈值,分别为 20,000 欧元/质量调整生命年(QALY)和 50,000 欧元/质量调整生命年:根据流行病学和监管信息,该设备在托斯卡纳的目标人群为 166 例。根据价值估算,CardioMEMS 的价格分别为 4,332 欧元和 16,662 欧元,WTP 临界值分别为 20,000 欧元/QALY 和 50,000 欧元/QALY。其目前在意大利的价格为 12,000 欧元:在我们地区,CardioMEMS 的引入可能是渐进式的,大约每年 50 名患者(或按当前价格计算每年 60 万欧元)。这个例子强调了根据当地情况调整国际文献中公布的信息的必要性,因为当地情况决定是否批准。在这种情况下,简化分析比复杂的马尔可夫模型更容易应用。
{"title":"Costs and benefits in patients with NYHA class III heart failure treated with CardioMEMS in Italy.","authors":"Andrea Messori, Maria Rita Romeo, Valeria Fadda, Francesca Collini, Sabrina Trippoli","doi":"10.33393/grhta.2024.3018","DOIUrl":"https://doi.org/10.33393/grhta.2024.3018","url":null,"abstract":"<p><strong>Background: </strong>CardioMEMS is a device suitable for telemedicine that is currently being evaluated by the Regional Health Technology Assessment (HTA) Committee of Tuscany. Two detailed HTA reports are available in the specialized literature, the results of which need to be transferred to our regional setting. These decisions in Tuscany are made by the so-called Centro Operativo HTA.</p><p><strong>Aim: </strong>To validate, with local cost-effectiveness data, the decision on CardioMEMS that will be made in the Tuscany region.</p><p><strong>Methods: </strong>Two detailed international HTA reports were rearranged and adapted to our regional setting to generate a simplified analysis that could form the basis of our decision. Two willingness-to-pay (WTP) thresholds of €20,000/quality-adjusted life year (QALY) and €50,000/QALY were considered.</p><p><strong>Results: </strong>Based on epidemiological and regulatory information, the target population in Tuscany for this device is 166 cases. The value-based price of CardioMEMS is estimated to be €4,332 and €16,662 at WTP thresholds of 20,000/QALY and 50,000/QALY, respectively. Its current price in Italy is €12,000.</p><p><strong>Conclusion: </strong>In our region, the introduction of CardioMEMS is likely to be gradual, around 50 patients/year (or €0.60 million/year at current price). This example highlights the need to adapt the information published in the international literature to the local context in which the approval decision is made. In this context, simplified analyses are easier to apply than complex Markov models.</p>","PeriodicalId":12627,"journal":{"name":"Global & Regional Health Technology Assessment","volume":null,"pages":null},"PeriodicalIF":0.5,"publicationDate":"2024-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11067868/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140862640","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Global & Regional Health Technology Assessment
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