Insurance, Health, Reimbursement

保险,健康,报销
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  • 文章类型: Journal Article
    中国社会医疗保险报销政策的最新变化影响了苯丙酮尿症(PKU)患者特殊食品的经济负担。然而,这一政策变化是否与他们的血液苯丙氨酸(PHE)浓度相关尚不清楚.
    研究PKU患者的报销政策与血液PHE浓度之间的关系。
    这项队列研究测量了2018年1月至2021年12月中国4个新生儿筛查中心167名PKU患者的血液PHE浓度。2019年取消了2个中心PKU患者特殊食品的报销政策,并从2020年起恢复。相比之下,其他两个中心一致执行该政策。对2023年9月10日至12月6日的数据进行了分析。
    实施和取消PKU患者特殊食品的报销政策。
    从2018年到2021年定期测量血液PHE浓度。使用单侧Z检验来比较不同年份之间的血液PHE浓度的平均值。
    在167例PKU患者中(平均[SD]年龄,84.4[48.3]个月;87名男性[52.1%]),从2018年至2021年,共收集了4285次血液PHE浓度测量值.对于2019年取消报销政策的中心患者,2019年血液PHE浓度的平均值(SD)为5.95(5.73)mg/dL,显著高于2018年的4.84(4.11)mg/dL(P<0.001),2020年为5.06(5.21)mg/dL(P=0.006),2021年为4.77(4.04)mg/dL(P<.001)。同样,对于2019年取消政策的其他中心的患者,2019年血液PHE浓度的平均值(SD)为5.95(3.43)mg/dL,2018年显著高于5.34(3.45)mg/dL(P=0.03),2020年5.13(3.15)mg/dL(P=0.003),2021年为5.39(3.46)mg/dL(P=0.03)。相反,在一贯实施该政策的2个中心的患者中,任何年份之间均未观察到显著差异.
    在这项来自多个中心的PKU患者的队列研究中,特殊食品报销政策的实施与控制血液PHE浓度相关.PKU患者特殊食品支出应纳入长期社会医疗保险报销范围。
    UNASSIGNED: Recent changes in China\'s social medical insurance reimbursement policy have impacted the financial burden of patients with phenylketonuria (PKU) for special foods. However, whether this policy change is associated with their blood phenylalanine (PHE) concentration is unclear.
    UNASSIGNED: To investigate the association between the reimbursement policy and blood PHE concentration in patients with PKU.
    UNASSIGNED: This cohort study measured the blood PHE concentrations of 167 patients with PKU across 4 newborn screening centers in China from January 2018 to December 2021. The reimbursement policy for special foods for patients with PKU at 2 centers was canceled in 2019 and restored from 2020 onwards. In contrast, the other 2 centers consistently implemented the policy. Data were analyzed from September 10 to December 6, 2023.
    UNASSIGNED: The implementation and cancelation of the reimbursement policy for special foods of patients with PKU.
    UNASSIGNED: The blood PHE concentration was regularly measured from 2018 to 2021. A 1-sided Z test was used to compare the mean of the blood PHE concentration between different years.
    UNASSIGNED: Among 167 patients with PKU (mean [SD] age, 84.4 [48.3] months; 87 males [52.1%]), a total of 4285 measurements of their blood PHE concentration were collected from 2018 to 2021. For patients at the center that canceled the reimbursement policy in 2019, the mean (SD) of the blood PHE concentrations in 2019 was 5.95 (5.73) mg/dL, significantly higher than 4.84 (4.11) mg/dL in 2018 (P < .001), 5.06 (5.21) mg/dL in 2020 (P = .006), and 4.77 (4.04) mg/dL in 2021 (P < .001). Similarly, for patients at the other center that canceled the policy in 2019, the mean (SD) of the blood PHE concentrations in 2019 was 5.95 (3.43) mg/dL, significantly higher than 5.34 (3.45) mg/dL in 2018 (P = .03), 5.13 (3.15) mg/dL in 2020 (P = .003), and 5.39 (3.46) mg/dL in 2021 (P = .03). On the contrary, no significant difference was observed between any of the years for patients at the 2 centers that consistently implemented the policy.
    UNASSIGNED: In this cohort study of patients with PKU from multiple centers, the implementation of the reimbursement policy for special foods was associated with controlling the blood PHE concentration. Special foods expenditure for patients with PKU should be included in the scope of long-term social medical insurance reimbursement.
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  • 文章类型: Journal Article
    背景:日益先进和昂贵的新医疗技术的可用性给公共资助的医疗保健系统带来了相当大的压力。决定不或不再从公共资金中偿还健康技术可能变得不可避免。尽管如此,政策制定者经常被迫修改或撤销负面的报销决定,因为公众通常会在这些决定之后产生分歧。在媒体上发布个别患者的照片可能会加剧公众的分歧。我们的目的是评估描绘受负面报销决定影响的患者对公众不同意该决定的影响。
    方法:我们在荷兰的一个具有代表性的公众样本(n=1008)中进行了一项离散选择实验,并评估了受访者“不同意政策制定者”决定不为两个患者组之一报销新药的可能性。我们为一个患者组提供了受决定影响的患者之一的图片,而另一组则为“无图片”。根据患者年龄对这些组进行描述,治疗前与健康相关的生活质量(HRQOL)和预期寿命(LE),以及HRQOL和LE从治疗中获得的收益。我们应用随机截距logit回归模型来分析数据。
    结果:我们的结果表明,当患者的照片出现时,受访者更有可能不同意否定的报销决定。与其他实证研究的结果一致,当患者相对年轻时,受访者也更有可能不同意这一决定,治疗前HRQOL和LE水平较高,和治疗带来的大量LE收益。
    结论:这项研究为描绘个体的效果提供了证据,受影响的患者在公众对医疗保健中的负面报销决定持不同意见。政策制定者最好意识到这种影响,以便他们能够预测这种影响并实施政策来减轻相关风险。
    BACKGROUND: The availability of increasingly advanced and expensive new health technologies puts considerable pressure on publicly financed healthcare systems. Decisions to not-or no longer-reimburse a health technology from public funding may become inevitable. Nonetheless, policymakers are often pressured to amend or revoke negative reimbursement decisions due to the public disagreement that typically follows such decisions. Public disagreement may be reinforced by the publication of pictures of individual patients in the media. Our aim was to assess the effect of depicting a patient affected by a negative reimbursement decision on public disagreement with the decision.
    METHODS: We conducted a discrete choice experiment in a representative sample of the public (n = 1008) in the Netherlands and assessed the likelihood of respondents\' disagreement with policymakers\' decision to not reimburse a new pharmaceutical for one of two patient groups. We presented a picture of one of the patients affected by the decision for one patient group and \"no picture available\" for the other group. The groups were described on the basis of patients\' age, health-related quality of life (HRQOL) and life expectancy (LE) before treatment, and HRQOL and LE gains from treatment. We applied random-intercept logit regression models to analyze the data.
    RESULTS: Our results indicate that respondents were more likely to disagree with the negative reimbursement decision when a picture of an affected patient was presented. Consistent with findings from other empirical studies, respondents were also more likely to disagree with the decision when patients were relatively young, had high levels of HRQOL and LE before treatment, and large LE gains from treatment.
    CONCLUSIONS: This study provides evidence for the effect of depicting individual, affected patients on public disagreement with negative reimbursement decisions in healthcare. Policymakers would do well to be aware of this effect so that they can anticipate it and implement policies to mitigate associated risks.
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  • 文章类型: Journal Article
    背景:急性细支气管炎,婴儿最常见的下呼吸道感染,主要是由呼吸道病毒引起的。然而,约有25%的急性细支气管炎患儿使用抗生素.这种对病毒感染不适当使用抗生素会引起抗生素耐药性。这项研究旨在确定韩国急性细支气管炎患儿的抗生素处方率和与抗生素使用相关的因素。抗生素使用和耐药率很高的地方。
    方法:2016年至2019年间被诊断为急性细支气管炎的24个月以下儿童的医疗保健数据来自国家健康保险系统报销索赔数据。评估抗生素处方率和相关因素。
    结果:共分析了3,638,424次就诊。抗生素处方率为51.8%,随着时间的推移而下降(P<0.001)。在多变量分析中,幼儿(与婴儿),非资本地区(与首都地区),初级诊所和非三级医院(vs.三级医院),住院患者(vs.门诊病人),和非儿科医生(vs.儿科医生)与抗生素处方显着相关(P<0.001)。非首都地区的十四个城市和省份的抗生素处方率范围从41.2%到65.4%,其中5人(35.7%)的抗生素处方率低于首都地区。
    结论:在韩国,急性细支气管炎的高抗生素处方率因患者年龄而异,区域,医疗设施类型,临床设置,和医师专业。在制定促进适当使用抗生素的策略时,应考虑这些因素。
    BACKGROUND: Acute bronchiolitis, the most common lower respiratory tract infection in infants, is mostly caused by respiratory viruses. However, antibiotics are prescribed to about 25% of children with acute bronchiolitis. This inappropriate use of antibiotics for viral infections induces antibiotic resistance. This study aimed to determine the antibiotic prescription rate and the factors associated with antibiotic use in children with acute bronchiolitis in Korea, where antibiotic use and resistance rates are high.
    METHODS: Healthcare data of children aged < 24 months who were diagnosed with acute bronchiolitis between 2016 and 2019 were acquired from the National Health Insurance system reimbursement claims data. Antibiotic prescription rates and associated factors were evaluated.
    RESULTS: A total of 3,638,424 visits were analyzed. The antibiotic prescription rate was 51.8%, which decreased over time (P < 0.001). In the multivariate analysis, toddlers (vs. infants), non-capital areas (vs. capital areas), primary clinics and non-tertiary hospitals (vs. tertiary hospitals), inpatients (vs. outpatients), and non-pediatricians (vs. pediatricians) showed a significant association with antibiotic prescription (P < 0.001). Fourteen cities and provinces in the non-capital area exhibited a wide range of antibiotic prescription rates ranging from 41.2% to 65.4%, and five (35.7%) of them showed lower antibiotic prescription rates than that of the capital area.
    CONCLUSIONS: In Korea, the high antibiotic prescription rates for acute bronchiolitis varied by patient age, region, medical facility type, clinical setting, and physician specialty. These factors should be considered when establishing strategies to promote appropriate antibiotic use.
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  • 文章类型: Journal Article
    肺康复(PR)是慢性呼吸系统疾病患者的有效干预措施,导致锻炼能力的提高,呼吸困难,与健康相关的生活质量,心情,减少住院,并改善COPD住院后的生存率和成本节约。尽管证明了有效性,公关没有得到充分利用,部分原因是缺乏意识,有限的访问,公关报销不足。糟糕的支付是公关金融稳定和准入的长期障碍。解决PR付款问题,access,利用是一个复杂的挑战,需要战略性的,有意义的解决方案的长期合作方法。克服支付差异的策略始于立法方法,以解决医疗保险和医疗补助服务中心覆盖范围的局限性。其他优先事项包括对远程医师和高级实践提供者(APP)PR监督的永久批准,APP的公关推荐,使用双向音频/视频技术的远程康复,和消除PR寿命最大限制72小时或单位/患者。需要将适当的PR处方和鼓励与初级保健提供者有效联系起来的方法,住院医生,案件经理,和医院导航员来优化公关推荐。在农村环境中,有必要解决公关访问不足的问题。改善PR转介和获取的潜在机会包括探索PR与基于价值的护理模式的协同作用,强调高质量的护理和成本节约。开发和使用有效的PR提供商工具和资源可能有助于解决上述挑战,并使PR计划在经济上受益。
    Pulmonary rehabilitation (PR) is a highly effective intervention for persons with chronic respiratory diseases, resulting in improvement in exercise capacity, dyspnea, health-related quality of life, mood, reduced hospitalization, and improved survival and cost savings post-COPD hospitalization. Despite demonstrated effectiveness, PR is underutilized in part due to lack of awareness, limited access, and inadequate PR reimbursement. Poor payment is a long-standing barrier to PR\'s financial stability and access. Addressing PR payment, access, and utilization is a complex challenge and requires strategic, collaborative long-term approaches to meaningful solutions. Strategies to overcome payment disparities begin with legislative approaches to address limitations of Centers for Medicare and Medicaid Services coverage. Additional priorities include permanent approval for remote physician and advanced practice provider (APP) PR supervision, PR referrals by APPs, telerehabilitation using two-way audio/video technology, and elimination of the PR lifetime maximum limit of 72 h or units/patient. Methods are needed to effectively link appropriate PR prescribing and encouragement with primary care providers, hospitalists, case managers, and hospital navigators to optimize PR referrals. There is an important need to address inadequate PR access in rural settings. Potential opportunities to improve PR referrals and access include exploration of PR synergies with value-based care models that emphasize high-quality care and cost savings. Development and use of effective PR provider tools and resources may help address the above challenges as well as financially benefit PR programs.
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  • 文章类型: Journal Article
    2018年11月,隐源性卒中(CS)的报销政策从复发性卒中扩大到首次卒中发作。没有报告显示此政策变更是否影响了植入式环路记录仪(ILR)利用率的趋势。
    我们使用韩国健康保险审查和评估服务数据库确定了在2016年7月至2021年10月期间接受ILR植入物的患者。符合以下所有标准的患者被认为具有CS适应症:1)既往卒中病史,2)既往无心房颤动或扑动(AF/AFL)病史,和3)ILR植入前一年内未维持口服抗凝剂≥4周。在植入ILR后3年内或去除ILR前诊断出的AF/AFL被认为是ILR驱动的。
    在3056名患者中,1,001(32.8%)有CS适应症。实施扩大的报销政策后,CS和非CS适应症的ILR植入总数逐渐增加,CS适应症的数量显着增加。在3年以上的CS患者中,AF/AFL的检出率为26.3%,卒中后2个月内植入ILR的患者明显高于之后植入ILR的患者。
    CS的扩大覆盖政策对CS适应症的ILR植入次数有重大影响。在2个月内植入ILR时,ILR对AF/AFL检测的诊断率似乎要好于以后。需要进一步研究以证明其他临床益处和最佳ILR植入时机。
    OBJECTIVE: The reimbursement policy for cryptogenic stroke (CS) was expanded in November 2018 from recurrent strokes to the first stroke episode. No reports have demonstrated whether this policy change has affected trends in implantable loop recorder (ILR) utilization.
    METHODS: We identified patients who received an ILR implant using the Korea Health Insurance Review and Assessment Service database between July 2016 and October 2021. Patients meeting all the following criteria were considered to have CS indication: 1) prior stroke history, 2) no previous history of atrial fibrillation or flutter (AF/AFL), and 3) no maintenance of oral anticoagulant for ≥4 weeks within a year before ILR implant. AF/AFL diagnosed within 3 years after ILR implant or before ILR removal was considered ILR-driven.
    RESULTS: Among 3,056 patients, 1,001 (32.8%) had CS indications. The total ILR implant number gradually increased for both CS and non-CS indications and the number of CS indication significantly increased after implementing the expanded reimbursement policy. The detection rate for AF/AFL was 26.3% in CS patients over 3 years, which was significantly higher in patients implanted with an ILR within 2 months after stroke than those implanted later.
    CONCLUSIONS: The expanded coverage policy for CS had a significant impact on the number of ILR implantation for CS indication. The diagnostic yield of ILR for AF/AFL detection seems better when ILR is implanted within 2 months than later. Further investigation is needed to demonstrate other clinical benefits and the optimal ILR implantation timing.
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  • 文章类型: Journal Article
    背景:在中国实施与报销挂钩的价格谈判后,研究抗癌药物的上市价格和临床价值与报销决策的关系。
    方法:2017年1月至2022年6月中国国家药监局批准的抗癌药物符合纳入条件。所包括的药物适应症的批准和报销日期是从公开可用的资源中检索的。我们收集了临床价值的测量,包括生存,生活质量,以及关键临床试验的总体反应率和启动时计算的治疗价格。单变量和多变量Cox比例风险模型被用来估计发射价格之间的关联,临床价值,和中国抗癌药物的报销决定。
    结果:对于随机对照试验支持的93种适应症,中位补偿滞后为579天(IQR:402-936),对于单组临床试验支持的42种适应症,中位补偿滞后为637天(IQR373-858)。60(65%)和23(55%)的适应症得到了随机对照和单臂临床试验的支持,分别。在多元回归分析中,抗癌药物的上市价格与报销决定无关。临床价值较高的随机对照试验支持的适应症更有可能获得报销(生存率HR=1.07,95CI:1.00-1.15,p=0.037),而单组临床试验支持的适应症的总体缓解率与获得报销的可能性无关(HR=2.09,95CI:0.14~32.28,p=0.595).
    结论:抗癌药的上市价格可能不会对报销决定产生重大影响,虽然在中国实施与报销挂钩的价格谈判,但优先考虑了具有较高临床价值的抗癌药物,但仅限于随机对照试验支持的适应症。需要努力优先考虑在价格谈判过程中具有更高价值的单臂临床试验支持的适应症。
    BACKGROUND: The potential role played by launch price and clinical value in reimbursement decisions has not been sufficiently established in China. This study aimed to investigate the association of launch price and clinical value with reimbursement decisions for anticancer drugs after the implementation of reimbursement-linked price negotiation in China.
    METHODS: Anticancer drugs approved by the National Medical Products Administration (NMPA) of China from January 2017 to June 2022 were eligible for inclusion. Approval and reimbursement dates of included drug indications were retrieved from publicly available resources. We collected measures of clinical value, including survival, quality of life (QoL), and overall response rate from pivotal clinical trials and calculated treatment price at launch. Univariate and multivariate Cox proportional hazards models were employed to estimate the association between launch price, clinical value, and reimbursement decisions of anticancer drugs in China.
    RESULTS: The median reimbursement lag was 579 days (interquartile range [IQR]: 402-936) for 93 indications supported by randomized controlled trials and 637 days (IQR: 373-858) for 42 indications supported by single-arm clinical trials. Reimbursement was granted to 60 (65%) and 23 (55%) indications supported by randomized controlled and single-arm clinical trials, respectively. The launch price of anticancer drugs was not associated with reimbursement decisions in multivariate regression analyses. Indications supported by randomized controlled trials with higher clinical value were more likely to be reimbursed (hazard ratio [HR] for survival=1.07, 95% CI: 1.00-1.15, P=.037), while the overall response rate of indications supported by single-arm clinical trials was not associated with the likelihood of being reimbursed (HR=2.09, 95% CI: 0.14-32.28, P=.595).
    CONCLUSIONS: The launch price of anticancer drugs may not have a significant impact on reimbursement decisions, while the implementation of reimbursement-linked price negotiation in China has prioritized anticancer drugs with higher clinical value, but only for indications supported by randomized controlled trials. Efforts are needed to prioritize indications supported by single-arm clinical trials that have higher value during the process of price negotiation.
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  • 文章类型: Journal Article
    加拿大拥有最复杂和最严格的药物批准和公共报销流程之一,不幸的是,是药物获取延误时间最长的国家之一。为了评估全身延迟获得癌症治疗的总体影响,进行了有针对性的文献综述(TLR)以确定与临床相关的研究,经济,以及延迟获得肿瘤药物对生活质量的影响。使用MEDLINE/PubMed数据库和滚雪球,四个独特的记录符合资格标准。结果显示,临床结果受肿瘤药物获得的系统性延迟影响最大(例如,失去了生命的岁月,总生存率,和无进展生存期)。TLR检索到的四篇文章特别说明,通过提高有关开发的系统效率,可以潜在地节省大量的生命年。批准,以及晚期恶性肿瘤新药的报销流程。当务之急是采取措施提高加拿大药品监管和卫生技术评估(HTA)流程的绩效和速度,特别是对于新的癌症疗法。本文提出的解决方案包括HTA和加拿大付款人之间更好的协调,以协调覆盖决策,国际合作,信息共享,和国家肿瘤药物准入及时性标准。
    Canada has one of the most complex and rigorous drug approval and public reimbursement processes and is, unfortunately, one of the countries with the longest delays in drug access. To assess the overall impact of systemic delays in access to cancer therapy, a targeted literature review (TLR) was performed to identify studies associated with the clinical, economic, and quality of life impacts of delayed access to oncology drugs. Using MEDLINE/PubMed databases and snowballing, four unique records met the eligibility criteria. Results revealed that clinical outcomes were the most impacted by systemic delays in access to oncology drugs (e.g., life years lost, overall survival, and progression-free survival). The four articles retrieved by the TLR specifically illustrated that a substantial number of life years could potentially be saved by increasing systemic efficiency regarding the development, approval, and reimbursement processes of new drugs for advanced malignancies. It is imperative that initiatives are put in place to improve the performance and speed of Canadian drug regulatory and health technology assessment (HTA) processes, especially for new cancer therapeutics. The proposed solutions in this paper include better coordination between HTA and Canadian payers to harmonize coverage decisions, international collaborations, information sharing, and national standards for timeliness in oncology drug access.
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  • 文章类型: Journal Article
    这项研究调查了2011年至2022年国家抗肥胖药物的医疗补助覆盖政策及其医疗补助报销趋势。
    This study examines state Medicaid coverage policies for antiobesity medications and their trends in Medicaid reimbursement from 2011 to 2022.
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