Insurance, Health, Reimbursement

保险,健康,报销
  • 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: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
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    背景:NVBP政策的实施大大降低了药品采购价格,并增加了NVBP药品的市场份额。本研究旨在调查武汉市患者对转向国家批量采购(NVBP)药物的态度,并确定其潜在影响因素。中国。
    方法:本研究纳入了武汉协和医院在2022年1月至2022年5月期间转用NVBP药物的21例符合条件的患者。进行半结构化面对面访谈,收集访谈信息,并采用Colaizzi七步法对访谈数据进行分析。
    结果:进行了21次半结构化面对面访谈。每次访谈的持续时间为25-35分钟,并提取与患者态度及其影响因素相关的三个主题,包括(1)患者对NVBP药物的认知;(2)家庭和社会对患者的影响;(3)患者的用药习惯。这项研究发现:1)71.4%的患者(15/21)对改用NVBP药物持积极态度;2)80.9%的患者(17/21)在实施NVBP政策后感到其药物成本显着降低;3)医疗保健专业人员和健康保险报销政策的建议对患者改用NVBP药物的态度有很大影响;4)在不同严重程度的患者中,改用NVBP药物的态度差异很大。
    结论:NVBP政策的实施显著降低了患者的医疗费用,并得到了71.4%(21个中的15个)患者的支持。然而,在这项研究中,政策的实施中发现了一些问题。卫生专业人员一般需要做出更多的努力,以改善患者对NVBP药物的成见,并增强他们对NVBP药物的信心。
    BACKGROUND: The implementation of the NVBP policy has generated considerable reductions in drug procurement prices and an increase in the market share of the NVBP drugs.This study aimed to investigate patients\' attitudes towards switching to drugs of national volume-based procurement (NVBP) and identify their underlying influencing factors in Wuhan, China.
    METHODS: A total of 21 eligible patients from the Wuhan Union Hospital who were switched to NVBP drugs between January 2022 and May 2022 were included in our study. Semi-structured face-to-face interviews were conducted to collect interview information and the interview data was analyzed by the Colaizzi seven-step method.
    RESULTS: Twenty-one semi-structured face-to-face interviews were conducted. The duration of each interview was 25-35 min and three themes related to patients\' attitudes and their influencing factors were extracted, including (1) Patients\' perception of the NVBP drugs; (2) Family and social influence to patients; (3) Medication habits of patients. This study found: 1) 71.4% patients (15/21) showed a positive attitude towards switching to NVBP medicines; 2)80.9% patients (17/21) have felt a significant reduction in their medication cost after the implementation of the NVBP policy; 3)Advices from healthcare professionals and health insurance reimbursement policies showed great impacts on patients\' attitude towards switching to NVBP drugs; 4)Attitudes towards switching to NVBP drugs varied considerably among patients with different severities of disease.
    CONCLUSIONS: The implementation of the NVBP policy has significantly reduced the cost of healthcare for patients and has been supported by71.4% (15 of 21) patients. However, some issues have been identified in the implementation of the policy in this study. Health professionals in general need to contribute more efforts to improve patients\' preconceptions about the NVBP drugs and boost their confidence in the NVBP drugs.
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  • 文章类型: Journal Article
    本回顾性介入病例系列的目的是比较根据台湾国家保险局报销政策,玻璃体内使用阿柏西普或雷珠单抗治疗的糖尿病性黄斑水肿(DME)和增生性糖尿病性视网膜病变(PDR)的功能和解剖结果。收集84只眼,所有眼睛都用光谱域光学相干断层扫描(SD-OCT)成像,彩色眼底照片(CFP),和荧光素血管造影(FA)。治疗开始后24个月,logMARBCVA从0.58±0.33提高到0.47±0.38(p<0.01),CRT从423.92±135.84下降到316.36±90.02(p<0.01),微动脉瘤的数量从142.14±57.23减少到75.32±43.86(p<0.01)。平均注射计数为11.74±5.44。logMARBCVA没有组间差异(p=0.96),CRT(p=0.69),或注射计数(p=0.81)。然而,在随访结束时用阿柏西普治疗的眼中,微动脉瘤的平均数量略有减少(p=0.06),补充全视网膜光凝(PRP)(p=0.04)和亚阈值微脉冲激光(SMPL)治疗(p=0.01)的发生率也降低。多因素分析显示,只有初始logMARBCVA影响最终的VA改善(比值比(OR)0.49,95%置信区间(CI)0.21〜0.93,p<0.01);相反,年龄(OR-0.38,95%CI-6.97〜-1.85,p<0.01)和初始CRT(OR0.56,95%CI0.34〜0.84,p<0.01)都影响了24个月时最终的CRT减少。总而言之,就VA而言,阿柏西普和雷珠单抗在PDR治疗DME方面均有效,CRT和MA计数。与接受雷珠单抗相比,接受阿柏西普治疗的眼睛需要更少的补充PRP和SMPL治疗。最初的VA影响了24个月时的最终VA改善,而年龄和初次CRT是24个月CRT减少的预后预测因子.
    The purpose of this retrospective interventional case series is to compare the functional and anatomical outcomes in eyes with diabetic macular edema (DME) and proliferative diabetic retinopathy (PDR) treated intravitreally with aflibercept or ranibizumab under the Taiwan National Insurance Bureau reimbursement policy. 84 eyes were collected and all eyes were imaged with spectral-domain optical coherence tomography (SD-OCT), color fundus photographs (CFPs), and fluorescein angiography (FA). At 24 months after therapy initiation, the logMAR BCVA improved from 0.58 ± 0.33 to 0.47 ± 0.38 (p < 0.01), the CRT decreased from 423.92 ± 135.84 to 316.36 ± 90.02 (p < 0.01), and the number of microaneurysms decreased from 142.14 ± 57.23 to 75.32 ± 43.86 (p < 0.01). The mean injection count was 11.74 ± 5.44. There was no intergroup difference in logMAR BCVA (p = 0.96), CRT (p = 0.69), or injection count (p = 0.81). However, the mean number of microaneurysms was marginally reduced (p = 0.06) in eyes treated with aflibercept at the end of the follow-up, and the incidence rates of supplementary panretinal photocoagulation (PRP) (p = 0.04) and subthreshold micropulse laser (SMPL) therapy sessions (p = 0.01) were also reduced. Multivariate analysis revealed that only initial logMAR BCVA influenced the final VA improvements (odds ratio (OR) 0.49, 95% confidence interval (CI) 0.21 ~ 0.93, p < 0.01); in contrast, age (OR - 0.38, 95% CI - 6.97 ~ - 1.85, p < 0.01) and initial CRT (OR 0.56, 95% CI 0.34 ~ 0.84, p < 0.01) both influenced the final CRT reduction at 24 months. To sum up, both aflibercept and ranibizumab are effective in managing DME with PDR in terms of VA, CRT and MA count. Eyes receiving aflibercept required less supplementary PRP and SMPL treatment than those receiving ranibizumab. The initial VA influenced the final VA improvements at 24 months, while age and initial CRT were prognostic predictors of 24-month CRT reduction.
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  • 文章类型: Journal Article
    Little is known about how health insurance policies, particularly in developing countries, influence breast cancer prognosis. Here, we examined the association between individual health insurance and breast cancer-specific mortality in China. We included 7436 women diagnosed with invasive breast cancer between 2009 and 2016, at West China Hospital, Sichuan University. The health insurance plan of patient was classified as either urban or rural schemes and was also categorized as reimbursement rate (ie, the covered/total charge) below or above the median. Breast cancer-specific mortality was the primary outcome. Using Cox proportional hazards models, we calculated hazard ratios (HRs) for cancer-specific mortality, contrasting rates among patients with a rural insurance scheme or low reimbursement rate to that of those with an urban insurance scheme or high reimbursement rate, respectively. During a median follow-up of 3.1 years, we identified 326 deaths due to breast cancer. Compared to patients covered by urban insurance schemes, patients covered by rural insurance schemes had a 29% increased cancer-specific mortality (95% CI 0%-65%) after adjusting for demographics, tumor characteristics and treatment modes. Reimbursement rate below the median was associated with a 42% increased rate of cancer-specific mortality (95% CI 11%-82%). Every 10% increase in the reimbursement rate is associated with a 7% (95% CI 2%-12%) reduction in cancer-specific mortality risk, particularly in patients covered by rural insurance schemes (26%, 95% CI 9%-39%). Our findings suggest that underinsured patients face a higher risk of breast cancer-specific mortality in developing countries.
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  • 文章类型: Journal Article
    WHO recommends that men who have sex with men (MSM) receive gonorrhoea and chlamydia testing, but many evidence-based preventive services are unaffordable. The pay-it-forward strategy offers an individual a gift (eg, a test for sexually transmitted diseases) and then asks whether they would like to give a gift (eg, a future test) to another person. This study examined the effectiveness of a pay-it-forward programme to increase gonorrhoea and chlamydia testing among MSM in China.
    We did a randomised controlled superiority trial at three HIV testing sites run by MSM community-based organisations in Guangzhou and Beijing, China. We included MSM aged 16 years or older who were seeking HIV testing and met indications for gonorrhoea and chlamydia testing. Restricted randomisation was done using computer-generated permuted blocks. 30 groups were randomised into three arms (1:1:1): a pay-it-forward arm in which men were offered free gonorrhoea and chlamydia testing and then asked whether they would like to donate for testing of prospective participants, a pay-what-you-want arm in which men were offered free testing and given the option to pay any desired amount for the test, and a standard-of-care arm in which testing was offered at ¥150 (US$22). There was no masking to arm assignment. The primary outcome was gonorrhoea and chlamydia test uptake ascertained by administrative records. We used generalised estimating equations to estimate intervention effects with one-sided 95% CIs and a prespecified superiority margin of 20%. The trial is registered with ClinicalTrials.gov, NCT03741725.
    Between Dec 8, 2018, and Jan 19, 2019, 301 men were recruited and included in the analysis. 101 were randomly assigned to the pay-it-forward group, 100 to the pay-what-you-want group, and 100 to the standard-of-care group. Test uptake for gonorrhoea and chlamydia was 56% (57 of 101 participants) in the pay-it-forward arm, 46% (46 of 100 participants) in the pay-what-you-want arm, and 18% (18 of 100 participants) in the standard-of-care arm. The estimated difference in test uptake between the pay-it-forward and standard-of-care group was 38·4% (95% CI lower bound 28·4%). Among men in the pay-it-forward arm, 54 of 57 (95%) chose to donate to support testing for others.
    The pay-it-forward strategy can increase gonorrhoea and chlamydia testing uptake among Chinese MSM and could be a useful tool for scaling up preventive services that carry a mandatory fee.
    US National Institute of Health; Special Programme for Research and Training in Tropical Diseases, sponsored by UNICEF, UNDP, World Bank, and WHO; the National Key Research and Development Program of China; Doris Duke Charitable Foundation; and Social Entrepreneurship to Spur Health.
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  • 文章类型: Journal Article
    In recent years, as the era of deepening healthcare reform in China progresses, there is a gradual development of ambulatory care pharmacy practice. This commentary reviews the current state of ambulatory care pharmacy practice in China and discusses future efforts to advance the practice. Areas of focus include practice standardization, transitions of care, and reimbursements of ambulatory care pharmacy practice.
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  • 文章类型: Journal Article
    背景:初级保健可能是增加艾滋病毒检测覆盖率的一种途径,但目前尚不清楚低收入和中等收入国家的初级保健专业人员面临哪些挑战。我们描述了社区卫生中心(CHC)的HIV检测实践,并探讨了工作人员对进一步发展中国初级保健水平的HIV检测服务的态度。
    方法:我们进行了一次全国,2015年对20个城市的CHC进行分层随机抽样的横断面调查。问卷调查由CHC的初级保健医生和护士完成,包括关于他们的人口统计的问题,临床经验以及他们对在CHC中提供HIV检测的促进者和障碍的看法。进行了多变量逻辑回归,以检查提供HIV检测的工作人员与其社会人口统计学特征之间的关联。
    结果:共有来自158个CHC的3580名员工参加。尽管大多数人(81%)同意艾滋病毒检测是医疗保健的重要组成部分,只有25%的人会在患者要求时提供艾滋病毒检测。大多数人(71%)担心报销,一半(47%)认为缺乏培训是主要障碍。几乎一半(44%)的人认为治疗属于高危人群的人会吓跑其他患者,6%的人公开表示不喜欢属于高风险人群的人。提供艾滋病毒检测的工作人员更年轻(调整后优势比(aOR)每年增加0.97,95%置信区间(CI):0.97-0.98);与护士相比,接受过医生培训(aOR1.79,95CI:1.46-2.15);拥有本科或以上学历(aOR1.34,95CI:1.11-1.62);并且以前接受过HIV培训(aOR1.55,95CI:1.27-1.89)。
    结论:改善CHC工作人员的艾滋病毒培训,包括解决污名化的态度,改善财务报销可能有助于增加中国的艾滋病毒检测覆盖率。
    BACKGROUND: Primary care may be an avenue to increase coverage of HIV testing but it is unclear what challenges primary healthcare professionals in low- and middle-income countries face. We describe the HIV testing practices in community health centres (CHCs) and explore the staff\'s attitude towards further development of HIV testing services at the primary care level in China.
    METHODS: We conducted a national, cross-sectional survey using a stratified random sample of CHCs in 20 cities in 2015. Questionnaires were completed by primary care doctors and nurses in CHCs, and included questions regarding their demographics, clinical experience and their views on the facilitators and barriers to offering HIV testing in their CHC. Multivariate logistic regression was conducted to examine the association between staff who would offer HIV testing and their sociodemographic characteristics.
    RESULTS: A total of 3580 staff from 158 CHCs participated. Despite the majority (81%) agreeing that HIV testing was an important part of healthcare, only 25% would provide HIV testing when requested by a patient. The majority (71%) were concerned about reimbursement, and half (47%) cited lack of training as a major barrier. Almost half (44%) believed that treating people belonging to high-risk populations would scare other patients away, and 6% openly expressed their dislike of people belonging to high-risk populations. Staff who would offer HIV testing were younger (adjusted odds ratio (aOR) 0.97 per year increase in age, 95% confidence interval (CI):0.97-0.98); trained as a doctor compared to a nurse (aOR 1.79, 95%CI:1.46-2.15); held a bachelor degree or above (aOR 1.34, 95%CI:1.11-1.62); and had previous HIV training (aOR 1.55, 95%CI:1.27-1.89).
    CONCLUSIONS: Improving HIV training of CHC staff, including addressing stigmatizing attitudes, and improving financial reimbursement may help increase HIV testing coverage in China.
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