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Bacterial vaginosis. 细菌性阴道炎
IF 9.4 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-06-02 DOI: 10.1503/cmaj.231688
Michal Braunstein, Amanda Selk
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引用次数: 0
Anorexie mentale masculine à l’adolescence. 青春期男性厌食症。
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-06-02 DOI: 10.1503/cmaj.230001-f
Basil Kadoura, Kyle T Ganson, Debra K Katzman
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引用次数: 0
Correction to "Projected estimates of cancer in Canada in 2024". 对 "2024 年加拿大癌症预测估计数 "的更正。
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-06-02 DOI: 10.1503/cmaj.240712
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引用次数: 0
Intraoral hemorrhagic bullae as the first sign of immunoglobulin light chain amyloidosis. 口腔内出血水泡是免疫球蛋白轻链淀粉样变性病的首发症状。
IF 9.4 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-05-26 DOI: 10.1503/cmaj.240119
Raquel María Dominguez-Lopez, Jorge Naharro-Rodriguez
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引用次数: 0
An empty heart. 一颗空洞的心
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.240008
Jacquelyn J Cragg
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引用次数: 0
Francophone patients. 法语病人。
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.231799
Mélanie Patrie, Danielle Barbeau-Rodrigue, Vanessa Morris
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引用次数: 0
Rougeole. 麻疹
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.240415-f
Sarah E Wilson, Marina I Salvadori, Michelle Science
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引用次数: 0
The impact of proposed price regulations on new patented medicine launches in Canada: a retrospective cohort study. 拟议的价格法规对加拿大新专利药品上市的影响:一项回顾性队列研究。
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.231485
Wei Zhang, Huiying Sun, Daphne P Guh, Paul Grootendorst, Aidan Hollis, Aslam H Anis

Background: The Patented Medicine Prices Review Board (PMPRB), the agency that regulates the prices of patented medicines in Canada, published proposed amendments to the regulatory framework in December 2017. Because of a series of changes and delays, the revised policy has not yet been finalized. We sought to evaluate the potential early impact of the uncertainty about the PMPRB policy on patented-medicine launches.

Methods: We developed a retrospective cohort of patented medicines (molecules) sold in Canada and the 13 countries that the PMPRB currently uses or has proposed to use as price comparators, from sales data from the IQVIA MIDAS database for 2012-2021. The outcome was whether a molecule was launched (i.e., sold) in a specific country within 2 years of its global first launch (2-yr launch). We compared the change of 2-year launch before (2012-2017) and after the proposed amendments were published ("uncertain period," 2018-2021) in Canada with the change in the United States and the other 12 countries as a group ("other-countries group"), using interrupted time series and logistic regressions, respectively. We further conducted analyses for each individual country and subgroups by molecule characteristics, such as therapeutic benefit, separately.

Results: We included 242 and 107 new molecules launched before publication of the proposed amendments and during the uncertain period, respectively. The corresponding 2-year launch proportions were 45.0% and 30.8% in Canada, 81.4% and 82.2% in the US, and 83.9% and 70.1% in the other-countries group. All analyses showed changes in 2-year launch during the uncertain period in the US and in the other-countries group that were similar to the changes in Canada. Greater decreases were observed in Norway and Sweden than in Canada. The 2-year launch proportion for molecules with major therapeutic benefit decreased from 45.8% to 31.3% in Canada during the uncertain period and from 87.5% to 62.5% in the other-countries group, but increased from 91.7% to 100% in the US.

Interpretation: No negative impact of the PMPRB-policy uncertainty on molecule launches was observed when comparing Canada with price-comparator countries, except for molecules with major therapeutic benefit. The reduction in launches of medicines with major therapeutic benefit in Canada requires continuing investigation.

背景:专利药品价格审查委员会(PMPRB)是加拿大专利药品价格的监管机构,于 2017 年 12 月发布了监管框架的拟议修正案。由于一系列修改和延迟,修订后的政策尚未最终确定。我们试图评估 PMPRB 政策的不确定性对专利药上市的潜在早期影响:我们根据 IQVIA MIDAS 数据库 2012-2021 年的销售数据,对在加拿大和 13 个国家销售的专利药品(分子)建立了一个回顾性队列,这些国家是 PMPRB 目前使用或建议用作价格比较对象的国家。结果是分子是否在全球首次上市(2 年上市)后 2 年内在特定国家上市(即销售)。我们分别采用间断时间序列和逻辑回归的方法,比较了加拿大在拟议修正案公布前(2012-2017 年)和公布后("不确定期",2018-2021 年)的 2 年上市变化情况,以及美国和其他 12 个国家组("其他国家组")的变化情况。我们还对每个国家进行了分析,并按分子特征(如治疗效果)分别进行了分组分析:我们分别纳入了 242 种和 107 种在拟议修正案公布前和不确定期间上市的新分子。相应的两年上市比例分别为:加拿大 45.0% 和 30.8%,美国 81.4% 和 82.2%,其他国家组 83.9% 和 70.1%。所有分析均显示,在不确定期间,美国和其他国家组的 2 年投放量变化与加拿大的变化相似。挪威和瑞典的下降幅度大于加拿大。在不确定期间,加拿大具有主要治疗效果的分子的 2 年上市比例从 45.8%下降到 31.3%,其他国家组从 87.5%下降到 62.5%,但美国从 91.7%上升到 100%:加拿大与价格参照国相比,除了具有重大治疗效果的分子药物外,PMPRB 政策的不确定性对分子药物的上市没有负面影响。加拿大具有重大治疗效果的药物上市量减少的情况需要继续调查。
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引用次数: 0
Vaccination contre la rougeole. 胭脂虫疫苗接种。
IF 14.6 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.240371-f
Samira Jeimy, Kyla J Hildebrand, Sabina Vohra-Miller
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引用次数: 0
Lisérés de Burton et ponctuations basophiles associés au saturnisme. 与铅中毒有关的伯顿李斯特菌和嗜碱性斑点。
IF 9.4 1区 医学 Q1 Medicine Pub Date : 2024-05-26 DOI: 10.1503/cmaj.231405-f
Takahide Morita, Toshinori Nishizawa, Toru Morikawa
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引用次数: 0
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