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Drug Coverage Policy and Legacy Prescribing: A Cross-Sectional Analysis in British Columbia 药物覆盖政策和遗留处方:不列颠哥伦比亚省的横断面分析。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71718
Aydan Con, Ivy Thrasher, Aaron M. Tejani
<p>Legacy drug-prescribing, the practice of continuing fixed-term drug therapy indefinitely without strong evidence of long-term therapeutic benefit, is a growing concern in healthcare [<span>1</span>]. Legacy drug prescribing can contribute to polypharmacy, which is associated with adverse health outcomes [<span>2</span>]. Several studies have highlighted significant proportions of elderly patients receiving legacy drug prescriptions for antidepressants, bisphosphonates, and proton-pump inhibitors (PPIs) [<span>1, 3, 4</span>]. In British Columbia, the provincial government operates the BC Pharmacare Drug Plan, which provides medication funding for individuals [<span>5</span>]. Within this plan, the Limited Coverage program (BCPLC) funds medications only when patients meet specific medical criteria, with coverage typically granted for defined durations [<span>5</span>].</p><p>Because such funding rules shape access, drug policy itself can influence prescribing patterns. Irish data show polypharmacy is more common among patients with subsidized coverage than those paying out-of-pocket [<span>4</span>]. Medicare Part D similarly increased both essential and low-value drug use [<span>3</span>], while British Columbia's reference pricing policy shifted patients to lower-cost equivalents without harm [<span>6</span>]. Together, this evidence suggests that funding arrangements can either reinforce problematic polypharmacy or promote more cost-effective prescribing. This study aims to assess whether BCPLC funding criteria contribute to legacy drug prescribing specifically and/or problematic polypharmacy.</p><p>We analyzed the 2022 BCPLC formulary, comprising 302 medications, focusing on the covered indications and duration of therapy (DOT) for each medication [<span>5</span>]. A multidisciplinary research group consisting of two pharmacist members of the BC Ministry of Health, a pharmacist and two research assistants developed a standardized data collection form. This form extracted the BCPLC covered indications and funding durations, as well as the listed indications and durations found in best-available evidence, such as systematic reviews, Health Canada drug monographs, Canadian Agency for Drugs and Technologies in Health (now known as Canada's Drug Agency) reimbursement recommendations, and clinical databases like UpToDate and Lexicomp [<span>7</span>]. We compared BCPLC criteria with referenced durations and indications and identified two types of mismatches: duration of therapy mismatch (DOTM) and indication mismatches (IM) [<span>5</span>]. We looked to see if medications with mismatches were listed as potentially inappropriate according to Beer's 2019 criteria [<span>8</span>]. All analyses were descriptive only; no statistical calculations were done. No Research Ethics Board approval was required as this was a quality assurance project.</p><p>Of 286 medications analyzed, 40% exhibited at least one mismatch (see Figure 1), predominantly DOTMs,
遗留药物处方,即在没有强有力证据表明长期治疗获益的情况下无限期地继续定期药物治疗的做法,是医疗保健领域日益关注的问题。遗留药物处方可能导致多种用药,这与不良健康结果有关。一些研究强调了接受抗抑郁药、双膦酸盐和质子泵抑制剂(PPIs)等遗留药物处方的老年患者的显著比例[1,3,4]。在不列颠哥伦比亚省,省政府实施了不列颠哥伦比亚省药品保险计划,为个人提供药品资金。在该计划中,有限保险计划(bccplc)仅在患者符合特定医疗标准时才为药物提供资金,通常在规定的持续时间内提供保险。由于此类资助规则决定了获取途径,药物政策本身也会影响处方模式。爱尔兰的数据显示,与自费医疗保险的患者相比,在有补贴的患者中,多药房更为常见。医疗保险D部分同样增加了基本药物和低价值药物的使用[3],而不列颠哥伦比亚省的参考定价政策将患者转移到低成本的等效药物而没有伤害[3]。总之,这一证据表明,资金安排可以强化有问题的综合用药或促进更具成本效益的处方。本研究旨在评估BCPLC资助标准是否有助于遗留药物处方,特别是和/或有问题的多药。我们分析了2022年bccp处方,包括302种药物,重点分析了每种药物的适应症和治疗时间(DOT)。由卑诗省卫生部的两名药剂师成员、一名药剂师和两名研究助理组成的多学科研究小组制定了一份标准化数据收集表。该表单提取了bccc涵盖的适应症和资助期限,以及在现有最佳证据中列出的适应症和期限,例如系统审查、加拿大卫生部药物专著、加拿大卫生药品和技术机构(现称为加拿大药品机构)报销建议,以及UpToDate和Lexicomp[7]等临床数据库。我们比较了bccc标准的参考时间和适应症,并确定了两种不匹配类型:治疗时间不匹配(DOTM)和适应症不匹配(IM)[5]。根据比尔2019年的标准,我们查看了不匹配的药物是否被列为可能不合适的药物。所有的分析都是描述性的;没有进行统计计算。不需要研究伦理委员会的批准,因为这是一个质量保证项目。在分析的286种药物中,40%表现出至少一种不匹配(见图1),主要是DOTMs,主要由非甾体抗炎药、PPIs和双膦酸盐组成。我们确定了DOTMs的四个子类别(见图2,n = 90):(a) bplc覆盖范围不确定的药物,只能在有限的时间内使用(n = 55), (b)建议的试验期短于bplc处方中列出的或未列出的药物(n = 15), (c) bplc覆盖范围固定的药物,超过我们的参考治疗持续时间(n = 8), (d)推荐用于固定周期治疗的药物,对最佳治疗持续时间缺乏共识(n = 13)。此外,根据Beer 2019年的标准,28种被认为可能不合适的药物的DOTMs为100。bccc覆盖标准显示不一致可能导致不适当的遗留处方和有问题的多药,特别是非甾体抗炎药、PPIs和双膦酸盐。根据我们的研究结果,我们建议将非甾体抗炎药的覆盖范围限制在有限的时间内,并对长期使用进行重新评估;将PPI覆盖范围限制在8-12周,并根据需要续保;并将无限期的双膦酸盐覆盖范围改为最初的5年,随后需要续保。这些较短的覆盖期鼓励定期重新评估,促进安全、适当和有时间限制的药物使用。虽然较短的覆盖期限可能促进更安全、有时间限制的处方,但它们也有风险。在不列颠哥伦比亚省持续的初级保健短缺中,更频繁的评估和处方续期请求可能会增加行政负担,为没有正规提供者的患者创造获取障碍,并延误必要的治疗。根据临床需要,一部分患者可能还需要更长时间的非甾体抗炎药、质子泵抑制剂或双膦酸盐。虽然这些变化可能会将工作量转移到初级保健,但频繁的治疗重新评估是标准护理,并且可以由其他授权提供者(包括社区药剂师或执业护士)支持更新。 为了防止意外伤害,默认为较短间隔的保险政策可以包括药剂师根据协议发起的续订,简化的电子重新评估,具有保险宽限期的自动提醒,以及明确扩大保险范围的标准(例如,巴雷特食管的PPI)。这些措施有助于平衡适当性与可及性,同时尽量减少可避免的治疗中断。我们的发现与药物覆盖政策影响处方的证据一致。获得补贴的患者往往会经历更多的多种用药,覆盖范围的变化可以增加低价值和高价值药物的使用,扩大的福利可以提高整体药物使用[3,4]。在不列颠哥伦比亚省,有限的BC药品保险可能会无意中鼓励潜在有害的处方。与之前的研究不同,我们专门研究了政策设计作为次优药物使用的驱动因素,解决了在理解资助规则的意外后果方面的差距。通过系统地评估BCPLC标准,我们提出了可操作的建议,这些建议得到了广泛使用的临床工具和监管指南bbb的支持。局限性包括缺乏实际处方模式或患者结果的数据,以及资源池较窄,无法捕捉到所有细微差别。未来的研究应该检查覆盖政策对处方行为和患者结果的影响。不列颠哥伦比亚省的政策制定者应该重新考虑有潜在危害的药物的无限期覆盖,包括非甾体抗炎药、质子泵抑制剂和双膦酸盐,以确保定期重新评估治疗并减少有问题的多药风险。艾丹·康:数据管理,形式分析,调查,方法论,项目管理,写作-原稿,写作-审查和编辑。Ivy Thrasher:数据管理,形式分析,方法论,项目管理。Aaron M. Tejani:概念化,数据管理,形式分析,方法论,项目管理,监督,验证,写作-原始草案,写作-审查和编辑。作者没有得到这项工作的特别资助。作者声明无利益冲突。通讯作者Aaron M. Tejani确认该手稿是对所报道的研究的诚实、准确和透明的描述;没有遗漏研究的重要方面;并且研究计划中的任何差异(如果相关的话,记录)都已得到解释。支持本研究结果的数据可向通讯作者索取。由于隐私或道德限制,这些数据不会公开。
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引用次数: 0
How Has the COVID-19 Pandemic Affected the Influenza Seasonality Patterns in Different Climate Regions?—A Time-Series Analysis COVID-19大流行如何影响不同气候区域的流感季节性模式?-时间序列分析。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71456
Ricardo Fonseca, Galana Mamo Ayana, Patricia Lee

Background and Aims

Due to the burden of influenza, significant efforts have been made to understand its geographical and temporal patterns to advise influenza prevention. Influenza temporal patterns have been affected since the emergence of COVID-19, presumably attributed to nonpharmacological interventions (NPIs). Understanding the changes in influenza activity before and during the COVID-19 pandemic in different climate regions is urgently needed to inform decision-making in future influenza control measures and prevention policies.

Methods

This study analysed influenza surveillance data (2012–2022) collected from the FluNet database to compare the patterns of long-term influenza activity in nine selected temperate and tropical countries. The long-term influenza activity in each country was compared before and after the emergence of COVID-19. The level of NPI stringency was measured using the stringency index (SI). Interrupted time series (ITS) analyses were performed to quantify the impact of COVID-19 NPIs on the changes in influenza patterns before and after the stringent implementation of NPIs in the selected countries.

Results

Before the COVID-19 pandemic, influenza activity in temperate countries appeared in winter, while the seasonality patterns in tropical countries were irregular and lasted longer than in temperate countries. During the pandemic, influenza cases decreased drastically in all selected countries, even though the amount of influenza testing remained adequate. The ITS results confirmed a significantly inverse relationship between stringency of NPIs and influenza activity. Although influenza cases have reemerged following the removal of NPIs, the patterns of influenza activity worldwide remain undergoing transitioning shifts post-pandemic. International collaboration is needed to continue monitoring future changes in influenza patterns to prevent large outbreaks.

Conclusion

There has been a change in the temporal patterns of influenza activity worldwide after the pandemic. NPIs have shown a significant effect in reducing influenza activity in all selected countries.

背景和目的:由于流感的负担,已作出重大努力了解其地理和时间格局,以便为流感预防提供建议。自COVID-19出现以来,流感时间模式受到了影响,这可能归因于非药物干预措施(npi)。迫切需要了解不同气候区域在COVID-19大流行之前和期间流感活动的变化,以便为未来流感控制措施和预防政策的决策提供信息。方法:本研究分析了从FluNet数据库收集的流感监测数据(2012-2022年),以比较9个选定的温带和热带国家的长期流感活动模式。比较了各国在COVID-19出现前后的长期流感活动性。NPI的严格程度用严格指数(SI)来衡量。通过中断时间序列(ITS)分析,量化选定国家在严格实施国家行动计划前后COVID-19国家行动计划对流感模式变化的影响。结果:2019冠状病毒病大流行前,温带国家的流感活动出现在冬季,而热带国家的季节性模式不规律,持续时间长于温带国家。在大流行期间,尽管流感检测的数量仍然充足,但所有选定国家的流感病例都急剧减少。ITS结果证实,npi的严格程度与流感活性之间存在显著的反比关系。虽然在取消国家预防措施后流感病例再次出现,但全球流感活动模式在大流行后仍在经历过渡转变。需要国际合作,继续监测未来流感形态的变化,以防止大规模疫情。结论:大流行后,世界范围内流感活动的时间模式发生了变化。在所有选定的国家,国家行动计划在减少流感活动方面显示出显著效果。
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引用次数: 0
Augmented Reality-Based Femur Registration With Head-Mounted Display and Infrared Tracking Device as Stand-Alone Navigation Tool: A Preclinical Validation Study 基于增强现实的股骨配准头戴式显示器和红外跟踪设备作为独立导航工具:临床前验证研究。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71723
Nicolas Himpe, Quentin Neuville, Taylor Frantz, Jef Vandemeulebroucke, Lieven Moke, Georges Vles, Stijn Ghijselings, Thierry Scheerlinck

Background and Aims

This study evaluated the accuracy of a standalone augmented reality (AR) navigation system using the Microsoft HoloLens 2 for total hip arthroplasty (THA). The system integrates infrared (IR) tracking and a preoperative 3D CT model for intraoperative visualization and guidance. The aim was to assess whether this AR-based solution could achieve clinically acceptable accuracy for use as a surgical navigation tool.

Methods

A dedicated AR application was developed to perform six-degrees-of-freedom pose estimation using inside-out tracking. Registration accuracy was assessed using six femur replicas with predefined target points. The registration pipeline combined landmark-based initialization with iterative surface refinement. Target registration error (TRE) was calculated for each point, and the influence of anatomical region, axis, surgical approach (anterior vs. posterior), and user experience level was analyzed.

Results

The system achieved a mean TRE of 3.61 ± 2.18 mm. Significant variations in accuracy were observed between anatomical regions (p = 0.019) and along different axes (p < 0.001), with the highest errors noted along the anteroposterior axis and in distal femoral regions. No significant differences were found between anterior and posterior approaches or among users with varying levels of experience, indicating operator-independent performance.

Conclusion

The AR navigation system demonstrated consistent and accurate registration performance across users and approaches. With a mean TRE of ~3 mm, the system meets accuracy requirements for potential clinical application in THA. Further cadaveric validation is recommended to confirm surgical feasibility and applicability.

背景和目的:本研究评估了使用微软HoloLens 2进行全髋关节置换术(THA)的独立增强现实(AR)导航系统的准确性。该系统集成了红外(IR)跟踪和术前3D CT模型,用于术中可视化和指导。目的是评估这种基于ar的解决方案是否可以达到临床可接受的精度,作为手术导航工具。方法:开发了一个专用的AR应用程序,使用由内向外跟踪进行六自由度姿态估计。使用六个具有预定目标点的股骨复制品评估配准精度。配准管道结合了基于地标的初始化和迭代曲面细化。计算每个点的目标配准误差(TRE),并分析解剖区域、轴、手术入路(前路vs后路)和用户体验水平的影响。结果:系统平均TRE为3.61±2.18 mm。在不同解剖区域之间(p = 0.019)和不同轴向上观察到准确率的显著差异(p)。结论:AR导航系统在不同用户和方法中表现出一致和准确的配准性能。该系统的平均TRE为~3 mm,满足THA潜在临床应用的精度要求。建议进一步的尸体验证以确认手术的可行性和适用性。
{"title":"Augmented Reality-Based Femur Registration With Head-Mounted Display and Infrared Tracking Device as Stand-Alone Navigation Tool: A Preclinical Validation Study","authors":"Nicolas Himpe,&nbsp;Quentin Neuville,&nbsp;Taylor Frantz,&nbsp;Jef Vandemeulebroucke,&nbsp;Lieven Moke,&nbsp;Georges Vles,&nbsp;Stijn Ghijselings,&nbsp;Thierry Scheerlinck","doi":"10.1002/hsr2.71723","DOIUrl":"10.1002/hsr2.71723","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and Aims</h3>\u0000 \u0000 <p>This study evaluated the accuracy of a standalone augmented reality (AR) navigation system using the Microsoft HoloLens 2 for total hip arthroplasty (THA). The system integrates infrared (IR) tracking and a preoperative 3D CT model for intraoperative visualization and guidance. The aim was to assess whether this AR-based solution could achieve clinically acceptable accuracy for use as a surgical navigation tool.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A dedicated AR application was developed to perform six-degrees-of-freedom pose estimation using inside-out tracking. Registration accuracy was assessed using six femur replicas with predefined target points. The registration pipeline combined landmark-based initialization with iterative surface refinement. Target registration error (TRE) was calculated for each point, and the influence of anatomical region, axis, surgical approach (anterior vs. posterior), and user experience level was analyzed.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The system achieved a mean TRE of 3.61 ± 2.18 mm. Significant variations in accuracy were observed between anatomical regions (<i>p</i> = 0.019) and along different axes (<i>p</i> &lt; 0.001), with the highest errors noted along the anteroposterior axis and in distal femoral regions. No significant differences were found between anterior and posterior approaches or among users with varying levels of experience, indicating operator-independent performance.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The AR navigation system demonstrated consistent and accurate registration performance across users and approaches. With a mean TRE of ~3 mm, the system meets accuracy requirements for potential clinical application in THA. Further cadaveric validation is recommended to confirm surgical feasibility and applicability.</p>\u0000 </section>\u0000 </div>","PeriodicalId":36518,"journal":{"name":"Health Science Reports","volume":"9 2","pages":""},"PeriodicalIF":2.1,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12838244/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146094511","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
High Prevalence of Active HDV Infection Among HBsAg-Positive Patients in Urban and Rural Areas in Gabon: A Cross-Sectional Retrospective Study 加蓬城乡hbsag阳性患者中高流行率的活动性HDV感染:一项横断面回顾性研究
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71535
Berthold Bivigou-Mboumba, Michelle Bignoumba, Pamela Moussavou-Boundzanga, Elsa-Luce Missoni Manga, Amahani Gafou, Yann Mouanga Ndzime, Dorothée Marielle Wora, Larissa F. Akombi, Jovanie-Dawen's Lendoye Zika Olembi, Rejane Manelle Betty Ndjila, Cyrille Bisseye, Augustin Mouinga Ondeme, Richard Onanga, Pascal Pineau

Background

HDV, a defective virus dependent on hepatitis B for assembly, can lead to severe liver diseases and an increased risk of progressing to complications such as hepatocellular carcinoma. Given the high prevalence of HDV in Gabon, especially in central Africa, understanding the epidemiology and associated risks is crucial.

Aim

This study aimed to assess the serological and molecular features of HDV among HBsAg-positive patients in the urban and rural areas of Gabon.

Method

The study was conducted from April 2019 to December 2022 in the Franceville area and from January to June 2023 in the Libreville area. We enrolled 145 newly diagnosed HBsAg-positive individuals in Franceville (101) and Libreville (44). Plasma samples were collected for serological and molecular analyses, including tests for HDV antibodies and RNA detection.

Result

The results showed an overall HDV prevalence of 26.2%, with higher rates in Libreville (18/44; 40.9%) compared to Franceville (20/101; 19.8%). Molecular analysis identified the circulation of genotypes I, VII, and VIII, with a predominance of replicative forms. The prevalence of replicative HDV RNA activity was 29.4%, indicating a need for accessible treatment options. Demographic analysis revealed a predominantly male population with an average age of 40.

Conclusion

These findings provide valuable insights into the epidemiology of HDV in Gabon and emphasise the importance of targeted interventions and further research to address public health challenges associated with HDV infection in the region.

背景:HDV是一种依赖于乙型肝炎进行组装的缺陷病毒,可导致严重的肝脏疾病,并增加进展为肝细胞癌等并发症的风险。鉴于HDV在加蓬,特别是在中非的高流行率,了解流行病学和相关风险至关重要。目的:本研究旨在评估加蓬城乡地区hbsag阳性患者HDV的血清学和分子特征。方法:研究于2019年4月至2022年12月在弗朗斯维尔地区进行,于2023年1月至6月在利伯维尔地区进行。我们在Franceville(101)和Libreville(44)招募了145名新诊断的hbsag阳性个体。收集血浆样本进行血清学和分子分析,包括检测HDV抗体和RNA检测。结果:结果显示,总HDV患病率为26.2%,其中利伯维尔(18/44;40.9%)高于弗朗斯维尔(20/101;19.8%)。分子分析确定了基因型I、VII和VIII的循环,以复制型为主。复制型HDV RNA活性的流行率为29.4%,表明需要可获得的治疗方案。人口统计分析显示,人口以男性为主,平均年龄为40岁。结论:这些发现为加蓬HDV流行病学提供了有价值的见解,并强调了有针对性的干预措施和进一步研究的重要性,以解决该地区与HDV感染相关的公共卫生挑战。
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引用次数: 0
Evaluation of Prevalence and Risk Factors of Possible Sarcopenia Based on SARC-F in Adults Over 60 in Tegucigalpa, Honduras: A Cross-Sectional Study 基于SARC-F对洪都拉斯特古西加尔巴60岁以上成年人可能的肌肉减少症患病率和危险因素的评估:一项横断面研究。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71761
Marcio Madrid, Jesus Perez, Joseph Gomez, Salvador Diaz, Yolly Molina, Emmely Henriquez, Gisela Mejia, Margiurie Sierra, Melania Madrid, Alicia Diaz, Martha Casco, Carlos Agudelo-Santos, Jorge Valle, Jose Zablah

Background and Aims

Sarcopenia, a progressive loss of skeletal muscle mass and function, poses a growing public health challenge in low and middle-income settings. We aimed to quantify its prevalence and identify sex-specific risk factors among older adults attending a public outpatient clinic in Tegucigalpa, Honduras.

Methods

In a hospital-based, age-stratified random sample, we enrolled 100 participants (73 women and 27 men; mean age = 69.7 ± 6.9 years) during July 2024. Possible sarcopenia and frailty were assessed using SARC-F and FRAIL questionnaires, respectively. Body mass index was calculated under standardized conditions and mean arterial pressure (MAP) was derived from blood pressure measurements. Normality of continuous variables was evaluated with the Shapiro–Wilk test. Between-sex differences were analyzed using Welch's t-test for continuous variables and χ2 test for categorical variables (α = 0.05). Pearson's correlation was employed to assess associations between SARC-F scores and clinical variables.

Results

Possible sarcopenia (SARC‑F ≥ 4) was present in 48% of participants (95% CI = 38–58), while 40% met criteria for frailty. Women showed a significantly higher mean BMI than men (28.0 ± 5.7 kg m−2 vs. 24.9 ± 4.5 kg m−2; t = 2.8, p = 0.007) yet a comparable MAP (102 ± 13 mmHg vs. 99 ± 13 mmHg; p = 0.33). Frailty prevalence remained higher in women across all age strata (42.5% vs. 37.0%), although the sex difference was not statistically significant (χ2 = 0.2, p = 0.9). SARC‑F scores correlated modestly with MAP (r = 0.3, p = 0.003) but not with age (r = 0.1, p = 0.3) or BMI (r = 0.1, p = 0.4).

Conclusions

Nearly half of older adults were at risk of sarcopenia and two-fifths were frail, with women more affected. Elevated blood pressure was linked to functional decline.

背景和目的:骨骼肌减少症是一种骨骼肌质量和功能的进行性损失,在低收入和中等收入环境中构成了越来越大的公共卫生挑战。我们的目的是量化在洪都拉斯特古西加尔巴一家公共门诊就诊的老年人的患病率,并确定性别特异性的危险因素。方法:在以医院为基础的年龄分层随机样本中,我们于2024年 月招募了100名参与者(73名女性和27名男性;平均 年龄= 69.7±6.9 岁)。分别使用SARC-F和虚弱问卷对可能的肌肉减少症和虚弱进行评估。体重指数在标准化条件下计算,平均动脉压(MAP)由血压测量得出。用Shapiro-Wilk检验评价连续变量的正态性。对连续变量采用Welch’st检验,对分类变量采用χ 2检验(α = 0.05)。采用Pearson相关法评估SARC-F评分与临床变量之间的相关性。结果:48%的参与者存在可能的肌肉减少症(SARC - F≥4)(95% CI = 38-58),而40%的参与者符合虚弱标准。女性的平均BMI明显高于男性(28.0±5.7 kg m-2 vs. 24.9±4.5 kg m-2; t = 2.8, p = 0.007), MAP也相当(102±13 mmHg vs. 99±13 mmHg; p = 0.33)。尽管性别差异无统计学意义(χ 2 = 0.2, p = 0.9),但在所有年龄段的女性中,虚弱患病率仍然较高(42.5% vs. 37.0%)。SARC - F评分与MAP (r = 0.3, p = 0.003)有一定相关性,但与年龄(r = 0.1, p = 0.3)或BMI (r = 0.1, p = 0.4)无关。结论:近一半的老年人有肌肉减少症的风险,五分之二的人身体虚弱,女性受影响更大。血压升高与功能衰退有关。
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引用次数: 0
Transferability of Real World Evidence to Support HTA Recommendations in Lower Income European Countries 支持HTA建议的真实世界证据在低收入欧洲国家的可转移性。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71534
Zoltán Kaló, Guenka Petrova, Bertalan Németh, Petra Došenović Bonča, Diana Delnoij, Alastair Bennett, Konstantin Tachkov, Yingying Zhang, Noemi Kreif, Saskia Knies, Iga Lipska, Tomas Tesar, Zornitsa Mitkova, Johan Ponten, Anders Viberg, Marian-Sorin Paveliu, Oresta Piniazkho, Adina Turcu-Stiolica, Tomáš Doležal, Michal Staňák, Alima Almadiyeva, Rok Hren, Dinko Vitezić, Zsuzsanna Petykó, Wim Goettsch, Andrea Manca

Background and Aims

Lower income European countries (LIECs) have more limited financial resources to cover high-cost technologies in rare diseases than higher income European countries (HIECs). Our study explores how treatment recommendations in myelodysplastic syndrome (MDS) can be supported in LIECS by transferring real-world evidence (RWE) generated by target trial emulation (TTE) method in HIECs.

Method

In the HTx project transferability aspects of the MDS case study were considered upfront. HTA agency consortium partners set expectations for the MDS case study team on how to integrate the new TTE methodology into the routine work of HTA bodies. In consecutive workshops consortium members and external HTA experts identified the main challenges of transferring evidence generated by TTE method to LIECs and made conclusions on how to overcome these challenges.

Results

The lack of local real-world data before making reimbursement decisions is an important challenge to apply the TTE method to LIECs. Differences in patient pathways and comparator technologies, limited expertise and resources for adapting international HTA methods are significant barriers of transferring RWE from other countries.

Still, transferring RWE to LIECs from other countries based on the TTE methodology represents an improvement to the current standard HTA methods, especially if joint clinical assessment provides the unbiased judgement on the relative effectiveness of orphan medicines. The TTE approach also provides an opportunity to LIECs to judge the value of high-cost technologies for different patient subgroups. However, HTA professionals in LIECs need training about advanced methodologies.

Conclusion

This is the first study to explore how RWE generated by the TTE method can be transferred to optimize treatment decisions of patients with a rare disease in countries with limited HTA capacities. Five general concluding statements were made on the novelty of the TTE method and on how to overcome main challenges of transferring TTE results to HTA systems in LIECs.

背景和目的:与高收入的欧洲国家相比,较低收入的欧洲国家(LIECs)用于支付罕见病高成本技术的财政资源更为有限。我们的研究探讨了如何通过转移HIECs中靶标试验模拟(TTE)方法产生的真实世界证据(RWE)来支持LIECS中骨髓增生异常综合征(MDS)的治疗建议。方法:在HTx项目中,首先考虑了MDS案例研究的可转移性方面。HTA机构联盟合作伙伴就如何将新的TTE方法纳入HTA机构的日常工作对MDS案例研究小组提出了期望。在连续的研讨会上,联盟成员和外部HTA专家确定了将TTE方法产生的证据转移给LIECs的主要挑战,并就如何克服这些挑战得出了结论。结果:在做出报销决策之前缺乏当地真实数据是将TTE方法应用于liec的一个重要挑战。患者途径和比较器技术的差异,适应国际HTA方法的专业知识和资源有限,是从其他国家转移RWE的重大障碍。尽管如此,根据TTE方法将RWE从其他国家转移到LIECs代表了对当前标准HTA方法的改进,特别是如果联合临床评估提供了对孤儿药相对有效性的公正判断。TTE方法还为liec提供了一个机会,以判断高成本技术对不同患者亚组的价值。然而,liec的HTA专业人员需要高级方法方面的培训。结论:这是第一个探索如何将TTE方法产生的RWE转移到HTA能力有限的国家,以优化罕见病患者的治疗决策的研究。就TTE方法的新颖性以及如何克服将TTE结果转移到liec的HTA系统的主要挑战发表了五项一般性结论性陈述。
{"title":"Transferability of Real World Evidence to Support HTA Recommendations in Lower Income European Countries","authors":"Zoltán Kaló,&nbsp;Guenka Petrova,&nbsp;Bertalan Németh,&nbsp;Petra Došenović Bonča,&nbsp;Diana Delnoij,&nbsp;Alastair Bennett,&nbsp;Konstantin Tachkov,&nbsp;Yingying Zhang,&nbsp;Noemi Kreif,&nbsp;Saskia Knies,&nbsp;Iga Lipska,&nbsp;Tomas Tesar,&nbsp;Zornitsa Mitkova,&nbsp;Johan Ponten,&nbsp;Anders Viberg,&nbsp;Marian-Sorin Paveliu,&nbsp;Oresta Piniazkho,&nbsp;Adina Turcu-Stiolica,&nbsp;Tomáš Doležal,&nbsp;Michal Staňák,&nbsp;Alima Almadiyeva,&nbsp;Rok Hren,&nbsp;Dinko Vitezić,&nbsp;Zsuzsanna Petykó,&nbsp;Wim Goettsch,&nbsp;Andrea Manca","doi":"10.1002/hsr2.71534","DOIUrl":"10.1002/hsr2.71534","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and Aims</h3>\u0000 \u0000 <p>Lower income European countries (LIECs) have more limited financial resources to cover high-cost technologies in rare diseases than higher income European countries (HIECs). Our study explores how treatment recommendations in myelodysplastic syndrome (MDS) can be supported in LIECS by transferring real-world evidence (RWE) generated by target trial emulation (TTE) method in HIECs.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Method</h3>\u0000 \u0000 <p>In the HTx project transferability aspects of the MDS case study were considered upfront. HTA agency consortium partners set expectations for the MDS case study team on how to integrate the new TTE methodology into the routine work of HTA bodies. In consecutive workshops consortium members and external HTA experts identified the main challenges of transferring evidence generated by TTE method to LIECs and made conclusions on how to overcome these challenges.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The lack of local real-world data before making reimbursement decisions is an important challenge to apply the TTE method to LIECs. Differences in patient pathways and comparator technologies, limited expertise and resources for adapting international HTA methods are significant barriers of transferring RWE from other countries.</p>\u0000 \u0000 <p>Still, transferring RWE to LIECs from other countries based on the TTE methodology represents an improvement to the current standard HTA methods, especially if joint clinical assessment provides the unbiased judgement on the relative effectiveness of orphan medicines. The TTE approach also provides an opportunity to LIECs to judge the value of high-cost technologies for different patient subgroups. However, HTA professionals in LIECs need training about advanced methodologies.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>This is the first study to explore how RWE generated by the TTE method can be transferred to optimize treatment decisions of patients with a rare disease in countries with limited HTA capacities. Five general concluding statements were made on the novelty of the TTE method and on how to overcome main challenges of transferring TTE results to HTA systems in LIECs.</p>\u0000 </section>\u0000 </div>","PeriodicalId":36518,"journal":{"name":"Health Science Reports","volume":"9 2","pages":""},"PeriodicalIF":2.1,"publicationDate":"2026-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12836872/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146094684","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
How to Better Assess the Real Role of the Environment in Pregnancy, From Past to Future: A Relational Open Data Infrastructure Covering 30,000 Births 如何更好地评估环境在怀孕中的真实作用,从过去到未来:一个涵盖30,000个新生儿的关系开放数据基础设施。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71668
Sophie Cot, Nadine Bernard, Berenger Martin, Honorine Gauthier-Manuel, Sophie Pujol, Frederic Mauny, Nicolas Mottet

Background and Aims

One of today's challenges in terms of understanding the real impact of the environment on pregnancy and its complications is the ability to work with real-life data that are correctly and extensively connected to data on the contamination of living environments and individualized exposures. We present a solution based on a data infrastructure that is directly usable for research. We describe (i) the methodological characteristics of the infrastructure, (ii) the geographical territory and environmental exposures covered by the infrastructure, and (iii) the initial description of the real-life health data of the included population.

Methods

The infrastructure is a relational database that integrates routine obstetric care data from CHUB with individual environmental exposure data linked via home addresses. The infrastructure includes all deliveries at Besançon University Hospital (CHUB) from January 1, 2010, to December 31, 2021.

Results

Our infrastructure included information on 20,376 women, 28,344 pregnancies, and 29,190 births. The infrastructure described includes 20% of deliveries in an administrative region of more than 1.5 million inhabitants. The quality of the data is linked to highly contrasted exposure of living areas within this region and temporal coverage of more than 10 years of obstetrical events. This infrastructure is a research tool with the capacity to incorporate data in the future.

Conclusion

This infrastructure can be used to address a wide range of questions aimed at describing the phenomena of environmental exposure during pregnancy, multiple exposures and their cumulative effects, particularly the phenomena of mediation, interaction, or confusion.

背景和目的:在了解环境对怀孕及其并发症的实际影响方面,当今面临的挑战之一是处理与生活环境污染和个体化暴露数据正确和广泛相关的现实数据的能力。我们提出了一个基于数据基础设施的解决方案,该解决方案可直接用于研究。我们描述了(i)基础设施的方法学特征,(ii)基础设施覆盖的地理领土和环境暴露,以及(iii)对纳入人口的真实健康数据的初步描述。方法:基础设施是一个关系数据库,它整合了来自CHUB的常规产科护理数据和通过家庭地址链接的个人环境暴露数据。该基础设施包括2010年1月1日至2021年12月31日在贝桑佩尔松大学医院(CHUB)分娩的所有产妇。结果:我们的基础设施包括20,376名妇女,28,344名孕妇和29,190名新生儿的信息。所描述的基础设施包括在一个拥有150多万居民的行政区域内20%的交付。数据的质量与该地区生活区域的高度对比暴露和超过10年的产科事件的时间覆盖有关。该基础设施是一种研究工具,具有将来合并数据的能力。结论:该基础设施可用于解决一系列旨在描述怀孕期间环境暴露现象、多重暴露及其累积效应的问题,特别是调解、相互作用或混淆现象。
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引用次数: 0
Portuguese Version of the PROMIS® Self-Efficacy for Managing Daily Activities for Patients With Chronic Conditions: Translation and Cross-Cultural Adaptation 葡萄牙语版PROMIS®管理慢性病患者日常活动的自我效能:翻译和跨文化适应。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-27 DOI: 10.1002/hsr2.71589
Sarah Joysi Almeida Leite, Thayla Amorim Santino, Sara Ahmed, João Carlos Alchieri, Joubert Barbosa, Karolinne Souza Monteiro, Karla Mendonça

Purpose

To translate and cross-culturally adapt the PROMIS® Self-Efficacy for Managing Daily Activities for Portuguese-speaking populations, ensuring linguistic and conceptual equivalence for future validation, while considering differences between Brazil and Portugal.

Methods

The Functional Assessment of Chronic Illness Therapy (FACIT) methodology was followed, including (1) independent translations by Brazilian and Portuguese native speakers; (2) reconciliation into a single version; (3) back-translation; (4) expert review; (5) cognitive debriefing with participants from both countries and (6) final approval by the PROMIS® Statistical Center. Ethical approval was obtained from the Federal University of Rio Grande do Norte.

Results

Minimal linguistic and cultural differences were found between Brazilian and European Portuguese. Vocabulary adjustments were made to ensure clarity (e.g., “tela” vs. “écrã,” “celular” vs. “telemóvel”). The cognitive debriefing involved seven participants (four from Brazil and three from Portugal). A new response option was added for individuals with mobility impairments. The final version preserved the scale's psychometric integrity while ensuring cultural relevance.

Conclusion

The adapted Portuguese version of the PROMIS® Self-Efficacy for Managing Daily Activities maintains its conceptual fidelity and usability across Portuguese-speaking populations. The item bank is ready for validation studies and clinical use in Lusophone healthcare settings.

目的:在考虑巴西和葡萄牙之间的差异的同时,翻译和跨文化适应葡萄牙语人群管理日常活动的PROMIS®自我效能感,确保未来验证的语言和概念等效。方法:采用慢性疾病治疗功能评估(FACIT)方法,包括:(1)由巴西和葡萄牙语母语人士独立翻译;(二)对账成单一版本;(3)反向翻译;(4)专家评审;(5)与两国参与者进行认知情况汇报;(6)获得PROMIS®统计中心的最终批准。获得了北格兰德联邦大学的伦理批准。结果:在巴西和欧洲葡萄牙语之间发现最小的语言和文化差异。对词汇进行了调整以确保清晰(例如,“tela”vs“tela”)。“écrã”,“cell”vs。“telemovel”)。认知汇报涉及七名参与者(四名来自巴西,三名来自葡萄牙)。为行动不便的个人增加了一个新的回应选项。最终版本保留了量表的心理测量完整性,同时确保了文化相关性。结论:葡萄牙语版本的PROMIS®日常活动管理自我效能在葡语人群中保持了其概念的保真度和可用性。该物项库已准备好在葡语医疗机构进行验证研究和临床使用。
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引用次数: 0
Exploring Coastal Male Knowledge, Perception, and Prioritization of Female Menstrual Health in Southern Bangladesh 探索沿海男性的知识,感知,并优先考虑女性月经健康在孟加拉国南部。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.1002/hsr2.71783
Farhana Yasmin, Jemima Jahan Meem, Shantanu Kumar Saha, Dilafroze Khanam

Background

Menstruation is a natural biological process, yet it remains heavily stigmatized and misunderstood in many communities, particularly in rural and coastal regions. In Bangladesh, gender norms, cultural taboos, and environmental challenges like saline water contribute to the neglect of menstrual health, especially in coastal areas.

Aim

This study aims to explore the knowledge, perceptions, and involvement of coastal males in women's menstrual health and hygiene, focusing on how environmental stressors, such as water salinity, impact menstrual practices.

Method

A phenomenological qualitative approach was used to conduct in-depth, semi-structured interviews with 50 adult males (aged 18 and above) from East Kharia village, Khulna District, Bangladesh. Data were analyzed thematically to uncover the key factors influencing men's understanding and support of menstrual health.

Results

The findings reveal that many participants had limited knowledge about the biological aspects of menstruation, largely influenced by myths and informal learning. Cultural silence surrounding menstruation was prevalent, with most men avoiding discussions on the topic. Environmental barriers, such as saline water, were identified as exacerbating menstrual health issues. Emotional detachment and lack of support for women during menstruation were common, though a subset of younger, more educated men showed emerging empathy and a shift toward recognizing menstruation as a shared family responsibility.

Conclusion

The study highlights significant gaps in male knowledge and involvement in menstrual health, compounded by cultural taboos and environmental stressors. It calls for gender-sensitive education and policies that encourage male participation in menstrual hygiene management, as well as addressing the unique challenges faced by coastal communities in managing menstrual health.

背景:月经是一个自然的生物过程,但在许多社区,特别是农村和沿海地区,它仍然被严重污名化和误解。在孟加拉国,性别规范、文化禁忌和咸水等环境挑战导致了对月经健康的忽视,特别是在沿海地区。目的:本研究旨在探讨沿海男性在女性月经健康和卫生方面的知识、观念和参与,重点关注环境压力因素(如水盐度)如何影响月经习惯。方法:采用现象学定性方法对来自孟加拉国库尔纳区东哈里亚村的50名成年男性(18岁及以上)进行深入的半结构化访谈。对数据进行专题分析,揭示影响男性对月经健康的理解和支持的关键因素。结果:研究结果显示,许多参与者对月经的生物学方面的知识有限,很大程度上受神话和非正式学习的影响。关于月经的文化沉默很普遍,大多数男性都避免讨论这个话题。环境障碍,如盐水,被认为加剧了月经健康问题。在月经期间,情感疏离和缺乏对女性的支持是很常见的,尽管一小部分受过更多教育的年轻男性表现出了同情心,并开始意识到月经是一项共同的家庭责任。结论:该研究突出了男性在月经健康知识和参与方面的显著差距,加上文化禁忌和环境压力因素。它呼吁开展对性别问题有敏感认识的教育和政策,鼓励男性参与经期卫生管理,并解决沿海社区在经期卫生管理方面面临的独特挑战。
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引用次数: 0
Peripheral Blood Skin-Homing T Cells Define Immunological Endotypes in Atopic Dermatitis: A Case–Control Study in a Mexican Population 外周血皮肤归巢T细胞定义特应性皮炎的免疫内型:墨西哥人群的病例对照研究。
IF 2.1 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-26 DOI: 10.1002/hsr2.71726
Zumaya-Pérez Luis Carlos, Velázquez-Sámano Guillermo, Velasco-Medina Andrea Aida, Garza-Velasco Raúl, Rangel-Castañeda Itzia Azucena, Moreno-Eutimio Mario Adán, Pastelin-Palacios Rodolfo

Background and Aims

Atopic dermatitis (AD) is a chronic inflammatory skin disease with marked immunological heterogeneity. T-cell subsets expressing CLA, CCR4, and CCR10 are involved in skin inflammation, but their frequency and expression patterns in AD remain poorly characterized. This study aimed to define distinct immunological endotypes of AD in the Mexican population by analyzing the frequency of CLA⁺ T cells expressing CCR4 and CCR10, along with their cytokine production profiles.

Methods

Flow cytometry quantified CD4⁺ and CD8⁺ T cells in 47 Mexican AD patients, 15 healthy controls, and 16 allergic individuals. Principal component analysis and unsupervised clustering were used to identify immunological patterns.

Results

Two AD endotypes were identified. Endotype 1 exhibited a higher frequency of CD4⁺CLA⁺ T cells (32.1% vs. 21.0%; p = 0.025) and a Th2/Th17-skewed profile, while Endotype 2 showed higher CD8⁺CLA⁺ T-cell frequencies (2.8% vs. 5.5%; p = 0.003) and increased chemokine receptor expression on CD4⁺ T cells (all p < 0.001). Clinically, Endotype 1 presented more active disease at examination (78.9% vs. 35.7%; p < 0.001). Total serum IgE was higher in Endotype 2 (5974 vs. 866 IU/mL; p = 0.032), and both endotypes showed higher IgE than healthy controls. SCORAD, POEM, and DLQI did not clearly separate the endotypes.

Conclusion

AD presents distinct immunological endotypes characterized by specific T-cell profiles, which may inform personalized treatment strategies. This study provides insights into the immunological heterogeneity of AD in the Mexican population and underscores the need for population-specific approaches in disease characterization and management.

背景与目的:特应性皮炎(AD)是一种具有明显免疫异质性的慢性炎症性皮肤病。表达CLA、CCR4和CCR10的t细胞亚群与皮肤炎症有关,但它们在AD中的频率和表达模式仍不清楚。这项研究旨在通过分析表达CCR4和CCR10的CLA + T细胞的频率,以及它们的细胞因子产生谱,来确定墨西哥人群中AD的不同免疫内型。方法:用流式细胞术定量检测47例墨西哥AD患者、15例健康对照者和16例过敏个体的CD4 +和CD8 + T细胞。主成分分析和无监督聚类用于识别免疫模式。结果:鉴定出两种AD内型。Endotype 1表现出更高的CD4 + CLA + T细胞频率(32.1% vs. 21.0%, p = 0.025)和Th2/ th17偏态,而Endotype 2表现出更高的CD8 + CLA + T细胞频率(2.8% vs. 5.5%, p = 0.003)和CD4 + T细胞上趋化因子受体表达增加(p p p = 0.032),两种Endotype均显示出高于健康对照组的IgE。SCORAD、POEM和DLQI未明确区分内型。结论:AD表现出独特的免疫内型,以特定的t细胞谱为特征,这可能为个性化的治疗策略提供信息。这项研究提供了对阿尔茨海默病在墨西哥人群中的免疫学异质性的见解,并强调了在疾病表征和管理中需要针对人群的方法。
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Health Science Reports
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