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Remove Oral Diphenhydramine From OTC-End the Status Quo. 将口服苯海拉明从otc下架——结束现状。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 DOI: 10.1001/jamainternmed.2025.7278
James H Clark, Eli O Meltzer, Robert M Naclerio
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引用次数: 0
Mobile Chat Messaging for Smoking Relapse Prevention: A Randomized Clinical Trial. 手机聊天信息预防吸烟复发:一项随机临床试验。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 DOI: 10.1001/jamainternmed.2025.7439
Tzu Tsun Luk, Xiaoyu Su, Vanessa Wong, Helan Ching-Han Chan, Grace Nga-Ting Wong, John Ka Hong Lee, Sai Yin Ho, Tai Hing Lam, Yee Tak Derek Cheung, Man Ping Wang

Importance: Most individuals attempting smoking cessation relapse, even with evidence-based treatment. Mobile interventions offer a potential but largely untested strategy to sustain cessation.

Objective: To test the effectiveness of mobile chat messaging for relapse prevention among individuals who recently quit smoking.

Design, setting, and participants: This randomized clinical trial was conducted from March 14, 2023, to August 15, 2024, at 2 clinic-based smoking cessation services in Hong Kong. Participants were adults who smoked daily and had abstained for 3 to 30 days; they were randomly assigned to an intervention group or a control group.

Interventions: All participants received usual smoking cessation treatment from the services. The intervention group additionally received 3 months of mobile relapse prevention intervention, including chat-based support delivered by a live counselor and access to a supportive chatbot via a messaging app. The control group received 8 text messages on generic smoking cessation advice over 3 months as a contact control.

Main outcomes and measures: The primary outcome was biochemically validated tobacco abstinence at 6 months after randomization, defined by an exhaled carbon monoxide level of less than 5 ppm or a negative salivary cotinine test result. Secondary outcomes at 6 months included self-reported prolonged abstinence, 7-day point prevalence abstinence, and relapse (7 consecutive days of smoking) rate. Intention-to-treat analyses were conducted, assuming participants with missing outcomes relapsed.

Results: Of 590 participants, 465 (78.8%) were male, and the mean (SD) age was 47.1 (11.2) years; 294 were randomized to the intervention group and 296 were randomized to the control group. The retention rate at 6-month follow-up was 98.0% (n = 578). Biochemically validated abstinence at 6 months was significantly higher in the intervention group than in the control group (45.9% [135 of 294] vs 35.5% [105 of 296]; relative risk [RR], 1.29; 95% CI, 1.06-1.58; P = .01). The intervention group also reported significantly higher prolonged abstinence (57.5% [169 of 294] vs 47.6% [141 of 296]; RR, 1.21; 95% CI, 1.03-1.41; P = .02), higher 7-day point prevalence abstinence (65.6% [193 of 294] vs 54.7% [162 of 296]; RR, 1.20; 95% CI, 1.05-1.37; P = .007), and lower relapse rate (33.0% [97 of 294] vs 44.9% [133 of 296]; RR, 0.73; 95% CI, 0.60-0.90; P = .003) at 6 months.

Conclusions and relevance: This randomized clinical trial found that mobile chat messaging for smoking relapse prevention increased validated abstinence by approximately 30%, offering a scalable approach to sustain abstinence among individuals who recently quit smoking.

Trial registration: ClinicalTrials.gov Identifier: NCT05370352.

重要性:大多数试图戒烟的人会复发,即使有循证治疗。移动干预为维持戒烟提供了一种潜在但基本上未经检验的策略。目的:检验手机聊天信息对新近戒烟者预防复吸的有效性。设计、环境和参与者:本随机临床试验于2023年3月14日至2024年8月15日在香港的两家戒烟诊所进行。参与者是每天吸烟并戒烟3至30天的成年人;他们被随机分配到干预组和对照组。干预措施:所有参与者都接受了常规的戒烟治疗。干预组还接受了3个月的移动预防复发干预,包括由现场咨询师提供的聊天支持,以及通过即时通讯应用程序访问支持性聊天机器人。对照组在3个月内收到8条关于一般戒烟建议的短信,作为联系控制。主要结局和措施:主要结局是随机分组后6个月生化验证的戒烟,以呼出的一氧化碳水平低于5ppm或唾液可替宁试验结果为阴性来定义。6个月时的次要结果包括自我报告的长期戒烟、7天点流行戒烟和复发率(连续7天吸烟)。假设结果缺失的参与者复发,进行意向治疗分析。结果:590名参与者中,465名(78.8%)为男性,平均(SD)年龄为47.1(11.2)岁;其中干预组294例,对照组296例。随访6个月,保留率为98.0% (n = 578)。干预组6个月时经生化验证的戒断率显著高于对照组(45.9% [135 / 294]vs 35.5%[105 / 296];相对危险度[RR], 1.29; 95% CI, 1.06-1.58; P = 0.01)。干预组也报告了更长的戒断时间(57.5% [294 / 169]vs 47.6% [296 / 141]); RR, 1.21; 95% CI, 1.03-1.41; P =。2002),较高的7天点患病率戒断(65.6% [294 / 193]vs 54.7% [296 / 162]; RR, 1.20; 95% CI, 1.05-1.37; P =。复发率较低(33.0%[294例中的97例]vs 44.9%[296例中的133例];RR, 0.73; 95% CI, 0.60-0.90; P =。003) 6个月。结论和相关性:这项随机临床试验发现,手机聊天信息预防吸烟复发使有效的戒烟率提高了约30%,为最近戒烟的个人提供了一种可扩展的方法来维持戒烟。试验注册:ClinicalTrials.gov标识符:NCT05370352。
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引用次数: 0
Navigating Postacute Care Options for Patients After Hospital Discharge: A Review. 出院后患者急性后护理选择:综述
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-20 DOI: 10.1001/jamainternmed.2025.7422
W James Deardorff, Robert E Burke, Anil N Makam

Importance: Approximately 25% to 40% of hospitalized adults are discharged to receive postacute care (PAC) either at home through home health (HH) or in skilled nursing facilities (SNFs), inpatient rehabilitation facilities (IRFs), or long-term acute care hospitals (LTACHs). An overview of various PAC settings is needed to help hospital-based clinicians collaborate most effectively with patients, caregivers, and an interdisciplinary care team to promote high-quality PAC and facilitate better PAC transitions.

Observations: PAC settings vary in their eligibility requirements and in the intensity and complexity of services they provide. HH provides intermittent in-home support for homebound individuals with skilled needs. SNFs provide housing, daily nursing care, rehabilitative services, and medical supervision, although the medical care provided is often a dramatic step down from hospital-based acute care. IRFs provide intensive rehabilitation, most commonly for individuals with specific diagnoses (eg stroke, hip fracture, or spinal cord injury). LTACHs care for patients with medically complex conditions who require prolonged hospital-level care for services (eg, ventilator weaning, complex wound management). Discharge planning to PAC should be guided by clinical needs, caregiver support, and the values and preferences of patients and caregivers; yet it is often opaque and influenced by external factors such as insurance coverage and geography. Clinicians should proactively recognize PAC needs, advocate for specific PAC settings for targeted situations, and assist on selecting an appropriate PAC facility, especially for patients with insurance restrictions. Moreover, PAC admissions frequently represent a pivotal time period for individuals with serious illness, during which a subsequent poor prognosis becomes clear. Therefore, PAC stays represent an opportunity for clinicians to revisit prognosis with patients and caregivers, engage in goals of care conversations, and clarify plans for the future.

Conclusions and relevance: To provide patient-centered care and help facilitate better transitions for patients and caregivers, hospital-based clinicians have a responsibility to understand the different types of PAC settings and actively participate in discharge planning.

重要性:大约25%至40%的住院成年人出院后通过家庭健康(HH)在家中或在熟练护理机构(snf)、住院康复机构(irf)或长期急性护理医院(LTACHs)接受急性后护理(PAC)。需要对各种PAC设置进行概述,以帮助医院临床医生与患者、护理人员和跨学科护理团队进行最有效的合作,以促进高质量PAC并促进更好的PAC过渡。观察:PAC设置在其资格要求以及所提供服务的强度和复杂性方面各不相同。HH为有技术需求的居家人士提供间歇性的家庭支持。snf提供住房、日常护理、康复服务和医疗监督,尽管所提供的医疗服务往往大大低于医院的急性护理。irf提供强化康复,最常见于有特定诊断的个体(如中风、髋部骨折或脊髓损伤)。ltahs为医疗条件复杂的患者提供护理,这些患者需要长期的医院护理服务(例如,呼吸机脱机、复杂的伤口处理)。PAC的出院计划应以临床需要、护理人员支持以及患者和护理人员的价值观和偏好为指导;然而,它往往是不透明的,并受到保险范围和地理等外部因素的影响。临床医生应主动认识到PAC需求,倡导针对特定情况的特定PAC设置,并协助选择适当的PAC设施,特别是对于有保险限制的患者。此外,PAC入院通常是严重疾病患者的关键时期,在此期间,随后的不良预后变得明显。因此,PAC停留为临床医生提供了一个机会,可以与患者和护理人员重新审视预后,参与护理目标对话,并明确未来的计划。结论和相关性:为了提供以患者为中心的护理,并帮助患者和护理人员更好地过渡,医院临床医生有责任了解不同类型的PAC设置,并积极参与出院计划。
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引用次数: 0
High-Dose vs Standard-Dose Influenza Vaccine in Older Adults With Diabetes: A Secondary Analysis of the DANFLU-2 Randomized Clinical Trial. 老年糖尿病患者的高剂量与标准剂量流感疫苗:DANFLU-2随机临床试验的二次分析
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-12 DOI: 10.1001/jamainternmed.2025.7286
Anne Bjerg Nielsen, Niklas Dyrby Johansen, Daniel Modin, Matthew M Loiacono, Rebecca C Harris, Marine Dufournet, Carsten Schade Larsen, Lykke Larsen, Lothar Wiese, Michael Dalager-Pedersen, Brian L Claggett, Kira Hyldekær Janstrup, Katja Vu Bartholdy, Katrine Feldballe Bernholm, Julie Inge-Marie Helene Borchsenius, Filip Søskov Davidovski, Lise Witten Davodian, Maria Dons, Lisa Steen Duus, Caroline Espersen, Frederik Holme Fussing, Anne Marie Reimer Jensen, Nino Emanuel Landler, Adam Cadovius Femerling Langhoff, Mats Christian Højbjerg Lassen, Camilla Ikast Ottosen, Morten Sengeløv, Kristoffer Grundtvig Skaarup, Manan Pareek, Dirk Müller-Wieland, Scott D Solomon, Martin J Landray, Gunnar H Gislason, Lars Køber, Pradeesh Sivapalan, Cyril Jean-Marie Martel, Jens Ulrik Stæhr Jensen, Tor Biering-Sørensen
<p><strong>Importance: </strong>Influenza infection poses a substantial risk of severe complications, particularly in older adults and high-risk populations, such as individuals with diabetes. The high-dose inactivated influenza vaccine (HD-IIV) has demonstrated superior efficacy against influenza infection compared with the standard-dose inactivated influenza vaccine (SD-IIV) among adults 65 years or older. However, there is limited evidence on its effectiveness in preventing severe respiratory and cardiovascular outcomes in individuals with diabetes.</p><p><strong>Objective: </strong>To investigate the relative vaccine effectiveness (rVE) of HD-IIV vs SD-IIV against severe respiratory and cardiovascular outcomes according to diabetes status and across diabetes subgroups.</p><p><strong>Design, setting, and participants: </strong>This was a prespecified secondary analysis of DANFLU-2, a pragmatic, open-label, individually randomized clinical trial conducted in Denmark during the 2022/2023 to 2024/2025 influenza seasons. Adults 65 years or older were eligible for inclusion regardless of comorbidities. Data were obtained from nationwide health registries and analyzed from June to October 2025.</p><p><strong>Interventions: </strong>Participants were randomly allocated 1:1 to receive HD-IIV or SD-IIV.</p><p><strong>Main outcomes and measures: </strong>Outcomes included respiratory and cardiovascular hospitalizations. The potential effect modification by diabetes status and across diabetes subgroups was tested.</p><p><strong>Results: </strong>Among 332 438 participants (mean [SD] age, 73.7 [5.8] years; 161 538 female individuals [48.6%]), 43 881 (13.2%) had diabetes. Overall, HD-IIV compared with SD-IIV was associated with reduced cardiorespiratory hospitalization, cardiovascular hospitalization, and influenza hospitalization. Effect estimates were similar for participants with and without diabetes for cardiorespiratory hospitalization (diabetes: rVE, 7.4%; 95% CI, -2.5% to 16.3%; no diabetes: rVE, 5.3%; 95% CI, 0.4%-10.0%; interaction P = .69), cardiovascular hospitalization (diabetes: rVE, 12.0%; 95% CI, -0.9% to 23.3%; no diabetes: rVE, 6.0%; 95% CI, -0.4% to 12.0%; interaction P = .38), and influenza hospitalization (diabetes: rVE, 41.6%; 95% CI, 5.0%-64.7%, vs no diabetes: rVE, 44.3%; 95% CI, 25.3%-58.7%; interaction P = .87). Duration of diabetes appeared to modify the effect of HD-IIV vs SD-IIV for cardiorespiratory hospitalization, with suggested benefit of HD-IIV in participants with diabetes duration longer than 5 years (rVE, 20.4%; 95% CI, 5.3%-33.1%), but not in those with shorter duration (rVE, -0.4%; 95% CI, -13.8% to 11.5%; interaction P = .03).</p><p><strong>Conclusions and relevance: </strong>The trial results suggest that, among adults 65 years or older, HD-IIV provided consistent benefit for cardiorespiratory, cardiovascular, and influenza hospitalizations compared with SD-IIV, regardless of diabetes status.</p><p><strong>Trial regi
重要性:流感感染具有严重并发症的巨大风险,特别是在老年人和高危人群中,如糖尿病患者。在65岁及以上的成年人中,与标准剂量流感灭活疫苗(sd - iv)相比,高剂量流感灭活疫苗(hd - iv)对流感感染的疗效更佳。然而,关于其在预防糖尿病患者严重呼吸和心血管后果方面的有效性的证据有限。目的:探讨hd - iv与sd - iv在不同糖尿病状态和不同糖尿病亚群中的相对疫苗有效性(rVE)。设计、环境和参与者:这是对danfu -2的预先指定的二次分析,danfu -2是一项实用的、开放标签的、单独随机的临床试验,于2022/2023至2024/2025年流感季节在丹麦进行。无论合并症如何,65岁或以上的成年人都有资格纳入。数据来自全国卫生登记处,并于2025年6月至10月进行了分析。干预措施:参与者按1:1随机分配接受hd - iv或sd - iv治疗。主要结局和测量:结局包括呼吸和心血管住院。对糖尿病状态和糖尿病亚组的潜在影响进行了测试。结果:在332 438名参与者(平均[SD]年龄73.7[5.8]岁;161 538名女性[48.6%])中,43 881名(13.2%)患有糖尿病。总体而言,与sd - iv相比,hd - iv与减少心肺住院、心血管住院和流感住院相关。有糖尿病和没有糖尿病的参与者在心肺住院治疗中的效果估计相似(糖尿病:rVE, 7.4%; 95% CI, -2.5%至16.3%;无糖尿病:rVE, 5.3%; 95% CI, 0.4%-10.0%;相互作用P =。69),心血管住院(糖尿病:rVE, 12.0%; 95% CI, -0.9%至23.3%;无糖尿病:rVE, 6.0%; 95% CI, -0.4%至12.0%;相互作用P =。38)和流感住院(糖尿病:rVE, 41.6%; 95% CI, 5.0%-64.7%, vs无糖尿病:rVE, 44.3%; 95% CI, 25.3%-58.7%;相互作用P = 0.87)。糖尿病病程似乎改变了HD-IIV vs SD-IIV在心肺住院治疗中的效果,糖尿病病程超过5年的患者使用HD-IIV获益(rVE, 20.4%; 95% CI, 5.3%-33.1%),但病程较短的患者没有获益(rVE, -0.4%; 95% CI, -13.8% - 11.5%;相互作用P = 0.03)。结论和相关性:试验结果表明,在65岁或以上的成年人中,与sd - iv相比,hd - iv对心肺、心血管和流感住院治疗具有一致的益处,而与糖尿病状况无关。试验注册:ClinicalTrials.gov标识符:NCT05517174。
{"title":"High-Dose vs Standard-Dose Influenza Vaccine in Older Adults With Diabetes: A Secondary Analysis of the DANFLU-2 Randomized Clinical Trial.","authors":"Anne Bjerg Nielsen, Niklas Dyrby Johansen, Daniel Modin, Matthew M Loiacono, Rebecca C Harris, Marine Dufournet, Carsten Schade Larsen, Lykke Larsen, Lothar Wiese, Michael Dalager-Pedersen, Brian L Claggett, Kira Hyldekær Janstrup, Katja Vu Bartholdy, Katrine Feldballe Bernholm, Julie Inge-Marie Helene Borchsenius, Filip Søskov Davidovski, Lise Witten Davodian, Maria Dons, Lisa Steen Duus, Caroline Espersen, Frederik Holme Fussing, Anne Marie Reimer Jensen, Nino Emanuel Landler, Adam Cadovius Femerling Langhoff, Mats Christian Højbjerg Lassen, Camilla Ikast Ottosen, Morten Sengeløv, Kristoffer Grundtvig Skaarup, Manan Pareek, Dirk Müller-Wieland, Scott D Solomon, Martin J Landray, Gunnar H Gislason, Lars Køber, Pradeesh Sivapalan, Cyril Jean-Marie Martel, Jens Ulrik Stæhr Jensen, Tor Biering-Sørensen","doi":"10.1001/jamainternmed.2025.7286","DOIUrl":"10.1001/jamainternmed.2025.7286","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Importance: &lt;/strong&gt;Influenza infection poses a substantial risk of severe complications, particularly in older adults and high-risk populations, such as individuals with diabetes. The high-dose inactivated influenza vaccine (HD-IIV) has demonstrated superior efficacy against influenza infection compared with the standard-dose inactivated influenza vaccine (SD-IIV) among adults 65 years or older. However, there is limited evidence on its effectiveness in preventing severe respiratory and cardiovascular outcomes in individuals with diabetes.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;To investigate the relative vaccine effectiveness (rVE) of HD-IIV vs SD-IIV against severe respiratory and cardiovascular outcomes according to diabetes status and across diabetes subgroups.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Design, setting, and participants: &lt;/strong&gt;This was a prespecified secondary analysis of DANFLU-2, a pragmatic, open-label, individually randomized clinical trial conducted in Denmark during the 2022/2023 to 2024/2025 influenza seasons. Adults 65 years or older were eligible for inclusion regardless of comorbidities. Data were obtained from nationwide health registries and analyzed from June to October 2025.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Interventions: &lt;/strong&gt;Participants were randomly allocated 1:1 to receive HD-IIV or SD-IIV.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main outcomes and measures: &lt;/strong&gt;Outcomes included respiratory and cardiovascular hospitalizations. The potential effect modification by diabetes status and across diabetes subgroups was tested.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Among 332 438 participants (mean [SD] age, 73.7 [5.8] years; 161 538 female individuals [48.6%]), 43 881 (13.2%) had diabetes. Overall, HD-IIV compared with SD-IIV was associated with reduced cardiorespiratory hospitalization, cardiovascular hospitalization, and influenza hospitalization. Effect estimates were similar for participants with and without diabetes for cardiorespiratory hospitalization (diabetes: rVE, 7.4%; 95% CI, -2.5% to 16.3%; no diabetes: rVE, 5.3%; 95% CI, 0.4%-10.0%; interaction P = .69), cardiovascular hospitalization (diabetes: rVE, 12.0%; 95% CI, -0.9% to 23.3%; no diabetes: rVE, 6.0%; 95% CI, -0.4% to 12.0%; interaction P = .38), and influenza hospitalization (diabetes: rVE, 41.6%; 95% CI, 5.0%-64.7%, vs no diabetes: rVE, 44.3%; 95% CI, 25.3%-58.7%; interaction P = .87). Duration of diabetes appeared to modify the effect of HD-IIV vs SD-IIV for cardiorespiratory hospitalization, with suggested benefit of HD-IIV in participants with diabetes duration longer than 5 years (rVE, 20.4%; 95% CI, 5.3%-33.1%), but not in those with shorter duration (rVE, -0.4%; 95% CI, -13.8% to 11.5%; interaction P = .03).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions and relevance: &lt;/strong&gt;The trial results suggest that, among adults 65 years or older, HD-IIV provided consistent benefit for cardiorespiratory, cardiovascular, and influenza hospitalizations compared with SD-IIV, regardless of diabetes status.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Trial regi","PeriodicalId":14714,"journal":{"name":"JAMA Internal Medicine","volume":" ","pages":""},"PeriodicalIF":23.3,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12797130/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145952108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Changes in US Skilled Nursing Facility Capacity Following the COVID-19 Pandemic. COVID-19大流行后美国熟练护理机构能力的变化
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-12 DOI: 10.1001/jamainternmed.2025.7197
Brian E McGarry, Andrew D Wilcock, Ashvin D Gandhi, David C Grabowski, Fangli Geng, Michael L Barnett

Importance: Skilled nursing facilities (SNFs) are the primary provider of institutional postacute care. Following the COVID-19 pandemic, there have been reports of SNFs reducing their capacity, affecting access to care and disrupting hospital discharges, yet little empirical evidence exists.

Objective: To describe changes in SNF capacity after 2020 and assess whether changes were associated with staffing shortages and hospital discharge outcomes.

Design, setting, and participants: In this cross-sectional study, data from the 2018-2024 Centers for Medicare & Medicaid Services Payroll-Based Journal on patient censuses in US skilled nursing facilities were assessed. Descriptive analyses characterized trends in SNF capacity from 2018 to 2024.

Main outcomes and measures: Main outcomes were SNF licensed bed count and estimated operating capacity. Secondary outcomes included SNF staffing shortages, mean hospital length of stay, percentage of hospital admissions lasting 28 days or more, and the median distance traveled to admitting SNFs. County-level regression analyses examined the association between changes in SNF capacity and the frequency of SNF staffing shortages. Hospital-level regressions examined the association between changes in nearby SNF capacity and discharge outcomes.

Results: Among US skilled nursing facilities, the number of licensed SNF beds declined by 2.5% between 2019 and 2024, while operating capacity declined by 5.0% over the same time period. There was substantial geographic variation-1 in 4 counties experienced operating capacity declines of 15.1% or more, with the largest declines being more common among rural counties. SNF capacity declines were larger in counties with more frequent reports of SNF staffing shortages-a 1-percentage point decline in county SNF capacity was associated with a 0.20-percentage point (95% CI, 0.11-0.29) increase in the frequency of reported shortages. Additionally, hospitals that experienced larger declines in nearby SNF capacity experienced greater increases in mean length of stay, percentage of stays lasting 28 or more days, and median distance traveled to admitting SNFs.

Conclusions and relevance: Results of this study suggest that SNF operating capacity declined following the pandemic and these declines were larger than the observed declines in licensed SNF bed counts, potentially because of staffing shortages. Greater loss of SNF capacity was associated with longer hospital stays and increased travel distances to SNFs, suggesting that declines in operating capacity may be impairing access to care.

重要性:熟练护理机构(snf)是机构急性后护理的主要提供者。在2019冠状病毒病大流行之后,有报告称snf降低了能力,影响了获得护理的机会并扰乱了医院的出院,但几乎没有经验证据。目的:描述2020年后SNF容量的变化,并评估变化是否与人员短缺和出院结果相关。设计、环境和参与者:在这项横断面研究中,评估了2018-2024年美国医疗保险和医疗补助服务中心基于工资的期刊中关于美国熟练护理机构患者人口普查的数据。描述性分析描述了2018 - 2024年SNF容量的趋势。主要结果和措施:主要结果是SNF许可的床位数和估计的运营能力。次要结局包括SNF人员短缺、平均住院时间、住院28天或更长时间的百分比,以及到SNF入院的中位距离。县级回归分析检验了SNF能力变化与SNF人员短缺频率之间的关系。医院水平的回归检验了附近SNF容量变化与出院结果之间的关系。结果:在美国专业护理机构中,2019年至2024年期间,获得许可的SNF床位数量下降了2.5%,而同期的运营能力下降了5.0%。有很大的地理差异- 4个县中有1个县的运营能力下降了15.1%或更多,其中最大的下降在农村县更为常见。在SNF人员短缺报告更频繁的县,SNF能力下降幅度更大——SNF能力下降1个百分点与报告短缺频率增加0.20个百分点(95% CI, 0.11-0.29)相关。此外,附近SNF容量下降幅度较大的医院在平均住院时间、28天或更长时间的住院百分比以及接收SNF的中位数距离方面均有较大的增加。结论和相关性:本研究的结果表明,在大流行之后,SNF的运营能力下降,而且这些下降幅度大于观察到的SNF许可床位数量的下降,可能是由于人员短缺。SNF能力损失越大,住院时间越长,前往SNF的路程越远,这表明运营能力的下降可能正在影响获得护理的机会。
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引用次数: 0
Skilled Nursing Facilities and Sufficient Bed Capacity-No Room at the Inn. 熟练的护理设施和充足的床位——酒店没有房间。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-12 DOI: 10.1001/jamainternmed.2025.7275
Mitchell H Katz, Lona Mody, Sharon K Inouye
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引用次数: 0
Inflammation's Impact on Ferritin in Iron Deficiency. 炎症对铁蛋白缺乏的影响。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-05 DOI: 10.1001/jamainternmed.2025.7127
Ye Shen, Peng Sun
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引用次数: 0
A Shark-Fin Pattern on the Electrocardiogram. 心电图上的鲨鱼鳍图案。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-05 DOI: 10.1001/jamainternmed.2025.7004
Samuel Chin Wei Tan, Zhen-Hua Liang, Shu-Qi Jin
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引用次数: 0
Steadying the Medical Education Pendulum-The Need for Experimental Studies. 稳住医学教育的钟摆——实验研究的必要性。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-05 DOI: 10.1001/jamainternmed.2025.7143
Alexander A Iyer, Leah Pierson, Richard M Schwartzstein
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引用次数: 0
Nudges to Clinicians and Patients for Influenza Vaccines During Visits: The BE IMMUNE Randomized Clinical Trial. 在就诊期间向临床医生和患者提示流感疫苗:BE IMMUNE随机临床试验。
IF 23.3 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL Pub Date : 2026-01-05 DOI: 10.1001/jamainternmed.2025.7133
Shivan J Mehta, Kimberly J Waddell, Kristin A Linn, Caitlin Brophy, Junning Liang, Sae-Hwan Park, Catherine Reitz, Keyirah Williams, Chaylin Couzens, Jonathan Staloff, Andrew A White, Corinne Rhodes, Joshua M Liao, Amol S Navathe

Importance: Annual influenza vaccination reduces burden of disease for older adults, but rates remain suboptimal.

Objective: To evaluate if a multicomponent nudge intervention to clinicians and patients increases vaccine completion during primary care visits.

Design, setting, and participants: The pragmatic BE IMMUNE (Behavioral Economics to Improve and Motivate Vaccination in Primary Care Using Nudges Through the Electronic Health Record) randomized clinical trial took place across 48 primary care clinics through Penn Medicine (Philadelphia, Pennsylvania) and UW Medicine (Seattle, Washington). Patients 50 years and older who were scheduled for a primary care visit and were due for an influenza vaccine within the active intervention period (September 25, 2023, to February 20, 2024) were included.

Interventions: Clinics were randomized in a 2:1 ratio to receive (1) previsit text message reminders to patients, (2) an automatic pended order, and (3) monthly comparisons of panel vaccination rates to peer clinicians, or usual care. Additionally, patients in the intervention arm who were identified as high risk for noncompletion were individually randomized 1:1 to receive previsit bidirectional text messaging or a standard text reminder.

Main outcomes and measures: The primary outcome was influenza vaccination during the visit.

Results: Among 80 039 patients across 47 clinics, the mean (SD) age was 65.8 (10.2) years, and 56.0% were female while 43.6% were male. The adjusted odds ratio (AOR) for vaccine completion comparing intervention to usual care was 1.28 (97.5% CI, 1.13-1.45; adjusted P < .001). The probability of completion in the intervention was 31.4% compared to 26.4% under usual care, with a risk difference of 5.1 percentage points (97.5% CI, 2.6-7.5 percentage points; adjusted P < .001). The adjusted odds ratio comparing bidirectional vs standard text messaging among high-risk patients was not statistically significant (1.00; 97.5% CI, 0.98-1.02; adjusted P = .92).

Conclusions and relevance: In this randomized clinical trial, the multicomponent nudge resulted in a statistically significant higher rate of influenza vaccination during the primary care visit, but the bidirectional text messaging did not further increase vaccination in the high-risk group.

Trial registration: ClinicalTrials.gov Identifier: NCT06057727.

重要性:每年接种流感疫苗可减少老年人的疾病负担,但接种率仍不理想。目的:评估临床医生和患者在初级保健就诊期间多成分轻推干预是否能提高疫苗完成率。设计、设置和参与者:实用的BE IMMUNE(通过电子健康记录推动改善和激励初级保健疫苗接种的行为经济学)随机临床试验通过宾夕法尼亚大学医学院(宾夕法尼亚州费城)和华盛顿大学医学院(华盛顿州西雅图)在48个初级保健诊所进行。纳入了在积极干预期间(2023年9月25日至2024年2月20日)计划进行初级保健就诊并应接种流感疫苗的50岁及以上患者。干预措施:诊所以2:1的比例随机分配,接收(1)就诊前短信提醒患者,(2)自动等待订单,(3)每月与同行临床医生或常规护理的小组疫苗接种率比较。此外,干预组中被确定为未完成高风险的患者按1:1的比例随机分组,分别接受就诊前双向短信或标准文本提醒。主要结局和措施:主要结局是在访问期间接种流感疫苗。结果:47个诊所80 039例患者中,平均(SD)年龄为65.8(10.2)岁,女性56.0%,男性43.6%。与常规护理相比,干预疫苗完成率的调整优势比(AOR)为1.28 (97.5% CI, 1.13-1.45);调整P值:结论和相关性:在这项随机临床试验中,多成分推动导致初级保健就诊期间流感疫苗接种率有统计学意义的提高,但双向短信并没有进一步增加高危组的疫苗接种率。试验注册:ClinicalTrials.gov标识符:NCT06057727。
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JAMA Internal Medicine
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