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Implementation of delirium screening in the emergency department: A qualitative study with early adopters 在急诊科实施谵妄筛查:对早期采用者的定性研究
IF 6.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-12 DOI: 10.1111/jgs.19188
Anita N. Chary, Annika R. Bhananker, Elise Brickhouse, Beatrice Torres, Ilianna Santangelo, Kyler M. Godwin, Aanand D. Naik, Christopher R. Carpenter, Shan W. Liu, Maura Kennedy
IntroductionDelirium affects 15% of older adults presenting to emergency departments (EDs) but is detected in only one‐third of cases. Evidence‐based guidelines for ED delirium screening exist, but are underutilized. Frontline staff perceptions about delirium and time and resource constraints are known barriers to ED delirium screening uptake. Early adopters of ED delirium screening can offer valuable lessons about successful implementation.MethodsWe conducted semi‐structured interviews with clinician‐administrators leading ED delirium screening initiatives from 20 EDs in the United States and Canada. Interviews focused on experiences of planning and implementing ED delirium screening. Interviews lasted 15 to 50 minutes and were digitally recorded and transcribed. To identify factors that commonly impacted implementation of ED delirium screening, we used constructs from the Consolidated Framework for Implementation Research (CFIR), an Implementation Science framework widely used to evaluate healthcare improvement initiatives.ResultsOverall, notable facilitators of successful implementation were having institutional and ED leadership support and designated clinical champions to longitudinally engage and educate frontline staff. We found specific examples of factors affecting implementation drawn from the following seven CFIR constructs: (1) intervention complexity, (2) intervention adaptability, (3) external policies and incentives, (4) peer pressure from other institutions, (5) the implementation climate of the ED, (6) staff knowledge and beliefs, and (7) engaging deliverers of intervention, that is, frontline ED staff.ConclusionImplementing ED delirium screening is complex and requires institutional resources as well as clinical champions to engage frontline staff in a sustained fashion.
导言:在急诊科(ED)就诊的老年人中,15%患有谵妄,但只有三分之一的病例能被发现。目前已有基于证据的急诊科谵妄筛查指南,但未得到充分利用。一线工作人员对谵妄的认识以及时间和资源的限制是阻碍急诊科接受谵妄筛查的已知障碍。我们对来自美国和加拿大 20 家急诊室的急诊室谵妄筛查项目负责人进行了半结构化访谈。访谈的重点是计划和实施急诊室谵妄筛查的经验。访谈持续了 15 到 50 分钟,并进行了数字录音和转录。为了确定通常影响急诊室谵妄筛查实施的因素,我们使用了实施研究综合框架(CFIR)中的构架,该框架是一个实施科学框架,被广泛用于评估医疗保健改进措施。结果总的来说,成功实施的显著促进因素是得到机构和急诊室领导的支持,以及指定临床倡导者纵向参与和教育一线员工。我们从以下七个 CFIR 构架中找到了影响实施因素的具体实例:(1)干预的复杂性,(2)干预的适应性,(3)外部政策和激励机制,(4)来自其他机构的同行压力,(5)急诊室的实施氛围,(6)员工的知识和信念,以及(7)干预实施者(即急诊室一线员工)的参与。
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引用次数: 0
Effect of hearing intervention on communicative function: A secondary analysis of the ACHIEVE randomized controlled trial. 听力干预对交流功能的影响:ACHIEVE 随机对照试验的二次分析。
IF 6.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-12 DOI: 10.1111/jgs.19185
Victoria A Sanchez,Michelle L Arnold,Emmanuel E Garcia Morales,Nicholas S Reed,Sarah Faucette,Sheila Burgard,Haley N Calloway,Josef Coresh,Jennifer A Deal,Adele M Goman,Lisa Gravens-Mueller,Kathleen M Hayden,Alison R Huang,Christine M Mitchell,Thomas H Mosley,James S Pankow,James R Pike,Jennifer A Schrack,Laura Sherry,Jacqueline M Weycker,Frank R Lin,Theresa H Chisolm,
BACKGROUNDThe Aging and Cognitive Health Evaluation in Elders (ACHIEVE) Study was designed to determine the effects of a best-practice hearing intervention on cognitive decline among community-dwelling older adults. Here, we conducted a secondary analysis of the ACHIEVE Study to investigate the effect of hearing intervention on self-reported communicative function.METHODSThe ACHIEVE Study is a parallel-group, unmasked, randomized controlled trial of adults aged 70-84 years with untreated mild-to-moderate hearing loss and without substantial cognitive impairment. Participants were randomly assigned (1:1) to a hearing intervention (audiological counseling and provision of hearing aids) or a control intervention of health education (individual sessions with a health educator covering topics on chronic disease prevention) and followed semiannually for 3 years. Self-reported communicative function was measured with the Hearing Handicap Inventory-Elderly Screening version (HHIE-S, range 0-40, higher scores indicate greater impairment). Effect of hearing intervention versus control on HHIE-S was analyzed through an intention-to-treat model controlling for known covariates.RESULTSHHIE-S improved after 6-months with hearing intervention compared to control, and continued to be better through 3-year follow-up. We estimated a difference of -8.9 (95% CI: -10.4, -7.5) points between intervention and control groups in change in HHIE-S score from baseline to 6 months, -9.3 (95% CI: -10.8, -7.9) to Year 1, -8.4 (95% CI: -9.8, -6.9) to Year 2, and - 9.5 (95% CI: -11.0, -8.0) to Year 3. Other prespecified sensitivity analyses that varied analytical parameters did not change the observed results.CONCLUSIONSHearing intervention improved self-reported communicative function compared to a control intervention within 6 months and with effects sustained through 3 years. These findings suggest that clinical recommendations for older adults with hearing loss should encourage hearing intervention that could benefit communicative function and potentially have positive downstream effects on other aspects of health.
背景老龄化与认知健康评估(ACHIEVE)研究旨在确定最佳听力干预对社区老年人认知能力下降的影响。在此,我们对 ACHIEVE 研究进行了二次分析,以调查听力干预对自我报告的交流功能的影响。方法ACHIEVE 研究是一项平行组、无掩蔽、随机对照试验,研究对象为 70-84 岁、患有轻度至中度听力损失且未接受治疗、无严重认知障碍的成年人。参与者被随机分配(1:1)到听力干预(听力咨询和提供助听器)或健康教育对照干预(由健康教育专家提供有关慢性疾病预防主题的个人课程)中,每半年进行一次跟踪,为期 3 年。听力障碍清单-老年人筛查版(HHIE-S,范围为 0-40,分数越高表示听力障碍越严重)对自我报告的交流功能进行了测量。通过意向治疗模型分析了听力干预与对照组相比对 HHIE-S 的影响,并控制了已知的协变量。结果与对照组相比,听力干预 6 个月后 HHIE-S 有所改善,并在 3 年的随访中持续改善。我们估计干预组和对照组的 HHIE-S 分数从基线到 6 个月的变化差异为 -8.9 (95% CI: -10.4, -7.5) 分,到第一年为 -9.3 (95% CI: -10.8, -7.9)分,到第二年为 -8.4 (95% CI: -9.8, -6.9)分,到第三年为 -9.5 (95% CI: -11.0, -8.0)分。结论与对照干预相比,听力干预能在 6 个月内改善自我报告的交流功能,且效果可持续 3 年。这些研究结果表明,针对听力损失老年人的临床建议应鼓励进行听力干预,这将有益于沟通功能,并可能对其他方面的健康产生积极的下游影响。
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引用次数: 0
Differences in opioid prescriptions by race among U.S. older adults with a hip fracture transitioning to community care 美国髋部骨折老年人过渡到社区护理时阿片类药物处方的种族差异
IF 6.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-11 DOI: 10.1111/jgs.19160
Kaleen N. Hayes, Meghan A. Cupp, Richa Joshi, Melissa R. Riester, Francesca L. Beaudoin, Andrew R. Zullo
BackgroundAppropriate pain management can facilitate rehabilitation after a hip fracture as patients transition back to the community setting. Differences in opioid prescribing by race may exist during this critical transition period.MethodsWe conducted a retrospective cohort study of older adult U.S. Medicare beneficiaries with a hip fracture to examine whether the receipt and dose of opioids differs between Black and White patients as they transitioned back to the community setting. We stratified beneficiaries by whether they received institutional post‐acute care (PAC). Outcomes were (1) receipt of an opioid and (2) opioid doses in the first 90 days in the community in milligram morphine equivalents (MMEs; also presented in mg oxycodone). We estimated relative rates and risk differences of opioid receipt and dose differences using Poisson and linear regression models, respectively, using the parametric g‐formula to standardize for age and sex.ResultsWe identified 164,170 older adults with hip fracture (mean age = 82.7 years; 75% female; 72% with PAC; 46% with opioid use after fracture). Overall use of opioids in the community was similar between Black and white beneficiaries. Black beneficiaries had lower average doses in their first 90 days in both total cumulative doses (PAC group: 165 [95% CI −264 to −69] fewer MMEs [−248 mg oxycodone]; no PAC: 167 [95% CI −274 to −62] fewer MMEs [−251 mg oxycodone]) and average MME per days' supply of medication (PAC: −3.0 [−4.6 to −1.4] fewer MMEs per day [−4.5 mg oxycodone]; no PAC: −4.7 [−4.6 to −1.4] fewer MMEs per day [−7.1 mg oxycodone]). In secondary analyses, Asian beneficiaries experienced the greatest differences (e.g., 617–653 fewer cumulative mg oxycodone).ConclusionRacial differences exist in pain management for Medicare beneficiaries after a hip fracture. Future work should examine whether these differences result in disparities in short‐ and long‐term health outcomes.
背景髋部骨折后,当患者重返社区环境时,适当的疼痛管理可促进康复。我们对髋部骨折的美国老年医疗保险受益人进行了一项回顾性队列研究,以考察黑人和白人患者在重返社区的过程中接受阿片类药物治疗的情况和剂量是否存在差异。我们根据受益人是否接受机构性急性期后护理 (PAC) 对他们进行了分层。结果包括:(1)接受阿片类药物治疗;(2)在社区的前 90 天内阿片类药物的剂量(以毫克吗啡当量(MMEs)为单位;也以毫克羟考酮(mg oxycodone)为单位)。我们使用泊松模型和线性回归模型分别估算了接受阿片类药物的相对比率和风险差异以及剂量差异,并使用参数 g 公式对年龄和性别进行了标准化处理。结果我们确定了 164170 名髋部骨折的老年人(平均年龄 = 82.7 岁;75% 为女性;72% 患有 PAC;46% 在骨折后使用过阿片类药物)。黑人和白人受益人在社区使用阿片类药物的总体情况相似。黑人受益人在最初 90 天内的平均总累积剂量较低(PAC 组:165 [95% CI -0.5 -0.6减少 165 [95% CI -264 至 -69]个 MME [-248 毫克羟考酮];无 PAC 组:减少 167 [95% CI -264 至 -69] 个 MME [-248 毫克羟考酮]:167[95%CI-274至-62]次[-251毫克羟考酮])和每日均用药量(PAC:-每天减少 3.0 [-4.6 至 -1.4] 次[-4.5 毫克羟考酮];无 PAC:-无 PAC:每天减少 4.7 [-4.6 至 -1.4] 个 MME [-7.1 毫克羟考酮])。在二次分析中,亚裔受益人的差异最大(例如,累计减少 617-653 毫克羟考酮)。未来的工作应研究这些差异是否会导致短期和长期健康结果的差异。
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引用次数: 0
Cover 封面
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-09-02 DOI: 10.1111/jgs.17869
Kathleen T. Unroe MD, MHA, MS, Debra Saliba MD, MPH, AGSF, Susan E. Hickman PhD, Sheryl Zimmerman PhD, Cari Levy MD, PhD, Jerry Gurwitz MD

Cover caption: Key elements for successful nursing home clinical trials. See the related article by Unroe et al., pages 2951–2956.

封面标题:疗养院临床试验成功的关键因素。参见 Unroe 等人的相关文章,第 2951-2956 页。
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引用次数: 0
More than dollars: Healthcare utilization among spouses of persons with dementia 不仅仅是金钱:痴呆症患者配偶的医疗保健使用情况。
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-29 DOI: 10.1111/jgs.19174
Molly J. Horstman MD, MS
<p>Being the spouse of a person with dementia can be a significant source of strain and can negatively impact one's health.<span><sup>1</sup></span> Although not all spouses serve as the primary caregiver, many spouses provide physical or emotional support to the person with dementia. Studies have shown that spouses of persons with dementia are more likely to have depression, anxiety, and sleep disturbances compared with spouses of persons who do not have dementia.<span><sup>2-4</sup></span> Identifying opportunities to improve health among spouses of persons with dementia is essential. In the United States, families provide most of the long-term care to persons with dementia.<span><sup>1</sup></span> Family members need to maintain sufficient health to fulfill caregiving roles and responsibilities to sustain this system. Spouses of a person with dementia may have less time and fewer financial resources to participate in recommended health behaviors and receive healthcare services, which, over time, may impact their ability to care for the person with dementia.<span><sup>5</sup></span></p><p>In this issue, <i>Ingraham</i> et al. present the results of a matched study examining Medicare Fee-for-Service expenditures for spouses of persons living with dementia compared with spouses of persons without dementia in the 5 years after the person with dementia was diagnosed with dementia.<span><sup>6</sup></span> Using the Health and Retirement Study with linked Medicare Claims, the authors measured three categories of health utilization costs: (1) inpatient or hospital expenditures; (2) outpatient or ambulatory expenditures, which included emergency room visits if a hospitalization did not follow the visit; and (3) skilled nursing facility, hospice, and home health expenditures. In the adjusted analysis, there was no difference in total Medicare expenditures between spouses of persons with dementia and spouses of persons without dementia in the 5 years after dementia was diagnosed. However, in Year 5, there was an increase in total Medicare expenditures among spouses of persons living with dementia driven by an increase in inpatient expenditures, with a total difference of $2748 (95% CI $321–$5447).</p><p>The results of this study differ from prior matched studies examining healthcare expenditures among spouses of persons living with dementia.<span><sup>3, 4, 7, 8</sup></span> As the authors note, prior studies had relied on claims data to identify persons with dementia, while the methods used by <i>Ingraham</i> et al. for identifying incident diagnoses of dementia from the Health and Retirement Study identified adults at an earlier stage of the disease. However, several other differences existed between this study and prior published studies. These include the methods by which spouses were identified, the type of insurance the spouse had, and the types of expenditures included in the total expenditures.<span><sup>3, 4, 7, 8</sup></span> In addition, <i>
作为痴呆症患者的配偶可能会承受巨大的压力,并对患者的健康产生负面影响。1 尽管并非所有的配偶都是主要的照顾者,但许多配偶都会为痴呆症患者提供身体或情感上的支持。研究表明,与非痴呆症患者的配偶相比,痴呆症患者的配偶更容易患抑郁症、焦虑症和睡眠障碍。在美国,大部分痴呆症患者的长期护理都是由家庭提供的。1 家庭成员需要保持足够的健康,以履行护理角色和责任,从而维持这一系统。痴呆症患者的配偶参与建议的健康行为和接受医疗保健服务的时间和财力可能较少,随着时间的推移,这可能会影响他们照顾痴呆症患者的能力。5 在本期杂志中,Ingraham 等人介绍了一项配对研究的结果,该研究对痴呆症患者的配偶与非痴呆症患者的配偶在痴呆症患者被诊断出患有痴呆症后 5 年内的医疗保险付费服务支出进行了比较。作者利用健康与退休研究(Health and Retirement Study)和关联的医疗保险索赔(Medicare Claims),测算了三类医疗利用成本:(1)住院病人或医院支出;(2)门诊病人或非住院病人支出,其中包括急诊就诊(如果就诊后没有住院);以及(3)专业护理机构、临终关怀和家庭医疗支出。在调整后的分析中,痴呆症患者的配偶与非痴呆症患者的配偶在痴呆症确诊后 5 年内的医疗保险总支出没有差异。然而,在第 5 年,痴呆症患者配偶的医疗保险总支出因住院费用的增加而增加,总差额为 2748 美元(95% CI 为 321 美元至 5447 美元)、4、7、8 正如作者所指出的,之前的研究依赖于索赔数据来识别痴呆症患者,而 Ingraham 等人从健康与退休研究(Health and Retirement Study)中使用的识别痴呆症事件诊断的方法则识别了处于疾病早期阶段的成年人。不过,这项研究与之前发表的研究还存在其他一些差异。3, 4, 7, 8 此外,Ingraham 等人还根据配偶是否需要帮助进行日常生活活动和工具性日常生活活动对配偶进行了匹配,而之前的研究并没有这样做。无论如何,Ingraham 等人的研究让我们进一步了解到,痴呆症患者配偶的医疗保健支出至少与非痴呆症患者配偶的医疗保健支出相同,某些类型的医疗保健支出可能更高。在一项针对患有多种慢性疾病的老年人的研究中,我们预计两组人都会有医疗保健支出。然而,两组之间相似的医疗支出并不意味着这两组接受了同等的医疗服务。9 在 20 年前发表的一项研究中,痴呆症患者的配偶与非痴呆症患者的配偶相比,去急诊室就诊的次数更多。4 目前的研究并未涉及这种情况是否仍然存在,但这确实提出了一个问题,即在所接受的医疗服务中是否存在未反映在总支出中的有意义的差异。了解两组患者在接受护理方面的差异可能会为干预措施提供启示,从而改善痴呆症患者配偶的健康状况。这与之前有关痴呆症患者照护者的文献一致,当照护者的损伤程度更严重、照护时间更长时,他们更有可能住院过夜。住院老年人常见的功能和认知能力下降可能会影响配偶履行护理责任的能力。
{"title":"More than dollars: Healthcare utilization among spouses of persons with dementia","authors":"Molly J. Horstman MD, MS","doi":"10.1111/jgs.19174","DOIUrl":"10.1111/jgs.19174","url":null,"abstract":"&lt;p&gt;Being the spouse of a person with dementia can be a significant source of strain and can negatively impact one's health.&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; Although not all spouses serve as the primary caregiver, many spouses provide physical or emotional support to the person with dementia. Studies have shown that spouses of persons with dementia are more likely to have depression, anxiety, and sleep disturbances compared with spouses of persons who do not have dementia.&lt;span&gt;&lt;sup&gt;2-4&lt;/sup&gt;&lt;/span&gt; Identifying opportunities to improve health among spouses of persons with dementia is essential. In the United States, families provide most of the long-term care to persons with dementia.&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; Family members need to maintain sufficient health to fulfill caregiving roles and responsibilities to sustain this system. Spouses of a person with dementia may have less time and fewer financial resources to participate in recommended health behaviors and receive healthcare services, which, over time, may impact their ability to care for the person with dementia.&lt;span&gt;&lt;sup&gt;5&lt;/sup&gt;&lt;/span&gt;&lt;/p&gt;&lt;p&gt;In this issue, &lt;i&gt;Ingraham&lt;/i&gt; et al. present the results of a matched study examining Medicare Fee-for-Service expenditures for spouses of persons living with dementia compared with spouses of persons without dementia in the 5 years after the person with dementia was diagnosed with dementia.&lt;span&gt;&lt;sup&gt;6&lt;/sup&gt;&lt;/span&gt; Using the Health and Retirement Study with linked Medicare Claims, the authors measured three categories of health utilization costs: (1) inpatient or hospital expenditures; (2) outpatient or ambulatory expenditures, which included emergency room visits if a hospitalization did not follow the visit; and (3) skilled nursing facility, hospice, and home health expenditures. In the adjusted analysis, there was no difference in total Medicare expenditures between spouses of persons with dementia and spouses of persons without dementia in the 5 years after dementia was diagnosed. However, in Year 5, there was an increase in total Medicare expenditures among spouses of persons living with dementia driven by an increase in inpatient expenditures, with a total difference of $2748 (95% CI $321–$5447).&lt;/p&gt;&lt;p&gt;The results of this study differ from prior matched studies examining healthcare expenditures among spouses of persons living with dementia.&lt;span&gt;&lt;sup&gt;3, 4, 7, 8&lt;/sup&gt;&lt;/span&gt; As the authors note, prior studies had relied on claims data to identify persons with dementia, while the methods used by &lt;i&gt;Ingraham&lt;/i&gt; et al. for identifying incident diagnoses of dementia from the Health and Retirement Study identified adults at an earlier stage of the disease. However, several other differences existed between this study and prior published studies. These include the methods by which spouses were identified, the type of insurance the spouse had, and the types of expenditures included in the total expenditures.&lt;span&gt;&lt;sup&gt;3, 4, 7, 8&lt;/sup&gt;&lt;/span&gt; In addition, &lt;i&gt;","PeriodicalId":17240,"journal":{"name":"Journal of the American Geriatrics Society","volume":null,"pages":null},"PeriodicalIF":4.3,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jgs.19174","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142116615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Clinical performance of existing diagnostic criteria for pneumonia in older emergency patients: A prospective cohort study 老年急诊患者肺炎现有诊断标准的临床表现:前瞻性队列研究。
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-24 DOI: 10.1111/jgs.19113
Katherine M. Hunold MD, MPH, Lorraine C. Mion PhD, RN, FAAN, Tanya R. Gure MD, Andrew L. Schwaderer MD, Matthew Exline MD, MPH, Courtney Hebert MD, MS, Brent C. Lampert DO, Lauren T. Southerland MD, Julie A. Stephens MS, Edward W. Boyer MD, PhD, Michael Hill RN, Ching-Min B. Chu BS, Carson Reider PhD, Jeffrey M. Caterino MD, MPH

Background

Pneumonia accounts for over half a million older adult emergency department (ED) visits annually, but ED pneumonia diagnosis is inaccurate. Geriatric-specific pneumonia diagnostic criteria exist for other settings; no prospective data exist to determine if application in the older adult ED population is feasible. The objective was to prospectively evaluate the utility of four current diagnostic criteria (Loeb; Modified McGeer; Infectious Disease Society of America/American Thoracic Society; American College of Emergency Physicians) in older adult ED patients.

Methods

This was a prospective, observational cohort study of older adult ED patients ≥65 years of age in two U.S. EDs with suspected pneumonia defined as having chest radiography ordered and treating physician suspicion. The standard we used for defining the presence, absence, or inability to determine a diagnosis of pneumonia diagnosis was expert physician chart adjudication. We report the summary statistics for demographic characteristics and symptoms/exam findings and sensitivity, specificity, and likelihood ratios with 95% confidence intervals of the existing diagnostic criteria. Pre-specified cutoff values of a positive LR >10 and a negative LR <0.3 were considered clinically significant.

Results

Of 135 patients enrolled, 27 had pneumonia by adjudicator review. Typical patient-reported pneumonia symptoms, such as fever (18.5%) and new/worse cough (51.9%), were not consistently present in pneumonia. The IDSA/ATS and ACEP criteria had positive LR >10 and negative LR <0.3; however, all confidence intervals included pre-specified cutoffs.

Conclusions

Older adults presented to the ED with low frequency of typical pneumonia symptoms. Although existing diagnostic definitions had promising test characteristics, they may not perform well enough for clinical application without refinement.

背景:每年有 50 多万老年人因肺炎到急诊科(ED)就诊,但急诊科肺炎诊断并不准确。目前已有针对其他环境的老年肺炎诊断标准,但尚无前瞻性数据来确定在老年人急诊室人群中应用这些标准是否可行。我们的目的是前瞻性地评估目前四种诊断标准(Loeb、修订版 McGeer、美国传染病学会/美国胸科学会、美国急诊医师学会)在老年急诊室患者中的实用性:这是一项前瞻性的观察性队列研究,研究对象是美国两家急诊室中年龄≥65 岁的老年急诊患者,其疑似肺炎的定义是已接受胸片检查且主治医生怀疑其患有肺炎。我们采用专家医师的病历判定标准来界定是否存在肺炎诊断或无法确定肺炎诊断。我们报告了现有诊断标准的人口统计学特征、症状/检查结果、灵敏度、特异性、似然比及 95% 置信区间的汇总统计。预设的临界值为阳性 LR >10 和阴性 LR 结果:在 135 名入选患者中,经评审员审查,27 人患有肺炎。患者报告的典型肺炎症状,如发热(18.5%)和新发/加重的咳嗽(51.9%),在肺炎中并不总是出现。IDSA/ATS 和 ACEP 标准的阳性 LR >10 和阴性 LR 结论:老年人在急诊室出现典型肺炎症状的频率较低。虽然现有的诊断定义具有很好的测试特性,但如果不加以改进,它们可能无法很好地应用于临床。
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引用次数: 0
Older women's perspectives on the ethics of persuasion in doctor-patient communication 老年妇女对医患沟通中说服伦理的看法。
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-14 DOI: 10.1111/jgs.19121
Nancy L. Schoenborn MD, MHS, Susan M. Hannum PhD, Sarah E. Gollust PhD, Rebekah H. Nagler PhD, Mara A. Schonberg MD, MPH, Craig E. Pollack MD, MHS, Cynthia M. Boyd MD, MPH, Qian-Li Xue PhD, Mary Catherine Beach MD

Background

Public health campaigns have often used persuasive techniques to promote healthy behaviors but the use of persuasion by doctors is controversial. We sought to examine older women's perspectives.

Methods

We conducted semi-structured interviews with 20 community-dwelling older women from the Baltimore metropolitan area. We asked whether participants thought it was ethically appropriate for doctors to try to persuade patients and explored their rationales. We probed about commonly used persuasive techniques and two example decisional contexts—stopping mammograms and moving out of one's house after multiple falls. We used qualitative thematic analysis to code the transcripts and summarized results into major themes.

Results

We found mixed views on the ethical appropriateness of persuasion (theme 1); supporters of persuasion were motivated by the potential benefit to patients' health, whereas opponents thought patients should be the ultimate decision-makers. Perspectives depended on the persuasive technique (theme 2), where emotional appeals elicited the most negative reactions while use of facts and patient stories were viewed more positively. Perspectives also varied by the decisional context (theme 3), where higher severity and certainty of harm influenced participants to be more accepting of persuasion. Participants suggested alternative communication approaches to persuasion (theme 4) that emphasized respect for patients.

Conclusions

Our findings suggest that the type of persuasive technique and the decisional context are important considerations in the ethical debate around the use of persuasion. Limiting the use of persuasion to high-stakes decisions and using facts and patient stories rather than emotional appeals are likely more acceptable.

背景:公共卫生运动经常使用说服技术来促进健康行为,但医生使用说服技术却存在争议。我们试图研究老年妇女的观点:我们对来自巴尔的摩大都会地区的 20 名居住在社区的老年妇女进行了半结构化访谈。我们询问参与者是否认为医生试图说服病人在道德上是适当的,并探讨了她们的理由。我们探究了常用的说服技巧和两个决策情境实例--停止乳房 X 光检查和多次跌倒后搬出自己的房子。我们使用定性主题分析法对记录誊本进行编码,并将结果归纳为主要的主题:我们发现,对于劝说的道德适当性(主题 1),人们看法不一;支持劝说者的动机是劝说对患者健康的潜在益处,而反对者则认为患者应该是最终的决策者。观点取决于说服技巧(主题 2),情感诉求引起的反应最为负面,而使用事实和患者故事则更受好评。观点也因决策环境而异(主题 3),危害的严重性和确定性越高,参与者对说服的接受度就越高。参与者建议采用其他沟通方式进行说服(主题 4),强调对患者的尊重:我们的研究结果表明,劝说技巧的类型和决策背景是围绕劝说使用的伦理辩论中的重要考虑因素。将劝说的使用限制在高风险决策中,使用事实和患者故事而非情感诉求可能更容易被接受。
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引用次数: 0
Surviving aging—An assets-based approach 度过老龄化--基于资产的方法。
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-13 DOI: 10.1111/jgs.19126
Brianna E. Morgan PhD, NP, Harriet Mather MD, Daniel David PhD, RN
<p>Rather than seeking time-bending bodies of water, today's scientists pursue the fountain of youth in older adults who demonstrate younger-than-expected attributes. SuperAgers, for example, exhibit signs of cognitive youth despite advanced age. Researchers seek to extract the fountain of youth from SuperAgers' modifiable risks. A 2020 Lancet Commission report found that addressing 12 modifiable risk factors could potentially prevent 40% of cases of dementia.<span><sup>2</sup></span> While promising, this approach centers around combating aging rather than building upon its inherent assets and opportunities. In this editorial, we discuss the strengths and weaknesses of contemporary conceptual models of aging, highlight an article published in this issue that characterizes factors associated with SuperAgers in a sample of African Americans, and propose a new model of aging (Table 1). We aim to conceptualize an assets-based approach that incorporates both the strengths and challenges faced by all older adults seeking to survive aging.</p><p>SuperAging describes older adults who maintain cognitive function equal to normative middle-aged cohorts and is the guiding framework of the Trammel study. While some heterogeneity exists, SuperAging most frequently characterizes a person who is 80+ years old and performs extremely well on a measure of episodic memory (the Rey Auditory Verbal Learning Task), a single aspect of cognition. SuperAgers resist age-related changes (i.e., display cognitive resilience) and demonstrate neuroanatomical features of adults who are decades younger. The concept of SuperAgers is limited by exclusivity (median—12% of older adults), singular dimension (only episodic memory), and stigmatization for those who fail to meet the criteria.<span><sup>3, 4</sup></span></p><p>Despite rising national awareness of racialized disparities in dementia, cognitive resilience in historically underrepresented racial and ethnic groups remains understudied. Using a nationally representative dataset, Trammel et al. explore differences among 1285 African American participants over 80 years old across three cohorts in the National Alzheimer's Coordinating Center dataset—SuperAgers, cognitively intact, and cognitively impaired. After accounting for gender and educational differences, classification as a SuperAger was associated with reduced prevalence of sleep disorders, decreased depression, and moderate alcohol usage. While SuperAgers exhibited vascular comorbidities comparable to non-SuperAgers, they were more likely to report taking medications, including antihypertensives and nonsteroidal anti-inflammatory drugs. Taken together, the results suggest that 80+-year-old African Americans who actively address chronic health conditions are most likely to demonstrate SuperAging status.</p><p>Research on SuperAgers has been a focus since 2012.<span><sup>5</sup></span> It is quite remarkable that a study investigating SuperAgers in African American cohort
此外,在超级老龄化和成功老龄化问世近 40 年后,罗和卡恩认为有必要对资源分配不公平、强化边缘化的制度以及结构性障碍对个人成功老龄化潜能的影响进行概念化研究,并加以解决。然而,正如美国桂冠诗人唐纳德-霍尔(Donald Hall)所言,"老年是一个失去的仪式"。8 事实上,在美国,85% 的 65 岁以上老人至少患有一种慢性疾病,三分之一患有 MCI 或痴呆症,三分之一有身体残疾。我们建议,现在是建立另一种老龄化框架--"生存老龄化 "的时候了。"生存老龄化 "与其他模式不同,它立足于当今美国老年人的老龄化现实。它是一种以资产为基础的方法,适用于所有步入老年的人,而不是少数有抱负的老年人。资产是一个人生态系统的各个方面,这些方面支持他们实现目标,并减轻对他们一生福祉的威胁。资产的概念可以贯穿个人、家庭、建设和服务、社会文化和政治层面的社会生态模式(图 1)。在这一模式中,资产是个人和环境所独有的,其结果植根于个人目标和价值观,而不是外部定义的。资产是动态的--在人的一生中,根据其经历和环境不断积累、变化和减少。健康时可以培养资产,生病时可以利用资产,甚至扩大资产。此外,以资产为基础的老龄化模式可以为解决长期存在的健康不平等问题提供信息,利用社区的优势而不是找茬。一些研究显示了其前景。CAPABLE、Positive Approach® to Care 和 Daily Engagement of Meaningful Activities 利用资产支持残疾和/或认知障碍人士实现个性化目标(如日常活动、互动),对自信心、满意度、身体功能和抑郁等结果产生影响12-14。首先,我们需要澄清 "老有所依 "的理论基础和假设。多个学科(如护理学、社会工作、心理学、职业疗法等)都对 "资产 "大加赞赏,但很少有学科对其方法的理论基础进行描述。健康起源(Salutogenesis)为创造健康而非预防疾病提供了坚实的理论基础。17 第三,我们需要与相关合作伙伴共同确定以资产为基础的成果,就像 LINC-AD 所做的努力一样。最后,我们需要对个人、家庭、社区、系统和政治方法的有效性进行评估,以支持老龄化并解决不平等问题。"老龄化生存 "是一个概念框架,它以面临老龄化挑战的美国人的生活经验为基础,与他们的意见相结合,并具有支持研究、实践和政策的潜力。研究人员将利用该框架开展高度相关和可操作的研究,为我们理解在当今世界 "安享晚年 "的含义提供基本见解。临床医生可以利用 "老龄化生存框架 "来确定每位美国老年人的目标(例如,在年度健康检查中)和资产(例如,通过资产分布图),并调整他们的临床工作,使之与这两个目标相一致。医疗系统、社区组织和支付方可以共同创建医疗服务和报销模式,这些模式以对美国老年人至关重要的结果为基础,并充分利用个人、社区和组织的各种可用资产。毕竟,有了激活的老龄资产,谁还需要青春之泉呢?HM:构思、撰写手稿、审阅、编辑。DD:构思、撰稿、审稿、编辑、监督。DD获得了康比亚健康基金会和国家姑息治疗研究中心的支持。BEM接受了美国国立卫生研究院(NIA P30 AG066512)的资助。
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引用次数: 0
Is more care recipient time at home also a family caregiver-centered quality of life measure? 更多接受护理者在家的时间也是以家庭护理者为中心的生活质量衡量标准吗?
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-13 DOI: 10.1111/jgs.19115
Courtney H. Van Houtven PhD, Karen M. Stechuchak MS, Paul A. Dennis PhD, MSA, Kasey Decosimo MPH, Chelsea L. Whitfield MPH, Nina R. Sperber PhD, S. Nicole Hastings MD, MHS, Megan Shepherd-Banigan PhD, MPH, Brystana G. Kaufman PhD, Valerie A. Smith DrPH

Background

Time in healthcare facilities is associated with worse patient quality of life (QoL); however, impact on family caregiver QoL is unknown. We evaluate care recipient days not at home—days in the emergency department (ED), inpatient (IP) care, and post-acute care (PAC)—to understand how care recipient days not at home correspond to family caregiver QoL.

Methods

Secondary data were linked to care recipient utilization data. Elastic net machine learning models were used to evaluate the impact of a single day of utilization in each setting on binary QoL outcomes. We also compared composite weighted and unweighted “days not at home” variables. Two time periods, 6 and 18 months, were used to predict three caregiver QoL measures (self-rated health, depressive symptoms, and subjective burden).

Results

In the 6-month timeframe, a single day of ED utilization was associated with increased likelihood of poor QoL for all three assessed outcomes (range: 1.4%–3.2%). A day of PAC was associated to a modest degree with increased likelihood of caregiver burden (0.2%) and depressive symptoms (0.1%), with a slight protective effect for self-rated health (−0.1%). An IP day had a slight protective effect (−0.2 to −0.1%). At 18 months, ED and IP had similar, albeit more muted, relationships with caregiver burden and depressive symptoms. PAC had a slight protective effect for caregiver burden (−0.1%). Cumulative days in all settings combined generally was not associated with caregiver QoL.

Conclusion

Whereas total care recipient time away from home had some negative spillovers to family caregivers, the countervailing effects of unique settings on caregiver QoL may mask net QoL effects. This finding limits the utility of a single care recipient home time measure as a valid caregiver-centered measure. Considering cumulative care recipient time in individual settings separately may be needed to reveal the true net effects on caregiver QoL.

背景:在医疗机构的时间与患者生活质量(QoL)的下降有关,但对家庭护理者生活质量的影响尚不清楚。我们评估了护理对象不在家的天数--在急诊科(ED)、住院(IP)护理和急性期后护理(PAC)的天数--以了解护理对象不在家的天数与家庭护理者 QoL 的对应关系:方法:将二级数据与接受护理者的使用数据联系起来。我们使用弹性网机器学习模型来评估在每种环境中使用一天护理服务对二元 QoL 结果的影响。我们还比较了综合加权和非加权 "不在家天数 "变量。我们使用 6 个月和 18 个月这两个时间段来预测三种照顾者 QoL 指标(自评健康、抑郁症状和主观负担):结果:在 6 个月的时间框架内,单日使用急诊室与所有三个评估结果的 QoL 较差可能性增加有关(范围:1.4%-3.2%)。一天的 PAC 与护理负担(0.2%)和抑郁症状(0.1%)的增加有一定程度的相关性,但对自评健康有轻微的保护作用(-0.1%)。IP 日也有轻微的保护作用(-0.2% 到 -0.1%)。在 18 个月时,ED 和 IP 与照顾者负担和抑郁症状的关系相似,但较为平淡。PAC 对照顾者的负担有轻微的保护作用(-0.1%)。在所有环境中的累计天数一般与护理者的 QoL 无关:虽然接受照护者离开家庭的总时间对家庭照护者有一些负面溢出效应,但独特环境对照护者 QoL 的反作用可能会掩盖 QoL 的净效应。这一发现限制了单一的受照护者在家时间测量作为以照护者为中心的有效测量方法的实用性。要揭示对照顾者 QoL 的真正净影响,可能需要单独考虑个别环境中照顾者的累计时间。
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引用次数: 0
A Thank You to JAGS Reviewers 感谢 JAGS 评论员
IF 4.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY Pub Date : 2024-08-12 DOI: 10.1111/jgs.19137
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引用次数: 0
期刊
Journal of the American Geriatrics Society
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