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PERSPECTIVE: A Path to Value-Based Insurance Design for Mental Health Services. PERSPECTIVE: A Path to Value-Based Insurance Design for Mental Health Services.
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2024-03-01
Michael C Freed, Jennifer L Humensky, Patricia A Arean

Background: Aligning cost of mental health care with expected clinical and functional benefits of that care would incentivize the delivery of high value treatments and services. In turn, ineffective or untested care could still be offered but at costs high enough to offset the delivery of high value care.

Aims: The authors comment on Benson and Fendrick's paper on Value-Based Insurance Design (VBID) for mental health in the September 2023 special issue of this journal. The authors also present a preliminary framework of key ingredients needed to consider VBID for mental health treatments and services.

Methods: The authors briefly review current and past efforts to contain costs and improve quality of mental health care, which include (for example) use of carve-out and carve-in programs, evaluation of cost sharing models, impact of accountable care organizations, and studying other benefit designs and impact of federal and state policies.

Results: Using PTSD as an example, key ingredients of VBID for mental health services were identified and include the following: tools for case identification and monitoring progress over time at the population level; specific treatments and services with evidence of clinical effectiveness, cost-effectiveness, and health equity; and an approach to document the specific treatment or service was delivered (versus another treatment or service that may lack evidence).

Discussion: The inability to afford mental health care is a top barrier to treatment seeking. People who do elect to spend time and money on mental health care are further disadvantaged by accessing care that is not well regulated and the quality at best is questionable. VBID could be an important lever for increasing access to and use of high value mental health care. Partnerships among the research, practice, and policy communities can help ensure research solutions meet needs of these two communities.

Implications for health care: VBID holds promise to make high value mental health care more affordable while discouraging low value treatments and services.

Implications for health policies: While evidence gaps remain, these gaps can be filled concurrently with pursuit of VBID for mental health services.

Implications for future research: This paper identifies important research opportunities to help make VBID a reality for mental health care.

背景:将心理健康护理的成本与该护理的预期临床和功能效益挂钩,将激励提供高价值的治疗和服务。反过来,无效或未经测试的医疗服务仍可提供,但其成本足以抵消高价值医疗服务的提供。目的:作者对本森和芬德瑞克在本刊 2023 年 9 月特刊上发表的关于心理健康价值型保险设计(VBID)的论文进行了评论。作者还提出了一个初步框架,其中包含了考虑心理健康治疗和服务的 VBID 所需的关键要素:作者简要回顾了当前和过去为控制成本和提高精神卫生保健质量所做的努力,其中包括(例如)使用 "退出 "和 "加入 "计划、成本分担模式评估、责任医疗组织的影响、研究其他福利设计以及联邦和州政策的影响:结果:以创伤后应激障碍为例,确定了心理健康服务 VBID 的关键要素,其中包括以下内容:病例识别工具和在人群层面监测随时间推移的进展情况;具有临床有效性、成本效益和健康公平性证据的特定治疗和服务;记录特定治疗或服务提供情况的方法(相对于可能缺乏证据的其他治疗或服务):无力负担心理健康医疗费用是寻求治疗的首要障碍。而那些选择花费时间和金钱在心理健康护理上的人,则会因为获得的护理没有得到很好的监管,充其量也只是质量有问题的护理而处于更加不利的地位。VBID 可以成为增加获取和使用高价值心理健康护理的重要杠杆。研究、实践和政策团体之间的合作有助于确保研究解决方案满足这两个团体的需求:VBID 有望使高价值的心理健康护理更加经济实惠,同时抑制低价值的治疗和服务:对未来研究的启示:本文指出了重要的研究机会,以帮助实现心理健康服务的 VBID。
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引用次数: 0
Effectiveness of Antidepressants in Combination with Psychotherapy. 抗抑郁药与心理疗法相结合的疗效。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2024-03-01
Farrokh Alemi, Tulay G Soylu, Mary Cannon, Conor McCandless
<p><strong>Background: </strong>Consensus-guidelines for prescribing antidepressants recommend that clinicians should be vigilant to match antidepressants to patient's medical history but provide no specific advice on which antidepressant is best for a given medical history.</p><p><strong>Aims of the study: </strong>For patients with major depression who are in psychotherapy, this study provides an empirically derived guideline for prescribing antidepressant medications that fit patients' medical history.</p><p><strong>Methods: </strong>This retrospective, observational, cohort study analyzed a large insurance database of 3,678,082 patients. Data was obtained from healthcare providers in the U.S. between January 1, 2001, and December 31, 2018. These patients had 10,221,145 episodes of antidepressant treatments. This study reports the remission rates for the 14 most commonly prescribed single antidepressants (amitriptyline, bupropion, citalopram, desvenlafaxine, doxepin, duloxetine, escitalopram, fluoxetine, mirtazapine, nortriptyline, paroxetine, sertraline, trazodone, and venlafaxine) and a category named "Other" (other antidepressants/combination of antidepressants). The study used robust LASSO regressions to identify factors that affected remission rate and clinicians' selection of antidepressants. The selection bias in observational data was removed through stratification. We organized the data into 16,770 subgroups, of at least 100 cases, using the combination of the largest factors that affected remission and selection bias. This paper reports on 2,467 subgroups of patients who had received psychotherapy.</p><p><strong>Results: </strong>We found large, and statistically significant, differences in remission rates within subgroups of patients. Remission rates for sertraline ranged from 4.5% to 77.86%, for fluoxetine from 2.86% to 77.78%, for venlafaxine from 5.07% to 76.44%, for bupropion from 0.5% to 64.63%, for desvenlafaxine from 1.59% to 75%, for duloxetine from 3.77% to 75%, for paroxetine from 6.48% to 68.79%, for escitalopram from 1.85% to 65%, and for citalopram from 4.67% to 76.23%. Clearly these medications are ideal for patients in some subgroups but not others. If patients are matched to the subgroups, clinicians can prescribe the medication that works best in the subgroup. Some medications (amitriptyline, doxepin, nortriptyline, and trazodone) always had remission rates below 11% and therefore were not suitable as single antidepressant therapy for any of the subgroups.</p><p><strong>Discussions: </strong>This study provides an opportunity for clinicians to identify an optimal antidepressant for their patients, before they engage in repeated trials of antidepressants.</p><p><strong>Implications for health care provision and use: </strong>To facilitate the matching of patients to the most effective antidepressants, this study provides access to a free, non-commercial, decision aid at http://MeAgainMeds.com.</p><p><strong>Implicati
背景:抗抑郁药物处方共识指南建议临床医生应根据患者的病史警惕性地选择抗抑郁药物,但并未就特定病史最适合哪种抗抑郁药物提供具体建议:研究目的:对于接受心理治疗的重度抑郁症患者,本研究为根据患者病史开具抗抑郁药物处方提供了经验性指导:这项回顾性、观察性、队列研究分析了一个包含 3,678,082 名患者的大型保险数据库。数据来自 2001 年 1 月 1 日至 2018 年 12 月 31 日期间美国的医疗服务提供者。这些患者共接受了 10,221,145 次抗抑郁治疗。本研究报告了14种最常处方的单一抗抑郁药(阿米替林、安非他酮、西酞普兰、去文拉法辛、多虑平、度洛西汀、艾司西酞普兰、氟西汀、米氮平、去甲替林、帕罗西汀、舍曲林、曲唑酮和文拉法辛)和一个名为 "其他 "的类别(其他抗抑郁药/抗抑郁药复方)的缓解率。研究采用稳健的LASSO回归法来确定影响缓解率和临床医生选择抗抑郁药物的因素。通过分层消除了观察性数据中的选择偏差。我们利用影响缓解率和选择偏差的最大因素组合,将数据分为 16,770 个至少有 100 个病例的亚组。本文报告了 2467 个接受过心理治疗的患者分组的情况:结果:我们发现,在亚组患者中,缓解率存在很大差异,而且在统计学上具有显著意义。舍曲林的缓解率从 4.5% 到 77.86%,氟西汀的缓解率从 2.86% 到 77.78%,文拉法辛的缓解率从 5.07% 到 76.44%,安非他酮的缓解率从 0.5% 到 64.63%,去文拉法辛从 1.59% 到 75%,度洛西汀从 3.77% 到 75%,帕罗西汀从 6.48% 到 68.79%,艾司西酞普兰从 1.85% 到 65%,西酞普兰从 4.67% 到 76.23%。显然,这些药物对某些亚组的患者来说是理想的选择,但对其他亚组的患者来说则不是。如果将患者与亚组相匹配,临床医生就可以为亚组患者开具疗效最好的药物。有些药物(阿米替林、多虑平、去甲替林和曲唑酮)的缓解率总是低于 11%,因此不适合作为任何亚组的单一抗抑郁治疗药物:讨论:这项研究为临床医生提供了一个机会,使他们能够在反复试验抗抑郁药之前,为患者确定最佳抗抑郁药:为便于将患者与最有效的抗抑郁药物相匹配,本研究提供了免费、非商业性的决策辅助工具,http://MeAgainMeds.com.Implications: 政策制定者应评估如何通过零散的医疗点电子健康记录提供研究结果。另外,政策制定者还可以建立一个人工智能系统,在家中向患者在线推荐抗抑郁药物,并鼓励他们在下次就诊时将推荐意见带给临床医生: 未来的研究可以调查(i)我们的建议在改变临床实践方面的有效性,(ii)提高抑郁症状的缓解率,以及(iii)降低护理成本。这些研究需要具有前瞻性,但要务实。随机临床试验不太可能解决影响缓解的大量因素。
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引用次数: 0
The Economic Burden of Chronic Psychotic Disorders: An Incidence-based Cost-of-Illness Approach. 慢性精神障碍的经济负担:基于发病率的疾病成本法》。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2024-03-01
Claire de Oliveira, Bryan Tanner

Background: The economic burden of chronic psychotic disorders is substantial. However, few studies have employed an incidence based approach to estimate the economic burden of chronic psychotic disorders. Furthermore, the existing work has mainly used models populated with data obtained from published literature, making several assumptions to estimate incidence-based costs.

Aims of the study: The objective of this study was to estimate the direct cumulative mean health care costs of chronic psychotic disorders, using an incidence-based, cost-of-illness approach and real-world data from a single-payer health care system.

Methods: Using health records from Ontario, Canada, all individuals with a valid health card number, residing in the province, and diagnosed with a chronic psychotic disorder between the ages of 16 and 45 from April 1st, 2006, to March 31st, 2021, were included in the analysis. Using a mix of bottom-up and top-down methodologies and a robust cost estimator, cumulative mean health care costs were estimated from diagnosis to death or the end of observation period. Cumulative mean health care costs, and respective 95% confidence intervals (CIs), were estimated for the 1-year period (i.e., first year post-diagnosis), overall, by sex, age groups and health service, and for the 5-, 10- and 15-periods, overall and by sex.

Results: One-, 5-, 10- and 15-year total discounted cumulative mean health care costs were estimated at USD 24,441.16, 95% CI (USD 24,166.13, USD 24,716.19), USD 70,754.69, 95% CI (USD 69,827.48-USD 71,681.89), USD 117,136.88, 95% CI (USD 115,370.40-USD 118,903.35), and USD 157,829.01 95% CI (USD 155,599.32.-USD 160,058.70), respectively. Total mean 1-year costs post-diagnosis were higher for younger individuals. Although females had higher 1-year costs, males had higher 5-, 10- and 15-year costs. Psychiatric hospitalisations made up the largest component of total costs across all cost estimates.

Discussion: These results suggest that the costs of chronic psychotic disorders are high in the year of diagnosis and then increase at a decreasing rate thereafter. Compared to previous work, the cost estimates from the present study suggest that the use of real-world data produces lower estimates of cumulative costs, albeit likely more accurate ones. However, these estimates do not account for costs of care provided in community-based agencies.

Implications for health policies: These estimates will serve as important inputs for policymakers looking to make decisions around resource allocation.

Implications for future research: Future research should seek to follow incident cases in administrative data over a longer time period to obtain cumulative costs of longer duration.

背景:慢性精神障碍造成的经济负担十分沉重。然而,很少有研究采用基于发病率的方法来估算慢性精神病的经济负担。此外,现有研究主要使用从公开发表的文献中获取的数据建立模型,并做出若干假设来估算基于发病率的成本:本研究的目的是使用基于发病率的疾病成本法和来自单一付费医疗系统的真实世界数据,估算慢性精神病性障碍的直接累积平均医疗成本:方法:利用加拿大安大略省的健康记录,将 2006 年 4 月 1 日至 2021 年 3 月 31 日期间所有拥有有效健康卡号、居住在该省并被诊断出患有慢性精神病性障碍的 16 至 45 岁人群纳入分析范围。通过混合使用自下而上和自上而下的方法以及稳健的成本估算器,估算了从诊断到死亡或观察期结束的累计平均医疗成本。按性别、年龄组和医疗服务估算了1年期(即诊断后第一年)的总体累计平均医疗成本和各自的95%置信区间(CIs),并按性别估算了5、10和15年期的总体累计平均医疗成本和各自的95%置信区间(CIs):1年、5年、10年和15年的总贴现累计平均医疗费用估计分别为24,441.16美元(95% CI为24,166.13美元,24,716.19美元)、70,754.69美元(95% CI为70,754.69美元)、70,754.69美元(95% CI为70,754.69美元)和70,754.69美元(95% CI为70,754.69美元)。69美元(95% CI,69,827.48-71,681.89美元)、117,136.88美元(95% CI,115,370.40-118,903.35美元)和157,829.01美元(95% CI,155,599.32-160,058.70美元)。年轻患者确诊后 1 年的平均总费用较高。虽然女性的 1 年费用较高,但男性的 5 年、10 年和 15 年费用较高。在所有成本估算中,精神科住院治疗占总成本的最大部分:讨论:这些结果表明,慢性精神障碍的成本在确诊当年较高,之后以递减的速度增长。与之前的研究相比,本研究的成本估算结果表明,使用真实世界的数据得出的累积成本估算结果较低,尽管可能更为准确。然而,这些估算并未考虑社区机构提供的护理成本:对未来研究的启示:这些估算值将作为决策者在资源分配方面决策的重要依据:未来研究的启示:未来的研究应寻求在更长的时间段内跟踪行政数据中的事件病例,以获得持续时间更长的累积成本。
{"title":"The Economic Burden of Chronic Psychotic Disorders: An Incidence-based Cost-of-Illness Approach.","authors":"Claire de Oliveira, Bryan Tanner","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>The economic burden of chronic psychotic disorders is substantial. However, few studies have employed an incidence based approach to estimate the economic burden of chronic psychotic disorders. Furthermore, the existing work has mainly used models populated with data obtained from published literature, making several assumptions to estimate incidence-based costs.</p><p><strong>Aims of the study: </strong>The objective of this study was to estimate the direct cumulative mean health care costs of chronic psychotic disorders, using an incidence-based, cost-of-illness approach and real-world data from a single-payer health care system.</p><p><strong>Methods: </strong>Using health records from Ontario, Canada, all individuals with a valid health card number, residing in the province, and diagnosed with a chronic psychotic disorder between the ages of 16 and 45 from April 1st, 2006, to March 31st, 2021, were included in the analysis. Using a mix of bottom-up and top-down methodologies and a robust cost estimator, cumulative mean health care costs were estimated from diagnosis to death or the end of observation period. Cumulative mean health care costs, and respective 95% confidence intervals (CIs), were estimated for the 1-year period (i.e., first year post-diagnosis), overall, by sex, age groups and health service, and for the 5-, 10- and 15-periods, overall and by sex.</p><p><strong>Results: </strong>One-, 5-, 10- and 15-year total discounted cumulative mean health care costs were estimated at USD 24,441.16, 95% CI (USD 24,166.13, USD 24,716.19), USD 70,754.69, 95% CI (USD 69,827.48-USD 71,681.89), USD 117,136.88, 95% CI (USD 115,370.40-USD 118,903.35), and USD 157,829.01 95% CI (USD 155,599.32.-USD 160,058.70), respectively. Total mean 1-year costs post-diagnosis were higher for younger individuals. Although females had higher 1-year costs, males had higher 5-, 10- and 15-year costs. Psychiatric hospitalisations made up the largest component of total costs across all cost estimates.</p><p><strong>Discussion: </strong>These results suggest that the costs of chronic psychotic disorders are high in the year of diagnosis and then increase at a decreasing rate thereafter. Compared to previous work, the cost estimates from the present study suggest that the use of real-world data produces lower estimates of cumulative costs, albeit likely more accurate ones. However, these estimates do not account for costs of care provided in community-based agencies.</p><p><strong>Implications for health policies: </strong>These estimates will serve as important inputs for policymakers looking to make decisions around resource allocation.</p><p><strong>Implications for future research: </strong>Future research should seek to follow incident cases in administrative data over a longer time period to obtain cumulative costs of longer duration.</p>","PeriodicalId":46381,"journal":{"name":"Journal of Mental Health Policy and Economics","volume":"27 1","pages":"13-21"},"PeriodicalIF":1.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140856280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
COVID-19, Mental Health, and Mental Health Treatment among Adults. COVID-19、心理健康和成人心理健康治疗。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-12-01
Samuel H Zuvekas

Background: The COVID-19 pandemic has been widely reported to have increased symptoms of anxiety, depression, and other mental health issues. It may also have significantly disrupted continuity of treatment for existing patients and made access for those newly seeking care more difficult at a time when treatment needs are higher.

Aims of the study: This study seeks to examine the impact of the COVID-19 pandemic on mental health status and mental health treatment among adults residing in the U.S. civilian, non-institutionalized population.

Methods: The data are drawn from the 2019-2020 Medical Expenditure Panel Survey (MEPS), a nationally representative household survey of the U.S. civilian non-institutionalized population conducted annually since 1996 and used extensively to study mental health treatment in the U.S. I examine unadjusted and regression-adjusted differences between 2019 and 2020 in perceived mental health status (excellent, very good, good, fair, poor) and in the K6 general psychological distress, the PHQ-2 depression screener, and the VR-12 mental component summary score. Similarly, using the detailed MEPS data on health care encounters and prescription drug fills, I examine differences in mental health use treatment between 2019 and 2020. I focus specifically on changes in continuity of treatment among those already in treatment in January and February, before the pandemic fully struck, as well differences in the initiation of new episodes of treatment after the pandemic began.

Results: All four mental health scales included in the MEPS show statistically significant declines in mental health between 2019 and 2020, particularly among younger adults. On balance, the percentage of US adults receiving mental health treatment did not change significantly. Continuity of treatment increased slightly in 2020, with 87.1% of adults in treatment January or February still receiving care in the second quarter, an increase of 2.5 percentage points (p=.025). However, there were significant declines in the initiation of new episodes of treatment, especially in the second quarter of 2020.

Discussion: While the continuity of treatment among adults already in care when the COVID pandemic first led to nationwide disruptions is welcome news, the decline in new episodes of mental health treatment among those not previously treated is of great concern. In a time of heightened need, the gap between need and treatment likely grew larger. IMPLICATIONS FOR HEALTH CARE PROVISION AND USE, AND IMPLICATIONS FOR HEALTH POLICIES: Continued long-term monitoring of the mental health needs and treatment gaps will be important, especially as many emergency measures designed to mitigate the effects of the pandemic on access to mental health treatment expire.

背景:据广泛报道,COVID-19 大流行增加了焦虑、抑郁和其他心理健康问题的症状。它还可能严重扰乱了现有患者治疗的连续性,并使新求医者在治疗需求较高时更难获得治疗:本研究旨在探讨 COVID-19 大流行对美国非住院成年人的心理健康状况和心理健康治疗的影响:数据来自 2019-2020 年医疗支出小组调查(MEPS),这是一项自 1996 年以来每年对美国平民非机构化人口进行的具有全国代表性的家庭调查,被广泛用于研究美国的心理健康治疗。我研究了 2019 年和 2020 年之间感知到的心理健康状况(极好、很好、好、一般、差)以及 K6 一般心理困扰、PHQ-2 抑郁筛查器和 VR-12 心理成分总分的未调整和回归调整差异。同样,我利用 MEPS 关于医疗保健就诊和处方药填写的详细数据,研究了 2019 年和 2020 年之间心理健康使用治疗方面的差异。我特别关注在大流行病全面爆发前的 1 月和 2 月已经接受治疗的人在治疗连续性方面的变化,以及在大流行病开始后开始新一轮治疗的差异:MEPS包含的所有四个心理健康量表均显示,2019年至2020年期间,心理健康水平在统计学上有显著下降,尤其是在年轻成年人中。总的来说,接受心理健康治疗的美国成年人的比例没有显著变化。治疗的持续性在 2020 年略有增加,1 月或 2 月接受治疗的成年人中有 87.1%在第二季度仍在接受治疗,增加了 2.5 个百分点(p=.025)。然而,开始新一轮治疗的人数明显减少,尤其是在 2020 年第二季度:在 COVID 大流行首次导致全国性混乱时,已经接受治疗的成年人继续接受治疗是一个值得欢迎的消息,但那些以前未接受过治疗的人的精神健康治疗的新发病率下降则令人十分担忧。在需求增加的时候,需求与治疗之间的差距可能会越来越大。对医疗服务的提供和使用的影响,以及对医疗政策的影响:继续对精神健康需求和治疗差距进行长期监测将是非常重要的,尤其是当许多旨在减轻大流行病对精神健康治疗影响的紧急措施到期时。
{"title":"COVID-19, Mental Health, and Mental Health Treatment among Adults.","authors":"Samuel H Zuvekas","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>The COVID-19 pandemic has been widely reported to have increased symptoms of anxiety, depression, and other mental health issues. It may also have significantly disrupted continuity of treatment for existing patients and made access for those newly seeking care more difficult at a time when treatment needs are higher.</p><p><strong>Aims of the study: </strong>This study seeks to examine the impact of the COVID-19 pandemic on mental health status and mental health treatment among adults residing in the U.S. civilian, non-institutionalized population.</p><p><strong>Methods: </strong>The data are drawn from the 2019-2020 Medical Expenditure Panel Survey (MEPS), a nationally representative household survey of the U.S. civilian non-institutionalized population conducted annually since 1996 and used extensively to study mental health treatment in the U.S. I examine unadjusted and regression-adjusted differences between 2019 and 2020 in perceived mental health status (excellent, very good, good, fair, poor) and in the K6 general psychological distress, the PHQ-2 depression screener, and the VR-12 mental component summary score. Similarly, using the detailed MEPS data on health care encounters and prescription drug fills, I examine differences in mental health use treatment between 2019 and 2020. I focus specifically on changes in continuity of treatment among those already in treatment in January and February, before the pandemic fully struck, as well differences in the initiation of new episodes of treatment after the pandemic began.</p><p><strong>Results: </strong>All four mental health scales included in the MEPS show statistically significant declines in mental health between 2019 and 2020, particularly among younger adults. On balance, the percentage of US adults receiving mental health treatment did not change significantly. Continuity of treatment increased slightly in 2020, with 87.1% of adults in treatment January or February still receiving care in the second quarter, an increase of 2.5 percentage points (p=.025). However, there were significant declines in the initiation of new episodes of treatment, especially in the second quarter of 2020.</p><p><strong>Discussion: </strong>While the continuity of treatment among adults already in care when the COVID pandemic first led to nationwide disruptions is welcome news, the decline in new episodes of mental health treatment among those not previously treated is of great concern. In a time of heightened need, the gap between need and treatment likely grew larger. IMPLICATIONS FOR HEALTH CARE PROVISION AND USE, AND IMPLICATIONS FOR HEALTH POLICIES: Continued long-term monitoring of the mental health needs and treatment gaps will be important, especially as many emergency measures designed to mitigate the effects of the pandemic on access to mental health treatment expire.</p>","PeriodicalId":46381,"journal":{"name":"Journal of Mental Health Policy and Economics","volume":"26 4","pages":"159-183"},"PeriodicalIF":1.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Employer-Provided and Self-Initiated Job Accommodations for Workers with Serious Mental Illness. 为患有严重精神疾病的工人提供雇主提供和自我发起的工作适应。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-12-01
Marjorie L Baldwin, Rebecca M B White, Steven C Marcus
<p><strong>Background: </strong>Many individuals with serious mental illness (SMI) are capable of employment in regular jobs (i.e. jobs paying at least minimum wage, not set aside for persons with disabilities, and not obtained with assistance from mental health services), but they may need job accommodations to be successful. The extant literature focuses almost exclusively on accommodations for workers with SMI who are receiving employment support, so we know almost nothing about the nature or frequency of accommodations needed by workers who are independently employed.</p><p><strong>Aims: </strong>Drawing on survey data from a sample of workers with diagnoses of SMI who are capable of regular, mainstream employment, we aim to: (i) describe the nature and frequency of job accommodations workers requested from their employer or initiated on their own; and (ii) identify individual- and work-related factors associated with the probabilities of requesting or initiating accommodations.</p><p><strong>Methods: </strong>The analysis sample includes 731 workers with diagnoses of schizophrenia, bipolar disorder, or major depressive disorder, who were employed in regular jobs post-onset of SMI. Workers identified any job accommodations requested from their employer, or initiated on their own. Summary statistics describe the nature and frequency of accommodations in four categories: scheduling, workspace, supervision, job modification. Logistic regression models estimate the relationship between workers' health- and job-related characteristics and the probabilities of requesting or self-initiating accommodations.</p><p><strong>Results: </strong>Whereas 84% of workers in our sample self-initiated accommodations, only 25% requested accommodations from their employer. The most frequent accommodations of either type involved flexibility in scheduling (63% self-initiated, 24% requested), or modifications to the workspace (58%, 19%). Factors significantly correlated with the probability of requesting accommodations include: supportive workplace culture, longer job tenure, more severe cognitive/social limitations. Factors significantly correlated with the probability of self-initiating accommodations include: younger age, more severe social limitations, greater job autonomy.</p><p><strong>Discussion: </strong>This is the first study of job accommodations among a cohort of persons with SMI independently employed in regular jobs. We identify a type of accommodation, self-initiated by the worker, that has not been studied before. These self-initiated accommodations are far more prevalent than employer-provided accommodations in our sample. Key factors associated with the probabilities of requesting/initiating accommodations reflect need (e.g. compromised health) and feasibility of implementation in a particular job. Limitations of the study include the cross-sectional design which limits our ability to identify causal relationships.</p><p><strong>Implications for he
背景:许多患有严重精神疾病(SMI)的人都有能力在普通工作岗位上就业(即至少支付最低工资的工作,这些工作不是为残障人士预留的,也不是在精神健康服务机构的帮助下获得的),但他们可能需要工作调整才能成功就业。现有文献几乎只关注那些接受就业支持的 SMI 工作者的工作调整,因此我们对独立就业的 SMI 工作者所需的工作调整的性质和频率几乎一无所知:(i) 描述工人要求雇主提供或自己主动提供工作便利的性质和频率;(ii) 确定与要求或主动提供便利的概率相关的个人和工作相关因素:分析样本包括 731 名被诊断为精神分裂症、双相情感障碍或重度抑郁障碍的工人,他们在患上精神分裂症后从事正规工作。工人们确认了他们向雇主提出的或自己主动提出的任何工作调整要求。摘要统计描述了四个类别的工作调整的性质和频率:时间安排、工作空间、监督和工作调整。逻辑回归模型估计了工人的健康和工作相关特征与要求或自行提出调整的概率之间的关系:在我们的样本中,84% 的工人自行提出调整要求,只有 25% 的工人向雇主提出调整要求。这两种类型中最常见的便利措施是灵活安排时间(63%为自己主动提出,24%为雇主要求)或改造工作空间(58%和19%)。与要求提供便利的可能性明显相关的因素包括:支持性的工作场所文化、较长的工作任期、较严重的认知/社会限制。与自行提出调整要求的概率明显相关的因素包括:年龄较小、社会限制较严重、工作自主性较强:这是首次对独立从事正常工作的 SMI 患者群体的工作适应情况进行研究。我们发现了一种以前未曾研究过的、由工人自我发起的适应类型。在我们的样本中,这些自我主动提供的便利远比雇主提供的便利更为普遍。与要求/主动提供便利的概率相关的关键因素反映了需求(如健康受损)和在特定工作中实施的可行性。研究的局限性包括横截面设计限制了我们确定因果关系的能力:为患有 SMI 的工人提供职业服务的提供者应该意识到,这些员工可以通过多种方式自行缓解病情,而无需向雇主披露 SMI:我们的研究结果建议制定支持披露和由雇主提供适应的工作场所政策,以及为员工创造灵活性,使其能够主动适应的政策:进一步研究的启示:鉴于员工自发调整的普遍性,针对患有严重精神疾病的员工的工作调整研究必须考虑到这些类型的调整。
{"title":"Employer-Provided and Self-Initiated Job Accommodations for Workers with Serious Mental Illness.","authors":"Marjorie L Baldwin, Rebecca M B White, Steven C Marcus","doi":"","DOIUrl":"","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Many individuals with serious mental illness (SMI) are capable of employment in regular jobs (i.e. jobs paying at least minimum wage, not set aside for persons with disabilities, and not obtained with assistance from mental health services), but they may need job accommodations to be successful. The extant literature focuses almost exclusively on accommodations for workers with SMI who are receiving employment support, so we know almost nothing about the nature or frequency of accommodations needed by workers who are independently employed.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Aims: &lt;/strong&gt;Drawing on survey data from a sample of workers with diagnoses of SMI who are capable of regular, mainstream employment, we aim to: (i) describe the nature and frequency of job accommodations workers requested from their employer or initiated on their own; and (ii) identify individual- and work-related factors associated with the probabilities of requesting or initiating accommodations.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;The analysis sample includes 731 workers with diagnoses of schizophrenia, bipolar disorder, or major depressive disorder, who were employed in regular jobs post-onset of SMI. Workers identified any job accommodations requested from their employer, or initiated on their own. Summary statistics describe the nature and frequency of accommodations in four categories: scheduling, workspace, supervision, job modification. Logistic regression models estimate the relationship between workers' health- and job-related characteristics and the probabilities of requesting or self-initiating accommodations.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Whereas 84% of workers in our sample self-initiated accommodations, only 25% requested accommodations from their employer. The most frequent accommodations of either type involved flexibility in scheduling (63% self-initiated, 24% requested), or modifications to the workspace (58%, 19%). Factors significantly correlated with the probability of requesting accommodations include: supportive workplace culture, longer job tenure, more severe cognitive/social limitations. Factors significantly correlated with the probability of self-initiating accommodations include: younger age, more severe social limitations, greater job autonomy.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Discussion: &lt;/strong&gt;This is the first study of job accommodations among a cohort of persons with SMI independently employed in regular jobs. We identify a type of accommodation, self-initiated by the worker, that has not been studied before. These self-initiated accommodations are far more prevalent than employer-provided accommodations in our sample. Key factors associated with the probabilities of requesting/initiating accommodations reflect need (e.g. compromised health) and feasibility of implementation in a particular job. Limitations of the study include the cross-sectional design which limits our ability to identify causal relationships.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Implications for he","PeriodicalId":46381,"journal":{"name":"Journal of Mental Health Policy and Economics","volume":"26 4","pages":"137-147"},"PeriodicalIF":1.6,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138812128","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Financial Sustainability of Novel Delivery Models in Behavioral Health Treatment. 行为健康治疗中新型交付模式的财务可持续性。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-12-01
Dominic Hodgkin, Constance M Horgan, Stephanie Jordan Brown, Gavin Bart, Maureen T Stewart
<p><strong>Background: </strong>In the US, much of the research into new intervention and delivery models for behavioral health care is funded by research institutes and foundations, typically through grants to develop and test the new interventions. The original grant funding is typically time-limited. This implies that eventually communities, clinicians, and others must find resources to replace the grant funding -otherwise the innovation will not be adopted. Diffusion is challenged by the continued dominance in the US of fee-for-service reimbursement, especially for behavioral health care.</p><p><strong>Aims: </strong>To understand the financial challenges to disseminating innovative behavioral health delivery models posed by fee-for-service reimbursement, and to explore alternative payment models that promise to accelerate adoption by better addressing need for flexibility and sustainability.</p><p><strong>Methods: </strong>We review US experience with three specific novel delivery models that emerged in recent years. The models are: collaborative care model for depression (CoCM), outpatient based opioid treatment (OBOT), and the certified community behavioral health clinic (CCBHC) model. These examples were selected as illustrating some common themes and some different issues affecting diffusion. For each model, we discuss its core components; evidence on its effectiveness and cost-effectiveness; how its dissemination was funded; how providers are paid; and what has been the uptake so far.</p><p><strong>Results: </strong>The collaborative care model has existed for longest, but has been slow to disseminate, due in part to a lack of billing codes for key components until recently. The OBOT model faced that problem, and also (until recently) a regulatory requirement requiring physicians to obtain federal waivers in order to prescribe buprenorphine. Similarly, the CCBHC model includes previously nonbillable services, but it appears to be diffusing more successfully than some other innovations, due in part to the approach taken by funders.</p><p><strong>Discussion: </strong>A common challenge for all three models has been their inclusion of services that were not (initially) reimbursable in a fee-for-service system. However, even establishing new procedure codes may not be enough to give providers the flexibility needed to implement these models, unless payers also implement alternative payment models.</p><p><strong>Implications for health care provision and use: </strong>For providers who receive time-limited grant funding to implement these novel delivery models, one key lesson is the need to start early on planning how services will be sustained after the grant ends.</p><p><strong>Implications for health policy: </strong>For research funders (e.g., federal agencies), it is clearly important to speed up the process of obtaining coverage for each novel delivery model, including the development of new billable service codes, and to plan for this
背景:在美国,对新的行为健康护理干预和提供模式的研究大多由研究机构和基金会资助,通常是通过拨款来开发和测试新的干预措施。最初的拨款通常是有时间限制的。这意味着社区、临床医生和其他人最终必须找到资源来替代拨款,否则创新就不会被采用。目的:了解收费服务对推广创新的行为健康服务模式所带来的财务挑战,并探索其他付费模式,这些模式有望通过更好地满足灵活性和可持续性的需求来加快创新的采用:方法:我们回顾了美国近年来出现的三种新型医疗服务模式的经验。这三种模式分别是:抑郁症协作护理模式(CoCM)、阿片类药物门诊治疗模式(OBOT)以及认证社区行为健康诊所模式(CCBHC)。选择这些例子是为了说明一些共同的主题和一些影响推广的不同问题。对于每种模式,我们都讨论了其核心组成部分、有效性和成本效益方面的证据、推广资金的筹措方式、提供者的薪酬支付方式以及迄今为止的采用情况:协作护理模式存在时间最长,但推广速度缓慢,部分原因是直到最近才为其关键组成部分制定了计费代码。OBOT 模式面临着这一问题,同时(直到最近)还面临着一项监管要求,即医生必须获得联邦豁免才能开丁丙诺啡处方。同样,CCBHC 模式也包括以前不计费的服务,但与其他一些创新相比,它的推广似乎更为成功,部分原因在于资助者采取的方法:这三种模式面临的一个共同挑战是,它们纳入了收费服务系统中(最初)无法报销的服务。然而,即使制定了新的程序代码,也可能不足以为医疗服务提供者提供实施这些模式所需的灵活性,除非支付者也实施替代支付模式:对医疗服务提供者而言,如果他们获得了有时间限制的补助资金来实施这些新的医疗服务模式,那么一个重要的经验就是需要尽早开始计划如何在补助结束后继续提供服务:对于研究资助者(如联邦机构)来说,加快为每种新型提供模式争取资助的进程,包括制定新的收费服务代码,并尽早为此制定计划,显然是非常重要的。资助者还需要在资助期的早期与医疗服务提供者合作,为资助后的环境制定可持续发展规划。对于支付方而言,一个重要的经验是需要将新模式纳入稳定的现有资金流,如医疗补助和商业保险,而不是任由有时间限制的循环拨款摆布,并为新支付模式下的创新提供签约途径:对研究人员而言,一个重要的建议是在设计新的提供模式和干预措施时,更多地关注支付环境。
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引用次数: 0
Value-Based Insurance Design: Clinically Nuanced Consumer Cost-Sharing for Mental Health Services. 基于价值的保险设计:心理健康服务的临床消费者成本分担。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-09-01
Nicole M Benson, A Mark Fendrick

Background: While consumer cost-sharing is a widely used strategy to mitigate health care spending, numerous studies have demonstrated that even modest levels of out-of-pocket cost are associated with lower use of medical care, including clinically necessary, high-value services. Within mental health care, increases in cost-sharing are associated with reductions in use of mental health care and psychotropic medication use. Further, these reductions in mental health services and treatments can lead to downstream consequences including worsening of psychiatric illness and increased need for acute care and psychiatric hospitalization. Thus, there is a need for clinically informed solutions that explicitly balance the need for appropriate access to essential mental health services and treatments with growing fiscal pressures faced by public and private payers. Value-Based Insurance Design (VBID) describes a model where consumer cost-sharing is based on the potential clinical benefit rather than the price of a specific health care service or treatment.

Aims of the study: Describe value-based insurance design and applications in mental health care.

Results, discussion and implications for health policies: For over two decades, clinically nuanced VBID programs have been implemented in an effort to optimize the use of high-value health services and enhance equity through reduced consumer cost-sharing. Overall, the evidence suggests that VBID has demonstrated success in reducing consumer out-of-pocket costs associated with specific, high value services. By reducing financial barriers to essential clinical services and medications, VBID has potential to enhance equity. However, the impact of VBID on overall mental health care spending and clinical outcomes remains uncertain.

背景:虽然消费者成本分担是一种广泛使用的减少医疗保健支出的策略,但许多研究表明,即使是适度的自付成本也与医疗保健的使用率较低有关,包括临床上必要的高价值服务。在精神卫生保健方面,费用分担的增加与精神卫生保健和精神药物使用的减少有关。此外,心理健康服务和治疗的减少可能会导致下游后果,包括精神疾病的恶化,以及对急性护理和精神病住院治疗的需求增加。因此,需要有临床知情的解决方案,明确平衡适当获得基本心理健康服务和治疗的需求与公共和私人付款人面临的日益增长的财政压力。基于价值的保险设计(VBID)描述了一种模型,其中消费者的成本分担是基于潜在的临床效益,而不是特定医疗服务或治疗的价格。研究目的:描述基于价值的保险设计和在心理健康护理中的应用。结果、讨论和对卫生政策的影响:20多年来,临床上细致入微的VBID计划一直在实施,以优化高价值卫生服务的使用,并通过减少消费者成本分担来提高公平性。总体而言,证据表明,VBID在降低与特定高价值服务相关的消费者自付成本方面取得了成功。通过减少基本临床服务和药物的财务障碍,VBID有可能提高公平性。然而,VBID对整体精神卫生保健支出和临床结果的影响仍不确定。
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引用次数: 0
LETTER: The Effect of Mental Disorders on Caregiver Workforce Participation: The Hidden Societal Cost. 信件:精神障碍对护理人员劳动力参与的影响:隐藏的社会成本。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-09-01
Jens Peter Eckardt

No abstract.

没有摘要。
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引用次数: 0
Perspectives on Financing Strategies for Evidence-Based Treatment Implementation in Youth Mental Health Systems. 青年心理健康系统循证治疗实施筹资策略展望。
IF 1 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-09-01
Maddison N North, Alex R Dopp, Jane F Silovsky, Marylou Gilbert, Jeanne S Ringel
<p><strong>Background: </strong>Evidence-based treatments (EBTs) are critical to effectively address mental health problems among children and adolescents, but costly for mental health service agencies to implement and sustain. Financing strategies help agencies overcome cost-related barriers by obtaining financial resources to support EBT implementation and/or sustainment.</p><p><strong>Aims: </strong>We sought to (i) understand how youth mental health system decision-makers involved with EBT implementation and sustainment view key features (e.g., relevance, feasibility) that inform financing strategy selection and (ii) compare service agency, funding agency, and intermediary representative perspectives.</p><p><strong>Method: </strong>Two surveys were disseminated to 48 representatives across U.S. youth mental health service agencies, funding agencies, and intermediaries who were participating in a larger study of financing strategies. Quantitative and qualitative data were gathered on 23 financing strategies through quantitative ratings and open-ended responses. Data were analyzed using descriptive statistics and rapid content analysis.</p><p><strong>Results: </strong>The financing strategies rated as most relevant include braided funding streams, contracts for EBTs, credentialing/rostering providers, fee-for-service reimbursement (regular and increased), and grant funding. All other strategies were unfamiliar to 1/3 to 1/2 of participants. The six strategies were rated between somewhat and quite available, feasible, and effective for EBT sustainment. For sustaining different EBT components (e.g., delivery, materials), the mix of financing strategies was rated as somewhat adequate. Qualitative analysis revealed challenges with strategies being non-recurring or unavailable in representatives' regions. Ratings were largely similar across participant roles, though funding agency representatives were the most familiar with financing strategies.</p><p><strong>Discussion: </strong>Despite the breadth of innovative financing strategies, expert representatives within the youth mental health services ecosystem had limited knowledge of most options. Experts relied on strategies that were familiar but often did not adequately support EBT implementation or sustainment. These findings underscore more fundamental issues with under-resourced mental health systems in the U.S.; financing strategies can help agencies navigate EBT use but must be accompanied by larger-scale system reforms. Limitations include difficulties generalizing results due to using a small sample familiar with EBTs, high agreement as a potential function of snowball recruiting, and limited responses to the open-ended survey questions.</p><p><strong>Implications for health care provision and use: </strong>Although EBTs have been found to effectively address mental health problems in children and adolescents, available strategies for financing their implementation and sustainment in mental h
背景:循证治疗(EBT)对于有效解决儿童和青少年的心理健康问题至关重要,但心理健康服务机构实施和维持成本高昂。融资战略通过获得财政资源来支持EBT的实施和/或维持,帮助各机构克服与成本相关的障碍。目的:我们试图(i)了解参与EBT实施和维持的青年心理健康系统决策者如何看待为融资战略选择提供信息的关键特征(如相关性、可行性),以及(ii)比较服务机构、融资机构和中介代表的观点。方法:将两项调查分发给美国青年心理健康服务机构、资助机构和中介机构的48名代表,他们正在参与一项更大规模的融资策略研究。通过定量评级和开放式答复,收集了23项融资战略的定量和定性数据。使用描述性统计和快速内容分析对数据进行分析。结果:被评为最相关的融资策略包括编织资金流、EBT合同、认证/名册提供者、服务费报销(定期和增加)和赠款。三分之一到二分之一的参与者不熟悉所有其他策略。这六种策略被评为在一定程度上和相当可用、可行和有效的EBT维持之间。为了维持不同的EBT组成部分(如交付、材料),融资策略的组合被评为在一定程度上足够。定性分析揭示了在代表所在地区不经常或不可用的战略所带来的挑战。参与者角色的评级基本相似,尽管融资机构代表最熟悉融资策略。讨论:尽管创新融资战略范围广泛,但青年心理健康服务生态系统中的专家代表对大多数选择的了解有限。专家们所依赖的战略是熟悉的,但往往不能充分支持EBT的实施或维持。这些发现强调了美国精神卫生系统资源不足的更根本问题。;融资策略可以帮助机构引导EBT的使用,但必须伴随着更大规模的系统改革。局限性包括由于使用熟悉EBT的小样本而难以概括结果,高度一致性是滚雪球招聘的潜在功能,以及对开放式调查问题的回答有限。对医疗保健提供和使用的影响:尽管EBT已被发现可以有效解决儿童和青少年的心理健康问题,但在心理健康系统中为其实施和维持提供资金的现有战略是不够的。这种限制使许多儿童和青少年无法获得高质量的服务。对卫生政策的影响:仅靠融资战略无法解决阻碍青年心理健康服务机构提供EBT的系统性问题。可能需要改变政策,例如美国政府增加对心理健康服务的财政投资,以支持基本的基础设施(如设施运营、衡量结果)。对进一步研究的影响:未来的工作应该审查专家对不同背景下EBT融资策略的看法(如药物使用服务),收集对鲜为人知的融资战略的有针对性的反馈,并探讨与EBT实施和维持相关的战略规划、资金稳定性和合作决策等主题。
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引用次数: 0
PERSPECTIVE: Economic and Policy Research Interests Highlighted in the 25th NIMH-Sponsored Mental Health Services Research Conference. 展望:在NIMH主办的第25届心理健康服务研究会议上强调的经济和政策研究兴趣。
IF 1.6 4区 医学 Q4 HEALTH POLICY & SERVICES Pub Date : 2023-09-01
Jennifer L Humensky, Michael C Freed, Susan T Azrin, Mary Acri, Denise Pintello
<p><strong>Background: </strong>The National Institute of Mental Health (NIMH) remains committed to addressing real-world challenges with delivering high quality mental health care to people in need by advancing a services research agenda to improve access, continuity, quality, equity, and value of mental healthcare nationwide, and to improve outcomes for people with serious mental illnesses (SMI). The NIMH-Sponsored Mental Health Services Research Conference (MHSR) is a highly productive venue for discussing topics of interest to NIMH audiences and disseminating NIMH's latest research findings directly to mental health clinicians, policy makers, administrators, advocates, consumers, and scientists who attend.</p><p><strong>Aims: </strong>This Perspective summarizes and provides highlights from the 25th MHSR. It also reviews three papers presented at the 25th MSHR and subsequently published in the June 2023 special issue of The Journal of Mental Health Policy and Economics (JMHPE).</p><p><strong>Methods: </strong>The authors review three papers published in the June 2023 special issue of JMHPE, identifying common themes across the papers and illustrating how the papers' findings promote key areas of NIMH research interests.</p><p><strong>Results: </strong>Three important areas are highlighted in this review: (i) service user engagement in the research enterprise, (ii) financing the implementation of the 988 Suicide and Crisis Lifeline, and (iii) methods to predict mental health workforce turnover.</p><p><strong>Discussion: </strong>These three papers illustrate key areas in which policy research can help to promote quality mental health care. One notable common theme across the papers is that of the role that end users play in the research enterprise. The papers focus on (i) service users and the value they bring to informing the practice of research, (ii) policy makers and the information they need to make evidence-informed decisions, and (iii) provider organization leadership, by using an innovative machine learning process to help organizations predict and address staff turnover.</p><p><strong>Implications for health care: </strong>NIMH encourages and often requires strong research practice partnerships to help ensure findings will be of value to end users and make their way into the practice setting. The three papers reviewed in this perspective are exemplars of how necessary stakeholder partnerships are to improve care for those with mental illness.</p><p><strong>Implications for health policies: </strong>The highlighted papers (i) provide recommendations for structural changes to research institutions to increase service user engagement in all aspects of the research enterprise, (ii) identify policy solutions to improve fiscal readiness to address increased demand of 988, and (iii) pilot a novel data-driven approach to predict mental health workforce turnover, a significant problem in community mental health clinics, offering health system
背景:美国国家心理健康研究所(NIMH)仍然致力于解决现实世界的挑战,通过推进服务研究议程,为有需要的人提供高质量的心理健康护理,以改善全国心理健康的可及性、连续性、质量、公平性和价值,并改善严重精神疾病患者的治疗效果。NIMH赞助的心理健康服务研究会议(MHSR)是一个高效的场所,可以讨论NIMH受众感兴趣的话题,并将NIMH的最新研究结果直接传播给参加会议的心理健康临床医生、政策制定者、管理者、倡导者、消费者和科学家。目标:本观点总结并提供了第25届MHSR的亮点。它还回顾了在第25届MSHR上发表的三篇论文,随后发表在2023年6月的《心理健康政策与经济学杂志》(JMHPE)特刊上。方法:作者回顾了发表在2023年6月的JMHPE特刊上的三篇论文,确定了论文中的共同主题,并说明了论文的发现如何促进NIMH研究兴趣的关键领域。结果:本综述强调了三个重要领域:(i)研究企业中的服务用户参与度,(ii)为988自杀和危机生命线的实施提供资金,以及(iii)预测心理健康劳动力流动的方法。讨论:这三篇论文说明了政策研究可以帮助促进高质量心理健康护理的关键领域。论文中一个值得注意的共同主题是最终用户在研究企业中扮演的角色。这些论文侧重于(i)服务用户及其为研究实践提供信息的价值,(ii)决策者及其做出证据知情决策所需的信息,以及(iii)提供者组织的领导力,通过使用创新的机器学习过程来帮助组织预测和解决员工流动问题。对医疗保健的影响:NIMH鼓励并经常要求建立强有力的研究与实践伙伴关系,以帮助确保研究结果对最终用户有价值,并进入实践环境。从这个角度回顾的三篇论文是利益相关者伙伴关系对改善精神疾病患者护理的必要性的例证。对卫生政策的影响:重点论文(i)为研究机构的结构变革提供建议,以提高研究企业各方面的服务用户参与度,这是社区心理健康诊所的一个重大问题,为卫生系统领导人和政策制定者提供了主动干预的机会,以帮助保持人员配置的连续性。对进一步研究的影响:与NIMH的研究战略计划和当前的资助公告一致,仍然迫切需要(i)制定战略,更好地实施、扩大和维持现有的证据支持的治疗和服务,特别是在历史上服务不足的社区,护理的连续性、质量、公平性和价值。ng和临床结果仍不确定。
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Journal of Mental Health Policy and Economics
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