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A Combined Analysis of Genetically Correlated Traits Identifies Genes and Brain Regions for Insomnia: Une analyse combinée de traits génétiquement corrélés identifie les gènes et les régions du cerveau pour l’insomnie 遗传相关性状的联合分析确定了失眠的基因和大脑区域:遗传相关性状的联合分析确定了失眠的基因和大脑区域
Pub Date : 2020-07-10 DOI: 10.25384/SAGE.C.5057221.V1
Kezhi Liu, Lingyi Zhu, Minglan Yu, X. Liang, Jin Zhang, Youguo Tan, Chao-hua Huang, Wenying He, W. Lei, J. Chen, Xiaochu Gu, Bo Xiang
Aims:Previous studies have inferred that there is a strong genetic component in insomnia. However, the etiology of insomnia is still unclear. This study systematically analyzed multiple genome-wide...
目的:以前的研究已经推断出失眠有很强的遗传成分。然而,失眠的病因尚不清楚。本研究系统分析了多个全基因组…
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引用次数: 0
mGluR5 Facilitates Long-Term Synaptic Depression in a Stress-Induced Depressive Mouse Model mGluR5促进应激诱导抑郁小鼠模型的长期突触抑制
Pub Date : 2020-05-01 DOI: 10.1177/0706743719874162
Xiangzhi Jiang, Wei Lin, Yuanyuan Cheng, Dongming Wang
Background Glutamatergic system has been known to play a role in the pathogenesis of major depression disorder by inducing N-methyl-d-aspartate receptor-dependent long-term depression (LTD) or metabotropic glutamate receptors (mGluR)-dependent LTD. Here, we characterized the LTD in a chronic social defeat stress (CSDS)-induced depressive mouse model. Methods CSDS was used to induce the depressive-like behaviors in C57BL/6 male mice, which were assessed using sucrose preference test and social interaction test. The synaptic strength including LTD and long-term potentiation (LTP) induced by paired-pulse low frequency stimulation (PP-LFS) was measured using whole-cell recording technique. Results CSDS induced depressive-like behaviors and facilitated PP-LFS-induced LTD in hippocampal CA3-CA1 pathway in the susceptible mice. Interestingly, mGluR5 but not N-methyl-d-aspartate receptor mediated the PP-LFS-induced LTD. In addition, mGluR5 agonist dihydroxyphenylglycine promoted PP-LFS-induced LTD specifically in susceptible mice, which was diminished by activating the BDNF/TrkB signaling pathway. Conclusions Our results suggest that mGluR5-dependent LTD might be responsible for the development of depressive-like behaviors in CSDS-induced depression mice model.
已知谷氨酸能系统通过诱导n -甲基-d-天冬氨酸受体依赖性长期抑郁(LTD)或代谢性谷氨酸受体(mGluR)依赖性长期抑郁(LTD)在重度抑郁症的发病机制中发挥作用。在这里,我们在慢性社会失败应激(CSDS)诱导的抑郁小鼠模型中表征了LTD。方法用CSDS诱导C57BL/6雄性小鼠抑郁样行为,采用蔗糖偏好测试和社会互动测试对其进行评价。采用全细胞记录技术测定配对脉冲低频刺激(PP-LFS)诱导的突触强度,包括LTP和LTP。结果CSDS诱导易感小鼠抑郁样行为,促进pp - lfs诱导的海马CA3-CA1通路的LTD。有趣的是,mGluR5而不是n -甲基-d-天冬氨酸受体介导pp - lfs诱导的LTD。此外,mGluR5激动剂二羟基苯基甘氨酸在易感小鼠中特异性地促进了pp - lfs诱导的LTD,通过激活BDNF/TrkB信号通路减少了LTD。结论mglur5依赖性LTD可能与csds诱导的抑郁小鼠模型中抑郁样行为的发生有关。
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引用次数: 9
Look Before You Leap: Representativeness of Those Completing Self-Reports in Early Psychosis Research 三思而后行:早期精神病研究中完成自我报告的代表性
Pub Date : 2020-01-01 DOI: 10.1177/0706743719879356
S. Iyer, S. Mustafa, S. Abadi, R. Joober, A. Malla
A randomized controlled trial (RCT) was conducted to compare the efficacy of early intervention (EI) for psychosis extended for 5 years with 2 years of EI followed by 3 years of regular care (details in prior publications). As secondary hypotheses, we postulated that the extended EI group (n 1⁄4 110) would have higher levels of alliance with their treatment providers than the control group (n 1⁄4 110) and that differences in medication adherence and retention in treatment between the two groups would be predicted by working alliance. Alliance was to be measured every 6 months after randomization (i.e., Months 30, 36, 42, 48, 54, and 60) with the Working Alliance Inventory (WAI), a self-report instrument. The average working alliance in the extended EI and regular care groups was 63.53 (SD 1⁄4 12.24, range: 24 to 84, N 1⁄4 85) and 59.35 (SD 1⁄4 12.30, range: 30 to 82, N 1⁄4 46), respectively, t(129) 1⁄4 1.862, P 1⁄4 0.065. The minimum score on the WAI is 12 and the maximum 84, indicating that in both arms, individuals reported moderate to high levels of alliance. Our results should not be interpreted as indicative of a true lack of difference in therapeutic alliance between persons receiving extended EI and regular care, given that individuals in the EI group were significantly likelier to have filled out the WAI at least once during follow-up than those receiving regular care (83% vs.44%, respectively; w 1⁄4 36.129, P < 0.001). We therefore chose not to conduct any additional analyses of the impact of alliance on group differences in medication adherence and retention. Willingness to fill out self-reports may in itself serve as an indicator of alliance/engagement with mental health systems/teams. Earlier, we reported that individuals receiving extended EI were likelier to remain engaged in their followup and have more contacts with their doctors and other treatment providers. That they were also likelier to complete the WAI may be an additional indicator of better “engagement” in the EI group. Assessments were conducted in both arms by the same research assistant. Nonetheless, some factors may have facilitated completion of measures in the EI group. Selfreports and structured interviews to assess symptoms were completed during in-person appointments with the research assistant who was in the same institution as the EI program, albeit in a separate pavilion. When individuals could not come in person, the research assistant completed the structured symptom interviews on the telephone. Self-reports, however, could not be done telephonically. This may have contributed to a higher rate of completion of symptom assessments (our primary outcome). If individuals consented, self-report measures were mailed to them, but very few mailed measures were returned. In the context of an RCT, it was important for the research assistant to be blind to treatment condition. This impeded us from adopting methods that prior research including in psychosis suggests may
进行了一项随机对照试验(RCT),比较早期干预(EI)治疗延长5年的精神病与2年的EI后3年的常规护理的疗效(详情见先前的出版物)。作为次要假设,我们假设扩展EI组(n 1⁄4 110)与治疗提供者的联盟水平高于对照组(n 1⁄4 110),并且两组在药物依从性和治疗保留方面的差异可以通过工作联盟来预测。随机化后每6个月(即第30、36、42、48、54和60个月)使用自我报告工具Working Alliance Inventory (WAI)测量一次联盟。扩展EI组和常规护理组的平均工作联盟分别为63.53 (SD 1⁄4 12.24,范围:24 ~ 84,N 1⁄4 85)和59.35 (SD 1⁄4 12.30,范围:30 ~ 82,N 1⁄4 46),t(129) 1⁄4 1.862,P 1⁄4 0.065。WAI的最低得分为12分,最高得分为84分,表明在两支队伍中,个体报告了中等到高度的联盟。我们的研究结果不应该被解释为表明接受延长EI和常规护理的患者之间的治疗联盟确实缺乏差异,因为EI组的个体在随访期间至少有一次填写WAI的可能性明显高于接受常规护理的个体(分别为83%对44%;w 1 / 4 36.129, P < 0.001)。因此,我们选择不进行任何额外的分析联盟对药物依从性和保留的组差异的影响。愿意填写自我报告本身可以作为与精神卫生系统/团队的联盟/参与的指标。早些时候,我们报告说,接受扩展EI的个体更有可能继续参与他们的随访,并与他们的医生和其他治疗提供者有更多的联系。他们也更有可能完成WAI,这可能是EI组更好的“参与”的另一个指标。两组的评估由同一名研究助理进行。尽管如此,一些因素可能促进了EI组测量的完成。自我报告和评估症状的结构化访谈是在与研究助理的面谈中完成的,该助理与EI项目在同一机构,尽管在不同的展馆。当个体无法亲自前来时,研究助理通过电话完成结构化的症状访谈。然而,自我报告不能通过电话进行。这可能有助于提高症状评估的完成率(我们的主要结果)。如果个人同意,自我报告量表将被邮寄给他们,但很少有邮寄的量表被退回。在随机对照试验中,研究助理对治疗条件不知情是很重要的。这阻碍了我们采用先前的研究方法,包括在精神病方面的研究表明,这些方法可能有助于完成自我报告,例如,要求人们在临床预约期间完成自我报告,以便完成的测量可以实时告知治疗决策。由于相当数量的个体从未填写过WAI,我们检查了在六个时间点中至少一个时间点(n1⁄4 139)完成WAI的个体与在任何时间点(n1⁄4 81)从未完成WAI的个体之间的差异,无论治疗情况如何。虽然有139人填写了该量表,但有8人遗漏了个人项目,因此总共有131人可以计算平均WAI。完成WAI的人之间没有显著差异
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引用次数: 0
Psychotherapies for Adolescents with Subclinical and Borderline Personality Disorder: A Systematic Review and Meta-Analysis 青少年亚临床和边缘型人格障碍的心理治疗:系统回顾和荟萃分析
Pub Date : 2020-01-01 DOI: 10.1177/0706743719878975
J. Wong, A. Bahji, S. Khalid-Khan
Background: Evidence regarding the efficacy of psychotherapy in adolescents with borderline personality disorder (BPD) symptomatology has not been previously synthesized. Objective: To conduct a systematic review and meta-analysis of the randomized controlled trials (RCTs) in order to assess the efficacy of psychotherapies in adolescents with BPD symptomatology. Methods: Seven electronic databases were systematically searched using the search terms BPD, adolescent, and psychotherapy from database inception to July 2019. Titles/abstracts and full-texts were screened by one reviewer; discrepancies were resolved via consensus. We extracted data on BPD symptomatology, including BPD symptoms, suicide attempts, nonsuicidal self-injury, general psychopathology, functional recovery, and treatment retention. Data were pooled using random-effects models. Results: Of 536 papers, seven trials (643 participants) were eligible. Psychotherapy led to significant short-term improvements in BPD symptomatology posttreatment (g = −0.89 [−1.75, −0.02]) but not in follow-up (g = 0.06 [−0.26, 0.39]). There was no significant difference in treatment retention between the experimental and control groups overall (odds ratio [OR] 1.02, 95% confidence interval [CI], 0.92 to 1.12, I 2 = 52%). Psychotherapy reduced the frequency of nonsuicidal self-injury (OR = 0.34, 95% CI, 0.16 to 0.74) but not suicide attempts (OR = 1.03, 95% CI, 0.46 to 2.30). Conclusions: There is a growing variety of psychotherapeutic interventions for adolescents with BPD symptomatology that appears feasible and effective in the short term, but efficacy is not retained in follow-up—particularly for frequency of suicide attempts.
背景:关于心理治疗对青少年边缘型人格障碍(BPD)症状的疗效的证据以前还没有合成。目的:对随机对照试验(RCTs)进行系统回顾和荟萃分析,以评估心理治疗对青少年BPD症状的疗效。方法:系统检索自数据库建立至2019年7月的7个电子数据库,检索词为BPD、青少年和心理治疗。题目/摘要和全文由一名审稿人筛选;分歧通过协商一致解决。我们提取了有关BPD症状学的数据,包括BPD症状、自杀企图、非自杀性自残、一般精神病理、功能恢复和治疗保留。使用随机效应模型汇总数据。结果:536篇论文中,有7项试验(643名受试者)符合条件。心理治疗导致治疗后BPD症状的短期显著改善(g = - 0.89[- 1.75, - 0.02]),但在随访中无显著改善(g = 0.06[- 0.26, 0.39])。试验组和对照组在治疗留置方面总体上无显著差异(优势比[OR] 1.02, 95%可信区间[CI], 0.92 ~ 1.12, i2 = 52%)。心理治疗降低了非自杀性自伤的频率(OR = 0.34, 95% CI, 0.16至0.74),但没有自杀企图(OR = 1.03, 95% CI, 0.46至2.30)。结论:对于有BPD症状的青少年,越来越多的心理治疗干预在短期内似乎是可行和有效的,但在随访中却不能保持疗效,尤其是对自杀企图的频率。
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引用次数: 40
Systematic Review and Meta-Analyses of Psychotherapies for Adolescents With Subclinical and Borderline Personality Disorder: Methodological Issues 青少年亚临床和边缘型人格障碍心理治疗的系统回顾和荟萃分析:方法学问题
Pub Date : 2019-12-09 DOI: 10.1177/0706743719893893
M. S. Jørgensen, O. J. Storebø, E. Simonsen
Dear Lakshmi N. Yatham, We thank Jennifer Wong, Anees Bahji, and Sarosh Khalid-Khan for a much needed systematic review of psychotherapies for adolescents with subclinical and borderline personality disorder (BPD). Previous reviews have largely excluded subclinical BPD presentations and therefore excluded the majority of the trials for this age-group. The authors found that psychotherapies for adolescents with subclinical and BPD are effective but that the efficacy was not statistically significant at follow-up. There are, however, some limitations to this review. First, we have not been able to retrieve any published protocol, which makes it difficult to determine whether the review could be prone to selective reporting bias. Second, the authors conclude that “the studies were rated as being of very high quality” (p. 5), but it is unclear on what ground this quality assessment was made. The use of tools like the Grading of Recommendations Assessment, Development and Evaluation could have increased the confidence of quality ratings. The authors conclude that the risk of bias was low on all domains except two instances with unclear risk of bias. However, the ratings on several domains may be too optimistic. For instance, it is left unaddressed that the developer of the experimental intervention was involved in four of the studies, which raises high risk of allegiance bias. Furthermore, all studies either did not publish a protocol or there were discrepancies between the protocols and the outcomes reported in the paper, thus warranting an unclear or high risk of selective outcome reporting bias. Concern about how missing data was handled, i.e. incomplete outcome data bias, in instances where no intention-to-treat analysis or multiple imputation were applied, only completers were included or there were extensive loss to follow-up are also not addressed. Instances of missing or unclear adherence ratings or skewed intensity between the experimental and control interventions are also not addressed even though these pose concerns for adherence or attention bias. Additionally, the review is prone to some methodological issues concerning clinical heterogeneity. The authors pooled experimental therapies and control therapies into metaanalyses not taking into consideration the heterogeneity of the experimental interventions, control treatments, type of outcome assessors, and time points. Lastly, the authors only searched seven electronic databases for relevant articles and used an English language restriction. This may have caused for some randomized controlled trials to be left out, for example, Santisteban et al., Salzer et al., and a pilot study by Gleeson et al. Valuable information have thus not been included. Publishing a systematic review with risk of bias assessments of psychological therapies for adolescents with BPD or subclinical BPD is an important first step to outline the evidence base. Early intervention and stage-linked care in potentially s
亲爱的Lakshmi N. Yatham:我们感谢Jennifer Wong, Anees Bahji和Sarosh Khalid-Khan对亚临床和边缘型人格障碍(BPD)青少年的心理治疗进行了非常需要的系统综述。先前的综述在很大程度上排除了亚临床BPD表现,因此排除了该年龄组的大多数试验。作者发现心理治疗对亚临床和BPD的青少年是有效的,但在随访中疗效无统计学意义。然而,这篇综述也有一些局限性。首先,我们无法检索任何已发表的方案,这使得很难确定该综述是否容易出现选择性报告偏倚。其次,作者得出结论,“这些研究被评为质量非常高”(第5页),但不清楚做出这种质量评估的依据是什么。使用建议分级评估、发展和评估等工具可以增加对质量评级的信心。作者得出结论,除了两个偏倚风险不明确的例子外,所有领域的偏倚风险都很低。然而,一些领域的评级可能过于乐观。例如,没有解决的是,实验干预的开发者参与了四项研究,这增加了忠诚偏见的高风险。此外,所有研究要么没有发表方案,要么方案与论文中报告的结果之间存在差异,因此可能存在不明确或高风险的选择性结果报告偏倚。关于如何处理缺失数据的担忧,即不完整的结果数据偏差,在没有意向治疗分析或多重输入的情况下,仅包括完成者或随访的大量损失也没有得到解决。缺失或不明确的依从性评级或实验和对照干预之间的倾斜强度的实例也没有得到解决,即使这些引起了对依从性或注意偏差的关注。此外,回顾容易出现一些关于临床异质性的方法学问题。作者将实验治疗和对照治疗合并为荟萃分析,没有考虑实验干预、对照治疗、结果评估者类型和时间点的异质性。最后,作者只在七个电子数据库中搜索了相关文章,并且使用了英语语言限制。这可能导致一些随机对照试验被遗漏,例如Santisteban等人,Salzer等人,以及Gleeson等人的一项试点研究。因此,没有列入有价值的资料。发表一篇有偏倚风险评估青少年BPD或亚临床BPD心理治疗的系统综述是概述证据基础的重要第一步。当我们关注青春期和成年期之间(包括非临床)发病的风险高峰时期时,早期干预和与BPD等潜在严重精神障碍阶段相关的护理是一个重要的目标。然而,上述限制可能会导致宝贵的信息被遗漏,也会对研究结果的质量得出过于乐观的结论。未来的审查应更彻底地解决这些限制。真诚地,
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引用次数: 6
Who Benefits from Physician Wellness? 谁从医生健康中受益?
Pub Date : 2019-12-09 DOI: 10.1177/0706743719890729
N. Lawson
In their recent Position Paper for the CPA’s Professional Standards and Practice Committee, Myers and Freeland state that there is a “clear relationship between physician wellness and competence to practice medicine.” This grounding assumption, and other questionable claims about the dangers posed by physicians with burnout and the effectiveness of physician health programs, is not helpful to physicianemployees with or without mental health disorders. Physician wellness policies and initiatives in general seem more likely to help hospital management. Myers and Freeland’s statement about physician wellness and competence is similar to statements in the new Accreditation Council for Graduate Medical Education program requirements on resident well-being. The requirements claim that programs “have the same responsibility to address well-being as other aspects of resident competence.” The American Psychiatric Association Publishing Textbook of Psychiatry also states that “Psychiatrists will play an increasingly important role as leaders in medicine in the future and can help to emphasize the links among physician well-being, clinical competence, and the importance of well-being as an ethical imperative. . . . ” “[P]hysician wellness [is a term] used interchangeably with physician well-being” that loosely refers to health. The effect of defining physicians’ competence in terms of well-being is to refocus appraisals of physicians’ abilities not on their performance, but on their health. Another problem with physician wellness is that studies suggest physician wellness initiatives are not effective. Even if they were, it is doubtful that even effective treatments could overcome the harm done to physicians with mental health disorders by such stigmatizing links between wellness and competence. In addition, what might be framed a “voluntary” physician-initiated participation in a wellness program may often be more accurately characterized as an employerinitiated requirement for assessment of potential impairment. Imagine a physician who checks a box on his initial employment paperwork asking, “Would you like to sign up for our free mindfulness and relaxation classes?” or “Would you like to work with wellness counselors and hospital management to evaluate and improve your mental health and work performance?” Follow-up contact from the wellness program and subsequent participation may be appropriately characterized as voluntary. But what if a resident is called into a meeting with program leadership, who to her surprise, express concerns about her performance and say they want to provide their residents with every available resource they need to succeed: “Do you feel that psychological testing— which we can offer right here at the hospital wellness program—might be helpful?” I would argue that the resident’s subsequent participation and any “voluntary” waiver of confidentiality in this setting would not actually be voluntary. Furthermore, the authors’ medica
在最近提交给注册会计师专业标准和实践委员会的意见书中,迈尔斯和弗里兰指出,“医生的健康和行医能力之间存在着明确的关系。”这种基本假设,以及其他关于医生职业倦怠带来的危险和医生健康项目有效性的可疑说法,对有或没有精神健康障碍的医生员工都没有帮助。一般来说,医生健康政策和倡议似乎更有可能帮助医院管理。迈尔斯和弗里兰关于医生健康和能力的声明与研究生医学教育新认证委员会对住院医师健康的要求类似。这些要求声称,项目“有同样的责任来解决居民能力的其他方面的福祉问题。”美国精神病学协会出版的精神病学教科书也指出,“精神科医生将在未来扮演越来越重要的角色,作为医学的领导者,可以帮助强调医生福祉,临床能力和福祉作为道德要求的重要性之间的联系. . . .。“[P]医师健康[是一个术语]与医师健康可互换使用”,泛指健康。从幸福感的角度来定义医生的能力,其效果是将对医生能力的评估重新聚焦于他们的健康,而不是他们的表现。医生健康的另一个问题是,研究表明医生健康倡议并不有效。即便如此,有效的治疗方法能否克服这种将健康和能力联系在一起的污名化对心理健康障碍医生造成的伤害,也是值得怀疑的。此外,医生发起的“自愿”参与健康计划可能更准确地描述为雇主发起的评估潜在损害的要求。想象一下,一位医生在他最初的雇佣文件中勾选了一个方框,问道:“你愿意报名参加我们的免费正念和放松课程吗?”或者“你愿意与健康咨询师和医院管理人员一起评估和改善你的心理健康和工作表现吗?”健康计划的后续接触和随后的参与可以适当地定性为自愿。但是,如果一位住院医生被叫去和项目领导开会,让她吃惊的是,他们对她的表现表示担忧,并说他们想为住院医生提供他们成功所需的一切可用资源:“你觉得心理测试——我们可以在医院的健康项目中提供——可能会有帮助吗?”我认为,在这种情况下,住院医生随后的参与和任何“自愿”放弃保密实际上都不是自愿的。此外,作者对破坏性行为的医学化,以及他们对“耻辱”的引用,本质上类似于“抵抗”,或者是医生雇员的一种有问题的信念,可能会迫使他们遵守这些评估。这是精神病学普遍存在的一个问题,在已经具有强制性的就业环境中,这个问题可能会更加严重。这些以及其他健康政策和做法的意想不到的后果是,它们让医生的雇主对医生的私生活有了更大的控制权。医生员工在医院内外所做的任何事情都可以说是干扰、损害或影响他们的健康,进而伤害病人。将医生的健康与能力联系起来,就为那些对某些治疗方法和生活方式有强烈个人意见的雇主打开了一扇门,他们通过暗示的威胁将这些偏好强加给他们的医生雇员,如果他们反抗就会被贴上无能的标签。这些医生健康政策不太可能真正帮助医生员工。他们甚至不太可能帮助心理健康障碍或残疾的医生。
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引用次数: 0
Burden of Mental, Neurological, Substance Use Disorders and Self-Harm: Counting the Cards, or Shuffling the Deck? 精神、神经、物质使用障碍和自残负担:算牌还是洗牌?
Pub Date : 2019-12-09 DOI: 10.1177/0706743719892706
S. Patten
In this issue’s paper entitled: “Burden of Mental, Neurological, Substance Use Disorders and Self-Harm in North America: A Comparative Epidemiology of Canada, Mexico, and the United States,” Vigo et al. provide an alternative perspective on disease-burden estimates from the Global Burden of Disease (GBD) Project. The authors criticize the GBD for what they consider to be an arbitrary reclassification of “mental health-related burden” into other categories and express concern that the GBD approach dilutes the apparent burden attributable to mental health issues. The authors base their reclassification on the creation of a new aggregate category that they call “mental, neurological, substance use disorders and self-harm” (MNSS). MNSS includes suicide mortality, some selected neurological conditions (neurocognitive disorders, epilepsy, and headaches), physical conditions attributable to alcohol, and a proportion of chronic pain issues (to capture the burden of somatic symptom disorders). Analysis of the reclassified data indicates that MNSS is the largest source of disease burden between the ages of 10 and 60. The GBD covers 359 diseases and injuries for 195 countries, with the most recently published estimates covering from 1990 to 2017. The GBD aggregates disease-specific estimates using four hierarchical levels. The fourth level includes burden related to specific disorders (e.g., major depression, dysthymia) although some conditions remain grouped (e.g., anxiety disorders are a Level 4 grouping as of 2017). The third level includes additional aggregation (e.g., depressive disorders), the second level includes a category called “mental disorders,” and at the top of the hierarchy, the first level includes only three overarching categories: noncommunicable diseases; injuries; and communicable, maternal, neonatal, and nutritional diseases. It is these aggregate groupings, and their labeling, that Vigo et al. consider problematic. They point out that the “mental disorders” category does not capture suicide deaths, some relevant neurological morbidity, alcohol-related morbidity, and somatic symptom disorders. Their concern is that the GBD’s approach may reduce “the visibility of the burden related to mental health.” For example, in the 2017 Canadian ranking of disease burden, “mental disorders” rank fifth (although they rank first in the 15 to 24 age range). The purpose of the GBD is to describe mortality and morbidity from health conditions (causes) and risk factors at global, national, and (in some countries, but not in Canada) subnational or regional levels. They make comparisons across populations that enable a better understanding of changing health across the world. While it is not the intention of the GBD to provide an arena in which healthcare sectors compete for resources and prestige, it is possible that naive decision makers, especially those who are unaware of the GBD methodology, could misinterpret GBD estimates in ways that undervalue me
在这期题为“北美精神、神经、物质使用障碍和自我伤害的负担:加拿大、墨西哥和美国的比较流行病学”的论文中,Vigo等人从全球疾病负担(GBD)项目的疾病负担估计中提供了另一种观点。作者批评GBD武断地将“精神健康相关负担”重新分类为其他类别,并表示关注GBD方法淡化了可归因于精神健康问题的明显负担。作者将他们的重新分类建立在一个新的汇总类别的基础上,他们称之为“精神、神经、物质使用障碍和自我伤害”(MNSS)。MNSS包括自杀死亡率、一些选定的神经系统疾病(神经认知障碍、癫痫和头痛)、可归因于酒精的身体疾病和一定比例的慢性疼痛问题(以捕捉躯体症状障碍的负担)。对重新分类数据的分析表明,MNSS是10至60岁人群疾病负担的最大来源。GBD涵盖了195个国家的359种疾病和伤害,最新公布的估计数涵盖了1990年至2017年。GBD使用四个层次来汇总特定疾病的估计。第四级包括与特定疾病相关的负担(例如,重度抑郁症、心境恶劣),尽管一些疾病仍然分组(例如,截至2017年,焦虑症是第4级分组)。第三级包括额外的汇总(例如,抑郁症),第二级包括一个称为“精神障碍”的类别,在层次结构的顶端,第一级仅包括三个总体类别:非传染性疾病;伤害;传染病、孕产妇、新生儿和营养性疾病。Vigo等人认为有问题的正是这些聚合分组及其标签。他们指出,“精神障碍”这一类别不包括自杀死亡、一些相关的神经系统疾病、酒精相关疾病和躯体症状障碍。他们担心GBD的方法可能会降低“与心理健康有关的负担的可见性”。例如,在2017年加拿大疾病负担排名中,“精神障碍”排名第五(尽管在15至24岁年龄段中排名第一)。GBD的目的是描述全球、国家和(在一些国家,但不是加拿大)国家以下或区域各级的健康状况(原因)和风险因素造成的死亡率和发病率。他们对不同人群进行比较,以便更好地了解世界各地不断变化的健康状况。虽然GBD的目的不是为医疗保健部门提供一个争夺资源和声望的舞台,但天真的决策者,特别是那些不了解GBD方法的决策者,可能会误解GBD的估计,低估心理健康的价值。例如,一些利益攸关方可能会认为,“精神障碍”第2级分组描述了或打算描述与精神健康有关的疾病负担。Vigo等人通过生成MNSS分类(一个排名第一的类别)来帮助应对这种风险。尽管Vigo等人对GBD提出了一些严厉的批评(例如,将汇总类别标记为“有偏见的”和缺乏“最低表面效度”),但将他们的重新分析视为诋毁GBD或纠正GBD所犯的错误是不明智的。在最初的GBD报告之前,卫生政策的重点确定主要基于特定病因的死亡率统计。随着……的普及
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引用次数: 0
Barriers to Brain Stimulation Therapies for Treatment-Resistant Depression: Beyond Cost Effectiveness 脑刺激疗法治疗难治性抑郁症的障碍:超越成本效益
Pub Date : 2019-12-09 DOI: 10.1177/0706743719893584
D. Goldbloom, D. Gratzer
In this issue of the journal, Fitzgibbon and colleagues create an elaborate simulation model based on a broad consideration of costs and treatment efficacies to determine the comparative cost-effectiveness of rapid transcranial magnetic stimulation (rTMS) and electroconvulsive therapy (ECT) in management of treatment-resistant depression (TRD). In so doing, they take the oldest continuing biological intervention in psychiatry, ECT—arguably our field’s most effective and most stigmatized treatment—and stack it up against one of our newer forms of brain stimulation. Even though rTMS has been subject to more than two decades of multiple randomized controlled trials in depression as well as network meta-analyses, it remains unknown or unfamiliar to many health professionals, patients, and families. While many generations of clinicians easily recall patients they knew who received and benefited from ECT, very few have a personal data bank of patients treated with rTMS. If ECT has secured a firm— if controversial—place in our therapeutic armamentarium and cultural history, rTMS is still virtually unavailable in most clinical settings and not yet a therapeutic skill that is a core part of psychiatry training. Depression is the leading cause of disability globally. In Ontario, depression alone represented a greater burden of disease (as reflected by years lived with disability and years lost due to premature death) than lung, prostate, colon, and breast cancer combined. Although we have reasonably effective psychological and pharmacological treatments for depression, too many people are left in a state of TRD after countless drug trials and drug combinations or extensive courses of psychotherapy. In the context of therapeutic frustration, it can even result in familiar patient-blaming verbal lapses such as, “the patient failed a trial of . . . ” We need to own the reality that our treatments fail some patients, not the other way around. There is both a clinical and economic imperative to develop new options as well as to use existing evidence-based options. ECT was developed over 80 years ago, spread rapidly around the globe, and remains for a number of psychiatrists the treatment they would want for themselves if they became severely depressed—a good yardstick to use when recommending treatments for other people. Jeff Daskalakis, co-director of the Temerty Centre for Therapeutic Brain Intervention at the Centre for Addiction and Mental Health (arguably the busiest center in the country for both ECT and rTMS), often states that the numbers needed to treat for ECT in TRD is 2 to 3 (based on a 65% remission rate for ECT in TRD vs. a 15% remission rate for placebo)—an astonishingly low number that very few treatments throughout medicine could match. However, it remains an intrusive and intensive treatment with significant cognitive sequelae, and the need for alternatives persists. In considering alternative forms of brain stimulation to ECT, the concept of
在这一期的杂志中,Fitzgibbon和他的同事基于成本和治疗效果的广泛考虑,创建了一个精心设计的模拟模型,以确定快速经颅磁刺激(rTMS)和电休克治疗(ECT)在治疗难治性抑郁症(TRD)方面的相对成本效益。在这样做的过程中,他们采用了精神病学中最古老的持续生物干预,ect——可以说是我们这个领域最有效的治疗方法,也是最被污名化的治疗方法——并将其与我们最新的一种大脑刺激方法相比较。尽管rTMS已经在抑郁症领域进行了超过20年的随机对照试验以及网络荟萃分析,但对于许多健康专业人员、患者和家庭来说,它仍然是未知的或不熟悉的。虽然几代临床医生很容易回忆起他们认识的接受过电痉挛疗法并从中受益的病人,但很少有人有接受过rTMS治疗的病人的个人数据库。如果说电痉挛疗法已经在我们的治疗设备和文化历史中获得了稳固的地位——如果有争议的话——那么rTMS在大多数临床环境中实际上仍然是不可用的,而且还不是精神病学培训的核心部分的治疗技能。抑郁症是全球致残的主要原因。在安大略省,仅抑郁症就代表着比肺癌、前列腺癌、结肠癌和乳腺癌加起来更大的疾病负担(以残疾生活年数和因过早死亡而损失的年数来反映)。虽然我们对抑郁症有相当有效的心理和药物治疗,但在无数的药物试验和药物组合或广泛的心理治疗课程之后,太多的人仍然处于TRD状态。在治疗挫折的背景下,它甚至会导致熟悉的患者指责言语失误,如“患者试验失败……”我们需要承认我们的治疗方法让一些病人失败的事实,而不是相反。在临床和经济上,开发新的选择以及使用现有的循证选择都是必要的。电痉挛疗法是在80多年前发展起来的,在全球范围内迅速传播开来,对于许多精神科医生来说,如果他们自己变得严重抑郁,这仍然是他们自己想要的治疗方法——在为其他人推荐治疗方法时,这是一个很好的标准。成瘾和心理健康中心(可以说是全国最繁忙的ECT和rTMS中心)的Temerty脑干预治疗中心的联合主任Jeff Daskalakis经常说,治疗TRD的ECT所需的数字是2到3(基于TRD中ECT的缓解率为65%,而安慰剂的缓解率为15%)-一个惊人的低数字,整个医学中很少有治疗方法可以达到。然而,它仍然是一种侵入性和强化治疗,具有显著的认知后遗症,并且仍然需要替代疗法。在考虑替代ECT的脑刺激形式时,阶梯式护理的概念是至关重要的。Fitzgibbon和他的同事们提出了一个模型和数据,表明对于TRD, rTMS途径是比ECT更划算的一线治疗方法,并且总的来说,最好的结果是TRD患者开始使用rTMS,然后只有在rTMS不起作用的情况下才进行ECT。这是阶梯式护理思维的本质:从一种更良性的治疗开始,即使它可能具有较低的狭义阳性临床结果率,然后只有在临床需要时才进行更具侵入性、破坏性和昂贵的治疗。由于rTMS很容易在门诊实施,术后不需要患者陪同回家,不需要麻醉,不需要诱导
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引用次数: 4
Protocol for Clozapine Rechallenge in a Case of Clozapine-Induced Myocarditis 氯氮平所致心肌炎1例氯氮平再灌注治疗方案
Pub Date : 2019-12-09 DOI: 10.1177/0706743719892709
G. Shivakumar, N. Thomas, Miranda Sollychin, A. Takács, S. Kolamunna, P. Melgar, Fiona Connally, C. Neil, C. Bousman, M. Jayaram, C. Pantelis
Objective: Protocol for clozapine rechallenge in patients with a history of clozapine-induced myocarditis. Method: Clozapine-related cardiovascular adverse effects including myocarditis and cardiomyopathy have limited its widespread use in treatment-resistant schizophrenia. Here, we present a case of clozapine-induced myocarditis and successful cautious rechallenge. Ms. AA, a young female patient with severe psychosis developed myocarditis during her initial clozapine titration phase, which was thus discontinued. Subsequent response to other medications was poor, and she remained significantly disabled. We reviewed blood-based biomarkers identified during the emergence of her index episode of myocarditis and developed a successful clozapine rechallenge protocol, based on careful monitoring of changes in these indices and a very slow clozapine re-titration. Results and Conclusions: This protocol may have utility in the management of patients with a history of clozapine-induced myocarditis.
目的:氯氮平诱发性心肌炎患者再用氯氮平治疗方案。方法:氯氮平相关的心血管不良反应,包括心肌炎和心肌病,限制了其在难治性精神分裂症中的广泛应用。在这里,我们报告一例氯氮平诱导的心肌炎和成功的谨慎再挑战。AA女士,一名患有严重精神病的年轻女性患者,在氯氮平初始滴药期出现心肌炎,因此停药。随后对其他药物的反应很差,她仍然明显残疾。我们回顾了在她出现心肌炎指数发作时发现的基于血液的生物标志物,并基于仔细监测这些指标的变化和非常缓慢的氯氮平再滴定,制定了成功的氯氮平再滴定方案。结果和结论:该方案可能对有氯氮平性心肌炎病史的患者有实用价值。
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引用次数: 10
Primary Care Practitioner Training in Child and Adolescent Psychiatry (PTCAP): A Cluster-Randomized Trial 初级保健从业者培训儿童和青少年精神病学(PTCAP):一项集群随机试验
Pub Date : 2019-12-09 DOI: 10.1177/0706743719890161
S. Espinet, Sandra Gotovac, Sommer Knight, L. Wissow, M. Zwarenstein, L. Lingard, M. Steele
Objectives Rural primary care practitioners (PCPs) have a pivotal role to play in frontline pediatric mental health care, given limited options for referral and consultation. Yet they report a lack of adequate training and confidence to provide this care. The aim of this study was to test the effectiveness of the Practitioner Training in Child and Adolescent Psychiatry (PTCAP) program, which was designed to enhance PCPs’ pediatric mental health care confidence. The program includes brief therapeutic skills and practice guidelines PCPs can use to address both subthreshold concerns and diagnosable conditions, themselves. Methods The study design was a pilot, cluster-randomized, multicenter trial. Practices were randomly assigned to intervention (n practices = 7; n PCPs = 42) or to wait-list control (n practices = 6; n PCPs = 34). The intervention involved 8 hr of training in practice guidelines and brief therapeutic skills for depression, anxiety, attention deficit hyperactivity disorder, and behavioral disorders with case discussion and video examples, while the control practiced as usual. A linear random-effects model controlling for clustering and baseline was carried out on the individual-level data to examine between-group differences in the primary (i.e., confidence) and secondary (i.e., attitude and knowledge) outcomes at 1-week follow-up. Results Findings were a statistically significant difference in the primary outcomes. Compared to the control group, the intervention group indicated significantly greater confidence in managing diagnosable conditions (d = 1.81) and general concerns (d = 1.73), as well as in making necessary referrals (d = 1.27) and obtaining consults (d = 0.74). While the intervention did not significantly impact secondary outcomes (attitudes and knowledge), regression analysis indicated that the intervention may have increased confidence, in part, by ameliorating the adverse impact of negative mental health care attitudes. Conclusion PTCAP enhances PCPs’ child/youth mental health care confidence in managing both general and diagnosable concerns. However, an 8-hr session focused on applying brief therapeutic skills was insufficient to significantly change attitudes and knowledge. Formal testing of PTCAP may be warranted, perhaps using more intensive training and including outcome assessments capable of determining whether increased PCP confidence translates to more effective management and better patient outcomes.
鉴于转诊和咨询的选择有限,农村初级保健从业人员(pcp)在一线儿科精神卫生保健中发挥着关键作用。然而,他们报告缺乏足够的培训和信心来提供这种护理。本研究的目的是检验儿童与青少年精神病学从业人员培训(PTCAP)计划的有效性,该计划旨在提高儿童与青少年精神病学从业人员对儿童精神卫生保健的信心。该计划包括简短的治疗技巧和实践指南,pcp可以用来解决阈值以下的问题和可诊断的条件。方法采用先导、集群随机、多中心试验设计。实践被随机分配到干预组(n实践= 7;n个pcp = 42)或等候名单控制(n个实践= 6;n pcp = 34)。干预包括8小时的实践指导和抑郁症、焦虑症、注意缺陷多动障碍和行为障碍的简短治疗技巧培训,并进行病例讨论和视频示例,而对照组则照常练习。采用控制聚类和基线的线性随机效应模型对个体水平数据进行1周随访,检验各组间主要(即信心)和次要(即态度和知识)结果的差异。结果两组的主要结局差异有统计学意义。与对照组相比,干预组在管理可诊断疾病(d = 1.81)和一般问题(d = 1.73)以及进行必要的转诊(d = 1.27)和获得咨询(d = 0.74)方面表现出更大的信心。虽然干预措施对次要结果(态度和知识)没有显著影响,但回归分析表明,干预措施可能通过改善消极精神卫生保健态度的不利影响,在一定程度上增加了信心。结论PTCAP提高了pcp在处理一般问题和可诊断问题方面的儿童/青少年心理保健信心。然而,专注于应用简短治疗技巧的8小时疗程不足以显著改变态度和知识。PTCAP的正式测试可能是有必要的,也许可以使用更密集的培训,并包括能够确定PCP信心增强是否转化为更有效的管理和更好的患者预后的结果评估。
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引用次数: 4
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The Canadian Journal of Psychiatry
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