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Accepting multiple conditions in psychiatry: From comorbidity to multimorbidity. 接受精神病学中的多重病症:从合并症到多病症。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-07 DOI: 10.1016/j.encep.2024.05.004
Christophe Gauld, Emmanuel D'Incau, Pauline Espi, Pierre Fourneret, Aileen McGonigal, Jean-Arthur Micoulaud-Franchi

The concept of multimorbidity in psychiatry refers to the coexistence of multiple health conditions without conceptualizing a central disorder referring to a patient-centered approach that views every diagnosis equally. It emphasizes a shift from focusing on an index disorder to considering interrelated symptoms crucial in psychiatry due to frequent multimorbidity patterns. In clinical practice, multimorbidity guides patient-centered care helping to address the holistic needs of patients and challenging the organization of mental health care. In research, multimorbidity reshapes study outcomes and promotes the development of patient-reported outcome questionnaires, also posing ethical challenges and advocating for the inclusion of multimorbid patients in personalized interventions. Finally, multimorbidity in psychiatry has public health implications aligning with the socioecological systems perspective. This notion aims to improve prognosis, care, and health costs while impacting global mortality and challenging the conceptualization and organization of psychiatric care.

精神病学中的多病症概念指的是多种健康状况并存,而没有将中心疾病概念化,指的是一种以患者为中心、平等看待每一种诊断的方法。它强调的是,由于多病共存模式的频繁出现,精神病学中至关重要的是要从关注一种指数性障碍转变为考虑相互关联的症状。在临床实践中,多病共存指导着以患者为中心的护理,有助于满足患者的整体需求,并对心理健康护理的组织形式提出了挑战。在研究中,多病模式重塑了研究结果,促进了患者报告结果问卷的开发,同时也带来了伦理挑战,并倡导将多病患者纳入个性化干预中。最后,精神病学中的多病症具有与社会生态系统观点一致的公共卫生意义。这一概念旨在改善预后、护理和医疗成本,同时影响全球死亡率,并对精神病护理的概念化和组织提出挑战。
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引用次数: 0
Obsessive-compulsive symptoms in dementia: Systematic review with meta-analysis. 痴呆症患者的强迫症状:系统回顾与荟萃分析。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.06.001
Filipe Peste Martinho, Tiago Filipe Ferreira, Daniela Magalhães, Rita Felício, Filipe Godinho

Dementia is a highly prevalent syndrome with various causes, characterized by cognitive deficit in one or more domains, with important impairment of functioning, which frequently presents with neuropsychiatric symptoms that may include obsessive-compulsive symptoms.

Objectives: The main goal of this meta-analysis was to describe and determine the prevalence of obsessive-compulsive symptoms in dementia.

Materials and methods: To accomplish that, MEDLINE, CENTRAL and Psycnet databases were searched from inception to March 2023. The Joanna Briggs Institute Critical Appraisal Checklist for Studies Reporting Prevalence Data was applied. The principal summary measures were the mean of prevalence of obsessive-compulsive symptoms in patients with dementia and the number of each type of obsession or compulsion.

Results: Of the 643 articles screened, 92 were accepted for full-text assessment. Of these, 30 with information on prevalence of obsessive-compulsive symptoms in dementia or any description of those were included, yielding a total of 37 cohorts (5 studies with two cohorts and 1 study with three cohorts). According to our results, obsessive-compulsive symptoms have considerable prevalence in dementia (35.3%, 23.1-47.6%), namely in frontotemporal dementia (48.4%, 29.8-67.0%); obsessive-compulsive symptoms were less frequent in other dementia diagnosis (17.6%, 9.1-26.2%). The more frequent obsessive contents are symmetry (28.6%) and somatic (20.0%); and the more frequent compulsions are checking (27.4%); hoarding is also a relevant symptom (27.8%).

Discussion: There was considerable heterogeneity in the prevalence of obsessive-compulsive symptoms in frontotemporal dementia, that is, in part related with diagnostic criteria for dementia, as well as obsessive-compulsive symptom assessment. A careful distinction between compulsions and compulsive-like symptoms is fundamental. Hypervigilance for somatic symptoms and concerns about disease and mortality, as well as deficits in cognitive domains like attention and memory may explain why somatic obsessions and checking compulsions are more prevalent.

Conclusions: The present results indicate that obsessive-compulsive symptoms may be prevalent in the clinical course of many patients with dementia, especially frontotemporal dementia. Better instruments are needed to describe obsessive-compulsive phenomena in a reliable and comparable way, particularly in a population such as dementia patients, whose subjectivity is difficult to access.

痴呆症是一种高发的综合征,其病因多种多样,以一个或多个领域的认知缺陷为特征,功能严重受损,常伴有神经精神症状,其中可能包括强迫症状:这项荟萃分析的主要目的是描述和确定痴呆症患者强迫症状的患病率:为此,研究人员检索了MEDLINE、CENTRAL和Psycnet数据库中从开始到2023年3月的数据。采用了乔安娜-布里格斯研究所(Joanna Briggs Institute)的流行率数据报告研究批判性评估核对表。主要汇总指标为痴呆症患者强迫症状的平均患病率以及每种强迫症状的数量:在筛选出的 643 篇文章中,有 92 篇接受了全文评估。结果:在筛选出的 643 篇文章中,有 92 篇接受了全文评估,其中 30 篇包含了痴呆症患者强迫症状的患病率或任何相关描述,共纳入了 37 个队列(5 项研究包含两个队列,1 项研究包含三个队列)。根据我们的研究结果,强迫症状在痴呆症(35.3%,23.1-47.6%),即额颞叶痴呆症(48.4%,29.8-67.0%)中的发病率相当高;强迫症状在其他痴呆症诊断中的发病率较低(17.6%,9.1-26.2%)。更常见的强迫内容是对称性(28.6%)和躯体性(20.0%);更常见的强迫症状是检查(27.4%);囤积也是一个相关症状(27.8%):讨论:强迫症状在额颞叶痴呆症中的患病率存在相当大的异质性,这在一定程度上与痴呆症的诊断标准以及强迫症状的评估有关。仔细区分强迫症状和类似强迫症状至关重要。对躯体症状的过度警惕、对疾病和死亡的担忧以及注意力和记忆力等认知领域的缺陷可能解释了为什么躯体强迫和检查强迫更为普遍:本研究结果表明,强迫症状可能在许多痴呆症患者的临床过程中普遍存在,尤其是额颞叶痴呆症患者。我们需要更好的工具,以可靠和可比较的方式描述强迫症现象,尤其是在痴呆症患者这类主观性难以获得的人群中。
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引用次数: 0
Psychological first aid in operation for military healthcare providers : a study on pre-deployment training. 军事医疗服务提供者在行动中的心理急救:关于部署前培训的研究。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.05.005
Frédérique Gignoux-Froment, Emeric Saguin, Cécile Gorin, Marianne Daudin, Sophie Annette, Julia Salomé, Mathieu Boutonnet, Luc Aigle, Pierre-Éric Schwartzbrod, Stéphane Travers, Bertrand Lahutte, Marie-Dominique Colas

Introduction: During operational missions, while the management of physical injuries in the field remains the priority, the identification of operational incapacity of psychological origin is necessary as it is equally crucial for the safety of the individual, the group and the mission. The French Military Health Service has developed a Psychological First Aid Training in Operation (PFATO) course based on relational simulations, for military service members. The aim is to identify the early signs of psychological distress in a comrade and to adopt an adapted and protective attitude. PFATO training is also offered to healthcare providers.

Methods: We conducted a descriptive cross-sectional study using a self-administered online questionnaire which was sent after deployment to all physicians or nurses trained in PFATO between July 2019 and July 2021 (n=80). The main objective of our work was to evaluate the relevance of this awareness training among physicians and nurses and to identify specific complementary expectations in operational psychiatry for this population.

Results: We obtained a response rate of 55%. Significantly, 21.62% of participants used PFATO during their last deployment and another 20% observed a team member using PFATO. The circumstances of use as reported by participants included acute stress related to combat, conflict with hierarchy or comrades, and suicidal crisis. Among those who used PFATO, the training helped 87.5% of them to identify signs of psychological distress and 100% of them to assist combatants . All respondents stressed the added value of practical simulations during PFATO education. Moreover, this study also makes it possible to identify adaptations needed to optimize this module for healthcare providers.

Conclusion: The results suggest the value for healthcare provider of training in first-response psychological care using relational simulation based on the model of raising awareness about PFATO.

导言:在执行任务期间,尽管处理战场上的身体伤害仍然是优先事项,但识别心理原因导致的行动能力丧失也是必要的,因为这对个人、团体和任务的安全同样至关重要。法国军事卫生局为军人开发了基于关系模拟的行动心理急救培训(PFATO)课程。其目的是识别战友心理困扰的早期迹象,并采取适应和保护态度。PFATO 培训也提供给医疗服务提供者:我们进行了一项描述性横断面研究,采用自填式在线问卷,在部署后向 2019 年 7 月至 2021 年 7 月期间接受过 PFATO 培训的所有医生或护士(n=80)发送问卷。我们工作的主要目的是评估医生和护士对这一意识培训的相关性,并确定这一人群对作战精神病学的具体补充期望:结果:我们获得了 55% 的回复率。值得注意的是,21.62% 的参与者在其上一次部署期间使用过 PFATO,另有 20% 的参与者观察到一名队员使用过 PFATO。参与者报告的使用情况包括与战斗有关的急性压力、与上级或战友的冲突以及自杀危机。在使用 PFATO 的人员中,87.5% 的人通过培训识别了心理困扰的迹象,100% 的人通过培训协助了战斗人员。所有受访者都强调了在 PFATO 教育过程中实际模拟的附加价值。此外,这项研究还有助于确定需要进行哪些调整,以优化医疗保健提供者的这一模块:结果表明,在提高对 PFATO 认识的模式基础上,利用关系模拟进行第一反应心理护理培训对医疗服务提供者很有价值。
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引用次数: 0
[Impact of the legalization of recreational cannabis on the risk of psychosis: A systematic review of the literature]. [娱乐性大麻合法化对精神病风险的影响:文献系统回顾]。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.05.003
Zélie Billion, Matthieu Hein
<p><strong>Introduction: </strong>Cannabis is the most consumed illicit substance in Europe. Although its sale and use remain generally prohibited, European public policies have evolved in recent years by legalizing cannabis for medical use and considering its legalization for recreational use. However, in the literature there are arguments in favor of a particular relationship between cannabis consumption and the development of psychotic symptoms. Thus, since cannabis consumption tends to increase with legalization, the aim of this review was to investigate the impact of the legalization of cannabis for recreational use on the risk of psychosis in regions of the world already concerned.</p><p><strong>Method: </strong>A systematic review of the literature was carried out in April 2024 in the PubMed-Medline database according to PRISMA criteria. The sequence of keywords used was as follows: ("Cannabis" [Mesh] or cannabis) AND (("Psychotic Disorders" [Mesh] or Psychotic Disorders) or ("Schizophrenia Spectrum and Other Psychotic Disorders" [Mesh]) or ("Schizophrenia" [Mesh] or Schizophrenia)) AND legal use. The inclusion criteria applied for the selection of articles in this systematic review were: (1) any article investigating the potential impact of the legalization of cannabis for recreational use on the risk of psychosis (any type of psychosis diagnosed according to ICD-9, ICD-10, DSM-4 or DSM-5) by the intermediary of epidemiological (incidence or prevalence) and/or clinical (ambulatory consultations, emergency visits or hospitalizations) criteria, (2) any type of study (cross-sectional, longitudinal, prospective, retrospective, interventional and experimental) with a methodology including a temporal and/or geographic comparison of the risk of psychosis associated with the legalization of cannabis for recreational use with the exception of literature reviews and clinical cases descriptions, (3) absence of limitation for the age of the populations studied and for the date of publication, and (4) articles written in English or French. After evaluation by the two authors of the 160 articles identified, seven studies investigating the impact of the legalization of cannabis for recreational use on the risk of psychosis were included in this systematic literature review.</p><p><strong>Results: </strong>Four of the studies showed no increase in the use of health services for psychosis following the legalization of cannabis for recreational use whereas three other studies highlighted a negative impact of the legalization of cannabis for recreational use on the risk of psychosis. All of these studies were carried out in North America and were characterized by a low level of scientific evidence.</p><p><strong>Conclusion: </strong>Given the complexity of assessing the impact of the legalization of cannabis for recreational use on the risk of psychosis, additional investigations through studies of better scientific quality are essential. However, based on
简介大麻是欧洲消费最多的非法物质。虽然大麻的销售和使用仍然普遍受到禁止,但近年来欧洲的公共政策已经发生了变化,大麻的医疗用途合法化,并考虑将其合法化用于娱乐用途。然而,文献中也有论点支持大麻消费与精神病症状发展之间的特殊关系。因此,由于大麻消费往往会随着大麻合法化而增加,本综述旨在调查大麻娱乐合法化对世界相关地区精神病风险的影响:根据 PRISMA 标准,于 2024 年 4 月在 PubMed-Medline 数据库中对文献进行了系统性综述。使用的关键词顺序如下:(大麻"[Mesh]或 "cannabis")和("精神障碍"[Mesh]或 "精神障碍")或("精神分裂症谱系和其他精神障碍"[Mesh])或("精神分裂症"[Mesh]或 "精神分裂症")和合法使用。本系统综述在选择文章时采用的纳入标准是(1) 以流行病学(发病率或流行率)和/或临床(门诊、急诊或住院)标准为中介,调查娱乐性使用大麻合法化对精神病(根据 ICD-9、ICD-10、DSM-4 或 DSM-5 诊断的任何类型的精神病)风险的潜在影响的任何文章,(2) 任何类型的研究(横断面研究、纵向研究、前瞻性研究、回顾性研究、干预性研究和实验性研究)、(2) 任何类型的研究(横断面研究、纵向研究、前瞻性研究、回顾性研究、干预性研究和实验性研究),研究方法包括对与娱乐性使用大麻合法化相关的精神病风险进行时间和/或地域比较,但文献综述和临床病例描述除外,(3) 对研究人群的年龄和发表日期没有限制,(4) 以英文或法文撰写的文章。经过两位作者对所确定的 160 篇文章进行评估后,本系统性文献综述纳入了七项研究,这些研究调查了娱乐性使用大麻合法化对精神病风险的影响:结果:其中四项研究表明,娱乐性吸食大麻合法化后,因精神病而使用医疗服务的情况没有增加,而另外三项研究则强调了娱乐性吸食大麻合法化对精神病风险的负面影响。所有这些研究都是在北美进行的,其特点是科学证据水平较低:鉴于评估娱乐用大麻合法化对精神病风险影响的复杂性,必须通过科学质量更高的研究开展更多调查。不过,根据现有数据,有一些证据表明,娱乐用大麻合法化可能会对精神健康产生负面影响。在这种情况下,如果娱乐性使用大麻合法化,似乎有必要建议降低使用大麻的风险(限制使用频率、推迟首次消费年龄、控制产品中四氢大麻酚的含量以及促进预防/教育)。最后,为了使公共卫生战略能够动态发展,随着大麻合法化的发展,建立持续监测至关重要。
{"title":"[Impact of the legalization of recreational cannabis on the risk of psychosis: A systematic review of the literature].","authors":"Zélie Billion, Matthieu Hein","doi":"10.1016/j.encep.2024.05.003","DOIUrl":"https://doi.org/10.1016/j.encep.2024.05.003","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Introduction: &lt;/strong&gt;Cannabis is the most consumed illicit substance in Europe. Although its sale and use remain generally prohibited, European public policies have evolved in recent years by legalizing cannabis for medical use and considering its legalization for recreational use. However, in the literature there are arguments in favor of a particular relationship between cannabis consumption and the development of psychotic symptoms. Thus, since cannabis consumption tends to increase with legalization, the aim of this review was to investigate the impact of the legalization of cannabis for recreational use on the risk of psychosis in regions of the world already concerned.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Method: &lt;/strong&gt;A systematic review of the literature was carried out in April 2024 in the PubMed-Medline database according to PRISMA criteria. The sequence of keywords used was as follows: (\"Cannabis\" [Mesh] or cannabis) AND ((\"Psychotic Disorders\" [Mesh] or Psychotic Disorders) or (\"Schizophrenia Spectrum and Other Psychotic Disorders\" [Mesh]) or (\"Schizophrenia\" [Mesh] or Schizophrenia)) AND legal use. The inclusion criteria applied for the selection of articles in this systematic review were: (1) any article investigating the potential impact of the legalization of cannabis for recreational use on the risk of psychosis (any type of psychosis diagnosed according to ICD-9, ICD-10, DSM-4 or DSM-5) by the intermediary of epidemiological (incidence or prevalence) and/or clinical (ambulatory consultations, emergency visits or hospitalizations) criteria, (2) any type of study (cross-sectional, longitudinal, prospective, retrospective, interventional and experimental) with a methodology including a temporal and/or geographic comparison of the risk of psychosis associated with the legalization of cannabis for recreational use with the exception of literature reviews and clinical cases descriptions, (3) absence of limitation for the age of the populations studied and for the date of publication, and (4) articles written in English or French. After evaluation by the two authors of the 160 articles identified, seven studies investigating the impact of the legalization of cannabis for recreational use on the risk of psychosis were included in this systematic literature review.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Four of the studies showed no increase in the use of health services for psychosis following the legalization of cannabis for recreational use whereas three other studies highlighted a negative impact of the legalization of cannabis for recreational use on the risk of psychosis. All of these studies were carried out in North America and were characterized by a low level of scientific evidence.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;Given the complexity of assessing the impact of the legalization of cannabis for recreational use on the risk of psychosis, additional investigations through studies of better scientific quality are essential. However, based on ","PeriodicalId":51042,"journal":{"name":"Encephale-Revue De Psychiatrie Clinique Biologique et Therapeutique","volume":null,"pages":null},"PeriodicalIF":1.2,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142146774","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
Retrospective study of hepatitis C screening and seroprevalence in the GHU Paris. 巴黎 GHU 的丙型肝炎筛查和血清阳性率回顾性研究。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.05.002
Alexandra Pham-Scottez, Valérie Dauriac-Le Masson, Oumeyma Ben Dahman, Armel Toquin, Amine Benmostefa, Nabil Hallouche

Objectives: The prevalence of hepatitis C virus (HCV) has been estimated to be approximately ten times higher in patients with psychiatric disorders, but European data are rare and only two French studies have recently been published on the subject. Our objective was to determine the HCV screening rate and the prevalence of HCV in adult patients hospitalised in the largest French psychiatric hospital.

Methods: We conducted a retrospective study of all adult patients hospitalised at GHU Paris, from 2019 to 2022, including age, gender, HCV screening, HCV serological status, and the existence of an ICD-10 diagnosis of psychoactive substance use disorder. Descriptive statistics used means±standard deviations and percentages. Bivariable comparisons used Student's t test and Chi-square test.

Results: The overall HCV screening rate was 55.4% and increased over the four years from 37.1% in 2019 to 69.4% in 2022. Patients screened were significantly younger people and with a substance use disorder than unscreened patients. The prevalence of HCV over this 4-year period was 2.8% and remained stable. The HCV-positive patients were significantly more male, older and more likely to have substance use disorders than the HCV-negative patients.

Conclusions: We found a prevalence rate of HCV ten times higher than the prevalence in the general population, in line with findings in many other European countries. The eradication of HCV will not be possible without the elimination of this "forgotten reservoir" of the virus. Efforts must be made in psychiatric hospitals to test all patients in order to treat patients suffering from hepatitis C with direct-acting antivirals.

研究目的据估计,丙型肝炎病毒(HCV)在精神障碍患者中的流行率大约是普通患者的十倍,但欧洲的相关数据非常罕见,最近也仅有两项法国研究公布了相关数据。我们的目标是确定法国最大的精神病医院中住院的成年患者的丙型肝炎病毒筛查率和丙型肝炎病毒感染率:我们对 2019 年至 2022 年在巴黎 GHU 住院的所有成年患者进行了一项回顾性研究,包括年龄、性别、HCV 筛查、HCV 血清学状态以及是否存在 ICD-10 精神活性物质使用障碍诊断。描述性统计采用均值±标准差和百分比。双变量比较采用学生 t 检验和卡方检验:总体HCV筛查率为55.4%,四年内从2019年的37.1%增至2022年的69.4%。与未接受筛查的患者相比,接受筛查的患者明显更年轻,且有药物使用障碍。在这 4 年中,HCV 感染率为 2.8%,并保持稳定。与 HCV 阴性患者相比,HCV 阳性患者中男性明显更多,年龄更大,更有可能患有药物使用障碍:我们发现,HCV 感染率是普通人群感染率的十倍,这与许多其他欧洲国家的研究结果一致。如果不消除这一 "被遗忘的病毒库",就不可能根除丙型肝炎病毒。精神病院必须努力对所有患者进行检测,以便用直接作用抗病毒药物治疗丙型肝炎患者。
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引用次数: 0
Should the French approval of baclofen for alcohol dependence be extended to abstinence maintenance? 法国批准将巴氯芬用于治疗酒精依赖症,是否应扩展至戒酒维持治疗?
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.05.001
Benjamin Rolland, Laurent Karila, Nicolas Franchitto, Camille Barrault, Mickael Naassila

Ever since 2018 France has been the only country to approve the gamma aminobutyric acid type B (GABA-B) receptor agonist baclofen for alcohol dependence. This authorization follows a ten-year period of intensive off-label use during which baclofen was used in doses of up to 300 and even 400mg per day to support the gradual reduction of alcohol consumption in patients suffering from alcohol dependence. However, in international clinical trials, baclofen has mainly been studied to support the maintenance of abstinence. The French use of baclofen was therefore somewhat atypical as it paved the way for drug-supported approaches to reducing alcohol consumption, even before nalmefene was marketed. In line with this specific use of baclofen, approval was granted only for alcohol reduction support. However, a recent Cochrane systematic review and meta-analysis by Agabio et al. found significant efficacy only for abstinence maintenance, while no significant effect was found on alcohol reduction outcomes and no dose-response relationship was identified in the analyses. The safety of baclofen was judged to be good. Based on these substantial new results, the Société française d'alcoologie (SFA) now considers that baclofen should also be approved for the maintenance of abstinence. The extension of approval should not lead to the removal of the initial indication or the possibility of using high doses, as some patients have found this therapeutic regimen particularly useful for them. France, which has been a open skies national laboratory on the use of baclofen in alcohol dependence for over ten years, should let this original therapeutic option available to patients. However, it should update the regulatory framework defining the main conditions of access to treatment for patients based on the latest and highest scientific evidence.

自2018年以来,法国一直是唯一一个批准γ-氨基丁酸B型(GABA-B)受体激动剂巴氯芬用于治疗酒精依赖症的国家。在此之前的十年间,巴氯芬在标签外被大量使用,每天的剂量高达 300 毫克甚至 400 毫克,以支持酒精依赖症患者逐渐减少饮酒量。不过,在国际临床试验中,巴氯芬主要用于支持维持戒酒。因此,法国对巴氯芬的使用在某种程度上是非典型性的,因为它甚至在纳美芬上市之前,就已经为减少酒精消费的药物支持方法铺平了道路。根据巴氯芬的这一特殊用途,该药物仅被批准用于支持减少饮酒。然而,Agabio 等人最近进行的一项 Cochrane 系统综述和荟萃分析发现,巴氯芬仅对维持戒酒有显著疗效,而对减少酒精结果没有显著效果,分析中也没有发现剂量-反应关系。巴氯芬的安全性被认为是良好的。基于这些重要的新结果,法国嗜酒者协会(SFA)现在认为,巴氯芬也应被批准用于维持戒酒。延长批准期限不应导致取消最初的适应症或使用大剂量的可能性,因为一些患者发现这种治疗方案对他们特别有用。十多年来,法国一直是巴氯芬治疗酒精依赖症的国家开放天空实验室,应该让患者能够使用这种原始的治疗方案。不过,法国应更新监管框架,根据最新和最高级别的科学证据,确定患者获得治疗的主要条件。
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引用次数: 0
Comments on "Anorexia nervosa: An addiction? Application of the addiction model to eating". 关于 "神经性厌食症:成瘾?成瘾模式在饮食中的应用"。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-09-06 DOI: 10.1016/j.encep.2024.05.006
Jônatas de Oliveira
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引用次数: 0
Pharmacological and nutraceutical treatments for borderline personality disorder 边缘型人格障碍的药物和营养治疗。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-10 DOI: 10.1016/j.encep.2024.04.001
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引用次数: 0
Financement de la psychiatrie en France, la question des médicaments onéreux : exemple de l’Esketamine dans l’épisode dépressif caractérisé résistant 法国精神病学的资金,昂贵药物的问题。艾氯胺酮在难治性抑郁发作中的应用实例]。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 DOI: 10.1016/j.encep.2023.09.007

In France, the funding of mental health institutions relies on an annual budget allocation. Esketamine, a non-competitive NMDA glutamate receptor antagonist, has been approved for adults with treatment-resistant major depressive disorder since 2019. However, due to its high cost (€200 per 28 mg device, excluding tax), the aim of this work was to evaluate whether the income received by an institution for the management of a patient treated with Esketamine could cover the purchase of devices, based on real clinical data. Within our institution, seven patients underwent treatment with Esketamine during the study period resulting in a total usage of 714 devices, amounting to a purchase cost of €142,800. Over the course of the follow-up period, the institution received €149,054 in revenue for the treatment of these patients. Our analysis reveals that the expense associated with Esketamine constitutes 95.8 % of the income generated from caring for these patients. This not only raises questions about the pricing of this drug but also highlights the lack of a funding system for costly psychiatric drugs. This concern extends to somatic treatments associated with psychiatric care.

在法国,精神卫生机构的资金依赖年度预算拨款。艾氯胺酮是一种非竞争性NMDA谷氨酸受体拮抗剂,自2019年以来已被批准用于治疗难治性重度抑郁症的成人。然而,由于其高昂的成本(每28毫克装置200欧元,不含税),这项工作的目的是评估一个机构为管理接受埃氯胺酮治疗的患者所收到的收入是否可以根据真实的临床数据支付设备的购买费用。在我们的机构内,在研究期间,有7名患者接受了艾氯胺酮治疗,总共使用了714台设备,购买成本为142800欧元。在随访期间,该机构为治疗这些患者获得了149,054欧元的收入。我们的分析显示,与艾氯胺酮相关的费用占照顾这些患者所产生收入的95.8%。这不仅引发了对这种药物定价的质疑,也凸显了昂贵的精神科药物缺乏资金体系。这种关注延伸到与精神科护理相关的躯体治疗。
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引用次数: 0
Concordance and validity between versions of the ADHD Conners scale for Parents ADHD 康纳斯家长量表各版本之间的一致性和有效性。
IF 1.2 4区 医学 Q4 NEUROSCIENCES Pub Date : 2024-08-01 DOI: 10.1016/j.encep.2023.07.006

Introduction

The Conners Scale for Parents (CRS-P) is one of the reference tools for the diagnostic assessment of Attention Deficit and Hyperactivity Disorders (ADHD). It is commonly used in both research and clinical practice. The latest edition of the Conners Parents Scale Long Version (CRS-P3L) has undergone extensive modifications but has never been compared with the 2nd edition (CRS-P2L). We aim to study the concordance between the last two editions of the CRS-P, their internal consistency, and their validity against the criteria of the ADHD-RS.

Methods

The study population was a cohort of 30 children diagnosed with ADHD participating in a clinical trial. The parents of these children completed both editions of the CRS (P2L and P3L), as well as a DSM-IV ADHD Diagnostic Criteria Rating Scale (ADHD-RS). A linear regression model with the calculation of Lin's concordance coefficient (LCC) was used to study the concordance between the scales. Internal validity was estimated with Cronbach's alpha and inter-criteria validity with Spearman's correlation coefficient.

Results

The internal consistency found was “correct” to “good” for both editions (Cronbach alpha 0.85 and 0.77), their correlation with the ADHD-RS was medium to low (Spearman's coefficient 0.25 and 0.09). Concordance between the overall score and the sub-scores of the two editions of the same Conners scale (CRS-P2L and CRS-P3L) was fair to medium (LCC 0.29 to 0.69).

Conclusions

The third edition of the long version of the CRS-P showed very poor concordance with the previous edition. The diagnostic profile of the children seems to have evolved with the new edition, which appears to affect the interpretation of the tests.

简介康纳斯家长量表(CRS-P)是诊断评估注意力缺陷和多动障碍(ADHD)的参考工具之一。它常用于研究和临床实践。最新版的康纳斯家长量表长版(CRS-P3L)经过了大量修改,但从未与第二版(CRS-P2L)进行过比较。我们的目的是研究最近两版 CRS-P 之间的一致性、内部一致性及其与 ADHD-RS 标准的有效性:研究对象是参与临床试验的 30 名被诊断为多动症的儿童。这些儿童的家长填写了两个版本的CRS(P2L和P3L)以及DSM-IV多动症诊断标准评定量表(ADHD-RS)。采用线性回归模型计算林氏一致性系数(LCC)来研究量表之间的一致性。用 Cronbach's alpha 估计内部效度,用 Spearman's 相关系数估计标准间效度:结果:两个版本的内部一致性均为 "正确 "至 "良好"(Cronbach alpha 分别为 0.85 和 0.77),与 ADHD-RS 的相关性为中低水平(斯皮尔曼系数分别为 0.25 和 0.09)。总分与同一康纳斯量表的两个版本(CRS-P2L 和 CRS-P3L)的分值之间的一致性为一般至中等(LCC 0.29 至 0.69):结论:长版康纳斯量表第三版与前一版的一致性很差。儿童的诊断特征似乎随着新版本的推出而发生了变化,这似乎会影响测试的解释。
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引用次数: 0
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Encephale-Revue De Psychiatrie Clinique Biologique et Therapeutique
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