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The WHO Flexible Interview for ICD-11 (FLII-11) 世卫组织 ICD-11 灵活访谈(FLII-11)
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21227
Geoffrey M. Reed, Karen T. Maré, Michael B. First, T.S. Jaisoorya, Girish N. Rao, John-Joe Dawson-Squibb, Christine Lochner, Mark van Ommeren, Dan J. Stein
<p>The movement to a descriptive, symptom-based diagnostic system that started with the DSM-III was in part a response to widespread concerns and criticisms regarding the reliability of psychiatric diagnoses. This fueled an emphasis on increasingly precise operationalization of diagnostic constructs and criteria, based on the assumption that this would produce successive improvements in reliability.</p><p>Clinician-administered structured diagnostic interviews were subsequently developed. For example, the Research Diagnostic Criteria were used to develop a Schedule for Affective Disorders and Schizophrenia<span><sup>1</sup></span>, while the DSM-III criteria were incorporated into the Structured Clinical Interview for DSM (SCID)<span><sup>2</sup></span>. In addition, the Diagnostic Interview Schedule<span><sup>3</sup></span> was developed for use by non-clinician interviewers in epidemiological surveys of mental disorders. These instruments have been widely used in research on mental disorders.</p><p>Structured diagnostic interviews have subsequently been developed or adapted for successive revisions of the DSM and the ICD. The SCID, a semi-structured interview – meaning that the interviewer probes unclear responses and makes certain clinical judgments – has been updated with each edition of the DSM<span><sup>4</sup></span>. The briefer and fully structured Mini International Neuropsychiatric Interview (MINI)<span><sup>5</sup></span> has also been widely employed. The Composite International Diagnostic Interview (CIDI)<span><sup>6</sup></span> incorporated both DSM and ICD diagnostic requirements and was used in the National Comorbidity Survey and the World Mental Health Surveys. Similarly, the Schedules for Clinical Assessment in Neuropsychiatry (SCAN), based on the Present State Examination, assessed for both DSM and ICD requirements<span><sup>7</sup></span>. Structured diagnostic interviews for children have also been developed, as have a range of more focused interviews that cover specific conditions or diagnostic groupings.</p><p>Based on an extensive program of field testing, the reliability of the diagnostic guidance provided in the Clinical Descriptions and Diagnostic Requirements for ICD-11 Mental, Behavioural and Neurodevelopmental Disorders (CDDR)<span><sup>8</sup></span> was found to be higher than that of other mental disorder classification systems, ranging from moderate to almost perfect according to the specific category. This finding was perhaps counterintuitive, insofar as the CDDR avoid highly prescriptive symptom counts and duration requirements, unless these are specifically supported scientifically, in order to facilitate clinical use.</p><p>These results, therefore, challenge the assumed relationship between operational precision and diagnostic reliability. They also suggest that the diagnoses based on the CDDR would be sufficiently reliable for certain types of research projects (e.g., studies focusing on diagnostic gr
从 DSM-III 开始的以症状为基础的描述性诊断系统的发展,在一定程度上是为了回应人们对精神病诊断可靠性的广泛关注和批评。这促使人们开始强调诊断结构和标准的日益精确的可操作性,并假定这将使诊断的可靠性不断提高。例如,"研究诊断标准 "被用于制定 "情感障碍和精神分裂症时间表 "1 ,而 "DSM-III 标准 "则被纳入了 "DSM 结构化临床访谈(SCID)"2。 此外,还制定了 "诊断访谈时间表 "3,供非临床医师访谈者在精神障碍流行病学调查中使用。这些工具已被广泛应用于精神障碍的研究中。结构化诊断访谈随后被开发或改编用于 DSM 和 ICD 的历次修订。SCID 是一种半结构化访谈--即访谈者对不明确的回答进行试探并做出某些临床判断--已随着 DSM4 的每一版进行了更新。更简短、完全结构化的迷你国际神经精神病学访谈(MINI)5 也被广泛采用。国际综合诊断访谈(CIDI)6 纳入了 DSM 和 ICD 的诊断要求,并被用于全国发病率调查和世界精神健康调查。同样,基于现状检查的神经精神病学临床评估表(SCAN)也同时评估了 DSM 和 ICD 的要求7。根据一项广泛的现场测试计划,《ICD-11 精神、行为和神经发育障碍临床描述和诊断要求》(CDDR)8 提供的诊断指导的可靠性高于其他精神障碍分类系统,根据具体类别从中等到几乎完美不等。这一结果可能与直觉相反,因为 CDDR 避免了高度规范化的症状计数和持续时间要求,除非这些要求得到科学的具体支持,以方便临床使用。这些结果还表明,基于 CDDR 的诊断对于某些类型的研究项目(例如,以医疗机构中的诊断群体为重点的研究)来说是足够可靠的。然而,在其他类型的研究中,标准化的诊断评估是可取的,以控制与不同技能水平、面谈风格和临床判断相关的临床医生层面的变异性。例如,在根据特定诊断要求选择参与者的药理学试验中,可靠、可重复地记录特定症状模式的能力往往非常重要。流行病学调查或其他基于人群的调查中,涉及非专业(即未接受过临床培训)访谈者时,也需要预设问题和严格的决策规则,因为这些调查不能依靠访谈者的临床知识来判断是否存在特定特征。因此,诊断访谈几乎从一开始就是 CDDR 相关工作计划的一部分。因此,诊断性访谈几乎从一开始就是 CDDR 相关工作计划的一部分。相关工作采用了严格的开发流程,并邀请了分类学和诊断性访谈领域的国际专家参与。自 2014 年以来,ICD-11 结构化临床访谈(SCII-11)的工作一直在进行。这是一个半结构化的诊断访谈--旨在由训练有素的临床医师进行--提供了一套标准化的问题,每个问题评估一个特定的诊断要求,以形成鉴别诊断。尽管 SCII-11 是为研究应用而开发的,但它也可用于培训目的和临床环境。由于 CDDR 对诊断要求的设定更加面向临床,因此在开发 SCII-11 时有必要增加可操作性。具体来说,SCII-11 用更精确的诊断阈值取代了 CDDR 中不那么规范的术语(例如,至少有三个而不是 "几个 "症状;至少有三个月而不是 "持续")。此外,还针对 CDDR 中可能以各种不同方式表现出来的内容(如精神分裂症中的 "持续妄想")开发了特定的问题。
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引用次数: 0
How the ICD-11 and the CDDR address the public health dimensions of substance use ICD-11 和 CDDR 如何解决药物使用的公共卫生问题
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21252
María Elena Medina-Mora, Rebeca Robles
<p>The use of psychoactive substances is highly prevalent and contributes substantially to risk behaviours, morbidity and mortality. The United Nations Office on Drugs and Crime World Drug Report<span><sup>1</sup></span> estimated that, in 2021, one in every 17 people aged 15-64 in the world had used an illicit drug in the year before. Users increased from 240 million in 2011 to 296 million in 2021, substantially more than accounted for by population growth.</p><p>Cannabis continued to be the most used illicit drug (219 million users, 4.3% of the global adult population); 36 million people had used amphetamines, 22 million cocaine, and 20 million methylenedioxymethamphetamine (MDMA or “ecstasy”) or related drugs in the previous year. An estimated 60 million people engaged in non-medical opioid use, 31.5 million of whom used opiates (i.e., non-synthetic opioids; mainly heroin).</p><p>Globally, there is very limited implementation of efficient and effective prevention strategies for substance use<span><sup>2</sup></span>, and there is a substantial treatment gap for disorders due to this use<span><sup>3</sup></span>. Global evidence has called attention to the need for a new and comprehensive conceptualization of substance use disorders that incorporates the full range of relevant conditions, from risky consumption to mental disorders linked to harmful drug use<span><sup>4</sup></span>.</p><p>In response to these challenges, the World Health Organization (WHO) adopted a public health approach to the development of the classification of disorders due to substance use in the ICD-11. By public health approach, we refer to a broader perspective that integrates health and social aspects, aiming to benefit affected individuals and their community, and focusing on population well-being<span><sup>5</sup></span>.</p><p>From a public health perspective, it is essential to identify persons who exhibit a hazardous use of substances that increases the risk of harmful psychological or medical consequences, but whose symptoms do not meet the diagnostic requirements for substance use disorders. These individuals can benefit from education, prevention, and community interventions. People with diagnosable disorders need harm reduction and treatment services of differing intensities and settings, depending on the nature of their condition and the substance involved. Those who suffer physical or psychological harm due to others’ substance use should also be identified and may require services<span><sup>6</sup></span>.</p><p>In line with this perspective, the range of psychoactive substances classified in the ICD-11 section on disorders due to substance use has been expanded, reflecting changes in the substances associated with public health impact in different parts of the world. An extended set of substance classes will help track patterns more accurately, in order to formulate appropriate clinical and social policy responses nationally and globally. For example
精神活性物质的使用非常普遍,是导致危险行为、发病率和死亡率的重要因素。据联合国毒品和犯罪问题办公室《世界毒品报告》1 估计,到 2021 年,全世界每 17 个 15-64 岁的人中就有一人在前一年使用过非法药物。大麻仍然是使用最多的非法药物(2.19 亿使用者,占全球成年人口的 4.3%);上一年有 3,600 万人使用过苯丙胺,2,200 万人使用过可卡因,2,000 万人使用过亚甲二氧基甲基苯丙胺(MDMA 或 "摇头丸")或相关药物。据估计,有 6,000 万人使用过非医用类阿片,其中 3,150 万人使用过阿片剂(即非合成类阿片;主要是海洛因)。在全球范围内,针对药物使用的高效和有效预防战略的实施非常有限2 ,而针对药物使用导致的失调症的治疗存在巨大差距3。全球证据表明,有必要对药物使用失调症进行新的、全面的概念化,将从危险消费到与有害药物使用相关的精神障碍等所有相关情况纳入其中4。为应对这些挑战,世界卫生组织(WHO)采用了公共卫生方法来制定 ICD-11 中药物使用失调症的分类。我们所说的公共卫生方法,指的是一种将健康和社会方面结合起来的更广阔的视角,旨在使受影响的个人及其社区受益,并关注人口福祉5。从公共卫生的角度来看,有必要识别那些表现出有害使用药物,从而增加了有害心理或医疗后果风险,但其症状并不符合药物使用失调诊断要求的人。这些人可以从教育、预防和社区干预中受益。有可诊断病症的人需要不同强度和环境的减低危害和治疗服务,这取决于他们的病症性质和所涉及的物质。那些因他人使用药物而遭受身体或心理伤害的人也应被识别出来,并可能需要服务6。根据这一观点,ICD-11 中关于药物使用引起的失调部分所分类的精神活性物质的范围已经扩大,反映了世界不同地区与公共健康影响相关的物质的变化。扩展后的物质类别将有助于更准确地跟踪模式,以便在国家和全球范围内制定适当的临床和社会政策应对措施。例如,新增了一组合成大麻素引起的失调类别。合成大麻素被喷洒在天然草药混合物上,以模仿大麻的兴奋效果,并可产生呼吸抑制作用7。高收入国家报告了合成大麻素的使用情况,但中低收入国家的资料很少1。正如《ICD-11 精神、行为和神经发育障碍的临床描述和诊断要求》(CDDR)8 中所述,每一类精神活性物质都有四种主要病症,这些病症按等级划分,相互排斥:a) 危险物质使用,其概念是一种在频率或数量上足以增加对使用者或他人的身体或精神 健康造成有害后果的风险的物质使用模式;由于它涉及尚未发生的伤害的递增风险,因 此不被视为精神障碍(相反,它出现在 ICD-11 关于 "影响健康状况或与医疗服务接触的因 素 "的章节中,便于医疗专业人员及早关注并提供建议);b) 有害药物使用发作,指已经对个人的身体或精神健康造成伤害,或导致伤害他人健康的行为,但不存在已知的药物使用模式;c) 有害的物质使用模式,这是一种亚依赖诊断,其特点是持续和重复的物质使用模式,通过个人行为直接对个人或他人造成伤害;以及 d) 物质依赖,即由于重复或持续使用某种物质而导致的物质使用调节障碍,通常伴有使用该物质的强烈内驱力。在 ICD-11 中,药物依赖诊断比 ICD-10 有所简化。它基于三个关键特征中至少两个特征的存在:a) 对药物使用的控制能力受损;b) 药物使用越来越优先于其他活动;c) 耐受或戒断的生理特征。
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引用次数: 0
Scientific validation of the ICD-11 CDDR ICD-11 CDDR 的科学验证
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21226
Mario Maj
<p>The process of scientific validation of the ICD-11 Clinical Descriptions and Diagnostic Requirements (CDDR) for Mental Disorders has spanned more than 10 years, being remarkably comprehensive and inclusive as well as truly international, with the involvement of many hundreds of clinicians and researchers from all regions of the world.</p><p>The field trials of the ICD-11 CDDR – contrary to those of the ICD-10 Clinical Descriptions and Diagnostic Guidelines (CDDG) and the DSM-5 diagnostic criteria – have been genuinely “developmental” (as opposed to “summative” or “evaluative”) in their nature<span><sup>1</sup></span>. That is, they have been conducted <i>before</i> the finalization of the relevant sets of criteria or guidelines – thus allowing the identification of conceptual or terminological problems in the proposed texts, the correction of those texts, and the further testing of the revised versions – rather than being conducted or concluded <i>after</i> the finalization of the relevant sets of criteria or guidelines, thus just providing information to clinicians about what they could expect from those products. As we will see, several amendments to the CDDR were actually implemented as a consequence of this design.</p><p>The CDDR field trials can be subdivided into two main groups: a) Internet-based trials, implemented through the Global Clinical Practice Network (involving, at the time when the trials were conducted, more than 15,000 mental health and primary health care professionals from more than 150 countries), which used a case vignette methodology to assess the effects of specific differences between the CDDR and the ICD-10 CDDG on the participants’ clinical decision making; b) clinic-based (or ecological) trials, assessing the reliability and clinical utility of the CDDR in real clinical contexts. The clinic-based trials differed from the DSM-5 field trials in that they used a joint-rater design (with two clinicians jointly interviewing each patient) rather than a test-retest design (with two clinicians separately interviewing each patient at different time points), thus controlling for information variance and more specifically testing the reliability of the proposed guidelines (rather than testing more generally the reliability of the relevant psychiatric diagnoses)<span><sup>2</sup></span>.</p><p>Among the Internet-based CDDR field trials, of special interest have been those focusing on disorders specifically associated with stress<span><sup>3</sup></span>, and on feeding and eating disorders<span><sup>4</sup></span>. A case-control field trial on the former grouping of disorders<span><sup>3</sup></span>, conducted with 1,738 mental health professionals from 76 countries, found that several changes introduced in the ICD-11 – including the addition of complex post-traumatic stress disorder (complex PTSD) and prolonged grief disorder – resulted in significantly improved diagnostic decisions. However, the trial also identified s
从《疾病分类与诊断登记表》初稿的编制到最终定稿,中间间隔了较长的一段时间,这也使得我们能够对《疾病分类与诊断登记表》中新引入的一些类别进行广泛而详细的验证。根据2024年2月8日在PubMed上进行的搜索,自2013年以来发表的关于长期悲伤障碍的具有原始数据的论文共有57篇。总体而言,这些论文证明了这一新类别的建构有效性、与其他疾病(如抑郁症和创伤后应激障碍)的区别、与明显功能障碍的关联(超越了伴随疾病的影响),以及与DSM-5持续性复杂丧亲障碍相比,在纵向研究中与长期悲伤模式的一致性更高。同日进行的PubMed搜索发现了自2013年以来发表的199篇关于复杂创伤后应激障碍的原始数据。总体而言,这些论文证明了这一新类别的有效性,并证明了它与创伤后应激障碍的不同之处,包括在广泛的文化背景下、在儿童和青少年以及成年人中、在多个遭受创伤的人群中7。ICD-11 CDDR 与经过国际测试的 DSM-5 诊断标准之间的另一个显著差异是关于儿童和青少年严重易激惹的分类。一项对来自 48 个国家8 的 196 名临床医生进行的研究发现,与 DSM-5 解决方案(引入了破坏性情绪调节障碍这一新类别)和 ICD-10 分类标准(将对立违抗障碍列为几种行为障碍之一,而不关注易激惹性)相比,CDDR 中提出的表述(将慢性易激惹-愤怒作为诊断对立违抗障碍的特指符)能更准确地识别严重易激惹性,并更好地与边界表现进行区分。通过在印度、英国和美国进行的一项国际研究(INCLUDE),ICD-11 CDDR 验证过程的另一个创新方面是通过经验让专家系统地参与进来9。这项研究收集了用户对抑郁发作、广泛性焦虑障碍、精神分裂症、双相 I 型障碍和人格障碍这五种诊断的意见。总的来说,CDDR 在许多情况下都被认为是有用的,与生活经验息息相关。当然,CDDR 科学验证中目前缺少的一个关键因素是其在普通临床实践中的表现。目前正在努力将 CDDR 翻译成尽可能多的语言,广泛传播 CDDR,并加快各国政府对 CDDR 的认可和实施。
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引用次数: 0
Ethics from the lens of the social dimension of psychiatry 从精神病学的社会维度透视伦理学
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21238
Sam Tyano
<p>From a historical perspective, Engel<span><sup>1</sup></span> conceptualized psychopathology as resulting from an interaction of three orders of factors: biological, psychological and social. The first half of the 20th century has been mostly devoted to conceptualizing the psychological component of mental disorders, the second half to the understanding of the biological component. We are now, in the 21st century, busy at better understanding the role of social processes that impact treatment approaches to psychopathology as well as the psychiatrist-patient relationship.</p><p>Even more than other medical disciplines, psychiatry is influenced by external events that plague society, such as epidemics, natural disasters and wars. These events often require the involvement of ethics committees that will determine the duties and rights of the physician in potentially conflictual ethical contexts, such as triage situations (i.e., choosing whom to treat first). The COVID-19 pandemic has shown how deeply interwoven the epidemiology of mental disorders and the access to mental health services are with both social factors and somatic health. Grief, isolation, loss of income and fear exacerbate existing mental health problems or create new ones. The pandemic has demonstrated that the biological and social dimensions of medicine and public health are inextricably linked<span><sup>2</sup></span>.</p><p>Profound changes in social values and norms, such as the legitimization of medical procedures for transgender individuals, or the availability of euthanasia in some countries, require a redefinition of the psychiatrist's role within the medical staff, and the development of ethical guidelines that take into account a variety of emotional, religious and ideological aspects pertaining to both the patient and the physician.</p><p>This changing scenario is extensively reflected in Galderisi et al's paper<span><sup>3</sup></span>. I will focus here on three of the issues discussed by the authors. The first is stigma related to mental disorders in society in general, and particularly in the medical world. Studies documenting the importance of social/environmental components in the development of psychopathology<span><sup>4</sup></span>, as well as those showing the close relationship between physical illness and emotional states, have contributed to reduce that stigma. The inclusion of psychiatric wards within general hospitals has been both a consequence and a further determinant of this evolution. Likewise, the importance of the psychiatrist's presence in transdisciplinary medical teams, as well as in hospital ethics committees, has become more obvious than in the past. It is also increasingly clear that codes of ethics of physical medicine and psychiatry overlap to a large extent, especially with regard to the therapist-patient relationship.</p><p>The second topic I wish to emphasize is the changing relationship between psychiatrists and representatives of
从历史的角度来看,恩格尔1 将精神病理学概念化为生物、心理和社会三种因素相互作用的结果。20 世纪上半叶主要致力于精神障碍的心理因素的概念化,下半叶则致力于对生物因素的理解。进入 21 世纪,我们正忙于更好地理解社会进程的作用,这些进程影响着精神病理学的治疗方法以及精神科医生与患者之间的关系。这些事件往往需要伦理委员会的参与,委员会将决定医生在分流(即选择先治疗谁)等可能发生冲突的伦理环境中的职责和权利。COVID-19 大流行表明,精神障碍的流行病学和心理健康服务的获取与社会因素和躯体健 康是多么紧密地交织在一起。悲伤、孤独、失去收入和恐惧会加剧现有的心理健康问题或产生新的问题。大流行病表明,医学和公共卫生的生物和社会层面有着千丝万缕的联系2。社会价值观和规范的深刻变化,如变性人医疗程序的合法化,或某些国家安乐死的可用性,都要求重新定义精神科医生在医务人员中的角色,并制定考虑到病人和医生情感、宗教和意识形态等多方面因素的伦理准则3。在此,我将重点讨论作者所讨论的三个问题。首先是整个社会,尤其是医学界对精神障碍的成见。有研究表明,社会/环境因素在精神病理学的发展过程中具有重要作用4 ,还有研究表明,身体疾病与情绪状态之间存在密切关系,这些都有助于减少这种成见。将精神科病房纳入综合医院既是这一演变的结果,也是其进一步的决定因素。同样,与过去相比,精神科医生在跨学科医疗团队以及医院伦理委员会中的重要性也变得更加明显。我想强调的第二个话题是精神科医生与患者和家属代表之间不断变化的关系。最近,我们目睹了前住院病人、他们的家人和人权组织举行的反对精神病学的示威活动。我们在社会层面的参与使得我们从家长式的立场转变为更加倾听、平等的立场。我们开始邀请这些示威者 "过马路",来参加我们的会议,与我们分享他们的观点,并在相互尊重的背景下,与我们讨论有关生活质量、患者权利、治疗效果与副作用以及胁迫情况等问题的困境。如今,在许多国家,精神病患者的代表被邀请参加讨论这些问题和分配研究资源的委员会。在一些国家,曾经的患者和/或其亲属也会参与医学生和住院医生的教学工作。这种合作提高了我们思维和工作方式的透明度,有助于减少精神病学所带来的耻辱感。这种态度的转变清楚地反映在了WPA的职业道德规范中2。其中一个仍然存在冲突并助长对精神科职业偏见的问题是强制措施的使用,这似乎剥夺了病人的自主权,而自主权是任何医疗职业道德规范的四项基本原则之一,其他三项原则分别是受益原则、非渎职原则和公正原则4。 自主权一词反映了病人拒绝接受治疗的权利。对于精神病患者而言,"自主 "的定义非常复杂,因为患者的 "自由 "意志受到其精神病症状和缺乏洞察力的影响。治疗(包括强制治疗)的目的是恢复病人独立工作所需的判断能力。
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引用次数: 0
Associations between physical diseases and subsequent mental disorders: a longitudinal study in a population-based cohort 身体疾病与后续精神障碍之间的关系:一项基于人群的队列纵向研究
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21242
Natalie C. Momen, Søren Dinesen Østergaard, Uffe Heide-Jorgensen, Henrik Toft Sørensen, John J. McGrath, Oleguer Plana-Ripoll
People with physical diseases are reported to be at elevated risk of subsequent mental disorders. However, previous studies have considered only a few pairs of conditions, or have reported only relative risks. This study aimed to systematically explore the associations between physical diseases and subsequent mental disorders. It examined a population-based cohort of 7,673,978 people living in Denmark between 2000 and 2021, and followed them for a total of 119.3 million person-years. The study assessed nine broad categories of physical diseases (cardiovascular, endocrine, respiratory, gastrointestinal, urogenital, musculoskeletal, hematological and neurological diseases, and cancers), encompassing 31 specific diseases, and the subsequent risk of mental disorder diagnoses, encompassing the ten ICD-10 groupings (organic, including symptomatic, mental disorders; mental disorders due to psychoactive substance use; schizophrenia and related disorders; mood disorders; neurotic, stress-related and somatoform disorders; eating disorders; personality disorders; intellectual disabilities; pervasive developmental disorders; and behavioral and emotional disorders with onset usually occurring in childhood and adolescence). Using Poisson regression, the overall and time-dependent incidence rate ratios (IRRs) for pairs of physical diseases and mental disorders were calculated, adjusting for age, sex and calendar time. Absolute risks were estimated with the Aalen-Johansen estimator. In total, 646,171 people (8.4%) were identified as having any mental disorder during follow-up. All physical diseases except cancers were associated with an elevated risk of any mental disorder. For the nine broad pairs of physical diseases and mental disorders, the median point estimate of IRR was 1.51 (range: 0.99-1.84; interquartile range: 1.29-1.59). The IRRs ranged from 0.99 (95% CI: 0.98-1.01) after cancers to 1.84 (95% CI: 1.83-1.85) after musculoskeletal diseases. Risks varied over time after the diagnosis of physical diseases. The cumulative mental disorder incidence within 15 years after diagnosis of a physical disease varied from 3.73% (95% CI: 3.67-3.80) for cancers to 10.19% (95% CI: 10.13-10.25) for respiratory diseases. These data document that most physical diseases are associated with an elevated risk of subsequent mental disorders. Clinicians treating physical diseases should constantly be alert to the possible development of secondary mental disorders.
据报道,患有躯体疾病的人罹患继发性精神障碍的风险较高。然而,以往的研究只考虑了几对疾病,或者只报告了相对风险。本研究旨在系统地探讨身体疾病与继发精神障碍之间的关联。研究调查了2000年至2021年期间居住在丹麦的7,673,978人,并对他们进行了总计1.193亿人年的跟踪调查。研究评估了九大类身体疾病(心血管疾病、内分泌疾病、呼吸系统疾病、胃肠道疾病、泌尿生殖系统疾病、肌肉骨骼疾病、血液和神经系统疾病以及癌症),包括 31 种具体疾病,以及随后诊断出精神障碍的风险,包括 10 个 ICD-10 分组(器质性精神障碍,包括症状性精神障碍;使用精神活性物质导致的精神障碍;精神分裂症及相关障碍;情绪障碍;神经症、压力相关障碍和躯体形式障碍;饮食障碍;人格障碍;智力障碍;广泛性发育障碍;以及通常在儿童和青少年时期发病的行为和情感障碍)。在对年龄、性别和日历时间进行调整后,采用泊松回归法计算了躯体疾病和精神障碍的总体发病率比和与时间相关的发病率比。绝对风险采用 Aalen-Johansen 估算法进行估算。在随访期间,共有 646 171 人(8.4%)被确认患有精神障碍。除癌症外,所有身体疾病都与任何精神障碍的风险升高有关。在九种躯体疾病和精神障碍的广泛配对中,IRR 的点估计中位数为 1.51(范围:0.99-1.84;四分位间范围:1.29-1.59)。癌症的 IRR 为 0.99(95% CI:0.98-1.01),肌肉骨骼疾病的 IRR 为 1.84(95% CI:1.83-1.85)。在确诊躯体疾病后,风险会随着时间的推移而变化。在确诊躯体疾病后的 15 年内,精神障碍的累积发病率从癌症的 3.73%(95% CI:3.67-3.80)到呼吸系统疾病的 10.19%(95% CI:10.13-10.25)不等。这些数据表明,大多数躯体疾病都与随后出现精神障碍的风险升高有关。治疗躯体疾病的临床医生应时刻警惕继发性精神障碍的可能发展。
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引用次数: 0
Human rights and early intervention: ethics as a positive force 人权与早期干预:伦理是一种积极的力量
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21236
Patrick D. McGorry
<p>As a medical student in the 1970s, my deep concern about the civil rights of the mentally ill was one of the main reasons for my interest in psychiatry and which ultimately inspired me to enter the field. These were “negative rights” which needed to be addressed and still do.</p><p>Galderisi et al<span><sup>1</sup></span> devote most of their paper to the protection of these civil rights. Less extensively addressed are the “positive rights”, that is the economic, social and cultural rights of the mentally ill. This includes the structural neglect of the mentally ill within the health care and medical research systems across all societies, including high-income countries<span><sup>2</sup></span>.</p><p>A global average of just around 2% of the health care budget is spent on the care of the mentally ill. Even in WEIRD (Western, Educated, Industrialized, Rich and Democratic) countries of the Global North, access to and quality of care are dramatically lower than for physical illness, such as cancer and cardiovascular diseases.</p><p>This gross global neglect is a major driver of coercive cultures of care, which in turn are an inevitable result of late intervention, with treatment only being offered as a last resort. Neglect also contributes to high rates of premature death from suicide and preventable and treatable medical causes, marginalization and immiseration.</p><p>In 2023, the World Mental Health Day celebrated mental health as a universal human right. However, the meaning of this – as eloquently argued by Patel<span><sup>3</sup></span> – is ideologically loaded. He points out that the population has the right to be protected from “known harms to mental health”. Such harms result from government policies and new megatrends that have created powerful structural forces which undermine mental health and produce higher levels of mental ill-health. They do so through creating increased poverty and marginalization, disproportionate exposure to violence and displacement, and surging wealth inequality.</p><p>The paradigm shift that began in the early 1990s to make early intervention a belated addition to the spectrum of treatment and care in psychiatry should be seen as part of the response to the above gross global neglect. Early intervention began within the field of schizophrenia and psychotic disorders and profoundly challenged and ultimately transformed this field. Subsequently it spread as a principle and goal across the full spectrum of mental disorders.</p><p>With K. Schaffner, I co-edited a special issue of <i>Schizophrenia Research</i> in 2001 on the ethics of early detection and intervention in schizophrenia. The main topic clearly is the balance between non-maleficence and beneficence, or risks versus benefits. Galderisi et al focus on the clinical high risk (CHR) for psychosis field in discussing the relevant issues. Ultra high risk (UHR) – or, in the US, CHR – is a concept that my colleagues and I introduced and operationally de
尽管如此,与我自己30多年来治疗这类病人的经验一致,作者最终得出的结论是,在适当的条件下,为寻求帮助的年轻人提供治疗是有明确价值的,因为他们确实有精神病的警告症状,同时还伴有其他合并症状和功能障碍,这可能是持续性精神病障碍的第一阶段。CHR概念的批评者提出的一个合理观点是,独立、"纯粹 "或狭隘的CHR门诊模式仅依赖于被动求助,这意味着只有一小部分表现出CHR表型并发展到持续或 "首次发作 "精神病的成熟阶段的患者能够参与其中,而其余的患者则是通过急诊科和其他途径进入治疗,此时他们已经越过了精神病的界限。Galderisi 等人正确地指出,普遍的、一步到位的筛查策略并不是解决这一问题的适当方案。相反,在澳大利亚以及随后在许多其他国家7 发展起来的强化初级保健或青少年综合服务护理模式才是一个潜在的解决方案。例如,我们能够在短短两年多的时间内,从当地的 "头部空间 "系统中招募到 310 名 CHR 患者参与一项临床试验8 ,而且我们估计,在所有接受 "头部空间 "服务的患者中,至少有 20%-30% 的患者的精神病症状有所减轻。它们可以对青少年新出现的各种精神疾病进行早期干预,减少对特定疾病轨迹的关注。我们可以更笼统地说明现在就采取行动的必要性,目的是防止症状和综合症恶化,或发展成其他或额外的问题。这种方法已被广泛接受,甚至在引入双相情感障碍或精神病等术语时,也不会像传统精神病学那样给人留下决定论和悲观主义的阴影。"心灵空间"(Headspace)已在澳大利亚运作了18年,目前已进入160多个社区。正如所有真正的改革一样,它也有反对者。然而,针对这些批评的反驳有时会被忽视。归根结底,这是一种得到消费者和社区大力支持的护理模式,最近的一项独立评估证实,这种模式是有效和具有成本效益的,尤其是对于早期和轻度至中度的失调9。在欧洲和加拿大的一系列服务环境中也开展了类似的研究。未来的进展将取决于加强这些一线初级保健平台的临床能力,并为其提供针对后期疾病的更专业的多学科护理方案。
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引用次数: 0
Sensitivity of the familial high-risk approach for the prediction of future psychosis: a total population study 家族高风险法预测未来精神病的灵敏度:全人群研究
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21243
Colm Healy, Ulla Lång, Kirstie O’Hare, Juha Veijola, Karen O'Connor, Marius Lahti-Pulkkinen, Eero Kajantie, Ian Kelleher
Children who have a parent with a psychotic disorder present an increased risk of developing psychosis. It is unclear to date, however, what proportion of all psychosis cases in the population are captured by a familial high-risk for psychosis (FHR-P) approach. This is essential information for prevention research and health service planning, as it tells us the total proportion of psychosis cases that this high-risk approach would prevent if an effective intervention were developed. Through a prospective cohort study including all individuals born in Finland between January 1, 1987 and December 31, 1992, we examined the absolute risk and total proportion of psychosis cases captured by FHR-P and by a transdiagnostic familial risk approach (TDFR-P) based on parental inpatient hospitalization for any mental disorder. Outcomes of non-affective psychosis (ICD-10: F20-F29) and schizophrenia (ICD-10: F20) were identified in the index children up to December 31, 2016. Of the index children (N=368,937), 1.5% (N=5,544) met FHR-P criteria and 10.3% (N=38,040) met TDFR-P criteria. By the study endpoint, 1.9% (N=6,966) of the index children had been diagnosed with non-affective psychosis and 0.5% (N=1,846) with schizophrenia. In terms of sensitivity, of all non-affective psychosis cases in the index children, 5.2% (N=355) were captured by FHR-P and 20.6% (N=1,413) by TDFR-P approaches. The absolute risk of non-affective psychosis was 6.4% in those with FHR-P, and 3.7% in those with TDFR-P. There was notable variation in the sensitivity and total proportion of FHR-P and TDFR-P cases captured based on the age at which FHR-P/TDFR-P were determined. The absolute risk for psychosis, however, was relatively time invariant. These metrics are essential to inform intervention strategies for psychosis risk requiring pragmatic decision-making.
父母一方患有精神病的儿童患精神病的风险会增加。然而,迄今为止,我们还不清楚家族性精神病高危因素(FHR-P)方法在所有精神病病例中所占的比例。这对于预防研究和健康服务规划来说是至关重要的信息,因为它告诉我们,如果开发出有效的干预措施,这种高风险方法可以预防的精神病病例的总比例。通过一项前瞻性队列研究(包括 1987 年 1 月 1 日至 1992 年 12 月 31 日期间在芬兰出生的所有个体),我们研究了 FHR-P 和基于父母因任何精神障碍住院治疗的跨诊断家族风险方法 (TDFR-P) 所捕获的精神病病例的绝对风险和总比例。截至 2016 年 12 月 31 日,在索引儿童中确定了非情感性精神病(ICD-10:F20-F29)和精神分裂症(ICD-10:F20)的结果。在指数儿童(N=368937)中,1.5%(N=5544)符合FHR-P标准,10.3%(N=38040)符合TDFR-P标准。到研究终点时,1.9%(N=6966)的指标儿童被诊断为非情感性精神病,0.5%(N=1846)被诊断为精神分裂症。就灵敏度而言,在指数儿童的所有非情感性精神病病例中,5.2%(样本数=355)被FHR-P方法捕获,20.6%(样本数=1413)被TDFR-P方法捕获。采用 FHR-P 方法的儿童患非情感性精神病的绝对风险为 6.4%,采用 TDFR-P 方法的儿童患非情感性精神病的绝对风险为 3.7%。根据测定FHR-P/TDFR-P的年龄,FHR-P和TDFR-P病例的敏感性和总比例存在显著差异。然而,精神病的绝对风险在时间上相对不变。这些指标对于制定需要务实决策的精神病风险干预策略至关重要。
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引用次数: 0
Development and temporal validation of a clinical prediction model of transition to psychosis in individuals at ultra-high risk in the UHR 1000+ cohort UHR 1000+ 队列中超高风险人群向精神病过渡的临床预测模型的开发和时间验证
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21240
Simon Hartmann, Dominic Dwyer, Blake Cavve, Enda M. Byrne, Isabelle Scott, Caroline Gao, Cassandra Wannan, Hok Pan Yuen, Jessica Hartmann, Ashleigh Lin, Stephen J. Wood, Johanna T.W. Wigman, Christel M. Middeldorp, Andrew Thompson, Paul Amminger, Monika Schlögelhofer, Anita Riecher-Rössler, Eric Y.H. Chen, Ian B. Hickie, Lisa J. Phillips, Miriam R. Schäfer, Nilufar Mossaheb, Stefan Smesny, Gregor Berger, Lieuwe de Haan, Merete Nordentoft, Swapna Verma, Dorien H. Nieman, Patrick D. McGorry, Alison R. Yung, Scott R. Clark, Barnaby Nelson
The concept of ultra-high risk for psychosis (UHR) has been at the forefront of psychiatric research for several decades, with the ultimate goal of preventing the onset of psychotic disorder in high-risk individuals. Orygen (Melbourne, Australia) has led a range of observational and intervention studies in this clinical population. These datasets have now been integrated into the UHR 1000+ cohort, consisting of a sample of 1,245 UHR individuals with a follow-up period ranging from 1 to 16.7 years. This paper describes the cohort, presents a clinical prediction model of transition to psychosis in this cohort, and examines how predictive performance is affected by changes in UHR samples over time. We analyzed transition to psychosis using a Cox proportional hazards model. Clinical predictors for transition to psychosis were investigated in the entire cohort using multiple imputation and Rubin's rule. To assess performance drift over time, data from 1995-2016 were used for initial model fitting, and models were subsequently validated on data from 2017-2020. Over the follow-up period, 220 cases (17.7%) developed a psychotic disorder. Pooled hazard ratio (HR) estimates showed that the Comprehensive Assessment of At-Risk Mental States (CAARMS) Disorganized Speech subscale severity score (HR=1.12, 95% CI: 1.02-1.24, p=0.024), the CAARMS Unusual Thought Content subscale severity score (HR=1.13, 95% CI: 1.03-1.24, p=0.009), the Scale for the Assessment of Negative Symptoms (SANS) total score (HR=1.02, 95% CI: 1.00-1.03, p=0.022), the Social and Occupational Functioning Assessment Scale (SOFAS) score (HR=0.98, 95% CI: 0.97-1.00, p=0.036), and time between onset of symptoms and entry to UHR service (log transformed) (HR=1.10, 95% CI: 1.02-1.19, p=0.013) were predictive of transition to psychosis. UHR individuals who met the brief limited intermittent psychotic symptoms (BLIPS) criteria had a higher probability of transitioning to psychosis than those who met the attenuated psychotic symptoms (APS) criteria (HR=0.48, 95% CI: 0.32-0.73, p=0.001) and those who met the Trait risk criteria (a first-degree relative with a psychotic disorder or a schizotypal personality disorder plus a significant decrease in functioning during the previous year) (HR=0.43, 95% CI: 0.22-0.83, p=0.013). Models based on data from 1995-2016 displayed good calibration at initial model fitting, but showed a drift of 20.2-35.4% in calibration when validated on data from 2017-2020. Large-scale longitudinal data such as those from the UHR 1000+ cohort are required to develop accurate psychosis prediction models. It is critical to assess existing and future risk calculators for temporal drift, that may reduce their utility in clinical practice over time.
几十年来,精神病超高风险(UHR)的概念一直处于精神病学研究的前沿,其最终目标是预防高风险人群中精神病性障碍的发生。Orygen 公司(澳大利亚墨尔本)在这一临床人群中开展了一系列观察和干预研究。这些数据集现已整合到 UHR 1000+ 队列中,该队列由 1,245 名 UHR 患者组成,随访时间从 1 年到 16.7 年不等。本文介绍了该队列,提出了该队列中向精神病过渡的临床预测模型,并研究了预测性能如何受到 UHR 样本随时间推移而发生的变化的影响。我们使用 Cox 比例危险模型分析了向精神病过渡的情况。我们使用多重估算和鲁宾法则调查了整个队列中精神病转归的临床预测因素。为评估随时间推移的性能漂移,1995-2016年的数据被用于初始模型拟合,随后模型在2017-2020年的数据中得到验证。在随访期间,220 例(17.7%)患者出现了精神障碍。汇总的危险比(HR)估计值显示,高危精神状态综合评估(CAARMS)言语紊乱子量表严重程度评分(HR=1.12,95% CI:1.02-1.24,P=0.024)、CAARMS异常思维内容子量表严重程度评分(HR=1.13,95% CI:1.03-1.24,P=0.009)、阴性症状评估量表(SANS)总评分(HR=1.02,95% CI:1.00-1.03,p=0.022)、社会与职业功能评估量表(SOFAS)得分(HR=0.98,95% CI:0.97-1.00,p=0.036)以及症状出现与进入 UHR 服务之间的时间(对数转换)(HR=1.10,95% CI:1.02-1.19,p=0.013)均可预测向精神病的转变。符合短暂局限性间歇性精神病性症状(BLIPS)标准的 UHR 患者比符合减轻精神病性症状(APS)标准的患者(HR=0.48,95% CI:0.32-0.73,p=0.001)和符合特质风险标准(直系亲属患有精神病性障碍或分裂型人格障碍,且前一年的功能显著下降)者(HR=0.43,95% CI:0.22-0.83,p=0.013)。基于1995-2016年数据的模型在初始模型拟合时显示出良好的校准性,但在对2017-2020年的数据进行验证时,校准性出现了20.2%-35.4%的漂移。要开发准确的精神病预测模型,需要大规模的纵向数据,如来自 UHR 1000+ 队列的数据。评估现有和未来风险计算器的时间漂移至关重要,因为随着时间的推移,时间漂移可能会降低其在临床实践中的效用。
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引用次数: 0
Ethical challenges in contemporary psychiatry: an overview and an appraisal of possible strategies and research needs 当代精神病学面临的伦理挑战:概述及评估可能的战略和研究需求
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21230
Silvana Galderisi, Paul S. Appelbaum, Neeraj Gill, Piers Gooding, Helen Herrman, Antonio Melillo, Keris Myrick, Soumitra Pathare, Martha Savage, George Szmukler, John Torous
Psychiatry shares most ethical issues with other branches of medicine, but also faces special challenges. The Code of Ethics of the World Psychiatric Association offers guidance, but many mental health care professionals are unaware of it and the principles it supports. Furthermore, following codes of ethics is not always sufficient to address ethical dilemmas arising from possible clashes among their principles, and from continuing changes in knowledge, culture, attitudes, and socio-economic context. In this paper, we identify topics that pose difficult ethical challenges in contemporary psychiatry; that may have a significant impact on clinical practice, education and research activities; and that may require revision of the profession's codes of ethics. These include: the relationships between human rights and mental health care, research and training; human rights and mental health legislation; digital psychiatry; early intervention in psychiatry; end-of-life decisions by people with mental health conditions; conflicts of interests in clinical practice, training and research; and the role of people with lived experience and family/informal supporters in shaping the agenda of mental health care, policy, research and training. For each topic, we highlight the ethical concerns, suggest strategies to address them, call attention to the risks that these strategies entail, and highlight the gaps to be narrowed by further research. We conclude that, in order to effectively address current ethical challenges in psychiatry, we need to rethink policies, services, training, attitudes, research methods and codes of ethics, with the concurrent input of a range of stakeholders, open minded discussions, new models of care, and an adequate organizational capacity to roll-out the implementation across routine clinical care contexts, training and research.
精神病学与其他医学分支有着相同的伦理问题,但也面临着特殊的挑战。世界精神病学协会的伦理守则提供了指导,但许多精神卫生保健专业人员并不了解该守则及其支持的原则。此外,遵循伦理守则并不总能解决因其原则之间可能存在的冲突,以及因知识、文化、态度和社会经济背景的不断变化而产生的伦理困境。在本文中,我们指出了在当代精神病学中对伦理提出挑战的课题,这些课题可能会对临床实践、教育和研究活动产生重大影响,并可能需要对该行业的伦理守则进行修订。这些议题包括:人权与心理健康护理、研究和培训之间的关系;人权与心理健康立法;数字精神病学;精神病学中的早期干预;精神疾病患者的临终决定;临床实践、培训和研究中的利益冲突;以及有生活经验者和家庭/非正式支持者在制定心理健康护理、政策、研究和培训议程中的作用。对于每一个主题,我们都强调了伦理方面的问题,提出了解决这些问题的策略,呼吁人们关注这些策略所带来的风险,并强调了需要通过进一步研究来缩小的差距。我们的结论是,为了有效应对当前精神病学面临的伦理挑战,我们需要重新思考政策、服务、培训、态度、研究方法和伦理准则,同时听取各利益相关方的意见,进行开放式讨论,建立新的护理模式,并具备足够的组织能力,以便在日常临床护理、培训和研究中推广实施。
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引用次数: 0
A broader approach to ethical challenges in digital mental health 以更广泛的方法应对数字心理健康领域的伦理挑战
IF 73.3 1区 医学 Q1 Medicine Pub Date : 2024-09-16 DOI: 10.1002/wps.21237
Nicole Martinez-Martin
<p>Galderisi et al<span><sup>1</sup></span> provide an insightful overview of current ethical challenges in psychiatry, including those presented by digital psychiatry, as well as recommendations for addressing these challenges. As they discuss, “digital psychiatry” encompasses an array of different digital tools, including mental health apps, chatbots, telehealth platforms, and artificial intelligence (AI). These tools hold promise for improving diagnosis and care, and could facilitate access to mental health services by marginalized populations. In particular, digital mental health tools can assist in expanding mental health support in lower-to-middle income countries.</p><p>Many of the ethical challenges identified by the authors in the use of digital tools reflect inequities and challenges within broader society. For example, in the US, lack of mental health insurance and insufficient representation of racialized minorities in medical research contribute to the difficulties with access and fairness in digital psychiatry. In many ways, the ethical challenges presented by digital psychiatry reflect long-standing concerns about who benefits, and who does not, from psychiatry. The array of forward-looking recommendations advanced by Galderisi et al show that these ethical challenges can also be seen as opportunities for moving towards greater equity and inclusion in psychiatry.</p><p>Discussions of the ethics of digital health benefit from broadening the scope of issues to include social context. Galderisi et al refer to inequities in how mental health care is researched, developed and accessed, and to historical power imbalances in psychiatry due to which patient voices are undervalued and overlooked. A broader approach to ethical challenges related to digital health technologies recognizes that issues affecting these technologies often emerge due to their interactions with the social institutions in which they are developed and applied<span><sup>2</sup></span>. For example, privacy and safety of digital psychiatry tools must be understood within the context of the specific regulatory environment and infrastructure (e.g., broadband, hardware) in which they are being used.</p><p>Digital health tools and medical AI are often promoted for improving cost-effectiveness, but this business-oriented emphasis can obscure discussion of what trade-offs in costs are considered acceptable, such as whether lesser-quality services are deemed acceptable for low-income groups. Institutions that regulate medical devices often struggle when they have to deal with softwares or AI. Consumers and patients too often find it difficult to obtain information that can help them decide which digital psychiatry tools are appropriate and effective for their needs.</p><p>There have been pioneering efforts to assist with evaluating effective digital mental health tools, such as American Psychiatric Association's mental health app evaluator<span><sup>3</sup></span>. However
这些数据行为对患者造成的影响可能是他们无法预料的。即使是去标识化的数据也会越来越多地被重新标识,而根据这些数据编制的用户档案可能会被用于针对目标人群的欺诈性营销计划,或导致对就业或教育机会的下游影响。此外,在美国等国家,许多人可能负担不起心理健康护理,人们实际上可能处于用数据换取健康护理的境地。由于公平性和偏见问题,数字和人工智能工具对不同人群的实际作用有多大也是个现实问题。一个常见的偏见来源是,用于训练和开发数字工具的数据可能不足以代表目标人群,例如不同种族、性别或残疾的参与者9。出现偏见的可能性不仅仅是算法偏见的问题,因为工具的设计方式可能根本无法对不同人群有效发挥作用,或者在特定情况下使用这些工具可能导致不公平的结果。要解决公平问题,就必须确保来自不同背景的研究人员和临床医生都能参与数字精神病学工具的开发和设计。正如加尔德里西等人所指出的,精神病学的学科和工具长期以来一直被用于社会控制,比如在刑事司法和教育系统中。数字精神病学工具的应用可能会使弱势和少数群体特别容易受到政府机构的惩罚性干预。因此,重要的是,精神病学专业的成员要深思熟虑,努力预测并解决在社会其他领域使用数字精神病学工具所带来的社会和法律影响。开发数字精神病学工具需要确定具体的伦理挑战,同时也要花时间反思和设想这些工具将帮助创建的系统和世界。加尔德里西等人提出了一系列行动项目,这些项目合在一起,为精神病学设想了一个更加公平和包容的未来。这是一个重要的时刻,我们应该抓住这些机会,为精神病学建立新的框架和系统,利用数字工具来支持人类的同理心和创造力,让心理健康蓬勃发展。
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