Pub Date : 2022-06-03DOI: 10.1177/00048674221103481
S. Suetani, Leshay Chong, Randall Frazer, C. Nelson, Lyle R. Turner, Marianna Serghi, A. Carson, H. Whiteford
the BiOC model, underpinned by an Indigenous practice framework and a partnership with a tertiary hospital, was able to close the gap against several perinatal health measures.
{"title":"The institute for urban indigenous health: The role of psychiatry in reducing health inequality","authors":"S. Suetani, Leshay Chong, Randall Frazer, C. Nelson, Lyle R. Turner, Marianna Serghi, A. Carson, H. Whiteford","doi":"10.1177/00048674221103481","DOIUrl":"https://doi.org/10.1177/00048674221103481","url":null,"abstract":"the BiOC model, underpinned by an Indigenous practice framework and a partnership with a tertiary hospital, was able to close the gap against several perinatal health measures.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"11 1","pages":"1376 - 1377"},"PeriodicalIF":0.0,"publicationDate":"2022-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86698258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-05-27DOI: 10.1177/00048674211031477
Juan Liu, Zhuang Liu, Yan-ge Wei, Yanbo Zhang, F. Womer, Duan Jia, Shengnan Wei, Feng Wu, Ling-tao Kong, Xiaowei Jiang, Luheng Zhang, Yanqing Tang, Xizhe Zhang, Fei Wang
Objective: Clinical heterogeneity in major depressive disorder likely reflects the range of etiology and contributing factors in the disorder, such as genetic risk. Identification of more refined subgroups based on biomarkers such as white matter integrity and lipid-related metabolites could facilitate precision medicine in major depressive disorder. Methods: A total of 148 participants (15 genetic high-risk participants, 57 patients with first-episode major depressive disorder and 76 healthy controls) underwent diffusion tensor imaging and plasma lipid profiling. Alterations in white matter integrity and lipid metabolites were identified in genetic high-risk participants and patients with first-episode major depressive disorder. Then, shared alterations between genetic high-risk and first-episode major depressive disorder were used to develop an imaging x metabolite diagnostic panel for genetically based major depressive disorder via factor analysis and logistic regression. A fivefold cross-validation test was performed to evaluate the diagnostic panel. Results: Alterations of white matter integrity in corona radiata, superior longitudinal fasciculus and the body of corpus callosum and dysregulated unsaturated fatty acid metabolism were identified in both genetic high-risk participants and patients with first-episode major depressive disorder. An imaging x metabolite diagnostic panel, consisting of measures for white matter integrity and unsaturated fatty acid metabolism, was identified that achieved an area under the receiver operating characteristic curve of 0.86 and had a significantly higher diagnostic performance than that using either measure alone. And cross-validation confirmed the adequate reliability and accuracy of the diagnostic panel. Conclusion: Combining white matter integrity in corpus callosum, superior longitudinal fasciculus and corona radiata, and unsaturated fatty acid profile may improve the identification of genetically based endophenotypes in major depressive disorder to advance precision medicine strategies.
{"title":"Combinatorial panel with endophenotypes from multilevel information of diffusion tensor imaging and lipid profile as predictors for depression","authors":"Juan Liu, Zhuang Liu, Yan-ge Wei, Yanbo Zhang, F. Womer, Duan Jia, Shengnan Wei, Feng Wu, Ling-tao Kong, Xiaowei Jiang, Luheng Zhang, Yanqing Tang, Xizhe Zhang, Fei Wang","doi":"10.1177/00048674211031477","DOIUrl":"https://doi.org/10.1177/00048674211031477","url":null,"abstract":"Objective: Clinical heterogeneity in major depressive disorder likely reflects the range of etiology and contributing factors in the disorder, such as genetic risk. Identification of more refined subgroups based on biomarkers such as white matter integrity and lipid-related metabolites could facilitate precision medicine in major depressive disorder. Methods: A total of 148 participants (15 genetic high-risk participants, 57 patients with first-episode major depressive disorder and 76 healthy controls) underwent diffusion tensor imaging and plasma lipid profiling. Alterations in white matter integrity and lipid metabolites were identified in genetic high-risk participants and patients with first-episode major depressive disorder. Then, shared alterations between genetic high-risk and first-episode major depressive disorder were used to develop an imaging x metabolite diagnostic panel for genetically based major depressive disorder via factor analysis and logistic regression. A fivefold cross-validation test was performed to evaluate the diagnostic panel. Results: Alterations of white matter integrity in corona radiata, superior longitudinal fasciculus and the body of corpus callosum and dysregulated unsaturated fatty acid metabolism were identified in both genetic high-risk participants and patients with first-episode major depressive disorder. An imaging x metabolite diagnostic panel, consisting of measures for white matter integrity and unsaturated fatty acid metabolism, was identified that achieved an area under the receiver operating characteristic curve of 0.86 and had a significantly higher diagnostic performance than that using either measure alone. And cross-validation confirmed the adequate reliability and accuracy of the diagnostic panel. Conclusion: Combining white matter integrity in corpus callosum, superior longitudinal fasciculus and corona radiata, and unsaturated fatty acid profile may improve the identification of genetically based endophenotypes in major depressive disorder to advance precision medicine strategies.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"1 1","pages":"1187 - 1198"},"PeriodicalIF":0.0,"publicationDate":"2022-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82072774","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-05-24DOI: 10.1177/00048674221100425
G. Murray, E. Bell, Darryl L Bassett, P. Boyce, R. Bryant, P. Hazell, M. Hopwood, B. Lyndon, R. Mulder, R. Porter, Ajeet B. Singh, G. Malhi
Australian & New Zealand Journal of Psychiatry, 56(9) career level have been women, and this significantly decreases to 3/40 (7.5%) at senior research level. An important consideration in gaining a deeper understanding of the systemic barriers underpinning this disparity is how career disruption and relative-toopportunity frameworks are applied in these award and grant schemes. We are not aware of a framework or guidelines supporting such considerations within the RANZCP and argue that this is urgently needed. On a positive note, Suetani et al. report that in 2021, the RANZCP established the Clinical Academic Psychiatry Steering Committee to ‘consult and advise the next generation of academic-psychiatrists’. We are hope ful that this Steering Committee is representative and consultative in its activities; inclusive in diversity across gender, academic level, colour and indigenous representation; and seeking cross-specialty and state, territory and binational perspectives. In summary, we reiterate Suetani et al.’s (2022) call for more data regarding the psychiatry research workforce, the need for greater clarity in the outcomes of research training efforts and finally, a national effort required to promote, implement and sustain the training of psychiatrist researchers.
{"title":"What works for whom when treating major depression with psychotherapy?","authors":"G. Murray, E. Bell, Darryl L Bassett, P. Boyce, R. Bryant, P. Hazell, M. Hopwood, B. Lyndon, R. Mulder, R. Porter, Ajeet B. Singh, G. Malhi","doi":"10.1177/00048674221100425","DOIUrl":"https://doi.org/10.1177/00048674221100425","url":null,"abstract":"Australian & New Zealand Journal of Psychiatry, 56(9) career level have been women, and this significantly decreases to 3/40 (7.5%) at senior research level. An important consideration in gaining a deeper understanding of the systemic barriers underpinning this disparity is how career disruption and relative-toopportunity frameworks are applied in these award and grant schemes. We are not aware of a framework or guidelines supporting such considerations within the RANZCP and argue that this is urgently needed. On a positive note, Suetani et al. report that in 2021, the RANZCP established the Clinical Academic Psychiatry Steering Committee to ‘consult and advise the next generation of academic-psychiatrists’. We are hope ful that this Steering Committee is representative and consultative in its activities; inclusive in diversity across gender, academic level, colour and indigenous representation; and seeking cross-specialty and state, territory and binational perspectives. In summary, we reiterate Suetani et al.’s (2022) call for more data regarding the psychiatry research workforce, the need for greater clarity in the outcomes of research training efforts and finally, a national effort required to promote, implement and sustain the training of psychiatrist researchers.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"42 1","pages":"1200 - 1202"},"PeriodicalIF":0.0,"publicationDate":"2022-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88662002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-05-21DOI: 10.1177/00048674221100947
Nicola Acevedo, D. Castle, Clare Groves, P. Bosanac, P. Mosley, S. Rossell
Deep brain stimulation is an emerging therapy for treatment-refractory obsessive-compulsive disorder patients. Yet, accessibility is limited, treatment protocols are heterogeneous and there is no guideline or consensus on the best practices. Here, we combine evidence from scientific investigations, expert opinions and our clinical expertise to propose several clinical recommendations from the pre-operative, surgical and post-operative phases of deep brain stimulation care for treatment-refractory obsessive-compulsive disorder patients. A person-centered and biopsychosocial approach is adopted. Briefly, we discuss clinical characteristics associated with response, the use of improved educational materials, an evaluative consent process, comprehensive programming by an expert clinician, a more global assessment of treatment efficacy, multi-disciplinary adjunct psychotherapy and the importance of peer support programs. Furthermore, where gaps are identified, future research suggestions are made, including connectome surgical targeting, scientific evaluation of hardware models and health economic data. In addition, we encourage collaborative groups of data and knowledge sharing by way of a clinical registry and a peer group of programming clinicians. We aim to commence a discussion on the determinants of deep brain stimulation efficacy for treatment-refractory obsessive-compulsive disorder patients, a rare and severe patient group, and contribute to more standardized and evidence-based practices.
{"title":"Clinical recommendations for the care of people with treatment-refractory obsessive-compulsive disorder when undergoing deep brain stimulation","authors":"Nicola Acevedo, D. Castle, Clare Groves, P. Bosanac, P. Mosley, S. Rossell","doi":"10.1177/00048674221100947","DOIUrl":"https://doi.org/10.1177/00048674221100947","url":null,"abstract":"Deep brain stimulation is an emerging therapy for treatment-refractory obsessive-compulsive disorder patients. Yet, accessibility is limited, treatment protocols are heterogeneous and there is no guideline or consensus on the best practices. Here, we combine evidence from scientific investigations, expert opinions and our clinical expertise to propose several clinical recommendations from the pre-operative, surgical and post-operative phases of deep brain stimulation care for treatment-refractory obsessive-compulsive disorder patients. A person-centered and biopsychosocial approach is adopted. Briefly, we discuss clinical characteristics associated with response, the use of improved educational materials, an evaluative consent process, comprehensive programming by an expert clinician, a more global assessment of treatment efficacy, multi-disciplinary adjunct psychotherapy and the importance of peer support programs. Furthermore, where gaps are identified, future research suggestions are made, including connectome surgical targeting, scientific evaluation of hardware models and health economic data. In addition, we encourage collaborative groups of data and knowledge sharing by way of a clinical registry and a peer group of programming clinicians. We aim to commence a discussion on the determinants of deep brain stimulation efficacy for treatment-refractory obsessive-compulsive disorder patients, a rare and severe patient group, and contribute to more standardized and evidence-based practices.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"58 1","pages":"1219 - 1225"},"PeriodicalIF":0.0,"publicationDate":"2022-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74207862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-05-06DOI: 10.1177/00048674221098632
Zoë E. Kristensen
{"title":"Inequity in psychiatry cannot be addressed without first embracing intersectionality","authors":"Zoë E. Kristensen","doi":"10.1177/00048674221098632","DOIUrl":"https://doi.org/10.1177/00048674221098632","url":null,"abstract":"","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"16 1","pages":"1046 - 1047"},"PeriodicalIF":0.0,"publicationDate":"2022-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82562282","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-04-30DOI: 10.1177/00048674221097037
Laurann Gilbertson, J. Kulkarni
Australian & New Zealand Journal of Psychiatry, 56(8) wayside. By instead accepting these issues as interconnected and embracing intersectionality by empowering and including these voices, we can find a solution which addresses the underlying issues once and for all. Our alternative is to spend decades repeating the process turn-wise providing half-measures to each marginalised group within our college.
{"title":"The need to take a trauma history in the acute psychiatry inpatient setting","authors":"Laurann Gilbertson, J. Kulkarni","doi":"10.1177/00048674221097037","DOIUrl":"https://doi.org/10.1177/00048674221097037","url":null,"abstract":"Australian & New Zealand Journal of Psychiatry, 56(8) wayside. By instead accepting these issues as interconnected and embracing intersectionality by empowering and including these voices, we can find a solution which addresses the underlying issues once and for all. Our alternative is to spend decades repeating the process turn-wise providing half-measures to each marginalised group within our college.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"14 1","pages":"1047 - 1047"},"PeriodicalIF":0.0,"publicationDate":"2022-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74156388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-04-30DOI: 10.1177/00048674221096617
Reuben White, M. Papadopoulos, P. Tibrewal
Selective serotonin reuptake inhibitors (SSRIs) can cause haemorrhage secondary to decreased platelet aggregation thus limiting pharmacological treatment options in Obsessive-compulsive disorder (OCD) patients with bleeding tendency (Laporte et al., 2017). We report a case where Clomipramine was better tolerated than SSRIs in a patient with recurrent epistaxis and recommend it as an alternative to SSRIs in patients susceptible to haemorrhagic complications. EL is a 59-year-old male, with a 15-year history of schizophrenia stable on Paliperidone 3 monthly depot and a 10-year history of OCD that responded well to Fluvoxamine but was selfceased due to recurrent epistaxis. In February 2021, EL was admitted to an acute psychiatric inpatient ward with obsessive ruminations about past social interactions where he would ‘replay conversations’ in his mind incessantly. The associated anxiety led to reduced self-care, isolation and disengagement with community mental health services. The psychotic symptoms were not dominant. EL was commenced on Sertraline 25 mg and titrated to 50 mg, but subsequently experienced recurrent episodes of severe epistaxis, which resolved with cessation. Naranjo Adverse Drug Reaction Probability Scale was applied to Sertraline and in retrospect to Fluvoxamine (Naranjo et al., 1981). The SSRIs scored 7 and 8, respectively, indicating probable adverse drug reaction (ADR). Further exploration of the aetiology of his epistaxis also revealed a nasal septal defect and Polycythemia Rubra Vera (PCV) for which he was commenced on Aspirin 100 mg/day and Hydroxyurea 1000 mg mane. PCV increases the risk of thrombosis and haemorrhage and Aspirin increases the risk of bleeding. Subsequent treatment with an SSRI would have further increased this risk. We therefore initiated a trial of Clomipramine which has a theoretical advantage over SSRIs of increased platelet aggregation (Alvarez et al., 1999). Clomipramine was gradually uptitrated to 175 mg/day with no further epistaxis during the admission. EL’s OCD symptoms improved with his Yale-Brown Obsessive Compulsive Scale score reducing from 22 at admission to 14 at discharge. He exhibited improved selfcare, social interactions and mood. Clomipramine is a third-line pharmacological treatment for OCD. Like SSRIs it can also increase the risk of haemorrhage via decreased platelet aggregation However, unlike SSRIs, Clomipramine is distinctly a 5-HT2 receptor antagonist which is proposed to lead to compensatory up-regulation of 5-HT2 receptors promoting platelet aggregation (Alvarez et al., 1999). It is possible that this mechanism helped prevent epistaxis in EL and led to better clinical outcome. To our knowledge, this is the first report comparing clomipramine and SSRIs in patients with haemorrhagic complications and provides the clinicians a safer alternative in such cases.
选择性5 -羟色胺再摄取抑制剂(SSRIs)可导致继发于血小板聚集减少的出血,从而限制了有出血倾向的强迫症(OCD)患者的药物治疗选择(Laporte等,2017)。我们报告了一个病例,氯丙咪嗪在复发性鼻出血患者中的耐受性优于SSRIs,并推荐其作为易发生出血并发症的患者的SSRIs的替代方案。EL是一名59岁男性,15年精神分裂症病史,服用帕利哌酮3个月稳定,10年强迫症病史,氟伏沙明反应良好,但因复发性鼻出血而自行停止。2021年2月,EL被送进了一家急性精神病住院病房,他对过去的社交互动进行了强迫性的反思,他会不断地在脑海中“回放对话”。相关的焦虑导致自我护理减少、孤立和脱离社区精神卫生服务。精神症状不明显。EL开始使用舍曲林25mg,然后滴定到50mg,但随后出现了反复发作的严重鼻出血,停药后消失。使用Naranjo药物不良反应概率量表评价舍曲林,回顾氟伏沙明(Naranjo et al., 1981)。SSRIs评分分别为7分和8分,提示可能的药物不良反应(ADR)。进一步检查其鼻出血的病因还发现鼻中隔缺损和红色红细胞增多症(PCV),他开始服用阿司匹林100毫克/天和羟脲1000毫克/天。PCV增加血栓形成和出血的风险,阿司匹林增加出血的风险。随后的SSRI治疗会进一步增加这种风险。因此,我们启动了氯丙咪嗪的试验,它在理论上比SSRIs具有增加血小板聚集的优势(Alvarez et al., 1999)。氯丙咪嗪逐渐增加至175 mg/天,入院期间无进一步出血。EL的强迫症症状有所改善,他的耶鲁-布朗强迫症量表得分从入院时的22分降至出院时的14分。他表现出更好的自我照顾、社交互动和情绪。氯丙咪嗪是治疗强迫症的三线药物。然而,与SSRIs不同的是,氯丙咪嗪明显是一种5-HT2受体拮抗剂,可导致5-HT2受体代偿性上调,促进血小板聚集(Alvarez et al., 1999)。这是可能的,这一机制有助于防止鼻出血在EL和导致更好的临床结果。据我们所知,这是第一份比较氯咪嗪和SSRIs在出血性并发症患者中的应用的报告,为临床医生提供了一种更安全的选择。
{"title":"Clomipramine as an alternative to selective serotonin reuptake inhibitors for patients at haemorrhagic risk","authors":"Reuben White, M. Papadopoulos, P. Tibrewal","doi":"10.1177/00048674221096617","DOIUrl":"https://doi.org/10.1177/00048674221096617","url":null,"abstract":"Selective serotonin reuptake inhibitors (SSRIs) can cause haemorrhage secondary to decreased platelet aggregation thus limiting pharmacological treatment options in Obsessive-compulsive disorder (OCD) patients with bleeding tendency (Laporte et al., 2017). We report a case where Clomipramine was better tolerated than SSRIs in a patient with recurrent epistaxis and recommend it as an alternative to SSRIs in patients susceptible to haemorrhagic complications. EL is a 59-year-old male, with a 15-year history of schizophrenia stable on Paliperidone 3 monthly depot and a 10-year history of OCD that responded well to Fluvoxamine but was selfceased due to recurrent epistaxis. In February 2021, EL was admitted to an acute psychiatric inpatient ward with obsessive ruminations about past social interactions where he would ‘replay conversations’ in his mind incessantly. The associated anxiety led to reduced self-care, isolation and disengagement with community mental health services. The psychotic symptoms were not dominant. EL was commenced on Sertraline 25 mg and titrated to 50 mg, but subsequently experienced recurrent episodes of severe epistaxis, which resolved with cessation. Naranjo Adverse Drug Reaction Probability Scale was applied to Sertraline and in retrospect to Fluvoxamine (Naranjo et al., 1981). The SSRIs scored 7 and 8, respectively, indicating probable adverse drug reaction (ADR). Further exploration of the aetiology of his epistaxis also revealed a nasal septal defect and Polycythemia Rubra Vera (PCV) for which he was commenced on Aspirin 100 mg/day and Hydroxyurea 1000 mg mane. PCV increases the risk of thrombosis and haemorrhage and Aspirin increases the risk of bleeding. Subsequent treatment with an SSRI would have further increased this risk. We therefore initiated a trial of Clomipramine which has a theoretical advantage over SSRIs of increased platelet aggregation (Alvarez et al., 1999). Clomipramine was gradually uptitrated to 175 mg/day with no further epistaxis during the admission. EL’s OCD symptoms improved with his Yale-Brown Obsessive Compulsive Scale score reducing from 22 at admission to 14 at discharge. He exhibited improved selfcare, social interactions and mood. Clomipramine is a third-line pharmacological treatment for OCD. Like SSRIs it can also increase the risk of haemorrhage via decreased platelet aggregation However, unlike SSRIs, Clomipramine is distinctly a 5-HT2 receptor antagonist which is proposed to lead to compensatory up-regulation of 5-HT2 receptors promoting platelet aggregation (Alvarez et al., 1999). It is possible that this mechanism helped prevent epistaxis in EL and led to better clinical outcome. To our knowledge, this is the first report comparing clomipramine and SSRIs in patients with haemorrhagic complications and provides the clinicians a safer alternative in such cases.","PeriodicalId":8576,"journal":{"name":"Australian & New Zealand Journal of Psychiatry","volume":"81 1","pages":"1045 - 1045"},"PeriodicalIF":0.0,"publicationDate":"2022-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74126187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-04-28DOI: 10.1177/00048674221096616
A. Pouchon, M. Polosan, C. Dondé
The term ‘interventional psychiatry’ was coined for the first time in 2014 to describe the growing field of psychiatry based on neuroscience-informed brain modulation devices (Williams et al., 2014). Since then, new interventional treatments have emerged and have been the subject of a large amount of encouraging published and ongoing trials. Some of these treatments were subsequently approved by the US Food and Drug Administration, the European Medicines Agency for Europe and the French Haute Autorité de Santé. Transcranial focused ultrasound stimulation, botulinum toxin injection devices, subcutaneous implants for prolonged psychotropic drugs delivery, infusion and intranasal therapies (Ketamine, Brexanolone) are among the most innovative interventional techniques that have been developed in the last few years. A growing use and demand for interventional approaches in clinical practice has led to individualization and labeling of ‘Interventional Psychiatry Centers’ in many countries, including the United States, Canada, Australia, Germany and Switzerland. Hereby, we strongly support the development and implementation of the ‘Interventional Psychiatry’ label for units that offer a range of services and expertise about these treatment options. We posit that the use of this umbrella term will lead to two following advances. First is stigma and misinformation reduction around interventional approaches with a special focus on neuromodulation techniques. Despite safe and ethical practice frameworks, these techniques continue to be stigmatized resulting in restriction and reduced accessibility. As an example, the name of electroconvulsive therapy has been demonstrated as having itself an impact on both its acceptability and effectiveness (Andrade and Thyagarajan, 2007). System atization of the ‘Interventional Psychiatry’ label would better meet the challenges of the underutilization of interventional – stigmatized – techniques by moving closer to the general, less-stigmatized, framework of interventional medicine. This is likely to improve the credibility and acceptability of interventional approaches in the eyes of patients, caregivers and health workers. Second, the use of interventional psychiatry umbrella term might lead to harmonized improvement of interventional psychiatric practice to a level of innovation and excellence that is recognized internationally. In this perspective, specialty tracks in interventional psychiatry including both neuroscience didactics and hands-on experiences must be generalized within residency curricula. Currently, most psychiatrists who use interventional techniques are trained in a very inconsistent manner. Few programs exist, but to our knowledge, such training is not mandatory to practice this subspecialty. Generalizing these programs will facilitate the identification of highly specialized practitioners, the implementations and visibility of specific Intervention Psychiatry Units and resources, and promote better
“介入精神病学”一词于2014年首次被创造出来,用来描述基于神经科学的脑调节设备的精神病学领域的发展(Williams et al., 2014)。从那时起,新的介入治疗方法出现了,并成为大量令人鼓舞的已发表和正在进行的试验的主题。其中一些治疗方法随后获得了美国食品和药物管理局(fda)、欧洲药品管理局(European Medicines Agency for Europe)和法国高级医疗机构(Haute autorit de sant)的批准。经颅聚焦超声刺激、肉毒杆菌毒素注射装置、用于长期精神药物输送的皮下植入物、输注和鼻内治疗(氯胺酮、布雷沙诺酮)是过去几年发展起来的最具创新性的介入技术。临床实践中对介入方法的使用和需求日益增长,导致了许多国家的个体化和“介入精神病学中心”的标签,包括美国、加拿大、澳大利亚、德国和瑞士。因此,我们强烈支持开发和实施“介入精神病学”标签,用于提供有关这些治疗选择的一系列服务和专业知识的单位。我们认为,使用这一总括性术语将导致以下两个进展。首先是减少围绕介入方法的污名和错误信息,特别关注神经调节技术。尽管有安全和道德的实践框架,但这些技术仍然受到歧视,导致限制和降低可及性。例如,电休克疗法的名称已被证明对其可接受性和有效性都有影响(Andrade和Thyagarajan, 2007)。“介入性精神病学”标签的系统化,通过向介入性医学的一般、较少的框架靠拢,可以更好地应对介入性——污名化——技术利用不足的挑战。这可能会提高介入方法在患者、护理人员和卫生工作者眼中的可信度和可接受性。第二,使用介入性精神病学总括术语可能会导致介入性精神病学实践的协调改进,达到国际公认的创新和卓越水平。从这个角度来看,介入精神病学的专业课程,包括神经科学教学和实践经验,必须在住院医师课程中进行推广。目前,大多数使用介入技术的精神科医生的训练方式非常不一致。很少有这样的项目存在,但据我们所知,这样的培训并不是强制性的。推广这些项目将有助于识别高度专业化的从业人员,特定干预精神病学单位和资源的实施和可见性,并促进干预技术的更好改进(Nikayin et al., 2022)。
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Pub Date : 2022-04-18DOI: 10.1177/00048674221089566
Charlotte Cox, M. George
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Pub Date : 2022-04-08DOI: 10.1177/00048674221091927
S. Suetani, S. Every-Palmer, M. Galbally, M. Berk, Neeraj S. Gill, D. Siskind
Australian & New Zealand Journal of Psychiatry, 56(5) Fostering the next generation of academic psychiatrists is crucial to maintaining our leading role in providing evidence-based care for the patients we serve. Embedding academic psychiatry into clinical services ensures the development of cutting edge clinical evidence and rapid translation into clinical practice, thus improving clinical outcomes (Burke et al., 2018). There is much to be loved about a career in academic psychiatry: self-determinism in terms of time and following interests; opportunities to teach and mentor; being able to influence policy and practice; connecting and collaborating with colleagues; asking difficult questions and sometimes finding answers; and long-term job satisfaction. It is often said that clinicians burn out but academics never retire – this may in turn improve recruitment and retention, especially in the public mental health sector. Despite these benefits, fewer psychiatrists are taking this career pathway, and those that do face significant challenges. Husain (2021) has argued that there is a genuine existential threat to clinical scientists who are ‘under pressure either to voluntarily seek extinction or to evolve into a set of desktop scientists who don’t run experimental studies but rather analyse big data’. Husain worried that such a shift away from experimental studies would have significant deleterious consequences for discovery science (Husain, 2021). In the United States, while the current COVID-19 pandemic has highlighted the critical importance of clinical scientists, it has also brought the decline of this workforce due to constraints on reimbursement, time and funding into stark relief – the percentage of physicians engaged in research has declined from 4.75% in the 1980s to 1.5% today (Utz et al., 2022). In New Zealand and Australia, we do not have far to look for inspiration in academic psychiatry. John Cade was a psychiatrist who discovered lithium in a kitchen at Bundoora Repatriation Mental Hospital in Melbourne. Mason Durie is a leader of Māori health and research world-renowned for the promotion of Indigenous knowledge. Beverley Raphael’s mentorship inspired a generation of academic psychiatrists, demonstrating the importance of creating a stimulating and supportive environment to help grow a culture of lifelong learning. So how can we build and grow the next generation of clinical academics? Utz et al. (2022) proposed the multipronged strategy of: (1) providing an immersive research experience for medical trainees (e.g. funding for a gap year in research laboratory), (2) lowering financial barriers to academic careers, (3) restoring the educators and mentors in clinical science and (4) building a leak-free physician-scientist network. These approaches are in keeping with the call by Scott Henderson et al. (2015) from Australia and Richard Porter from New Zealand, along with 19 other senior academic psychiatrists across Australasia, for u
澳大利亚和新西兰精神病学杂志,56(5):培养下一代学术精神科医生对于保持我们在为我们所服务的病人提供循证护理方面的领导地位至关重要。将学术精神病学纳入临床服务,可确保前沿临床证据的发展和快速转化为临床实践,从而改善临床结果(Burke等人,2018)。从事精神病学学术工作有很多值得热爱的地方:在时间和兴趣方面的自我决定论;教学和指导的机会;能够影响政策和实践;与同事联系和协作;提出困难的问题,有时找到答案;以及长期的工作满意度。人们常说,临床医生会精疲力竭,但学者永远不会退休——这可能反过来改善招聘和留住,尤其是在公共精神卫生部门。尽管有这些好处,很少有精神科医生走上这条职业道路,而那些走上这条道路的人面临着重大挑战。Husain(2021)认为,临床科学家面临着真正的生存威胁,他们“要么在压力下自愿寻求灭绝,要么进化成一群不进行实验研究、而是分析大数据的桌面科学家”。Husain担心这种远离实验研究的转变会对发现科学产生重大的有害后果(Husain, 2021)。在美国,虽然当前的COVID-19大流行凸显了临床科学家的重要性,但由于报销、时间和资金方面的限制,这一劳动力的减少也凸显出来——从事研究的医生比例从20世纪80年代的4.75%下降到今天的1.5% (Utz et al., 2022)。在新西兰和澳大利亚,我们不必在学术精神病学中寻找灵感。约翰·凯德是一名精神病学家,他在墨尔本邦杜拉遣返精神病院的一间厨房里发现了锂。梅森·杜里(Mason Durie)是Māori健康与研究的领导者,以促进土著知识而闻名于世。贝弗利·拉斐尔的指导激励了一代学术精神科医生,证明了创造一个激励和支持的环境对于帮助培养终身学习文化的重要性。那么我们如何才能建立和发展下一代临床学者呢?Utz等人(2022)提出了多管齐下的策略:(1)为医学学员提供身临其境的研究体验(例如为研究实验室的间隔年提供资金),(2)降低学术生涯的财务障碍,(3)恢复临床科学中的教育工作者和导师,(4)建立一个无泄漏的医生-科学家网络。这些方法与澳大利亚的Scott Henderson等人(2015)和新西兰的Richard Porter以及澳大利亚其他19名资深学术精神病学家的呼吁一致,要求采取紧急行动。他们建议(1)创建报酬充足的学术精神病学途径,(2)改善精神病学的招聘,并增加在澳大利亚和新西兰从事复兴学术精神病学的机会
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