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Economic evaluation of screening, treatment, and prevention interventions for perinatal mood and anxiety disorders: a systematic review 围产期情绪和焦虑障碍筛查、治疗和预防干预的经济评价:一项系统综述。
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.11.005
Sabrina Alam , Brian Christman , Emma McNeill , Man Tang , Rong Rong , Qing Li , William Hillegass , Janice Hall , Laura Wright , Chisa Lanier , Xu Xiong , Lizheng Shi , Abigail Gamble

Objective

This systematic review synthesized evidence on the cost-effectiveness and economic favorability of interventions for the detection, treatment, and prevention of perinatal mood and anxiety disorders (PMADs).

Methods

This protocol is registered on PROSPERO (CRD42024528777). PubMed, EMBASE, Web of Science, EconLit, Scopus, PsycINFO, and the National Health Service economic evaluation databases were searched from inception through April 2025. Intervention studies reporting quality-adjusted life years, incremental cost-effectiveness ratios, or equivalent cost analyses during pregnancy or up to one year postpartum were included. Risk of bias was assessed using the Consensus on Health Economics Criteria and Bias in Economic Evaluation checklists. Data were synthesized by study design, intervention type, and economic perspective.

Findings

The search identified 3863 records; 1820 deduplicated titles and abstracts, and 75 full texts were assessed for eligibility. Thirty-seven studies were included (n = 218,525 participants). Thirty-two (86.5 %) interventions were cost-effective or economically favorable, including prevention-only (28.1 %), treatment-only (34.3 %), screening-only (18.7 %), and screening plus treatment and/or prevention (18.7 %). Cost-effective evaluations were primarily from the healthcare system (46.8 %) or payer (25 %) perspectives. Twenty-two (68.7 %) cost-effective interventions included time horizons of one year or greater. Five of six (83.3 %) non-cost-effective interventions included time horizons of less than one year. Studies were heterogeneous in design, population, and intervention types.

Interpretation

Findings support the integration of PMAD interventions into perinatal clinical care. Evidence-based policy and payment models are needed for scaling sustainable uptake. Research priorities include standardization in economic evaluation methods, longer-term modeling, and inclusion of diverse populations.
目的:本系统综述综合了围产期情绪和焦虑障碍(PMADs)检测、治疗和预防干预措施的成本效益和经济效益的证据。方法:该协议在PROSPERO (CRD42024528777)上注册。检索了PubMed、EMBASE、Web of Science、EconLit、Scopus、PsycINFO和National Health Service经济评估数据库,检索时间从数据库建立到2025年4月。干预研究报告了质量调整生命年、增量成本-效果比或怀孕期间或产后一年的等效成本分析。偏倚风险采用卫生经济学标准共识和经济评价偏倚清单进行评估。根据研究设计、干预类型和经济角度综合数据。结果:检索到3863条记录;1820个重复的标题和摘要以及75个全文被评估为合格。纳入37项研究(n = 218,525名受试者)。32项(86.5%)干预措施具有成本效益或经济效益,包括仅预防(28.1%)、仅治疗(34.3%)、仅筛查(18.7%)和筛查加治疗和/或预防(18.7%)。成本效益评价主要是从医疗系统(46.8%)或付款人(25%)的角度进行的。22项(68.7%)具有成本效益的干预措施包括一年或更长时间。6项不具成本效益的干预措施中有5项(83.3%)包括不到一年的时间范围。研究在设计、人群和干预类型上是异质的。解释:研究结果支持将PMAD干预纳入围产期临床护理。需要基于证据的政策和支付模式来扩大可持续吸收。研究重点包括经济评估方法的标准化、长期建模和包括不同人群。
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引用次数: 0
Effectiveness of mental health triage systems in reducing psychiatric emergency department admissions 心理健康分诊系统在减少精神病急诊科入院率方面的有效性
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.11.007
L.W. Mokhwelepa , G.O. Sumbane , R. Mukhinindi
Psychiatric emergency department (PEDs) face significant challenges such as overcrowding, prolonged wait times, and resource constraints, often resulting in suboptimal care. Mental health triage systems have been developed to prioritize urgent cases, optimize resource allocation, and reduce unnecessary admissions, yet their effectiveness remains variably reported. This scoping review aimed to systematically synthesize empirical evidence on the effectiveness of mental health triage systems in reducing psychiatric emergency department admissions and identify factors influencing their success. Following Arksey and O'Malley's framework and PRISMA-ScR guidelines, a comprehensive search was conducted across PubMed, PsycINFO, Scopus, and Web of Science for studies published between 2000 and 2025. Included studies evaluated triage interventions in psychiatric emergency settings with reported outcomes on admission rates. Data were extracted and synthesized narratively. Twenty-three studies from diverse international settings met inclusion criteria. Findings indicate that structured triage systems, particularly nurse-led models employing validated assessment scales, contribute to reductions in avoidable PED admissions. Multi-disciplinary approaches further enhanced decision-making complexity and patient outcomes. Key facilitators included rigorous staff training and integration with community mental health services. Barriers such as inconsistent triage application, limited alternative care options, and staff resistance impeded effectiveness. Mental health triage systems show promise in optimizing psychiatric emergency care by reducing unnecessary admissions and improving prioritization. Their effectiveness depends on standardized protocols, comprehensive training, and strong community linkages. Future research should focus on rigorous, longitudinal evaluations to inform evidence-based triage frameworks.
精神科急诊科(PEDs)面临着巨大的挑战,如过度拥挤、等待时间延长和资源限制,往往导致次优护理。精神卫生分诊系统已开发优先处理紧急情况,优化资源分配,并减少不必要的入院,但其有效性仍有不同的报告。本综述旨在系统地综合精神卫生分诊系统在减少精神科急诊科入院率方面的有效性的经验证据,并确定影响其成功的因素。按照Arksey和O'Malley的框架和PRISMA-ScR指南,在PubMed、PsycINFO、Scopus和Web of Science上进行了全面的搜索,以获取2000年至2025年间发表的研究。纳入的研究评估了精神科急诊环境中的分诊干预措施,并报告了入院率的结果。数据提取和综合叙述。来自不同国际环境的23项研究符合纳入标准。研究结果表明,结构化的分诊系统,特别是采用有效评估量表的护士主导模式,有助于减少可避免的PED入院。多学科方法进一步提高了决策的复杂性和患者的预后。关键的促进因素包括严格的工作人员培训和与社区精神卫生服务的结合。诸如不一致的分诊应用、有限的替代护理选择和工作人员阻力等障碍阻碍了有效性。心理健康分诊系统显示出通过减少不必要的入院和提高优先级来优化精神科急诊护理的希望。它们的有效性取决于标准化的协议、全面的培训和强有力的社区联系。未来的研究应该集中在严谨的纵向评估上,为循证分类框架提供信息。
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引用次数: 0
Effectiveness of probiotic supplements on cognitive function in mild cognitive impairment and Alzheimer’s disease: A meta-analysis of randomized controlled trials 益生菌补充剂对轻度认知障碍和阿尔茨海默病患者认知功能的影响:随机对照试验的荟萃分析
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.11.004
Tzu-Rong Peng , Hung-Hong Lin , Tzu-Ling Tseng , Ta-Wei Wu

Background

Cognitive impairment, encompassing mild cognitive impairment (MCI) and Alzheimer's disease (AD), poses a significant public health challenge worldwide. Emerging evidences suggest that probiotics, through modulation of the gut–brain axis, may improve cognitive function. However, their efficacy in individuals with cognitive impairment remains unclear.

Methods

This meta-analysis adhered to PRISMA guidelines, systematically reviewing randomized controlled trials (RCTs) investigating the effects of probiotics for individuals with cognitive impairment. Data were extracted from the PubMed, Embase, and Cochrane databases. Subgroup analyses were conducted based on different measurement scales (MMSE, MoCA, and RBANS), population types (cognitive impairment vs. no cognitive impairment), multiple or single strain and intervention duration. Effect sizes were expressed as standardized mean differences (SMDs) using random-effects models.

Results

Fifteen RCTs involving 994 participants were included. Probiotic supplementation significantly improved cognitive function compared to placebo (SMD = 0.57; 95 % CI, 0.19–0.94; P = 0.003). Subgroup analyses revealed that both single-strain and multi-strain probiotics were effective; however, multi-strain probiotics demonstrated greater heterogeneity and variability in efficacy. Cognitive improvements were most pronounced with supplementation durations of at least 12 weeks (SMD = 0.73; 95 % CI, 0.30–1.16; P = 0.0009) and higher probiotic doses (>1 × 109 CFU/g; SMD = 0.93; 95 % CI, 0.36–1.49; P < 0.01).

Conclusion

Probiotic supplementations significantly enhance cognitive function in individuals with cognitive impairment, particularly with single-strain formulations, higher doses, and a minimum duration of 12 weeks.
认知障碍,包括轻度认知障碍(MCI)和阿尔茨海默病(AD),是全球范围内重大的公共卫生挑战。新出现的证据表明,益生菌通过调节肠-脑轴,可以改善认知功能。然而,它们对认知障碍患者的疗效尚不清楚。方法本荟萃分析遵循PRISMA指南,系统回顾了调查益生菌对认知障碍患者影响的随机对照试验(rct)。数据从PubMed、Embase和Cochrane数据库中提取。根据不同的测量量表(MMSE、MoCA和rban)、种群类型(认知障碍与无认知障碍)、多菌株或单菌株以及干预时间进行亚组分析。效应量使用随机效应模型表示为标准化平均差异(SMDs)。结果共纳入15项随机对照试验,994名受试者。与安慰剂相比,益生菌补充剂显著改善了认知功能(SMD = 0.57; 95% CI, 0.19-0.94; P = 0.003)。亚群分析显示,单菌种和多菌种益生菌均有效;然而,多菌株益生菌在功效上表现出更大的异质性和可变性。补充至少12周(SMD = 0.73; 95% CI, 0.30-1.16; P = 0.0009)和较高益生菌剂量(1 × 109 CFU/g; SMD = 0.93; 95% CI, 0.36-1.49; P < 0.01)的认知改善最为明显。结论补充益生菌可显著提高认知功能障碍患者的认知功能,特别是单品系配方、高剂量和最少持续12周。
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引用次数: 0
Stigma and health: an urgent need in the training of health professionals 耻辱与健康:迫切需要培训卫生专业人员。
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.10.019
Matías E. Rodríguez-Rivas , Sanndy Infante
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引用次数: 0
Open-label study of the efficacy, safety and tolerability of Brexanolone in the treatment of adult women with postpartum psychosis Brexanolone治疗成年女性产后精神病的疗效、安全性和耐受性的开放标签研究。
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.10.017
Riah Patterson , Holly Krohn , Elizabeth Richardson , Cecilia Pearson , Kai Xia , Mary Kimmel , Samantha Meltzer-Brody

Objective

Postpartum psychosis (PPP) is a rare but severe postpartum psychiatric emergency that occurs during a critical time in mother-infant attachment. This study investigated the efficacy, safety, and tolerability of brexanolone, a neuroactive steroid and synthetic form of allopregnanolone, for adult females with PPP.

Methods

In this open-label, proof-of-concept study, ten patients with PPP received brexanolone as a single, continuous, 60-h intravenous infusion titrated to a target dose of 90 μg/kg/h over a period of 2.5 days. Primary outcomes were change in total score on the Young Mania Rating Scale (YMRS) and Positive and Negative Syndrome Scale (PANSS); Secondary outcomes included change in Hamilton Depression Rating Scale (HAMD) from baseline to Day 7. Adverse events were monitored. Patients were followed through Day 90.

Results

All ten patients completed the treatment protocol without dose reductions and without intolerable adverse side effects. Change in mean PANSS total score from baseline to Day 7 was statistically significant (p = 0.00006; 95 % CI [19.60–38.40]), as were YMRS scores (p = 0.01; 95 % CI [2.69–16.01]) and HAM-D scores (p = 0.0003; 95 % CI [5.22–11.98]).

Conclusions

This study suggests the potential for neuroactive steroids as rapid-acting, adjunctive treatment for PPP and provides support for future research to assess the role of neuroactive steroids and synthetic forms of allopregnanolone in the treatment of PPP.
目的:产后精神病(PPP)是一种罕见但严重的产后精神疾病,发生在母婴依恋的关键时期。本研究调查了布雷沙诺酮(一种神经活性类固醇和异孕酮的合成形式)对患有PPP的成年女性的疗效、安全性和耐受性。方法:在这项开放标签的概念验证研究中,10例PPP患者接受布雷沙诺酮单次连续60小时静脉滴注,在2.5天的时间内滴注目标剂量为90 μg/kg/h。主要结局为青年躁狂症评定量表(YMRS)和阳性与阴性综合征量表(PANSS)总分的变化;次要结局包括汉密尔顿抑郁评定量表(HAMD)从基线到第7天的变化。监测不良事件。患者随访至第90天。结果:10例患者均完成了治疗方案,无减量,无不可忍受的不良反应。从基线到第7天,平均PANSS总分的变化具有统计学意义(p = 0.00006; 95% CI [19.60-38.40]), YMRS评分(p = 0.01; 95% CI[2.69-16.01])和HAM-D评分(p = 0.0003; 95% CI[5.22-11.98])也具有统计学意义。结论:本研究提示神经活性类固醇作为PPP的速效辅助治疗的潜力,并为未来研究评估神经活性类固醇和合成异孕酮在PPP治疗中的作用提供了支持。
{"title":"Open-label study of the efficacy, safety and tolerability of Brexanolone in the treatment of adult women with postpartum psychosis","authors":"Riah Patterson ,&nbsp;Holly Krohn ,&nbsp;Elizabeth Richardson ,&nbsp;Cecilia Pearson ,&nbsp;Kai Xia ,&nbsp;Mary Kimmel ,&nbsp;Samantha Meltzer-Brody","doi":"10.1016/j.genhosppsych.2025.10.017","DOIUrl":"10.1016/j.genhosppsych.2025.10.017","url":null,"abstract":"<div><h3>Objective</h3><div>Postpartum psychosis (PPP) is a rare but severe postpartum psychiatric emergency that occurs during a critical time in mother-infant attachment. This study investigated the efficacy, safety, and tolerability of brexanolone, a neuroactive steroid and synthetic form of allopregnanolone, for adult females with PPP.</div></div><div><h3>Methods</h3><div>In this open-label, proof-of-concept study, ten patients with PPP received brexanolone as a single, continuous, 60-h intravenous infusion titrated to a target dose of 90 μg/kg/h over a period of 2.5 days. Primary outcomes were change in total score on the Young Mania Rating Scale (YMRS) and Positive and Negative Syndrome Scale (PANSS); Secondary outcomes included change in Hamilton Depression Rating Scale (HAM<img>D) from baseline to Day 7. Adverse events were monitored. Patients were followed through Day 90.</div></div><div><h3>Results</h3><div>All ten patients completed the treatment protocol without dose reductions and without intolerable adverse side effects. Change in mean PANSS total score from baseline to Day 7 was statistically significant (<em>p</em> = 0.00006; 95 % CI [19.60–38.40]), as were YMRS scores (<em>p</em> = 0.01; 95 % CI [2.69–16.01]) and HAM-D scores (<em>p</em> = 0.0003; 95 % CI [5.22–11.98]).</div></div><div><h3>Conclusions</h3><div>This study suggests the potential for neuroactive steroids as rapid-acting, adjunctive treatment for PPP and provides support for future research to assess the role of neuroactive steroids and synthetic forms of allopregnanolone in the treatment of PPP.</div></div>","PeriodicalId":12517,"journal":{"name":"General hospital psychiatry","volume":"97 ","pages":"Pages 237-240"},"PeriodicalIF":3.7,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145458266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Cognitive function among stable schizophrenia patients receiving an mHealth app-based cognitive remediation therapy: randomized controlled trial with mediation analysis 接受基于移动健康应用程序的认知修复治疗的稳定型精神分裂症患者的认知功能:随机对照试验与中介分析
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.10.013
Min Wen , Xiaoyao Liu , Ying He , Weiguo Xu , Yongling Zhou , Juan Liu , Xiaodan Zhu

Objective

To explore the application effect and underlying mechanisms of mHealth app-based cognitive remediation therapy on the cognitive function of patients with stable schizophrenia.

Methods

This study was a randomized controlled trial, patients received either treatment as usual or mHealth app-based cognitive remediation therapy. Guided by the theoretical framework integrating the MCI theoretical model of rehabilitation, we examined the mediating roles of self-efficacy and negative emotion in the relationship between intervention subgroups and cognitive functioning. These outcome indicators were assessed at baseline, the primary endpoint, and the follow-up endpoint. Linear mixed-effects modeling was employed to compare these measures between the two patient groups, with all analyses adhering to the intention-to-treat principle. Mediation analyses were conducted using the PROCESS. The significance of mediation effects was assessed through bias-corrected nonparametric percentile bootstrap analysis.

Results

Linear mixed-effects models revealed statistically significant group*time interaction effects at both the primary endpoint (post-intervention) and the follow-up endpoint (3-month post-intervention) for cognitive functioning (P = 0.001), psychiatric symptoms (P < 0.001), self-efficacy (P < 0.001), and negative emotions (P < 0.001). Analysis of these interactions indicated that, compared to the TAU group, the CRT group demonstrated significantly greater improvement in cognitive function and self-efficacy, and significantly greater reduction in psychiatric symptoms and negative emotions over time. Mediation analyses further indicated that self-efficacy scores partially mediated the relationship between the intervention groupings and cognitive function scores (indirect effect of 0.237, 95 % CI [0.073, 0.414]). Similarly, negative emotion scores were found to partially mediate this relationship (indirect effect of 0.154, 95 % CI [0.029, 0.323]).

Conclusion

Cognitive remediation therapy delivered through mHealth app for patients with stable schizophrenia has been shown to effectively improve cognitive functioning. Moreover, this intervention may exert an indirect positive effect on cognitive performance mediated by negative emotions and self-efficacy.
目的:探讨基于移动健康app的认知修复疗法对稳定型精神分裂症患者认知功能的应用效果及其机制。方法:本研究是一项随机对照试验,患者接受常规治疗或基于移动健康应用程序的认知修复治疗。在整合MCI康复理论模型的理论框架指导下,我们考察了自我效能感和负性情绪在干预亚组与认知功能关系中的中介作用。这些结局指标在基线、主要终点和随访终点进行评估。采用线性混合效应模型比较两组患者的这些措施,所有分析均遵循意向治疗原则。使用PROCESS进行中介分析。通过偏差校正的非参数百分位自举分析评估中介效应的显著性。结果:线性混合效应模型显示,在主要终点(干预后)和随访终点(干预后3个月),认知功能(P = 0.001)和精神症状(P)方面,组*时间交互作用具有统计学意义(P = 0.001)。结论:通过移动健康应用程序对稳定型精神分裂症患者进行认知修复治疗已被证明可以有效改善认知功能。此外,这种干预可能对负性情绪和自我效能介导的认知表现产生间接的积极影响。
{"title":"Cognitive function among stable schizophrenia patients receiving an mHealth app-based cognitive remediation therapy: randomized controlled trial with mediation analysis","authors":"Min Wen ,&nbsp;Xiaoyao Liu ,&nbsp;Ying He ,&nbsp;Weiguo Xu ,&nbsp;Yongling Zhou ,&nbsp;Juan Liu ,&nbsp;Xiaodan Zhu","doi":"10.1016/j.genhosppsych.2025.10.013","DOIUrl":"10.1016/j.genhosppsych.2025.10.013","url":null,"abstract":"<div><h3>Objective</h3><div>To explore the application effect and underlying mechanisms of mHealth app-based cognitive remediation therapy on the cognitive function of patients with stable schizophrenia.</div></div><div><h3>Methods</h3><div>This study was a randomized controlled trial, patients received either treatment as usual or mHealth app-based cognitive remediation therapy. Guided by the theoretical framework integrating the MCI theoretical model of rehabilitation, we examined the mediating roles of self-efficacy and negative emotion in the relationship between intervention subgroups and cognitive functioning. These outcome indicators were assessed at baseline, the primary endpoint, and the follow-up endpoint. Linear mixed-effects modeling was employed to compare these measures between the two patient groups, with all analyses adhering to the intention-to-treat principle. Mediation analyses were conducted using the PROCESS. The significance of mediation effects was assessed through bias-corrected nonparametric percentile bootstrap analysis.</div></div><div><h3>Results</h3><div>Linear mixed-effects models revealed statistically significant group*time interaction effects at both the primary endpoint (post-intervention) and the follow-up endpoint (3-month post-intervention) for cognitive functioning (<em>P</em> = 0.001), psychiatric symptoms (<em>P</em> &lt; 0.001), self-efficacy (<em>P</em> &lt; 0.001), and negative emotions (<em>P</em> &lt; 0.001). Analysis of these interactions indicated that, compared to the TAU group, the CRT group demonstrated significantly greater improvement in cognitive function and self-efficacy, and significantly greater reduction in psychiatric symptoms and negative emotions over time. Mediation analyses further indicated that self-efficacy scores partially mediated the relationship between the intervention groupings and cognitive function scores (indirect effect of 0.237, 95 % CI [0.073, 0.414]). Similarly, negative emotion scores were found to partially mediate this relationship (indirect effect of 0.154, 95 % CI [0.029, 0.323]).</div></div><div><h3>Conclusion</h3><div>Cognitive remediation therapy delivered through mHealth app for patients with stable schizophrenia has been shown to effectively improve cognitive functioning. Moreover, this intervention may exert an indirect positive effect on cognitive performance mediated by negative emotions and self-efficacy.</div></div>","PeriodicalId":12517,"journal":{"name":"General hospital psychiatry","volume":"97 ","pages":"Pages 225-234"},"PeriodicalIF":3.7,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145451359","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
The relationship between cognitive function and depressive symptoms in Chinese older adults: A cross-lagged panel network analysis 中国老年人认知功能与抑郁症状的关系:一个交叉滞后面板网络分析
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-11-01 DOI: 10.1016/j.genhosppsych.2025.10.016
Shuaichen Li , Jinglan Tan , Yanwei Guo , Junyao Li , Renqin Hu , Jiayi Ge , Yiran Feng , Wenjing Zhao , Qinghua Luo

Background

The bidirectional association between depressive symptoms and cognitive decline has been extensively studied in Western populations, yet empirical evidence from non-Western contexts, particularly among Chinese older adults, remains limited. This study aimed to examine the longitudinal and symptom-level dynamics between depressive symptoms and cognitive functioning using a cross-lagged panel network (CLPN) approach.

Methods

Data were drawn from two waves (2015, 2018) of the China Health and Retirement Longitudinal Study (CHARLS), including 6824 individuals aged 50 years and above. Cognitive performance was assessed via the China Mini-Mental State Examination (CMMSE), and depressive symptoms were measured using the 8-item Center for Epidemiological Studies Depression Scale (CESD-8). A CLPN model was estimated to identify temporally predictive pathways and symptom-level interactions, with LASSO regularization ensuring model sparsity. Model stability was evaluated through nonparametric bootstrapping.

Results

Findings revealed a reciprocal, predominantly negative relationship between cognitive decline and depressive symptoms over time. “Mental State” (orientation, processing, and visuospatial skills) emerged as the central network hub and primary bridge from cognition to depression, while lack of motivation (“ I felt everything was an effort”) was the pivotal bridge symptom from depression to cognition. Specifically, “I felt everything was an effort” predicted subsequent declines in memory function, whereas better mental state predicted reduced depressive symptoms, including feeling depressed, trouble concentrating, and restless sleep. The network model highlighted symptom-specific pathways not observable in traditional latent variable models.

Conclusions

This study underscores the clinical and public health value of integrated screening and interventions targeting both depressive symptoms and cognitive impairment in older adults. Motivational deficits and mental state deficits may serve as actionable transdiagnostic targets. Future interventions should be symptom-specific, modular, and culturally sensitive. Longitudinal neurobiological studies are warranted to elucidate underlying mechanisms.
背景:在西方人群中,抑郁症状与认知能力下降之间的双向关联已被广泛研究,但非西方背景下的经验证据,特别是在中国老年人中,仍然有限。本研究旨在使用交叉滞后面板网络(CLPN)方法检查抑郁症状和认知功能之间的纵向和症状水平动态。方法:数据来源于中国健康与退休纵向研究(CHARLS)的两波(2015年、2018年),共6824名50岁及以上的个体。通过中国简易精神状态检查(CMMSE)评估认知能力,使用8项流行病学研究中心抑郁量表(csd -8)测量抑郁症状。估计CLPN模型用于识别时间预测途径和症状水平的相互作用,使用LASSO正则化确保模型稀疏性。通过非参数自举评估模型的稳定性。结果:研究结果显示,随着时间的推移,认知能力下降和抑郁症状之间存在相互的、主要为负的关系。“精神状态”(定向、处理和视觉空间技能)是认知到抑郁的中心网络枢纽和主要桥梁,而缺乏动机(“我觉得一切都是努力”)是从抑郁到认知的关键桥梁症状。具体来说,“我觉得一切都是一种努力”预示着随后记忆功能的下降,而更好的精神状态预示着抑郁症状的减少,包括情绪低落、注意力难以集中和睡眠不安。网络模型强调了传统潜在变量模型中无法观察到的症状特异性途径。结论:本研究强调了针对老年人抑郁症状和认知障碍的综合筛查和干预的临床和公共卫生价值。动机缺陷和精神状态缺陷可以作为可操作的跨诊断目标。未来的干预措施应针对具体症状,采取模块化措施,并具有文化敏感性。纵向神经生物学研究有必要阐明潜在的机制。
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引用次数: 0
A guideline-based perspective on neurostimulation in treatment-resistant obsessive-compulsive disorder: An international overview 基于指南的神经刺激治疗难治性强迫症:国际综述
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-21 DOI: 10.1016/j.genhosppsych.2025.10.014
Nadine D. Wolf , Martin Jakobs , R. Christian Wolf

Background

Obsessive-compulsive disorder (OCD) is a severe psychiatric illness associated with substantial psychosocial burden. Although evidence-based first- and second-line treatments are often effective, a significant proportion of patients continue to experience treatment-resistant symptoms. In such cases, brain neurostimulation is gaining increasing attention. This study aims to provide a structured overview of national and international clinical guidelines for the management of treatment-resistant OCD, with a particular focus on neurostimulation techniques.

Materials and methods

Relevant clinical guidelines were identified and compared with respect to their recommendations on various neurostimulatory procedures. Among the approaches examined were transcranial magnetic stimulation (TMS), electroconvulsive therapy (ECT), Deep Brain Stimulation (DBS), ablative neurosurgical procedures, and further techniques such as transcranial direct current stimulation (tDCS).

Results

Across guidelines, DBS is regarded as a potentially effective treatment option for carefully selected, severely affected patients. Its use is restricted to specialized centers and requires an interdisciplinary treatment approach. Ablative procedures are endorsed by certain guidelines solely in exceptionally severe cases. The evidence basis for TMS remains inconsistent, though certain stimulation protocols have shown short-term efficacy. For ECT and tDCS, current evidence is insufficient to support their use in targeting core OCD symptoms.

Conclusions

Overall, the reviewed guidelines emphasize the need for clearly defined indications, standardized treatment protocols, and continuous scientific evaluation. Invasive procedures are not considered standard treatment but represent highly specialized therapeutic options within interdisciplinary care frameworks.
背景:强迫症(OCD)是一种严重的精神疾病,伴有严重的社会心理负担。尽管循证一线和二线治疗通常有效,但仍有很大一部分患者出现治疗抵抗症状。在这种情况下,脑神经刺激正获得越来越多的关注。本研究旨在为治疗难治性强迫症的管理提供国家和国际临床指南的结构化概述,特别关注神经刺激技术。材料和方法确定了相关的临床指南,并比较了它们对各种神经刺激手术的推荐。研究的方法包括经颅磁刺激(TMS)、电休克治疗(ECT)、深部脑刺激(DBS)、烧蚀性神经外科手术以及进一步的技术,如经颅直流电刺激(tDCS)。结果:在指南中,DBS被认为是精心挑选的严重影响患者的潜在有效治疗选择。它的使用仅限于专业中心,需要跨学科的治疗方法。消融手术只有在特别严重的情况下才得到某些指导方针的认可。尽管某些刺激方案显示出短期疗效,但颅磁刺激的证据基础仍不一致。对于ECT和tDCS,目前的证据不足以支持它们用于治疗核心强迫症症状。结论总的来说,修订后的指南强调了明确适应症、标准化治疗方案和持续科学评价的必要性。侵入性手术不被认为是标准治疗,但在跨学科护理框架中代表了高度专业化的治疗选择。
{"title":"A guideline-based perspective on neurostimulation in treatment-resistant obsessive-compulsive disorder: An international overview","authors":"Nadine D. Wolf ,&nbsp;Martin Jakobs ,&nbsp;R. Christian Wolf","doi":"10.1016/j.genhosppsych.2025.10.014","DOIUrl":"10.1016/j.genhosppsych.2025.10.014","url":null,"abstract":"<div><h3>Background</h3><div>Obsessive-compulsive disorder (OCD) is a severe psychiatric illness associated with substantial psychosocial burden. Although evidence-based first- and second-line treatments are often effective, a significant proportion of patients continue to experience treatment-resistant symptoms. In such cases, brain neurostimulation is gaining increasing attention. This study aims to provide a structured overview of national and international clinical guidelines for the management of treatment-resistant OCD, with a particular focus on neurostimulation techniques.</div></div><div><h3>Materials and methods</h3><div>Relevant clinical guidelines were identified and compared with respect to their recommendations on various neurostimulatory procedures. Among the approaches examined were transcranial magnetic stimulation (TMS), electroconvulsive therapy (ECT), Deep Brain Stimulation (DBS), ablative neurosurgical procedures, and further techniques such as transcranial direct current stimulation (tDCS).</div></div><div><h3>Results</h3><div>Across guidelines, DBS is regarded as a potentially effective treatment option for carefully selected, severely affected patients. Its use is restricted to specialized centers and requires an interdisciplinary treatment approach. Ablative procedures are endorsed by certain guidelines solely in exceptionally severe cases. The evidence basis for TMS remains inconsistent, though certain stimulation protocols have shown short-term efficacy. For ECT and tDCS, current evidence is insufficient to support their use in targeting core OCD symptoms.</div></div><div><h3>Conclusions</h3><div>Overall, the reviewed guidelines emphasize the need for clearly defined indications, standardized treatment protocols, and continuous scientific evaluation. Invasive procedures are not considered standard treatment but represent highly specialized therapeutic options within interdisciplinary care frameworks.</div></div>","PeriodicalId":12517,"journal":{"name":"General hospital psychiatry","volume":"97 ","pages":"Pages 196-202"},"PeriodicalIF":3.7,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145358707","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Efficacy and safety of quetiapine prophylaxis for delirium in hospitalized adult patients: A systematic review and meta-analysis of randomized controlled trials 奎硫平预防住院成年患者谵妄的疗效和安全性:随机对照试验的系统回顾和荟萃分析
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-21 DOI: 10.1016/j.genhosppsych.2025.10.011
Raj Kiran Donthu , Sneha Mary Minz , Mamidipalli Sai Spoorthy , R. Dyuthy , A. Balaji , P.S. Sethu , Libnus B. Varghese , Shahul Ameen , Brijesh Sathian , Vikas Menon

Objective

We aimed to compare summary estimates of efficacy and safety of quetiapine versus comparator treatments in preventing delirium among hospitalized adult patients by pooling evidence from parallel-group randomized controlled trials (RCTs).

Methods

We searched MEDLINE, Embase, Scopus, and clinical trial registers from inception till January 31st, 2025. Our primary outcome was between-group incidence of delirium. Secondary outcomes included 10-day mortality, duration of hospital stay, duration of delirium, severity of delirium, readmission rates (efficacy outcomes), and reported adverse effects (safety outcomes).

Results

Six eligible RCTs (pooled N = 491) were identified; of these, five were included in the meta-analysis. The pooled RR for preventing the incidence of delirium was 0.61 (95 % CI, 0.45–0.83;5 RCTs; I2 = 0;p = .001), favoring quetiapine (dose range 12.5-75 mg/day). The SMD for duration of delirium was −1.21 (95 % CI, −2.08 to −0.35; 3 RCTs; I2 = 86 %; p = .006), again favoring quetiapine. No significant between-group differences were noted on other outcomes. Adverse effects with quetiapine were absent in four studies and minimal in the other two. The findings were robust to sensitivity analyses.

Conclusion

Low-dose quetiapine prophylaxis may be a safe and effective treatment option for preventing delirium. These conclusions are tempered by the small number and size of existing trials.
目的:我们旨在通过汇集平行组随机对照试验(rct)的证据,比较奎硫平与比较药物治疗在预防住院成年患者谵妄方面的有效性和安全性的总结估计。方法:检索MEDLINE、Embase、Scopus和临床试验注册库,检索时间从成立到2025年1月31日。我们的主要结局是组间谵妄的发生率。次要结局包括10天死亡率、住院时间、谵妄持续时间、谵妄严重程度、再入院率(疗效结局)和报告的不良反应(安全性结局)。结果:共纳入6项符合条件的rct(共N = 491);其中5例纳入meta分析。预防谵谵症发生率的合并RR为0.61 (95% CI, 0.45-0.83;5个rct; I2 = 0;p = .001),支持喹硫平(剂量范围12.5-75 mg/天)。谵妄持续时间的SMD为-1.21 (95% CI, -2.08至-0.35;3个rct; I2 = 86%; p = 0.006),再次有利于喹硫平。其他结果组间无显著差异。四项研究没有喹硫平的不良反应,另外两项研究的不良反应最小。这些发现在敏感性分析中是稳健的。结论:低剂量喹硫平预防谵妄可能是一种安全有效的治疗选择。这些结论受到现有试验数量和规模较小的影响。
{"title":"Efficacy and safety of quetiapine prophylaxis for delirium in hospitalized adult patients: A systematic review and meta-analysis of randomized controlled trials","authors":"Raj Kiran Donthu ,&nbsp;Sneha Mary Minz ,&nbsp;Mamidipalli Sai Spoorthy ,&nbsp;R. Dyuthy ,&nbsp;A. Balaji ,&nbsp;P.S. Sethu ,&nbsp;Libnus B. Varghese ,&nbsp;Shahul Ameen ,&nbsp;Brijesh Sathian ,&nbsp;Vikas Menon","doi":"10.1016/j.genhosppsych.2025.10.011","DOIUrl":"10.1016/j.genhosppsych.2025.10.011","url":null,"abstract":"<div><h3>Objective</h3><div>We aimed to compare summary estimates of efficacy and safety of quetiapine versus comparator treatments in preventing delirium among hospitalized adult patients by pooling evidence from parallel-group randomized controlled trials (RCTs).</div></div><div><h3>Methods</h3><div>We searched MEDLINE, Embase, Scopus, and clinical trial registers from inception till January 31st, 2025. Our primary outcome was between-group incidence of delirium. Secondary outcomes included 10-day mortality, duration of hospital stay, duration of delirium, severity of delirium, readmission rates (efficacy outcomes), and reported adverse effects (safety outcomes).</div></div><div><h3>Results</h3><div>Six eligible RCTs (pooled <em>N</em> = 491) were identified; of these, five were included in the meta-analysis. The pooled RR for preventing the incidence of delirium was 0.61 (95 % CI, 0.45–0.83;5 RCTs; I<sup>2</sup> = 0;<em>p</em> = .001), favoring quetiapine (dose range 12.5-75 mg/day). The SMD for duration of delirium was −1.21 (95 % CI, −2.08 to −0.35; 3 RCTs; I<sup>2</sup> = 86 %; <em>p</em> = .006), again favoring quetiapine. No significant between-group differences were noted on other outcomes. Adverse effects with quetiapine were absent in four studies and minimal in the other two. The findings were robust to sensitivity analyses.</div></div><div><h3>Conclusion</h3><div>Low-dose quetiapine prophylaxis may be a safe and effective treatment option for preventing delirium. These conclusions are tempered by the small number and size of existing trials.</div></div>","PeriodicalId":12517,"journal":{"name":"General hospital psychiatry","volume":"97 ","pages":"Pages 192-195"},"PeriodicalIF":3.7,"publicationDate":"2025-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145354394","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"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
Treatment of cannabinoid hyperemesis syndrome: A systematic review and treatment algorithm for consultation-liaison psychiatrists 大麻素呕吐综合征的治疗:会诊-联络精神科医生的系统回顾和治疗算法。
IF 3.7 2区 医学 Q1 PSYCHIATRY Pub Date : 2025-10-17 DOI: 10.1016/j.genhosppsych.2025.10.012
Jennifer Hsu , Saurabh Kashyap , Cheryl Hurd , Lauren McCormack , Zachary Herrmann , Ann C. Schwartz , Joshua Jackson , Dustin DeMoss

Background

Cannabinoid Hyperemesis Syndrome (CHS) is a cyclical vomiting syndrome associated with chronic cannabis use and is often resistant to anti-emetics. Despite increasing incidence of suspected CHS, literature regarding its treatment is limited, and there are no established treatment guidelines.

Objectives

With the goal of establishing treatment guidelines for consultation-liaison (C-L) psychiatrists managing CHS, the authors systematically reviewed existing literature for pharmacologic treatment strategies using Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. With the results of the review, the authors propose a treatment algorithm for CHS.

Methods

We searched PubMed, PyschINFO & PsychARTICLES, Embase, and Web of Science from inception to July 2021 to identify literature describing treatment of CHS. We included cases of CHS where patient-level data describing the treatment of CHS was available. Pharmacologic treatments were considered beneficial if the patient's nausea, hyperemesis, and urge to take hot showers resolved. Non-independent review of exclusion criteria assisted in reducing individual bias of the literature.

Results

The authors identified 34 eligible articles, consisting of 63 individual cases. Among these articles and cases, capsaicin cream, antipsychotics, and benzodiazepines were reported to improve CHS more effectively than other, more frequently used anti-emetics, such as promethazine, ondansetron, and metoclopramide.

Conclusion

An examination of treatment strategies for CHS can allow for more effective care while providing a foundation for further research in treatment. This proposed algorithm is designed to aid in establishing treatment strategies for C-L psychiatrists who assist with managing CHS for patients in general medical settings. The goal of this research is to establish evidence-based treatment guidelines for C-L psychiatrists who are managing patients with CHS in general medical settings. Recognizing the limitations of this algorithm being based on case reports adds to the necessity of further research in this area.

Registration

PROSPERO (https://www.crd.york.ac.uk/PROSPERO/view/CRD42021254888) registration number CRD42021254888.
背景:大麻素呕吐综合征(CHS)是一种周期性呕吐综合征,与慢性大麻使用有关,通常对止吐药有抗性。尽管疑似CHS的发病率越来越高,但有关其治疗的文献有限,也没有既定的治疗指南。目的:为了建立咨询联络(C-L)精神科医生管理CHS的治疗指南,作者使用系统评价和荟萃分析(PRISMA)指南的首选报告项目系统地回顾了现有的药物治疗策略文献。根据综述的结果,作者提出了一种治疗CHS的算法。方法:我们检索PubMed, PyschINFO & PsychARTICLES, Embase和Web of Science从成立到2021年7月,以确定描述CHS治疗的文献。我们纳入了描述CHS治疗的患者水平数据可用的CHS病例。如果患者的恶心、呕吐和洗热水澡的冲动得到缓解,药物治疗被认为是有益的。排除标准的非独立评价有助于减少文献的个体偏倚。结果:作者确定了34篇符合条件的文章,包括63例个案。在这些文章和病例中,辣椒素乳膏、抗精神病药物和苯二氮卓类药物被报道比其他更常用的止吐药,如异丙嗪、昂丹西琼和甲氧氯普胺更有效地改善CHS。结论:对CHS的治疗策略进行研究可以提供更有效的治疗,同时为进一步的治疗研究提供基础。该算法旨在帮助在一般医疗环境中协助管理CHS患者的C-L精神科医生建立治疗策略。本研究的目的是为在一般医疗环境中管理CHS患者的C-L精神科医生建立循证治疗指南。认识到该算法基于病例报告的局限性,增加了在该领域进一步研究的必要性。报名:普洛斯彼罗(https://www.crd.york.ac.uk/PROSPERO/view/CRD42021254888)注册号CRD42021254888。
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引用次数: 0
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General hospital psychiatry
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