Centre for Youth Mental Health - Research Publications

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    Validation of a brief tool to assess and monitor suicidal ideation: The Youth Suicide Ideation Screen (YSIS-3)
    Hetrick, SE ; Gao, CX ; Filia, KM ; Menssink, JM ; Rickwood, DJ ; Herrman, H ; Hickie, I ; McGorry, P ; Telford, N ; Parker, AG ; Cotton, SM (ELSEVIER, 2021-12-01)
    BACKGROUND: . Suicidal ideation is common in young people. Assessment and monitoring can help to understand its dynamic nature and inform treatment planning. AIMS: . The aims were to evaluate psychometric properties of a brief screening tool - the Youth Suicide Ideation Screen-3 item (YSIS-3) and determine its correlation with the Suicidal Ideation Question-Junior (SIQ-JR) and measures of depressive and anxiety symptoms a. METHOD: . Cronbach's alpha (α) was used to evaluate internal consistency of the YSIS-3 in 1107 young people. Convergent validity was evaluated using network analysis based on individual item polychoric correlations. Structural equation modelling was used to understand latent constructs; pearson product moment correlations to validate the integrity of the underlying construct. and two-way mixed Intraclass Correlation Coefficient to examine longitudinal stability and Cohen's d to assess sensitivity to change. RESULTS: . The YSIS-3 was found to have internal consistency, convergent validity and criteria validity almost identical to the 15-item SIQ-JR. There was a high correlation (0.91) between the latent factor underpinning YSIS-3 and SIQ-JR. The YSIS-3 was more sensitive to change among those presenting with suicidal ideation at baseline. CONCLUSIONS: . The YSIS-3 is a valid measure for the assessment and monitoring of suicidal ideation, and is sensitive to change. This brief measure can contribute to regular monitoring of the presence and nature of suicidal ideation, which when included in comprehensive assessment, will inform the clinical management of those at risk of suicide.
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    A Systematic Review and Synthesis of Trauma-Informed Care Within Outpatient and Counseling Health Settings for Young People
    Bendall, S ; Eastwood, O ; Cox, G ; Farrelly-Rosch, A ; Nicoll, H ; Peters, W ; Bailey, AP ; McGorry, PD ; Scanlan, F (SAGE PUBLICATIONS INC, 2021-08)
    There is growing consensus that outpatient health services for young people (aged 12-25 years) need to deliver trauma-informed care to ameliorate the effects of trauma, offer safe treatments, and avoid retraumatization. Trauma-informed care has become a familiar term for many professionals; however, its operating definition lacks clarity. MEDLINE, Embase, and PsycINFO were systematically searched to clarify what trauma-informed care is, and what it should achieve in these settings. We reviewed 3,381 unique records, of which 13 met criteria for inclusion. Content analysis identified 10 components of trauma-informed care as it has been operationalized in practice: seven of these occurred at the system-level (interagency collaboration; service provider training; safety; leadership, governance and agency processes; youth and family/carer choice in care; cultural and gender sensitivity; youth and family/carer participation), and three involved trauma-specific clinical practices (screening and assessment; psychoeducation; therapeutic interventions). There is a need for greater consensus regarding an operating definition of trauma-informed care and further research into outcomes for young people and their families/carers.
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    [Early Intervention for Psychosis from Past to Future: Overcoming Implementation Challenges to Maximize its Impact?].
    Malla, A ; Roy, M-A ; Abdel-Baki, A ; Conus, P ; McGorry, P (Consortium Erudit, 2021)
    Objectives The emergence of early intervention for first episode psychosis (FEP) in the 1990s represents a major advance in mental health. It was demonstrated that by providing intensive interventions tailored to the specific needs of youth at the onset of FEP, it became possible to sustainably improve their subsequent course. This model of early intervention for psychosis (EIP) is accompanied by a major revision of conceptions of psychotic disorders and a major change in philosophy of care. The purpose of this article is to provide a historical perspective on the development of EIP, to discuss the challenges associated with its implementation, and to offer possible solutions. Methods Experts consensus identifying the most salient challenges in implementing Early intervention for psychosis, and proposing the most feasible solutions, based on their assessment of the literature to address them. Results To optimize the implementation and efficiency of EIP programs, 7 avenues were identified: 1) Better targeting of hard-to-reach populations and systematizing the admission of all FEP patients in EIP programs. 2) Reducing the duration of untreated psychosis should be a major goal of EIP programs, requiring early detection efforts through public awareness, training of front-line professionals, and improving treatment access processes and delays. 3) Measures to maintain patient engagement in a follow-up should be implemented systematically. 4) Family involvement should be more actively supported by teams throughout follow-up, including strategies to promote patient acceptance of their involvement. 5) Future research will provide a better understanding of how to modulate the duration and intensity of EIP follow-up according to patient profiles, in particular in order to maintain the results achieved during PPEP over the longer term. 6) The modalities for managing at-risk mental states remain to be clarified, both in terms of the approaches to be offered to them and the health care structure that would be most appropriate to accommodate them. 7) The implementation of EIP programs must be continued, particularly in the French-speaking world, which is at very different stages from one country to another and even within each country. Conclusion EIP improve the outcomes of youth with FEP in terms of recovery, mortality and suicide. Solutions to challenges encountered in their widespread implementation must be operationalized to ensure that this care is accessible to the greatest number of people in a timely manner to maximize its impact at the population level.
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    Association of Structural Magnetic Resonance Imaging Measures With Psychosis Onset in Individuals at Clinical High Risk for Developing Psychosis An ENIGMA Working Group Mega-analysis
    Jalbrzikowski, M ; Hayes, RA ; Wood, SJ ; Nordholm, D ; Zhou, JH ; Fusar-Poli, P ; Uhlhaas, PJ ; Takahashi, T ; Sugranyes, G ; Kwak, YB ; Mathalon, DH ; Katagiri, N ; Hooker, CI ; Smigielski, L ; Colibazzi, T ; Via, E ; Tang, J ; Koike, S ; Rasser, PE ; Michel, C ; Lebedeva, I ; Hegelstad, WTV ; de la Fuente-Sandoval, C ; Waltz, JA ; Mizrahi, R ; Corcoran, CM ; Resch, F ; Tamnes, CK ; Haas, SS ; Lemmers-Jansen, ILJ ; Agartz, I ; Allen, P ; Amminger, GP ; Andreassen, OA ; Atkinson, K ; Bachman, P ; Baeza, I ; Baldwin, H ; Bartholomeusz, CF ; Borgwardt, S ; Catalano, S ; Chee, MWL ; Chen, X ; Cho, KIK ; Cooper, RE ; Cropley, VL ; Dolz, M ; Ebdrup, BH ; Fortea, A ; Glenthoj, LB ; Glenthoj, BY ; de Haan, L ; Hamilton, HK ; Harris, MA ; Haut, KM ; He, Y ; Heekeren, K ; Heinz, A ; Hubl, D ; Hwang, WJ ; Kaess, M ; Kasai, K ; Kim, M ; Kindler, J ; Klaunig, MJ ; Koppel, A ; Kristensen, TD ; Kwon, JS ; Lawrie, SM ; Lee, J ; Leon-Ortiz, P ; Lin, A ; Loewy, RL ; Ma, X ; McGorry, P ; McGuire, P ; Mizuno, M ; Moller, P ; Moncada-Habib, T ; Munoz-Samons, D ; Nelson, B ; Nemoto, T ; Nordentoft, M ; Omelchenko, MA ; Oppedal, K ; Ouyang, L ; Pantelis, C ; Pariente, JC ; Raghava, JM ; Reyes-Madrigal, F ; Roach, BJ ; Rossberg, JI ; Rossler, W ; Salisbury, DF ; Sasabayashi, D ; Schall, U ; Schiffman, J ; Schlagenhauf, F ; Schmidt, A ; Sorensen, ME ; Suzuki, M ; Theodoridou, A ; Tomyshev, AS ; Tor, J ; Vaernes, TG ; Velakoulis, D ; Venegoni, GD ; Vinogradov, S ; Wenneberg, C ; Westlye, LT ; Yamasue, H ; Yuan, L ; Yung, AR ; van Amelsvoort, TAMJ ; Turner, JA ; van Erp, TGM ; Thompson, PM ; Hernaus, D (AMER MEDICAL ASSOC, 2021-07)
    IMPORTANCE: The ENIGMA clinical high risk (CHR) for psychosis initiative, the largest pooled neuroimaging sample of individuals at CHR to date, aims to discover robust neurobiological markers of psychosis risk. OBJECTIVE: To investigate baseline structural neuroimaging differences between individuals at CHR and healthy controls as well as between participants at CHR who later developed a psychotic disorder (CHR-PS+) and those who did not (CHR-PS-). DESIGN, SETTING, AND PARTICIPANTS: In this case-control study, baseline T1-weighted magnetic resonance imaging (MRI) data were pooled from 31 international sites participating in the ENIGMA Clinical High Risk for Psychosis Working Group. CHR status was assessed using the Comprehensive Assessment of At-Risk Mental States or Structured Interview for Prodromal Syndromes. MRI scans were processed using harmonized protocols and analyzed within a mega-analysis and meta-analysis framework from January to October 2020. MAIN OUTCOMES AND MEASURES: Measures of regional cortical thickness (CT), surface area, and subcortical volumes were extracted from T1-weighted MRI scans. Independent variables were group (CHR group vs control group) and conversion status (CHR-PS+ group vs CHR-PS- group vs control group). RESULTS: Of the 3169 included participants, 1428 (45.1%) were female, and the mean (SD; range) age was 21.1 (4.9; 9.5-39.9) years. This study included 1792 individuals at CHR and 1377 healthy controls. Using longitudinal clinical information, 253 in the CHR-PS+ group, 1234 in the CHR-PS- group, and 305 at CHR without follow-up data were identified. Compared with healthy controls, individuals at CHR exhibited widespread lower CT measures (mean [range] Cohen d = -0.13 [-0.17 to -0.09]), but not surface area or subcortical volume. Lower CT measures in the fusiform, superior temporal, and paracentral regions were associated with psychosis conversion (mean Cohen d = -0.22; 95% CI, -0.35 to 0.10). Among healthy controls, compared with those in the CHR-PS+ group, age showed a stronger negative association with left fusiform CT measures (F = 9.8; P < .001; q < .001) and left paracentral CT measures (F = 5.9; P = .005; q = .02). Effect sizes representing lower CT associated with psychosis conversion resembled patterns of CT differences observed in ENIGMA studies of schizophrenia (ρ = 0.35; 95% CI, 0.12 to 0.55; P = .004) and individuals with 22q11.2 microdeletion syndrome and a psychotic disorder diagnosis (ρ = 0.43; 95% CI, 0.20 to 0.61; P = .001). CONCLUSIONS AND RELEVANCE: This study provides evidence for widespread subtle, lower CT measures in individuals at CHR. The pattern of CT measure differences in those in the CHR-PS+ group was similar to those reported in other large-scale investigations of psychosis. Additionally, a subset of these regions displayed abnormal age associations. Widespread disruptions in CT coupled with abnormal age associations in those at CHR may point to disruptions in postnatal brain developmental processes.
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    Preventive interventions for individuals at ultra high risk for psychosis: An updated and extended meta-analysis
    Mei, C ; van der Gaag, M ; Nelson, B ; Smit, F ; Yuen, HP ; Berger, M ; Krcmar, M ; French, P ; Amminger, GP ; Bechdolf, A ; Cuijpers, P ; Yung, AR ; McGorry, PD (PERGAMON-ELSEVIER SCIENCE LTD, 2021-06)
    Intervention at the earliest illness stage, in ultra or clinical high-risk individuals, or indicated prevention, currently represents the most promising strategy to ameliorate, delay or prevent psychosis. We review the current state of evidence and conduct a broad-spectrum meta-analysis of various outcomes: transition to psychosis, attenuated positive and negative psychotic symptoms, mania, depression, anxiety, general psychopathology, symptom-related distress, functioning, quality of life, and treatment acceptability. 26 randomized controlled trials were included. Meta-analytically pooled interventions reduced transition rate (risk ratio [RR] = 0.57, 95%CI 0.41-0.81) and attenuated positive psychotic symptoms at 12-months (standardized mean difference = -0.15, 95%CI = -0.28--0.01). When stratified by intervention type (pharmacological, psychological), only the pooled effect of psychological interventions on transition rate was significant. Cognitive behavioral therapy (CBT) was associated with a reduction in incidence at 12-months (RR = 0.52, 95%CI = 0.33-0.82) and 18-48-months (RR = 0.60, 95%CI = 0.42-0.84), but not 6-months. Findings at 12-months and 18-48-months were robust in sensitivity and subgroup analyses. All other outcomes were non-significant. To date, effects of trialed treatments are specific to transition and, a lesser extent, attenuated positive symptoms, highlighting the future need to target other symptom domains and functional outcomes. Sound evidence supports CBT in reducing transition and the value of intervening at this illness stage. STUDY REGISTRATION: Research Registry ID: reviewregistry907.
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    The associations between migrant status and ethnicity and the identification of individuals at ultra-high risk for psychosis and transition to psychosis: a systematic review
    Moore, D ; Castagnini, E ; Mifsud, N ; Geros, H ; Sizer, H ; Addington, J ; van der Gaag, M ; Nelson, B ; McGorry, P ; O'Donoghue, B (SPRINGER HEIDELBERG, 2021-11)
    PURPOSE: Migrant and ethnic minority populations exhibit a higher incidence of psychotic disorders. The Ultra-High Risk for psychosis (UHR) paradigm provides an opportunity to explore the stage at which such factors influence the development of psychosis. In this systematic review, we collate and appraise the literature on the association between ethnicity and migrant status and the rate of identification of individuals at UHR, as well as their rate of transition to psychosis. METHODS: We conducted a systematic review in the Ovid Medline, PsychINFO, Pubmed, CINAHL and EMBASE databases according to PRISMA guidelines. We included studies written in English that included an UHR cohort, provided a measure of ethnicity or migrant status, and examined the incidence, rate, or risk of UHR identification or transition to psychosis. RESULTS: Of 2182 unique articles identified, seven fulfilled the criteria. One study found overrepresentation of UHR individuals from black ethnic groups, while another found underrepresentation. Two studies found increased rates of transition among certain ethnic groups and a further two found no association. Regarding migrant status, one study found that first-generation migrants were underrepresented in an UHR sample. Lastly, a lower transition rate in migrant populations was identified in one study, while two found no association. CONCLUSION: Rates of UHR identification and transition according to ethnic and migrant status were inconsistent and insufficient to conclusively explain higher incidences of psychotic disorders among these groups. We discuss the clinical implications and avenues for future research, which is required to clarify the nature of the associations.
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    Cognitive functioning throughout adulthood and illness stages in individuals with psychotic disorders and their unaffected siblings
    Velthorst, E ; Mollon, J ; Murray, RM ; de Haan, L ; Germeys, IM ; Glahn, DC ; Arango, C ; van der Ven, E ; Di Forti, M ; Bernardo, M ; Guloksuz, S ; Delespaul, P ; Mezquida, G ; Amoretti, S ; Bobes, J ; Saiz, PA ; Garcia-Portilla, MP ; Santos, JL ; Jimenez-Lopez, E ; Sanjuan, J ; Aguilar, EJ ; Arrojo, M ; Carracedo, A ; Lopez, G ; Gonzalez-Penas, J ; Parellada, M ; Atbasoglu, C ; Saka, MC ; Ucok, A ; Alptekin, K ; Akdede, B ; Binbay, T ; Altinyazar, V ; Ulas, H ; Yalincetin, B ; Gumus-Akay, G ; Beyaz, BC ; Soygur, H ; Cankurtaran, ES ; Kaymak, SU ; Maric, NP ; Mihaljevic, MM ; Petrovic, SA ; Mirjanic, T ; Del-Ben, CM ; Ferraro, L ; Gayer-Anderson, C ; Jones, PB ; Jongsma, HE ; Kirkbride, JB ; La Cascia, C ; Lasalvia, A ; Tosato, S ; Llorca, P-M ; Menezes, PR ; Morgan, C ; Quattrone, D ; Menchetti, M ; Selten, J-P ; Szoke, A ; Tarricone, I ; Tortelli, A ; McGuire, P ; Valmaggia, L ; Kempton, MJ ; van der Gaag, M ; Riecher-Rossler, A ; Bressan, RA ; Barrantes-Vidal, N ; Nelson, B ; McGorry, P ; Pantelis, C ; Krebs, M-O ; Ruhrmann, S ; Sachs, G ; Rutten, BPF ; van Os, J ; Alizadeh, BZ ; van Amelsvoort, T ; Bartels-Velthuis, AA ; Bruggeman, R ; van Beveren, NJ ; Luykx, JJ ; Cahn, W ; Simons, CJP ; Kahn, RS ; Schirmbeck, F ; van Winkel, R ; Reichenberg, A (SPRINGERNATURE, 2021-08)
    Important questions remain about the profile of cognitive impairment in psychotic disorders across adulthood and illness stages. The age-associated profile of familial impairments also remains unclear, as well as the effect of factors, such as symptoms, functioning, and medication. Using cross-sectional data from the EU-GEI and GROUP studies, comprising 8455 participants aged 18 to 65, we examined cognitive functioning across adulthood in patients with psychotic disorders (n = 2883), and their unaffected siblings (n = 2271), compared to controls (n = 3301). An abbreviated WAIS-III measured verbal knowledge, working memory, visuospatial processing, processing speed, and IQ. Patients showed medium to large deficits across all functions (ES range = -0.45 to -0.73, p < 0.001), while siblings showed small deficits on IQ, verbal knowledge, and working memory (ES = -0.14 to -0.33, p < 0.001). Magnitude of impairment was not associated with participant age, such that the size of impairment in older and younger patients did not significantly differ. However, first-episode patients performed worse than prodromal patients (ES range = -0.88 to -0.60, p < 0.001). Adjusting for cannabis use, symptom severity, and global functioning attenuated impairments in siblings, while deficits in patients remained statistically significant, albeit reduced by half (ES range = -0.13 to -0.38, p < 0.01). Antipsychotic medication also accounted for around half of the impairment in patients (ES range = -0.21 to -0.43, p < 0.01). Deficits in verbal knowledge, and working memory may specifically index familial, i.e., shared genetic and/or shared environmental, liability for psychotic disorders. Nevertheless, potentially modifiable illness-related factors account for a significant portion of the cognitive impairment in psychotic disorders.
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    The association between migrant status and transition in an ultra-high risk for psychosis population
    O'Donoghue, B ; Geros, H ; Sizer, H ; Addington, J ; Amminger, GP ; Beaden, CE ; Cadenhead, KS ; Cannon, TD ; Cornblatt, BA ; Berger, GE ; Chen, EYH ; de Haan, L ; Hartmann, JA ; Hickie, IB ; Ising, HK ; Lavoie, S ; Lin, A ; Markulev, C ; Mathalon, DH ; McGlashan, TH ; Mifsud, NG ; Mossaheb, N ; Nieman, DH ; Nordentoft, M ; Perkins, DO ; Riecher-Roessler, A ; Schaefer, MR ; Schloegelhofer, M ; Seidman, LJ ; Smesny, S ; Thompson, A ; Tsuang, MT ; van der Gaag, M ; Verma, S ; Walker, EF ; Wood, SJ ; Woods, SW ; Yuen, HP ; Yung, AR ; McGorry, PD ; Nelson, B (SPRINGER HEIDELBERG, 2021-06)
    PURPOSE: Migrant status is one of the most replicated and robust risk factors for developing a psychotic disorder. This study aimed to determine whether migrant status in people identified as Ultra-High Risk for Psychosis (UHR) was associated with risk of transitioning to a full-threshold psychotic disorder. METHODS: Hazard ratios for the risk of transition were calculated from five large UHR cohorts (n = 2166) and were used to conduct a meta-analysis using the generic inverse-variance method using a random-effects model. RESULTS: 2166 UHR young people, with a mean age of 19.1 years (SD ± 4.5) were included, of whom 221 (10.7%) were first-generation migrants. A total of 357 young people transitioned to psychosis over a median follow-up time of 417 days (I.Q.R.147-756 days), representing 17.0% of the cohort. The risk of transition to a full-threshold disorder was not increased for first-generation migrants, (HR = 1.08, 95% CI 0.62-1.89); however, there was a high level of heterogeneity between studies The hazard ratio for second-generation migrants to transition to a full-threshold psychotic disorder compared to the remainder of the native-born population was 1.03 (95% CI 0.70-1.51). CONCLUSIONS: This meta-analysis did not find a statistically significant association between migrant status and an increased risk for transition to a full-threshold psychotic disorder; however, several methodological issues could explain this finding. Further research should focus on examining the risk of specific migrant groups and also ensuring that migrant populations are adequately represented within UHR clinics.
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    Pre-training inter-rater reliability of clinical instruments in an international psychosis research project
    Berendsen, S ; Kapitein, P ; Schirmbeck, F ; van Tricht, MJ ; McGuire, P ; Morgan, C ; Gayer-Anderson, C ; Kempton, MJ ; Valmaggia, L ; Quattrone, D ; di Forti, M ; van der Gaag, M ; Kirkbride, JB ; Jongsma, HE ; Jones, PB ; Parellada, M ; Arango, C ; Arrojo, M ; Bernardo, M ; Sanjuan, J ; Santos, JL ; Szoke, A ; Tortelli, A ; Llorca, P-M ; Tarricone, I ; Tripoli, G ; Ferraro, L ; La Cascia, C ; Lasalvia, A ; Tosato, S ; Menezes, PR ; Del-Ben, CM ; Nelson, B ; Riecher-Rossler, A ; Bressan, R ; Barrantes-Vidal, N ; Krebs, M-O ; Nordentoft, M ; Ruhrmann, S ; Sachs, G ; Rutten, BPF ; van Os, J ; Velthorst, E ; de Haan, L (ELSEVIER, 2021-04)
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    The utility of a fidelity measure to monitor implementation of new early psychosis services across Australia
    Williams, G ; Farrelly, S ; Thompson, A ; Stavely, H ; Albiston, D ; van der El, K ; McGorry, P ; Killackey, E (WILEY, 2021-10)
    AIM: Early psychosis delivery models have proliferated worldwide, but there is limited research into establishing model fidelity. In this context, this article aims to describe the development and implementation of a fidelity tool in a national network of early psychosis services across Australia-the headspace Early Psychosis program. METHODS: Following a detailed consultation process, and based on the Australian Early Psychosis model, an 80-item Early Psychosis Prevention and Intervention Centre Model Integrity Tool (EMIT) was developed along with predefined thresholds for fidelity. The tool was used to assess adherence to the model in six clusters of service sites across Australia. Ratings on the EMIT were informed by interviews with site staff and young people receiving the service, routinely collected data and site policies and procedures. RESULTS: All six clusters of headspace Early Psychosis programs participated in five fidelity assessments across a period of two and a half years. In the initial two visits, the average fidelity score was in the 'low' fidelity range (i.e., <75%). By the fifth fidelity visit, the network average improved to 92.35%, reflecting 'superior' fidelity. CONCLUSIONS: Results of the longitudinal fidelity assessments indicate the successful implementation of the Australian Early Psychosis model across the headspace Early Psychosis program. Utilisation of ongoing fidelity assessments has proved an effective method to improve and maintain adherence to the model.