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Antidepressant, antipsychotic and psychological interventions in subjects at high clinical risk for psychosis: OASIS 6-year naturalistic study

Published online by Cambridge University Press:  22 October 2014

P. Fusar-Poli*
Affiliation:
King's College London, Institute of Psychiatry, London, UK OASIS team, South London and Maudsley NHS Foundation Trust, London, UK
M. Frascarelli
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy
L. Valmaggia
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy
M. Byrne
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy
D. Stahl
Affiliation:
King's College London, Institute of Psychiatry, London, UK
M. Rocchetti
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy
L. Codjoe
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy
L. Weinberg
Affiliation:
King's College London, Institute of Psychiatry, London, UK Department of Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy
S. Tognin
Affiliation:
King's College London, Institute of Psychiatry, London, UK
L. Xenaki
Affiliation:
King's College London, Institute of Psychiatry, London, UK
P. McGuire
Affiliation:
King's College London, Institute of Psychiatry, London, UK
*
*Address for correspondence: P. Fusar-Poli, Department of Psychosis Studies, Institute of Psychiatry PO63, De Crespigny Park, London SE5 8AF, UK. (Email: [email protected])

Abstract

Background.

Recent randomized controlled trials suggest some efficacy for focused interventions in subjects at high risk (HR) for psychosis. However, treating HR subjects within the real-world setting of prodromal services is hindered by several practical problems that can significantly make an impact on the effect of focused interventions.

Method.

All subjects referred to Outreach and Support in South London (OASIS) and diagnosed with a HR state in the period 2001–2012 were included (n = 258). Exposure to focused interventions was correlated with sociodemographic and clinical characteristics at baseline. Their association with longitudinal clinical and functional outcomes was addressed at follow-up.

Results.

In a mean follow-up time of 6 years (s.d. = 2.5 years) a transition risk of 18% was observed. Of the sample, 33% were treated with cognitive behavioural therapy (CBT) only; 17% of subjects received antipsychotics (APs) in addition to CBT sessions. Another 17% of subjects were prescribed with antidepressants (ADs) in addition to CBT. Of the sample, 20% were exposed to a combination of interventions. Focused interventions had a significant relationship with transition to psychosis. The CBT + AD intervention was associated with a reduced risk of transition to psychosis, as compared with the CBT + AP intervention (hazards ratio = 0.129, 95% confidence interval 0.030–0.565, p = 0.007).

Conclusions.

There were differential associations with transition outcome for AD v. AP interventions in addition to CBT in HR subjects. These effects were not secondary to baseline differences in symptom severity.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2014 

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References

Addington, J, Cornblatt, BA, Cadenhead, KS, Cannon, TD, McGlashan, TH, Perkins, DO, Seidman, LJ, Tsuang, MT, Walker, EF, Woods, SW, Heinssen, R (2011 a). At clinical high risk for psychosis: outcome for nonconverters. American Journal of Psychiatry 168, 800805.CrossRefGoogle ScholarPubMed
Addington, J, Epstein, I, Liu, L, French, P, Boydell, KM, Zipursky, RB (2011 b). A randomized controlled trial of cognitive behavioral therapy for individuals at clinical high risk of psychosis. Schizophrenia Research 125, 5461.Google Scholar
Amminger, GP, Schafer, MR, Papageorgiou, K, Klier, CM, Cotton, SM, Harrigan, SM, Mackinnon, A, McGorry, PD, Berger, GE (2010). Long-chain omega-3 fatty acids for indicated prevention of psychotic disorders: a randomized, placebo-controlled trial. Archives of General Psychiatry 67, 146154.CrossRefGoogle ScholarPubMed
Angrist, J, Imbens, G, Rubin, D (1996). Identification of causal effects using instrumental variables. Journal of the American Statistical Association 91, 444455.Google Scholar
Bechdolf, A, Wagner, M, Ruhrmann, S, Harrigan, S, Putzfeld, V, Pukrop, R, Brockhaus-Dumke, A, Berning, J, Janssen, B, Decker, P, Bottlender, R, Maurer, K, Moller, HJ, Gaebel, W, Hafner, H, Maier, W, Klosterkotter, J (2012). Preventing progression to first-episode psychosis in early initial prodromal states. British Journal of Psychiatry 200, 2229.CrossRefGoogle ScholarPubMed
Cannon, TD, Cadenhead, K, Cornblatt, B, Woods, SW, Addington, J, Walker, E, Seidman, LJ, Perkins, D, Tsuang, M, McGlashan, T, Heinssen, R (2008). Prediction of psychosis in youth at high clinical risk: a multisite longitudinal study in North America. Archives of General Psychiatry 65, 2837.CrossRefGoogle ScholarPubMed
Cornblatt, BA, Lencz, T, Smith, CW, Olsen, R, Auther, AM, Nakayama, E, Lesser, ML, Tai, JY, Shah, MR, Foley, CA, Kane, JM, Correll, CU (2007). Can antidepressants be used to treat the schizophrenia prodrome? Results of a prospective, naturalistic treatment study of adolescents. Journal of Clinical Psychiatry 68, 546557.Google Scholar
First, MB, Spitzer, RL, Gibbon, M, Williams, JBW (2002). Structured Clinical Interview for DSM-IV-TR Axis I Disorders, Research Version, Patient Edition (SCID-I/P) . Biometrics Research: New York, NY.Google Scholar
Fusar-Poli, P, Bechdolf, A, Taylor, MJ, Bonoldi, I, Carpenter, WT, Yung, AR, McGuire, P (2013 a). At risk for schizophrenic or affective psychoses? A meta-analysis of DSM/ICD diagnostic outcomes in individuals at high clinical risk. Schizophrenia Bulletin 39, 923932.CrossRefGoogle ScholarPubMed
Fusar-Poli, P, Bonoldi, I, Yung, AR, Borgwardt, S, Kempton, MJ, Valmaggia, L, Barale, F, Caverzasi, E, McGuire, P (2012). Predicting psychosis: meta-analysis of transition outcomes in individuals at high clinical risk. Archives of General Psychiatry 69, 220229.Google Scholar
Fusar-Poli, P, Borgwardt, S, Bechdolf, A, Addington, J, Riecher-Rossler, A, Schultze-Lutter, F, Keshavan, M, Wood, S, Ruhrmann, S, Seidman, LJ, Valmaggia, L, Cannon, T, Velthorst, E, De Haan, L, Cornblatt, B, Bonoldi, I, Birchwood, M, McGlashan, T, Carpenter, W, McGorry, P, Klosterkotter, J, McGuire, P, Yung, A (2013 b). The psychosis high-risk state: a comprehensive state-of-the-art review. JAMA Psychiatry 70, 107120.CrossRefGoogle Scholar
Fusar-Poli, P, Byrne, M, Badger, S, Valmaggia, LR, McGuire, PK (2013 c). Outreach and support in South London (OASIS), 2001–2011: ten years of early diagnosis and treatment for young individuals at high clinical risk for psychosis. European Psychiatry 28, 315326.Google Scholar
Fusar-Poli, P, Carpenter, WT Woods, S, McGlashan, T (2014 a). Attenuated psychosis syndrome: ready for DSM-5.1? Annual Review of Clinical Psychology 10, 155192.Google Scholar
Fusar-Poli, P, Nelson, B, Valmaggia, L, Yung, AR, McGuire, PK (2014 b). Comorbid depressive and anxiety disorders in 509 individuals with an at-risk mental state: impact on psychopathology and transition to psychosis. Schizophrenia Bulletin 40, 120131.CrossRefGoogle ScholarPubMed
Fusar-Poli, P, Smieskova, R, Kempton, MJ, Ho, BC, Andreasen, NC, Borgwardt, S (2013 d). Progressive brain changes in schizophrenia related to antipsychotic treatment? A meta-analysis of longitudinal MRI studies. Neuroscience and Biobehavioural Reviews 37, 16801691.CrossRefGoogle ScholarPubMed
Fusar-Poli, P, Valmaggia, L, McGuire, P (2007). Can antidepressants prevent psychosis? Lancet 370, 17461748.Google Scholar
Fusar-Poli, P, Van Os, J (2013). Lost in transition: setting the psychosis threshold in prodromal research. Acta Psychiatrica Scandinavica 127, 248252.Google Scholar
Hall, RC (1995). Global Assessment of Functioning. A modified scale. Psychosomatics 36, 267275.Google Scholar
Ho, BC, Andreasen, NC, Ziebell, S, Pierson, R, Magnotta, V (2011). Long-term antipsychotic treatment and brain volumes: a longitudinal study of first-episode schizophrenia. Archives of General Psychiatry 68, 128137.Google Scholar
Hutton, P, Taylor, PJ (2014). Cognitive behavioural therapy for psychosis prevention: a systematic review and meta-analysis. Psychological Medicine 44, 449468.Google Scholar
Kim, E, Jang, JH, Park, HY, Shim, G, Hwang, JY, Kim, SN, Kwon, JS (2012). Pharmacotherapy and clinical characteristics of ultra-high-risk for psychosis according to conversion status: a naturalistic observational study. Early Intervention Psychiatry 6, 3037.Google Scholar
Kirkbride, JB, Fearon, P, Morgan, C, Dazzan, P, Morgan, K, Tarrant, J, Lloyd, T, Holloway, J, Hutchinson, G, Leff, JP, Mallett, RM, Harrison, GL, Murray, RM, Jones, PB (2006). Heterogeneity in incidence rates of schizophrenia and other psychotic syndromes: findings from the 3-center AeSOP study. Archives of General Psychiatry 63, 250258.CrossRefGoogle ScholarPubMed
Kraemer, HC (2000). Pitfalls of multisite randomized clinical trials of efficacy and effectiveness. Schizophrenia Bulletin 26, 533541.Google Scholar
McGlashan, TH, Zipursky, RB, Perkins, D, Addington, J, Miller, T, Woods, SW, Hawkins, KA, Hoffman, RE, Preda, A, Epstein, I, Addington, D, Lindborg, S, Trzaskoma, Q, Tohen, M, Breier, A (2006). Randomized, double-blind trial of olanzapine versus placebo in patients prodromally symptomatic for psychosis. American Journal of Psychiatry 163, 790799.Google Scholar
McGlashan, TH, Zipursky, RB, Perkins, D, Addington, J, Miller, TJ, Woods, SW, Hawkins, KA, Hoffman, R, Lindborg, S, Tohen, M, Breier, A (2003). The PRIME North America randomized double-blind clinical trial of olanzapine versus placebo in patients at risk of being prodromally symptomatic for psychosis. I. Study rationale and design. Schizophrenia Research 61, 718.Google Scholar
McGorry, PD, Yung, AR, Bechdolf, A, Amminger, P (2008). Back to the future: predicting and reshaping the course of psychotic disorder. Archives of General Psychiatry 65, 2527.CrossRefGoogle Scholar
McGorry, PD, Yung, AR, Phillips, LJ, Yuen, HP, Francey, S, Cosgrave, EM, Germano, D, Bravin, J, McDonald, T, Blair, A, Adlard, S, Jackson, H (2002). Randomized controlled trial of interventions designed to reduce the risk of progression to first-episode psychosis in a clinical sample with subthreshold symptoms. Archives of General Psychiatry 59, 921928.Google Scholar
Middleton, H, Shaw, I, Hull, S, Feder, G (2005). NICE guidelines for the management of depression. British Medical Journal 330, 267268.CrossRefGoogle ScholarPubMed
Modinos, G, Allen, P, Frascarelli, M, Tognin, S, Valmaggia, L, Xenaki, L, Keedwell, P, Broome, M, Valli, I, Woolley, J, Stone, JM, Mechelli, A, Phillips, ML, McGuire, P, Fusar-Poli, P (2014). Are we really mapping psychosis risk? Neuroanatomical signature of affective disorders in subjects at ultra high risk. Psychological Medicine. Published online 30 April 2014. doi:10.1017/S0033291714000865.Google Scholar
Morrison, AP, French, P, Walford, L, Lewis, SW, Kilcommons, A, Green, J, Parker, S, Bentall, RP (2004). Cognitive therapy for the prevention of psychosis in people at ultra-high risk: randomised controlled trial. British Journal of Psychiatry 185, 291297.Google Scholar
Morrison, AP, Stewart, SL, French, P, Bentall, RP, Birchwood, M, Byrne, R, Davies, LM, Fowler, D, Gumley, AI, Jones, PB, Lewis, SW, Murray, GK, Patterson, P, Dunn, G (2011). Early detection and intervention evaluation for people at high-risk of psychosis-2 (EDIE-2): trial rationale, design and baseline characteristics. Early Intervention Psychiatry 5, 2432.Google Scholar
National Collaborating Centre For Mental Health (2013). Psychosis and Schizophrenia in Children and Young People. Recognition and Management. National Clinical Guideline Number 155. British Psychological Society and Royal College of Psychiatrists: London.Google Scholar
Nelson, B, Yuen, HP, Wood, SJ, Lin, A, Spiliotacopoulos, D, Bruxner, A, Broussard, C, Simmons, M, Foley, DL, Brewer, WJ, Francey, SM, Amminger, GP, Thompson, A, McGorry, PD, Yung, AR (2013). Long-term follow-up of a group at ultra high risk (“prodromal”) for psychosis: the PACE 400 study. JAMA Psychiatry 70, 793802.Google Scholar
Nieman, DH, Rike, WH, Becker, HE, Dingemans, PM, van Amelsvoort, TA, de Haan, L, van der Gaag, M, Denys, DA, Linszen, DH (2009). Prescription of antipsychotic medication to patients at ultra high risk of developing psychosis. International Clinical Psychopharmacology 24, 223228.CrossRefGoogle ScholarPubMed
Nordentoft, M, Petersen, L, Jeppesen, P, Thorup, AA, Abel, MB, Ohlenschlaeger, J, Christensen, TO, Krarup, G, Jorgensen, P (2006). OPUS: a randomised multicenter trial of integrated versus standard treatment for patients with a first-episode psychosis – secondary publication [article in Danish]. Ugeskrift for Laeger 168, 381384.Google Scholar
Phillips, LJ, Nelson, B, Yuen, HP, Francey, SM, Simmons, M, Stanford, C, Ross, M, Kelly, D, Baker, K, Conus, P, Amminger, P, Trumpler, F, Yun, Y, Lim, M, McNab, C, Yung, AR, McGorry, PD (2009). Randomized controlled trial of interventions for young people at ultra-high risk of psychosis: study design and baseline characteristics. Australian and New Zealand Journal of Psychiatry 43, 818829.CrossRefGoogle ScholarPubMed
Ruhrmann, S, Bechdolf, A, Kuhn, KU, Wagner, M, Schultze-Lutter, F, Janssen, B, Maurer, K, Hafner, H, Gaebel, W, Moller, HJ, Maier, W, Klosterkotter, J (2007). Acute effects of treatment for prodromal symptoms for people putatively in a late initial prodromal state of psychosis. British Journal of Psychiatry Supplement 51, s88s95.Google Scholar
Schennach-Wolff, R, Jager, M, Seemuller, F, Obermeier, M, Messer, T, Laux, G, Pfeiffer, H, Naber, D, Schmidt, LG, Gaebel, W, Huff, W, Heuser, I, Maier, W, Lemke, MR, Ruther, E, Buchkremer, G, Gastpar, M, Moller, HJ, Riedel, M (2009). Defining and predicting functional outcome in schizophrenia and schizophrenia spectrum disorders. Schizophrenia Research 113, 210217.CrossRefGoogle ScholarPubMed
Schultze-Lutter, F, Schimmelmann, BG, Ruhrmann, S (2011). The near Babylonian speech confusion in early detection of psychosis. Schizophrenia Bulletin 37, 653655.CrossRefGoogle Scholar
Stafford, MR, Jackson, H, Mayo-Wilson, E, Morrison, AP, Kendall, T (2013). Early interventions to prevent psychosis: systematic review and meta-analysis. British Medical Journal 346, f185.Google Scholar
van der Gaag, M, Nieman, DH, Rietdijk, J, Dragt, S, Ising, HK, Klaassen, RM, Koeter, M, Cuijpers, P, Wunderink, L, Linszen, DH (2012). Cognitive behavioral therapy for subjects at ultrahigh risk for developing psychosis: a randomized controlled clinical trial. Schizophrenia Bulletin 38, 11801188.CrossRefGoogle ScholarPubMed
Walker, EF, Cornblatt, BA, Addington, J, Cadenhead, KS, Cannon, TD, McGlashan, TH, Perkins, DO, Seidman, LJ, Tsuang, MT, Woods, SW, Heinssen, R (2009). The relation of antipsychotic and antidepressant medication with baseline symptoms and symptom progression: a naturalistic study of the North American Prodrome Longitudinal Sample. Schizophrenia Research 115, 5057.CrossRefGoogle ScholarPubMed
Woods, SW, Addington, J, Bearden, CE, Cadenhead, KS, Cannon, TD, Cornblatt, BA, Mathalon, DH, Perkins, DO, Seidman, LJ, Tsuang, MT, Walker, EF, McGlashan, TH (2013). Psychotropic medication use in youth at high risk for psychosis: comparison of baseline data from two research cohorts 1998–2005 and 2008–2011. Schizophrenia Research 148, 99104.CrossRefGoogle ScholarPubMed
Woods, SW, Carlson, JP, McGlashan, TH (2010). DSM-5 and the ‘psychosis risk syndrome’: the DSM-5 proposal is better than DSM-IV. Psychosis 2, 187190.Google Scholar
Yung, AR, Philips, L McGorry, PD (2004). Treating Schizophrenia in the Prodromal Phase. Taylor & Francis: London.CrossRefGoogle Scholar
Yung, AR, Woods, SW, Ruhrmann, S, Addington, J, Schultze-Lutter, F, Cornblatt, BA, Amminger, GP, Bechdolf, A, Birchwood, M, Borgwardt, S, Cannon, TD, de Haan, L, French, P, Fusar-Poli, P, Keshavan, M, Klosterkotter, J, Kwon, JS, McGorry, PD, McGuire, P, Mizuno, M, Morrison, AP, Riecher-Rossler, A, Salokangas, RK, Seidman, LJ, Suzuki, M, Valmaggia, L, van der Gaag, M, Wood, SJ, McGlashan, TH (2012). Whither the attenuated psychosis syndrome? Schizophrenia Bulletin 38, 11301134.Google Scholar
Yung, AR, Yuen, HP, McGorry, PD, Phillips, LJ, Kelly, D, Dell'Olio, M, Francey, SM, Cosgrave, EM, Killackey, E, Stanford, C, Godfrey, K, Buckby, J (2005). Mapping the onset of psychosis: the Comprehensive Assessment of At-Risk Mental States. Australian and New Zealand Journal of Psychiatry 39, 964971. Google Scholar
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