Nervenheilkunde 2006; 25(01/02): 17-27
DOI: 10.1055/s-0038-1626435
Arbeiten zum Schwerpunkt - Theme Articles
Schattauer GmbH

Frühinterventionen vor schizophrenen Ersterkrankungen

Early intervention in the prodromal phase of schizophrenia
A. Bechdolf
1   Früherkennungs-und Therapiezentrum für psychische Krisen FETZ, Klinik für Psychiatrie und Psychotherapie, Klinikum der Universität zu Köln (Direktor: Prof. Dr. J. Klosterkötter)
,
S. Ruhrmann
1   Früherkennungs-und Therapiezentrum für psychische Krisen FETZ, Klinik für Psychiatrie und Psychotherapie, Klinikum der Universität zu Köln (Direktor: Prof. Dr. J. Klosterkötter)
,
M. Wagner
2   Zentrum für Beratung und Behandlung bei erhöhtem Psychoserisiko – ZeBB, Klinik für Psychiatrie und Psychotherapie, Universitätsklinikum Bonn (Direktor: Prof. Dr. W. Maier)
,
W. Maier
2   Zentrum für Beratung und Behandlung bei erhöhtem Psychoserisiko – ZeBB, Klinik für Psychiatrie und Psychotherapie, Universitätsklinikum Bonn (Direktor: Prof. Dr. W. Maier)
,
J. Klosterkötter
1   Früherkennungs-und Therapiezentrum für psychische Krisen FETZ, Klinik für Psychiatrie und Psychotherapie, Klinikum der Universität zu Köln (Direktor: Prof. Dr. J. Klosterkötter)
› Author Affiliations
Further Information

Publication History

Publication Date:
22 January 2018 (online)

Zusammenfassung

Eine Reihe von Erkenntnissen hat in den letzten Jahren dazu beigetragen, dass eine Frühintervention bei schizophrenen Erkrankungen vor dem Auftreten erster psychotischer Symptomen begründet und aussichtsreich erscheint. Aus internationalen Studien gibt es erste Hinweise für die Effektivität einer Frühintervention bei Personen mit erhöhtem Psychoserisiko. In Erweiterung der internationalen Forschung wurde in den Interventionsstudien des Kompetenznetz Schizophrenie zwischen einem psychosenahen und einem psychosefernen Prodrom unterschieden und hierauf bezogene differenzielle Interventionen mit kognitiver Verhaltenstherapie im psychosefernen Prodrom und mit atypischem Antipsychotikum im psychosenahen Prodrom entwickelt. Obwohl die Datenlage abschließend noch nicht zu beurteilen ist, stimmen die Zwischenauswertungen der Interventionsstudien des Kompetenznetzes Schizophrenie und die vorliegenden Ergebnisse internationaler Studien optimistisch für die Entwicklung einer indizierten Prävention bei schizophrenen Störungen.

Summary

In recent years new clinical findings suggested that early intervention in the prodromal phase of schizophrenia may be possible. First pilot data from international studies indicated that early intervention in persons at ultra-high risk of developing psychosis may be effective. Asa further development of the international approaches within the German Research Network on Schizophrenia we defined an early anda late initial prodromal state and developeda related differential intervention. A comprehensive cognitive-behavioural therapy is evaluated in persons in the early initial prodromal whereas clinical management and atypical neuroleptics combined are explored in persons in the late initial prodromal state. Although we have to await the final results of the ongoing trials, the preliminary data and findings from international studies are suggesting that indicated prevention may become a new perspective in the treatment of schizophrenia.

 
  • Literatur

  • 1 Andreasen NC, Flaum M. Schizophrenia: the characteristic symptoms. Schizophr Bull 1991; 17: 27-49.
  • 2 Bechdolf A, Maier S, Knost B, Wagner M, Hambrecht M. Psychologisches Frühinterventionsprogramm bei psychosefernen Prodromen. Ein Fallbericht. Nervenarzt 2003; 74: 436-9.
  • 3 Bechdolf A, Ruhrmann S, Wagner M, Kuhn KU, Janssen B, Bottlender R, Wieneke A, Schultze-Lutter F, Maier W, Klosterkötter J. Interventions in the initial prodromal states of psychosis in Germany: Concept and recruitment. Br J Psychiatry Suppl 2005; 48: S45-8.
  • 4 Bechdolf A, Veith V, Schwarzer D, Schormann M, Stamm E, Janssen B, Berning J, Wagner M, Klosterkötter J. Cognitive-behavioural therapy in the pre-psychotic phase: An exploratory pilot study. Psychiatry Research 2005; 136: 2-3.
  • 5 Bechdolf A, Phillips LJ, Francey SM, Leicester S, Morrison AP, Klosterkötter J, McGorry PD. Recent approaches to psychological interventions for people at risk of psychosis. European-Archives of Psychiatry and Neuroscience. 2005 (in press).
  • 6 Bell RQ. Multiple-risk cohorts and segmenting risk soluztions to the problem of false positives in the risk for major psychoses. Psychiatry 1992; 150: 370-81.
  • 7 Cohen J. Statistical power analysis for the behavioral sciences (rev ed). Hillsdale, NJ: Erlbaum; 1988
  • 8 Cornblatt B, Lencz T, Obuchowski M. The schizophrenia prodrome: treatment and high-risk perspectives. Schizophr Res 2002; 54: 177-86.
  • 9 Genduso LA, Haley JC. Cost of illness studies for schizophrenia: components, benefits, results, and implications. Am J Managed Care 1997; 03: 873-7.
  • 10 Gould RA, Mueser KT, Bolton E. et al. Cognitive therapy for psychosis in schizophrenia. An effect size analysis. Schizophr Res 2002; 48: 335-42.
  • 11 Häfner H, Nowotny B, Löffler W, an der Heiden W, Maurer K. When and how does schizophrenia produce social deficits?. Eur Arch Psychiatr Clin Neurosci 1995; 246: 17-28.
  • 12 Häfner H, Maurer K, Löffler W, an der Heiden W, Könnecke R, Hambrecht M. The early course of schizophrenia. In: Häfner H. (ed). Risk and Protective Factors in Schizophrenia– Towards a Conceptual Model of the Disease Process. Darmstadt: Steinkopff; 2002: 207-28.
  • 13 Häfner H, Maurer K, Ruhrmann S, Bechdolf A, Klosterkötter J, Wagner M, Maier W, Bottlender R, Möller HJ, Gaebel W, Wölwer W. Are early detection and secondary prevention feasible? Facts and visions. Eur Arch Psychiatry Clin Neurosci 2004; 254: 117-28.
  • 14 Helgason L. Twenty years follow-up of first psychiatric presentation for schizophrenia: what could have been prevented?. Acta Psychiatr Scand 1990; 81: 231-5.
  • 15 Huber G. Psychiatrische Aspekte des Basisstörungskonzepts. In: Süllwold L, Huber G. (Hrsg). Schizophrene Basisstörungen. Berlin, Heidelberg, New York: Springer; 1986: 39-143.
  • 16 Huber G, Gross G, Schüttler R. Schizophrenie. Verlaufs-und sozialpsychiatrische Langzeituntersuchung an den 1945–1959 in Bonn hospitalisierten schizophrenen Kranken. Berlin: Springer; 1979
  • 17 Humphreys MS, Johnstone EC, Macmillan JF, Taylor PJ. Dangerous behaviour preceeding first admission for schizophrenia. Br J Psychiatry 1992; 161: 501-5.
  • 18 Johnstone EC, Crow TJ, Johnson AL, MacMillan JF. The Northwick Park Study of first episodes of schizophrenia. I. Presentation of the illness and problems relating to admission. Br J Psychiatry 1986; 148: 115-20.
  • 19 Kissling W, Hoffler J. et al. Direct and indirect costs of schizophrenia. Fortschr Neurol Psychiatr 1999; 67: 29-36.
  • 20 Klosterkötter J, Hellmich M, Steinmeyer EM, Schultze-Lutter F. Diagnosing schizophrenia in the initial prodromal phase. Arch Gen Psychiatr 2001; 58: 158-64.
  • 21 Larsen TK, Bechdolf A, Bichwood M. The concept of schizophrenia and phase specific treatment. Psychological treatment in pre-psychosis and non-responders. Journal of the American-Academy of Psychoanalysis and Dynamic Psychiatry 2003; 31: 209-28.
  • 22 Lieberman JA, Kinon BJ, Loebel AD. Dopaminergic mechanisms in idiopathic and drug-induced psychoses. Schizophr Bull 1990; 16: 97-110.
  • 23 Loebel AD, Lieberman JA, Alvir JM, Mayerhoff DI, Geisler SH, Szymanski SR. Duration of psychosis and outcome in first-episode schizophrenia. Am J Psychiatry 1992; 149: 1183-8.
  • 24 Mason O, Startup M, Halpin S. et al. Risk factors for transition to first episode psychosis among individuals with ‘at-risk mental states’. Schizophrenia Research 2004; 71: 227-37.
  • 25 McGlashan TH, Johannessen JO. Early detection and intervention with schizophrenia: rationale. Schizophrenia Bulletin 1996; 22: 201-22.
  • 26 McGlashan TH, Zipursky RB, Perkins DO, Addington J, Woods SW, Miller TJ, Lindborg S, Marquez E, Hawkins K, Hoffmann RE, Tohen M, Breier A. 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 rational and design. Schizophr Res 2003; 61: 7-18.
  • 27 McGlashan TH. et al. Olanzapine vs. placebo for prodromal schizophrenia. Schizophr Res 2004; 67: 6.
  • 28 McGorry PD, Yung AR, Phillips LJ, Yuen HP, Francey S, Cosgrave EM, Germano D, Bravin J, McDonald T, Blair A, Adlard S, Jackson H. Randomized controlled trial of interventions designed to reduce the risk of progression to first-episode psychosis in a clinical sample with subthreshold symptoms. Arch Gen Psychiatry 2002; 59: 921-8.
  • 29 McGorry PD, Yung AR, Phillips LJ. The „closein” or ultra high-risk model: a safe and effective strategy for research and clinical intervention in prepsychotic mental disorder. Schizophrenia Bulletin 2003; 29: 771-90.
  • 30 Miller TJ, McGlashan TH, Rosen JL, Somjee L, Markovich PJ, Stein K, Woods SW. Prospective diagnosis of the initial prodrome for schizophrenia based on the structured interview for prodromal syndromes: preliminary evidence of interrater reliability and predictive validity. Am J Psychiatry 2002; 159: 863-5.
  • 31 Morrison AP, French P, Walford L, Lewis SW, Kilcommons A, Green J, Parker S, Bentall RP. A randomised controlled trial of early detection and cognitive therapy for the prevention of psychosis in people at ultra-high risk. Br J Psychiatry 2004; 185: 291-7.
  • 32 Murray CJ, Lopez AD. Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet 1997; 349: 1436-42.
  • 33 Pantelis C, Velakoulis D, McGorry PD, Wood SJ, Suckling J, Phillips LJ, Yung AR, Bullmore ET, Brewer W, Soulsby B, Desmond P, McGuire P. Neuroanatomical abnormalities before and after onset of psychosis: a cross-sectional and longitudinal MRI comparison. Lancet 2003; 361: 281-8.
  • 34 Phillips LJ, Yung AR, McGorry PD. Identification of young people at risk of psychosis: validation of personal assessment and crisis evaluation clinic intake criteria. Aust NZ J Psychiatry 2000; 34 (Suppl.): S164-S169.
  • 35 Rector N, Beck AT. Cognitive behavioural therapy for schizophrenia: An empirical review. J Nerv Ment Dis 2001; 189: 278-87.
  • 36 Ruhrmann S, Schultze-Lutter F, Klosterkotter J. Early detection and intervention in the initial prodromal phase of schizophrenia. Pharmacopsychiatry 2003; (Suppl. 03) 162-7.
  • 37 Schultze-Lutter F, Wieneke A. et al. The Schizophrenia Prediction Instrument, Adult version (SPI-A). Schizophr Res 2004; 70 (Suppl. 01) 76-7.
  • 38 Tsuang MT, Stone WS, Seidman LJ, Faraone SV, Zimmet S, Wojcik J, Kelleher JP, Green AI. Treatment of nonpsychotic relatives of patients with schizophrenia: four case studies. Biol Psychiatry 1999; 45: 1412-8.
  • 39 Woods SW, D´Souza DC, Wexler BE, Hoffman RE, McGlashan TH. Novel early interventions for prodromal states. Paper presented at the 3rd International Early Psychosis Conference, Copenhagen, 25-28 September, 2002..
  • 40 Woods SW, Breier A, Zipursky RB, Perkins DO, Addington J, Miller TJ, Hawkins KA, Marquez E, Lindborg SR, Tohen M, McGlashan TH. Randomized trial of Olanzapine vs placebo in the symptomatic acute treatment of the schizophrenic prodrome. Biol Psychiatry 2003; 54: 453-64.
  • 41 Yung AR, Phillips L, McGorry PD, McFarlane CA, Francey S, Harrigan S, Patton G, Jackson HJ. Prediction of psychosis. A step towards indicated prevention of schizophrenia. Br J Psychiatry 1998; 172: 14-20.
  • 42 Yung AR, Phillips LJ, Yuen HP, Francey SM, McFarlane CA, Hallgren M, McGorry PD. Psychosis prediction: 12-month follow up ofa highrisk (“prodromal”) group. Schizophr Res 2003; 60: 21-3.
  • 43 Yung AR, Phillips LJ, Yuen HP, McGorry PD. Risk factors for psychosis in an ultra high-risk group: psychopathology and clinical features. Schizophr Res 2004; 67: 131-42.