Früherkennung von Psychosen bei Kindern und Adoleszenten
Sind entwicklungsbezogene Besonderheiten ausreichend berücksichtigt?
Abstract
Die Früherkennung und Frühbehandlung von Personen mit erhöhtem Psychoserisiko gilt derzeit als vielversprechende Strategie, die weitreichenden negativen Konsequenzen psychotischer Störungen zu reduzieren. Die beiden derzeitigen Risikokriteriensätze, die «ultra-high risk» und die Basissymptom-Kriterien, wurden vorwiegend an Erwachsenenstichproben entwickelt. Erste Studien sprechen dafür, dass diese Kriterien nur eingeschränkt auf Kinder und Jugendliche übertragbar sein könnten. Für die «ultra-high risk»-Kriterien gibt es Hinweise, dass einige attenuierte psychotische Symptome im Jugendalter möglicherweise nicht ausreichend spezifisch und, wenn beobachtbare Verhaltenskorrelate fehlen, kurze intermittierende psychotische Symptome im Kindesalter schwer klassifizierbar sind. Auch für die Basissymptom-Kriterien liegen nur sehr vorläufige Hinweise auf ihre Eignung bei Kindern und Adoleszenten vor. Da entwicklungsbezogene Besonderheiten auch bei der Erhebung von Basissymptomen berücksichtigt werden sollten, wurde eine Kinder- und Jugendversion des Schizophrenia Proneness Instrument (SPI-CY) entwickelt, die in der vorgelegten Arbeit vorgestellt wird. Somit sind gezielte Studien zur Validierung und ggf. Adaptation der Risikokriterien für Kinder und Jugendliche dringend erforderlich, insbesondere wenn ein «Prodromal Risk Syndrome for Psychosis» oder «Attenuated Psychotic Symptoms Syndrome» in das DSM-5 aufgenommen wird. In diesem Fall müsste betont werden, dass die klinisch-prognostische Validität dieses Risikosyndroms für Kinder und Jugendliche noch unzureichend geklärt ist.
The early detection and treatment of persons at risk for psychosis is currently regarded as a promising strategy in fighting the devastating consequences of psychotic disorders. The two current favored at-risk approaches, i.e., the «ultra high risk» and the «basic symptom» criteria, were developed mainly using adult samples. Initial evidence suggests, however, that they cannot simply be applied to children and adolescents. For «ultra-high risk» criteria, there is indication of some attenuated psychotic symptoms being potentially nonspecific in adolescents, and of brief limited intermittent symptoms being difficult to clinically classify in children when observable behavioral correlates are missing. For basic symptoms, too, only a preliminary indication of their usefulness in children and adolescents exists. Since developmental peculiarities in the assessment of basic symptoms should be considered, a child and youth version of the Schizophrenia Proneness Instrument (SPI-CY) was developed. In conclusion, research on the clinical-prognostic validity of the at-risk criteria and their potential adaption to the special needs of children and adolescents is needed. If a «Prodromal Risk Syndrome for Psychosis» or «Attenuated Psychotic Symptoms Syndrome» are included in the upcoming DSM-5, it should be highlighted that its suitability for children and adolescents is only insufficiently known.
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