AIM: Early identification and better characterization of the prodromal phase of psychotic illness can lead to targeted treatment and, perhaps, prevention of many of the devastating effects of a first psychotic episode. The primary aim of this manuscript is to describe the treatment histories of a large cohort of individuals who entered into one of seven prodromal research programs in a North American Prodrome Longitudinal Study consortium. METHODS: Treatment histories from 372 clinical high-risk subjects are described along with demographic, symptom, diagnostic and functional variables that may have contributed to treatment decisions for this group of individuals. RESULTS: Of all subjects included, 82.1% had received psychosocial and/or pharmacologic treatment prior to entry. Psychosocial interventions were more common in the attenuated psychotic syndrome prodromal sample, especially those with more negative, disorganized or general symptoms and more impaired functioning. Psychotropic medication had been administered to individuals with a history of Axis I disorders. CONCLUSIONS: Given the many potential clinical presentations, treatments and ethical issues connected with the psychosis-risk syndrome, it is not surprising that clinicians administered a broad range of interventions to study participants prior to their entry into the various research programs. Those individuals with milder and non-specific symptoms were more likely to have received psychosocial treatments, whereas those with more severe symptoms received pharmacologic intervention. Clinical treatment research is needed that addresses the complexities of these psychosis-risk states and helps to specify appropriate treatment at different stages of the psychosis prodrome.
AIM: Early identification and better characterization of the prodromal phase of psychotic illness can lead to targeted treatment and, perhaps, prevention of many of the devastating effects of a first psychotic episode. The primary aim of this manuscript is to describe the treatment histories of a large cohort of individuals who entered into one of seven prodromal research programs in a North American Prodrome Longitudinal Study consortium. METHODS: Treatment histories from 372 clinical high-risk subjects are described along with demographic, symptom, diagnostic and functional variables that may have contributed to treatment decisions for this group of individuals. RESULTS: Of all subjects included, 82.1% had received psychosocial and/or pharmacologic treatment prior to entry. Psychosocial interventions were more common in the attenuated psychotic syndrome prodromal sample, especially those with more negative, disorganized or general symptoms and more impaired functioning. Psychotropic medication had been administered to individuals with a history of Axis I disorders. CONCLUSIONS: Given the many potential clinical presentations, treatments and ethical issues connected with the psychosis-risk syndrome, it is not surprising that clinicians administered a broad range of interventions to study participants prior to their entry into the various research programs. Those individuals with milder and non-specific symptoms were more likely to have received psychosocial treatments, whereas those with more severe symptoms received pharmacologic intervention. Clinical treatment research is needed that addresses the complexities of these psychosis-risk states and helps to specify appropriate treatment at different stages of the psychosis prodrome.
Authors: Patrick D McGorry; Ian B Hickie; Alison R Yung; Christos Pantelis; Henry J Jackson Journal: Aust N Z J Psychiatry Date: 2006-08 Impact factor: 5.744
Authors: Barbara A Cornblatt; Todd Lencz; Christopher W Smith; Ruth Olsen; Andrea M Auther; Emilie Nakayama; Martin L Lesser; Julia Y Tai; Manoj R Shah; Carmel A Foley; John M Kane; Christoph U Correll Journal: J Clin Psychiatry Date: 2007-04 Impact factor: 4.384
Authors: Thomas H McGlashan; Robert B Zipursky; Diana Perkins; Jean Addington; Tandy Miller; Scott W Woods; Keith A Hawkins; Ralph E Hoffman; Adrian Preda; Irvin Epstein; Donald Addington; Stacy Lindborg; Quynh Trzaskoma; Mauricio Tohen; Alan Breier Journal: Am J Psychiatry Date: 2006-05 Impact factor: 18.112
Authors: Anthony P Morrison; Paul French; Lara Walford; Shôn W Lewis; Aoiffe Kilcommons; Joanne Green; Sophie Parker; Richard P Bentall Journal: Br J Psychiatry Date: 2004-10 Impact factor: 9.319
Authors: Jadon R Webb; Jean Addington; Diana O Perkins; Carrie E Bearden; Kristin S Cadenhead; Tyrone D Cannon; Barbara A Cornblatt; Robert K Heinssen; Larry J Seidman; Sarah I Tarbox; Ming T Tsuang; Elaine F Walker; Thomas H McGlashan; Scott W Woods Journal: Schizophr Bull Date: 2015-09 Impact factor: 9.306
Authors: Joya N Hampton; Hanan D Trotman; Jean Addington; Carrie E Bearden; Kristin S Cadenhead; Tyrone D Cannon; Barbara A Cornblatt; Daniel H Mathalon; Thomas H McGlashan; Ming T Tsuang; Diana O Perkins; Larry J Seidman; Scott W Woods; Elaine F Walker Journal: Stress Health Date: 2018-06-28 Impact factor: 3.519
Authors: Deanna M Barch; Ian H Gotlib; Robert M Bilder; Daniel S Pine; Jordan W Smoller; C Hendricks Brown; Wayne Huggins; Carol Hamilton; Adam Haim; Gregory K Farber Journal: Biol Psychiatry Date: 2016-02-19 Impact factor: 13.382
Authors: Sandra M Goulding; Carrie W Holtzman; Hanan D Trotman; Arthur T Ryan; Allison N Macdonald; Daniel I Shapiro; Joy L Brasfield; Elaine F Walker Journal: Child Adolesc Psychiatr Clin N Am Date: 2013-06-18
Authors: Megan S Farris; Glenda MacQueen; Benjamin I Goldstein; JianLi Wang; Sidney H Kennedy; Signe Bray; Catherine Lebel; Jean Addington Journal: Can J Psychiatry Date: 2018-08-02 Impact factor: 4.356
Authors: Tracy Alderman; Jean Addington; Carrie Bearden; Tyrone D Cannon; Barbara A Cornblatt; Thomas H McGlashan; Diana O Perkins; Larry J Seidman; Ming T Tsuang; Elaine F Walker; Scott W Woods; Kristin S Cadenhead Journal: Early Interv Psychiatry Date: 2014-02-27 Impact factor: 2.732