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1.
Eur Psychiatry ; 52: 29-37, 2018 08.
Article in English | MEDLINE | ID: mdl-29614389

ABSTRACT

BACKGROUND: The duration of untreated psychosis (DUP) has been associated with negative outcomes in psychosis; however, few studies have focused on the duration of active psychotic symptoms after commencing treatment (DAT). In this study, we aimed to evaluate the effect of DUP and DAT on functional long-term outcomes (3 years) in patients with early psychosis. METHODS: We evaluated the Scale for the Assessment of Positive Symptoms (SAPS) at frequent intervals for 3 years after presentation to determine the DAT for 307 individuals with first-episode psychosis together with DUP and clinical variables. The functional outcomes were assessed using the Disability Assessment Scale (DAS) at three years, and functional recovery was defined as minimal impairment and return to activity. Associated variables, DAT and DUP were included in logistic regression models to predict functional outcomes. Receiver operating characteristic curves and Youden's index were applied to assess the best cut-off values. RESULTS: DAT, (Wald: 13.974; ExpB: 1.097; p < 0.001), premorbid adjustment, initial BPRS score, gender, age of onset and schizophrenia diagnosis were significant predictors of social functioning, whereas only premorbid adjustment (Wald: 11.383; ExpB:1.009), DAT (Wald: 4.850; ExpB: 1.058; p = 0.028) and education were significant predictors of recovery. The optimal cut-off of DAT for predicting social functioning was 3.17 months for DAT (sensitivity: 0.68; specificity: 0.64; Youden's index: 0.314). CONCLUSIONS: DAT is strongly related to functional outcomes independent of the DUP period or other variables. As a modifiable variable, the reduction of the DAT should be considered a main focus of intervention from the onset of the illness to improve long-term outcomes.


Subject(s)
Psychotic Disorders/psychology , Schizophrenia/diagnosis , Schizophrenic Psychology , Social Adjustment , Activities of Daily Living/psychology , Adult , Antipsychotic Agents/therapeutic use , Cohort Studies , Disability Evaluation , Female , Humans , Male , Prospective Studies , Psychiatric Status Rating Scales , Psychotic Disorders/diagnosis , Psychotic Disorders/diagnostic imaging , Schizophrenia/drug therapy , Time Factors , Treatment Outcome
2.
Eur Arch Psychiatry Clin Neurosci ; 267(4): 315-323, 2017 Jun.
Article in English | MEDLINE | ID: mdl-27796500

ABSTRACT

Relapses may represent a critical hazard in schizophrenia spectrum disorders as they are associated with an increased risk of a clinical and functional deterioration. Preventing relapse after recovering from a first psychotic episode has become a major challenge due to its critical impact on lifelong functionality. This study explored the rate of first and second relapses and the predictors associated with these relapses in a large cohort of non-affective psychosis patients during a period of 3 years after the first break of the illness. From February 2001 to May 2014, sociodemographic and clinical data from an epidemiological cohort of 341 non-affective first-episode psychosis patients at risk of relapse were analysed at a specialized early intervention service. Logistic regression, Cox regression, and Kaplan-Meier survival analyses were performed to compare non-relapsed and relapsed patients. One hundred and sixty-six (48.7%) individuals relapsed at least once. Median time to relapse was 17.0 months in non-adherent patients and 40.0 months in adherent patients (log-rankχ 2: 51.36; p < 0.001). Non-adherence to medication (odds ratio-OR 2.979; p < 0.001), schizophrenia diagnosis (OR 2.173; p = 0.002), and age of onset (OR 1.020; p = 0.033) were the main predictors of the first relapse. Fifty-six subjects experienced a second relapse (33.73%) predicted by diagnosis (OR 1.975; p = 0.074), age of onset (OR 1.078; p = 0.003), and positive symptoms (OR 0.863; p = 0.03), but not adherence. Non-adherence is the main predictive factor of first relapse after a first episode of psychosis. Second relapses were not often and not related to modifiable factors, suggesting that multiple relapsed patients may comprise a subgroup with a higher biological risk.


Subject(s)
Psychotic Disorders/diagnosis , Psychotic Disorders/epidemiology , Adolescent , Adult , Antipsychotic Agents/therapeutic use , Female , Humans , Logistic Models , Longitudinal Studies , Male , Middle Aged , Patient Compliance/psychology , Patient Compliance/statistics & numerical data , Predictive Value of Tests , Psychiatric Status Rating Scales , Psychotic Disorders/drug therapy , Recurrence , Retrospective Studies , Risk Factors , Young Adult
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