Introduction: There has been considerable support for the observation that atypical antipsychotics have a broader range of therapeutic effects than traditional antipsychotics. Specifically, they appear to be superior in terms of improvement of negative, cognitive, and affective symptoms in patients with schizophrenia. The purpose of this study was to compare the long-term efficacy of SGAs (Clozapine, Olanzapine, Risperidone) and FGAs (Haloperidol) on the different symptoms of schizophrenia. The analysis had 2 principal objectives: 1. to assess whether a significant change over time occurred in any of the 4 treatment groups; 2. to test whether there is a slope difference between the 4 medication groups in syndrome change trajectories over time. Materials and method: A multicentric open-study has been carried out in Italy, in seven University centres (Catanzaro, Chieti, Florence, L'Aquila, Pescara, Rome and Trieste). The study population comprised 126 patients with DSM-IV schizophrenia disorder diagnosis, 81 males (64.3%) and 45 females (35.7%), mean age 34.2 ± 10.1 years (range 18-64) (Tabs. I-II). Patients were assigned to treatment with Clozapine, Olanzapine, Risperidone, or Haloperidol, according to the judgment of a senior Psychiatric Specialist (Tab. III). The efficacy evaluation was assessed by means of Positive and Negative Syndrome Scales (PANSS), 3-THREE, CGI and Hamilton Rating Scales for Depression (HAM-D). The subjects were evaluated at first visit (T0), after 30 days (T30), 60 days (T60), 90 days (T90) and 120 days (T120). The measures of efficacy were analysed with a repeated measures analysis variance (MANOVA), with the technique of the contrast group of treatment, including the basal score in the model. Results: The efficacy analysis showed a statistically significant difference in the PANSS total (Tab. IV), Positive (Tab. V) and General subscale (Tab. VI) scores in all assessments of the four groups. PANSS Negative subscale score (Tab. VII) differences were statistically significant for Clozapine, Risperidone and Olanzapine, but not for Haloperidol. The intergroup analysis showed that the Negative subscale improvement, at 120 days, was greater in the Clozapine, Risperidone and Olanzapine groups than in the Haloperidol group. The HAM-D total scores efficacy analysis (Tab. VIII) indicated that the symptoms improved in all assessments in the four groups. The improvement in the SGAs groups at 90 and 120 days' evaluations was significantly greater than in the Haluperidol group. The 3-THREE analysis showed a significant improvement in T60, T90 and T120 total scores and Positive subscale in all four groups. The improvement of Negative and Behavioural 3-THREE subscale was statistically significant for SGAs, but not for Haloperidol. The Negative symptoms improvement after 120 days' treatment, assessed by the Negative and Behavioural 3-THREE subscale was greater in the SGAs groups than in the Haloperidol group and the improvement after 30 days' treatment was greater for Clozapine than for all the other three groups (Fig. 1). The seventy CGJ scores at T30 assessment was lower for Olanzapine and Risperidone than for Clozapine and Haloperidol. Conclusion: In conclusion, our data confirm that all 3 SGAs were associated with significant improvements in the positive, negative and affective symptoms of schizophrenia. In contrast, Haloperidol had only a marginally significant effect on the positive domain while the effect on the negative domain worsened.

L’“isteria” è stata dichiarata un’interpretazione arcaica di processi patologici (Slater, 1965) ma, nonostante che sia stata oscurata, smembrata, nelle definizioni diagnostiche ad esempio del DSM, il termine e il suo significato di esperienza vissuta si sono mantenuti nel tempo. Isteria è un termine che ha assunto via via diversi significati così come differenti sono state le cure di questa malattia nell’evolversi temporale e nello spirito dei tempi. Verso la metà del ventesimo secolo l’isteria è diventata: una summa specifica di caratteristiche di personalità, un complesso psicoanalitico, sintomi somatici psicogeni fino a comportamenti che richiamavano la riprovazione pubblica. Nel DSM-III e nel DSM-III-R (American Psychiatric Association, 1980, 1987) l’ambiguità semantica si è risolta nello smembramento dei contenuti diagnostici: la fenomenologia ha deciso la classificazione diagnostica. Osserviamo il disturbo istrionico di personalità, il disturbo somatoforme con il disturbo di somatizzazione e i disturbi dissociativi mentre le reazione isteriche di conversione si osservano nel disturbo algico e nel disturbo di conversione. L’Obiettivo del presente contributo si focalizzerà, dopo una digressione storica sulle terapie dell’isteria, sulla presentazione di diverse modalità terapeutiche (psicoterapeutiche, psicofarmacologiche) derivate da pazienti curati sia nel servizio pubblico con psicoterapia psicoanalitica (Servizio di Psicoterapia, Università di Milano) che privatamente con un’analisi junghiana.

L'isteria : quali terapie? / C. Bressi. - In: GIORNALE ITALIANO DI PSICOPATOLOGIA. - ISSN 1592-1107. - 12:S1(2006 Feb), pp. 194-194. ((Intervento presentato al convegno Terapia psichiatrica. Un problema di libertà : Congresso Nazionale della Società Italiana di Psicopatologia tenutosi a Roma nel 2006.

L'isteria : quali terapie?

C. Bressi
Primo
2006

Abstract

Introduction: There has been considerable support for the observation that atypical antipsychotics have a broader range of therapeutic effects than traditional antipsychotics. Specifically, they appear to be superior in terms of improvement of negative, cognitive, and affective symptoms in patients with schizophrenia. The purpose of this study was to compare the long-term efficacy of SGAs (Clozapine, Olanzapine, Risperidone) and FGAs (Haloperidol) on the different symptoms of schizophrenia. The analysis had 2 principal objectives: 1. to assess whether a significant change over time occurred in any of the 4 treatment groups; 2. to test whether there is a slope difference between the 4 medication groups in syndrome change trajectories over time. Materials and method: A multicentric open-study has been carried out in Italy, in seven University centres (Catanzaro, Chieti, Florence, L'Aquila, Pescara, Rome and Trieste). The study population comprised 126 patients with DSM-IV schizophrenia disorder diagnosis, 81 males (64.3%) and 45 females (35.7%), mean age 34.2 ± 10.1 years (range 18-64) (Tabs. I-II). Patients were assigned to treatment with Clozapine, Olanzapine, Risperidone, or Haloperidol, according to the judgment of a senior Psychiatric Specialist (Tab. III). The efficacy evaluation was assessed by means of Positive and Negative Syndrome Scales (PANSS), 3-THREE, CGI and Hamilton Rating Scales for Depression (HAM-D). The subjects were evaluated at first visit (T0), after 30 days (T30), 60 days (T60), 90 days (T90) and 120 days (T120). The measures of efficacy were analysed with a repeated measures analysis variance (MANOVA), with the technique of the contrast group of treatment, including the basal score in the model. Results: The efficacy analysis showed a statistically significant difference in the PANSS total (Tab. IV), Positive (Tab. V) and General subscale (Tab. VI) scores in all assessments of the four groups. PANSS Negative subscale score (Tab. VII) differences were statistically significant for Clozapine, Risperidone and Olanzapine, but not for Haloperidol. The intergroup analysis showed that the Negative subscale improvement, at 120 days, was greater in the Clozapine, Risperidone and Olanzapine groups than in the Haloperidol group. The HAM-D total scores efficacy analysis (Tab. VIII) indicated that the symptoms improved in all assessments in the four groups. The improvement in the SGAs groups at 90 and 120 days' evaluations was significantly greater than in the Haluperidol group. The 3-THREE analysis showed a significant improvement in T60, T90 and T120 total scores and Positive subscale in all four groups. The improvement of Negative and Behavioural 3-THREE subscale was statistically significant for SGAs, but not for Haloperidol. The Negative symptoms improvement after 120 days' treatment, assessed by the Negative and Behavioural 3-THREE subscale was greater in the SGAs groups than in the Haloperidol group and the improvement after 30 days' treatment was greater for Clozapine than for all the other three groups (Fig. 1). The seventy CGJ scores at T30 assessment was lower for Olanzapine and Risperidone than for Clozapine and Haloperidol. Conclusion: In conclusion, our data confirm that all 3 SGAs were associated with significant improvements in the positive, negative and affective symptoms of schizophrenia. In contrast, Haloperidol had only a marginally significant effect on the positive domain while the effect on the negative domain worsened.
L’“isteria” è stata dichiarata un’interpretazione arcaica di processi patologici (Slater, 1965) ma, nonostante che sia stata oscurata, smembrata, nelle definizioni diagnostiche ad esempio del DSM, il termine e il suo significato di esperienza vissuta si sono mantenuti nel tempo. Isteria è un termine che ha assunto via via diversi significati così come differenti sono state le cure di questa malattia nell’evolversi temporale e nello spirito dei tempi. Verso la metà del ventesimo secolo l’isteria è diventata: una summa specifica di caratteristiche di personalità, un complesso psicoanalitico, sintomi somatici psicogeni fino a comportamenti che richiamavano la riprovazione pubblica. Nel DSM-III e nel DSM-III-R (American Psychiatric Association, 1980, 1987) l’ambiguità semantica si è risolta nello smembramento dei contenuti diagnostici: la fenomenologia ha deciso la classificazione diagnostica. Osserviamo il disturbo istrionico di personalità, il disturbo somatoforme con il disturbo di somatizzazione e i disturbi dissociativi mentre le reazione isteriche di conversione si osservano nel disturbo algico e nel disturbo di conversione. L’Obiettivo del presente contributo si focalizzerà, dopo una digressione storica sulle terapie dell’isteria, sulla presentazione di diverse modalità terapeutiche (psicoterapeutiche, psicofarmacologiche) derivate da pazienti curati sia nel servizio pubblico con psicoterapia psicoanalitica (Servizio di Psicoterapia, Università di Milano) che privatamente con un’analisi junghiana.
Antipsychotic Agents; FGAs; Schizophrenia; SGAs; Treatment Outcome
Settore MED/25 - Psichiatria
feb-2006
Società Italiana di Psicopatologia
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/32370
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