Presentation is loading. Please wait.

Presentation is loading. Please wait.

Ron Beasley, PharmD Candidate Preceptor: Soheyla Mahdavian, PharmD

Similar presentations


Presentation on theme: "Ron Beasley, PharmD Candidate Preceptor: Soheyla Mahdavian, PharmD"— Presentation transcript:

1 Ron Beasley, PharmD Candidate Preceptor: Soheyla Mahdavian, PharmD
CUtLASS TRIAL Ron Beasley, PharmD Candidate Preceptor: Soheyla Mahdavian, PharmD

2 CUtLASS TRIAL Cost Utility of the Latest Antipsychotic Drugs in Schizophrenia Study Tested at Fourteen community psychiatric services in the English National Health Service. Published in Archives of General Psychiatry in 2006

3 Objectives To test the hypothesis that in people with schizophrenia SGAs improve quality of life across 1 year compared with FGAs. Multisite, randomized controlled trial of antipsychotic drug classes, with Blind assessments at 12, 26, and 56 weeks using intention-to-treat analysis.

4 Methods 227 people aged 18 to 65 years with DSM-IV schizophrenia and related disorders assessed for medication review because of inadequate response or adverse effects. Following randomization, the referring psychiatrists would choose a medication from the assigned class to administer for up to 1 year's duration.

5 Methods Cont. The FGAs were *Not in the USA
Chlorpromazine hydrochloride, Flupenthixol * Haloperidol Loxapine Methotrimeprazine* Sulpiride* Trifluoperazine hydrochloride Zuclopenthixol* Depot Preperations Fluphenazine decanoate, Flupentixol decanoate * Haloperidol decanoate Pipothiazine palmitate * Zuclopenthixol decanoate * *Not in the USA

6 Methods Cont. SGAs were Risperidone Olanzapine Amisulpride* Zotepine*
Quetiapine *Not in the USA

7 Criteria Inclusion Exclusion
DSM-IV schizophrenia, schizoaffective disorder, or delusional disorder Age 18 to 65 years At least 1 month since the first onset of positive psychotic symptoms Psychiatrist electing to change the current FGA or SGA treatment because of inadequate clinical response or in- tolerance. Substance misuse or a medical disorder considered clinically to be the major cause of positive psychotic symptoms and a history of neuroleptic malignant syndrome.

8 Outcome Measurements The primary outcome measure was total score on the Quality of Life Scale (QLS), assessed blindly at baseline and at Weeks 12, 26, and 52 of the study. Secondary outcome measures included: Positive and Negative Syndrome Scale (PANSS) Calgary Depression Scale Various scales looking at adverse medication effects Participant satisfaction

9 Results SGAs did not show superiority in improvement in the QLS. In fact, there was a numerical trend toward greater improvement with the FGA cohort. Healthcare costs were similar in both groups with psychiatric inpatient hospitalization responsible for the majority of the expense. Although SGAs were more expensive than FGAs, total antipsychotic medication cost was a relatively small proportion of total expenses (2.1% and 3.8% for FGAs and SGAs, respectively).

10 Results cont. There was no measurable difference between the 2 cohorts in: Positive or negative symptoms Depressive symptoms Adverse effects

11 Critique (Pros) It is consistent with several other recent studies showing minimal to no clinical or cost-savings advantage of SGAs over FGAs It is a practical, blinded, well-designed trial that contains discussion about why the original premise (SGA superior to FGA) could not be proven Effect size, sample size, statistical power, utility of the QLS all were assed for bias

12 Critique (Cons) This study fails to answer key questions:
Are second-generation antipsychotic medications overrated? Do SGA’s really provide patients with an advantage over first-generation antipsychotics? Limited sample size and statistical power Psychiatrists may have been less ready to change from SGAs compared with FGAs in treating the patients skewing results.

13 References 1. Voruganti L, Cortese L, Oyewumi L, Cernovsky Z, Awad A. Comparative evalu- ation of conventional and novel antipsychotic drugs with reference to their sub- jective tolerability, side-effect profile and impact on quality of life. Schizophr Res. 2000;43: 2. National Collaborating Centre for Mental Health. Guidance on the Use of Newer (Atypical) Antipsychotic Drugs for the Treatment of Schizophrenia. London, En- gland: National Institute for Clinical Excellence; 2002. 3. Davis JM, Chen N, Glick ID. A meta-analysis of the efficacy of second- generation antipsychotics. Arch Gen Psychiatry. 2003;60:


Download ppt "Ron Beasley, PharmD Candidate Preceptor: Soheyla Mahdavian, PharmD"

Similar presentations


Ads by Google