Early access to clozapine in Early Intervention in Psychosis: Hope vs reality. A mixed method service analysis.

Early Interv Psychiatry

Early Intervention in Psychosis Service, Sussex Partnership NHS Foundation Trust, Worthing, UK.

Published: February 2021

AI Article Synopsis

  • The study focuses on improving access to clozapine in Early Intervention in Psychosis Services (EIPS) in the UK, emphasizing identifying treatment-resistant psychosis early on.
  • It involved screening 150 service users, with 79% retained, and found that factors like two or more hospital admissions and age at first episode were significantly associated with clozapine eligibility.
  • The conclusion recommends that EIP services should proactively screen for treatment resistance, focusing on patients with negative symptoms, younger age at onset, and a history of multiple hospital admissions and antipsychotic trials.

Article Abstract

Aim: Improving access to clozapine is a recognized priority nationally across Early Intervention in Psychosis Services (EIPS) in the UK. Treatment resistance (TR) may be identifiable from early episode psychosis and appears to be characterized by negative symptoms and younger age of onset. This mixed method cross-sectional snapshot analysis of antipsychotic (AP) prescribing in an EIPS, explored clozapine eligibility (CE) and prioritization of AP prescribing based on choice, selectivity and appropriateness.

Method: We screened 150 service users and 79% (n = 119) were retained after inclusion criteria were applied. We explored CE in all service users who were indicated clozapine based on the product licence (n = 78), and whether there was association between CE and number of hospital admissions, AP trials, age at first episode and duration of untreated psychosis.

Results: Following multidisciplinary clinical discussions, we found that 23 service users were CE; 8 were offered and declined clozapine. When compared to non-CE service users, significant factors associated with CE were history of two or more hospital admissions (Mann-Whitney U = 269, P = .008), more than two trials of two different APs (Mann-Whitney U = 517, P ≤ .01), and younger age first episode (independent-samples t-test, P = .047). A total of 47.5% of all service users had been started on olanzapine as their first AP, despite high risk of cardiometabolic syndrome.

Conclusion: We propose that EIP services adopt a proactive approach in screening for TR, taking into account negative symptoms and young age at onset, prioritizing service users with two or more hospital admissions and AP trials.

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Source
http://dx.doi.org/10.1111/eip.12962DOI Listing

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