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--- | ||
abstract: | | ||
Expansion of early intervention services to identify and clinically | ||
manage at-risk mental state for psychosis has been recently | ||
commissioned by NHS England. Although this is a welcome development | ||
for preventive psychiatry, further clarity is required on thresholds | ||
for definition of such risk states and their ability to predict | ||
subsequent outcomes. Intervention studies for these risk states have | ||
demonstrated that a variety of interventions, including those with | ||
fewer adverse effects than antipsychotic medication, may potentially | ||
be effective but they should be interpreted with caution. | ||
author: | ||
- Richard Whale | ||
- Andrew Thompson | ||
- Rick FraserCorrespondence to Richard Whale | ||
(<richard.whale@brighton.ac.uk>) [^1] | ||
date: 2017-2 | ||
institute: | ||
- 1Early Intervention Service, Sussex Partnership NHS Foundation Trust, | ||
UK | ||
- 2Brighton and Sussex Medical School, UK | ||
- 3Division of Mental Health and Wellbeing, Warwick Medical School, | ||
University of Warwick, Coventry, UK | ||
- 4North Warwickshire Early Intervention in Psychosis Service, Coventry | ||
and Warwickshire Partnership NHS Trust, UK | ||
references: | ||
- id: R1 | ||
- id: R2 | ||
- id: R3 | ||
- id: R4 | ||
- id: R5 | ||
- id: R6 | ||
- id: R7 | ||
- id: R8 | ||
- id: R9 | ||
- id: R10 | ||
- id: R11 | ||
- id: R12 | ||
title: "The access and waiting-time standard for first-episode | ||
psychosis: an opportunity for identification and treatment of | ||
psychosis risk states?" | ||
--- | ||
|
||
With the advent of the new access and waiting-time standard for | ||
first-episode psychosis published by NHS England in February 2015, | ||
^[@R1]^ there is now a definite move to adopt service models aimed at | ||
preventing transition to psychosis in vulnerable individuals, as | ||
originally developed in 1994 by the Personal Assistance and Crisis | ||
Evaluation clinic in Melbourne. ^[@R2]^ There is an expectation that | ||
early intervention in psychosis services will now also offer | ||
interventions for at-risk mental state for psychosis (ARMS), based on | ||
our evolving understanding of best practice in this area. | ||
|
||
This move is exciting for a number of reasons. It represents a | ||
commitment from the Government to support mental health service | ||
development and reform, especially preventive approaches, at a time when | ||
many services are experiencing cuts. Cost-effectiveness of ARMS services | ||
has been demonstrated. ^[@R3]^ Second, as a treatment paradigm the | ||
preventive strategy represents a possibility that we can alter the | ||
trajectory of a potentially serious condition and improve outcomes in | ||
all domains, including symptoms and functioning. Third, we may be able | ||
to use, at an earlier stage of illness, more benign treatments that are | ||
potentially less costly, less stigmatising and better tolerated. ^[@R2]^ | ||
This preventive model also represents an opportunity to broaden | ||
treatment paradigms within mental health, not just for psychosis but for | ||
other disorders, fitting perfectly with another current health | ||
development strategy -- low-stigma, accessible and responsive youth | ||
mental health services. Debate continues as to whether such services are | ||
appropriately placed within established early intervention for psychosis | ||
or whether new, dedicated teams with a more public health emphasis | ||
should be created. However, existing services have expertise in both | ||
defining first-episode psychosis thresholds and offering relevant | ||
clinical support packages for both ARMS and first-episode psychosis. | ||
^[@R4]^ | ||
|
||
The criteria commonly used in the UK for ARMS depend on the presenting | ||
clinical features, relative functional impairment and help-seeking. | ||
^[@R2]^ Consistent quantification of distress relating to these features | ||
is currently lacking. It also remains unclear how these clinical risk | ||
features differ from more widespread psychotic phenomena in the general | ||
population. Psychotic experiences in non-help-seeking populations appear | ||
relatively common, affecting about 5%, ^[@R5]^ and higher in child and | ||
adolescent samples; ^[@R6]^ there is apparent sharing of aetiological | ||
risk factors with schizophrenia. Clinical outcomes of this | ||
non-help-seeking group are unknown. Psychosis transition threshold is | ||
commonly defined by three Positive and Negative Syndrome Scale items | ||
(delusions, hallucinations or conceptual disorganisation) achieving | ||
adequate severity for at least 7 days, ^[@R7]^ but such psychosis | ||
thresholds are not without controversy. ^[@R8]^ The large majority of | ||
those identified as ARMS do not cross this severity threshold within 3 | ||
years of follow-up, although many remain functionally impaired or | ||
develop other disorders. ^[@R2]^ Whether other transition criteria, or | ||
modifications of existing criteria, are better able to predict | ||
longer-term outcome remains to be established. The reliability of | ||
identifying such thresholds in clinical practice is also less than in | ||
research settings, ^[@R9]^ despite using widely available tools. ^[@R2]^ | ||
This is further complicated by concurrent substance misuse, common in | ||
such clinical populations. However, the definition and adoption of such | ||
thresholds is clearly necessary to educate clinicians, decide when to | ||
appropriately intervene and support research. The complexity of the | ||
psychosis sub-syndrome groups (including individuals with a family | ||
history of psychotic illness, those with schizotypal disorder or the | ||
attenuated psychosis syndrome, those with brief limited intermittent | ||
notable severity psychotic episodes and those help-seeking or not) and | ||
their undetermined probable outcomes may lead to services primarily | ||
adopting a more discrete threshold for inception, such as the DSM-5 | ||
research-appendix-defined attenuated psychosis syndrome, which has | ||
marked clinical overlap with ARMS-defined populations. ^[@R9]^ | ||
|
||
Without clear diagnostic robustness of a condition, and with a wide | ||
variation in clinical outcome, interpretation of intervention studies is | ||
problematic. Initially, randomised studies of diverse interventions for | ||
operationally defined ARMS (termed ultra high risk for psychosis) seemed | ||
to show similar beneficial effects *v.* control. Reviews pooling | ||
outcomes of these studies clearly advocated intervention. ^[@R7],[@R10]^ | ||
More recent randomised studies have demonstrated less clear benefits | ||
over control than earlier studies, as is often seen in health research | ||
(arguably 'active' controls were used in many of these studies). Primary | ||
intervention recommendations of supportive counselling/case management | ||
for this clinical group have emerged, as previously used as a control | ||
intervention. Several factors will need to be considered, with future | ||
investigations including previous low sample size due to recruitment | ||
problems, use of robust and consistent thresholds for group inclusion, | ||
and transition to psychosis to reduce heterogeneity of outcome, | ||
consistent inclusion of functional outcomes, translation of findings to | ||
usual clinical care (away from research clinics), ensuring timely | ||
publication of results and the importance of replication of existing | ||
findings. | ||
|
||
While considerable progress has been made in this area, we remain at the | ||
early stages of defining a risk syndrome for psychosis. The currently | ||
adopted clinical threshold for ARMS seems to be a valid construct to | ||
identify clinical need but the heterogeneity of subsequent clinical | ||
outcomes is wide. Specific interventions for ARMS are unclear, aside | ||
from those for commonly identified comorbidities (such as anxiety, | ||
depression and substance misuse). Intervention studies to date highlight | ||
the importance of methodological rigour and consistency of diagnostic | ||
thresholds used, to which end the DSM-5 attenuated psychosis syndrome | ||
may be a positive step. ^[@R9]^ Biological models for psychosis risk | ||
need replication, clinical validation and combining with clinical | ||
markers in larger, longitudinal studies to enhance risk determination. | ||
^[@R2],[@R11],[@R12]^ | ||
|
||
Despite these caveats, this field of study represents an important | ||
advance in the development of preventive psychiatry. The current move to | ||
incorporate earlier psychosis states in more widespread clinical | ||
services, with appropriate threshold definition and outcome monitoring, | ||
may also have important societal impact. | ||
|
||
[^1]: **Richard Whale** is Principal Lecturer at Brighton and Sussex | ||
Medical School and a Consultant Psychiatrist with the Early | ||
Intervention Services at Sussex Partnership NHS Foundation Trust. | ||
**Andrew Thompson** is Associate Clinical Professor in Psychiatry at | ||
the University of Warwick and a Consultant Psychiatrist in the North | ||
Warwickshire Early Intervention in Psychosis Service. **Rick | ||
Fraser** is Honorary Senior Lecturer at Brighton and Sussex Medical | ||
School and Lead Psychiatrist with the Early Intervention Services at | ||
Sussex Partnership NHS Foundation Trust. |
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