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Psychiatric advance directives facilitated by peer workers among people with mental illness: economic evaluation of a randomized controlled trial (DAiP study)

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Aims: We aimed to assess the cost-effectiveness of psychiatric advance directives (PAD) facilitated by peer workers (PW-PAD) in the management of patients with mental disorders in France. Methods: In a prospective multicentre randomized controlled trial, we randomly assigned adults with a Diagnostic and Statistical Manual of Mental Disorders, fifth edition diagnosis of schizophrenia, bipolar I disorder or schizoaffective disorders, who were compulsorily hospitalized in the past 12 months, to either fill out a PAD form and meet a peer worker for facilitation or receive usual care. We assessed differences in societal costs in euros (€) and quality-adjusted life-years (QALYs) over a year-long follow-up to estimate the incremental cost-effectiveness ratio of the PW-PAD strategy. We conducted multiple sensitivity analyses to assess the robustness of our results. Results: Among the 394 randomized participants, 196 were assigned to the PW-PAD group and 198 to the control group. Psychiatric inpatient costs were lower in the PW-PAD group than the control group (relative risk, -0.22; 95% confidence interval, [-0.33 to -0.11]; P < 0.001), and 1-year cumulative savings were obtained for the PW-PAD group (mean difference, -€4,286 [-4,711 to -4,020]). Twelve months after PW-PAD implementation, we observed improved health utilities (difference, 0.040 [0.003-0.077]; P = 0.032). Three deaths occurred. QALYs were higher in the PW-PAD group (difference, 0.045 [0.040-0.046]). In all sensitivity analyses, taking into account sampling uncertainty and unit variable variation, PW-PAD was likely to remain a cost-effective use of resources. Conclusion: PW-PAD was strictly dominant, that is, less expensive and more effective compared with usual care for people living with mental illness.
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Epidemiology and Psychiatric
Sciences
cambridge.org/eps
Original Article
Cite this article: Loubière S, Loundou A,
Auquier P, Tinland A (2023). Psychiatric
advance directives facilitated by peer workers
among people with mental illness: economic
evaluation of a randomized controlled trial
(DAiP study). Epidemiology and Psychiatric
Sciences 32, e27, 1–9. https://doi.org/10.1017/
S2045796023000197
Received: 27 September 2022
Revised: 10 March 2023
Accepted: 25 March 2023
Keywords:
health economics; mental health; other
psychosocial techniques/treatments;
psychiatric services; randomized controlled
trials
Corresponding author: S. Loubière,
Email: sandrine.loubiere@univ-amu.fr
© The Author(s), 2023. Published by
Cambridge University Press. This is an Open
Access article, distributed under the terms of
the Creative Commons Attribution licence
(http://creativecommons.org/licenses/by/4.0),
which permits unrestricted re-use,
distribution and reproduction, provided the
original article is properly cited.
Psychiatric advance directives facilitated by
peer workers among people with mental
illness: economic evaluation of a randomized
controlled trial (DAiP study)
S. Loubière1,2, A. Loundou1,2, P. Auquier1,2and A. Tinland2,3
1Department of Clinical Research and Innovation, Support Unit for Clinical Research and Economic Evaluation,
Assistance Publique Hôpitaux de Marseille, Marseille, France; 2Health Service Research and Quality of Life
Center (UR 3279), Aix-Marseille University, School of Medicine, Marseille, France and 3Department of Psychiatry,
Assistance Publique Hôpitaux de Marseille, Marseille, France
Abstract
Aims. We aimed to assess the cost-eectiveness of psychiatric advance directives (PAD) facil-
itated by peer workers (PW-PAD) in the management of patients with mental disorders in
France.
Methods. In a prospective multicentre randomized controlled trial, we randomly assigned
adults with a Diagnostic and Statistical Manual of Mental Disorders, h edition diagnosis
of schizophrenia, bipolar I disorder or schizoaective disorders, who were compulsorily hos-
pitalized in the past 12 months, to either ll out a PAD form and meet a peer worker for
facilitation or receive usual care. We assessed dierences in societal costs in euros (€) and
quality-adjusted life-years (QALYs) over a year-long follow-up to estimate the incremental
cost-eectiveness ratio of the PW-PAD strategy. We conducted multiple sensitivity analyses
to assess the robustness of our results.
Results. Among the 394 randomized participants, 196 were assigned to the PW-PAD group
and 198 to the control group. Psychiatric inpatient costs were lower in the PW-PAD group than
the control group (relative risk, −0.22; 95% condence interval, [−0.33 to −0.11]; P<0.001),
and 1-year cumulative savings were obtained for the PW-PAD group (mean dierence, −€4,286
[−4,711 to −4,020]). Twelve months aer PW-PAD implementation, we observed improved
health utilities (dierence, 0.040 [0.003–0.077]; P=0.032). ree deaths occurred. QALYs
were higher in the PW-PAD group (dierence, 0.045 [0.040–0.046]). In all sensitivity analyses,
taking into account sampling uncertainty and unit variable variation, PW-PAD was likely to
remain a cost-eective use of resources.
Conclusion. PW-PAD was strictly dominant, that is, less expensive and more eective com-
pared with usual care for people living with mental illness.
Introduction
Involuntary treatment and care is common and increasing in high-income countries, with vari-
ation by country (Wasserman et al., 2020). Compulsory hospital admissions, whether or not
associated with other coercive measures, are important causes of trauma and negative treat-
ment outcomes among people with mental disorders. Several studies show that these episodes
of deprivation of liberty constitute a very negative experience (Nyttingnes et al., 2016; Sibitz
et al., 2011), aecting quality of life (Swanson et al., 2003), with little evidence of eectiveness
in terms of health status, social functioning and use of services (Hofmann et al., 2022). e
overall cost of compulsory hospitalizations has scarcely been studied (Venturini et al., 2017).
Dierent models of interventions to reduce compulsory admissions have been developed. Of
these, psychiatric advance directives (PADs) or joint crisis plans (JCPs) are written documents
that allow adults with mental illness and with temporary decision-making incapacity to state
their will and preferences in advance, to be applied if further mental health crises impair their
decision-making capacity (Henderson et al., 2008).
Behind this common objective, PADs and JCPs dier in several ways, including their legal
force or with whom they are fullled (Atkinson et al., 2003). On the one hand, the speci-
city of PADs is that they emphasize that they are legal documents, on the other hand, JCPs
rather emphasize that they are on an agreement signed by the person, the healthcare pro-
fessionals and possibly the relatives. Authors have highlighted profound dierences in the
way peoples autonomy is represented in JCPs and PADs: more absolute for PADs advo-
cates and more assisted for JCPs advocates (Ambrosini and Crocker, 2010). Despite these
dierences, PADs and JCPs have so much in common that they are routinely categorized as a
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
2 S. Loubière et al.
similar intervention and analysed together in systematic reviews,
which all rank them among the most eective interventions for
reducing compulsory admission (Barbui et al., 2021; Bone et al.,
2019; DeJong et al., 2016). A meta-analysis evaluated that PADs
and JCPs reduced compulsory admission by 25% (Molyneaux et al.,
2019).
Inherently, PADs promote user’s involvement and dialogue
(Murray and Wortzel, 2019). e benets in terms of autonomy
of PADs were at rst only theoretical but have gradually gained
ground as studies have shown that PADs improve user involve-
ment, empowerment and recovery; the therapeutic alliance and
integration of care, but these positive results are still low in evi-
dence (Nicaise et al., 2013). Recently, a randomized controlled trial
that we conducted showed that PADs facilitated by peer workers
were associated with fewer symptoms (eect size [95% condence
interval, CI]: −0.20 [−0.40 to 0.00]), higher empowerment (0.30
[0.10 to 0.50]) and higher recovery (0.44 [0.24 to 0.65]) compared
to the control group (Tinland et al., 2022).
e model of PADs that we have experimented in this trial had
the originality of being facilitated by peer workers, that is, peo-
ple with personal experiences of mental distress who are trained
to assist users in lling their PAD statement and sharing it with
relatives and psychiatrists. We observed that this model of PADs
was associated with a signicant reduction of over 32% in the pro-
portion of compulsory hospitalized people (main criterion of our
trial) (Tinland et al., 2022). As in the Molyneaux’ meta-analysis,
we found a less clear eect on voluntary hospitalizations and on
the total number of hospital admissions. e latter result raises
the question of the cost-eectiveness of PADs facilitated by peer
workers.
To our knowledge, and despite its societal importance, PAD
interventions have received little attention in terms of costs, and
only two of the randomized trials on the topic have explored
this parameter, exclusively in the UK (Barrett et al., 2013; Flood
et al., 2006), and the dierence in costs was not signicant. Despite
counting its eectiveness among people with mental illness, it is
unclear whether reducing compulsory admissions results in cost
savings or a shi in care to non-compulsory admissions amount-
ing to the same length of stay. e main objective of this study
was to conduct an economic evaluation of psychiatric advance
directives facilitated by peer workers (PW-PAD) as part of a lon-
gitudinal randomized clinical trial for people with severe mental
illness.
Methods
Trial design
e ‘Peer-Worker-Facilitated Psychiatric Advance Directive’ study
(DAiP) was a multicentre randomized controlled trial conducted
in seven mental health facilities of three cities in France (Lyon,
Paris and Marseille) between January 2019 and June 2021. Forty
treating psychiatrists checked the eligibility criteria and referred
eligible participants to research assistants, who validated inclu-
sion criteria, obtained written consent and conducted interviews at
inclusion, 6 and 12 months. According to the principle of ‘sector’,
which has organized most public psychiatric care in France since
the 1960s, the participating psychiatrists were both inpatient and
outpatient (the same team ensures continuity). Only six of them
were strictly outpatient. All psychiatrists at each participating men-
tal health facility were fully informed about the study at the time
of its implementation. No special training or incentives were given
to participating psychiatrists. e follow-up period was 12 months
aer an 18-month recruitment.
e study was registered on Clinicaltrials (NCT03630822).
e study was conducted in compliance with the Declaration of
Helsinki, sixth revision; Good Clinical Practice guidelines and
local regulatory requirements. e trial was approved by the local
ethics committee (2018-A00146-49).
Population
e inclusion criteria were being over 18 years of age; with
experience of involuntary admission to hospital within the past
12 months; with a diagnosis of schizophrenia, bipolar I dis-
order or schizoaective disorders according to Diagnostic and
Statistical Manual of Mental Disorders, h edition criteria; with
decision-making capacity assessed by a psychiatrist according to
the MacArthur Competence AssessmentTool for Clinical Research
(Appelbaum and Grisso, 1995) and with French government health
insurance. e exclusion criteria included being considered unable
to provide informed consent and being under the highest level of
guardianship. At the time of inclusion, most participants were dis-
charged from the hospital; nevertheless, a few participants were
included as inpatients.
Randomization
Participants were randomly assigned using a web-based system at
a 1:1 ratio. Treating clinicians, participants and research assistants
were aware of the assigned randomization group.
Intervention group: PW-PAD
All PW-PAD participants received the PW-PAD document from
research assistants, consisting of future treatment and support
preference options, description of early signs of relapse and cop-
ing strategies (English translation in the Supplementary material).
Depending on their wishes, the PW-PAD participants could (i)
meet a peer worker in a place of their choice; (ii) be supported
by this peer worker in draing the PAD document with as many
meetings as necessary and (iii) be supported by the peer worker
during the sharing of PAD with the healthcare agent and the psy-
chiatrist. Peer support workers were recruited specically for this
study and trained at a Recovery college (Centre de Formation
au Rétablissement CoFoR). Regular exchanges were organized
between them (intervisions) and with the whole research team,
both remote and face-to-face.
Hard PADs were stored by the health worker or psychiatrist
depending on the participant’s choice and in electronic format if
available and requested. In case of crisis, reporting of the exis-
tence of PADs was done by patients, their entourage or informed
caregivers.
Control group
People assigned to the control group were treated as usual.
Depending on the persons needs, the usual treatment includes
psychological, pharmaceutical and social support. In France, espe-
cially at the time of this study, JCPs were only used locally by a
few pioneering teams, and there was very little chance that peo-
ple in the control group would access to crisis plans. Nonetheless,
they received comprehensive information about the PAD con-
cept during the inclusion step and were free to ll out a PAD,
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
Epidemiology and Psychiatric Sciences 3
but with no connection to the study’s peer worker. Figure S1 (see
Supplementary material) reports the number of PAD (PW-PAD or
other) completion and PAD use in each group.
Cost-eectiveness analysis
We performed a cost-utility analysis based on the societal per-
spective, including hospital, outpatient and community care, and
productivity losses due to illness. Incremental cost-eectiveness
ratios (ICERs) were expressed in terms of costs per quality-
adjusted life-year (QALY) gained, in accordance with Consolidated
Health Economic Evaluation Reporting Standards (CHEERS) and
the French National Authority for Health (HAS) guidelines for
economic evaluation (HAS, 2020; Husereau et al., 2022).
Eectiveness measure
Utilities for health states were assessed using the EuroQol-
5 Dimensions, three-level version (EQ-5D-3L) (Brooks, 1996;
Chevalier and de Pouvourville, 2013). is questionnaire is a
validated questionnaire that assesses a participant’s health status
through ve dimensions: mobility, personal care, routine occu-
pations, pain and discomfort and anxiety and depression. Each
dimension has three levels: no problems, some problems and severe
problems. e index score ranges from 0 (worst utility) to 1 (best
utility). Quality-of-life measures at baseline, 6 and 12 months
were summed as QALYs using an area under the curve approach
(Hunter et al., 2015; Husereau et al., 2022) and compared between
the PW-PAD and control groups.
Costs measure
We considered all direct and indirect healthcare costs in rela-
tion with care management during the follow-up. Resource use
data were retrieved from two sources: hospital-based administra-
tive databases and patients self-reported measures. Resource use
for each collaborative hospital was retrieved for all randomized
patients. To measure ambulatory and community care, and at the
margin to supplement hospital registry data, interview grids were
built to assist participants in reporting individual and prospective
resource use, based on previous studies of service use among peo-
ple with mental illness (Latimer et al., 2017; Loubière et al., 2020).
Resource utilization included those relating to the intervention,
including training of peer workers and time spent for PAD sup-
port, visits to the emergency department (ED), psychiatric hospital
admissions and total number of days at hospital, as well as outpa-
tient care. ese latter costs were assessed through consultations
with general practitioners, referring psychiatrists and other spe-
cialists. Indirect costs were investigated based on the number of
days of work absenteeism and compared between groups where
relevant.
Unit costs for hospital resources were estimated using data from
the French National Hospital Database (https://www.atih.sante.
fr/). e training of peer workers consisted in two half-day ses-
sions per week for 6 weeks, with an estimated cost of €1,215. We
observed the real cost of recruiting a peer worker at each site, either
a full-time or part-time contract over the duration of the study. e
average salary scales at the participating facilities were used to esti-
mate the monthly salary of the peer workers. No overhead costs
were charged to the intervention: the oce room and equipment
(i.e., computer and telephone) were already present and shared
with the care/administrative team. In the city of Paris (i.e., for
two health facilities), transportation costs were taken into account
(intra-city transportation card). For outpatient and community
care costs, national taris were used (Source: National databases
for medical and paramedical acts). All resources were valued in
2019 euros (see Supplementary Table S1) and discounting was not
applied.
Statistical analyses
An intention-to-treat analysis was conducted in the present study
and included all participants randomized in each group whether
or not they received the intervention or were lost to follow-up. To
detect a reduction of 30% in the rate of compulsory admissions to
psychiatric hospitals during the 12-month follow-up, the planned
sample was 200 per group, i.e., 400 in total. is number of sub-
jects allowed for a minimum cost dierence of €320 with a standard
deviation of 1,000, at a statistical power of 90%.
Missing data were addressed using multiple imputations
(van Buuren, 2007), under the assumption of missing at random
(Ware et al., 2012). Markov chain Monte Carlo multiple imputation
was used, which creates multiple complete’ datasets by predictions
for each missing value. Fiy imputed datasets were implemented
using Multivariate Imputation by Chained Equations and mitools
R packages. We ran a sensitivity analysis for only the observed data
(excluding missing data).
A mixed model for longitudinal utility values was used to con-
trol for potential bias due to intra-patient correlated data and
the existence of co-variates inuencing quality of life. Between-
group dierences in service use and total costs were estimated
using generalized estimating equations (GENLIN function) apply-
ing a Poisson distribution with a link log due to skewness. Mean
dierences and beta coecients with 95% CI were provided.
We used non-parametric bootstrapping (with 5,000
replications) to resample observations. e bootstrap results
were combined to calculate the mean values for costs and utilities,
and the SEs for the imputed values were used to calculate 95%
CIs. e incremental cost per QALY gained was then calculated
as mean incremental costs divided by mean incremental QALYs
and reported where relevant. Uncertainty in the cost-eectiveness
results was analysed using both univariate deterministic and
probabilistic sensitivity analyses.
Statistical analyses were performed using R Studio (R version
4.0.2, RStudio, Inc., Massachusetts, USA) and TreeAgePro 2019.
Results
A total of 394 participants were included in the analysis: 196 were
assigned to the intervention group and 198 to the control group.
Interviews at the 12-month follow-up were completed for 127
(65%) in the PW-PAD group (four participants withdrew) and 139
(70%) in the control group (including ve withdrawals) (see details
in Supplementary Figure S2). Baseline characteristics and primary
clinical outcomes are reported in Table 1. Gender, age, comor-
bidities and experience of previous hospital admissions were well
balanced between the two groups. PW-PAD participants showed
signicantly improved self-reported mental symptoms, recovery
and empowerment scores over the 12-month follow-up compared
with the control group.
Eectiveness
e mean utility at baseline (standard error [SE]) for the PW-PAD
and control groups were, respectively, 0.798 (0.015) and 0.757
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
4 S. Loubière et al.
(0.020) (P=0.101) (Table 2). Participants in the PW-PAD group
reported higher health utilities at month 12 (0.814 vs. 0.755;
P=0.017). From baseline to 12 months of follow-up, health util-
ities improved more in the PW-PAD group than in the control
group (mean dierence, 0.040; 95% CI, 0.003–0.077; P=0.032).
Based on complete data, the mean dierence in health utilities
Table 1. Socio-demographic and clinical characteristics of participants
(N=394)
Characteristics
PW-PAD goup
(n=196)
Control group
(n=198)
Gender, N(%)
Men 127 (64.8) 112 (56.6)
Age mean (SD), y 37.4 (11.7) 41.0 (12.7)
Median (IQR) 36 (28–44) 40 (31–49)
Nationality, N(%)
French 184 (93.9) 180 (91.8)
Education, N(%)
Less than high school
(<bac)
57 (29.2) 75 (37.9)
Completed or postsec-
ondary school
138 (70.8) 123 (62.1)
Marital status, N(%)
Single 132 (67.3) 128 (64.6)
Married/partnered 38 (19.4) 35 (17.7)
Divorced/separated/widow 26 (13.3) 35 (17.7)
Work activity, N(%)
Yes 33 (18.8) 37 (19.9)
EPICES score mean (SD) 40.6 (19.9) 42.8(20.9)
Median (IQR) 40.8 (24–57) 44.6 (26–59)
DSM-5 diagnosis, N(%)
Bipolar I disorder 66 (33.8) 73 (36.9)
Schizophrenia 86 (44.1) 92 (46.5)
Schizoaective disorders 43 (22.1) 33 (16.7)
Alcohol dependence, N(%)
Yes 6 (3.4) 6 (3.5)
Substance dependence, N(%)
Yes 22 (12.6) 24 (13.6)
With at least one somatic
comorbidity, N(%)
Yes 120 (61.2) 137 (69.2)
CGI score mean (SD) 4.1 (1.2) 4.3 (1.1)
Median (IQR) 4.0 (3–5) 4.0 (4–5)
Number of admissions in the
previous year, mean (SD)
1.5 (0.9) 1.4 (0.8)
1 132 (67.3) 148 (75.5)
2 45 (23.0) 37 (18.9)
3 17 (8.7) 11 (5.6)
(Continued)
Table 1. (Continued.)
Characteristics
PW-PAD goup
(n=196)
Control group
(n=198)
Clinical outcomes
MCSI score, mean (SD) 11.49 (11.91) 13.87 (10.99)
ES score, mean (SD) 16.80 (26.32) 10.20 (16.04)
RAS score, mean (SD) 72.60 (14.13) 65.55 (13.92)
PW-PAD: peer worker–facilitated psychiatric advance directive; SD: standard deviation; IQR:
interquartile range; DSM-5: Diagnostic and Statistical Manual of Mental Disorders, fih
edition; CGI: Clinical Global Impression scale.
Recovery was assessed using the Recovery Assessment Scale (RAS) (Corrigan et al., 2004),
which measures various aspects of recovery from the perspective of the consumer, with
a particular emphasis on hope and self-determination. This self-administered instrument
comprises 24 items, exploring five domains: personal confidence and hope, willingness
to ask for help, goal and success orientation, reliance on others and no domination by
symptoms. A higher score indicates better recovery.
Mental health symptomatology was assessed using the self-report modified Colorado
Symptom Index (MCSI; Conrad et al., 2001). The MCSI contains 14 items, which evaluate
how oen in the past month an individual has experienced a variety of mental health
symptoms, including loneliness, depression, anxiety and paranoia. Higher scores indicate a
greater likelihood of mental health problems.
Empowerment was assessed using the Empowerment Scale (ES) (Rogers et al., 1997). The
ES comprises 28 items, split into five dimensions: community activism and autonomy, self-
esteem and eicacy, optimism and control over the future, righteous anger and power
and powerlessness. The index score is 0 to 100, where higher scores correspond to higher
empowerment.
was 0.045 (95% CI, 0.002–0.088; P=0.039) (see Supplementary
Table S2).
ree (0.76%) patients died during the 12-month follow-up:
two (1.01%) patients in the TAU group and one (0.51%) patient
in the PW-PAD group.
Service use and costs
Details of service resource use and mean costs are provided in
Table 3. Table S2 (see Supplementary material) reports total psy-
chiatric hospital admissions and length of stay in both compulsory
and voluntary settings. e PW-PAD group experienced less psy-
chiatric hospital days over 1 year compared to the control group
(45.4 vs. 57.1; P=0.026). No signicant dierences were found
in the mean number of ED visits or consultations (P=0.056 and
P=0.309; respectively). Similarly, the rates of patients having
working activity at the end of follow-up did not show signicant
dierence between the PW-PAD and control groups (36.6% vs.
28.2%; P=0.184). No signicant dierences were found in the
mean number of days o work between the PW-PAD and control
groups (3.75 vs. 2.54 days; P=0.383).
Compared with the control group, PW-PAD exhibited a sta-
tistically signicant cost dierence in total costs (€22,094.27 vs.
26,382.39; P=0.001) (Table 4).
Cost-eectiveness
e incremental benet of PW-PAD versus control group was
0.045 QALY (95% CI, 0.040 to 0.046); the incremental cost
was −€4,286 (95% CI, −4,711 to −4,020) (Table 4). e cost-
eectiveness analysis showed that the PW-PAD intervention was
strictly dominant, that is, less expensive and more eective com-
pared to the usual care.
e bootstrap distribution of the ICER showed that 100% of the
5,000 replicates of ICER were located in the lower-right quadrant
of the scatterplot plan (Fig. 1).
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
Epidemiology and Psychiatric Sciences 5
Table 2. Change in health utilities score (EQ5D-3L) during follow-up in the DAiP trial
Baseline Month 6 Month 12
PW-PAD group Control group PW-PAD group Control group PW-PAD group Control group Mean dierenceb(95% CI)
Mean utility 0.798 0.757 0.774 0.753 0.814 0.755 0.040 (0.003–0.077)
Standard error 0.015 0.020 0.019 0.021 0.017 0.018
Pvaluea0.101 0.459 0.017 0.032b
PW-PAD: peer worker–facilitated psychiatric advance directive; SE: standard error; 95% CI: 95% confidence interval.
aP-values at each time were provided by t-test analysis (independent samples test) based on imputed data.
bMixed linear models (MIXED) for repeated-measure analyses were applied, using a restricted maximum likelihood approach for variance estimation, with a repeated variable ln(t+1),
where tis the time from baseline. An unstructured covariance matrix for repeated measures was used. The interaction between group and time was tested and was not kept because none
achieved statistical significance.
Values in italic indicate a statistically significant dierence from the group variable (PW-PAD vs. control groups)
Table 3. Mean healthcare utilization and costs at 12 months of follow-up
Utilization Costs
PW-PAD
group
(n=196)
Control
group
(n=198)
PW-PAD
group
(n=196)
Control
group
(n=198)
Outcomes Mean (SE) Mean (SE)
Mean dierence
(95% CI) Mean (SE) Mean (SE)
Relative risk
(95% CI)a
No. of days
in psychiatric
hospitalization
45.41 (3.28) 57.08 (4.09) −11.67 (−21.95
to –1.39)
Total
inpatient
costs
20,127.25 (867.27) 25,062.54 (800.41) −0.22 (−0.33
to –0.11)
No. of emergency
department visits
1.61 (0.36) 0.90 (0.23) 0.71 (−0.02 to 1.44) Emergency
department
costs
278.75 (58.67) 158.21 (36.32) 0.59 (0.11
to 1.08)
No. of ambulatory
visits
13.79 (1.05) 12.35 (0.93) 1.44 (−1.33 to 4.20) Ambulatory
costs
1,290.95 (28.48) 1,168.66 (19.29) 0.10 (0.05
to 0.16)
Intervention
costs
399.66 (3.63)
Total costs 22,094.27 (873.36) 26,382.39 (836.15) −0.18 (−0.28
to –0.08)
PW-PAD: peer worker–facilitated psychiatric advance directive; SE: standard error; 95% CI: 95% confidence interval.
aA Poisson distribution with a link log was used.
Generalized linear models were used to address mean dierence and 95% CI for the groups.
Values in italic indicate a statistically significant dierence in pooled imputation dataset from the group variable (PW-PAD vs. control groups), P<0.05.
Table 4. Mean and incremental costs and QALYs for patients receiving PW-PAD
versus usual care
PW-PAD group,
mean (95% CI)
Control group,
mean (95% CI)
Incremental,
mean (95% CI)
QALYs 0.789 (0.783–0.794) 0.746 (0.740–0.752) 0.045 (0.040–0.046)
Costs 22,095
(21,498–24,436)
26,382
(25,695–27,981)
−4,286 (−4,711
to –4,020)
ICER −99,977 (−113,378
to −91,035)
PW-PAD: peer worker–facilitated psychiatric advance directive; QALY: quality-adjusted life-
years; CI: confidence interval.
e graph contains axes that represent the incremental cost
(y-axis) and incremental eectiveness (x-axis). Each point in the
graph represents the incremental cost and incremental eective-
ness values (PW-PAD vs. control) from a single recalculation from
the database.
e willingness to pay (WTP), or ICER threshold, is used
as the slope of a line intersecting the origin of the plot. e
WTP line in the graph intersects points having the specied
ICER value, and the region below and to the right of the
line includes points where the intervention/PW-PAD is more
cost-eective than the usual care/control. e ellipsis shows the
95% CI.
Sensitivity analyses
Sensitivity analyses with complete cases yielded similar results to
imputed datasets (Table S3). e tornado diagram (Fig. 2) indi-
cated that cost-eectiveness was most strongly aected by utility
values altered over their 95% CI and inpatient costs varying from
±30%. is was followed by the mortality rates in the PW-PAD
and control groups. Regardless of the change in these parame-
ters, the higher eectiveness and cost savings were maintained for
PW-PAD. In addition, increasing or decreasing the costs of the
intervention by 50% had less eects on the ICER.
Taking sampling uncertainty into consideration, the cost-
eectiveness acceptability curve for the base-case analysis
(Figure S3) shows a 100% probability that PW-PAD was cost-
eective by comparison with usual care at the threshold of €1,000
WTP per QALY gained.
Discussion
Our study is the largest prospective study on PADs including peo-
ple living with mental illness who were compulsorily admitted
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
6 S. Loubière et al.
Fig. 1. Cost-eectiveness plane associated with the 12-month cost per QALY analysis.
PW-PAD: peer worker–facilitated psychiatric advance directive; QALY: quality-adjusted life year; WTP: willingness to pay.
Fig. 2. One-way sensitivity analysis of cost-eectiveness associated with PW-PAD intervention.
PW-PAD: peer worker–facilitated psychiatric advance directive; QALY: quality-adjusted life year; CI: confidence interval; ICER: incremental cost-eectiveness ratio.
during the past year. It is also the rst to evaluate the costs and
benets of peer worker–facilitated PADs for the management of a
patient’s mental disorder. In our study, for the overall population,
PW-PAD was strictly dominant. e intervention was associated
with a higher number of QALYs at a lower cost compared to usual
care.
PW-PAD was associated with a signicant decrease in total
psychiatric inpatient days/nights and with a signicant improve-
ment in compulsory admissions, with no signicant reduction in
the rate of overall psychiatric admissions (Tinland et al., 2022).
Our hypothesis is that, rather than preventing psychiatric hospital
admissions, PADs may reduce compulsory admissions by making
participants more willing to consider voluntary admission when a
crisis occurs. e economic analysis goes further and shows, based
on a detailed measure of health service utilization and cost analysis,
that the use of PW-PAD reduces the overall length of stay and costs
compared to usual care. Our ndings are consistent with nonran-
domized studies showing improvement in length of stay and costs
associated with a shi from coercive measures (Dimitri et al., 2018,
Kallert et al., 2008; McLaughlin et al., 2016, Salias and Fenton,
2000).
Few multicentre and randomized controlled studies have eval-
uated the eectiveness of advance directives in psychiatry, none
incorporating facilitation by peer workers (Henderson et al., 2004;
Molyneaux et al., 2019; Papageorgiou et al., 2002; Ruchlewska et al.,
2014; Swanson et al., 2006; ornicro et al., 2013). Of these,
only two had assessed their economic outcomes (Barrett et al.,
2013; Flood et al., 2006). Flood et al. could not nd any dier-
ences in admissions or total costs per participant over a 15-month
follow-up. Similarly, Barrett et al. could not nd any dierences
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
Epidemiology and Psychiatric Sciences 7
in compulsory admissions or total societal costs per participant
over an 18-month follow-up. Neither of these studies found signi-
cant intervention eects on inpatient stays (i.e., number of nights).
Our results show that the French participants spent considerable
amount of time in hospital, regardless of the group, compared
with those from UK studies with the same inclusion criteria. As
an example, over 1 year, participants in both French study groups
spent, on average, 2.5 times more days in hospital than partici-
pants in Barret’s UK-b ased study. e initial lengthy hospitalization
duration, combined with its sharp fall over 1 year, explains the
majority of our observed cost savings. is is consistent with the
conclusion of Burns meta-analysis, which showed that interven-
tions that reduce hospital admissions (in his paper. it is case man-
agement) are more eective when participants are high consumers
of hospital care at baseline (Burns et al., 2007). Dierences between
the interventions could also explain these results: PW-PAD dier
from Flood and Barret’s intervention in that they are PADs, and
peer workers facilitate them. On the one hand, PADs are unique
tools to promote self-determination (Elbogen et al., 2007), and part
of the results could be due to this law-oriented form; on the other
hand, peer workers involvement in healthcare has been shown to
be associated with improvements in quality of life, self-ecacy,
hope and empowerment (e.g., Fuhr et al., 2014; Lloyd-Evans et al.,
2014; Mahlke et al., 2017; Vayshenker et al., 2016), which is con-
sistent with our results. Unfortunately, our study does not allow
us to identify the relative role of each ingredient in achieving good
clinical or economic outcomes. PW-PAD is a complex intervention
where the meeting with a peer worker and crisis reection likely
interact with each other.
Over the follow-up period, participants in the PW-PAD group
gained more health utilities than their counterparts in the con-
trol group, with similar EQ5D-3L scores at baseline and 6 months.
is nding could suggest a learning period with PW-PAD, with
the eects in terms of quality of life appearing only aer the rst
6 months following the initiation of the advance directives, sug-
gesting that this could be maintained in the long term. Further
investigations are needed to understand the factors that inu-
ence the early benets of the intervention and to help inform
decision-making.
Even when the PW-PAD intervention was considered to cost
double, the intervention still remained dominant compared to
usual care. In fact, regardless of the variations considered in cost
parameters, the PW-PAD group remained dominant, presenting a
100% chance of being cost-eective at small WTP thresholds for
mental health programmes.
Such results are important because they inform decision mak-
ers and, perhaps more critically, they contribute to international
guidelines on the economic eciency of programmes in men-
tal health. Indeed, cost analyses oer a perspective for policy
changes. e PW-PAD is an intervention, which can be imple-
mented in a fairly straightforward manner and can be very quickly
cost-eective for the healthcare system.
Strengths and limitations
e strengths of our study lie in our design and methodol-
ogy. First, this research was deployed through seven psychiatric
facilities, each with several services. e wide range of practices
across these services reects the diversity of practice in France.
Between and within countries and regions, large variations have
been found between services in rates of inpatient admissions and
compulsion (Gandré et al., 2018b,2018a; Hofstad et al., 2021;
Weich et al., 2017), and these variations are not yet fully under-
stood by the scientic literature (Rugkåsa, 2017). e diversity
of participating centres, associated with broad inclusion criteria
and limited exclusion criteria, enhances our condence in the
generalizability of our results. Second, we captured a measure of
benet expressed in terms of participants quality of life rather
than simply a measure of resource use. Our approach is in accor-
dance with international guidelines and avoids the double counting
of resource use in both the denominator and numerator of the
ICER (Neumann et al., 2016). ird, resource use was based on
the data collected from hospital-based databases that captured the
entire hospital pathway associated with the management of mental
illness.
is trial had several limitations. First among them is the short
follow-up period. Given the short-term nature of PAD fullment,
the uncertainty surrounding long-term use and long-term conse-
quences on health utility of PADs and the limited impact of PADs
on survival, the 12-month randomized controlled trial timeline
was deemed appropriate to capture most of the relevant costs and
benets associated with the intervention. Most of the incremental
cost of PW-PAD is spent in the rst 3 months, so this intervention
might become even more cost-eective aer 1 year if participants
receiving the intervention continue to improve more than those
receiving usual care without additional costs.
Second, we assumed the same costs for compulsory and stan-
dard hospitalizations. We may have underestimated the costs in
the control group, although this reinforces the conservative costing
approach. e accounting costs provided by French health agen-
cies for hospitalization are not dierentiated between compulsory
or freely admitted patients, whereas compulsory hospitalization
appears more expensive, especially at the beginning, oen requir-
ing more sta and special facilities such as isolation rooms (Flood
et al., 2008; LeBel and Goldstein 2005). With 32% more compul-
sory admissions in the control group, total costs would be even
higher if the associated containment and seclusion costs had been
valued. At the same time, we did not account for the impact of dis-
charge to the community on people other than the study patient
(e.g., family or partners providing care to the patient) or measure
costs of pharmaceuticals, the latter being assumed to be higher at
entry in compulsory admission (Brown et al., 2010).
Finally, discontinuation rates were around one-third in both
groups. Unfortunately, the COVID-19 pandemic generated a crisis
that suddenly widened the gap in access to healthcare, especially
for vulnerable populations. Our attrition rates were mainly due to
lost to follow-up in periods of lockdown.
Conclusions
Among people living with mental illness, the elaboration of PADs
with the support of a peer worker was associated with a signi-
cant improvement in health utility in parallel to cost-savings over a
12-month period. ese ndings support a national-scale promul-
gation of this type of intervention and an implementation study of
these tools to measure the level of adoption in common practice
and to identify barriers and facilitators.
Supplementary material. e supplementary material for this article can
be found at https://doi.org/10.1017/S2045796023000197.
Data availability statement. Not all the data are freely accessible because
no informed consent was given by the participants for open data sharing, but
we can provide the data used in this study to researchers who want to use them,
following approval by the ethics committee of the Aix Marseille University.
https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
8 S. Loubière et al.
Acknowledgements. Jean Dhorne provided help to monitor this clinical
trial, with the assistance of Marika Larose. Sophie Tardosky and Richard
Malkoun contributed to the data management of the study. Magali Pontier
had the idea to develop DAP in Marseille and provided preliminary results
about the limits of facilitation by professionals. Nicolas Ordener, Julien Grard,
Celine Letailleur, EUTOPIA, MARSS team and the CoFoR Recovery College
provided help and advices to develop the practice of facilitation by peer work-
ers. Lee Antoine, Camille Niard, Nicholas Armstrong, Elsa Castot and Iannis
Mc Cluskey contributed as peer workers. Frederic Mougeot, Emmanuelle
Jouet, Magali Pontier, Nicolas Franck, Juliette Robert, Antoine Simon, Aurélien
Troisoeufs, Julien Grard and Karine Baumstarck were member of the steering
committee. Owen Taylor provided English proofreading. We thank them for
their grateful help.
Financial support. is work was supported by an institutional grant from
the French 2017 National Program of Health Services Research (Programme de
Recherche sur la Performance du système de Soins, PREPS-17-0575, FINESS
number 130786049).
Competing interest. None.
Ethical standards. e authors assert that all procedures contributing to this
work complywith the et hical standardsof the relevant national and institutional
committees on human experimentation and with the Helsinki Declaration of
1975, as revised in 2000.
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https://doi.org/10.1017/S2045796023000197 Published online by Cambridge University Press
... There were 13 studies that investigated the impact of facilitated treatment planning interventions on psychiatric symptoms as measured by the Brief Psychiatric Rating Scale (BPRS) [56,57], the Health of the Nation Outcome Scale (HoNOS) [54,58], the modified Colorado Symptom Index (CSI) [59,60], or a variety of other self-report and clinician-rated scales including the: EuropASI [55], CGI [61], SQ-48 [62], FARS [63] and GHQ scales/questionnaires [39], among others. The studies investigated mostly different intervention types over a range of followup periods (2-24 months). ...
... Eight (8) of the 13 studies reported significant improvements in psychiatric symptoms, in intervention compared to control groups [54,55,57,59,60,62], or after the intervention compared to before [58,61]. A further two studies reported improvements that were not significant over the study period [63,64]. ...
... The best-studied category was Quality of Life, with 9 studies (10 articles) quantitatively investigating this outcome measure [38, 47, 51, 52, 55, 59-61, 65, 69]. All other categories were less well studied, they included: Self-efficacy/management (7 studies) [34,45,54,56,61,70,71]; Functioning (6 studies) [45,57,58,63,65,72]; Work (6 studies) [57,58,60,61,63,73]; Recovery (6 studies, 7 articles) [51,52,56,59,60,66,74]; Attitudes (5 studies) [46,64,69,70,75]; Wellbeing (5 studies, 6 articles) [38,51,52,54,58,66]; Social functioning (5 studies) [38,39,56,76,77]; Empowerment (5 studies) [59,60,71,78,79]; Knowledge (3 studies, 4 articles) [46,70,80,81]; Independence/Control (2 studies) [76,82]; Activation (2 studies) [61,79]; and Sense of coherence (1 study) [61]. ...
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Background Most people with mental ill health want to be involved in decision‐making about their care, many mental health professionals now recognise the importance of this (at least in‐principle) and the Convention on the Rights of Persons with Disabilities enshrines the ethical imperative to support people in making their own treatment decisions. Nonetheless, there are widespread reports of people with mental ill health being excluded from decision‐making about their treatment in practice. Objectives We conducted a systematic review of quantitative, qualitative and mixed method research on interventions to improve opportunities for the involvement of mental healthcare service users in treatment planning. We sought to consolidate and understand the evidence on the outcomes of shared and supported decision‐making for people with mental ill health. Methods Seven databases were searched and 5137 articles were screened. Articles were included if they reported on an intervention for adult service users, were published between 2008 and October 2023 and were in English. Evidence in the 140 included articles was synthesised according to the JBI guidance on Mixed Methods Systematic Reviews. Results There was evidence relating to the effects of these interventions on a range of outcomes for people with mental ill health, including on: suicidal crisis, symptoms, recovery, hospital admissions, treatment engagement and on the use of coercion by health professionals. There is favourable evidence for these types of interventions in improving some outcomes for people with mental ill health, more so than treatment‐as‐usual. For other outcomes, the evidence is preliminary but promising. Some areas for caution are also identified. Conclusions The review indicates that when the involvement of people with mental ill health in treatment planning is supported, there can be improved outcomes for their health and care. Areas for future research are highlighted. Patient or Public Contribution This systematic review has been guided at all stages by a researcher with experience of mental health service use, who does not wish to be identified at this point in time. The findings may inform organisations, researchers and practitioners on the benefits of implementing supported decision‐making, for the greater involvement of people with mental ill health in their healthcare.
... Based on the concept of shared decision-making [8], it defines the modalities of intervention in case of a crisis by outlining the individual's treatment preferences (e.g., preferred alternative intervention to coercion), refusal of treatment, as well as crisis triggers and early warning signs [9][10][11][12]. A study by Loubière, Loundou, Auquier and Tinland [13] suggests that the use of JCPs could result in cost savings associated with a decrease in total psychiatric inpatients days/nights. The JCP also has the potential to reduce compulsory admissions [14][15][16]. ...
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Background/Objectives: Coercion in mental health is challenged, prompting reduction interventions. Among those, the Joint Crisis Plan (JCP), which aims to document individuals’ treatment preferences in case of future de-compensation, regardless of the potential loss of discernment, has been identified as a key path to study. Identified challenges related to its implementation highlight the need to adapt this intervention to the local context. Considering that in Quebec (Canada), the JCP is not widely used, but the scientific literature supports its adoption and corroborates its potential impact on reducing coercion, this study evaluates the feasibility, acceptability, and preliminary outcomes of the JCP among psychiatric and forensic inpatient settings. Methods: A pilot mixed-methods study was conducted through 16 individual interviews with inpatients and healthcare providers, combined with a pre–post analysis of seclusion and restraint use and the violence prevention climate (VPC) based on healthcare providers’ (n = 57) and inpatients’ perspectives (n = 53). Results: Although the challenging implementation of the JCP complicated the evaluation of its effects on seclusion and restraint use, a moderate change (d = 0.40) in the VPC was identified based on healthcare providers’ perspectives. Qualitative findings are also insightful to understand the acceptability and feasibility of the JCP use. A tension emerged between the perspectives of inpatients and healthcare providers: while inpatients valued the reflective process of completing the plan, providers focused more on its technical aspects. Conclusions: The results support the integration of the JCP into patient care pathways, as it provides a tool to amplify patients’ voices, promote patient empowerment, facilitate open dialog on alternatives to coercion, and foster more collaborative and humane mental health care.
... Peers with personal experiences of mental illness and recovery can provide unique insights, empathy and understanding of the developmental process. Peer support contributes to a more trusting and compassionate environment, which positively affects the mental health outcomes of service users (Loubière et al., 2023;Tinland et al., 2022). ...
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This article discusses advance statements in mental health care, which allow individuals with mental disorders to express their preferences for treatment during mental health crises. Despite the evidence supporting their effectiveness, their implementation in clinical practice remains limited. This article explores variations among advance statements, such as psychiatric advance directives (PADs), joint crisis plans (JCPs) and self-binding directives (SBDs), highlighting their content, development process and legal status. We outline the benefits of advance statements, including empowerment, early intervention, improved therapeutic relationships and reduced compulsory admissions. We then draw attention to the challenges that may contribute to their lack of implementation, including legal complexities, communication issues, cultural factors, potential inequities, healthcare provider knowledge, changing preferences, resource constraints, crisis responses, data privacy, family involvement, and long-term evaluation. In conclusion, advance statements offer significant benefits but require addressing these critical aspects to ensure ethical and effective use. Bridging the evidence-to-practice gap is essential, with a focus on implementation science. Integrating these tools into routine clinical practice can significantly benefit individuals with severe mental disorders and mental health systems.
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Importance: Reducing the use of coercion in mental health care is crucial from a human rights and public health perspective. Psychiatric advance directives (PADs) are promising tools that may reduce compulsory admissions. Assessments of PADs have included facilitation by health care agents but not facilitation by peer workers. Objective: To determine the efficacy of PADs facilitated by peer workers (PW-PAD) in people with mental disorders. Design, setting, and participants: A multicenter randomized clinical trial was conducted in 7 French mental health facilities. Adults with a DSM-5 diagnosis of schizophrenia, bipolar I disorder, or schizoaffective disorder who had a compulsory admission in the past 12 months and the capacity to consent were enrolled between January 2019 and June 2020 and followed up for 12 months. Interventions: The PW-PAD group was invited to fill out a PAD form and meet a peer worker who was trained to assist in completing and sharing the form with relatives and psychiatrists. Main outcomes and measures: The primary outcome was the rate of compulsory admission at 12 months after randomization. The overall psychiatric admission rate, therapeutic alliance, quality of life, mental health symptoms, empowerment, and recovery outcomes were also investigated. Results: Among 394 allocated participants (median age, 39 years; 39.3% female; 45% with schizophrenia, 36% bipolar I disorder, and 19% schizoaffective disorder), 196 were assigned to the PW-PAD group and 198 to the control group. In the PW-PAD group, 27.0% had compulsory admissions compared with 39.9% in the control group (risk difference, -0.13; 95% CI, -0.22 to -0.04; P = .007). No significant differences were found in the rate of overall admissions, therapeutic alliance score, and quality of life. Participants in the PW-PAD group exhibited fewer symptoms (effect size, -0.20; 95% CI, -0.40 to 0.00), greater empowerment (effect size, 0.30; 95% CI, 0.10 to 0.50), and a higher recovery score (effect size, 0.44; 95% CI, 0.24 to 0.65), compared with those in the control group. Conclusions and relevance: Peer worker-facilitated PADs are effective in decreasing compulsory hospital admissions and increasing some mental health outcomes (self-perceived symptoms, empowerment, and recovery). Involving peer workers in the completion of PADs supports the current shift of mental health care from substitute decision-making to supported decision-making. Trial registration: ClinicalTrials.gov Identifier: NCT03630822.
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Background: Despite multiple ethical issues and little evidence of their efficacy, compulsory admission and treatment are still common psychiatric practice. Therefore, we aimed to assess potential differences in treatment and outcome between voluntarily and compulsorily admitted patients. Methods: We extracted clinical data from inpatients treated in an academic hospital in Zurich, Switzerland between January 1, 2013 and December 31, 2019. Observation time started upon the first admission and ended after a one-year follow-up after the last discharge. Several sociodemographic and clinical characteristics, including Health of the Nation Outcome Scales (HoNOS) scores, were retrospectively obtained. We then identified risk factors of compulsory admission using logistic regression in order to perform a widely balanced propensity score matching. Altogether, we compared 4,570 compulsorily and 4,570 voluntarily admitted propensity score-matched patients. Multiple differences between these groups concerning received treatment, coercive measures, clinical parameters, and service use outcomes were detected. Results: Upon discharge, compulsorily admitted patients reached a similar HoNOS sum score in a significantly shorter duration of treatment. They were more often admitted for crisis interventions, were prescribed less pharmacologic treatment, and received fewer therapies. During the follow-up, voluntarily admitted patients were readmitted more often, while the time to readmission did not differ. Conclusions: Under narrowly set circumstances, compulsory admissions might be helpful to avert and relieve exacerbations of severe psychiatric disorders.
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Background: Compulsory hospitalisation in mental healthcare is contested. For ethical and legal reasons, it should only be used as a last resort. Geographical variation could indicate that some areas employ compulsory hospitalisation more frequently than is strictly necessary. Explaining variation in compulsory hospitalisation might contribute to reducing overuse, but research on associations with service characteristics remains patchy. Objectives: We aimed to investigate the associations between the levels of compulsory hospitalisation and the characteristics of primary mental health services in Norway between 2015 and 2018 and the amount of variance explained by groups of explanatory variables. Methods: We applied random-effects within–between Poisson regression of 461 municipalities/city districts, nested within 72 community mental health centre catchment areas (N = 1,828 municipality-years). Results: More general practitioners, mental health nurses, and the total labour-years in municipal mental health and addiction services per population are associated with lower levels of compulsory hospitalisations within the same areas, as measured by both persons (inpatients) and events (hospitalisations). Areas that, on average, have more general practitioners and public housing per population have lower levels of compulsory hospitalisation, while higher levels of compulsory hospitalisation are seen in areas with a longer history of supported employment and the systematic gathering of service users' experiences. In combination, all the variables, including the control variables, could account for 39–40% of the variation, with 5–6% related to municipal health services. Conclusion: Strengthening primary mental healthcare by increasing the number of general practitioners and mental health workers can reduce the use of compulsory hospitalisation and improve the quality of health services.
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Background Coercive treatment comprises a broad range of practices, ranging from implicit or explicit pressure to accept certain treatment to the use of forced practices such as involuntary admission, seclusion and restraint. Coercion is common in mental health services. Aims To evaluate the strength and credibility of evidence on the efficacy of interventions to reduce coercive treatment in mental health services. Protocol registration: https://doi.org/10.17605/OSF.IO/S76T3 . Method Systematic literature searches were conducted in MEDLINE, Cochrane Central, PsycINFO, CINAHL, Campbell Collaboration, and Epistemonikos from January 2010 to January 2020 for meta-analyses of randomised studies. Summary effects were recalculated using a common metric and random-effects models. We assessed between-study heterogeneity, predictive intervals, publication bias, small-study effects and whether the results of the observed positive studies were more than expected by chance. On the basis of these calculations, strength of associations was classified using quantitative umbrella review criteria, and credibility of evidence was assessed using the GRADE approach. Results A total of 23 primary studies (19 conducted in European countries and 4 in the USA) enrolling 8554 participants were included. The evidence on the efficacy of staff training to reduce use of restraint was supported by the most robust evidence (relative risk RR = 0.74, 95% CI 0.62–0.87; suggestive association, GRADE: moderate), followed by evidence on the efficacy of shared decision-making interventions to reduce involuntary admissions of adults with severe mental illness (RR = 0.75, 95% CI 0.60–0.92; weak association, GRADE: moderate) and by the evidence on integrated care interventions (RR = 0.66, 95% CI 0.46–0.95; weak association, GRADE: low). By contrast, community treatment orders and adherence therapy had no effect on involuntary admission rates. Conclusions Different levels of evidence indicate the benefit of staff training, shared decision-making interventions and integrated care interventions to reduce coercive treatment in mental health services. These different levels of evidence should be considered in the development of policy, clinical and implementation initiatives to reduce coercive practices in mental healthcare, and should lead to further studies in both high- and low-income countries to improve the strength and credibility of the evidence base.
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Background.: Compulsory admission procedures of patients with mental disorders vary between countries in Europe. The Ethics Committee of the European Psychiatric Association (EPA) launched a survey on involuntary admission procedures of patients with mental disorders in 40 countries to gather information from all National Psychiatric Associations that are members of the EPA to develop recommendations for improving involuntary admission processes and promote voluntary care. Methods.: The survey focused on legislation of involuntary admissions and key actors involved in the admission procedure as well as most common reasons for involuntary admissions. Results.: We analyzed the survey categorical data in themes, which highlight that both medical and legal actors are involved in involuntary admission procedures. Conclusions.: We conclude that legal reasons for compulsory admission should be reworded in order to remove stigmatization of the patient, that raising awareness about involuntary admission procedures and patient rights with both patients and family advocacy groups is paramount, that communication about procedures should be widely available in lay-language for the general population, and that training sessions and guidance should be available for legal and medical practitioners. Finally, people working in the field need to be constantly aware about the ethical challenges surrounding compulsory admissions.
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Background: Mental health services lack a strong evidence base on the most effective interventions to reduce compulsory admissions. However, some research suggests a positive impact of crisis-planning interventions in which patients are involved in planning for their future care during a mental health crisis. Aims: This review aimed to synthesise randomised controlled trial (RCT) evidence on the effectiveness of crisis-planning interventions (for example advance statements and joint crisis plans) in reducing rates of compulsory hospital admissions for people with psychotic illness or bipolar disorder, compared with usual care (PROSPERO registration number: CRD42018084808). Method: Six online databases were searched in October 2018. The primary outcome was compulsory psychiatric admissions and secondary outcomes included other psychiatric admissions, therapeutic alliance, perceived coercion and cost-effectiveness. Bias was assessed using the Cochrane collaboration tool. Results: The search identified 1428 studies and 5 RCTs were eligible. One study had high risk of bias because of incomplete primary outcome data. Random-effects meta-analysis showed a 25% reduction in compulsory admissions for those receiving crisis-planning interventions compared with usual care (risk ratio 0.75, 95% CI 0.61-0.93, P = 0.008; from five studies). There was no statistical evidence that the intervention reduced the risk of voluntary or combined voluntary and compulsory psychiatric admissions. Few studies assessed other secondary outcomes. Conclusions: Our meta-analysis suggests that crisis-planning interventions substantially reduce the risk of compulsory admissions among individuals with psychotic illness or bipolar disorder. Despite common components, interventions varied in their content and intensity across the trials. The optimal models and implementation of these interventions require further investigation. Declaration of interest: E.M., S.L., S.J. and B.L.-E. received funding from the National Institute for Health Research during the conduct of the study.
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Background: Compulsory mental health hospital admissions are increasing in several European countries but are coercive and potentially distressing. It is important to identify which mental health service models and interventions are effective in reducing compulsory admissions. Methods: We conducted a rapid evidence synthesis to explore whether there is any evidence for an effect on compulsory admissions for 15 types of psychosocial intervention, identified by an expert group as potentially relevant to reducing compulsory admission. A search for randomised controlled trials (RCTs) reporting compulsory admission as a primary or secondary outcome or adverse event was carried out using clinical guidelines, recent systematic reviews, and database searches postdating these reviews. Findings: We found 949 RCTs reporting on the interventions of interest, of which 19 reported on compulsory admission. Our narrative synthesis found some evidence for the effectiveness of crisis planning and self-management, while evidence for early intervention services was mixed. We did not find evidence to support adherence therapy, care from crisis resolution teams and assertive community treatment, but numbers of relevant studies were very small. We found no trials which tested effects on compulsory admission of the nine other intervention types. Interpretation: Crisis planning and self-management interventions with a relapse prevention element are most promising for preventing compulsory admissions. Given our broad search strategy, the lack of evidence demonstrates that there is an urgent need for more research on interventions which may reduce compulsory admissions. Funding: Independent research commissioned and funded by the National Institute for Health Research Policy Research Programme.
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Health economic evaluations are comparative analyses of alternative courses of action in terms of their costs and consequences. The Consolidated Health Economic Evaluation Reporting Standards (CHEERS) statement, published in 2013, was created to ensure health economic evaluations are identifiable, interpretable, and useful for decision making. It was intended as guidance to help authors report accurately which health interventions were being compared and in what context, how the evaluation was undertaken, what the findings were, and other details that may aid readers and reviewers in interpretation and use of the study. The new CHEERS 2022 statement replaces previous CHEERS reporting guidance. It reflects the need for guidance that can be more easily applied to all types of health economic evaluation, new methods and developments in the field, as well as the increased role of stakeholder involvement including patients and the public. It is also broadly applicable to any form of intervention intended to improve the health of individuals or the population, whether simple or complex, and without regard to context (such as health care, public health, education, social care, etc). This summary article presents the new CHEERS 2022 28-item checklist and recommendations for each item. The CHEERS 2022 statement is primarily intended for researchers reporting economic evaluations for peer reviewed journals as well as the peer reviewers and editors assessing them for publication. However, we anticipate familiarity with reporting requirements will be useful for analysts when planning studies. It may also be useful for health technology assessment bodies seeking guidance on reporting, as there is an increasing emphasis on transparency in decision making.
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Objectives There is limited evidence available on the health-seeking behaviours of individuals in relation to determinants of healthcare use. This study aimed to analyse the determinants of healthcare use (including both hospital and outpatient services) among homeless people with severe mental health illnesses. Study design The study used data from a multicentre, randomised, controlled trial conducted in four large French cities (the French Housing First Study). Methods Data were drawn from 671 homeless people enrolled in the study between August 2011 and April 2014. Mobile mental health outreach teams recruited homeless individuals with severe mental health illnesses who were living on the street or in emergency shelters, hospitals or prisons. Data collection was performed during face-to-face interviews. Healthcare service use included hospitalisations, mental health and regular emergency department (ED) visits and outpatient visits to healthcare facilities or physicians’ offices over a 6-month follow-up period. The data were analysed with zero-inflated (ZI) two-part models. Results In total, 61.1% of participants had at least one hospitalisation stay over the previous 6 months, with a mean of 25 (+/− 39.2) hospital days, and the majority (51%) had visited the ED (either for regular or mental health issues) during the same time period. The results confirmed the role of financial barriers (resources and health insurance) in seeking hospital care (P < 0.05). The main predictors for hospital use in the study population were a better social functioning score (odds ratio [OR]: 1.03; P < 0.001) and having schizophrenia (OR: 1.39; P < 0.01). Higher mental health scores (assessed by the Medical Outcomes Study 36-item Short Form Health Survey) (OR: 1.03, P < 0.01) and alcohol dependence (OR: 2.13; P < 0.01) were associated with not using ED healthcare services. Being ‘absolutely homeless’ predicted an increased use of the ED and a zero use of outpatient services. Inversely, no association with factors related to the homelessness trajectory was found in hospital ZI negative binomial models. Conclusion This study is important because a comprehensive understanding of the determinants of healthcare use enables healthcare systems to adapt and develop. The efficiency of medicosocial interventions targeting the homeless population with mental health illnesses must also be assessed. Clinical trial number NCT01570712.
Article
Psychiatric advance directives (PADs) are legal documents that allow individuals with psychiatric illness to designate decisions, while competent, about their future psychiatric care were they to lose competency due to psychiatric illness in the future. Among other items, these documents often include preferences regarding a surrogate decision-maker, types of medications, doses and routes of medications, seclusion and restraints, electroconvulsive therapy, and instructions for care of their property while incapacitated. While the concept and legal recognition of PADs has existed in the United States for several decades, use of PADs by patients and familiarity with PADs among mental health providers remain limited. This column reviews the origin of PADs, discusses several commonly considered arguments for and against the use of these documents, and concludes with a discussion of how PADs are currently used in the United States and their potential future role in mental health treatment.