Hostname: page-component-6766d58669-6mz5d Total loading time: 0 Render date: 2026-05-14T22:41:29.222Z Has data issue: false hasContentIssue false
  • English
  • Français

Treating patients with severe mental illness with narrative exposure therapy for comorbid post-traumatic stress disorder

Published online by Cambridge University Press:  09 December 2020

Maria W. Mauritz Open the ORCID record for Maria W. Mauritz [Opens in a new window] ,
Betsie G.I. van Gaal ,
Peter J.J. Goossens ,
Ruud A. Jongedijk  and
Hester Vermeulen
Maria W. Mauritz*
Affiliation:
GGNet Center for Mental Health Care, The Netherlands; Radboud University Medical Center, Radboud Institute for Health Sciences, IQ Healthcare, The Netherlands
Betsie G.I. van Gaal
Affiliation:
Radboud University Medical Center, Radboud Institute for Health Sciences, IQ Healthcare, The Netherlands; HAN University for Applied Sciences, Nursing Studies, Nijmegen, The Netherlands
Peter J.J. Goossens
Affiliation:
Dimence Group, Center for Mental Health Care, Specialistisch Centrum Bipolaire Stoornissen, The Netherlands; and University Centre for Nursing and Midwifery, Department of Public Health and Primary Care, Faculty of Medicine and Health Sciences, Ghent University, Belgium
Ruud A. Jongedijk
Affiliation:
ARQ Centrum ’45; and ARQ National Psychotrauma Center, The Netherlands
Hester Vermeulen
Affiliation:
Radboud University Medical Center, Radboud Institute for Health Sciences, IQ Healthcare, The Netherlands; and HAN University for Applied Sciences, Nursing studies, Nijmegen, The Netherlands
*
Correspondence: Maria W. Mauritz. Email: m.mauritz@ggnet.nl
Rights & Permissions [Opens in a new window]

Abstract

Background

Interpersonal trauma and post-traumatic stress disorder (PTSD) in patients with severe mental illness (SMI) negatively affect illness course. Narrative exposure therapy (NET) is effective in vulnerable patient groups, but its efficacy and applicability has not been studied in out-patients with SMI.

Aims

We aimed to evaluate the efficacy and applicability of NET in SMI on changes in PTSD, dissociation, SMI symptoms, care needs, quality of life, global functioning and care consumption.

Method

The study had a single-group, pre-test–post-test, repeated-measures design and was registered in The Netherlands National Trial Register (identifier TR571). Primary outcomes were assessed at pre-treatment (T0), 1 month post-treatment (T1) and 7 months’ follow-up (T2), with a structured interview for PTSD and dissociation screening. Secondary outcomes followed routinely SMI measurements and medical data. Mixed models were used for data analysis.

Results

The majority of the 23 participants was female (82%). Mean age was 49.9 years (s.d. 9.8) and mean PTSD duration was 24.1 years (s.d. 14.5). Mean PTSD severity decreased from 37.9 at T0 to 31.9 at T1 (−6.0 difference, 95%CI −10.0 to −2.0), and decreased further to 24.5 at T2 (−13.4 difference, 95%CI −17.4 to −9.4). Dissociation, SMI symptoms, duration of contacts, and medication decreased; global functioning increased; and quality of life and perceived needs did not change. Eleven participants were in remission for PTSD at T2, of which five were also in remission for major depression.

Conclusions

NET appeared efficacious and applicable to out-patients with SMI and PTSD, and was well tolerated.

Keywords

post-traumatic stress disordersevere mental illnessnarrative exposure therapysingle grouprepeated-measures

Information

Type
Papers
Information
BJPsych Open , Volume 7 , Issue 1 , January 2021 , e12
Check for updates
Creative Commons
Creative Common License - CCCreative Common License - BY
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 in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press on behalf of the Royal College of Psychiatrists

In the past decade, the high prevalence of interpersonal trauma and post-traumatic stress disorder (PTSD) in patients with severe mental illness (SMI) has received considerable attention. Trauma and PTSD are still underdiagnosed in patients with SMI, and have a negative influence on the illness course,Reference Grubaugh, Zinzow, Paul, Egede and Frueh1–Reference Stumbo, Paulson and Green3 specifically for psychotic disorders,Reference Misiak, Krefft, Bielawski, Moustafa, Sasiadek and Frydecka4 bipolar disordersReference Aas, Henry, Andreassen, Bellivier, Melle and Etain5 and major depressive disorders.Reference Flory and Yehuda6 That is why clinicians and researchers emphasise the importance of adequate screening for trauma and PTSD to counteract undertreatment in this vulnerable population.Reference Bateman, Henderson and Kezelman7 Controlled intervention studies have shown that PTSD in patients with SMI can be treated effectively by the following trauma-focused treatment (TFT) options: cognitive–behavioural treatment, prolonged exposure (PE) and eye movement desensitisation reprocessing (EMDR).Reference Hagenaars, van Minnen and Hoogduin8–Reference van den Berg, de Bont, van der Vleugel, de Roos, de Jongh and van Minnen12 An alternative TFT is narrative exposure therapy (NET) for patients who are exposed to repeated traumatic events during their life cycle. NET integrates prolonged exposure into the life story and includes attention to positive meaningful events.Reference Schauer, Neuner and Elbert13,Reference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14 NET has been proven particularly effective in vulnerable patient groups such as refugeesReference Lely, Smid, Jongedijk, Knipscheer and Kleber15,Reference Jongedijk16 and patients with a history of interpersonal trauma including child and adult abuse.Reference Pabst, Schauer, Bernhardt, Ruf, Goder and Elbert17 At this moment, NET has not yet been studied in patients with SMI who are receiving community mental healthcare. Therefore, to underpin the use of NET in clinical practice, this study evaluates the efficacy and applicability of NET in out-patients with SMI with comorbid PTSD associated with repeated interpersonal trauma.

Method

Design

This study was a single-group, pre-test–post-test study with repeated-measures, and was part of a larger mixed-methods study.Reference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14 The study was registered in The Netherlands National Trial Register (identifier TR5714).18

Ethics statement

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. All procedures involving patients were approved by the Committee on Research Involving Human Subjects, Arnhem-Nijmegen (approval number 1843–2015).Reference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14 The study started in April 2016 and ended in January 2019.

Participants

We included adult (age 21–65 years) out-patients with SMI and a history of repeated interpersonal trauma and comorbid PTSD, who received NET in a community mental healthcare context. The inclusion criteria were out-patients with (a) the existence of SMI, defined as the presence of a bipolar, major depressive, schizophrenia spectrum or personality disorder, according to the Mini-International Neuropsychiatric Interview (MINI-plus)Reference Sheehan, Lecrubier, Sheehan, Amorim, Janavs and Weiller19,Reference van Vliet and de Beurs20 and/or the Structured Clinical Interview for DSM-IV Personality Disorders (SCID-II),Reference First, Spitzer, Gibbon and Williams21 with reduced global functioning according the Global Assessment of Functioning (GAF; score <60)Reference Pedersen and Karterud22,23 during ≥2 years, according to chart diagnosis; (b) a trauma history including repeated physical and/or sexual abuse according to the Life of Events Checklist for DSM-5 (LEC-5);Reference Boeschoten, Bakker, Jongedijk and Olff24,Reference Weathers, Blake, Schnurr, Kaloupek, Marx and Keane25 and (c) the existence of PTSD according to the Clinical-Administered PTSD Scale for DSM-5 (CAPS-5).26-28 The exclusion criteria were out-patients with (a) provision of other trauma-focused treatment within 12 months before the study; (b) antisocial personality disorder; (c) dissociative identity disorder or (d) the provision of involuntary treatment following the Dutch Mental Health Law.

Recruitment

The study was carried out in 10 local flexible assertive community treatment (FACT) teamsReference van Veldhuizen29 located in five geographic regions of a large mental health centre in The Netherlands. FACT team professionals (mainly psychiatrists and specialised psychiatric nurses) screened their patients for trauma and PTSD with the Trauma Screening Questionnaire (TSQ).Reference Brewin, Rose, Andrews, Green, Tata and McEvedy30 After positive screening on the TSQ, the PTSD Checklist for the DSM-5 (PCL-5) was used to verify all PTSD symptoms,30-32 and 27 patients with repeated interpersonal trauma and PTSD were selected.

Patients received oral information about NET from their therapists and were asked to participate in the study. The researcher then provided written information and called after 1 week to check whether information was clearly explained and ask for oral consent. Written consent was obtained from all patients before the inclusion interview. Considering the vulnerable position of patients with SMI, FACT team members who knew their patients, were asked to recruit possible eligible patients. They were informed that they could stop with NET and/or participating in the study at any time, without reason. Information included a statement that personal and clinical data were processed anonymously.Reference Badu, O'Brien and Mitchell33 There was no reward for participating. The recruitment lasted from April 2016 to January 2018.

Intervention

The NET was conducted according to the Dutch NET manual,Reference Jongedijk and Mauritz34,Reference Jongedijk35 which is based on the manual outlined by Schauer et al.Reference Schauer, Neuner and Elbert13 NET was offered by five therapists (three nurse practitioners and two clinical psychologists) in a maximum of 16 weekly sessionsReference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14 from May 2016 to October 2018. The therapists were recruited from different FACT teams at the mental health centre and followed a 3-day NET training by qualified trainers in 2015–2016.36 They completed additional group video supervision in 10 90-min sessions by a trained NET supervisor during the study. FACT was continued during NET, and comprised the usual coordinated, multidisciplinary treatment interventions for out-patients with SMI, including pharmacotherapy alongside collaborative care, which comprised case management, crisis interventions and outreach nursing care.Reference Drukker, Visser, Sytema and van Os37,Reference van Veldhuizen38 During NET treatment, minimal biweekly supportive interventions by other FACT team members was requested as an important condition, because of the vulnerability of patients with SMI. In this period, the patients with SMI did not receive any other psychological treatment or benefits.

Outcomes

The primary outcomes were PTSD and dissociative symptoms. Remission of PTSD was based on the number and severity of symptoms, according to CAPS-5 rules.26-28 The secondary outcomes were SMI symptoms, care needs, quality of life, global functioning and care consumption.

Assessments

At baseline, demographic data were collected via the electronic patient record (EPR) and included gender, age, marital status, cultural background, education, living condition and employment. Clinical characteristics consisted of the verification of the primary SMI diagnosis, duration of illness, suicide risk, suicide attempts and substance misuse were collected with the MINI-plus.Reference Sheehan, Lecrubier, Sheehan, Amorim, Janavs and Weiller19,Reference van Vliet and de Beurs20 During the study, it was decided to monitor long-term changes in diagnosis, substance misuse and suicide risk by a second assessment with the MINI-plus at follow-up (T2). Therefore, additional ethical approval was obtained from the Committee on Research Involving Human Subjects, Arnhem-Nijmegen. The number and duration of interpersonal traumatic event types were collected with the LEC-5.Reference Boeschoten, Bakker, Jongedijk and Olff24,Reference Weathers, Blake, Schnurr, Kaloupek, Marx and Keane25 PTSD subtype and duration information were collected according to the CAPS-5.Reference Boeschoten, Bakker, Jongedijk, van Minnen, Elzinga and Rademaker26,Reference Weathers, Blake, Schnurr, Kaloupek, Marx and Keane27

Data for the primary and secondary outcomes were collected at three time points: at baseline (T0), and 1 month (T1) and 7 months (T2) after NET. PTSD symptoms and severity were assessed with the CAPS-5,Reference Boeschoten, Bakker, Jongedijk, van Minnen, Elzinga and Rademaker26,Reference Weathers, Blake, Schnurr, Kaloupek, Marx and Keane27 and dissociative symptoms were assessed with the Dissociative Experiences Scale (DES).Reference Bernstein and Putnam39 SMI symptoms were assessed with the Health of the Nation Outcome Scale (HoNOS),Reference Orrell, Yard, Handysides and Schapira40 care needs were assessed with the Camberwell Assessment of Needs (CAN),Reference Phelan, Thornicroft, Dunn, Holloway, Wykes and Strathdee41 quality of life was assessed with the Manchester Short Assessment of Quality of Life (MANSA)Reference Priebe, Huxley, Knight and Evans42 and global functioning was assessed with the GAF.23 These assessments were performed by a trained and independent research assistant, who was supervised by the first author. The HoNOS was assessed by the primary care provider because this instrument is focused on long-term observation. For detailed information on content, validity and reliability of the mentioned diagnostic instruments, consult the study protocol.Reference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14

Care consumption was defined as the number of therapeutic contacts, including duration in minutes and prescribed medications. These data were collected via the EPR by the first author from 6 months before T0 up to and including T2. The prescribed medications comprised four groups of psychiatric medication. For each group, a standard equivalent was calculated for: (a) benzodiazepines: diazepam;43 (b) antidepressants: fluoxetine;44,45 (c) antipsychotics: haloperidolReference Andreasen, Pressler, Nopoulos, Miller and Ho46,47 and (4) mood stabilisers: topiramate, because this medication was most commonly prescribed.48 The cumulative dose for each group of medication was calculated for each participant in the defined periods.

Sample size and statistical methods

The intended sample size was 25 participants. This size was based on the clinical feasibility of performing the intervention in the mental health centre. It was assumed that each of the five therapists in their geographic region could provide NET to five participants within 2 years. A sample size was not calculated because the great degree of uncertainty, but the chosen number is in line with other feasibility trials with a continuous end-point.Reference Billingham, Whitehead and Julious49,Reference Sim50

To describe demographics and clinical characteristics at baseline, means (s.d.) or median (interquartile range) were used for continuous data, depending on whether there was a normal distribution. Percentages were obtained for categorical data.

Because of the hierarchical structure of our study (repeated-measures nested within participants) we performed a linear mixed models for the analysis of the continuous course of illness outcomes. The duration of contacts had a skewed distribution and therefore a log transformation was performed. The log-transformed outcome was also analysed with a linear mixed model. The number of contacts was analysed with a generalised linear mixed model with a negative binomial distribution. For all these analyses, we used a model with a random intercept and all other variables fixed. A P-value of <0.05 was considered to be statistically significant, based on two-sided tests. The analysis was done with IBM SPSS Statistics version 25 for Windows. Table 2 presents back-transformed results.

For the use of psychiatric medication, the cumulative dose was calculated for the following periods: 6 months before T0; between T0 and T1; and 6 months thereafter, at T2. Medications were prescribed once a month to once every 3 months. Therefore, dosages were expressed in daily per month.

Results

Participant flow

In total, 27 eligible patients were contacted and all accepted NET treatment. One man (age 59 years) and one women (age 56 years) received NET, but did not consent to participate in the study. The other 25 patients did consent to participate in the study. Of these, two patients (both female, ages 23 and 39 years) withdrew before inclusion because of somatic illness and family circumstances, respectively. The remaining 23 patients started with NET within 1 week after inclusion. Most of them had never received TFT in the past. Two female patients dropped out during NET, but no serious events occurred (Fig. 1).

Fig. 1

Flow diagram, adapted to single-group design (CONSORT 2010).Reference Schulz, Altman and Moher51 SMI, severe mental illness.

Baseline demographics and clinical characteristics

The mean age of the participants (n = 23) was 49.9 years (s.d. 9.81). The majority were women (n = 19). Four participants had a non-Western cultural background. Of all of the participants, 14 had a middle education (above elementary school), two had a high education (vocational and academic) and only one was employed. Twelve participants were married or lived together, seven lived alone and four were living in sheltered housing.

Clinical characteristics show that the participants experienced 3–8 years (median) emotional, physical and/or sexual abuse during childhood and/or adulthood. The mean duration of PTSD was 24.1 years (s.d. 14.48).

Major depressive disorder was overrepresented among the participants (n = 15), in contrast to schizophrenia spectrum disorder (n = 4) and bipolar disorder (n = 4). Personality disorder did not appear in this group. The mean duration of SMI was 26.2 (s.d. 12.2). Thirteen participants had attempted suicide in the past and ten participants had current high suicide risk. Substance misuse was relatively low. See Table 1 for further details.

Table 1

Demographic and clinical characteristics (n = 23)

MINI-Plus, Mini-International Neuropsychiatric Interview; LEC-5, Life Events Checklist for DSM-5; CAPS-5, Clinician-Administered PTSD Scale for DSM-5.

Provision of NET

Of the 23 participants who started with NET, two of them discontinued treatment prematurely after one session and four sessions, respectively. The other 21 participants received 8–15 (median 11, interquartile range 2.5) weekly NET sessions. Duration of NET was 10–43 weeks (median 15), including four cases with interrupted treatment because of somatic problems (one participant), family circumstances (one participant), experienced stress from the therapy (one participant) and change of therapist (one participant), but eventually all finished NET after these breaks.

Analysis with mixed models included 23 participants, based on the intention-to-treat principle and taking missing values into account. Twenty-one participants completed the intervention and the study. There was no measurement of one participant at T1, and another at T2. Also missed were two HoNOS measurements at T2. These participants were in remission for PTSD and major depressive disorder and left the mental health centre after treatment; therefore, they could not be observed by the primary care provider. All other measures were completed by the research assistant.

PTSD and dissociative symptoms

The number of PTSD symptoms and PTSD severity (CAPS-5) decreased over time between baseline, post-treatment and follow-up. The number and severity of each PTSD cluster symptoms decreased over time between baseline and follow-up. Intrusion, avoidance, cognition and mood symptoms decreased during and after treatment, whereas arousal and reactivity were decreased at follow-up (see Table 2). Severity of dissociative symptoms (DES) also decreased between baseline, post-treatment and follow-up. Eight participants were in remission for PTSD at post-treatment and three other participants were in remission at follow-up. Remission rates in the diagnostic subgroups were almost similar: 8 out of 15 for depressive disorder, 2 out of 4 for bipolar disorder and 1out of 4 for schizophrenia spectrum disorder.

Table 2

Results of primary and secondary outcomes based on a mixed model analysis for repeated measures of the full analysis setReference Grubaugh, Zinzow, Paul, Egede and Frueh1

NET, Narrative Exposure Therapy; LSMD, least squares mean difference; CAPS-5, Clinician Administered PTSD Scale for DSM-5; DES, Dissociative Experiences Scale; SMI, severe mental illness; HoNOS, Health of the Nation Outcome Scale; CAN, Camberwell Assessment of Needs; MANSA, Manchester Short Assessment of Quality of Life; GAF, Global Assessment of Functioning scale.

a. Results for the number and duration of contacts (obtained from the electronic record) are based on analyses on a logarithmic scale; table presents back-transformed results. The columns T0, T1 and T2 refer to the period before, during and after treatment.

SMI symptoms, care needs, quality of life and global functioning

Severity of SMI symptoms (HoNOS) decreased between baseline (T0) and follow-up (T2). No significant changes occurred in quality of life (MANSA) and care needs (CAN). Global functioning (GAF) increased over time, between post-treatment and follow-up (see Table 2).

Between T0 and T2, suicide risk shifted from high (44% to 35%) and medium risk (13% to 5%) to low risk (26% to 35%). In the group as a whole, substance misuse decreased from 30% to 24%. One participant had alcohol and substance use at baseline, but was abstinent for both at follow-up. Of the 11 participants in remission for PTSD, five were also in remission for major depression at follow-up (MINI-plus).

Care consumption

The number of contacts changed from 35 in the 6 months before treatment (T0), to 40 during treatment (T0 to T1), and to 31 during the 6 months after treatment (T1 to T2), although this was not statistically significant (overall P = 0.572). However, the geometric mean of the duration of the contacts increased 1.85 times (95%CI 1.35–2.55) from 2021 min (34 h) in the 6 months before treatment (T0) to 3749 min (62 h) for the treatment period T1–T0, whereas it decreased by a factor 0.63 (95%CI 0.48–0.86) to 1271 min (21 h) in the 6 months after treatment (T2) compared with the 6 months before treatment (T0; overall P = <0.001).

Before and during the study, 21 participants received psychiatric medication. Prescribed doses of antipsychotics (n = 13) and benzodiazepines (n = 16) were the most reduced. Mood stabilisers (n = 5) also decreased, but the number of consumers was small. Antidepressant (n = 15) doses increased during NET and did not decrease between post-treatment and follow-up. The trends in medication are shown in Fig. 2.

Fig. 2

Average medication dose before baseline (6 months before T0), during treatment (T0 to T1) and after treatment (T1 to T2).

Harms

No serious events occurred during NET and follow-up. In addition, none of the participants were admitted to hospital or needed crisis management during the study.Reference Mauritz, Van Gaal, Jongedijk, Schoonhoven, Nijhuis-van der Sanden and Goossens14

Discussion

Main findings

To the best of our knowledge, this is the first study to examine the feasibility and applicability of NET for comorbid PTSD in out-patients with SMI. PTSD symptoms and severity reduced significantly at post-treatment and follow-up. All four PTSD clusters showed significant reduction of symptoms, whereas intrusions, arousal and reactivity decreased more slowly than symptoms of avoidance, cognition and mood. These results are in line with other controlled NET studies in vulnerable patients, such as children and adolescents,Reference Peltonen and Kangaslampi52 patients with borderline personality,Reference Pabst, Schauer, Bernhardt, Ruf, Goder and Elbert17 the elderly,Reference Lely, Knipscheer, Moerbeek, Heide, Bout and Kleber53 refugeesReference Lely, Smid, Jongedijk, Knipscheer and Kleber15 and asylum-seeking refugees with PTSD and depressive disorder.Reference Stenmark, Catani, Neuner, Elbert and Holen54 Of the 23 participants, 11 (48%) were in remission for PTSD at follow-up. This corresponds to other NET studies that reported 38%, 55% and 71%.Reference Mørkved, Hartmann, Aarsheim, Holen, Milde and Bomyea55,Reference Steuwe, Rullkötte, Ert, Berg, Neune and Beblo56

Our results suggests that patients with SMI may benefit from NET just like other patient groups. So far, NET has not studied specifically in patients with SMI. Until now, most NET studies excluded patients with psychosis, bipolar disorder, substance misuse and suicidal ideations.Reference Pabst, Schauer, Bernhardt, Ruf, Goder and Elbert17,52-54 One case study reported positive results of NET in a refugee with PTSD and psychotic features.Reference Katsounari57 Mørkved et al Reference Mørkved, Hartmann, Aarsheim, Holen, Milde and Bomyea55 compared NET and prolonged exposure therapy for PTSD and argued that NET and prolonged exposure have several commonalities when it comes to the principles of exposure. An important feature of NET is that trauma-processing is never an isolated event, but is always embedded in the context of a traumatic event and in the life history as a whole. Given this focus on the autobiographical elaboration of traumatic experiences, NET is particularly suited for populations with multiple trauma and complex mental health conditions.Reference Jongedijk16

Comparing NET with prolonged exposure makes sense to the extent that it has shown to be effective in patients with SMI and psychotic disorders, including schizophrenia, bipolar and depressive disorders, in a controlled study. Dissociation, substance use and suicidality risk were not excluded in this study. Results showed that there was no increase of hallucinations, dissociation or suicidality.Reference van den Berg, de Bont, van der Vleugel, de Roos, de Jongh and van Minnen9,Reference van den Berg, de Bont, van der Vleugel, de Roos, de Jongh and van Minnen12 The findings in our study are in line with these results: dissociation, suicidality risk and substance misuse were also not excluded, and all showed reduction during and after NET. Severity of dissociative symptoms also declined significantly at post-treatment and follow-up. These findings are in line with some other NET studies and other TFT studies.Reference Pabst, Schauer, Bernhardt, Ruf, Goder and Elbert17,Reference Steuwe, Rullkötte, Ert, Berg, Neune and Beblo56,Reference Hoeboer, De Kleine, Molendijk, Schoorl, Oprel and Mouthaan58 Also, a meta-analysis on the effect of dissociation suggests that pre-treatment dissociation does not determine trauma-focused psychotherapy outcomes in PTSD.Reference Hoeboer, De Kleine, Molendijk, Schoorl, Oprel and Mouthaan58

SMI symptoms were assessed with generic measures to allow for comparisons across diagnostic groups.Reference de Beurs, Vissers, Schoever, Carlie, van Hemert and Meesters59 The coherence of the SMI outcomes was low: a slight improvement in SMI was seen based on HoNOS, there were no significant changes in perceived care needs (CAN) and quality of life (MANSA) based on self-reporting, and care providers concluded that global functioning (GAF) was significantly increased.

The MINI-plus is a diagnostic and more specific instrument to measure mental disorders, which, in this study, showed remission in 5 out of the 15 participants with major depression, and over all lower disease burden, suicide risk and less substance use. This is partly comparable with the results of a systematic review of outcomes for psychological interventions for PTSD in psychosis. For prolonged exposure and EMDR, secondary outcomes for psychopathology and distress showed significant reduction, especially for depression and anxiety, but social functioning did not improve. The long duration of SMI and additional social isolation are supposed to be influencing factors.Reference Swan, Keen, Reynolds and Onwumere60

The duration of contacts increased during NET (T0 to T1), but decreased significantly during the 6 months’ follow-up (T1 to T2), which might reflect less burden of disease. Doses of prescribed benzodiazepines, antipsychotics and mood stabilisers also decreased during and after NET. This suggests that patients experienced less anxiety, irritability, arousal, reactivity and showed reduction of psychotic and bipolar symptoms. In contrast, doses of antidepressants slightly increased during NET and did not change at follow-up. Antidepressants were indicated for both depression and PTSD, and are more difficult to phase out, particularly selective serotonin reuptake inhibitors.Reference Horowitz and Taylor61 To our knowledge, this is the first study on psychological interventions for PTSD in SMI that takes into account care consumption, expressed as contacts and prescribed medication.Reference Swan, Keen, Reynolds and Onwumere60,Reference Sin, Spain, Furuta, Murrells and Norman62

Findings in context: treating PTSD in out-patients with SMI

Our results support the notion that out-patients with SMI with comorbid PTSD can tolerate intensive trauma-focused therapy like NET. The long-standing clinical perception of vulnerability in patients with SMI has not only resulted in appropriate psychiatric care, but unfortunately in the underestimation of the resilience of these patients. This perception may influence underdiagnosis, overlooking trauma histories and not recognising comorbid PTSD, all contributing to undertreatment.Reference Grubaugh, Zinzow, Paul, Egede and Frueh1,Reference Mauritz, Goossens, Draijer and van Achterberg2,Reference Bateman, Henderson and Kezelman7,Reference Sweeney, Filson, Kennedy, Collinson and Gillard63 Patients and care providers have to balance resilience and vulnerability in careful conversations, to consider the right time and circumstances for treatment. This study was therefore embedded in clinical practice where optimal care and support by FACT team members was an important condition. Given that the overall disease burden was high and TFT is often perceived as intensive, most of the participants could endure and tolerate NET. As no serious adverse events occurred, no crisis management was required and no patients were admitted to hospital, this underlines the applicability and safety of NET in this population.

Strengths and limitations

A strength of this study is that it was conducted in the real-life clinical context. NET was provided to out-patients with SMI in a familiar environment, with support from their known care providers from the certified FACT teams. Diagnostic assessments (i.e. PTSD and SMI) were in line with clinical practice and, in addition, routine outcome measurements for SMI were used. NET also fits well in the workflow of the involved professional, which is helpful for future implementation. Furthermore, this strategy avoids extra diagnostic burden and ensures its applicability and implementation in clinical practice.

A second strength of the study was that the five trained and certified NET therapists were all FACT team members and experienced with out-patients with SMI. They followed the NET protocol and received group supervision from a trained NET supervisor.36 Because of this, they were able to discuss questions and dilemmas among NET for out-patients with SMI.

The use of the EPR to monitor prescribed medication and contacts is a third strength, because these objective data were not influenced by oral assessments.

Despite these strengths, the limitations of this study are that it was conducted in a small study population without a control group. Moreover, most participants were female; therefore caution is warranted for statements about effectiveness for men. However, for all participants together, the observed changes are in line with the proven effect of prolonged exposure, which shares important principles with NET.

Second, generalisability is limited, as no subgroup analysis could be done by age, gender or primary diagnosis. However, prolonged exposure and EMDR have be shown to be effective in psychosisReference Swan, Keen, Reynolds and Onwumere60 and SMI,Reference Sin, Spain, Furuta, Murrells and Norman62 whereas NET is effective in major depressive disorder.Reference Stenmark, Catani, Neuner, Elbert and Holen54

Third, the used routine outcome measurements are possibly not responsive and distinctive enough with regard to SMI symptoms, care needs and quality of life.Reference de Beurs, Blankers, Delespaul, van Duijn, Mulder and Nugter64 Finally, implementing this intervention in daily clinical practice also meant that the NET protocol and the agreed biweekly FACT support were not always strictly followed. This concerns mostly interruptions during NET and replacement of FACT care providers.

Interpretation and recommendations

In conclusion, our results support that NET is feasible and applicable to SMI out-patients in a FACT setting. NET seems to be a valuable addition to other evidence-based, trauma-focused therapies (i.e. cognitive–behavioural treatment, prolonged exposure and eye movement desensitisation reprocessing) and is specifically indicated for PTSD related to repeated interpersonal trauma. Given the high prevalence of repeated interpersonal trauma and PTSD in patients with SMIReference Mauritz, Goossens, Draijer and van Achterberg2,Reference Stumbo, Paulson and Green3 and the burden of disease, offering TFT to these patients is important. Relevant screening by means of structured diagnostic interviews for trauma history, PTSD and primary SMI disorder are recommended in this group. Using more specific diagnostic instruments to evaluate changes in SMI could help to implement appropriate care. These strategies require sufficient training for therapists and supporting FACT team members. In this context, it is helpful and encouraging that national health institutes are increasingly convinced of the importance of developing trauma-informed care policies in mental health systems.Reference Bateman, Henderson and Kezelman7

Data availability

The data that support the findings of this study are available from the corresponding author, M.W.M., upon reasonable request.

Acknowledgements

This study was carried out as part of an internal project at GGNet Mental Health Center, to improve the treatment of complex trauma-related disorders in severe mental illness.

We thank Wanda Pol, MSc, for data collection and descriptive analysis; Enzo Boeijen, MSc, for data analysis with mixed models; and Reinier Akkermans, PhD, for statistical advice.

Author contributions

M.W.M., B.G.I.v.G., and P.J.J.G. designed the study. R.A.J. advised on NET and, with M.W.M., made a substantive contribution toward knowledge and training. M.W.M. carried out the study and analysed the data with B.G.I.v.G., and P.J.J.G. advised on SMI. B.G.I.v.G. and H.V. supervised the study. M.W.M. wrote the first draft of the article. All authors made critical revisions of the manuscript and approved the final version.

Funding

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Declaration of interest

None.

ICMJE forms are in the supplementary material, available online at https://doi.org/10.1192/bjo.2020.124

References

Grubaugh, AL, Zinzow, HM, Paul, L, Egede, LE, Frueh, BC. Trauma exposure and posttraumatic stress disorder in adults with severe mental illness: a critical review. Clin Psychol Rev 2011; 31: 883–99.CrossRefGoogle ScholarPubMed
Mauritz, MW, Goossens, PJ, Draijer, N, van Achterberg, T. Prevalence of interpersonal trauma exposure and trauma-related disorders in severe mental illness. Eur J Psychotraumatol 2013; 4, 19985.CrossRefGoogle ScholarPubMed
Stumbo, SP, Paulson, RI, Green, CA. The impact of adverse child and adult experiences on recovery from serious mental illness. Psychiatr Rehabil J 2015; 38(4): 320–7.CrossRefGoogle ScholarPubMed
Misiak, B, Krefft, M, Bielawski, T, Moustafa, AA, Sasiadek, MM, Frydecka, D. Toward a unified theory of childhood trauma and psychosis: a comprehensive review of epidemiological, clinical, neuropsychological and biological findings. Neurosci Biobehav Rev 2017; 75: 393–406.Google Scholar
Aas, M, Henry, C, Andreassen, OA, Bellivier, F, Melle, I, Etain, B. The role of childhood trauma in bipolar disorders. Int J Bipolar Disord 2016; 4: 2.CrossRefGoogle ScholarPubMed
Flory, JD, Yehuda, R. Comorbidity between post-traumatic stress disorder and major depressive disorder: alternative explanations and treatment considerations. Dialogues Clin Neurosci 2015; 17(2): 141–50.Google ScholarPubMed
Bateman, J, Henderson, C, Kezelman, C. Trauma-informed care and practice: towards a cultural shift in policy reform across mental health and human services in Australia - a national strategic direction. Mental Health Coordinating Council (MHCC) and NSW Australia Adults Surviving Child Abuse (ASCA), 2013.Google Scholar
Hagenaars, MA, van Minnen, A, Hoogduin, KAL. The impact of dissociation and depression on the efficacy of prolonged exposure treatment for PTSD. Behav Res Ther 2010; 48: 19–27.CrossRefGoogle ScholarPubMed
van den Berg, DP, de Bont, PA, van der Vleugel, BM, de Roos, C, de Jongh, A, van Minnen, A, et al. Trauma-focused treatment in PTSD patients with psychosis: symptom exacerbation, adverse events, and revictimization. Schizophr Bull 2016; 42(3): 693–702.CrossRefGoogle ScholarPubMed
Otto, MW, Perlman, CA, Wernicke, R, Reese, HE, Bauer, MS, Pollack, HH. Posttraumatic stress disorder in patients with bipolar disorder: a review of prevalence, correlates, and treatment strategies. Bipolar Disord 2004; 6(6): 470–9.CrossRefGoogle ScholarPubMed
Lu, W, Fite, R, Kim, E, Hyer, L, Yanos, PT, Mueser, KT. Cognitive-behavioral treatment of PTSD in severe mental illness. Am J Psychiatr Rehabil 2009; 12(1): 73–91.Google Scholar
van den Berg, DPG, de Bont, PAJM, van der Vleugel, BM, de Roos, C, de Jongh, A, van Minnen, A, et al. Prolonged exposure vs eye movement desensitization and reprocessing vs waiting list for posttraumatic stress disorder in patients with a psychotic disorder a randomized clinical trial. JAMA Psychiatry 2015; 72(3): 259–67.Google ScholarPubMed
Schauer, M, Neuner, F, Elbert, T. Narrative Exposure Therapy. A Short-Term Treatment for Traumatic Stress Disorders (2nd revised and expanded edn). Hogrefe Publishers, 2011.Google Scholar
Mauritz, MW, Van Gaal, BGI, Jongedijk, RA, Schoonhoven, L, Nijhuis-van der Sanden, MWG, Goossens, PJ. Narrative exposure therapy for posttraumatic stress disorder associated with repeated interpersonal trauma in patients with severe mental illness: a mixed methods design. Eur J Psychotraumatol 2016; 7: 32473.Google ScholarPubMed
Lely, JCG, Smid, GE, Jongedijk, R, Knipscheer, JW, Kleber, RJ. The effectiveness of narrative exposure therapy: a review, meta-analysis and meta-regression analysis. Eur J Psychotraumatol 2019; 10(1): 1–13.CrossRefGoogle ScholarPubMed
Jongedijk, RA. Narrative exposure therapy: an evidence-based treatment for multiple and complex trauma. Eur J Psychotraumatol 2014; 5(1): 26522.CrossRefGoogle ScholarPubMed
Pabst, A, Schauer, M, Bernhardt, K, Ruf, M, Goder, R, Elbert, T, et al. Evaluation of narrative exposure therapy (NET) for borderline personality disorder with comorbid posttraumatic stress disorder. Clin Neuropsychiatry 2014; 11(4): 108–17.Google Scholar
Dutch Cochrane Centre. Netherlands Trial Register. Dutch Cochrane Centre, 2016 (https://www.trialregister.nl/).Google Scholar
Sheehan, DV, Lecrubier, Y, Sheehan, KH, Amorim, P, Janavs, J, Weiller, E, et al. The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 1998; 59(suppl 20): 22–33; quiz 4–57.Google ScholarPubMed
van Vliet, IM, de Beurs, E. The Mini-International Neuropsychiatric Interview. A brief structured diagnostic psychiatric interview for DSM-IV and ICD-10 psychiatric disorders. Dutch J Psychiatry 2007; 49(6): 393–7.Google ScholarPubMed
First, MB, Spitzer, RL, Gibbon, M, Williams, JBW. The Structured Clinical Interview for DSM-III-R Personality Disorders (SCID-II). Part I: Description. J Pers Disord 1995; 9(2): 83–91.CrossRefGoogle Scholar
Pedersen, G, Karterud, S. The symptom and function dimensions of the Global Assessment of Functioning (GAF) scale. Compr Psychiatry 2012; 53: 292–8.CrossRefGoogle ScholarPubMed
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders(4th edn, text revision). American Psychiatric Association, 2000.Google Scholar
Boeschoten, MA, Bakker, A, Jongedijk, RA, Olff, M. Life Events Checklist for the DSM-5. Stichting Centrum ‘45, ARQ Psychotrauma Expert Groep, 2014 (https://www.psychotraumadiagnostics.centrum45.nl/nl/ptss).Google Scholar
Weathers, FW, Blake, DD, Schnurr, PP, Kaloupek, DG, Marx, BP, Keane, TM. The Life Events Checklist for DSM-5 (LEC-5). National Center for PTSD, 2013 (https://www.ptsd.va.gov/).Google Scholar
Boeschoten, MA, Bakker, A, Jongedijk, RA, van Minnen, A, Elzinga, BM, Rademaker, AR, et al. Clinician Administered PTSD Scale for DSM-5 – Dutch Version. Stichting Centrum ‘45, ARQ Psychotrauma Expert Groep, 2014 (http://www.psychotraumadiagnostics.centrum45.nl/nl/ptss).Google Scholar
Weathers, FW, Blake, DD, Schnurr, PP, Kaloupek, DG, Marx, BP, Keane, TM. The Clinician-Administered PTSD Scale for DSM-5 (CAPS-5). National Center for PTSD, 2013 (https://www.ptsd.va.gov).Google Scholar
Boeschoten, MA, Van der Aa, N, Bakker, A, Ter Heide, FJJ, Hoofwijk, MC, Jongedijk, RA, et al. Development and evaluation of the Dutch clinician-administered PTSD scale for DSM-5 (CAPS-5). Eur J Psychotraumatol 2018; 9(1): 1546085.CrossRefGoogle Scholar
van Veldhuizen, JR. FACT: a Dutch version of ACT. Community Ment Health J 2007; 43(4): 421–33.CrossRefGoogle ScholarPubMed
Brewin, R, Rose, S, Andrews, B, Green, J, Tata, P, McEvedy, C, et al. Brief screening instrument for post-traumatic stress disorder. BrJ Psychiatry 2002; 181: 158–62.CrossRefGoogle ScholarPubMed
Weathers, FW, Litz, BT, Keane, TM, Palmieri, PA, Marx, BP, Schnurr, PP. PTSD Checklist for the DSM-5 (PCL-5). National Center for PTSD, 2013 (https://www.ptsd.va.gov).Google Scholar
Boeschoten, MA, Bakker, A, Jongedijk, RA, Olff, M. PTSS Checklist voor de DSM-5 (PCL-5) – Dutch Version. Stichting Centrum ‘45, ARQ Psychotrauma Expert Groep, 2014 (https://www.psychotraumadiagnostics.centrum45.nl/nl/ptss).Google Scholar
Badu, E, O'Brien, AP, Mitchell, R. An integrative review on methodological considerations in mental health research – design, sampling, data collection procedure and quality assurance. Arch Public Health 2019; 77: 37.CrossRefGoogle ScholarPubMed
Jongedijk, RA, Mauritz, MW. Narrative Exposure Therapy: Treatment Manual. Oegstgeest/Diemen/Warnsveld: Centrum '45/ARQ Psychotrauma Expert Groep/GGNet, 2016.Google Scholar
Jongedijk, RA. Life Stories and Psychotrauma. Narrative Exposure Therapy in Practice. Boom, 2014.Google Scholar
ARQ National Psychotrauma Centre. Narrative Exposure Therapy. ARQ National Psychotrauma Centre, 2016 (https://academy.arq.org/ggz-professionals-cursus-2/narratieve-exposure-therapie-net).Google Scholar
Drukker, M, Visser, E, Sytema, S, van Os, J. Flexible assertive community treatment, severity of symptoms and psychiatric health service use, a real life observational study. Clin Pract Epidemiol Ment Health 2013; 9: 202–9.CrossRefGoogle ScholarPubMed
van Veldhuizen, JR. FACT: a Dutch version of ACT. Community Health J 2007; 43: 421–33.Google ScholarPubMed
Bernstein, EM, Putnam, FW. Development, reliability and validity of a dissociation scale. J Nerv Ment Dis 1986; 174: 727–35.Google ScholarPubMed
Orrell, M, Yard, P, Handysides, J, Schapira, R. Validity and reliability of the Health of the Nation Outcome Scales in psychiatric patients in the community. Br J Psychiatry 1999; 174: 409–12.CrossRefGoogle Scholar
Phelan, M, Thornicroft, G, Dunn, G, Holloway, F, Wykes, T, Strathdee, G, et al. The Camberwell Assessment of Need: the validity and reliability of an instrument to assess the needs of people with severe mental illness. Br J Psychiatry 1995; 167: 589–95.CrossRefGoogle ScholarPubMed
Priebe, S, Huxley, P, Knight, S, Evans, S. Application and results of the Manchester Short Assessment of Quality of Life (MANSA). Int J Soc Psychiatry 1999; 45: 7–12.CrossRefGoogle Scholar
Anonymous. Calculation of a Benzodiazepine Switch, Psychiatrienet 2014. (visited 2019, http://wiki.psychiatrienet.nl/index.php/Special:RunQuery/CalcBenzo).Google Scholar
Health Alliance. Antidepressants Comparison Guide Most Commonly Prescribed How to Switch Antidepressants, 2019 (https://www.healthalliance.org/media/Resources/generic-antidepressants-chart.pdf).Google Scholar
Anonymous. Switching Antidepressants. Psychiatrienet 2014 (visited 2019, http://wiki.psychiatrienet.nl/index.php/SwitchAntidepressants).Google Scholar
Andreasen, NC, Pressler, M, Nopoulos, P, Miller, D, Ho, BC. Antipsychotic dose equivalents and dose-years: a standardized method for comparing exposure to different drugs. Biol Psychiatry 2010; 67(3): 255–62.CrossRefGoogle ScholarPubMed
Anonymous. Switching Antipsychotics, 2014. Psychiatrienet 2014 (visited 2019, http://wiki.psychiatrienet.nl/index.php/SwitchAntipsychotics).Google Scholar
National Health Care Institute. Pharmacotherapeutic Compass. National Health Care Institute, 2019 (https://www.farmacotherapeutischkompas.nl/).Google Scholar
Billingham, SAM, Whitehead, AL, Julious, SA. An audit of sample sizes for pilot and feasibility trials being undertaken in the United Kingdom registered in the United Kingdom Clinical Research Network database. BMC Med Res Methodol 2013; 13: 104.CrossRefGoogle ScholarPubMed
Sim, J. Should treatment effects be estimated in pilot and feasibility studies? BMC Pilot Feasibility Stud 2019; 5: 107.CrossRefGoogle ScholarPubMed
Schulz, K F, Altman, D G, Moher, D. CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMC Med 2010; 8(18).CrossRefGoogle ScholarPubMed
Peltonen, K, Kangaslampi, S. Treating children and adolescents with multiple traumas: a randomized clinical trial of narrative exposure therapy. Eur J Psychotraumatol 2019; 10: 1558708.CrossRefGoogle ScholarPubMed
Lely, JCG, Knipscheer, JW, Moerbeek, M, Heide, F, Bout, J, Kleber, RJ. Randomised controlled trial comparing narrative exposure therapy with present-centred therapy for older patients with post-traumatic stress disorder. Br J Psychiatry 2019; 214: 369–77.CrossRefGoogle ScholarPubMed
Stenmark, H, Catani, C, Neuner, F, Elbert, T, Holen, A. Treating PTSD in refugees and asylum seekers within the general health care system. A randomized controlled multicenter study. Behav Res Ther 2013; 51: 641–7.CrossRefGoogle ScholarPubMed
Mørkved, N, Hartmann, K, Aarsheim, LM, Holen, D, Milde, AM, Bomyea, J, et al. A comparison of narrative exposure therapy and prolonged exposure therapy for PTSD. Clin Psychol Rev 2014; 34: 453–67.CrossRefGoogle ScholarPubMed
Steuwe, C, Rullkötte, N, Ert, V, Berg, M, Neune, F, Beblo, T, et al. Effectiveness and feasibility of narrative exposure therapy (NET) in patients with borderline personality disorder and posttraumatic stress disorder – a pilot study. BMC Psychiatry 2016; 16: 254.CrossRefGoogle ScholarPubMed
Katsounari, I. Narrative exposure therapy for treating PTSD with psychotic features: a case study. Clin Case Stud 2014; 14(5): 342–56.CrossRefGoogle Scholar
Hoeboer, CM, De Kleine, RA, Molendijk, ML, Schoorl, M, Oprel, DAC, Mouthaan, J, et al. Impact of dissociation on the effectiveness of psychotherapy for post-traumatic stress disorder: meta-analysis. BJPsych Open 2020; 6(3): e53.CrossRefGoogle ScholarPubMed
de Beurs, E, Vissers, E, Schoever, R, Carlie, IVE, van Hemert, AM, Meesters, Y. Comparative responsiveness of generic versus disorder-specific instruments for depression: an assessment in three longitudinal datasets. Depress Anxiety 2018; 36: 93–102.CrossRefGoogle ScholarPubMed
Swan, S, Keen, N, Reynolds, N, Onwumere, J. Psychological interventions for post-traumatic stress symptoms in psychosis: a systematic review of outcomes. Front Psychol 2017; 8: 341.CrossRefGoogle ScholarPubMed
Horowitz, MA, Taylor, D. Tapering of SSRI treatment to mitigate withdrawal symptoms. Lancet Psychiatry 2019; 6(6): 538–46.CrossRefGoogle ScholarPubMed
Sin, J, Spain, D, Furuta, M, Murrells, T, Norman, I. Psychological Interventions for Post-Traumatic Stress Disorder (PTSD) in People with Severe Mental Illness. The Cochrane Collaboration, 2017 (https://www.cochrane.org/CD011464/SCHIZ_psychological-interventions-post-traumatic-stress-disorder-ptsd-people-severe-mental-illness).CrossRefGoogle Scholar
Sweeney, A, Filson, B, Kennedy, A, Collinson, L, Gillard, S. A paradigm shift: relationships in trauma-informed mental health services. BJPsych Adv 2018; 24: 319–33.CrossRefGoogle ScholarPubMed
de Beurs, E, Blankers, M, Delespaul, PE, van Duijn, E, Mulder, N, Nugter, A, et al. Treatment results for severe psychiatric illness: which method is best suited to denote the outcome of mental health care? BMC Psychiatry 2018; 18: 225.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1 Flow diagram, adapted to single-group design (CONSORT 2010).51 SMI, severe mental illness.

Figure 1

Table 1 Demographic and clinical characteristics (n = 23)

Figure 2

Table 2 Results of primary and secondary outcomes based on a mixed model analysis for repeated measures of the full analysis set1

Figure 3

Fig. 2 Average medication dose before baseline (6 months before T0), during treatment (T0 to T1) and after treatment (T1 to T2).

Supplementary material: File

Mauritz et al. supplementary material

Mauritz et al. supplementary material

Download Mauritz et al. supplementary material(File)
File 5.8 MB
Submit a response

eLetters

No eLetters have been published for this article.