| Literature DB >> 34836461 |
Denisa A Clisu1,2, Imogen Layther3, Deborah Dover2, Russell M Viner1, Tina Read2, David Cheesman2, Sally Hodges4, Lee D Hudson1,3.
Abstract
Background: Many children and young people (CYP) presenting with mental health crises are admitted to hospital due to concerns around illness severity and risk. Whilst inpatient admissions have an important role for such children, there are a number of burdens associated with them, and safe avoidance of admissions is favourable. We systematically reviewed the literature for studies of interventions reported as alternatives to a hospital admission in CYP presenting with mental health crises, in any inpatient setting.Entities:
Keywords: Child; adolescent; crisis; inpatient admissions; mental health
Mesh:
Year: 2021 PMID: 34836461 PMCID: PMC8811329 DOI: 10.1177/13591045211044743
Source DB: PubMed Journal: Clin Child Psychol Psychiatry ISSN: 1359-1045 Impact factor: 2.544
Figure 1.PRISMA flow diagram of included and excluded studies.
Summary of the studies included.
| Author (year), country | Design | Sample | N (%male, %female) | Age range (mean, | Outcome measure(s) | Intervention (duration) | Intervention details | Comparison condition | Main findings | Conclusions | Overall risk of bias |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Single-session interventions for emergency department crisis presentations | |||||||||||
| Service evaluation | Adolescents admitted for emergency hospitalisation evaluation | 48 (45.83%, 54.17%) | 12–18 (modal age: 16.5) | Inpatient admission rate | Emergency evaluation interview + brief therapeutic intervention (max. 24 hours) | Semi-structured interview and mental status evaluation. After that, a supportive, reality-based, present-focused therapeutic intervention was offered. Adolescents could be helped for up to 24 hours if necessary | N/A | 5 patients were hospitalised right after the evaluation (10%). 0 patients were hospitalised in the following month. 4.2% ( | The majority of the adolescents referred to emergency hospitalisation were maintained in the community after receiving the emergency evaluation and brief therapeutic intervention | Critical | |
| Service Evaluation | Adolescents with psychiatric crisis | n.s. | n.s. | Admission rate and length of inpatient stay | Rapid response model (single-session offered max 48 hours post-referral) | Brief interview focused on crisis and risk | Pre-implementation | Site 1: RRM phase had no significant impact on number of consultations leading to admission. RRM phase had a significant effect on the monthly average length of inpatient stay (F(1,42) = 3.1, | Suggestion of lower admission rate and length of stay associated with RRM implementation, although each was true or investigated only for one site rather than both | Serious | |
| Cohort external historical retrospective control group | Suicidal adolescents at the ED | In experimental condition: 100 (24%, 76%) | 13–18 (15.6, 1.5) | Admission rate | Family-based crisis intervention (FBCI) in the emergency room (single-session) | CBT- and family-based session using psychoeducation, therapeutic readiness and safety planning | Suicidal adolescents ( | Significant decrease in admission rate from pre-FBCI (55%) to post-FBCI (35%): | FBCI was associated with a lower percentage of patients admitted to hospital in comparison to a control group attending the clinic before its implementation | Low | |
| Exclusively in-home interventions | |||||||||||
| RCT | Adolescents referred to emergency psychiatric hospitalisation | 113 (65%, 35%) | 10–17 (13, n.s.) | GSI-BSI, CBCL, PEI, self-esteem subscale of FFS | Multisystemic therapy (3–6 months) | Family and behavioural therapy strategies used to intervene in the key social systems | Hospitalisation ( | Both groups reported pre- to post-treatment improvements in GSI-BSI (child and caregiver-reported), CBCL internalising (caregiver-reported) and CBCL-social functioning (caregiver-reported), and a deterioration in FACES-III family adaptability (caregiver) ( | While both treatments improved child’s self-reported and caregiver-reported symptoms severity, caregiver-reported internalising symptoms and social functioning and family adaptability as reported by youths, MST proved to be superior to hospitalisation in many areas. For example, MST was better than hospitalisation at improving externalising symptoms (caregiver and teacher-reports), family adaptability (youth-reported) and cohesion (caregiver-reported) and was associated with less days spent out of school. Hospitalisation was however superior to MST in improving youth self-esteem | Low | |
| RCT | Adolescents referred to emergency psychiatric hospitalisation | 113 (65%, 35%) | 10–17 (12.9, 2.1) | GSI-BSI, CBCL, PEI, self-esteem subscale of FFS | Multisystemic therapy (3–6 months) | Family and behavioural therapy strategies used to intervene in the key social systems | Hospitalisation ( | Clinical improvements were maintained until the 12-months follow-up point, but the group differences which were initially found in | Both MST and hospitalisation were effective at improving the of CYP in crises on the long-term, but initial differences seen between groups dissipated at 1-year post-treatment | Low | |
| RCT | Adolescents referred to emergency psychiatric hospitalisation | 113 (65%, 35%) | 10–17 (12.9, 2.1) | FFS, BSI, CBCL, HSC, YRBSS | Multisystemic therapy (3–6 months) | Family and behavioural therapy strategies used to intervene in the key social systems | Hospitalisation ( | A significant time effect was found in both groups for most measures, with patients scoring lower at follow-up than pre-treatment in CBCL caregiver-rated attempted suicide (t = −5.25, | Compared to hospitalisation, MST was found to be more effective in reducing youth-reported suicide attempts. Both treatments were equally effective in decreasing caregiver-reported attempted suicide, suicidal ideation, hopelessness and depression and anxiety symptoms | Low | |
| Uncontrolled pre-post study | CYP with externalising psychiatric disorders requiring inpatient admission | 50 (74%, 26%) | 5–16 (9.8, 2.4) | SGKJ, MEI, non-involved clinician in the care of the child ratings on: symptom load, level of functioning, psychosocial environment | Home-treatment (1–2/week for 2 hours for 3.5 months) | Utilised principles of behaviour modification and parent training: reinforcement schedules, training of social skills and therapeutic exercises | N/A | A significant decrease was reported in the MEI total symptoms score from pre-treatment (M = 11.9) to post-treatment (M = 8.1): | The home-treatment was associated with a decrease in psychological symptoms and psychosocial adjustment, showing positive results in almost all areas of functioning considered | Serious | |
| Uncontrolled pre-post study | CYP who require restrictive and intensive mental health services | 104 (62%, 38%) | 4–17 (n.s.) | Y-OQ | In-home family centered treatment | 24/7 access to services, exploring areas to improve as a family system | N/A | Scores on the Y-OQ decreased from pre-treatment through the intervention: pre-treatment M = 106.53 | The in-home family treatment was suggested to lead to improvements or even recovery for a number of patients, from pre-treatment to throughout the treatment and finalisation. When compared to a group of patients receiving outpatient treatment, no evidence was found for superiority of the in-home intervention | Serious | |
| RCT | CYP at risk of out-of-home placement | 31 (58%, 42%) | n.s. (14.5, n.s.) | Out-of-home placement (including admission), CBCL, YRBSS, PEI, criminal activity, SRD, school placement, FACES-III, SSQ | Multisystemic therapy (3–6 months) | Family and behavioural therapy strategies used to intervene in the key social systems | Usual care | A significantly higher change was reported in externalising symptoms for MST in comparison to usual care (F(1, 25) = 4.62, | MST was reported to be superior to usual care in improving youth-rated externalising and internalising symptoms, self-reported minor delinquencies, days spent in general education and monthly days in out-of-home placement by the end of treatment | Some concerns | |
| RCT | Adolescents referred to emergency psychiatric hospitalisation | 113 (65%, 35%) | 10–17 (13, n.s.) | Admission rate and length of stay | Multisystemic therapy (3–6 months) | Family and behavioural therapy strategies used to intervene in the key social systems | Hospitalisation ( | 44% of the patients receiving MST were admitted to hospital by the end of treatment. The mean days hospitalised was significantly lower for patients in the MST group (M = 2.39, | The majority of patients receiving MST avoided admission by the end of treatment. It was suggested that MST was superior at decreasing the number of overall days hospitalised and days hospitalised per episode in comparison to admission | Low | |
| Matched sample control group | CYP requiring psychiatric hospitalisation | 105 (n.s.) | 6–17 (n.s.) | MEI, behaviour changes (child, parents, therapist) | Home-treatment (3 months) | Child-centred tailored, home-based and family-focused treatment | Hospitalisation | Both groups achieved significant positive pre-treatment to follow-up changes in the total MEI symptom score ( | CYP admitted had higher significant improvements reported in the total symptoms score ( | Moderate | |
| RCT | CYP with emotional and behavioural disorders (EBDs) | 65 (n.s., n.s.) | 6–14 (n.s., n.s.) | SCIS, SSRS | Family preservation program (up to 12 hours/week, 12 weeks) | Flexible and intensive in-home support available using problem-solving and CBT-based techniques | 5-day residential program (5DR) (5 days/week, 3 months). Individualised and flexible day treatment | A significantly higher decrease in internalising symptoms in the family therapy group was detected from pre- treatment (M = 69.76; | Although both treatments improved externalising and behavioural problems and social competence, the family programme was superior in improving internalising symptoms in comparison to the residential treatment, which was reported to worsen the problems | Some concerns | |
| Outside of the home but outside of hospital clinics | |||||||||||
| Service Evaluation | CYP with complex psychological needs | 42 (n.s.) | n.s. | Admission rate | Community intensive therapy (CITT) (n.s.) | Services offered were similar to inpatient setting but delivered in the community. Strong emphasis on interagency network and especially with educational services. Individual and family therapy were offered flexibly, limited group therapy activities, and dieticians, and clinical psychologists were available if needed | A similar sample attending the service before the implementation of the CITT | Number of inpatient admissions decreased considerably after CITT implementation: 5–6 CYP were admitted the year before implementation at any one time while for the 5 years after implementation, 0–1 CYP were admitted every year | CITT was suggested to be effective in reducing the likelihood of inpatient psychiatric admission of CYP with complex mental health needs | Serious | |
| Service Evaluation | CYP in psychiatric crisis | n.s. | n.s. | The Ohio scale | Emergency mobile psychiatric services (EMPSs) (average of 20.8 days of help, maximum 45 days) | Emergency crises service delivered at various locations 24/7: crisis stabilisation and support, screening and assessment, suicide assessment and prevention, brief solution-focused interventions, and referral and linkage to ongoing care | N/A | Significant pre- to post-treatment changes occurred in parent- and clinician-rated child functioning and problem severity. Parent-rated functioning scores increased from M = 42.94 at pre-treatment to M = 45.52 at post-treatment (t = 4.70, | EMPS improved psychological outcomes and social functioning and led to clinically significant results for some children | Critical | |
| RCT | CYP with severe behaviour disorders referred to admission | 49 (84%, 16%) | 5–13 (n.s.) | BRS, DESB, DCB, MAT, SESAT, PSS (in mothers), FFC | Community treatment (6 months) | Highlight on support for the parents and involvement of social services for the family. Distinguishing characteristic of the program: continuous availability of staff, persistent advocacy and treatment flexibility. Pharmacology or individual therapy provided where needed | Inpatient hospitalisation (6 months) | A significant decrease in scores for all measures was detected for all factors in the community treatment group. A decrease from M = 2.40 ( | Community treatment was reported to improve more psychological symptoms than hospitalisation, however no statistical tests were conducted to investigate the difference in change between the two groups. Both groups reported similar achievements in arithmetic and reading by the end of treatment and parental mental health was not impacted (neither positively nor negatively) by either of the two treatments | High | |
| Exclusively clinic-based interventions, including day treatment | |||||||||||
| Uncontrolled pre-post study | Adolescent suicide attempters | 35 (14%, 86%) | n.s. (14.89, 1.60) | NIMH DISC-IV, HASS, CES-D, BHS, SAS | SAFETY program (M total sessions = 10.14) | Based on cognitive-behavioural techniques, aims to enhance safety and reduce suicide risk. Included individual, parental and family sessions | N/A | Significant pre-treatment to follow-up differences were reported on all scales. HASS suicide attempt scores decreased from M = 0.89 ( | The SAFET program was reported to be effective in improving all clinical, functioning and family outcomes | Moderate | |
| Cohort external historical retrospective control group | CYP in crisis referred from the emergency department | 980 (n.s.) | n.s. | Admission rate | Emergency room follow-up team (ERFUT) | Immediate, intensive (daily if needed), short-term, family and psycho-dynamically oriented treatment in addition to other interventions | CYP presenting to the emergency room in crisis before the implementation of the service | A 16% reduction in the proportion of patients admitted was recorded after the implementation of the ERFUT in comparison to a period before its implementation: | In comparison to a period before its implementation, ERFUT was associated with a decrease in admissions for CYP presenting to the emergency department in psychological crisis | Serious | |
| RCT | Psychotic children and adolescents that require psychiatric hospitalisation | 48 (69%, 31%) | 4.16–17 (10.33, n.s.) | Rate of inpatient admission, hospitalisation requests, police difficulties, out of regular school placements | Parental counselling with or without medication (1 hr/week) | n.s. | No counselling with or without medication | Most of the patients were maintained in the community and no significant differences were reported between the 4 groups in regard to the number of patients hospitalised ( | The majority of the patients in the trial were maintained in the community, did not provoke hospitalisation requests, did not get into police difficulties and remained in their regular classroom. Neither parental counselling nor medication proved to be more effective in comparison to each other or in comparison to no treatment | High | |
| Uncontrolled pre-post | CYP moderately to severely affected by a diagnosable psychiatric disorder | 114 (n.s.) | 5–18 (11.6, n.s.) | CBCL, YRS, utilization of mental health services. Intake and follow-up questionnaire (parent report of child functioning), FAD | Partial hospitalisation (12–397 days, M = 115.9) | Individual therapy, family therapy, group psychotherapy, psychoeducational groups | N/A | Treatment significantly decreased scores on all CBCL subscales from intake to follow-up apart from sex problems (from M = 59.36 to M = 55.92, t = 1.33, | The partial hospitalisation was successful in improving all clinical outcomes (apart from sex problems as rated by the child) and some school, peer relations and community integration functioning outcomes. Both parents and children reported that affective involvement and behaviour control improved in the family by end of treatment. The treatment also decreased the use of mental health inpatient services | Critical | |
Note: CBCL = Child Behaviour Checklist; GSI-BSI = The Global Severity Index of the Brief Symptom Inventory; BSI = Brief Symptom Inventory; PEI = Personal Experiences Inventory; FFS = Family, Friend and Self Scale; HSC = Hopelessness Scale for Children; YRBSS = Youth Risk Behaviour Survey; SGKJ = Skala zur Gesamtbeurteilung von Kindern und Jugendlichen; MEI = Mannheim Parent Interview; SRD = Self-report Delinquency Scale; FACES-III = Family Adaptability and Cohesion Evaluation Scales - Third Edition; SSQ = Social Support Questionnaire; SCIS = Standardized Client Information System; SSRS = Social Skills Rating System; The Ohio Scale; BRS = The Conners Behaviour Rating Scale; DESB = The Devereux Elementary School Behaviour Rating Scale; DCB = Devereux Child Behaviour Rating Scale; MAT = Metropolitan Achievement Test; SESAT = Stanford Early School Achievement Test; PSS = Psychiatric Status Schedule; FFC = Family Functioning Checklist; YRS = Youth Self-Report; FAD = McMaster Family Assessment Device; Y-OQ = Youth Outcome Questionnaire; NIMH DISC-IV = NIMH Diagnostic Interview Schedule for Children Version IV; Columbia Suicide History Form; HASS = Harkavy–Asnis Suicide Survey; CES-D = Center for Epidemiological Studies-Depression Scale; BHS = Beck Hopelessness Scale; SAS = Social Adjustment Scale.
Results of risk of bias assessment for randomised-controlled trials using the ROB2 tool.
| Author (year, country) | Randomisation process | Notes | Deviations from intended interventions | Notes | Missing outcome data | Notes | Measurements of the outcome | Notes | Selection of the reported results | Notes | Overall bias |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Low | No significant baselines differences reported between the two groups. Participants were randomly assigned to groups | Low | No deviations mentioned | Low | No significant missing data reported | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Low | |
| Low | No significant baselines differences reported between the two groups. Participants were randomly assigned to groups | Low | No deviations mentioned | Low | No significant missing data reported | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Low | |
| Low | No significant baselines differences reported between the two groups. Participants were randomly assigned to groups | Low | No deviations mentioned | Low | No significant missing data reported | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Low | |
| Some concerns | Baseline differences were found for child delinquency with the treatment group scoring higher than the usual services group | Low | No deviations mentioned | Some concerns | Follow-up data only available for 31 out of the 55 people that initially consented to take part in the study. No reason was given for why this happened for the majority of the patients whose data was not available | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Some concerns | |
| No information | No statistical tests were conducted to investigate baseline group differences although descriptive statistics were reported. Participants were randomly assigned to groups | Low | No deviations mentioned | Low | No significant missing data reported | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Low | |
| No information | No statistical tests were conducted to investigate baseline group differences although descriptive statistics were reported. Participants were randomly assigned to groups | Some concerns | The intervention plan was not described in detail and the paper did not mention if treatment protocol was adhered to | Low | No significant missing data reported | High | Test-retest reliability and validity of some of the measures used not mentioned | Low | Results for all measured were reported, regardless to their statistical significance | High | |
| Low | No statistical tests were conducted to investigate baseline group differences although descriptive statistics were reported. Participants were randomly assigned to groups | Low | No deviations mentioned | Some concerns | The paper mentions that a high proportion of teacher-rated and youth-rated data are missing. Although a clear explanation was given for the missingness of teacher data, no explanation was given for the missingness of youth-rated data | Low | Used validated outcome measures | Low | Results for all measured were reported, regardless to their statistical significance | Some concerns | |
| Low | No significant baselines differences reported between the two groups. Participants were randomly assigned to groups | Low | No deviations mentioned | Low | No significant missing data reported | Low | Used validate outcome measures | High | Results on 2 of the subscales of the behaviour rating scale were not presented | High |
Results of risk of bias assessment for non-randomised trials using the ROBINS-I tool.
| Reference | Confounding | Notes | Selection of participants | Notes | Classification of interventions | Notes | Deviations from intended intervention | Notes | Missing data | Notes | Measurement of outcome | Notes | Selection of reported results | Notes | Overall bias |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Moderate | Single group study but standardization used to control for possible confounders | Moderate | Some pre-established eligibility criteria used | Not applicable | Single group design | Low | No deviations mentioned | Moderate | Although substantial missing data were reported, the authors used an appropriate statistical analysis to account for it | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Moderate | |
| Critical | Retrospective control group and no statistical analysis conducted to determine baseline group differences | Serious | No pre-established eligibility criteria used | Moderate | Retrospective study of different time periods in which patients attending a clinic either received or did not receive the new intervention | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Serious | |
| Critical | Single group design – potential for confounding | Serious | No pre-established eligibility criteria used | Not applicable | Single group design | Low | No deviations mentioned | Low | No significant missing data report | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Critical | |
| Critical | Retrospective control group and no statistical analysis conducted to determine baseline group differences | Serious | No pre-established eligibility criteria used | Moderate | Retrospective study of different time periods in which patients attending a clinic either received or did not receive the new intervention | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Serious | |
| Critical | Single group design – potential for confounding | Serious | No pre-established eligibility criteria used | Not applicable | Single group design | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Critical | |
| Critical | Single group design – potential for confounding | Low | Clear pre-established eligibility criteria used | Not applicable | Single group deign | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Serious | |
| Serious | Single group design but statistical analysis conducted to determine baseline group differences in comparison to normative scores on the same scale for a sample receiving inpatient/outpatient treatment | Serious | No pre-established eligibility criteria used | Not applicable | Single group design | Low | No deviations mentioned | Moderate | Although substantial missing data was reported, the authors used an appropriate statistical analysis to account for it | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Serious | |
| Critical | Retrospective study – potential for confounding | Serious | No pre-established eligibility criteria used | Moderate | Retrospective study of different time periods in which patients attending a clinic either received or did not receive the new intervention | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Serious | |
| Moderate | Although matched samples were used in the trial, the authors could not recruit the same number of patients in the control group as the experimental condition | Low | Clear pre-established eligibility criteria used | Low | Treatment and control groups used | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Moderate | |
| Critical | Single group design – potential for confounding | Serious | No pre-established eligibility criteria used | Not applicable | Single group design | Low | No deviations mentioned | Low | No clear information on whether there was any missing data or not | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Critical | |
| Low | Matched control group used, and statistical analysis were conducted to determine differences between groups at baseline. No differences were found | Low | Clear pre-established eligibility criteria used | Moderate | Matched retrospective comparison group | Low | No deviations mentioned | Low | No significant missing data reported | Low | Validated and reliable outcome measures used | Low | No potential bias identified | Low |