| Literature DB >> 21057974 |
L R Cornelius1, J J L van der Klink, J W Groothoff, S Brouwer.
Abstract
INTRODUCTION In the past few decades, mental health problems have increasingly contributed to sickness absence and long-term disability. However, little is known about prognostic factors of return to work (RTW) and disability of persons already on sick leave due to mental health problems. Understanding these factors may help to develop effective prevention and intervention strategies to shorten the duration of disability and facilitate RTW. METHOD We reviewed systematically current scientific evidence about prognostic factors for mental health related long term disability, RTW and symptom recovery. Searching PubMed, PsycINFO, Embase, Cinahl and Business Source Premier, we selected articles with a publication date from January 1990 to March 2009, describing longitudinal cohort studies with a follow-up period of at least 1 year. Participants were persons on sick leave or receiving disability benefit at baseline. We assessed the methodological quality of included studies using an established criteria list. Consistent findings in at least two high quality studies were defined as strong evidence and positive findings in one high quality study were defined as limited evidence. RESULTS Out of 796 studies, we included seven articles, all of high methodological quality describing a range of prognostic factors, according to the ICF-model categorized as health-related, personal and external factors. We found strong evidence that older age (>50 years) is associated with continuing disability and longer time to RTW. There is limited evidence for the association of other personal factors (gender, education, history of previous sickness absence, negative recovery expectation, socio-economic status), health related (stress-related and shoulder/back pain, depression/anxiety disorder) and external i.e., job-related factors (unemployment, quality and continuity of occupational care, supervisor behavior) with disability and RTW. We found limited evidence for the association of personal/external factors (education, sole breadwinner, partial/full RTW, changing work tasks) with symptom recovery. CONCLUSION This systematic review identifies a number of prognostic factors, some more or less consistent with findings in related literature (mental health factors, age, history of previous sickness absence, negative recovery expectation, socio-economic status, unemployment, quality and continuity of occupational care), while other prognostic factors (gender, level of education, sole breadwinner, supervisor support) conflict with existing evidence. There is still great need for research on modifiable prognostic factors of continuing disability and RTW among benefit claimants with mental health problems. Recommendations are made as to directions and methodological quality of further research, i.e., prognostic cohort studies.Entities:
Mesh:
Year: 2011 PMID: 21057974 PMCID: PMC3098343 DOI: 10.1007/s10926-010-9261-5
Source DB: PubMed Journal: J Occup Rehabil ISSN: 1053-0487
Search terms (a = truncated)
| Terms linked to | MeSH | Subheading | Free text words |
|---|---|---|---|
| Diagnosis | Mental disorders | Mental illness | |
| Mental morbidity | |||
| Mental comorbidity | |||
| Psychiatric disordera | |||
| Psychiatric diagnosa | |||
| Psychiatric morbidity | |||
| Psychiatric comorbidity | |||
| Mental problems | |||
| Psychiatric problems | |||
| Population | Sick leave | Sick-listed | |
| Insurance, disability | Disability pensiona | ||
| Pensions | Sickness benefita | ||
| Study design | Cohort study, case control study | Epidemiology | |
| Economics | |||
| Statistics and numerical data |
In- and exclusion criteria
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| Observational studies, i.e., case–control studies, cohort studies, follow-up studies or longitudinal studies with a minimum follow-up period of 1 year |
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| Wholly or partially disabled persons in the age bracket 18–64 years who are on sick leave, who claim disability benefits or who are receiving disability pensions at baseline, because of disability due to mental disorders. Duration of sick leave or disability is not an in- or exclusion criterion in order to include all durations |
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| Dependent variables: symptom recovery, improvement of functioning; reduction of disability; expanding of activities; heightening of social participation; return to work. Independent variables: nature and severity of mental disorder focusing on depression, anxiety disorder and substance use disorder; demographics; health service use; adequacy of treatment; coping strategies and social support |
Operationalization of criteria list for quality assessment
| Study population | A Inception cohort |
| One point if patients are identified at an early uniform point in the course of their disability e.g., uniform period after first day of sick leave | |
| Zero point if it is not clear if an inception cohort was used | |
| B Description of source population | |
| One point if the source population is described in terms of place of recruitment (for example: Groningen, the Netherlands), time-period of recruitment and sampling frame of source population (for example: occupational health service, organization for social security) | |
| Zero point if ≤2 features of source population are given | |
| C Description of relevant inclusion and exclusion criteria | |
| One point if >2 criteria are formulated | |
| Zero point if ≤2 criteria are formulated | |
| Follow-up | D Follow-up at least 12 months |
| One point if the follow-up period is at least 12 month and data are provided for this moment in time | |
| E Drop-outs/loss to follow-up <20% | |
| One point if total number of drop-outs/loss to follow up <20% at 12 months | |
| F Information completers versus loss to follow-up/drop-outs | |
| One point if sociodemographic information is presented for completers and those lost to follow-up/drop outs at baseline, or no loss to follow-up/drop outs. Reasons for loss to follow-up/drop outs have to be unrelated to the outcome. Loss to follow-up/drop outs: all patients of the assembled cohort minus the number of patients at the main moment of measurement for the main outcome measure, divided by the total number of patients of the assembled cohort | |
| G Prospective data collection | |
| One point if a prospective design is used, or a historical cohort when the prognostic factors are measured before the outcome is determined | |
| Zero point if a historical cohort is used, considering prognostic factors at time zero which are not related to the primary research question for which the cohort is created, or in case of an ambispective design | |
| Treatment | H Treatment in cohort is fully described/standardized |
| One point if treatment subsequent to inclusion into cohort, is fully described and standardized, or in case of no treatment is given, or if multi-variate correction for treatment is performed in analysis | |
| Zero point if different treatment is given and if it is not clear how outcome is influenced by it, or if it is not clear whether any treatment is given | |
| Prognostic factors | I Clinically relevant potential prognostic factors |
One point if besides socio-demographic factors (age, gender) at least one other factor of the following is described at baseline:
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| (congenital or acquired vulnerability, psychiatric diagnosis, comorbidity, psychotrauma, physical condition) | |
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| (cognition, attitude, beliefs, efficacy, activity, avoidance behavior, coping, therapy compliance, employment, education, income, marital status, residence) | |
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| (physical or psychosocial job characteristics, employer characteristics, social support, health care system, social security system, social benefit) | |
| J Standardized or valid measurements | |
| One point if at least one of the factors of I, excluding age and gender, are reported in a standardized or valid way (for example: questionnaire, structured interview, register, patient-status of occupational/insurance physician) | |
| K Data presentation of most important prognostic factors | |
| One point if frequencies, or percentages, or mean (and standard deviation/confidence interval), or median (and Inter Quartile Range) are reported for the three most important factors of I, namely age, gender and at least one other factor, for the most important follow-up measurements | |
| Outcome | L Clinically relevant outcome measures |
| One point if at least one of the following outcome criteria for change is reported: symptom, functioning, daily life activities, disability, return to work | |
| M Standardized or valid measurements | |
| One point if one or more of the main outcome measures of L are reported in a standardized or valid way (for example: questionnaire, structured interview, registration, patient-status of occupational/insurance physician) | |
| N Data presentation of most important outcome measures | |
| One point if frequencies, or percentages, or mean (and standard deviation/confidence interval), or median (and Inter Quartile Range) are reported for one or more of the main outcome for the most important follow-up measurements | |
| Analysis | O Appropriate univariate crude estimates |
| One point if univariate crude estimates (RR, OR, HRR) between prognostic factors separately and outcome are presented | |
| Zero point if only | |
| P Appropriate multivariate analysis techniques | |
| One point if logistic regression analysis is used, or survival analysis for dichotomous outcomes, or linear regression analysis for continuous outcomes | |
| Zero point if no multivariate techniques are performed at all |
Levels of evidence for prognostic factors
| Level | |
|---|---|
| Strong | Consistent findings (≥80%) in at least two high quality studies |
| Moderate | One high quality study and consistent findings (≥80%) in one or more low quality studies |
| Limited | Findings of one high quality study or consistent findings (≥80%) in one or more low quality studies |
| Inconclusive | Inconsistent findings irrespective of study quality |
Flow diagram of study selection
Results of methodological assessment
| Study | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Score (%) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Brenninkmeijer et al. [ | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 15 (93.7) |
| Engström and Janson [ | 0 | 1 | 1 | 1 | 1 | 0 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 13 (81.3) |
| Nieuwenhuijsen et al. [ | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 16 (100) |
| Nieuwenhuijsen et al. [ | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 15 (93.7) |
| Nieuwenhuijsen et al. [ | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 16 (100) |
| Nieuwenhuijsen et al. [ | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 14 (87.5) |
| Vaez et al. [ | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 14 (87.5) |
| Total | 5 | 7 | 7 | 7 | 7 | 5 | 7 | 3 | 7 | 7 | 7 | 6 | 7 | 7 | 7 | 7 |
See Appendix Table 8 for operationalization of items A–P
Study characteristics
| Study | Score | Design | Recruitment and source population | Case definition | Response | Numbers enrolled | Measurement | Follow-up | % Lost to follow-up |
|---|---|---|---|---|---|---|---|---|---|
| Brenninkmeijer et al. [ | 15 | Prospective cohort study; 2 measurements: T1 after 13 weeks of sickness; T2 after 1 year | Three social insurance companies, Utrecht, The Netherlands; inclusion in 2002; source population: | Sick-listed 12–20 weeks; high level of psychological distress (GHQ-12 ≥ 5); sickness due to psychological complaints; cause of sickness: work situation and private life | Screening: 42% 1st interview T1: 93% 2nd interview T2: 79% |
| (1) Screening: GHQ-12a (2) Telephone interview: SCL-90b JCQc Self report | 1 year | 14% |
| Engström and Janson [ | 13 | Prospective cohort study; 3 annual measurements after 1, 2 and 3 years of follow-up | Social insurance office Värmland, Sweden; all individuals sick registered one November week 2000; | Sickness absence >28 days; stress-related psychiatric disorder | 100% (registry data) |
| Registry data | 3 years | 1.9% |
| Nieuwenhuijsen et al. [ | 16 | Retrospective cohort study | 35 Different occupational physicians (OP) | Medical files of first 100 patients on sick leave due to adjustment disorders visiting OP in 1999 and 2000; first time visit since onset; 100% absent from work; no major psychiatric disorder; no prominent somatic disorder | 100% (registry data) |
| (1) File: Length of sickness absence (2) OP guideline: 10 OP performance indicators | 1 year | 0% |
| Nieuwenhuijsen et al. [ | 15 | Part of longitudinal cohort study; measurements: Employees: at baseline, 3, 6, 12 months Supervisors: 6 months | Consecutive patients reported by 30 occupational physicians of 9 occupational health services; Amsterdam, The Netherlands; inclusion: march 2001–february 2002; source pop.: | Employees with self reported psychological symptoms; on sick leave <6 weeks | Consent to participate: 76%; baseline questionnaire: 71%; consent to contact supervisor: 48% (of | Employees: Supervisors: | Employee: Questionnaired Supervisor: Telephone interviewe | Employee: 1 year; Supervisor: no follow up | Employee: not provided; Supervisor: not applicable |
| Nieuwenhuijsen et al. [ | 16 | Part of longitudinal cohort study; measurements at baseline, 3, 6, 12 months | Consecutive patients reported by 30 occupational physicians of 9 occupational health services; Amsterdam, The Netherlands; inclusion: march 2001–february 2002; source population | Employees on sick leave <6 weeks due to mental health problemsf; last visit to OP >3 months | Consent to participate: 76%; baseline questionnaire: 71% |
| (1) RTW: Questionnaire Register (2) Diagnosis: Telephone version of CIDI versus 2.1g DASS-depressionh (3) Other predictors: Questionnaire | 1 year | 1.1% |
| Nieuwenhuijsen et al. [ | 14 | Part of longitudinal cohort study; measurements at baseline, 3, 6, 12 months | Consecutive patients reported by 30 occupational physicians of 9 occupational health services; Amsterdam, The Netherlands; inclusion: march 2001–february 2002; source population | Employees on sick leave <6 weeks due to mental health problemsi; last visit to OP >3 months | Consent to participate: 76%; baseline questionnaire: 71% |
| (1) Irrational belief: IBIj (2) Diagnosis: Telephone version of CIDI versus 2.11a (3) Psychological symptoms: DASSl | 1 year | 1,1% |
| Vaez et al. [ | 14 | Retrospective and prospective cohort study | Insurance company, Sweden; inclusion in 1999; random selection ( | Employees living in Sweden; aged 20–65 years; new sick-leave spell ≥90 days in 1999 due to psychiatric diagnosis, burnout or exhaustion; | 100% (registry data) | Included: | Registry data 1996–2002 from: Insurance company Social insurance board | Retrospective: 1996–1999 Prospective: 1999–2002 | 0% |
aGeneral Health Questionnaire (12 items)
bDepression subscale (16 items) of Symptom Check List (90 items)
cJob Content Questionnaire
dBaseline: age, gender, occupation, self reported cause of mental health problem; Depression Anxiety Stress Scale (DASS): severity of psychological symptoms; during follow up: absence data
eStandardized, with 19 questions
fPsychological symptoms not caused by a somatic disorder
gSections: major depressive disorder, panic disorder, social phobia, somatoform disorder, bipolar disorder, obsessive–compulsive disorder, post-traumatic stress disorder, psychotic disorder
hDepression Anxiety Stress Scale; cut-off >12
iPsychological symptoms not caused by a somatic disorder
jIrrational Beliefs Inventory 50-item
kSections: major depressive disorder, panic disorder, social phobia, somatoform disorder, bipolar disorder, obsessive–compulsive disorder, post-traumatic stress disorder, psychotic disorder
l42-item
Outcome, prognostic factors and results
| Study | Outcome (dependent variables) | Prognostic factors (independent variables) | Results |
|---|---|---|---|
| Brenninkmeijer et al. [ | Depressive symptoms | (1) Demographicsa (2) Work characteristicsb (2) Work resumptionc (3) Actions by employersd | Significant factors ( (1) Increased risk: Lower education: β = 0.10 Sole breadwinner: β = 0.14 (2) Decreased risk: Partial or full work resumption: resp. β = 0.13, β = 0.30 Changing work tasks: β = 0.10 |
| Engström and Janson [ | Dependency on sickness insurance c.q. full/partial (healthy state) or no work resumption (unhealthy state) | (1) Demographicse (2) Labour market dataf (3) History of previous sickness absence | Logistic regression to estimate ORs; significant risk factors healthy versus unhealthy state 3 years after initial sickness absence: (1) Healthy: Male gender: OR 1.637 ( (2) Unhealthy: Age: OR 16.961 (16–29 years, Unemployment: OR 0.468 ( History of previous sickness absence OR 0.617 ( Multiple diagnosis (stress-related and shoulder/back pain) OR 0.576 ( |
| Nieuwenhuijsen et al. [ | Time to full/partial return to work (RTW) | Performance indicator (PI)g of occupational physician (OP) | Kaplan–Meier survival analysis to estimate univariate relations: (1) Longer time to first RTW: Deviant PI interventions aimed at organization ( Deviant PI continuity of care ( (2) Longer time to full RTW: Age >50 ( Cox proportional hazard ratio (HR, 95% CI) analysis to estimate multivariate associations: (1) Longer time to first RTW: Deviant PI interventions aimed at organization: HR 0.5 (0.3–0.9) Deviant PI continuity of care: HR 0.3 (0.2–0.5) (2) Longer time to full RTW: Deviant PI continuity of care: HR 0.3 (0.2–0.5) |
| Nieuwenhuijsen et al. [ | Time to full/partial RTW | (1) Supervisor behaviourh (2) Conditional factorsi | Cox regression analysis to estimate hazard ratios (HR, 95% CI) indicating time to RTW: (1) Shorter time to full RTW: Communication with employee (non-depressed only): HR 3.5 (1.4–8.9) (2) Longer time to full/partial RTW: Consulting with professionals: HR 0.4 (0.2–0.9) |
| Nieuwenhuijsen et al. [ | Time to full RTW | (1) Disorder related factorsj (2) Personal factorsk (3) Environmental factorsl | Cox regression analysis to estimate hazard ratios (HR, 95% CI) indicating time to full RTW: Longer time: Age ≥50: HR 0.5 (0.3–0.8) Expectation of duration >3 months: HR 0.5 (0.3–0.8) Educational level medium/high Depression/anxiety disorder: HR 0.7 (0.4–0.9) |
| Nieuwenhuijsen et al. [ | Symptom recovery | Change in irrational beliefs | Repeated measurements MANOVAs to describe relation of change in irrational beliefs and symptom recovery: Magnitude/direction of change in irrational beliefs are related to magnitude of recovery of depressive, anxiety, stress symptoms over time Design not suited to assess temporal relationship beliefs/symptoms |
| Vaez et al. [ | (1) Sickness absence (2) Disability pension (DP) | (1) Demographicsm (2) Previous sickness absencen | To predict DP: logistic regression to estimate adjusted ORs (95% CI): Higher risk: Age 55–61: OR 6.30 (4.80–8.09) Low SES: OR 3.40 (2.28–5.08) |
aGender, age, education, care for children, breadwinner’s role, marital status
bVariable work schedule, management function, reorganization, job insecurity, leadership quality, years in organization, years in function, working hours, overtime work, travelling hours, size of organization, physical load/risk, chemical risk, decision latitude, task demands, work atmosphere
cPartial or full work resumption
dChange of tasks, reduction of tasks, reduction of hours, equipment/aids/courses, showing interest, change of position/department
eAge, gender
fOccupation, employer type, full- or part-time work, work-related diagnosis
gAssessment of symptoms, correct diagnosis, evaluation of curative care, assessment of work related causes, assessment of impediments, interventions aimed at individual, interventions aimed at organization, interventions aimed at providers of care in the curative sector, timing of first consultation, continuity of care
hCommunication with the employee, promoting gradual return to work, consulting with professionals
iFinancial consequences, rehabilitation, responsibility, motivation, work performance, work relationship
jDiagnosis, level of depressive symptoms, work-relatedness of the diagnosis, pre-baseline duration of the disorder, pre-baseline sick leave days
kGender, age, marital status, recovery expectations, educational level
lJob demands, supervisory support, co-worker support
mGender, age, occupation, socio-economic status
n4 levels: <17 days (short); 17–90 days (intermediate); 91–365 days (long term); granted disability pension
Overall level of evidence
| Category | Prognostic factor | Outcome | Studies | Pos. findings (increase) | High quality | Neg. findings (decrease) | High quality | Level of evidence | Modifiable |
|---|---|---|---|---|---|---|---|---|---|
| Health | Stress-related and shoulder/back pain | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + |
| Depression/anxiety disorder | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Personal | Older age | Disability | 4 | 4/4 (100%) | 4 | Strong | – | ||
| Gender (male) | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | – | |
| Medium/higher education | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | – | |
| Lower education | Symptoms | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Sole breadwinner | Symptoms | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Partial/full RTW | Symptoms | 1 | – | – | 1/1 (100%) | 1 | Limited | + | |
| History of previous sickness absence | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | – | |
| Own expectation of duration >3 months | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Low socio-economic status | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| External | Changing work tasks | Symptoms | 1 | – | – | 1/1 (100%) | 1 | Limited | + |
| Unemployment | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Deviant OP interventions aimed at organization | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Deviant continuity of OP care | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + | |
| Supervisor communication with employee | Disability | 1 | – | – | 1/1 (100%) | 1 | Limited | + | |
| Supervisor consulting with professional | Disability | 1 | 1/1 (100%) | 1 | – | – | Limited | + |