| Literature DB >> 22476607 |
Nicole Hoefsmit1, Inge Houkes, Frans J N Nijhuis.
Abstract
INTRODUCTION: In many Western countries, a vast amount of interventions exist that aim to facilitate return to work (RTW) after sickness absence. These interventions are usually focused on specific target populations such as employees with low back pain, stress-related complaints or adjustment disorders. The aim of the present study is to detect and identify characteristics of RTW interventions that generally facilitate return to work (i.e. in multiple target populations and across interventions). This type of knowledge is highly relevant to policy makers and health practitioners who want to deliver evidence based care that supports the employee's health and participation in labour.Entities:
Mesh:
Year: 2012 PMID: 22476607 PMCID: PMC3484272 DOI: 10.1007/s10926-012-9359-z
Source DB: PubMed Journal: J Occup Rehabil ISSN: 1053-0487
Databases, search terms, hits and included publications
| Database | Key words | Number of hits | Number included |
|---|---|---|---|
| Pubmed (MeSH) | Sick leave | 310 | 6 |
| Sick leave AND intervention studies | 8 | 0 | |
| Absenteeism | 214 | 0 | |
| Absenteeism AND intervention studies | 7 | 0 | |
| Pubmed | Return to work | 4560 | 7 |
| Sickness absence | 1065 | 2 | |
| Cinahl | Return to work | 248 | 1 |
| Cochrane library | Return to work | 63 | 1 |
| Google scholar | Return to work | About 625.000 | 3 |
| Return AND to AND work AND intervention | About 111.000 | 2 | |
| Early AND return AND to AND work | About 190.000 | 1 | |
| Total | 23 |
Criteria for evaluating the quality of empirical research
| Research | Criteria | Evaluation | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Quantitativea | Design (A), measurements (B) | A | Randomized controlled trial (++) | Cluster randomized trial (++) | Controlled trial or quasi-experiment (+) | Longitudinal observational study (+) | Cross sectional study (−+) | Ex-post facto chart review (−+) | Case/case series study (−+) | |||
| B | >1 pre or post (++) | 1 pre or post (+) | Multiple (+) | No (−+) | ||||||||
| Study population | ≥100 respondents (yes: ++, no: −+) | Heterogeneous: respondents of different ages, gender and/or educational levels (yes: ++, no: −+) | ||||||||||
| When applicable: control group | Description (yes: ++/no: −+) | Appropriate to draw conclusions: control group received nothing or care as usual differed from the intervention (yes: ++/no: −+) | Expected group difference described (yes: ++/no: −+) | |||||||||
| Outcomes, measurement instruments | Outcomes described (yes: +/no: −+) | Outcomes match study aims (yes: +/no: −+) | Instruments described (yes: +/no: −+) | Validity and reliability of instruments described or logically no description (yes: ++/no: −+) | Instruments are likely to be accepted in the profession under concern (yes: +/no: −+) | References given for instruments (yes: +/no: −+) | ||||||
| Data analysis (scoring of most advanced method applied in study under concern) | Hierarchical regression with all variables measured at all moments (++) | Hierarchical regression without measurement of all variables at all moments (+) | Multiple regression analysis or multivariate analysis of variance (+) | Survival analysis (+) | Ex-post factor chart (+) | Descriptive statistics (−+) | Logistical regression (−+) | Regression analysis or analysis of variance (−+) | Correlation (−+) | Chi-square (−+) | T-test (−+) | |
| Reviewb | Research question includes | Patient (yes: ++/no: −) | Intervention (yes: ++/no: −) | Comparison (yes: ++/no: −) | Outcome (yes: ++/no: −) | |||||||
| Search, selection | Sufficient terms (yes: ++/no: −) | Terms relevant for research question (yes: ++/no: −) | Search in databases as Medline (yes: ++/no: −) | Restrictions described (yes: ++/no: −) | Inclusion criteria described (yes: ++/no: −) | Inclusion criteria match research question (yes: ++/no: −+) | Selection by multiple researchers (yes: ++/no: −+) | Multiple researchers selected the articles independently (yes: ++/no: −+) | Selection process well described (yes: ++/no: −) | |||
| Quality rating | Quality rated (yes: ++/no: −) | Rating criteria described (yes: ++/no: −) | Multiple researchers (yes: ++/no: −+) | Multiple researchers rated the articles independently (yes: ++/no: −+) | Consensus seeking process between researchers described (yes: ++/no: −+) | Results reported for each included article separately (yes: ++/no: −) | ||||||
| Data extraction | Described (yes: ++/no: −) | Multiple researchers (yes: ++/no: −+) | ||||||||||
| Description original methods | Study population (yes: ++/no: −+) | Intervention (yes: ++/no: −+) | Outcomes (yes: ++/no: −+) | Confounders (yes: ++/no: −+) | Results (yes: ++/no: −+) | |||||||
| Description meta-analysis | Meta-analysis performed or heterogeneity described (yes: ++/no: −) | Potential sources of heterogeneity described (yes: ++/no: −) | ||||||||||
− = Minus one, insufficient; −+ = zero, neutral/sufficient; + = one, good; ++ = two, very good. A criterion is also ranked with a −+ in case it was inapplicable to the article or in case it cannot be identified based on the text in the article
aEffective Public Health Practice Project, n.d.
bCochrane, n.d.
Criteria for evaluating the characteristics of the included interventions
| Intervention characteristic | Evaluation | |||
|---|---|---|---|---|
| 1. Timing of intervention, early which starts within first 6 weeks of absence | Yes | No or timing not restricted | ||
| 2. Care professionals involved, multidisciplinary, involving multiple professionals (care providers) from more than one discipline | Yes | No | ||
| 3. Planning of activities to support RTW, time-contingent, activities followed pre-defined time schedule | Yes | No | ||
| 4. Target population | Generic: all employees on sickness absence irrespective of their specific medical diagnosis | Specific: only employees with specific diagnosis | ||
| 5. Character of activities to support RTW, interventions including explicit actions to stimulate the employee to RTW | A: making decisions about actual RTW (when and/or how) | B: gradual exposure to the workplace (for example when employees resume work for a limited but increasing number of hours per week) | C: implemented work-related adaptations, e.g. workplace (such as ergonomic improvements of furniture) | |
| Yes/no | Yes/no | Yes/no | ||
| 6. Intensity | High: ≥10 h divided over multiple sessions | Moderate: <10 h, multiple sessions | Low: once | Variable |
| 7. Employee and employer role, decision latitude of the employee and/or employer about activities to support medical recovery or RTW and (the timing of) RTW | Yes | No | ||
Not described means that a certain characteristic is either not a part of the intervention or not described in the article. Not described is evaluated as a ‘no’
Systematic reviews were evaluated by reading the descriptions of original studies that were included in the reviews. A ‘no’ was also attached in case original intervention studies varied largely or in the case of doubt
Methodological quality of the included studies
| Quantitative study (in order of quality) | Design | Population | Control group | Outcomes, instruments | Data analysis | Scorea |
|---|---|---|---|---|---|---|
| Brouwers et al. [ | ++ | ++ | ++ | + | + | 8 (Good) |
| van der Feldtz-Cornelis et al. [ | ++ | ++ | ++ | + | + | 8 (Good) |
| Mortelmans et al. [ | ++ | ++ | ++ | + | + | 8 (Good) |
| Bogefeldt et al. [ | ++ | ++ | + | + | + | 7 (Good) |
| Bültmann et al. [ | ++ | ++ | ++ | + | −+ | 7 (Good) |
| Fleten and Johnsen [ | ++ | ++ | + | + | + | 7 (Good) |
| van der Klink et al. [ | ++ | ++ | + | + | + | 7 (Good) |
| Arnetz et al. [ | ++ | ++ | + | + | −+ | 6 (Good) |
| Bakker et al. [ | ++ | + | + | + | + | 6 (Good) |
| Drews et al. [ | + | ++ | + | + | + | 6 (Good) |
| Hagen et al. [ | ++ | ++ | + | + | −+ | 6 (Good) |
| Nystuen and Hagen [ | ++ | ++ | + | + | −+ | 6 (Good) |
| Braathen et al. [ | + | ++ | + | + | −+ | 5 (Moderate) |
| Marhold et al. [ | ++ | −+ | + | + | + | 5 (Moderate) |
| Grossi and Santell [ | ++ | −+ | + | + | −+ | 4 (Moderate) |
| Godges et al. [ | + | + | −+ | + | −+ | 3 (Moderate) |
| Matheson and Brophy [ | −+ | ++ | −+ | + | −+ | 3 (Moderate) |
| Weiler et al. [ | + | −+ | −+ | + | + | 3 (Moderate) |
− = Minus one, insufficient; −+ = zero, neutral/sufficient; + = one, good; ++ = two, very good. A criteria is also ranked with a −+ in case it was inapplicable to the article or in case it cannot be identified based on the text in the article
Methodological quality score of quantitative studies: −1 to 2 (insufficient), 3–5 (moderate), 6–8 (good), 9–11 (very good). Methodological quality of systematic reviews: −4 to 0 (insufficient), 1–4 (moderate), 5–8 (good), 9–12 (very good)
Methodological quality ranges: quantitative studies from −1 to 11, systematic literature reviews ranges from −4 to 12. Mean scores are calculated when a criteria existed of multiple sub criteria. These mean scores were taken into account in the overall calculation of quality
aFinal quality scores are calculated by adding up all pluses and subtracting all minuses
Description and effectiveness of the interventions
| Study | Target population | Intervention and care as usual | Study outcomes most relevant for this review (operationalisation of return to work/sickness absence) | Effectiveness (on outcomes relevant to this study) |
|---|---|---|---|---|
| Brouwers et al. [ | Specific: only employees with specific diagnosis (emotional and stress related complaints) | Activating counselling/control group: care as usual | Sick leave duration (days): period between first day of absence and return to work | No effect on sick leave duration |
| van der Feldtz-Cornelis et al. [ | Specific: only employees with specific diagnosis (depressive, anxiety and somatoform disorders) | (1) Training of occupational physicians in diagnosis and treatment (2) supportive psychiatric consultations (3) training of psychiatrist/Control group: care as usual | Time to return to work: period between onset of sickness leave due to mental disorder and full return to work, for at least 4 weeks without relapse | Full RTW at 3 months follow up** survival analysis: return to work occurred 122 (intervention) and 190 days (control) after intervention |
| Mortelmans et al. [ | Generic: all employees on sickness absence irrespective of their specific medical diagnosis | Structured and circular information exchange by communication form/control group: occupational physician filled out the communication form and delivered to the researcher. | Return to work rate/median gradual return to work duration in days | No effect on return to work rate. Relative risk: 1.03 (95% CI 0.93–1.13)/no effect on gradual return to work rate. Relative risk: 1.24 (95% CI 0.52–2.97). No difference in median duration of gradual return to work (62 days) |
| Bogefeldt et al. [ | Specific: only employees with specific diagnosis (low back pain) |
| Return to work rate./Sick leave in days (number of days times sick leave extent) | Increase return to work after 10 weeks** (hazard ratio 1.62, 95% CI, 1.006–2.60, |
| Bültmann et al. [ | Specific: only employees with specific diagnosis (musculoskeletal complaints or low back pain) | Systematic multidisciplinary work disability screening, development and implementation of work rehabilitation plan/control group: care as usual | Cumulative sickness absence hours, time intervals: 0–3, 3–6, 6–12, 0–6, 0–12 months | Lower number of sickness absence hours during intervals 0–6, 6–12 and 0–12**/no effect during intervals 0–3–3–6 |
| Fleten and Johnsen [ | Specific: only employees with specific diagnosis (musculoskeletal or mental disorders) | General information letter on possible work related measures if sick-listed/control group: care as usual | Length of sick leaves in calendar days | Reduction mean length of sick leaves in subgroups with mental disorders, rheumatic disorders, arthritis and in overall sick leaves lasting 12 weeks or more** |
| van der Klink et al. [ | Specific: only employees with specific diagnosis (adjustment disorders) | Graded activity/control group: care as usual by the occupational physician | Return to work rate: percentage return to work (partial or full) at 3 months/duration of sick leave: days lost until full return to work with correction for partial return to work | Increase return to work rate at 3 months*** shorter duration of sick leave** rate ratio: 2.39 (95% CI 1.15–4.95) |
| Arnetz et al. [ | Specific: only employees with specific diagnosis (musculoskeletal complaints) | (A) Semistructured interview with employee on social and occupational situation. (B) worksite visits by team for ergonomic assessment and improvements and/or personal vocational training schedule/control group: care as usual | Sick leave: number of sick days at 6 months and at 12 months | Shorter sick leave***/likelihood return to work (odds ratio, OR) at 6 months: 1.9; 95% C.I. 1.0; 3.6, |
| Bakker et al. [ | Specific: only employees with specific diagnosis (emotional and stress related complaints) | Communications by general practitioner to promote functional recovery (e.g. in informing and advising the employee)/control group: care as usual | Sick leave duration (calendar days) from the first day of sick leave until full RTW | No effect on sickness absence duration/hazard ratio: 1.06 (95% CI 0.87–1.29) |
| Drews et al. [ | Generic: all employees on sickness absence irrespective of their specific medical diagnosis | Social medicine examination and counselling/control group: care as usual | Duration of sick leave period from first day until at least 315 days/regular employment 1 year after intervention | No effect on sickness absence duration/no effect on likelihood of regular employment at follow up/odds ratio intervention group: 0.76 (95% CI 0.45–1.28) |
| Hagen et al. [ | Specific: only employees with specific diagnosis (low back pain) | Physical exercise program, besides control treatment/control group: control treatment | Length of sick leave | No (additional) effect on sick leave |
| Nystuen and Hagen [ | Specific: only employees with specific diagnosis (musculoskeletal complaints) | Solution-focused intervention/control group: care as usual | Sick leave: mean length after 12 months/work status (at work or not) 6 months after intervention | No effect on sick leave/no effect on work status |
| Braathen et al. [ | Generic: all employees on sickness absence irrespective of their specific medical diagnosis | Multidisciplinary rehabilitation programme/control group: treatment of persons’ own choice | Return to work: percentage of population who resumed work | No effect on return to work |
| Marhold et al. [ | Specific: only employees with specific diagnosis (musculoskeletal complaints) | Pain coping skills training, focus on: how to return to work and apply coping skills to occupational risk factors/control group: care as usual | Sick leave (days) over periods of 2 months (2 months before treatment and 6 months follow up) | Patients short-term sick leave (2–6 months): shorter sick leave**/patients long-term sick leave (>12 months): no effect on sick leave |
| Grossi and Santell [ | Specific: only employees with specific diagnosis (females on sick leave due to work-related psychological complaints) | Coping with psychological/somatic symptoms of stress/control group: standard individual treatment for stress | Return to work rate: percentage of population who resumed work | No effect on return to work rate |
| Godges et al. [ | Specific: only employees with specific diagnosis (low back pain) | Education, counselling on pain management tactics and value of physical activity besides conventional physical therapy/control group: conventional physical therapy | Sick leave duration (days) | Shorter sickness absence duration** |
| Matheson and Brophy [ | Specific: only employees with specific diagnosis (low back pain) | Early return to work in transitional light duty work, immediate identification and treatment during work hours/Control group: not applicable | Return to work rate: percentage of population who resumed work/days lost from work | Within 30 days, 94% of all subjects had return to work/increase return to work rate compared to other studies/mean number of days lost from work: 8.8 |
| Weiler et al. [ | Specific: only employees with specific diagnosis (musculoskeletal complaints) | Outpatient rehabilitation and determination of return to work (regular, assisted or individualised procedure), multidisciplinary team conferences (therapists and Airbus health professionals)/control group: not described | Return to work ratios/annual sick leave days (as compared to before sick leave period) | 97% of the Patients returned to their original job at the workplace. Reduction annual sick leave days from 48.8 ± 32.8 days to 34.2 ± 37.3 days***. Intervention stabilised low level annual sick leave days during first 2 years of follow-up |
| van Oostrom et al. [ | Specific: only employees with specific diagnosis (musculoskeletal complaints, mental and other health problems) | Interventions directed at work/control group: care as usual or clinical interventions | Time until a lasting return to work: a period of absence from the first day of sick leave to full return to work in previous or equal work for at least 4 weeks without dropping out/Time until first return to work: period of absence from work because of sickness, preceded and followed by period of at least 1 day at work/Cumulative duration of sickness absence: total days of sick leave during follow-up period | Shorter sickness absence duration among workers with musculoskeletal disorders (moderate evidence)/no conclusions on effectiveness in mental health problems and other conditions due to lack of studies/workplace interventions: days until lasting return to work, relative effect hazard ratio 1.70 (CI 95% 1.23–2.35), days until first return to work, relative effect hazard ratio 1.55 (CI 95% 1.32–2.16)/mean cumulative duration of sickness absence: −39.06 days |
| Carroll et al. [ | Specific: only employees with specific diagnosis (back pain) | Interventions involving workplace/control group: interventions not involving workplace | Multiple operationalisations of return to work among which time to return to work | Interventions involving employee, health practitioner and employer working together to implement work modifications, were more consistently effective than other workplace-linked interventions |
| Meijer et al. [ | Specific: only employees with specific diagnosis (non-specific musculoskeletal complaints) | Several interventions/control group: care as usual or control treatment | Difference in sick leave after treatment as compared to sick leave preceding treatment | Shorter sick leave duration (significance not described): 7 out of 22 treatment programs (inconsistent findings). Essential to effective treatment: knowledge, psychological, physical and work conditioning, possibly supplemented with relaxation exercises |
| Norlund et al. [ | Specific: only employees with specific diagnosis (low back pain) | Multidisciplinary interventions/control group: variable | Return to work (measured either directly or indirectly as days of sick leave after start of rehabilitation, with the opportunity to turn sick leave into RTW) | Return to work: difference of effect 21%, relative risk 1.21, 95% CI in favour of the intervention groups (only Scandinavian studies) |
| Tveito et al. [ | Specific: only employees with specific diagnosis (low back pain) | Workplace interventions/control group: not described | Lost work days or sick leave due to low back pain | Exercise significantly reduced sick leave duration (limited evidence, level of significance not described)/interventions to treat low back pain have positive effects on sick leave (moderate evidence, levels of significance not described)/no evidence of effect on sick leave from educational intervention, pamphlet, back belts/limited evidence that multidisciplinary interventions have no effect on sick leave (level of significance not described) |
** P < 0.05. *** P < 0.01
Studies are listed in order of methodological quality
Intervention characteristics
| Study | Timing of intervention, early intervention: starts within 6 weeks of absence | Care professionals involved, multidisciplinary | Planning of activities to support RTW, time contingency, activities followed time schedule | Target population | Character of activities to support RTW, explicit actions to stimulate RTWa | Intensityb | Employee and employer role, decision authority |
|---|---|---|---|---|---|---|---|
| Brouwers et al. [ | No/no restrictiction | No | Yes | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Moderate | Yes |
| van der Feldtz-Cornelis et al. [ | No/no restrictiction | Yes | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Mortelmans et al. [ | No/no restrictiction | Yes | No | Generic: all absent employees | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Bogefeldt et al. [ | No/no restrictiction | Yes | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Bültmann et al. [ | No/no restrictiction | Yes | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: yes | High | Yes |
| Fleten and Johnsen [ | No/no restrictiction | No | Yes | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | Yes |
| van der Klink et al. [ | Yes | Yes | Yes | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High/moderate | Yes |
| Arnetz et al. [ | No/no restrictiction | Yes | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: yes | Low or variable | No |
| Bakker et al. [ | No/no restrictiction | No | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High | Yes |
| Drews et al. [ | No/no restrictiction | No | No | Generic: all absent employees | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | Yes |
| Hagen et al. [ | No/no restrictiction | Uncertain | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High | No |
| Nystuen and Hagen [ | No/no restrictiction | No | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High | Yes |
| Braathen et al. [ | No/no restrictiction | Yes | Yes | Generic: all absent employees | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High | Yes |
| Marhold et al. [ | No/no restrictiction | No | Yes | Specific diagnosis | Decision RTW: yes Gradual exposure: no Work-related adaptations: no | High | No |
| Grossi and Santell [ | No/no restrictiction | Yes | Yes | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | High | Yes |
| Godges et al. [ | No/no restrictiction | No | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Matheson and Brophy [ | No/no restrictiction | Yes | Yes | Specific diagnosis | Decision RTW: yes Gradual exposure: yes Work-related adaptations: no | Low or variable | No |
| Weiler et al. [ | No/no restrictiction | Yes | Yes | Specific diagnosis | Decision RTW: yes Gradual exposure: no Work-related adaptations: yes | High | No |
| van Oostrom et al. [ | No/no restrictiction | Yes | No | Specific diagnosis | Decision RTW: yes Gradual exposure: yes Work-related adaptations: yes | Low or variable | No |
| Carroll et al. [ | Yes | Yes | No | Specific diagnosis | Decision RTW: yes Gradual exposure: yes Work-related adaptations: no | Low or variable | No |
| Meijer et al. [ | No/no restrictiction | Uncertain | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Norlund et al. [ | No/no restrictiction | Uncertain | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
| Tveito et al. [ | No/no restrictiction | Uncertain | No | Specific diagnosis | Decision RTW: no Gradual exposure: no Work-related adaptations: no | Low or variable | No |
RTW return to work
Criteria and sub criteria of a characteristic (for example A, B) are in line with the criteria for evaluating the composition of the included interventions (Table 3)
Studies are listed in order of methodological quality
aThree types of actions to stimulate the employee to return to work, which are: making a decision about actual return to work (when and/or how it takes place), gradual exposure to the workplace (for example when employees resume work for a limited but increasing number of hours per week) and implemented work-related adaptations, e.g. workplace (such as ergonomic improvements of furniture)
bHigh: ≥10 h, more than 1 session/moderate: <10 h, more than 1 session/low: once or variable