| Literature DB >> 23185429 |
Stefan Schandelmaier1, Shanil Ebrahim, Susan C A Burkhardt, Wout E L de Boer, Thomas Zumbrunn, Gordon H Guyatt, Jason W Busse, Regina Kunz.
Abstract
BACKGROUND: The dramatic rise in chronically ill patients on permanent disability benefits threatens the sustainability of social security in high-income countries. Social insurance organizations have started to invest in promising, but costly return to work (RTW) coordination programmes. The benefit, however, remains uncertain. We conducted a systematic review to determine the long-term effectiveness of RTW coordination compared to usual practice in patients at risk for long-term disability. METHODS ANDEntities:
Mesh:
Year: 2012 PMID: 23185429 PMCID: PMC3501468 DOI: 10.1371/journal.pone.0049760
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Characteristics of outcomes.
| Study | Follow-up | Return to work outcomes (definition); patient reported outcomes (assigned outcome group) |
| Bültmann 2009 | 12 months |
|
| Davey 1994 | 6 months |
|
| Donceel 1999 | 12 months |
|
| Feuerstein 2003 | 16 months |
|
| Lambeek 2010 | 12 months |
|
| Lindh 1998 | 60 months |
|
| Purdon 2006 | 20 to 36 weeks |
|
| Rossignol 2000 | 6 months |
|
| Van der Feltz-Cornelis 2010 | 6 months |
|
RTW = return to work, PROs = patient reported outcomes, n.r. = not reported.
Data source: 1administrative data,
diary, interview, or survey, 3combination of diary or interview and administrative data,
not reported.
SD not reported. We imputed missing standard deviations (SDs) with the weighted average of the SDs of the remaining trials.
Hazard ratio estimated from log-rank test.
From personal correspondence.
Data extracted from graph.
Time between a claimant’s initial evaluation by a case manager (not randomization) and RTW.
Missing or unclear number of participants.
Cessation of disability benefits as surrogate for RTW (Rossignol, Feuerstein).
Data presented for two subgroups (immigrant and swedes) which we recombined. Only the number of patients who started the intervention reported. To prevent attrition bias at 60 month, we used 18 month data (ensuring a slightly longer follow up than other studies) and conducted sensitivity analysis using 15 or 12 months.
Data in graph conflicting with text or table.
RTW for at least 2, 6 or 13 weeks reported. We disregarded the 13 weeks outcome which most participants could not achieve due to short follow-up. To ensure longest follow-up, we used 2 weeks and conducted sensitivity analysis using 6 weeks.
Data presented in groups, variance not estimable.
Full-time and part-time RTW reported separately. We used full time RTW and conducted sensitivity analyses using part-time combined with full-time.
End scores.
Change scores.
Figure 1Study selection.
Last update of electronic search to April 2, 2012.
Characteristics of studies and populations (at time of randomisation).
| Trial (country) | Sample size | Year(s), method of recruitment | Health condition | mean age (SD)[years] | % men | type of claim | length of work absence [months] |
| Bültmann 2009 (Denmark) | 119 | 2004/2005, consecutive cases of sick leave registers of 4 municipalities | Musculoskeletal, not mental disorder | 43.7 (11.3) | 45 | Full sick leave, not permanent disability | 1 to 3 |
| Davey 1994 (United Kingdom) | 50 | 1990/1991, review of personal injury claimfiles of four participating personalinjury insurances | Injuries likely to result in absences fromwork of six months or more | 39.4 (11.5) | 75 | Full sick-leave, not permanent disability | median 20 (range 3 to 55) |
| Donceel 1999 (Belgium) | 710 in 60 clusters | 1997/1997, consecutive cases of insuranceoffices ( = clusters) | Surgery for disc herniation | 39.2 (n.r.) | 65 | Full sick leave | 2 to 2.5 |
| Feuerstein 2003 (Unites States of America) | 205 | 1999/2000, claim database of the Departmentof Labour’s Office of Workers’ Compensation Programs | Work related upper extremity disorder | 46.0 (8.6) | 22 | Full or part-time sick-leave | 1 to 6 |
| Lambeek 2010 (Netherlands) | 134 | 2005-2007, visitors of 4 outpatient clinics | Non-specific chronic low back pain, not mental disorder | 46.2 (9.1) | 58 | Full or part-time sick leave, not permanent disability | 3 or more |
| Lindh 1998 (Sweden) | 611 | 1995/1996, consecutive cases of 7 socialinsurance offices | Non-specific chronic musculoskeletal pain | 39.5 (n.r.) | 38 | Full sick-leave | 3 or more |
| Purdon 2006 (United Kingdom) | 1423 | 2003/2004, attracted by marketing of RTW-coordination-providers | Any condition likely to result in a<50% chance to returnto work without intervention, 1/3mental and 1/3 musculoskeletal disorders | 44 (n.r.) | 43 | Full sick leave, not permanent disability | 1,5 to 6 |
| Rossignol 2000 (Canada) | 110 | 1995/1996, consecutive casesof regional office of the Quebec Workers' CompensationBoard | Any work-related injury to the middle or lower vertebral column, not surgery or multiple injuries | 37.6 (10.1) | 72 | Full sick-leave, not permanent disability | 1 to 2 |
| Van der Feltz-Cornelis 2010 (Netherlands) | 60 in 24 clusters | 2007, review of medical files and prospective selection by occupational physicians( = clusters) | Anxiety, depression, somatoform disorder | 42, range 24–59 (n.r.) | 42 | Full sick leave, not permanent disability | mean 4.7, range 0.25 to 10.6 |
RTW = return to work, n.r. = not reported.
As inferred from a subsample of 131 participants.
From personal correspondence.
Characteristics of interventions and comparisons.
| Study: intervention title | Provider(s) of RTW-coordination: | Affiliation of RTW-coordinator(s) | Process of RTW-coordination | Duration | Consumption of health care and other services | Adherence of RTW-coordinators and participants | Usual practice |
| Bültmannn 2009: | 1 rehab. team: OP, occupational PT, chiropractor, psychologist, social worker, experience and training n.r. | N.r. | Standardised assessment of disability and functioning, identification of barriers for RTW; individually tailored RTW-plan, actions directed at worker, workplace, and environment. Social worker coordinates with workplace and municipality case manager | Maximal 3 month | Increase | all patients received RTW-plan | Optional case management from municipal case managers |
| Davey 1994: “Rehabilitation co-ordinator service” | 1 coordinator: PT, experience in care coordination, no specific training | Academic rehab. unit | Assessment at the participant's home, RTW-plan with focus on involving each claimant to the fullest possible extent, coordinator discussed plan with a psychologist and a physician, monitoring, making changes as appropriate | 6 month | Increase | N.r. | No restriction |
| Donceel 1999: | 30 medical advisers: social insurance physicians, experience and training n.r. | One private insurer | Monthly follow-up: Clinical and functional assessment, exploration of barriers for RTW, advice on legal criteria, gradual RTW, exercise, and normal course of work incapacity, encouragement of rehab., communication with treating physicians; case discussion with colleagues; referral to rehab. if no RTW after 3-4 months | As long as participant on disability benefit | N.r. | no drop-outs | 30 medical advisors, focus on corporal damage, little rehab. efforts |
| Feuerstein 2003: “ | 32 nurse case managers: 2 day training in ergonomic assessment and workplace accommodations, problem solving approach, experience in coordination of medical care | US Department of Labour | Semi structured interview, ergonomic worksite assessment, case management plan with workplace accommodation, applying problem solving process, monitoring, coordination of medical care (detailed list of workplace accommodations reported | 4 month, variable | N.r. | N.r. | 33 Nurse case managers, focus on medical care, no training in a structured protocol |
| Lambeek 2010: | 2 case managers: OPs, 2-day training program | University hospital | Individualised RTW-plan, coordination of care, communication with occupational therapists (mandatory workplace intervention based on participatory ergonomics) and physical therapists (mandatory graded activity program using cognitive behavioural principles). Conference calls every three weeks, strict timing. | 67 (SD 32) calendar days | Decrease | N.r. | Guidance from OPs, GPs and other health professionals. averagely 0.2 visits to case managers |
| Lindh 1998: “ | 1 rehab. team: rehab. physician, nurse, physical therapist, psychotherapist, psychologist, occupational therapist, social worker, vocational counsellor, experience and training n.r. | Outpatient rehab. clinic | Medical, functional, psychological and social assessment, RTW-plan, weekly team conferences, regular meetings with participant and spouse | Individually regulated | N.r. | N.r. | Physical therapy and other rehab. measures |
| Purdon 2006 | Case managers, experience and training n.r. | 4 third-party case management providers | Point of contact for clients, giving advice, gate keeping to other services, sometimes providing services, coordination of medical care, rehab., employer, ergonomic workplace assessment, occupational therapy, advising on welfare rights, career, CV preparation, and job search. | 20 to 36 weeks | No change | 88% received RTW-plan, 72% of those followed the plan | No systematic aid; low levels of work support |
| Rossignol 2000: “P | 1 team: 2 primary care physicians, 1 nurse, experience and training n.r. | N.r. | Standardised medical assessment, RTW-plan according to clinical guideline for back pain. Assisting the treating physicians in finding and scheduling diagnostic and therapeutic procedures, cooperation with Worker's Compensation, standardised weekly telephone talk | Until RTW | No change | N.r. | Instruction to continue with treating physician |
| Van der Feltz-Cornelis 2010: “ | 12 OPs, training in diagnosis and treatment of mental disorders. consulted by 2 psychiatrist trained in improvement of work functioning | Company of participant | Psychiatric assessment, collaborative RTW-plan, coordination of plan and monitoring by OP | Until RTW | N.r. | N.r. | Care from OP |
RTW = return to work, n.r. = not reported, OP = occupational physician, PT = physical therapist, GP = general practitioner, rehab. = rehabilitation.
The trial compared three intervention arms with usual practice. We considered only the arm “combined intervention” because the other arms were restricted to either workplace or health care interventions.
In the Dutch system, each company is obliged to have company insurance for sick leave and to offer their employees access to occupational health care. Occupational physicians provide social-medical guidance for sick listed employees with the aim to return to work (RTW) as quickly as possible. Usually, occupational physicians are organised as third party service providers.
From personal correspondence.
Methodological components.
| Study | Random sequence adequately generated? | Allocation concealed? | Participants and RTW-coordinators blinded? | RTW-outcome assessor blinded? | PRO- outcome assessor blinded? | Loss to follow-up of RTW-outcomes [%] | Loss to follow-up of PROs [%] | Intention to treat analysis | Selective reporting | Other |
| Bültmann 2009 | Y | Y | N | Y | N | 5 | 34 | Y | ? | |
| Davey 1994 | Y | Y | N | N | N | 0 | 0 | Y | ? | |
| Donceel 1999 | Y | Y | N | N | n.a. | 0 | n.a. | (Y) | ? |
|
| Feuerstein 2003 | Y | N | N | (N) | N | 40 | 36–61 | (N) | Y | |
| Lambeek 2010 | Y | Y | N | N | N | 7 | 13 | Y | N | |
| Lindh 1998 | (N) | (N) | N | Y | n.a. | ? | n.a. | Y | Y | |
| Purdon 2006 | Y | Y | N | N | N | 28 | 29 | Y | ? | |
| Rossignol 2000 | Y | Y | N | Y | N | 0 | 18 | Y | ? | |
| V. d. Feltz-Cornelis 2010 | Y | Y | N | Y | N | 18 | 27 | Y | Y |
|
RTW = return to work, PRO = patient reported outcomes, Y = yes, (Y) = probably Yes, N = No, (N) = probably no, ? = unclear, n.a. = not applicable.
Participants analysed in the group to which they were initially assigned.
“No” if protocol published and all outcomes correctly reported; “?” if no protocol published and selective reporting not obvious.
From personal correspondence.
Participants were probably not aware of the intervention.
RTW-outcomes not published, incomplete outcome information (see table 3).
Results presented in subgroups, incomplete outcome information (see table 3).
Primary outcome not mentioned in protocol.
Incomplete outcome information (see table 3).
Cluster randomised trials: No risk of recruitment bias. Baseline information of individual clusters not reported. Effects of RTW-outcomes not corrected for possible design effects (risk of inflated precision).
Evidence Profile, relevant outcomes.
| Quality assessment | No of participants | Effect | Confidence in estimate | Importance | |||||||||
| No of studies | Design | Risk of bias | Inconsistency | Indirectness | Imprecision | RTW-coordination | Usual care | Relative (95% CI) | Absolute | ||||
|
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| 6 | randomised trials | serious | no serious inconsistency | no serious indirectness | no serious imprecision | 794/1279 (62.1%) | 656/1138 (57.6%) | RR 1.08 (1.03 to 1.13) | 5 more per 100(from 2 more to 7 more) | ⊕⊕⊕ MODERATE | CRITICAL | ||
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| 4 | randomised trials | serious | no serious inconsistency | no serious indirectness | no serious imprecision | 716 | 558 | – | MD 5.2 higher(2.4 to 8.0 higher) | ⊕⊕⊕ MODERATE | IMPORTANT | ||
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| 5 | randomised trials | serious | no serious inconsistency | no serious indirectness | no serious imprecision | 729 | 619 | – | MD 5.3 higher(1.4 to 9.1 higher) | ⊕⊕⊕ MODERATE | IMPORTANT | ||
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| 6 | randomised trials | serious | no serious inconsistency | no serious indirectness | no serious imprecision | 784 | 646 | – | MD 6.1 lower(3.1 to 9.2 lower) | ⊕⊕⊕ MODERATE | IMPORTANT | ||
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| 2 | randomised trials | serious | no serious inconsistency | no serious indirectness | serious | 589 | 470 | – | MD 3.1 higher (0.6 lower to 6.8 higher) | ⊕⊕ LOW | IMPORTANT | ||
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| 2 | randomised trials | serious | no serious inconsistency | no serious indirectness | no serious imprecision | 599 | 512 | – | MD 3.1 higher (0.7 to 5.6higher) | ⊕⊕⊕ MODERATE | IMPORTANT | ||
Risk of attrition bias.
Risk of reporting bias.
Total population size less than 400.
Use of unvalidated instruments.
Confidence interval encloses no effect and meaningful difference.
Figure 2RTW-outcomes.
RTW coord. = return to work coordination.
Figure 3Patient reported outcomes.
Individual trials’ outcomes expressed on a 0 to 100 scale. RTW coord. = return to work coordination. MID = minimal important difference.