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旨在改善病假员工复工情况的复工协调计划。

Return-to-work coordination programmes for improving return to work in workers on sick leave.

作者信息

Vogel Nicole, Schandelmaier Stefan, Zumbrunn Thomas, Ebrahim Shanil, de Boer Wout El, Busse Jason W, Kunz Regina

机构信息

Department Clinical Research, EbIM Evidence-based Insurance Medicine, University of Basel Hospital, Spitalstrasse 8+12, Basel, Switzerland, 4031.

Leonardo, Hirslanden Klinik Birshof, Reinacherstrasse 28, Münchenstein, Switzerland, 4142.

出版信息

Cochrane Database Syst Rev. 2017 Mar 30;3(3):CD011618. doi: 10.1002/14651858.CD011618.pub2.

Abstract

BACKGROUND

To limit long-term sick leave and associated consequences, insurers, healthcare providers and employers provide programmes to facilitate disabled people's return to work. These programmes include a variety of coordinated and individualised interventions. Despite the increasing popularity of such programmes, their benefits remain uncertain. We conducted a systematic review to determine the long-term effectiveness of return-to-work coordination programmes compared to usual practice in workers at risk for long-term disability.

OBJECTIVES

To assess the effects of return-to-work coordination programmes versus usual practice for workers on sick leave or disability.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 11), MEDLINE, Embase, CINAHL and PsycINFO up to 1 November 2016.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) that enrolled workers absent from work for at least four weeks and randomly assigned them to return-to-work coordination programmes or usual practice.

DATA COLLECTION AND ANALYSIS

Two review authors independently screened titles, abstracts and full-text articles for study eligibility; extracted data; and assessed risk of bias from eligible trials. We contacted authors for additional data where required. We conducted random-effects meta-analyses and used the GRADE approach to rate the quality of the evidence.

MAIN RESULTS

We identified 14 studies from nine countries that enrolled 12,568 workers. Eleven studies focused on musculoskeletal problems, two on mental health and one on both. Most studies (11 of 14) followed workers 12 months or longer. Risk of bias was low in 10 and high in 4 studies, but findings were not sensitive to their exclusion.We found no benefits for return-to-work coordination programmes on return-to-work outcomes.For short-term follow-up of six months, we found no effect on time to return to work (hazard ratio (HR) 1.32, 95% confidence interval (CI) 0.93 to 1.88, low-quality evidence), cumulative sickness absence (mean difference (MD) -16.18 work days per year, 95% CI -32.42 to 0.06, moderate-quality evidence), the proportion of participants at work at end of the follow-up (risk ratio (RR) 1.06, 95% CI 0.86 to 1.30, low-quality evidence) or on the proportion of participants who had ever returned to work, that is, regardless of whether they had remained at work until last follow-up (RR 0.87, 95% CI 0.63 to 1.19, very low-quality evidence).For long-term follow-up of 12 months, we found no effect on time to return to work (HR 1.25, 95% CI 0.95 to 1.66, low-quality evidence), cumulative sickness absence (MD -14.84 work days per year, 95% CI -38.56 to 8.88, low-quality evidence), the proportion of participants at work at end of the follow-up (RR 1.06, 95% CI 0.99 to 1.15, low-quality evidence) or on the proportion of participants who had ever returned to work (RR 1.03, 95% CI 0.97 to 1.09, moderate-quality evidence).For very long-term follow-up of longer than 12 months, we found no effect on time to return to work (HR 0.93, 95% CI 0.74 to 1.17, low-quality evidence), cumulative sickness absence (MD 7.00 work days per year, 95% CI -15.17 to 29.17, moderate-quality evidence), the proportion of participants at work at end of the follow-up (RR 0.94, 95% CI 0.82 to 1.07, low-quality evidence) or on the proportion of participants who had ever returned to work (RR 0.95, 95% CI 0.88 to 1.02, low-quality evidence).We found only small benefits for return-to-work coordination programmes on patient-reported outcomes. All differences were below the minimal clinically important difference (MID).

AUTHORS' CONCLUSIONS: Offering return-to-work coordination programmes for workers on sick leave for at least four weeks results in no benefits when compared to usual practice. We found no significant differences for the outcomes time to return to work, cumulative sickness absence, the proportion of participants at work at end of the follow-up or the proportion of participants who had ever returned to work at short-term, long-term or very long-term follow-up. For patient-reported outcomes, we found only marginal effects below the MID. The quality of the evidence ranged from very low to moderate across all outcomes.

摘要

背景

为限制长期病假及相关后果,保险公司、医疗服务提供者和雇主提供了促进残疾人重返工作岗位的项目。这些项目包括各种协调一致的个性化干预措施。尽管此类项目越来越受欢迎,但其益处仍不明确。我们进行了一项系统评价,以确定与常规做法相比,重返工作岗位协调项目对有长期残疾风险的工人的长期有效性。

目的

评估重返工作岗位协调项目与常规做法对休病假或残疾工人的影响。

检索方法

我们检索了截至2016年11月1日的考克兰对照试验中央注册库(CENTRAL;2016年第11期)、MEDLINE、Embase、CINAHL和PsycINFO。

入选标准

我们纳入了随机对照试验(RCT),这些试验招募了至少四周未上班的工人,并将他们随机分配到重返工作岗位协调项目或常规做法组。

数据收集与分析

两位综述作者独立筛选标题、摘要和全文文章以确定研究的合格性;提取数据;并评估合格试验的偏倚风险。必要时,我们联系作者获取更多数据。我们进行了随机效应荟萃分析,并使用GRADE方法对证据质量进行评级。

主要结果

我们从九个国家识别出14项研究,共纳入12568名工人。11项研究聚焦于肌肉骨骼问题,2项关注心理健康,1项两者兼顾。大多数研究(14项中的11项)对工人进行了12个月或更长时间的随访。10项研究的偏倚风险较低,4项较高,但排除这些研究后结果并不敏感。我们发现重返工作岗位协调项目对重返工作结果没有益处。

对于六个月的短期随访,我们发现对重返工作时间没有影响(风险比(HR)1.32,95%置信区间(CI)0.93至1.88,低质量证据),对累计病假天数没有影响(平均差(MD)-16.18个工作日/年,95%CI -32.42至0.06,中等质量证据),对随访结束时工作的参与者比例没有影响(风险比(RR)1.06,95%CI 0.86至1.30,低质量证据),对曾经重返工作岗位的参与者比例也没有影响,即无论他们是否一直工作到最后一次随访(RR 0.87,95%CI 0.63至1.19)(极低质量证据)。

对于12个月的长期随访,我们发现对重返工作时间没有影响(HR 1.25,95%CI 0.95至1.66,低质量证据),对累计病假天数没有影响(MD -14.84个工作日/年,95%CI -38.56至8.88,低质量证据),对随访结束时工作的参与者比例没有影响(RR 1.06,95%CI 0.99至1.15,低质量证据),对曾经重返工作岗位的参与者比例也没有影响(RR 1.03,95%CI 0.97至1.09,中等质量证据)。

对于超过12个月的极长期随访,我们发现对重返工作时间没有影响(HR 0.93,95%CI 0.74至1.17,低质量证据),对累计病假天数没有影响(MD 7.00个工作日/年,95%CI -15.17至29.17,中等质量证据),对随访结束时工作的参与者比例没有影响(RR 0.94,95%CI 0.82至1.07,低质量证据),对曾经重返工作岗位的参与者比例也没有影响(RR 0.95,95%CI 0.88至1.02,低质量证据)。

我们发现重返工作岗位协调项目对患者报告的结果只有微小益处。所有差异均低于最小临床重要差异(MID)。

作者结论

与常规做法相比,为休病假至少四周的工人提供重返工作岗位协调项目没有益处。我们发现在短期、长期或极长期随访中,在重返工作时间、累计病假天数、随访结束时工作的参与者比例或曾经重返工作岗位的参与者比例这些结果方面没有显著差异。对于患者报告的结果,我们仅发现低于MID的微小效应。所有结果的证据质量从极低到中等不等。

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