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治疗职业性哮喘的工作场所干预措施。

Workplace interventions for treatment of occupational asthma.

作者信息

Henneberger Paul K, Patel Jenil R, de Groene Gerda J, Beach Jeremy, Tarlo Susan M, Pal Teake M, Curti Stefania

机构信息

Respiratory Health Division, National Institute for Occupational Safety and Health, 1095 Willowdale Road, Morgantown, West Virginia, USA, 26505.

出版信息

Cochrane Database Syst Rev. 2019 Oct 8;10(10):CD006308. doi: 10.1002/14651858.CD006308.pub4.

Abstract

BACKGROUND

The impact of workplace interventions on the outcome of occupational asthma is not well understood.

OBJECTIVES

To evaluate the effectiveness of workplace interventions on occupational asthma.

SEARCH METHODS

We searched the Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE (PubMed); EMBASE(Ovid); NIOSHTIC-2; and CISILO (CCOHS) up to July 31, 2019.

SELECTION CRITERIA

We included all eligible randomized controlled trials, controlled before and after studies and interrupted time-series of workplace interventions for occupational asthma.

DATA COLLECTION AND ANALYSIS

Two authors independently assessed study eligibility and risk of bias, and extracted data.

MAIN RESULTS

We included 26 non-randomized controlled before and after studies with 1,695 participants that reported on three comparisons: complete removal from exposure and reduced exposure compared to continued exposure, and complete removal from exposure compared to reduced exposure. Reduction of exposure was achieved by limiting use of the agent, improving ventilation, or using protective equipment in the same job; by changing to another job with intermittent exposure; or by implementing education programs. For continued exposure, 56 per 1000 workers reported absence of symptoms at follow-up, the decrease in forced expiratory volume in one second as a percentage of a reference value (FEV1 %) was 5.4% during follow-up, and the standardized change in non-specific bronchial hyperreactivity (NSBH) was -0.18.In 18 studies, authors compared removal from exposure to continued exposure. Removal may increase the likelihood of reporting absence of asthma symptoms, with risk ratio (RR) 4.80 (95% confidence interval (CI) 1.67 to 13.86), and it may improve asthma symptoms, with RR 2.47 (95% CI 1.26 to 4.84), compared to continued exposure. Change in FEV1 % may be better with removal from exposure, with a mean difference (MD) of 4.23 % (95% CI 1.14 to 7.31) compared to continued exposure. NSBH may improve with removal from exposure, with standardized mean difference (SMD) 0.43 (95% CI 0.03 to 0.82).In seven studies, authors compared reduction of exposure to continued exposure. Reduction of exposure may increase the likelihood of reporting absence of symptoms, with RR 2.65 (95% CI 1.24 to 5.68). There may be no considerable difference in FEV1 % between reduction and continued exposure, with MD 2.76 % (95% CI -1.53 to 7.04) . No studies reported or enabled calculation of change in NSBH.In ten studies, authors compared removal from exposure to reduction of exposure. Following removal from exposure there may be no increase in the likelihood of reporting absence of symptoms, with RR 6.05 (95% CI 0.86 to 42.34), and improvement in symptoms, with RR 1.11 (95% CI 0.84 to 1.47), as well as no considerable change in FEV1 %, with MD 2.58 % (95% CI -3.02 to 8.17). However, with all three outcomes, there may be improved results for removal from exposure in the subset of patients exposed to low molecular weight agents. No studies reported or enabled calculation of change in NSBH.In two studies, authors reported that the risk of unemployment after removal from exposure may increase compared with reduction of exposure, with RR 14.28 (95% CI 2.06 to 99.16). Four studies reported a decrease in income of 20% to 50% after removal from exposure.The quality of the evidence is very low for all outcomes.

AUTHORS' CONCLUSIONS: Both removal from exposure and reduction of exposure may improve asthma symptoms compared with continued exposure. Removal from exposure, but not reduction of exposure, may improve lung function compared to continued exposure. When we compared removal from exposure directly to reduction of exposure, the former may improve symptoms and lung function more among patients exposed to low molecular weight agents. Removal from exposure may also increase the risk of unemployment. Care providers should balance the potential clinical benefits of removal from exposure or reduction of exposure with potential detrimental effects of unemployment. Additional high-quality studies are needed to evaluate the effectiveness of workplace interventions for occupational asthma.

摘要

背景

工作场所干预措施对职业性哮喘结局的影响尚未得到充分了解。

目的

评估工作场所干预措施对职业性哮喘的有效性。

检索方法

我们检索了截至2019年7月31日的Cochrane对照试验中心注册库(CENTRAL)、MEDLINE(PubMed)、EMBASE(Ovid)、NIOSHTIC - 2和CISILO(CCOHS)。

入选标准

我们纳入了所有符合条件的随机对照试验、前后对照研究以及职业性哮喘工作场所干预措施的中断时间序列研究。

数据收集与分析

两位作者独立评估研究的入选资格和偏倚风险,并提取数据。

主要结果

我们纳入了26项前后对照的非随机对照研究,共1695名参与者,这些研究报告了三项比较:与持续暴露相比,完全脱离暴露和减少暴露;与减少暴露相比,完全脱离暴露。减少暴露是通过限制制剂的使用、改善通风或在同一工作岗位使用防护设备来实现的;通过更换为间歇性暴露的另一工作岗位;或通过实施教育计划。对于持续暴露,每1000名工人中有56人在随访时报告无症状,随访期间一秒用力呼气量作为参考值的百分比(FEV1%)下降了5.4%,非特异性支气管高反应性(NSBH)的标准化变化为 - 0.18。在18项研究中,作者比较了脱离暴露与持续暴露。与持续暴露相比,脱离暴露可能增加报告无哮喘症状的可能性,风险比(RR)为4.80(95%置信区间(CI)为1.67至13.86),并且可能改善哮喘症状,RR为2.47(95%CI为1.26至4.84)。与持续暴露相比,脱离暴露时FEV1%的变化可能更好,平均差(MD)为4.23%(95%CI为1.14至7.31)。NSBH可能随着脱离暴露而改善,标准化平均差(SMD)为0.43(95%CI为0.03至0.82)。在7项研究中,作者比较了减少暴露与持续暴露。减少暴露可能增加报告无症状的可能性,RR为2.65(95%CI为1.24至5.68)。减少暴露与持续暴露之间FEV1%可能没有显著差异,MD为2.76%(95%CI为 - 1.53至7.04)。没有研究报告或能够计算NSBH的变化。在10项研究中,作者比较了脱离暴露与减少暴露。脱离暴露后报告无症状的可能性可能没有增加,RR为6.05(95%CI为0.86至42.34),症状改善,RR为1.11(95%CI为0.84至1.47),FEV1%也没有显著变化,MD为2.58%(95%CI为 - 3.02至8.17)。然而,对于所有这三个结局,在暴露于低分子量制剂的患者亚组中,脱离暴露可能会有更好的结果。没有研究报告或能够计算NSBH的变化。在两项研究中,作者报告与减少暴露相比,脱离暴露后失业风险可能增加,RR为14.28(95%CI为2.06至99.16)。四项研究报告脱离暴露后收入下降了20%至50%。所有结局的证据质量都非常低。

作者结论

与持续暴露相比,脱离暴露和减少暴露都可能改善哮喘症状。与持续暴露相比,脱离暴露而非减少暴露可能改善肺功能。当我们直接比较脱离暴露与减少暴露时,在暴露于低分子量制剂的患者中,前者可能更能改善症状和肺功能。脱离暴露也可能增加失业风险。医疗服务提供者应权衡脱离暴露或减少暴露的潜在临床益处与失业的潜在不利影响。需要更多高质量研究来评估工作场所干预措施对职业性哮喘的有效性。

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