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一项整群随机对照试验的研究方案,旨在评估针对患有慢性下腰痛的年轻初级保健患者的轴性脊柱关节炎转诊策略;一项影响研究。

Study protocol for a cluster randomized controlled trial to evaluate a referral strategy for axial spondyloarthritis in young primary care patients with chronic low back pain; an impact study.

作者信息

van Hoeven Lonneke, Vergouwe Yvonne, Koes Bart W, Hazes Johanna M W, Weel Angelique E A M

机构信息

Erasmus MC, Department of Rheumatology, Wytemaweg 80, 3015, CN, Rotterdam, The Netherlands.

Maasstad Hospital, Department of Rheumatology, Maasstadweg 21, 3079, DZ, Rotterdam, The Netherlands.

出版信息

BMC Musculoskelet Disord. 2016 Jul 12;17:278. doi: 10.1186/s12891-016-1132-6.

Abstract

BACKGROUND

Axial spondyloarthritis (axSpA) is a disabling inflammatory joint disease with chronic low back pain (CLBP) as leading symptom. Recognizing axSpA in the large amount of CLBP patients is difficult for general practioners (GP). This evaluation aims to assess the effect of a referral strategy for axSpA in young primary care patients with CLBP by comparing the use of the strategy with usual care. The effect is measured at three different levels; by patient reported outcomes (the clinical effect), process and costs evaluation.

METHODS/DESIGN: This study design is a cluster randomized controlled trial with GP as clusters. GPs throughout the Netherlands are invited to participate and randomized to either the intervention or the control group. Patients from participating GPs are invited to participate if they have ever been registered with low back pain, without radiation (ICPC L03) and aged 18-45 years. To be included in the study, patients need to have current low back pain and chronic low back pain (>12 weeks). In the intervention arm a referral strategy for axSpA will be applied in CLBP patients, in the control arm care as usual will be provided for CLBP patients. The referral strategy consists of four easy to use variables. All are questions about the back pain complaints of the patients. Data is prospectively collected in an online database at baseline (T0), 4 months (T1), 12 months (T2) and 24 months (T3). After time point T1 (4 months) patients from the control group will also receive the intervention i.e. the application of a referral strategy for axSpA. The effect of the referral strategy is measured at three different levels, by patient outcomes (e.g. pain scores, quality of life), process measures (e.g. number of axSpA diagnoses by rheumatologists) and by costs (work productivity and health care resources use). Our primary outcome is the Roland Morris Disability Questionnaire after 4 months, secondary outcomes are pain and quality of life. Costs will be assessed before and after the use of the referral strategy, to estimate if the use of the strategy will lead to a reduction in health care costs and improvement in work participation.

DISCUSSION

It is anticipated that using the axSpA referral strategy for primary care CLBP patients will increase the quality of life of CLBP patients, will result in more (correct) diagnoses of axSpA by the rheumatologists, and will be cost-effective. Ultimately, the results of this study may contribute to the startup of a national implementation of the axSpA referral strategy to identify timely CLBP patients with axSpA.

TRIAL REGISTRATION

NCT01944163 , date of registration; September 6, 2013 (Clinicaltrials.gov).

摘要

背景

轴性脊柱关节炎(axSpA)是一种导致残疾的炎性关节疾病,以慢性腰痛(CLBP)为主要症状。对于全科医生(GP)而言,在大量CLBP患者中识别axSpA具有一定难度。本评估旨在通过比较该策略与常规护理的使用情况,评估针对年轻的原发性CLBP患者的axSpA转诊策略的效果。该效果在三个不同层面进行衡量:患者报告的结果(临床效果)、过程和成本评估。

方法/设计:本研究设计为一项以GP为群组的整群随机对照试验。邀请荷兰各地的GP参与并随机分为干预组或对照组。如果参与的GP的患者曾有过无放射性的腰痛记录(国际初级保健分类L03)且年龄在18 - 45岁之间,就邀请他们参与。要纳入研究,患者需目前患有腰痛且为慢性腰痛(>12周)。在干预组,将对CLBP患者应用axSpA转诊策略,在对照组,将为CLBP患者提供常规护理。转诊策略包含四个易于使用的变量。所有这些都是关于患者背痛主诉的问题。数据在基线(T0)、4个月(T1)、12个月(T2)和24个月(T3)时前瞻性地收集到一个在线数据库中。在时间点T1(4个月)之后,对照组的患者也将接受干预,即应用axSpA转诊策略。转诊策略的效果在三个不同层面进行衡量,通过患者结果(例如疼痛评分、生活质量)、过程指标(例如风湿病学家诊断的axSpA病例数)和成本(工作生产力和医疗资源使用)。我们的主要结局是4个月后的罗兰·莫里斯残疾问卷,次要结局是疼痛和生活质量。将在使用转诊策略之前和之后评估成本,以估计该策略的使用是否会导致医疗成本降低和工作参与度提高。

讨论

预计对初级保健CLBP患者使用axSpA转诊策略将提高CLBP患者的生活质量,使风湿病学家能做出更多(正确的)axSpA诊断,并且具有成本效益。最终,本研究结果可能有助于启动axSpA转诊策略的全国实施,以便及时识别患有axSpA的CLBP患者。

试验注册

NCT01944163,注册日期:2013年9月6日(Clinicaltrials.gov)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb4c/4942916/41002243a6e9/12891_2016_1132_Fig1_HTML.jpg

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