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慢性疲劳综合征/肌痛性脑脊髓炎的专科治疗:一项针对英格兰成年患者的队列研究。

Specialist treatment of chronic fatigue syndrome/ME: a cohort study among adult patients in England.

作者信息

Collin Simon M, Crawley Esther

机构信息

School of Social & Community Medicine, Oakfield House, University of Bristol, Oakfield Grove, Bristol, BS8 2BN, UK.

出版信息

BMC Health Serv Res. 2017 Jul 14;17(1):488. doi: 10.1186/s12913-017-2437-3.

Abstract

BACKGROUND

NHS specialist chronic fatigue syndrome (CFS/ME) services in England treat approximately 8000 adult patients each year. Variation in therapy programmes and treatment outcomes across services has not been described.

METHODS

We described treatments provided by 11 CFS/ME specialist services and we measured changes in patient-reported fatigue (Chalder, Checklist Individual Strength), function (SF-36 physical subscale, Work & Social Adjustment Scale), anxiety and depression (Hospital Anxiety & Depression Scale), pain (visual analogue rating), sleep (Epworth, Jenkins), and overall health (Clinical Global Impression) 1 year after the start of treatment, plus questions about impact of CFS/ME on employment, education/training and domestic tasks/unpaid work. A subset of these outcome measures was collected from former patients 2-5 years after assessment at 7 of the 11 specialist services.

RESULTS

Baseline data at clinical assessment were available for 952 patients, of whom 440 (46.2%) provided 1-year follow-up data. Treatment data were available for 435/440 (98.9%) of these patients, of whom 175 (40.2%) had been discharged at time of follow-up. Therapy programmes varied substantially in mode of delivery (individual or group) and number of sessions. Overall change in health 1 year after first attending specialist services was 'very much' or 'much better' for 27.5% (115/418) of patients, 'a little better' for 36.6% (153/418), 'no change' for 15.8% (66/418), 'a little worse' for 12.2% (51/418), and 'worse' or 'very much worse' for 7.9% (33/418). Among former patients who provided 2- to 5-year follow-up (30.4% (385/1265)), these proportions were 30.4% (117/385), 27.5% (106/385), 11.4% (44/385), 13.5% (52/385), and 17.1% (66/385), respectively. 85.4% (327/383) of former patients responded "Yes" to "Do you think that you are still suffering from CFS/ME?" 8.9% (34/383) were "Uncertain", and 5.7% (22/383) responded "No".

CONCLUSIONS

This multi-centre NHS study has shown that, although one third of patients reported substantial overall improvement in their health, CFS/ME is a long term condition that persists for the majority of adult patients even after receiving specialist treatment.

摘要

背景

英国国家医疗服务体系(NHS)的慢性疲劳综合征(CFS/ME)专科服务每年治疗约8000名成年患者。各服务机构的治疗方案和治疗结果差异尚未见描述。

方法

我们描述了11个CFS/ME专科服务机构提供的治疗方法,并在治疗开始1年后测量了患者报告的疲劳程度(查尔德疲劳量表、个体力量清单)、功能(SF-36身体分量表、工作与社会适应量表)、焦虑和抑郁(医院焦虑抑郁量表)、疼痛(视觉模拟评分)、睡眠(爱泼沃斯嗜睡量表、詹金斯睡眠问卷)以及总体健康状况(临床总体印象),还询问了CFS/ME对就业、教育/培训和家务/无薪工作的影响。在11个专科服务机构中的7个,对部分患者在评估后2至5年收集了这些结果指标的子集数据。

结果

952例患者有临床评估时的基线数据,其中440例(46.2%)提供了1年随访数据。440例患者中的435例(98.9%)有治疗数据,其中175例(40.2%)在随访时已出院。治疗方案在提供方式(个体或团体)和疗程数量上差异很大。首次就诊专科服务机构1年后,27.5%(115/418)的患者总体健康状况“非常”或“好多了”,36.6%(153/418)的患者“稍好一些”,15.8%(66/418)的患者“无变化”,12.2%(51/418)的患者“稍差一些”,7.9%(33/418)的患者“更差”或“差得多”。在提供2至5年随访的既往患者中(30.4%(385/1265)),这些比例分别为30.4%(117/385)、27.5%(106/385)、11.4%(44/385)、13.5%(52/385)和17.1%(66/385)。85.4%(327/383)的既往患者对“你认为自己仍患有CFS/ME吗?”回答“是”。8.9%(34/383)的患者“不确定”,5.7%(22/383)的患者回答“否”。

结论

这项NHS多中心研究表明,虽然三分之一的患者报告总体健康状况有显著改善,但CFS/ME是一种长期病症,即使接受专科治疗后,大多数成年患者的病情仍会持续。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/921f/5513420/e3854185c5d1/12913_2017_2437_Fig1_HTML.jpg

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