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一项关于由物理治疗师通过教学 DVD 或面对面授课教授呼吸训练练习对成人哮喘管理的有效性的随机对照研究。

A randomised controlled study of the effectiveness of breathing retraining exercises taught by a physiotherapist either by instructional DVD or in face-to-face sessions in the management of asthma in adults.

机构信息

Faculty of Medicine, University of Southampton, Southampton, UK.

Faculty of Health Sciences, University of Southampton, Southampton, UK.

出版信息

Health Technol Assess. 2017 Sep;21(53):1-162. doi: 10.3310/hta21530.

Abstract

BACKGROUND

Asthma control is suboptimal, resulting in quality of life (QoL) impairment and costs. Breathing retraining exercises have evidence of effectiveness as adjuvant treatment, but are infrequently used.

OBJECTIVES

To transfer the contents of a brief (three-session) physiotherapist-delivered breathing retraining programme to a digital versatile disc (DVD) and booklet format; to compare the effectiveness of the self-guided intervention with that of 'face-to-face' physiotherapy and usual care for QoL and other asthma-related outcomes; to perform a health economic assessment of both interventions; and to perform a process evaluation using quantitative and qualitative methods.

DESIGN

Parallel-group three-arm randomised controlled trial.

SETTING

General practice surgeries in the UK.

PARTICIPANTS

In total, 655 adults currently receiving asthma treatment with impaired asthma-related QoL were randomly allocated to the DVD ( = 261), physiotherapist ( = 132) and control (usual care) ( = 262) arms in a 2 : 1 : 2 ratio. It was not possible to blind participants but data collection and analysis were performed blinded.

INTERVENTIONS

Physiotherapy-based breathing retraining delivered through three 'face-to-face' respiratory physiotherapist sessions or a self-guided programme (DVD plus our theory-based behaviour change booklet) developed by the research team, with a control of usual care.

MAIN OUTCOME MEASURES

The primary outcome measure was asthma-specific QoL, measured using the Asthma Quality of Life Questionnaire (AQLQ). Secondary outcomes included asthma symptom control [Asthma Control Questionnaire (ACQ)], psychological state [Hospital Anxiety and Depression Scale (HADS)], hyperventilation symptoms (Nijmegen questionnaire), generic QoL [EuroQol-5 Dimensions (EQ-5D)], assessments of airway physiology (spirometry) and inflammation (exhaled nitric oxide) and health resource use and costs. Assessments were carried out at baseline and at 3, 6 and 12 months post randomisation. Patient engagement and experience were also assessed using quantitative and qualitative methods.

RESULTS

Primary efficacy analysis was between-group comparison of changes in AQLQ scores from baseline to 12 months in the intention-to-treat population with adjustments for prespecified covariates. Significant improvements occurred in the DVD group compared with the control group [adjusted mean difference 0.28, 95% confidence interval (CI) 0.11 to 0.44;  < 0.001] and in the face-to-face physiotherapy group compared with the control group (adjusted mean difference 0.24, 95% CI 0.04 to 0.44;  < 0.05), with equivalence between the DVD and the face-to-face physiotherapy groups (adjusted mean difference 0.04, 95% CI -0.16 to 0.24). In all sensitivity analyses, both interventions remained significantly superior to the control and equivalence between the interventions was maintained. In other questionnaire outcome measures and in the physiological measures assessed, there were no significant between-group differences. Process evaluations showed that participants engaged well with both of the active interventions, but that some participants in the DVD arm would have liked to receive tuition from a professional. Asthma health-care costs were lower in both intervention arms than in the control group, indicating 'dominance' for both of the interventions compared with the control, with lowest costs in the DVD arm. The rate of adverse events was lower in the DVD and face-to-face physiotherapy groups than in the control group.

CONCLUSIONS

Only 10% of the potentially eligible population responded to the study invitation. However, breathing retraining exercises improved QoL and reduced health-care costs in adults with asthma whose condition remains uncontrolled despite standard pharmacological therapy, were engaged with well by patients and can be delivered effectively as a self-guided intervention. The intervention should now be transferred to an internet-based platform and implementation studies performed. Interventions for younger patients should be developed and trialled.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN88318003.

FUNDING

This project was primarily funded by the NIHR Health Technology Assessment programme and will be published in full in ; Vol. 21, No. 53. See the NIHR Journals Library website for further project information. Additional financial support was received from Comprehensive Local Research Networks.

摘要

背景

哮喘控制不佳导致生活质量受损和成本增加。呼吸训练在辅助治疗方面具有一定的效果,但应用较少。

目的

将简短(三节课)物理治疗师提供的呼吸训练计划的内容转移到数字多功能光盘(DVD)和手册格式中;比较自我指导干预与“面对面”物理治疗和常规护理对生活质量和其他哮喘相关结果的有效性;对两种干预措施进行健康经济评估;并使用定量和定性方法进行过程评估。

设计

平行组三臂随机对照试验。

地点

英国的普通外科手术室。

参与者

总共 655 名目前正在接受哮喘治疗且生活质量受损的成年人被随机分配到 DVD 组( = 261)、物理治疗师组( = 132)和对照组(常规护理)( = 262),比例为 2:1:2。参与者无法被蒙蔽,但数据收集和分析是盲法进行的。

干预措施

通过三次“面对面”呼吸物理治疗师会议或由研究团队开发的自我指导计划(DVD 加我们基于理论的行为改变手册)提供基于生理的呼吸训练,对照组为常规护理。

主要结果测量

主要结局测量指标是哮喘特异性生活质量,使用哮喘生活质量问卷(AQLQ)进行测量。次要结局包括哮喘症状控制(哮喘控制问卷(ACQ))、心理状态(医院焦虑和抑郁量表(HADS))、过度通气症状(尼姆根问卷)、一般生活质量(EuroQol-5 维度(EQ-5D))、气道生理评估(肺活量测定)和炎症(呼气一氧化氮)以及健康资源使用和成本。在随机分组后 3、6 和 12 个月进行评估。还使用定量和定性方法评估患者的参与度和体验。

结果

主要疗效分析是在意向治疗人群中,从基线到 12 个月时 AQLQ 评分的组间变化,同时调整了预设协变量。与对照组相比,DVD 组(调整后的平均差异 0.28,95%置信区间(CI)0.11 至 0.44; < 0.001)和面对面物理治疗组(调整后的平均差异 0.24,95%CI 0.04 至 0.44; < 0.05)都有显著改善,且 DVD 组和面对面物理治疗组之间具有等效性(调整后的平均差异 0.04,95%CI -0.16 至 0.24)。在所有敏感性分析中,两种干预措施均显著优于对照组,且干预措施之间保持等效性。在其他问卷调查结果测量和生理测量中,组间没有显著差异。过程评估表明,参与者对两种主动干预措施都有很好的参与度,但 DVD 组的一些参与者希望接受专业人士的指导。与对照组相比,两种干预组的哮喘保健费用都较低,表明与对照组相比,两种干预措施均具有“优势”,而 DVD 组的成本最低。DVD 组和面对面物理治疗组的不良事件发生率低于对照组。

结论

只有 10%的潜在合格人群对研究邀请做出了回应。然而,呼吸训练可以改善生活质量并降低哮喘患者的医疗保健成本,这些患者的病情尽管经过标准药物治疗仍未得到控制,并且患者参与度高,并且可以作为自我指导干预措施有效地实施。现在应该将该干预措施转移到互联网平台上,并进行实施研究。应该为年轻患者开发和试验干预措施。

试验注册

当前对照试验 ISRCTN88318003。

资金

该项目主要由英国国家卫生与临床优化研究所健康技术评估计划资助,全文将在 ; 第 21 卷,第 53 期发表。有关该项目的更多信息,请访问 NIHR 期刊库网站。该项目还获得了综合地方研究网络的额外财政支持。

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