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使用电子方法监测单独使用或联合使用长效β2-激动剂(LABA)的常规吸入皮质类固醇(ICS)的依从性对哮喘结局的影响:叙述性系统评价。

Effect of monitoring adherence to regular inhaled corticosteroid (ICS) alone or in combination with a long-acting β2-agonist (LABA) using electronic methods on asthma outcomes: a narrative systematic review.

机构信息

College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK

Department of Pharmacy Practice, College of Pharmacy, Qassim University, Buraidah, Saudi Arabia.

出版信息

BMJ Open. 2023 Aug 16;13(8):e074127. doi: 10.1136/bmjopen-2023-074127.

Abstract

OBJECTIVES

To evaluate through a systematic review the effectiveness of electronic methods in monitoring adherence to regular inhaled corticosteroids (ICS) alone or in combination with long-acting β2-agonists (LABAs) and their effect on clinical outcomes.

DESIGN

A narrative systematic review.

DATA SOURCES

MEDLINE, EMBASE, Cochrane Database of Systematic Reviews and Web of Science were searched through up to 10 July 2022.

ELIGIBILITY CRITERIA

We included peer-reviewed studies of qualitative and quantitative outcomes that compared the effect of electronic methods to routine non-electronic monitoring intervention or placebo among children and adults with asthma on medication adherence rates to regular ICS alone or in combination with LABA, asthma control and asthma exacerbations.

DATA EXTRACTION AND SYNTHESIS

Data extraction was performed according to a predetermined sheet specific to the review objectives. The risk of bias was assessed using the Cochrane Risk of Bias Tool for randomised controlled trials and the Risk of Bias in Systematic Reviews tool for systematic reviews. Meta-analysis was not possible based on the findings of the scoping search; however, a narrative review was performed to allow for the grouping of results based on asthma inhaler adherence rates, asthma control and exacerbations.

RESULTS

Six articles comprising 98 studies published from 1998 to 2022 in the USA, Canada and the UK were included. Compared with the control, electronic monitoring devices (EMDs) showed a 23% adherence improvement, mean difference (MD) of 23%, 95% CI 10.84 to 34.16, p=0.0002. Asthmatic children were 1.5 times more likely to be adherent using EMDs compared with non-EMD users (RR=1.5, 95% CI 1.19 to 1.9) (p<0.001). Mobile devices and text message reminders (MHealth) showed a 12% adherence improvement (MD 12%, 95% CI 6.22 to 18.03) (p<0.0001), alongside a small to medium improvement in asthma control (standardised mean difference (SMD) 0.31, 95% CI 0.17 to 0.44), small improvement in asthma-related quality of life (SMD 0.26) (p=0.007) and variable risk reduction in asthma exacerbations for digital health (risk ratio 0.53, 95% CI 0.32 to 0.91) (p=0.02) compared with EMDs, which showed insignificant differences (risk ratio 0.89, 95% CI 0.45 to 1.75) (p=0.72). Technologies combined yielded variable adherence effects, with an SMD for eHealth of 0.41, 95% CI 0.02 to 0.79, and MD for digital health was 14.66% higher than the control, 95% CI 7.74 to 21.57. Heterogeneity between studies was significant (eHealth I=98%, digital I=94%).

CONCLUSION

Electronic methods improved adherence to inhaled medications in asthma. EMDs appear to be the most effective technology, followed by mHealth. The adherence improvement was associated with a small clinical improvement. There was inconsistent overlapping of terminology describing electronic methods that require standardisation. Data on the cost-effectiveness of electronic devices and their utilisation in severe asthma are lacking and require further research.

PROSPERO REGISTRATION NUMBER

CRD42022303069.

摘要

目的

通过系统评价评估电子方法在监测单独使用或与长效β2-激动剂(LABA)联合使用的常规吸入皮质激素(ICS)的依从性方面的有效性,以及其对临床结果的影响。

设计

叙述性系统评价。

资料来源

截至 2022 年 7 月 10 日,通过 MEDLINE、EMBASE、Cochrane 系统评价数据库和 Web of Science 进行检索。

入选标准

我们纳入了比较电子方法与常规非电子监测干预或安慰剂在儿童和成人哮喘患者对单独使用 ICS 或与 LABA 联合使用的 ICS 药物依从率、哮喘控制和哮喘恶化方面效果的定性和定量结局的同行评审研究。

资料提取与综合

根据特定于审查目标的预定表格进行数据提取。使用 Cochrane 随机对照试验偏倚风险工具和系统评价偏倚风险工具评估偏倚风险。由于范围搜索的结果,无法进行荟萃分析;然而,进行了叙述性综述,以便根据哮喘吸入器依从率、哮喘控制和恶化的结果进行分组。

结果

纳入了 6 篇文章,共 98 项研究,发表于 1998 年至 2022 年,来自美国、加拿大和英国。与对照组相比,电子监测设备(EMD)显示依从性提高了 23%,平均差异(MD)为 23%,95%CI 为 10.84 至 34.16,p=0.0002。与非 EMD 用户相比,哮喘儿童使用 EMD 更有可能依从(RR=1.5,95%CI 1.19 至 1.9)(p<0.001)。移动设备和短信提醒(MHealth)显示依从性提高了 12%(MD 12%,95%CI 6.22 至 18.03)(p<0.0001),同时哮喘控制有较小到中等程度的改善(标准化均数差(SMD)0.31,95%CI 0.17 至 0.44),哮喘相关生活质量有较小程度的改善(SMD 0.26)(p=0.007),数字健康对哮喘恶化的风险降低(风险比 0.53,95%CI 0.32 至 0.91)(p=0.02),与 EMD 相比,差异无统计学意义(风险比 0.89,95%CI 0.45 至 1.75)(p=0.72)。联合使用技术产生了不同的依从性效果,电子健康的 SMD 为 0.41,95%CI 0.02 至 0.79,数字健康的 MD 比对照组高 14.66%,95%CI 为 7.74 至 21.57。研究之间的异质性显著(电子健康 I=98%,数字 I=94%)。

结论

电子方法改善了哮喘患者吸入药物的依从性。EMD 似乎是最有效的技术,其次是 MHealth。依从性的提高与临床改善相关。描述电子方法的术语不一致,需要标准化。缺乏关于电子设备的成本效益及其在严重哮喘中的应用的数据,需要进一步研究。

PROSPERO 注册号:CRD42022303069。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/879e/10432637/3393c7305919/bmjopen-2023-074127f01.jpg

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