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Device errors in asthma and COPD: systematic literature review and meta-analysis

机译:哮喘和COPD的设备错误:系统的文献综述和荟萃分析

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摘要

Inhaler device errors are common and may impact the effectiveness of the delivered drug. There is a paucity of up-to-date systematic reviews (SRs) or meta-analyses (MAs) of device errors in asthma and chronic obstructive pulmonary disease (COPD) patients. This SR and MA provides an estimate of overall error rates (both critical and non-critical) by device type and evaluates factors associated with inhaler misuse. The following databases from inception to July 23, 2014 (Embase®, MEDLINE®, MEDLINE® In-Process and CENTRAL) were searched, using predefined search terms. Studies in adult males and females with asthma or COPD, reporting at least one overall or critical error, using metered dose inhalers and dry powder inhalers were included. Random-effect MAs were performed to estimate device error rates and to compare pairs of devices. Overall and critical error rates were high across all devices, ranging from 50-100% and 14-92%, respectively. However, between-study heterogeneity was also generally >90% (I-squared statistic), indicating large variability between studies. A trend towards higher error rates with assessments comprising a larger number of steps was observed; however no consistent pattern was identified. This SR and MA highlights the relatively limited body of evidence assessing device errors and the lack of standardised checklists. There is currently insufficient evidence to determine differences in error rates between different inhaler devices and their impact on clinical outcomes. A key step in improving our knowledge on this topic would be the development of standardised checklists for each device. CHRONIC LUNG DISEASES CALL TO STANDARDISE RESEARCH INTO INHALER DEVICE ERRORS: Researchers should adopt a standardised approach to investigate the incorrect use of inhalers and its associated clinical implications. Henry Chrystyn at Plymouth University, together with scientists across the UK and the Netherlands, conducted a review of research related to inhaled medication errors made by patients with asthma or chronic obstructive pulmonary disease. It is widely acknowledged that many patients with lung conditions don't use their inhaler devices correctly, which affects drug effectiveness and disease control. While Chrystyn's team found high critical error rates reported across all devices, their meta-analysis and systematic review highlighted significant gaps in knowledge regarding different inhalers and associated error rates, and how these affect clinical outcomes. The researchers call for in-depth studies into device use, alongside standardised checklists and definitions for such studies to use to ensure consistency.
机译:吸入器设备错误很常见,可能会影响所输送药物的有效性。哮喘和慢性阻塞性肺疾病(COPD)患者中缺乏针对设备错误的最新系统评价(SR)或荟萃分析(MAs)。该SR和MA提供了按设备类型估算的总体错误率(严重和非严重),并评估了与吸入器滥用相关的因素。使用预定义的搜索词搜索了从开始到2014年7月23日的以下数据库(Embase®,MEDLINE®,MEDLINE®In-Process和CENTRAL)。纳入了使用计量吸入器和干粉吸入器对患有哮喘或COPD的成年男性和女性进行的研究,报告了至少一项总体或严重误差。执行随机效应MA来估计设备错误率并比较设备对。所有设备的总体和严重错误率很高,分别为50-100%和14-92%。但是,研究之间的异质性通常也> 90%(I平方统计),表明研究之间的差异很大。观察到错误率趋于更高的趋势,评估包括更多的步骤;但是,没有发现一致的模式。此SR和MA强调了评估设备错误的证据相对有限,并且缺乏标准化的检查清单。当前尚无足够的证据来确定不同吸入器设备之间的错误率差异及其对临床结果的影响。改善我们对此主题知识的关键一步是为每个设备开发标准化清单。慢性肺病会导致吸入器设备错误的标准化研究:研究人员应采用标准化方法来调查吸入器的不正确使用及其相关的临床意义。普利茅斯大学的亨利·克莱斯汀(Henry Chrystyn)与英国和荷兰的科学家一起,对与哮喘或慢性阻塞性肺病患者吸入药物错误有关的研究进行了回顾。众所周知,许多患有肺部疾病的患者未正确使用其吸入器,这会影响药物疗效和疾病控制。尽管Chrystyn的团队发现所有设备报告的严重错误率很高,但他们的荟萃分析和系统的评估突出了有关不同吸入器和相关错误率以及这些错误如何影响临床结果的知识方面的重大空白。研究人员呼吁对设备的使用进行深入研究,并提供标准化的检查表和定义,以确保一致性。

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