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Device use errors with soft mist inhalers: A global systematic literature review and meta-analysis

机译:设备使用软雾吸入器的错误:全球系统文献综述和META分析

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Inhaled bronchodilators are the cornerstone of treatment for chronic obstructive pulmonary disease (COPD). Soft mist inhalers (SMIs) are devices that deliver bronchodilators. Although correct device use is paramount to successful medication delivery, patient errors are common. This global systematic literature review and meta-analysis examined device use errors with SMIs among patients with obstructive lung diseases. PubMed, EMBASE, PsycINFO, Cochrane, and Google Scholar were searched to identify studies published between 2010 and 2019 that met the following inclusion criteria: (a) English language; (b) a diagnosis of COPD, bronchitis, or emphysema; and (c) reported device use errors among adults receiving long-acting bronchodilator treatment with Respimat? SMI (i.e. Spiriva?, Stiolto?, Spiolto?, and Striverdi?). Descriptive statistics examined sociodemographics, clinical characteristics, and device use errors. Meta-analysis techniques were employed with random-effects models to generate pooled mean effect sizes and 95% confidence intervals (CIs) for overall and step-by-step errors. The I sup2/sup statistic measured heterogeneity. Twelve studies (n = 1288 patients) were included in this meta-analysis. Eighty-eight percent of patients had COPD, and most had moderate/very severe airflow limitation (Global Initiative for Chronic Obstructive Lung Disease spirometric stages II to IV). Aggregate results revealed that 58.9% (95% CI: 42.4–75.5; I sup2/sup = 92.8%) of patients made ≥1 device use errors. Among 11 studies with step-by-step data, the most common errors were failure to (1) exhale completely and away from the device (47.8% (95% CI: 33.6–62.0)); (2) hold breath for up to 10 seconds (30.6% (95% CI: 17.5–43.7)); (3) take a slow, deep breath while pressing the dose release button (27.9% (95% CI: 14.5–41.2)); (4) hold the inhaler upright (22.6% (95% CI: 6.2–39.0)); and (5) turn the base toward the arrows until it clicked (17.6% (95% CI: 3.0–32.2)). Device use errors occurred in about 6 of 10 patients who used SMIs. An individualized approach to inhalation device selection and ongoing training and monitoring of device use are important in optimizing bronchodilator treatment.
机译:吸入支气管扩张剂是慢性阻塞性肺病(COPD)治疗的基石。软雾吸入器(SMIS)是提供支气管扩张剂的装置。虽然正确的设备使用对于成功的药物交付至关重要,但患者误差是常见的。这种全球系统文献综述和META分析检查了阻塞性肺病患者中的SMIS误差。搜索PUBMED,EMBASE,PSYCINFO,COCHRANE和GELOW SECRER,识别2010年至2019年期间发布的研究,符合以下纳入标准:(a)英语; (b)COPD,支气管炎或肺气肿的诊断; (c)报告的设备在成人中使用患有妊娠期支气管扩张剂治疗的成人误差? smi(即spiriva?,stiolto?,spiolto?,striverdi?)。描述性统计数据检查了社会主干,临床特征和设备使用错误。使用随机效应模型使用元分析技术,以产生总体和逐步误差的汇总平均效应大小和95%置信区间(CIS)。 I 2 统计测量异质性。该荟萃分析中包括12项研究(n = 1288名患者)。八十八百名患者患有COPD,大多数具有中等/非常严重的气流限制(全球慢性阻塞性肺病血液计量阶段II至IV)。总结果表明,58.9%(95%CI:42.4-75.5; I 2 = 92.8%)患者≥1装置使用误差。在11项研究中,逐步数据的研究中,最常见的误差失败(1)完全呼气并远离设备(47.8%(95%CI:33.6-62.0)); (2)呼吸长达10秒(30.6%(95%CI:17.5-43.7)); (3)按下剂量释放按钮时缓慢,深呼吸(27.9%(95%CI:14.5-41.2)); (4)持有吸入器直立(22.6%(95%CI:6.2-39.0)); (5)将底座转向箭头直至其点击(17.6%(95%CI:3.0-32.2))。设备使用错误发生在10名使用SMIS的10名患者中发生。在优化支气管扩张剂处理方面,一种个性化的吸入设备选择和持续培训和监测的方法。

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