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严重哮喘生物制剂和热塑疗法时代的不依从性。

Nonadherence in the era of severe asthma biologics and thermoplasty.

机构信息

Allergy, Asthma and Clinical Immunology, The Alfred Hospital, Melbourne, Australia.

School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia.

出版信息

Eur Respir J. 2018 Apr 4;51(4). doi: 10.1183/13993003.01836-2017. Print 2018 Apr.

Abstract

Nonadherence to inhaled preventers impairs asthma control. Electronic monitoring devices (EMDs) can objectively measure adherence. Their use has not been reported in difficult asthma patients potentially suitable for novel therapies, biologics and bronchial thermoplasty.Consecutive patients with difficult asthma were assessed for eligibility for novel therapies. Medication adherence, defined as taking >75% of prescribed doses, was assessed by EMD and compared with standardised clinician assessment over an 8-week period.Among 69 difficult asthma patients, adherence could not be analysed in 13, due to device incompatibility or malfunction. Nonadherence was confirmed in 20 out of 45 (44.4%) patients. Clinical assessment of nonadherence was insensitive (physician 15%, nurse 28%). Serum eosinophils were higher in nonadherent patients. Including 11 patients with possible nonadherence (device refused or not returned) increased the nonadherence rate to 31 out of 56 (55%) patients. Severe asthma criteria were fulfilled by 59 out of 69 patients. 47 were eligible for novel therapies, with confirmed nonadherence in 16 out of 32 (50%) patients with EMD data; including seven patients with possible nonadherence increased the nonadherence rate to 23 out of 39 (59%).At least half the patients eligible for novel therapies were nonadherent to preventers. Nonadherence was often undetectable by clinical assessments. Preventer adherence must be confirmed objectively before employing novel severe asthma therapies.

摘要

吸入性预防药物的不依从会损害哮喘控制。电子监测设备(EMD)可以客观地测量依从性。它们在潜在适合新型疗法、生物制剂和支气管热成形术的难治性哮喘患者中尚未得到报道。

连续评估难治性哮喘患者是否适合新型疗法。通过 EMD 评估药物依从性,定义为服用> 75%规定剂量,并与 8 周期间标准化临床医生评估进行比较。

在 69 例难治性哮喘患者中,由于设备不兼容或故障,无法对 13 例患者进行分析。在 45 例(44.4%)患者中证实存在不依从性。临床评估的不依从性不敏感(医生 15%,护士 28%)。不依从的患者血清嗜酸性粒细胞水平更高。包括 11 例可能不依从的患者(设备拒绝或未归还),使不依从率从 56 例中的 31 例(55%)增加到 56 例中的 56 例(31 例)。

69 例患者中有 59 例符合严重哮喘标准。47 例患者有资格接受新型疗法,其中 32 例(50%)患者的 EMD 数据证实存在不依从,包括 7 例可能不依从的患者,使不依从率从 39 例增加到 39 例(59%)。

至少有一半有资格接受新型疗法的患者对预防药物不依从。临床评估往往无法检测到不依从。在使用新型严重哮喘疗法之前,必须客观地确认预防药物的依从性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2573/5884695/0304090a4849/ERJ-01836-2017.01.jpg

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