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评估社区药剂师与肺病专家合作,在真实数据中使用吸入器设备的情况,包括患者的满意度和治疗依从性。

Evaluation of real-life data on the use of inhaler devices, including satisfaction and adherence to treatment, by community pharmacists in partnership with pulmonary disease specialists.

机构信息

Cerrahpaşa Faculty of Medicine, Department of Pulmonary Diseases, Istanbul University-Cerrahpaşa, Istanbul, Turkey.

Cerrahpaşa Faculty of Medicine, Department of Public Health, Istanbul University-Cerrahpaşa, Istanbul, Turkey.

出版信息

J Asthma. 2023 Jul;60(7):1326-1335. doi: 10.1080/02770903.2022.2144355. Epub 2022 Dec 1.

Abstract

OBJECTIVE

The use of inhaler device (UID) and the satisfaction and adherence of patients to treatment were evaluated by Istanbul city community pharmacists to obtain real-life data from patients with asthma or chronic obstructive pulmonary disease (COPD).

METHODS

Pharmacists educated by pulmonary disease specialists asked patients who combined medications with inhaler devices to fill out a questionnaire prepared by the specialists. Each patient's UID was checked, and their errors were corrected by showing them the already prepared standard video of their inhaler device. Afterward, the UID was repeated and rechecked. The visual analog scale (VAS), feeling of satisfaction with the inhaler (FSI-10) questionnaire, and the Morisky Green Levine (MGL) scale were used for symptom control, satisfaction, and adherence, respectively. Then, we compared the results of three different types of inhalers: metered dose inhalers (MDI), dry powder inhalers (DPI), and dry powder inhalation capsules (DPI Caps).

RESULTS

Twenty-seven (19.3%) patients used MDI, 42 (30%) used DPI caps, and 71 (50.7%) used DPI. UID before training was better in patients with DPI than in those with MDI and DPI Cap ( < 0.001). After training, the UID increased in all three groups ( < 0.001). The VAS scores were high in the DPI Caps group than the other groups ( < 0.001). The FSI-10 score was not significantly different among the groups ( > 0.05). Full-adherence was observed in 36.8% of the MDI group, 39.1% of the DPI Caps group, and 21.7% of the DPI groups ( > 0.05).

CONCLUSION

The partnership between community pharmacists and pulmonary disease specialists improved patients' UID.

摘要

目的

伊斯坦布尔市社区药剂师通过评估吸入器设备(UID)的使用情况以及患者对治疗的满意度和依从性,从哮喘或慢性阻塞性肺疾病(COPD)患者中获得真实数据。

方法

肺病专家培训的药剂师要求同时使用药物和吸入器设备的患者填写肺病专家准备的问卷。检查每位患者的 UID,并通过展示已经准备好的他们吸入器设备标准视频来纠正他们的错误。之后,重复并再次检查 UID。视觉模拟量表(VAS)、对吸入器的满意度(FSI-10)问卷和 Morisky Green Levine(MGL)量表分别用于症状控制、满意度和依从性。然后,我们比较了三种不同类型的吸入器的结果:计量吸入器(MDI)、干粉吸入器(DPI)和干粉吸入胶囊(DPI 胶囊)。

结果

27 名(19.3%)患者使用 MDI,42 名(30%)使用 DPI 胶囊,71 名(50.7%)使用 DPI。在培训前,DPI 患者的 UID 优于 MDI 和 DPI 帽组(<0.001)。培训后,所有三组的 UID 均增加(<0.001)。DPI 胶囊组的 VAS 评分高于其他组(<0.001)。各组间 FSI-10 评分无显著差异(>0.05)。MDI 组的完全依从率为 36.8%,DPI 胶囊组为 39.1%,DPI 组为 21.7%(>0.05)。

结论

社区药剂师与肺病专家的合作提高了患者的 UID。

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