Hogan Alice, Bonney Mary-Ann, Brien Jo-Anne, Karamy Rita, Aslani Parisa
Faculty of Pharmacy, Pharmacy and Bank Building A15, The University of Sydney, Broadway, NSW, 2006, Australia.
Int J Clin Pharm. 2015 Feb;37(1):86-93. doi: 10.1007/s11096-014-0043-6. Epub 2014 Nov 29.
Nebulised medicines contribute to the high treatment burden experienced by patients with cystic fibrosis (CF).
This study explored experiences of adult patients with CF when using nebulised medicines, factors impacting on their adherence to nebulised therapy and strategies they used to facilitate adherence.
Community setting, in Sydney, Australia.
Ten patients with CF were recruited through a CF patient organisation. Semi-structured face-to-face interviews were conducted, addressing the study objectives. Interviews were audio-recorded, transcribed verbatim and content analysed for anticipated and emergent themes.
Experiences with using nebulised medicines; and barriers and facilitators of adherence to nebulised medicines.
Participants' age ranged from 22 to 45 years, with half being male. Four broad themes (with more specific sub-themes) were identified from the interviews: experiences with using nebulised medicines (cleaning nebuliser, time taken to use nebuliser medicine, flexibility in use of nebuliser); feelings about using nebulised medicines (necessary/important, dislike, part of life); factors impacting non-adherence (time consuming therapy, side effects/effects of medicine, work/social demands, lack of perceived importance); factors and strategies facilitating adherence (perceived medicine importance, habit/routine, support, health benefits, technology/medicine dose form, timetabling).
Nebulised therapy for cystic fibrosis patients takes a substantial amount of time, with patients trying to alter their routine to incorporate nebulising into their daily lives. However there are still many factors that lead to low adherence, including work/social demands and travelling. Patients balance the necessity for nebulised therapy against the barriers, and engage in intentional non-adherence at times. Future strategies and resources should target and address specific factors identified by patients with CF as being important and impacting their adherence to nebulised medicines.
雾化药物增加了囊性纤维化(CF)患者的治疗负担。
本研究探讨成年CF患者使用雾化药物的体验、影响其坚持雾化治疗的因素以及他们用来促进坚持治疗的策略。
澳大利亚悉尼的社区环境。
通过一个CF患者组织招募了10名CF患者。进行了半结构化面对面访谈,以探讨研究目标。访谈进行了录音,逐字转录,并对预期和新出现的主题进行了内容分析。
使用雾化药物的体验;坚持雾化药物治疗的障碍和促进因素。
参与者年龄在22至45岁之间,一半为男性。从访谈中确定了四个广泛的主题(以及更具体的子主题):使用雾化药物的体验(清洁雾化器、使用雾化药物所需时间、使用雾化器的灵活性);对使用雾化药物的感受(必要/重要、不喜欢、生活的一部分);影响不坚持治疗的因素(治疗耗时、药物副作用/效应、工作/社会需求、缺乏重要性认知);促进坚持治疗的因素和策略(药物重要性认知、习惯/常规、支持、健康益处、技术/药物剂型、时间安排)。
CF患者的雾化治疗需要大量时间,患者试图改变日常生活习惯以将雾化纳入其中。然而,仍有许多因素导致坚持率低,包括工作/社会需求和旅行。患者在雾化治疗的必要性与障碍之间进行权衡,有时会故意不坚持治疗。未来的策略和资源应针对CF患者确定的重要且影响其坚持雾化药物治疗的具体因素。