Alfred Hospital, Melbourne, VIC.
Centre for Healthy Lungs, University of Newcastle, Newcastle, NSW.
Med J Aust. 2020 Oct;213(7):316-320. doi: 10.5694/mja2.50758. Epub 2020 Sep 9.
To estimate the level of dispensing of oral corticosteroids (OCS) for managing asthma in Australia, with a particular focus on the cumulative dispensing of doses associated with long term toxicity (≥ 1000 mg prednisolone-equivalent).
Retrospective cohort study; analysis of 10% random sample of Pharmaceutical Benefits Scheme (PBS) dispensing data.
PARTICIPANTS, SETTING: People aged 12 years or more treated for asthma during 2014-2018, according to dispensing of controller inhaled corticosteroids (ICS).
Number of people dispensed OCS for managing asthma during 2014-2018; proportion who were cumulatively dispensed at least 1000 mg prednisolone-equivalent. The secondary outcome was the number of people dispensed at least 1000 mg prednisolone-equivalent during 2018, stratified by inhaler controller dose and use.
124 011 people had been dispensed at least two prescriptions of ICS during 2014-2018 and met the study definition for asthma, of whom 64 112 (51.7%) had also been dispensed OCS, including 34 580 (27.9% of the asthma group) cumulatively dispensed 1000 mg prednisolone-equivalent or more. Of 138 073 people dispensed OCS at this level, 68 077 (49%) were patients with airway diseases. Dispensing of diabetes and osteoporosis medications was more common for people cumulatively dispensed 1000 mg prednisolone-equivalent or more. During 2018, 4633 people with asthma using high dose ICS controllers were dispensed 1000 mg prednisolone-equivalent or more, for 2316 of whom (50%) controller use was inadequate.
Cumulative exposure to OCS in Australia reaches levels associated with toxicity in one-quarter of patients with asthma using ICS. Cumulative dispensing of potentially toxic OCS amounts often accompanies inadequate inhaler controller dispensing. Better approaches are needed to improve adherence to controller therapy, improve outcomes for people with asthma, and to minimise the use and toxicity of OCS.
评估澳大利亚管理哮喘的口服皮质类固醇(OCS)的配药水平,特别关注与长期毒性相关的累积配药量(≥1000mg 泼尼松龙当量)。
回顾性队列研究;分析药品福利计划(PBS)配药数据的 10%随机样本。
参与者、设置:根据控制器吸入皮质类固醇(ICS)的配药情况,2014-2018 年期间治疗哮喘的年龄在 12 岁或以上的人群。
2014-2018 年期间因哮喘管理而配给 OCS 的人数;累积配给至少 1000mg 泼尼松龙当量的比例。次要结局是 2018 年至少配给 1000mg 泼尼松龙当量的人数,按吸入器控制器剂量和使用情况分层。
在 2014-2018 年期间,有 124011 人至少配给了两次 ICS 处方,并符合哮喘研究定义,其中 64112 人(哮喘组的 51.7%)也配给了 OCS,包括 34580 人(27.9%)累积配给了 1000mg 泼尼松龙当量或以上。在配给这一水平 OCS 的 138073 人中,68077 人(49%)为气道疾病患者。累积配给 1000mg 泼尼松龙当量或以上的患者更常配给糖尿病和骨质疏松症药物。在 2018 年,使用高剂量 ICS 控制器的 4633 名哮喘患者配给了 1000mg 泼尼松龙当量或以上,其中 2316 人(50%)控制器使用不足。
澳大利亚 OCS 的累积暴露水平达到了使用 ICS 的哮喘患者中与毒性相关的水平的四分之一。潜在毒性 OCS 累积配给量通常伴随着吸入器控制器配给不足。需要更好的方法来提高对控制器治疗的依从性,改善哮喘患者的结局,并尽量减少 OCS 的使用和毒性。