Pulmonary Research Institute at Lung Clinic Grosshansdorf, Airway Research Center North, Member of the German Center of Lung Research, Grosshansdorf, Germany.
Respiratory Effectiveness Group, Ely, UK.
Respir Res. 2021 Jan 21;22(1):25. doi: 10.1186/s12931-021-01615-0.
Inhaled corticosteroids (ICS) are indicated for prevention of exacerbations in patients with COPD, but they are frequently overprescribed. ICS withdrawal has been recommended by international guidelines in order to prevent side effects in patients in whom ICS are not indicated.
Observational comparative effectiveness study aimed to evaluate the effect of ICS withdrawal versus continuation of triple therapy (TT) in COPD patients in primary care. Data were obtained from the Optimum Patient Care Research Database (OPCRD) in the UK.
A total of 1046 patients who withdrew ICS were matched 1:4 by time on TT to 4184 patients who continued with TT. Up to 76.1% of the total population had 0 or 1 exacerbation the previous year. After controlling for confounders, patients who discontinued ICS did not have an increased risk of moderate or severe exacerbations (adjusted HR: 1.04, 95% confidence interval (CI) 0.94-1.15; p = 0.441). However, rates of exacerbations managed in primary care (incidence rate ratio (IRR) 1.33, 95% CI 1.10-1.60; p = 0.003) or in hospital (IRR 1.72, 95% CI 1.03-2.86; p = 0.036) were higher in the cessation group. Unsuccessful ICS withdrawal was significantly and independently associated with more frequent courses of oral corticosteroids the previous year and with a blood eosinophil count ≥ 300 cells/μL.
In this primary care population of patients with COPD, composed mostly of infrequent exacerbators, discontinuation of ICS from TT was not associated with an increased risk of exacerbation; however, the subgroup of patients with more frequent courses of oral corticosteroids and high blood eosinophil counts should not be withdrawn from ICS. Trial registration European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (EUPAS30851).
吸入性皮质类固醇(ICS)适用于预防 COPD 患者的恶化,但它们经常被过度开具。国际指南建议停用 ICS,以预防不适用 ICS 的患者出现副作用。
这是一项观察性比较有效性研究,旨在评估 COPD 患者在初级保健中停用 ICS 与继续三联疗法(TT)的效果。数据来自英国 Optimum Patient Care Research Database(OPCRD)。
共有 1046 名停用 ICS 的患者按照 TT 时间进行了 1:4 匹配,共匹配到 4184 名继续使用 TT 的患者。在总人群中,多达 76.1%的人在过去一年中有 0 次或 1 次恶化。在控制了混杂因素后,停用 ICS 的患者发生中重度恶化的风险并未增加(调整后的 HR:1.04,95%置信区间(CI)0.94-1.15;p=0.441)。然而,在初级保健中管理的恶化发生率(发病率比(IRR)1.33,95%CI 1.10-1.60;p=0.003)或在医院(IRR 1.72,95%CI 1.03-2.86;p=0.036)更高。不成功的 ICS 停药与过去一年中更频繁的口服皮质类固醇疗程以及血液嗜酸性粒细胞计数≥300 细胞/μL 显著相关。
在这个由 COPD 患者组成的初级保健人群中,大多数是不频繁恶化者,从 TT 中停用 ICS 与恶化风险增加无关;然而,血液嗜酸性粒细胞计数较高且更频繁使用口服皮质类固醇的患者亚组不应停用 ICS。试验注册欧洲药物流行病学和药物警戒网络(EUPAS30851)。