BioPharmaceuticals Medical, Respiratory & Immunology, AstraZeneca, Gaithersburg, MD, USA.
Pneumology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, CIBER de Enfermedades Respiratorias (CIBERES), Barcelona, Spain.
Int J Chron Obstruct Pulmon Dis. 2022 Sep 9;17:2187-2200. doi: 10.2147/COPD.S378649. eCollection 2022.
Some patients with chronic obstructive pulmonary disease (COPD) experience frequent exacerbations despite maximal inhaled therapy ("triple therapy"), possibly leading to high health care resource utilization (HCRU).
Describe characteristics, future HCRU, and mortality of patients with COPD who experience frequent exacerbations despite triple therapy; characterize individuals who may be candidates for biologic therapies.
This descriptive observational study used primary care data of patients aged ≥40 years in the United Kingdom receiving maintenance therapy for COPD who had ≥1 year of data prior to index date and ≥1 year of follow-up data. We described these patients' clinical and demographic characteristics, including blood eosinophil counts (BEC), pattern of exacerbations, hospitalizations, and corticosteroid exposure, as well as future exacerbations, hospitalizations, and death.
Of 43,753 patients with maintenance-treated COPD, 6480 experienced exacerbations despite ≥3 months of triple therapy. Of these, 5669 had available BEC: 1287 (22.7%) had BEC ≥250 cells/µL and ≥3 exacerbations in the year prior to the index date; 471 (36.6%) received ≥4 acute courses of oral corticosteroids. Patients with a pattern of high disease burden continued to have high disease burden: 51.1% experienced ≥3 exacerbations and 2.6% experienced ≥3 hospitalizations. Patients who experienced exacerbations despite triple therapy had a significantly higher risk of COPD-related death than other maintenance-treated patients (5.8% vs 2.1%).
Nearly one-quarter of patients receiving triple therapy for COPD who experienced frequent exacerbations had elevated BEC and ≥3 exacerbations, suggesting a potential mechanism of persistent eosinophilic inflammation that could be a target for eosinophil-depleting biologic therapy.
一些患有慢性阻塞性肺疾病(COPD)的患者尽管接受了最大吸入疗法(“三联疗法”),仍会频繁发作,这可能导致高卫生保健资源利用(HCRU)。
描述尽管接受三联疗法仍频繁发作的 COPD 患者的特征、未来 HCRU 和死亡率;描述可能适合接受生物疗法的个体的特征。
本描述性观察研究使用了英国接受 COPD 维持治疗的年龄≥40 岁患者的初级保健数据,这些患者在指数日期前有≥1 年的数据,并且有≥1 年的随访数据。我们描述了这些患者的临床和人口统计学特征,包括血嗜酸性粒细胞计数(BEC)、发作模式、住院和皮质类固醇暴露情况,以及未来的发作、住院和死亡情况。
在 43753 名接受维持治疗的 COPD 患者中,有 6480 名患者尽管接受了≥3 个月的三联疗法仍发生了发作。其中,5669 名患者有可用的 BEC:1287 名(22.7%)在指数日期前 1 年内 BEC≥250 细胞/µL 和≥3 次发作;471 名(36.6%)接受了≥4 次急性口服皮质类固醇治疗。具有高疾病负担模式的患者继续具有高疾病负担:51.1%的患者经历了≥3 次发作,2.6%的患者经历了≥3 次住院治疗。尽管接受三联疗法治疗但仍发生发作的患者 COPD 相关死亡的风险明显高于其他接受维持治疗的患者(5.8%比 2.1%)。
近四分之一接受 COPD 三联疗法治疗且频繁发作的患者 BEC 升高且≥3 次发作,提示持续嗜酸性粒细胞炎症的潜在机制可能是嗜酸性粒细胞耗竭生物疗法的靶点。