Reduction in systemic glucocorticoid utilization among COPD patients with type 2 inflammation treated with biologics.

IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM
Truong-An A Ho, Stephen Dachert, Anugya Mittal, Gerard J Criner
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Abstract

Background: Systemic glucocorticoids are associated with significant side effects, however, are essential in the treatment of acute exacerbations of chronic obstructive pulmonary disease (COPD). Biologic therapies in COPD with type 2 (T2) inflammation have shown benefit in reducing exacerbations, but their impact on glucocorticoid utilization remains unclear. We aim to examine if use of biologics in COPD patients reduces glucocorticoid burden.

Methods: A retrospective review of the electronic medical record (2016-2023) was performed. Patients with COPD that were treated with biologics were included. Data collected included demographics, baseline comorbidities, eosinophil count, pulmonary function testing and dispense reports for glucocorticoids. The primary outcomes were a change in the number of glucocorticoid dispenses and total cumulative systemic glucocorticoid dosage, in the year prior and post initiation of therapy.

Results: 56 patients (mean age 71 ± 8.5) were included in the study. 55% had coronary artery disease, 25% had heart failure, 71% had hypertension, 14% had stroke and 30% had diabetes. Biologics significantly reduced annual glucocorticoid dispenses (3.38 ± 2.58 vs. 2.22 ± 2.33, mean reduction 1.16, 95% CI 0.45-1.87, p = 0.002) and cumulative dosage (1073 ± 831 mg vs. 659 ± 723 mg, mean reduction 413.2 mg, 95% CI 180.8-645.6, p = 0.001). There was no strong association between baseline eosinophil count and glucocorticoid utilization.

Conclusions: In this real-world cohort of COPD patients with T2 inflammation, the addition of biologic therapies was associated with a significant reduction in systemic glucocorticoid usage, both in terms of dispense frequency and overall total dosage of systemic glucocorticoids. This highlights the potential of biologics to reduce glucocorticoid-related adverse effects in COPD patients.

生物制剂治疗慢性阻塞性肺病2型炎症患者系统性糖皮质激素使用的降低
背景:全身糖皮质激素与显著的副作用相关,然而,在慢性阻塞性肺疾病(COPD)急性加重期的治疗中是必不可少的。慢性阻塞性肺病2型(T2)炎症的生物治疗已显示出减少加重的益处,但其对糖皮质激素使用的影响尚不清楚。我们的目的是研究慢性阻塞性肺病患者使用生物制剂是否能减轻糖皮质激素负担。方法:对2016-2023年电子病历进行回顾性分析。接受生物制剂治疗的COPD患者也被纳入其中。收集的数据包括人口统计学、基线合并症、嗜酸性粒细胞计数、肺功能测试和糖皮质激素分配报告。主要结果是在治疗开始前和开始后一年糖皮质激素分配数量和总累积全身糖皮质激素剂量的变化。结果:56例患者(平均年龄71±8.5岁)纳入研究。55%患有冠状动脉疾病,25%患有心力衰竭,71%患有高血压,14%患有中风,30%患有糖尿病。生物制剂显著减少糖皮质激素年用量(3.38±2.58 vs. 2.22±2.33,平均减少1.16,95% CI 0.45 ~ 1.87, p = 0.002)和累积剂量(1073±831 mg vs. 659±723 mg,平均减少413.2 mg, 95% CI 180.8 ~ 645.6, p = 0.001)。基线嗜酸性粒细胞计数和糖皮质激素使用之间没有很强的关联。结论:在这个真实世界的T2炎症COPD患者队列中,生物治疗的增加与全身糖皮质激素使用的显著减少相关,无论是在分配频率还是全身糖皮质激素的总剂量方面。这突出了生物制剂在COPD患者中减少糖皮质激素相关不良反应的潜力。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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