Nordon Clementine, Carstens Donna, Fagerås Malin, Müllerová Hana, Veeranki Phani S, Alves João André, Germack Hayley D, Barnes Timothy L, McCormack Meredith C
Respiratory Evidence Strategy, BioPharmaceuticals Medical, AstraZeneca, Cambridge, UK.
US Medical Evidence, Biopharmaceuticals, AstraZeneca, Wilmington, DE, USA.
Int J Chron Obstruct Pulmon Dis. 2025 Jun 11;20:1851-1864. doi: 10.2147/COPD.S513573. eCollection 2025.
Many people with chronic obstructive pulmonary disease (COPD) continue to experience frequent moderate/severe exacerbations despite treatment with inhaled triple therapy (TT). We evaluated the baseline characteristics and outcomes (exacerbation rate, mortality, and healthcare resource utilization [HCRU]) of this COPD population, overall and by smoking status.
A retrospective real-world cohort study of US patients was conducted using Optum's deidentified Market Clarity Data, an integrated claims and electronic health record database (study period: 2015-2019). Patients eligible for inclusion were aged ≥40 years, with a COPD diagnosis, continuous 12-month (baseline) period of treatment with TT, and record of ≥2 moderate or ≥1 severe exacerbation during baseline. Follow-up was either variable (from end of baseline to death, loss to follow-up, or end of 2019) or fixed (12 months). Baseline characteristics and treatment patterns, crude incidence rates (IRs) for exacerbations and mortality (per 100 person-years [PYs]; variable follow-up), and HCRU and costs (12-month follow-up) were summarized descriptively.
Of 4,920 patients in the TT cohort, mean (SD) age was 62.3 (9.7) years, 60.9% were female, and 68.0% were white; 46.5% of TT cohort patients with a history of smoking were current smokers. Hypertension (92.7%), ischemic heart disease (52.1%), and heart failure (40.1%) were the most prevalent cardiovascular comorbidities. Most patients received oral corticosteroids (89.6%) or antibiotics (92.8%) for exacerbation management during baseline. Add-on therapies included phosphodiesterase-4 inhibitors (10.4%) and leukotriene receptor antagonists (26.4%). During follow-up, IRs (95% CI) were 108.2 (104.7-111.8) per 100 PY for any moderate/severe exacerbation and 8.0 (7.4-8.6) per 100 PY for mortality. Exacerbation risk was similar by smoking status. During the 12-month follow-up, mean (SD) all-cause and COPD costs were $63,178 ($77,061) and $26,153 ($47,085), respectively.
There is high mortality and considerable HCRU and healthcare costs incurred by people with COPD experiencing frequent moderate/severe exacerbations while on TT. Optimization of COPD management and new therapies are needed to reduce disease burden in this population.
许多慢性阻塞性肺疾病(COPD)患者尽管接受了吸入三联疗法(TT)治疗,但仍频繁经历中度/重度急性加重。我们评估了这一COPD人群的基线特征和结局(急性加重率、死亡率和医疗资源利用[HCRU]),总体情况以及按吸烟状况分类的情况。
使用Optum的去识别化市场清晰度数据(一个综合的索赔和电子健康记录数据库)对美国患者进行了一项回顾性真实世界队列研究(研究期:2015 - 2019年)。符合纳入标准的患者年龄≥40岁,患有COPD诊断,接受TT连续治疗12个月(基线期),且在基线期间有≥2次中度或≥1次重度急性加重记录。随访时间为可变(从基线结束到死亡、失访或2019年底)或固定(12个月)。对基线特征和治疗模式、急性加重和死亡率的粗发病率(IRs)(每100人年[PYs];可变随访)以及HCRU和费用(12个月随访)进行描述性总结。
在TT队列的4920名患者中,平均(标准差)年龄为62.3(9.7)岁,60.9%为女性,68.0%为白人;TT队列中有吸烟史的患者中46.5%为当前吸烟者。高血压(92.7%)、缺血性心脏病(52.1%)和心力衰竭(40.1%)是最常见的心血管合并症。大多数患者在基线期间因急性加重管理接受了口服糖皮质激素(89.6%)或抗生素(92.8%)治疗。附加治疗包括磷酸二酯酶-4抑制剂(10.4%)和白三烯受体拮抗剂(26.4%)。在随访期间,任何中度/重度急性加重的IRs(95%CI)为每100 PY 108.2(104.7 - 111.8),死亡率为每100 PY 8.0(7.4 - 8.)。急性加重风险按吸烟状况相似。在12个月的随访期间,平均(标准差)全因和COPD费用分别为63,178美元(77,061美元)和26,153美元(47,085美元)。
接受TT治疗但仍频繁经历中度/重度急性加重的COPD患者死亡率高,HCRU和医疗费用可观。需要优化COPD管理和新疗法以减轻该人群的疾病负担。