Cardiovascular Medication Use and Risk of Acute Exacerbation in Patients With Asthma-COPD Overlap (CVACO Study)

被引:3
作者
Su, Vincent Yi-Fong [1 ,2 ,3 ]
Ko, Szu-Wen [4 ,5 ]
Chang, Yuh-Lih [4 ,5 ,6 ]
Chou, Yueh-Ching [4 ,5 ,6 ,7 ]
Lee, Hsin-Chen [5 ]
Yang, Kuang-Yao [2 ,3 ,8 ,9 ]
Chou, Kun-Ta [2 ,3 ,10 ]
Hsu, Chia-Chen [4 ,6 ]
机构
[1] Taipei City Hosp, Dept Internal Med, Taipei, Taiwan
[2] Taipei Vet Gen Hosp, Dept Chest Med, Taipei, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Fac Med, Sch Med, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Pharm, 201,Sec 2,Shi Pai Rd, Taipei 112, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Coll Med, Inst Pharmacol, Taipei, Taiwan
[6] Natl Yang Ming Chiao Tung Univ, Coll Pharmaceut Sci, Dept Pharm, Taipei, Taiwan
[7] Taipei Med Univ, Sch Pharm, Taipei, Taiwan
[8] Natl Yang Ming Chiao Tung Univ, Sch Med, Inst Emergency & Crit Care Med, Taipei, Taiwan
[9] Natl Yang Ming Chiao Tung Univ, Canc Progress Res Ctr, Taipei, Taiwan
[10] Taipei Vet Gen Hosp, Ctr Sleep Med, Taipei, Taiwan
关键词
Asthma; chronic obstructive pulmonary disease; beta-adrenergic blockers; angiotensin converting enzyme inhibitors; angiotensin II receptor blockers; calcium channel blockers; CHRONIC OBSTRUCTIVE PULMONARY; CARDIOSELECTIVE BETA-BLOCKERS; DISEASE; COUGH; INHIBITORS; CHANNELS;
D O I
10.4168/aair.2022.14.3.314
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: Current clinical guidelines are unclear regarding the association of cardiovascular medication with the risk of acute exacerbation (AE) in patients with asthma-chronic obstructive pulmonary disease (COPD) overlap (ACO). Methods: We conducted a retrospective cohort study by interrogating the claims database of Taipei Veterans General Hospital. Patients with coexistent fixed airflow limitation and asthma were enrolled as an ACO cohort between 2009 and 2017. Exposure to cardiovascular medications, including angiotensin converting enzyme inhibitors (ACEIs), angiotensin II receptor blockers (ARBs), non-selective beta-blockers, cardioselective beta-blockers, dihydropyridine (DHP) calcium channel blockers (CCBs), and non-DHP CCBs, in 3-month period each served as time-dependent covariates. Patients receiving a cardiovascular medication >= 28 cumulative daily doses were defined as respective cardiovascular medication users. Patients were followed up until December 31, 2018. The primary endpoint was severe AE, defined as hospitalization or emergency department visit for either asthma, COPD, or respiratory failure. The secondary outcome was moderate AE. Results: The final study cohort consisted of 582 ACO subjects, with a mean follow-up period of 2.98 years. After adjustment, ARB (hazard ratio [HR], 0.64, 95% confidence interval [CI], 0.44-0.93, P = 0.019), cardioselective beta-blocker (HR, 0.29, 95% CI, 0.11-0.72, P = 0.008) and DHP CCB (HR, 0.66, 95% CI, 0.45-0.97, P = 0.035) therapies were associated with lower risks of severe AE. ARB (HR, 0.42, 95% CI, 0.30-0.62, P < 0.001) and DHP CCB (HR, 0.55, 95% CI, 0.38-0.80, P = 0.002) therapies were associated with lower risks of moderate AE.Cardioselective beta-blockers, ARBs, and DHP CCBs were associated with lower risks of severe AE in frequent exacerbators. ACEI, non-selective beta-blocker, or non-DHP CCB use did not change the risk of severe AE. Conclusions: ARB, cardioselective beta-blocker, and DHP CCB therapies may lower the risk of AE in patients with ACO.
引用
收藏
页码:314 / 327
页数:14
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