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支气管扩张剂、类固醇、抗心律失常药物、抗抑郁药和苯二氮䓬类药物与以支气管扩张和哮喘为主的患者的心脏病和缺血性中风之间的关系。

Relationships Between Bronchodilators, Steroids, Antiarrhythmic Drugs, Antidepressants, and Benzodiazepines and Heart Disease and Ischemic Stroke in Patients With Predominant Bronchiectasis and Asthma.

作者信息

Yeh Jun-Jun, Lai Mei-Chu, Yang Yu-Cih, Hsu Chung-Y, Kao Chia-Hung

机构信息

Department of Family Medicine, Chest Medicine, Geriatric Medicine and Medical Research, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi, Taiwan.

College of Medicine, China Medical University, Taichung, Taiwan.

出版信息

Front Cardiovasc Med. 2022 Feb 17;9:797623. doi: 10.3389/fcvm.2022.797623. eCollection 2022.

Abstract

OBJECTIVE

We investigated the effects of medication on heart disease and ischemic stroke (HDS) risk in patients with predominant bronchiectasis-asthma combination (BCAS).

METHODS

BCAS and non-BCAS cohorts ( = 588 and 1,118, respectively) were retrospectively enrolled. The cumulative incidence of HDS was analyzed using Cox proportional regression; propensity scores were estimated using non-parsimonious multivariable logistic regression. Adjusted hazard ratios (aHRs) and 95% confidence intervals (CIs) for HDS were calculated, adjusting for sex, age, comorbidities, and medication {long- and short-acting β2 agonists and muscarinic antagonists (LABAs/SABAs and LAMAs/SAMAs), steroids [inhaled corticosteroid steroids (ICSs), oral steroids (OSs)], antiarrhythmics, antidepressants (fluoxetine), benzodiazepines (alprazolam, fludiazepam), statins and antihypertensive drugs (diuretics, cardioselective beta blockers, calcium channel blockers (CCBs) and angiotensin converting enzyme inhibitors (ACEi), angiotensin II blockers)}.

RESULTS

Compared with the non-BCAS cohort, the BCAS cohort taking LABAs, SABAs, SAMAs, ICSs, OSs, antiarrhythmics, and alprazolam had an elevated HDS risk [aHRs (95% CIs): 2.36 (1.25-4.33), 2.65 (1.87-3.75), 2.66 (1.74-4.05), 2.53 (1.61-3.99), 1.76 (1.43-2.18), 9.88 (3.27-30.5), and 1.73 (1.15-2.58), respectively except fludiazepam 1.33 (0.73-2.40)]. The aHRs (95% CIs) for LABAs ≤ 30 days, DDDs <415, ICSs ≤ 30 days were 1.10 (0.38-3.15), 2.95 (0.22-38.8), 1.45 (0.76-2.77). The aHRs (95% CIs) for current and recent alprazolam were 1.78 (1.09-2.93) and 777.8 (1.34-451590.0); for current and past fludiazepam were 1.39 (0.75-2.59) and 1.29 (0.42-4.01) and for past alprazolam was 1.57 (0.55-4.46); respectively. The aHRs (95% CIs) for alprazolam >30 DDDs, fludiazepam >20 DDDs, ICSs ≦415 DDDs, and OSs DDDs ≦15 were 1.60 (0.78-3.29), 2.43 (0.90-6.55), 5.02 (1.76-14.3), and 2.28 (1.43-3.62), respectively.

CONCLUSION

The bronchodilators, steroids, and antiarrhythmics were associated with higher risk of HDS, even low dose use of steroids. However, the current use of LABAs/ICSs were not associated with HDS. Benzodiazepines were relatively safe, except for current or recent alprazolam use. Notably, taking confounders into account is crucial in observational studies.

摘要

目的

我们研究了药物治疗对以支气管扩张 - 哮喘为主的组合(BCAS)患者心脏病和缺血性中风(HDS)风险的影响。

方法

回顾性纳入BCAS队列和非BCAS队列(分别为588例和1118例)。使用Cox比例回归分析HDS的累积发病率;使用非简约多变量逻辑回归估计倾向得分。计算HDS的调整后风险比(aHRs)和95%置信区间(CIs),并对性别、年龄、合并症和药物进行调整{长效和短效β2激动剂及毒蕈碱拮抗剂(LABAs/SABAs和LAMAs/SAMAs)、类固醇[吸入性糖皮质激素(ICSs)、口服类固醇(OSs)]、抗心律失常药、抗抑郁药(氟西汀)、苯二氮䓬类药物(阿普唑仑、氟地西泮)、他汀类药物和抗高血压药物(利尿剂、心脏选择性β受体阻滞剂、钙通道阻滞剂(CCBs)和血管紧张素转换酶抑制剂(ACEi)、血管紧张素II受体阻滞剂)}。

结果

与非BCAS队列相比,服用LABAs、SABAs、SAMAs、ICSs、OSs、抗心律失常药和阿普唑仑的BCAS队列HDS风险升高[aHRs(95% CIs):分别为2.36(1.25 - 4.33)、2.65(1.87 - 3.75)、2.66(1.74 - 4.05)、2.53(1.61 - 3.99)、1.76(1.43 - 2.18)、9.88(3.27 - 30.5)和1.73(1.15 - 2.58),氟地西泮除外,为1.33(0.73 - 2.40)]。LABAs使用≤30天、用药频度(DDDs)<415、ICSs使用≤30天的aHRs(95% CIs)分别为1.10(0.38 - 3.15)、2.95(0.22 - 38.8)、1.45(0.76 - 2.77)。当前和近期使用阿普唑仑的aHRs(95% CIs)分别为1.78(1.09 - 2.93)和777.8(1.34 - 451590.0);当前和过去使用氟地西泮的分别为1.39(0.75 - 2.59)和1.29(0.42 - 4.01),过去使用阿普唑仑的为1.57(0.55 - 4.46);阿普唑仑>30 DDDs、氟地西泮>20 DDDs、ICSs≤415 DDDs和OSs DDDs≤15的aHRs(95% CIs)分别为1.60(0.78 - 3.29)、2.43(0.90 - 6.55)、5.02(1.76 - 14.3)和2.28(1.43 - 3.62)。

结论

支气管扩张剂、类固醇和抗心律失常药与较高的HDS风险相关,即使是低剂量使用类固醇。然而,当前使用LABAs/ICSs与HDS无关。苯二氮䓬类药物相对安全,但当前或近期使用阿普唑仑除外。值得注意的是,在观察性研究中考虑混杂因素至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e31/8893278/c84cccb61860/fcvm-09-797623-g0001.jpg

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