他汀类药物预处理对无症状患者颈动脉支架置入并发症的影响:观察性研究。
Impact of statin pretreatment on the complications of carotid stenting in asymptomatic patients: observational study.
机构信息
Department of Neurology, Keimyung University Dongsan Hospital, Keimyung University School of Medicine, 1095 Dalgubeol-daero, Dalseo-gu, Daegu, 42601, South Korea.
Department of Neurology, Seoul National University Bundang Hospital, Seoul National University School of Medicine, Seongnam, South Korea.
出版信息
BMC Neurol. 2021 Feb 15;21(1):75. doi: 10.1186/s12883-021-02104-z.
BACKGROUND
Carotid stenosis is a known risk factor for ischemic stroke, and carotid artery stenting is an effective preventive procedure. However, the stroke risk reduction for asymptomatic patients is small. Therefore, it is important to reduce the risk of complications, particularly in asymptomatic carotid stenosis. Statins are known to reduce the overall risk of periprocedural complications, although there is a lack of data focusing on asymptomatic patients. We aimed to investigate whether different doses of statin pretreatment can reduce periprocedural complications of carotid artery stenting (CAS) in patients with asymptomatic carotid artery stenosis.
METHODS
Between July 2003 and June 2013, 276 consecutive patients received CAS for asymptomatic carotid stenosis. Periprocedural complications included the outcome of stroke, myocardial infarction, or death within 30 days of CAS. Statin pretreatment was categorized as no-statin (n = 87, 31.5%), standard-dose (< 40 mg, n = 139, 50.4%), and high-dose statin (≥40 mg, n = 50, 18.1%) according to the atorvastatin equivalent dose. The Cochran-Armitage (CA) trend test was performed to investigate the association of periprocedural complications with statin dose.
RESULTS
The overall periprocedural complication rate was 3.3%. There was no significant difference in the risk of periprocedural complications between the three groups (no statin: n = 3 [3.4%]; standard-dose: n = 4 [2.9%]; high-dose n = 2 [4.0%] p = 0.923). The CA trend test did not demonstrate a trend in the proportion of periprocedural complications across increasing statin equivalent doses (p = 0.919).
CONCLUSIONS
Statin pretreatment before CAS showed neither absolute nor dose-dependent effects against periprocedural complications in asymptomatic patients undergoing CAS.
背景
颈动脉狭窄是缺血性中风的已知危险因素,颈动脉支架置入术是一种有效的预防措施。然而,无症状患者的中风风险降低幅度较小。因此,重要的是要降低并发症的风险,特别是在无症状颈动脉狭窄患者中。他汀类药物已被证明可以降低围手术期并发症的总体风险,尽管缺乏专门针对无症状患者的相关数据。我们旨在研究不同剂量的他汀类药物预处理是否可以降低无症状颈动脉狭窄患者颈动脉支架置入术(CAS)围手术期的并发症。
方法
2003 年 7 月至 2013 年 6 月期间,276 例连续接受 CAS 治疗的无症状颈动脉狭窄患者纳入本研究。围手术期并发症包括 CAS 术后 30 天内的中风、心肌梗死或死亡结局。根据阿托伐他汀等效剂量,他汀类药物预处理分为无他汀类药物(n=87,31.5%)、标准剂量(<40mg,n=139,50.4%)和高剂量他汀类药物(≥40mg,n=50,18.1%)。采用 Cochran-Armitage(CA)趋势检验来研究围手术期并发症与他汀类药物剂量之间的关系。
结果
总的围手术期并发症发生率为 3.3%。三组之间围手术期并发症的风险无显著差异(无他汀类药物组:n=3[3.4%];标准剂量组:n=4[2.9%];高剂量组:n=2[4.0%],p=0.923)。CA 趋势检验也未显示随着他汀类药物等效剂量的增加,围手术期并发症的比例呈趋势性变化(p=0.919)。
结论
在接受 CAS 的无症状患者中,CAS 术前他汀类药物预处理既没有绝对效果,也没有剂量依赖性效果来预防围手术期并发症。
相似文献
J Vasc Surg. 2018-6-15
Eur J Vasc Endovasc Surg. 2014-9-16
引用本文的文献
Ther Adv Neurol Disord. 2023-5-10
本文引用的文献
J Am Heart Assoc. 2018-8-21
J Endovasc Ther. 2018-8-13
N Engl J Med. 2016-2-17
Eur J Vasc Endovasc Surg. 2014-9-16