蛋白转化酶枯草菌素/kexin 9型抑制剂启动后他汀类药物停药与随后的动脉粥样硬化性心血管疾病事件的关系

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Samuel K Peasah, Tiffany Lee, Duy Do, Yan Huang, Angela Inneh, Urvashi Patel, Aryan N Aiyer, Chester B Good
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引用次数: 0

摘要

背景:临床指南推荐在动脉粥样硬化性心血管疾病(ASCVD)和非最佳低密度脂蛋白患者中使用蛋白转化酶枯草杆菌素/克辛蛋白9型抑制剂(PCSK9is)。目的:评估PCSK9i启动后停止他汀类药物使用与随后ASCVD事件的关系。方法:这项前后回顾性比较研究使用了PCSK9i指数(2019年1月1日至2021年4月30日)、既往ASCVD诊断的成人他汀类药物使用者(年龄≥18岁)的国家行政数据,并进行了2年的随访。比较停用他汀类药物(停用队列)和继续使用他汀类药物(继续队列)的患者的指数后(PCSK9i)与指数前(PCSK9i) ASCVD事件的比例和概率。倾向评分加权用于平衡患者的基线特征。多变量泊松回归和时间-事件Cox回归模型用于评估他汀类药物停药与ASCVD事件之间的关系。结果:继续组和停止组分别有294例和46例患者。未加权结果显示,继续队列中的患者更有可能接受高强度他汀类药物(32% vs 22%;P = 0.4),并且Charlson合并症指数评分为3分或以上(62% vs 54%;P = 0.5)。在停止治疗的队列中,基线他汀类药物依从性较低(6.7% vs 59%;随访24个月,P < 0.05, P < 0.9)。任何ASCVD事件的发生率在两个队列之间具有可比性(参考:持续队列;优势比= 1.88;95% ci = 0.28-14.6;p = 0.51)。两组间Cox回归分析差异无统计学意义(P = 0.47)。结论:两组患者的ASCVD后事件发生率均显著降低,但停用他汀类药物与不利的ASCVD结果无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between statin discontinuation after proprotein convertase subtilisin/kexin type 9 inhibitor initiation and subsequent atherosclerotic cardiovascular disease events.

Background: Clinical guidelines recommend the use of proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9is) in patients with atherosclerotic cardiovascular disease (ASCVD) and nonoptimal low-density lipoprotein.

Objective: To evaluate the association between discontinuation of statin use after PCSK9i initiation and subsequent ASCVD events.

Methods: This pre-post retrospective comparative study used national administrative data of adult statin medication users (age ≥18 years) with an index PCSK9i claim (January 1, 2019, to April 30, 2021), prior ASCVD diagnosis, and a 2-year follow-up period. Proportions and probability of ASCVD events post-index (PCSK9i) vs pre-index (PCSK9i) for patients who discontinued statins (discontinued cohort) and those who continued statins (continued cohort) were compared. Propensity score weighting was used to balance patient baseline characteristics. Multivariate Poisson regression and time-to-event Cox regression models were used to assess the association between statin discontinuation and ASCVD events.

Results: There were 294 and 46 patients in the continued and discontinued cohorts, respectively. Unweighted results showed that patients in the continued cohort were more likely to receive high-intensity statins (32% vs 22%; P = 0.4) and have a Charlson Comorbidity Index score of 3 or more (62% vs 54%; P  =  0.5) at baseline. Baseline statin adherence was lower in the discontinued cohort (6.7% vs 59%; P < 0.001) but 30% each in the propensity 1:1 matched cohort. The 2 cohorts (after matching) had similar ASCVD event prevalence (discontinued cohort: 24% vs continued cohort: 26%) in the baseline and the same lower prevalence (6.5% each; P > 0.9) in the 24-month follow-up period. The odds of any ASCVD event post-index was comparable between the 2 cohorts (reference: continued cohort; odds ratio = 1.88; 95% CI = 0.28-14.6; P = 0.51). There were no statistically significant differences between the 2 groups in the Cox regression (P = 0.47).

Conclusions: Post-ASCVD event rates were significantly lower in both cohorts, but discontinuation of statins was not associated with unfavorable ASCVD outcomes.

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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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