Heart Center, Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, Location AMC, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Department of Cardiology, Maastricht University Medical Center, Maastricht, The Netherlands.
Am J Cardiovasc Drugs. 2021 Mar;21(2):219-229. doi: 10.1007/s40256-020-00427-9.
Unlike neighboring countries, the Netherlands does not have a national acute coronary syndrome (ACS) registry to evaluate quality of care.
We conducted a pilot registry in two hospitals to assess the prescription of guideline-recommended therapies in Dutch patients with ACS.
We included all consecutive patients with ST-elevation myocardial infarction (STEMI) and non-STEMI (NSTEMI) (n = 1309) admitted to two Dutch percutaneous coronary intervention centers between March 2015 and February 2016. We collected follow-up medication use and reasons for discontinuation at discharge and 1, 6, and 12 months post-discharge. We assessed the use of optimal medical therapy (OMT), defined as the combined prescription of aspirin, P2Y12 inhibitors, statins, β-blockers, and angiotensin-converting enzyme inhibitors or angiotensin-receptor blockers.
OMT prescription was 43.2% at discharge, 60.1% at 1 month, and 28.7% at 12 months. At 1 month, OMT prescription was significantly lower in patients with NSTEMI (51.8 vs. 65.7% for STEMI; p < 0.001). OMT prescription was lower in women (6 months: 55.4 vs. 62.0%, p = 0.036) and in elderly patients.
In this pilot study that aimed to extend a national Dutch ACS registry to patients with STEMI and NSTEMI, OMT prescription was comparable to that in other local registries, was lower in women and patients with NSTEMI, and decreased with increasing age.
与邻国不同,荷兰没有国家急性冠状动脉综合征(ACS)登记处来评估护理质量。
我们在两家医院开展了一项试点登记研究,以评估荷兰 ACS 患者指南推荐治疗方案的应用情况。
我们纳入了 2015 年 3 月至 2016 年 2 月期间在荷兰两家经皮冠状动脉介入治疗中心连续收治的所有 ST 段抬高型心肌梗死(STEMI)和非 ST 段抬高型心肌梗死(NSTEMI)患者(n=1309)。我们收集了出院时及出院后 1、6 和 12 个月的随访用药情况和停药原因。我们评估了优化药物治疗(OMT)的应用情况,定义为阿司匹林、P2Y12 抑制剂、他汀类药物、β受体阻滞剂和血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂的联合应用。
出院时 OMT 处方率为 43.2%,1 个月时为 60.1%,12 个月时为 28.7%。1 个月时,NSTEMI 患者的 OMT 处方率显著较低(STEMI 为 51.8% vs. 65.7%;p<0.001)。女性(6 个月:55.4% vs. 62.0%,p=0.036)和老年患者的 OMT 处方率较低。
在这项旨在将荷兰全国 ACS 登记研究扩展到 STEMI 和 NSTEMI 患者的试点研究中,OMT 处方率与其他本地登记研究相当,在女性和 NSTEMI 患者中较低,且随年龄增长而降低。