Ho Charles Yao-Cheng, Lee Mildred, El-Jack Seif, Barr Peter, Simmonds Mark, Devlin Gerry, Adamson Philip D, Williams Michael, Kerr Andrew J
Department of Cardiology, Counties Manukau District Health Board, New Zealand.
Department of Cardiology, Waitematā District Health Board, New Zealand.
N Z Med J. 2021 Jun 25;134(1537):43-55.
The last two decades in New Zealand have seen increased availability of primary percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI) and early invasive coronary angiography (ICA) for other high-risk acute coronary syndrome (ACS) patients. One metric to assess the clinical appropriateness of these invasive strategies is to examine the false-positive rate for the investigation (ie, the rate of non-ACS diagnoses).
All patients presenting to New Zealand public hospitals with suspected ACS who underwent ICA between 2015 and 2019 were recorded prospectively in the All New Zealand Acute Coronary Syndrome Quality Improvement registry. The cohort was divided according to clinical impression at presentation: (1) suspected STEMI <24h and (2) other suspected ACS. The final discharge diagnosis for each patient were obtained from the registry.
There were 6,059 (20%) patients with suspected STEMI <24h and 24,258 (80%) with other suspected ACS. Of the suspected STEMIs <24h, 90.6% had a final diagnosis of STEMI, 3.5% non-ST segment elevation ACS (NSTEACS) and only 5.9% had a non-ACS diagnosis. Of those with other suspected ACS, 80.7% had a final ACS diagnosis. Across all New Zealand district health boards (DHBs), the proportion of non-ACS diagnoses was similar for suspected STEMI presentations. However, for other suspected ACS, the proportions were higher in DHBs with rapid access to coronary interventional facilities than in those without (17.6% vs 7.0%, p<0.001).
False-positive catheter laboratory activations for suspected STEMI patients are low across New Zealand. The differences in the proportion of non-ACS diagnoses according to DHB interventional capability for other suspected ACS requires further investigation.
在过去二十年里,新西兰用于ST段抬高型心肌梗死(STEMI)的直接经皮冠状动脉介入治疗(PCI)以及用于其他高危急性冠状动脉综合征(ACS)患者的早期有创冠状动脉造影(ICA)的可及性有所提高。评估这些有创治疗策略临床合理性的一个指标是检查检查的假阳性率(即非ACS诊断率)。
2015年至2019年间在新西兰公立医院因疑似ACS接受ICA检查的所有患者均被前瞻性记录在全新西兰急性冠状动脉综合征质量改进登记册中。该队列根据就诊时的临床印象分为:(1)疑似STEMI<24小时和(2)其他疑似ACS。每位患者的最终出院诊断均从登记册中获取。
有6059例(20%)疑似STEMI<24小时的患者和24258例(80%)其他疑似ACS的患者。在疑似STEMI<24小时的患者中,90.6%最终诊断为STEMI,3.5%为非ST段抬高型ACS(NSTEACS),只有5.9%为非ACS诊断。在其他疑似ACS的患者中,80.7%最终诊断为ACS。在新西兰所有地区卫生委员会(DHB)中,疑似STEMI患者的非ACS诊断比例相似。然而,对于其他疑似ACS患者,能够快速获得冠状动脉介入设施的DHB中的比例高于没有这些设施的DHB(17.6%对7.0%,p<0.001)。
在新西兰,疑似STEMI患者导管实验室激活的假阳性率较低。根据DHB对其他疑似ACS的介入能力,非ACS诊断比例的差异需要进一步研究。