Department of Emergency Medicine, Wake Forest School of Medicine, 1 Medical Center Boulevard, Winston-Salem, NC 27157, USA.
Am J Emerg Med. 2021 Dec;50:196-201. doi: 10.1016/j.ajem.2021.08.006. Epub 2021 Aug 8.
Nitroglycerin (NTG) is a vasodilator used in the prehospital setting with chest pain patients. Potential adverse effects include hypotension, bradycardia or tachycardia, and mental status change. However, it is unclear which factors, if any, are associated with patients having an adverse event after receiving NTG. The objective of this study was to determine demographic and clinical factors associated with adverse events after prehospital NTG administration.
The ESO Data Collaborative (Austin, TX), containing records from 1322 EMS agencies, was queried for 911 encounters where NTG was administered to patients ≥18 years old by EMS. Adverse event outcomes were defined as a new systolic blood pressure (SBP) < 90, heart rate (HR) < 50 or > 120, mean arterial pressure (MAP) < 65, or change in mental status following NTG administration. Descriptive statistics and logistic regression models adjusting for age, sex, race, ethnicity, intravenous (IV) access, and initial vital signs were used to assess for adverse event-related factors.
Among 80,760 encounters, the mean age was 61 (IQR 50-72), with 52% males, 71% white race, and 7% Hispanic ethnicity. Adverse events occurred in 7% of encounters. Adverse events were found to be less common among Black patients (OR = 0.74, 95%CI:0.69-0.80). IV access obtained prior to NTG administration was associated with fewer adverse events (OR = 0.92, 95%CI:0.85-0.99). Increasing age (OR = 1.02, 95%CI:1.01-1.02) and HR (OR = 1.03, 95%CI:1.02-1.03) were associated with increased odds of adverse events while SBP (OR = 0.99, 95%CI:0.98-0.99) was inversely associated.
Adverse events following prehospital NTG administration were rare, especially in patients with an SBP > 110 and a HR < 100, and less frequent in those with existing IV access. Demographics were not found to be clinically significant.
硝酸甘油(NTG)是一种在胸痛患者的院前环境中使用的血管扩张剂。潜在的不良反应包括低血压、心动过缓或心动过速以及精神状态改变。然而,尚不清楚哪些因素(如果有的话)与接受 NTG 后发生不良反应的患者有关。本研究的目的是确定与院前 NTG 给药后发生不良反应相关的人口统计学和临床因素。
ESO Data 协作(奥斯汀,德克萨斯州)查询了来自 1322 个 EMS 机构的记录,其中包括 18 岁以上患者由 EMS 给予 NTG 的 911 次就诊。不良反应结局定义为新的收缩压(SBP)<90、心率(HR)<50 或>120、平均动脉压(MAP)<65 或 NTG 给药后精神状态改变。使用描述性统计和调整年龄、性别、种族、民族、静脉(IV)通路和初始生命体征的逻辑回归模型来评估与不良反应相关的因素。
在 80760 次就诊中,平均年龄为 61(IQR 50-72),男性占 52%,白人占 71%,西班牙裔占 7%。7%的就诊发生不良反应。黑人患者发生不良反应的可能性较小(OR=0.74,95%CI:0.69-0.80)。在给予 NTG 之前获得 IV 通路与不良反应减少相关(OR=0.92,95%CI:0.85-0.99)。年龄增加(OR=1.02,95%CI:1.01-1.02)和 HR 增加(OR=1.03,95%CI:1.02-1.03)与不良反应的可能性增加相关,而 SBP 降低(OR=0.99,95%CI:0.98-0.99)与不良反应的可能性降低相关。
院前 NTG 给药后发生不良反应的情况很少见,尤其是 SBP>110 和 HR<100 的患者,并且在已经存在 IV 通路的患者中发生的频率较低。人口统计学因素没有显示出临床意义。