ACTRN12622001474741尚未招募未知
Queensland introduction of the Siemen's Atellica high sensitivity troponin and its effect on time to emergency department discharge in patients presenting to the emergency department with suspected acute coronary syndrome: A health services evaluation
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 120,000
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patients will be eligible for enrolment if they are 18 years of age or older and have at least one troponin test ordered within 3 hours of their presentation to the ED. Participants will be included in the pre-implementation group if presenting to a Queensland ED prior to implementation of the Siemen's Atellica assay between April 2021 and February 2022. Participants will be included in the post-implementation group if presenting to a Queensland ED where the Siemen's Atellica assay was implemented between April 2022 and February 2023.
排除标准
- •Patients will be excluded if they presented to the ED with troponin testing during the block-out implementation period relevant for each facility occurring between October 2021 and July 2022.
研究者
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