ARTICA RCT primary outcome ...
BACKGROUND: Patients with suspected non-ST-segment elevation acute coronary syndrome (NSTE-ACS) are routinely transferred to theemergency department (ED). A clinical risk score with point-of-care (POC) troponin measurement might enable ambulance paramedics to identify low-risk patients in whom ED ev...
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Online Access: | https://dx.doi.org/10.17026/dans-xd2-3zpg https://lifesciences.datastations.nl/citation?persistentId=doi:10.17026/dans-xd2-3zpg |
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ftdatacite:10.17026/dans-xd2-3zpg 2024-04-28T08:12:49+00:00 ARTICA RCT primary outcome ... Camaro, C 2019 https://dx.doi.org/10.17026/dans-xd2-3zpg https://lifesciences.datastations.nl/citation?persistentId=doi:10.17026/dans-xd2-3zpg en eng DANS Data Station Life Sciences dataset Dataset 2019 ftdatacite https://doi.org/10.17026/dans-xd2-3zpg 2024-04-02T12:24:47Z BACKGROUND: Patients with suspected non-ST-segment elevation acute coronary syndrome (NSTE-ACS) are routinely transferred to theemergency department (ED). A clinical risk score with point-of-care (POC) troponin measurement might enable ambulance paramedics to identify low-risk patients in whom ED evaluation is unnecessary. The aim was to assess safety and healthcare costs of a pre-hospital rule-out strategy using a POC troponin measurement in low-risk suspected NSTE-ACS patients.METHODS AND RESULTS:This investigator-initiated, randomized clinical trial was conducted in five ambulance regions in the Netherlands. Suspected NSTE-ACS patients with HEAR (History, ECG, Age, Risk factors) score ≤3 were randomized to pre-hospital rule-out with POC troponin measurement or direct transfer to the ED. The sample size calculation was based on the primary outcome of 30-day healthcare costs. Secondary outcome was safety, defined as 30-day major adverse cardiac events (MACE), consisting of ACS, unplanned revascularization ... Dataset artica DataCite Metadata Store (German National Library of Science and Technology) |
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Open Polar |
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DataCite Metadata Store (German National Library of Science and Technology) |
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ftdatacite |
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English |
description |
BACKGROUND: Patients with suspected non-ST-segment elevation acute coronary syndrome (NSTE-ACS) are routinely transferred to theemergency department (ED). A clinical risk score with point-of-care (POC) troponin measurement might enable ambulance paramedics to identify low-risk patients in whom ED evaluation is unnecessary. The aim was to assess safety and healthcare costs of a pre-hospital rule-out strategy using a POC troponin measurement in low-risk suspected NSTE-ACS patients.METHODS AND RESULTS:This investigator-initiated, randomized clinical trial was conducted in five ambulance regions in the Netherlands. Suspected NSTE-ACS patients with HEAR (History, ECG, Age, Risk factors) score ≤3 were randomized to pre-hospital rule-out with POC troponin measurement or direct transfer to the ED. The sample size calculation was based on the primary outcome of 30-day healthcare costs. Secondary outcome was safety, defined as 30-day major adverse cardiac events (MACE), consisting of ACS, unplanned revascularization ... |
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Camaro, C |
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Camaro, C ARTICA RCT primary outcome ... |
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Camaro, C |
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Camaro, C |
title |
ARTICA RCT primary outcome ... |
title_short |
ARTICA RCT primary outcome ... |
title_full |
ARTICA RCT primary outcome ... |
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ARTICA RCT primary outcome ... |
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ARTICA RCT primary outcome ... |
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artica rct primary outcome ... |
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DANS Data Station Life Sciences |
publishDate |
2019 |
url |
https://dx.doi.org/10.17026/dans-xd2-3zpg https://lifesciences.datastations.nl/citation?persistentId=doi:10.17026/dans-xd2-3zpg |
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artica |
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artica |
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https://doi.org/10.17026/dans-xd2-3zpg |
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1797579570494308352 |