Author:
Tada Masafumi,Azuma Hiroyuki,Yamada Naoki,Kano Ken-ichi,Nagai Hideya,Maeda Shigenobu,Ishida Hiroshi,Aoyama Takahiko,Okada Ryota,Kawano Takahisa,Kobuchi Taketsune,Uzui Hiroyasu,Matano Hideyuki,Iwasaki Hose,Maeno Koji,Shimada Yoshimitsu,Yoshida Hiroyuki,Ando Masaki,Murakami Yoshimasa,Iwakami Naotsugu,Kishimoto Sanae,Iwami Taku,Tada Hiroshi,Chapman Andrew,Mills Nicholas,Hayashi Hiroyuki,Furukawa Toshi A,Watanabe Norio
Abstract
IntroductionRecent advances in troponin sensitivity enabled early and accurate judgement of ruling-out myocardial infarction, especially non-ST elevation myocardial infarction (NSTEMI) in emergency departments (EDs) with development of various prediction-rules and high-sensitive-troponin-based strategies (hs-troponin). Reliance on clinical impression, however, is still common, and it remains unknown which of these strategies is superior. Therefore, our objective in this prospective cohort study is to comprehensively validate the diagnostic accuracy of clinical impression-based strategies, prediction-rules and hs-troponin-based strategies for ruling-out NSTEMIs.Methods and analysisIn total, 1500 consecutive adult patients with symptoms suggestive of acute coronary syndrome will be prospectively recruited from five EDs in two tertiary-level, two secondary-level community hospitals and one university hospital in Japan. The study has begun in July 2018, and recruitment period will be about 1 year. A board-certified emergency physician will complete standardised case report forms, and independently perform a clinical impression-based risk estimation of NSTEMI. Index strategies to be compared will include the clinical impression-based strategy; prediction rules and hs-troponin-based strategies for the following types of troponin (Roche Elecsys hs-troponin T; Abbott ARCHITECT hs-troponin I; Siemens ADVIA Centaur hs-troponin I; Siemens ADVIA Centaur sensitive-troponin I). The reference standard will be the composite of type 1 MI and cardiac death within 30 days after admission to the ED. Outcome measures will be negative predictive value, sensitivity and effectiveness, defined as the proportion of patients categorised as low risk for NSTEMI. We will also evaluate inter-rater reliability of the clinical impression-based risk estimation.Ethics and disseminationThe study is approved by the Ethics Committees of the Kyoto University Graduate School and Faculty of Medicine and of the five hospitals where we will recruit patients. We will disseminate the study results through conference presentations and peer-reviewed journals.
Funder
Radiometer
Nakatani Foundation for Advancement of Measuring Technologies in Biomedical Engineering
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