Literature DB >> 27823689

Safety and efficacy of the 0 h/3 h protocol for rapid rule out of myocardial infarction.

Karin Wildi1, Berit Nelles2, Raphael Twerenbold3, Maria Rubini Giménez4, Tobias Reichlin3, Hélène Singeisen3, Sophie Druey3, Philip Haaf3, Zaid Sabti3, Petra Hillinger3, Cedric Jaeger3, Isabel Campodarve5, Philip Kreutzinger3, Christian Puelacher3, Zoraida Moreno Weidmann3, Mathias Gugala3, Gilles Pretre3, Stephanie Doerflinger3, Max Wagener3, Fabio Stallone3, Michael Freese3, Claudia Stelzig3, Katharina Rentsch6, Stefano Bassetti7, Roland Bingisser8, Stefan Osswald3, Christian Mueller9.   

Abstract

BACKGROUND: The early and accurate diagnosis of acute myocardial infarction (AMI) is an important medical and economic challenge. We aimed to prospectively evaluate the performance of the new European Society of Cardiology rapid 0-hour/3-hour (0 h/3 h) rule out protocol for AMI.
METHODS: We enrolled 2,727 consecutive patients presenting with suspected AMI without persistent ST-segment elevation to the emergency department in a prospective international multicenter study. The final diagnosis was adjudicated by 2 independent cardiologists. The performance of the 0 h/3 h rule out protocol was evaluated using 4 high-sensitivity (primary analysis) and 3 sensitive cardiac troponin (cTn) assays.
RESULTS: Acute myocardial infarction was the final diagnosis in 473 patients (17.3%). Using the 4 high-sensitivity cTn assays, the 0-hour rule out protocol correctly ruled out 99.8% (95% [confidence interval] CI, 98.7%-100%), 99.6% (95% CI, 98.5%-99.9%), 100% (95% CI, 97.9%-100%), and 100% (95% CI, 98.0%-100%) of late presenters (>6 h from chest pain onset). The 3-hour rule out protocol correctly ruled out 99.9% (95% CI, 99.1%-100%), 99.5% (95% CI, 98.3%-99.9%), 100% (95% CI, 98.1%-100%), and 100% (95% CI, 98.2%-100%) of early presenters (<6 h from chest pain onset). Using the 3 sensitive cTn assays, the 0-hour rule out protocol correctly ruled out 99.6% (95% CI, 98.6%-99.9%), 99.0% (95% CI, 96.9%-99.7%), and 99.1% (95% CI, 97.2%-99.8%) of late presenters; and the 3-hour rule out protocol correctly ruled out 99.4% (95% CI, 98.3%-99.8%), 99.2% (95% CI, 97.3%-99.8%), and 99.0% (95% CI, 97.2%-99.7%) of early presenters. Overall, the 0 h/3 h rule out protocol assigned 40% to 60% of patients to rule out. None of the patients assigned rule out died during 3-months follow-up.
CONCLUSIONS: The 0 h/3 h rule out protocol seems to allow the accurate rule out of AMI using both high-sensitivity and sensitive cTn measurements in conjunction with clinical assessment. Additional studies are warranted for external validation.
Copyright © 2016 Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27823689     DOI: 10.1016/j.ahj.2016.07.013

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  10 in total

1.  Five steps for use and interpretation of troponin in the Emergency Department.

Authors:  Ludovico Furlan; Anna Maria Rusconi; Elisa Ceriani
Journal:  Intern Emerg Med       Date:  2017-07-08       Impact factor: 3.397

2.  Implementation of High-Sensitivity Cardiac Troponin: Challenges From the International Experience.

Authors:  Stacey J Howell; Ezra A Amsterdam; Bryn E Mumma; Javier E López; Nam K Tran
Journal:  Crit Pathw Cardiol       Date:  2018-12

Review 3.  Association of High-Sensitivity Cardiac Troponin I Concentration With Cardiac Outcomes in Patients With Suspected Acute Coronary Syndrome.

Authors:  Andrew R Chapman; Kuan Ken Lee; David A McAllister; Louise Cullen; Jaimi H Greenslade; William Parsonage; Andrew Worster; Peter A Kavsak; Stefan Blankenberg; Johannes Neumann; Nils A Sörensen; Dirk Westermann; Madelon M Buijs; Gerard J E Verdel; John W Pickering; Martin P Than; Raphael Twerenbold; Patrick Badertscher; Zaid Sabti; Christian Mueller; Atul Anand; Philip Adamson; Fiona E Strachan; Amy Ferry; Dennis Sandeman; Alasdair Gray; Richard Body; Brian Keevil; Edward Carlton; Kim Greaves; Frederick K Korley; Thomas S Metkus; Yader Sandoval; Fred S Apple; David E Newby; Anoop S V Shah; Nicholas L Mills
Journal:  JAMA       Date:  2017-11-21       Impact factor: 56.272

4.  Is high-sensitivity troponin, alone or in combination with copeptin, sensitive enough for ruling out NSTEMI in very early presenters at admission? A post hoc analysis performed in emergency departments.

Authors:  Camille Chenevier-Gobeaux; Mustapha Sebbane; Christophe Meune; Sophie Lefebvre; Anne-Marie Dupuy; Guillaume Lefèvre; Nicolas Peschanski; Patrick Ray
Journal:  BMJ Open       Date:  2019-06-16       Impact factor: 2.692

5.  Cardiac Troponin Assays With Improved Analytical Quality: A Trade-Off Between Enhanced Diagnostic Performance and Reduced Long-Term Prognostic Value.

Authors:  Hilde L Tjora; Ole-Thomas Steiro; Jørund Langørgen; Rune Bjørneklett; Ottar K Nygård; Øyvind Skadberg; Vernon V S Bonarjee; Paul Collinson; Torbjørn Omland; Kjell Vikenes; Kristin M Aakre
Journal:  J Am Heart Assoc       Date:  2020-11-26       Impact factor: 5.501

6.  Higher Frequency of Undetected Acute Coronary Syndrome in Elderly Patients with Chest Pain Who Visited the Emergency Department: A Large-Cohort Retrospective Study.

Authors:  Ki Hun Hong; Sung Jin Bae; Dong Hoon Lee; Choung Ah Lee; Sang Hyun Park; Duk Ho Kim; Eui Chung Kim; Jee Yong Lim; Sangsoo Han; Yoon Hee Choi
Journal:  Biomed Res Int       Date:  2021-04-10       Impact factor: 3.411

7.  Multi-centre evaluation of recent troponin assays for the diagnosis of NSTEMI.

Authors:  Camille Chenevier-Gobeaux; Louis Deweerdt; Anne-Valérie Cantero; Bertrand Renaud; Bruno Desmaizières; Sandrine Charpentier; Aline Leroy; Emmanuelle Adelaïde; Delphine Collin-Chavagnac; Eric Bonnefoy-Cudraz; Laurence Estepa; Akli Chekroune; Sylvie Basco; Stéphane Andrieu; Stéphane Bourgeois; Marie-Agnès Costa; Christine Vallejo; Tiphaine Robert; Siham Ouahabi; Bruno Baudin; Benedicte Beneteau-Burnat; Anne-Marie Gorce-Dupuy; Patrick Ray; Claire Gast; Monique Dehoux; Guillaume Lefèvre
Journal:  Pract Lab Med       Date:  2018-02-26

8.  Absolute Change in High-Sensitivity Cardiac Troponin I at Three Hours After Presentation is Useful for Diagnosing Acute Myocardial Infarction in the Emergency Department.

Authors:  Jong Won Kim; Hanah Kim; Yeo-Min Yun; Kyeong Ryong Lee; Hyun Joong Kim
Journal:  Ann Lab Med       Date:  2020-06-17       Impact factor: 3.464

9.  Critical appraisal of the 2020 ESC guideline recommendations on diagnosis and risk assessment in patients with suspected non-ST-segment elevation acute coronary syndrome.

Authors:  Evangelos Giannitsis; Stefan Blankenberg; Robert H Christenson; Norbert Frey; Stephan von Haehling; Christian W Hamm; Kenji Inoue; Hugo A Katus; Chien-Chang Lee; James McCord; Martin Möckel; Jack Tan Wei Chieh; Marco Tubaro; Kai C Wollert; Kurt Huber
Journal:  Clin Res Cardiol       Date:  2021-02-26       Impact factor: 5.460

10.  High-Sensitivity Cardiac Troponin I and Clinical Risk Scores in Patients With Suspected Acute Coronary Syndrome.

Authors:  Andrew R Chapman; Kerrick Hesse; Jack Andrews; Kuan Ken Lee; Atul Anand; Anoop S V Shah; Dennis Sandeman; Amy V Ferry; Jack Jameson; Simran Piya; Stacey Stewart; Lucy Marshall; Fiona E Strachan; Alasdair Gray; David E Newby; Nicholas L Mills
Journal:  Circulation       Date:  2018-10-16       Impact factor: 29.690

  10 in total

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