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HEART Score Recalibration Using Higher Sensitivity Troponin T - 20/09/23

Doi : 10.1016/j.annemergmed.2023.04.024 
Aleem U. Khand, MRCP, MD a, b, c, , Barbra Backus, MD d, Michael Campbell, MBChB a, Freddy Frost, MBChB, MD c, Liam Mullen, MBBS b, Michael Fisher, FRCP, PhD a, b, Konstantinos C. Theodoropoulos, MBBS b, Mohammed Obeidat, MBBS a, Kate Batouskaya, MBChB a, Edward W. Carlton, PhD e, Kirsten Van Meerten, MD f, Kai Neoh, BMBS a, Ahmed Dakshi, MBChB a, Bryn E. Mumma, MD, MAS g
a Liverpool University Hospital, Liverpool, UK 
b Liverpool Heart and Chest Hospital, Liverpool, UK 
c Liverpool Centre for Cardiovascular Diseases, University of Liverpool, Liverpool, UK 
d Erasmus Medical Center, Rotterdam, Netherlands 
e North Bristol NHS Trust, Bristol, UK 
f Albert Schweitzer Hospital, Dordrecht, The Netherlands 
g Department of Emergency Medicine, University of California, Davis School of Medicine, Sacramento, CA 

Corresponding Author.

Abstract

Study objective

We examined the diagnostic performance of a recalibrated History, Electrocardiogram, Age, Risk factors, Troponin (HEART), and Thrombolysis in Myocardial Infarction (TIMI) score in patients with suspected acute cardiac syndrome (ACS). Recalibration of troponin thresholds was performed, including shifting from the 99th percentile to the limit of detection (LOD) or to the limit of quantification (LOQ)

We compared the discharge potential and safety of the recalibrated composite scores using a single presentation high-sensitivity cardiac troponin (hs-cTn) T to the conventional scores and with a LOD/LOQ troponin strategy alone.

Methods

We undertook a 2-center prospective cohort study in the United Kingdom (UK) (2018) (Clinicaltrials.gov NCT03619733) to specifically assess recalibrated risk scores (shifting the troponin subset scoring from 99th percentile to LOD [UK]) and combined the results of this with secondary analyses of 2 prospective cohort studies in the UK (2011) and the United States (2018, using LOQ rather than LOD). The primary outcome was major adverse cardiovascular events (MACE), defined as adjudicated type 1 myocardial infarction (MI), urgent coronary revascularization, and all-cause death, at 30 days. We evaluated the original scores using hs-cTn below the 99th percentile and recalibrated scores using hs-cTn <LOD/LOQ and compared these composite scores with a single hs-cTnT less than LOD/LOQ combined with a nonischemic ECG. For each discharge strategy, an assessment of clinical effectiveness was also made, defined as the proportion of patients eligible for discharge from the emergency department without the need for further inpatient testing.

Results

We studied 3,752 patients (3,003 in the UK and 749 in the United States). Median age was 58 years, and 48% were female. At 30 days, 330/3,752 (8.8%) experienced MACE. The sensitivities of the original HEART less or equal to 3 and recalibrated HEART less or equal to 3 scores for rule-out were 96.1% (95% confidence interval [CI], 93.4 to 97.9) and 98.6% (95% CI, 96.5 to 99.5) respectively; the original TIMI less or equal to 1 and recalibrated TIMI less or equal to 1 scores’ sensitivities were 79.7% (95% CI, 74.9 to 83.9) and 96.1% (95% CI, 93.4 to 97.9) respectively; and nonischemic ECG with hs-cTn T below the 99th percentile and hs-cTn T less than LOD/LOQ was 79.7% (95%CI, 0.749 to 0.839) and 99.1% (95% CI, 0.974 to 0.998), respectively. Recalibrated HEART less or equal to 3 was projected to discharge 14% more patients than hs-cTn T less than LOD/LOQ. The improved sensitivity of rule-out for recalibrated HEART less than or equal to 3 came at the cost of reduced specificity (50.8% versus 53.8% for recalibrated HEART and conventional HEART respectively).

Conclusion

This study indicates that recalibrated HEART score of less or equal to 3 is a feasible and safe early discharge strategy using a single presentation hs-cTnT. This finding should be further tested using competitor hs-cTn assays in independent prospective cohorts before implementation.

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Plan


 Please see page 450 for the Editor’s Capsule Summary of this article.
 Supervising editor: Keith A. Marill, MD, MS. Specific detailed information about possible conflicts of interest for individual editors is available at editors.
 Author contributions: AK, FF, LM, KM, BB developed the concept. MC, FF, LM, KT, MO, KB, AD, KN were researchers entering data for the study. AK, MF, LM were principal adjudicators for type 1/2 MI. BM provided US cohort data and provided intellectual input. AK wrote the paper with input from BM. AK is the guarantor of the data. AK takes responsibility for the paper as a whole.
 All authors attest to meeting the four ICMJE.org authorship criteria: (1) Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; AND (2) Drafting the work or revising it critically for important intellectual content; AND (3) Final approval of the version to be published; AND (4) Agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
 Funding and support: By Annals policy, all authors are required to disclose any and all commercial, financial, and other relationships in any way related to the subject of this article as per ICMJE conflict of interest guidelines (see www.icmje.org). This research was supported by a grant from Bayer (pharmaceutical division), an innovation award from Liverpool University hospital NHS Foundation trust and Northwest Educational Cardiac Group from the United Kingdom, and by the Alpha Phi Foundation Grant Support: Heart to Heart Grant (BEM); the UC Davis Collaborative for Diagnostic Innovation Improving Diagnosis in Healthcare Award (BEM); an investigator-initiated grant from Roche Diagnostics (BEM); and the National Heart, Lung, and Blood Institute through grant #5K08HL130546 (BEM)—from the United States. These funders had no role in study design, data collection, data analysis, data interpretation, or writing of the manuscript.
 BEM has no relevant conflicts of interest. Dr. A Khand: Speaker/ expert panel fees: Bayer, Daiichi Sankyo, Astra Zeneca, Menarini, St Jude, Abbot Vascular. Research funds: Bayer Medical, Menarini. Research contracts: Abbott Diagnostics, Siemens diagnostics, Quidel. Other (A Khand: director): NWECG (northwest educational cardiac group, a not-for-profit medical educational group) received sponsorship for educational courses from Bayer, Astra Zeneca, Genzyme (Sanofi), Daiichi Sankyo, Circle Cardiovascular, Menarini, Circle. Innovation agency, Northwest: clinical Champion for high sensitive troponins. Liam Mullen: secretary NWECG (northwest educational cardiac group, a not-for-profit medical educational group) received sponsorship for educational courses from Bayer, Astra Zeneca, Genzyme (Sanofi), Daiichi Sankyo, Circle Cardiovascular, Menarini, Circle.
 All other authors declare no conflict of interest. AK is the guarantor of the data.
 Trial Number: Clinicaltrials.gov NCT03619733.
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 A podcast for this article is available at www.annemergmed.com.


© 2023  American College of Emergency Physicians. Publié par Elsevier Masson SAS. Tous droits réservés.
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Vol 82 - N° 4

P. 449-462 - octobre 2023 Retour au numéro
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