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The relative merits of using a high-sensitivity cardiac Troponin T assay compared to a nonhigh-sensitivity troponin T assay after noncardiac surgery - 16/08/24

Doi : 10.1016/j.ahj.2024.05.020 
Flavia K. Borges, MD, PhD a, b, c, , Daniel I. Sessler, MD d, Maria Tiboni, MD b, Ameen Patel, MD b, Yannick LeManach, MD, PhD a, b, c, Diane Heels-Ansdell, BSc, MSc c, Sadeesh Srinathan, MD e, Chew Yin Wang, MBChB f, Clara Chow, MD, PhD g, h, Emmanuelle Duceppe, MD, PhD a, i, Peter Kavsak, BSc, PhD j, Sandra N. Ofori, MBBS, MSc a, b, Shirley Pettit, RN a, Otavio Berwanger, MD, PhD k, Andrea Kurz, MD l, m, Alparslan Turan, MD l, Ana Claudia Tonelli, MD, PhD n, o, PJ Devereaux, MD, PhD a, b, c
On behalf of

VISION Study Investigators

a Perioperative Medicine and Surgical Research Unit, Population Health Research Institute, Hamilton, Canada 
b Department of Medicine, McMaster University, Hamilton, Canada 
c Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Canada 
d Department of Outcomes Research, Cleveland Clinic, Cleveland, USA 
e Department of Surgery, University of Manitoba, Winnipeg, Canada 
f Department of Anaesthesiology, University of Malaya, Kuala Lumpur, Wilayah Persekutuan, Malaysia 
g Department of Cardiology, Westmead Applied Research Centre (WARC), University of Sydney, Westmead, New South Wales, Australia 
h Westmead Hospital, Westmead, New South Wales, Australia 
i Department of Medicine, University of Montreal, Montreal, Canada 
j Department of Pathology and Molecular Medicine, McMaster University 
k George Institute for Global Health UK and Imperial College London, London, UK 
l Departments of General Anesthesiology and Outcomes Research, Anesthesiology Institute, Cleveland Clinic, Ohio, USA 
m Department of General Anesthesiology, Emergency and Intensive Care Medicine, Medical University Graz, Austria 
n Department of Medicine, Unisinos University, São Leopoldo, Brazil 
o Department of Internal Medicine, Internal Medicine Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil 

Reprint requests: Flavia Kessler Borges, Population Health Research Institute, David Braley Cardiac, Vascular, and Stroke Research Institute, Room C1-109, Perioperative Medicine and Surgical Research Unit, c/o Hamilton General Hospital, 237 Barton Street East, Hamilton, ON, Canada, L8L 2 × 2.Population Health Research InstituteDavid Braley CardiacVascularand Stroke Research InstituteRoom C1-109, Perioperative Medicine and Surgical Research Unit, c/o Hamilton General Hospital, 237 Barton Street EastHamiltonONCanada

Riassunto

Introduction

Troponin elevation after noncardiac surgery is associated with an elevated risk of 30-day mortality. Little is known about relative merit of using a high-sensitivity Troponin T (hsTnT), the fifth-generation assay, vs the nonhigh sensitivity Troponin T (non-hsTnT), the fourth-generation assay, in the noncardiac surgery setting. We aimed to identify whether hsTnT can identify additional patients at risk that would have gone undetected with non-hsTnT measurement.

Methods

The VISION Study included 40,004 noncardiac surgery patients with postoperative troponin measurements. Among them, 1,806 patients had both fourth-generation non-hsTnT and fifth-generation hsTnT concomitant measurements (4,451 paired results). We compared the absolute concentrations, the timing, and the impact of different thresholds on predicting 30-day major cardiovascular complications (composite of death, nonfatal cardiac arrest, coronary revascularization, and congestive heart failure).

Results

Based on the manufacturers’ threshold of 14 ng/L, 580 (32.1%) patients had postoperative hsTnT concentrations greater than the threshold, while their non-hsTnT concentrations were below the manufacturer's threshold. These 580 patients had higher risk of major cardiovascular events (OR 2.33; CI 95% 1.04-5.23; P = .049) than patients with hsTnT concentrations below the manufacturer threshold. Among patients with myocardial injury after noncardiac surgery, only 50% would be detected by the fourth-generation non-hsTnT assay at 6 to 12 hours postoperative as compared to 85% with the fifth-generation hsTnT assay (P-value < .001).

Conclusions

Within the first 3 postoperative days, fifth-generation hsTnT identified at least 1 in 3 patients with troponin elevation that would have gone undetected by fourth-generation non-hsTnT using published thresholds in this setting. Furthermore, fifth-generation hsTnT identified patients with an elevation earlier than fourth-generation non-hsTnT, indicating potential to improve postoperative risk stratification.

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