@article{fdb5bd59887f4d44b6f2ba48c0d30167,
title = "High-Sensitivity Cardiac Troponin and the Diagnosis of Myocardial Infarction in Patients with Renal Impairment",
abstract = "The benefit and utility of high-sensitivity cardiac troponin in the diagnosis of myocardial infarction (MI) in patients with renal impairment is unclear. Here, we describe the implementation of high-sensitivity cardiac troponin testing on the diagnosis, management, and outcomes of MI in patients with and without renal impairment. Consecutive patients with suspected acute coronary syndrome enrolled in a stepped-wedge, cluster-randomised controlled trial were included in this pre-specified secondary analysis. Renal impairment was defined as an eGFR <60mL/min/1.73m2. The index diagnosis and primary outcome of type 1/4b MI or cardiovascular death at one year were compared in patients with and without renal impairment following implementation of a high-sensitivity cardiac troponin I assay with 99th centile sex-specific diagnostic thresholds. Serum creatinine concentrations were available in 46,927 (97%) patients (61±17years; 47% women), of whom 9,080 (19%) had renal impairment. Cardiac troponins were >99th centile in 46% and 16% of patients with and without renal impairment. Implementation increased the diagnosis of type 1 MI from 12.4% to 17.8%, and from 7.5% to 9.4% in patients with and without renal impairment (P<0.001 [both]). Patients with renal impairment and type 1 MI were less likely to undergo coronary revascularisation (26% versus 53%; P<0.001) or receive dual anti-platelets (40% versus 68%;P<0.001) than those without renal impairment, and this did not change post-implementation. In patients with cardiac troponins >99th centile, the primary outcome occurred twice as often in those with renal impairment compared to those without (24% versus 12%, HR 1.53, 95%CI 1.31 to 1.78). Implementation increased the identification of myocardial injury and infarction but failed to address disparities in management and outcomes between those with and without renal impairment.",
author = "{High-STEACS Investigators} and Gallacher, {Peter J} and Eve Miller-Hodges and Shah, {Anoop S.v.} and Tariq Farrah and Nynke Halbesma and Blackmur, {James P} and Chapman, {Andrew R} and Adamson, {Philip D} and Atul Anand and Strachan, {Fiona E} and Ferry, {Amy V} and Lee, {Kuan Ken} and Colin Berry and Iain Findlay and Anne Cruickshank and Alan Reid and Alasdair Gray and Collinson, {Paul O} and Apple, {Fred S} and McAllister, {David A} and Donogh Maguire and Fox, {Keith AA} and Catriona Keerie and Weir, {Christopher J} and Newby, {David E} and Mills, {Nicholas L} and Neeraj Dhaun",
note = "Funding Information: ASVS and ARC have received honoraria from Abbott Diagnostics. NLM has received honoraria from Abbott Diagnostics, Siemens Healthineers, Roche Diagnostics, and LumiraDx; and the University of Edinburgh has received research grants from Abbott Diagnostics and Siemens Healthineers. FSA has received honoraria (advisory board) from Siemens Healthineers and LumiraDx; nonsalaried research through research foundation from Abbott Diagnostics, Abbott PC, Beckman Coulter, Siemens Healthineers, Quidel, Ortho-Clinical Diagnostics, Roche Diagnostics; and has served on the board of directors of HyTest. CB is named on institutional research and/or consultancy agreements between the University of Glasgow and Abbot Vascular, AstraZeneca, Coroventis, GSK, HeartFlow, Menarini, Novartis, and Siemens Healthcare. All the other authors declared no competing interests. Funding Information: This trial was funded by a Special Project Grant from the British Heart Foundation (BHF; SP/12/10/29922) with additional support from a BHF-Turing Cardiovascular Data Science Award (BCDSA/100003) and BHF Research Excellence Award (RE/18/5/34216; RE/18/6/34217). PJG is supported by the Mason Medical Research Foundation and a BHF Clinical Research Training Fellowship (FS/CRTF/20/24079). ARC, NLM, and DEN are supported by Clinical Research Training Fellowship (FS/16/75/32533), Butler Senior Clinical Research Fellowship (FS/16/14/32023), and Chair (CH/09/002) awards from the BHF. TEF is supported by a Medical Research Council Clinical Research Training Fellowship (MR/R017840/1). NH is supported by a BHF Intermediate Basic Science Research Fellowship (FS/16/36/32205). PDA is supported by a National Heart Foundation of New Zealand Senior Fellowship (1844). CJW was supported by National Health Service Lothian through the Edinburgh Clinical Trials Unit. Abbott Laboratories provided cardiac troponin assay reagents, calibrators, and controls without charge. The funders played no role in the design, conduct, data collection, analysis, or reporting of the trial. The companies listed in the disclosures had no involvement in this manuscript. We would like to thank researchers from the Emergency Medicine Research Group Edinburgh for their support during the conduct of this trial. The High-Sensitivity Troponin in the Evaluation of Patients With Acute Coronary Syndrome (High-STEACS) trial is registered as NCT01852123 with ClinicalTrials.gov. The High-STEACS Investigators contributed to the conception or design of the work or the acquisition, analysis, or interpretation of data for the work. They were involved in drafting and revising the manuscript and have given final approval of the version to be published. The High-STEACS investigators are accountable for the work. Funding Information: This trial was funded by a Special Project Grant from the British Heart Foundation (BHF; SP/12/10/29922) with additional support from a BHF -Turing Cardiovascular Data Science Award (BCDSA/100003) and BHF Research Excellence Award (RE/18/5/34216; RE/18/6/34217). PJG is supported by the Mason Medical Research Foundation and a BHF Clinical Research Training Fellowship (FS/CRTF/20/24079). ARC, NLM, and DEN are supported by Clinical Research Training Fellowship (FS/16/75/32533), Butler Senior Clinical Research Fellowship (FS/16/14/32023), and Chair (CH/09/002) awards from the BHF . TEF is supported by a Medical Research Council Clinical Research Training Fellowship (MR/R017840/1). NH is supported by a BHF Intermediate Basic Science Research Fellowship (FS/16/36/32205). PDA is supported by a National Heart Foundation of New Zealand Senior Fellowship (1844). CJW was supported by National Health Service Lothian through the Edinburgh Clinical Trials Unit. Abbott Laboratories provided cardiac troponin assay reagents, calibrators, and controls without charge. The funders played no role in the design, conduct, data collection, analysis, or reporting of the trial. The companies listed in the disclosures had no involvement in this manuscript. Publisher Copyright: {\textcopyright} 2022 International Society of Nephrology",
year = "2022",
month = mar,
day = "7",
doi = "10.1016/j.kint.2022.02.019",
language = "English",
journal = "Kidney International",
issn = "0085-2538",
publisher = "Elsevier",
}