The Relationship Between Cardiac Troponin in People Hospitalised for Exacerbation of COPD and Major Adverse Cardiac Events (MACE) and COPD Readmissions

Constantinos Kallis; Amit Kaura; Nathan A Samuel; Abdulrahim Mulla; Ben Glampson; Kevin O'Gallagher; Jim Davies; Dimitri Papadimitriou; Kerrie J Woods; Anoop D Shah; Bryan Williams; Folkert W Asselbergs; Erik K Mayer; Richard W Lee; Christopher Herbert; Stuart W Grant; Nick Curzen; Iain B Squire; Thomas Johnson; Ajay M Shah; Divaka Perera; Rajesh K Kharbanda; Riyaz S Patel; Keith M Channon; Jamil Mayet; Jennifer K Quint

doi:10.2147/COPD.S432166

The Relationship Between Cardiac Troponin in People Hospitalised for Exacerbation of COPD and Major Adverse Cardiac Events (MACE) and COPD Readmissions

Int J Chron Obstruct Pulmon Dis. 2023 Nov 6:18:2405-2416. doi: 10.2147/COPD.S432166. eCollection 2023.

Authors

Constantinos Kallis^{1

2

3}, Amit Kaura^{1

3}, Nathan A Samuel⁴, Abdulrahim Mulla³, Ben Glampson³, Kevin O'Gallagher⁵, Jim Davies⁴, Dimitri Papadimitriou³, Kerrie J Woods⁴, Anoop D Shah^{6

7}, Bryan Williams^{6

7}, Folkert W Asselbergs^{6

7}, Erik K Mayer^{3

8}, Richard W Lee^{1

9}, Christopher Herbert¹⁰, Stuart W Grant¹¹, Nick Curzen¹², Iain B Squire¹³, Thomas Johnson¹⁴, Ajay M Shah¹⁵, Divaka Perera⁵, Rajesh K Kharbanda⁴, Riyaz S Patel⁶, Keith M Channon⁴, Jamil Mayet^{1

3}, Jennifer K Quint^{1

2

3}

Affiliations

¹ National Heart and Lung Institute, Imperial College London, London, UK.
² School of Public Health, Imperial College London, London, UK.
³ NIHR Imperial Biomedical Research Centre, Imperial College London and Imperial College Healthcare NHS Trust, London, UK.
⁴ NIHR Oxford Biomedical Research Centre, University of Oxford and Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
⁵ NIHR King's Biomedical Research Centre, King's College London and King's College Hospital NHS Foundation Trust, London, UK.
⁶ NIHR University College London Biomedical Research Centre, University College London and University College London Hospitals NHS Foundation Trust, London, UK.
⁷ Institute of Health Informatics, University College London, London, UK.
⁸ Imperial Clinical Analytics, Research & Evaluation (iCARE) and Department of Surgery & Cancer, Imperial College London, London, UK.
⁹ Early Diagnosis and Detection Centre, NIHR BRC at The Royal Marsden and Institute of Cancer Research, London, UK.
¹⁰ NIHR Leeds Clinical Research Facility, Leeds Teaching Hospitals Trust and University of Leeds, Leeds, UK.
¹¹ NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust and the University of Manchester, Manchester, UK.
¹² NIHR Southampton Clinical Research Facility and Biomedical Research Centre, Faculty of Medicine, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, UK.
¹³ NIHR Leicester Biomedical Research Centre, Glenfield Hospital, and Department of Cardiovascular Sciences, University of Leicester, Leicester, UK.
¹⁴ NIHR Bristol Biomedical Research Centre, University of Bristol and University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
¹⁵ NIHR Guys & St Thomas' Hospital Clinical Research Facility, King's College Hospital, and King's College London British Heart Foundation Centre of Excellence, London, UK.

Abstract

Background: No single biomarker currently risk stratifies chronic obstructive pulmonary disease (COPD) patients at the time of an exacerbation, though previous studies have suggested that patients with elevated troponin at exacerbation have worse outcomes. This study evaluated the relationship between peak cardiac troponin and subsequent major adverse cardiac events (MACE) including all-cause mortality and COPD hospital readmission, among patients admitted with COPD exacerbation.

Methods: Data from five cross-regional hospitals in England were analysed using the National Institute of Health Research Health Informatics Collaborative (NIHR-HIC) acute coronary syndrome database (2008-2017). People hospitalised with a COPD exacerbation were included, and peak troponin levels were standardised relative to the 99th percentile (upper limit of normal). We used Cox Proportional Hazard models adjusting for age, sex, laboratory results and clinical risk factors, and implemented logarithmic transformation (base-10 logarithm). The primary outcome was risk of MACE within 90 days from peak troponin measurement. Secondary outcome was risk of COPD readmission within 90 days from peak troponin measurement.

Results: There were 2487 patients included. Of these, 377 (15.2%) patients had a MACE event and 203 (8.2%) were readmitted within 90 days from peak troponin measurement. A total of 1107 (44.5%) patients had an elevated troponin level. Of 1107 patients with elevated troponin at exacerbation, 256 (22.8%) had a MACE event and 101 (9.0%) a COPD readmission within 90 days from peak troponin measurement. Patients with troponin above the upper limit of normal had a higher risk of MACE (adjusted HR 2.20, 95% CI 1.75-2.77) and COPD hospital readmission (adjusted HR 1.37, 95% CI 1.02-1.83) when compared with patients without elevated troponin.

Conclusion: An elevated troponin level at the time of COPD exacerbation may be a useful tool for predicting MACE in COPD patients. The relationship between degree of troponin elevation and risk of future events is complex and requires further investigation.

Keywords: COPD; CVD; exacerbation.

MeSH terms

Cardiovascular Diseases* / etiology
Hospitalization
Humans
Patient Readmission
Pulmonary Disease, Chronic Obstructive*
Troponin

Substances

Troponin

Abstract

MeSH terms

Substances

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