Published online Dec 26, 2021. doi: 10.4330/wjc.v13.i12.745
Peer-review started: August 26, 2021
First decision: October 17, 2021
Revised: October 23, 2021
Accepted: December 3, 2021
Article in press: December 3, 2021
Published online: December 26, 2021
Processing time: 124 Days and 15.9 Hours
Evaluation of suspected stable angina patients with probable coronary artery disease (CAD) in the community is challenging. In the United Kingdom, patients with suspected stable angina are referred by community physicians to be assessed by specialists within the hospital system in rapid access chest pain clinics (RACPC). The role of a highly sensitive troponin I (uscTnI) assay in the diagnosis of suspected CAD in a RACPC in a “real-life” setting in a non-academic hospital has not been explored.
To examine the diagnostic value of uscTnI (detection limit 0.12 ng/L, upper reference range 8.15 ng/L, and detected uscTnI in 96.8% of the reference population), in the evaluation of stable CAD in a non-selected patient group, with several co-morbidities, who presented to the RACPC.
One hundred and seventy two RACPC patients were assigned to either functional or anatomical testing according to the hospital protocol.
The investigations offered to patients were exercise tolerance test 7.6%, 24 h ECG 1.2%, Echocardiogram 14.5%, stress echocardiogram 8.1%, coronary computed tomography angiography (CCTA) 12.8%, coronary angiogram 13.4%, 17.4% were diagnosed with non-cardiac chest pain, 3.5% treated as stable angina, 8.2% reviewed by cardiologists, electronic medical records were not available in 10.4%. Receiver operating characteristic curves for CAD used uscTnI values measured in patients who underwent functional testing, angiogram or CCTA. Values > 0.52 ng/L showed 100% sensitivity and at > 11.6 ng/L showed 100% specificity. In the range > 0.52-11.6 ng/L, uscTnI may not have the same diagnostic potential. In patients assigned to coronary angiogram higher concentrations of uscTnI was associated with severe CAD. Low levels of uscTnI and low pre-test probability of CAD (QRISK3) may decrease patient numbers assigned to CCTA.
The uscTnI diagnostic cut-off values in a RACPC will depend on patient population and their presenting co-morbidity. In the presence of clinical comorbidities and previous CAD the uscTnI needs to be used in conjunction with clinical assessment.
Core Tip: In the United Kingdom, patients with suspected stable angina are referred to rapid access chest pain clinic (RACPC) by community physicians for assessment by hospital specialist medical practitioners. We evaluated the value of a new highly sensitive cardiac troponin I assay in the management of patients with suspected coronary artery disease (CAD) in a RACPC. Patients admitted for further assessment and preselected for either coronary computed tomography angiography or coronary angiogram the assay may indicate the severity of CAD. The diagnostic cut-off values of the assay is determined by the patient population and existing co-morbidities.