Stable angina remains a high-risk diagnosis in patients with recent-onset symptoms, highlighting the need for larger population-based studies to define prognostic differences across phenotypes.
Highlights the discrepancy in stable angina prognosis between clinical trials and real-world cohorts, calling for larger population studies with higher endpoint resolution.
The prognosis of angina was described as "unhappy" by the Framingham investigators and as little different from that of 1-year survivors of acute myocardial infarction. Yet recent clinical trials now report that angina has a good prognosis with adverse outcomes reduced to "normal levels". These disparate prognostic assessments may not be incompatible, applying as they do to population cohorts (Framingham) and selected participants in clinical trials. Comparisons between studies are further complicated by the absence of agreed case definitions for stable angina (contrast this with acute coronary syndromes). Our recent data show that for patients with recent onset symptoms attending chest pain clinics, angina remains a high-risk diagnosis and although many patients receive symptomatic benefit from revascularisation, prognosis is usually unaffected. This leaves little room for complacency and, with angina the commonest initial manifestation of coronary artery disease, there is the opportunity for early detection, risk stratification and treatment to modify outcomes. Meanwhile, larger population-based studies are needed to define the patient journey from earliest presentation through the various syndrome transitions to coronary or noncardiac death in order to increase understanding of the aetiological and prognostic differences between the different coronary disease phenotypes.
Timmis et al. (Mon,) conducted a editorial in Stable angina pectoris. Stable angina remains a high-risk diagnosis in patients with recent-onset symptoms, highlighting the need for larger population-based studies to define prognostic differences across phenotypes.
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