Why the study?
The accepted <65 μm fibrous cap thickness threshold was derived from postmortem studies and may not be appropriate for in vivo rupture-prone plaques.
What is the in vivo critical fibrous cap thickness for rupture-prone coronary plaques assessed by OCT?
What is the in vivo critical fibrous cap thickness for rupture-prone coronary plaques assessed by OCT?
In vivo OCT assessment suggests that the critical fibrous cap thickness for rupture-prone plaques is <80 μm for the thinnest cap and <188 μm for the most representative cap, extending beyond the traditional <65 μm postmortem threshold.
Answers are grounded in this paper and cite their sources.
May warrant higher OCT thresholds than 65 μm for identifying rupture-prone plaques; leaves open the optimal in vivo cutoff for risk stratification.
AIMS: The widely accepted threshold of <65 μm for coronary plaque fibrous cap thickness was derived from postmortem studies of ruptured plaques and may not be appropriate for in vivo rupture-prone plaques. We investigated the relationship between fibrous cap thickness and plaque rupture using optical coherence tomography (OCT). METHODS AND RESULTS: We studied 266 lesions (103 from patients with acute coronary syndrome and 163 from patients with stable angina) before percutaneous coronary intervention using OCT. Ruptured and non-ruptured lipid-rich plaques were identified and the thinnest and most representative fibrous cap thickness were determined. Cap thickness was reliably measured in 71 ruptured and 111 non-ruptured plaques. From the ruptured plaques, the median thinnest cap thickness was 54 μm (50-60). The median most representative cap thickness was 116 μm (103-136). For non-ruptured plaques, the median thinnest cap thickness was 80 μm (67-104) and 182 μm (156-216) for most representative cap thickness. In 95% of ruptured plaques, the thinnest cap thickness and most representative cap thickness were <80 and <188 μm, respectively. The best cut-offs for predicting rupture were <67 μm (OR: 16.1, CI: 7.5-34.4, P < 0.001) for the thinnest cap thickness and <151 μm (OR: 35.6, CI: 15.0-84.3, P < 0.001) for most representative cap thickness. These two measures were modestly correlated (r(2) = 0.39) and both independently associated with rupture. CONCLUSION: In vivo critical cap thicknesses were <80 μm for the thinnest and <188 μm for most representative fibrous cap thickness. Prospective imaging studies are required to establish the significance of these values.
No takes yet. Share an insight, caveat, or question.
Yonetsu et al. (2011) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: