CLINICAL: VH IVUS Clinical Paper Summaries

VH IVUS / PROSPECT

Providing Regional Observations to Study Predictors of Events in the Coronary Tree (PROSPECT).

Stone GW, Serruys P, de Bruyne B.

TCT 2009

OBJECTIVES:

Prospective assessment of the event rate attributable to the progression of vulnerable plaque.

METHODS:
  • 697 patients
  • 40 European and U.S. cen-ters
  • IVUS and Virtual Histology post PCI on the 3 primary coronary arteries
  • Prospective registry of acute coronary syndromes (ACS) patients

SUMMARY:
  • Approximately 20 % of patients with ACS successfully treated with stents and contemporary medical Rx develop MACE within 3 years.
  • Approximately 12 % of patients develop MACE from non culprit lesions during 3 years of follow-up.
  • While plaques which are responsible for unanticipated future MACE are frequently angiographically mild, most untreated plaques which become symptomatic have a large plaque burden and a small lumen area.
  • The patients had on average 0.83 lesions with < 4 mm² MLA that were left untreated.
  • The prospective identification of non culprit lesions prone to develop MACE within 3 years can be enhanced by characterization of underlying plaque morphology with virtual histology, with VH-TCFAs representing the highest risk lesion type.
  • In 52 % of the patients at least one VH thin-cap fibroatheroma (TCFA) that was left behind was identified.
  • The combination of large plaque burden by IVUS and large necrotic core without visible cap (VH-TCFA) identifies high risk lesions for MACE (15.3 %) within 3 years.
  • The combination of large plaque burden by IVUS and pathological intimal thickening (PIT) has a lower risk for MACE within 3 years compared to high plaque burden lesions in general (2.6 % vs. 9.2 %).

CONCLUSIONS:

The highest risk plaque type is VH thin-cap fibroatheroma (VH-TCFA) with a minimum lumen area of ≤ 4 mm² and a plaque burden ≥ 70 %. The current practice of using angiography alone cannot measure plaque burden or the presence of VH-TCFAs, which were the two most signifi-cant predictors of lesion risk for events within 3 years. The plaque type pathological intimal thickening (PIT) with a plaque burden of ≥ 70 % is associated with a reduced risk of MACE.

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