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Updated: Jun 8, 2025

Imaging In-Stent Restenosis: An Inexpensive, Reliable, and Rapid Preclinical Model
Published on: September 14, 2009
Diagnostic performance of CCTA and CTP imaging for clinically suspected in-stent restenosis: A meta-analysis
Jorge Dahdal1, Ruurt A Jukema2, Sharon Remmelzwaal3
1Department of Cardiology, Amsterdam Cardiovascular Sciences, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands; Departamento de Enfermedades Cardiovasculares, Clínica Alemana de Santiago, Facultad de Medicina, Clínica Alemana Universidad Del Desarrollo, Santiago, Chile.
Aims:
The objective of this study is to conduct a meta-analysis to assess the diagnostic performance of Coronary Computed Tomography Angiography (CCTA) and a hybrid approach that incorporates Computed Tomography Perfusion (CTP) in addition to CCTA (CCTA + CTP) for the detection of in-stent restenosis (ISR), as defined by angiography.
Methods:
A comprehensive search of articles identified 18,513 studies. After removing duplicates, title/abstract screening, and full-text review, 17 CCTA and 3 CCTA + CTP studies were included. Only studies using ≥64-slices multidetector computed tomography (CT) were considered eligible.
Results:
The per-patient ISR prevalence was 43 %, with 92 % of stents fully interpretable with CCTA. Meta-analysis exhibited a per-stent CCTA (n = 2674) sensitivity of 90 % (95 % CI; 84-94 %), specificity of 89 % (95 % CI; 86-92 %), positive likelihood ratio of 7.17 (95 % CI; 5.24-9.61), negative likelihood ratio of 0.17 (95 % CI; 0.10-0.25), and diagnostic odds ratio of 45.7 (95 % CI; 22.71-82.43). Additional sensitivity analyses revealed no influence of stent diameter or strut thickness on the diagnostic yield of CCTA. The per-stent diagnostic performance of CCTA + CTP (n = 752) did not show differences compared to CCTA.
Conclusions:
With currently utilized scanners, CCTA and CCTA + CTP demonstrated high diagnostic performance for in-stent restenosis evaluation. Consequently, a history of previous stent implantation should not be an argument to preclude using these methods in clinically suspected patients.
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