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Updated: May 11, 2026

Imaging In-Stent Restenosis: An Inexpensive, Reliable, and Rapid Preclinical Model
Published on: September 14, 2009
Duplex Ultrasound in Evaluating Transplanted Renal Artery In-Stent Restenosis
Fu-Shun Pan1, Dao-Peng Yang1, Rong-Hai Deng2
1Department of Medical Ultrasonics, Institute of Diagnostic and Interventional Ultrasound, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Objective:
To evaluate the diagnosis performance of duplex ultrasound (DUS) in predicting transplanted renal artery (TRA) in-stent restenosis (ISR).
Methods:
In this retrospective study, 112 consecutive patients underwent stenting due to TRA stenosis. DUS were performed within 1 week after stenting for baseline value, and after ≥3 months follow-up for surveillance of ISR. The DUS measurements included peak systolic velocity (PSV) and PSV ratio of renal artery stent to iliac artery (RIR). Receiver operating characteristic (ROC) curves were applied to evaluate the diagnosis performance of DUS parameters in predicting ISR.
Results:
There were 69 patients (28 men; age, 38.3 ± 15.1 years) who obtained 92 adequate paired DUS and CTA after stenting, which were classified as ISR group (26 TRAs) and non-ISR group (66 TRAs). There was no difference between the two groups for baseline DUS features, including PSVB and RIRB. The late DUS features including stent PSVL (475.5 vs 261.9 cm/s), RIRL (4.10 vs 2.18), and stent PSVL/PSVB (2.72 vs 1.14) were significantly higher in the ISR group than the non-ISR group (all P < .0001). Stent PSVL, RIRL, and PSVL/PSVB demonstrated comparable AUCs in predicting ISR. However, the sensitivity and specificity of PSVL/PSVB in predicting ISR were 92.3 and 93.5%, respectively, demonstrating higher specificity with equivalent sensitivity than PSVL and higher sensitivity with equivalent specificity than RIRL.
Conclusions:
DUS is an accurate technique to identify TRA-ISR. We suggest all patients should undergo DUS immediately after stenting to establish baseline value and aid in evaluating ISR at late follow-up.
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