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Published on: December 11, 2017
Practical Graft Sizing Strategy Based on True Lumen Diameter Distal to the LSA in Fenestrated Frozen Elephant Trunk
Norimasa Haijima1, Mikihiko Kudo1, Satoru Murata1
1Department of Cardiovascular Surgery, National Hospital Organization Saitama Hospital, Saitama, Japan.
Background:
We aimed to describe a pragmatic graft-sizing strategy for fenestrated frozen elephant trunk procedures that aligns the sizing index with the proximal sealing or transition zone using the true lumen (TL) long-axis immediately distal to the left subclavian artery (LSA). This approach was evaluated against a pre-specified comparator at the seventh thoracic vertebral level (Th7).
Methods:
In this single-center retrospective cohort study (N = 24), the Frozenix graft diameter was determined by matching the device size to the LSA TL long-axis on centerline-orthogonal computed tomography. A virtual Th7 comparator was defined as the equivalent diameter (circumference/π) × 0.9, with sensitivity assessed using the Th7 long-axis × 0.9. The primary outcome was the agreement proportion (|Δ%|≤10%) between the actual and virtual sizes. Interobserver reliability was evaluated using the intraclass correlation coefficient (ICC; 2, 1) and Bland-Altman analysis. Safety outcomes included the type Ia endoleak, stent-graft-induced new entry (SINE), and staged thoracic endovascular aortic repair (TEVAR).
Results:
The median age of the cohort was 61.0 years (interquartile range (IQR): 56.0-66.0), and 66.7% were men. The median follow-up period was 682.0 days. The most frequently used graft size was 27 mm. Agreement between the actual and virtual Th7 (equivalent × 0.9) diameters was 4.2%, with a median Δ% of 30.5% (IQR: 18.3-39.5%), indicating systematic undersizing. Th7 diameter increased postoperatively, consistent with downstream remodeling. All staged TEVARs were preplanned (14/14, 100%). No type Ia endoleak or SINE occurred. Interobserver reliability was excellent (ICC: 0.98-0.99).
Conclusion:
LSA-based sizing appears simple, reproducible, and anatomically aligned, warranting prospective multicenter validation.

