Objective: The use of duplex ultrasound (DUS) examinations for surveillance after fenestrated endovascular aneurysm repair (FEVAR) is not well-studied. Our objective was to further characterize normal and abnormal duplex findings in renal branch grafts after FEVAR. Methods: We retrospectively reviewed a single-center experience involving consecutive patients treated with Cook ZFEN devices between 2012 and 2017. Postoperative imaging consisted of a computed tomography (CT) scan at 1 month, 6 months, 1 year, and annually thereafter. As experienced progressed, DUS examination with or without concurrent CT scans were obtained in a nonstandardized protocol, particularly for patients with decreased renal function. Renal patency loss was defined as occlusion or stenosis of greater than 50% evaluated on 3-day renal artery center-line imaging. Results: A total of 116 patients were treated with FEVAR, of which 60 (51.7%) had concurrent CT and renal DUS images available for review. Six patients (10%) had limited ultrasound studies owing to bowel gas and were excluded. The study cohort therefore included 54 patients receiving of 94 renal fenestrated stents with a mean follow-up of 23 months. Twelve cases of renal patency loss in 10 patients (9 stenoses, 3 occlusions) were found on CT scanning, 11 (91.6%) of which had concurrent abnormalities found on ultrasound examination. Stents with compression at the junction of the main body exhibited significantly elevated mean Peak systolic velocities (PSV) compared with nonstenosed stents (349.2 cm/s vs 115.3 cm/s; P = .003). Stenosis in the most proximal portion of the stent (ie, within the main body) showed no difference in proximal PSV (86.0 cm/s vs 131.9 cm/s; P = .257); however, dampened PSV showed significant differences in the mid (17.5 cm/s vs 109.9 cm/s; P = .027) and distal (19.0 cm/s vs 78.3 cm/s; P = .028) segments compared with nonstenosed stents. All occluded stents demonstrated no flow detection. Proximal PSV served as a strong classifier for junctional stenosis (area under the curve, 0.98). A combined criterion of proximal PSV of greater than 215 cm/s or distal PSV of less than 25 cm/s resulted in a sensitivity of 91.6% and specificity of 85.3% for detecting patency loss. All stents that were compromised underwent successful secondary reintervention and restoration of patency. Conclusions: DUS imaging is a clinically useful modality for surveillance of renal branch grafts after FEVAR. Patterns of segmental velocity elevation (proximal PSV, >215 cm/s) and dampening in the distal renal indicate potential hemodynamic compromise and should prompt more aggressive workup or imaging and likely be considered for secondary intervention.
机构:
Gunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
Schaeffer, Jacob S.
Shakhnovich, Irina
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Gundersen Hlth Syst, Dept Gen & Vasc Surg, 1900 South Ave,C05-001, La Crosse, WI 54601 USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
Shakhnovich, Irina
Sieck, Kyle N.
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Gunderson Med Fdn, Dept Med Res, La Crosse, WI USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
Sieck, Kyle N.
Kallies, Kara J.
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Gunderson Med Fdn, Dept Med Res, La Crosse, WI USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
Kallies, Kara J.
Davis, Clark A.
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Gundersen Hlth Syst, Dept Gen & Vasc Surg, 1900 South Ave,C05-001, La Crosse, WI 54601 USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
Davis, Clark A.
Cogbill, Thomas H.
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Gundersen Hlth Syst, Dept Gen & Vasc Surg, 1900 South Ave,C05-001, La Crosse, WI 54601 USAGunderson Med Fdn, Dept Med Educ, Gen Surg Residency, La Crosse, WI USA
机构:
Stanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USAStanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USA
Kenneth Tran
Fajardo, Andres
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Indiana Univ, Div Vasc Surg, Indianapolis, IN 46204 USAStanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USA
Fajardo, Andres
Ullery, Brant W.
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Stanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USAStanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USA
Ullery, Brant W.
Goltz, Christopher
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Indiana Univ, Div Vasc Surg, Indianapolis, IN 46204 USAStanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USA
Goltz, Christopher
Lee, Jason T.
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Stanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USAStanford Univ, Med Ctr, Div Vasc Surg, 300 Pasteur Dr,Ste H3600, Stanford, CA 94305 USA
机构:
CHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Royal Free London NHS Fdn Trust, Aort Team, London, EnglandCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Maurel, B.
Lounes, Y.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Lounes, Y.
Amako, M.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Amako, M.
Fabre, D.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Fabre, D.
Hertault, A.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Hertault, A.
Sobocinski, J.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Sobocinski, J.
Spear, R.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Spear, R.
Azzaoui, R.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Azzaoui, R.
Mastracci, T. M.
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Royal Free London NHS Fdn Trust, Aort Team, London, EnglandCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France
Mastracci, T. M.
Haulon, S.
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CHRU Lille, Hop Cardiol, Aort Ctr, Lille, FranceCHRU Lille, Hop Cardiol, Aort Ctr, Lille, France