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Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II

BACKGROUND: Catheter‐based occlusion of patent ductus arteriosus (PDA) can be performed using different devices. Transvenous embolization using the Amplatzer vascular plug II (AVP‐II) has been studied in humans, but it has not been described in dogs. OBJECTIVE: Evaluate the feasibility and success o...

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Autores principales: Hildebrandt, Nicolai, Stosic, Andreas, Henrich, Estelle, Wiedemann, Nicola, Wurtinger, Gabriel, Schneider, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783350/
https://www.ncbi.nlm.nih.gov/pubmed/34914141
http://dx.doi.org/10.1111/jvim.16342
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author Hildebrandt, Nicolai
Stosic, Andreas
Henrich, Estelle
Wiedemann, Nicola
Wurtinger, Gabriel
Schneider, Matthias
author_facet Hildebrandt, Nicolai
Stosic, Andreas
Henrich, Estelle
Wiedemann, Nicola
Wurtinger, Gabriel
Schneider, Matthias
author_sort Hildebrandt, Nicolai
collection PubMed
description BACKGROUND: Catheter‐based occlusion of patent ductus arteriosus (PDA) can be performed using different devices. Transvenous embolization using the Amplatzer vascular plug II (AVP‐II) has been studied in humans, but it has not been described in dogs. OBJECTIVE: Evaluate the feasibility and success of transvenous embolization of PDA using the AVP‐II in dogs. ANIMALS: Nineteen client‐owned dogs with left‐to‐right shunting PDA, with minimal ductal diameter >2.5 mm. METHODS: Prospective observational study using AVP‐II with transvenous access for PDA closure in dogs. RESULTS: Angiography showed a conical ductus with a long (n = 17) or short (n = 2) ampulla. The minimal diameter of the duct was 4.34 ± 1.11 mm, and the maximal diameter of the ampulla was 13.18 ± 3.47 mm. Technical success was achieved in 18 of the 19 (94.7%) patients after the first intervention and in all 19 (100%) patients after the second intervention. Postrelease angiography documented complete occlusion of the PDA in 10 of 19 (52.6%) dogs. Mild flow acceleration or stenosis of the left pulmonary artery was found in 6 and 1 of the 17 analyzed cases, respectively, by Doppler examination. The closure rate 24 hours after intervention was 94.7% (18/19). The remaining dog had a moderate residual shunt, and delayed complete closure after 3 months led to a 100% closure rate. CONCLUSION AND CLINICAL IMPORTANCE: The AVP‐II is a safe and effective device for transvenous embolization in dogs with moderate to large PDA.
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spelling pubmed-87833502022-02-01 Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II Hildebrandt, Nicolai Stosic, Andreas Henrich, Estelle Wiedemann, Nicola Wurtinger, Gabriel Schneider, Matthias J Vet Intern Med SMALL ANIMAL BACKGROUND: Catheter‐based occlusion of patent ductus arteriosus (PDA) can be performed using different devices. Transvenous embolization using the Amplatzer vascular plug II (AVP‐II) has been studied in humans, but it has not been described in dogs. OBJECTIVE: Evaluate the feasibility and success of transvenous embolization of PDA using the AVP‐II in dogs. ANIMALS: Nineteen client‐owned dogs with left‐to‐right shunting PDA, with minimal ductal diameter >2.5 mm. METHODS: Prospective observational study using AVP‐II with transvenous access for PDA closure in dogs. RESULTS: Angiography showed a conical ductus with a long (n = 17) or short (n = 2) ampulla. The minimal diameter of the duct was 4.34 ± 1.11 mm, and the maximal diameter of the ampulla was 13.18 ± 3.47 mm. Technical success was achieved in 18 of the 19 (94.7%) patients after the first intervention and in all 19 (100%) patients after the second intervention. Postrelease angiography documented complete occlusion of the PDA in 10 of 19 (52.6%) dogs. Mild flow acceleration or stenosis of the left pulmonary artery was found in 6 and 1 of the 17 analyzed cases, respectively, by Doppler examination. The closure rate 24 hours after intervention was 94.7% (18/19). The remaining dog had a moderate residual shunt, and delayed complete closure after 3 months led to a 100% closure rate. CONCLUSION AND CLINICAL IMPORTANCE: The AVP‐II is a safe and effective device for transvenous embolization in dogs with moderate to large PDA. John Wiley & Sons, Inc. 2021-12-16 2022 /pmc/articles/PMC8783350/ /pubmed/34914141 http://dx.doi.org/10.1111/jvim.16342 Text en © 2021 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC. on behalf of the American College of Veterinary Internal Medicine. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle SMALL ANIMAL
Hildebrandt, Nicolai
Stosic, Andreas
Henrich, Estelle
Wiedemann, Nicola
Wurtinger, Gabriel
Schneider, Matthias
Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title_full Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title_fullStr Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title_full_unstemmed Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title_short Transvenous embolization of moderate to large patent ductus arteriosus in dogs using the Amplatzer vascular plug II
title_sort transvenous embolization of moderate to large patent ductus arteriosus in dogs using the amplatzer vascular plug ii
topic SMALL ANIMAL
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8783350/
https://www.ncbi.nlm.nih.gov/pubmed/34914141
http://dx.doi.org/10.1111/jvim.16342
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