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Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study
PURPOSE: Thoracic central venous obstruction is commonly associated with the use of central venous catheters. The Surfacer System to Facilitate Access in Venous Occlusions Study was an Food and Drug Administration–approved US Investigational Device Exemption study designed to evaluate the performanc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897784/ https://www.ncbi.nlm.nih.gov/pubmed/32597356 http://dx.doi.org/10.1177/1129729820937121 |
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author | Razavi, Mahmood K Peden, Eric K Sorial, Ehab Ross, John R Aruny, John E Pflederer, Timothy A Wasse, Haimanot Haskal, Ziv J |
author_facet | Razavi, Mahmood K Peden, Eric K Sorial, Ehab Ross, John R Aruny, John E Pflederer, Timothy A Wasse, Haimanot Haskal, Ziv J |
author_sort | Razavi, Mahmood K |
collection | PubMed |
description | PURPOSE: Thoracic central venous obstruction is commonly associated with the use of central venous catheters. The Surfacer System to Facilitate Access in Venous Occlusions Study was an Food and Drug Administration–approved US Investigational Device Exemption study designed to evaluate the performance and safety of the Surfacer System when used to facilitate central venous access in patients with thoracic central venous obstruction. METHODS: Thirty patients were enrolled in this prospective, multicenter, single-arm study between December 2017 and May 2019. Device performance and adverse events were collected peri-procedurally and at discharge. Enrollment included 15 female and 15 male subjects with a mean age of 55.5 ± 12.9 (range: 30–79) years. Twenty-eight patients (93.3%) required central venous access for hemodialysis access. Locations of thoracic central venous obstruction were graded from 1 to 4 based on severity and extension of venous occlusions. Seven patients (23.3%) had type 1, 6 (20.0%) type 2, 16 (53.3%) type 3, and 1 (3.3%) type 4 obstruction. RESULTS: Successful central venous catheter placement was achieved in 27 of 30 patients (90.0%). The procedure was discontinued in three (10.0%) due to tortuous anatomy discovered intraprocedurally. All 27 patients with successful CVC placement achieved adequate catheter patency and tip positioning with a mean overall procedural time and time to achieve central venous access with the Surfacer System being 44.1 ± 30.6 and 19.1 ± 25.1 min, respectively. There were no device-related adverse events or catheter malposition. CONCLUSION: The results of the SAVEUS Study confirm the safety and efficacy of the Surfacer System and the Inside-Out procedure when used for the placement of right-sided central venous access in patients with thoracic central venous obstruction. |
format | Online Article Text |
id | pubmed-7897784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-78977842021-03-10 Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study Razavi, Mahmood K Peden, Eric K Sorial, Ehab Ross, John R Aruny, John E Pflederer, Timothy A Wasse, Haimanot Haskal, Ziv J J Vasc Access Original Research Articles PURPOSE: Thoracic central venous obstruction is commonly associated with the use of central venous catheters. The Surfacer System to Facilitate Access in Venous Occlusions Study was an Food and Drug Administration–approved US Investigational Device Exemption study designed to evaluate the performance and safety of the Surfacer System when used to facilitate central venous access in patients with thoracic central venous obstruction. METHODS: Thirty patients were enrolled in this prospective, multicenter, single-arm study between December 2017 and May 2019. Device performance and adverse events were collected peri-procedurally and at discharge. Enrollment included 15 female and 15 male subjects with a mean age of 55.5 ± 12.9 (range: 30–79) years. Twenty-eight patients (93.3%) required central venous access for hemodialysis access. Locations of thoracic central venous obstruction were graded from 1 to 4 based on severity and extension of venous occlusions. Seven patients (23.3%) had type 1, 6 (20.0%) type 2, 16 (53.3%) type 3, and 1 (3.3%) type 4 obstruction. RESULTS: Successful central venous catheter placement was achieved in 27 of 30 patients (90.0%). The procedure was discontinued in three (10.0%) due to tortuous anatomy discovered intraprocedurally. All 27 patients with successful CVC placement achieved adequate catheter patency and tip positioning with a mean overall procedural time and time to achieve central venous access with the Surfacer System being 44.1 ± 30.6 and 19.1 ± 25.1 min, respectively. There were no device-related adverse events or catheter malposition. CONCLUSION: The results of the SAVEUS Study confirm the safety and efficacy of the Surfacer System and the Inside-Out procedure when used for the placement of right-sided central venous access in patients with thoracic central venous obstruction. SAGE Publications 2020-06-27 2021-01 /pmc/articles/PMC7897784/ /pubmed/32597356 http://dx.doi.org/10.1177/1129729820937121 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Articles Razavi, Mahmood K Peden, Eric K Sorial, Ehab Ross, John R Aruny, John E Pflederer, Timothy A Wasse, Haimanot Haskal, Ziv J Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title | Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title_full | Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title_fullStr | Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title_full_unstemmed | Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title_short | Efficacy and safety associated with the use of the Surfacer(®) Inside-Out(®) Access Catheter System: Results from a prospective, multicenter Food and Drug Administration–approved Investigational Device Exemption study |
title_sort | efficacy and safety associated with the use of the surfacer(®) inside-out(®) access catheter system: results from a prospective, multicenter food and drug administration–approved investigational device exemption study |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7897784/ https://www.ncbi.nlm.nih.gov/pubmed/32597356 http://dx.doi.org/10.1177/1129729820937121 |
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