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The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery

INTRODUCTION: Percutaneous fetoscopic surgery is hampered by an increased risk of preterm prelabor rupture of membranes (PPROM). Recent surgical techniques have shown that suturing the chorioamniotic membranes following laparotomy and uterine exteriorization is associated with a lower risk of PPROM...

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Autores principales: Byju, Achu G., Diemer, Ashley, Luk, Christine, Heffernan, Michael J., Belfort, Michael A., Simons, Brian W., Koh, Chester J., Haridas, Balakrishna, Espinoza, Jimmy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691532/
https://www.ncbi.nlm.nih.gov/pubmed/35785761
http://dx.doi.org/10.1159/000525768
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author Byju, Achu G.
Diemer, Ashley
Luk, Christine
Heffernan, Michael J.
Belfort, Michael A.
Simons, Brian W.
Koh, Chester J.
Haridas, Balakrishna
Espinoza, Jimmy
author_facet Byju, Achu G.
Diemer, Ashley
Luk, Christine
Heffernan, Michael J.
Belfort, Michael A.
Simons, Brian W.
Koh, Chester J.
Haridas, Balakrishna
Espinoza, Jimmy
author_sort Byju, Achu G.
collection PubMed
description INTRODUCTION: Percutaneous fetoscopic surgery is hampered by an increased risk of preterm prelabor rupture of membranes (PPROM). Recent surgical techniques have shown that suturing the chorioamniotic membranes following laparotomy and uterine exteriorization is associated with a lower risk of PPROM compared to percutaneous in utero surgery. This study presents the ChorioAnchor, a novel resorbable device that percutaneously anchors the chorioamniotic membranes to the uterine wall. METHODS: Human factors testing and peel tests were used to simulate the worst-case in-use loading conditions, establishing the device strength requirements. Tensile testing was used to measure the time-zero strength of the device. Porcine cadaver testing was used to examine ultrasound visibility and acute handling characteristics. Short-term host response was examined through an acute 7-day implantation study in a rabbit model. RESULTS: With a time-zero tensile strength of 47 N, the ChorioAnchor exceeded the established 4 N strength requirement. Both the ChorioAnchor and delivery device were seen to be clearly visible under ultrasound imaging. Short-term host response to the device was well within the range expected for this type of device. CONCLUSION: The ChorioAnchor meets its engineering requirements in the early stages of implantation. Future studies will examine the kinetics of degradation of the device in vitro and in vivo.
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spelling pubmed-96915322023-07-04 The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery Byju, Achu G. Diemer, Ashley Luk, Christine Heffernan, Michael J. Belfort, Michael A. Simons, Brian W. Koh, Chester J. Haridas, Balakrishna Espinoza, Jimmy Fetal Diagn Ther Fetal Therapy INTRODUCTION: Percutaneous fetoscopic surgery is hampered by an increased risk of preterm prelabor rupture of membranes (PPROM). Recent surgical techniques have shown that suturing the chorioamniotic membranes following laparotomy and uterine exteriorization is associated with a lower risk of PPROM compared to percutaneous in utero surgery. This study presents the ChorioAnchor, a novel resorbable device that percutaneously anchors the chorioamniotic membranes to the uterine wall. METHODS: Human factors testing and peel tests were used to simulate the worst-case in-use loading conditions, establishing the device strength requirements. Tensile testing was used to measure the time-zero strength of the device. Porcine cadaver testing was used to examine ultrasound visibility and acute handling characteristics. Short-term host response was examined through an acute 7-day implantation study in a rabbit model. RESULTS: With a time-zero tensile strength of 47 N, the ChorioAnchor exceeded the established 4 N strength requirement. Both the ChorioAnchor and delivery device were seen to be clearly visible under ultrasound imaging. Short-term host response to the device was well within the range expected for this type of device. CONCLUSION: The ChorioAnchor meets its engineering requirements in the early stages of implantation. Future studies will examine the kinetics of degradation of the device in vitro and in vivo. S. Karger AG 2022-11 2022-07-04 /pmc/articles/PMC9691532/ /pubmed/35785761 http://dx.doi.org/10.1159/000525768 Text en The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission.
spellingShingle Fetal Therapy
Byju, Achu G.
Diemer, Ashley
Luk, Christine
Heffernan, Michael J.
Belfort, Michael A.
Simons, Brian W.
Koh, Chester J.
Haridas, Balakrishna
Espinoza, Jimmy
The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title_full The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title_fullStr The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title_full_unstemmed The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title_short The ChorioAnchor: Design and Testing of a Novel Chorioamniotic Anchoring Device to Enable Percutaneous Fetoscopic Surgery
title_sort chorioanchor: design and testing of a novel chorioamniotic anchoring device to enable percutaneous fetoscopic surgery
topic Fetal Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9691532/
https://www.ncbi.nlm.nih.gov/pubmed/35785761
http://dx.doi.org/10.1159/000525768
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