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Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation
INTRODUCTION: Bioresorbable stent has the theoretical advantage in the pediatric age group; however, experience in the literature is very limited. OBJECTIVES: This pilot study sought to evaluate the feasibility, safety, and performance of iron bioresorbable scaffold (IBS Angel™) as short-term pallia...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564399/ https://www.ncbi.nlm.nih.gov/pubmed/36246748 http://dx.doi.org/10.4103/apc.apc_187_21 |
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author | Mood, Marhisham Che Niazy, Khalil Ahmad Alwi, Mazeni Samion, Hasri Tiong, Koh Ghee Sivalingam, Sivakumar Zhang, Deyuan |
author_facet | Mood, Marhisham Che Niazy, Khalil Ahmad Alwi, Mazeni Samion, Hasri Tiong, Koh Ghee Sivalingam, Sivakumar Zhang, Deyuan |
author_sort | Mood, Marhisham Che |
collection | PubMed |
description | INTRODUCTION: Bioresorbable stent has the theoretical advantage in the pediatric age group; however, experience in the literature is very limited. OBJECTIVES: This pilot study sought to evaluate the feasibility, safety, and performance of iron bioresorbable scaffold (IBS Angel™) as short-term palliation in lesions with noncomplex patent ductus arteriosus (PDA). MATERIALS AND METHODS: Nine neonates with duct dependent but dual-source pulmonary blood flow (PBF) were included. Major stent-related complications, in-hospital course, stent patency up to 6 months, and unplanned re-interventions were studied, as well the percentage of stent material resorbed in patients in whom the stents were explanted at the surgery. RESULTS: IBS Angel™ was successfully implanted in all nine patients (mean weight range 3.4 ± 0.4 kg). Six were pulmonary atresia with an intact ventricular septum and 1 critical pulmonary stenosis patients where PDA stenting was done together or after balloon dilation. The mean procedure and fluoroscopy times were 89 ± 39 min and 16.3 ± 6.9 min, respectively. There were no major complications such as stent thrombosis or embolization and there were no in-hospital deaths. Post procedure overshunting and prolonged ventilatory support was a prominent feature. The median ventilation days was 3 (1–11 days). One patient died after 1 month due to respiratory syncytial virus pneumonia at the referring hospital. At 6 months follow-up, four had patent stents and four had blocked or restrictive stent flow. One patient received re-stenting at 4 months for restrictive stent flow. In three patients where microcomputed tomography of explanted stent was available, resorption of iron was 15% at 6 months and >65% at 16 months. CONCLUSIONS: Ductal stenting with IBS Angel™ is feasible and safe in selected patients. Because of early luminal loss, its use may be recommended for lesions with dual-source PBF with noncomplex PDA morphology that requires a short duration of palliation. |
format | Online Article Text |
id | pubmed-9564399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-95643992022-10-15 Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation Mood, Marhisham Che Niazy, Khalil Ahmad Alwi, Mazeni Samion, Hasri Tiong, Koh Ghee Sivalingam, Sivakumar Zhang, Deyuan Ann Pediatr Cardiol Original Article INTRODUCTION: Bioresorbable stent has the theoretical advantage in the pediatric age group; however, experience in the literature is very limited. OBJECTIVES: This pilot study sought to evaluate the feasibility, safety, and performance of iron bioresorbable scaffold (IBS Angel™) as short-term palliation in lesions with noncomplex patent ductus arteriosus (PDA). MATERIALS AND METHODS: Nine neonates with duct dependent but dual-source pulmonary blood flow (PBF) were included. Major stent-related complications, in-hospital course, stent patency up to 6 months, and unplanned re-interventions were studied, as well the percentage of stent material resorbed in patients in whom the stents were explanted at the surgery. RESULTS: IBS Angel™ was successfully implanted in all nine patients (mean weight range 3.4 ± 0.4 kg). Six were pulmonary atresia with an intact ventricular septum and 1 critical pulmonary stenosis patients where PDA stenting was done together or after balloon dilation. The mean procedure and fluoroscopy times were 89 ± 39 min and 16.3 ± 6.9 min, respectively. There were no major complications such as stent thrombosis or embolization and there were no in-hospital deaths. Post procedure overshunting and prolonged ventilatory support was a prominent feature. The median ventilation days was 3 (1–11 days). One patient died after 1 month due to respiratory syncytial virus pneumonia at the referring hospital. At 6 months follow-up, four had patent stents and four had blocked or restrictive stent flow. One patient received re-stenting at 4 months for restrictive stent flow. In three patients where microcomputed tomography of explanted stent was available, resorption of iron was 15% at 6 months and >65% at 16 months. CONCLUSIONS: Ductal stenting with IBS Angel™ is feasible and safe in selected patients. Because of early luminal loss, its use may be recommended for lesions with dual-source PBF with noncomplex PDA morphology that requires a short duration of palliation. Wolters Kluwer - Medknow 2022 2022-08-19 /pmc/articles/PMC9564399/ /pubmed/36246748 http://dx.doi.org/10.4103/apc.apc_187_21 Text en Copyright: © 2022 Annals of Pediatric Cardiology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Mood, Marhisham Che Niazy, Khalil Ahmad Alwi, Mazeni Samion, Hasri Tiong, Koh Ghee Sivalingam, Sivakumar Zhang, Deyuan Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title | Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title_full | Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title_fullStr | Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title_full_unstemmed | Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title_short | Feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
title_sort | feasibility, safety, and efficacy of iron bioresorbable scaffold in neonates with duct-dependent pulmonary circulation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564399/ https://www.ncbi.nlm.nih.gov/pubmed/36246748 http://dx.doi.org/10.4103/apc.apc_187_21 |
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