Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy

BACKGROUND: Nintedanib (previously known as BBIF 1120) was approved by the United States Food and Drug Administration and European Medical Agency to treat idiopathic lung fibrosis in the year 2014 and 2015, respectively. It is now gaining interest for its anti-fibrotic activity in other organs and d...

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Main Authors: Sourav Mathur, Indrani Hazra, Aditya Konar, Sarbani Hazra
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2024-12-01
Series:International Journal of Abdominal Wall and Hernia Surgery
Subjects:
Online Access:https://doi.org/10.4103/ijawhs.ijawhs_41_24
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author Sourav Mathur
Indrani Hazra
Aditya Konar
Sarbani Hazra
author_facet Sourav Mathur
Indrani Hazra
Aditya Konar
Sarbani Hazra
author_sort Sourav Mathur
collection DOAJ
description BACKGROUND: Nintedanib (previously known as BBIF 1120) was approved by the United States Food and Drug Administration and European Medical Agency to treat idiopathic lung fibrosis in the year 2014 and 2015, respectively. It is now gaining interest for its anti-fibrotic activity in other organs and disease conditions. Although a surgical mesh is used as a mainstay therapy for herniorrhaphy, postoperative peritoneal adhesion with a polypropylene mesh is a significant drawback. This study aims to assess the efficacy of nintedanib in preventing postoperative adhesion incited with a polypropylene mesh in a rabbit model of ventral hernia. MATERIALS AND METHODS: Ventral hernia was induced surgically in ten adult healthy New Zealand White rabbits of either sex. Hernioplasty was performed with a polypropylene mesh, and the rabbits were randomly allocated into two groups to receive either oral 1 mL sterile water or 100 mg nintedanib in 1 mL of sterile water for 7 days. The adhesion of the implanted mesh with the intra-abdominal organs was assessed clinically, by histological and ultrastructural studies with scanning electron microscopy (SEM) at 30 days postoperatively. RESULTS: All rabbits were clinically healthy for 30 days post-surgery with no complication at the site of surgery. The incidence of peritoneal adhesion and tenacity was less in the nintedanib group versus the control group (P = 0.00105). Histopathological and SEM evaluations also indicated less fibrosis and adhesion in the nintedanib-treated group versus control. CONCLUSION: Our results show successful prevention of mesh-associated adhesion with nintedanib, but further studies on the mechanistic pathway, pharmacokinetics, dose standardization, and evaluation of systemic side effects are warranted.
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series International Journal of Abdominal Wall and Hernia Surgery
spelling doaj-art-109cd7103f6846d2948d3defaf40570a2025-01-17T10:51:27ZengWolters Kluwer Medknow PublicationsInternational Journal of Abdominal Wall and Hernia Surgery2589-87362589-80782024-12-017416016410.4103/ijawhs.ijawhs_41_24Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphySourav MathurIndrani HazraAditya KonarSarbani HazraBACKGROUND: Nintedanib (previously known as BBIF 1120) was approved by the United States Food and Drug Administration and European Medical Agency to treat idiopathic lung fibrosis in the year 2014 and 2015, respectively. It is now gaining interest for its anti-fibrotic activity in other organs and disease conditions. Although a surgical mesh is used as a mainstay therapy for herniorrhaphy, postoperative peritoneal adhesion with a polypropylene mesh is a significant drawback. This study aims to assess the efficacy of nintedanib in preventing postoperative adhesion incited with a polypropylene mesh in a rabbit model of ventral hernia. MATERIALS AND METHODS: Ventral hernia was induced surgically in ten adult healthy New Zealand White rabbits of either sex. Hernioplasty was performed with a polypropylene mesh, and the rabbits were randomly allocated into two groups to receive either oral 1 mL sterile water or 100 mg nintedanib in 1 mL of sterile water for 7 days. The adhesion of the implanted mesh with the intra-abdominal organs was assessed clinically, by histological and ultrastructural studies with scanning electron microscopy (SEM) at 30 days postoperatively. RESULTS: All rabbits were clinically healthy for 30 days post-surgery with no complication at the site of surgery. The incidence of peritoneal adhesion and tenacity was less in the nintedanib group versus the control group (P = 0.00105). Histopathological and SEM evaluations also indicated less fibrosis and adhesion in the nintedanib-treated group versus control. CONCLUSION: Our results show successful prevention of mesh-associated adhesion with nintedanib, but further studies on the mechanistic pathway, pharmacokinetics, dose standardization, and evaluation of systemic side effects are warranted.https://doi.org/10.4103/ijawhs.ijawhs_41_24adhesionhernianintedanibpolypropylene meshprevention
spellingShingle Sourav Mathur
Indrani Hazra
Aditya Konar
Sarbani Hazra
Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
International Journal of Abdominal Wall and Hernia Surgery
adhesion
hernia
nintedanib
polypropylene mesh
prevention
title Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
title_full Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
title_fullStr Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
title_full_unstemmed Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
title_short Nintedanib alleviates polypropylene mesh-induced adhesion in rabbit ventral herniorrhaphy
title_sort nintedanib alleviates polypropylene mesh induced adhesion in rabbit ventral herniorrhaphy
topic adhesion
hernia
nintedanib
polypropylene mesh
prevention
url https://doi.org/10.4103/ijawhs.ijawhs_41_24
work_keys_str_mv AT souravmathur nintedaniballeviatespolypropylenemeshinducedadhesioninrabbitventralherniorrhaphy
AT indranihazra nintedaniballeviatespolypropylenemeshinducedadhesioninrabbitventralherniorrhaphy
AT adityakonar nintedaniballeviatespolypropylenemeshinducedadhesioninrabbitventralherniorrhaphy
AT sarbanihazra nintedaniballeviatespolypropylenemeshinducedadhesioninrabbitventralherniorrhaphy