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Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy
Objectives: To analyze the efficacy and tolerability of diflunisal for the treatment of acquired amyloid neuropathy in domino liver transplant recipients. Methods: We performed a retrospective longitudinal study of prospectively collected data for all domino liver transplant recipients with acquired...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044119/ https://www.ncbi.nlm.nih.gov/pubmed/35497887 http://dx.doi.org/10.3389/ti.2022.10454 |
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author | Nedkova-Hristova, Velina Baliellas, Carmen González-Costello, José Lladó, Laura González-Vilatarsana, Emma Vélez-Santamaría, Valentina Casasnovas, Carlos |
author_facet | Nedkova-Hristova, Velina Baliellas, Carmen González-Costello, José Lladó, Laura González-Vilatarsana, Emma Vélez-Santamaría, Valentina Casasnovas, Carlos |
author_sort | Nedkova-Hristova, Velina |
collection | PubMed |
description | Objectives: To analyze the efficacy and tolerability of diflunisal for the treatment of acquired amyloid neuropathy in domino liver transplant recipients. Methods: We performed a retrospective longitudinal study of prospectively collected data for all domino liver transplant recipients with acquired amyloid neuropathy who received diflunisal at our hospital. Neurological deterioration was defined as an score increase of ≥2 points from baseline on the Neurological Impairment Scale/Neurological Impairment Scale-Lower Limbs. Results: Twelve patients who had received compassionate use treatment with diflunisal were identified, of whom seven had follow-up data for ≥12 months. Five patients (71.4%) presented with neurological deterioration on the Neurological Impairment Scale after 12 months (p = 0.0382). The main adverse effects were cardiovascular and renal, leading to diflunisal being stopped in five patients and the dose being reduced in two patients. Conclusion: Our study suggests that most domino liver transplant recipients with acquired amyloid neuropathy will develop neurological deterioration by 12 months of treatment with diflunisal. This therapy was also associated with a high incidence of adverse effects and low treatment retention. The low efficacy and low tolerability of diflunisal treatment encourage the search for new therapeutic options. |
format | Online Article Text |
id | pubmed-9044119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90441192022-04-28 Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy Nedkova-Hristova, Velina Baliellas, Carmen González-Costello, José Lladó, Laura González-Vilatarsana, Emma Vélez-Santamaría, Valentina Casasnovas, Carlos Transpl Int Health Archive Objectives: To analyze the efficacy and tolerability of diflunisal for the treatment of acquired amyloid neuropathy in domino liver transplant recipients. Methods: We performed a retrospective longitudinal study of prospectively collected data for all domino liver transplant recipients with acquired amyloid neuropathy who received diflunisal at our hospital. Neurological deterioration was defined as an score increase of ≥2 points from baseline on the Neurological Impairment Scale/Neurological Impairment Scale-Lower Limbs. Results: Twelve patients who had received compassionate use treatment with diflunisal were identified, of whom seven had follow-up data for ≥12 months. Five patients (71.4%) presented with neurological deterioration on the Neurological Impairment Scale after 12 months (p = 0.0382). The main adverse effects were cardiovascular and renal, leading to diflunisal being stopped in five patients and the dose being reduced in two patients. Conclusion: Our study suggests that most domino liver transplant recipients with acquired amyloid neuropathy will develop neurological deterioration by 12 months of treatment with diflunisal. This therapy was also associated with a high incidence of adverse effects and low treatment retention. The low efficacy and low tolerability of diflunisal treatment encourage the search for new therapeutic options. Frontiers Media S.A. 2022-04-13 /pmc/articles/PMC9044119/ /pubmed/35497887 http://dx.doi.org/10.3389/ti.2022.10454 Text en Copyright © 2022 Nedkova-Hristova, Baliellas, González-Costello, Lladó, González-Vilatarsana, Vélez-Santamaría and Casasnovas. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Health Archive Nedkova-Hristova, Velina Baliellas, Carmen González-Costello, José Lladó, Laura González-Vilatarsana, Emma Vélez-Santamaría, Valentina Casasnovas, Carlos Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title | Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title_full | Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title_fullStr | Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title_full_unstemmed | Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title_short | Treatment With Diflunisal in Domino Liver Transplant Recipients With Acquired Amyloid Neuropathy |
title_sort | treatment with diflunisal in domino liver transplant recipients with acquired amyloid neuropathy |
topic | Health Archive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9044119/ https://www.ncbi.nlm.nih.gov/pubmed/35497887 http://dx.doi.org/10.3389/ti.2022.10454 |
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