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Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study()
INTRODUCTION: Data indicates there are 4 main pulmonary sarcoidosis duration/treatment phenotypes: asymptomatic, acute (disease duration <1–2 years), chronic and advanced. There are no data about disease duration/treatment phenotypes of cardiac sarcoidosis patients. Our study had 2 main aims (i)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333413/ https://www.ncbi.nlm.nih.gov/pubmed/37441681 http://dx.doi.org/10.1016/j.ahjo.2022.100224 |
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author | Wiefels, Christiane Weng, Willy Beanlands, Rob deKemp, Rob Nery, Pablo B. Boczar, Kevin Mesquita, Claudio Tinoco Birnie, David |
author_facet | Wiefels, Christiane Weng, Willy Beanlands, Rob deKemp, Rob Nery, Pablo B. Boczar, Kevin Mesquita, Claudio Tinoco Birnie, David |
author_sort | Wiefels, Christiane |
collection | PubMed |
description | INTRODUCTION: Data indicates there are 4 main pulmonary sarcoidosis duration/treatment phenotypes: asymptomatic, acute (disease duration <1–2 years), chronic and advanced. There are no data about disease duration/treatment phenotypes of cardiac sarcoidosis patients. Our study had 2 main aims (i) to assess the response to corticosteroids and (ii) to assess the incidence of relapse after a one-year course of corticosteroids (thereby classifying patients as acute or chronic treatment phenotype). METHODS: Consecutive, treatment naive patients with CS were prospectively recruited and treated with 0.5 mg/kg prednisone, to a maximum dose of 40 mg/day. Patients had a follow-up PET after 3–6 months of therapy (PET 2). In the responders (PET definition of response) the prednisone was then weaned and stopped after 12 months. Three months after stopping, the PET was repeated to look for disease relapse (PET 3). RESULTS: Twenty-one consecutive patients were included, and all patients showed a reduction in cardiac FDG uptake after 3–6 months and 19/21 (90.5 %) met the PET definition of response. Of these, 12/19 (63.1 %) relapsed after prednisone was stopped. There were no serious adverse effects during the trial of therapy cessation and there were no later relapses in the 7 non-relapsers during over 4 years of subsequent follow-up. CONCLUSION: The initial response rate to prednisone was high with all patients showing a reduction in FDG uptake and 19/21 meeting a PET definition of >25 % response. Secondly, a trial of therapy discontinuation was able to classify 7/19 patients as acute treatment phenotype and 12/19 as chronic. |
format | Online Article Text |
id | pubmed-10333413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103334132023-07-12 Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() Wiefels, Christiane Weng, Willy Beanlands, Rob deKemp, Rob Nery, Pablo B. Boczar, Kevin Mesquita, Claudio Tinoco Birnie, David Am Heart J Plus Research Paper INTRODUCTION: Data indicates there are 4 main pulmonary sarcoidosis duration/treatment phenotypes: asymptomatic, acute (disease duration <1–2 years), chronic and advanced. There are no data about disease duration/treatment phenotypes of cardiac sarcoidosis patients. Our study had 2 main aims (i) to assess the response to corticosteroids and (ii) to assess the incidence of relapse after a one-year course of corticosteroids (thereby classifying patients as acute or chronic treatment phenotype). METHODS: Consecutive, treatment naive patients with CS were prospectively recruited and treated with 0.5 mg/kg prednisone, to a maximum dose of 40 mg/day. Patients had a follow-up PET after 3–6 months of therapy (PET 2). In the responders (PET definition of response) the prednisone was then weaned and stopped after 12 months. Three months after stopping, the PET was repeated to look for disease relapse (PET 3). RESULTS: Twenty-one consecutive patients were included, and all patients showed a reduction in cardiac FDG uptake after 3–6 months and 19/21 (90.5 %) met the PET definition of response. Of these, 12/19 (63.1 %) relapsed after prednisone was stopped. There were no serious adverse effects during the trial of therapy cessation and there were no later relapses in the 7 non-relapsers during over 4 years of subsequent follow-up. CONCLUSION: The initial response rate to prednisone was high with all patients showing a reduction in FDG uptake and 19/21 meeting a PET definition of >25 % response. Secondly, a trial of therapy discontinuation was able to classify 7/19 patients as acute treatment phenotype and 12/19 as chronic. Elsevier 2022-12 /pmc/articles/PMC10333413/ /pubmed/37441681 http://dx.doi.org/10.1016/j.ahjo.2022.100224 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Wiefels, Christiane Weng, Willy Beanlands, Rob deKemp, Rob Nery, Pablo B. Boczar, Kevin Mesquita, Claudio Tinoco Birnie, David Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title | Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title_full | Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title_fullStr | Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title_full_unstemmed | Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title_short | Investigating the treatment phenotypes of cardiac sarcoidosis: A prospective cohort study() |
title_sort | investigating the treatment phenotypes of cardiac sarcoidosis: a prospective cohort study() |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333413/ https://www.ncbi.nlm.nih.gov/pubmed/37441681 http://dx.doi.org/10.1016/j.ahjo.2022.100224 |
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