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Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis
BACKGROUND AND OBJECTIVE: We recently noted a dramatic increase in the number of patients with accelerated silicosis associated with exposure to artificial stone dust. Therefore, the natural history of artificial stone‐associated silicosis was compared with that of natural stone‐associated silicosis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187561/ https://www.ncbi.nlm.nih.gov/pubmed/31828940 http://dx.doi.org/10.1111/resp.13744 |
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author | Wu, Na Xue, Changjiang Yu, Shiwen Ye, Qiao |
author_facet | Wu, Na Xue, Changjiang Yu, Shiwen Ye, Qiao |
author_sort | Wu, Na |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: We recently noted a dramatic increase in the number of patients with accelerated silicosis associated with exposure to artificial stone dust. Therefore, the natural history of artificial stone‐associated silicosis was compared with that of natural stone‐associated silicosis. METHODS: A total of 18 patients with artificial stone‐associated silicosis and 63 with natural stone‐associated silicosis were diagnosed sequentially in 2018 and followed up for a period of 6–12 months. Data were collected from clinical charts. RESULTS: The median duration of exposure prior to onset of symptoms of silicosis was shorter for patients who had been exposed to artificial stone dust (6.4 vs 29.3 years, P < 0.01). Four of the 18 patients experienced rapid deterioration in lung function over the follow‐up period, with declines in pre‐bronchodilator FVC of 587 (210–960) mL/year and FEV(1) of 625 (360–860) mL/year. GGO, PMF, emphysema and pulmonary artery widening were more frequently observed on computed tomography scans of patients with artificial stone‐associated silicosis than of those with natural stone‐associated silicosis. Approximately 38.9% of the patients with artificial stone‐associated silicosis were lung transplant candidates and 27.8% died, both rates being significantly higher than in patients with natural stone‐associated silicosis (3.2% and 0%, both P < 0.01). CONCLUSION: Compared to natural stone‐associated silicosis, artificial stone‐associated silicosis was characterized by short latency, rapid radiological progression, accelerated decline in lung function and high mortality. |
format | Online Article Text |
id | pubmed-7187561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-71875612020-04-29 Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis Wu, Na Xue, Changjiang Yu, Shiwen Ye, Qiao Respirology ORIGINAL ARTICLES BACKGROUND AND OBJECTIVE: We recently noted a dramatic increase in the number of patients with accelerated silicosis associated with exposure to artificial stone dust. Therefore, the natural history of artificial stone‐associated silicosis was compared with that of natural stone‐associated silicosis. METHODS: A total of 18 patients with artificial stone‐associated silicosis and 63 with natural stone‐associated silicosis were diagnosed sequentially in 2018 and followed up for a period of 6–12 months. Data were collected from clinical charts. RESULTS: The median duration of exposure prior to onset of symptoms of silicosis was shorter for patients who had been exposed to artificial stone dust (6.4 vs 29.3 years, P < 0.01). Four of the 18 patients experienced rapid deterioration in lung function over the follow‐up period, with declines in pre‐bronchodilator FVC of 587 (210–960) mL/year and FEV(1) of 625 (360–860) mL/year. GGO, PMF, emphysema and pulmonary artery widening were more frequently observed on computed tomography scans of patients with artificial stone‐associated silicosis than of those with natural stone‐associated silicosis. Approximately 38.9% of the patients with artificial stone‐associated silicosis were lung transplant candidates and 27.8% died, both rates being significantly higher than in patients with natural stone‐associated silicosis (3.2% and 0%, both P < 0.01). CONCLUSION: Compared to natural stone‐associated silicosis, artificial stone‐associated silicosis was characterized by short latency, rapid radiological progression, accelerated decline in lung function and high mortality. John Wiley & Sons, Ltd 2019-12-11 2020-05 /pmc/articles/PMC7187561/ /pubmed/31828940 http://dx.doi.org/10.1111/resp.13744 Text en © 2019 The Authors. Respirology published by John Wiley & Sons Australia, Ltd on behalf of Asian Pacific Society of Respirology. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | ORIGINAL ARTICLES Wu, Na Xue, Changjiang Yu, Shiwen Ye, Qiao Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title | Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title_full | Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title_fullStr | Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title_full_unstemmed | Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title_short | Artificial stone‐associated silicosis in China: A prospective comparison with natural stone‐associated silicosis |
title_sort | artificial stone‐associated silicosis in china: a prospective comparison with natural stone‐associated silicosis |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7187561/ https://www.ncbi.nlm.nih.gov/pubmed/31828940 http://dx.doi.org/10.1111/resp.13744 |
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