| Literature DB >> 31557149 |
Cecile Rose, Amy Heinzerling, Ketki Patel, Coralynn Sack, Jenna Wolff, Lauren Zell-Baran, David Weissman, Emily Hall, Robbie Sooriash, Ronda B McCarthy, Heidi Bojes, Brian Korotzer, Jennifer Flattery, Justine Lew Weinberg, Joshua Potocko, Kirk D Jones, Carolyn K Reeb-Whitaker, Nicholas K Reul, Claire R LaSee, Barbara L Materna, Ganesh Raghu, Robert Harrison.
Abstract
Silicosis is an incurable occupational lung disease caused by inhaling particles of respirable crystalline silica. These particles trigger inflammation and fibrosis in the lungs, leading to progressive, irreversible, and potentially disabling disease. Silica exposure is also associated with increased risk for lung infection (notably, tuberculosis), lung cancer, emphysema, autoimmune diseases, and kidney disease (1). Because quartz, a type of crystalline silica, is commonly found in stone, workers who cut, polish, or grind stone materials can be exposed to silica dust. Recently, silicosis outbreaks have been reported in several countries among workers who cut and finish stone slabs for countertops, a process known as stone fabrication (2-5). Most worked with engineered stone, a manufactured, quartz-based composite material that can contain >90% crystalline silica (6). This report describes 18 cases of silicosis, including the first two fatalities reported in the United States, among workers in the stone fabrication industry in California, Colorado, Texas, and Washington. Several patients had severe progressive disease, and some had associated autoimmune diseases and latent tuberculosis infection. Cases were identified through independent investigations in each state and confirmed based on computed tomography (CT) scan of the chest or lung biopsy findings. Silica dust exposure reduction and effective regulatory enforcement, along with enhanced workplace medical and public health surveillance, are urgently needed to address the emerging public health threat of silicosis in the stone fabrication industry.Entities:
Mesh:
Year: 2019 PMID: 31557149 PMCID: PMC6762184 DOI: 10.15585/mmwr.mm6838a1
Source DB: PubMed Journal: MMWR Morb Mortal Wkly Rep ISSN: 0149-2195 Impact factor: 35.301
Demographic, occupational, and clinical features of 18 silicosis cases in stone fabrication workers — California, Colorado, Texas, and Washington, 2017–2019
| State-Patient no. | Age range (yrs) at diagnosis | Decade of first exposure* (total yrs) | Chest CT abnormalities | Pulmonary function test findings (FEV1, FVC, and DLCO percentage predicted; FEV1/FVC ratio) | Other associated conditions |
|---|---|---|---|---|---|
| CA-1† | 30–39 | 2000s (9 yrs) | Diffuse ground glass and solid centrilobular nodules; mediastinal lymphadenopathy | FEV1: 35%§ | Scleroderma |
| FVC: 33%§ | |||||
| FEV1/FVC: 86% | |||||
| DLCO: 13%§ | |||||
| CA-2†,¶ | 30–39 | 2000s (13 yrs) | Bilateral ground glass opacities and nodules | Not performed | Rheumatoid arthritis |
| CA-3 | 30–39 | 2000s (11 yrs) | Diffuse, upper lung predominant perilymphatic nodules | FEV1: 77%§ | None |
| FVC: 83% | |||||
| FEV1/FVC: 76% | |||||
| DLCO: 70%§ | |||||
| CA-4 | 40–49 | 2000s (14 yrs) | Subpleural nodules with upper lobe predominance; mild mediastinal lymphadenopathy | FEV1: 73%§ | None |
| FVC: 79%§ | |||||
| FEV1/FVC: 75% | |||||
| DLCO: 57%§ | |||||
| CA-5 | 30–39 | 2000s (14 yrs) | Upper lobe architectural distortion and ground glass micronodules; mediastinal lymphadenopathy. | FEV1: 58%§ | None |
| FVC: 71%§ | |||||
| FEV1/FVC: 67%§ | |||||
| DLCO: 73%§ | |||||
| CA-6 | 50–59 | 2000s (16 yrs) | Bilateral upper lobe fibronodular scarring; calcified mediastinal lymphadenopathy. | FEV1: 94% | None |
| FVC: 96% | |||||
| FEV1/FVC: 98% | |||||
| CO-1 | 40–49 | 2000s (12 yrs) | Upper lung predominant perilymphatic nodules | FEV1: 86% | Latent tuberculosis infection |
| FVC: 92% | |||||
| FEV1/FVC: 76% | |||||
| DLCO: 96% | |||||
| CO-2 | 60–69 | 1980s (23 yrs) | Diffuse perilymphatic nodules; calcified mediastinal lymphadenopathy | FEV1: 57%§ | Rheumatoid arthritis |
| FVC: 48%§ | |||||
| FEV1/FVC: 91% | |||||
| DLCO: 62%§ | |||||
| CO-3 | 50–59 | 2000s (13 yrs) | Upper lung predominant nodules; calcified mediastinal lymphadenopathy | FEV1: 82% | Latent tuberculosis infection |
| FVC: 82% | |||||
| FEV1/FVC: 80% | |||||
| DLCO: 102% | |||||
| CO-4 | 40–49 | 2000s (17 yrs) | Diffuse centrilobular nodules; upper lung ground glass opacities; calcified mediastinal lymphadenopathy | FEV1: 96% | None |
| FVC: 92% | |||||
| FEV1/FVC: 82% | |||||
| DLCO: 74%§ | |||||
| CO-5 | 50–59 | 1980s (23 yrs) | Upper lung predominant nodules; calcified mediastinal lymphadenopathy | FEV1: 105% | Rheumatoid arthritis |
| FVC: 104% | |||||
| FEV1/FVC: 80% | |||||
| DLCO: 90% | |||||
| CO-6 | 40–49 | 1990s (22 yrs) | Upper and middle lung predominant nodules | FEV1: 105% | None |
| FVC: 103% | |||||
| FEV1/FVC: 82% | |||||
| DLCO: 102% | |||||
| CO-7 | 40–49 | 1990s (24 yrs) | Upper lung predominant nodules; mild paraseptal emphysema; calcified mediastinal lymphadenopathy | FEV1: 90% | Rheumatoid arthritis |
| FVC: 83% | |||||
| FEV1/FVC: 86% | |||||
| DLCO: 77%§ | |||||
| TX-1 | 50–59 | 2010s (2 yrs) | Bilateral lower lobe ground glass opacities and scattered nodules | FEV1: 65%§ | None |
| FVC: 70%§ | |||||
| FEV1/FVC: 73% | |||||
| TX-2 | 50–59 | 1980s (31 yrs) | Multiple bilateral pulmonary nodules; ground glass opacities in lower lobes and calcified hilar lymphadenopathy | FEV1: 118% | None |
| FVC: 115% | |||||
| FEV1/FVC: 80% | |||||
| TX-3 | 50–59 | 1980s (31 yrs) | Upper lobe predominant reticular and partially calcified nodular opacities with bilateral partially calcified hilar and mediastinal lymphadenopathy | FEV1: 89% | None |
| FVC: 102% | |||||
| FEV1/FVC: 69%§ | |||||
| TX-4 | 40–49 | 2010s (2 yrs) | Upper lobe predominant nodules with bilateral hilar and mediastinal lymphadenopathy | FEV1: 54%§ | None |
| FVC: 55%§ | |||||
| FEV1/FVC: 79% | |||||
| WA-1 | 30–39 | 2010s (6 yrs) | Diffuse, upper lung predominant nodules with early conglomeration; mediastinal lymphadenopathy | FEV1: 41%§ | None |
| FVC: 44%§ | |||||
| FEV1/FVC: 77% | |||||
| DLCO: 32%§ |
Abbreviations: CA = California; CO = Colorado; CT = computed tomography; DLCO = diffusing capacity for carbon monoxide; FEV1 = forced expiratory volume in 1 second; FVC = forced vital capacity; TX = Texas; WA = Washington.
* Exact years of employment suppressed for patient confidentiality.
† Patient died from silicosis.
§ Abnormal pulmonary function test defined as FEV1<80% predicted, FVC<80% predicted, FEV1/FVC<70%, and DLCO <80% predicted. Global Lung Function Initiative reference values (2012) were used to calculate percentage predicted values for spirometry; DLCO was based on reference values in Crapo RO, Morris AH. Standardized single-breath normal values for carbon monoxide diffusing capacity. Am Rev Respir Dis 1981;123:185–9. For some cases, only spirometry was performed; therefore, DLCO is not reported.
¶ Silicosis diagnosed based on postmortem review of lung tissue.