RESPIRATORY AND SYSTEMIC REACTION FOLLOWING EXPOSURE TO HEATED ELECTROSTATIC POLYESTER PAINT

Citation
A. Cartier et al., RESPIRATORY AND SYSTEMIC REACTION FOLLOWING EXPOSURE TO HEATED ELECTROSTATIC POLYESTER PAINT, The European respiratory journal, 7(3), 1994, pp. 608-611
Citations number
12
Categorie Soggetti
Respiratory System
ISSN journal
09031936
Volume
7
Issue
3
Year of publication
1994
Pages
608 - 611
Database
ISI
SICI code
0903-1936(1994)7:3<608:RASRFE>2.0.ZU;2-C
Abstract
A 39 year old nonatopic man developed episodes of cough, dyspnoea, swe ating and shivers within 2-3 weeks of starting a new job in a factory where metallic boards were treated with an electrostatic powder paint, made of an epoxy resin and a carboxylated polyester containing polyet hylene terephthalate and polybutylene terephthalate. The subject spray ed the metallic boards which were then heated in 200-degrees-C ovens. The subject was first seen in an emergency room after being at work fo r 4 h. The physical examination revealed bilateral wheezing with fever (39-degrees-C), hypoxaemia (arterial oxygen tension (PaO2) 58 torr (7 .7 kPa), leucocytosis (white blood count cells.mm-3 17,000 (17x10(9) c ells.l-1) and severe airway obstruction (forced expiratory volume in o ne second (FEV1)/forced vital capacity, (FVC) 1.3/2.4 1, improving to 2.2/3.8 l after bronchodilator; predicted values = 3.4/4.1 l). The sub jects condition improved after being treated with oral steroids. His s pirometry was normal two weeks later, although he showed mild bronchia l hyperresponsiveness to methacholine with the (provocative concentrat ion producing a 20% fall in FEV1 (PC20) being 1.7 mg.ml-1). The subjec t underwent specific inhalation challenges at the workplace 4 months l ater. After being exposed at work for 4 h, he developed a significant fall in FEV1 (40%), fever, leucocytosis, and a fall in diffusing capac ity. Lung function tests were back to normal two weeks later. Exposing the subject to heated granulated polyester for one hour in a hospital laboratory produced a fall in FEV1 of 41%, fever, leucocytosis and a fall in diffusing capacity. Nine months later, the subject still had s ymptoms of mild asthma and his PC20 was 0.2 mg.ml-1. To the best of ou r knowledge, this is the first account of occupational asthma and an a lveolitis-type reaction after exposure to polyester.