CASE REPORT
Acute Pulmonary Toxicity Linked to Use of a Leather Protector From the CentreAnti-Poisondu Quebec, Sainte-Foy, Quebec, Canada. Receivedfor publicationJune 3, 1994. Revision received October25, 1994. Acceptedfor publication November 15, 1994.
Martin Lalibertd, MD, FRCP(C) Guy Sanfa~on, PhD Rend Blais, MD, FRCP(C)
Copyright © by the American College of Emergency Physicians.
Leather protectors are used extensively for waterproofing leather garments. Inhalation exposure to this type of product is usually considered a benign incident. We report two cases of acute pulmonary toxicity associated with the use of a new leather protector recently introduced to the Canadian market. Emergency physicians must be aware of the potential acute toxicity of new leather protectors. [Lalibert6 M, Sanfa~,on (3, Blais R: Acute pulmonary toxicity linked to use of a leather protector. Ann EmergMeclJune 1995;25:841-844.]
INTRODUCTION Leather protectors are used extensively for waterproofing leather garments. Inhalation exposure to a leather protector is usually considered a benign event with little evidence of toxic effects reported in the medical literature. We report two cases of acute pulmonary toxicity associated with the use of a new formulation of leather protector that was introduced to the Canadian market. In 1 month, 16 people reported the occurrence of acute respiratory symptoms after the use of this new leather protector
CASE REPORTS Patient 1 A 27-year-old man called the Quebec Poison Control Center complaining of acute respiratory symptoms after the use of a leather protector called Oiled Nubuck Leather Protector. Earlier that day he had sprayed a pair of shoes with this leather protector in a large apartment with the windows and doors closed. Fifteen minutes later, acute respiratory symptoms of dyspnea, a dry cough, and anterior chest pain developed. The patient felt dizzy and chilly; his temperature at that time was 38.5°C. He went outside for fresh air, but came back inside as he felt more dyspneic. A few minutes later, his 26-year-old wife, who had been sitting within several feet of her husband when the leather protector was used, began to feel ill with
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similar respiratory symptoms. Both patients were advised by the poison center to seek medical care immediately. Medical evaluation on arrival in the emergency department later that day showed a man in moderate respiratory distress. His medical history was negative for asthma or chronic respiratory disorders. The history of acute respiratory symptoms occurring minutes after the use of the leather protector was confirmed. His symptoms included dyspnea at rest, dry cough, palpitations, and anterior chest pain. The patient appeared to be in moderate respiratory distress without evidence of cyanosis. Vital signs were blood pressure, 120/70 mm Hg; pulse, 108; respirations, 28; and temperature, 37°C. Head and neck examination was normal. Cardiac examination showed tachycardia without murmurs. Lung auscultation showed good air entry with diffuse bilateral wheezing. The chest radiograph was normal. Portable spirometry was performed before treatment and showed a mild obstructive syndrome (Table 1). The patient was treated with supplemental oxygen, 5 mg nebulized salbutamol in normal saline solution, and 40 mg of prednisone orally. His peak expiratory flow rate (PEFR) improved rapidly from 396 Umin before treatment to 560 L/rain after treatment. The patient was discharged home after 8 hours. Outpatient treatment included a salbutamol metered-dose inhaler and oral prednisone. One week later, the patient complained only of mild shortness of breath on exercise. His physical examination was normal. Four weeks later, he was asymptomatic and his medication was discontinued. Pulmonary function tests obtained at 1 week were normal (Table 1). Patient 2 The patient's wife also had a medical history negative for respiratory disorders. She reported acute respiratory symptoms--severe shortness of breath at rest, dry cough, palpitations, and diaphoresis--that began a few minutes after her husband used the leather protector.
Physical examination revealed a young woman in moderate respiratory distress with tachypnea, diaphoresis, and mild cyanosis. Vital signs were blood pressure, 140/80 mm Hg; pulse, 120; respirations, 32; and temperature, 37.8°C. Oxygen saturation was not recorded, but the cyanosis corrected rapidly after administration of 100% oxygen. Cardiac examination showed tachycardia without murmurs. Lung auscultation showed good air entry with diffuse, bilateral wheezing. A chest radiograph showed diffuse bilateral interstitial infiltrates consistent with pulmonary edema. The patient's PEFR was 250 L/min. She was treated with supplemental oxygen, 5 mg nebulized salbutamol in normal saline solution, and 40 mg IV methylprednisolone every 6 hours. Her subjective response to treatment was rapid, and her PEFR increased to 320 L/min 1 hour after admission. A second chest radiograph 24 hours later was normal. The patient's total leukocyte count on admission was 19,800 mm 3 with 81% neutrophils; it rose to 29,300 mm 3 at 24 hours with 88% neutrophils. The patient was discharged approximately 24 hours later on a salbutamol metered-dose inhaler and oral prednisone. Four weeks after the event, the patient remained asymptomatic, physical examination was normal and her medication was discontinued. Pulmonary function tests at that time were normal (Table 1). Oiled Nubuck Leather Protector (Panita Entreprises, Vancouver, British Columbia) was a new formulation first distributed in Canada in late 1993 and sold primarily in Quebec. This leather protector also was manufactured in the United States by Vanguard Chemical Corporation (St Louis, Missouri). The product was sold in Quebec in 237mL pump spray containers under different store brand names (Simard et Voyer, Transit, Pegabo, Aldo, and Panita). According to the Canadian distributor, the formulation of the leather protector was 95% Soltrol-10 iso-
Table 1.
Pulmonaryfunction tests. Patient I Admission Parameter
Vital capacity (L) Forced vital capacity (L) Forced expiratory volume in 1 second (L) Forced expiratory volume in 1 second (L)/ forced vital capacity (L) Peak expiratory flow rate (L/sec)
842
Patient 2 1 Week After Exposure
4 Weeks After Exposure
Measured
% Predicted
Measured
% Predicted
Measured
% Predicted
4.18 3.85 2.96 77
67 62 57 -6
4.90 5.02 3.94 77
84 86 79 -7
3.11 3.32 2.92 88
76 81 84 +4
396
63
548
90
349
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octane (of which 70% was 2-2-4 trimethylpentane and 30% was C7 and C8 isoparaffins), 2% FS 4565 (made of unknown concentrations of Stoddard's solvent, heptane, fluoropolymer resin, and a copolymer), 1% of a silicon resin, and 1% of polymerized C10 alkenes. We identified 14 additional calls to Quebec Poison Control Center from individuals complaining of acute respiratory symptoms associated with the use of Oiled Nubuck Leather Protector over a 5-week period (Table 2). These cases involved young healthy people (ages 11 to 41 years) using the leather protector indoors on leather goods (eg, shoes and jackets) over short periods. Exposed individuals rapidly developed a variety of acute respiratory symptoms, including dyspnea, dry cough, chest pain, nausea, and vomiting. In seven cases, a medical evaluation was performed and pulmonary edema was documented in one case. These patients received supportive care with supplemental oxygen; some received nebulized salbutamol and IV corticosteroids. All recovered and were discharged within 24 hours. In the seven remaining cases, no medical evaluation was performed. These patients stayed home and complications were not found on telephone follow-up. On November 23, 1993, the Canadian Ministry of Health published a press bulletin warning Canadian consumers against the use of Oiled Nubuck Leather Protector. This publication followed the voluntary with-
drawal of the leather protector from the market by the distributor. DISCUSSION
Our cases are very similar to the 29 reported in December 1992.1 The cases were associated with the use of another new leather protector named Wilson's Leather Protector. Its formulation is very similar to that of Oiled Nubuck Leather Protector. Both include isooctane as a solvent and a fluoropolymer resin as the active ingredient. In November 1993, an additional three cases of acute respiratory illness related to the use of an aerosolized leather-shoe conditioner were reported. 2 These three patients developed severe cough, shortness of breath, and tachypnea. Two had interstitial infiltrates on chest radiography. All treated patients responded well to bronchodilator therapy. The formulation was also similar to that of Oiled Nubuck Leather Protector and included 2-2-4 trimethylpentane, isooctane, and FS-4565. These leather conditioners have been reformulated by manufacturers to eliminate the use of trichloroethane as a solvent. The clinical findings in our patients suggested either a chemical or hypersensitivity pneumonitis. A possible explanation for their respiratory illness is polymer-fume fever, a syndrome caused by the inhalation of fumes containing products of pyrolysis released when fluoropolymers are exposed to high temperatures. 3 Another possible explanation
Table 2.
Data on additional 14 cases of leather protector pulmonary toxicity. Patient Age (yr)
Symptoms
Medical Evaluation
Treatment
Outcome
18 34
Cough,chest pain, vomiting Cough, dyspnea,chest pain
Oxygen,salbutamol* Oxygen,salbutamol, IV steroidst
Home at 8 hr Home at 8 hr
39
Cough,dyspnea,chest pain, vomiting
Oxygen,salbutamol, IV steroids
Home at 12 hr
30 11 20 30 30 28 27 36 14 41 23
Cough,dyspnea Cough,dyspnea Cough, dyspnea,chest pain Cough, dyspnea,chest pain Cough, dyspnea Cough,dyspnea,nausea Cough,dyspnea Cough,dyspnea Cough,dyspnea Cough, dyspnea,chest pain Cough,dyspnea,headache
Tachypnea,wheezing;chest radiographnormal Tachypnea,wheezing;oxygensaturation normal; chest radiographnormal wheezing; oxygensaturation normal; chest radiographshowed pulmonaryedema Tachypnea,wheezing;chest radiographnormal Tachypnea,wheezing,chest radiographnormal Normal Normal None None None None None None None
Oxygen,salbutamol Oxygen,salbutamol Oxygen Oxygen None None None None None None None
Home at 8 hr Home at 8 hr Home at 2 hr Home at 1 hr Stayed home Stayed home Stayed home Stayed home Stayed home Stayed home Stayed home
*Satbutamol 5 mg nebulizer in repeated doses. tMethylprednisolone 40 mg IV every 6 hours.
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for their illness is direct pulmonary toxicity of one or more of the ingredients. Hydrocarbons, namely trimethylpentane or C7 and C8 isoparaffins, or the fluoropolymer resin might have played a role in the pulmonary toxicity. Other commercially available leather protectors are made of various concentrations of trichloroethane as well as other hydrocarbons and chemical substances. Inhalation of trichloroethane is known to cause central nervous system symptoms, but there is little evidence of pulmonary toxicity. Woo et al4 described acute respiratory symptoms and hypoxemia in a 25-year-old man after the use of a waterproofing aerosol product containing trichloroethane and a fluorocarbon resin. 4 The authors attributed these effects to the trichloroethane portion of the formulation. Other descriptions of pulmonary toxicity secondary to inhalational exposure to hydrocarbons can be found; some occurred in the context of professional exposures to kerosene 5 or to naphtha distillate vapors. 6 In the cases described in our report, the leather protector was used indoors in areas with limited ventilation, thereby increasing the risk of pulmonary toxicity. Customers should be advised by manufacturers of sprayed leather protectors against indoor use of their products; a large, easily seen warning label should be placed on the can for this purpose. The information we report was obtained primarily by telephone. Other unknown environmental factors may have played a role in the acute pulmonary toxicity reported.
5. Perrone H, Passero MA: Hydrocarbon aerosol pneumonitis in an adult. Arch InternMed 1983;143:1607-1608. 6. Wilson FVV:Toxicology of petroleum naphtha distillate vapors. J OccupMed 1976;18:821.
Reprint no. 47/1/64104 Address for reprints: Martin Lalibert&MD, FRCP(C) Departmentof EmergencyMedicine RoyalVictoriaHospital 687 West PineAvenue Montreal,Quebec Oanada H3A 1A1 514-842-1231ext 4277 Fax514-843-1638
SUMMARY
Two cases of acute pulmonary toxicity associated with the use of a new leather protector are reported. We speculate that the effects of this exposure were secondary to direct pulmonary injury by the hydrocarbon ingredients or the fluoropolymer resin. Both cases responded rapidly to supportive treatment with bronchodilators and corticosteroids. More cases involving similar formulations of leather protectors have been reported. Emergency physicians should be aware of the potential acute pulmonary toxicity of leather protectors. REFERENCES 1. Smilkstein M J, Burton BT, Keene W: Acute respiratory illness linked to use of aerosol leather conditioner. MMWR1993;41:965-967. 2. Kulig K, Brent J, Phillips S: Severe acute respiratory illness linked to use of shoe spray. MMWR1993;42:885-887. 3. Albrecht WN, Bryant CJ: Polymer fume fever associated with smoking and use of a moldrelease spray containing polytetrafluoroethylene. J &cup Med 1987;29:817-819. 4. Woo OF, Healy KM, Sheppard D: Chest pain and hypexemia from inhalation of a trichloroethane aerosol product. J ToxicolClin Toxico11983;26:333-341.
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