Dennis Shusterman, MD, MPH Professor of Clinical Medicine, Emeritus - - PDF document

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Dennis Shusterman, MD, MPH Professor of Clinical Medicine, Emeritus - - PDF document

3/10/16 Scenarios for the De Novo Generation of Toxic Substances Dennis Shusterman, MD, MPH Professor of Clinical Medicine, Emeritus UCSF Division of Occupational & Environmental Medicine Disclosures I have nothing to disclose 1


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Scenarios for the De Novo Generation 


  • f Toxic Substances

Dennis Shusterman, MD, MPH Professor of Clinical Medicine, Emeritus UCSF Division of Occupational & Environmental Medicine

Disclosures

I have nothing to disclose

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Objectives

  • To review the range of de novo toxicants
  • To highlight DDX issues
  • To promote 1
  • and 2
  • prevention

Background

  • Definition of de novo toxicants

Toxic agents that are generated (or transformed) in the workplace or environment.

  • Classes of de novo toxicants

ü Pyrolysis / combustion products ü Mixing incompatibilities ü Environmental activation of toxic agents

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Pyrolysis & Combustion Products

Definitions

  • Pyrolysis

ü Non-oxidative thermal decomposition of

  • rganic materials
  • Combustion

ü Oxidative thermal decomposition of organic

materials

Dorland’s Illustrated Medical Dictionary. 2012

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Combustion Toxicology: Fire Science

C + ½ O2 à CO Δ

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C + ½ O2 à CO Δ C + ½ O2 à CO Δ

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Combustion Toxicology: Fire Science

Scenario 1

An electronics assembly factory reports an

  • utbreak of episodic febrile illness among

workers and consults a university clinic to identify the cause. You are on the team that

  • responds. On arrival, you meet with

management and some symptomatic workers. What do you want to know?

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Scenario 1

  • A. What is produced in the factory?
  • B. With what materials and processes?
  • C. What were the symptoms and their

timing?

  • D. Who was affected?
  • E. Did anything change pre-outbreak?
  • F. All of the above

Scenario 1

ü What is produced in the factory?

Ø Encapsulated electronic circuit boards

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Scenario 1

ü What is produced in the factory?

Ø Encapsulated electronic circuit boards

ü With what materials and processes?

Ø Circuit boards are placed in a mold to be

encapsulated (“potted”) with an epoxy

  • resin. Prior to encapsulation, the interior
  • f the molds are sprayed with a parting

agent

Scenario 1

Ø What were the symptoms and their timing?

Ø Acute (following afternoon break)

  • Chest tightness
  • Sore throat
  • Cough
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Scenario 1

Ø What were the symptoms and their timing?

Ø Acute (following afternoon break)

  • Chest tightness
  • Sore throat
  • Cough

Ø Delayed (by another 5-6 hours)

  • Malaise
  • Headache
  • Chills
  • Fever

Scenario 1

ü Who was affected?

Ø All-male workforce Ø 36 of 61 (59%) of workers symptomatic Ø 34 of 61 (56%) smokers

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Scenario 1

ü Who was affected?

Ø All-male workforce Ø 36 of 61 (59%) of workers symptomatic Ø 34 of 61 (56%) smokers

OR = 7.7; χ2 = 13.2; p < 0.001

Smoker? Symptomatic? Yes No Yes 27 7 No 9 18

Scenario 1

ü Did anything change pre-outbreak?

Ø Yes…

The mold release spray (parting agent) was changed to one containing a short- chain polytetrafluoroethylene (TeflonR) compound.

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Scenario 1

Ø Interpretation -- What happened?

Ø The majority of symptomatic workers

(smokers) contaminated their hands (thence cigarettes) with PTFE dust and subsequently pyrolyzed the PTFE.

Scenario 1

ü Diagnosis?

Ø Polymer fume fever Source: Lewis CE, Kerby GR. An epidemic of polymer-fume fever. JAMA 1965; 191: 103-6.

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Fume Fevers

Polymer Fume Fever

  • 1st described by Harris (1951)
  • Agent

ü Polytetrafluoroethylene (PTFE /TeflonR) fume

  • Exposure scenarios

ü Smoking PTFE-contaminated cigarettes

̵

Electronics / textiles / ski wax

ü Welding near PTFE-containing parts

  • Variants / sequelae

ü Veterinary cases (birds) ü ? COPD with repeated episodes (Kales, 1994) ü Chemical pneumonitis (very high temperature)

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Polymer Fume Fever

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Inhalation Fevers

  • Polymer fume fever
  • Metal fume fever
  • Inhalation fevers from contaminated
  • rganic material (e.g., ODTS)
  • Inhalation fevers from contaminated 


H2O (e.g. humidifier fever)

Inhalation Fevers: Common Features

  • Inhalation of specific types of fine PM
  • Latency period for systemic symptoms

ü ~ 2-8 hours

  • Symptoms

ü Systemic: Chills, fever, myalgias, headache ü Pulmonary & GI: Sx’s variable

  • Spontaneous resolution (~ 24-48 hrs)
  • Negative CXR
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Inhalation Fevers: Natural history

  • Key Concepts

ü Does not involve sensitization

à may occur on initial exposure

ü High attack rate among comparably exposed

persons

Inhalation Fevers: Natural history

  • Key Concepts

ü Does not involve sensitization

à may occur on initial exposure

ü High attack rate among comparably exposed

persons

  • Clinical Syndromes

ü May be mistaken for viral URI ü Tachyphylaxis is common (“Monday fever”)

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Metal Fume Fever Metal Fume Fever

  • 1st described by Thakrah (1831)
  • Agent = ZnO fume; other metals not proven
  • Synonyms

ü “Brass-founder’s ague” ü “Monday fever” ü “Spelter’s chills”

  • Variants / sequelae

ü “Cadmium fume fever” à pneumonitis

ü Possible bronchospasm (Malo & Cartier, 1987)

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Metal Fume Fever

  • Pathophysiology (Blanc et al.; 2003-2007)

ü Nascent ZnO fume reaches alveoli…

à PMN influx into BAL fluid

à Cytokine release (TNF; IL-6; IL-8) in BAL fluid

Nascent ZnO Fume

Electron micrograph courtesy Prof. Lung-Chi Chen, NYU.

100 nm

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Inhalation Injury

Spectrum of inhalation injury

ü Rhino-conjunctivitis; Pharyngitis ü Laryngitis ü Tracheo-bronchitis ü Chemical pneumonitis

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Spectrum of inhalation injury

ü Rhino-conjunctivitis; Pharyngitis

→ Sinusitis

ü Laryngitis ü Tracheo-bronchitis ü Chemical pneumonitis

Spectrum of inhalation injury

ü Rhino-conjunctivitis; Pharyngitis

→ Sinusitis

ü Laryngitis

→ Vocal cord dysfunction (VCD)

ü Tracheo-bronchitis ü Chemical pneumonitis

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Spectrum of inhalation injury

ü Rhino-conjunctivitis; Pharyngitis

→ Sinusitis

ü Laryngitis

→ Vocal cord dysfunction (VCD)

ü Tracheo-bronchitis

→ Irritant-induced asthma

ü Chemical pneumonitis

Spectrum of inhalation injury

ü Rhino-conjunctivitis; Pharyngitis

→ Sinusitis

ü Laryngitis

→ Vocal cord dysfunction (VCD)

ü Tracheo-bronchitis

→ Irritant-induced asthma

ü Chemical pneumonitis

→ Bronchiolitis obliterans

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Chemical Pneumonitis Chemical pneumonitis

  • Synonyms

ü Non-cardiogenic pulmonary edema ü Acute respiratory distress syndrome (ARDS) ü Acute lung injury (ALI)

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Chemical pneumonitis

  • Synonyms

ü Non-cardiogenic pulmonary edema ü Acute respiratory distress syndrome (ARDS) ü Acute lung injury (ALI)

  • Radiographic features

ü CXR: “Butterfly” infiltrates with normal cardio-


thoracic ratio

ü HRCT: Centrilobular ground-glass attenuation

Source: Fraser & Pare: Diagnosis of Diseases of the Chest. Philadelphia, Saunders, 1970: p. 951

Chemical pneumonitis

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Source: Akira M. High-resolution CT in the evaluation of occupational and environmental disease. Radiologic Clin North Am 2002; 40: 43-59.

Chemical pneumonitis Chemical pneumonitis

  • Synonyms

ü Non-cardiogenic pulmonary edema ü Acute respiratory distress syndrome (ARDS) ü Acute lung injury (ALI)

  • Radiographic features

ü CXR: “Butterfly” infiltrates with normal cardio-


thoracic ratio

ü HRCT: Centrilobular ground-glass attenuation

  • Etiologic agents (de novo):

ü Cadmium oxide fume ü Irritant gases & vapors

ü Chlorinated solvent pyrolysis à phosgene ü High-temperature atmospheric chemistry (O3 + NOx)

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3 O2 à 2 O3

N2 + O2 à NOx

Δ

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Water solubility & initial level of impact

Source: Shusterman Current Allergy Asthma Rep 2003;3:258.

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2 NO2 + H2O → HNO3 + HNO2

In vivo fate: NO2 à disproportionation: In vivo fate: Phosgene à hydrolysis:

COCl2 + H2O → CO2 + 2 HCl

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Mixing Incompatibilities Scenario 2

A 40 year-old-female presents to her primary care physician with a history of transient eye, nose and throat irritation, as well as cough,

  • ccurring after mixing a window cleaner with

bleach in a poorly ventilated room. Symptoms resolved quickly, but she wants to know what

  • ccurred and how to avoid it in the future.

What do you want to know?

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Questions re: exposure

√ What was in the window cleaner? √ Are the product constituents known to be

incompatible? If so, what kind of reaction products were likely formed?

√ Were there any warning labels? √ All of the above

Answers re: exposure

√ What was in the window cleaner?

Ø CAN’T TELL YOU

√ Was there ammonia in the window cleaner?

Ø CAN’T TELL YOU

√ Possibility of chloramine generation if

ammonia is present?

Ø CAN’T TELL YOU IF AMMONIA IS PRESENT BUT

CAN SAY YOU DON’T HAVE TO WORRY ABOUT THAT PARTICULAR REACTION.

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Mixing Incompatibilities

Na+ClO- (sodium hypochlorite) plus…

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Mixing Incompatibilities

Na+ClO- (sodium hypochlorite) plus… NH3 (ammonia) -> NHxCly (chloramines)

Chloramines

NaClO + NH3 -> NHxCly

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Mixing Incompatibilities

Na+ClO- (sodium hypochlorite) plus… H+ (acids) -> Cl2 (chlorine gas)

Chlorine gas

NaClO + 2 HCl -> NaCl + H2O + Cl2

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Arsine (AsH3) gas generation

√ Mixing acids with metallic slags √ Immersion of an aluminum ladder in a tank

containing sodium arsenite (NaAsO2)

√ Potential formation in electronics industry

GaAs + 3 HCl à GaCl3 + AsH3

Environmental activation of toxicants

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Air Pollutants

Credit: Nick Lammers, Oakland Tribune

H2SO7 + H2O à 2 H2SO4

General Chemical Oleum Release:

July 26, 1993

Cloud enveloped parts of Richmond, San Pablo, El Sobrante, Pinole ~ 24,000 people sought medical attention or claimed health effects

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Water Pollutants

Minamata, Japan…

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Minamata, Japan… Minamata, Japan…

?

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HgCl2 ¡+ ¡bacteria ¡-­‑> ¡CH3Hg+ ¡+ ¡Cl-­‑ ¡

Minamata, Japan…

HgCl2 ¡+ ¡bacteria ¡-­‑> ¡CH3Hg+ ¡+ ¡Cl-­‑ ¡

Minamata, Japan…

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HgCl2 ¡+ ¡bacteria ¡-­‑> ¡CH3Hg+ ¡+ ¡Cl-­‑ ¡

Minamata, Japan… Minamata, Japan…

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Minamata, Japan… Minamata, Japan…

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Pesticides Metam Sodium Spill


Dunsmuir, CA – July 1991

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DOT status of Metam Sodium

√ NOT considered a hazardous substance

Ø NO placarding Ø NO double-walled tank cars required

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DOT status of Metam Sodium

√ NOT considered a hazardous substance

Ø NO placarding Ø NO double-walled tank cars required

Ø “The liquid fumigant is transported at an elevated

  • pH. When it comes in contact with water/soil

moisture it releases into a gas killing the little

  • critters. For the Railroad at that time placarding

something as hazardous, the substance had to be immediately toxic to humans, it exploded on release, or caught on fire upon release.”

SOURCE: George Day, PE, Region 5 RWQCB, 11/5/15

Metam sodium

H C–N–C–S–, Na+ S = H –

H2S

CH3–N=C=S Methyl isothiocyanate CH3–N=C=S Methyl isothiocyanate

hydrolysis

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CH3-N=C=O

Summary

√ Toxic substances can be generated (or activated)

by the action of heat, inappropriate mixing, or biological processes in the environment.

√ The resulting de novo toxicants can be qualitatively

and/or quantitatively more toxic than the starting products.

√ Fume fevers can mimic viral illnesses. √ Foreknowledge of these potential reactions can

hasten the recognition of exposure hazards.

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Resource:

  • 1. Inhalation fevers are characterized by

all of the following except:

  • A. Inhalation of fine particles
  • B. A lag-time between exposure and Sxs
  • C. Systemic Sxs (chills and fever)
  • D. Characteristic CXR findings
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  • 2. Clinical features of chemical

pneumonitis include all except:

  • A. Hypoxemia
  • B. Symmetrical (“butterfly”) infiltrates
  • C. Specific IgG antibodies (“precipitins”)
  • D. Peripheral leukocytosis
  • 3. Identified mixing incompatibilities

include all except:

  • A. Bleach + ammonia à Chloramines (NHxCly)
  • B. Bleach + acids à Chorine gas (Cl2)
  • C. Bleach + detergent à Phosgene gas (COCl2)
  • D. Gallium arsenide + HCl à Arsine gas (AsH3)