ASTHMA
Case Definitions
“Reversible airway obstruction with airway
inflammation and increased airways
responsiveness to a variety of stimuli”
Samet JM, Marbury MC, Spengler JD.
Health effects and sources of indoor air
pollution. Part II. Am Rev Respir Dis. 1988
Jan;137(1):221–242.
Measuring airway obstruction:
Spirometry
• PEF = Peak Expiratory Flow
– Greatest flow sustained 10 milliseconds with a forced
expiration
• FEV1 = Forced Expiratory Volume
– Volume of air expelled in 1st second of forced
expiration
• FVC = Forced Vital Capacity
– Maximum volume of air exhaled with forced expiration
after a maximum inhalation
• FEF25-75 = Forced Expiratory Flow between 25%
and 75% of FVC
– Detects small-airways obstruction
Reversible airway obstruction
http://www.sbpt.org.br/downloads/arquivos/
Dir_Asma_Int/Practical_Guide_Diagnosis_
Management_Asthma_NIH_2002.pdf
Council of State and Territorial
Epidemiologists
Asthma Surveillance Case
Definition Work Group
Mortality/Hospitalization Case Definition
Confirmed:
· No confirmed case classification for mortality and hospital
discharge data.
Probable:
· death certificates/records listing the asthma diagnostic code (ICD-9
Code: 493; or ICD-10 Codes: J45, J46) as the underlying cause of
death.
· hospital records listing the asthma diagnostic code (ICD-9-CM
Codes: 493.0- 493.9;ICD-10-CM Codes: J45.0-J45.9) as the primary
diagnosis.
Possible:
· death certificates/records listing the asthma diagnostic code as a
contributing cause of death.
· hospital records listing the asthma diagnostic code as a secondary
diagnosis.
· 466(acute bronchitis and bronchiolitis), *** in children < 12 years***
· 491.20 and 491.21 (chronic bronchitis), *** in children < 12
years***
Prevalent Case Definition
Confirmed:
· There is no confirmed case classification for self-report.
Probable:
· A positive response:
“Did a doctor (or other health professional) ever tell you that you had
asthma?” and “Do you still have asthma?”
OR
“Have you taken prescription medications for asthma (such as albuterol,
inhaled steroids, cromolyn, theophylline, etc) during the past year?”
OR
“Have you had a wheeze episode in the past year?”
Possible:
· A positive response
“Have you used over-the-counter medications for asthma during the
past year?”,
OR
“Have you experienced episodes of wheezing during the past year?
Clinical and functional criteria
• Clinical criteria
– Wheezing 2 consecutive days
– Chronic cough persisting 3-6 weeks responding to
bronchodilators in absence of allergic rhinitis or
sinusitis
– Nocturnal awakening with dyspnea, cough/wheezing
(w/o other medical condition)
• Laboratory criteria – Spirometry (FEV1, FVC)
– 12%  > short-acting bronchodilator challenge
– 20%  FEV1 w/histamine/methacholine/exercise/cold
– 20% diurnal variation in PEF over 1-2 weeks
Clinical and functional case definitions
Confirmed: any of the clinical symptoms at least 3 times during the past
year AND at least one of the laboratory criteria.
Probable: In the absence of supporting
· laboratory criteria, presence of any of the clinical symptoms which have
been reversed by physician treatment with asthma medications and have
occurred at least 3 times during the past year.
· clinical criteria, at least one of the laboratory criteria during the past year.
· laboratory or clinical criteria, taken medications in the past year that were
prescribed by a physician for asthma.
Possible: the presence of any of the following during the past year:
· shortness of breath on exertion, presence of wheezing or chronic cough in
the absence of obvious respiratory infection, presence of increased nasal
secretion, mucosal swelling, nasal polyps, or chronic sinusitis, hyper
expansion of the thorax, sounds of wheezing during normal breathing,
prolonged phase of forced exhalation, chest x ray showing hyper
expansion, FEV1 less than 80% of predicted value
Asthma Case Definition
Epidemiologic Issues
• Overlap with other COPD’s
• Partially a diagnosis of exclusion
• Different etiologies?
• Continuum of symptoms?
• More difficult to diagnose in young children
• Symptoms & lung function change over time,
related to environmental triggers, medication,
and age
• Definitions based on self-report or medical
records depend on physician diagnosis
– Diagnostic criteria not standardized
Pathogenesis of Asthma:
IgE-mediated Inflammation
Allergen
IgE Antibodies
Activate Inflammatory Cells
Mast cells
Lymphocytes
Eosinophils
Platelets
Macrophages
Inflammatory Mediators Released
Histamine
Leukotrines
Cytokines
Early Response
Bronchospasm
Edema
Airflow Obstruction
Late Response
Airway Inflammation
Airflow Obstruction
Airway Hyperresponsiveness
Remodelling
Adapted from Busse WW, Lemanske RF NEJM 2001;344
Asthma Risk Factors
• Genetic
– Atopy : IgE-mediated response to common
environmental allergens
• Strong genetic component
• 50% of asthma attributable to atopy
– Family history of asthma
• Environmental
– House dust mites, cat dander
– Environmental tobacco smoke in pre-school children
– Ambient air pollution (RR<2)
– Fungi
– Cockroaches
Primary Prevention?:
Clinical Trials in High-Risk Infants
• Prenatal intervention (allergen avoidance) in
infants from birth through one year of age with
first-degree relatives who have diagnosed
asthma
(Chan-Yeung et al. Archives of Ped Adol Med
2000;54:667-63)
• Primary prevention of asthma and atopy during
childhood by allergen avoidance in infancy (birth
through age 8 years)
(Arshad et al. Thorax 2003;58:489-93)
Primary Prevention?:
Hygiene Hypothesis
• Newborn immune system skewed to type 2 T-
helper cell type (Th2)
• Need timely and appropriate environmental
stimuli to create balanced immune response
– Th1: cellular defense, autoimmune diseases
• Viral & bacterial infections, older siblings, early day care,
rural environments
– Th2: humoral defense, allergies, IgE
• Antibiotics, parasites, house-dust mites, cockroaches, urban
environment, diet
• Vaccination, antibiotics, hygiene, fewer siblings
=> Skewed to Th2 => increased atopy / asthma
Risk Factors for
Asthma Exacerbations
• Biologic
– Causal: cat, cockroach, house dust mite, pollens
– Associated: dog, fungi/molds, rhinovirus
– Suggestive: domestic birds, respiratory infections
• Chemical
– Causal: environmental tobacco smoke (pre-school)
– Associated: pollutants
– Suggestive: ETS (older children, adults),
formaldehyde, fragrances
• Other
– Exercise, cold air
IOM 2000, Clearing the Air: Asthma and Indoor Air Exposures
Environmental Epidemiology
• Indoor environment (Chapman, NHANES)
– Self-report of smokers in family, use of gas stove,
having a dog or cat
• Occupational airborne exposure (Bakke)
– Self-report on survey of past or present dust or gas
exposure
– Imputation based on occupational titles
• Low-level ozone – Gent et al. JAMA 2003
– Longitudinal study of asthma exacerbations
– Hourly ozone concentrations from monitoring sites
– Asthmatic children vulnerable to ozone at levels
below current EPA air quality standards
Source: CDC. Surveillance for asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
Source: CDC. Surveillance for asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
Source: CDC. Surveillance for asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
Source: CDC. Surveillance for asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
Source: CDC. Surveillance for asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
Societal Impact of Asthma
Source: CDC. Surveillance for asthma – United States, 1980-1999. MMWR 2002;51(SS-01)
• In 1998, the cost of asthma to the U.S. economy was
estimated to be $12.7 billion
Primary Prevention?:
NIH RFA 2003
• Hypothesis: early life changes in immune
function induced by environmental factors
determine likelihood of developing asthma
– Early cellular/molecular markers of asthma
onset
– Effect of timing, dose and route of antigen
exposure on asthma susceptibility
– Effects of maternal & environmental asthma
risk factors on immune function early in life
– Etc.
Secondary Prevention of Asthma:
• Expert Panel Report 2: Guidelines for the Diagnosis and
Management of Asthma (NHLBI 1997, 2002)
– Stepwise approach based on symptom severity
• Quick-acting bronchodilator (e.g. ß-agonists)
• Prophylactic anti-inflammatory (e.g., steroids)
– Control factors contributing to asthma severity
• Avoid triggers (allergens, tobacco smoke,
• Annual influenza vaccination with persistent asthma
– Assessment and monitoring
– Patient involvement
– written plan for self-management, PEF monitoring
• Environmental controls (e.g. reduced air pollution – see Gent et al.)
• What proportion of medically-attended asthma-related exacerbations
are preventable through proper management?
• How does access to and quality of asthma management vary by
region, socioeconomic status, and race/ethnicity?

Asthma lecture

  • 1.
  • 2.
    Case Definitions “Reversible airwayobstruction with airway inflammation and increased airways responsiveness to a variety of stimuli” Samet JM, Marbury MC, Spengler JD. Health effects and sources of indoor air pollution. Part II. Am Rev Respir Dis. 1988 Jan;137(1):221–242.
  • 3.
    Measuring airway obstruction: Spirometry •PEF = Peak Expiratory Flow – Greatest flow sustained 10 milliseconds with a forced expiration • FEV1 = Forced Expiratory Volume – Volume of air expelled in 1st second of forced expiration • FVC = Forced Vital Capacity – Maximum volume of air exhaled with forced expiration after a maximum inhalation • FEF25-75 = Forced Expiratory Flow between 25% and 75% of FVC – Detects small-airways obstruction
  • 4.
  • 5.
    Council of Stateand Territorial Epidemiologists Asthma Surveillance Case Definition Work Group
  • 6.
    Mortality/Hospitalization Case Definition Confirmed: ·No confirmed case classification for mortality and hospital discharge data. Probable: · death certificates/records listing the asthma diagnostic code (ICD-9 Code: 493; or ICD-10 Codes: J45, J46) as the underlying cause of death. · hospital records listing the asthma diagnostic code (ICD-9-CM Codes: 493.0- 493.9;ICD-10-CM Codes: J45.0-J45.9) as the primary diagnosis. Possible: · death certificates/records listing the asthma diagnostic code as a contributing cause of death. · hospital records listing the asthma diagnostic code as a secondary diagnosis. · 466(acute bronchitis and bronchiolitis), *** in children < 12 years*** · 491.20 and 491.21 (chronic bronchitis), *** in children < 12 years***
  • 7.
    Prevalent Case Definition Confirmed: ·There is no confirmed case classification for self-report. Probable: · A positive response: “Did a doctor (or other health professional) ever tell you that you had asthma?” and “Do you still have asthma?” OR “Have you taken prescription medications for asthma (such as albuterol, inhaled steroids, cromolyn, theophylline, etc) during the past year?” OR “Have you had a wheeze episode in the past year?” Possible: · A positive response “Have you used over-the-counter medications for asthma during the past year?”, OR “Have you experienced episodes of wheezing during the past year?
  • 8.
    Clinical and functionalcriteria • Clinical criteria – Wheezing 2 consecutive days – Chronic cough persisting 3-6 weeks responding to bronchodilators in absence of allergic rhinitis or sinusitis – Nocturnal awakening with dyspnea, cough/wheezing (w/o other medical condition) • Laboratory criteria – Spirometry (FEV1, FVC) – 12%  > short-acting bronchodilator challenge – 20%  FEV1 w/histamine/methacholine/exercise/cold – 20% diurnal variation in PEF over 1-2 weeks
  • 9.
    Clinical and functionalcase definitions Confirmed: any of the clinical symptoms at least 3 times during the past year AND at least one of the laboratory criteria. Probable: In the absence of supporting · laboratory criteria, presence of any of the clinical symptoms which have been reversed by physician treatment with asthma medications and have occurred at least 3 times during the past year. · clinical criteria, at least one of the laboratory criteria during the past year. · laboratory or clinical criteria, taken medications in the past year that were prescribed by a physician for asthma. Possible: the presence of any of the following during the past year: · shortness of breath on exertion, presence of wheezing or chronic cough in the absence of obvious respiratory infection, presence of increased nasal secretion, mucosal swelling, nasal polyps, or chronic sinusitis, hyper expansion of the thorax, sounds of wheezing during normal breathing, prolonged phase of forced exhalation, chest x ray showing hyper expansion, FEV1 less than 80% of predicted value
  • 10.
    Asthma Case Definition EpidemiologicIssues • Overlap with other COPD’s • Partially a diagnosis of exclusion • Different etiologies? • Continuum of symptoms? • More difficult to diagnose in young children • Symptoms & lung function change over time, related to environmental triggers, medication, and age • Definitions based on self-report or medical records depend on physician diagnosis – Diagnostic criteria not standardized
  • 11.
    Pathogenesis of Asthma: IgE-mediatedInflammation Allergen IgE Antibodies Activate Inflammatory Cells Mast cells Lymphocytes Eosinophils Platelets Macrophages Inflammatory Mediators Released Histamine Leukotrines Cytokines Early Response Bronchospasm Edema Airflow Obstruction Late Response Airway Inflammation Airflow Obstruction Airway Hyperresponsiveness Remodelling Adapted from Busse WW, Lemanske RF NEJM 2001;344
  • 13.
    Asthma Risk Factors •Genetic – Atopy : IgE-mediated response to common environmental allergens • Strong genetic component • 50% of asthma attributable to atopy – Family history of asthma • Environmental – House dust mites, cat dander – Environmental tobacco smoke in pre-school children – Ambient air pollution (RR<2) – Fungi – Cockroaches
  • 14.
    Primary Prevention?: Clinical Trialsin High-Risk Infants • Prenatal intervention (allergen avoidance) in infants from birth through one year of age with first-degree relatives who have diagnosed asthma (Chan-Yeung et al. Archives of Ped Adol Med 2000;54:667-63) • Primary prevention of asthma and atopy during childhood by allergen avoidance in infancy (birth through age 8 years) (Arshad et al. Thorax 2003;58:489-93)
  • 15.
    Primary Prevention?: Hygiene Hypothesis •Newborn immune system skewed to type 2 T- helper cell type (Th2) • Need timely and appropriate environmental stimuli to create balanced immune response – Th1: cellular defense, autoimmune diseases • Viral & bacterial infections, older siblings, early day care, rural environments – Th2: humoral defense, allergies, IgE • Antibiotics, parasites, house-dust mites, cockroaches, urban environment, diet • Vaccination, antibiotics, hygiene, fewer siblings => Skewed to Th2 => increased atopy / asthma
  • 16.
    Risk Factors for AsthmaExacerbations • Biologic – Causal: cat, cockroach, house dust mite, pollens – Associated: dog, fungi/molds, rhinovirus – Suggestive: domestic birds, respiratory infections • Chemical – Causal: environmental tobacco smoke (pre-school) – Associated: pollutants – Suggestive: ETS (older children, adults), formaldehyde, fragrances • Other – Exercise, cold air IOM 2000, Clearing the Air: Asthma and Indoor Air Exposures
  • 17.
    Environmental Epidemiology • Indoorenvironment (Chapman, NHANES) – Self-report of smokers in family, use of gas stove, having a dog or cat • Occupational airborne exposure (Bakke) – Self-report on survey of past or present dust or gas exposure – Imputation based on occupational titles • Low-level ozone – Gent et al. JAMA 2003 – Longitudinal study of asthma exacerbations – Hourly ozone concentrations from monitoring sites – Asthmatic children vulnerable to ozone at levels below current EPA air quality standards
  • 18.
    Source: CDC. Surveillancefor asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
  • 19.
    Source: CDC. Surveillancefor asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
  • 20.
    Source: CDC. Surveillancefor asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
  • 22.
    Source: CDC. Surveillancefor asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
  • 23.
    Source: CDC. Surveillancefor asthma – United States, 1980-2004. MMWR 2007;56(SS-08)
  • 25.
    Societal Impact ofAsthma Source: CDC. Surveillance for asthma – United States, 1980-1999. MMWR 2002;51(SS-01) • In 1998, the cost of asthma to the U.S. economy was estimated to be $12.7 billion
  • 26.
    Primary Prevention?: NIH RFA2003 • Hypothesis: early life changes in immune function induced by environmental factors determine likelihood of developing asthma – Early cellular/molecular markers of asthma onset – Effect of timing, dose and route of antigen exposure on asthma susceptibility – Effects of maternal & environmental asthma risk factors on immune function early in life – Etc.
  • 27.
    Secondary Prevention ofAsthma: • Expert Panel Report 2: Guidelines for the Diagnosis and Management of Asthma (NHLBI 1997, 2002) – Stepwise approach based on symptom severity • Quick-acting bronchodilator (e.g. ß-agonists) • Prophylactic anti-inflammatory (e.g., steroids) – Control factors contributing to asthma severity • Avoid triggers (allergens, tobacco smoke, • Annual influenza vaccination with persistent asthma – Assessment and monitoring – Patient involvement – written plan for self-management, PEF monitoring • Environmental controls (e.g. reduced air pollution – see Gent et al.) • What proportion of medically-attended asthma-related exacerbations are preventable through proper management? • How does access to and quality of asthma management vary by region, socioeconomic status, and race/ethnicity?