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Transcript
Bronchial Asthma
Ayman A Hamid Farghaly
MD FCCP
Definition of Asthma

A chronic inflammatory disorder of the
airways

Many cells and cellular elements play a role

Chronic inflammation is associated with
airway hyperresponsiveness that leads to
recurrent episodes of wheezing,
breathlessness, chest tightness, and
coughing

Widespread, variable, and often reversible
airflow limitation
Asthma Inflammation: Cells and Mediators
Source: Peter J. Barnes, MD
Mechanisms: Asthma Inflammation
Source: Peter J. Barnes, MD
Asthma Inflammation: Cells and Mediators
Source: Peter J. Barnes, MD
Airway Remodeling
Environment
Normal
Airway
Function
Repair
Remodeling
Smooth muscle
hypertrophy/hyper
plasia
Matrix deposition
Angiogenesis Epithelial and goblet cell
phenotype alterations
Genetic
predispositi
on
Asthma
Injury
Genetic
predisposition for
remodeling
Burden of Asthma

Asthma is one of the most common chronic
diseases worldwide with an estimated 300
million affected individuals

Prevalence increasing in many countries,
especially in children

A major cause of school/work absence
Asthma Prevalence and Mortality
Risk Factors for Asthma

Host factors: predispose individuals to, or
protect them from, developing asthma

Environmental factors: influence
susceptibility to development of asthma in
predisposed individuals, precipitate
asthma exacerbations, and/or cause
symptoms to persist
Factors that Influence Asthma
Development and Expression
Host Factors
 Genetic
- Atopy
- Airway
hyperresponsiveness
 Gender
 Obesity
Environmental Factors
 Indoor allergens
 Outdoor allergens
 Occupational sensitizers
 Tobacco smoke
 Air Pollution
 Respiratory Infections
 Diet
Genetics of Asthma
While it is generally agreed that there is
a major hereditary contribution to the
etiology of asthma, the inheritance
patterns are complex, and asthma
cannot be simply classified as having
an autosomal-dominant, recessive, or
sex-linked mode of inheritance.
Genetics & Asthma ..
Chromosomes 2q, 3p, 5q, 6p, 12q,
13q, 19q, and 21q are likely to
contain genes for allergy and
asthma.
Factors that Exacerbate Asthma

Allergens
Respiratory infections
Exercise and
hyperventilation
Weather changes
Sulfur dioxide

Food additives , drugs




Asthma Diagnosis


History and patterns of symptoms
Measurements of lung function
- Spirometry
- Peak expiratory flow

Measurement of airway responsiveness

Measurements of allergic status to identify risk
factors

Extra measures may be required to diagnose
asthma in children 5 years and younger and the
elderly
Is it Asthma?

Recurrent episodes of wheezing

Troublesome cough at night

Cough or wheeze after exercise

Cough, wheeze or chest tightness
after exposure to airborne allergens
or pollutants

Colds “go to the chest” or take more
than 10 days to clear
Typical Spirometric (FEV1)
Tracings
Volume
FEV1
Normal Subject
Asthmatic (After Bronchodilator)
Asthmatic (Before Bronchodilator)
1
2
3
4
Time (sec)
5
Note: Each FEV1 curve represents the highest of three repeat measurements
Nonatopic Asthma




Patients who have none of the typical features of
atopy.
Older .
Intrinsic asthma may involve activation by an
as-yet-unidentified antigen.
Putative nonallergic antigens that may cause
such reactions include viral antigens or
inappropriately recognized “self-antigens.”
Clinical Control of Asthma
 No (or minimal)* daytime symptoms
 No limitations of activity
 No nocturnal symptoms
 No (or minimal) need for rescue medication
 Normal lung function
 No exacerbations
_________
* Minimal = twice or less per week
Levels of Asthma Control
Characteristic
Controlled
(All of the
following)
Partly controlled
(Any present in any
week)
Daytime symptoms
None (2 or less /
week)
More than
twice / week
Limitations of
activities
None
Any
Nocturnal symptoms
/ awakening
None
Any
Need for rescue /
“reliever” treatment
None (2 or less /
week)
More than
twice / week
Lung function
(PEF or FEV1)
Normal
< 80% predicted or
personal best (if
known) on any day
Exacerbation
None
One or more / year
Uncontrolled
3 or more
features of
partly
controlled
asthma
present in any
week
1 in any week
Asthma Management and Prevention
Program: Five Interrelated Components
1. Develop Patient/Doctor Partnership
2. Identify and Reduce Exposure to
Risk Factors
3. Assess, Treat and Monitor Asthma
4. Manage Asthma Exacerbations
5. Special Considerations
Component 1: Develop
Patient/Doctor Partnership

Educate continually

Include the family

Provide information about asthma

Provide training on self-management skills

Emphasize a partnership among health
care providers, the patient, and the patient’s
family
Education
Component 2: Identify and Reduce
Exposure to Risk Factors

Reduce exposure to indoor allergens

Avoid tobacco smoke

Avoid vehicle emission

Identify irritants in the workplace

Explore role of infections on asthma
development, especially in children and
young infants
Influenza Vaccination
 Influenza vaccination should be
provided to patients with asthma when
vaccination of the general population is
advised
 However, routine influenza vaccination
of children and adults with asthma
does not appear to protect them from
asthma exacerbations or improve
asthma control
Asthma Management and Prevention Program
Factors Involved in Non-Adherence
Medication Usage

Difficulties associated
with inhalers

Complicated regimens

Fears about, or actual
side effects

Cost

Distance to pharmacies
Non-Medication Factors

Misunderstanding/lack of
information

Fears about side-effects

Inappropriate expectations

Underestimation of severity

Attitudes toward ill health

Cultural factors

Poor communication
Component 3: Assess, Treat
and Monitor Asthma
The goal of asthma treatment, to
achieve and maintain clinical control,
can be achieved in a majority of
patients with a pharmacologic
intervention strategy developed in
partnership between the
patient/family and the health care
professional
Component 4: Asthma Management and Prevention Program
Controller Medications









Inhaled glucocorticosteroids
Leukotriene modifiers
Long-acting inhaled β2-agonists
Systemic glucocorticosteroids
Theophylline
Cromones
Long-acting oral β2-agonists
Anti-IgE
Systemic glucocorticosteroids
Estimate Comparative Daily Dosages for
Inhaled Glucocorticosteroids by Age
Drug
Low Daily Dose (g)
> 5 y Age < 5 y
Medium Daily Dose (g)
> 5 y Age < 5 y
Beclomethasone
200-500
100-200
>500-1000
>200-400
Budesonide
200-600
100-200
600-1000
>200-400
Budesonide-Neb
Inhalation Suspension
Ciclesonide
250-500
80 – 160
High Daily Dose (g)
> 5 y Age < 5 y
>1000
>1000
>500-1000
>400
>400
>1000
80-160
>160-320
>160-320
>320-1280
>320
Flunisolide
500-1000
500-750
>1000-2000
>750-1250
>2000
>1250
Fluticasone
100-250
100-200
>250-500
>200-500
>500
>500
Mometasone furoate
200-400
100-200
> 400-800
>200-400
>800-1200
Triamcinolone acetonide
400-1000
400-800
>1000-2000
>800-1200
>2000
>400
>1200
Component 4: Asthma Management and Prevention Program
Reliever Medications
 Rapid-acting inhaled β2-agonists
 Systemic glucocorticosteroids
 Anticholinergics
 Theophylline
 Short-acting oral β2-agonists
Component 4: Asthma Management and Prevention Program
Allergen-specific Immunotherapy

Greatest benefit of specific immunotherapy
using allergen extracts has been obtained in
the treatment of allergic rhinitis

The role of specific immunotherapy in asthma is
limited

Specific immunotherapy should be considered
only after strict environmental avoidance and
pharmacologic intervention, including inhaled
glucocorticosteroids, have failed to control
asthma

Perform only by trained physician
REDUCE
LEVEL OF CONTROL
TREATMENT OF ACTION
maintain and find lowest
controlling step
partly controlled
consider stepping up to
gain control
INCREASE
controlled
uncontrolled
exacerbation
step up until controlled
treat as exacerbation
REDUCE
INCREASE
TREATMENT STEPS
STEP
STEP
STEP
STEP
STEP
1
2
3
4
5
Treating to Maintain Asthma Control
 When control as been achieved,
ongoing monitoring is essential to:
- maintain control
- establish lowest step/dose treatment
 Asthma control should be monitored
by the health care professional and
by the patient
Treating to Maintain Asthma Control
Stepping down treatment when asthma is
controlled
 When controlled on medium- to
high-dose inhaled
glucocorticosteroids: 50% dose
reduction at 3 month intervals
(Evidence B)
 When controlled on low-dose
inhaled glucocorticosteroids: switch
to once-daily dosing (Evidence A)
Component 3: Assess, Treat and Monitor
Asthma – Children 5 Years and Younger
Many asthma medications (e.g.
glucocorticosteroids, β2- agonists,
theophylline) are metabolized faster in
children than in adults, and younger
children tend to metabolize medications
faster than older children
Component 3: Assess, Treat and Monitor
Asthma – Children 5 Years and Younger


Long-term treatment with inhaled
glucocorticosteroids has not been shown
to be associated with any increase in
osteoporosis or bone fracture
Studies including a total of over 3,500
children treated for periods of 1 – 13 years
have found no sustained adverse effect of
inhaled glucocorticosteroids on growth
Bronchial Thermoplasty
Special Considerations
Special considerations are required to
manage asthma in relation to:
 Pregnancy
 Surgery
 Rhinitis, sinusitis, and nasal polyps
 Occupational asthma
 Respiratory infections
 Gastroesophageal reflux
 Aspirin-induced asthma
 Anaphylaxis and Asthma
Neutrophilic inflammation in
asthma



The release of IL-8 and GRO-α from airway epithelial cells
may be stimulated by viral infection.
Allergens may stimulate dendritic cells to release IL-23,
activating Th17 cells to release TNF-α. This enhances
inflammation and stimulates the release of IL-8 and GRO-α,
which recruit neutrophils into the airways.
These release further IL-8 plus transforming growth factorβ (TGF-β), which activates fibroblasts to cause fibrosis, and
neutrophil elastase and matrix metalloproteinase (MMP)-9
which stimulate mucus hypersecretion from goblet cells.
Neutrophils & Asthma
Is asthma a Neutrophilic disease?


Asthmatic patients who show an
increased neutrophil count in the
airways tend to be older, and have
an overall increase in the total
number of inflammatory cells
compared to patients with an
eosinophilic pattern of asthma.
They are also more likely to be
female and non-atopic.


An increased neutrophil count is also
found in the induced sputum of patients
with asthma who smoke, and sputum
neutrophils are also increased in asthmatic
patients during exacerbations, which are
mostly due to infections of the upper
respiratory tract.
In children with asthma, a marked
increase in neutrophils is also seen in
induced sputum during exacerbations.

An increase in neutrophil numbers is
now a recognised feature in patients
with asthma, particularly in those
with more severe disease, and in
exacerbations.

The increase in neutrophil numbers
is likely to be a contributing factor to
loss of asthma control, indicating
that there may be a therapeutic
benefit to targeting neutrophils.

Neutrophil asthma appears to be
poorly responsive to corticosteroids
even when given at high doses,
suggesting that other therapies may
be needed.


LABA have recently been shown to
reduce neutrophilic inflammation in
asthma, an effect that may be
mediated via inhibition of IL-8 or
other related chemokines.
This provides a rationale for the use
of combination inhalers in asthma
treatment,
Asthma & Pregnancy

Asthma is one of the most common
conditions that can complicate a
pregnancy, and the question whether
the asthma itself or the medications
used to treat it have any negative
effects on the unborn baby or infant
has become increasingly urgent.

Asthma in itself does not increase
the risk of having a premature
birth.

but taking steroid tablets or
theophylline does. No increased risk
was seen with taking inhaled
corticosteroids.

The risk of low birth weight or size
increases with the severity of the
asthma symptoms, regardless of the
medication.


The recommended is a more active
treatment of pregnant women with
mild or moderate asthma,
Add steroid tablets only if the
asthma gets considerably worse.