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Optimizing management of asthma and COPD

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Title: Optimizing management of asthma and COPD


1
Optimizing Management of Asthma and COPD
  • Dr. Surinder K Jindal
  • www.jindalchest.com

2
Definition of COPD Asthma
  • COPD is a preventable and treatable disease with
    some significant extrapulmonary effects that may
    contribute to the severity in individual
    patients.
  • It is characterized by airflow limitation that is
    not fully reversible. The airflow limitation is
    usually progressive and associated with an
    abnormal inflammatory response of the lung to
    noxious particles or gases.
  • Asthma - Chronic Inflammatory disorder of
    airways
  • characterized by Episodic, Reversible
    bronchospasm
  • resulting from an exaggerated
    bronchoconstrictor response
  • to various stimuli.

3
COPD IS NOT ASTHMA
  • Different causes
  • Different inflammatory cells
  • Different mediators
  • Different inflammatory consequences
  • Different sites
  • Different response to treatment

4
Inflammation
Asthma COPD
Inflammatory cells Mast cell, Eosinophil Neutrophil
CD4 cells CD8 cells
Macrophages Macrophages
Inflammatory LTB4, histamine LTB4
mediators IL-4, IL-5, IL-13 TNF-a
Oxidative stress Oxidative stress
Inflammatory effect All airways Peripheral airways
AHR AHR
Epithelial shedding Epithelial metaplasia
Fibrosis Fibrosis
No parenchymal involvement Parenchymal destruction
Mucus secretion Mucus secretion
Response to steroid
5
Pathogenesis of COPD
Cigarette smoke Biomass particles Particulates
Host factors Amplifying mechanisms
LUNG INFLAMMATION
Anti-oxidants
Anti-proteinases
Oxidative stress
Proteinases
Repair mechanisms
COPD PATHOLOGY
Source Peter J. Barnes, MD
6
Asthma Pathogenesis
INFLAMMATION
7
Investigations
Asthma COPD
Chest radiograph Normal Suggestive
Spirometry Obstructive defect Obstructive defect
Good reversibility Poor reversibility
AHR Very common May be present
DLCO Normal / Increased Decreased
Lung elastic recoil Normal Increased
Thoracic CT scan Airway wall thickening Airway wall thickening
Mucus plugs (ABPA) Emphysema
Air trapping Air trapping
In general, investigations are poor discriminators
8
(No Transcript)
9
Basic Principles of Management of Asthma And COPD
  • Removal/ Avoidance of risk-factor/s
  • Pharmacotherapy
  • Bronchodilators
  • Anti-inflammatory drugs
  • (Corticosteroids)
  • Supportive therapy
  • Non-pharmacological managements
  • Management of Acute Exacerbations
  • Management of Complications

10
Bronchodilators
  • Bronchodilator medications - central to symptom
    management
  • Reduce breathlessness, improve lung function,
    improve HRQOL
  • Inhaled therapy is preferred
  • Choice between ß2-agonist (short acting and
    long-acting), anticholinergic agents,
    theophylline or a combination of these drugs

11
Inhalers vs Oral drugs
  • Inhalation route preferred
  • MDI, DPI, or nebulized aerosol
  • MDI with spacer - preferred device
  • DPI easier to use, but costlier
  • Patients should be instructed regarding proper
    use of the inhaler device and technique should be
    checked regularly

Cochrane Database Syst Rev 2002 1 CD002170
12
Bronchodilators
  • Therapy - availability and individual response in
    terms of symptom relief and side effects
  • Prescribed - on as-needed or regular basis to
    prevent or reduce symptoms
  • Long-acting drugs are more convenient
  • Combination of ß2-agonist and anticholinergic
    agents - better than either drug given alone
    (lung function)

Eur Respir J 2005 25 1084-1106
13
Anti-inflammatory Drugs
  • Corticosteroids
  • Inhaled (Beclomethasone, Budesonide,
  • Fluticasone, Mometasone,
    Triamcinalone)
  • Oral (Prednisone, Prednisolone,
  • Dexamethasone,
    Methylprednisolone)
  • Parenteral (Hydrocortisone,
  • Methylprednisolone,
    Dexamethasone etc)
  • Immunosuppressants
  • Immunomodulators

14
What are your objectives while treating a patient
with COPD?
No treatment has shown to reverse the
pre-existing changes that have occurred in COPD
15
Four Components of COPD Management
  • Assess and monitor disease
  • Reduce risk factors
  • Manage stable COPD
  • Education
  • Pharmacologic
  • Non-pharmacologic
  • Manage exacerbations

16
Objectives
  • Prevent disease progression
  • Relieve symptoms
  • Improve exercise tolerance
  • Improve health status
  • Prevent and treat exacerbations
  • Prevent and treat complications
  • Reduce mortality
  • Minimize side effects from treatment

Am J Respir Crit Care Med 2001 163 1256-1276
17
Management of stable COPD
  • None of the existing medications for COPD has
    been shown to modify the long-term decline in
    lung function that is the hallmark of this
    disease (Evidence A)
  • Therefore, pharmacotherapy for COPD is used to
    decrease symptoms and/or complications

18
Basic considerations
  • Heterogeneous condition
  • All patients should be viewed as individuals -
    presentation, history, symptoms, disability
    response to drugs
  • Important factors - acceptability, adverse
    effects, efficacy
  • Drug titration - airflow obstruction, symptoms,
    exercise tolerance, frequency of exacerbations

19
Which bronchodilator???1. Theophylline2.
Ipratropium3. Tiotropium4. Beta-2 agonists
20
Bronchodilator in COPD
  • Predominant parasympathetic tone first choice
    anticholinergic
  • Tiotropium or Ipratropium
  • Tiotropium reduced the COPD exacerbation (OR
    0.74 95 CI 0.66 to 0.83) and hospitalizations
    (OR 0.64 95 CI 0.51 to 0.82) compared to
    placebo or ipratropium
  • Combination of tiotropium and formoterol ideal

Cochrane Database Syst Rev 2005 2 CD002876
21
Cochrane Database Syst Rev 2005 2 CD002876
22
Commonly used bronchodilators
  • Drugs MDI/DPI (µg/dose) Oral (mg)
  • Beta agonists
  • Salbutamol 100-200 2-4mg tid/qid
  • Terbutaline 250-500 2.5-5 mg tid
  • Salmeterol 25-50
  • Formoterol 6-12
  • Bambuterol 10-20mg/day
  • Anticholinergics
  • Ipratropium 40-160
  • Tiotropium 18
  • Methylxanthines
  • Theophyllines 200-600 mg/day

23
Is there a role for ICS in COPD?
  • Is there a role for ICS in COPD?
  • Yes
  • No
  • Limited
  • Acute exacerbation

24
Inhaled corticosteroids in COPD
Anti-inflammatory effects with ICS in COPD
include Attenuation of neutrophil activation
recruitment Reduction of neutrophil
chemotaxis Reduction in the CD8/CD4
ratio Reduction in IL-8 levels Reduction in
eosinophils RANTES, associated with
exacerbations of COPD.
Decreased symptoms Decreased number and severity
of exacerbations Improved health status Reduction
of cardiac events - IHD Decreased mortality (?)
Options beclomethasone, budesonide, fluticasone,
triamcinolone Oral glucocorticosteroids not
recommended for long-term use in COPD
25
Cochrane review on efficacy of the use of ICS in
COPD
Forty-seven primary studies with 13,139
participants met the inclusion criteria. Long
term use of ICS (gt six months) did not
significantly reduce the rate of decline in FEV1
in COPD patients Long term use of ICS reduced
the mean rate of exacerbations There was an
increased risk of oropharyngeal candidiasis and
hoarseness. No major effect on fractures and
bone mineral density over 3 years.
Cochrane Database Syst Rev. 2007 Apr
18(2)CD002991.
26
30 reduction in exacebations
Am J Med 2002 113 59-65
27
Pooled analysis of randomized trials of ICS on
mortality in COPD
27 reduction
27 risk reduction
Thorax 2005 60 992-997
28
What other therapies can be used in patients with
COPD?
  1. Mucolytics
  2. Immunomodulators
  3. Antibiotics
  4. Respiratory stimulants

29
Other drugs
  • Vaccines Influenza and Pneumococcus in all
    patients
  • Oral mucolytics - reduce the viscosity of sputum,
    no effect on lung function
  • Oral immunostimulatory agent OM-85 BV (extract
    of 8 bacteria) - recurrent exacerbations
  • Antioxidants - N-acetylcysteine- no clear role

Am J Respir Crit Care Med 2001 163 1256-1276
30
Other drugs
  • Respiratory stimulants almitrine and doxapram
    no role
  • Antibiotics no role in stable COPD
  • Others - Nedocromil, leukotriene modifiers and
    alternate forms of medicine - no clear role

Am J Respir Crit Care Med 2001 163 1256-1276
31
Therapy at Each Stage of COPD
IV Very Severe
III Severe
II Moderate
I Mild
FEV1/FVC lt 70 FEV1 lt 30 predicted or FEV1 lt 50 predicted plus chronic respiratory failure
FEV1/FVC lt 70 30 lt FEV1 lt 50 predicted
FEV1/FVC lt 70 50 lt FEV1 lt 80 predicted
FEV1/FVC lt 70 FEV1 gt 80 predicted
Add regular treatment with one or more
long-acting bronchodilators (when needed) Add
rehabilitation
Add inhaled glucocorticosteroids if repeated
exacerbations
Add long term oxygen if chronic respiratory
failure. Consider surgical treatments
32
Management of Stable COPD Non-Pharmacologic
Treatments
  • Rehabilitation All COPD patients benefit from
    exercise training programs, improving with
    respect to both exercise tolerance and symptoms
    of dyspnea and fatigue (Evidence A).
  • Oxygen Therapy The long-term administration of
    oxygen (gt 15 hours per day) to patients with
    chronic respiratory failure has been shown to
    increase survival (Evidence A).

33
ExacerbationsWhat are they?
  • An event which in the natural course of the
    disease characterized by a change in the
    patients baseline dyspnea, cough and/or sputum
    and beyond the normal day-to-day variations
  • Acute in onset
  • May warrant a change in regular medication
  • Patients are living with daily breathlessness and
    cough
  • Fear about worsening
  • Unpredictable

34
Exacerbations result in worsening of quality of
life Data from GLOBE study
Am J Med 2006119(10A)S38-S45
35
Treatment of exacerbation
  • Inhaled bronchodilators salbutamol/ ipratropium
  • Oral prednisolone 30-40 mg for 7-10 days
  • Antibiotics
  • respiratory quinolones, macrolides, co-amoxyclav,
    2o or 3o cephalosporins
  • FEV1lt 35 with recurrent courses of oral steroids
    etc FQ with antipseudomonal activity

36
Acute exacerbations are defining moments in a
COPD patient particularly if hospitalization is
needed
Disease Accelerated progression Enhanced airway
inflammation Adverse effects of oral steroids
Patient Death Worsening quality of life Costs
It is no less serious than an acute myocardial
infarction
37
Goals of Asthma Management
  1. Minimal (ideally no) symptoms
  2. Minimal (or no) symptoms on exercise
  3. Minimal need for relievers
  4. No exacerbations
  5. No limitation of physical activity
  6. Normal (or near normal) PFT
  7. Minimal side effects of drugs
  8. Prevention of irreversible obstruction
  9. Prevent asthma related mortality

38
Stage-wise Control
  • Day time symptoms lt 1/week
    Relievers
  • and night time lt 2/month
  • Need for relievers lt 1/week
    Controllers
  • Need for relievers lt 3/day
    Doctor visit
  • Requirement for drugs (as per table)
  • Maintenance of goals for
    Step down
  • at least 3 months
    (25 reduction in dosages)

39
Anti-asthma Drugs
  • Controllers
  • Glucocorticoids Inhaled/Systemic
  • Inhaled long acting ?-2 agonists
  • Oral theophyllines
  • Leukotriene receptor antagonists
  • Cromones
  • Oral long acting ?-2 agonist
  • Relievers
  • Rapid acting ? 2 agonists
  • Oral glucocorticoids
  • Inhaled anticholinergics
  • Oral short acting ?2 agonists

40
GINA Guidelines for Asthma
  • Mild intermittent
  • Mild persistent
  • Moderate persistent
  • Severe Persistent

SOS bronchodilators
ICS/LTRA
ICS LABA/LTRA combination
ICS LABA LTRA AC OS
At each step SOS bronchodilator therapy is
required
GINA 2004
41
Asthma Control vs. Severity
  • Asthma Control
  • Clinical status of disease (with ongoing therapy)
  • Patient-centered approach
  • Asthma Severity
  • Underlying disease (asthma)
  • (in absence of any treatment)
  • Physician-centered approach

42
Asthma Levels of Control
Controlled (All of the following) Partly Controlled (Any measure present) Un-controlled
Nocturnal symptoms or awakening None Any 3 features of partly controlled asthma
Daytime symptoms 2 per week gt 2 per week 3 features of partly controlled asthma
Limitation of activities None Any 3 features of partly controlled asthma
Need for reliever or rescue treatment 2 per week gt 2 per week 3 features of partly controlled asthma
FEV1 or PEF Normal lt80 predicted 3 features of partly controlled asthma
Adapted from GINA (Global Initiative for Asthma)
guidelines 2010
43
Asthma Management
  • Maintain well controlled state
  • Add drugs, step-wise, determined by control
  • ICS LABAs constitute the cornerstone of
    treatment
  • Use of SABA, as needed
  • SMART approach (Use of single inhaler for
    maintenance and SOS use)

44
Difficult Asthma
  • Asthma which is difficult to control with maximum
    treatment recommended as appropriate for that
    stage
  • Persistence of symptoms, frequent exacerbations
    or airway obstruction despite high (or optimum)
    medication

45
Considerations in Management of SR/SD Asthma
  • Correct diagnostic work up
  • SR asthmatics do respond to bronchodilator
    therapy and such medications should be instituted
    early as rescue therapy.
  • Presence of persistent airway inflammation
    predisposes them to airway remodeling and long
    term irreversible airways diseases. Thus it is of
    paramount importance to treat their inflammation
    early and effectively.

46
SUMMARY- Asthma
  • Airway inflammation, a prominent feature in
    asthma, needs to be targeted with effective
    medication to achieve asthma control.
  • Appropriate guidelines need to be followed for
    best results. ICS ina combination with LABAs
    remain the cornerstone of treatment.
  • A major unmet need is to treat patients with
    severe asthma who are relatively
    corticosteroid-resistant more effectively.
  • A number of pharmaceutical approaches currently
    in clinical development, show promise in
    targeting specific cytokines, inflammatory cells,
    or inflammatory mechanisms.

47
Summary - COPD
Current therapy for COPD remains
sub-optimal Concomitant use of LABAs with ICS
influences both airflow obstruction airway
inflammation. The use of ICS LABA in
combination for severe COPD help in achieving
patient centered outcomes. The clinical benefits
are manifested by the reduction in the number and
severity of exacerbations, lung function
improvement improved health status of COPD
patients
48
Conclusion
  • Budesonide/formoterol was shown to be an
    effective treatment for the management of
    moderate-to-severe COPD in
  • Reducing severe exacerbations
  • Providing early and sustained improvements in
    lung function and symptoms, Improvements in
    health-related quality of life.
  • Budesonide/formoterol demonstrated a similar
    safety profile to placebo.

Szafransky Eu Resp J 20032174-81
49
Important Treatment Recommendations
GINA NIH BTS
1 Management steps 4 4 5
2 Inhaled CS Steps 2 to 4 Low doses Step 2 Steps 2 to 5
3 Add on Therapies
LABA Steps 3 and 4 Step 2 onwards Step 3 onwards
SR Theophylline Step 4 -do- -do-
LT modifiers -do- -do- -do-
Oral CS -do- -do- Step 5
50
PDE-4 Inhibitors
  • Roflumilast, orally active PDE-4 inhibitor,
    dose-related inhibition of late-phase
    bronchospasm following allergen challenge in mild
    asthma
  • Improvements in lung function ( FEV1) , asthma
    symptoms, and reductions in rescue medication
    use, vs ICS
  • Ciclamilast - mediates AHR through inhibition of
    PDE-4D mRNA expression and down-modulation of
    PDE-4 activity, reduced inflammation and mucus
    hypersecretion

Ann Allergy Asthma Immunol 2006 96679686 Eur J
Pharmacol 2006 547125135
51
A new paradigm A systemic disease, needs a
systemic approach
  • Asthma is a systemic disease
  • Required
  • New classes that are effective in severe poorly
    controlled asthma
  • An oral treatment that is as effective as inhaled
    corticosteroids without any side effects
  • Drugs that modify or even cure the disease

J Allergy Clin Immunol 2007
52
Well Controlled asthma
  • No or minimal symptoms
  • Minimal use of rescue medication
  • No significant limitation in activity
  • (Near) normal lung function
  • GINA-2006

53
Algorithmic Management of Acute Severe
Asthma Unable to complete a sentence in one
breath, RR gt 30/minute, use of accessory muscles
of respiration, HR gt 120/minute, pulsus paradoxus
gt 25 mm Hg, extensive wheeze, PEFR lt 50, PaO2 lt
60 mm Hg, PaCO2 gt 45 mm Hg
Salbutamol 2.5 mg q 15 minutes Ipratropium 250
mcg q 15 minutes PO prednisolone 40-60 mg/day
Sustained improvement at 1hour- Discharge on oral
steroids and bronchodilators
No improvement- ADMISSION IN HOSPITAL OR ICU
54
Management of SRA/SDA
  • High dose inhaled corticosteroids are the first
    line option
  • Omalizumab is effective in reducing oral
    corticosteroid requirements in allergic asthma
  • Methotrexate, gold, and cyclosporine have
    corticosteroidsparing effects clinically that
    must be weighed against a serious adverse effect
    profile
  • Nebulized diuretics and lidocaine, with a low
    adverse effect profile, offer promising results
    but require further study

Randhawa et al. 30 yrs review
55
Acute asthma Algorithmic management
56
Use of ACT
  • Different populations and sub-populations
    (Literacy, language, socio-economic factors,
    urban/rural residence, age, sex etc.)
  • Primary health-care settings
  • Abandoning lung function measurements
  • Under-assessment and under treatment

57
GINA Classification of Control
  • Controlled
  • No or minimal symptoms
  • Minimal use of rescue medication
  • No significant limitation in activity
  • (Near) normal lung function
  • Partly controlled
  • Poorly controlled


  • GINA-2006

58
A new paradigm A systemic diseaseneeds a
systemic approach
  • Asthma is a systemic disease
  • New classes that are effective in severe poorly
    controlled asthma
  • An oral treatment that is as effective as inhaled
    corticosteroids without any side effects
  • Drugs that modify or even cure the disease

J Allergy Clin Immunol 20071201269-75
59
Instruments for control measurements
  • Asthma Control Test (ACT)
  • Asthma Control Questionnaire (ACQ)
  • Asthma Therapy Assessment Questionnaire (ATAQ)
  • Asthma Control Scoring System (ACSS)
  • Asthma-symptom diary

60
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