Professional Documents
Culture Documents
Program Objectives
Increase appreciation of asthma as a global public health problem
Present key recommendations for diagnosis and management of asthma Provide strategies to adapt recommendations to varying health needs, services, and resources
Identify areas for future investigation of particular significance to the global community
GINA Structure
Executive Committee
Chair: Tim Clark, MD
Dissemination Committee
Chair: Martyn Partridge, MD
Science Committee
Chair: Paul OByrne, MD
GINA reports prepared during workshops conducted in cooperation with the U.S. National Heart, Lung, and Blood Institute, NIH and the World Health Organization.
GINA Sponsors
AstraZeneca
Aventis Bayer Byk Gulden Chiesi GlaxoSmithKline
Executive Committee
T. Clark, UK, Chair J. Bousquet, France W. Busse, USA S. Holgate, UK C. Lenfant, USA P. OByrne, Canada K. Ohta, Japan M. Partridge, UK S. Pedersen, Denmark R. Singh, India A. Sheffer, USA W. Tan, Singapore
Science Committee
P. OByrne, Canada, Chair P. Barnes, UK P. Gibson, Australia E. Bateman, S. Africa S. Holgate, UK J. Bousquet, France J. Kips, Belgium W. Busse, USA K. Ohta, Japan J. Drazen, USA S. Pedersen, Denmark M. FitzGerald, Canada E. von Mutius, Germany
With the Dissemination Committee, develop methods to disseminate new scientific findings that impact on GINA documents
Dissemination Committee
M. Partridge, UK, chair G. Anabwani, Botswana R. Beasley, N. Zealand H. Campos, Brazil Y. Chen, China F. Gallefoss, Norway M. Haida, Japan J. Khan, Pakistan R. Neville, UK A. Sheffer, USA J. Sinnadurai, Malaysia R. Singh, India W. Tan, Singapore R. Tomlins, Australia O. van Schyack, Netherlands H. Zar, S. Africa
GINA Documents
Workshop Report: Global Strategy for
Asthma Management and Prevention
(updated 2002)
Pocket guide for health care providers Pocket guide for management of pediatric
asthma (available mid-2002)
Randomized clinical trials Rich body of data Randomized clinical trials Limited body of data Non-randomized trials Observational studies Panel judgment consensus
B
C D
Definition of Asthma
Definition of Asthma
Asthma is a chronic inflammatory disorder of the airways in which many cells and cellular elements play a role
Chronic inflammation causes an associated increase in airway hyperresponsiveness that leads to recurrent episodes of wheezing, breathlessness, chest tightness, and coughing, particularly at night or in the early morning
These episodes are usually associated with widespread but variable airflow obstruction that is often reversible either spontaneously or with treatment
INFLAMMATION
Airway Hyperresponsiveness Airflow Obstruction
Symptoms
Burden of Asthma
An overall increase in severity of asthma increases the pool of patients at risk for death
Burden of Asthma
(Omran et al)
(NHIS)
(Shaw et al)
(Peat et al)
10
15
20
25
30
35
Prevalence (%)
Countries should enter their own data on burden of asthma. The following three slides are US data on prevalence, hospitalization rates and mortality.
Age (years)
<18 18-44
45-64
65+ Total (All Ages)
30
25 20
15
10 5 0 74 76 78 80 82 84 86 Year 88 90 92 94 96
1985
1990 Year
1995
2000
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
Allergens Air Pollutants Respiratory infections Exercise and hyperventilation Weather changes Sulfur dioxide Food, additives, drugs
Environmental Factors
Indoor allergens Outdoor allergens Occupational sensitizers Tobacco smoke Air Pollution Respiratory Infections Parasitic infections Socioeconomic factors Family size Diet and drugs Obesity
Is it Asthma?
Asthma Diagnosis
Classification of Severity
CLASSIFY SEVERITY
Clinical Features Before Treatment
Symptoms STEP 4 Severe Persistent STEP 3 Continuous Limited physical activity Daily Attacks affect activity Nocturnal Symptoms FEV1 or PEF 60% predicted
Frequent
> 1 time a week but < 1 time a day < 1 time a week Asymptomatic and normal PEF between attacks
Variability 20 - 30%
2 times a month
80% predicted
The presence of one feature of severity is sufficient to place patient in that category.
Achieve and maintain control of symptoms Prevent asthma episodes or attacks Maintain pulmonary function as close to normal levels as possible Maintain normal activity levels, including exercise Avoid adverse effects from asthma medications Prevent development of irreversible airflow limitation Prevent asthma mortality
Control of Asthma
2-agonist
The most effective management is to prevent airway inflammation by eliminating the causal factors Asthma can be effectively controlled in most patients, although it can not be cured The major factors contributing to asthma morbidity and mortality are underdiagnosis and inappropriate treatment
Any asthma more severe than intermittent asthma is more effectively controlled by treatment to suppress and reverse airway inflammation than by treatment only of acute bronchoconstriction and symptoms
Part 1: Educate Patients to Develop a Partnership Patient education involves a partnership between the patient and health care professional(s) with frequent revision and reinforcement
Aim is guided self-management giving patients the ability to control their asthma
Interventions, including use of written action plans, have been shown to reduce morbidity in both children and adults
Part 1: Educate Patients to Develop a Partnership Guidelines on asthma management should be available but adapted and adopted for local use by local asthma planning teams
Clear communication between health care professionals and asthma patients is key to enhancing compliance
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 patients family
Patient/Physician
Misunderstanding/lack of information
Complicated regimens
Fears about, or actual side effects
Cost
Poor communication
Part 2: Assess and Monitor Asthma Severity with Symptom Reports and Measures of Lung Function
Symptom
reports
Spirometry
follow-up:
PEF
monitoring at home
Important for those with poor perception of symptoms Daily measurement recorded in a diary Assesses the severity and predicts worsening Guides the use of a zone system for asthma self-management
Arterial
Normal Subject
2 3 4 Time (sec)
Note: Each FEV1 curve represents the highest of three repeat measurements
PEF (L/min)
Days
Part 3: Avoid Exposure to Risk Factors Methods to prevent onset of asthma are not yet available but this remains an important goal Measures to reduce exposure to causes of asthma exacerbations (e.g. allergens, pollutants, foods and medications) should be implemented whenever possible
Part 4: Establish Medication Plans for Long-Term Asthma Management in Infants and Children
At present, inhaled glucocorticosteroids are the most effective controller medications and are recommended for persistent asthma at any step of severity Long-term treatment with inhaled glucocorticosteroids markedly reduces the frequency and severity of exacerbations
A stepwise approach to pharmacological therapy is recommended The aim is to accomplish the goals of therapy with the least possible medication Although in many countries traditional methods of healing are used, their efficacy has not yet been established and their use can therefore not be recommended
Pharmacologic Therapy
Controller Medications:
Inhaled glucocorticosteroids Systemic glucocorticosteroids Cromones Methylxanthines Long-acting inhaled 2-agonists Long-acting oral 2-agonists Leukotriene modifiers
Pharmacologic Therapy
Reliever Medications:
Anticholinergics
Methylxanthines Short-acting oral 2-agonists
Controller:
Controller: Controller:
None
Controller:
Daily inhaled corticosteroid
Daily inhaled corticosteroid Daily long acting inhaled 2-agonist plus (if needed)
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Allergen-specific Immunotherapy
Greatest benefit of specific immunotherapy using allergen extracts has been obtained in the treatment of allergic rhinitis
A number of questions must be addressed regarding the role of specific immunotherapy in asthma therapy
Specific immunotherapy should be considered only after strict environmental avoidance and pharmacologic intervention, including inhaled glucocorticosteroids, have failed to control asthma
Part 4: Establish Medication Plans for Long-Term Asthma Management in Infants and Children
Childhood and adult asthma share the same underlying mechanisms. However, because of processes of growth and development, effects of asthma treatments in children differ from those in adults.
Part 4: Establish Medication Plans for Long-Term Asthma Management in Infants and Children
Many asthma medications (e.g. glucocorticosteroids, 2- agonists, theophylline) are metabolized faster in children than in adults, and younger children tend to metabolize medications faster than older children
Part 4: Establish Medication Plans for Long-Term Asthma Management in Infants and Children
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
Part 4: Establish Medication Plans for Long-Term Asthma Management in Infants and Children
Rapid-acting inhaled 2- agonists are the most effective reliever therapy for children These medications are the most effective bronchodilators available and are the treatment of choice for acute asthma symptoms
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Leukotriene modifier
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Inhaled glucocorticosteroid Inhaled glucocorticosteroid (< 800 g ( 400 800 g budesonide budesonide or equivalent) plus sustained-release theophylline, or or equivalent) Inhaled glucocorticosteroid (< 800 g budesonide or equivalent) plus longacting inhaled 2- agonist, or Inhaled glucocorticosteroid at higher doses (> 800 g budesonide or equivalent), or Inhaled glucocorticosteroid (< 800 g budesonide or equivalent) plus leukotriene modifier
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Reliever Medication: Rapid-acting inhaled 2- agonist prn, not more than 3-4 times a day. Once control is achieved and maintained for at least 3 months, gradual reduction of therapy should be tried.
Part 5: Establish Plans for Managing Exacerbations Treatment of exacerbations depends on: The patient Experience of the health care professional Therapies that are the most effective for the particular patient Availability of medications Emergency facilities
Part 5: Establish Plans for Managing Exacerbations Primary therapies for exacerbations: Repetitive administration of rapid-acting inhaled 2-agonist Early introduction of systemic glucocorticosteroids Oxygen supplementation Closely monitor response to treatment with serial measures of lung function
Part 5: Managing Severe Asthma Exacerbations Severe exacerbations are lifethreatening medical emergencies
Care must be expeditious and treatment is often most safely undertaken in a hospital or hospital-based emergency department
Acute Asthma
Initial Assessment History, Physical Examination, PEF or FEV1 Initial Therapy Bronchodilators; O2 if needed Good Response Observe for at least 1 hour Incomplete/Poor Response Add Systemic Glucocorticosteroids Good Response If Stable, Discharge to Home Poor Response Respiratory Failure
Discharge
Admit to Hospital
Admit to ICU
Special Considerations
Special considerations are required to manage asthma in relation to: Pregnancy Surgery Physical activity Rhinitis, sinusitis, and nasal polyps Occupational asthma Respiratory infections Gastroesophageal reflux Aspirin-induced asthma
Effective asthma management programs include education, objective measures of lung function, environmental control, and pharmacologic therapy A stepwise approach to pharmacologic therapy is recommended. The aim is to accomplish the goals of therapy with the least possible medication
Anything more than mild, occasional asthma is more effectively controlled by suppressing inflammation than by only treating acute bronchospasm The availability of varying forms of treatment, cultural preferences, and differing health care systems need to be considered
http://www.ginasthma.com
Controller:
Controller: Controller:
None
Controller:
Daily inhaled corticosteroid
Daily inhaled corticosteroid Daily long acting inhaled 2-agonist plus(if needed)
Reliever Medications
Rapid-acting inhaled 2-agonist for symptoms (but < once a week) Rapid-acting inhaled 2-agonist, cromone, or leukotriene modifier before exercise or exposure to allergen
Continuously review medication technique, compliance and environmental control Review treatment every three months. Step up if control is not achieved; step down if control is sustained for at least 3 months Preferred treatments are in bold print
Reliever Medications
Rapid-acting inhaled 2-agonist for symptoms (but < 3-4 times/day) Other options: inhaled anticholinergic, or short-acting oral 2-agonist, or short-acting theophylline
Continuously review medication technique, compliance and environmental control. Review treatment every three months Step up if control is not achieved; Step down if control is sustained for at least 3 months Preferred treatments are in bold print
Inhaled glucocorticosteroid, (200 1000 g BDP or Rapid-acting inhaled equivalent) plus long-acting inhaled 2agonist 2-agonist for symptoms Other options (order by cost): (but < 3 - 4 times/day) Inhaled glucocorticosteroid (500 1000 g BDP equivalent) plus sustained-release theophylline, or Other options: Inhaled glucocorticosteroid (500 1000 g BDP inhaled anticholinergic or equivalent) plus long-acting inhaled 2- agonist, or short-acting oral inhaled glucocorticosteroid at higher doses 2-agonist or (> 1000 g BDP equivalent), or short-acting theophylline Inhaled glucocorticosteroid (500 1000 g BDP
equivalent) plus leukotriene modifier
Continuously review medication technique, compliance and environmental control. Review treatment every three months. Step up if control is not achieved; Step down if control is sustained for at least 3 months. Preferred treatments are in bold print.
Reliever Medications
Rapid-acting inhaled 2-agonist for symptoms (but < 3-4 times/day)
plus one or more of the following, if needed (order by cost): sustained-release theophylline, or leukotriene modifier or oral glucocorticosteroid
Continuously review medication technique, compliance and environmental control. Review treatment every three months. Step up if control is not achieved; Step down if control is sustained for at least 3 months. Preferred treatments are in bold print.