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ASTHMATIC
ANTI
PREPARED BY : ABDUSSAMI MOULVI
DEFINATION
• ASTHMA IS CHARACTERIZED INCREASED
RESPONSIVENESS BY OF TRACHEA AND
BRONCHI TO VARIOUS STIMULI AND BY
NARROWING OF THE AIRWAYS.
• ANTIASTHMATIC ARE DRUGS USED TO TREAT
ASTHMATIC CONDITIONS.
• Bronchodilators
CLASSIFICATION
• These are the drugs
used in bronchial
asthma and relax the
spasm of bronchi by
sympathetic nervous
system stimulation.
• Leukotriene antagonists
• Leukotrienes are
inflammatory
chemicals the body
releases after coming in
contact with an
allergen or allergy
trigger.
• Mast cell stabilizers
• Mast cell stabilizers are
used to prevent disorders.
or control allergic
• They block a calcium
channel essential for mast
cell degranulation, stabilizing
the cell.
• Anti-IgE antibody
• Anti-inflammatory agents
Anti-IgE is a form of
treatment for allergic
conditions that has been
approved for the treatment
of moderate to severe
persistent asthma and
chronic idiopathic urticaria
A drug or substance that
reduces inflammation
(redness, swelling, and pain)
in the body
BRONCHODILATOR
• Classified as -
• Beta 2 sympathomimetics
• Methylxanthines
• Anticholinergics
BETA 2
SYMAPATHOMIMETICS
• The Symapathomimetic drugs, whose mimic that of sympathetic
stimulation.
• The Symapathomimetic agents or beta adrenergic receptor agonists
are widely used for treatment of asthma.
• There are two type of receptors- beta 1 and beta 2.
• The beta 1 adrenergic receptors are present in the heart and beta 2 receptors are
present in lungs.
• By stimulation of beta 2 adrenergic receptors these agents ;
relax bronchial muscles, inhibit the release of mediators from
mast cells, enhance mucociliary activity and effect
composition of mucus.
So when receptor beta- adrenergic agonists are administered,
adverse effects are caused by stimulation of beta-1 receptors in
heart, which cause cardiac stimulation.
• Thus, now drugs having greater affinity to beta 2 adrenergic
receptors has been developed.
• Adenergic that effect the primarily beta 2 adrenergic receptors
are called selective beta 2 adrenergic agonists.
• But selectivity is lost at sufficiently high concentration of these
drugs.
BETA 2 SYMPATHOMIMETICS
DRUGS
• Terbutaline
• Salbutamol
• salmetrol
• 1.catecholamines
Beta 2 sympathomimetic agents are
classified under 2 broad categories.
• 2. noncatecholamines
• For the purpose of simplify the understanding, the important beta 2
sympathomimetic discussed under drugs are
• 1.selective beta 2 receptor agonist and
• 2.non-selective beta 2 receptor agonist categories.
• It is a short acting
beta 2 adrenergic
receptor agonist used
for the relief of
bronchospasm in
conditions such as
asthma and COPD.
01
• SALBUTAMOL
(ALBUTEROL):
02 03
• Airway smooth muscle
has little sympathetic
nervous supply but
contain lots of beta 2
adrenoreceptors that
respond to circulating
adrenaline.
SALBUTAMOL
MOA
• The stimulation of
beta 2 receptors leads
to rise in intracellular
cyclic adenine
monophosphate (cAMP)
levels and the
subsequent bronchial
smooth muscle
relaxation.
• Oral (children)
• 2-6 years: 0.1-0.2
mg/kg/dose three times
/ day, maximum does
not exceed 12 mg/day
(divided doses)
DOSE
• 1.SELECTIVE BETA 2 RECEPTOR AGONIST
• 6-12 years : 2mg/dose 3-4
times/day; maximum does not
exceed 24 mg/day (divided
doses)
• Extended release: 4 mg every 12
hours; maximum dose not to
exceed 24 mg/day ( divided
doses).
04
2-4 mg 3-4 times /day,
not to exceed 32 mg/day
• Extended release: 8 mg
every 12 hours, not to
exceed 32 mg/day
• Elderly: 2 mg 3-4
times/day, maximum 8
mg 4 times/day.
DOSE
ABOVE 12 YEARS
AND ADULTS
• Children: > 2-12 years:
0.63-1.25 mg every 4-6
hours.
• Children 4 years :
• - quick relief: 0.63-2.5 mg
every 4- 6 hours.
• Exacerbation of asthma :
0.15 mg/kg every 20 min for 3
doses.
Children 5-11 years
• Quick relief: 1.25-5mg
every 4-8 hours
• Exacerbation of
asthma : 0.15mg/kg
every 20 min 3 times.
• 1.SELECTIVE BETA 2 RECEPTOR AGONIST
05
NEBULIZATION
Above 12 years and adults
• Quick relief: 1.25-5mg every 20
min for 3 doses
• Continuous infusion :
• Adults: severe bronchospasm
and status asthmaticus.
• Asthma
• COPD
• Exercise induced
bronchospasm
• 1.SELECTIVE BETA 2 RECEPTOR AGONIST
06
INDICATIONS
• 2.NON-SELECTIVE BETA 2 RECEPTOR
AGONIST CATEGORIES.
Ephedrine (ΕΡΗ) is a sympathomimetic amine used as a
stimulant, decongestant, treating allergic asthma and
bronchodilator.
Ephedrine releases tissue stores of norepinephrine
and there by produces an alpha and beta adrenergic
stimulation longer acting and less potent than
epinephrine.
• EPHEDRINE
• EPHEDRINE MOA
• Children: oral, 3mg/kg/day
• IM, slow IV push: 0.2-0.3 mg/kg
• Adults: oral: 25-50 mg every 3-4 hours
• Sc:25-50 mg
• IV: 5-25mg/dose slow IV push
DOSE INDUCATION
Treatment of bronchial asthma and broncospasm
METHYLXANTHINES
THEOPHYLLINE
• Theophylline known as
dimethylxanthine drug used for
COPD or asthma.
• THEOPHYLLINE
• AMINOPHYLLINE
• HYDROXYETHYL
THEOPHYLLINE
Theophylline MOA
• It causes bronchodilatation, which increase tissue
concentrations of CAMP, (cyclic adenine
monophosphate (cAMP) which in turn promotes
catecholamine of lipolysis, glycogenolysis and
gluconeogenesis and induces release of
epinephrine from adrenal medulla cells.
Dosage
• Adult minimum / maximum dose :
6.0 mg/kg/24.0 mg/kg
• Paediatric minimum / maximum
dose: 2.0mg/kg/24.0mg/kg
ANTICHOLINERGICS (MUSCARINIC ANTAGONIST)
ANTICHOLINERGIC
DRUGS
• Ipratropium
bromide
• Tiotropium
bromide
IPRATROPIUM
BROMIDE
Ipratropium bromide
- Ipratropium bromide
is an anticholinergic
drug,
- chemically related to
atropine.
IPRATROPIUM
BROMIDE MOA
• It blocks muscarinic
cholinergic receptors,
• Resulting in a decrease
in the formation of
cyclic guanosine
monophosphate (cGMP).
• This results in
decreased contractility
of smooth muscle.
An anticholinergic agent substance that blocks is a the
neurotransmitter acetylcholine in the central and the
peripheral nervous system.
Dosage
• 1.Aerosol inhalation
two inhalations four
times daily. Do not
exceed 12 inhalations in
24 hours.
• Spray 0.03 formulation
:2 sprays per nostril 3 or
4 times daily.
DOSAGE
DOSAGE
LEUKOTRIENE ANTAGONISTS
• Leukotrienes are
inflammatory
chemicals the body
releases after
coming in contact
with an allergen or
allergy trigger.
Leukotriene antagonists
• Montelukast
• Zafirlukast
Montelukast
• A leukotriene antagonist is
a drug that inhibits
leukotrienes.
Montelukast MOA
• That inhibits the cysteinyl
leukotrine receptor.
Dosage
• Oral (children)
• 6-11 months: Asthma: 4mg
once daily
• 6-23 months: allergic
rhinitis : 4mg once daily
• 12-23 months: Asthma: 4
mg once daily.
MAST CELL STABILIZER
MAST CELL
• A mast cell is
a type of white
blood cell and
part of immune
and
neuroimmune
system
contains
histamine.
Mast cell stabilizers
• Mast cell stabilizers
are used to prevent
disorders. or control
allergic
• They block a calcium
channel essential for
mast cell
degranulation,
stabilizing the cell.
Mast cell
stabilizers
• Sodium
cromoglyc
ate
• Ketotifen
Sodium
cromoglycate MOA
• It prevents
mediators the
release of that
inflammatory cells
attract
• And because it
stabilizes the
inflammatory cells.
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Anti Asthmatic Drugs PPT PreparedBy Abdussami Moulvi

  • 1. ASTHMATIC ANTI PREPARED BY : ABDUSSAMI MOULVI
  • 2. DEFINATION • ASTHMA IS CHARACTERIZED INCREASED RESPONSIVENESS BY OF TRACHEA AND BRONCHI TO VARIOUS STIMULI AND BY NARROWING OF THE AIRWAYS. • ANTIASTHMATIC ARE DRUGS USED TO TREAT ASTHMATIC CONDITIONS.
  • 3. • Bronchodilators CLASSIFICATION • These are the drugs used in bronchial asthma and relax the spasm of bronchi by sympathetic nervous system stimulation. • Leukotriene antagonists • Leukotrienes are inflammatory chemicals the body releases after coming in contact with an allergen or allergy trigger. • Mast cell stabilizers • Mast cell stabilizers are used to prevent disorders. or control allergic • They block a calcium channel essential for mast cell degranulation, stabilizing the cell. • Anti-IgE antibody • Anti-inflammatory agents Anti-IgE is a form of treatment for allergic conditions that has been approved for the treatment of moderate to severe persistent asthma and chronic idiopathic urticaria A drug or substance that reduces inflammation (redness, swelling, and pain) in the body
  • 4. BRONCHODILATOR • Classified as - • Beta 2 sympathomimetics • Methylxanthines • Anticholinergics
  • 5. BETA 2 SYMAPATHOMIMETICS • The Symapathomimetic drugs, whose mimic that of sympathetic stimulation. • The Symapathomimetic agents or beta adrenergic receptor agonists are widely used for treatment of asthma. • There are two type of receptors- beta 1 and beta 2. • The beta 1 adrenergic receptors are present in the heart and beta 2 receptors are present in lungs. • By stimulation of beta 2 adrenergic receptors these agents ; relax bronchial muscles, inhibit the release of mediators from mast cells, enhance mucociliary activity and effect composition of mucus. So when receptor beta- adrenergic agonists are administered, adverse effects are caused by stimulation of beta-1 receptors in heart, which cause cardiac stimulation. • Thus, now drugs having greater affinity to beta 2 adrenergic receptors has been developed. • Adenergic that effect the primarily beta 2 adrenergic receptors are called selective beta 2 adrenergic agonists. • But selectivity is lost at sufficiently high concentration of these drugs.
  • 6. BETA 2 SYMPATHOMIMETICS DRUGS • Terbutaline • Salbutamol • salmetrol
  • 7. • 1.catecholamines Beta 2 sympathomimetic agents are classified under 2 broad categories. • 2. noncatecholamines • For the purpose of simplify the understanding, the important beta 2 sympathomimetic discussed under drugs are • 1.selective beta 2 receptor agonist and • 2.non-selective beta 2 receptor agonist categories.
  • 8. • It is a short acting beta 2 adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and COPD. 01 • SALBUTAMOL (ALBUTEROL): 02 03 • Airway smooth muscle has little sympathetic nervous supply but contain lots of beta 2 adrenoreceptors that respond to circulating adrenaline. SALBUTAMOL MOA • The stimulation of beta 2 receptors leads to rise in intracellular cyclic adenine monophosphate (cAMP) levels and the subsequent bronchial smooth muscle relaxation. • Oral (children) • 2-6 years: 0.1-0.2 mg/kg/dose three times / day, maximum does not exceed 12 mg/day (divided doses) DOSE • 1.SELECTIVE BETA 2 RECEPTOR AGONIST
  • 9. • 6-12 years : 2mg/dose 3-4 times/day; maximum does not exceed 24 mg/day (divided doses) • Extended release: 4 mg every 12 hours; maximum dose not to exceed 24 mg/day ( divided doses). 04 2-4 mg 3-4 times /day, not to exceed 32 mg/day • Extended release: 8 mg every 12 hours, not to exceed 32 mg/day • Elderly: 2 mg 3-4 times/day, maximum 8 mg 4 times/day. DOSE ABOVE 12 YEARS AND ADULTS • Children: > 2-12 years: 0.63-1.25 mg every 4-6 hours. • Children 4 years : • - quick relief: 0.63-2.5 mg every 4- 6 hours. • Exacerbation of asthma : 0.15 mg/kg every 20 min for 3 doses. Children 5-11 years • Quick relief: 1.25-5mg every 4-8 hours • Exacerbation of asthma : 0.15mg/kg every 20 min 3 times. • 1.SELECTIVE BETA 2 RECEPTOR AGONIST 05 NEBULIZATION
  • 10. Above 12 years and adults • Quick relief: 1.25-5mg every 20 min for 3 doses • Continuous infusion : • Adults: severe bronchospasm and status asthmaticus. • Asthma • COPD • Exercise induced bronchospasm • 1.SELECTIVE BETA 2 RECEPTOR AGONIST 06 INDICATIONS
  • 11. • 2.NON-SELECTIVE BETA 2 RECEPTOR AGONIST CATEGORIES. Ephedrine (ΕΡΗ) is a sympathomimetic amine used as a stimulant, decongestant, treating allergic asthma and bronchodilator. Ephedrine releases tissue stores of norepinephrine and there by produces an alpha and beta adrenergic stimulation longer acting and less potent than epinephrine. • EPHEDRINE • EPHEDRINE MOA • Children: oral, 3mg/kg/day • IM, slow IV push: 0.2-0.3 mg/kg • Adults: oral: 25-50 mg every 3-4 hours • Sc:25-50 mg • IV: 5-25mg/dose slow IV push DOSE INDUCATION Treatment of bronchial asthma and broncospasm
  • 12. METHYLXANTHINES THEOPHYLLINE • Theophylline known as dimethylxanthine drug used for COPD or asthma. • THEOPHYLLINE • AMINOPHYLLINE • HYDROXYETHYL THEOPHYLLINE Theophylline MOA • It causes bronchodilatation, which increase tissue concentrations of CAMP, (cyclic adenine monophosphate (cAMP) which in turn promotes catecholamine of lipolysis, glycogenolysis and gluconeogenesis and induces release of epinephrine from adrenal medulla cells. Dosage • Adult minimum / maximum dose : 6.0 mg/kg/24.0 mg/kg • Paediatric minimum / maximum dose: 2.0mg/kg/24.0mg/kg
  • 13. ANTICHOLINERGICS (MUSCARINIC ANTAGONIST) ANTICHOLINERGIC DRUGS • Ipratropium bromide • Tiotropium bromide IPRATROPIUM BROMIDE Ipratropium bromide - Ipratropium bromide is an anticholinergic drug, - chemically related to atropine. IPRATROPIUM BROMIDE MOA • It blocks muscarinic cholinergic receptors, • Resulting in a decrease in the formation of cyclic guanosine monophosphate (cGMP). • This results in decreased contractility of smooth muscle. An anticholinergic agent substance that blocks is a the neurotransmitter acetylcholine in the central and the peripheral nervous system. Dosage • 1.Aerosol inhalation two inhalations four times daily. Do not exceed 12 inhalations in 24 hours. • Spray 0.03 formulation :2 sprays per nostril 3 or 4 times daily. DOSAGE DOSAGE
  • 14. LEUKOTRIENE ANTAGONISTS • Leukotrienes are inflammatory chemicals the body releases after coming in contact with an allergen or allergy trigger. Leukotriene antagonists • Montelukast • Zafirlukast Montelukast • A leukotriene antagonist is a drug that inhibits leukotrienes. Montelukast MOA • That inhibits the cysteinyl leukotrine receptor. Dosage • Oral (children) • 6-11 months: Asthma: 4mg once daily • 6-23 months: allergic rhinitis : 4mg once daily • 12-23 months: Asthma: 4 mg once daily.
  • 15. MAST CELL STABILIZER MAST CELL • A mast cell is a type of white blood cell and part of immune and neuroimmune system contains histamine. Mast cell stabilizers • Mast cell stabilizers are used to prevent disorders. or control allergic • They block a calcium channel essential for mast cell degranulation, stabilizing the cell. Mast cell stabilizers • Sodium cromoglyc ate • Ketotifen Sodium cromoglycate MOA • It prevents mediators the release of that inflammatory cells attract • And because it stabilizes the inflammatory cells.