What are the goals of asthma treatment?
What are the types of treatment of asthma?
Describe reliever treatments?
Drugs that provide relief from a asthma symptoms. Normally paid onset but short duration, cause airway smooth-muslce relaxation. Only take during attack.
Describe preventer treatments?
Do not provide relief for an acute asthma attack. Still need to take even if there are no symptoms.
What are the benefits for using inhaled beta-agonist in the management of asthma?
Describe the mechanism of relaxation of bronchial smooth muscle?
Beta 2 stimulant will bind to the Beta 2 receptor on the cell membrane. It will activate the Gs which activates AC. AC will convert ATP to cAMP. cAMP increases which increases PKA. This will activate:
What is the route of administration of asthma treatment?
What are the types of inhalers?
2. Dry powder device.
Why use a spacer with an inhaler?
Allows you to deliver more of the drug to the lung. Largely reduce the chance of systemic adverse effects.
What are nebulisers?
Warm and moisture can comfort the airway. usually combine 2 or 3 medications together. Need a machine to do ti.
Describe short acting Beta-2-adrenoreceptor aganoists?
Rapid onset but short duration - maximum effect occurs within 30 minutes and the duration is around 4-6 hours. Effective in preventing - exercise induced asthma, cold air and allergen triggered asthma. Also used for acute severe asthma. use on an “As needed” basis.
What are the adverse effects of the Beta2 agonists?
Describe Long-acting beta2 agonists (LABA)?
The duration of action is longer than 12 hours. Use on a regular basis. Used to prevent bronchospasm in patients requiring long-term bronchodilator therapy. Inhaled corticosteroid (ICS) and LABA can be used as combined therapy.
What are the FDA recommendations for asthma treatment?
What are anticholinergic agents?
Each can cause broncho-constriction and mucus secretion. Currently available are non-selective.
Describe ipratropium bromide?
Slow onset (60-90minute) and a shorter duration (6-8h). use on a regular basis. Low side effect, less tachyphylaxis. Problems - reduced mucocillary clearance.
Describe tiotropium bromide?
Long lasting muscarinic antagonist (>25 hours). Equal affinity for M1, M2 and M3 receptors. Dissociates rapidly from m2 receptors. Approximately 10-fold more potent than ipratropium bromide. Problems with dry mouth in 10-15% (systemic absorption of the drug is low but sufficient to cause it). Can cause constipation, blurred vision and urinary retention.
Describe Xanthine drug?
It is non-selective inhibition of phosphodiesterase - cause broncho-dilation. Activation of histone deacetylases (HDAC): related to anti-inflammatory effects. Non-selective antagonism of adenosine receptors.
what does theophylline do?
Prevents PDE3,4,7 from converting cAMP to AMP.
what does theophylline do?
Prevents PDE3,4,7 from converting cAMP to AMP. Increase in cAMP will increase broncho-dilation.
What are the side effects of theophylline?
Narrow therapeutic range (10-20microgram/mL). Toxicity can occur within the therapeutic range.
Serum level monitoring is the only reliable method of preventing toxicity.
What are the side effects of theophylline?
Narrow therapeutic range (10-20microgram/mL). Toxicity can occur within the therapeutic range. Serum level monitoring is the only reliable method of preventing toxicity. -Nausea/vomiting. -Headache. -Diarrhoea. -Insomnia. -Hyperglycaemia (from overdose). -Seizures (from overdose). -Arrhythmias (from overdose).
Describe the clearance of theophylline?
Heart failure, erythromycin, beta blocker, CYP1A2 polymorphism and ciprofloaxcin will decrease clearance.
smoking and phenytoin will increase clearance.
Describe glucocorticoids (GCs)?
They reduce inflammation and immune responses. Used clinically since 1948 and the market size in the US per year is around $10,000,000,000.