Location via proxy:   [ UP ]  
[Report a bug]   [Manage cookies]                

Aerosol Therapy TMK 1

Download as ppt, pdf, or txt
Download as ppt, pdf, or txt
You are on page 1of 34

Aerosol therapy

A review
AEROSOLS
Suspension of fine liquid or solid particle in air
Key to aerosol therapy is aerosol particle
Aerosol emerge at a velocity of 100km/h
80% drugs deposited in oropharynx
10% in the walls of the inhaler
10% in the lungs
Particle size important :2-5µ undergo impaction &
sedimentation in the lungs & submicronic
particles go in and out
Indications
Deposition of bronchoactive aerosols
Enhancement of secretion clearance
Sputum induction
Humidification of respired gases
Prevent dehydration
Prevent or relieve bronchospasm or upper
airway inflammation
Hazards of therapy
Bronchospasm
Over hydration
Overheating of inspired gases
Delivery of contaminated aerosol
Tubing condensation draining into the
airway
Aerosol delivery systems
The three principle types of devices widely
used are:
MDI: Metered dose inhalers
DPI: Dry powder inhalers
Accuhalers
Nebulizers
Metered dose inhalers

Most widely used


Propellants were chlorofluorocarbons[CFC]
May be freon/archon
Aerosol flow rate 30m/s or 100km/h
Advantages of MDI
Inexpensive
Light,compact,resistant to moisture
Quick delivery of drugs
Precise and consistent doses
Available with most anti asthmatic drugs
Disadvantage of MDI
Difficulty in coordination of activation&
inspiration
Time consuming to teach
Cold freon effect i.e. inability to continue to
breathe when propellant is released into
mouth
Contains CFC
Spacers
Holding chambers or reservoirs
Attachment to a MDI
2 Types:
1. small volume spacer-tube spacer
2. large volume spacer-conical spacer
Advantages 1.no need to activate coordination with
Advantages:
inspiration 2.increases drug deposition in the
lungs[130%]. 3.reduces drug deposition in the mouth.
4.used in children with face mask 5.eliminates cold
freon effect 6.decreases the incidence of oral thrush
7.multiple doses can be given.
Dry powder inhalers
Introduced in 1960’s
No propellent
Requires patient’s own inspiratory effort to form aerosol
Powder is delivered only when the patient inhales
Useful in children above 5 years, teenagers & arthritic
patients
Advantages: 1. light weight 2. no hand breath co-
ordination 3. no CFC 4. quick delivery of drugs
Disadvantages: 1. Require high inspiration
flow>28/l/min 2. available with only few anti asthma
drugs
Comparison between MDI & DPI
contains CFC No CFC
High velocity aerosols Aerosol velocity depends
on inspiratory flow rate
Requires hand breath co
No hand breath co
ordination ordination needed
Delivery of medicines Delivery of medication
independent of external largely dependent on
factors external factors
Time consuming to teach Easy to teach
Requires deep& slow Requires high inspiratory
breathing only flow>28L/min
Nebulizers
Turns an aqueous solution of drug into fine
mist
Drug will be inhaled with normal
respiration
Medication reaches lower airways more
effectively
Two types: jet & ultrasonic
Differences between jet nebulizer
& ultrasonic nebulizer

JET ULTRASONIC
Cools during operation Heats up during
Small aerosol particle operation
size Larger aerosol particle
Less expensive More expensive
More noise Less noise
Indications for nebulizers
Useful in children
Handicapped person
Acute severe asthma
Bronchial challenge tests
Lung ventilation scans
Ventilated patient
High doses can be given
Combination drugs can be given
Disadvantages: nebulizer
Expensive
Requires regular maintenance
High doses result in toxicity
Airborne infections may be transmitted
Produces lot of noise
Requires a power source
Choice of inhalation therapy
Infants Nebulizer
Children
< 4 years Nebulizer
4 year DPI/MDI/Spacer
7 years DPI/MDI
Adults MDI/DPI
Acute episodes Nebulizer
Drugs available:MDI
ß agonists
Salbutamol, terbutalin, fenoterol, salmetrol,
pibuterol, veproterol, fometerol, nimeterol
Steroids
Beclomethazone, budesonide, flucoticasone
• Antimucarinics:
Ipratropium bromide/oxitropium bromide
• Mast cell stabilizers:
Diisodium cromoglycoate, nedocromial sodium
DRUGS AVAILBLE FOR NEBULIZATION

Beta 2 agonists:salbutamol, terbutalin, feneterol


Antimuscaranics: ipratropium bromide
Steroids:budoneside
Sodium cromoglycoate
Antibiotics
Antifungals: pentamidine
Mucolytics: acetyl cysteine, mistabron
Beta 2 adrenergic agonists
Mechanism of action
• Beta receptor stimulation- increased C
AMP in bronchial muscle cell –relaxation

• Increased C AMP in mast cells- reduced


Ag:Ab reaction induced mediater release
Albuterol
Short acting
A high selective beta 2 agonist
Selectively increased by inhalation route
Peak bronchodilation in 10 min
Long term use leads to decreased
responsiveness
Terbutalin

Similar to salbutamol in properties & use


Are all short acting albuterol preparations same?

Commonly used beta 2 agonist is racemic


albuterol
Mixture of R mirror image isomers R albuterol &
S albuterol
R has rapid bronchodilator effect & S has no
bronchodilator effect
Pharmokinetics of both are different
S metabolized 10 times slowly & decreased
responsiveness in long term use
Long acting beta 2 agonists : Fometerol &
salmeterol

Both are potent & selective


Duration of action >12 hours due to lipophilicity
Salmeterol has delayed onset of action
Fometerol rpid onset of action
Fometerol in a dose dependent fashion more
protective against bronchospasm than salmeterol
Fometerol produce more finger tremor than
salmeterol
More helpful in nocturnal asthma
Why combine beta 2 agonists & steroids ?

Complementary effects
Steroids increase beta 2 receptor gene expression
and decrease the potential for desensitization
Long acting beta 2 agonists prime the
glucocorticoid-receptors making them more
sensitive to steroid dependent activation
In steroid responsive systems the addition of long
acting beta 2 agonist increases steroid potency
Proven or widely accepted beneficial effects of steroids

Improvement in pulmonary function


Decrease in diurnal variation of lung
function
Decreased requirement of oral steroids
Protection against antigen induced
bronchoconstriction when used chronically
Decrease in exacerbation rate
Beneficial effects of inhaled steroids

Probable decrease in hospital admission rate


Possible decrease in asthma death rate
Possible prevention of long term lung
damage leading to irreversible airflow
obstruction
Possible decrease in rate of decline of lung
function in asthma of long duration
Side effects of inhaled steroids

Depression of adrenocortical function


Effects on bone metabolism
Effects of growth in children
Easy bruising & skin thinning
Cataract formation
Inhaled steroids
Most widely used are beclamethasone &
budesonide.
Both are potent & absorbed from GIT and partial
first-pass metabolism in liver
When used up to 1000 µg –day no adrenocortical
function effects
Fluticasone propionate highly selective, poorly
absorbed from GIT, subject to 100% first pass
metabolism in liver. Safer in children
Treatment strategies in children
The step up strategy The step down strategy
• Uses inhaled steroids late in • Inhaled steroids early in all
treatment children with chronic
• Reserves steroids in severe cases symptoms
only
• Inhaled steroids up to 800µg
• Only minority of children (10-
day with inhaled beta-2
20%) are on steroids
agonists up to 6-8 weeks. then
• Starts with beta-2 agonists
gradual reduction depending
increasing in doses adding
theophyllin or oral beta-2 agonists on pulmonary function
or sodium cromoglycoate / long • Improved quality of life
acting beta-2 agonists • Most children end up with
• Lastly inhaled steroids long term steroids.
Chronic management of asthma

Step1: mild symptoms - <1-2 times a week,


nocturnal asthma, asymptomatic between
exacerbations, PEF or FEV1>80%
Short acting inhaled beta-2 Agonist not
more than 3 times a week
Sodium cromoglycoate or beta-2 agonists
before exposure to antigen or exercise
Chronic management of asthma
Step 2: moderate - exacerbations >2 times a week,
affects activity & sleep, nocturnal asthma >2 times
a month, requires short acting beta-2 agonists
daily, PEF or FEV1 60-80% predicted
Inhaled anti inflammatory therapy daily: initially
corticosteroid 200-600µg /day or sodium
cromoglycoate (children)- if not controlled , long
acting beta-2 agonist
Step3: moderate - add sustained release theophyllin
or inhaled cholinergics or inhaled beta 2 agonist
Chronic management of asthma
Step 4 : severe -frequent exacerbations, continuous
symptoms, frequent nocturnal asthma, PEF or
FEV1 <60%
Inhaled steroids daily 800-1000µg
Sustained release theophyllin and or oral beta 2
agonist or long acting
Oral steroids (alternate day or single daily dose)
with short or long acting beta-2 agonists
Particle deposition
Thank you
Thank you

You might also like