BRONCHIAL ASTHMA
CLINICAL FEATURES AND MANAGEMENT
Nanditha Aravind,Navya ak
Roll no:69 and 70
BRONCHIAL ASTHMA
• It is a group of disorders characterized by an increased
responsiveness of the airways to various stimuli.
• It manifests by widespread narrowing of the airways causing
paroxysmal dyspnea, wheezing or cough.
BRONCHIAL ASTHMA
PATHOPHYSIOLOGY
Airway obstruction in asthma is caused by
i) edema and inflammation of mucous membrane lining the airways
ii) excessive secretion of mucus, inflammatory cells and cellular debris
iii) spasm of the smooth muscle of bronchi. Obstruction is diffuse but not
uniform
BRONCHIAL ASTHMA
PATHOPHYSIOLOGY
Asthma has been classified as
1. atopic (lgE mediated, triggered by allergens)
2. nonatopic (non lgE mediated, triggered by infection)
3. mixed
4. exercise induced or aspirin induced
Inhalation of an allergen leads to a biphasic response with early and late
reactions ultimately causing bronchoconstriction.
BRONCHIAL ASTHMA
EARLY REACTION
BRONCHIAL ASTHMA
LATE REACTION
• develops 3-4 hr later and peaks at 8-12 hr.
• The release of mast cell mediators is not prevented by premedication
with beta2 -agonist.
• it is inhibited by premedication with steroids suggesting that airway
narrowing is mainly due to an inflammatory reaction and mucosal
edema.
This phase presents as clinical asthma.
BRONCHIAL ASTHMA
TRIGGERS
• Viral Infections
• Exercise
• Weather Changes
• Emotional factors
• Food
• Endocrine Factors
BRONCHIAL ASTHMA
• Dyspnea
• May develop cyanosis
• Restless
• Chest becomes barrel
shaped
• Hyperinflation of chest
• Clubbing of fingers
• Recurrent Cough
• Wheezing
• Air Hunger
• Hyper resonant chest due to air
trapping
• Prolonged Respiratory phase
• Feeble breath sounds
O Symptoms occur with change in season , aggravated by
exercise,and more in nights
O Acute asthma usually begins with a cold ,bouts of spasmodic
coughing
BRONCHIAL ASTHMA
DIFFERENTIAL DIAGNOSIS
• Bronchiolitis
• Congenital Malformation
• Aspiration of foreign body
• Hypersensitivity Pneumonitis
• Cystic Fibrosis
GRADING OF SEVERITY OF ACUTE
ASTHMA
BRONCHIAL ASTHMA
INVESTIGATIONS
• Complete blood count,ESR(normal values are expected ;may have eosinophilia
• Pulse oximetry –mild ->955,moderate-90-95%,severe<90%
• Chest X Ray-normal or show bilateral symmetric air trapping
• Patches of atelectasis of varying sizes due to mucus plugs
• Allergy Test- blood IgE elevated in atopic asthma and normal in non atopic
asthma
• Spirometry-mild ->80%,moderate -60-80%,severe<60%
BRONCHIAL ASTHMA
MANAGEMENT
The goals of the therapy are
1. Maintenance of near normal pulmonary function
2. Maintenance of near normal physical activity
3. Prevention of night time cough/wheeze with minimal chronic
symptoms
4. Prevention of exacerbation
5. Avoiding adverse effects of medications
O Management
1. Identification and elimination of exacerbating factors
2. Pharmacotherapy
i. Acute exacerbation management
ii. Long term mangement
ACUTE EXACERABATION OF ASTHMA
MILD
O Nebulization- salbutamol 150 mcg/kg/dose n 3 ml of saline once
O Assess for response
O Response is adequate and child is comfortable discharge on oral
salbutamol ,0.1-0.2 mg/kg/dose,6hrly or salbutamol inhaler
puffs ,2 puffs 4-6hrly
O if the child is not improving a adequately shift to the
management protocol of moderate exacerbation
MODERATE
Nebulized salbutamol every 20 minutes for 3 times in one hour.
Assess for response
the if the response is adequate, space out nebulization intervals
2-4hrly . observe the child for six to eight hours if the relief is
sustained discharge the child on oral salbutamol or salbutamol
inhaler 2puffs 4-6hrly
response is only partial start oral steroids prednisolone 1 to 2 mg /
kg / day continue nebulization .when improved (usually takes 1 to 2
days ),discharge the child on Oral salbutamol and steroid for 3 to 5
days. the child is fit for discharge if he feeds well and sleeps well
In case of deterioration manage as severe exacerbation.
if the nebulizer is not available, 2 to 4 puffs of salbutamol by MDI
every 20 minute for 3 times or subcutaneous injection of terbutaline
may be considered
SEVERE
Admit in the ICU
Connect to Pulse oxymeter
oxygen inhalation
oxygen driven nebulization with salbutamol and ipratropium
(125 mcg for infants and toddlers ,250 mcg for > 5 years, 500
mcg for adolescence) every 20 minutes for 3 doses .
IV hydrocortisone 10 mg/kg initially followed by 4 to 5
mg/kg/dose every 6hrly or IV methylprednisolone 2
mg/kg/dose or oral prednisolone 2mg/kg/day
IV MgSO4 ;0.1ml/kg 50% MgSO4 in normal infusion over 30
minute. injection aminophylline 5mg/kg/dose diluted as IV
infusion 6 hourly
if improvement is inadequate ,consider continuous oxygen driven nebulization
with salbutamol ,0.5 mg/kg or hourly nebulization. ipratropium can be spaced
out to 4 hourly, mixed with the corresponding doses of salbutamol
IV TERBUTALINE 10 Mcg /kg bolus infusion over 30 minute, followed by 0.4
mcg/kg/min increasing gradually, to maximum 4 mcg/kg/min
ketamine
Mechanical ventilation
Pharmacological
-long term
i. Assessment of symptom control
ii. Assessment of risk of exacerbation
iii. Selection of medication
iv. Selection of appropriate inhalational device
v. monitoring
ASSESSMENT OF SYMPTOM CONTROL
characteristics controlled Partially controlled uncontrolled
Day time symptoms none >2 per week 3 or more features of pa
rtially controlled prese
nt in week
Limitation of activity none any
nocturnal sumptoms none any
Reliever or rescue drug none >2 per week
Assessment of risk of
exacerbation
 MODIFIABLE
o Uncontrolled asthma symptoms
o Previous history(1 or more)
o Exposures:tobacco smoke,indoor or outdoor air
pollution,indoor allergens
o Psychological or socioeconomic problems
o Poor adherence with controlled medication
o Co- morbidities:obesity,rhinosinusitis and food allergy
 Non modifiable
o Ever intubated :PICU admissions
o >1 severe exacerbation requiring hospitalization in last 12
months
Selection of medication
O Infrequent symptoms –- No controlled medication ,short
acting beta agonist with inhaled steroids
O Asthma with any risk factors,>twice a month--low dose
inhaled steroids as and when required short acting beta
agonist
Montelukast(other choice)
O Troublesome – low dose inhaled steroids +long acting beta
agonist or medium dose inhaled steroids
Low or medium dose inhaled steroids +LTRA or sustained
release theophylline
O Severely uncontrolled – medium to high dose inhaled
steroids+long acting beta agonist
short course oral steroid and high dose inhaled steroids or
moderate dose inhaled steroids and long acting beta agonist
Selection of appropriate inhalation
device
O Metered dose inhaler(MDI)
O MDI with spacer
O With face mask
O Dry powder inhaler
O Nebulizer
monitoring
O Every 4-12 wks
O Detailed history(frequency of symptoms ,sleep
disturbance,physical activity,school absenteeism,visit to
doctors,need for bronchodialators)
O maintain Symptom diary
O Assessed as being controlled,partially or uncontrolled
O Poor compliance ,wrong technique of inhalation
inappropriate dose ,infections
O No cause is found-step up
O Control is sustained for 3-6 months,and gradual reduction-
step down
Step wise management
OLife threatening asthma:
o Cyanosis
o Silent chest
o Poor respiratory efforts
o fatigue
o Altered sensorium
o PEFR< 30 %
o Oxygen saturation <90%
O MDI
o Fixed amount of medication
o Aerosol form –activated
o Exacerbation and maintanance therapy
o Coordination (press and breath)
o Pressure ,oropharynx
o spacer
BRONCHIAL ASTHMA PEDIATRICS SLIDESHAReee
How to use
MDI with spacer
O Large portion being deposited in lung ,with less impaction on
oropharynx
O Advantage- overcome coordination
O Limitations-being bulky ,costly,young infants and toddlers
BRONCHIAL ASTHMA PEDIATRICS SLIDESHAReee
How to use
1. Remove cap ,shake ,insert into spacer
2. Place mouth piece of spacer
3. Start breathing in and out-valve
4. Breathing pattern established press canister and continue
to breath—5-10
5. Wait for 30 sec
With mask
O Below 2-3 yrs
HOW TO USE
O Attach baby mask
O Shake mdi inserted to mdi end
O Mouth and nose
O Press canister and encourage child to take breathing mouth
open
O 30-60
BRONCHIAL ASTHMA PEDIATRICS SLIDESHAReee
Nebulizer
O Acute severe asthma in young irritable and hypoxic children
O Bulky and inefficient aerosol delivery system
IMPROVE THE AMOUNT OF DRUG DELIVERED
o Total fill volume -3-5 ml
o Tapping the side of nebulizer
o Optimal flow rate -6-12L/min
o Slow,deep inhalation and breath holding
BRONCHIAL ASTHMA PEDIATRICS SLIDESHAReee
O Below 4 yrs-MDI with spacer and Face mask
O Above 4 yrs-MDI with spacer
O Above 12 yrs-MDI may be used directly
THANK YOU

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BRONCHIAL ASTHMA PEDIATRICS SLIDESHAReee

  • 1. BRONCHIAL ASTHMA CLINICAL FEATURES AND MANAGEMENT Nanditha Aravind,Navya ak Roll no:69 and 70
  • 2. BRONCHIAL ASTHMA • It is a group of disorders characterized by an increased responsiveness of the airways to various stimuli. • It manifests by widespread narrowing of the airways causing paroxysmal dyspnea, wheezing or cough.
  • 3. BRONCHIAL ASTHMA PATHOPHYSIOLOGY Airway obstruction in asthma is caused by i) edema and inflammation of mucous membrane lining the airways ii) excessive secretion of mucus, inflammatory cells and cellular debris iii) spasm of the smooth muscle of bronchi. Obstruction is diffuse but not uniform
  • 4. BRONCHIAL ASTHMA PATHOPHYSIOLOGY Asthma has been classified as 1. atopic (lgE mediated, triggered by allergens) 2. nonatopic (non lgE mediated, triggered by infection) 3. mixed 4. exercise induced or aspirin induced Inhalation of an allergen leads to a biphasic response with early and late reactions ultimately causing bronchoconstriction.
  • 6. BRONCHIAL ASTHMA LATE REACTION • develops 3-4 hr later and peaks at 8-12 hr. • The release of mast cell mediators is not prevented by premedication with beta2 -agonist. • it is inhibited by premedication with steroids suggesting that airway narrowing is mainly due to an inflammatory reaction and mucosal edema. This phase presents as clinical asthma.
  • 7. BRONCHIAL ASTHMA TRIGGERS • Viral Infections • Exercise • Weather Changes • Emotional factors • Food • Endocrine Factors
  • 8. BRONCHIAL ASTHMA • Dyspnea • May develop cyanosis • Restless • Chest becomes barrel shaped • Hyperinflation of chest • Clubbing of fingers • Recurrent Cough • Wheezing • Air Hunger • Hyper resonant chest due to air trapping • Prolonged Respiratory phase • Feeble breath sounds
  • 9. O Symptoms occur with change in season , aggravated by exercise,and more in nights O Acute asthma usually begins with a cold ,bouts of spasmodic coughing
  • 10. BRONCHIAL ASTHMA DIFFERENTIAL DIAGNOSIS • Bronchiolitis • Congenital Malformation • Aspiration of foreign body • Hypersensitivity Pneumonitis • Cystic Fibrosis
  • 11. GRADING OF SEVERITY OF ACUTE ASTHMA
  • 12. BRONCHIAL ASTHMA INVESTIGATIONS • Complete blood count,ESR(normal values are expected ;may have eosinophilia • Pulse oximetry –mild ->955,moderate-90-95%,severe<90% • Chest X Ray-normal or show bilateral symmetric air trapping • Patches of atelectasis of varying sizes due to mucus plugs • Allergy Test- blood IgE elevated in atopic asthma and normal in non atopic asthma • Spirometry-mild ->80%,moderate -60-80%,severe<60%
  • 13. BRONCHIAL ASTHMA MANAGEMENT The goals of the therapy are 1. Maintenance of near normal pulmonary function 2. Maintenance of near normal physical activity 3. Prevention of night time cough/wheeze with minimal chronic symptoms 4. Prevention of exacerbation 5. Avoiding adverse effects of medications
  • 14. O Management 1. Identification and elimination of exacerbating factors 2. Pharmacotherapy i. Acute exacerbation management ii. Long term mangement
  • 15. ACUTE EXACERABATION OF ASTHMA MILD O Nebulization- salbutamol 150 mcg/kg/dose n 3 ml of saline once O Assess for response O Response is adequate and child is comfortable discharge on oral salbutamol ,0.1-0.2 mg/kg/dose,6hrly or salbutamol inhaler puffs ,2 puffs 4-6hrly O if the child is not improving a adequately shift to the management protocol of moderate exacerbation
  • 16. MODERATE Nebulized salbutamol every 20 minutes for 3 times in one hour. Assess for response the if the response is adequate, space out nebulization intervals 2-4hrly . observe the child for six to eight hours if the relief is sustained discharge the child on oral salbutamol or salbutamol inhaler 2puffs 4-6hrly
  • 17. response is only partial start oral steroids prednisolone 1 to 2 mg / kg / day continue nebulization .when improved (usually takes 1 to 2 days ),discharge the child on Oral salbutamol and steroid for 3 to 5 days. the child is fit for discharge if he feeds well and sleeps well In case of deterioration manage as severe exacerbation. if the nebulizer is not available, 2 to 4 puffs of salbutamol by MDI every 20 minute for 3 times or subcutaneous injection of terbutaline may be considered
  • 18. SEVERE Admit in the ICU Connect to Pulse oxymeter oxygen inhalation oxygen driven nebulization with salbutamol and ipratropium (125 mcg for infants and toddlers ,250 mcg for > 5 years, 500 mcg for adolescence) every 20 minutes for 3 doses .
  • 19. IV hydrocortisone 10 mg/kg initially followed by 4 to 5 mg/kg/dose every 6hrly or IV methylprednisolone 2 mg/kg/dose or oral prednisolone 2mg/kg/day IV MgSO4 ;0.1ml/kg 50% MgSO4 in normal infusion over 30 minute. injection aminophylline 5mg/kg/dose diluted as IV infusion 6 hourly
  • 20. if improvement is inadequate ,consider continuous oxygen driven nebulization with salbutamol ,0.5 mg/kg or hourly nebulization. ipratropium can be spaced out to 4 hourly, mixed with the corresponding doses of salbutamol IV TERBUTALINE 10 Mcg /kg bolus infusion over 30 minute, followed by 0.4 mcg/kg/min increasing gradually, to maximum 4 mcg/kg/min ketamine Mechanical ventilation
  • 21. Pharmacological -long term i. Assessment of symptom control ii. Assessment of risk of exacerbation iii. Selection of medication iv. Selection of appropriate inhalational device v. monitoring
  • 22. ASSESSMENT OF SYMPTOM CONTROL characteristics controlled Partially controlled uncontrolled Day time symptoms none >2 per week 3 or more features of pa rtially controlled prese nt in week Limitation of activity none any nocturnal sumptoms none any Reliever or rescue drug none >2 per week
  • 23. Assessment of risk of exacerbation  MODIFIABLE o Uncontrolled asthma symptoms o Previous history(1 or more) o Exposures:tobacco smoke,indoor or outdoor air pollution,indoor allergens o Psychological or socioeconomic problems o Poor adherence with controlled medication o Co- morbidities:obesity,rhinosinusitis and food allergy
  • 24.  Non modifiable o Ever intubated :PICU admissions o >1 severe exacerbation requiring hospitalization in last 12 months
  • 25. Selection of medication O Infrequent symptoms –- No controlled medication ,short acting beta agonist with inhaled steroids O Asthma with any risk factors,>twice a month--low dose inhaled steroids as and when required short acting beta agonist Montelukast(other choice)
  • 26. O Troublesome – low dose inhaled steroids +long acting beta agonist or medium dose inhaled steroids Low or medium dose inhaled steroids +LTRA or sustained release theophylline O Severely uncontrolled – medium to high dose inhaled steroids+long acting beta agonist short course oral steroid and high dose inhaled steroids or moderate dose inhaled steroids and long acting beta agonist
  • 27. Selection of appropriate inhalation device O Metered dose inhaler(MDI) O MDI with spacer O With face mask O Dry powder inhaler O Nebulizer
  • 28. monitoring O Every 4-12 wks O Detailed history(frequency of symptoms ,sleep disturbance,physical activity,school absenteeism,visit to doctors,need for bronchodialators) O maintain Symptom diary O Assessed as being controlled,partially or uncontrolled O Poor compliance ,wrong technique of inhalation inappropriate dose ,infections
  • 29. O No cause is found-step up O Control is sustained for 3-6 months,and gradual reduction- step down
  • 31. OLife threatening asthma: o Cyanosis o Silent chest o Poor respiratory efforts o fatigue o Altered sensorium o PEFR< 30 % o Oxygen saturation <90%
  • 32. O MDI o Fixed amount of medication o Aerosol form –activated o Exacerbation and maintanance therapy o Coordination (press and breath) o Pressure ,oropharynx o spacer
  • 35. MDI with spacer O Large portion being deposited in lung ,with less impaction on oropharynx O Advantage- overcome coordination O Limitations-being bulky ,costly,young infants and toddlers
  • 37. How to use 1. Remove cap ,shake ,insert into spacer 2. Place mouth piece of spacer 3. Start breathing in and out-valve 4. Breathing pattern established press canister and continue to breath—5-10 5. Wait for 30 sec
  • 38. With mask O Below 2-3 yrs HOW TO USE O Attach baby mask O Shake mdi inserted to mdi end O Mouth and nose O Press canister and encourage child to take breathing mouth open O 30-60
  • 40. Nebulizer O Acute severe asthma in young irritable and hypoxic children O Bulky and inefficient aerosol delivery system IMPROVE THE AMOUNT OF DRUG DELIVERED o Total fill volume -3-5 ml o Tapping the side of nebulizer o Optimal flow rate -6-12L/min o Slow,deep inhalation and breath holding
  • 42. O Below 4 yrs-MDI with spacer and Face mask O Above 4 yrs-MDI with spacer O Above 12 yrs-MDI may be used directly