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Tables
Table 1. Prevalence of asthma in adults and children in studies from India
| Region |
No. |
Age and setting |
Method |
Prevalence |
Salient Features |
| Mumbai
(Chowgule et al, 1998) 3 |
2,313 |
20-44 yrs
Population based |
ECRHS |
3.5% by physician diagnosis |
9-12% symptom prevalence without diagnosis of asthma |
| Chandigarh
(Jindal et al, 2000) 4 |
2,116 |
>18 yrs
Population based |
IUATLD based questionnaire |
3.9% (M)
1.3% (F)
Equal in urban and rural |
Questionnaire standardized against physician diagnosis |
| Chandigarh
(Gupta et al, 2001) 5 |
9,090 |
9-20 yrs
School based |
IUATLD based questionnaire |
2.6% (M)
1.9% (F) |
Questionnaire standardized against physician diagnosis
|
| Delhi
(Chhabra et al, 1999) 6 |
18,955 |
5-17 yrs
School based |
Questionnaire on wheeze |
3.4% (Past wheeze)
11.9% (Current wheeze)
12.8% (M)
10.7% (F) |
2.1% (Exercise Induced Asthma)
2.4% (Cold Associated Asthma) |
| Ludhiana
(Singh et al, 2002) 7 |
2,275 |
1-15 yrs
Population based |
Questionnaire on symptoms of asthma |
2.6% (Rural) |
Modified ATS criteria used for diagnosis |
| Lucknow
(Awasthi et al, 2004) 8 |
6,000 |
6-7 and 13-14 yrs School based |
ISAAC Questionnaire |
6.2% and 7.8% (Wheeze)
2.3% and 3.3% (Asthma) |
Part of multicentric (ISAAC III) trial |
| Multicentric
(ISAAC Steering Committee, 1998) 9,10 |
37,171 |
6-7 and 13-14 yrs
School Based |
ISAAC Questionnaire |
6.0% (Wheeze)
4.5% (Ever asthma) |
Wide variations in different regions worldwide (including within India) |
| Multicentric (ICMR)
(Jindal et al, Unpublished data) 11 |
73,605 |
>15 yrs
Population based |
IUATLD based Questionnaire |
2.4%
(1.7-3.5% range) |
Questionnaire standardized against physician diagnosis |
ATS American Thoracic Society, ECRHS European Community Respiratory Health Survey, ICMR Indian Council of Medical Research, ISAAC International Study of Asthma and Allergies in Childhood, IUATLD International Union Against Tuberculosis and Lung Diseases
Table 2. Role of tobacco smoke in asthma 19
| Active Smoking |
Passive Smoking (environmental tobacco smoke exposure) |
| Increased bronchial responsiveness |
Aggravation and occurrence of increased prevalence of respiratory symptoms |
| Frequent bronchial irritation symptoms |
Bronchial hyper-responsiveness in adults |
| Increased sensitization to occupational agents |
Aggravation of asthma symptoms |
| Aggravation of acute episodes |
Precipitation of acute episodes |
| Association with asthma severity |
Risk factor for development of asthma (both children and adults) |
| Risk factor for asthma? |
|
| Exaggerated decline in lung functions |
|
| Role in development of fixed airway obstruction and chronic obstructive pulmonary disease? |
|
Table 3 : Categorization of severity of asthma
|
Mild |
Moderate |
Severe |
| Symptoms disturbing sleep |
< Once per week |
> Once per week |
Daily |
| Daytime symptoms |
< Daily |
Daily |
Daily |
| Limitation of accustomed activities |
Nil |
<1 per week |
>1 per week |
| Use of rescue medication * |
<1 dose per day |
1-2 doses per day |
>2 doses per day |
| FEV1 |
Normal |
60-80% |
<60% |
| Peak expiratory flow |
Normal |
60-80% |
<60% |
A patient should be placed in the highest category of severity based on any one of the clinical features or lung function test.
FEV1 Forced expiratory volume in first second
* Each rescue medication dose = 200 µg inhaled salbutamol = 500 µg terbutaline = 2 mg oral salbutamol = 2.5 mg oral terbutaline.
Table 4. Equivalent doses of inhaled corticosteroids (in micrograms/day)
| Drug |
Low-dose ICS |
Medium-dose ICS |
High-dose ICS |
| Adults |
Children |
Adults |
Children |
Adults |
Children |
| Beclomethasone |
200-400 |
100-200 |
400-1000 |
200-400 |
>1000 |
>400 |
| Budesonide |
200-400 |
100-200 |
400-800 |
200-400 |
>800 |
>400 |
| Fluticasone |
125-250 |
50-125 |
250-500 |
125-250 |
>500 |
>250 |
Medication inserts for hydrofluoroalkane (HFA) preparations should be carefully reviewed for the correct dosage level. In general, the dose of dry powder inhalers with filler (such as lactose) is double than that of pressurized metered dose inhalers.
Table 5. Management of asthma in different stages
| Stage |
Daily controller medications |
Other treatment options |
| Mild |
Low-dose ICS* |
Sustained-release theophylline or Cromones |
| Moderate |
Moderate dose ICS + inhaled LABA** and/or LTRA |
- Moderate dose ICS + either sustained-release theophylline or LTRA or oral LABA
- High-dose ICS |
| Severe |
High dose ICS + inhaled LABA plus one or more of the following if needed: sustained-release theophylline, leukotriene modifiers, oral LABA, oral glucocorticoid |
|
At all steps of severity SABA can be added on as needed basis for symptom relief.
See text for additional details
* Inhaled LABA optional; ** Optional in children
ICS Inhaled corticosteroids; LABA Long-acting beta-2 agonist; LTRA Leukotriene receptor antagonists, SABA Short acting beta-2 agonists
Table 6. Dosages of different anti-asthma drugs
|
Adult |
Children |
| |
|
|
| Long-acting beta-2 agonists |
|
|
| pMDI/DPI |
|
|
| Salmeterol |
50-100 µg/day |
50-100 µg/day (>5 years) |
| Formoterol |
12-24 µg/day |
12-24 µg/day (>5 years) |
| Oral |
|
|
| Bambuterol |
10-20 mg/day |
- |
| |
|
|
| Systemic steroids |
|
|
| Prednisolone |
|
|
| For acute exacerbations |
40-60 mg/day for 7-10 days in single or divided doses |
1-2 mg/kg/day for 3-10 days in single or divided doses |
| For long-term control |
Administer lowest dose required to control symptoms Preferably single a.m. dose; alternate day if possible |
Administer lowest dose required to control symptoms Preferably single a.m. dose; alternate day if possible |
| Intravenous Hydrocortisone |
|
|
| For acute exacerbations |
100 mg stat and 50 mg q6 hourly |
4-8 mg/kg/day |
| |
|
|
| Theophyllines |
Starting dose 10mg/kg/day (max. 300 mg/day); usual maximum 600-800 mg/day |
Starting dose 10mg/kg/day; usual maximum dose age > 1 year- 16 mg/kg/day age < 1 year- [0.2 (age in weeks) + 5] mg/kg/day |
| |
|
|
| Leukotriene modifiers |
|
|
| Montelukast |
10 mg/day |
2-5 years 4 mg/day |
|
|
6-14 years 5 mg/day |
| |
|
|
| Short-acting beta-2 agonists |
|
|
| Salbutamol |
|
|
| pMDI/DPI |
100-200 µg/dose |
100 µg/dose |
| Nebulized |
2.5 to 5 mg q 4-6 hourly |
0.05 mg/kg/dose, (min. 1.25 mg, max. 2.5 mg) q 4-6 hourly |
| Oral |
2-8 mg q 6-8 hourly |
1-4 mg q 6-8 hourly |
| Intravenous |
3-20 µg/minute adjusted to bronchospasm and heart rate |
0.1-0.2 µg/kg/minute adjusted to bronchospasm and heart rate |
| Subcutaneous |
8 µg/kg |
Not recommended |
| Terbutaline |
|
|
| pMDI/DPI |
250 µg/dose |
250 µg/dose |
| Nebulized |
10 mg q 4-6 hourly |
0.3 mg/kg/dose, (max. 10 mg/dose) q 4-6 hourly |
| Oral |
2.5 mg q 6-8 hourly |
0.25 µg/kg/dose q 6-8 hourly (Not recommended below 2 y of age) |
| Intravenous/Subcutaneous/ Intramuscular |
0.25-0.5 mg q 4-6 hourly |
10 µg/kg/dose (max. 300 µg) |
| |
|
|
| Anticholinergic drugs |
|
|
| Ipratropium |
|
|
| pMDI/DPI |
20 µg/dose |
20 µg/dose |
| Nebulized |
0.25 mg q 4-6 hourly |
0.25 mg q 4-6 hourly |
| Tiotropium (pMDI/DPI) |
12 µg/day |
|
DPI Dry powder inhaler; pMDI Pressurized metered dose inhaler
Table 7. Normal respiratory and pulse rates in awake children
| Age |
Normal respiratory rate |
| < 2 months |
< 60/min |
| 2-12 months |
< 50/min |
| 1-5 years |
< 40/min |
| 6-8 years |
< 30/min |
| Age |
Normal pulse rate |
| 2-12 months |
< 160/min |
| 1-2 years |
< 120/min |
| 2-8 years |
< 110/min |
Appendix: Levels of evidence used for classification in this document
|
Description |
| Level 1 |
Randomized controlled trials with statistically significant results |
| Level 2 |
Randomized controlled trials with substantial threats to validity (small numbers, inadequate blinding, weak methodology) |
| Level 3 |
Observational study with a concurrent control group |
| Level 4 |
Observational study with a historical control group; consensus opinion |
| Level 5 |
Bench study, animal study, case series |
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