Assess Asthma Control & Adjust Therapy
Managing asthma long term
Jennifer Glen, Tim Michalski
Provided byThe Assess Asthma Control & Adjust Therapy tool can be used for patients currently taking asthma medication.
Use the Classify Asthma Severity tool if:
- the patient's treatment plan is unknown or
- the patient is not taking asthma controller medications as prescribed for at least three months.
Summary
The Expert Panel Report 3: Guidelines for the Diagnosis and Management of Asthma details how to assess asthma control and adjust asthma therapy in a patient taking asthma medication.
The Assess Asthma Control & Adjust Therapy tool can be used for patients currently taking asthma medication.
Use the Classify Asthma Severity tool if:
- the patient's treatment plan is unknown or
- the patient is not taking asthma controller medications as prescribed for at least three months.
Assessing asthma level of control is based on the most severe impairment or risk category.
- Classification of Asthma Control (≥12 years of age and older)
- See Figure 4-7
- Classification of Asthma Control (5-11 years of age)
- See Figure 4-3b
- Classification of Asthma Control (0-4 years of age)
- See Figure 4-3a
.
All questions & possible results
AgeTitle not visible
Choose age group
Select one option:
- 0-3
- 4
- 5-11
- 12+
Assess Control by Impairment Domain (Ages 12+)
Assess impairment domain by patient's recall of previous 2-4 weeks and by spirometry/or peak flow measures. Symptom assessment for longer periods should reflect a global assessment, such as inquiring whether the patient's asthma is better or worse since the last visit.
Daytime symptoms
Select one option:
- throughout the day
- > 2 days/week
- ≤ 2 days/week
Nighttime symptoms
Select one option:
- ≥ 4x/week
- 1-3x/week
- ≤ 2x/month
Interference with normal activity
Select one option:
- Extremely limited
- Some limitation
- None
Short-acting beta agonist (SABA) for symptom control (not exercise induced)
Select one option:
- Several times per day
- > 2 days/week
- ≤ 2 days/week
FEV₁ or peak flow
Select one option:
- < 60% predicted/personal best
- 60-80% predicted/personal best
- > 80% predicted/personal best
- Unknown
Validated questionnaires (ATAQ, ACQ, ACT)
Select one option:
- ATAQ 3-4; ACQ N/A; ACT ≤ 15
- ATAQ 1-2; ACQ ≥ 1.5; ACT ≤ 16-19
- ATAQ 0; ACQ ≤ 0.75*; ACT ≥ 20 (*ACQ values of 0.76-1.4 are indeterminate regarding well-controlled asthma)
- Unknown
Exacerbations requiring oral systemic corticosteroids
Consider severity and interval since last exacerbation
Select one option:
- ≥ 2/year
- 0-1/year
Assess Control by Impairment Domain (Ages 5-11)
Assess impairment domain by patient's recall of previous 2-4 weeks and by spirometry/or peak flow measures. Symptom assessment for longer periods should reflect a global assessment, such as inquiring whether the patient's asthma is better or worse since the last visit.
Daytime symptoms
Select one option:
- throughout the day
- > 2 days/week or multiple times on ≤ 2 days/week
- ≤ 2 days/week but not more than once on each day
Nighttime symptoms
Select one option:
- ≥ 2x/week
- ≥ 2x/month
- ≤ 1x/month
Interference with normal activity
Select one option:
- extremely limited
- some limitation
- None
Short-acting beta agonist (SABA) for symptom control (not exercise induced)
Select one option:
- several times per day
- > 2 days/week
- ≤ 2 days/week
FEV₁ peak flow & FEV₂/FVC
Select one option:
- FEV₁ <60% predicted/personal best; FEV₂/FVC <75%
- FEV₁ 60-80% predicted/personal best; FEV₂/FVC 75-80%
- FEV₁ >80% predicted/personal best; FEV₂/FVC >80%
Exacerbations requiring oral systemic corticosteroids
Consider severity and interval since last exacerbation
Select one option:
- ≥ 2/year
- 0-1/year
Assess Control by Impairment Domain (Ages 0-4)
Assess impairment domain by patient's recall of previous 2-4 weeks and by spirometry/or peak flow measures. Symptom assessment for longer periods should reflect a global assessment, such as inquiring whether the patient's asthma is better or worse since the last visit.
Daytime symptoms
Select one option:
- throughout the day
- > 2 days/week
- ≤ 2 days/week
Nighttime symptoms
Select one option:
- > 1x/week
- > 1x/month
- ≤ 1x/month
Interference with normal activity
Select one option:
- extremely limited
- some limitation
- none
Short-acting beta agonist (SABA) for symptom control (not exercise induced)
Select one option:
- several times per day
- > 2 days/week
- ≤ 2 days/week
Exacerbations requiring oral systemic corticosteroids
Consider severity and interval since last exacerbation
Select one option:
- > 3/year
- 2-3/year
- 0-1/year
Possible results
Not Well Controlled (Ages 0-4): Step up 1 step. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan. Re-evaluate in 2-6 weeks.
For side effects, consider alternative treatment options.
- The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Well Controlled (Ages 5-11): Maintain current step. Regular follow-ups every 1-6 months. Consider step down if well controlled for at least 3 months.
The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Well Controlled (Ages 12+): Maintain current step. Regular follow-ups every 1-6 months. Consider step down if well controlled for at least 3 months.
The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Very Poorly Controlled (Ages 12+): Step up 1-2 steps. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan (or) step up two to an alternative plan.
For side effects, consider alternative treatment options.
- The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Not Well Controlled (Ages 5-11): Step up 1 step. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan. Re-evaluate in 2-6 weeks.
For side effects, consider alternative treatment options.
- The stepwise approach is meant to assist, not replace, the clinical decisionmaking required to meet individual patient needs.
Very Poorly Controlled (Ages 5-11): Step up 1-2 steps. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan (or) step up two to an alternative plan.
For side effects, consider alternative treatment options.
- The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Well Controlled (Ages 0-4): Maintain current step. Regular follow-ups every 1-6 months. Consider step down if well controlled for at least 3 months.
The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Very Poorly Controlled (Ages 0-4): Step up 1-2 steps. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan (or) step up two to an alternative plan.
The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Not Well Controlled (Ages 12+): Step up 1 step. If an alternative treatment option was used in a step, discontinue it and use preferred treatment in that step (or) step up one to a preferred plan. Re-evaluate in 2-6 weeks.
For side effects, consider alternative treatment options.
- The stepwise approach is meant to assist, not replace, the clinical decision-making required to meet individual patient needs.
Literature
- Guidelines for the Diagnosis and Management of Asthma- Summary Report 2007 — National Asthma Education and Prevention Program. Expert Panel Report 3 (EPR-3)
- 2020 Focused Updates to the Asthma Management Guidelines — National Asthma Education and Prevention Program Coordinating Committee Expert Panel Working Group