Treatment algorithm

Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer

ACUTE

life-threatening exacerbation or impending respiratory failure

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intensive care unit admission

Children with signs of a life-threatening exacerbation (e.g., drowsiness, confusion, silent chest) are admitted to the paediatric intensive care unit for treatment and respiratory support (e.g., high-flow humidified nasal cannulae, non-invasive ventilation, or intubation and mechanical ventilation).[7][72]

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nebulised short-acting beta-2 agonist

Treatment recommended for ALL patients in selected patient group

An inhaled short-acting beta-2 agonist (SABA) is delivered by continuous oxygen-driven nebuliser to patients with life-threatening exacerbations.[7][57]​​[87][88] Maintain saturations of 94% to 98%.[7]

Further oxygen desaturation is possible due to pulmonary vasodilation in areas of poorly ventilated lung.[7][57]​​ Frequent administration of a beta-2 agonist can cause transient decreases in potassium, magnesium, and phosphate levels. Potassium levels should be monitored and replaced, as needed, when giving a SABA very frequently.[57]​ Use SABA with caution in children with pre-existing cardiac disease.

Primary options

salbutamol inhaled: children ≤5 years of age: 2.5 mg nebulised every 20-30 minutes or when required according to response; children 6-11 years of age: 2.5 to 5 mg nebulised every 20-30 minutes or when required according to response

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Plus – 

oral or parenteral corticosteroid

Treatment recommended for ALL patients in selected patient group

Intravenous or intramuscular corticosteroids are often required in life-threatening exacerbations, but oral corticosteroids have comparable effectiveness and are preferred when tolerated. Oral dexamethasone and oral prednisolone have comparable outcomes, although oral dexamethasone is associated with lower non-compliance and vomiting rates.[96]​ Concerns about metabolic adverse effects limit the use of oral dexamethasone to no more than two days, at which point changing to prednisolone should be considered (i.e., if symptoms persist or relapse).[7][96]

Consider parenteral corticosteroids when patients are too dyspnoeic to swallow, are vomiting, or require non-invasive ventilation or intubation.[7] Corticosteroids produce a treatment response by 4-6 hours.[7][82] 

Systemic corticosteroids have the potential to cause severe adverse effects (e.g., gastrointestinal bleeding, sepsis, pneumonia, and adrenal suppression), with systemic adverse effects more common with parenteral or long-acting corticosteroids.[101][102]

Treat patients with systemic corticosteroids, typically prednisolone, for 3 days and then review.[7][57]​​​​​​[105][106][107]​​​​​ Parenteral corticosteroids required for severe and life-threatening exacerbations can be given for up to 10 days with regular review.[104]

Primary options

prednisolone: 1-2 mg/kg/day orally, maximum 20 mg/day (children <2 years of age) or 30 mg/day (children 2-5 years of age) or 40 mg/day (children 6-11 years of age)

Secondary options

dexamethasone sodium phosphate: 0.6 mg/kg orally/intramuscularly/intravenously once daily

OR

methylprednisolone sodium succinate: 1 mg/kg intravenously every 6 hours

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Plus – 

controlled oxygen

Treatment recommended for ALL patients in selected patient group

Oxygen is given to maintain saturations of 94% to 98%.[7][57]​​

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Consider – 

nebulised anticholinergic

Additional treatment recommended for SOME patients in selected patient group

Children aged 6-11 years are routinely given a nebulised anticholinergic. Children aged 5 years and younger only receive a nebulised anticholinergic if there is poor response to initial treatment with beta-2 agonists, corticosteroids, and oxygen. The benefits and risks in children <2 years are unclear and anticholinergics are not recommended, except for children with bronchiolitis and chronic lung disease of prematurity.[7][57]​​[86]​​  [ Cochrane Clinical Answers logo ]

Anticholinergics are given by oxygen-driven nebuliser every 20 minutes for the first hour and then reassessed.[7][57]​​ Nebulised anticholinergics produce a weaker bronchodilation response with a slower onset of action (30-90 minutes) than beta-2 agonists (5-15 minutes).[85] Their addition can improve both cholinergic bronchomotor tone and secretions.

Cardiac stimulation occurs but is less marked than that produced by beta-2 agonists.

Primary options

ipratropium inhaled: children ≤5 years of age: 250 micrograms nebulised every 20 minutes for 3 doses; children 6-11 years of age: 250-500 micrograms nebulised every 20 minutes for 3 doses

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Consider – 

intravenous bronchodilator or nebulised magnesium sulfate

Additional treatment recommended for SOME patients in selected patient group

Consider intravenous bronchodilator therapy if there is poor response to inhaled bronchodilators and corticosteroids.[7][57]​​[59]​​ Criteria for starting include no response to initial therapies, persistent hypoxaemia, and an FEV₁ <60% predicted at 1 hour.[7]

Intravenous magnesium sulfate is preferred by GINA (children 6-11 years old) and BTS/NICE/SIGN (children 2-11 years old) for exacerbations unresponsive to first-line therapy.[7][57]​​[59][75][76] [ Cochrane Clinical Answers logo ] ​​​​ Its use can reduce the length of hospital stay.[83] However, it does not have an established role in children 5 years and younger due to a lack of evidence.[7] Nebulised magnesium sulfate can be considered if there is no intravenous access, but this offers only modest benefit in severe exacerbations.[7][57]​​[78]​​​​​[79][80] [ Cochrane Clinical Answers logo ] ​​​​​ 

Nebulised magnesium sulfate can be added to a nebulised short-acting beta-2 agonist and anticholinergic in the first hour of treatment for children 2-5 years with severe asthma (e.g., oxygen saturation <92%), particularly if symptoms have lasted <6 hours.[7][57]​​​​ However, this may not be as effective as intravenous therapy.[7]​​​​​​[73]​​[74] [ Cochrane Clinical Answers logo ]

Intravenous SABA (salbutamol or subcutaneous terbutaline where intravenous salbutamol is not available) or a methylxanthine (aminophylline or theophylline) are listed as second-line intravenous bronchodilators by the BTS/NICE/SIGN guideline for use in children 2-11 years old, but only under expert supervision and with extreme caution.[57]​​[59]​​ Neither approach is recommended by GINA.[7]

Treatment with intravenous magnesium sulfate requires close monitoring for respiratory depression. During intravenous treatment with beta-2 agonists, monitor and replace potassium levels as required.[57]​ If patients receive intravenous aminophylline, adverse effects are more likely in those taking sustained-release theophylline as part of their chronic management.[7] Serum theophylline levels should be checked regularly and the dose adjusted accordingly if patients receive continuous therapy.

Primary options

magnesium sulfate: children ≥2 years of age: 40-50 mg/kg intravenously by slow infusion over 20-60 minutes, maximum 2000 mg/dose

Secondary options

salbutamol: consult specialist for guidance on dose

OR

terbutaline: consult specialist for guidance on dose

OR

magnesium sulfate: children ≥2 years of age: 150 mg nebulised every 20 minutes for 3 doses

More

Tertiary options

aminophylline: consult specialist for guidance on dose

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Consider – 

antibiotic therapy

Additional treatment recommended for SOME patients in selected patient group

Antibiotics are rarely required and should not be given routinely unless there is fever, purulent sputum, or radiographic evidence of pneumonia.[7][71]

If bacterial pneumonia is diagnosed, antibiotic selection and dosing should be according to local institutional protocols. Mycoplasma pneumoniae is most common.

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Consider – 

intramuscular adrenaline (epinephrine)

Additional treatment recommended for SOME patients in selected patient group

Administer intramuscular adrenaline if signs of angio-oedema or anaphylaxis are present.[7][117]

Primary options

adrenaline (epinephrine): consult specialist for guidance on dose

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Consider – 

ventilation

Additional treatment recommended for SOME patients in selected patient group

Clinical symptoms of exhaustion, cyanosis, or drowsiness with hypoxaemia and hypercapnia are indications for intubation and mechanical ventilation. The paediatric intensive care team and/or anaesthetist with paediatric training should be alerted early for children with life-threatening exacerbations.

Non-invasive ventilation has a role in the management of acute asthma and may help to avoid the subsequent need for invasive ventilation.[118]

Humidified high-flow nasal cannulae (HFNC) are well tolerated and may be appropriate in some settings, but their use is not supported by data from randomised controlled trials and they may offer no benefits over aerosol masks.[119][120][121]

The application of positive pressure in the setting of severe acute bronchospasm may prevent airway collapse and reduce the mechanical load on already tired respiratory muscles.[120] Non-invasive positive pressure ventilation (NPPV) may be used as a rescue therapy to avoid intubation. Continuous positive airways pressure (CPAP) or bi-level non-invasive ventilation can be applied using either a nasal or full-face mask interface. However, one Cochrane review found that current evidence is insufficient to recommend for or against the use of NPPV in children with acute asthma.[122] Sedation is occasionally necessary for patient tolerance, but should be used with caution.

Intubation is preferred before the onset of respiratory arrest. If intubation is required, the ventilation strategy should ensure adequate expiratory time to aid gas exchange. Muscle relaxation may be necessary. Fluid replacement will be required because these patients are often fluid depleted and the initiation of positive pressure ventilation may trigger hypotension.

severe exacerbation

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1st line – 

hospital admission and nebulised short-acting beta-2 agonist

An inhaled short-acting beta-2 agonist (SABA) is delivered by continuous oxygen-driven nebuliser to patients with life-threatening exacerbations.[7][57]​​[87][88] Maintain saturations of 94% to 98%.[7]

Further oxygen desaturation is possible due to pulmonary vasodilation in areas of poorly ventilated lung.[7][57]​​ Frequent administration of a beta-2 agonist can cause transient decreases in potassium, magnesium, and phosphate levels. Potassium levels should be monitored and replaced, as needed, when giving a SABA very frequently.[57]​ Use SABA with caution in children with pre-existing cardiac disease.

All patients with severe exacerbations should be admitted to the hospital.

Primary options

salbutamol inhaled: children ≤5 years of age: 2.5 mg nebulised every 20-30 minutes or when required according to response; children 6-11 years of age: 2.5 to 5 mg nebulised every 20-30 minutes or when required according to response

Back
Plus – 

oral or parenteral corticosteroid

Treatment recommended for ALL patients in selected patient group

Intravenous or intramuscular corticosteroids are often required in severe exacerbations, but oral corticosteroids have comparable effectiveness and are preferred when tolerated. Oral dexamethasone and oral prednisolone have comparable outcomes, although oral dexamethasone is associated with lower non-compliance and vomiting rates.[96]​ Concerns about metabolic adverse effects limit the use of oral dexamethasone to no more than two days, at which point changing to prednisolone should be considered (i.e., if symptoms persist or relapse).[7][96]

Consider parenteral corticosteroids when patients are too dyspnoeic to swallow, are vomiting, or require non-invasive ventilation or intubation.[7] Corticosteroids produce a treatment response by 4-6 hours.[7][82]

Systemic corticosteroids have the potential to cause severe adverse effects (e.g., gastrointestinal bleeding, sepsis, pneumonia, and adrenal suppression), with systemic adverse effects more common with parenteral or long-acting corticosteroids.[101][102]

Treat patients with systemic corticosteroids, usually prednisolone, for 3 days and then review the need for a longer course.[7][57]​​​​​​[105][106][107]​​​​​ Where parenteral corticosteroids are required for severe and life-threatening exacerbations, they can be continued for a maximum of 10 days with regular review.[104]

Primary options

prednisolone: 1-2 mg/kg/day orally, maximum 20 mg/day (children <2 years of age) or 30 mg/day (children 2-5 years of age) or 40 mg/day (children 6-11 years of age)

Secondary options

dexamethasone sodium phosphate: 0.6 mg/kg orally/intramuscularly/intravenously once daily

OR

methylprednisolone sodium succinate: 1 mg/kg intravenously every 6 hours

Back
Plus – 

controlled oxygen

Treatment recommended for ALL patients in selected patient group

Oxygen may be required in some children to maintain oxygen saturation at a target of 94% to 98%.[7][57]​​

Back
Consider – 

nebulised anticholinergic

Additional treatment recommended for SOME patients in selected patient group

Children aged 6-11 years are routinely given a nebulised anticholinergic. Children aged 5 years and younger only receive a nebulised anticholinergic if there is poor response to initial treatment with beta-2 agonists, corticosteroids, and oxygen. The benefits and risks in children <2 years are unclear and anticholinergics are not recommended, except for children with bronchiolitis and chronic lung disease of prematurity.[7]​​[57]​​[86] [ Cochrane Clinical Answers logo ]

Anticholinergics are given by oxygen-driven nebuliser every 20 minutes for the first hour and then reassessed.[7][57]​​ Nebulised anticholinergics produce a weaker bronchodilation response with a slower onset of action (30-90 minutes) than beta-2 agonists (5-15 minutes).[85] Their addition can improve both cholinergic bronchomotor tone and secretions.

Cardiac stimulation occurs but is less marked than that produced by beta-2 agonists.

Primary options

ipratropium inhaled: children ≤5 years of age: 250 micrograms nebulised every 20 minutes for 3 doses; children 6-11 years of age: 250-500 micrograms nebulised every 20 minutes for 3 doses

Back
Consider – 

intravenous bronchodilator or nebulised magnesium sulfate

Additional treatment recommended for SOME patients in selected patient group

Consider intravenous bronchodilator therapy if there is poor response to inhaled bronchodilators and corticosteroids.[7][57]​​[59]​​ Criteria for starting include no response to initial therapies, persistent hypoxaemia, and an FEV₁ <60% predicted at 1 hour.[7]

Intravenous magnesium sulfate is preferred by GINA (children 6-11 years old) and BTS/NICE/SIGN (children 2-11 years old) for exacerbations unresponsive to first-line therapy.[7][57]​​[59][75][76] [ Cochrane Clinical Answers logo ] ​​​ Its use can reduce the length of hospital stay.[83]​ However, it does not have an established role in children 5 years and younger due to a lack of evidence.[7] Nebulised magnesium sulfate can be considered if there is no intravenous access, but this offers only modest benefit in severe exacerbations.[7][57]​​[78]​​​​[79][80] [ Cochrane Clinical Answers logo ] ​​​​ 

Nebulised magnesium sulfate can be added to a nebulised short-acting beta-2 agonist and anticholinergic in the first hour of treatment for children 2-5 years with severe asthma (e.g., oxygen saturation <92%), particularly if symptoms have lasted <6 hours.[7][57]​​​However, this may not be as effective as intravenous therapy.[7]​​​​​​[73]​​[74] [ Cochrane Clinical Answers logo ]

Intravenous SABA (salbutamol or subcutaneous terbutaline where intravenous salbutamol is not available) or a methylxanthine (aminophylline or theophylline) are listed as second-line intravenous bronchodilators by the BTS/NICE/SIGN guideline for use in children 2-11 years old, but only under expert supervision and with extreme caution.[57]​​[59]​​ Neither approach is recommended by GINA.[7]

Treatment with intravenous magnesium sulfate requires close monitoring for respiratory depression. During intravenous treatment with beta-2 agonists, monitor and replace potassium levels as required.[57]​ If patients receive intravenous aminophylline, adverse effects are more likely in those taking sustained-release theophylline as part of their chronic management.[7] Serum theophylline levels should be checked regularly and the dose adjusted accordingly if patients receive continuous therapy.

Primary options

magnesium sulfate: children ≥2 years of age: 40-50 mg/kg intravenously by slow infusion over 20-60 minutes, maximum 2000 mg/dose

Secondary options

salbutamol: consult specialist for guidance on dose

OR

terbutaline: consult specialist for guidance on dose

OR

magnesium sulfate: children ≥2 years of age: 150 mg nebulised every 20 minutes for 3 doses

More

Tertiary options

aminophylline: consult specialist for guidance on dose

Back
Consider – 

antibiotic therapy

Additional treatment recommended for SOME patients in selected patient group

Antibiotics are rarely required and should not be given routinely unless there is fever, purulent sputum, or radiographic evidence of pneumonia.[7][71]

If bacterial pneumonia is diagnosed, antibiotic selection and dosing should be according to local institutional protocols. Mycoplasma pneumoniae is most common.​​

Back
Consider – 

intramuscular adrenaline (epinephrine)

Additional treatment recommended for SOME patients in selected patient group

Administer intramuscular adrenaline if signs of angio-oedema or anaphylaxis are present.[7][117]

Primary options

adrenaline (epinephrine): consult specialist for guidance on dose

Back
Consider – 

ventilation

Additional treatment recommended for SOME patients in selected patient group

Involve the anaesthetic or paediatric intensive care team involved early. If children with severe asthma develop signs of impending respiratory failure (confusion or marked agitation, loss of respiratory effort, pulsus paradoxus, cyanosis, hypoxaemia, or respiratory acidosis) despite aggressive treatment (e.g., intravenous bronchodilators and magnesium sulfate), they may require intubation and mechanical ventilation with 100% oxygen.

Non-invasive ventilation has a role in the management of acute asthma and may help to avoid the subsequent need for invasive ventilation.[118]

Humidified high-flow nasal cannulae (HFNC) are well tolerated and may be appropriate in some settings, but their use is not supported by data from randomised controlled trials and they may offer no benefits over aerosol masks.[119][120][121]

The application of positive pressure in the setting of severe acute bronchospasm may prevent airway collapse and reduce the mechanical load on already tired respiratory muscles.[120] Non-invasive positive pressure ventilation (NPPV) may be used as a rescue therapy to avoid intubation. Continuous positive airways pressure (CPAP) or bi-level non-invasive ventilation can be applied using either a nasal or full-face mask interface. However, one Cochrane review found that current evidence is insufficient to recommend for or against the use of NPPV in children with acute asthma.[122] Sedation is occasionally necessary for patient tolerance, but should be used with caution.

Intubation is preferred before the onset of respiratory arrest. If intubation is required, the ventilation strategy should ensure adequate expiratory time to aid gas exchange. Muscle relaxation may be necessary. Fluid replacement will be required because these patients are often fluid depleted and the initiation of positive pressure ventilation may trigger hypotension.

mild to moderate exacerbation

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1st line – 

inhaled short-acting beta-2 agonist

Give an inhaled short-acting beta-2 agonist (SABA) immediately, reassess after 15-20 minutes, and give a further dose if response is inadequate (up to three doses in the first hour). The response to treatment should be immediate and sustained for 3-4 hours.[7]

A metered-dose inhaler plus a spacer is just as effective as a nebuliser for mild to moderate exacerbations.​[81]​​​ [ Cochrane Clinical Answers logo ] ​​ Use a face mask for children aged <3 years and a mouthpiece used for older children.[7]

Mild exacerbations do not usually require hospital admission and can be treated appropriately at home using the child's personalised asthma action plan. Some moderate exacerbations may require hospital admission.[7][57]​​[72] [ Cochrane Clinical Answers logo ]

Primary options

salbutamol inhaled: (100 micrograms/dose metered-dose inhaler) children ≤5 years of age: 200-600 micrograms (2-6 puffs) every 20 minutes for 3 doses, then adjust dose according to response; children 6-11 years of age: 400-1000 micrograms (4-10 puffs) every 20 minutes for 3 doses, followed by 4-10 puffs every 3-4 hours to 6-10 puffs every 1-2 hours

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Consider – 

oral corticosteroid

Additional treatment recommended for SOME patients in selected patient group

Oral corticosteroids are not usually required in a mild exacerbation, but may be needed to prevent deterioration when response to an inhaled short-acting beta-2 agonist (SABA) is incomplete. For children 5 years and younger with mild to moderate exacerbations, a systemic corticosteroid should only be given if symptoms recur within 3-4 hours of treatment with a SABA.[7]

Corticosteroids produce a treatment response by 4-6 hours.[7][82] Early administration within the first hour of arrival reduces admission rates compared with placebo.[82] 

A pragmatic approach is to prescribe treatment for 3 days and then review the need for a longer course.[7][57]​​

Adjusting the ICS dose may be considered on a case-by-case basis to reduce hospitalisations (e.g., adding a short course of daily ICS to a SABA reliever at the onset of a respiratory illness in children aged 0-4 years), but this is not recommended routinely.[7][55][89]​​[90][91][92]​​​​[94][95] [ Cochrane Clinical Answers logo ]

Primary options

prednisolone: 1-2 mg/kg/day orally, maximum 20 mg/day (children <2 years of age) or 30 mg/day (children 2-5 years of age) or 40 mg/day (children 6-11 years of age)

Back
Consider – 

inhaled anticholinergic

Additional treatment recommended for SOME patients in selected patient group

An inhaled anticholinergic can be added to the short-acting beta-2 agonist if there is a poor response to initial treatment in children with a moderate to severe exacerbation.[7][57]​​ [ Cochrane Clinical Answers logo ] [ Cochrane Clinical Answers logo ]

Anticholinergics produce a weaker bronchodilation response with a slower onset of action (30-90 minutes) than beta-2 agonists (5-15 minutes).[85] Give the anticholinergic at 20 minute intervals and reassess response.[7]

The use of spacers with pressurised metered-dose inhalers is recommended, especially for young children (i.e., ≤5 years old).[7] Use a face mask if <3 years old and a mouthpiece if older.

Routine use of an anticholinergic is not recommended in children <2 years of age, except for those with bronchiolitis or chronic lung disease of prematurity.[86]

Cardiac stimulation occurs but is less marked than that produced by beta-2 agonists.

Primary options

ipratropium inhaled: consult specialist for guidance on dose

Back
Consider – 

controlled oxygen

Additional treatment recommended for SOME patients in selected patient group

Oxygen may be required in some children to maintain oxygen saturation at a target of 94% to 98%.[7][57]​​

Back
Consider – 

antibiotic therapy

Additional treatment recommended for SOME patients in selected patient group

Antibiotics are rarely required and should not be given routinely unless there is fever, purulent sputum, or radiographic evidence of pneumonia.[7]​​[71]

If bacterial pneumonia is diagnosed, antibiotic selection and dosing should be according to local institutional protocols. Mycoplasma pneumoniae is the most common.

ONGOING

acute exacerbation resolved

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1st line – 

arrange ongoing treatment

In the acute care setting, patients are assessed for hospitalisation or discharge based on their clinical status (including the ability to lie flat), oxygen saturation, and lung function 1 hour after starting treatment. These outcomes more reliably predict the need for hospitalisation than the patient’s status on arrival. If recorded, decisions can be based on peak expiratory flow (PEF) and/or forced expiratory volume in the first second of expiration (FEV₁).[7] Hospitalisation is recommended if pre-treatment FEV₁ or PEF is <25% predicted or personal best; post-treatment FEV₁ or PEF is <40% predicted or personal best. Discharge possible if post-treatment lung function 40% to 60% predicted. Discharge is recommended if post-treatment lung function is >60% predicted or personal best.

Only consider discharge from the acute care setting after assessing the patient’s risk factors and the availability of follow-up care. Risk factors for admission include: female sex, older age, and non-white race; use of >8 beta-2 agonist puffs in 24 hours; life threatening or severe exacerbations (may be considered if moderate); past history of severe exacerbations (e.g., intubations, asthma admissions); and previous unscheduled office and emergency department visits requiring oral corticosteroids.[7]

Discharge from hospital can be considered when the child is stable on inhaled bronchodilators every 3-4 hours that can be used at home; if recorded, the peak expiratory flow (PEF) and/or forced expiratory volume in the first second of expiration (FEV₁) is >75% of best or predicted; and oxygen saturations are >94% in room air.[57]​​

Update the treatment plan before discharge from hospital or acute care settings. Include the following: start inhaled corticosteroid (ICS)-containing controller treatment or increase the dose of an existing ICS-containing treatment, and aim for step-up treatment to last 2-4 weeks; guide patients to reduce their use of reliever therapies to as-needed; review symptom control and risk factors for exacerbations; if not already done, step-up the patient’s treatment; update or provide a written asthma action plan; provide advice about avoiding triggers; and check inhaler technique and adherence.

Arrange early follow-up after hospital discharge for any exacerbation (i.e., 1-2 days) to assess progress and update the treatment plan, as appropriate.

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Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer

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