Secondary severity assessment
Following the initial severity assessment and initiation of treatment, perform a more detailed secondary severity assessment as outlined in Secondary severity assessment of acute asthma to determine ongoing management.
Assessment of response to treatment is an ongoing process; tailor the frequency of assessment to the severity of the exacerbation. Repeat secondary severity assessment frequently within the first hour (eg after each dose of salbutamol). In more severe cases, remain at the bedside until the patient is stabilised.
Secondary assessment of acute asthma should also take into account any risk factors for fatal asthma—see Risk factors for potentially fatal asthma.
Mild to moderate: all of the following |
Severe: any of the following |
Life-threatening: any of the following |
---|---|---|
consciousness | ||
alert |
may be the same as mild to moderate and does not determine severity |
reduced consciousness (eg drowsy or unconscious) |
speech | ||
can finish a sentence in one breath |
children 1 to 5 years: may be the same as mild to moderate and does not determine severity adults: unable to complete sentences in one breath |
can’t speak or can only speak single words because of dyspnoea |
posture | ||
can walk (or, if an infant, crawl) |
difficulty lying flat because of dyspnoea sitting hunched forward (‘tripoding’) tiring |
collapsed or exhausted |
breathing | ||
respiratory distress is not severe |
increased work of breathing with use of accessory muscles (eg tracheal tug, intercostal or subcostal recession, marked abdominal breathing, chest wall recession in children) |
severe respiratory distress or poor respiratory effort |
skin colour | ||
normal |
may be the same as mild to moderate and does not determine severity |
cyanosis (not always present) |
respiratory rate [NB1] | ||
normal |
tachypnoea |
tachypnoea bradypnoea (indicates respiratory exhaustion) |
heart rate [NB1] | ||
normal |
tachycardia |
cardiac arrhythmia or bradycardia (may occur just before respiratory arrest) |
chest auscultation | ||
wheeze persistent cough (not always present) |
may be the same as mild to moderate and does not determine severity |
‘silent chest’ due to reduced air entry |
oxygen saturation (pulse oximetry) | ||
SpO2 more than 94% |
SpO2 90 to 94% |
SpO2 less than 90% or clinical cyanosis |
arterial blood gas analysis (only applicable to adults) | ||
not indicated |
may be indicated if not improving as expected [NB2] |
PaO2 lower than 60 mmHg on room air PaCO2 higher than 45 mmHg or PaCO2 within normal range [NB2] pH less than 7.35 [NB3] |
lung function tests (only applicable to adults) | ||
FEV1 or PEF more than 40% predicted or personal best |
FEV1 or PEF less than 40% predicted or personal best |
not indicated (usually not able to be performed) |
asthma history | ||
assess risk factors for asthma-related death; see Risk factors for potentially fatal asthma | ||
chest X-ray | ||
not usually required; indicated if pneumonia, atelectasis, pneumothorax or pneumomediastinum is suspected, or if sudden deterioration | ||
Note:
FEV1 = forced expiratory volume in 1 second; PaCO2 = partial pressure of carbon dioxide; PaO2 = partial pressure of oxygen; PEF = peak expiratory flow; SpO2 = oxygen saturation measured by pulse oximetry NB1: Normal values for heart rate and respiratory rate in children vary with age; see The Royal Children’s Hospital (Melbourne) website. NB2: Do not be reassured by a normal PaCO2 in a patient with an elevated respiratory rate. The presence of hypercapnia or normocapnia indicates that the patient is tiring and may need ventilatory support. NB3: Metabolic acidosis (often associated with hypokalaemia) may occur with increased work of breathing and with high-dose salbutamol. Adapted from the Australian Asthma Handbook © 2020 National Asthma Council Australia. Accessed 31 August 2020. |
Risk factors for potentially fatal asthma include:
- previous ventilation or admission to an intensive care unit for asthma
- hospital admission for asthma in the last year
- repeated emergency-department attendances in the last year
- frequent short-acting beta2 agonist use (eg more than one canister per month)
- requirement for three or more classes of asthma maintenance medication
- poor lung function
- history of ‘brittle asthma’ (ie sudden and severe exacerbations)
- confirmed food allergy
- current or recent requirement for oral corticosteroid
- rural or remote location.
The above factors often coexist with adverse psychosocial or behavioural factors, such as:
- poor adherence to drug therapy
- poor attendance at follow-up appointments
- depression or other psychiatric illness
- substance misuse, including smoking
- denial of the serious nature of asthma or the need for regular treatment
- social isolation
- learning difficulties
- financial or domestic problems.