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. 2016 Aug 12;9:26. doi: 10.1186/s40413-016-0117-0

Table 5.

Indications for initial low-dose ICS controller therapy in children aged 5 years and below

Indication to start low-dose ICS:
Symptom pattern consistent with asthma (Box 1) and asthma symptoms not well-controlled (Box 2), or at least 3 exacerbations per year
OR
Symptom pattern not consistent with asthma, but wheezing episodes occur frequently (e.g. every 6–8 weekly)
BOX 1: Features suggesting a diagnosis of asthma in children 5 years and younger
Feature Characteristics suggesting asthma
Cough Recurrent or persistent non-productive cough that may be worse at night or accompanied by some wheezing and breathing difficulties
Cough occurring with exercise, laughing, crying or exposure to tobacco smoke in the absence of an apparent respiratory infection
Wheezing Recurrent wheezing, including sleep or with triggers such as activity, laughing, crying or exposure to tobacco smoke or air pollution
Difficult or heavy breathing or shortness of breath Occurring with exercise, laughing or crying
Reduced activity Not running, playing or laughing at the same intensity as other children; tires earlier during walks (wants to be carried)
Past or family history Other allergic disease (atopic dermatitis or allergic rhinitis)
Asthma in first-degree relatives
Therapeutic trial with low dose ICS and as-needed SABA Clinical improvement during 2–3 months of controller treatment and worsening when treatment is stopped
BOX 2: GINA assessment of asthma control in children 5 years and younger
Symptoms in the last 4 weeks Level of control
Well controlled Partly controlled Uncontrolled
Daytime asthma symptoms for more than a few minutes, more than once a week None 1–2 of these 3–4 of these
Any activity limitation due to asthma (Runs/plays less than other children, tires easily when walking/playing)
Reliever medication (excludes reliever taken before exercise) needed more than once a week
Any night waking or night coughing due to asthma

Legend:

SABA short acting beta2-agonist

Evidence A – data from randomized controlled trials and meta-analyses, rich body of data

Evidence B – data from randomized controlled trials and meta-analyses, limited data

Evidence C – data from nonrandomized trials/observational studies

Evidence D – panel consensus judgment

modified from GINA 2015 [3]