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Factors Associated with Failure of Intermittent Nebulization with Short-Acting Beta-Agonists in Children with Severe
Prapasri Kulalert1, Phichayut Phinyo2,3, Jayanton Patumanond3
1Department of Clinical Epidemiology, Faculty of Medicine, Thammasat University, Pathum Thani, Thailand.
Insights
Children with severe asthma exacerbation (SAE) may not respond to initial SABA treatment. Predictors of treatment failure include prior intubation, low oxygen saturation, and pneumonia triggers.
Area of Science:
- Pediatric Emergency Medicine
- Respiratory Medicine
- Clinical Research
Background:
- Short-acting beta-agonists (SABA) are the first-line treatment for pediatric asthma exacerbations.
- Children with severe asthma exacerbations (SAE) may require advanced treatment strategies due to inadequate response to initial therapy.
Purpose of the Study:
- To identify factors predicting poor response to intermittent nebulized SABA in children experiencing SAE.
- To inform clinical decision-making for managing severe pediatric asthma.
Main Methods:
- Retrospective cohort study of children with SAE admitted between 2015-2017.
- Treatment failure was defined as the need for escalated therapy.
- Logistic regression analysis was employed to determine predictors of treatment failure.
Main Results:
- Previous intubation history was significantly associated with treatment failure (aOR 6.46).
- Receiving fewer than 3 doses of nebulized salbutamol in the ER predicted failure (aOR 3.21).
- Low emergency room oxygen saturation (SpO2 <92%) and pneumonia as a trigger were also significant predictors (aOR 3.02 and 2.67, respectively).
Conclusions:
- Four key prognostic factors for treatment failure in pediatric SAE were identified: prior intubation, insufficient initial SABA dosage, low SpO2, and pneumonia.
- These findings highlight critical indicators for closer monitoring and potential escalation of care in severe pediatric asthma cases.
Purpose:
Intermittent nebulization of short-acting beta-agonists (SABA) is the initial treatment of choice for children with asthma exacerbation. However, children with severe asthma exacerbation (SAE) may not show an adequate response and need aggressive stepwise therapy. We aimed to explore factors associated with a poor response to intermittent nebulized SABA in children with SAE.
Methods:
A retrospective cohort study of children with SAE diagnosed according to the definition of the British Guidelines on the Management of Asthma, who were admitted at Hat Yai Hospital from January 1, 2015, to December 31, 2017. All children were treated with intermittent SABA nebulization. Treatment failure was defined as children needing escalated therapy. Logistic regression with confounding score adjustment was used to explore the predictors of treatment failure.
Results:
One hundred thirty-three children were included in the analysis, 59 were in the failure group and 74 were in the success group. After adjusting for potential confounders, they were significantly associated with a previous history of intubation (adjusted OR 6.46, 95% CI 1.13 to 36.79, p=0.036), receiving <3 doses of nebulized salbutamol in the emergency room (ER, aOR 3.21, 95% CI 1.15 to 9.02, p=0.027), ER measured oxygen saturation (SpO2) <92% (adjusted OR 3.02, 95% CI 1.18 to 7.75, p=0.022), and exacerbation triggered by pneumonia (adjusted OR 2.67, 95% CI 1.19 to 6.00, p=0.017).
Conclusion:
We identified four prognostic factors of treatment failure in children with SAE: a previous history of intubation; receiving <3 doses of nebulized salbutamol in the ER, SpO2 at ER <92%; and exacerbation triggered by pneumonia. Further prospective studies are required to confirm our findings before clinical implementation.
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