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The relationship of asthma medication use to perinatal outcomes
Michael Schatz1, Mitchell P Dombrowski, Robert Wise
1Allergy Department, Kaiser Permanente Medical Center, 7060 Clairemont Mesa Boulevard, San Diego, CA 92111, USA. michael.x.schatz@kp.org
Insights
Maternal asthma medication use was studied in pregnant women. Inhaled asthma drugs showed no increased risk, but oral corticosteroids were linked to preterm birth and low birth weight.
Area of Science:
- Obstetrics and Gynecology
- Pulmonology
- Perinatal Medicine
Background:
- Maternal asthma is linked to adverse perinatal outcomes like preeclampsia and low birth weight.
- Mechanisms connecting maternal asthma to these outcomes are not fully understood.
Purpose of the Study:
- To investigate the association between contemporary asthma medication use during pregnancy and adverse perinatal outcomes.
- To determine if specific asthma treatments pose risks to pregnancy.
Main Methods:
- A cohort of 2123 asthmatic pregnant women was recruited across 16 centers.
- Gestational medication use was recorded via patient history.
- Perinatal outcomes including preterm birth, low birth weight, and malformations were assessed via chart review.
Main Results:
- No significant link was found between inhaled beta-agonists, inhaled corticosteroids, or theophylline and adverse perinatal outcomes.
- Maternal use of oral corticosteroids was significantly associated with preterm birth (OR 1.54) and low birth weight (OR 1.80).
Conclusions:
- Contemporary inhaled asthma medications (beta-agonists, corticosteroids) and theophylline do not appear to elevate perinatal risks.
- The association between oral corticosteroid use and prematurity requires further investigation to determine the underlying mechanisms.
Background:
Maternal asthma has been reported to increase the risk of preeclampsia, preterm deliveries, and lower-birth-weight infants, but the mechanisms of this effect are not defined.
Objective:
We sought to evaluate the relationship between the use of contemporary asthma medications and adverse perinatal outcomes.
Methods:
Asthmatic patients were recruited from the 16 centers of the National Institute of Child Health and Human Development Maternal Fetal Medicine Units Network from December 1994 through February 2000. Gestational medication use was determined on the basis of patient history at enrollment and at monthly visits during pregnancy. Perinatal data were obtained at postpartum chart reviews. Perinatal outcome variables included gestational hypertension, preterm births, low-birth-weight infants, small-for-gestational-age infants, and major malformations.
Results:
The final cohort included 2123 asthmatic participants. No significant relationships were found between the use of inhaled beta-agonists (n=1828), inhaled corticosteroids (n=722), or theophylline (n=273) and adverse perinatal outcomes. After adjusting for demographic and asthma severity covariates, oral corticosteroid use was significantly associated with both preterm birth at less than 37 weeks' gestation (odds ratio, 1.54; 95% CI, 1.02-2.33) and low birth weight of less than 2500 g (odds ratio, 1.80; 95% CI, 1.13-2.88).
Conclusions:
Use of inhaled beta-agonists, inhaled steroids, and theophylline do not appear to increase perinatal risks in pregnant asthmatic women. The mechanism of the association between maternal oral corticosteroid use and prematurity remains to be determined.
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