TY - JOUR
T1 - Safety of leukotriene receptor antagonists in pregnancy
AU - Bakhireva, Ludmila N.
AU - Jones, Kenneth Lyons
AU - Schatz, Michael
AU - Klonoff-Cohen, Hillary S.
AU - Johnson, Diana
AU - Slymen, Donald J.
AU - Chambers, Christina D.
N1 - Funding Information:
Supported by a grant from Aventis Pharmaceutical.
Funding Information:
Disclosure of potential conflict of interest: K. L. Jones has consulting arrangements with Merck and has received grant support from Sanofi-Aventis, Sanofi-Pasteur, Abbott Laboratories, Amgen, Apotex, Barr Laboratories, Kali Laboratories, Sandoz Pharmaceutical, and Teva Pharmaceutical. M. Schatz has received grant support from GlaxoSmithKline and Sanofi-Aventis and has received honoraria from GlaxoSmithKline, Genentech, and Merck. C. D. Chambers has consulting arrangements with Cephalom Pharmaceutical and has received grant support from Sanofi-Aventis, Sanofi-Pasteur, Abbott Laboratories, Amgen, Apotex, Barr Laboratories, Kali, Laboratories, Sandoz Pharmaceutical, and Teva Pharmaceutical. The rest of the authors have declared that they have no conflict of interest.
PY - 2007/3
Y1 - 2007/3
N2 - Background: Asthma is a chronic disorder that affects about 8% of pregnant women and may complicate pregnancy. Adequate asthma therapy in pregnancy is crucial but challenging because of safety concerns for the fetus. Objective: To evaluate the safety of gestational asthma therapy with leukotriene receptor antagonists (LTRAs) for the mother and fetus/newborn. Methods: Subjects were participants of the Organization of Teratology Information Specialists Asthma Medications in Pregnancy Study. Perinatal outcomes among 96 women who took LTRAs (montelukast or zafirlukast) were compared with women who exclusively took short-acting β2-agonists (n = 122) and women without asthma (n = 346). Results: Use of LTRAs was not associated with an increased risk of pregnancy loss, gestational diabetes, preeclampsia, low maternal weight gain, preterm delivery, low Apgar scores, or reduced measures of birth length and head circumference in infants (P > .05). Slightly decreased birth weight in infants born to LTRA users could be attributed to maternal asthma severity/control. The birth prevalence of major structural defects in the LTRA group (5.95%) was significantly higher compared with controls without asthma (P = .007), but not different from the comparison group with asthma (P = .524). Furthermore, the defects observed in the LTRA group did not represent a consistent pattern. Conclusions: Use of LTRAs in pregnancy was not associated with a specific pattern of major structural anomalies in offspring or a large risk of other adverse perinatal outcomes. Clinical implications: This study suggests that LTRAs do not appear to be a major human teratogen; however, results should be interpreted with caution because of limited sample size.
AB - Background: Asthma is a chronic disorder that affects about 8% of pregnant women and may complicate pregnancy. Adequate asthma therapy in pregnancy is crucial but challenging because of safety concerns for the fetus. Objective: To evaluate the safety of gestational asthma therapy with leukotriene receptor antagonists (LTRAs) for the mother and fetus/newborn. Methods: Subjects were participants of the Organization of Teratology Information Specialists Asthma Medications in Pregnancy Study. Perinatal outcomes among 96 women who took LTRAs (montelukast or zafirlukast) were compared with women who exclusively took short-acting β2-agonists (n = 122) and women without asthma (n = 346). Results: Use of LTRAs was not associated with an increased risk of pregnancy loss, gestational diabetes, preeclampsia, low maternal weight gain, preterm delivery, low Apgar scores, or reduced measures of birth length and head circumference in infants (P > .05). Slightly decreased birth weight in infants born to LTRA users could be attributed to maternal asthma severity/control. The birth prevalence of major structural defects in the LTRA group (5.95%) was significantly higher compared with controls without asthma (P = .007), but not different from the comparison group with asthma (P = .524). Furthermore, the defects observed in the LTRA group did not represent a consistent pattern. Conclusions: Use of LTRAs in pregnancy was not associated with a specific pattern of major structural anomalies in offspring or a large risk of other adverse perinatal outcomes. Clinical implications: This study suggests that LTRAs do not appear to be a major human teratogen; however, results should be interpreted with caution because of limited sample size.
KW - Asthma
KW - asthma medications
KW - leukotriene receptor antagonists
KW - major structural anomalies
KW - montelukast
KW - pregnancy
KW - zafirlukast
UR - http://www.scopus.com/inward/record.url?scp=33847288181&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33847288181&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2006.12.618
DO - 10.1016/j.jaci.2006.12.618
M3 - Article
C2 - 17336611
AN - SCOPUS:33847288181
SN - 0091-6749
VL - 119
SP - 618
EP - 625
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 3
ER -