The safety of dextromethorphan in pregnancy - Results of a controlled study

被引:22
作者
Einarson, A [1 ]
Lyszkiewicz, D [1 ]
Koren, G [1 ]
机构
[1] Univ Toronto, Div Clin Pharmacol, Motherisk Program, Hosp Sick Children, Toronto, ON M5G 1X8, Canada
关键词
birth defects; dextromethorphan; pregnancy;
D O I
10.1378/chest.119.2.466
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Dextromethorphan (DM), the d-isomer of the codeine analog levorphanol, is an active ingredient present in a variety of cough and cold remedies. Recently, data generated from a study in chick embryos were extrapolated to suggest that pregnant women should not use this drug because of the risk of birth defects. We conducted a controlled study of pregnant women who used DM, to examine the possible teratogenic risk in humans. Materials and methods: We followed up women who used DM and had been counseled by the Motherisk Program during their pregnancy. A control group of women was matched for age, smoking, alcohol use, and disease state (upper respiratory tract infection, not treated with DM). Results: We were able to ascertain pregnancy outcome in 184 women. There were 172 live births, 10 spontaneous abortions, 1 therapeutic abortion, and 1 stillbirth. One hundred twenty-eight of the women used the drug during the first trimester of pregnancy. There were three major malformations (2.3%) among the babies of women who used DM in die first trimester, seven minor malformations, and the mean (+/- SD) birth weight was 3,381 +/- 670 g. In the control group, there were 17 live births, 8 spontaneous abortions, and 2 therapeutic abortions. There were five major malformations, one of which was a chromosomal abnormality (2.8%), eight minor malformations, and the mean birth weight was 3,446 +/- 571 g. Conclusion: This study fails to show that DM use during pregnancy increases the rates of major malformations above the expected baseline rate of 1% to 3%.
引用
收藏
页码:466 / 469
页数:4
相关论文
共 15 条
[1]   Dextromethorphan and other N-methyl-D-aspartate receptor antagonists are teratogenic in the avian embryo model [J].
Andaloro, VJ ;
Monaghan, DT ;
Rosenquist, TH .
PEDIATRIC RESEARCH, 1998, 43 (01) :1-7
[2]  
BERGLUND F, 1984, ACTA OBSTET GYN SCAN, P1
[3]  
Brent RL, 1998, PEDIATR RES, V44, P415, DOI 10.1203/00006450-199809000-00026
[4]  
*CAN PHARM ASS, 1998, COMP NONPR PROD, P167
[5]   A prospective controlled multicentre study of clarithromycin in pregnancy [J].
Einarson, A ;
Phillips, E ;
Mawji, F ;
D'Alimonte, D ;
Schick, B ;
Addis, A ;
Mastroiacova, P ;
Mazzone, T ;
Matsui, D ;
Koren, G .
AMERICAN JOURNAL OF PERINATOLOGY, 1998, 15 (09) :523-525
[6]  
HEINONEN OP, 1997, BIRTH DEFECTS DRUGS
[7]   Untitled - Commentary [J].
Holmes, LB .
PEDIATRIC RESEARCH, 1999, 45 (02) :286-287
[8]   Drug therapy - Drugs in pregnancy [J].
Koren, G ;
Pastuszak, A ;
Ito, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (16) :1128-1137
[9]   CONGENITAL ANOMALIES IN NEWBORN INFANT INCLUDING MINOR VARIATIONS - STUDY OF 4412 BABIES BY SURFACE EXAMINATION FOR ANOMALIES + BUCCAL SMEAR FOR SEX CHROMATIN [J].
MARDEN, PM ;
SMITH, DW ;
MCDONALD, MJ .
JOURNAL OF PEDIATRICS, 1964, 64 (03) :357-+
[10]   TERATOGEN UPDATE - CLINICAL ASPECTS OF THALIDOMIDE EMBRYOPATHY - A CONTINUING PREOCCUPATION [J].
NEWMAN, CGH .
TERATOLOGY, 1985, 32 (01) :133-144