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Volume 95, Issue 1, Pages 66-72 (October 2006)


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Alcohol abuse — A persistent preventable risk for congenital anomalies

P. BaumannaCorresponding Author Informationemail address, C. Schildb, R.F. Humec, R.J. Sokold

Received 6 March 2006; received in revised form 11 May 2006; accepted 17 May 2006. published online 04 July 2006.

Abstract 

Objective

To examine whether alcohol abuse (ALC) continued to be a health hazard to pregnant women in the 1990s.

Study design

Analysis of a perinatal data base comprising 170,258 women with singleton pregnancies. Univariate cross table analysis and logistic regression were conducted to examine the association between alcohol abuse and congenital malformations coded according to the International Classification of Diseases (ICD).

Results

14,727/170,258 mothers (8.6%) admitted to ALC during pregnancy and 36,705/170,258 (21.6%) to smoking. Anomaly rates for ALC (365/14,092, 4.3%) vs. Non-ALC (6187/149,344, 4.0%) differed significantly (p<0.001). The rates of specific anomalies varied between <0.1% and 1.1%. Odds ratios for 16 ICD 9 anomaly categories were >1 in 14 instances overall (Sign test, p=0.004), in 12 instances in women <30 years (p=0.08), and in 13 instances in women over 30 years (p=0.02). Congenital anomalies of the “respiratory system” (ICD9 748), of “genital organs” (ICD9 752.1), of the “integument” (ICD9 757), and “other anomalies of limbs/other musculoskeletal anomalies” (ICD 755/756) were statistically significantly associated with ALC, especially in women>30 years.

Conclusion

ALC in pregnancy continued to be an important factor independently associated with an increased incidence of a broader range of congenital anomalies than previously recognized. Risk for anatomic anomalies was increased in offspring of ALC women over age 30, consistent with previous reports of increased risk of neurobehavioral abnormality in offspring of women over 30.

a Department of Obstetrics and Gynecology, Hutzel Women's Hospital, Wayne State University, Detroit, Michigan, USA

b Department of Obstetrics and Gynecology, Medical University Lübeck, Lübeck, Germany

c Department of Obstetrics and Gynecology, Division of Reproductive Genetics, Hutzel Women's Hospital, Wayne State University, Detroit, Michigan, USA

d Department of Obstetrics and Gynecology, C.S. Mott Center for Human Growth and Development, Detroit, Michigan, USA

Corresponding Author InformationCorresponding author. Tel.: +1 313 993 4043; fax: +1 313 993 4132.

 This study was conducted at the state of Schleswig-Holstein, Germany, and Wayne State University, Detroit, Michigan.

 This manuscript was presented as a poster at the 2005 Annual Meeting of the Society of Gynecologic Investigation, March 23–26, 2005, Los Angeles, CA.

PII: S0020-7292(06)00273-6

doi:10.1016/j.ijgo.2006.05.033


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