Underuse of pregnancy testing for women prescribed teratogenic medications in the emergency department
- PMID: 25639672
- PMCID: PMC4399487
- DOI: 10.1111/acem.12578
Underuse of pregnancy testing for women prescribed teratogenic medications in the emergency department
Abstract
Objectives: The objectives were to estimate the frequency of pregnancy testing in emergency department (ED) visits by reproductive-aged women administered or prescribed teratogenic medications (Food and Drug Administration categories D or X) and to determine factors associated with nonreceipt of a pregnancy test.
Methods: This was a retrospective cross-sectional study using 2005 through 2009 National Hospital Ambulatory Medical Care Survey data of ED visits by females ages 14 to 40 years. The number of visits was estimated where teratogenic medications were administered or prescribed and pregnancy testing was not conducted. The association of demographic and clinical factors with nonreceipt of pregnancy testing was assessed using multivariable logistic regression.
Results: Of 39,859 sampled visits, representing an estimated 141.0 million ED visits by reproductive-aged females nationwide, 10.1 million (95% confidence interval [CI] = 8.9 to 11.3 million) estimated visits were associated with administration or prescription of teratogenic medications. Of these, 22.0% (95% CI = 19.8% to 24.2%) underwent pregnancy testing. The most frequent teratogenic medications administered without pregnancy testing were benzodiazepines (52.2%; 95% CI = 31.1% to 72.7%), antibiotics (10.7%; 95% CI = 5.0% to 16.3%), and antiepileptics (7.7%; 95% CI = 0.12% to 15.5%). The most common diagnoses associated with teratogenic drug prescription without pregnancy testing were psychiatric (16.1%; 95% CI = 13.6% to 18.6%), musculoskeletal (12.7%; 95% CI = 10.8% to 14.5%), and cardiac (9.5%; 95% CI = 7.6% to 11.3%). In multivariable analyses, visits by older (adjusted odds ratio [AOR] = 0.57, 95% CI = 0.42 to 0.79), non-Hispanic white females (AOR = 0.71; 95% CI = 0.54 to 0.93); visits in the Northeast region (AOR = 0.60; 95% CI = 0.42 to 0.86); and visits during which teratogenic medications were administered in the ED only (AOR = 0.74; 95% CI = 0.57 to 0.97) compared to prescribed at discharge only were less likely to have pregnancy testing.
Conclusions: A minority of ED visits by reproductive-aged women included pregnancy testing when patients were prescribed category D or X medications. Interventions are needed to ensure that pregnancy testing occurs before women are prescribed potentially teratogenic medications, as a preventable cause of infant morbidity.
© 2015 by the Society for Academic Emergency Medicine.
Conflict of interest statement
Figures
Comment in
-
In reply.Acad Emerg Med. 2015 Jun;22(6):770. doi: 10.1111/acem.12690. Epub 2015 May 20. Acad Emerg Med. 2015. PMID: 25996558 Free PMC article. No abstract available.
-
Defining a medication class as a teratogen: may the evidence be with you and not the FDA Pregnancy Risk Categories.Acad Emerg Med. 2015 Jun;22(6):769. doi: 10.1111/acem.12691. Epub 2015 May 21. Acad Emerg Med. 2015. PMID: 25999059 No abstract available.
References
-
- Schwarz EB, Maselli J, Norton M, Gonzales R. Prescription of teratogenic medications in United States ambulatory practices. Am J Med. 2005;118:1240–1249. - PubMed
-
- Andrade SE, Gurwitz JH, Davis RL, et al. Prescription drug use in pregnancy. Am J Obstet Gynecol. 2004;191:398–407. - PubMed
-
- Koren G. The way women perceive teratogenic risk. Can J Clin Pharmacol. 2007;14:e10–e16. - PubMed
-
- Todd CS, Mountvarner G, Lichenstein R. Unintended pregnancy risk in an emergency department population. Contraception. 2005;71:35–39. - PubMed
-
- Ramoska EA, Sacchetti AD, Nepp M. Reliability of patient history in determining the possibility of pregnancy. Ann Emerg Med. 1989;18:48–50. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
