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Treat to Target: Rheumatoid Arthritis in Pregnant Patients

Eliza F. Chakravarty, MD, MS  |  Issue: October 2012  |  October 1, 2012

Both chronic HTN and DM have provided an excellent framework for the treat-to-target principle in nonpregnant individuals who may suffer fewer irreversible complications from undertreated disease as a result of achieving a low-disease state. This paradigm has been nicely translated to RA, with goals of low disease state/remission becoming increasingly possible with a growing arsenal of targeted drug therapy. With the adoption of treat to target, we can expect to see slowing or halting of RA-related damage accrual, including joint destruction, accelerated cardiovascular disease, and malignancy. In HTN and DM, however, treat-to-target goals extend into pregnancy, as it has been widely recognized that tight disease control during pregnancy improves both maternal and fetal outcomes. It is recognized that some therapeutic agents are “safer” than others during pregnancy, so that the medication regimen may need to be adjusted prior to conception, but the benefits of tight disease control far outweigh the risks of antenatal exposure to “safer” medications. Just as the rheumatology community has adopted the treat-to-target paradigm in the nonpregnant state, we should perhaps strongly consider similarly including these concepts during the peripregnancy period in female RA patients. Within the past few years, adverse pregnancy outcomes have been associated with RA, with some suggestion that these are directly related to increased disease activity. At the same time, effective medications that may be considered “safer” have become part of routine RA management. Because RA has been shown to improve during pregnancy, many women can hope to achieve good disease control without medical intervention. However, for the unlucky subset of women with moderate to severe disease during pregnancy, medical intervention may be warranted. The development of specific guidelines for RA control during pregnancy may aid in more widespread acceptance of medication use by both physicians and patients.

Disclosure

Dr. Chakravarty is a consultant for UCB and Genentech

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Dr. Chakravarty is an associate member in Arthritis and Clinical Immunology at Oklahoma Medical Research Foundation in Oklahoma City.

References

  1. Smolen JS, Aletaha D, Bijlsma JW, et al. Treating rheumatoid arthritis to target: Recommendations of an international task force. Ann Rheum Dis. 2010 Apr; 69(4):631-637.
  2. Hazes JMW, Coulie PG, Geenen V, et al. Rheumatoid arthritis and pregnancy: Evolution of disease activity and pathophysiological considerations for drug use. Rheumatology. 2011;50:1955-1968.
  3. De Man YA, Dolhain RJ, van de Geijn FE, Willemsen SP, Hazes JM. Disease activity of rheumatoid arthritis during pregnancy: Results from a nationwide prospective study. Arthritis Rheum. 2008;59:1241-1248.
  4. Jawaheer D, Zhu JL, Nohr EA, Olsen J. Time to pregnancy among women with rheumatoid arthritis. Arthritis Rheum. 2011;63:1517-1521.
  5. Schoels M, Knevel R, Aletaha D, et al. Evidence for treating rheumatoid arthritis to target: Results of a systematic literature search. Ann Rheum Dis. 2010;69:638-643.
  6. Chakravarty EF. Rheumatoid arthritis and pregnancy: Beyond smaller and preterm babies. Arthritis Rheum. 2011;63:1469-1471.
  7. de Man YA, Hazes JMW, van der Heide H, et al. Association of higher rheumatoid arthritis disease activity during pregnancy with lower birth weight. Arthritis Rheum. 2009;60:3196-3206.
  8. McIntire DD, Leveno KJ. Neonatal mortality and morbidity rates in late preterm births compared with births at term. Obstet Gynecol. 2008;111:35-41.
  9. Quinn D. Teratology risk assessment and counseling. In: Diseases, Complications, and Drug Therapy in Obstetrics: A Guide for Clinicians. Briggs GG, Mageotte M, Eds. Bethesda, Md.:American Society of Health-System Pharmacists, Inc., 2009.
  10. Shahin I, Einarson A. Knowledge transfer and translocation: Examining how teratogen information is disseminated. Birth Def Res (Part A). 2011;91:956-961.
  11. Buhimschi CS, Weiner CP. Medications in pregnancy and lactation. Part 1. Teratology. Obstet Gynecol. 2009;113:166-188.
  12. Carter JD. Ladhani A, Ricca LR, Valeriano J. Vasey FB. A safety assessment of tumor necrosis factor antagonists during pregnancy: A review of the Food and Drug Administration database. J Rheumatol. 2009;36:635-641.
  13. El Mourabet M, El-Hachem S, Harrison JR, Binion DG. Anti-TNF antibody therapy for inflammatory bowel disease during pregnancy: A clinical review. Curr Drug Targets. 2010 Feb;11(2):234-241.
  14. Clowse ME. The use of anti-TNFa medications for rheumatologic disease in pregnancy. Int J Womens Health. 2010;2:199-209.
  15. Chronic hypertension in pregnancy. Practice Bulletin No. 125. American College of Obstetricians and Gynecologists. Obstet Gynecol. 2012;119:396-407.
  16. Ali S, Dornhorst A. Diabetes in pregnancy: Health risks and management. Postgrad Med J. 2011;87:417-427.
  17. Garne E, Loane M, Dolk H, et al. Spectrum of congenital anomalies in pregnancies with pregestational diabetes. Birth Defect Res (Part A). 2012; 94:134-140.

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