Considerations in using registry and health plan data for studying pregnancy in rheumatic diseases

Curr Opin Rheumatol. 2014 May;26(3):315-20. doi: 10.1097/BOR.0000000000000056.

Abstract

Purpose of review: The purpose of this review is to critically evaluate the strengths and limitations of different data sources for pregnancy-related research in patients with rheumatic diseases. We describe challenges in studying adverse pregnancy outcomes in the setting of observational research, with a particular focus on the studies of maternal drug exposures.

Recent findings: We discuss potential threats to validity in the assessment of exposure and outcomes and controlling for confounding; present findings from selected pregnancy-related observational studies conducted using data from registries and health plans; and highlight future research opportunities for pregnancy research.

Summary: Registry and health plan data contribute complementary information to each other. Used together, linked data sources may allow clinicians, researchers, and patients to obtain a more complete understanding of the risk and benefits associated with maternal drug exposure and of the risk factors associated with adverse birth outcomes in women with rheumatic disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Antirheumatic Agents / adverse effects*
  • Antirheumatic Agents / therapeutic use
  • Female
  • Humans
  • Maternal-Fetal Exchange
  • Medical Record Linkage
  • Medical Records
  • Pregnancy
  • Pregnancy Complications / drug therapy*
  • Pregnancy Outcome
  • Prenatal Exposure Delayed Effects
  • Registries
  • Rheumatic Diseases / drug therapy*
  • Sample Size

Substances

  • Antirheumatic Agents