Elective Termination of Pregnancy in Autoimmune Rheumatic Diseases: Experience From Two Databases. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: To provide reference data regarding the frequency and safety of elective termination of pregnancy in women with autoimmune rheumatic diseases followed up in 2 referral databases. METHODS: Two large databases, one from an autoimmune rheumatic disease referral clinical practice with a known interest in pregnancy (the Barbara Volcker Center for Women and Rheumatic Disease [BVC]), and one from an observational study of systemic lupus erythematosus- and antiphospholipid antibody-associated pregnancies (Predictors of Pregnancy Outcome: Biomarkers in Antiphospholipid Antibody Syndrome and Systemic Lupus Erythematosus [PROMISSE]), were interrogated for histories of prior elective termination of pregnancy and complications related to incident pregnancy termination. RESULTS: Of women who had had prior pregnancies, 21.7% of 1,307 in the BVC database and 25.3% of 297 in the PROMISSE database gave histories of 1-5 prior elective terminations of pregnancy; BVC patients reported no flares or hospitalizable complications due to pregnancy termination. Of 674 incident pregnancies, termination for fetal or maternal reasons was recommended for 15 (2%); of these, 2 fetuses died before the procedure was carried out and 1 woman declined termination and, though gravely ill, successfully delivered. She died of cardiomyopathy 3 years later. CONCLUSION: Many patients with autoimmune rheumatic disease undergo elective termination of pregnancy; few report complications. In medically indicated termination of pregnancy, there are no adverse signals of unusual complications or disease flare.

publication date

  • June 17, 2020

Research

keywords

  • Abortion, Induced
  • Autoimmune Diseases
  • Pregnancy Complications
  • Rheumatic Diseases

Identity

PubMed Central ID

  • PMC7486237

Scopus Document Identifier

  • 85088605241

Digital Object Identifier (DOI)

  • 10.1002/art.41249

PubMed ID

  • 32162838

Additional Document Info

volume

  • 72

issue

  • 8