Pregnancy outcomes before and after a diagnosis of systemic lupus erythematosus

The purpose of this study was to evaluate pregnancy outcomes before and after diagnosis of lupus. Successive selection criterion applied to 148 lupus and 78,905 non-lupus pregnancies, generated 3 groups: lupus group, 84 pregnancies (not-yet-diagnosed group, 15 women; already-diagnosed group, 69 wome...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of obstetrics and gynecology 2005-10, Vol.193 (4), p.1444-1455
Hauptverfasser: Dhar, J. Patricia, Essenmacher, Lynnette M., Ager, Joel W., Sokol, Robert J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The purpose of this study was to evaluate pregnancy outcomes before and after diagnosis of lupus. Successive selection criterion applied to 148 lupus and 78,905 non-lupus pregnancies, generated 3 groups: lupus group, 84 pregnancies (not-yet-diagnosed group, 15 women; already-diagnosed group, 69 women), and control group, 51,000 pregnancies. Three-way analysis of variance and the chi-squared test were used for analyses. Stillbirth outcome was increased in the lupus group compared with the control group (odds ratio, 4.84 [95% CI, 1.72,11.08]); the not-yet-diagnosed group (odds ratio, 9.89 [95% CI, 1.09,42.63]), and the already-diagnosed group (odds ratio, 3.85 [95% CI, 1.02,10.31]). Considering >1 pregnancy per patient would have overestimated the stillbirth rate. Stillbirth risk was increased significantly in severe maternal disease that was marked by central nervous system involvement. The already-diagnosed group had more hypertensive complications ( P = .001 and .0001). Both lupus groups showed a significantly greater proportion of preterm births ( P = .03), growth restriction ( P = .019), and infants in the very low birth weight category ( P = .021) compared with the control group. Poor fetal outcomes are seen in pregnancies that are complicated by lupus, even before clinical appearance of disease, which supports a predisease state.
ISSN:0002-9378
1097-6868
DOI:10.1016/j.ajog.2005.02.104