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      Predictors of Pregnancy Outcome in a Prospective, Multiethnic Cohort of Lupus Patients

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          Abstract

          Background

          Since systemic lupus erythematosus (SLE) affects women of reproductive age, pregnancy is a major concern.

          Objective

          To identify predictors of adverse pregnancy outcome (APO) in inactive or stable active SLE patients

          Design

          Prospective Cohort

          Setting

          Multicenter

          Patients

          385 patients (49% non-Hispanic White; 31% prior nephritis) with SLE in PROMISSE. Exclusion criteria were: proteinuria >1000 mg/24 hour, creatinine >1.2 mg/dL, prednisone >20 mg/day, or multi-fetal pregnancy.

          Measurements

          APO included: fetal/neonatal death; birth <36 weeks due to placental insufficiency, hypertension, or preeclampsia; and small for gestational age (SGA) <5%. Disease activity was assessed by SLEPDAI and physician's global assessment (PGA).

          Results

          APO occurred in 19.0% (95% CI: 15.2% - 23.2%) of pregnancies, fetal death (4%), neonatal death (1%), preterm delivery (9%), and SGA (10%). Severe flares in the second and third trimester occurred in 2.5% and 3.0%, respectively. Baseline predictors of APO included lupus anticoagulant positive (OR = 8.32, 95% CI: 3.59-19.26), antihypertensive use (OR = 7.05, 95% CI: 3.05 - 16.31), PGA>1 (OR = 4.02, 95% CI: 1.84 - 8.82) and platelets (OR = 1.33 per 50K decrease, 95% CI:1.09-1.63); non-Hispanic White was protective (OR = 0.45, 95% CI: 0.24-0.84). Maternal flares, higher disease activity, and smaller increase in C3 later in pregnancy also predicted APO. Among women without baseline risk factors, the APO rate was 7.8%. For those either LAC positive, or LAC negative but non-White or Hispanic and taking antihypertensives, APO rate was 58%; fetal/neonatal mortality 22%.

          Limitations

          Excluded patients with high disease activity.

          Conclusions

          In pregnant SLE patients with inactive or stable mild/moderate disease, severe flares are infrequent, and absent specific risk factors, outcomes are favorable.

          Primary Funding Source

          National Institutes of Health

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          Author and article information

          Contributors
          Journal
          0372351
          596
          Ann Intern Med
          Ann. Intern. Med.
          Annals of internal medicine
          0003-4819
          1539-3704
          4 November 2016
          4 August 2015
          17 November 2016
          : 163
          : 3
          : 153-163
          Affiliations
          New York University School of Medicine, New York
          Albert Einstein College of Medicine, New York
          Hospital for Special Surgery, New York
          University of Toronto, Toronto
          Johns Hopkins University School of Medicine, Baltimore
          Hospital for Special Surgery and Weill Cornell Medical College, New York
          Hospital for Special Surgery and Weill Cornell Medical College, New York
          University of Utah Health Sciences Center and Intermountain Healthcare, Salt Lake City
          University of Utah Health Sciences Center and Intermountain Healthcare, Salt Lake City
          University of Utah Health Sciences Center, Salt Lake City
          Oklahoma Medical Research Foundation and the University of Oklahoma Health Sciences Center, Oklahoma City
          University of Illinois at Chicago, Chicago
          Hospital for Special Surgery, New York
          Hospital for Special Surgery, New York, Oest fold Hospital Trust, Fredrikstad, Norway
          Hospital for Special Surgery and Weill Cornell Medical College, New York
          Author notes
          [* ]To whom correspondence should be addressed
          Article
          PMC5113288 PMC5113288 5113288 nihpa826877
          10.7326/M14-2235
          5113288
          26098843
          f23169c5-36cb-4188-be95-f612ff40ad7f
          History
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