Evidence map›Paper›PMID 32188491›Full record

ArticleArthritis research & therapy2020

Low frequency of flares during pregnancy and post-partum in stable lupus patients.

Julia Davis-Porada, Mimi Y Kim, Marta M Guerra, Carl A Laskin, Michelle Petri, Michael D Lockshin, Lisa R Sammaritano, D Ware Branch, Allen Sawitzke, Joan T Merrill and 2 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
7.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 66 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 2 countries.

Julia Davis-PoradaHospital for Special Surgery, 535 E 70th Street, New York, NY, 10021, USA.
Mimi Y KimAlbert Einstein College of Medicine, New York, NY, USA.
Marta M GuerraHospital for Special Surgery, 535 E 70th Street, New York, NY, 10021, USA.
Carl A LaskinMount Sinai Hospital Toronto, Toronto, Ontario, Canada.
Michelle PetriJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Michael D LockshinHospital for Special Surgery, 535 E 70th Street, New York, NY, 10021, USA.
Lisa R SammaritanoHospital for Special Surgery, 535 E 70th Street, New York, NY, 10021, USA.
D Ware BranchIntermountain Healthcare, Salt Lake City, UT, USA.
Allen SawitzkeUniversity of Utah Health Sciences Center, Salt Lake City, UT, USA.
Joan T MerrillUniversity of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
Jill P BuyonNew York University School of Medicine, 550 1st Avenue, New York, NY, 10016, USA. jill.buyon@nyumc.org.
Jane E SalmonHospital for Special Surgery, 535 E 70th Street, New York, NY, 10021, USA. salmon@hss.edu.ORCID 0000-0001-9113-7122
Hospital for Special Surgery · USAlbert Einstein College of Medicine · USIntermountain Healthcare · USJohns Hopkins University · USMount Sinai Hospital · CANew York University · USOklahoma Medical Research Foundation · USUniversity of Utah · US

Funding

Predictors of Pregnancy Outcome In SLE and APSR01AR049772 · NIAMS · HOSPITAL FOR SPECIAL SURGERY · PI SALMON, JANE E · 2003 to 2012
$12.6M
Hopkins Lupus CohortR01AR069572 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI PETRI, MICHELLE A · 2016 to 2020
$3.4M
NIAMS NIH HHS R01 AR049772NIAMS NIH HHS R01 AR069572
6 · The paper itself

Abstract

backgroundLupus patients are at risk for pregnancy loss, and it has been generally accepted that women with SLE should have low disease activity prior to conception. However, there are conflicting results regarding the effect of pregnancy on SLE flares. This study aims to identify predictors of flares during and after pregnancy in SLE patients with inactive or stable disease activity during the first trimester and to characterize and estimate the frequency of post-partum flares in these patients.

methodsSLE patients in the multicenter, prospective PROMISSE (Predictors of Pregnancy Outcome: Biomarkers in Antiphospholipid Antibody Syndrome and Systemic Lupus Erythematosus) study were evaluated for flares during and after pregnancy using the SELENA-SLEDAI Flare Index. Flares during pregnancy were assessed in all 384 patients and post-partum flares in 234 patients with study visits 2-6 months post-partum. Logistic regression models were fit to the data to identify independent risk factors for flare.

resultsDuring pregnancy, 20.8% of patients had mild/moderate flares and 6.25% had severe. Post-partum, 27.7% of patients had mild/moderate flares and 1.7% had severe. The mild flares rarely required treatment. Younger age, low C4 and higher PGA at baseline were independently associated with higher risk of having at least one mild/moderate or severe flare during pregnancy. Older patients were at decreased risk of flare, as well as those with quiescent disease at baseline. No variables evaluated at baseline or the visit most proximal to delivery was significantly associated with risk of flare post-partum. Medications were not associated with flare during or after pregnancy.

conclusionIn patients with inactive or stable mild disease activity at the time of conception, lupus disease flares during and after pregnancy are typically mild and occur at similar rates. Flares during pregnancy are predicted by the patients' age and clinical and serological activity at baseline.

Indexed as

AdultAntibodies, AntinuclearBiomarkersDisease ProgressionFemaleHumansLogistic ModelsLupus Erythematosus, SystemicPostpartum PeriodPregnancyPregnancy ComplicationsPregnancy Trimester, FirstProspective StudiesRisk FactorsSeverity of Illness IndexAntibodies, AntinuclearBiomarkersFlaresPregnancySLE

Identifiers

PMID32188491
PMCPMC7081564
OpenAlexW3012872161

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.