Evidence map›Paper›PMID 22933738›Full record

SynthesisNeurology2012

Disease-modifying drugs for multiple sclerosis in pregnancy: a systematic review.

Ellen Lu, Bing Wei Wang, Colleen Guimond, Anne Synnes, Dessa Sadovnick, Helen Tremlett

Open access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in Neurology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 3 pooled it
9.4field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 3 syntheses or guidelines pooled it, 158 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Updated Perspectives on the Challenges of Managing Multiple Sclerosis During Pregnancy.Degenerative neurological and neuromuscular disease · 2022
    Review
  11. Treatment of Women with Multiple Sclerosis Planning Pregnancy.Current treatment options in neurology · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Sex effects across the lifespan in women with multiple sclerosis.Therapeutic advances in neurological disorders · 2020
    Review
  16. Review
  17. Review
  18. Caring for Women with Multiple Sclerosis Across the Lifespan.Current neurology and neuroscience reports · 2018
    Review
  19. Review
  20. Management of pregnancy-related issues in multiple sclerosis patients: the need for an interdisciplinary approach.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
    Article
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

6 authors at 1 institution in 1 country.

Ellen LuDepartment of Medicine, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
Bing Wei Wang
Colleen Guimond
Anne Synnes
Dessa Sadovnick
Helen Tremlett
University of British Columbia · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

objectiveTo systematically review the literature regarding safety of disease-modifying drug (DMD) use during pregnancy on perinatal and developmental outcomes in offspring of patients with multiple sclerosis (MS).

methodsA PubMed and EMBASE search up to February 2012 was conducted with a manual search of references from relevant articles. Selected studies were evaluated using internationally accepted criteria.

resultsFifteen studies identified 761 interferon β-, 97 glatiramer acetate-, and 35 natalizumab-exposed pregnancies. Study quality ranged from poor to good; no study was rated excellent. Small sample sizes limited most studies. Compared with data for unexposed pregnancies, fair- to good-quality prospective cohort studies reported that interferon β exposure was associated with lower mean birth weight, shorter mean birth length, and preterm birth (<37 weeks), but not low birth weight (<2,500 g), cesarean delivery, congenital anomaly (including malformation), or spontaneous abortion. Fewer studies of fair quality were available for glatiramer acetate and natalizumab. Glatiramer acetate exposure was not associated with lower mean birth weight, congenital anomaly, preterm birth, or spontaneous abortion. Natalizumab exposure did not appear to be associated with shorter mean birth length, lower mean birth weight, or lower mean gestational age. No studies examined mitoxantrone or fingolimod exposure. One study of paternal DMD use during conception found no effect on gestational age or birth weight. Few studies examined longer-term developmental outcomes.

conclusionFurther studies are needed to determine the potential risks associated with preconceptional and in utero DMD exposure in patients with MS. Discontinuation of DMDs before conception is still recommended.

Indexed as

Antibodies, Monoclonal, HumanizedFemaleGlatiramer AcetateHumansImmunologic FactorsInterferon-betaMultiple SclerosisNatalizumabPeptidesPregnancyPregnancy ComplicationsAntibodies, Monoclonal, HumanizedGlatiramer AcetateImmunologic FactorsInterferon-betaNatalizumabPeptides

Identifiers

PMID22933738
PMCPMC3525300
OpenAlexW2157759118

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.