Evidence map›Paper›PMID 33055080›Full record

ArticleAnnals of the rheumatic diseases2021

EULAR recommendations for a core data set for pregnancy registries in rheumatology.

Yvette Meissner, Rebecca Fischer-Betz, Laura Andreoli, Nathalie Costedoat-Chalumeau, Diederik De Cock, Radboud J E M Dolhain, Frauke Forger, Doreen Goll, Anna Molto, Catherine Nelson-Piercy and 8 more

Open access · hybridAbstract readConsensus Statement
In one paragraph

Article in Annals of the rheumatic diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 2 pooled it
7.6field-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

26 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 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

18 authors at 12 institutions in 9 countries.

Yvette MeissnerEpidemiology and Health Care Research, German Rheumatism Research Center Berlin, Berlin, Germany y.meissner@drfz.de.ORCID 0000-0003-0147-4112
Rebecca Fischer-BetzDepartment for Rheumatology and Hiller Research Institute, Heinrich Heine University Düsseldorf, Dusseldorf, Germany.
Laura AndreoliDepartment of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.ORCID 0000-0002-9107-3218
Nathalie Costedoat-ChalumeauInternal Medicine Department, Referral Center for Rare Autoimmune and Systemic Diseases, Hospital Cochin, Paris, France.ORCID 0000-0002-1555-9021
Diederik De CockDepartment of Development and Regeneration KU, KU Leuven, Leuven, Belgium.
Radboud J E M DolhainMedical Centre, Department of Rheumatology, Erasmus University Rotterdam, Rotterdam, Netherlands.
Frauke ForgerDepartment of Rheumatology, Immunology and Allergology, Inselspital University Hospital Bern, Bern, Switzerland.
Doreen GollPatient research partner, Berlin, Germany.
Anna MoltoRheumatology Department, Hospital Cochin, Paris, France.ORCID 0000-0003-2246-1986
Catherine Nelson-PiercyObstetric Medicine Service, Queen Charlotte's and Chelsea Hospital, London, UK.
Rebecca ÖzdemirPatient research partner, Duisburg, Germany.
Luigi RaioDepartment of Obstetrics and Gynaecology, Inselspital University Hospital Bern, Bern, Switzerland.
Sebastian Cruz Rodríguez-GarcíaRheumatology Department, Hospital Universitario de la Princesa, Madrid, Spain.ORCID 0000-0002-7773-151X
Savino SciasciaDipartimento di Malattie Rare, Immunologiche, Ematologiche ed Immunoematologiche. Centro di Ricerche di Immunopatologia e Documentazione su Malattie Rare (CMID). Struttura Complessa a Direzione Universitaria di Immunologia Clinica, Ospedale Torino Nord Emergenza San G. Bosco ed Università di Torino, Torino, Italy.ORCID 0000-0003-1266-9441
Marianne WalleniusInstitute of Neuromedicine and Movement Science, Faculty of Medicine and Health Sciences, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Astrid ZbindenDepartment of Rheumatology, Immunology and Allergology, Inselspital University Hospital Bern, Bern, Switzerland.
Angela ZinkEpidemiology and Health Care Research, German Rheumatism Research Center Berlin, Berlin, Germany.
Anja StrangfeldEpidemiology and Health Care Research, German Rheumatism Research Center Berlin, Berlin, Germany.ORCID 0000-0002-6233-022X
German Rheumatism Research Centre · DEUniversity Hospital of Bern · CHInserm · FRAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITBG Klinikum Duisburg · DEErasmus University Rotterdam · NLGuy's and St Thomas' NHS Foundation Trust · GBHeinrich Heine University Düsseldorf · DEHospital Universitario de La Princesa · ESKU Leuven · BENorwegian University of Science and Technology · NOOspedale San Giovanni Bosco · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveThere is an urgent need for robust data on the trajectories and outcomes of pregnancies in women with inflammatory rheumatic diseases (IRD). In particular when rare outcomes or rare diseases are to be investigated, collaborative approaches are required. However, joint data analyses are often limited by the heterogeneity of the different data sources.To facilitate future research collaboration, a European League Against Rheumatism (EULAR) Task Force defined a core data set with a minimum of items to be collected by pregnancy registries in rheumatology covering the period of pregnancy and the 28-day neonatal phase in women with any underlying IRD.

methodsA stepwise process included a two-round Delphi survey and a face-to-face meeting to achieve consensus about relevant items.

resultsA total of 64 multidisciplinary stakeholders from 14 different countries participated in the two rounds of the Delphi process. During the following face-to-face meeting of the EULAR Task Force, consensus was reached on 51 main items covering 'maternal information', 'pregnancy' and 'treatment'. Generic instruments for assessment are recommended for every item. Furthermore, for the five most frequent IRDs rheumatoid arthritis, spondyloarthritis, juvenile idiopathic arthritis, systemic lupus erythematosus and other connective tissue diseases, disease-specific laboratory markers and disease activity measurements are proposed.

conclusionThis is the first consensus-based core data set for prospective pregnancy registries in rheumatology. Its purpose is to stimulate and facilitate multinational collaborations that aim to increase the knowledge about pregnancy course and safety of treatment in women with IRDs during pregnancy.

Indexed as

Data CollectionPregnancy OutcomeRegistriesAdvisory CommitteesAntirheumatic AgentsArthritis, JuvenileArthritis, RheumatoidConnective Tissue DiseasesDelphi TechniqueEuropeFemaleHumansLupus Erythematosus, SystemicPostnatal CarePreconception CarePregnancyAntirheumatic Agentsantirheumatic agentsautoimmune diseasesbiological therapyepidemiologyhealth careoutcome assessment

Identifiers

PMID33055080
PMCPMC7788063
OpenAlexW3092756703

What OpenQuestion holds

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Registered trials

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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.