Evidence map›Paper›PMID 40323420›Full record

ArticleZeitschrift fur Rheumatologie2025

[Annual report 2025 from the National Database of the Regional Collaborative Rheumatology Centers in Germany].

Katinka Albrecht, Katja Thiele, Tobias Alexander, Martin Aringer, Jacqueline Detert, Thorsten Eidner, Martin Feuchtenberger, Jörg Henes, Kirsten Karberg, Uta Kiltz and 8 more

Abstract readEnglish Abstract
In one paragraph

Article in Zeitschrift fur Rheumatologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

18 authors.

Katinka AlbrechtProgrammbereich Epidemiologie und Versorgungsforschung, Deutsches Rheuma Forschungszentrum Berlin, Charitéplatz1, 10117, Berlin, Deutschland. albrecht@drfz.de.
Katja ThieleProgrammbereich Epidemiologie und Versorgungsforschung, Deutsches Rheuma Forschungszentrum Berlin, Charitéplatz1, 10117, Berlin, Deutschland.
Tobias AlexanderMedizinische Klinik m.S. Rheumatologie und Klinische Immunologie, Charité - Universitätsmedizin Berlin, corporate member Freie Universität Berlin, Humboldt-Universität zu Berlin, und Berlin Institute of Health (BIH), Berlin, Deutschland.
Martin AringerBereich Rheumatologie, Medizinische Klinik und Poliklinik III und UniversitätsCentrum für Autoimmun- und Rheumatische Erkrankungen (UCARE) Universitätsklinikum und Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Deutschland.
Jacqueline DetertRheumapraxis Templin, Templin, Templin, Deutschland.
Thorsten EidnerKlinik für Innere Medizin III - Rheumatologie/Osteologie, Universitätsklinikum Jena, Jena, Deutschland.
Martin FeuchtenbergerRheumatologie, MVZ MED BAYERN OST, Burghausen, Deutschland.
Jörg HenesZentrum für Interdisziplinäre Rheumatologie, klinische Immunologie und Autoimmunerkrankungen (INDIRA), Department für Innere Medizin II, Universitätsklinik Tübingen, Tübingen, Deutschland.
Kirsten KarbergRheumatologisches Versorgungszentrum Steglitz, Berlin, Deutschland.
Uta KiltzRuhr-Universität Bochum, Bochum, Deutschland.
Benjamin KöhlerRheumazentrum Ratingen, Rheumatologische Gemeinschaftspraxis, Ratingen, Deutschland.
Andreas KrauseRheumatologie, klinische Immunologie und Osteologie, Immanuel-Krankenhaus Berlin, Berlin, Deutschland.
Jutta G RichterKlinik für Rheumatologie, Medizinische Fakultät, Universitätsklinikum Düsseldorf, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Deutschland.
Susanna Späthling-MestekemperRheumapraxis München-Pasing, München, Deutschland.
Mirko SteinmüllerRheumateam Lahn-Dill-Siegerland - Wetzlar/Burbach, Wetzlar/Burbach, Deutschland.
Silke ZinkeRheumatologische Schwerpunktpraxis Berlin, Berlin, Deutschland.
Anja StrangfeldProgrammbereich Epidemiologie und Versorgungsforschung, Deutsches Rheuma Forschungszentrum Berlin, Charitéplatz1, 10117, Berlin, Deutschland.
Johanna CallhoffProgrammbereich Epidemiologie und Versorgungsforschung, Deutsches Rheuma Forschungszentrum Berlin, Charitéplatz1, 10117, Berlin, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData of patients with inflammatory rheumatic diseases are annually recorded within the National Database of the German Collaborative Rheumatology Centers.

methodsFor rheumatoid arthritis (RA), psoriatic arthritis (PsA), axial spondylarthritis (axSpA), systemic lupus erythematosus (SLE), systemic sclerosis (SSc), Sjögren's syndrome (SjS), idiopathic inflammatory myositis (IIM), polymyalgia rheumatica (PMR), giant cell arteritis (GCA), ANCA-associated vasculitis (AAV), Behçet's disease (BD), adult onset Still's disease (AOSD) and autoinflammatory diseases (AID) data are reported from 2023. Information includes physician-reported disease activity on a numeric rating scale (NRS) of 0-10, treatment and patient-reported outcomes. For selected diagnoses, developments from 2010 to 2023 are presented regarding physicians' assessments of disease activity and treatment.

resultsA total of 13,884 patients were documented from 14 rheumatology centers, most frequently with RA (5734), PsA (1741) and axSpA (1494). The mean age ranged from 45 years (BD) to 73 years (GCA) and the median disease duration ranged from 3 years (PMR) to 16 years (axSpA). Disease activity was predominantly low, with 6% (BD) to 15% (axSpA) rated moderate to high (> 4 on the NMR) by rheumatologists. Biological disease-modifying antirheumatic drugs (bDMARD) were most frequently prescribed for axSpA (65%), AOSD (58%), PsA (53%) and GCA (41%). Tumor necrosis factor (TNF) inhibitors were frequently used in axSpA (53%), BD (30%) and PsA (28%), interleukin (IL)-1 inhibitors in AOSD (51%) and AID (50%), IL-6Ri in GCA (38%), IL17i in PsA (17%) and rituximab in AAV (29%). Higher levels of pain, fatigue, sleep disturbances and reduced well-being were reported by patients with IIM, SSc, axSpA and AID. Among those younger than 65 years, 58% (SSc) to 77% (axSpA) were employed. The percentage of early retirement due to rheumatic diseases was 5% (AOSD) to 18% (AAV). Since 2010 the development in the proportion of patients in remission or with very low disease activity (NRS 0-1) has increased across all diagnoses. In terms of treatment there has been an increase in b/tsDMARDs and a decrease in glucocorticoids for various diagnoses.

conclusionThe results show the diversity of inflammatory rheumatic diagnoses and the continuously growing range of treatment in rheumatology along with good disease control in many patients.

Indexed as

Databases, FactualRegistriesRheumatic DiseasesRheumatologyAdultAgedAntirheumatic AgentsFemaleGermanyHumansMaleMiddle AgedYoung AdultAntirheumatic AgentsDMARD therapyHealth services researchLong-term observational researchRheumatic diseasesRheumatology

Identifiers

PMID40323420
PMCPMC12605611

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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.