Evidence map›Paper›PMID 29124397›Full record

ArticleRheumatology international2018

Long-term glucocorticoid treatment in patients with polymyalgia rheumatica, giant cell arteritis, or both diseases: results from a national rheumatology database.

Katinka Albrecht, Dörte Huscher, Frank Buttgereit, Martin Aringer, Guido Hoese, Wolfgang Ochs, Katja Thiele, Angela Zink

Abstract read
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
3.9field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Observational
  16. Article
  17. Review
  18. Review
  19. Article
  20. Polymyalgia Rheumatica.Deutsches Arzteblatt international · 2022
    Review
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

8 authors at 3 institutions in 1 country.

Katinka AlbrechtEpidemiology Unit, German Rheumatism Research Center, A Leibniz Institute, Charitéplatz 1, 10117, Berlin, Germany. albrecht@drfz.de.ORCID http://orcid.org/0000-0003-0886-0294
Dörte HuscherEpidemiology Unit, German Rheumatism Research Center, A Leibniz Institute, Charitéplatz 1, 10117, Berlin, Germany.ORCID http://orcid.org/0000-0001-9070-0761
Frank ButtgereitDepartment of Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany.
Martin AringerDepartment of Rheumatology and Clinical Immunology, TU Dresden, Dresden, Germany.
Guido HoesePrivate Specialty Practice for Rheumatology, Stadthagen, Germany.
Wolfgang OchsPrivate Specialty Practice for Rheumatology, Bayreuth, Germany.
Katja ThieleEpidemiology Unit, German Rheumatism Research Center, A Leibniz Institute, Charitéplatz 1, 10117, Berlin, Germany.
Angela ZinkEpidemiology Unit, German Rheumatism Research Center, A Leibniz Institute, Charitéplatz 1, 10117, Berlin, Germany.ORCID http://orcid.org/0000-0001-7072-9022
German Rheumatism Research Centre · DECharité - Universitätsmedizin Berlin · DETechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study was to evaluate glucocorticoid (GC) use in patients with polymyalgia rheumatica (PMR), giant cell arteritis (GCA) or both diseases (PMR + GCA) under rheumatological care. Data from patients with PMR (n = 1420), GCA (n = 177) or PMR + GCA (n = 261) from the National Database of the German Collaborative Arthritis Centers were analyzed regarding GCs and related comorbidities (osteoporosis, diabetes and cardiovascular disease), stratified by disease duration (DD). Longitudinal data were analyzed for all patients with a DD ≤ 2 years at database entry (n = 1397). Three-year data were available for 256 patients. Predictors of GC use ≥ 3 years were examined by logistic regression analyses. A total of 76% received GCs, and 19% (PMR) to 40% (GCA) received methotrexate. Median GC doses were 12.5 mg (PMR), 11.3 mg (GCA), and 20.0 mg/day (PMR + GCA) in a 0-6-month DD. Median GC doses ≤ 5 mg/day were reached at a 13-18-month DD in PMR patients and at a 19-24-month DD in GCA or PMR + GCA patients. In the multivariate analysis, baseline methotrexate (OR 2.03, [95% CI 1.27-3.24]), GCs > 10 mg/day (OR 1.65, [1.07-2.55]), higher disease activity (OR 1.12, [1.02-1.23]) (median 0.6 years DD), and female sex (OR 1.63 [1.09-2.43]) were predictive for GC therapy at ≥ 3 years. Of the examined comorbidities, only osteoporosis prevalence increased within 3 years. GC use for ≥ 3 years was reported in one-fourth of all the patients. A difficult-to-control disease activity within the first year was a good predictor of long-term GC need.

Indexed as

RheumatologyAgedAged, 80 and overComorbidityCross-Sectional StudiesDatabases, FactualDrug Administration ScheduleFemaleGermanyGiant Cell ArteritisGlucocorticoidsHumansLogistic ModelsLongitudinal StudiesMaleMultivariate AnalysisGlucocorticoidsComorbiditiesGiant cell arteritisGlucocorticoidsImmunosuppressive agentsPolymyalgia rheumatica

Identifiers

PMID29124397
OpenAlexW2767898276

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.