Evidence map›Paper›PMID 35927387›Full record

ReviewZeitschrift fur Rheumatologie2022

[Sarcoidosis as prime example of a granulomatous disease].

Tim Oqueka, Sören Galow, Marcel Simon, Anna Weidmann, Nicole Stübiger, Elvin Zengin-Sahm, Christoph Sinning, Martin Krusche, Nikolas Ruffer, Stefan Steurer and 9 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Zeitschrift fur Rheumatologie, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. [Granulomatous dermatoses].Zeitschrift fur Rheumatologie · 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

19 authors.

Tim OquekaAbteilung für Pneumologie, Zentrum für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland. t.oqueka@uke.de.
Sören GalowAbteilung für Pneumologie, Zentrum für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.
Marcel SimonAbteilung für Pneumologie, Zentrum für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.
Anna WeidmannAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Nicole StübigerAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Elvin Zengin-SahmAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Christoph SinningAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Martin KruscheAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Nikolas RufferIII. Medizinische Klinik und Poliklinik, Nephrologie und Sektion Rheumatologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Stefan SteurerAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Xenia Schick-BengardtAbteilung für Pneumologie, Zentrum für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.
Marcial SebodeAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Ludwig Jesse HorstI. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Oliver M SteinmetzIII. Medizinische Klinik und Poliklinik, Nephrologie und Sektion Rheumatologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Simon MelderisIII. Medizinische Klinik und Poliklinik, Nephrologie und Sektion Rheumatologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Sina Cathérine RosenkranzAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Katharina MöllerAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Holger JantkeAmbulante spezialfachärztliche Versorgung (ASV) Sarkoidose, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
Hans KloseAbteilung für Pneumologie, Zentrum für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcoidosis is the most frequent immunologically related granulomatous disease and can serve as a model for understanding diseases within this category. The evidence on the diagnostics and treatment is so far limited. It is therefore all the more important that two new and significant guidelines on diagnosis and treatment of sarcoidosis were published during the last 2 years. Additionally, there were more new publications, which were considered for this review article. In this context, this review article provides a current update and overview of sarcoidosis. Pathophysiologically, there is an increasing understanding of the complex processes and interactions involved in the inflammatory processes and granuloma formation. The probability of a diagnosis of sarcoidosis is determined by compatible histology, the exclusion of differential diagnoses and if possible evidence of a multiorgan manifestation. The clinical course is variable and ranges from an asymptomatic manifestation to severe life-threatening organ failure. The most frequently affected organ are the lungs. Pulmonary fibrosis is the most severe form and is also decisive for mortality. An increasing focus is on the extrapulmonary organ manifestations, in particular, cardiac, hepatosplenic, gastrointestinal, renal, ocular and neurological involvement. Treatment, which consists primarily of immunosuppression, should be initiated in cases of organ-threatening or quality of life-impairing activity of the disease. Additional organ-specific management must also be evaluated. In cases of organ failure transplantation should be considered. Due to the limited evidence especially for the treatment of multiorgan sarcoidosis, when possible, patients with this disease should be included in clinical trials.

Indexed as

Pulmonary FibrosisSarcoidosisDiagnosis, DifferentialGranulomaHumansLungQuality of LifeGranulomatosisImmunosuppressionOrgan involvementPulmonary fibrosisSystemic disease

Identifiers

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.