Evidence map›Paper›PMID 35683507›Full record

ArticleJournal of clinical medicine2022

Patients' Baseline Characteristics, but Not Tocilizumab Exposure, Affect Severe Outcomes Onset in Giant Cell Arteritis: A Real-World Study.

Cyril Dumain, Jonathan Broner, Erik Arnaud, Emmanuel Dewavrin, Jan Holubar, Myriam Fantone, Benoit de Wazières, Simon Parreau, Pierre Fesler, Philippe Guilpain and 2 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2022. 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

12 authors.

Cyril DumainInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.ORCID 0000-0002-2804-3307
Jonathan BronerInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.
Erik ArnaudInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.
Emmanuel DewavrinIntensive Care Medicine Department, Lapeyronie Hospital, CHU Montpellier, 34090 Montpellier, France.
Jan HolubarInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.
Myriam FantoneInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.
Benoit de WazièresDepartment of Internal Medicine and Geriatrics, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.
Simon ParreauDepartment of Internal Medicine, Limoges University Hospital Center, 87042 Limoges, France.
Pierre FeslerDepartment of Internal Medicine, Lapeyronie Hospital, CHU Montpellier, 34090 Montpellier, France.ORCID 0000-0002-7831-6545
Philippe GuilpainDepartment of Internal Medicine and Multi-Organic Diseases, St. Eloi Hospital, CHU Montpellier, 34295 Montpellier, France.ORCID 0000-0002-7673-2561
Camille RoubilleDepartment of Internal Medicine, Lapeyronie Hospital, CHU Montpellier, 34090 Montpellier, France.ORCID 0000-0002-5268-1704
Radjiv GoulabchandInternal Medicine Department, CHU Nîmes, University of Montpellier, 30029 Nîmes, France.ORCID 0000-0002-7328-4097

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Giant cell arteritis (GCA) is associated with severe outcomes such as infections and cardiovascular diseases. We describe here the impact of GCA patients’ characteristics and treatment exposure on the occurrence of severe outcomes. Methods: Data were collected retrospectively from real-world GCA patients with a minimum of six-months follow-up. We recorded severe outcomes and treatment exposure. In the survival analysis, we studied the predictive factors of severe outcomes occurrence, including treatment exposure (major glucocorticoids (GCs) exposure (>10 g of the cumulative dose) and tocilizumab (TCZ) exposure), as time-dependent covariates. Results: Among the 77 included patients, 26% were overweight (BMI ≥ 25 kg/m2). The mean cumulative dose of GCs was 7977 ± 4585 mg, 18 patients (23%) had a major GCs exposure, and 40 (52%) received TCZ. Over the 48-month mean follow-up period, 114 severe outcomes occurred in 77% of the patients: infections—29%, cardiovascular diseases—18%, hypertension—15%, fractural osteoporosis—8%, and deaths—6%. Baseline diabetes and overweight were predictive factors of severe outcomes onset (HR, 2.41 [1.05−5.55], p = 0.039; HR, 2.08 [1.14−3.81], p = 0.018, respectively) independently of age, sex, hypertension, and treatment exposure. Conclusion: Diabetic and overweight GCA patients constitute an at-risk group requiring tailored treatment, including vaccination. The effect of TCZ exposure on the reduction of severe outcomes was not proved here.

Indexed as

cardiovascular eventsdiabetesgiant cell arteritisglucocorticoidsinfectionsoverweighttocilizumab

Identifiers

PMID35683507
PMCPMC9181652

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.