Evidence map›Paper›PMID 39974589›Full record

ArticleMediterranean journal of rheumatology2024

Difficult-to-Treat Spondyloarthritis in Morocco: A Real-World Study.

Salma Zemrani, Bouchra Amine, Imane ElBinoune, Samira Rostom, Rachid Bahiri

Abstract read
In one paragraph

Article in Mediterranean journal of rheumatology, 2024. 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

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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

5 authors.

Salma ZemraniDepartment of Rheumatology A, El Ayachi Hospital, University Hospital Centre Ibn Sina, Rabat-Sale, Morocco.
Bouchra AmineDepartment of Rheumatology A, El Ayachi Hospital, University Hospital Centre Ibn Sina, Rabat-Sale, Morocco.
Imane ElBinouneDepartment of Rheumatology A, El Ayachi Hospital, University Hospital Centre Ibn Sina, Rabat-Sale, Morocco.
Samira RostomDepartment of Rheumatology A, El Ayachi Hospital, University Hospital Centre Ibn Sina, Rabat-Sale, Morocco.
Rachid BahiriDepartment of Rheumatology A, El Ayachi Hospital, University Hospital Centre Ibn Sina, Rabat-Sale, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: High biologic requirement in inflammatory rheumatic diseases (IRD) may indicate a difficult to treat (D2T) condition. In axial spondyloarthritis (axSpA), a consensual definition for this concept is still lacking. Our objectives are to identify the prevalence and characteristics of multiswitcher patients with axSpA, and to analyse the number and reasons for switches. Methods: This is a longitudinal observational study including patients treated with biologic agents for axSpA. We propose to define D2T patients as those who required more than 2 b/tsDMARD. Patients who did not fulfil this definition were used as controls. The prevalence of multiswitchers was calculated, and characteristics were compared between the two groups. The number and reasons for switches were analysed in the D2T group. Results: 124 patients were included. The prevalence of multiswitchers was 24.19%. There were no significant differences between the two groups in the age, sex, and comorbidities. D2T patients have more arthritis (p=0.01), and fibromyalgia (p=0.04), and higher disease activity before initiating biotherapy, (BASDAI:p=0.04), (ASDAS:p=0.04). Additionally, the time from diagnosis to the first use of biologic was longer (p=0.04). In the multivariate analysis, the D2T condition was found to be associated with fibromyalgia (p=0.01). Among this group, the prevalence of those treated with 3, 4, and 5 b/tsDMARD was 86%, 9%, and 5%, respectively, the primary and secondary failures were the most common reasons for switching. Conclusion: We suggest that D2T-axSpA present several characteristics. Identification of this category in large studies is necessary to establish a consensus definition.

Indexed as

axial spondyloarthritisbiological therapydifficult-to-treat

Identifiers

PMID39974589
PMCPMC11834991

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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.