Evidence map›Paper›PMID 36033132›Full record

ArticleDrug design, development and therapy2022

A Real-World Study on the Effect of Imrecoxib for Patients with Axial Spondyloarthritis.

He-Xiang Zong, Sheng-Qian Xu, Jian-Xiong Wang, Yi-Ran Chu, Ke-Ming Chen, Cong Wang, Wan-Qiu Tong, Xi-le Wang

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Imrecoxib: Advances in Pharmacology and Therapeutics.Drug design, development and therapy · 2024
    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 1 institution in 1 country.

He-Xiang ZongDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Sheng-Qian XuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0000-0002-9559-1143
Jian-Xiong WangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0000-0002-6888-934X
Yi-Ran ChuDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Ke-Ming ChenDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0000-0003-3775-9902
Cong WangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Wan-Qiu TongDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Xi-le WangDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.
Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Non-steroidal anti-inflammatory drugs (NSAIDs) have generally been viewed as first-line therapy for axial spondyloarthritis (axSpA). Imrecoxib is a selective COX-2 inhibitor developed independently in China. At present, only one single-center RCT trial has shown that imrecoxib is equally effective as celecoxib in treating axSpA. Based on real-world data, our study aims to explore the efficiency of imrecoxib and TNF inhibitor (TNFi) combined with imrecoxib in treating axSpA. Patients and Methods: A total of 163 patients with axSpA who had more than two follow-up records in 6 months and treated with imrecoxib/celecoxib/TNFi combined with imrecoxib/TNFi combined with celecoxib from the First Affiliated Hospital of Anhui Medical University SpA Real World Database (AHSpA) were selected for analysis of our study. The linear mixed model was used to compare efficacy indexes before and after treatment and between different groups, adjust baseline measurement value and follow-up time. The Kaplan-Meier survival analysis was used to identify the differences in cumulative clinical remission rates between groups with different treatment at the follow-up period. Results: Results showed that after treatment ASDAScrp was slightly improved in imrecoxib group and celecoxib group within 6 months (p < 0.05). CRP, ESR, BASDAI, ASDAScrp, BASFI, occiput to wall distance and finger floor distance all significantly improved in TNFi combined with imrecoxib group and TNFi combined with celecoxib group within 6 months (all p < 0.05). According to the Kaplan-Meier survival curve and Log rank test analysis, the clinical remission rate was not significantly different between different treatment during 24-month follow-up (all p > 0.05). Conclusion: ASDAScrp improved slightly within 6 months after treatment with imrecoxib, and TNFi combined with imrecoxib significantly improved multiple effect indexes in axSpA patients. The efficacy of imrecoxib and celecoxib in the treatment of axSpA is equivalent. Also, they have the same efficacy after being combined with TNFi.

Indexed as

Axial SpondyloarthritisPyrrolesSulfidesCelecoxibHumansTreatment OutcomeTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsCelecoxibImrecoxibPyrrolesSulfidesTumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorsaxial spondyloarthritiscelecoxibimrecoxibTNF inhibitor

Identifiers

PMID36033132
PMCPMC9416422
OpenAlexW4292553229

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.