Evidence map›Paper›PMID 39133368›Full record

ArticleClinical and experimental medicine2024

Abatacept versus tumor necrosis factor inhibitors on mortality and medical utilizations in the treatment of rheumatoid arthritis associated interstitial lung disease: a large-scale real-world retrospective cohort study.

Po-Cheng Shih, Chih-Cheng Lai, Qing-Hua Zou, Shiow-Ing Wang, Xiang-Yang Huang, James Cheng Chung Wei

Abstract readComparative Study
In one paragraph

Article in Clinical and experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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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

6 authors.

Po-Cheng Shih *Institute of Medicine, Chung Shan Medical University, South District, No. 110, Section 1, Jianguo North Road, 402, Taichung, Taiwan.
Chih-Cheng LaiDivision of Hospital Medicine, Department of Internal Medicine, Chi Mei Medical Center, Tainan, Taiwan.
Qing-Hua Zou *Department of Rheumatology and Immunology, First Affiliated Hospital of Army Medical University, Chongqing, People's Republic of China.
Shiow-Ing WangInstitute of Medicine, Chung Shan Medical University, South District, No. 110, Section 1, Jianguo North Road, 402, Taichung, Taiwan.
Xiang-Yang HuangDepartment of Rheumatology and Immunology, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu, 610041, People's Republic of China. yangyang1029@aliyun.com.
James Cheng Chung WeiInstitute of Medicine, Chung Shan Medical University, South District, No. 110, Section 1, Jianguo North Road, 402, Taichung, Taiwan. jccwei@gmail.com.

Funding

Chung Shan Medical University Hospital CSH-2021-D-001Chung Shan Medical University Hospital CSH-2022-A-001
6 · The paper itself

Abstract

Rheumatoid arthritis is a chronic inflammatory disease, and interstitial lung disease is one of the important extra-articular manifestations. There is limited evidence comparing abatacept (ABA) and tumor necrosis factor inhibitors (TNFi) regarding the risk of mortality among patients with rheumatoid arthritis associated interstitial lung disease (RA-ILD). The aim of this study is to investigate the risk of mortality in patients with RA-ILD treated with ABA compared to TNFi. This retrospective cohort study utilized TriNetX electronic health record database. We enrolled patients who were diagnosed with RA-ILD and had received a new prescription for either ABA or TNFi. Patients were categorized into two cohorts based on their initial prescription. The primary outcome was all-cause mortality, and secondary outcomes were healthcare utilizations, including hospitalization, critical care services, and mechanical ventilation. Subgroup analyses were performed on age, presence of anti-citrullinated peptide antibodies (ACPA), and cardiovascular risk. Among 34,388 RA-ILD patients, 895 were selected for each group (ABA and TNFi) following propensity score matching. The ABA group exhibited a higher all-cause mortality risk. (HR 1.296, 95% CI 1.006-1.671). Subgroup analysis showed a heightened risk of receiving mechanical ventilation in ABA-treated patients aged 18-64 years old (HR 1.853, 95% CI 1.002-3.426), and those with cardiovascular risk factors (HR 2.015, 95% CI 1.118-3.630). Another subgroup analysis indicated a higher risk of mortality among ABA-treated patients with positive-ACPA. (HR 4.138 95% CI 1.343-12.75). This real-world data research demonstrated a higher risk of all-cause mortality in RA-ILD patients treated with ABA compared to TNFi, particularly those aged 18-64 years, lacking cardiovascular risk factors, and positive-ACPA. ABA was associated with an increased risk of mechanical ventilation in patients aged 18-64 years and those with cardiovascular risk factors.

Indexed as

AbataceptArthritis, RheumatoidLung Diseases, InterstitialAdultAgedAntirheumatic AgentsFemaleHospitalizationHumansMaleMiddle AgedRetrospective StudiesTumor Necrosis Factor InhibitorsAbataceptAntirheumatic AgentsTumor Necrosis Factor InhibitorsAbataceptCritical careInterstitial lung diseaseMortalityRheumatoid arthritisTNF inhibitors

Identifiers

PMID39133368
PMCPMC11319376

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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.