Evidence map›Paper›PMID 34717762›Full record

SynthesisEuropean journal of medical research2021

The effects and safety of pirfenidone in the treatment of idiopathic pulmonary fibrosis: a meta-analysis and systematic review.

Chenchen Zang, Yan Zheng, Yanqing Wang, Lisha Li

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in European journal of medical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Multi-omics insights into the mechanisms and prognosis of IPF.Genes and environment : the official journal of the Japanese Environmental Mutagen Society · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Pirfenidone use in fibrotic diseases: What do we know so far?Immunity, inflammation and disease · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. 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

4 authors at 2 institutions in 1 country.

Chenchen Zang *Department of Respiratory and Critical Care Medicine, Qingdao Hospital of Traditional Chinese Medicine(Qingdao Hiser Hospital), No.4 Renmin Road, Shibei District, Qingdao, 266000, Shandong Province, China.
Yan Zheng *Department of General Practice, Qingdao Hospital of Traditional Chinese Medicine(Qingdao Hiser hospital), Qingdao, China.
Yanqing WangDepartment of Respiratory and Critical Care Medicine, Qingdao Hospital of Traditional Chinese Medicine(Qingdao Hiser Hospital), No.4 Renmin Road, Shibei District, Qingdao, 266000, Shandong Province, China.
Lisha LiDepartment of Respiratory and Critical Care Medicine, Qingdao Hospital of Traditional Chinese Medicine(Qingdao Hiser Hospital), No.4 Renmin Road, Shibei District, Qingdao, 266000, Shandong Province, China. ktchidn7048952@163.com.
Qingdao Municipal Hospital · CNQingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt is necessary to systematically evaluate the efficacy and adverse reactions of pirfenidone in the treatment of patients with idiopathic pulmonary fibrosis (IPF).

methodsPubmed et al. databases were searched up to March 15, 2021 for randomized controlled trials (RCT) of pirfenidone in the treatment of IPF. Two authors collected and compared the indicators including progression-free survival (PFS), vital capacity (VC), forced vital capacity (FVC), and adverse reactions. RevMan 5.3 software and Stata 15.0 software were used for meta-analysis.

resultsA total of 8 reports with 9 RCTs involving 1824 IPF patients were included. Meta-analysis results showed that compared with the control group, pirfenidone could prolong the PFS phase of IPF patients (HR = 0.65, 95% CI 0.55 ~ 0.76, P < 0.001), slow down the VC of IPF patients (SMD = 0.43, 95% CI 0.21 ~ 0.66, P < 0.001), and decrease FVC (SMD = 0.31, 95% CI 0.14 ~ 0.48, P < 0.001). The main adverse reactions of pirfenidone were gastrointestinal reactions, photosensitivity and skin rashes.

conclusionPirfenidone is beneficial to prolong the PFS of IPF patients, improve lung function, and it is safe for clinical use. However, more high-quality RCTs are still needed to provide reliable evidence for the treatment of IPF.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalDiarrheaExanthemaHumansIdiopathic Pulmonary FibrosisLungNauseaProgression-Free SurvivalPyridonesTreatment OutcomeVital CapacityAnti-Inflammatory Agents, Non-SteroidalpirfenidonePyridonesEffectIdiopathic pulmonary fibrosisPirfenidoneSafetyTreatment

Identifiers

PMID34717762
PMCPMC8557612
OpenAlexW3210227467

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.