Evidence map›Paper›PMID 28992174›Full record

ReviewRheumatology (Oxford, England)2017

Interstitial lung disease points to consider for clinical trials in systemic sclerosis.

Dinesh Khanna, James Seibold, Jonathan Goldin, Donald P Tashkin, Daniel E Furst, Athol Wells

Abstract readReview
In one paragraph

Review in Rheumatology (Oxford, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

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

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Observational
  7. Drugs in phase I and phase II clinical trials for systemic sclerosis.Expert opinion on investigational drugs · 2020
    Review
  8. Article
  9. Observational
  10. Review
  11. Article
  12. Article
  13. Review
  14. 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

6 authors.

Dinesh KhannaDepartment of Medicine, University of Michigan Scleroderma Program, University of Michigan, Ann Arbor, MI.
James SeiboldScleroderma Consultants LLC, Litchfield, CT.
Jonathan GoldinDepartment of Radiological Science.
Donald P TashkinDepartment of Medicine-Pulmonology.
Daniel E FurstDepartment of Rheumatology, David Geffen School of Medicine, Los Angeles, CA, USA.
Athol WellsDepartment of Medicine, Royal Brompton Hospital, Faculty of Medicine, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial lung disease causes major morbidity and mortality in patients with systemic sclerosis (SSc-ILD). Large randomized clinical trials in SSc-ILD have provided important information regarding the feasibility, reliability and validity of outcome measures. Forced vital capacity percentage predicted should be considered as a primary outcome measure, with inclusion of appropriate radiological and patient-reported measures. We provide practical recommendations for trial design in SSc-ILD.

Indexed as

Disease ManagementLung Diseases, InterstitialClinical Trials as TopicGlobal HealthHumansScleroderma, SystemicSurvival Rateinterstitial lung disease clinical trialslung diseasescleroderma

Identifiers

PMID28992174
PMCPMC5850349

What OpenQuestion holds

Textmetadata
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.