Evidence map›Paper›PMID 30876420›Full record

ArticleRespiratory research2019

The clinical course of idiopathic pulmonary fibrosis and its association to quality of life over time: longitudinal data from the INSIGHTS-IPF registry.

Michael Kreuter, Jeff Swigris, David Pittrow, Silke Geier, Jens Klotsche, Antje Prasse, Hubert Wirtz, Dirk Koschel, Stefan Andreas, Martin Claussen and 16 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Respiratory research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01695408 (Investigating Significant Health Trends in IPF), which is not on this map. Cited by 69 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 4 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.

NCT01695408 completednot on this map

Investigating Significant Health Trends in IPF (INSIGHTS-IPF). Nationwide Prospective Registry.

TypeobservationalSponsorTechnische Universität DresdenRan2012 to 2021Enrolled1,232ConditionsIdiopathic Pulmonary Fibrosis
3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Health-related quality of life of patients with idiopathic pulmonary fibrosis: a systematic review and meta-analysis.European respiratory review : an official journal of the European Respiratory Society · 2020
    Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Article
  12. Article
  13. Review
  14. Article
  15. Progressive pulmonary fibrosis: the importance of identification and intervention.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  16. Article
  17. Article
  18. Observational
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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

26 authors.

Michael KreuterCenter for interstitial and rare lung diseases, Thoraxklinik, University of Heidelberg, Röntgenstr 1, D-69126, Heidelberg, Germany. kreuter@uni-heidelberg.de.
Jeff SwigrisInterstitial Lung Disease Program, National Jewish Health, Denver, CO, USA.
David PittrowInstitut für Klinische Pharmakologie, Medizinische Fakultät, Technische Universität Dresden, Dresden, Germany.
Silke GeierDepartment Market Access, Boehringer Ingelheim, Ingelheim am Rhein, Germany.
Jens KlotscheEpidemiologie, Deutsches Rheuma-Forschungsinstitut, Berlin, Germany.
Antje PrasseKlinik für Pneumologie, Medizinische Hochschule Hannover, Hannover, Germany.
Hubert WirtzAbteilung für Pneumologie, Department Innere Medizin, Neurologie und Dermatologie, Universitätsklinikum Leipzig AöR, Leipzig, Germany.
Dirk KoschelZentrum für Pneumologie und Bereich Pneumologie, Fachkrankenhaus Coswig und Uniklinikum Dresden, Coswig, Germany.
Stefan AndreasLungenfachklinik Immenhausen and Universitätsmedizin Göttingen, Kardiologie und Pneumologie, Göttingen, Germany.
Martin ClaussenLungen Clinic Grosshansdorf, Grosshansdorf, Germany.
Christian GrohéKlinik für Pneumologie - ELK, Berlin Buch, Berlin, Germany.
Henrike WilkensKlinik für Innere Medizin V, Pneumologie, Universitätsklinikum Universitätskliniken des Saarlandes, Homburg, Germany.
Lars HagmeyerKrankenhaus Bethanien, Solingen, Germany.
Dirk SkowaschMedizinische Klinik und Poliklinik II, Universitätsklinikum Bonn, Bonn, Germany.
Joachim F MeyerLungenzentrum München, LZM Bogenhausen-Harlaching, Städtisches Klinikum München GmbH, Munich, Germany.
Joachim KirschnerCenter for Internal Medical Studies CIMS, Bamberg, Germany.
Sven GläserKlinik und Poliklinik für Innere Medizin B, Forschungsbereich Pneumologie und Pneumologische Epidemiologie, Universitätsmedizin Greifswald, Greifswald, Germany.
Nicolas KahnCenter for interstitial and rare lung diseases, Thoraxklinik, University of Heidelberg, Röntgenstr 1, D-69126, Heidelberg, Germany.
Tobias WelteKlinik für Pneumologie, Medizinische Hochschule Hannover, Hannover, Germany.
Claus NeurohrMedizinische Klinik und Poliklinik V, Klinikum der LMU, Munich, Germany.
Martin SchwaiblmairMedizinische Klinik, Klinikum Augsburg, Augsburg, Germany.
Matthias HeldKlinikum Würzburg Mitte, Standort Missioklinik, Abteilung Innere Medizin, Pneumologie, Würzburg, Germany.
Thomas BahmerLungen Clinic Grosshansdorf, Grosshansdorf, Germany.
Tim OquekaUniversitätsklinikum Hamburg, Hamburg, Germany.
Marion FrankenbergerMedizinische Klinik und Poliklinik V, Klinikum der LMU, Munich, Germany.
Jürgen BehrMedizinische Klinik und Poliklinik V, Klinikum der LMU, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundQuality of life (QoL) is profoundly impaired in patients with idiopathic pulmonary fibrosis (IPF). However, data is limited regarding the course of QoL. We therefore analysed longitudinal data from the German INSIGHTS-IPF registry.

methodsClinical status and QoL were assessed at enrollment and subsequently at 6- to 12-months intervals. A range of different QoL questionnaires including the St. George's Respiratory Questionnaire (SGRQ) were used.

resultsData from 424 patients were included; 76.9% male; mean age 68.7 ± 9.1 years, mean FVC% predicted 75.9 ± 19.4, mean DL

conclusionsQoL assessments in the INSIGHTS-IPF registry demonstrate a close relationship between QoL and clinically meaningful changes in lung function, comorbidities, disease duration and clinical course of IPF, including hospitalisation and mortality.

Indexed as

Disease ProgressionRegistriesAgedCohort StudiesDatabases, FactualFemaleHumansIdiopathic Pulmonary FibrosisLongitudinal StudiesMaleMiddle AgedQuality of LifeTime FactorsVital CapacityCohort studyIdiopathic pulmonary fibrosisPatient-related outcomesSQRQ

Identifiers

PMID30876420
PMCPMC6420774

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.