Evidence map›Paper›PMID 9659357›Full record

ReviewThorax1998

New ideas on the pathophysiology and treatment of lung disease.

D F Rogers, G J Laurent

Abstract readReview
In one paragraph

Review in Thorax, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Novel drugs for treating asthma.Current allergy and asthma reports · 2001
    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

2 authors.

D F RogersNational Heart and Lung Institute, Imperial College, London, UK.
G J Laurent

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a continuing need for development of new treatments for lung disease. Basic scientific investigations are identifying novel targets for the development of new approaches to therapy of a range of respiratory conditions. Coupled with the advances in technology being harnessed by the pharmaceutical and biotechnological industries, there is now an impressive range of potential treatments including gene therapy, not just for cystic fibrosis but also for a range of inflammatory lung conditions, anti-cytokine and anti-adhesion molecule approaches, and targeting of intracellular signal transduction pathways including cyclic AMP metabolism, tyrosine kinases and MAP kinases. "Old" molecules such as heparin and secretory leukoprotease inhibitor (SLPI) are demonstrating new beneficial activities. Simple molecules such as nitric oxide (NO) gas may be involved in the pathophysiology of different airway conditions. It is an exciting time for respiratory science and a time for optimism for those seeking new approaches to the treatment of lung diseases.

Indexed as

AsthmaCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorGenetic TherapyHumansLungLung DiseasesProteinase Inhibitory Proteins, SecretoryProteinsPulmonary FibrosisSecretory Leukocyte Peptidase InhibitorSerine Proteinase InhibitorsCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorProteinase Inhibitory Proteins, SecretoryProteinsSecretory Leukocyte Peptidase InhibitorSerine Proteinase InhibitorsSLPI protein, human

Identifiers

PMID9659357
PMCPMC1745171

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.