Evidence map›Paper›PMID 8787430›Full record

Trial reportArchives of disease in childhood1996

Alteration of lung diffusion capacity in IgA nephropathy.

S Ravilly, M Chaussain, J L Iniguez, A Lenhert, G Kalifa, P Brun, P Niaudet, D Gendrel

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Archives of disease in childhood, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 85% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

S RavillyDepartment of Paediatrics, Hôpital Saint Vincent de Paul, Paris, France.
M Chaussain
J L Iniguez
A Lenhert
G Kalifa
P Brun
P Niaudet
D Gendrel
Hôpital Saint-Vincent-de-Paul · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo establish whether changes of lung transfer for carbon monoxide (TLCO) are related to the phase of IgA nephropathy.

methodsRespiratory function was tested in 12 children with IgA nephropathy assessed by percutaneous renal biopsy. This was done during acute exacerbations or haematuria-free phases of the disease.

resultsTLCO was low in 12/13 measurements made in the haematuric phase of IgA nephropathy or during the month following gross haematuria (mean TLCO 64% of expected values). Lung volumes and blood gas values were normal and only minor radiological signs of interstial lung involvement were observed in 11/12 patients. When respiratory tests were performed more than three months after gross haematuria, TLCO was low in 4/9 patients, with no relation to the significance of residual proteinuria or severity of findings at renal biopsy. There was a significant difference between tests performed when haematuria was present or recent and those performed more than three months after an episode of gross haematuria (p < 0.01).

conclusionsThe decrease of TLCO in the acute phases of the disease is probably related to alterations of the lung alveolarcapillary membrane by immune complexes containing IgA. This non-invasive technique, easy to perform and repeat, could be of value in the diagnosis of IgA nephropathy in haematuric children.

Indexed as

Acute DiseaseAdolescentCarbon MonoxideChildChild, PreschoolFemaleFunctional Residual CapacityGlomerulonephritis, IGAHematuriaHumansLungMaleProspective StudiesCarbon Monoxide

Identifiers

PMID8787430
PMCPMC1511411
OpenAlexW2099831017

What OpenQuestion holds

Textmetadata
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Registered trials

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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.