Evidence map›Paper›PMID 42166414›Full record

ArticleRespiration; international review of thoracic diseases2026

Usefulness of the S

Zubair Owadally, Mathilde Guillemot, Romain Barthes, Dan Adler, Jean-Christian Borel, Marius Lebret, Mehdi Rahim, Joëlle Texereau, Sandrine Pontier

Abstract read
In one paragraph

Article in Respiration; international review of thoracic diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Zubair OwadallyDepartment of Respiratory and Allergic Diseases, Toulouse University Hospital, Toulouse, France.
Mathilde GuillemotAir Liquide R&D, Innovation Campus Paris, Loges-en-Josas, France.
Romain BarthesDepartment of Respiratory and Allergic Diseases, Toulouse University Hospital, Toulouse, France.
Dan AdlerDivision of Lung Diseases, Hôpital de la Tour, Geneva, Switzerland.
Jean-Christian BorelHenri Bazire Respiratory Centre, La Sûre en Chartreuse, France.
Marius LebretMed2Lab Laboratory - Air Liquide Medical Systems, Antony, France.
Mehdi RahimAir Liquide R&D, Innovation Campus Paris, Loges-en-Josas, France.
Joëlle TexereauAir Liquide Healthcare, Bagneux, France.
Sandrine PontierDepartment of Respiratory and Allergic Diseases, Toulouse University Hospital, Toulouse, France, pontier.s@chu-toulouse.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOptimal management of long-term home noninvasive ventilation (NIV) therapy is not clearly defined. This study determined whether patient experience of disease and NIV therapy (S3-NIV score) in the first month was associated with successful NIV delivery and termination rate at 6 months.

methodsParticipants were adults starting home nocturnal NIV for chronic respiratory failure in 2019-2022, who used telemonitoring, completed ≥1 S3-NIV questionnaire in the first month of NIV, and were followed by the same home service provider. As no S3-NIV score thresholds are defined, participants were grouped by S3-NIV score quartiles (Q) (Q1 = most negative impact of symptoms/NIV; Q4 = lowest impact of disease/treatment). Factors associated with successful NIV delivery at 6 months were determined using multivariate logistic regression analysis.

resultsOne hundred fifty-three patients were included (mean age 65.9 ± 12.9 years, 60% male). The proportion of patients with successful NIV delivery at 6 months increased as initial S3-NIV score increased: Q1 42%, Q2 60%, Q3 63%, and Q4 63% (p = 0.007). Individuals with lower S3-NIV scores had more home interventions and mask changes during follow-up, regardless of whether NIV was successful or not. Termination rate was higher in S3-NIV score Q1 versus Q4 (29% vs. 11%). The probability of successful NIV delivery at 6 months increased by 1.14-fold for each 1-point increase in the initial S3-NIV score, independent of the association between the score and NIV data at 1 month.

conclusionThe S3-NIV questionnaire helped identify patients at higher risk of therapy termination more effectively than relying only on objective ventilator data.

Indexed as

Chronic respiratory failureHome service providerNoninvasive ventilationPatient-reported outcomesTelemonitoring

Identifiers

PMID42166414
PMCPMC13421290

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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.