Evidence map›Paper›PMID 32093612›Full record

ArticleBMC infectious diseases2020

Late viral or bacterial respiratory infections in lung transplanted patients: impact on respiratory function.

Marie Dubert, Benoit Visseaux, André Birgy, Pierre Mordant, Anne-Cécile Metivier, Gaelle Dauriat, Nadhira Fidouh, Yazdan Yazdanpanah, Nathalie Grall, Yves Castier and 3 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

13 authors.

Marie DubertAP-HP, Hôpital Bichat, Service de maladies infectieuses et tropicales, 46 Rue Henri Huchard, F-75018, Paris, France. marie.dubert@aphp.fr.
Benoit VisseauxINSERM, IAME, UMR 1137, F-75018, Paris, France.
André BirgyINSERM, IAME, UMR 1137, F-75018, Paris, France.
Pierre MordantAP-HP, Hôpital Bichat, Service de chirurgie thoracique, F-75018, Paris, France.
Anne-Cécile MetivierAP-HP, Hôpital Bichat, Service de pneumologie, F-75018, Paris, France.
Gaelle DauriatAP-HP, Hôpital Bichat, Service de pneumologie, F-75018, Paris, France.
Nadhira FidouhAP-HP, Hôpital Bichat, Laboratoire de virologie, F-75018, Paris, France.
Yazdan YazdanpanahAP-HP, Hôpital Bichat, Service de maladies infectieuses et tropicales, 46 Rue Henri Huchard, F-75018, Paris, France.
Nathalie GrallINSERM, IAME, UMR 1137, F-75018, Paris, France.
Yves CastierAP-HP, Hôpital Bichat, Service de chirurgie thoracique, F-75018, Paris, France.
Hervé MalAP-HP, Hôpital Bichat, Service de pneumologie, F-75018, Paris, France.
Gabriel ThabutAP-HP, Hôpital Bichat, Service de pneumologie, F-75018, Paris, France.
François-Xavier LescureAP-HP, Hôpital Bichat, Service de maladies infectieuses et tropicales, 46 Rue Henri Huchard, F-75018, Paris, France. xavier.lescure@aphp.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRespiratory infections are a major threat for lung recipients. We aimed to compare with a monocentric study the impact of late viral and bacterial respiratory infections on the graft function.

methodsPatients, who survived 6 months or more following lung transplantation that took place between 2009 and 2014, were classified into three groups: a viral infection group (VIG) (without any respiratory bacteria), a bacterial infection group (BIG) (with or without any respiratory viruses), and a control group (CG) (no documented infection). Chronic lung allograft dysfunction (CLAD) and acute rejection were analysed 6 months after the inclusion in the study.

resultsAmong 99 included lung recipients, 57 (58%) had at least one positive virological respiratory sample during the study period. Patients were classified as follows: 38 in the VIG, 25 in the BIG (among which 19 co-infections with a virus) and 36 in the CG. The BIG presented a higher initial deterioration in lung function (p = 0.05) than the VIG. But 6 months after the infection, only the VIG presented a median decrease of forced expiratory volume in 1 s; - 35 mL (IQR; - 340; + 80) in the VIG, + 140 mL (+ 60;+ 330) in the BIG and + 10 (- 84;+ 160) in the CG, p < 0.01. Acute rejection was more frequent in the VIG (n = 12 (32%)), than the BIG (n = 6 (24%)) and CG (n = 3 (8%)), p < 0.05, despite presenting no more CLAD (p = 0.21).

conclusionsDespite a less severe initial presentation, single viral respiratory infections seem to lead to a greater deterioration in lung function, and to more acute rejection, than bacterial infections.

Indexed as

Lung TransplantationBacterial InfectionsFemaleForced Expiratory VolumeGraft RejectionHumansLungMaleMiddle AgedPicornaviridaePseudomonas aeruginosaRespiratory Tract InfectionsVirus DiseasesBacterial respiratory infectionChronic lung allograft dysfunctionLung graft acute rejectionLung graft patientsViral respiratory infections

Identifiers

PMID32093612
PMCPMC7041086

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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.