Evidence map›Paper›PMID 27917877›Full record

ArticleScientific reports2016

Ascites' neutrophil function is significantly impaired in patients with decompensated cirrhosis but can be restored by autologous plasma incubation.

Cornelius Engelmann, Christina Becker, Andreas Boldt, Toni Herta, Albrecht Boehlig, Katrin Splith, Moritz Schmelzle, Niklas Mueller, Sandra Krohn, Hans-Michael Tautenhahn and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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  4. Review
  5. 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

13 authors at 2 institutions in 1 country.

Cornelius EngelmannUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Christina BeckerUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Andreas BoldtUniversity Hospital Leipzig; Institute of Clinical Immunology, Johannisalle 30, 04103 Leipzig, Germany.
Toni HertaUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Albrecht BoehligUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Katrin SplithCharité - Universitätsmedizin Berlin; Department for General, Visceral and Transplantation Surgery, Augustenburger Platz 1, 13353 Berlin, Germany.
Moritz SchmelzleCharité - Universitätsmedizin Berlin; Department for General, Visceral and Transplantation Surgery, Augustenburger Platz 1, 13353 Berlin, Germany.
Niklas MuellerUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Sandra KrohnUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
Hans-Michael TautenhahnUniversity Hospital of Leipzig; Department for General, Visceral and Transplantation Surgery, Liebigstrasse 20, 04103 Leipzig.
Michael BartelsUniversity Hospital of Leipzig; Department for General, Visceral and Transplantation Surgery, Liebigstrasse 20, 04103 Leipzig.
Ulrich SackUniversity Hospital Leipzig; Institute of Clinical Immunology, Johannisalle 30, 04103 Leipzig, Germany.
Thomas BergUniversity Hospital Leipzig; Section of Hepatology; Department of Internal Medicine, Neurology, Dermatology, Liebigstrasse 20, 04103 Leipzig, Germany.
University Hospital Leipzig · DEAuguste-Viktoria-Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic immune cell dysfunction is a typical feature of liver diseases and increases the risk of bacterial infection, especially spontaneous bacterial peritonitis. We evaluated functional properties of neutrophil granulocytes in blood and ascites of patients both with and without decompensated cirrhosis. We collected blood and ascites samples from 63 patients with cirrhosis and eight without cirrhosis. Phagocytosis activity (PA) and oxidative burst activity (OBA) were evaluated after ex vivo stimulation with E. coli, while fluorescence signals were measured by flow cytometry. Ascites' neutrophil function tests were repeated after incubation with autologous plasma. Ascites' neutrophils showed an impaired PA and OBA (median blood PA 98.1% (86.8-99.8) vs. ascites' PA 50.5% (0.4-97.3), p < 0.0001; median blood OBA 98.7% (27.5-100) vs. ascites' OBA 27.5% (0.3-96.7), p < 0.0001). Patients with non-cirrhotic ascites showed higher PA but equally suppressed OBA. Ascites' neutrophil function could be partially restored after incubation with autologous plasma (median increase PA: 22.5% (-49.7 - +93.2), p = 0.002; OBA: 22.8% (-10.4 - +48.8), p = 0.002). Ascites' neutrophils of patients with cirrhosis are functionally impaired, but could be partially restored after incubation with plasma. Further investigations are needed to identify the factors in ascites that are associated with neutrophils' function.

Indexed as

AgedAged, 80 and overBlood Transfusion, AutologousFemaleHumansLiver CirrhosisMaleMiddle AgedNeutrophilsPhagocytosisRespiratory Burst

Identifiers

PMID27917877
PMCPMC5137075
OpenAlexW2559749117

What OpenQuestion holds

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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.