Evidence map›Paper›PMID 37855751›Full record

ArticleBJS open2023

Histology and transcriptome insights into the early processes of intestinal anastomotic healing: a rat model.

Claire P M van Helsdingen, Aurelia C L Wildeboer, Konstantina Zafeiropoulou, Audrey C H M Jongen, Joanna W A M Bosmans, Camille Gallé, Theodorus B M Hakvoort, Marion J J Gijbels, Wouter J de Jonge, Nicole D Bouvy and 2 more

Open access · goldAbstract read
In one paragraph

Article in BJS open, 2023. 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
1.8field-weighted citation impact, top 13% 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, 8 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Claire P M van HelsdingenEmma Children's Hospital, Amsterdam UMC, location University of Amsterdam, Paediatric Surgery, Amsterdam, The Netherlands.ORCID 0000-0001-6508-0214
Aurelia C L WildeboerEmma Children's Hospital, Amsterdam UMC, location University of Amsterdam, Paediatric Surgery, Amsterdam, The Netherlands.ORCID 0000-0002-9056-6838
Konstantina ZafeiropoulouEmma Children's Hospital, Amsterdam UMC, location University of Amsterdam, Paediatric Surgery, Amsterdam, The Netherlands.
Audrey C H M JongenDepartment of Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.
Joanna W A M BosmansDepartment of Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.
Camille GalléDepartment of General Surgery, Maastricht University, Maastricht, The Netherlands.
Theodorus B M HakvoortAmsterdan UMC, location University of Amsterdam, Tytgat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands.
Marion J J GijbelsDepartment of Pathology, Maastricht University Medical Center, Maastricht, The Netherlands.ORCID 0000-0002-4906-0384
Wouter J de JongeAmsterdan UMC, location University of Amsterdam, Tytgat Institute for Liver and Intestinal Research, Amsterdam, The Netherlands.
Nicole D BouvyDepartment of Surgery, Maastricht University Medical Center, Maastricht, The Netherlands.
Andrew Y F Li YimEmma Children's Hospital, Amsterdam UMC, location University of Amsterdam, Paediatric Surgery, Amsterdam, The Netherlands.ORCID 0000-0002-0754-0953
Joep P M DerikxEmma Children's Hospital, Amsterdam UMC, location University of Amsterdam, Paediatric Surgery, Amsterdam, The Netherlands.
Maastricht University · NLEmma Kinderziekenhuis · NLUniversity of Amsterdam · NLUniversity of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnderstanding the early processes underlying intestinal anastomotic healing is crucial to comprehend the pathophysiology of anastomotic leakage. The aim of this study was to assess normal intestinal anastomotic healing and disturbed healing in rats to investigate morphological, cellular and intrinsic molecular changes in the anastomotic tissue.

methodAnastomoses were created in two groups of Wistar rats, using four sutures or 12 sutures to mimic anastomotic leakage and anastomotic healing respectively. At 6, 12, 24 hours and 2, 3, 5 and 7 days, anastomotic tissue was assessed macroscopically using the anastomotic complication score and histologically using the modified Ehrlich-Hunt score. Transcriptome analysis was performed to assess differences between anastomotic leakage and anastomotic healing at the first three time points to find affected genes and biological processes.

resultsNinety-eight rats were operated on (49 animals in the anastomotic leakage and 49 in the anastomotic healing group) and seven rats analysed at each time point. None of the animals with 12 sutures developed anastomotic leakage macroscopically, whereas 35 of the 49 animals with four sutures developed anastomotic leakage. Histological analysis showed increasing influx of inflammatory cells up to 3 days in anastomotic healing and up to 7 days in anastomotic leakage, and this increase was significantly higher in anastomotic leakage at 5 (P = 0.041) and 7 days (P = 0.003). Transcriptome analyses revealed large differences between anastomotic leakage and anastomotic healing at 6 and 24 hours, mainly driven by an overall downregulation of genes in anastomotic leakage.

conclusionTranscriptomic analyses revealed large differences between normal and disturbed healing at 6 hours after surgery, which might eventually serve as early-onset biomarkers for anastomotic leakage.

Indexed as

Anastomotic LeakTranscriptomeAnastomosis, SurgicalAnimalsHumansRatsRats, WistarWound Healing

Identifiers

PMID37855751
PMCPMC10586197
OpenAlexW4387764773

What OpenQuestion holds

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LicenceCC BY
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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.