Evidence map›Paper›PMID 25622967›Full record

ArticleJournal of translational medicine2015

Postconditioning in major vascular surgery: prevention of renal failure.

Peter Aranyi, Zsolt Turoczi, David Garbaisz, Gabor Lotz, Janos Geleji, Viktor Hegedus, Zoltan Rakonczay, Zsolt Balla, Laszlo Harsanyi, Attila Szijarto

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2015. 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
0.4field-weighted citation impact, top 33% 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, 2 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

10 authors at 3 institutions in 1 country.

Peter Aranyi1st Department of Surgery, Semmelweis University, Budapest, Hungary. aranyi.p@gmail.com.
Zsolt Turoczi1st Department of Surgery, Semmelweis University, Budapest, Hungary. zsturoczi@gmail.com.
David Garbaisz1st Department of Surgery, Semmelweis University, Budapest, Hungary. garbaiszdavid@t-online.hu.
Gabor Lotz2nd Department of Pathology, Semmelweis University, Budapest, Hungary. lotz.gabor@med.semmelweis-univ.hu.
Janos GelejiEötvös Loránd University, Faculty of Science, Institute of Mathematics, Budapest, Hungary. janos@geleji.hu.
Viktor Hegedus1st Department of Surgery, Semmelweis University, Budapest, Hungary. viktolhegedus@gmail.com.
Zoltan RakonczayFirst Department of Internal Medicine, University of Szeged, Szeged, Hungary. zrakonczay@gmail.com.
Zsolt BallaFirst Department of Internal Medicine, University of Szeged, Szeged, Hungary. ballatanar@gmail.com.
Laszlo Harsanyi1st Department of Surgery, Semmelweis University, Budapest, Hungary. harsanyi.laszlo@med.semmelweis-univ.hu.
Attila Szijarto1st Department of Surgery, Semmelweis University, Budapest, Hungary. szijartoattila@gmail.com.
Semmelweis University · HUUniversity of Szeged · HUEötvös Loránd University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPostconditioning is a novel reperfusion technique to reduce ischemia-reperfusion injuries. The aim of the study was to investigate this method in an animal model of lower limb revascularization for purpose of preventing postoperative renal failure.

methodsBilateral lower limb ischemia was induced in male Wistar rats for 3 hours by infrarenal aorta clamping under narcosis. Revascularization was allowed by declamping the aorta. Postconditioning (additional 10 sec reocclusion, 10 sec reperfusion in 6 cycles) was induced at the onset of revascularization. Myocyte injury and renal function changes were assessed 4, 24 and 72 hours postoperatively. Hemodynamic monitoring was performed by invasive arterial blood pressure registering and a kidney surface laser Doppler flowmeter.

resultsMuscle viability studies showed no significant improvement with the use of postconditioning in terms of ischemic rhabdomyolysis (4 h: ischemia-reperfusion (IR) group: 42.93 ± 19.20% vs. postconditioned (PostC) group: 43.27 ± 27.13%). At the same time, renal functional laboratory tests and kidney myoglobin immunohistochemistry demonstrated significantly less expressed kidney injury in postconditioned animals (renal failure index: 4 h: IR: 2.37 ± 1.43 mM vs. PostC: 0.92 ± 0.32 mM; 24 h: IR: 1.53 ± 0.45 mM vs. PostC: 0.77 ± 0.34 mM; 72 h: IR: 1.51 ± 0.36 mM vs. PostC: 0.43 ± 0.28 mM), while systemic hemodynamics and kidney microcirculation significantly improved (calculated reperfusion area: IR: 82.31 ± 12.23% vs. PostC: 99.01 ± 2.76%), and arterial blood gas analysis showed a lesser extent systemic acidic load after revascularization (a defined relative base excess parameter: 1(st) s: IR: 2.25 ± 1.14 vs. PostC: 1.80 ± 0.66; 2(nd) s: IR: 2.14 ± 1.44 vs. PostC: 2.44 ± 1.14, 3(rd) s: IR: 3.99 ± 3.09 vs. PostC: 2.07 ± 0.82; 4(th) s: IR: 3.28 ± 0.32 vs. PostC: 2.05 ± 0.56).

conclusionsThe results suggest a protective role for postconditioning in major vascular surgeries against renal complications through a possible alternative release of nephrotoxic agents and exerting a positive effect on hemodynamic stability.

Indexed as

Ischemic PostconditioningAnimalsHemodynamicsHSP72 Heat-Shock ProteinsImmunohistochemistryKidney CortexKidney Function TestsLaser-Doppler FlowmetryLipid PeroxidationLower ExtremityMaleMicrocirculationMusclesMyoglobinRats, WistarRenal InsufficiencyHSP72 Heat-Shock ProteinsMyoglobin

Identifiers

PMID25622967
PMCPMC4314807
OpenAlexW2138465585

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.